United States et al. v. The Charlotte-Mecklenburg Hospital Authority, d/b/a Carolinas Healthcare System; Proposed Final Judgment and Competitive Impact Statement, 63674-63685 [2018-26755]
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Lisa Barton,
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[FR Doc. 2018–26740 Filed 12–10–18; 8:45 am]
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BILLING CODE 7020–02–P
DEPARTMENT OF JUSTICE
Antitrust Division
United States et al. v. The CharlotteMecklenburg Hospital Authority, d/b/a
Carolinas Healthcare System;
Proposed Final Judgment and
Competitive Impact Statement
Notice is hereby given pursuant to the
Antitrust Procedures and Penalties Act,
15 U.S.C. § 16(b)–(h), that a proposed
Final Judgment, Stipulation, and
Competitive Impact Statement have
been filed with the United States
District Court for the Western District of
North Carolina in United States and
State of North Carolina. v. The
Charlotte-Mecklenburg Hospital
Authority, d/b/a Carolinas HealthCare
System, Civil Action No. 3:16–cv–
00311–RJC–DCK. On June 6, 2016, the
United States and the State of North
Carolina filed a Complaint alleging that
The Charlotte-Mecklenburg Hospital
Authority formerly known as Carolinas
HealthCare System (or CHS) and now
doing business as Atrium Health
(‘‘Atrium’’) included provisions in its
contracts with health insurers that
restricted insurers from steering their
members to lower-cost, high-quality
providers, in violation of Section 1 of
the Sherman Act, 15 U.S.C. § 1. The
proposed Final Judgment, filed
November 15, 2018, enjoins Atrium
from (1) enforcing provisions in its
current insurer contracts that restrict
steering and transparency; (2) having
contract provisions with an insurer that
would prohibit, prevent or significantly
restrain the insurer from using certain
steering methods or providing
transparency; and (3) penalizing, or
threatening to penalize, any insurer for
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its use of certain steering methods and
transparency.
Copies of the Complaint, proposed
Final Judgment, and Competitive Impact
Statement are available for inspection
on the Antitrust Division’s website at
https://www.justice.gov/atr and at the
Office of the Clerk of the United States
District Court for the Western District of
North Carolina. Copies of these
materials may be obtained from the
Antitrust Division upon request and
payment of the copying fee set by
Department of Justice regulations.
Public comment is invited within 60
days of the date of this notice. Such
comments, including the name of the
submitter, and responses thereto, will be
posted on the Antitrust Division’s
website, filed with the Court, and, under
certain circumstances, published in the
Federal Register. Comments should be
directed to Peter J. Mucchetti, Chief,
Healthcare and Consumer Products
Section, Antitrust Division, Department
of Justice, 450 Fifth Street NW, Suite
4100, Washington, DC 20530
(telephone: 202–307–0001).
Patricia A. Brink,
Director of Civil Enforcement.
United States District Court for the Western
District of North Carolina Charlotte Division
United States of America and the State of
North Carolina, Plaintiffs, v. The CharlotteMecklenburg Hospital Authority, d/b/a
Carolinas Healthcare System, Defendant.
Case No. 3:16–cv–00311–RJC–DCK
Judge Robert J. Conrad, Jr.
COMPLAINT
The United States of America and the State
of North Carolina bring this civil antitrust
action to enjoin Defendant, The CharlotteMecklenburg Hospital Authority, d/b/a
Carolinas HealthCare System (‘‘CHS’’), from
using unlawful contract restrictions that
prohibit commercial health insurers in the
Charlotte area from offering patients financial
benefits to use less-expensive healthcare
services offered by CHS’s competitors. These
steering restrictions reduce competition
resulting in harm to Charlotte area
consumers, employers, and insurers.
I. CHS AND ITS UNLAWFUL STEERING
RESTRICTIONS
1. CHS is a North Carolina not-for-profit
corporation providing healthcare services
with its principal place of business in
Charlotte. Its flagship facility is Carolinas
Medical Center, a large general acute-care
hospital located in downtown Charlotte. It
also operates nine other general acute-care
hospitals in the Charlotte area.
2. CHS is the dominant hospital system in
the Charlotte area, with approximately a 50
percent share of the relevant market, and
2014 revenue of approximately $8.7 billion.
Its closest competitor by size is Novant,
which owns five general acute care hospitals
in the Charlotte area and has less than half
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of CHS’s revenue. After Novant, the nextlargest hospital in the Charlotte area is
CaroMont Regional Medical Center, which
has less than one tenth of CHS’s revenue.
3. CHS exerts market power in its dealings
with commercial health insurers (‘‘insurers’’).
CHS’s market power results from its large
size, the comprehensive range of healthcare
services that it offers, its high market share,
and insurers’ need to include access to CHS’s
hospitals–as well as its other facilities and
providers–in at least some of their provider
networks in insurance plans that cover
people in the Charlotte area. CHS’s market
power is further evidenced by its ability to
profitably charge prices to insurers that are
higher than competitive levels across a range
of services, and to impose on insurers
restrictions that reduce competition.
4. CHS’s market power has enabled it to
negotiate high prices (in the form of high
‘‘reimbursement rates’’) for treating insured
patients. CHS has long had a reputation for
being a high-priced healthcare provider. In a
2013 presentation, CHS’s internal strategy
group recognized that CHS ‘‘has enjoyed
years of annual reimbursement rate increases
that are premium to the market, with those
increases being applied to rates that are also
premium to the market.’’
5. Steering is a method by which insurers
offer consumers of healthcare services
options to reduce some of their healthcare
expenses. Steering typically occurs when an
insurer offers consumers a financial incentive
to use a lower-cost provider or lower-cost
provider network, in order to lower their
healthcare expenses.
6. Steering–and the competition from
lower-priced healthcare providers that
steering animates–threatens CHS’s high
prices and revenues. In 2013, CHS’s internal
strategy group surveyed a dozen of CHS’s
senior leaders, asking them to list the
‘‘biggest risks to CHS revenue streams.’’ Nine
of the twelve leaders polled identified the
steering of patients away from CHS as one of
the biggest risks to CHS’s revenues.
7. To protect itself against steering that
would induce price competition and
potentially require CHS to lower its high
prices, CHS has imposed steering restrictions
in its contracts with insurers. These
restrictions impede insurers from providing
financial incentives to patients to encourage
them to consider utilizing lower-cost but
comparable or higher-quality alternative
healthcare providers.
8. Tiered networks are a popular type of
steering that insurers use in healthcare
markets. Typically, insurers using tiered
networks place healthcare providers that
offer better value healthcare services (lower
cost, higher quality) in top tiers. Patients who
use top-tier providers pay lower out-ofpocket costs. For example, for a procedure
costing $10,000, a patient might be
responsible for paying $3,600 in coinsurance
at a lower-tier hospital, but only $1,800
coinsurance to have the same procedure
performed at a top-tier hospital.
9. Narrow-network insurance plans are
another popular steering tool. Typically,
narrow networks consist of a subset of all the
healthcare providers that participate in an
insurer’s conventional network. A consumer
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who chooses a narrow-network insurance
plan typically pays lower premiums, and
lower out-of-pocket expenses than a
conventional broad-network insurance plan
as long as the consumer is willing to choose
from the smaller network of providers for his
or her healthcare needs.
10. Providers are motivated to have
insurers steer towards them, including
through an insurer’s narrow or tiered
network, because of the increased patient
volume that accompanies steering. Thus, the
ability of insurers to steer gives providers a
powerful incentive to be as efficient as
possible, maintain low prices, and offer high
quality and innovative services. By doing so,
providers induce insurers to steer patient
volume to them. Individuals and employers
that provide health insurance to their
employees benefit tremendously from this
because they can lower their healthcare
expenses.
11. CHS has gained patient volume from
insurers steering towards CHS, and has
obtained higher revenues as a result. CHS
encourages insurers to steer patients toward
itself by offering health insurers modest
concessions on its market-power driven,
premium prices.
12. However, CHS forbids insurers from
allowing CHS’s competitors to do the same.
CHS prevents insurers from offering tiered
networks that feature hospitals that compete
with CHS in the top tiers, and prevents
insurers from offering narrow networks that
include only CHS’s competitors. By
restricting its competitors from competing
for–and benefitting from–steered
arrangements, CHS uses its market power to
impede insurers from negotiating lower
prices with its competitors and offering
lower-premium plans.
13. CHS also imposes restrictions in its
contracts with insurers that impede insurers
from providing truthful information to
consumers about the value (cost and quality)
of CHS’s healthcare services compared to
CHS’s competitors. CHS’s restrictions on
insurers’ price and quality transparency are
an indirect restriction on steering, because
they prevent patients from accessing
information that would allow them to make
healthcare choices based on available price
and quality information.
14. Because CHS’s steering restrictions
prevent its competitors from attracting more
patients through lower prices, CHS’s
competitors have less incentive to remain
lower priced and to continue to become more
efficient. As a result, CHS’s restrictions
reduce the competition that CHS faces in the
marketplace. In the instances in which
insurers have steered in other markets and in
the few instances in which insurers have
steered in the Charlotte area despite CHS’s
restrictions, insurers have reduced health
insurance costs for consumers.
15. Four insurers provide coverage to more
than 85 percent of the commerically-insured
residents of the Charlotte area. They are:
Aetna Health of the Carolinas, Inc., Blue
Cross Blue Shield of North Carolina, Cigna
Healthcare of North Carolina, Inc., and
United Healthcare of North Carolina, Inc.
16. CHS maintains and enforces steering
restrictions in its contracts with all four of
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these insurers. In some instances, the
contract language prohibits steering outright.
For example, CHS secured a contractual
obligation from one insurer that it ‘‘shall not
directly or indirectly steer business away
from’’ CHS. In other instances, the contract
language gives CHS the right to terminate its
agreement with the insurer if the insurer
engages in steering, providing CHS the ability
to deny the insurer and its enrollees access
to its dominant hospital system unless the
steering ends. Although the contractual
language that CHS has imposed varies with
each insurer, it consistently creates
disincentives that deter insurers from
providing to their enrollees truthful
information about their healthcare options
and the benefits of price and quality
competition among healthcare providers that
the insurers could offer if they had full
freedom to steer.
II. RELEVANT MARKET AND
COMPETITIVE EFFECTS
17. The sale of general acute care inpatient
hospital services to insurers (‘‘acute inpatient
hospital services’’) is a relevant product
market. The market includes sales of such
services to insurers’ individual, group, fullyinsured and self-funded health plans.
18. The relevant market does not include
sales of acute inpatient hospital services to
government payers, e.g., Medicare (covering
the elderly and disabled), Medicaid (covering
low-income persons), and TRICARE
(covering military personnel and families)
because a healthcare provider’s negotiations
with an insurer are separate from the process
used to determine the rates paid by
government payers.
19. Acute inpatient hospital services
consist of a broad group of medical and
surgical diagnostic and treatment services
that include a patient’s overnight stay in the
hospital. Although individual acute inpatient
hospital services are not substitutes for each
other (e.g., obstetrics is not a substitute for
cardiac services), insurers typically contract
for the various individual acute inpatient
hospital services as a bundle, and CHS’s
steering restrictions have an adverse impact
on the sale of all acute inpatient hospital
services. Therefore, acute inpatient hospital
services can be aggregated for analytical
convenience.
20. There are no reasonable substitutes or
alternatives to acute inpatient hospital
services. Consequently, a hypothetical
monopolist of acute inpatient hospital
services would likely profitably impose a
small but significant price increase for those
services over a sustained period of time.
21. The relevant geographic market is no
larger than the Charlotte area. In this
Complaint, the Charlotte area means the
Charlotte Combined Statistical Area, as
defined by the U.S. Office of Management
and Budget, which consists of Cabarrus,
Cleveland, Gaston, Iredell, Lincoln,
Mecklenburg, Rowan, Stanly, and Union
counties in North Carolina, and Chester,
Lancaster, and York counties in South
Carolina. The Charlotte area has a population
of about 2.6 million people.
22. Insurers contract to purchase acute
inpatient hospital services from hospitals
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within the geographic area where their
enrollees are likely to seek medical care.
Such hospitals are typically close to their
enrollees’ homes or workplaces. Insurers who
seek to sell insurance plans to individuals
and employers in the Charlotte area must
include Charlotte area hospitals in their
provider networks because people who live
and work in the Charlotte area strongly prefer
to obtain acute inpatient hospital services in
the Charlotte area. Charlotte area consumers
have little or no willingness to enroll in an
insurance plan that provides no network
access to hospitals located in the Charlotte
area.
23. For these reasons, it is not a viable
alternative for insurers that sell health
insurance plans to consumers in the
Charlotte area to purchase acute inpatient
hospital services from providers outside the
Charlotte area. Consequently, competition
from providers of acute inpatient hospital
services located outside the Charlotte area
would not likely be sufficient to prevent a
hypothetical monopolist provider of acute
inpatient hospital services located in the
Charlotte area from profitably imposing small
but significant price increases for those
services over a sustained period of time.
24. An insurer selling health insurance
plans to individuals and employers in the
Charlotte area must have CHS as a
participant in at least some of its provider
networks, in order to have a viable health
insurance business in the Charlotte area. This
gives CHS the ability to impose steering
restrictions in its contracts with insurers.
When CHS negotiates with insurers for CHS’s
network participation, CHS typically
negotiates the prices and terms of
participation for acute inpatient hospital
services and other healthcare services, such
as outpatient, ancillary, and physician
services, at the same time, including services
that are located outside the Charlotte area. As
a result, CHS’s anticompetitive steering
restrictions typically apply to all the
negotiated services.
25. CHS’s maintenance and enforcement of
its steering restrictions lessen competition
between CHS and the other providers of
acute inpatient hospital services in the
Charlotte area that would, in the absence of
the restrictions, likely reduce the prices paid
for such services by insurers. Thus, the
restrictions help to insulate CHS from
competition, by limiting the ability of CHS’s
competitors to win more commerciallyinsured business by offering lower prices.
26. Insurers want to steer towards lowercost providers and to offer innovative
insurance plans that steer. For years, insurers
have tried to negotiate the removal of steering
restrictions from their contracts with CHS,
but cannot because of CHS’s market power.
In the absence of the steering restrictions,
insurers would likely steer consumers to
lower-cost providers more than their current
contracts with CHS presently permit.
27. As a result of this reduced competition
due to CHS’s steering restrictions,
individuals and employers in the Charlotte
area pay higher prices for health insurance
coverage, have fewer insurance plans from
which to choose, and are denied access to
consumer comparison shopping and other
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cost-saving innovative and more efficient
health plans that would be possible if
insurers could steer freely. Deprived of the
option to benefit from choosing more costefficient providers, Charlotte area patients
incur higher out-of-pocket costs for their
healthcare. Insurers are directly harmed by
CHS’s imposition of steering restrictions.
28. CHS restricts steering to help insulate
itself from price competition, which enables
CHS to maintain high prices and preserve its
dominant position, and not for any
procompetitive purpose. Indeed, when asked
under oath whether CHS should limit the
ability of insurers to offer tiered networks or
narrow networks that exclude CHS, Carol
Lovin, CHS’s Chief Strategy Officer, said that
CHS should not. And when asked her view
about the possibility of eliminating CHS’s
steering restrictions, she testified, ‘‘Would I
personally be okay with getting rid of them?
Yes, I would.’’ CHS’s steering restrictions do
not have any procompetitive effects. CHS can
seek to avoid losses of revenues and market
share from lower cost competitors by
competing to offer lower prices and better
value than its competitors, rather than
imposing rules on insurers that reduce the
benefit to its rivals from competing on price.
III. JURISDICTION, VENUE AND
INTERSTATE COMMERCE
29. The Court has subject-matter
jurisdiction over this action under Section 4
of the Sherman Act, 15 U.S.C. § 4 (as to the
claim by the United States); Section 16 of the
Clayton Act, 15 U.S.C. § 26 (as to the claim
by the State of North Carolina); and 28 U.S.C.
§§ 1331, 1337(a), and 1345.
30. The Court has personal jurisdiction
over CHS under Section 12 of the Clayton
Act, 15 U.S.C. § 22. CHS maintains its
principal place of business and transacts
business in this District.
31. Venue is proper under 28 U.S.C. § 1391
and Section 12 of the Clayton Act, 15 U.S.C.
§ 22. CHS transacts business and resides in
this District and the events giving rise to the
claims occurred in this District.
32. CHS engages in interstate commerce
and in activities substantially affecting
interstate commerce. CHS provides
healthcare services for which employers,
insurers, and individual patients remit
payments across state lines. CHS also
purchases supplies and equipment that are
shipped across state lines, and it otherwise
participates in interstate commerce.
IV. CHS’S VIOLATION OF SECTION 1 OF
THE SHERMAN ACT
33. Plaintiffs incorporate paragraphs 1
through 32 of this Complaint.
34. CHS has market power in the sale of
acute inpatient hospital services in the
Charlotte area.
35. CHS has and likely will continue to
negotiate and enforce contracts containing
steering restrictions with insurers in the
Charlotte area. The contracts containing the
steering restrictions are contracts,
combinations, and conspiracies within the
meaning of Section 1 of the Sherman Act, 15
U.S.C. § 1.
36. These steering restrictions have had,
and will likely to continue to have, the
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following substantial anticompetitive effects
in the relevant product and geographic
market, among others:
a. protecting CHS’s market power and
enabling CHS to maintain at
supracompetitive levels the prices of acute
inpatient hospital services;
b. substantially lessening competition
among providers in their sale of acute
inpatient hospital services;
c. restricting the introduction of innovative
insurance products that are designed to
achieve lower prices and improved quality
for acute inpatient hospital services;
d. reducing consumers’ incentives to seek
acute inpatient hospital services from more
cost-effective providers; and
e. depriving insurers and their enrollees of
the benefits of a competitive market for their
purchase of acute inpatient hospital services.
37. Entry or expansion by other hospitals
in the Charlotte area has not counteracted the
actual and likely competitive harms resulting
from CHS’s steering restrictions. And in the
future, such entry or expansion is unlikely to
be rapid enough and sufficient in scope and
scale to counteract these harms to
competition. Building a hospital with a
strong reputation that is capable of attracting
physicians and patients is difficult, timeconsuming, and expensive. Additionally,
new facilities and programs, and typically
the expansion of existing facilities and
programs, are subject to lengthy licensing
requirements, and in North Carolina, to
certificate-of-need laws.
38. CHS did not devise its strategy of using
steering restrictions for any procompetitive
purpose. Nor do the steering restrictions have
any procompetitive effects. Any arguable
benefits of CHS’s steering restrictions are
outweighed by their actual and likely
anticompetitive effects.
39. The challenged steering restrictions
unreasonably restrain trade in violation of
Section 1 of the Sherman Act, 15 U.S.C. § 1.
V. REQUEST FOR RELIEF
40. The United States and the State of
North Carolina request that the Court:
a. adjudge that all of the steering
restrictions in the contracts between CHS and
any insurer violate Section 1 of the Sherman
Act, 15 U.S.C. § 1;
b. enjoin CHS, its officers, directors, agents,
employees, and successors, and all other
persons acting or claiming to act on its
behalf, directly or indirectly, from seeking,
agreeing to, or enforcing any provision in any
agreement that prohibits or restricts an
insurer from engaging, or attempting to
engage, in steering towards any healthcare
provider;
c. enjoin CHS from retaliating, or
threatening to retaliate, against any insurer
for engaging or attempting to engage in
steering; and
d. award Plaintiffs their costs in this action
and such other relief as the Court may deem
just and proper.
Dated: June 9, 2016
Respectfully Submitted,
FOR PLAINTIFF UNITED STATES OF
AMERICA
lllllllllllllllllllll
Renata B. Hesse,
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Principal Deputy Assistant Attorney General
for Antitrust.
David I. Gelfand,
Deputy Assistant Attorney General.
Patricia A. Brink,
Director of Civil Enforcement.
Peter J. Mucchetti,
Chief, Litigation I.
Jill Westmoreland Rose,
United States Attorney.
lllllllllllllllllllll
Paul B. Taylor,
Assistant United States Attorney, Chief, Civil
Division, N.C. Bar Number 10067, Room 233,
U.S. Courthouse, 100 Otis Street, Asheville,
NC 28801–2611, (828) 271–4661(phone),
paul.taylor@usdoj.gov.
lllllllllllllllllllll
Paul Torzilli,
Karl D. Knutsen,
Richard Martin,
John R. Read,
Antitrust Division, U.S. Department of
Justice, 450 Fifth Street N.W., Suite 4100,
Washington, DC 20530, (202) 514–8349
(phone), (202 514–7308 (fax), Paul.Torzill@
usdoj.gov.
FOR PLAINTIFF STATE OF NORTH
CAROLINA
Roy Cooper,
Attorney General of North Carolina.
lllllllllllllllllllll
K.D. Sturgis,
Special Deputy Attorney General, North
Carolina Department of Justice, N.C. Bar
Number 9486, P.O. Box 629, Raleigh, NC
27602, Tel. 919–716–6011, Fax 919–716–
6050, ksturgis@ncdoj.gov.
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United States District Court for the Western
District of North Carolina Charlotte Division
United States of America and State of
North Carolina, Plaintiffs, v. The CharlotteMecklenburg Hospital Authority d/b/a
Carolinas Healthcare System, Defendant.
Case No. 3:16–cv–00311–RJC–DCK
Judge Robert J. Conrad, Jr.
[PROPOSED] FINAL JUDGMENT
WHEREAS, Plaintiffs, the United States of
America and the State of North Carolina
(collectively ‘‘Plaintiffs’’), filed their
Complaint on June 9, 2016; Plaintiffs and
Defendant The Charlotte-Mecklenburg
Hospital Authority d/b/a Atrium Health f/k/
a Carolinas HealthCare System (collectively
the ‘‘Parties’’), by their respective attorneys,
have consented to the entry of this Final
Judgment without trial or adjudication of any
issue of fact or law;
AND WHEREAS, this Final Judgment does
not constitute any evidence against or
admission by any party regarding any issue
of fact or law;
AND WHEREAS, the Plaintiffs and
Defendant agree to be bound by the
provisions of this Final Judgment pending its
approval by this Court;
AND WHEREAS, the essence of this Final
Judgment is to enjoin Defendant from
prohibiting, preventing, or penalizing
steering as defined in this Final Judgment;
NOW THEREFORE, before any testimony
is taken, without trial or adjudication of any
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issue of fact or law, and upon consent of the
parties, it is ORDERED, ADJUDGED, AND
DECREED:
I. JURISDICTION
The Court has jurisdiction over the subject
matter of and each of the Parties to this
action. The Complaint states a claim upon
which relief may be granted against
Defendant under Section 1 of the Sherman
Act, as amended, 15 U.S.C. § 1.
II. DEFINITIONS
For purposes of this Final Judgment, the
following definitions apply:
A. ‘‘Benefit Plan’’ means a specific set of
health care benefits and Healthcare Services
that is made available to members through a
health plan underwritten by an Insurer, a
self-funded benefit plan, or Medicare Part C
plans. The term ‘‘Benefit Plan’’ does not
include workers’ compensation programs,
Medicare (except Medicare Part C plans),
Medicaid, or uninsured discount plans.
B. ‘‘Carve-out’’ means an arrangement by
which an Insurer unilaterally removes all or
substantially all of a particular Healthcare
Service from coverage in a Benefit Plan
during the performance of a networkparticipation agreement.
C. ‘‘Center of Excellence’’ means a feature
of a Benefit Plan that designates Providers of
certain Healthcare Services based on
objective quality or quality-and-price criteria
in order to encourage patients to obtain such
Healthcare Services from those designated
Providers.
D. ‘‘Charlotte Area’’ means Cabarrus,
Cleveland, Gaston, Iredell, Lincoln,
Mecklenburg, Rowan, Stanly, and Union
counties in North Carolina and Chester,
Lancaster, and York counties in South
Carolina.
E. ‘‘Co-Branded Plan’’ means a Benefit
Plan, such as Blue Local with Carolinas
HealthCare System, arising from a joint
venture, partnership, or a similar formal type
of alliance or affiliation beyond that present
in broad network agreements involving
value-based arrangements between an Insurer
and Defendant in any portion of the Charlotte
Area whereby both Defendant’s and Insurer’s
brands or logos appear on marketing
materials.
F. ‘‘Defendant’’ means The CharlotteMecklenburg Hospital Authority d/b/a
Atrium Health f/k/a Carolinas HealthCare
System, a North Carolina hospital authority
with its headquarters in Charlotte, North
Carolina; and its directors, commissioners,
officers, managers, agents, and employees; its
successors and assigns; and any controlled
subsidiaries (including Managed Health
Resources), divisions, partnerships, and joint
ventures, and their directors, commissioners,
officers, managers, agents, and employees;
and any Person on whose behalf Defendant
negotiates contracts with, or consults in the
negotiation of contracts with, Insurers. For
purposes of this Final Judgment, an entity is
controlled by Defendant if Defendant holds
50% or more of the entity’s voting securities,
has the right to 50% or more of the entity’s
profits, has the right to 50% or more of the
entity’s assets on dissolution, or has the
contractual power to designate 50% or more
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of the directors or trustees of the entity. Also
for purposes of this Final Judgment, the term
‘‘Defendant’’ excludes MedCost LLC and
MedCost Benefits Services LLC, but it does
not exclude any Atrium Health director,
commissioner, officer, manager, agent, or
employee who may also serve as a director,
member, officer, manager, agent, or employee
of MedCost LLC or MedCost Benefit Services
LLC when such director, commissioner,
officer, manager, agent, or employee is acting
within the course of his or her duties for
Atrium Health. MedCostLLC and MedCost
Benefits Services LLC will remain excluded
from the definition of ‘‘Defendant’’ as long as
Atrium does not acquire any greater
ownership interest in these entities than it
has at the time that this Final Judgment is
lodged with the Court.
G. ‘‘Healthcare Provider’’ or ‘‘Provider’’
means any Person delivering any Healthcare
Service.
H. ‘‘Healthcare Services’’ means all
inpatient services (i.e., acute-care diagnostic
and therapeutic inpatient hospital services),
outpatient services (i.e., acute-care diagnostic
and therapeutic outpatient services,
including but not limited to ambulatory
surgery and radiology services), and
professional services (i.e., medical services
provided by physicians or other licensed
medical professionals) to the extent offered
by Defendant and within the scope of
services covered on an in-network basis
pursuant to a contract between Defendant
and an Insurer. ‘‘Healthcare Services’’ does
not mean management of patient care, such
as through population health programs or
employee or group wellness programs.
I. ‘‘Insurer’’ means any Person providing
commercial health insurance or access to
Healthcare Provider networks, including but
not limited to managed-care organizations,
and rental networks (i.e., entities that lease,
rent, or otherwise provide direct or indirect
access to a proprietary network of Healthcare
Providers), regardless of whether that entity
bears any risk or makes any payment relating
to the provision of healthcare. The term
‘‘Insurer’’ includes Persons that provide
Medicare Part C plans, but does not include
Medicare (except Medicare Part C plans),
Medicaid, or TRICARE, or entities that
otherwise contract on their behalf.
J. ‘‘Narrow Network’’ means a network
composed of a significantly limited number
of Healthcare Providers that offers a range of
Healthcare Services to an Insurer’s members
for which all Providers that are not included
in the network are out of network.
K. ‘‘Penalize’’ or ‘‘Penalty’’ is broader than
‘‘prohibit’’ or ‘‘prevent’’ and is intended to
include any contract term or action with the
likely effect of significantly restraining
steering through Steered Plans or
Transparency. In determining whether any
contract provision or action ‘‘Penalizes’’ or is
a ‘‘Penalty,’’ factors that may be considered
include: the facts and circumstances relating
to the contract provision or action; its
economic impact; and the extent to which
the contract provision or action has potential
or actual procompetitive effects in the
Charlotte Area.
L. ‘‘Person’’ means any natural person,
corporation, company, partnership, joint
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venture, firm, association, proprietorship,
agency, board, authority, commission, office,
or other business or legal entity.
M. ‘‘Reference-Based Pricing’’ means a
feature of a Benefit Plan by which an Insurer
pays up to a uniformly-applied defined
contribution, based on an external price
selected by the Insurer, toward covering the
full price charged for a Healthcare Service,
with the member being required to pay the
remainder. For avoidance of doubt, a Benefit
Plan with Reference-Based Pricing as a
feature may permit an Insurer to pay a
portion of this remainder.
N. ‘‘Steered Plan’’ means any Narrow
Network Benefit Plan, Tiered Network
Benefit Plan, or any Benefit Plan with
Reference-Based Pricing or a Center of
Excellence as a component.
O. ‘‘Tiered Network’’ means a network of
Healthcare Providers for which (i) an Insurer
divides the in-network Providers into
different sub-groups based on objective price,
access, and/or quality criteria; and (ii)
members receive different levels of benefits
when they utilize Healthcare Services from
Providers in different sub-groups.
P. ‘‘Transparency’’ means communication
of any price, cost, quality, or patient
experience information directly or indirectly
by an Insurer to a client, member, or
consumer.
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III. APPLICABILITY
This Final Judgment applies to Defendant,
as defined above, and all other Persons in
active concert with, or participation with,
Defendant who receive actual notice of this
Final Judgment by personal service or
otherwise.
IV. PROHIBITED CONDUCT
A. The contract language reproduced in
Exhibit A is void, and Defendant shall not
enforce or attempt to enforce it. The contract
language reproduced in Exhibit B shall not be
used to prohibit, prevent, or penalize Steered
Plans or Transparency, but could remain
enforceable for protection against Carve-outs.
For the Network Participation Agreement
between Blue Cross and Blue Shield of North
Carolina and Defendant’s wholly-owned
subsidiary Managed Health Resources,
effective January 1, 2014, as amended,
Defendant shall exclude from the calculation
of total cumulative impact pursuant to
Section 6.14 of that agreement any impact to
Defendant resulting from Blue Cross and
Blue Shield of North Carolina disfavoring
Defendant through Transparency or through
the use of any Steered Plan.
B. For Healthcare Services in the Charlotte
Area, Defendant will not seek or obtain any
contract provision which would prohibit,
prevent, or penalize Steered Plans or
Transparency including:
1. express prohibitions on Steered Plans or
Transparency;
2. requirements of prior approval for the
introduction of new benefit plans (except in
the case of Co-Branded Plans); and
3. requirements that Defendant be included
in the most-preferred tier of Benefit Plans
(except in the case of Co-Branded Plans).
However, notwithstanding this Paragraph
IV(B)(3), Defendant may enter into a contract
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with an Insurer that provides Defendant with
the right to participate in the most-preferred
tier of a Benefit Plan under the same terms
and conditions as any other Charlotte Area
Provider, provided that if Defendant declines
to participate in the most-preferred tier of
that Benefit Plan, then Defendant must
participate in that Benefit Plan on terms and
conditions that are substantially the same as
any terms and conditions of any thenexisting broad-network Benefit Plan (e.g.,
PPO plan) in which Defendant participates
with that Insurer. Additionally,
notwithstanding Paragraph IV(B)(3), nothing
in this Final Judgment prohibits Defendant
from obtaining any criteria used by the
Insurer to (i) assign Charlotte Area Providers
to each tier in any Tiered Network; and/or (ii)
designate Charlotte Area Providers as a
Center of Excellence.
C. Defendant will not take any actions that
penalize, or threaten to penalize, an Insurer
for (i) providing (or planning to provide)
Transparency, or (ii) designing, offering,
expanding, or marketing (or planning to
design, offer, expand, or market) a Steered
Plan.
I. PERMITTED CONDUCT
A. Defendant may exercise any contractual
right it has, provided it does not engage in
any Prohibited Conduct as set forth above.
B. For any Co-Branded Plan or Narrow
Network in which Defendant is the mostprominently featured Provider, Defendant
may restrict steerage within that Co-Branded
Plan or Narrow Network. For example,
Defendant may restrict an Insurer from
including at inception or later adding other
Providers to any (i) Narrow Network in
which Defendant is the most-prominently
featured Provider, or (ii) any Co-Branded
Plan.
C. With regard to information
communicated as part of any Transparency
effort, nothing in this Final Judgment
prohibits Defendant from reviewing its
information to be disseminated, provided
such review does not delay the dissemination
of the information. Furthermore, Defendant
may challenge inaccurate information or seek
appropriate legal remedies relating to
inaccurate information disseminated by third
parties. Also, for an Insurer’s dissemination
of price or cost information (other than
communication of an individual consumer’s
or member’s actual or estimated out-ofpocket expense), nothing in the Final
Judgment will prevent or impair Defendant
from enforcing current or future provisions,
including but not limited to confidentiality
provisions, that (i) prohibit an Insurer from
disseminating price or cost information to
Defendant’s competitors, other Insurers, or
the general public; and/or (ii) require an
Insurer to obtain a covenant from any third
party that receives such price or cost
information that such third party will not
disclose that information to Defendant’s
competitors, another Insurer, the general
public, or any other third party lacking a
reasonable need to obtain such competitively
sensitive information. Defendant may seek all
appropriate remedies (including injunctive
relief) in the event that dissemination of such
information occurs.
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V. REQUIRED CONDUCT
Within fifteen (15) business days of entry
of this Final Judgment, Defendant, through
its designated counsel, must notify in writing
Aetna, Blue Cross and Blue Shield of North
Carolina, Cigna, MedCost, and
UnitedHealthcare, that:
A. This Final Judgment has been entered
(enclosing a copy of this Final Judgment) and
that it prohibits Defendant from entering into
or enforcing any contract term that would
prohibit, prevent, or penalize Steered Plans
or Transparency, or taking any other action
that violates this Final Judgment; and
B. For the term of this Final Judgment
Defendant waives any right to enforce any
provision listed in Exhibit A and further
waives the right to enforce any provision
listed in Exhibit B to prohibit, prevent, or
penalize Steered Plans and Transparency.
VII. COMPLIANCE
A. It shall be the responsibility of the
Defendant’s designated counsel to undertake
the following:
1. within fifteen (15) calendar days of entry
of this Final Judgment, provide a copy of this
Final Judgment to each of Defendant’s
commissioners and officers, and to each
employee whose job responsibilities include
negotiating or approving agreements with
Insurers for the purchase of Healthcare
Services, including personnel within the
Managed Health Resources subsidiary (or any
successor organization) of Defendant;
2. distribute in a timely manner a copy of
this Final Judgment to any person who
succeeds to, or subsequently holds, a
position of commissioner, officer, or other
position for which the job responsibilities
include negotiating or approving agreements
with Insurers for the purchase of Healthcare
Services, including personnel within the
Managed Health Resources subsidiary (or any
successor organization) of Defendant; and
3. within sixty (60) calendar days of entry
of this Final Judgment, develop and
implement procedures necessary to ensure
Defendant’s compliance with this Final
Judgment. Such procedures shall ensure that
questions from any of Defendant’s
commissioners, officers, or employees about
this Final Judgment can be answered by
counsel (which may be outside counsel) as
the need arises. Paragraph 21.1 of the
Amended Protective Order Regarding
Confidentiality shall not be interpreted to
prohibit outside counsel from answering
such questions.
B. For the purposes of determining or
securing compliance with this Final
Judgment, or any related orders, or
determining whether the Final Judgment
should be modified or vacated, and subject
to any legally-recognized privilege, from time
to time authorized representatives of the
United States or the State of North Carolina,
including agents and consultants retained by
the United States or the State of North
Carolina, shall, upon written request of an
authorized representative of the Assistant
Attorney General in charge of the Antitrust
Division or the Attorney General for the State
of North Carolina, and on reasonable notice
to Defendant, be permitted:
1. access during Defendant’s office hours to
inspect and copy, or at the option of the
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United States, to require Defendant to
provide electronic copies of all books,
ledgers, accounts, records, data, and
documents in the possession, custody, or
control of Defendant, relating to any matters
contained in this Final Judgment; and
2. to interview, either informally or on the
record, Defendant’s officers, employees, or
agents, who may have their individual
counsel present, regarding such matters. The
interviews shall be subject to the reasonable
convenience of the interviewee and without
restraint or interference by Defendant.
C. Within 270 calendar days of entry of this
Final Judgment, Defendant must submit to
the United States and the State of North
Carolina a written report setting forth its
actions to comply with this Final Judgment,
specifically describing (1) the status of all
negotiations between Managed Health
Resources (or any successor organization)
and an Insurer relating to contracts that cover
Healthcare Services rendered in the Charlotte
Area since the entry of the Final Judgment,
and (2) the compliance procedures adopted
under Paragraph VII(A)(3) of this Final
Judgment.
D. Upon the written request of an
authorized representative of the Assistant
Attorney General in charge of the Antitrust
Division or the Attorney General for the State
of North Carolina, Defendant shall submit
written reports or responses to written
interrogatories, under oath if requested,
relating to any of the matters contained in
this Final Judgment as may be requested.
E. The United States may share
information or documents obtained under
Paragraph VII with the State of North
Carolina subject to appropriate
confidentiality protections. The State of
North Carolina shall keep all such
information or documents confidential.
F. No information or documents obtained
by the means provided in Paragraph VII shall
be divulged by the United States or the State
of North Carolina to any Person other than
an authorized representative of (1) the
executive branch of the United States or (2)
the Office of the North Carolina Attorney
General, except in the course of legal
proceedings to which the United States or the
State of North Carolina is a party (including
grand jury proceedings), for the purpose of
securing compliance with this Final
Judgment, or as otherwise required by law.
G. If at the time that Defendant furnishes
information or documents to the United
States or the State of North Carolina,
Defendant represents and identifies in
writing the material in any such information
or documents to which a claim of protection
may be asserted under Rule 26(c)(1)(G) of the
Federal Rules of Civil Procedure, and
Defendant marks each pertinent page of such
material, ‘‘Subject to claim of protection
under Rule 26(c)(1)(G) of the Federal Rules
of Civil Procedure,’’ the United States and
the State of North Carolina shall give
Defendant ten (10) calendar days’ notice
prior to divulging such material in any legal
proceeding (other than a grand jury
proceeding).
H. For the duration of this Final Judgment,
Defendant must provide to the United States
and the State of North Carolina a copy of
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17:51 Dec 10, 2018
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each contract and each amendment to a
contract that covers Healthcare Services in
the Charlotte Area that it negotiates with any
Insurer within thirty (30) calendar days of
execution of such contract or amendment.
Defendant must also notify the United States
and the State of North Carolina within thirty
(30) calendar days of having reason to believe
that a Provider which Defendant controls has
a contract with any Insurer with a provision
that prohibits, prevents, or penalizes any
Steered Plans or Transparency.
VIII. Retention of Jurisdiction
The Court retains jurisdiction to enable any
Party to this Final Judgment to apply to the
Court at any time for further orders and
directions as may be necessary or appropriate
to carry out or construe this Final Judgment,
to modify any of its provisions, to enforce
compliance, and to punish violations of its
provisions.
IX. Enforcement of Final Judgment
A. The United States retains and reserves
all rights to enforce the provisions of this
Final Judgment, including the right to seek
an order of contempt from the Court.
Defendant agrees that in any civil contempt
action, any motion to show cause, or any
similar action brought by the United States
regarding an alleged violation of this Final
Judgment, the United States may establish a
violation of the decree and the
appropriateness of any remedy therefor by a
preponderance of the evidence, and
Defendant waives any argument that a
different standard of proof should apply.
B. The Final Judgment should be
interpreted to give full effect to the
procompetitive purposes of the antitrust laws
and to restore all competition Plaintiffs
alleged was harmed by the challenged
conduct. Defendant agrees that it may be held
in contempt of, and that the Court may
enforce, any provision of this Final Judgment
that, as interpreted by the Court in light of
these procompetitive principles and applying
ordinary tools of interpretation, is stated
specifically and in reasonable detail, whether
or not it is clear and unambiguous on its face.
In any such interpretation, the terms of this
Final Judgment should not be construed
against either Party as the drafter.
C. In any enforcement proceeding in which
the Court finds that Defendant has violated
this Final Judgment, the United States may
apply to the Court for a one-time extension
of this Final Judgment, together with such
other relief as may be appropriate. In
connection with any successful effort by the
United States to enforce this Final Judgment
against Defendant, whether litigated or
resolved prior to litigation, Defendant agrees
to reimburse the United States for the fees
and expenses of its attorneys, as well as any
other costs including experts’ fees, incurred
in connection with that enforcement effort,
including in the investigation of the potential
violation.
X. Expiration of Final Judgment
Unless the Court grants an extension, this
Final Judgment shall expire ten (10) years
from the date of its entry, except that after
five (5) years from the date of its entry, this
Final Judgment may be terminated upon
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notice by the United States to the Court and
Defendant that the continuation of the Final
Judgment is no longer necessary or in the
public interest.
XI. Public Interest Determination
Entry of this Final Judgment is in the
public interest. The Parties have complied
with the requirements of the Antitrust
Procedures and Penalties Act, 15 U.S.C. § 16,
including making copies available to the
public of this Final Judgment, the
Competitive Impact Statement, any
comments thereon, and the United States’
responses to comments. Based upon the
record before the Court, which includes the
Competitive Impact Statement and any
comments and responses to comments filed
with the Court, entry of this Final Judgment
is in the public interest.
Date: llllllllllllllllll
[Court approval subject to procedures of
Antitrust Procedures and Penalties Act, 15
U.S.C. § 16]
lllllllllllllllllllll
Robert J. Conrad, Jr.
United States District Judge.
Exhibit A
Aetna
Section 2.8 of the Physician Hospital
Organization Agreement between and among
Aetna Health of the Carolinas, Inc., Aetna
Life Insurance Company, Aetna Health
Management, LLC, and Defendant states in
part:
‘‘Company may not . . . steer Members
away from Participating PHO Providers other
than instances where services are not deemed
to be clinically appropriate, subject to the
terms of Section 4.1.3 of this Agreement.’’
In addition, Section 2.11 of the abovereferenced agreement states in part:
‘‘Company reserves the right to introduce
in new Plans . . . and products during the
term of this Agreement and will provide PHO
with ninety (90) days written notice of such
new Plans, Specialty Programs and products.
. . . For purposes under (c) and (d) above,
Company commits that Participating PHO
Providers will be in-network Participating
Providers in Company Plans and products as
listed on the Product Participation Schedule.
If Company introduces new products or
benefit designs in PHO’s market that have the
effect of placing Participating PHO Providers
in a non-preferred position, PHO will have
the option to terminate this Agreement in
accordance with Section 6.3.
Notwithstanding the foregoing, if Company
introduces an Aexcel performance network
in PHO Provider’s service area, all PHO
Providers will be placed in the most
preferred benefit level. As long as such Plans
or products do not directly or indirectly steer
Members away from a Participating PHO
Provider to an alternative Participating
Provider for the same service in the same
level of care or same setting, the termination
provision would not apply.’’
Blue Cross and Blue Shield of North Carolina
The Benefit Plan Exhibit to the Network
Participation Agreement between Blue Cross
and Blue Shield of North Carolina and
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Defendant (originally effective January 1,
2014), as replaced by the Fifth Amendment,
states in part:
‘‘After meeting and conferring, if parties
cannot reach agreement, then,
notwithstanding Section 5.1, this Agreement
will be considered to be beyond the initial
term, and you may terminate this Agreement
upon not less than 90 days’ prior Written
Notice to us, pursuant to Section 5.2.’’
Cigna
Section II.G.5 of the Managed Care
Alliance Agreement between Cigna
HealthCare of North Carolina, Inc. and
Defendant states in part:
‘‘All MHR entities as defined in Schedule
1 will be represented in the most preferred
benefit level for any and all CIGNA products
for all services provided under this
Agreement unless CIGNA obtains prior
written consent from MHR to exclude any
MHR entities from representation in the most
preferred benefit level for any CIGNA
product. . . . As a MHR Participating
Provider, CIGNA will not steer business away
from MHR Participating Providers.’’
Medcost
Section 3.6 of the Participating Physician
Hospital Organization agreement between
Medcost, LLC and Defendant states in part:
‘‘Plans shall not directly or indirectly steer
patients away from MHR Participating
Providers.’’
UnitedHealthcare
Section 2 of the Hospital Participation
Agreement between UnitedHealthcare of
North Carolina, Inc. and Defendant states in
part:
‘‘As a Participating Provider, Plan shall not
directly or indirectly steer business away
from Hospital.’’
Exhibit B
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Cigna
Section II.G.5 of the Managed Care
Alliance Agreement between Cigna
HealthCare of North Carolina, Inc. and
Defendant states in part:
‘‘CIGNA may not exclude a MHR
Participating Provider as a network provider
for any product or Covered Service that MHR
Participating Provider has the capability to
provide except those carve-out services as
outlined in Exhibit E attached hereto, unless
CIGNA obtains prior written consent from
MHR to exclude MHR Participating Provider
as a network provider for such Covered
Services.’’
UnitedHealthcare
Section 2 of the Hospital Participation
Agreement between UnitedHealthcare of
North Carolina, Inc. and Defendant states in
part:
‘‘Plan may not exclude Hospital as a
network provider for any Health Service that
Hospital is qualified and has the capability
to provide and for which Plan and Hospital
have established a fee schedule or fixed rate,
as applicable, unless mutually agreed to in
writing by Plan and Hospital to exclude
Hospital as a network provider for such
Health Service.’’
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In addition, Section 3.6 of the abovereferenced agreement states in part:
‘‘During the term of this Agreement,
including any renewal terms, if Plan creates
new or additional products, which product
otherwise is or could be a Product Line as
defined in this Agreement, Hospital shall be
given the opportunity to participate with
respect to such new Product Line.’’
United States District Court for the Western
District of North Carolina Charlotte Division
United States of America and the State of
North Carolina, Plaintiffs, v. The CharlotteMecklenburg Hospital Authority, d/b/a
Carolinas Healthcare System, Defendant.
Case No. 3:16–cv–00311–RJC–DCK
Judge Robert J. Conrad, Jr.
COMPETITIVE IMPACT STATEMENT
Plaintiff United States of America (‘‘United
States’’), pursuant to Section 2(b) of the
Antitrust Procedures and Penalties Act
(‘‘APPA’’ or ‘‘Tunney Act’’), 15 U.S.C.
§§ 16(b)–(h), files this Competitive Impact
Statement relating to the proposed Final
Judgment submitted for entry in this civil
antitrust proceeding.
I. NATURE AND PURPOSE OF THE
PROCEEDING
On June 9, 2016, the United States and the
State of North Carolina filed a civil antitrust
lawsuit against The Charlotte-Mecklenburg
Hospital Authority, formerly known as
Carolinas HealthCare System and now doing
business as Atrium Health (‘‘Atrium’’), to
enjoin it from using steering restrictions in its
agreements with health insurers in the
Charlotte, North Carolina area. The
Complaint alleges that Atrium’s steering
restrictions are anticompetitive and violate
Section 1 of the Sherman Act, 15 U.S.C. § 1,
because the restrictions have detrimental
effects on competition among healthcare
providers in the Charlotte area.
Healthcare providers charge health
insurers a wide variety of prices for the same
service, but insurers have generally not
passed these price differences on to
consumers because most commercial health
plans offer coverage that is the same no
matter which provider a patient chooses.
This weakens the connection between price
and quantity that is the essence of
competition because it allows a provider to
charge a high price without losing business
to rivals. To control escalating healthcare
costs, insurers have developed health plans
and plan features that ‘‘steer’’ members by
providing financial incentives that enable
members to share savings by choosing more
cost-effective providers, which stimulates
competition between providers. To enable
patients to choose more cost-effective
providers, insurers also provide members
with transparency about the prices, quality,
patient experience, or anticipated out-ofpocket costs at different healthcare providers.
Atrium is the largest health system in the
Charlotte area. For an insurer to maintain a
competitive health insurance business in the
Charlotte area, it needs to have a contractual
relationship with Atrium that gives
employers and consumers the option of
purchasing insurance that covers care there.
Atrium has used its dominant position to
demand contractual restrictions on steering
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and transparency that interfere with the
competitive process. Insurers that contract
with Atrium are prohibited from providing
financial incentives or information that
would encourage consumers to obtain
healthcare services from competing
providers. These contract provisions
significantly reduce the number of additional
patients that Atrium’s competitors can hope
to attract by agreeing to lower prices or
otherwise providing greater value. These
restrictions have been in Atrium’s contracts
for years, and remain to this day.
Atrium’s steering restrictions reduce the
competitive incentive that Atrium’s
competitors would otherwise have to lower
prices in order to win more business. This
interference in the competitive process has
reduced competition between Atrium and
other healthcare providers in the Charlotte
area. In addition, because many of the most
innovative healthcare plans in the country
today are based on steering to more efficient
providers, Atrium’s steering restrictions have
also curbed the introduction of such plans,
and reduced choices for Charlotte-area
consumers.
Plaintiffs and Atrium have entered into a
Stipulation and proposed Final Judgment.
The proposed Final Judgment enjoins Atrium
from (1) enforcing provisions in its current
insurer contracts that restrict steering and
transparency; (2) seeking or obtaining
contract provisions with an insurer that
would prohibit, prevent, or penalize the
insurer from using popular steering methods
or providing transparency; and (3)
penalizing, or threatening to penalize, any
insurer for its use of these popular steering
methods and transparency. The proposed
Final Judgment is described in detail
beginning with Section III below. In the
Stipulation, Atrium agrees to abide by the
injunctive provisions of the proposed Final
Judgment while awaiting its entry by the
Court.
The United States (unless it has withdrawn
its consent), the State of North Carolina, and
Atrium have stipulated that the Court may
enter the proposed Final Judgment at any
time after compliance with the APPA. Entry
of the proposed Final Judgment would
terminate this action, except that the Court
would retain jurisdiction to construe, modify,
or enforce the provisions of the proposed
Final Judgment and to punish violations
thereof.
II. DESCRIPTION OF THE ALLEGED
VIOLATION
A. Atrium and other Charlotte-Area
Hospitals
Atrium is the largest healthcare system in
North Carolina and one of the largest not-forprofit healthcare systems in the United
States. It is the dominant hospital system in
the Charlotte area. Its flagship facility is
Carolinas Medical Center, a general acutecare hospital located near downtown
Charlotte and the largest hospital in North
Carolina. Atrium also operates nine
additional general acute-care hospitals in the
Charlotte area. Atrium owns, manages, or has
strategic affiliations with over 40 hospitals in
the Carolinas, and sells healthcare services
throughout the Carolinas, including in
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freestanding emergency departments, urgent
care centers, physician practices, outpatient
surgery centers, imaging centers, nursing
homes, and laboratories. In 2017, Atrium’s
owned, managed, and affiliated hospitals and
other healthcare providers earned net
operating revenue of close to $10 billion.
In addition to Atrium’s ten Charlotte-area
hospitals, there are eleven other general
acute-care hospitals in the Charlotte area.
The next largest hospital system, Novant
Health (‘‘Novant’’), owns five general acutecare hospitals located in that area and had
operating revenue of approximately $4.6
billion in 2017, making Novant less than half
the size of Atrium. Novant’s largest hospital
in the Charlotte area is Novant Presbyterian
Medical Center, which is the second-largest
hospital in Charlotte. After Novant, the nextlargest hospital in the Charlotte area is
CaroMont Regional Medical Center.
CaroMont Regional Medical Center is a 370bed hospital in Gastonia, North Carolina, and
is owned and operated by CaroMont Health,
an independent community hospital system.
In 2016, CaroMont Health had net operating
revenue of approximately $529 million. The
remaining hospitals in the Charlotte area are
operated by Community Health Systems,
Inc., Tenet Healthcare Corporation, and
Iredell Health System.
B. The Relevant Market
The Complaint alleges that Atrium has
market power in a relevant market for the
sale of general acute care inpatient hospital
services sold to commercial health insurers
(‘‘GAC inpatient hospital services’’) in the
Charlotte area. GAC inpatient hospital
services consist of a broad group of medical
and surgical diagnostic and treatment
services that includes a patient’s overnight
stay in the hospital. Although individual
GAC inpatient hospital services are not
substitutes for each other (e.g., a patient who
needs heart surgery cannot elect instead to
have her knee replaced), GAC inpatient
hospital services can be aggregated for
analytical convenience because the
competitive conditions for each of the
individual services is largely the same.
The relevant geographic market for the sale
of GAC inpatient hospital services is no
larger than the Charlotte area.1 Insurers
contract to purchase GAC inpatient hospital
services from hospitals within the geographic
area where their members are likely to seek
medical care because consumers prefer to
seek medical care near the places where they
work and live. As a result, insurers doing
business in the Charlotte area must include
in their provider networks hospitals located
in the Charlotte area. Charlotte-area
consumers have little or no willingness to
enroll in an insurance plan that provides no
network access to hospitals located in the
Charlotte area. For these reasons, it is not a
viable alternative for insurers that sell health
plans to consumers in the Charlotte area to
1 As used in this case, the Charlotte area means
the Charlotte Combined Statistical Area, as defined
by the U.S. Office of Management and Budget,
which consists of Cabarrus, Cleveland, Gaston,
Iredell, Lincoln, Mecklenburg, Rowan, Stanly, and
Union counties in North Carolina, and Chester,
Lancaster, and York counties in South Carolina.
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contract for GAC inpatient hospital services
from providers outside the Charlotte area.
C. Anticompetitive Effects of the Steering
Restrictions
1. Atrium is the dominant hospital system in
the Charlotte area
Atrium is the dominant seller of GAC
inpatient hospital services in the Charlotte
area. Atrium has market power in this
market. The market for GAC inpatient
hospital services in the Charlotte area is
highly concentrated, and Atrium’s market
share is more than 55 percent. By
comparison, Atrium’s largest rival, Novant
Health, has approximately 17 percent of the
licensed hospital beds in the Charlotte area.
Without an attractive broad-network plan
that includes Atrium, insurers would not be
viable in the Charlotte area because they
would not be able to attract the business of
employers. Atrium’s size and breadth give it
significant market power because it can
decline to participate in an insurer’s network
unless it obtains high prices and
advantageous contract terms.
As a result of its market power, Atrium has
been able to secure from insurers high prices
relative to other hospital systems in the
Charlotte area and relative to other advanced
medical centers in North Carolina. These
higher prices are not explained by any
measure of relative high-quality. Because of
high provider prices, patients’ out-of-pocket
healthcare costs in the Charlotte area are
among the highest in North Carolina.
2. Steering is part of the competitive process
Employers in Charlotte and elsewhere
around the country have approached health
insurers about ways to address rising
healthcare costs. One approach of increasing
interest is the introduction of steering
mechanisms into the health plans that
employers offer. Steering can be one way of
fostering competition among hospitals.
Steering can be accomplished in several
ways. Popular types of steering in healthcare
are narrow networks and tiered networks,
reference-based pricing, and centers of
excellence.2 Transparency into hospitals’ or
physicians’ relative prices and quality is also
important to help effectuate steering.
a. Narrow networks and tiered networks
In addition to offering the broad-network
plans that are most popular with employers,
insurers in Charlotte want to introduce
narrow network and tiered insurance
options. Narrow networks are formed by
using cost and/or quality criteria to select
and contract with a subset of healthcare
providers in an area. For example, a health
plan sold in the Charlotte area that consists
of hospitals and physicians only at Novant,
CaroMont, and Community Health Systems
would be a narrow-network plan. Because
using an in-network provider costs a member
less than using an out-of-network provider, a
consumer that enrolls in a narrow-network
plan is choosing to be steered to participating
2 The proposed Final Judgment defines narrow
networks, tiered networks, and health plans with
reference-based pricing or centers of excellence as
‘‘Steered Plans.’’
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providers. The likely increase in patient
volume realized by providers in the narrow
network can help the insurer to negotiate
lower prices, and then to pass those savings
along in the form of lower premiums.
Tiered networks are typically created by
designating network providers into different
levels (or tiers) based mostly on quality and
price. Tiered networks typically have two or
more tiers of in-network providers: a
preferred tier and one or more secondary innetwork tiers. There may also be providers
that remain out-of-network. In tiered
networks, members are free to use any of the
providers, but receive the most substantial
benefits when they choose a provider in the
preferred tier. This tier typically includes the
providers with the best mix of quality and
price. Tiered and narrow network plans are
increasingly popular with employers and
consumers. For example, in 2017, 19 percent
of large employers that offered healthcare
coverage provided a narrow-network plan to
their employees and 31 percent offered a
tiered plan.3 A large majority of the plans
offered on the individual healthcare
exchanges are narrow network plans. Narrow
and tiered networks can effectively reduce
healthcare costs and make insurance more
affordable.
b. Reference-based pricing and centers of
excellence
Reference-based pricing and centers of
excellence are forms of steering that can be
used as a feature of a health benefit plan. For
reference-based pricing, the insurer
establishes a market-wide standard, or
‘‘reference,’’ price for a service. The reference
price can be established by drawing from
average local prices or from other sources
such as the reimbursement amounts
established by Medicare rules. The benefit
plan covers the member’s expenses up to the
‘‘reference price.’’ Reference-based pricing
steers members towards the providers that
have prices at or below the reference price.
This gives higher-priced providers an
incentive to reduce their prices to be closer
to the reference price.4
A center of excellence is a designation that
an insurer applies to a provider for its quality
and/or cost efficiency in delivering a
particular healthcare service. The insurer
often provides a financial incentive to
consumers to select the center of excellence.
For example, an insurer may designate a
particular hospital in a metropolitan area as
3 Kaiser Family Foundation, 2017 Employer
Health Benefits Survey, 213–214, https://files.kff.org/
attachment/Report-Employer-Health-BenefitsAnnual-Survey-2017.
4 The California Public Employees’ Retirement
System (‘‘CalPERS’’) has successfully used
reference-based pricing to lower expenses on hip
and knee replacements. A study of the first year
after implementation of the reference-based pricing
program indicates that surgical volumes at lowprice facilities increased while volumes at highprice facilities decreased. Prices declined at both
high and low price facilities. As a result CalPERS
and its employees saved approximately $3 million.
James C. Robinson and Timothy T. Brown,
Increases in Consumer Cost Sharing Redirect
Patient Volumes and Reduce hospital Prices for
Orthopedic Surgery, 32 Health Affairs 1392, 1394–
97 (2013).
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its center of excellence in bariatric surgery
because the hospital has superior expertise or
is particularly cost effective. To incent
members to obtain bariatric surgery there, the
insurer may reduce or eliminate out-ofpocket expenses for members who choose
that hospital. Members remain free to obtain
bariatric surgery elsewhere and pay the outof-pocket expenses prescribed under the
plan. Members are steered towards a center
of excellence by virtue of the designation and
the cost savings.
c. Transparency
Transparency is the communication of
price, cost, quality, or patient experience
information to a member. Transparency
makes steered plans more effective by
providing consumers with information to
enable them to comparison shop before
selecting a provider. Transparency may also
be a form of steering even in the absence of
differential benefits because information that
identifies one provider as more cost effective
than another provider may prompt
consumers to choose the more cost-effective
provider.
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3. To insulate itself from competition, Atrium
required that steering restrictions be included
in its insurer contracts
To protect its dominant share and high
prices and insulate itself from competition,
Atrium has used its market power to require
every major insurer in the Charlotte area—
Aetna Health of the Carolinas, Inc. (‘‘Aetna’’),
Blue Cross and Blue Shield of North Carolina
(‘‘BCBS–NC’’), Cigna Healthcare of North
Carolina, Inc. (‘‘Cigna’’), and United
Healthcare of North Carolina, Inc.
(‘‘UnitedHealthcare’’) 5— to accept contract
terms that restrict the insurers from steering
their members to Atrium’s lower-cost
competitors.
Atrium’s contracts with each of these
insurers contain steering restrictions that
either expressly prohibit the insurer from
steering their members away from Atrium, or
impede steering through other means, such
as by imposing a financial penalty on any
steering against Atrium that exceeds a
specified amount or by allowing Atrium to
promptly terminate the insurer’s contract if
the insurer steers against Atrium. Atrium
used its market power to require that insurers
agree to these contract provisions that restrict
steering, and thereby restrict competition.
Atrium’s steering restrictions restrain
insurers from offering consumers the choice
of narrow-network plans that do not include
Atrium, and tiered-network plans that do not
place Atrium in the most favorable tier.
Atrium’s steering restrictions also prevent
insurers from offering reference-based pricing
because if the reference price for a service is
5 These four major insurers cover over 90 percent
of the commercially-insured residents of the
Charlotte area. MedCost is the next-largest health
plan in the Charlotte area. MedCost provides
administrative services and access to its healthcare
provider networks to employers that self-fund their
employees’ healthcare benefits. Employers that are
self-funded pay the healthcare benefit claims from
the assets of their business, rather than purchase
health insurance policies for the benefit of their
employees. Atrium owns 50 percent of MedCost.
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lower than the price that Atrium charges for
that service, members will be steered away
from Atrium. Insurers are also prevented
from offering financial incentives for
members to obtain services at non-Atrium
providers that are designated centers of
excellence.
These restrictions also prevent insurers
from providing members transparency into
the price, quality, patient experience, and
anticipated out-of-pocket costs of Atrium’s
healthcare services compared to Atrium’s
competitors. Atrium’s restrictions on
transparency indirectly restrict steering
because they inhibit consumers from
accessing information that would allow them
to make better-informed healthcare provider
choices.
Deprived of any mechanism to reward low
prices with more patient volume, insurers
cannot create incentives for Atrium’s rivals to
compete on price. Atrium’s steering
restrictions, therefore, reduce competition for
GAC inpatient hospital services in the
Charlotte area by impeding its competitors’
ability to attract patients by offering lower
prices to insurers and their members. The
steering restrictions prevent consumers from
benefitting from lower prices, so they protect
Atrium from losing patient volume in
response to high prices. This reduction in
competition causes prices to be higher than
they would be in the absence of Atrium’s
steering restrictions.
III. EXPLANATION OF THE PROPOSED
FINAL JUDGMENT
The purpose of the proposed Final
Judgment is to prevent Atrium from
impeding insurers’ steered plans and
transparency, and to restore competition
among healthcare providers in the Charlotte
area. The proposed Final Judgment will
accomplish this objective through injunctive,
compliance, and enforcement provisions.
Atrium has market power in GAC inpatient
hospital services, but the proposed Final
Judgment applies to the broad range of
healthcare services that Atrium provides and
to which its steering restrictions apply. The
additional healthcare services covered by the
proposed Final Judgment include outpatient
services (such as ambulatory surgeries and
radiological services), professional services
rendered by physicians, and ancillary
services such as imaging and lab services.
The full scope of services covered by the
proposed Final Judgment falls within the
proposed Final Judgment’s definition of
‘‘Healthcare Services.’’ Because Atrium uses
its market power to restrict steering away
from it for any healthcare service, the
proposed Final Judgment provides relief that
is broader than the set of services in the
relevant market.
The proposed Final Judgment also applies
to a broad range of benefit plans. This
includes health insurance policies sold to
individuals, fully-insured and self-funded
health plans sold to employers and other
groups, and Medicare Advantage plans.
A. Prohibited Conduct
The proposed Final Judgment seeks to
restore competition by prohibiting Atrium
from engaging in specific conduct. There are
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three main provisions. The first stops Atrium
from enforcing the current contract
provisions at issue in this suit. The second
stops Atrium from enforcing similar or new
contractual provisions that would restrict
steering in the Charlotte area. The third stops
Atrium from retaliating against insurers for
steering in the Charlotte area.
1. Eliminating the anticompetitive contract
provisions
The proposed Final Judgment eliminates
the contractual language that Plaintiffs
alleged is anticompetitive. The proposed
Final Judgment voids the contractual
provisions listed in Exhibit A to the proposed
Final Judgment that expressly prevent
steering. For example, a provision stating that
an insurer ‘‘will not steer business away
from’’ Atrium is voided from that insurer’s
contract. Additionally, a part of a contract
between Atrium and an insurer that required
the insurer to give Atrium 90 days’ notice
before bringing a plan to market that would
steer patients away from Atrium is also
voided. Further, the proposed Final
Judgment eliminates a provision in one
insurer’s contract that allows Atrium to
terminate the contract on 90 days’ notice if
the insurer offers a plan that would steer
away from Atrium.
In addition, Atrium’s contracts with
commercial insurers contain other provisions
that require the insurer to include Atrium in
all of its benefit plans. Each such provision
prevents the insurer from creating narrow
networks that feature Atrium’s rivals, but
exclude Atrium. The proposed Final
Judgment lists that language in Exhibit B, and
prohibits Atrium from enforcing or
attempting to enforce such contractual
provisions to prevent, prohibit, or penalize
steered plans and transparency.6
Finally, the proposed Final Judgment
prevents Atrium from enforcing a ‘‘material
impact’’ provision in its contract with BCBS–
NC in a manner that reduces BCBS–NC’s
incentives to steer to more efficient
providers.
2. Preventing new contractual provisions that
harm steering
The proposed Final Judgment also prevents
Atrium from seeking or obtaining similar or
new contract provisions that would prohibit,
prevent, or penalize steering through steered
plans or transparency in the Charlotte area.
Paragraph IV(B) of the proposed Final
Judgment identifies three types of contractual
provisions that, among others, would
prohibit, prevent, or penalize steering
through steered plans and would thus violate
the terms of the proposed Final Judgment.
First, Atrium may not expressly prohibit
6 The contract provisions appearing in Exhibit B
could remain enforceable to prevent insurers from
‘‘carving out’’ certain Atrium procedures from their
benefits plans. A ‘‘carve-out’’ is an industry term
defined in the proposed Final Judgment as an
arrangement by which an insurer unilaterally
removes all or substantially all of a particular
healthcare service from coverage in a benefit plan
during the performance of a network-participation
agreement. Insurers are free to negotiate carve-outs
as part of a contract, but Atrium may prohibit
insurers from carving additional services out of a
contract after it is signed.
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steered plans or transparency. Second,
Atrium may not require prior approval of
new benefit plans. Third, Atrium may not
demand to be included in the most-preferred
tier of benefit plans regardless of price.
The Final Judgment’s injunction against
steering restrictions also reaches beyond
these three existing provisions to include any
contract provision that prohibits, prevents, or
penalizes steering. ‘‘Penalize’’ is a term in the
proposed Final Judgment that includes
within its definition anything that would
significantly restrain an insurer’s steering.
Because steering away from Atrium
necessarily reduces its volume and revenues,
terms that punish such reductions with
higher prices or other detrimental
consequences may be penalties. Whether a
provision or action is likely to significantly
restrain steering depends on the facts and
circumstances, including but not limited to
its economic impact, and any procompetitive
effects that would tend to lower healthcare
costs or otherwise benefit consumers in the
Charlotte area.
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3. Atrium may not retaliate against steering
Under the terms of the proposed Final
Judgment Atrium also may not seek or obtain
any contract provision, or take any other
action that would penalize an insurer for
steering away from Atrium through steered
plans or transparency. For example, Atrium
may not threaten to terminate its
participation in an insurer’s healthcare
networks because the insurer was planning to
introduce a tiered-network plan that steered
away from Atrium.
B. Conduct That is Not Prohibited by the
Final Judgment
Paragraph V of the proposed Final
Judgment sets forth conduct that Atrium may
undertake without violating the terms of the
proposed Final Judgment. Paragraph V(A)
makes clear that nothing in the proposed
Final Judgment prohibits Atrium from
exercising any of its contractual rights
provided it does not engage in any conduct
that would violate the terms of the proposed
Final Judgment.
If Atrium is the most-prominently featured
provider in a narrow-network plan or cobranded plan,7 Paragraph V(B) of the
proposed Final Judgment allows Atrium to
restrict an insurer from steering away from
Atrium in that plan. Such restrictions may
help narrow networks and co-branded plans
be more effective, and this provision allows
Atrium to participate in plans that steer
towards it.
Paragraph V(C) makes clear that the
proposed Final Judgment does not prohibit
Atrium from negotiating with insurers for the
ability to review the information about
Atrium that an insurer disseminates through
transparency, as long as any provision for
review does not delay dissemination of the
information. The proposed Final Judgment
does not prevent Atrium from challenging
7 A co-branded plan is a benefit plan created by
a formal and substantial level of alliance or
affiliation, such as a partnership or joint venture,
between a provider and an insurer. A co-branded
plan has the logos of both the insurer and provider
on the plan’s marketing materials.
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information that it believes is inaccurate,
including pursuing legal remedies available
to it.
Paragraph V(C) also makes clear that the
proposed Final Judgment does not prohibit
Atrium from seeking certain safeguards
regarding the insurer’s dissemination of the
prices Atrium has negotiated with insurers.
Atrium may seek contractual provisions with
an insurer prohibiting the insurer from
disseminating Atrium’s negotiated prices to
Atrium’s competitors, other insurers, or the
general public. Atrium may also seek
contractual provisions with an insurer
requiring the insurer to obtain a covenant
from any third party receiving Atrium’s
negotiated prices that such third party will
not disclose that information to Atrium’s
competitors, another insurer, the general
public, or another third party lacking a
reasonable need to know such information.
Atrium may also seek all appropriate
remedies in the event that dissemination of
such information occurs.
C. Required Conduct
The proposed Final Judgment also
prescribes conduct that Atrium is required to
undertake in order to facilitate prompt and
effective relief. Paragraph VI of the proposed
Final Judgment requires Atrium to provide
Aetna, BCBS–NC, Cigna, MedCost and
UnitedHealthcare with a copy of the Final
Judgment and notify them in writing within
15 business days of the Court’s entry of the
proposed Final Judgment that (1) the Final
Judgment has been entered; (2) the Final
Judgment prohibits Atrium from entering
into or enforcing any agreement provision
that violates the Final Judgment; (3) Atrium
waives the right to enforce any contract
language reproduced in Exhibit A; and (4)
Atrium waives the right to enforce any
contract language reproduced in Exhibit B to
the extent such language prohibits, prevents,
or penalizes steered plans or transparency.
D. Compliance
Under Paragraph VII of the proposed Final
Judgment, within 15 calendar days of the
entry of the Final Judgment, Atrium must
provide a copy of the Final Judgment to each
of its commissioners and officers as well as
each employee who has responsibility to
negotiate or approve contracts with insurers.
Within 60 calendar days of the entry of the
proposed Final Judgment, Atrium must
develop and implement procedures
necessary to ensure Atrium’s compliance
with the proposed Final Judgment, including
procedures to answer questions from
Atrium’s commissioners and employees
about abiding by the terms of the proposed
Final Judgment.
Within 270 calendar days of entry of the
proposed Final Judgment, Atrium must
submit to the United States and the State of
North Carolina a written report setting forth
its actions to comply with the proposed Final
Judgment. Atrium must also submit to the
United States and the State of North Carolina
a copy of any new or revised agreement or
amendment to any agreement with any
insurer that is executed during the term of
the proposed Final Judgment no later than 30
calendar days after the date the agreement or
amendment is executed.
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Atrium must also notify the United States
and the State of North Carolina within 30
calendar days of having reason to believe that
a provider which Atrium controls has a
contract with any insurer with a provision
that prohibits, prevents, or penalizes
transparency or any steered plan.
To facilitate monitoring Atrium’s
compliance with the proposed Final
Judgment, Paragraphs VII(B) and VII(D) of the
proposed Final Judgment require Atrium to
grant the United States access, upon
reasonable notice, to Atrium’s records and
documents relating to matters contained in
the proposed Final Judgment. In addition
Atrium must make its employees available
for interviews or depositions and answer
interrogatories and prepare written reports
relating to matters contained in the proposed
Final Judgment upon request.
The proposed Final Judgment also contains
provisions that promote compliance and
make the enforcement of the proposed Final
Judgment as effective as possible. Paragraph
IX(A) provides that the United States retains
and reserves all rights to enforce the
provisions of the proposed Final Judgment,
including its rights to seek an order of
contempt from the Court. Under the terms of
this Paragraph, Atrium has agreed that in any
civil contempt action, any motion to show
cause, or any similar action brought by the
United States regarding an alleged violation
of the proposed Final Judgment, the United
States may establish the violation and the
appropriateness of any remedy by a
preponderance of the evidence and that
Atrium has waived any argument that a
different standard of proof should apply.
This provision aligns the standard for
compliance obligations with the standard of
proof that applies to the underlying offense
that the compliance commitments address.
Paragraph IX(B) sets forth the parties’
agreed-upon rules for interpreting the
proposed Final Judgment’s provisions.
Because consent decrees share many
attributes with ordinary contracts, they
should be construed as contracts for purposes
of enforcement. See Anita’s New Mexico
Style Mexican Food v. Anita’s Mexican Foods
Corp., 201 F.3d 314, 319 (4th Cir. 2000)
(quoting United States v. ITT Continental
Baking Co., 420 U.S. 223, 236–37 (1975)).
The parties have agreed that the Court should
employ ordinary tools of interpretation to
enforce the proposed Final Judgment. In
Paragraph IX(B), the parties make clear the
purpose of the proposed Final Judgment that
can be used as an interpretive tool. The
proposed Final Judgment was drafted with
the purpose of resolving this litigation and
restoring all competition that Plaintiffs
alleged was harmed by the challenged
conduct. Paragraph IX(B) says that the
provisions of the proposed Final Judgment
are to be interpreted to give effect to the
procompetitive purpose of the federal
antitrust laws, and to restore this lost
competition.
Atrium also agrees that the Court may
enforce any provision of the proposed Final
Judgment that is stated specifically and in
reasonable detail, see Fed.R.Civ.P. 65(d)
(requiring specific terms and ‘‘reasonable
detail’’), even if the provision is not clear and
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unambiguous on its face, by applying these
procompetitive principles and ordinary tools
of interpretation. See Martin’s Herend
Imports, Inc. v. Diamond & Gem Trading, 195
F.3d 765, 771 (5th Cir. 1999) (‘‘The mere fact
that interpretation is necessary does not
render the injunction so vague and
ambiguous that a party cannot know what is
expected of him.’’ (internal citation and
quotation omitted)). When interpreting the
proposed Final Judgment, the Court should
not construe the language of the proposed
Final Judgment against either party as the
drafter.
Paragraph IX(C) of the proposed Final
Judgment provides that should the Court find
in an enforcement proceeding that Atrium
has violated the proposed Final Judgment,
the United States may apply to the Court for
a one-time extension of the proposed Final
Judgment, together with such other relief as
may be appropriate. In addition, in order to
compensate American taxpayers for any costs
associated with the investigation and
enforcement of violations of the proposed
Final Judgment, Paragraph IX(C) further
provides that in any successful effort by the
United States to enforce the proposed Final
Judgment against Atrium, whether litigated
or resolved prior to litigation, Atrium agrees
to reimburse the United States for attorneys’
fees, experts’ fees, or costs incurred in
connection with any enforcement effort,
including the investigation of the potential
violation.
Finally, Paragraph X of the proposed Final
Judgment provides that the proposed Final
Judgment shall expire ten years from the date
of its entry, except that after five years from
the date of its entry, the proposed Final
Judgment may be terminated upon notice by
the United States to the Court and Atrium
that the continuation of the proposed Final
Judgment is no longer necessary or in the
public interest.
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IV. REMEDIES AVAILABLE TO POTENTIAL
PRIVATE LITIGANTS
Section 4 of the Clayton Act, 15 U.S.C.
§ 15, provides that any person who has been
injured as a result of conduct prohibited by
the antitrust laws may bring suit in federal
court to recover three times the damages the
person has suffered, as well as costs and
reasonable attorneys’ fees. Entry of the
proposed Final Judgment will neither impair
nor assist any private antitrust damage
action. Under the provisions of Section 5(a)
of the Clayton Act, 15 U.S.C. § 16(a), the
proposed Final Judgment has no prima facie
effect in any subsequent private lawsuit that
may be brought against Atrium.
V. PROCEDURES AVAILABLE FOR
MODIFICATION OF THE PROPOSED
FINAL JUDGMENT
The United States, the State of North
Carolina, and Atrium have stipulated that the
proposed Final Judgment may be entered by
the Court after compliance with the
provisions of the APPA, provided that the
United States has not withdrawn its consent.
The APPA conditions entry upon the Court’s
determination that the proposed Final
Judgment is in the public interest.
The APPA provides a period of at least 60
calendar days preceding the effective date of
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the proposed Final Judgment within which
any person may submit to the United States
written comments regarding the proposed
Final Judgment. Any person who wishes to
comment should do so within 60 calendar
days of the date of publication of this
Competitive Impact Statement in the Federal
Register, or the last date of publication in a
newspaper of the summary of this
Competitive Impact Statement, whichever is
later. All comments received during this
period will be considered by the United
States Department of Justice, which remains
free to withdraw its consent to the entry of
the proposed Final Judgment at any time
prior to the Court’s entry of the judgment.
The comments and the response of the
United States will be filed with the Court. In
addition, comments will be posted on the
U.S. Department of Justice, Antitrust
Division’s internet website and, under certain
circumstances, published in the Federal
Register.
Written comments should be submitted to:
Peter J. Mucchetti
Chief, Healthcare and Consumer Products
Section
Antitrust Division
United States Department of Justice
450 Fifth Street, NW, Suite 4100
Washington, DC 20530
The proposed Final Judgment provides that
the Court retains jurisdiction over this action,
and the parties may apply to the Court for
any order necessary or appropriate for the
modification, interpretation, or enforcement
of the proposed Final Judgment.
VI. ALTERNATIVES TO THE PROPOSED
FINAL JUDGMENT
As an alternative to the proposed Final
Judgment, the United States considered
continuing this litigation, and proceeding to
trial in May 2019 against Atrium. While the
proposed Final Judgment represents a
negotiated resolution to the action that
necessitated compromises by Plaintiffs and
Atrium, the United States is satisfied that the
relief contained in the proposed Final
Judgment will remedy the anticompetitive
conduct identified in the Complaint. The
proposed Final Judgment would achieve all
or substantially all of the relief the United
States would have obtained through litigation
but avoids the time, expense, and uncertainty
of a full trial on the merits.
VII. APPA’s STANDARD OF REVIEW FOR
THE PROPOSED FINAL JUDGMENT
The Clayton Act, as amended by the APPA,
requires that proposed consent judgments in
antitrust cases brought by the United States
be subject to a 60-day comment period, after
which the Court shall determine whether
entry of the proposed Final Judgment ‘‘is in
the public interest.’’ 15 U.S.C. § 16(e)(1). In
making that determination, the Court, in
accordance with the statute as amended in
2004, is required to consider:
(A) the competitive impact of such
judgment, including termination of alleged
violations, provisions for enforcement and
modification, duration of relief sought,
anticipated effects of alternative remedies
actually considered, whether its terms are
ambiguous, and any other competitive
PO 00000
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considerations bearing upon the adequacy of
such judgment that the court deems
necessary to a determination of whether the
consent judgment is in the public interest;
and
(B) the impact of entry of such judgment
upon competition in the relevant market or
markets, upon the public generally and
individuals alleging specific injury from the
violations set forth in the complaint
including consideration of the public benefit,
if any, to be derived from a determination of
the issues at trial.
15 U.S.C. § 16(e)(1)(A) & (B). In considering
these statutory factors, the Court’s inquiry is
necessarily a limited one as the government
is entitled to ‘‘broad discretion to settle with
the defendant within the reaches of the
public interest.’’ United States v. Microsoft
Corp., 56 F.3d 1448, 1461 (D.C. Cir. 1995);
see generally United States v. SBC
Commc’ns, Inc., 489 F. Supp. 2d 1 (D.D.C.
2007) (assessing public interest standard
under the Tunney Act); United States v. U.S.
Airways Group, Inc., 38 F. Supp. 3d 69, 75
(D.D.C. 2014) (explaining that the ‘‘court’s
inquiry is limited’’ in Tunney Act
settlements).
As the United States Court of Appeals for
the District of Columbia Circuit has held,
under the APPA a court considers, among
other things, the relationship between the
remedy secured and the specific allegations
in the government’s complaint, whether the
decree is sufficiently clear, whether its
enforcement mechanisms are sufficient, and
whether the decree may positively harm
third parties. See Microsoft, 56 F.3d at 1458–
62. With respect to the adequacy of the relief
secured by the decree, a court may not
‘‘engage in an unrestricted evaluation of what
relief would best serve the public.’’ United
States v. BNS, Inc., 858 F.2d 456, 462 (9th
Cir. 1988) (quoting United States v. Bechtel
Corp., 648 F.2d 660, 666 (9th Cir. 1981)); see
also Microsoft, 56 F.3d at 1460–62; United
States v. Alcoa, Inc., 152 F. Supp. 2d 37, 40
(D.D.C. 2001). Instead:
[t]he balancing of competing social and
political interests affected by a proposed
antitrust consent decree must be left, in the
first instance, to the discretion of the
Attorney General. The court’s role in
protecting the public interest is one of
insuring that the government has not
breached its duty to the public in consenting
to the decree. The court is required to
determine not whether a particular decree is
the one that will best serve society, but
whether the settlement is ‘‘within the reaches
of the public interest.’’ More elaborate
requirements might undermine the
effectiveness of antitrust enforcement by
consent decree.
Bechtel, 648 F.2d at 666 (emphasis added)
(citations omitted).8
In determining whether a proposed
settlement is in the public interest, a district
8 See also BNS, 858 F.2d at 464 (holding that the
court’s ‘‘ultimate authority under the [APPA] is
limited to approving or disapproving the consent
decree’’); United States v. Gillette Co., 406 F. Supp.
713, 716 (D. Mass. 1975) (noting that, in this way,
the court is constrained to ‘‘look at the overall
picture not hypercritically, nor with a microscope,
but with an artist’s reducing glass’’).
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Federal Register / Vol. 83, No. 237 / Tuesday, December 11, 2018 / Notices
amozie on DSK3GDR082PROD with NOTICES1
court ‘‘must accord deference to the
government’s predictions about the efficacy
of its remedies, and may not require that the
remedies perfectly match the alleged
violations.’’ SBC Commc’ns, 489 F. Supp. 2d
at 17; see also U.S. Airways, 38 F. Supp. 3d
at 74–75 (noting that a court should not reject
the proposed remedies because it believes
others are preferable and that room must be
made for the government to grant
concessions in the negotiation process for
settlements); Microsoft, 56 F.3d at 1461
(noting the need for courts to be ‘‘deferential
to the government’s predictions as to the
effect of the proposed remedies’’); United
States v. Archer-Daniels-Midland Co., 272 F.
Supp. 2d 1, 6 (D.D.C. 2003) (noting that the
court should grant ‘‘due respect to the
government’s prediction as to the effect of
proposed remedies, its perception of the
market structure, and its views of the nature
of the case’’). The ultimate question is
whether ‘‘the remedies [obtained in the
decree are] so inconsonant with the
allegations charged as to fall outside of the
‘reaches of the public interest.’’’ Microsoft, 56
F.3d at 1461. To meet this standard, the
United States ‘‘need only provide a factual
basis for concluding that the settlements are
reasonably adequate remedies for the alleged
harms.’’ SBC Commc’ns, 489 F. Supp. 2d at
17.
Moreover, a court’s role under the APPA is
limited to reviewing the remedy in
relationship to the violations that the United
States has alleged in its complaint, and does
not authorize a court to ‘‘construct [its] own
hypothetical case and then evaluate the
decree against that case.’’ Microsoft, 56 F.3d
at 1459; see also U.S. Airways, 38 F. Supp.
3d at 75 (noting that the court must simply
determine whether there is a factual
foundation for the government’s decisions
such that its conclusions regarding the
proposed settlements are reasonable).
Because the ‘‘court’s authority to review the
decree depends entirely on the government’s
exercising its prosecutorial discretion by
bringing a case in the first place,’’ it follows
that ‘‘the court is only authorized to review
the decree itself,’’ and not to ‘‘effectively
redraft the complaint’’ to inquire into other
matters that the United States did not pursue.
Microsoft, 56 F.3d at 1459–60. As the court
confirmed in SBC Communications, courts
‘‘cannot look beyond the complaint in
making the public interest determination
unless the complaint is drafted so narrowly
as to make a mockery of judicial power.’’ SBC
Commc’ns, 489 F. Supp. 2d at 15.
In its 2004 amendments,9 Congress made
clear its intent to preserve the practical
benefits of utilizing consent decrees in
antitrust enforcement, adding the
unambiguous instruction that ‘‘[n]othing in
this section shall be construed to require the
court to conduct an evidentiary hearing or to
9 The 2004 amendments substituted ‘‘shall’’ for
‘‘may’’ in directing relevant factors for a court to
consider and amended the list of factors to focus on
competitive considerations and to address
potentially ambiguous judgment terms. Compare 15
U.S.C. § 16(e) (2004), with 15 U.S.C. § 16(e)(1)
(2006); see also SBC Commc’ns, 489 F. Supp. 2d at
11 (concluding that the 2004 amendments ‘‘effected
minimal changes’’ to Tunney Act review).
VerDate Sep<11>2014
17:51 Dec 10, 2018
Jkt 247001
require the court to permit anyone to
intervene.’’ 15 U.S.C. § 16(e)(2); see also U.S.
Airways, 38 F. Supp. 3d at 76 (indicating that
a court is not required to hold an evidentiary
hearing or to permit intervenors as part of its
review under the Tunney Act). This language
explicitly wrote into the statute what
Congress intended when it first enacted the
Tunney Act in 1974. As Senator Tunney
explained: ‘‘[t]he court is nowhere compelled
to go to trial or to engage in extended
proceedings which might have the effect of
vitiating the benefits of prompt and less
costly settlement through the consent decree
process.’’ 119 Cong. Rec. 24,598 (1973)
(statement of Sen. Tunney). Rather, the
procedure for the public interest
determination is left to the discretion of the
court, with the recognition that the court’s
‘‘scope of review remains sharply proscribed
by precedent and the nature of Tunney Act
proceedings.’’ SBC Commc’ns, 489 F. Supp.
2d at 11. A court can make its public interest
determination based on the competitive
impact statement and response to public
comments alone. U.S. Airways, 38 F. Supp.
3d at 76. See also United States v. Enova
Corp., 107 F. Supp. 2d 10, 17 (D.D.C. 2000)
(noting that the ‘‘Tunney Act expressly
allows the court to make its public interest
determination on the basis of the competitive
impact statement and response to comments
alone’’); S. Rep. No. 93–298 93d Cong., 1st
Sess., at 6 (1973) (‘‘Where the public interest
can be meaningfully evaluated simply on the
basis of briefs and oral arguments, that is the
approach that should be utilized.’’).
63685
Subcommittee on Quantum Information
Science (SCQIS) release of the ‘‘National
Strategic Overview for Quantum
Information Science’’ (hereafter
‘‘Strategic Overview’’) calls upon
agencies to develop plans to address six
key policy areas to enable continued
American leadership in quantum
information science. The National
Science Foundation (NSF), working
with the NSTC, is requesting
information from the research and
development community around
quantum information science (QIS) to
inform the subcommittee as the
Government develops potential means
of addressing specific policy
recommendations.
DATES: Interested persons are invited to
submit comments on or before 11:59
p.m. (ET) on January 25, 2019.
ADDRESSES: Comments submitted in
response to this notice may be sent by
either of the following methods:
• Email: nsfscqis@nsf.gov. Email
submissions should be machinereadable and not be copyright-protected.
Submissions should include ‘‘RFI
Response: National Strategic Overview
for Quantum Information Science’’ in
the subject line of the message.
• Direct input to the website: https://
www.nsfscqis.org
Instructions: Response to this RFI is
VIII. DETERMINATIVE DOCUMENTS
voluntary. Each individual or institution
There are no determinative materials or
is requested to submit only one
documents within the meaning of the APPA
response. Submissions must not exceed
that were considered by the United States in
the equivalent of one page for each
formulating the proposed Final Judgment.
question, or eight pages total, in 12
Respectfully submitted,
point or larger font, with a page number
Dated: December 4, 2018
provided on each page. Responses
FOR PLAINTIFF UNITED STATES OF
should include the name of the
AMERICA:
person(s) or organization(s) filing the
lllllllllllllllllllll comment.
John R. Read
Responses to this RFI may be posted
Karl D. Knutsen
online as discussions proceed.
Natalie Melada
Therefore, we request that no business
Catherine R. Reilly
proprietary information, copyrighted
David Stolzfus
information, or personally identifiable
Paul Torzilli
information be submitted in response to
Antitrust Division, U.S. Department of
this RFI.
Justice, 450 Fifth Street NW, Suite 4100,
In accordance with FAR 15.202(3),
Washington, D.C. 20530, (p) 202/307.0468,
responses to this notice are not offers
John.Read@usdoj.gov.
[FR Doc. 2018–26755 Filed 12–10–18; 8:45 am]
and cannot be accepted by the
Government to form a binding contract.
BILLING CODE 4410–11–P
Responders are solely responsible for all
expenses associated with responding to
this RFI.
NATIONAL SCIENCE FOUNDATION
FOR FURTHER INFORMATION CONTACT: C.
Request for Information on National
Denise Caldwell at (703)-292–7371 or
Strategic Overview for Quantum
nsfscqis@nsf.gov. Individuals who use a
Information Science
telecommunications device for the deaf
(TDD) may call the Federal Information
AGENCY: National Science Foundation.
Relay Service (FIRS) at 1–800–877–8339
ACTION: Notice of request for
between 8 a.m. and 8 p.m., Eastern time,
information.
Monday through Friday.
SUMMARY: The National Science and
SUPPLEMENTARY INFORMATION: The
Technology Council (NSTC)
National Science and Technology
PO 00000
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Agencies
[Federal Register Volume 83, Number 237 (Tuesday, December 11, 2018)]
[Notices]
[Pages 63674-63685]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-26755]
=======================================================================
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DEPARTMENT OF JUSTICE
Antitrust Division
United States et al. v. The Charlotte-Mecklenburg Hospital
Authority, d/b/a Carolinas Healthcare System; Proposed Final Judgment
and Competitive Impact Statement
Notice is hereby given pursuant to the Antitrust Procedures and
Penalties Act, 15 U.S.C. Sec. 16(b)-(h), that a proposed Final
Judgment, Stipulation, and Competitive Impact Statement have been filed
with the United States District Court for the Western District of North
Carolina in United States and State of North Carolina. v. The
Charlotte-Mecklenburg Hospital Authority, d/b/a Carolinas HealthCare
System, Civil Action No. 3:16-cv-00311-RJC-DCK. On June 6, 2016, the
United States and the State of North Carolina filed a Complaint
alleging that The Charlotte-Mecklenburg Hospital Authority formerly
known as Carolinas HealthCare System (or CHS) and now doing business as
Atrium Health (``Atrium'') included provisions in its contracts with
health insurers that restricted insurers from steering their members to
lower-cost, high-quality providers, in violation of Section 1 of the
Sherman Act, 15 U.S.C. Sec. 1. The proposed Final Judgment, filed
November 15, 2018, enjoins Atrium from (1) enforcing provisions in its
current insurer contracts that restrict steering and transparency; (2)
having contract provisions with an insurer that would prohibit, prevent
or significantly restrain the insurer from using certain steering
methods or providing transparency; and (3) penalizing, or threatening
to penalize, any insurer for its use of certain steering methods and
transparency.
Copies of the Complaint, proposed Final Judgment, and Competitive
Impact Statement are available for inspection on the Antitrust
Division's website at https://www.justice.gov/atr and at the Office of
the Clerk of the United States District Court for the Western District
of North Carolina. Copies of these materials may be obtained from the
Antitrust Division upon request and payment of the copying fee set by
Department of Justice regulations.
Public comment is invited within 60 days of the date of this
notice. Such comments, including the name of the submitter, and
responses thereto, will be posted on the Antitrust Division's website,
filed with the Court, and, under certain circumstances, published in
the Federal Register. Comments should be directed to Peter J.
Mucchetti, Chief, Healthcare and Consumer Products Section, Antitrust
Division, Department of Justice, 450 Fifth Street NW, Suite 4100,
Washington, DC 20530 (telephone: 202-307-0001).
Patricia A. Brink,
Director of Civil Enforcement.
United States District Court for the Western District of North Carolina
Charlotte Division
United States of America and the State of North Carolina,
Plaintiffs, v. The Charlotte-Mecklenburg Hospital Authority, d/b/a
Carolinas Healthcare System, Defendant.
Case No. 3:16-cv-00311-RJC-DCK
Judge Robert J. Conrad, Jr.
COMPLAINT
The United States of America and the State of North Carolina
bring this civil antitrust action to enjoin Defendant, The
Charlotte-Mecklenburg Hospital Authority, d/b/a Carolinas HealthCare
System (``CHS''), from using unlawful contract restrictions that
prohibit commercial health insurers in the Charlotte area from
offering patients financial benefits to use less-expensive
healthcare services offered by CHS's competitors. These steering
restrictions reduce competition resulting in harm to Charlotte area
consumers, employers, and insurers.
I. CHS AND ITS UNLAWFUL STEERING RESTRICTIONS
1. CHS is a North Carolina not-for-profit corporation providing
healthcare services with its principal place of business in
Charlotte. Its flagship facility is Carolinas Medical Center, a
large general acute-care hospital located in downtown Charlotte. It
also operates nine other general acute-care hospitals in the
Charlotte area.
2. CHS is the dominant hospital system in the Charlotte area,
with approximately a 50 percent share of the relevant market, and
2014 revenue of approximately $8.7 billion. Its closest competitor
by size is Novant, which owns five general acute care hospitals in
the Charlotte area and has less than half
[[Page 63675]]
of CHS's revenue. After Novant, the next-largest hospital in the
Charlotte area is CaroMont Regional Medical Center, which has less
than one tenth of CHS's revenue.
3. CHS exerts market power in its dealings with commercial
health insurers (``insurers''). CHS's market power results from its
large size, the comprehensive range of healthcare services that it
offers, its high market share, and insurers' need to include access
to CHS's hospitals-as well as its other facilities and providers-in
at least some of their provider networks in insurance plans that
cover people in the Charlotte area. CHS's market power is further
evidenced by its ability to profitably charge prices to insurers
that are higher than competitive levels across a range of services,
and to impose on insurers restrictions that reduce competition.
4. CHS's market power has enabled it to negotiate high prices
(in the form of high ``reimbursement rates'') for treating insured
patients. CHS has long had a reputation for being a high-priced
healthcare provider. In a 2013 presentation, CHS's internal strategy
group recognized that CHS ``has enjoyed years of annual
reimbursement rate increases that are premium to the market, with
those increases being applied to rates that are also premium to the
market.''
5. Steering is a method by which insurers offer consumers of
healthcare services options to reduce some of their healthcare
expenses. Steering typically occurs when an insurer offers consumers
a financial incentive to use a lower-cost provider or lower-cost
provider network, in order to lower their healthcare expenses.
6. Steering-and the competition from lower-priced healthcare
providers that steering animates-threatens CHS's high prices and
revenues. In 2013, CHS's internal strategy group surveyed a dozen of
CHS's senior leaders, asking them to list the ``biggest risks to CHS
revenue streams.'' Nine of the twelve leaders polled identified the
steering of patients away from CHS as one of the biggest risks to
CHS's revenues.
7. To protect itself against steering that would induce price
competition and potentially require CHS to lower its high prices,
CHS has imposed steering restrictions in its contracts with
insurers. These restrictions impede insurers from providing
financial incentives to patients to encourage them to consider
utilizing lower-cost but comparable or higher-quality alternative
healthcare providers.
8. Tiered networks are a popular type of steering that insurers
use in healthcare markets. Typically, insurers using tiered networks
place healthcare providers that offer better value healthcare
services (lower cost, higher quality) in top tiers. Patients who use
top-tier providers pay lower out-of-pocket costs. For example, for a
procedure costing $10,000, a patient might be responsible for paying
$3,600 in coinsurance at a lower-tier hospital, but only $1,800
coinsurance to have the same procedure performed at a top-tier
hospital.
9. Narrow-network insurance plans are another popular steering
tool. Typically, narrow networks consist of a subset of all the
healthcare providers that participate in an insurer's conventional
network. A consumer who chooses a narrow-network insurance plan
typically pays lower premiums, and lower out-of-pocket expenses than
a conventional broad-network insurance plan as long as the consumer
is willing to choose from the smaller network of providers for his
or her healthcare needs.
10. Providers are motivated to have insurers steer towards them,
including through an insurer's narrow or tiered network, because of
the increased patient volume that accompanies steering. Thus, the
ability of insurers to steer gives providers a powerful incentive to
be as efficient as possible, maintain low prices, and offer high
quality and innovative services. By doing so, providers induce
insurers to steer patient volume to them. Individuals and employers
that provide health insurance to their employees benefit
tremendously from this because they can lower their healthcare
expenses.
11. CHS has gained patient volume from insurers steering towards
CHS, and has obtained higher revenues as a result. CHS encourages
insurers to steer patients toward itself by offering health insurers
modest concessions on its market-power driven, premium prices.
12. However, CHS forbids insurers from allowing CHS's
competitors to do the same. CHS prevents insurers from offering
tiered networks that feature hospitals that compete with CHS in the
top tiers, and prevents insurers from offering narrow networks that
include only CHS's competitors. By restricting its competitors from
competing for-and benefitting from-steered arrangements, CHS uses
its market power to impede insurers from negotiating lower prices
with its competitors and offering lower-premium plans.
13. CHS also imposes restrictions in its contracts with insurers
that impede insurers from providing truthful information to
consumers about the value (cost and quality) of CHS's healthcare
services compared to CHS's competitors. CHS's restrictions on
insurers' price and quality transparency are an indirect restriction
on steering, because they prevent patients from accessing
information that would allow them to make healthcare choices based
on available price and quality information.
14. Because CHS's steering restrictions prevent its competitors
from attracting more patients through lower prices, CHS's
competitors have less incentive to remain lower priced and to
continue to become more efficient. As a result, CHS's restrictions
reduce the competition that CHS faces in the marketplace. In the
instances in which insurers have steered in other markets and in the
few instances in which insurers have steered in the Charlotte area
despite CHS's restrictions, insurers have reduced health insurance
costs for consumers.
15. Four insurers provide coverage to more than 85 percent of
the commerically-insured residents of the Charlotte area. They are:
Aetna Health of the Carolinas, Inc., Blue Cross Blue Shield of North
Carolina, Cigna Healthcare of North Carolina, Inc., and United
Healthcare of North Carolina, Inc.
16. CHS maintains and enforces steering restrictions in its
contracts with all four of these insurers. In some instances, the
contract language prohibits steering outright. For example, CHS
secured a contractual obligation from one insurer that it ``shall
not directly or indirectly steer business away from'' CHS. In other
instances, the contract language gives CHS the right to terminate
its agreement with the insurer if the insurer engages in steering,
providing CHS the ability to deny the insurer and its enrollees
access to its dominant hospital system unless the steering ends.
Although the contractual language that CHS has imposed varies with
each insurer, it consistently creates disincentives that deter
insurers from providing to their enrollees truthful information
about their healthcare options and the benefits of price and quality
competition among healthcare providers that the insurers could offer
if they had full freedom to steer.
II. RELEVANT MARKET AND COMPETITIVE EFFECTS
17. The sale of general acute care inpatient hospital services
to insurers (``acute inpatient hospital services'') is a relevant
product market. The market includes sales of such services to
insurers' individual, group, fully-insured and self-funded health
plans.
18. The relevant market does not include sales of acute
inpatient hospital services to government payers, e.g., Medicare
(covering the elderly and disabled), Medicaid (covering low-income
persons), and TRICARE (covering military personnel and families)
because a healthcare provider's negotiations with an insurer are
separate from the process used to determine the rates paid by
government payers.
19. Acute inpatient hospital services consist of a broad group
of medical and surgical diagnostic and treatment services that
include a patient's overnight stay in the hospital. Although
individual acute inpatient hospital services are not substitutes for
each other (e.g., obstetrics is not a substitute for cardiac
services), insurers typically contract for the various individual
acute inpatient hospital services as a bundle, and CHS's steering
restrictions have an adverse impact on the sale of all acute
inpatient hospital services. Therefore, acute inpatient hospital
services can be aggregated for analytical convenience.
20. There are no reasonable substitutes or alternatives to acute
inpatient hospital services. Consequently, a hypothetical monopolist
of acute inpatient hospital services would likely profitably impose
a small but significant price increase for those services over a
sustained period of time.
21. The relevant geographic market is no larger than the
Charlotte area. In this Complaint, the Charlotte area means the
Charlotte Combined Statistical Area, as defined by the U.S. Office
of Management and Budget, which consists of Cabarrus, Cleveland,
Gaston, Iredell, Lincoln, Mecklenburg, Rowan, Stanly, and Union
counties in North Carolina, and Chester, Lancaster, and York
counties in South Carolina. The Charlotte area has a population of
about 2.6 million people.
22. Insurers contract to purchase acute inpatient hospital
services from hospitals
[[Page 63676]]
within the geographic area where their enrollees are likely to seek
medical care. Such hospitals are typically close to their enrollees'
homes or workplaces. Insurers who seek to sell insurance plans to
individuals and employers in the Charlotte area must include
Charlotte area hospitals in their provider networks because people
who live and work in the Charlotte area strongly prefer to obtain
acute inpatient hospital services in the Charlotte area. Charlotte
area consumers have little or no willingness to enroll in an
insurance plan that provides no network access to hospitals located
in the Charlotte area.
23. For these reasons, it is not a viable alternative for
insurers that sell health insurance plans to consumers in the
Charlotte area to purchase acute inpatient hospital services from
providers outside the Charlotte area. Consequently, competition from
providers of acute inpatient hospital services located outside the
Charlotte area would not likely be sufficient to prevent a
hypothetical monopolist provider of acute inpatient hospital
services located in the Charlotte area from profitably imposing
small but significant price increases for those services over a
sustained period of time.
24. An insurer selling health insurance plans to individuals and
employers in the Charlotte area must have CHS as a participant in at
least some of its provider networks, in order to have a viable
health insurance business in the Charlotte area. This gives CHS the
ability to impose steering restrictions in its contracts with
insurers. When CHS negotiates with insurers for CHS's network
participation, CHS typically negotiates the prices and terms of
participation for acute inpatient hospital services and other
healthcare services, such as outpatient, ancillary, and physician
services, at the same time, including services that are located
outside the Charlotte area. As a result, CHS's anticompetitive
steering restrictions typically apply to all the negotiated
services.
25. CHS's maintenance and enforcement of its steering
restrictions lessen competition between CHS and the other providers
of acute inpatient hospital services in the Charlotte area that
would, in the absence of the restrictions, likely reduce the prices
paid for such services by insurers. Thus, the restrictions help to
insulate CHS from competition, by limiting the ability of CHS's
competitors to win more commercially-insured business by offering
lower prices.
26. Insurers want to steer towards lower-cost providers and to
offer innovative insurance plans that steer. For years, insurers
have tried to negotiate the removal of steering restrictions from
their contracts with CHS, but cannot because of CHS's market power.
In the absence of the steering restrictions, insurers would likely
steer consumers to lower-cost providers more than their current
contracts with CHS presently permit.
27. As a result of this reduced competition due to CHS's
steering restrictions, individuals and employers in the Charlotte
area pay higher prices for health insurance coverage, have fewer
insurance plans from which to choose, and are denied access to
consumer comparison shopping and other cost-saving innovative and
more efficient health plans that would be possible if insurers could
steer freely. Deprived of the option to benefit from choosing more
cost-efficient providers, Charlotte area patients incur higher out-
of-pocket costs for their healthcare. Insurers are directly harmed
by CHS's imposition of steering restrictions.
28. CHS restricts steering to help insulate itself from price
competition, which enables CHS to maintain high prices and preserve
its dominant position, and not for any procompetitive purpose.
Indeed, when asked under oath whether CHS should limit the ability
of insurers to offer tiered networks or narrow networks that exclude
CHS, Carol Lovin, CHS's Chief Strategy Officer, said that CHS should
not. And when asked her view about the possibility of eliminating
CHS's steering restrictions, she testified, ``Would I personally be
okay with getting rid of them? Yes, I would.'' CHS's steering
restrictions do not have any procompetitive effects. CHS can seek to
avoid losses of revenues and market share from lower cost
competitors by competing to offer lower prices and better value than
its competitors, rather than imposing rules on insurers that reduce
the benefit to its rivals from competing on price.
III. JURISDICTION, VENUE AND INTERSTATE COMMERCE
29. The Court has subject-matter jurisdiction over this action
under Section 4 of the Sherman Act, 15 U.S.C. Sec. 4 (as to the
claim by the United States); Section 16 of the Clayton Act, 15
U.S.C. Sec. 26 (as to the claim by the State of North Carolina);
and 28 U.S.C. Sec. Sec. 1331, 1337(a), and 1345.
30. The Court has personal jurisdiction over CHS under Section
12 of the Clayton Act, 15 U.S.C. Sec. 22. CHS maintains its
principal place of business and transacts business in this District.
31. Venue is proper under 28 U.S.C. Sec. 1391 and Section 12 of
the Clayton Act, 15 U.S.C. Sec. 22. CHS transacts business and
resides in this District and the events giving rise to the claims
occurred in this District.
32. CHS engages in interstate commerce and in activities
substantially affecting interstate commerce. CHS provides healthcare
services for which employers, insurers, and individual patients
remit payments across state lines. CHS also purchases supplies and
equipment that are shipped across state lines, and it otherwise
participates in interstate commerce.
IV. CHS'S VIOLATION OF SECTION 1 OF THE SHERMAN ACT
33. Plaintiffs incorporate paragraphs 1 through 32 of this
Complaint.
34. CHS has market power in the sale of acute inpatient hospital
services in the Charlotte area.
35. CHS has and likely will continue to negotiate and enforce
contracts containing steering restrictions with insurers in the
Charlotte area. The contracts containing the steering restrictions
are contracts, combinations, and conspiracies within the meaning of
Section 1 of the Sherman Act, 15 U.S.C. Sec. 1.
36. These steering restrictions have had, and will likely to
continue to have, the following substantial anticompetitive effects
in the relevant product and geographic market, among others:
a. protecting CHS's market power and enabling CHS to maintain at
supracompetitive levels the prices of acute inpatient hospital
services;
b. substantially lessening competition among providers in their
sale of acute inpatient hospital services;
c. restricting the introduction of innovative insurance products
that are designed to achieve lower prices and improved quality for
acute inpatient hospital services;
d. reducing consumers' incentives to seek acute inpatient
hospital services from more cost-effective providers; and
e. depriving insurers and their enrollees of the benefits of a
competitive market for their purchase of acute inpatient hospital
services.
37. Entry or expansion by other hospitals in the Charlotte area
has not counteracted the actual and likely competitive harms
resulting from CHS's steering restrictions. And in the future, such
entry or expansion is unlikely to be rapid enough and sufficient in
scope and scale to counteract these harms to competition. Building a
hospital with a strong reputation that is capable of attracting
physicians and patients is difficult, time-consuming, and expensive.
Additionally, new facilities and programs, and typically the
expansion of existing facilities and programs, are subject to
lengthy licensing requirements, and in North Carolina, to
certificate-of-need laws.
38. CHS did not devise its strategy of using steering
restrictions for any procompetitive purpose. Nor do the steering
restrictions have any procompetitive effects. Any arguable benefits
of CHS's steering restrictions are outweighed by their actual and
likely anticompetitive effects.
39. The challenged steering restrictions unreasonably restrain
trade in violation of Section 1 of the Sherman Act, 15 U.S.C. Sec.
1.
V. REQUEST FOR RELIEF
40. The United States and the State of North Carolina request
that the Court:
a. adjudge that all of the steering restrictions in the
contracts between CHS and any insurer violate Section 1 of the
Sherman Act, 15 U.S.C. Sec. 1;
b. enjoin CHS, its officers, directors, agents, employees, and
successors, and all other persons acting or claiming to act on its
behalf, directly or indirectly, from seeking, agreeing to, or
enforcing any provision in any agreement that prohibits or restricts
an insurer from engaging, or attempting to engage, in steering
towards any healthcare provider;
c. enjoin CHS from retaliating, or threatening to retaliate,
against any insurer for engaging or attempting to engage in
steering; and
d. award Plaintiffs their costs in this action and such other
relief as the Court may deem just and proper.
Dated: June 9, 2016
Respectfully Submitted,
FOR PLAINTIFF UNITED STATES OF AMERICA
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Renata B. Hesse,
[[Page 63677]]
Principal Deputy Assistant Attorney General for Antitrust.
David I. Gelfand,
Deputy Assistant Attorney General.
Patricia A. Brink,
Director of Civil Enforcement.
Peter J. Mucchetti,
Chief, Litigation I.
Jill Westmoreland Rose,
United States Attorney.
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Paul B. Taylor,
Assistant United States Attorney, Chief, Civil Division, N.C. Bar
Number 10067, Room 233, U.S. Courthouse, 100 Otis Street, Asheville,
NC 28801-2611, (828) 271-4661(phone), [email protected].
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Paul Torzilli,
Karl D. Knutsen,
Richard Martin,
John R. Read,
Antitrust Division, U.S. Department of Justice, 450 Fifth Street
N.W., Suite 4100, Washington, DC 20530, (202) 514-8349 (phone), (202
514-7308 (fax), [email protected].
FOR PLAINTIFF STATE OF NORTH CAROLINA
Roy Cooper,
Attorney General of North Carolina.
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K.D. Sturgis,
Special Deputy Attorney General, North Carolina Department of
Justice, N.C. Bar Number 9486, P.O. Box 629, Raleigh, NC 27602, Tel.
919-716-6011, Fax 919-716-6050, [email protected].
United States District Court for the Western District of North Carolina
Charlotte Division
United States of America and State of North Carolina,
Plaintiffs, v. The Charlotte-Mecklenburg Hospital Authority d/b/a
Carolinas Healthcare System, Defendant.
Case No. 3:16-cv-00311-RJC-DCK
Judge Robert J. Conrad, Jr.
[PROPOSED] FINAL JUDGMENT
WHEREAS, Plaintiffs, the United States of America and the State
of North Carolina (collectively ``Plaintiffs''), filed their
Complaint on June 9, 2016; Plaintiffs and Defendant The Charlotte-
Mecklenburg Hospital Authority d/b/a Atrium Health f/k/a Carolinas
HealthCare System (collectively the ``Parties''), by their
respective attorneys, have consented to the entry of this Final
Judgment without trial or adjudication of any issue of fact or law;
AND WHEREAS, this Final Judgment does not constitute any
evidence against or admission by any party regarding any issue of
fact or law;
AND WHEREAS, the Plaintiffs and Defendant agree to be bound by
the provisions of this Final Judgment pending its approval by this
Court;
AND WHEREAS, the essence of this Final Judgment is to enjoin
Defendant from prohibiting, preventing, or penalizing steering as
defined in this Final Judgment;
NOW THEREFORE, before any testimony is taken, without trial or
adjudication of any issue of fact or law, and upon consent of the
parties, it is ORDERED, ADJUDGED, AND DECREED:
I. JURISDICTION
The Court has jurisdiction over the subject matter of and each
of the Parties to this action. The Complaint states a claim upon
which relief may be granted against Defendant under Section 1 of the
Sherman Act, as amended, 15 U.S.C. Sec. 1.
II. DEFINITIONS
For purposes of this Final Judgment, the following definitions
apply:
A. ``Benefit Plan'' means a specific set of health care benefits
and Healthcare Services that is made available to members through a
health plan underwritten by an Insurer, a self-funded benefit plan,
or Medicare Part C plans. The term ``Benefit Plan'' does not include
workers' compensation programs, Medicare (except Medicare Part C
plans), Medicaid, or uninsured discount plans.
B. ``Carve-out'' means an arrangement by which an Insurer
unilaterally removes all or substantially all of a particular
Healthcare Service from coverage in a Benefit Plan during the
performance of a network-participation agreement.
C. ``Center of Excellence'' means a feature of a Benefit Plan
that designates Providers of certain Healthcare Services based on
objective quality or quality-and-price criteria in order to
encourage patients to obtain such Healthcare Services from those
designated Providers.
D. ``Charlotte Area'' means Cabarrus, Cleveland, Gaston,
Iredell, Lincoln, Mecklenburg, Rowan, Stanly, and Union counties in
North Carolina and Chester, Lancaster, and York counties in South
Carolina.
E. ``Co-Branded Plan'' means a Benefit Plan, such as Blue Local
with Carolinas HealthCare System, arising from a joint venture,
partnership, or a similar formal type of alliance or affiliation
beyond that present in broad network agreements involving value-
based arrangements between an Insurer and Defendant in any portion
of the Charlotte Area whereby both Defendant's and Insurer's brands
or logos appear on marketing materials.
F. ``Defendant'' means The Charlotte-Mecklenburg Hospital
Authority d/b/a Atrium Health f/k/a Carolinas HealthCare System, a
North Carolina hospital authority with its headquarters in
Charlotte, North Carolina; and its directors, commissioners,
officers, managers, agents, and employees; its successors and
assigns; and any controlled subsidiaries (including Managed Health
Resources), divisions, partnerships, and joint ventures, and their
directors, commissioners, officers, managers, agents, and employees;
and any Person on whose behalf Defendant negotiates contracts with,
or consults in the negotiation of contracts with, Insurers. For
purposes of this Final Judgment, an entity is controlled by
Defendant if Defendant holds 50% or more of the entity's voting
securities, has the right to 50% or more of the entity's profits,
has the right to 50% or more of the entity's assets on dissolution,
or has the contractual power to designate 50% or more of the
directors or trustees of the entity. Also for purposes of this Final
Judgment, the term ``Defendant'' excludes MedCost LLC and MedCost
Benefits Services LLC, but it does not exclude any Atrium Health
director, commissioner, officer, manager, agent, or employee who may
also serve as a director, member, officer, manager, agent, or
employee of MedCost LLC or MedCost Benefit Services LLC when such
director, commissioner, officer, manager, agent, or employee is
acting within the course of his or her duties for Atrium Health.
MedCostLLC and MedCost Benefits Services LLC will remain excluded
from the definition of ``Defendant'' as long as Atrium does not
acquire any greater ownership interest in these entities than it has
at the time that this Final Judgment is lodged with the Court.
G. ``Healthcare Provider'' or ``Provider'' means any Person
delivering any Healthcare Service.
H. ``Healthcare Services'' means all inpatient services (i.e.,
acute-care diagnostic and therapeutic inpatient hospital services),
outpatient services (i.e., acute-care diagnostic and therapeutic
outpatient services, including but not limited to ambulatory surgery
and radiology services), and professional services (i.e., medical
services provided by physicians or other licensed medical
professionals) to the extent offered by Defendant and within the
scope of services covered on an in-network basis pursuant to a
contract between Defendant and an Insurer. ``Healthcare Services''
does not mean management of patient care, such as through population
health programs or employee or group wellness programs.
I. ``Insurer'' means any Person providing commercial health
insurance or access to Healthcare Provider networks, including but
not limited to managed-care organizations, and rental networks
(i.e., entities that lease, rent, or otherwise provide direct or
indirect access to a proprietary network of Healthcare Providers),
regardless of whether that entity bears any risk or makes any
payment relating to the provision of healthcare. The term
``Insurer'' includes Persons that provide Medicare Part C plans, but
does not include Medicare (except Medicare Part C plans), Medicaid,
or TRICARE, or entities that otherwise contract on their behalf.
J. ``Narrow Network'' means a network composed of a
significantly limited number of Healthcare Providers that offers a
range of Healthcare Services to an Insurer's members for which all
Providers that are not included in the network are out of network.
K. ``Penalize'' or ``Penalty'' is broader than ``prohibit'' or
``prevent'' and is intended to include any contract term or action
with the likely effect of significantly restraining steering through
Steered Plans or Transparency. In determining whether any contract
provision or action ``Penalizes'' or is a ``Penalty,'' factors that
may be considered include: the facts and circumstances relating to
the contract provision or action; its economic impact; and the
extent to which the contract provision or action has potential or
actual procompetitive effects in the Charlotte Area.
L. ``Person'' means any natural person, corporation, company,
partnership, joint
[[Page 63678]]
venture, firm, association, proprietorship, agency, board,
authority, commission, office, or other business or legal entity.
M. ``Reference-Based Pricing'' means a feature of a Benefit Plan
by which an Insurer pays up to a uniformly-applied defined
contribution, based on an external price selected by the Insurer,
toward covering the full price charged for a Healthcare Service,
with the member being required to pay the remainder. For avoidance
of doubt, a Benefit Plan with Reference-Based Pricing as a feature
may permit an Insurer to pay a portion of this remainder.
N. ``Steered Plan'' means any Narrow Network Benefit Plan,
Tiered Network Benefit Plan, or any Benefit Plan with Reference-
Based Pricing or a Center of Excellence as a component.
O. ``Tiered Network'' means a network of Healthcare Providers
for which (i) an Insurer divides the in-network Providers into
different sub-groups based on objective price, access, and/or
quality criteria; and (ii) members receive different levels of
benefits when they utilize Healthcare Services from Providers in
different sub-groups.
P. ``Transparency'' means communication of any price, cost,
quality, or patient experience information directly or indirectly by
an Insurer to a client, member, or consumer.
III. APPLICABILITY
This Final Judgment applies to Defendant, as defined above, and
all other Persons in active concert with, or participation with,
Defendant who receive actual notice of this Final Judgment by
personal service or otherwise.
IV. PROHIBITED CONDUCT
A. The contract language reproduced in Exhibit A is void, and
Defendant shall not enforce or attempt to enforce it. The contract
language reproduced in Exhibit B shall not be used to prohibit,
prevent, or penalize Steered Plans or Transparency, but could remain
enforceable for protection against Carve-outs. For the Network
Participation Agreement between Blue Cross and Blue Shield of North
Carolina and Defendant's wholly-owned subsidiary Managed Health
Resources, effective January 1, 2014, as amended, Defendant shall
exclude from the calculation of total cumulative impact pursuant to
Section 6.14 of that agreement any impact to Defendant resulting
from Blue Cross and Blue Shield of North Carolina disfavoring
Defendant through Transparency or through the use of any Steered
Plan.
B. For Healthcare Services in the Charlotte Area, Defendant will
not seek or obtain any contract provision which would prohibit,
prevent, or penalize Steered Plans or Transparency including:
1. express prohibitions on Steered Plans or Transparency;
2. requirements of prior approval for the introduction of new
benefit plans (except in the case of Co-Branded Plans); and
3. requirements that Defendant be included in the most-preferred
tier of Benefit Plans (except in the case of Co-Branded Plans).
However, notwithstanding this Paragraph IV(B)(3), Defendant may
enter into a contract with an Insurer that provides Defendant with
the right to participate in the most-preferred tier of a Benefit
Plan under the same terms and conditions as any other Charlotte Area
Provider, provided that if Defendant declines to participate in the
most-preferred tier of that Benefit Plan, then Defendant must
participate in that Benefit Plan on terms and conditions that are
substantially the same as any terms and conditions of any then-
existing broad-network Benefit Plan (e.g., PPO plan) in which
Defendant participates with that Insurer. Additionally,
notwithstanding Paragraph IV(B)(3), nothing in this Final Judgment
prohibits Defendant from obtaining any criteria used by the Insurer
to (i) assign Charlotte Area Providers to each tier in any Tiered
Network; and/or (ii) designate Charlotte Area Providers as a Center
of Excellence.
C. Defendant will not take any actions that penalize, or
threaten to penalize, an Insurer for (i) providing (or planning to
provide) Transparency, or (ii) designing, offering, expanding, or
marketing (or planning to design, offer, expand, or market) a
Steered Plan.
I. PERMITTED CONDUCT
A. Defendant may exercise any contractual right it has, provided
it does not engage in any Prohibited Conduct as set forth above.
B. For any Co-Branded Plan or Narrow Network in which Defendant
is the most-prominently featured Provider, Defendant may restrict
steerage within that Co-Branded Plan or Narrow Network. For example,
Defendant may restrict an Insurer from including at inception or
later adding other Providers to any (i) Narrow Network in which
Defendant is the most-prominently featured Provider, or (ii) any Co-
Branded Plan.
C. With regard to information communicated as part of any
Transparency effort, nothing in this Final Judgment prohibits
Defendant from reviewing its information to be disseminated,
provided such review does not delay the dissemination of the
information. Furthermore, Defendant may challenge inaccurate
information or seek appropriate legal remedies relating to
inaccurate information disseminated by third parties. Also, for an
Insurer's dissemination of price or cost information (other than
communication of an individual consumer's or member's actual or
estimated out-of-pocket expense), nothing in the Final Judgment will
prevent or impair Defendant from enforcing current or future
provisions, including but not limited to confidentiality provisions,
that (i) prohibit an Insurer from disseminating price or cost
information to Defendant's competitors, other Insurers, or the
general public; and/or (ii) require an Insurer to obtain a covenant
from any third party that receives such price or cost information
that such third party will not disclose that information to
Defendant's competitors, another Insurer, the general public, or any
other third party lacking a reasonable need to obtain such
competitively sensitive information. Defendant may seek all
appropriate remedies (including injunctive relief) in the event that
dissemination of such information occurs.
V. REQUIRED CONDUCT
Within fifteen (15) business days of entry of this Final
Judgment, Defendant, through its designated counsel, must notify in
writing Aetna, Blue Cross and Blue Shield of North Carolina, Cigna,
MedCost, and UnitedHealthcare, that:
A. This Final Judgment has been entered (enclosing a copy of
this Final Judgment) and that it prohibits Defendant from entering
into or enforcing any contract term that would prohibit, prevent, or
penalize Steered Plans or Transparency, or taking any other action
that violates this Final Judgment; and
B. For the term of this Final Judgment Defendant waives any
right to enforce any provision listed in Exhibit A and further
waives the right to enforce any provision listed in Exhibit B to
prohibit, prevent, or penalize Steered Plans and Transparency.
VII. COMPLIANCE
A. It shall be the responsibility of the Defendant's designated
counsel to undertake the following:
1. within fifteen (15) calendar days of entry of this Final
Judgment, provide a copy of this Final Judgment to each of
Defendant's commissioners and officers, and to each employee whose
job responsibilities include negotiating or approving agreements
with Insurers for the purchase of Healthcare Services, including
personnel within the Managed Health Resources subsidiary (or any
successor organization) of Defendant;
2. distribute in a timely manner a copy of this Final Judgment
to any person who succeeds to, or subsequently holds, a position of
commissioner, officer, or other position for which the job
responsibilities include negotiating or approving agreements with
Insurers for the purchase of Healthcare Services, including
personnel within the Managed Health Resources subsidiary (or any
successor organization) of Defendant; and
3. within sixty (60) calendar days of entry of this Final
Judgment, develop and implement procedures necessary to ensure
Defendant's compliance with this Final Judgment. Such procedures
shall ensure that questions from any of Defendant's commissioners,
officers, or employees about this Final Judgment can be answered by
counsel (which may be outside counsel) as the need arises. Paragraph
21.1 of the Amended Protective Order Regarding Confidentiality shall
not be interpreted to prohibit outside counsel from answering such
questions.
B. For the purposes of determining or securing compliance with
this Final Judgment, or any related orders, or determining whether
the Final Judgment should be modified or vacated, and subject to any
legally-recognized privilege, from time to time authorized
representatives of the United States or the State of North Carolina,
including agents and consultants retained by the United States or
the State of North Carolina, shall, upon written request of an
authorized representative of the Assistant Attorney General in
charge of the Antitrust Division or the Attorney General for the
State of North Carolina, and on reasonable notice to Defendant, be
permitted:
1. access during Defendant's office hours to inspect and copy,
or at the option of the
[[Page 63679]]
United States, to require Defendant to provide electronic copies of
all books, ledgers, accounts, records, data, and documents in the
possession, custody, or control of Defendant, relating to any
matters contained in this Final Judgment; and
2. to interview, either informally or on the record, Defendant's
officers, employees, or agents, who may have their individual
counsel present, regarding such matters. The interviews shall be
subject to the reasonable convenience of the interviewee and without
restraint or interference by Defendant.
C. Within 270 calendar days of entry of this Final Judgment,
Defendant must submit to the United States and the State of North
Carolina a written report setting forth its actions to comply with
this Final Judgment, specifically describing (1) the status of all
negotiations between Managed Health Resources (or any successor
organization) and an Insurer relating to contracts that cover
Healthcare Services rendered in the Charlotte Area since the entry
of the Final Judgment, and (2) the compliance procedures adopted
under Paragraph VII(A)(3) of this Final Judgment.
D. Upon the written request of an authorized representative of
the Assistant Attorney General in charge of the Antitrust Division
or the Attorney General for the State of North Carolina, Defendant
shall submit written reports or responses to written
interrogatories, under oath if requested, relating to any of the
matters contained in this Final Judgment as may be requested.
E. The United States may share information or documents obtained
under Paragraph VII with the State of North Carolina subject to
appropriate confidentiality protections. The State of North Carolina
shall keep all such information or documents confidential.
F. No information or documents obtained by the means provided in
Paragraph VII shall be divulged by the United States or the State of
North Carolina to any Person other than an authorized representative
of (1) the executive branch of the United States or (2) the Office
of the North Carolina Attorney General, except in the course of
legal proceedings to which the United States or the State of North
Carolina is a party (including grand jury proceedings), for the
purpose of securing compliance with this Final Judgment, or as
otherwise required by law.
G. If at the time that Defendant furnishes information or
documents to the United States or the State of North Carolina,
Defendant represents and identifies in writing the material in any
such information or documents to which a claim of protection may be
asserted under Rule 26(c)(1)(G) of the Federal Rules of Civil
Procedure, and Defendant marks each pertinent page of such material,
``Subject to claim of protection under Rule 26(c)(1)(G) of the
Federal Rules of Civil Procedure,'' the United States and the State
of North Carolina shall give Defendant ten (10) calendar days'
notice prior to divulging such material in any legal proceeding
(other than a grand jury proceeding).
H. For the duration of this Final Judgment, Defendant must
provide to the United States and the State of North Carolina a copy
of each contract and each amendment to a contract that covers
Healthcare Services in the Charlotte Area that it negotiates with
any Insurer within thirty (30) calendar days of execution of such
contract or amendment. Defendant must also notify the United States
and the State of North Carolina within thirty (30) calendar days of
having reason to believe that a Provider which Defendant controls
has a contract with any Insurer with a provision that prohibits,
prevents, or penalizes any Steered Plans or Transparency.
VIII. Retention of Jurisdiction
The Court retains jurisdiction to enable any Party to this Final
Judgment to apply to the Court at any time for further orders and
directions as may be necessary or appropriate to carry out or
construe this Final Judgment, to modify any of its provisions, to
enforce compliance, and to punish violations of its provisions.
IX. Enforcement of Final Judgment
A. The United States retains and reserves all rights to enforce
the provisions of this Final Judgment, including the right to seek
an order of contempt from the Court. Defendant agrees that in any
civil contempt action, any motion to show cause, or any similar
action brought by the United States regarding an alleged violation
of this Final Judgment, the United States may establish a violation
of the decree and the appropriateness of any remedy therefor by a
preponderance of the evidence, and Defendant waives any argument
that a different standard of proof should apply.
B. The Final Judgment should be interpreted to give full effect
to the procompetitive purposes of the antitrust laws and to restore
all competition Plaintiffs alleged was harmed by the challenged
conduct. Defendant agrees that it may be held in contempt of, and
that the Court may enforce, any provision of this Final Judgment
that, as interpreted by the Court in light of these procompetitive
principles and applying ordinary tools of interpretation, is stated
specifically and in reasonable detail, whether or not it is clear
and unambiguous on its face. In any such interpretation, the terms
of this Final Judgment should not be construed against either Party
as the drafter.
C. In any enforcement proceeding in which the Court finds that
Defendant has violated this Final Judgment, the United States may
apply to the Court for a one-time extension of this Final Judgment,
together with such other relief as may be appropriate. In connection
with any successful effort by the United States to enforce this
Final Judgment against Defendant, whether litigated or resolved
prior to litigation, Defendant agrees to reimburse the United States
for the fees and expenses of its attorneys, as well as any other
costs including experts' fees, incurred in connection with that
enforcement effort, including in the investigation of the potential
violation.
X. Expiration of Final Judgment
Unless the Court grants an extension, this Final Judgment shall
expire ten (10) years from the date of its entry, except that after
five (5) years from the date of its entry, this Final Judgment may
be terminated upon notice by the United States to the Court and
Defendant that the continuation of the Final Judgment is no longer
necessary or in the public interest.
XI. Public Interest Determination
Entry of this Final Judgment is in the public interest. The
Parties have complied with the requirements of the Antitrust
Procedures and Penalties Act, 15 U.S.C. Sec. 16, including making
copies available to the public of this Final Judgment, the
Competitive Impact Statement, any comments thereon, and the United
States' responses to comments. Based upon the record before the
Court, which includes the Competitive Impact Statement and any
comments and responses to comments filed with the Court, entry of
this Final Judgment is in the public interest.
Date:------------------------------------------------------------------
[Court approval subject to procedures of Antitrust Procedures and
Penalties Act, 15 U.S.C. Sec. 16]
-----------------------------------------------------------------------
Robert J. Conrad, Jr.
United States District Judge.
Exhibit A
Aetna
Section 2.8 of the Physician Hospital Organization Agreement
between and among Aetna Health of the Carolinas, Inc., Aetna Life
Insurance Company, Aetna Health Management, LLC, and Defendant
states in part:
``Company may not . . . steer Members away from Participating
PHO Providers other than instances where services are not deemed to
be clinically appropriate, subject to the terms of Section 4.1.3 of
this Agreement.''
In addition, Section 2.11 of the above-referenced agreement
states in part:
``Company reserves the right to introduce in new Plans . . . and
products during the term of this Agreement and will provide PHO with
ninety (90) days written notice of such new Plans, Specialty
Programs and products. . . . For purposes under (c) and (d) above,
Company commits that Participating PHO Providers will be in-network
Participating Providers in Company Plans and products as listed on
the Product Participation Schedule. If Company introduces new
products or benefit designs in PHO's market that have the effect of
placing Participating PHO Providers in a non-preferred position, PHO
will have the option to terminate this Agreement in accordance with
Section 6.3. Notwithstanding the foregoing, if Company introduces an
Aexcel performance network in PHO Provider's service area, all PHO
Providers will be placed in the most preferred benefit level. As
long as such Plans or products do not directly or indirectly steer
Members away from a Participating PHO Provider to an alternative
Participating Provider for the same service in the same level of
care or same setting, the termination provision would not apply.''
Blue Cross and Blue Shield of North Carolina
The Benefit Plan Exhibit to the Network Participation Agreement
between Blue Cross and Blue Shield of North Carolina and
[[Page 63680]]
Defendant (originally effective January 1, 2014), as replaced by the
Fifth Amendment, states in part:
``After meeting and conferring, if parties cannot reach
agreement, then, notwithstanding Section 5.1, this Agreement will be
considered to be beyond the initial term, and you may terminate this
Agreement upon not less than 90 days' prior Written Notice to us,
pursuant to Section 5.2.''
Cigna
Section II.G.5 of the Managed Care Alliance Agreement between
Cigna HealthCare of North Carolina, Inc. and Defendant states in
part:
``All MHR entities as defined in Schedule 1 will be represented
in the most preferred benefit level for any and all CIGNA products
for all services provided under this Agreement unless CIGNA obtains
prior written consent from MHR to exclude any MHR entities from
representation in the most preferred benefit level for any CIGNA
product. . . . As a MHR Participating Provider, CIGNA will not steer
business away from MHR Participating Providers.''
Medcost
Section 3.6 of the Participating Physician Hospital Organization
agreement between Medcost, LLC and Defendant states in part:
``Plans shall not directly or indirectly steer patients away
from MHR Participating Providers.''
UnitedHealthcare
Section 2 of the Hospital Participation Agreement between
UnitedHealthcare of North Carolina, Inc. and Defendant states in
part:
``As a Participating Provider, Plan shall not directly or
indirectly steer business away from Hospital.''
Exhibit B
Cigna
Section II.G.5 of the Managed Care Alliance Agreement between
Cigna HealthCare of North Carolina, Inc. and Defendant states in
part:
``CIGNA may not exclude a MHR Participating Provider as a
network provider for any product or Covered Service that MHR
Participating Provider has the capability to provide except those
carve-out services as outlined in Exhibit E attached hereto, unless
CIGNA obtains prior written consent from MHR to exclude MHR
Participating Provider as a network provider for such Covered
Services.''
UnitedHealthcare
Section 2 of the Hospital Participation Agreement between
UnitedHealthcare of North Carolina, Inc. and Defendant states in
part:
``Plan may not exclude Hospital as a network provider for any
Health Service that Hospital is qualified and has the capability to
provide and for which Plan and Hospital have established a fee
schedule or fixed rate, as applicable, unless mutually agreed to in
writing by Plan and Hospital to exclude Hospital as a network
provider for such Health Service.''
In addition, Section 3.6 of the above-referenced agreement
states in part:
``During the term of this Agreement, including any renewal
terms, if Plan creates new or additional products, which product
otherwise is or could be a Product Line as defined in this
Agreement, Hospital shall be given the opportunity to participate
with respect to such new Product Line.''
United States District Court for the Western District of North Carolina
Charlotte Division
United States of America and the State of North Carolina,
Plaintiffs, v. The Charlotte-Mecklenburg Hospital Authority, d/b/a
Carolinas Healthcare System, Defendant.
Case No. 3:16-cv-00311-RJC-DCK
Judge Robert J. Conrad, Jr.
COMPETITIVE IMPACT STATEMENT
Plaintiff United States of America (``United States''), pursuant
to Section 2(b) of the Antitrust Procedures and Penalties Act
(``APPA'' or ``Tunney Act''), 15 U.S.C. Sec. Sec. 16(b)-(h), files
this Competitive Impact Statement relating to the proposed Final
Judgment submitted for entry in this civil antitrust proceeding.
I. NATURE AND PURPOSE OF THE PROCEEDING
On June 9, 2016, the United States and the State of North
Carolina filed a civil antitrust lawsuit against The Charlotte-
Mecklenburg Hospital Authority, formerly known as Carolinas
HealthCare System and now doing business as Atrium Health
(``Atrium''), to enjoin it from using steering restrictions in its
agreements with health insurers in the Charlotte, North Carolina
area. The Complaint alleges that Atrium's steering restrictions are
anticompetitive and violate Section 1 of the Sherman Act, 15 U.S.C.
Sec. 1, because the restrictions have detrimental effects on
competition among healthcare providers in the Charlotte area.
Healthcare providers charge health insurers a wide variety of
prices for the same service, but insurers have generally not passed
these price differences on to consumers because most commercial
health plans offer coverage that is the same no matter which
provider a patient chooses. This weakens the connection between
price and quantity that is the essence of competition because it
allows a provider to charge a high price without losing business to
rivals. To control escalating healthcare costs, insurers have
developed health plans and plan features that ``steer'' members by
providing financial incentives that enable members to share savings
by choosing more cost-effective providers, which stimulates
competition between providers. To enable patients to choose more
cost-effective providers, insurers also provide members with
transparency about the prices, quality, patient experience, or
anticipated out-of-pocket costs at different healthcare providers.
Atrium is the largest health system in the Charlotte area. For
an insurer to maintain a competitive health insurance business in
the Charlotte area, it needs to have a contractual relationship with
Atrium that gives employers and consumers the option of purchasing
insurance that covers care there.
Atrium has used its dominant position to demand contractual
restrictions on steering and transparency that interfere with the
competitive process. Insurers that contract with Atrium are
prohibited from providing financial incentives or information that
would encourage consumers to obtain healthcare services from
competing providers. These contract provisions significantly reduce
the number of additional patients that Atrium's competitors can hope
to attract by agreeing to lower prices or otherwise providing
greater value. These restrictions have been in Atrium's contracts
for years, and remain to this day.
Atrium's steering restrictions reduce the competitive incentive
that Atrium's competitors would otherwise have to lower prices in
order to win more business. This interference in the competitive
process has reduced competition between Atrium and other healthcare
providers in the Charlotte area. In addition, because many of the
most innovative healthcare plans in the country today are based on
steering to more efficient providers, Atrium's steering restrictions
have also curbed the introduction of such plans, and reduced choices
for Charlotte-area consumers.
Plaintiffs and Atrium have entered into a Stipulation and
proposed Final Judgment. The proposed Final Judgment enjoins Atrium
from (1) enforcing provisions in its current insurer contracts that
restrict steering and transparency; (2) seeking or obtaining
contract provisions with an insurer that would prohibit, prevent, or
penalize the insurer from using popular steering methods or
providing transparency; and (3) penalizing, or threatening to
penalize, any insurer for its use of these popular steering methods
and transparency. The proposed Final Judgment is described in detail
beginning with Section III below. In the Stipulation, Atrium agrees
to abide by the injunctive provisions of the proposed Final Judgment
while awaiting its entry by the Court.
The United States (unless it has withdrawn its consent), the
State of North Carolina, and Atrium have stipulated that the Court
may enter the proposed Final Judgment at any time after compliance
with the APPA. Entry of the proposed Final Judgment would terminate
this action, except that the Court would retain jurisdiction to
construe, modify, or enforce the provisions of the proposed Final
Judgment and to punish violations thereof.
II. DESCRIPTION OF THE ALLEGED VIOLATION
A. Atrium and other Charlotte-Area Hospitals
Atrium is the largest healthcare system in North Carolina and
one of the largest not-for-profit healthcare systems in the United
States. It is the dominant hospital system in the Charlotte area.
Its flagship facility is Carolinas Medical Center, a general acute-
care hospital located near downtown Charlotte and the largest
hospital in North Carolina. Atrium also operates nine additional
general acute-care hospitals in the Charlotte area. Atrium owns,
manages, or has strategic affiliations with over 40 hospitals in the
Carolinas, and sells healthcare services throughout the Carolinas,
including in
[[Page 63681]]
freestanding emergency departments, urgent care centers, physician
practices, outpatient surgery centers, imaging centers, nursing
homes, and laboratories. In 2017, Atrium's owned, managed, and
affiliated hospitals and other healthcare providers earned net
operating revenue of close to $10 billion.
In addition to Atrium's ten Charlotte-area hospitals, there are
eleven other general acute-care hospitals in the Charlotte area. The
next largest hospital system, Novant Health (``Novant''), owns five
general acute-care hospitals located in that area and had operating
revenue of approximately $4.6 billion in 2017, making Novant less
than half the size of Atrium. Novant's largest hospital in the
Charlotte area is Novant Presbyterian Medical Center, which is the
second-largest hospital in Charlotte. After Novant, the next-largest
hospital in the Charlotte area is CaroMont Regional Medical Center.
CaroMont Regional Medical Center is a 370-bed hospital in Gastonia,
North Carolina, and is owned and operated by CaroMont Health, an
independent community hospital system. In 2016, CaroMont Health had
net operating revenue of approximately $529 million. The remaining
hospitals in the Charlotte area are operated by Community Health
Systems, Inc., Tenet Healthcare Corporation, and Iredell Health
System.
B. The Relevant Market
The Complaint alleges that Atrium has market power in a relevant
market for the sale of general acute care inpatient hospital
services sold to commercial health insurers (``GAC inpatient
hospital services'') in the Charlotte area. GAC inpatient hospital
services consist of a broad group of medical and surgical diagnostic
and treatment services that includes a patient's overnight stay in
the hospital. Although individual GAC inpatient hospital services
are not substitutes for each other (e.g., a patient who needs heart
surgery cannot elect instead to have her knee replaced), GAC
inpatient hospital services can be aggregated for analytical
convenience because the competitive conditions for each of the
individual services is largely the same.
The relevant geographic market for the sale of GAC inpatient
hospital services is no larger than the Charlotte area.\1\ Insurers
contract to purchase GAC inpatient hospital services from hospitals
within the geographic area where their members are likely to seek
medical care because consumers prefer to seek medical care near the
places where they work and live. As a result, insurers doing
business in the Charlotte area must include in their provider
networks hospitals located in the Charlotte area. Charlotte-area
consumers have little or no willingness to enroll in an insurance
plan that provides no network access to hospitals located in the
Charlotte area. For these reasons, it is not a viable alternative
for insurers that sell health plans to consumers in the Charlotte
area to contract for GAC inpatient hospital services from providers
outside the Charlotte area.
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\1\ As used in this case, the Charlotte area means the Charlotte
Combined Statistical Area, as defined by the U.S. Office of
Management and Budget, which consists of Cabarrus, Cleveland,
Gaston, Iredell, Lincoln, Mecklenburg, Rowan, Stanly, and Union
counties in North Carolina, and Chester, Lancaster, and York
counties in South Carolina.
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C. Anticompetitive Effects of the Steering Restrictions
1. Atrium is the dominant hospital system in the Charlotte area
Atrium is the dominant seller of GAC inpatient hospital services
in the Charlotte area. Atrium has market power in this market. The
market for GAC inpatient hospital services in the Charlotte area is
highly concentrated, and Atrium's market share is more than 55
percent. By comparison, Atrium's largest rival, Novant Health, has
approximately 17 percent of the licensed hospital beds in the
Charlotte area. Without an attractive broad-network plan that
includes Atrium, insurers would not be viable in the Charlotte area
because they would not be able to attract the business of employers.
Atrium's size and breadth give it significant market power because
it can decline to participate in an insurer's network unless it
obtains high prices and advantageous contract terms.
As a result of its market power, Atrium has been able to secure
from insurers high prices relative to other hospital systems in the
Charlotte area and relative to other advanced medical centers in
North Carolina. These higher prices are not explained by any measure
of relative high-quality. Because of high provider prices, patients'
out-of-pocket healthcare costs in the Charlotte area are among the
highest in North Carolina.
2. Steering is part of the competitive process
Employers in Charlotte and elsewhere around the country have
approached health insurers about ways to address rising healthcare
costs. One approach of increasing interest is the introduction of
steering mechanisms into the health plans that employers offer.
Steering can be one way of fostering competition among hospitals.
Steering can be accomplished in several ways. Popular types of
steering in healthcare are narrow networks and tiered networks,
reference-based pricing, and centers of excellence.\2\ Transparency
into hospitals' or physicians' relative prices and quality is also
important to help effectuate steering.
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\2\ The proposed Final Judgment defines narrow networks, tiered
networks, and health plans with reference-based pricing or centers
of excellence as ``Steered Plans.''
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a. Narrow networks and tiered networks
In addition to offering the broad-network plans that are most
popular with employers, insurers in Charlotte want to introduce
narrow network and tiered insurance options. Narrow networks are
formed by using cost and/or quality criteria to select and contract
with a subset of healthcare providers in an area. For example, a
health plan sold in the Charlotte area that consists of hospitals
and physicians only at Novant, CaroMont, and Community Health
Systems would be a narrow-network plan. Because using an in-network
provider costs a member less than using an out-of-network provider,
a consumer that enrolls in a narrow-network plan is choosing to be
steered to participating providers. The likely increase in patient
volume realized by providers in the narrow network can help the
insurer to negotiate lower prices, and then to pass those savings
along in the form of lower premiums.
Tiered networks are typically created by designating network
providers into different levels (or tiers) based mostly on quality
and price. Tiered networks typically have two or more tiers of in-
network providers: a preferred tier and one or more secondary in-
network tiers. There may also be providers that remain out-of-
network. In tiered networks, members are free to use any of the
providers, but receive the most substantial benefits when they
choose a provider in the preferred tier. This tier typically
includes the providers with the best mix of quality and price.
Tiered and narrow network plans are increasingly popular with
employers and consumers. For example, in 2017, 19 percent of large
employers that offered healthcare coverage provided a narrow-network
plan to their employees and 31 percent offered a tiered plan.\3\ A
large majority of the plans offered on the individual healthcare
exchanges are narrow network plans. Narrow and tiered networks can
effectively reduce healthcare costs and make insurance more
affordable.
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\3\ Kaiser Family Foundation, 2017 Employer Health Benefits
Survey, 213-214, https://files.kff.org/attachment/Report-Employer-Health-Benefits-Annual-Survey-2017.
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b. Reference-based pricing and centers of excellence
Reference-based pricing and centers of excellence are forms of
steering that can be used as a feature of a health benefit plan. For
reference-based pricing, the insurer establishes a market-wide
standard, or ``reference,'' price for a service. The reference price
can be established by drawing from average local prices or from
other sources such as the reimbursement amounts established by
Medicare rules. The benefit plan covers the member's expenses up to
the ``reference price.'' Reference-based pricing steers members
towards the providers that have prices at or below the reference
price. This gives higher-priced providers an incentive to reduce
their prices to be closer to the reference price.\4\
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\4\ The California Public Employees' Retirement System
(``CalPERS'') has successfully used reference-based pricing to lower
expenses on hip and knee replacements. A study of the first year
after implementation of the reference-based pricing program
indicates that surgical volumes at low-price facilities increased
while volumes at high-price facilities decreased. Prices declined at
both high and low price facilities. As a result CalPERS and its
employees saved approximately $3 million. James C. Robinson and
Timothy T. Brown, Increases in Consumer Cost Sharing Redirect
Patient Volumes and Reduce hospital Prices for Orthopedic Surgery,
32 Health Affairs 1392, 1394-97 (2013).
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A center of excellence is a designation that an insurer applies
to a provider for its quality and/or cost efficiency in delivering a
particular healthcare service. The insurer often provides a
financial incentive to consumers to select the center of excellence.
For example, an insurer may designate a particular hospital in a
metropolitan area as
[[Page 63682]]
its center of excellence in bariatric surgery because the hospital
has superior expertise or is particularly cost effective. To incent
members to obtain bariatric surgery there, the insurer may reduce or
eliminate out-of-pocket expenses for members who choose that
hospital. Members remain free to obtain bariatric surgery elsewhere
and pay the out-of-pocket expenses prescribed under the plan.
Members are steered towards a center of excellence by virtue of the
designation and the cost savings.
c. Transparency
Transparency is the communication of price, cost, quality, or
patient experience information to a member. Transparency makes
steered plans more effective by providing consumers with information
to enable them to comparison shop before selecting a provider.
Transparency may also be a form of steering even in the absence of
differential benefits because information that identifies one
provider as more cost effective than another provider may prompt
consumers to choose the more cost-effective provider.
3. To insulate itself from competition, Atrium required that
steering restrictions be included in its insurer contracts
To protect its dominant share and high prices and insulate
itself from competition, Atrium has used its market power to require
every major insurer in the Charlotte area-- Aetna Health of the
Carolinas, Inc. (``Aetna''), Blue Cross and Blue Shield of North
Carolina (``BCBS-NC''), Cigna Healthcare of North Carolina, Inc.
(``Cigna''), and United Healthcare of North Carolina, Inc.
(``UnitedHealthcare'') \5\-- to accept contract terms that restrict
the insurers from steering their members to Atrium's lower-cost
competitors.
---------------------------------------------------------------------------
\5\ These four major insurers cover over 90 percent of the
commercially-insured residents of the Charlotte area. MedCost is the
next-largest health plan in the Charlotte area. MedCost provides
administrative services and access to its healthcare provider
networks to employers that self-fund their employees' healthcare
benefits. Employers that are self-funded pay the healthcare benefit
claims from the assets of their business, rather than purchase
health insurance policies for the benefit of their employees. Atrium
owns 50 percent of MedCost.
---------------------------------------------------------------------------
Atrium's contracts with each of these insurers contain steering
restrictions that either expressly prohibit the insurer from
steering their members away from Atrium, or impede steering through
other means, such as by imposing a financial penalty on any steering
against Atrium that exceeds a specified amount or by allowing Atrium
to promptly terminate the insurer's contract if the insurer steers
against Atrium. Atrium used its market power to require that
insurers agree to these contract provisions that restrict steering,
and thereby restrict competition.
Atrium's steering restrictions restrain insurers from offering
consumers the choice of narrow-network plans that do not include
Atrium, and tiered-network plans that do not place Atrium in the
most favorable tier. Atrium's steering restrictions also prevent
insurers from offering reference-based pricing because if the
reference price for a service is lower than the price that Atrium
charges for that service, members will be steered away from Atrium.
Insurers are also prevented from offering financial incentives for
members to obtain services at non-Atrium providers that are
designated centers of excellence.
These restrictions also prevent insurers from providing members
transparency into the price, quality, patient experience, and
anticipated out-of-pocket costs of Atrium's healthcare services
compared to Atrium's competitors. Atrium's restrictions on
transparency indirectly restrict steering because they inhibit
consumers from accessing information that would allow them to make
better-informed healthcare provider choices.
Deprived of any mechanism to reward low prices with more patient
volume, insurers cannot create incentives for Atrium's rivals to
compete on price. Atrium's steering restrictions, therefore, reduce
competition for GAC inpatient hospital services in the Charlotte
area by impeding its competitors' ability to attract patients by
offering lower prices to insurers and their members. The steering
restrictions prevent consumers from benefitting from lower prices,
so they protect Atrium from losing patient volume in response to
high prices. This reduction in competition causes prices to be
higher than they would be in the absence of Atrium's steering
restrictions.
III. EXPLANATION OF THE PROPOSED FINAL JUDGMENT
The purpose of the proposed Final Judgment is to prevent Atrium
from impeding insurers' steered plans and transparency, and to
restore competition among healthcare providers in the Charlotte
area. The proposed Final Judgment will accomplish this objective
through injunctive, compliance, and enforcement provisions.
Atrium has market power in GAC inpatient hospital services, but
the proposed Final Judgment applies to the broad range of healthcare
services that Atrium provides and to which its steering restrictions
apply. The additional healthcare services covered by the proposed
Final Judgment include outpatient services (such as ambulatory
surgeries and radiological services), professional services rendered
by physicians, and ancillary services such as imaging and lab
services. The full scope of services covered by the proposed Final
Judgment falls within the proposed Final Judgment's definition of
``Healthcare Services.'' Because Atrium uses its market power to
restrict steering away from it for any healthcare service, the
proposed Final Judgment provides relief that is broader than the set
of services in the relevant market.
The proposed Final Judgment also applies to a broad range of
benefit plans. This includes health insurance policies sold to
individuals, fully-insured and self-funded health plans sold to
employers and other groups, and Medicare Advantage plans.
A. Prohibited Conduct
The proposed Final Judgment seeks to restore competition by
prohibiting Atrium from engaging in specific conduct. There are
three main provisions. The first stops Atrium from enforcing the
current contract provisions at issue in this suit. The second stops
Atrium from enforcing similar or new contractual provisions that
would restrict steering in the Charlotte area. The third stops
Atrium from retaliating against insurers for steering in the
Charlotte area.
1. Eliminating the anticompetitive contract provisions
The proposed Final Judgment eliminates the contractual language
that Plaintiffs alleged is anticompetitive. The proposed Final
Judgment voids the contractual provisions listed in Exhibit A to the
proposed Final Judgment that expressly prevent steering. For
example, a provision stating that an insurer ``will not steer
business away from'' Atrium is voided from that insurer's contract.
Additionally, a part of a contract between Atrium and an insurer
that required the insurer to give Atrium 90 days' notice before
bringing a plan to market that would steer patients away from Atrium
is also voided. Further, the proposed Final Judgment eliminates a
provision in one insurer's contract that allows Atrium to terminate
the contract on 90 days' notice if the insurer offers a plan that
would steer away from Atrium.
In addition, Atrium's contracts with commercial insurers contain
other provisions that require the insurer to include Atrium in all
of its benefit plans. Each such provision prevents the insurer from
creating narrow networks that feature Atrium's rivals, but exclude
Atrium. The proposed Final Judgment lists that language in Exhibit
B, and prohibits Atrium from enforcing or attempting to enforce such
contractual provisions to prevent, prohibit, or penalize steered
plans and transparency.\6\
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\6\ The contract provisions appearing in Exhibit B could remain
enforceable to prevent insurers from ``carving out'' certain Atrium
procedures from their benefits plans. A ``carve-out'' is an industry
term defined in the proposed Final Judgment as an arrangement by
which an insurer unilaterally removes all or substantially all of a
particular healthcare service from coverage in a benefit plan during
the performance of a network-participation agreement. Insurers are
free to negotiate carve-outs as part of a contract, but Atrium may
prohibit insurers from carving additional services out of a contract
after it is signed.
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Finally, the proposed Final Judgment prevents Atrium from
enforcing a ``material impact'' provision in its contract with BCBS-
NC in a manner that reduces BCBS-NC's incentives to steer to more
efficient providers.
2. Preventing new contractual provisions that harm steering
The proposed Final Judgment also prevents Atrium from seeking or
obtaining similar or new contract provisions that would prohibit,
prevent, or penalize steering through steered plans or transparency
in the Charlotte area.
Paragraph IV(B) of the proposed Final Judgment identifies three
types of contractual provisions that, among others, would prohibit,
prevent, or penalize steering through steered plans and would thus
violate the terms of the proposed Final Judgment. First, Atrium may
not expressly prohibit
[[Page 63683]]
steered plans or transparency. Second, Atrium may not require prior
approval of new benefit plans. Third, Atrium may not demand to be
included in the most-preferred tier of benefit plans regardless of
price.
The Final Judgment's injunction against steering restrictions
also reaches beyond these three existing provisions to include any
contract provision that prohibits, prevents, or penalizes steering.
``Penalize'' is a term in the proposed Final Judgment that includes
within its definition anything that would significantly restrain an
insurer's steering. Because steering away from Atrium necessarily
reduces its volume and revenues, terms that punish such reductions
with higher prices or other detrimental consequences may be
penalties. Whether a provision or action is likely to significantly
restrain steering depends on the facts and circumstances, including
but not limited to its economic impact, and any procompetitive
effects that would tend to lower healthcare costs or otherwise
benefit consumers in the Charlotte area.
3. Atrium may not retaliate against steering
Under the terms of the proposed Final Judgment Atrium also may
not seek or obtain any contract provision, or take any other action
that would penalize an insurer for steering away from Atrium through
steered plans or transparency. For example, Atrium may not threaten
to terminate its participation in an insurer's healthcare networks
because the insurer was planning to introduce a tiered-network plan
that steered away from Atrium.
B. Conduct That is Not Prohibited by the Final Judgment
Paragraph V of the proposed Final Judgment sets forth conduct
that Atrium may undertake without violating the terms of the
proposed Final Judgment. Paragraph V(A) makes clear that nothing in
the proposed Final Judgment prohibits Atrium from exercising any of
its contractual rights provided it does not engage in any conduct
that would violate the terms of the proposed Final Judgment.
If Atrium is the most-prominently featured provider in a narrow-
network plan or co-branded plan,\7\ Paragraph V(B) of the proposed
Final Judgment allows Atrium to restrict an insurer from steering
away from Atrium in that plan. Such restrictions may help narrow
networks and co-branded plans be more effective, and this provision
allows Atrium to participate in plans that steer towards it.
---------------------------------------------------------------------------
\7\ A co-branded plan is a benefit plan created by a formal and
substantial level of alliance or affiliation, such as a partnership
or joint venture, between a provider and an insurer. A co-branded
plan has the logos of both the insurer and provider on the plan's
marketing materials.
---------------------------------------------------------------------------
Paragraph V(C) makes clear that the proposed Final Judgment does
not prohibit Atrium from negotiating with insurers for the ability
to review the information about Atrium that an insurer disseminates
through transparency, as long as any provision for review does not
delay dissemination of the information. The proposed Final Judgment
does not prevent Atrium from challenging information that it
believes is inaccurate, including pursuing legal remedies available
to it.
Paragraph V(C) also makes clear that the proposed Final Judgment
does not prohibit Atrium from seeking certain safeguards regarding
the insurer's dissemination of the prices Atrium has negotiated with
insurers. Atrium may seek contractual provisions with an insurer
prohibiting the insurer from disseminating Atrium's negotiated
prices to Atrium's competitors, other insurers, or the general
public. Atrium may also seek contractual provisions with an insurer
requiring the insurer to obtain a covenant from any third party
receiving Atrium's negotiated prices that such third party will not
disclose that information to Atrium's competitors, another insurer,
the general public, or another third party lacking a reasonable need
to know such information. Atrium may also seek all appropriate
remedies in the event that dissemination of such information occurs.
C. Required Conduct
The proposed Final Judgment also prescribes conduct that Atrium
is required to undertake in order to facilitate prompt and effective
relief. Paragraph VI of the proposed Final Judgment requires Atrium
to provide Aetna, BCBS-NC, Cigna, MedCost and UnitedHealthcare with
a copy of the Final Judgment and notify them in writing within 15
business days of the Court's entry of the proposed Final Judgment
that (1) the Final Judgment has been entered; (2) the Final Judgment
prohibits Atrium from entering into or enforcing any agreement
provision that violates the Final Judgment; (3) Atrium waives the
right to enforce any contract language reproduced in Exhibit A; and
(4) Atrium waives the right to enforce any contract language
reproduced in Exhibit B to the extent such language prohibits,
prevents, or penalizes steered plans or transparency.
D. Compliance
Under Paragraph VII of the proposed Final Judgment, within 15
calendar days of the entry of the Final Judgment, Atrium must
provide a copy of the Final Judgment to each of its commissioners
and officers as well as each employee who has responsibility to
negotiate or approve contracts with insurers. Within 60 calendar
days of the entry of the proposed Final Judgment, Atrium must
develop and implement procedures necessary to ensure Atrium's
compliance with the proposed Final Judgment, including procedures to
answer questions from Atrium's commissioners and employees about
abiding by the terms of the proposed Final Judgment.
Within 270 calendar days of entry of the proposed Final
Judgment, Atrium must submit to the United States and the State of
North Carolina a written report setting forth its actions to comply
with the proposed Final Judgment. Atrium must also submit to the
United States and the State of North Carolina a copy of any new or
revised agreement or amendment to any agreement with any insurer
that is executed during the term of the proposed Final Judgment no
later than 30 calendar days after the date the agreement or
amendment is executed.
Atrium must also notify the United States and the State of North
Carolina within 30 calendar days of having reason to believe that a
provider which Atrium controls has a contract with any insurer with
a provision that prohibits, prevents, or penalizes transparency or
any steered plan.
To facilitate monitoring Atrium's compliance with the proposed
Final Judgment, Paragraphs VII(B) and VII(D) of the proposed Final
Judgment require Atrium to grant the United States access, upon
reasonable notice, to Atrium's records and documents relating to
matters contained in the proposed Final Judgment. In addition Atrium
must make its employees available for interviews or depositions and
answer interrogatories and prepare written reports relating to
matters contained in the proposed Final Judgment upon request.
The proposed Final Judgment also contains provisions that
promote compliance and make the enforcement of the proposed Final
Judgment as effective as possible. Paragraph IX(A) provides that the
United States retains and reserves all rights to enforce the
provisions of the proposed Final Judgment, including its rights to
seek an order of contempt from the Court. Under the terms of this
Paragraph, Atrium has agreed that in any civil contempt action, any
motion to show cause, or any similar action brought by the United
States regarding an alleged violation of the proposed Final
Judgment, the United States may establish the violation and the
appropriateness of any remedy by a preponderance of the evidence and
that Atrium has waived any argument that a different standard of
proof should apply. This provision aligns the standard for
compliance obligations with the standard of proof that applies to
the underlying offense that the compliance commitments address.
Paragraph IX(B) sets forth the parties' agreed-upon rules for
interpreting the proposed Final Judgment's provisions. Because
consent decrees share many attributes with ordinary contracts, they
should be construed as contracts for purposes of enforcement. See
Anita's New Mexico Style Mexican Food v. Anita's Mexican Foods
Corp., 201 F.3d 314, 319 (4th Cir. 2000) (quoting United States v.
ITT Continental Baking Co., 420 U.S. 223, 236-37 (1975)). The
parties have agreed that the Court should employ ordinary tools of
interpretation to enforce the proposed Final Judgment. In Paragraph
IX(B), the parties make clear the purpose of the proposed Final
Judgment that can be used as an interpretive tool. The proposed
Final Judgment was drafted with the purpose of resolving this
litigation and restoring all competition that Plaintiffs alleged was
harmed by the challenged conduct. Paragraph IX(B) says that the
provisions of the proposed Final Judgment are to be interpreted to
give effect to the procompetitive purpose of the federal antitrust
laws, and to restore this lost competition.
Atrium also agrees that the Court may enforce any provision of
the proposed Final Judgment that is stated specifically and in
reasonable detail, see Fed.R.Civ.P. 65(d) (requiring specific terms
and ``reasonable detail''), even if the provision is not clear and
[[Page 63684]]
unambiguous on its face, by applying these procompetitive principles
and ordinary tools of interpretation. See Martin's Herend Imports,
Inc. v. Diamond & Gem Trading, 195 F.3d 765, 771 (5th Cir. 1999)
(``The mere fact that interpretation is necessary does not render
the injunction so vague and ambiguous that a party cannot know what
is expected of him.'' (internal citation and quotation omitted)).
When interpreting the proposed Final Judgment, the Court should not
construe the language of the proposed Final Judgment against either
party as the drafter.
Paragraph IX(C) of the proposed Final Judgment provides that
should the Court find in an enforcement proceeding that Atrium has
violated the proposed Final Judgment, the United States may apply to
the Court for a one-time extension of the proposed Final Judgment,
together with such other relief as may be appropriate. In addition,
in order to compensate American taxpayers for any costs associated
with the investigation and enforcement of violations of the proposed
Final Judgment, Paragraph IX(C) further provides that in any
successful effort by the United States to enforce the proposed Final
Judgment against Atrium, whether litigated or resolved prior to
litigation, Atrium agrees to reimburse the United States for
attorneys' fees, experts' fees, or costs incurred in connection with
any enforcement effort, including the investigation of the potential
violation.
Finally, Paragraph X of the proposed Final Judgment provides
that the proposed Final Judgment shall expire ten years from the
date of its entry, except that after five years from the date of its
entry, the proposed Final Judgment may be terminated upon notice by
the United States to the Court and Atrium that the continuation of
the proposed Final Judgment is no longer necessary or in the public
interest.
IV. REMEDIES AVAILABLE TO POTENTIAL PRIVATE LITIGANTS
Section 4 of the Clayton Act, 15 U.S.C. Sec. 15, provides that
any person who has been injured as a result of conduct prohibited by
the antitrust laws may bring suit in federal court to recover three
times the damages the person has suffered, as well as costs and
reasonable attorneys' fees. Entry of the proposed Final Judgment
will neither impair nor assist any private antitrust damage action.
Under the provisions of Section 5(a) of the Clayton Act, 15 U.S.C.
Sec. 16(a), the proposed Final Judgment has no prima facie effect
in any subsequent private lawsuit that may be brought against
Atrium.
V. PROCEDURES AVAILABLE FOR MODIFICATION OF THE PROPOSED FINAL JUDGMENT
The United States, the State of North Carolina, and Atrium have
stipulated that the proposed Final Judgment may be entered by the
Court after compliance with the provisions of the APPA, provided
that the United States has not withdrawn its consent. The APPA
conditions entry upon the Court's determination that the proposed
Final Judgment is in the public interest.
The APPA provides a period of at least 60 calendar days
preceding the effective date of the proposed Final Judgment within
which any person may submit to the United States written comments
regarding the proposed Final Judgment. Any person who wishes to
comment should do so within 60 calendar days of the date of
publication of this Competitive Impact Statement in the Federal
Register, or the last date of publication in a newspaper of the
summary of this Competitive Impact Statement, whichever is later.
All comments received during this period will be considered by the
United States Department of Justice, which remains free to withdraw
its consent to the entry of the proposed Final Judgment at any time
prior to the Court's entry of the judgment. The comments and the
response of the United States will be filed with the Court. In
addition, comments will be posted on the U.S. Department of Justice,
Antitrust Division's internet website and, under certain
circumstances, published in the Federal Register.
Written comments should be submitted to:
Peter J. Mucchetti
Chief, Healthcare and Consumer Products Section
Antitrust Division
United States Department of Justice
450 Fifth Street, NW, Suite 4100
Washington, DC 20530
The proposed Final Judgment provides that the Court retains
jurisdiction over this action, and the parties may apply to the
Court for any order necessary or appropriate for the modification,
interpretation, or enforcement of the proposed Final Judgment.
VI. ALTERNATIVES TO THE PROPOSED FINAL JUDGMENT
As an alternative to the proposed Final Judgment, the United
States considered continuing this litigation, and proceeding to
trial in May 2019 against Atrium. While the proposed Final Judgment
represents a negotiated resolution to the action that necessitated
compromises by Plaintiffs and Atrium, the United States is satisfied
that the relief contained in the proposed Final Judgment will remedy
the anticompetitive conduct identified in the Complaint. The
proposed Final Judgment would achieve all or substantially all of
the relief the United States would have obtained through litigation
but avoids the time, expense, and uncertainty of a full trial on the
merits.
VII. APPA's STANDARD OF REVIEW FOR THE PROPOSED FINAL JUDGMENT
The Clayton Act, as amended by the APPA, requires that proposed
consent judgments in antitrust cases brought by the United States be
subject to a 60-day comment period, after which the Court shall
determine whether entry of the proposed Final Judgment ``is in the
public interest.'' 15 U.S.C. Sec. 16(e)(1). In making that
determination, the Court, in accordance with the statute as amended
in 2004, is required to consider:
(A) the competitive impact of such judgment, including
termination of alleged violations, provisions for enforcement and
modification, duration of relief sought, anticipated effects of
alternative remedies actually considered, whether its terms are
ambiguous, and any other competitive considerations bearing upon the
adequacy of such judgment that the court deems necessary to a
determination of whether the consent judgment is in the public
interest; and
(B) the impact of entry of such judgment upon competition in the
relevant market or markets, upon the public generally and
individuals alleging specific injury from the violations set forth
in the complaint including consideration of the public benefit, if
any, to be derived from a determination of the issues at trial.
15 U.S.C. Sec. 16(e)(1)(A) & (B). In considering these statutory
factors, the Court's inquiry is necessarily a limited one as the
government is entitled to ``broad discretion to settle with the
defendant within the reaches of the public interest.'' United States
v. Microsoft Corp., 56 F.3d 1448, 1461 (D.C. Cir. 1995); see
generally United States v. SBC Commc'ns, Inc., 489 F. Supp. 2d 1
(D.D.C. 2007) (assessing public interest standard under the Tunney
Act); United States v. U.S. Airways Group, Inc., 38 F. Supp. 3d 69,
75 (D.D.C. 2014) (explaining that the ``court's inquiry is limited''
in Tunney Act settlements).
As the United States Court of Appeals for the District of
Columbia Circuit has held, under the APPA a court considers, among
other things, the relationship between the remedy secured and the
specific allegations in the government's complaint, whether the
decree is sufficiently clear, whether its enforcement mechanisms are
sufficient, and whether the decree may positively harm third
parties. See Microsoft, 56 F.3d at 1458-62. With respect to the
adequacy of the relief secured by the decree, a court may not
``engage in an unrestricted evaluation of what relief would best
serve the public.'' United States v. BNS, Inc., 858 F.2d 456, 462
(9th Cir. 1988) (quoting United States v. Bechtel Corp., 648 F.2d
660, 666 (9th Cir. 1981)); see also Microsoft, 56 F.3d at 1460-62;
United States v. Alcoa, Inc., 152 F. Supp. 2d 37, 40 (D.D.C. 2001).
Instead:
[t]he balancing of competing social and political interests affected
by a proposed antitrust consent decree must be left, in the first
instance, to the discretion of the Attorney General. The court's
role in protecting the public interest is one of insuring that the
government has not breached its duty to the public in consenting to
the decree. The court is required to determine not whether a
particular decree is the one that will best serve society, but
whether the settlement is ``within the reaches of the public
interest.'' More elaborate requirements might undermine the
effectiveness of antitrust enforcement by consent decree.
Bechtel, 648 F.2d at 666 (emphasis added) (citations omitted).\8\
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\8\ See also BNS, 858 F.2d at 464 (holding that the court's
``ultimate authority under the [APPA] is limited to approving or
disapproving the consent decree''); United States v. Gillette Co.,
406 F. Supp. 713, 716 (D. Mass. 1975) (noting that, in this way, the
court is constrained to ``look at the overall picture not
hypercritically, nor with a microscope, but with an artist's
reducing glass'').
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In determining whether a proposed settlement is in the public
interest, a district
[[Page 63685]]
court ``must accord deference to the government's predictions about
the efficacy of its remedies, and may not require that the remedies
perfectly match the alleged violations.'' SBC Commc'ns, 489 F. Supp.
2d at 17; see also U.S. Airways, 38 F. Supp. 3d at 74-75 (noting
that a court should not reject the proposed remedies because it
believes others are preferable and that room must be made for the
government to grant concessions in the negotiation process for
settlements); Microsoft, 56 F.3d at 1461 (noting the need for courts
to be ``deferential to the government's predictions as to the effect
of the proposed remedies''); United States v. Archer-Daniels-Midland
Co., 272 F. Supp. 2d 1, 6 (D.D.C. 2003) (noting that the court
should grant ``due respect to the government's prediction as to the
effect of proposed remedies, its perception of the market structure,
and its views of the nature of the case''). The ultimate question is
whether ``the remedies [obtained in the decree are] so inconsonant
with the allegations charged as to fall outside of the `reaches of
the public interest.''' Microsoft, 56 F.3d at 1461. To meet this
standard, the United States ``need only provide a factual basis for
concluding that the settlements are reasonably adequate remedies for
the alleged harms.'' SBC Commc'ns, 489 F. Supp. 2d at 17.
Moreover, a court's role under the APPA is limited to reviewing
the remedy in relationship to the violations that the United States
has alleged in its complaint, and does not authorize a court to
``construct [its] own hypothetical case and then evaluate the decree
against that case.'' Microsoft, 56 F.3d at 1459; see also U.S.
Airways, 38 F. Supp. 3d at 75 (noting that the court must simply
determine whether there is a factual foundation for the government's
decisions such that its conclusions regarding the proposed
settlements are reasonable). Because the ``court's authority to
review the decree depends entirely on the government's exercising
its prosecutorial discretion by bringing a case in the first
place,'' it follows that ``the court is only authorized to review
the decree itself,'' and not to ``effectively redraft the
complaint'' to inquire into other matters that the United States did
not pursue. Microsoft, 56 F.3d at 1459-60. As the court confirmed in
SBC Communications, courts ``cannot look beyond the complaint in
making the public interest determination unless the complaint is
drafted so narrowly as to make a mockery of judicial power.'' SBC
Commc'ns, 489 F. Supp. 2d at 15.
In its 2004 amendments,\9\ Congress made clear its intent to
preserve the practical benefits of utilizing consent decrees in
antitrust enforcement, adding the unambiguous instruction that
``[n]othing in this section shall be construed to require the court
to conduct an evidentiary hearing or to require the court to permit
anyone to intervene.'' 15 U.S.C. Sec. 16(e)(2); see also U.S.
Airways, 38 F. Supp. 3d at 76 (indicating that a court is not
required to hold an evidentiary hearing or to permit intervenors as
part of its review under the Tunney Act). This language explicitly
wrote into the statute what Congress intended when it first enacted
the Tunney Act in 1974. As Senator Tunney explained: ``[t]he court
is nowhere compelled to go to trial or to engage in extended
proceedings which might have the effect of vitiating the benefits of
prompt and less costly settlement through the consent decree
process.'' 119 Cong. Rec. 24,598 (1973) (statement of Sen. Tunney).
Rather, the procedure for the public interest determination is left
to the discretion of the court, with the recognition that the
court's ``scope of review remains sharply proscribed by precedent
and the nature of Tunney Act proceedings.'' SBC Commc'ns, 489 F.
Supp. 2d at 11. A court can make its public interest determination
based on the competitive impact statement and response to public
comments alone. U.S. Airways, 38 F. Supp. 3d at 76. See also United
States v. Enova Corp., 107 F. Supp. 2d 10, 17 (D.D.C. 2000) (noting
that the ``Tunney Act expressly allows the court to make its public
interest determination on the basis of the competitive impact
statement and response to comments alone''); S. Rep. No. 93-298 93d
Cong., 1st Sess., at 6 (1973) (``Where the public interest can be
meaningfully evaluated simply on the basis of briefs and oral
arguments, that is the approach that should be utilized.'').
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\9\ The 2004 amendments substituted ``shall'' for ``may'' in
directing relevant factors for a court to consider and amended the
list of factors to focus on competitive considerations and to
address potentially ambiguous judgment terms. Compare 15 U.S.C.
Sec. 16(e) (2004), with 15 U.S.C. Sec. 16(e)(1) (2006); see also
SBC Commc'ns, 489 F. Supp. 2d at 11 (concluding that the 2004
amendments ``effected minimal changes'' to Tunney Act review).
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VIII. DETERMINATIVE DOCUMENTS
There are no determinative materials or documents within the
meaning of the APPA that were considered by the United States in
formulating the proposed Final Judgment.
Respectfully submitted,
Dated: December 4, 2018
FOR PLAINTIFF UNITED STATES OF AMERICA:
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John R. Read
Karl D. Knutsen
Natalie Melada
Catherine R. Reilly
David Stolzfus
Paul Torzilli
Antitrust Division, U.S. Department of Justice, 450 Fifth Street NW,
Suite 4100, Washington, D.C. 20530, (p) 202/307.0468,
[email protected].
[FR Doc. 2018-26755 Filed 12-10-18; 8:45 am]
BILLING CODE 4410-11-P