United States et al. v. United Regional Health Care System; Public Comments and Response on Proposed Final Judgment, 35017-35022 [2011-14628]
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[FR Doc. 2011–14726 Filed 6–14–11; 8:45 am]
BILLING CODE 4410–FY–P
DEPARTMENT OF JUSTICE
Antitrust Division
United States et al. v. United Regional
Health Care System; Public Comments
and Response on Proposed Final
Judgment
Pursuant to the Antitrust Procedures
and Penalties Act, 15 U.S.C. 16(b)–(h),
the United States hereby publishes
below the comment received on the
proposed Final Judgment in United
States and State of Texas v. United
Regional Health Care System, Civil
Action No. 7:11–cv–00030–0, which
was filed in the United States District
Court for the Northern District of Texas,
Wichita Falls Division, on June 6, 2011,
together with the response of the United
States to the comment.
Copies of the comment and the
response are available for inspection at
the U.S. Department of Justice, Antitrust
Division, Antitrust Documents Group,
450 Fifth Street, NW., Suite 1010,
Washington, DC 20530 (telephone: 202–
514–2481); on the Department of
Justice’s Web site at https://
www.usdoj.gov/atr; and at the Office of
the Clerk of the United States District
Court for the Northern District of Texas,
Wichita Falls Division. Copies of any of
these materials may be obtained upon
request and payment of a copying fee.
Patricia A. Brink,
Director of Civil Enforcement.
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In The United States District Court for
the Northern District of Texas, Wichita
Falls Division
United States Of America And State Of
Texas, (RCO) Plaintiffs, V. United
Regional Health Care System,
Defendant.
Case No.: 7:11–cv–00030
Response Of Plaintiff United States To
Public Comment On The Proposed
Final Judgment
Pursuant to the requirements of the
Antitrust Procedures and Penalties Act,
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15 U.S.C. § 16(b)–(h) (‘‘APPA7 or
‘‘Tunney Act’’), the United States
hereby responds to the public comment
received regarding the proposed Final
Judgment in this case. The single
comment received agrees that the
proposed Final Judgment will provide
an effective and appropriate remedy for
the antitrust violations alleged in the
Complaint. The United States will move
the Court for entry of the proposed Final
Judgment after the public comment and
this response have been published in
the Federal Register, pursuant to 15
U.S.C. § 16(d).
On February 25, 2011, the United
States and the State of Texas filed a civil
antitrust lawsuit against Defendant
United Regional Health Care System
(‘‘United Regional’’) challenging United
Regional’s contracts with commercial
health insurers that effectively
prevented insurers from contracting
with United Regional’s competitors
(‘‘exclusionary contracts’’). The
Complaint alleged that United Regional
had unlawfully used those contracts to
maintain its monopoly for hospital
services, in violation of Section 2 of the
Sherman Act, 15 U.S.C. § 2. By
effectively preventing most commercial
health insurers from including in their
networks other inpatient and outpatient
facilities, the Complaint alleged that
United Regional (1) delayed and
prevented the expansion and entry of its
competitors, likely leading to higher
health-care costs and higher health
insurance premiums; (2) limited price
competition for price-sensitive patients,
likely leading to higher health-care costs
for those patients; and (3) reduced
quality competition between United
Regional and its competitors. The
Complaint sought to enjoin United
Regional from entering exclusionary
contracts with insurers.
Simultaneously with the filing of the
Complaint, the United States and the
State of Texas filed a proposed Final
Judgment and Stipulation signed by the
plaintiffs and United Regional
consenting to entry of the proposed
Final Judgment after compliance with
the requirements of the Tunney Act, 15
U.S.C. § 16. Pursuant to those
requirements, the United States also
filed its Competitive Impact Statement
(‘‘CIS’’) with the Court on February 25,
2011; published the proposed Final
Judgment and CIS in the Federal
Register on March 10, 2011, see 76 Fed.
Reg. 13209; and had summaries of the
terms of the proposed Final Judgment
and CIS, together with directions for the
submission of written comments
relating to the proposed Final Judgment,
published in The Washington Post and
Times Record News for seven days
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beginning on March 9, 2011, and ending
on March 15, 2011. The sixty-day period
for public comment ended on May 14,
2011. One comment was received, as
described below and attached hereto.
I. THE INVESTIGATION AND
PROPOSED RESOLUTION
The proposed Final Judgment is the
culmination of an investigation by the
Antitrust Division of the United States
Department of Justice (‘‘Department’’) of
United Regional’s contracting practices
with commercial insurers. As part of its
investigation, the Department issued
more than fifteen Civil Investigative
Demands for documents. The
Department reviewed the documents
and other materials received, conducted
more than 80 interviews, and took oral
testimony of United Regional personnel.
The Department carefully analyzed the
information obtained and thoroughly
considered all of the issues presented.
The Department found that beginning
in 1998, United Regional responded to
the competitive threat posed by the
entry of a competing hospital, Kell
West; and other outpatient-surgery
facilities by systematically entering into
exclusionary contracts with commercial
health insurers. The precise terms of
these contracts varied, but all shared the
same anticompetitive feature: a
significant pricing penalty if an insurer
contracts with competing facilities
within a region that is no larger than
Wichita County. In general, the
contracts offered a substantially larger
discount off billed charges (e.g., 25%) if
United Regional was the only local
hospital or outpatient surgical provider
in the insurer’s network; and the
contracts provided for a much smaller
discount (e.g., 5% off billed charges) if
the insurer contracted with one of
United Regional’s rivals.
Within three months after Kell West
opened in January 1999, United
Regional had entered into exclusionary
contracts with five commercial health
insurers, and by 2010, it had
exclusionary contracts with eight
insurers. In each instance, United
Regional-not the insurer-required the
exclusionary provisions in the contract.
The only major insurer that did not sign
an exclusionary contract with United
Regional was Blue Cross Blue Shield of
Texas (‘‘Blue Cross’’), by far the largest
insurer in Wichita Falls and Texas.
Because United Regional is a ‘‘must
have’’ hospital for any insurer that
wants to sell health insurance in the
Wichita Falls area, and because the
penalty for contracting with United
Regional’s rivals was so significant,
most insurers entered into exclusionary
contracts with United Regional.
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Consequently, United Regional’s rivals
could not obtain contracts with most
insurers, except Blue Cross, which
substantially hindered their ability to
compete and helped United Regional
maintain its monopoly in the relevant
markets, to the detriment of consumers.
After reviewing the investigative
materials, the Department determined
that United Regional’s conduct violated
Section 2 of the Sherman Act, 15 U.S.C.
§ 2, as alleged in the Complaint. The
proposed Final Judgment is designed to
restore competition between health-care
providers in the Wichita Falls MSA.
Section IV of the proposed Final
Judgment prohibits United Regional
from using exclusivity terms in its
contracts with commercial health
insurers. In particular, United Regional
is prohibited from (1) conditioning the
prices or discounts that it offers to
commercial health insurers on whether
those insurers contract with other
health-care providers, such as Kell
West; and (2) preventing insurers from
entering into agreements with United
Regional’s rivals. United Regional is
also prohibited from taking any
retaliatory actions against an insurer
that enters (or seeks to enter) into an
agreement with a rival health-care
provider.
In addition, the proposed Final
Judgment prohibits United Regional
from offering other types of ‘‘conditional
volume discounts’’ that could have the
same anticompetitive effects as the
challenged conduct. ‘‘Conditional
volume discounts’’ are prices,
discounts, or rebates offered to a
commercial health insurer on condition
that the volume of that insurer’s
purchases from United Regional meets
or exceeds a specified threshold.
Similarly, United Regional may not offer
market-share discounts, e.g., discounts
conditioned on an insurer’s purchases at
United Regional meeting a specified
percentage of that insurer’s total
purchases, whether they apply
retroactively or not, because such
discounts can also be a form of
anticompetitive pricing. Finally, United
Regional may not use provisions in its
insurance contracts that discourage
insurers from offering products that
encourage members to use other innetwork providers (besides United
Regional).
The proposed Final Judgment does,
however, allow price discounts that are
likely to be procompetitive. Section V of
the proposed Final Judgment permits
United Regional to offer above-cost
incremental volume discounts. By
permitting such discounts, the proposed
Final Judgment ensures that United
Regional can engage in procompetitiye
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efforts to compete for additional patient
volume, while preventing United
Regional from offering ‘discounts that
have the potential to exclude an equally
efficient competitor.
II. STANDARD OF JUDICIAL REVIEW
The APPA requires that proposed
consent judgments in antitrust cases
brought by the United States be subject
to a sixty-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
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 also United States
v. SBC Commc’ns, Inc., 489 F. Supp. 2d
1 (D.D.C. 2007) (assessing publicinterest standard under the Tunney
Act); United States v. InBev N.V./S.A.,
No. 08–1965 (JR), 2009 U.S. Dist. LEXIS
84787, at *3 (D.D.C. Aug. 11, 2009)
(noting that the court’s review of a
consent judgment is limited and only
inquires ‘‘into whether the government’s
determination that the proposed
remedies will cure the antitrust
violations alleged in the complaint was
reasonable, and whether the
mechanisms to enforce the final
judgment are clear and manageable.’’).
As the United States Court of Appeals
for the District of Columbia Circuit has
held, a court considers under the APPA,
among other things, the relationship
between the remedy secured and the
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specific allegations set forth in the
United States’ complaint, whether the
decree is sufficiently clear, whether
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) (citing United States v.
Bechtel Corp., 648 F.2d 660, 666 (9th
Cir. 1981)); see also Microsoft, 56 F.3d
at 1460–62; InBev, 2009 U.S. Dist.
LEXIS 84787, at *3; United States v.
Alcoa, Inc., 152 F. Supp. 2d 37, 40
(D.D.C. 2001). Courts have held that:
[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).1 In
determining whether a proposed
settlement is in the public interest, a
district 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 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-DanielsMidland Co., 272 F. Supp. 2d I, 6
(D.D.C. 2003) (noting that the court
should grant due respect to the United
States’ ‘‘prediction as to the effect of
proposed remedies, its perception of the
1 Cf 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’’); see generally Microsoft, 56
F.3d at 1461 (discussing 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’ ’’).
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market structure, and its views of the
nature of the case’’).
Courts have greater flexibility in
approving proposed consent decrees
than in crafting their own decrees
following a finding of liability in a
litigated matter. ‘‘[A] proposed decree
must be approved even if it falls short
of the remedy the court would impose
on its own, as long as it falls within the
range of acceptability or is ‘within the
reaches of public interest.’’’ United
States v. Am. Tel. & Tel. Co., 552 F.
Supp. 131, 151 (D.D.C. 1982) (citations
omitted) (quoting United States v.
Gillette Co., 406 F. Supp. 713, 716 (D.
Mass. 1975)), aff’d sub nom. Maryland
v. United States, 460 U.S. 1001 (1983);
see also United States v. Akan
Aluminum Ltd., 605 F. Supp. 619, 622
(W.D. Ky. 1985) (approving the consent
decree even though the court would
have imposed a greater remedy). 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, the 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 the
court to ‘‘construct [its] own
hypothetical case and then evaluate the
decree against that case.’’ Microsoft, 56
F.3d at 1459; see also InBev, 2009 U.S.
Dist. LEXIS 84787, at *20 (‘‘the ‘public
interest’ is not to be measured by
comparing the violations alleged in the
complaint against those the court
believes could have, or even should
have, been alleged’’). 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
United States District Court for the
District of Columbia 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 to the
Tunney Act,2 Congress made clear its
2 The 2004 amendments substituted ‘‘shall’’ for
‘‘may’’ in directing relevant factors for courts to
consider and amended the list of factors to focus on
competitive considerations and to address
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intent to preserve the practical benefits
of using 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. § 16(e)(2). This
language effectuates what Congress
intended when it enacted the Tunney
Act in 1974. As Senator Tunney
explained: ‘‘Mlle 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 Senator 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 11.3
III. SUMMARY OF PUBLIC COMMENT
AND THE UNITED STATES’
RESPONSE
During the sixty-day comment period,
the United States received only one
comment, submitted by the American
Medical Association (‘‘AMA’’), which is
attached to this Response. In its
comment, the AMA expressed its
support for the United States’ and the
State of Texas’s analysis as well as the
remedy articulated in the proposed
Final Judgment, stating that the action,
against United Regional ‘‘represents an
important step towards [reining] in
hospitals that use their monopoly power
to force exclusive dealing arrangements
onto health insurers.’’ AMA Comment at
1. The United States has carefully
reviewed the comment and has
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).
3 See 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’’); United States v. Mid-Am.
Dairymen, Inc., 1977–1 Trade Cas. (CCH)11 61,508,
at 71,980 (W.D. Mo. 1977) (‘‘Absent a showing of
corrupt failure of the government to discharge its
duty, the Court, in making its public interest
finding, should * * * carefully consider the
explanations of the government in the competitive
impact statement and its responses to comments in
order to determine whether those explanations are
reasonable under the circumstances.’’); S. Rep. No.
93–298 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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determined that the proposed Final
Judgment remains in the public interest.
The AMA is the largest association of
physicians and medical students in the
United States. The AMA’s comment
states that it concurs with several
central points made in the Complaint
and CIS. First, the AMA agreed with the
Department’s conclusion that the
relevant product markets should be
limited to inpatient hospital and
outpatient surgical services sold to
commercial health insurers. Although
hospitals serve patients covered by both
commercial health insurers and the
government plans (Medicare, Medicaid,
and TRICARE), the AMA agreed that a
market limited to hospital services sold
to commercial health insurers is well
defined because ‘‘[i]ndividuals who
have commercial health insurance
cannot switch over to Medicare or
Medicaid because of price increases or
output reductions in the commercial
market.’’ AMA Comment at 3. Thus,
health-care providers can target a price
increase to commercial health insurers
because the insurers cannot shift to
government rates.
Second, the AMA agreed that while
the relevant product markets are limited
to hospital services sold to commercial
health insurers, the competitive-effects
analysis should account for the ability
of health-care providers to serve
patients covered by other sources of
payments—including the government
plans. The AMA agreed that Medicare
and Medicaid pay providers
substantially less than commercial
health insurers in the Wichita Falls
MSA. Thus, as the Complaint and CIS
make clear, the appropriate method to
assess the contracts’ effect on
competition is to assess the degree to
which the contracts have foreclosed
access to payments for commercially
insured patients and account for the
foreclosed percentage of profits from all
payers.
Third, the AMA agreed with the
method used by the Department to
determine whether United Regional’s
discounts tied to exclusivity were
procompetitive or anticompetitive.
According to the AMA, in this case ‘‘the
Antitrust Division correctly looked at
United Regional’s costs, as opposed to
its rivals’ costs.’’ AMA Comment at 5. In
this case, the Department applied the
total discount United Regional offered
to health insurers to the patient volume
that United Regional would actually be
at risk of losing if an insurer were to
choose non-exclusivity (the ‘‘contestable
volume’’). In applying this ‘‘price-cost’’
test, which was similar to the ‘‘discountattribution’’ test adopted in Cascade
Health Solutions v. PeaceHealth, 515
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F.3d 883, 906–909 (9th Cir. 2008), the
Department determined that the prices
charged by United Regional in exchange
for exclusivity were below any plausible
measure of United Regional’s
incremental costs.
Finally, the AMA endorsed the
proposed Final Judgment, noting that it
strikes the right balance between
preventing United Regional from
engaging in anticompetitive conduct
while assuring that United Regional’s
rivals must still provide their services in
an efficient manner in order to compete.
IV. CONCLUSION
After reviewing the AMA’s public
comment, the United States continues to
believe that the proposed Final
Judgment, as drafted, provides an
effective and appropriate remedy for the
antitrust violations alleged in the
Complaint, and is therefore in the
public interest. The United States will
move this Court to enter the proposed
Final Judgment after the AMA’s
comment and this response are
published in the Federal Register.
Dated: June 6, 2011.
Respectfully submitted,
s/Scott I. Fitzgerald
Scott I. Fitzgerald (WA Bar #39716)
Amy R. Fitzpatrick (DC Bar #458680)
Attorneys for the United States, U.S.
Department of Justice, Antitrust
Division, Litigation I, 450 Fifth Street,
NW., Suite 4100, Washington, DC
20530, (202) 353–3863,
Scott.Fitzgerald@usdoj.gov
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CERTIFICATE OF SERVICE
On June 6, 2011, I, Scott I. Fitzgerald,
electronically submitted a copy of the
foregoing document with the clerk of
court for the U.S. District Court,
Northern District of Texas, using the
electronic case filing system for the
court. I hereby certify that I caused a
copy of the foregoing document to be
served upon Defendant United Regional
Health Care System electronically or by
another means authorized by the Court
or the Federal Rules of Civil Procedure.
s/Scott I. Fitzgerald
Scott I. Fitzgerald (WA Bar #39716)
Attorney for the United States, U.S.
Department of Justice, Antitrust
Division, Litigation I, 450 Fifth Street,
NW., Suite 4100, Washington, DC
20530
April 20, 2011.
BY E-MAIL
Mr. Joshua H. Soven, Chief of the
Litigation I Section, Antitrust
Division, United States Department of
Justice, 450 5th Street, N.W., Suite
4700, Washington, D.C. 20001.
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Re: Comments to Proposed Consent
Judgment in U.S. v. United Regional
Health Care System
Dear Mr. Soven:
The action by the Antitrust Division
of the Department of Justice (‘‘Antitrust
Division’’) against United Regional
Health Care System (‘‘United Regional’’)
represents an important step towards
reigning in hospitals that use their
monopoly power to force exclusive
dealing arrangements onto health
insurers in order to prevent entry by
firms that would compete against the
monopoly hospital.1 In United States, et
al., v. United Regional Health Care
System, 7:11-cv-00030 the Antitrust
Division alleged that United Regional
offered discriminatory bundled price
discounts to health insurers in order to
obtain exclusive dealing arrangements
that prevented or delayed entry into the
market. Specifically, health insurers
agreeing to an exclusive arrangement
with United Regional would received a
large discount on all of the services
purchased from United Regional. Health
insurers that did not agree to an
exclusive arrangement would receive a
significantly smaller discount from
United Regional. Not surprisingly, every
commercial health insurer operating in
United Regional’s market (except for
Blue Cross Blue Shield of Texas (‘‘Blue
Cross’’) chose an exclusive dealing
arrangement with United Regional. The
Antitrust Division alleged that these
exclusive dealing arrangements played
an important role in maintaining United
Regional’s monopoly power.
On February 25, 2011 the Antitrust
Division filed a Proposed Final
Judgment that is designed to end United
Regional’s use of discriminatory
bundled price discounts. The American
Medical Association (‘‘AMA’’) supports
the Proposed Final Judgment and the
Antitrust Division’s efforts to prevent
hospitals with monopoly power from
foreclosing entry through the use of the
discriminatory bundled price discounts.
The United Regional matter highlights
how hospitals with monopoly power
can use certain types of price discounts
to make it impossible for physicians to
compete on a level playing field. The
Antitrust Division’s action against
1 The American Medical Association understands
that no hearing or trial has occurred in United
Regional, and that United Regional has not
admitted the truth of the allegations contained in
the Antitrust Divisions’ Complaint or Competitive
Impact Statement. Indeed, the AMA understands
that United Regional denies many of the facts
alleged by the Antitrust Division. The AMA is not
taking a position, one way or the other, concerning
the truth of the allegations made by the Antitrust
Division against United Regional. The AMA’s
comments are based on and limited to the
allegations made by the Antitrust Division.
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United Regional shows how this lack of
competition ultimately hurts consumers
by locking in place high prices and
lower quality.
A. The Structure of Competition In
Health Care Markets
Throughout the country, physicians
play a crucial role in facilitating the
entry of new facilities that compete
against hospitals with entrenched
monopoly power. In order to compete
against an entrenched monopolist,
however, physicians need access to
commercial health insurers that control
access to patients.
Providers of medical services compete
for contracts with health insurers.
Because patients either cannot or will
not use out-of-network providers,
competition between providers for
patients is significantly affected by the
outcome of competition between
providers for health insurance contracts.
Health care markets cannot function in
a competitive manner if either form of
competition is monopolized or distorted
by anticompetitive agreements.
Competition for health insurance
contracts is particularly susceptible to
anticompetitive conduct because
commercial health insurance markets
and hospital markets have experienced
significant consolidation over the last 20
years. The consolidation by hospital and
health insurance markets has given each
side opportunities to limit the
competition they face. Throughout the
country, there are bilateral monopolies
in which hospitals and health insurers
jointly agree not to contract with each
other’s rivals in order to prevent entry
into either the hospital or the health
insurer market. Such arrangements are
becoming more common and have the
effect of mutually reinforcing the market
power wielded by hospitals and health
insurers.
The exclusive dealing arrangements
challenged in United Regional were
one-sided, in that they protected the
hospital from entry, but were not
designed to also prevent entry into the
health insurance market. The
anticompetitive effects created by
United Regional’s actions were still
significant, and the Antitrust Division’s
enforcement action represents a definite
step in the right direction.
B. Provider Access to Medicare and
Medicaid Is Not a Substitute for Access
to Commercial Health Insurance
An important issue raised by the
Antitrust Division’s action against
United Regional is the relevance of
Medicare and Medicaid in the antitrust
analysis of health care markets. The
Antitrust Division correctly concluded
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that the existence of Medicare and
Medicaid did not prevent United
Regional from possessing monopoly
power. Further, access to those
government programs by providers did
not prevent United Regional’s exclusive
dealing arrangements from barring
entry, and, thus, from limiting the
provider choices available to
consumers.
The Antitrust Division defined the
relevant product markets affected by
United Regional’s anticompetitive
practices as (a) ‘‘general acute-care
inpatient services * * * sold to
commercial health insurers,’’ and (b)
‘‘the market for outpatient surgical
services sold to commercial health
insurers.’’ The Antitrust Division
correctly concluded that the existence of
Medicare and Medicaid do not prevent
the exercise of monopoly power by a
hospital against commercial health
insurers or patients.
Individuals who have commercial
health insurance cannot switch over to
Medicare or Medicaid because of price
increases or output reductions in the
commercial market. Thus, if a health
insurer excludes various providers from
its provider panel, patients cannot
defeat those limitations by switching to
Medicare or Medicaid. Access to the
Medicare and Medicaid programs is
defined by federal law, and does not
turn on the quality, price or
comprehensiveness of commercial
health insurance products.
Defining a relevant product market,
however, is only part of the analysis.
While Medicare and Medicaid will not
prevent a hospital from imposing
onerous terms on health insurers that
adversely affect patient choice, the
Antitrust Division was correct in asking
the next question as to whether this
conduct actually could prevent rival
hospital and outpatient centers from
entering the market. One could argue
that programs such as Medicare and
Medicaid provide a large source of
patients upon which a new potential
rival hospital or outpatient center could
base a business plan. Such an argument,
however, is fallacious because Medicare
and Medicaid cannot fund new entry
given the way those programs are
currently structured.
Medicare and Medicaid pay providers
substantially less than commercial
health insurers, and in many instances,
pay providers less than the actual cost
of providing a medical service. It is
commonly recognized that hospitals and
outpatient centers have to crosssubsidize their Medicare and Medicaid
services with the profits earned from
patients covered by commercial health
insurance. Medicare and Medicaid,
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therefore, cannot function as facilitators
of new entry into the market.
The Antitrust Division was correct in
concluding that ‘‘foreclosure analysis
properly focuses on the profitability of
the various payment sources available to
health-care providers.’’ Without access
to the profitable sources of business in
the health care market, potential or
actual competitors cannot expand into
new markets or grow to a level where
they can seriously challenge the
incumbent monopolist. The Antitrust
Division was equally correctly when it
concluded that access to Medicare and
Medicaid by United Regional’s actual or
potential rivals was not an adequate
substitute to the private commercial
health insurers that United Regional
locked up with exclusive contracts.
The Antitrust Division stated, for
example, that the insurers with whom
United Regional had exclusive contracts
‘‘account for approximately 30% to 35%
of the profits that United Regional earns
from all payer-including the government
payers-even though they account for
only about 8% of United Regional’s total
patient volume.’’ Without access to the
most profitable segment of the health
care market, United Regional’s primary
rival, Kell West, could not hope to
develop into an effective competitor:
* * * without the exclusionary
contracts, Kell West likely would have
used the profits that it obtained from
contracts with the excluded commercial
health insurers to expand sooner, and
would also likely have added more beds
and additional services, such as
additional intensive-care capabilities,
cardiology services, and obstetric
services. Kell West has considered
expansion into additional services on
numerous occasions, but has been
limited in its ability to expand due to its
lack of access to commercially insured
patients.
C. United Regional’s Bundled Discounts
Were Anticompetitive
The Antitrust Division alleged that
United Regional used its market power
to make it ‘‘one of the most expensive
hospitals in Texas.’’ United Regional
understood that its monopoly pricing
would attract new entry, and it took
steps to maintain its monopoly position
by creating barriers to entry by using
discriminatory bundled price discounts
to obtain exclusive dealing
arrangements from commercial health
insurers.
According to the Antitrust Division,
United Regional established a dual track
pricing structure for health insurers. If
a health insurer agreed to exclusivity,
the health insurer received a premium
discount on all of the services provided
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by United Regional. If a health insurer
did not agree to exclusivity, the health
insurer would receive a significantly
smaller discount on all of the services
it paid for on behalf of its policyholders.
United Regional’s bundled discount
arrangement led to exclusive dealing
arrangements with health insurers
because United Regional’s rivals did not
and could not offer the full line of
services that United Regional provided.
United Regional’s rivals could not
match the total value of the discount
United Regional offered. While the
health insurer would get a comparable
price discount on the services on which
United Regional and its rival competed,
the health insurer would lose the United
Regional discount on all of United
Regional’s services if the health insurer
abandoned exclusivity. As a result, a
rival would have to offer a health
insurer a discount substantially higher
than the discount offered by United
Regional. Only in this manner could a
rival compete against the total value of
the discount offered by United Regional.
None of United Regional’s actual or
potential rivals could offer health
insurers a discount large enough to
make the health insurer abandon its
exclusive dealing arrangement with
United Regional. In fact, the total value
of the discount United Regional offered
was so large that its rivals would have
to offer health insurers prices that
would almost certainly be substantially
below cost, and therefore would be
unsustainable.
The Antitrust Division claims that
United Regional’s exclusive dealingdependent pricing structure largely
succeeded in foreclosing competition.
All of the commercial health insurers in
the area entered into exclusive
arrangements, except for Blue Cross.
Blue Cross was apparently large enough
that it could off-set United Regional’s
market power and negotiated discounts
without having to agree to an exclusive
arrangement. The ability of United
Regional’s rivals to contract with Blue
Cross apparently allowed them to
survive in the market, but did not give
them the ability to effectively compete
against United Regional.
There is nothing inherently wrong
with offering attractive price discounts
to customers, and in many cases price
discounts are procompetitive. Courts
and economists, however, have
recognized that price discounts are
sometimes anticompetitive. The
Antitrust Division correctly
distinguished United Regional’s
anticompetitive bundled price discounts
from procompetitive price discounts. To
do this, the Antitrust Division correctly
looked at United Regional’s costs, as
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opposed to its rivals’ costs. Specifically,
the Antitrust Division determined the
patient volume for which United
Regional and its rivals actually
competed, and then applied the total
discount United Regional offered to
health insurers to that ‘‘contestable
volume.’’ If the total discount, when
applied to the contestable volume,
results in the contestable volume being
sold at a loss, a portion of the discount
is then equivalent to a market control
premium. The Antitrust Division was
correct in concluding that United
Regional was offering health insurance
companies a market control premium in
order to maintain its monopoly.
Finally, the AMA supports the
narrowly tailored limitations the
Antitrust Division set forth in the
Proposed Final Judgment. Overall, the
Proposed Final Judgment will prevent
United Regional from ceding back to
commercial health insurers a portion of
its monopoly profits in order to
maintain its monopoly power. The
Proposed Final Judgment, however,
does not prevent United Regional from
offering incremental price discounts
that allow it to offer discounted prices
that are in line with its cost structure.
Thus, potential rivals to United
Regional will have to provide their
services in an efficient manner in order
to compete against United Regional on
price when trying to strike deals with
commercial health insurers. United
Regional will also have to compete on
the basis of the efficiencies it can offer,
rather than on the raw use of its market
power.
Overall, the Proposed Final Judgment
will not have the effect of propping up
inefficient firms that can only survive in
the market because United Regional is
unable to freely reduce its prices.
Instead, the pricing restraints placed on
United Regional should prevent it from
using bundled discounts in order to
limit the competition it faces from truly
efficient firms.
Sincerely,
Henry S. Allen, Jr.
Senior Attorney, Advocacy
[FR Doc. 2011–14628 Filed 6–14–11; 8:45 am]
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DEPARTMENT OF JUSTICE
Federal Bureau of Investigation
[OMB Number 1110–NEW]
Agency Information Collection
Activities; Proposed Collection,
Comments Requested; Applicant
Information Form (1–783)
60-day Notice of Information
Collection for Review.
ACTION:
The Department of Justice (DOJ),
Federal Bureau of Investigation (FBI),
Criminal Justice Information Services
(CJIS) Division will be submitting the
following information collection
renewal to the Office of Management
and Budget (OMB) for review in
accordance with established review
procedures of the Paperwork Reduction
Act of 1995. The information collection
is published to obtain comments from
the public and affected agencies.
Comments are encouraged and will be
accepted for ‘‘sixty days’’ until August
15, 2011. This process is conducted in
accordance with 5 CFR 1320.10.
All comments, suggestions, or
questions regarding additional
information, to include obtaining a copy
of the proposed information collection
instrument with instructions, should be
directed to Rachel K. Hurst,
Management Program Analyst, FBI, CJIS
Division, Biometric Services Section
(BSS), Support Services Unit (SSU),
Module E–1, 1000 Custer Hollow Road,
Clarksburg, West Virginia, 26306; or by
facsimile to (304) 625–5392.
Written comments concerning this
information collection should be sent to
the Office of Information and Regulatory
Affairs, Office of Management and
Budget, Attn: DOJ Desk Officer. The best
way to ensure your comments are
received is to e-mail them to
oira_submission@omb.eop.gov or fax
them to 202–395–7285. All comments
should reference the 8-digit OMB
number for the collection or the title of
the collection. If you have questions
concerning the collection, please call
Rachel Hurst at 1–304–625–2000 or the
DOJ Desk Officer at 202–395–3176.
Written comments and suggestions
from the public and affected agencies
concerning the proposed collection of
information are encouraged. Comments
should address one or more of the
following four points:
(1) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have a
practical utility;
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(2) Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(3) Enhance the quality, utility, and
clarity of the information to be
collected; and
(4) Minimize the burden of the
collection of information on those who
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques of
other forms of information technology,
e.g., permitting electronic submission of
responses.
Overview of this information
collection:
(1) Type of information collection:
Approval of existing collection in use
without an OMB control number.
(2) The title of the form/collection:
Applicant Information Form.
(3) The agency form number, if any,
and the applicable component of the
department sponsoring the collection:
1–783; CJIS Division, FBI, DOJ.
(4) Affected public who will be asked
or required to respond, as well as a brief
abstract: Primary: Individuals. This
collection is necessary for an individual
to request a copy of their personal
identification record to review it or to
obtain a change, correction, or an
update to the record.
(5) An estimate of the total number of
respondents and the amount of time
estimated for an average respondent to
respond: Annually, the FBI receives
225,000 identification requests,
therefore there are 225,000 respondents.
The form requires three minutes to
complete.
(6) An estimate of the total public
burden (in hours) associated with this
collection: There are approximately
11,250 burden hours associated with
this collection.
If additional information is required
contact: Jerri Murray, Department
Clearance Officer, Justice Management
Division, United States Department of
Justice, Policy and Planning Staff, 145 N
Street, NE., Room 2E–808, Washington,
DC 20530.
Jerri Murray,
Department Clearance Officer, United States
Department of Justice.
[FR Doc. 2011–14727 Filed 6–9–11; 8:45 am]
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Agencies
[Federal Register Volume 76, Number 115 (Wednesday, June 15, 2011)]
[Notices]
[Pages 35017-35022]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-14628]
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DEPARTMENT OF JUSTICE
Antitrust Division
United States et al. v. United Regional Health Care System;
Public Comments and Response on Proposed Final Judgment
Pursuant to the Antitrust Procedures and Penalties Act, 15 U.S.C.
16(b)-(h), the United States hereby publishes below the comment
received on the proposed Final Judgment in United States and State of
Texas v. United Regional Health Care System, Civil Action No. 7:11-cv-
00030-0, which was filed in the United States District Court for the
Northern District of Texas, Wichita Falls Division, on June 6, 2011,
together with the response of the United States to the comment.
Copies of the comment and the response are available for inspection
at the U.S. Department of Justice, Antitrust Division, Antitrust
Documents Group, 450 Fifth Street, NW., Suite 1010, Washington, DC
20530 (telephone: 202-514-2481); on the Department of Justice's Web
site at https://www.usdoj.gov/atr; and at the Office of the Clerk of the
United States District Court for the Northern District of Texas,
Wichita Falls Division. Copies of any of these materials may be
obtained upon request and payment of a copying fee.
Patricia A. Brink,
Director of Civil Enforcement.
In The United States District Court for the Northern District of Texas,
Wichita Falls Division
United States Of America And State Of Texas, (RCO) Plaintiffs, V.
United Regional Health Care System, Defendant.
Case No.: 7:11-cv-00030
Response Of Plaintiff United States To Public Comment On The Proposed
Final Judgment
Pursuant to the requirements of the Antitrust Procedures and
Penalties Act, 15 U.S.C. Sec. 16(b)-(h) (``APPA7 or ``Tunney Act''),
the United States hereby responds to the public comment received
regarding the proposed Final Judgment in this case. The single comment
received agrees that the proposed Final Judgment will provide an
effective and appropriate remedy for the antitrust violations alleged
in the Complaint. The United States will move the Court for entry of
the proposed Final Judgment after the public comment and this response
have been published in the Federal Register, pursuant to 15 U.S.C.
Sec. 16(d).
On February 25, 2011, the United States and the State of Texas
filed a civil antitrust lawsuit against Defendant United Regional
Health Care System (``United Regional'') challenging United Regional's
contracts with commercial health insurers that effectively prevented
insurers from contracting with United Regional's competitors
(``exclusionary contracts''). The Complaint alleged that United
Regional had unlawfully used those contracts to maintain its monopoly
for hospital services, in violation of Section 2 of the Sherman Act, 15
U.S.C. Sec. 2. By effectively preventing most commercial health
insurers from including in their networks other inpatient and
outpatient facilities, the Complaint alleged that United Regional (1)
delayed and prevented the expansion and entry of its competitors,
likely leading to higher health-care costs and higher health insurance
premiums; (2) limited price competition for price-sensitive patients,
likely leading to higher health-care costs for those patients; and (3)
reduced quality competition between United Regional and its
competitors. The Complaint sought to enjoin United Regional from
entering exclusionary contracts with insurers.
Simultaneously with the filing of the Complaint, the United States
and the State of Texas filed a proposed Final Judgment and Stipulation
signed by the plaintiffs and United Regional consenting to entry of the
proposed Final Judgment after compliance with the requirements of the
Tunney Act, 15 U.S.C. Sec. 16. Pursuant to those requirements, the
United States also filed its Competitive Impact Statement (``CIS'')
with the Court on February 25, 2011; published the proposed Final
Judgment and CIS in the Federal Register on March 10, 2011, see 76 Fed.
Reg. 13209; and had summaries of the terms of the proposed Final
Judgment and CIS, together with directions for the submission of
written comments relating to the proposed Final Judgment, published in
The Washington Post and Times Record News for seven days beginning on
March 9, 2011, and ending on March 15, 2011. The sixty-day period for
public comment ended on May 14, 2011. One comment was received, as
described below and attached hereto.
I. THE INVESTIGATION AND PROPOSED RESOLUTION
The proposed Final Judgment is the culmination of an investigation
by the Antitrust Division of the United States Department of Justice
(``Department'') of United Regional's contracting practices with
commercial insurers. As part of its investigation, the Department
issued more than fifteen Civil Investigative Demands for documents. The
Department reviewed the documents and other materials received,
conducted more than 80 interviews, and took oral testimony of United
Regional personnel. The Department carefully analyzed the information
obtained and thoroughly considered all of the issues presented.
The Department found that beginning in 1998, United Regional
responded to the competitive threat posed by the entry of a competing
hospital, Kell West; and other outpatient-surgery facilities by
systematically entering into exclusionary contracts with commercial
health insurers. The precise terms of these contracts varied, but all
shared the same anticompetitive feature: a significant pricing penalty
if an insurer contracts with competing facilities within a region that
is no larger than Wichita County. In general, the contracts offered a
substantially larger discount off billed charges (e.g., 25%) if United
Regional was the only local hospital or outpatient surgical provider in
the insurer's network; and the contracts provided for a much smaller
discount (e.g., 5% off billed charges) if the insurer contracted with
one of United Regional's rivals.
Within three months after Kell West opened in January 1999, United
Regional had entered into exclusionary contracts with five commercial
health insurers, and by 2010, it had exclusionary contracts with eight
insurers. In each instance, United Regional-not the insurer-required
the exclusionary provisions in the contract. The only major insurer
that did not sign an exclusionary contract with United Regional was
Blue Cross Blue Shield of Texas (``Blue Cross''), by far the largest
insurer in Wichita Falls and Texas.
Because United Regional is a ``must have'' hospital for any insurer
that wants to sell health insurance in the Wichita Falls area, and
because the penalty for contracting with United Regional's rivals was
so significant, most insurers entered into exclusionary contracts with
United Regional.
[[Page 35018]]
Consequently, United Regional's rivals could not obtain contracts with
most insurers, except Blue Cross, which substantially hindered their
ability to compete and helped United Regional maintain its monopoly in
the relevant markets, to the detriment of consumers.
After reviewing the investigative materials, the Department
determined that United Regional's conduct violated Section 2 of the
Sherman Act, 15 U.S.C. Sec. 2, as alleged in the Complaint. The
proposed Final Judgment is designed to restore competition between
health-care providers in the Wichita Falls MSA. Section IV of the
proposed Final Judgment prohibits United Regional from using
exclusivity terms in its contracts with commercial health insurers. In
particular, United Regional is prohibited from (1) conditioning the
prices or discounts that it offers to commercial health insurers on
whether those insurers contract with other health-care providers, such
as Kell West; and (2) preventing insurers from entering into agreements
with United Regional's rivals. United Regional is also prohibited from
taking any retaliatory actions against an insurer that enters (or seeks
to enter) into an agreement with a rival health-care provider.
In addition, the proposed Final Judgment prohibits United Regional
from offering other types of ``conditional volume discounts'' that
could have the same anticompetitive effects as the challenged conduct.
``Conditional volume discounts'' are prices, discounts, or rebates
offered to a commercial health insurer on condition that the volume of
that insurer's purchases from United Regional meets or exceeds a
specified threshold. Similarly, United Regional may not offer market-
share discounts, e.g., discounts conditioned on an insurer's purchases
at United Regional meeting a specified percentage of that insurer's
total purchases, whether they apply retroactively or not, because such
discounts can also be a form of anticompetitive pricing. Finally,
United Regional may not use provisions in its insurance contracts that
discourage insurers from offering products that encourage members to
use other in-network providers (besides United Regional).
The proposed Final Judgment does, however, allow price discounts
that are likely to be procompetitive. Section V of the proposed Final
Judgment permits United Regional to offer above-cost incremental volume
discounts. By permitting such discounts, the proposed Final Judgment
ensures that United Regional can engage in procompetitiye efforts to
compete for additional patient volume, while preventing United Regional
from offering `discounts that have the potential to exclude an equally
efficient competitor.
II. STANDARD OF JUDICIAL REVIEW
The APPA requires that proposed consent judgments in antitrust
cases brought by the United States be subject to a sixty-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 also 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. InBev N.V./S.A., No. 08-1965 (JR), 2009 U.S. Dist. LEXIS
84787, at *3 (D.D.C. Aug. 11, 2009) (noting that the court's review of
a consent judgment is limited and only inquires ``into whether the
government's determination that the proposed remedies will cure the
antitrust violations alleged in the complaint was reasonable, and
whether the mechanisms to enforce the final judgment are clear and
manageable.'').
As the United States Court of Appeals for the District of Columbia
Circuit has held, a court considers under the APPA, among other things,
the relationship between the remedy secured and the specific
allegations set forth in the United States' complaint, whether the
decree is sufficiently clear, whether 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) (citing
United States v. Bechtel Corp., 648 F.2d 660, 666 (9th Cir. 1981)); see
also Microsoft, 56 F.3d at 1460-62; InBev, 2009 U.S. Dist. LEXIS 84787,
at *3; United States v. Alcoa, Inc., 152 F. Supp. 2d 37, 40 (D.D.C.
2001). Courts have held that:
[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).\1\ In
determining whether a proposed settlement is in the public interest, a
district 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 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 I, 6 (D.D.C. 2003) (noting that
the court should grant due respect to the United States' ``prediction
as to the effect of proposed remedies, its perception of the
[[Page 35019]]
market structure, and its views of the nature of the case'').
---------------------------------------------------------------------------
\1\ Cf 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''); see
generally Microsoft, 56 F.3d at 1461 (discussing 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' '').
Courts have greater flexibility in approving proposed consent
decrees than in crafting their own decrees following a finding of
liability in a litigated matter. ``[A] proposed decree must be approved
even if it falls short of the remedy the court would impose on its own,
as long as it falls within the range of acceptability or is `within the
reaches of public interest.''' United States v. Am. Tel. & Tel. Co.,
552 F. Supp. 131, 151 (D.D.C. 1982) (citations omitted) (quoting United
States v. Gillette Co., 406 F. Supp. 713, 716 (D. Mass. 1975)), aff'd
sub nom. Maryland v. United States, 460 U.S. 1001 (1983); see also
United States v. Akan Aluminum Ltd., 605 F. Supp. 619, 622 (W.D. Ky.
1985) (approving the consent decree even though the court would have
imposed a greater remedy). 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, the 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 the court to
``construct [its] own hypothetical case and then evaluate the decree
against that case.'' Microsoft, 56 F.3d at 1459; see also InBev, 2009
U.S. Dist. LEXIS 84787, at *20 (``the `public interest' is not to be
measured by comparing the violations alleged in the complaint against
those the court believes could have, or even should have, been
alleged''). 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 United States District Court for the District of Columbia
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 to the Tunney Act,\2\ Congress made clear
its intent to preserve the practical benefits of using 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). This language effectuates
what Congress intended when it enacted the Tunney Act in 1974. As
Senator Tunney explained: ``Mlle 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 Senator 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.\3\
---------------------------------------------------------------------------
\2\ The 2004 amendments substituted ``shall'' for ``may'' in
directing relevant factors for courts 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).
\3\ See 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'');
United States v. Mid-Am. Dairymen, Inc., 1977-1 Trade Cas. (CCH)11
61,508, at 71,980 (W.D. Mo. 1977) (``Absent a showing of corrupt
failure of the government to discharge its duty, the Court, in
making its public interest finding, should * * * carefully consider
the explanations of the government in the competitive impact
statement and its responses to comments in order to determine
whether those explanations are reasonable under the
circumstances.''); S. Rep. No. 93-298 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.'').
---------------------------------------------------------------------------
III. SUMMARY OF PUBLIC COMMENT AND THE UNITED STATES' RESPONSE
During the sixty-day comment period, the United States received
only one comment, submitted by the American Medical Association
(``AMA''), which is attached to this Response. In its comment, the AMA
expressed its support for the United States' and the State of Texas's
analysis as well as the remedy articulated in the proposed Final
Judgment, stating that the action, against United Regional ``represents
an important step towards [reining] in hospitals that use their
monopoly power to force exclusive dealing arrangements onto health
insurers.'' AMA Comment at 1. The United States has carefully reviewed
the comment and has determined that the proposed Final Judgment remains
in the public interest.
The AMA is the largest association of physicians and medical
students in the United States. The AMA's comment states that it concurs
with several central points made in the Complaint and CIS. First, the
AMA agreed with the Department's conclusion that the relevant product
markets should be limited to inpatient hospital and outpatient surgical
services sold to commercial health insurers. Although hospitals serve
patients covered by both commercial health insurers and the government
plans (Medicare, Medicaid, and TRICARE), the AMA agreed that a market
limited to hospital services sold to commercial health insurers is well
defined because ``[i]ndividuals who have commercial health insurance
cannot switch over to Medicare or Medicaid because of price increases
or output reductions in the commercial market.'' AMA Comment at 3.
Thus, health-care providers can target a price increase to commercial
health insurers because the insurers cannot shift to government rates.
Second, the AMA agreed that while the relevant product markets are
limited to hospital services sold to commercial health insurers, the
competitive-effects analysis should account for the ability of health-
care providers to serve patients covered by other sources of payments--
including the government plans. The AMA agreed that Medicare and
Medicaid pay providers substantially less than commercial health
insurers in the Wichita Falls MSA. Thus, as the Complaint and CIS make
clear, the appropriate method to assess the contracts' effect on
competition is to assess the degree to which the contracts have
foreclosed access to payments for commercially insured patients and
account for the foreclosed percentage of profits from all payers.
Third, the AMA agreed with the method used by the Department to
determine whether United Regional's discounts tied to exclusivity were
procompetitive or anticompetitive. According to the AMA, in this case
``the Antitrust Division correctly looked at United Regional's costs,
as opposed to its rivals' costs.'' AMA Comment at 5. In this case, the
Department applied the total discount United Regional offered to health
insurers to the patient volume that United Regional would actually be
at risk of losing if an insurer were to choose non-exclusivity (the
``contestable volume''). In applying this ``price-cost'' test, which
was similar to the ``discount-attribution'' test adopted in Cascade
Health Solutions v. PeaceHealth, 515
[[Page 35020]]
F.3d 883, 906-909 (9th Cir. 2008), the Department determined that the
prices charged by United Regional in exchange for exclusivity were
below any plausible measure of United Regional's incremental costs.
Finally, the AMA endorsed the proposed Final Judgment, noting that
it strikes the right balance between preventing United Regional from
engaging in anticompetitive conduct while assuring that United
Regional's rivals must still provide their services in an efficient
manner in order to compete.
IV. CONCLUSION
After reviewing the AMA's public comment, the United States
continues to believe that the proposed Final Judgment, as drafted,
provides an effective and appropriate remedy for the antitrust
violations alleged in the Complaint, and is therefore in the public
interest. The United States will move this Court to enter the proposed
Final Judgment after the AMA's comment and this response are published
in the Federal Register.
Dated: June 6, 2011.
Respectfully submitted,
s/Scott I. Fitzgerald
Scott I. Fitzgerald (WA Bar 39716)
Amy R. Fitzpatrick (DC Bar 458680)
Attorneys for the United States, U.S. Department of Justice, Antitrust
Division, Litigation I, 450 Fifth Street, NW., Suite 4100, Washington,
DC 20530, (202) 353-3863, Scott.Fitzgerald@usdoj.gov
CERTIFICATE OF SERVICE
On June 6, 2011, I, Scott I. Fitzgerald, electronically submitted a
copy of the foregoing document with the clerk of court for the U.S.
District Court, Northern District of Texas, using the electronic case
filing system for the court. I hereby certify that I caused a copy of
the foregoing document to be served upon Defendant United Regional
Health Care System electronically or by another means authorized by the
Court or the Federal Rules of Civil Procedure.
s/Scott I. Fitzgerald
Scott I. Fitzgerald (WA Bar 39716)
Attorney for the United States, U.S. Department of Justice, Antitrust
Division, Litigation I, 450 Fifth Street, NW., Suite 4100, Washington,
DC 20530
April 20, 2011.
BY E-MAIL
Mr. Joshua H. Soven, Chief of the Litigation I Section, Antitrust
Division, United States Department of Justice, 450 5th Street, N.W.,
Suite 4700, Washington, D.C. 20001.
Re: Comments to Proposed Consent Judgment in U.S. v. United Regional
Health Care System
Dear Mr. Soven:
The action by the Antitrust Division of the Department of Justice
(``Antitrust Division'') against United Regional Health Care System
(``United Regional'') represents an important step towards reigning in
hospitals that use their monopoly power to force exclusive dealing
arrangements onto health insurers in order to prevent entry by firms
that would compete against the monopoly hospital.\1\ In United States,
et al., v. United Regional Health Care System, 7:11-cv-00030 the
Antitrust Division alleged that United Regional offered discriminatory
bundled price discounts to health insurers in order to obtain exclusive
dealing arrangements that prevented or delayed entry into the market.
Specifically, health insurers agreeing to an exclusive arrangement with
United Regional would received a large discount on all of the services
purchased from United Regional. Health insurers that did not agree to
an exclusive arrangement would receive a significantly smaller discount
from United Regional. Not surprisingly, every commercial health insurer
operating in United Regional's market (except for Blue Cross Blue
Shield of Texas (``Blue Cross'') chose an exclusive dealing arrangement
with United Regional. The Antitrust Division alleged that these
exclusive dealing arrangements played an important role in maintaining
United Regional's monopoly power.
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\1\ The American Medical Association understands that no hearing
or trial has occurred in United Regional, and that United Regional
has not admitted the truth of the allegations contained in the
Antitrust Divisions' Complaint or Competitive Impact Statement.
Indeed, the AMA understands that United Regional denies many of the
facts alleged by the Antitrust Division. The AMA is not taking a
position, one way or the other, concerning the truth of the
allegations made by the Antitrust Division against United Regional.
The AMA's comments are based on and limited to the allegations made
by the Antitrust Division.
---------------------------------------------------------------------------
On February 25, 2011 the Antitrust Division filed a Proposed Final
Judgment that is designed to end United Regional's use of
discriminatory bundled price discounts. The American Medical
Association (``AMA'') supports the Proposed Final Judgment and the
Antitrust Division's efforts to prevent hospitals with monopoly power
from foreclosing entry through the use of the discriminatory bundled
price discounts.
The United Regional matter highlights how hospitals with monopoly
power can use certain types of price discounts to make it impossible
for physicians to compete on a level playing field. The Antitrust
Division's action against United Regional shows how this lack of
competition ultimately hurts consumers by locking in place high prices
and lower quality.
A. The Structure of Competition In Health Care Markets
Throughout the country, physicians play a crucial role in
facilitating the entry of new facilities that compete against hospitals
with entrenched monopoly power. In order to compete against an
entrenched monopolist, however, physicians need access to commercial
health insurers that control access to patients.
Providers of medical services compete for contracts with health
insurers. Because patients either cannot or will not use out-of-network
providers, competition between providers for patients is significantly
affected by the outcome of competition between providers for health
insurance contracts. Health care markets cannot function in a
competitive manner if either form of competition is monopolized or
distorted by anticompetitive agreements.
Competition for health insurance contracts is particularly
susceptible to anticompetitive conduct because commercial health
insurance markets and hospital markets have experienced significant
consolidation over the last 20 years. The consolidation by hospital and
health insurance markets has given each side opportunities to limit the
competition they face. Throughout the country, there are bilateral
monopolies in which hospitals and health insurers jointly agree not to
contract with each other's rivals in order to prevent entry into either
the hospital or the health insurer market. Such arrangements are
becoming more common and have the effect of mutually reinforcing the
market power wielded by hospitals and health insurers.
The exclusive dealing arrangements challenged in United Regional
were one-sided, in that they protected the hospital from entry, but
were not designed to also prevent entry into the health insurance
market. The anticompetitive effects created by United Regional's
actions were still significant, and the Antitrust Division's
enforcement action represents a definite step in the right direction.
B. Provider Access to Medicare and Medicaid Is Not a Substitute for
Access to Commercial Health Insurance
An important issue raised by the Antitrust Division's action
against United Regional is the relevance of Medicare and Medicaid in
the antitrust analysis of health care markets. The Antitrust Division
correctly concluded
[[Page 35021]]
that the existence of Medicare and Medicaid did not prevent United
Regional from possessing monopoly power. Further, access to those
government programs by providers did not prevent United Regional's
exclusive dealing arrangements from barring entry, and, thus, from
limiting the provider choices available to consumers.
The Antitrust Division defined the relevant product markets
affected by United Regional's anticompetitive practices as (a)
``general acute-care inpatient services * * * sold to commercial health
insurers,'' and (b) ``the market for outpatient surgical services sold
to commercial health insurers.'' The Antitrust Division correctly
concluded that the existence of Medicare and Medicaid do not prevent
the exercise of monopoly power by a hospital against commercial health
insurers or patients.
Individuals who have commercial health insurance cannot switch over
to Medicare or Medicaid because of price increases or output reductions
in the commercial market. Thus, if a health insurer excludes various
providers from its provider panel, patients cannot defeat those
limitations by switching to Medicare or Medicaid. Access to the
Medicare and Medicaid programs is defined by federal law, and does not
turn on the quality, price or comprehensiveness of commercial health
insurance products.
Defining a relevant product market, however, is only part of the
analysis. While Medicare and Medicaid will not prevent a hospital from
imposing onerous terms on health insurers that adversely affect patient
choice, the Antitrust Division was correct in asking the next question
as to whether this conduct actually could prevent rival hospital and
outpatient centers from entering the market. One could argue that
programs such as Medicare and Medicaid provide a large source of
patients upon which a new potential rival hospital or outpatient center
could base a business plan. Such an argument, however, is fallacious
because Medicare and Medicaid cannot fund new entry given the way those
programs are currently structured.
Medicare and Medicaid pay providers substantially less than
commercial health insurers, and in many instances, pay providers less
than the actual cost of providing a medical service. It is commonly
recognized that hospitals and outpatient centers have to cross-
subsidize their Medicare and Medicaid services with the profits earned
from patients covered by commercial health insurance. Medicare and
Medicaid, therefore, cannot function as facilitators of new entry into
the market.
The Antitrust Division was correct in concluding that ``foreclosure
analysis properly focuses on the profitability of the various payment
sources available to health-care providers.'' Without access to the
profitable sources of business in the health care market, potential or
actual competitors cannot expand into new markets or grow to a level
where they can seriously challenge the incumbent monopolist. The
Antitrust Division was equally correctly when it concluded that access
to Medicare and Medicaid by United Regional's actual or potential
rivals was not an adequate substitute to the private commercial health
insurers that United Regional locked up with exclusive contracts.
The Antitrust Division stated, for example, that the insurers with
whom United Regional had exclusive contracts ``account for
approximately 30% to 35% of the profits that United Regional earns from
all payer-including the government payers-even though they account for
only about 8% of United Regional's total patient volume.'' Without
access to the most profitable segment of the health care market, United
Regional's primary rival, Kell West, could not hope to develop into an
effective competitor:
* * * without the exclusionary contracts, Kell West likely would have
used the profits that it obtained from contracts with the excluded
commercial health insurers to expand sooner, and would also likely have
added more beds and additional services, such as additional intensive-
care capabilities, cardiology services, and obstetric services. Kell
West has considered expansion into additional services on numerous
occasions, but has been limited in its ability to expand due to its
lack of access to commercially insured patients.
C. United Regional's Bundled Discounts Were Anticompetitive
The Antitrust Division alleged that United Regional used its market
power to make it ``one of the most expensive hospitals in Texas.''
United Regional understood that its monopoly pricing would attract new
entry, and it took steps to maintain its monopoly position by creating
barriers to entry by using discriminatory bundled price discounts to
obtain exclusive dealing arrangements from commercial health insurers.
According to the Antitrust Division, United Regional established a
dual track pricing structure for health insurers. If a health insurer
agreed to exclusivity, the health insurer received a premium discount
on all of the services provided by United Regional. If a health insurer
did not agree to exclusivity, the health insurer would receive a
significantly smaller discount on all of the services it paid for on
behalf of its policyholders. United Regional's bundled discount
arrangement led to exclusive dealing arrangements with health insurers
because United Regional's rivals did not and could not offer the full
line of services that United Regional provided. United Regional's
rivals could not match the total value of the discount United Regional
offered. While the health insurer would get a comparable price discount
on the services on which United Regional and its rival competed, the
health insurer would lose the United Regional discount on all of United
Regional's services if the health insurer abandoned exclusivity. As a
result, a rival would have to offer a health insurer a discount
substantially higher than the discount offered by United Regional. Only
in this manner could a rival compete against the total value of the
discount offered by United Regional. None of United Regional's actual
or potential rivals could offer health insurers a discount large enough
to make the health insurer abandon its exclusive dealing arrangement
with United Regional. In fact, the total value of the discount United
Regional offered was so large that its rivals would have to offer
health insurers prices that would almost certainly be substantially
below cost, and therefore would be unsustainable.
The Antitrust Division claims that United Regional's exclusive
dealing-dependent pricing structure largely succeeded in foreclosing
competition. All of the commercial health insurers in the area entered
into exclusive arrangements, except for Blue Cross. Blue Cross was
apparently large enough that it could off-set United Regional's market
power and negotiated discounts without having to agree to an exclusive
arrangement. The ability of United Regional's rivals to contract with
Blue Cross apparently allowed them to survive in the market, but did
not give them the ability to effectively compete against United
Regional.
There is nothing inherently wrong with offering attractive price
discounts to customers, and in many cases price discounts are
procompetitive. Courts and economists, however, have recognized that
price discounts are sometimes anticompetitive. The Antitrust Division
correctly distinguished United Regional's anticompetitive bundled price
discounts from procompetitive price discounts. To do this, the
Antitrust Division correctly looked at United Regional's costs, as
[[Page 35022]]
opposed to its rivals' costs. Specifically, the Antitrust Division
determined the patient volume for which United Regional and its rivals
actually competed, and then applied the total discount United Regional
offered to health insurers to that ``contestable volume.'' If the total
discount, when applied to the contestable volume, results in the
contestable volume being sold at a loss, a portion of the discount is
then equivalent to a market control premium. The Antitrust Division was
correct in concluding that United Regional was offering health
insurance companies a market control premium in order to maintain its
monopoly.
Finally, the AMA supports the narrowly tailored limitations the
Antitrust Division set forth in the Proposed Final Judgment. Overall,
the Proposed Final Judgment will prevent United Regional from ceding
back to commercial health insurers a portion of its monopoly profits in
order to maintain its monopoly power. The Proposed Final Judgment,
however, does not prevent United Regional from offering incremental
price discounts that allow it to offer discounted prices that are in
line with its cost structure. Thus, potential rivals to United Regional
will have to provide their services in an efficient manner in order to
compete against United Regional on price when trying to strike deals
with commercial health insurers. United Regional will also have to
compete on the basis of the efficiencies it can offer, rather than on
the raw use of its market power.
Overall, the Proposed Final Judgment will not have the effect of
propping up inefficient firms that can only survive in the market
because United Regional is unable to freely reduce its prices. Instead,
the pricing restraints placed on United Regional should prevent it from
using bundled discounts in order to limit the competition it faces from
truly efficient firms.
Sincerely,
Henry S. Allen, Jr.
Senior Attorney, Advocacy
[FR Doc. 2011-14628 Filed 6-14-11; 8:45 am]
BILLING CODE 4410-11-M