Carilion Clinic; Analysis of Agreement Containing Consent Orders To Aid Public Comment, 53252-53254 [E9-24949]
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53252
Federal Register / Vol. 74, No. 199 / Friday, October 16, 2009 / Notices
remains in ‘‘not current’’ status on
Commerce’s website.
The proposed order applies to
ExpatEdge’s representations about its
membership in any privacy, security, or
any other compliance program
sponsored by the government or any
other third party. It contains provisions
designed to prevent ExpatEdge from
engaging in the future in practices
similar to those alleged in the
complaint.
Part I of the proposed order prohibits
ExpatEdge from making
misrepresentations about its
membership in any privacy, security, or
any other compliance program
sponsored by the government or any
other third party.
Parts II through VI of the proposed
order are reporting and compliance
provisions. Part II requires ExpatEdge to
retain documents relating to its
compliance with the order for a fiveyear period. Part III requires
dissemination of the order now and in
the future to persons with
responsibilities relating to the subject
matter of the order. Part IV ensures
notification to the FTC of changes in
corporate status. Part V mandates that
ExpatEdge submit an initial compliance
report to the FTC, and make available to
the FTC subsequent reports. Part VI is
a provision ‘‘sunsetting’’ the order after
twenty (20) years, with certain
exceptions.
The purpose of the analysis is to
facilitate public comment on the
proposed order. It is not intended to
constitute an official interpretation of
the agreement and proposed order or to
modify in any way their terms.
By direction of the Commission.
Donald S. Clark,
Secretary.
[FR Doc. E9–24997 Filed 10–15–09; 8:45 am]
BILLING CODE 6750–01–S
FEDERAL TRADE COMMISSION
[Docket No. 9338]
Carilion Clinic; Analysis of Agreement
Containing Consent Orders To Aid
Public Comment
Federal Trade Commission.
Proposed consent agreement.
AGENCY:
jlentini on DSKJ8SOYB1PROD with NOTICES
ACTION:
SUMMARY: The consent agreement in this
matter settles alleged violations of
federal law prohibiting unfair or
deceptive acts or practices or unfair
methods of competition. The attached
Analysis to Aid Public Comment
describes both the allegations in the
complaint and the terms of the consent
VerDate Nov<24>2008
16:37 Oct 15, 2009
Jkt 220001
order — embodied in the consent
agreement — that would settle these
allegations.
DATES: Comments must be received on
or before November 6, 2009.
ADDRESSES: Interested parties are
invited to submit written comments
electronically or in paper form.
Comments should refer to ‘‘Carilion
Clinic, Docket No. 9338’’ to facilitate the
organization of comments. Please note
that your comment — including your
name and your state — will be placed
on the public record of this proceeding,
including on the publicly accessible
FTC website, at (https://www.ftc.gov/os/
publiccomments.shtm).
Because comments will be made
public, they should not include any
sensitive personal information, such as
an individual’s Social Security Number;
date of birth; driver’s license number or
other state identification number, or
foreign country equivalent; passport
number; financial account number; or
credit or debit card number. Comments
also should not include any sensitive
health information, such as medical
records or other individually
identifiable health information. In
addition, comments should not include
any ‘‘[t]rade secret or any commercial or
financial information which is obtained
from any person and which is privileged
or confidential . . . .,’’ as provided in
Section 6(f) of the FTC Act, 15 U.S.C.
46(f), and Commission Rule 4.10(a)(2),
16 CFR 4.10(a)(2). Comments containing
material for which confidential
treatment is requested must be filed in
paper form, must be clearly labeled
‘‘Confidential,’’ and must comply with
FTC Rule 4.9(c), 16 CFR 4.9(c).1
Because paper mail addressed to the
FTC is subject to delay due to
heightened security screening, please
consider submitting your comments in
electronic form. Comments filed in
electronic form should be submitted by
using the following weblink: (https://
public.commentworks.com/ftc/
carilionclinic) and following the
instructions on the web-based form. To
ensure that the Commission considers
an electronic comment, you must file it
on the web-based form at the (https://
public.commentworks.com/ftc/
carilionclinic.). If this Notice appears at
(https://www.regulations.gov/search/
index.jsp), you may also file an
1 The comment must be accompanied by an
explicit request for confidential treatment,
including the factual and legal basis for the request,
and must identify the specific portions of the
comment to be withheld from the public record.
The request will be granted or denied by the
Commission’s General Counsel, consistent with
applicable law and the public interest. See FTC
Rule 4.9(c), 16 CFR 4.9(c).
PO 00000
Frm 00040
Fmt 4703
Sfmt 4703
electronic comment through that
website. The Commission will consider
all comments that regulations.gov
forwards to it. You may also visit the
FTC website at (https://www.ftc.gov/) to
read the Notice and the news release
describing it.
A comment filed in paper form
should include the ‘‘Carilion, Docket
No. 9338’’ reference both in the text and
on the envelope, and should be mailed
or delivered to the following address:
Federal Trade Commission, Office of the
Secretary, Room H-135 (Annex D), 600
Pennsylvania Avenue, NW, Washington,
DC 20580. The FTC is requesting that
any comment filed in paper form be sent
by courier or overnight service, if
possible, because U.S. postal mail in the
Washington area and at the Commission
is subject to delay due to heightened
security precautions.
The Federal Trade Commission Act
(‘‘FTC Act’’) and other laws the
Commission administers permit the
collection of public comments to
consider and use in this proceeding as
appropriate. The Commission will
consider all timely and responsive
public comments that it receives,
whether filed in paper or electronic
form. Comments received will be
available to the public on the FTC
website, to the extent practicable, at
(https://www.ftc.gov/os/
publiccomments.shtm). As a matter of
discretion, the Commission makes every
effort to remove home contact
information for individuals from the
public comments it receives before
placing those comments on the FTC
website. More information, including
routine uses permitted by the Privacy
Act, may be found in the FTC’s privacy
policy, at (https://www.ftc.gov/ftc/
privacy.shtm).
FOR FURTHER INFORMATION CONTACT:
Jeffrey Perry, Bureau of Competition,
600 Pennsylvania Avenue, NW,
Washington, D.C. 20580, (202) 3262331.
SUPPLEMENTARY INFORMATION: Pursuant
to section 6(f) of the Federal Trade
Commission Act, 38 Stat. 721, 15 U.S.C.
46(f), and § 3.25(f) the Commission
Rules of Practice, 16 CFR 3.25(f), notice
is hereby given that the above-captioned
consent agreement containing a consent
order to cease and desist, having been
filed with and accepted, subject to final
approval, by the Commission, has been
placed on the public record for a period
of thirty (30) days. The following
Analysis to Aid Public Comment
describes the terms of the consent
agreement, and the allegations in the
complaint. An electronic copy of the
full text of the consent agreement
E:\FR\FM\16OCN1.SGM
16OCN1
Federal Register / Vol. 74, No. 199 / Friday, October 16, 2009 / Notices
package can be obtained from the FTC
Home Page (for October 7, 2009), on the
World Wide Web, at (https://
www.ftc.gov/os/actions.shtm). A paper
copy can be obtained from the FTC
Public Reference Room, Room 130-H,
600 Pennsylvania Avenue, NW,
Washington, D.C. 20580, either in
person or by calling (202) 326-2222.
Public comments are invited, and may
be filed with the Commission in either
paper or electronic form. All comments
should be filed as prescribed in the
ADDRESSES section above, and must be
received on or before the date specified
in the DATES section.
Analysis of Agreement Containing
Consent Order To Aid Public Comment
I. Introduction
The Federal Trade Commission
(‘‘Commission’’) has accepted for public
comment, subject to final approval, an
Agreement Containing Consent Orders
(‘‘Consent Agreement’’) from Carilion
Clinic (‘‘Carilion’’). The purpose of the
proposed Consent Agreement is to
remedy the competitive harm resulting
from Carilion’s acquisition of two
independent outpatient centers,
Odyssey IV, L.L.C. d/b/a The Center for
Advanced Imaging (‘‘CAI’’), and The
Center for Surgical Excellence, L.L.C.
(‘‘CSE’’). Under the terms of the
proposed Consent Agreement, Carilion
is required to divest both acquired
centers, together with related assets
sufficient to ensure that the buyer(s) of
the divested centers will replace fully
the competition eliminated by the
acquisition.
The proposed Consent Agreement has
been placed on the public record for
thirty (30) days to solicit comments
from interested persons. Comments
received during this period will become
part of the public record. After thirty
(30) days, the Commission again will
review the proposed Consent Agreement
and comments received, and decide
whether it should withdraw the Consent
Agreement or make it final.
The sole purpose of this analysis is to
facilitate public comment on the
Consent Agreement; it is not intended to
constitute an official interpretation of
the Consent Agreement or modify its
terms in any way.
jlentini on DSKJ8SOYB1PROD with NOTICES
Background
Carilion is the largest provider of
healthcare services in the Roanoke,
Virginia area, controlling nearly 80
percent of the hospital beds in the
Roanoke area. On August 28, 2008,
Carilion acquired CAI and CSE, the only
two independent (non-hospital-owned)
providers of advanced outpatient
VerDate Nov<24>2008
16:37 Oct 15, 2009
Jkt 220001
imaging and outpatient surgical services
in the Roanoke area. Advanced
outpatient imaging services are a cluster
of imaging services, including Magnetic
Resonance Imaging (‘‘MRI’’) and
Computerized Tomographic Imaging
(‘‘CT’’) scanning, used to obtain images
of the internal anatomy. Outpatient
surgical services are surgical
procedures, such as interventional spine
surgeries or vascular access surgeries,
that do not require an overnight stay at
a hospital.
Prior to the acquisition, CAI and CSE
were direct competitors to Carilion for
these services in the Roanoke area,
competing on price as well as non-price
terms. Notably, the freestanding centers’
charges were significantly lower than
Carilion’s charges for the same services.
In many cases, CAI’s procedures were
also more convenient and accessible
than those performed at a hospital. In
response to this competition, Carilion
took steps to compete and maintain
market share, including improving the
accessibility of its services and reducing
wait times for scheduling services. This
competition provided real benefits,
financial and otherwise, for patients in
the Roanoke area.
Carilion’s acquisition of CAI and CSE
eliminated this price and non-price
competition, and threatened substantial
competitive harm in the markets for
advanced outpatient imaging and
outpatient surgical services in the
Roanoke area. First, the acquisition
reduced from three to two the number
of competitors for both outpatient
services, and reduced the incentives to
compete for the remaining firms,
Carilion and HCA Lewis-Gale (‘‘HCA’’),
a similarly-situated hospital provider.
Second, the acquisition eliminated
health plans’ and patients’ only
independent alternative to Carilion and
HCA, and thus substantially reduced
competition and enhanced Carilion’s
power to impose a unilateral price
increase. Staff’s investigation confirmed
that repositioning by existing healthcare
providers or new entry would be
insufficient to deter or counteract this
harm to competition.
Having reason to believe the proposed
transaction would result in competitive
harm, the Commission authorized staff
to commence an administrative trial
under Part 3 of the Commission’s Rules
of Practice. The administrative
complaint alleged that the combined
entity would increase prices and
decrease non-price competition in the
markets for advanced outpatient
imaging and outpatient surgical services
in the Roanoke area.
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53253
Litigation History
On July 23, 2009, the Commission
issued an administrative complaint
pursuant to Part 3 of the Commission’s
Rules of Practice challenging Carilion’s
acquisition of CAI and CSE. On August
7, 2009, the parties filed an amended
joint motion to withdraw the matter
from administrative litigation, together
with a proposed settlement agreement
that the parties asserted would
‘‘completely restore the competition that
was alleged to have been eliminated by
the acquisition.’’The Commission
granted the amended joint motion on
August 11, 2009, and temporarily
withdrew the matter from adjudication
for 30 days. The withdrawal was
subsequently extended until October 14,
2009, as Carilion and Commission staff
continued to negotiate a remedy in
settlement of the ongoing litigation.
The Proposed Consent Agreement
The proposed Consent Agreement
remedies the anticompetitive effects of
the acquisition by requiring the
divestiture of all of the acquired assets
to a Commission-approved buyer (or
buyers) within three months. The assets
to be divested include not only the two
acquired centers, but also the associated
assets – such as patient and physician
records, government permits, medical
equipment, and payor and supplier
contracts – necessary for a Commissionapproved buyer to independently and
effectively operate each center. The
Commission may appoint a divestiture
trustee if Carilion has not completed the
required divestitures within three
months.
In addition to requiring the
divestiture of both centers and all
related assets, the Consent Agreement
includes several provisions designed to
accelerate the Commission-approved
buyer(s)’ ability to replicate the
competition that was eliminated by the
acquisition. For example, the Consent
Agreement prohibits Carilion from
soliciting for employment any physician
or physician practice that has referred
patients to CAI since the acquisition.
The prohibition is effective for six
months as of the date Carilion signs the
Agreement Containing Consent Orders,
and will allow the Commissionapproved buyer sufficient time to
develop CAI’s referral base by
preventing Carilion from seeking out
and acquiring referring physicians and
physician practices. The Consent
Agreement also prohibits Carilion from
restricting its employed physicians who
have referred patients to CAI since the
acquisition from continuing to refer
patients to CAI. The prohibition is in
E:\FR\FM\16OCN1.SGM
16OCN1
53254
Federal Register / Vol. 74, No. 199 / Friday, October 16, 2009 / Notices
effect for one year, and is designed to
ensure that any Carilion-employed
physician who previously referred
patients to CAI will continue to be able
to do so.
Finally, incorporated into the Consent
Agreement is an Order to Maintain
Assets (‘‘OMA’’). The OMA preserves
the viability, marketability, and
competitiveness of the assets to be
divested, and prohibits Carilion from
using or disclosing competitively
sensitive information. The OMA also
allows the Commission to appoint a
Monitor to ensure Carilion’s compliance
with the Consent Agreement. In
addition, the OMA requires Carilion to
offer financial incentives to CAI and
CSE personnel to remain with each
business before the sale, during the
transition period, and at the option of
the buyer(s), after the transition. Under
the Consent Agreement, Carilion also
must remove any contractual
impediments that may deter CAI or CSE
staff from accepting a Commissionapproved buyer’s offer of employment.
The proposed Consent Agreement
will resolve fully the competitive issues
raised by the acquisition by
reestablishing price, quality, and service
competition in the markets for advanced
outpatient imaging and outpatient
surgical services in the Roanoke area.
Moreover, acceptance of the proposed
Consent Agreement will bring
immediate and certain relief to
Roanoke-area consumers by avoiding
the expense and uncertainty inherent in
continuing litigation.
By direction of the Commission.
Donald S. Clark,
Secretary.
[FR Doc. E9–24949 Filed 10–15–09; 9:29 am]
BILLING CODE 6750–01–S
FEDERAL TRADE COMMISSION
[File No. 092 3142]
Collectify, Inc.; Analysis of Proposed
Consent Orders To Aid Public
Comment
Federal Trade Commission.
Proposed consent agreement.
AGENCY:
jlentini on DSKJ8SOYB1PROD with NOTICES
ACTION:
SUMMARY: The consent agreement in this
matter settles alleged violations of
federal law prohibiting unfair or
deceptive acts or practices or unfair
methods of competition. The attached
Analysis to Aid Public Comment
describes both the allegations in the
draft complaint and the terms of the
consent order — embodied in the
consent agreement — that would settle
these allegations.
VerDate Nov<24>2008
16:37 Oct 15, 2009
Jkt 220001
DATES: Comments must be received on
or before November 5, 2009.
ADDRESSES: Interested parties are
invited to submit written comments
electronically or in paper form.
Comments should refer to ‘‘Collectify,
File No. 092 3142’’ to facilitate the
organization of comments. Please note
that your comment — including your
name and your state — will be placed
on the public record of this proceeding,
including on the publicly accessible
FTC website, at (https://www.ftc.gov/os/
publiccomments.shtm).
Because comments will be made
public, they should not include any
sensitive personal information, such as
an individual’s Social Security Number;
date of birth; driver’s license number or
other state identification number, or
foreign country equivalent; passport
number; financial account number; or
credit or debit card number. Comments
also should not include any sensitive
health information, such as medical
records or other individually
identifiable health information. In
addition, comments should not include
any ‘‘[t]rade secret or any commercial or
financial information which is obtained
from any person and which is privileged
or confidential . . . .,’’ as provided in
Section 6(f) of the FTC Act, 15 U.S.C.
46(f), and Commission Rule 4.10(a)(2),
16 CFR 4.10(a)(2). Comments containing
material for which confidential
treatment is requested must be filed in
paper form, must be clearly labeled
‘‘Confidential,’’ and must comply with
FTC Rule 4.9(c), 16 CFR 4.9(c).1
Because paper mail addressed to the
FTC is subject to delay due to
heightened security screening, please
consider submitting your comments in
electronic form. Comments filed in
electronic form should be submitted by
using the following weblink: (https://
public.commentworks.com/ftc/
collectify) and following the instructions
on the web-based form. To ensure that
the Commission considers an electronic
comment, you must file it on the webbased form at the weblink: (https://
public.commentworks.com/ftc/
collectify). If this Notice appears at
(https://www.regulations.gov/search/
index.jsp), you may also file an
electronic comment through that
website. The Commission will consider
all comments that regulations.gov
1 The comment must be accompanied by an
explicit request for confidential treatment,
including the factual and legal basis for the request,
and must identify the specific portions of the
comment to be withheld from the public record.
The request will be granted or denied by the
Commission’s General Counsel, consistent with
applicable law and the public interest. See FTC
Rule 4.9(c), 16 CFR 4.9(c).
PO 00000
Frm 00042
Fmt 4703
Sfmt 4703
forwards to it. You may also visit the
FTC website at (https://www.ftc.gov/) to
read the Notice and the news release
describing it.
A comment filed in paper form
should include the ‘‘Collectify, File No.
092 3142’’ reference both in the text and
on the envelope, and should be mailed
or delivered to the following address:
Federal Trade Commission, Office of the
Secretary, Room H-135 (Annex D), 600
Pennsylvania Avenue, NW, Washington,
DC 20580. The FTC is requesting that
any comment filed in paper form be sent
by courier or overnight service, if
possible, because U.S. postal mail in the
Washington area and at the Commission
is subject to delay due to heightened
security precautions.
The Federal Trade Commission Act
(‘‘FTC Act’’) and other laws the
Commission administers permit the
collection of public comments to
consider and use in this proceeding as
appropriate. The Commission will
consider all timely and responsive
public comments that it receives,
whether filed in paper or electronic
form. Comments received will be
available to the public on the FTC
website, to the extent practicable, at
(https://www.ftc.gov/os/
publiccomments.shtm). As a matter of
discretion, the Commission makes every
effort to remove home contact
information for individuals from the
public comments it receives before
placing those comments on the FTC
website. More information, including
routine uses permitted by the Privacy
Act, may be found in the FTC’s privacy
policy, at (https://www.ftc.gov/ftc/
privacy.shtm).
FOR FURTHER INFORMATION CONTACT:
Molly Crawford (202-326-3076) or Katie
´
Ratte (202-326-3514), Bureau of
Consumer Protection, 600 Pennsylvania
Avenue, NW, Washington, D.C. 20580.
SUPPLEMENTARY INFORMATION: Pursuant
to section 6(f) of the Federal Trade
Commission Act, 38 Stat. 721, 15 U.S.C.
46(f), and § 2.34 the Commission Rules
of Practice, 16 CFR 2.34, notice is
hereby given that the above-captioned
consent agreement containing a consent
order to cease and desist, having been
filed with and accepted, subject to final
approval, by the Commission, has been
placed on the public record for a period
of thirty (30) days. The following
Analysis to Aid Public Comment
describes the terms of the consent
agreement, and the allegations in the
complaint. An electronic copy of the
full text of the consent agreement
package can be obtained from the FTC
Home Page (for October 6, 2009), on the
World Wide Web, at (https://
E:\FR\FM\16OCN1.SGM
16OCN1
Agencies
[Federal Register Volume 74, Number 199 (Friday, October 16, 2009)]
[Notices]
[Pages 53252-53254]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-24949]
-----------------------------------------------------------------------
FEDERAL TRADE COMMISSION
[Docket No. 9338]
Carilion Clinic; Analysis of Agreement Containing Consent Orders
To Aid Public Comment
AGENCY: Federal Trade Commission.
ACTION: Proposed consent agreement.
-----------------------------------------------------------------------
SUMMARY: The consent agreement in this matter settles alleged
violations of federal law prohibiting unfair or deceptive acts or
practices or unfair methods of competition. The attached Analysis to
Aid Public Comment describes both the allegations in the complaint and
the terms of the consent order -- embodied in the consent agreement --
that would settle these allegations.
DATES: Comments must be received on or before November 6, 2009.
ADDRESSES: Interested parties are invited to submit written comments
electronically or in paper form. Comments should refer to ``Carilion
Clinic, Docket No. 9338'' to facilitate the organization of comments.
Please note that your comment -- including your name and your state --
will be placed on the public record of this proceeding, including on
the publicly accessible FTC website, at (https://www.ftc.gov/os/publiccomments.shtm).
Because comments will be made public, they should not include any
sensitive personal information, such as an individual's Social Security
Number; date of birth; driver's license number or other state
identification number, or foreign country equivalent; passport number;
financial account number; or credit or debit card number. Comments also
should not include any sensitive health information, such as medical
records or other individually identifiable health information. In
addition, comments should not include any ``[t]rade secret or any
commercial or financial information which is obtained from any person
and which is privileged or confidential . . . .,'' as provided in
Section 6(f) of the FTC Act, 15 U.S.C. 46(f), and Commission Rule
4.10(a)(2), 16 CFR 4.10(a)(2). Comments containing material for which
confidential treatment is requested must be filed in paper form, must
be clearly labeled ``Confidential,'' and must comply with FTC Rule
4.9(c), 16 CFR 4.9(c).\1\
---------------------------------------------------------------------------
\1\ The comment must be accompanied by an explicit request for
confidential treatment, including the factual and legal basis for
the request, and must identify the specific portions of the comment
to be withheld from the public record. The request will be granted
or denied by the Commission's General Counsel, consistent with
applicable law and the public interest. See FTC Rule 4.9(c), 16 CFR
4.9(c).
---------------------------------------------------------------------------
Because paper mail addressed to the FTC is subject to delay due to
heightened security screening, please consider submitting your comments
in electronic form. Comments filed in electronic form should be
submitted by using the following weblink: (https://public.commentworks.com/ftc/carilionclinic) and following the
instructions on the web-based form. To ensure that the Commission
considers an electronic comment, you must file it on the web-based form
at the (https://public.commentworks.com/ftc/carilionclinic.). If this
Notice appears at (https://www.regulations.gov/search/index.jsp), you
may also file an electronic comment through that website. The
Commission will consider all comments that regulations.gov forwards to
it. You may also visit the FTC website at (https://www.ftc.gov/) to read
the Notice and the news release describing it.
A comment filed in paper form should include the ``Carilion, Docket
No. 9338'' reference both in the text and on the envelope, and should
be mailed or delivered to the following address: Federal Trade
Commission, Office of the Secretary, Room H-135 (Annex D), 600
Pennsylvania Avenue, NW, Washington, DC 20580. The FTC is requesting
that any comment filed in paper form be sent by courier or overnight
service, if possible, because U.S. postal mail in the Washington area
and at the Commission is subject to delay due to heightened security
precautions.
The Federal Trade Commission Act (``FTC Act'') and other laws the
Commission administers permit the collection of public comments to
consider and use in this proceeding as appropriate. The Commission will
consider all timely and responsive public comments that it receives,
whether filed in paper or electronic form. Comments received will be
available to the public on the FTC website, to the extent practicable,
at (https://www.ftc.gov/os/publiccomments.shtm). As a matter of
discretion, the Commission makes every effort to remove home contact
information for individuals from the public comments it receives before
placing those comments on the FTC website. More information, including
routine uses permitted by the Privacy Act, may be found in the FTC's
privacy policy, at (https://www.ftc.gov/ftc/privacy.shtm).
FOR FURTHER INFORMATION CONTACT: Jeffrey Perry, Bureau of Competition,
600 Pennsylvania Avenue, NW, Washington, D.C. 20580, (202) 326-2331.
SUPPLEMENTARY INFORMATION: Pursuant to section 6(f) of the Federal
Trade Commission Act, 38 Stat. 721, 15 U.S.C. 46(f), and Sec. 3.25(f)
the Commission Rules of Practice, 16 CFR 3.25(f), notice is hereby
given that the above-captioned consent agreement containing a consent
order to cease and desist, having been filed with and accepted, subject
to final approval, by the Commission, has been placed on the public
record for a period of thirty (30) days. The following Analysis to Aid
Public Comment describes the terms of the consent agreement, and the
allegations in the complaint. An electronic copy of the full text of
the consent agreement
[[Page 53253]]
package can be obtained from the FTC Home Page (for October 7, 2009),
on the World Wide Web, at (https://www.ftc.gov/os/actions.shtm). A paper
copy can be obtained from the FTC Public Reference Room, Room 130-H,
600 Pennsylvania Avenue, NW, Washington, D.C. 20580, either in person
or by calling (202) 326-2222.
Public comments are invited, and may be filed with the Commission
in either paper or electronic form. All comments should be filed as
prescribed in the ADDRESSES section above, and must be received on or
before the date specified in the DATES section.
Analysis of Agreement Containing Consent Order To Aid Public Comment
I. Introduction
The Federal Trade Commission (``Commission'') has accepted for
public comment, subject to final approval, an Agreement Containing
Consent Orders (``Consent Agreement'') from Carilion Clinic
(``Carilion''). The purpose of the proposed Consent Agreement is to
remedy the competitive harm resulting from Carilion's acquisition of
two independent outpatient centers, Odyssey IV, L.L.C. d/b/a The Center
for Advanced Imaging (``CAI''), and The Center for Surgical Excellence,
L.L.C. (``CSE''). Under the terms of the proposed Consent Agreement,
Carilion is required to divest both acquired centers, together with
related assets sufficient to ensure that the buyer(s) of the divested
centers will replace fully the competition eliminated by the
acquisition.
The proposed Consent Agreement has been placed on the public record
for thirty (30) days to solicit comments from interested persons.
Comments received during this period will become part of the public
record. After thirty (30) days, the Commission again will review the
proposed Consent Agreement and comments received, and decide whether it
should withdraw the Consent Agreement or make it final.
The sole purpose of this analysis is to facilitate public comment
on the Consent Agreement; it is not intended to constitute an official
interpretation of the Consent Agreement or modify its terms in any way.
Background
Carilion is the largest provider of healthcare services in the
Roanoke, Virginia area, controlling nearly 80 percent of the hospital
beds in the Roanoke area. On August 28, 2008, Carilion acquired CAI and
CSE, the only two independent (non-hospital-owned) providers of
advanced outpatient imaging and outpatient surgical services in the
Roanoke area. Advanced outpatient imaging services are a cluster of
imaging services, including Magnetic Resonance Imaging (``MRI'') and
Computerized Tomographic Imaging (``CT'') scanning, used to obtain
images of the internal anatomy. Outpatient surgical services are
surgical procedures, such as interventional spine surgeries or vascular
access surgeries, that do not require an overnight stay at a hospital.
Prior to the acquisition, CAI and CSE were direct competitors to
Carilion for these services in the Roanoke area, competing on price as
well as non-price terms. Notably, the freestanding centers' charges
were significantly lower than Carilion's charges for the same services.
In many cases, CAI's procedures were also more convenient and
accessible than those performed at a hospital. In response to this
competition, Carilion took steps to compete and maintain market share,
including improving the accessibility of its services and reducing wait
times for scheduling services. This competition provided real benefits,
financial and otherwise, for patients in the Roanoke area.
Carilion's acquisition of CAI and CSE eliminated this price and
non-price competition, and threatened substantial competitive harm in
the markets for advanced outpatient imaging and outpatient surgical
services in the Roanoke area. First, the acquisition reduced from three
to two the number of competitors for both outpatient services, and
reduced the incentives to compete for the remaining firms, Carilion and
HCA Lewis-Gale (``HCA''), a similarly-situated hospital provider.
Second, the acquisition eliminated health plans' and patients' only
independent alternative to Carilion and HCA, and thus substantially
reduced competition and enhanced Carilion's power to impose a
unilateral price increase. Staff's investigation confirmed that
repositioning by existing healthcare providers or new entry would be
insufficient to deter or counteract this harm to competition.
Having reason to believe the proposed transaction would result in
competitive harm, the Commission authorized staff to commence an
administrative trial under Part 3 of the Commission's Rules of
Practice. The administrative complaint alleged that the combined entity
would increase prices and decrease non-price competition in the markets
for advanced outpatient imaging and outpatient surgical services in the
Roanoke area.
Litigation History
On July 23, 2009, the Commission issued an administrative complaint
pursuant to Part 3 of the Commission's Rules of Practice challenging
Carilion's acquisition of CAI and CSE. On August 7, 2009, the parties
filed an amended joint motion to withdraw the matter from
administrative litigation, together with a proposed settlement
agreement that the parties asserted would ``completely restore the
competition that was alleged to have been eliminated by the
acquisition.''The Commission granted the amended joint motion on August
11, 2009, and temporarily withdrew the matter from adjudication for 30
days. The withdrawal was subsequently extended until October 14, 2009,
as Carilion and Commission staff continued to negotiate a remedy in
settlement of the ongoing litigation.
The Proposed Consent Agreement
The proposed Consent Agreement remedies the anticompetitive effects
of the acquisition by requiring the divestiture of all of the acquired
assets to a Commission-approved buyer (or buyers) within three months.
The assets to be divested include not only the two acquired centers,
but also the associated assets - such as patient and physician records,
government permits, medical equipment, and payor and supplier contracts
- necessary for a Commission-approved buyer to independently and
effectively operate each center. The Commission may appoint a
divestiture trustee if Carilion has not completed the required
divestitures within three months.
In addition to requiring the divestiture of both centers and all
related assets, the Consent Agreement includes several provisions
designed to accelerate the Commission-approved buyer(s)' ability to
replicate the competition that was eliminated by the acquisition. For
example, the Consent Agreement prohibits Carilion from soliciting for
employment any physician or physician practice that has referred
patients to CAI since the acquisition. The prohibition is effective for
six months as of the date Carilion signs the Agreement Containing
Consent Orders, and will allow the Commission-approved buyer sufficient
time to develop CAI's referral base by preventing Carilion from seeking
out and acquiring referring physicians and physician practices. The
Consent Agreement also prohibits Carilion from restricting its employed
physicians who have referred patients to CAI since the acquisition from
continuing to refer patients to CAI. The prohibition is in
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effect for one year, and is designed to ensure that any Carilion-
employed physician who previously referred patients to CAI will
continue to be able to do so.
Finally, incorporated into the Consent Agreement is an Order to
Maintain Assets (``OMA''). The OMA preserves the viability,
marketability, and competitiveness of the assets to be divested, and
prohibits Carilion from using or disclosing competitively sensitive
information. The OMA also allows the Commission to appoint a Monitor to
ensure Carilion's compliance with the Consent Agreement. In addition,
the OMA requires Carilion to offer financial incentives to CAI and CSE
personnel to remain with each business before the sale, during the
transition period, and at the option of the buyer(s), after the
transition. Under the Consent Agreement, Carilion also must remove any
contractual impediments that may deter CAI or CSE staff from accepting
a Commission-approved buyer's offer of employment.
The proposed Consent Agreement will resolve fully the competitive
issues raised by the acquisition by reestablishing price, quality, and
service competition in the markets for advanced outpatient imaging and
outpatient surgical services in the Roanoke area. Moreover, acceptance
of the proposed Consent Agreement will bring immediate and certain
relief to Roanoke-area consumers by avoiding the expense and
uncertainty inherent in continuing litigation.
By direction of the Commission.
Donald S. Clark,
Secretary.
[FR Doc. E9-24949 Filed 10-15-09; 9:29 am]
BILLING CODE 6750-01-S