Findings of Research Misconduct, 15127 [2014-05921]
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Federal Register / Vol. 79, No. 52 / Tuesday, March 18, 2014 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
Findings of Research Misconduct
Office of the Secretary, HHS.
Notice.
AGENCY:
ACTION:
Notice is hereby given that
the Office of Research Integrity (ORI)
has taken final action in the following
case:
Parag Patel, D.O., Advocate Health
Care Network d/b/a Advocate Health
Care: Based on an investigation
conducted by Advocate Health Care
Network d/b/a Advocate Health Care
(Advocate Health Care) and additional
analysis conducted by ORI in its
oversight review, ORI and Advocate
Health Care found that Dr. Parag Patel,
Cardiologist, Department of Medicine,
Advocate Health and Hospitals
Corporation d/b/a Advocate Lutheran
General Hospital, Park Ridge, Illinois,
engaged in research misconduct in
research supported by National Heart,
Lung, and Blood Institute (NHLBI),
National Institutes of Health (NIH),
grant U01 HL089458.
ORI and Advocate Health Care found
that the Respondent engaged in research
misconduct by directing or intimidating
fellows and others to influence left
ventricular ejection fraction (LVEF)
scores of ≤ 35% and requesting
attending physicians to reassess scores
of LVEF to be reported as ≤ 35% for
research subjects after being diagnosed
with acute myocardial infarction,
thereby causing and being responsible
for falsification of research records.
These falsifications made subjects
eligible for enrollment into the ‘‘Vest
Prevention of Early Sudden Death Trial’’
(VEST) when they otherwise may not
have been eligible.
The Respondent, Advocate Health
Care, and the U.S. Department of Health
and Human Services (HHS) want to
conclude this matter without further
expenditure of time or other resources
and have entered into a Voluntary
Settlement Agreement (Agreement) to
resolve this matter. Respondent neither
admits nor denies ORI’s and Advocate
Health Care’s findings of research
misconduct. This settlement does not
constitute an admission of liability on
the part of the Respondent.
Dr. Patel has voluntarily agreed for a
period of two (2) years, beginning on
February 21, 2014:
(1) To have any U.S. Public Health
Service (PHS)-supported research in
which he is involved be supervised;
Respondent agreed that prior to the
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SUMMARY:
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18:34 Mar 17, 2014
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submission of an application for PHS
support for a research project on which
the Respondent’s participation is
proposed and prior to Respondent’s
participation in any capacity on PHSsupported research, Respondent shall
ensure that a plan for supervision of
Respondent’s duties is submitted to ORI
for approval; the supervision plan must
be designed to ensure the scientific
integrity of Respondent’s research
contribution as outlined below;
Respondent agreed that he shall not
participate in any PHS-supported
research until such a supervision plan is
submitted to and approved by ORI;
Respondent agreed to maintain
responsibility for compliance with the
agreed-upon supervision plan;
(2) That the requirements for
Respondent’s supervision plan are as
follows:
• A committee of two to three
qualified physicians at the institution’s
discretion, who are familiar with
Respondent’s field of research, but not
including Respondent’s supervisor or
collaborators, will provide oversight and
guidance; the committee will review
primary data from Respondent’s
participation in PHS-supported research
on a quarterly basis and submit a report
to ORI at six (6) month intervals setting
forth the committee’s meeting dates,
Respondent’s compliance with
appropriate research standards, and
confirming the integrity of Respondent’s
research contribution; and
• The committee will conduct an
advance review of any PHS grant
applications (including supplements,
resubmissions, etc.), manuscripts
reporting PHS-funded research
submitted for publication, and abstracts;
the review will include a discussion
with Respondent of the primary data
represented in those documents and
will include a certification to ORI that
the data presented in the proposed
application/publication are supported
by the research record;
(3) That any institution employing
him shall submit, in conjunction with
each application for PHS funds, or
report, manuscript, or abstract involving
PHS-supported research in which
Respondent is involved, a certification
to ORI that the data provided by
Respondent are based on actual
experiments or are otherwise
legitimately derived and that the data,
procedures, and methodology are
accurately reported in the application,
report, manuscript, or abstract; and
(4) To exclude himself voluntarily
from serving in any advisory capacity to
PHS including, but not limited to,
service on any PHS advisory committee,
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15127
board, and/or peer review committee, or
as a consultant.
FOR FURTHER INFORMATION CONTACT:
Acting Director, Office of Research
Integrity, 1101 Wootton Parkway,
Suite 750, Rockville, MD 20852, (240)
453–8800.
Donald Wright,
Acting Director, Office of Research Integrity.
[FR Doc. 2014–05921 Filed 3–17–14; 8:45 am]
BILLING CODE 4150–31–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–14–0263]
Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
proposed projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–7570 or send
comments to Leroy Richardson, 1600
Clifton Road, MS–D74, Atlanta, GA
30333 or send an email to omb@cdc.gov.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (d) ways to minimize the
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on respondents, including through the
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or other forms of information
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be received within 60 days of this
notice.
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Nonhuman Primates into the United
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0263, expiration date: 4/30/2016)—
National Center for Emerging and
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Division of Global Migration and
Quarantine (DGMQ), Centers for Disease
Control and Prevention (CDC).
E:\FR\FM\18MRN1.SGM
18MRN1
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[Federal Register Volume 79, Number 52 (Tuesday, March 18, 2014)]
[Notices]
[Page 15127]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-05921]
[[Page 15127]]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
Findings of Research Misconduct
AGENCY: Office of the Secretary, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: Notice is hereby given that the Office of Research Integrity
(ORI) has taken final action in the following case:
Parag Patel, D.O., Advocate Health Care Network d/b/a Advocate
Health Care: Based on an investigation conducted by Advocate Health
Care Network d/b/a Advocate Health Care (Advocate Health Care) and
additional analysis conducted by ORI in its oversight review, ORI and
Advocate Health Care found that Dr. Parag Patel, Cardiologist,
Department of Medicine, Advocate Health and Hospitals Corporation d/b/a
Advocate Lutheran General Hospital, Park Ridge, Illinois, engaged in
research misconduct in research supported by National Heart, Lung, and
Blood Institute (NHLBI), National Institutes of Health (NIH), grant U01
HL089458.
ORI and Advocate Health Care found that the Respondent engaged in
research misconduct by directing or intimidating fellows and others to
influence left ventricular ejection fraction (LVEF) scores of <= 35%
and requesting attending physicians to reassess scores of LVEF to be
reported as <= 35% for research subjects after being diagnosed with
acute myocardial infarction, thereby causing and being responsible for
falsification of research records. These falsifications made subjects
eligible for enrollment into the ``Vest Prevention of Early Sudden
Death Trial'' (VEST) when they otherwise may not have been eligible.
The Respondent, Advocate Health Care, and the U.S. Department of
Health and Human Services (HHS) want to conclude this matter without
further expenditure of time or other resources and have entered into a
Voluntary Settlement Agreement (Agreement) to resolve this matter.
Respondent neither admits nor denies ORI's and Advocate Health Care's
findings of research misconduct. This settlement does not constitute an
admission of liability on the part of the Respondent.
Dr. Patel has voluntarily agreed for a period of two (2) years,
beginning on February 21, 2014:
(1) To have any U.S. Public Health Service (PHS)-supported research
in which he is involved be supervised; Respondent agreed that prior to
the submission of an application for PHS support for a research project
on which the Respondent's participation is proposed and prior to
Respondent's participation in any capacity on PHS-supported research,
Respondent shall ensure that a plan for supervision of Respondent's
duties is submitted to ORI for approval; the supervision plan must be
designed to ensure the scientific integrity of Respondent's research
contribution as outlined below; Respondent agreed that he shall not
participate in any PHS-supported research until such a supervision plan
is submitted to and approved by ORI; Respondent agreed to maintain
responsibility for compliance with the agreed-upon supervision plan;
(2) That the requirements for Respondent's supervision plan are as
follows:
A committee of two to three qualified physicians at the
institution's discretion, who are familiar with Respondent's field of
research, but not including Respondent's supervisor or collaborators,
will provide oversight and guidance; the committee will review primary
data from Respondent's participation in PHS-supported research on a
quarterly basis and submit a report to ORI at six (6) month intervals
setting forth the committee's meeting dates, Respondent's compliance
with appropriate research standards, and confirming the integrity of
Respondent's research contribution; and
The committee will conduct an advance review of any PHS
grant applications (including supplements, resubmissions, etc.),
manuscripts reporting PHS-funded research submitted for publication,
and abstracts; the review will include a discussion with Respondent of
the primary data represented in those documents and will include a
certification to ORI that the data presented in the proposed
application/publication are supported by the research record;
(3) That any institution employing him shall submit, in conjunction
with each application for PHS funds, or report, manuscript, or abstract
involving PHS-supported research in which Respondent is involved, a
certification to ORI that the data provided by Respondent are based on
actual experiments or are otherwise legitimately derived and that the
data, procedures, and methodology are accurately reported in the
application, report, manuscript, or abstract; and
(4) To exclude himself voluntarily from serving in any advisory
capacity to PHS including, but not limited to, service on any PHS
advisory committee, board, and/or peer review committee, or as a
consultant.
FOR FURTHER INFORMATION CONTACT:
Acting Director, Office of Research Integrity, 1101 Wootton Parkway,
Suite 750, Rockville, MD 20852, (240) 453-8800.
Donald Wright,
Acting Director, Office of Research Integrity.
[FR Doc. 2014-05921 Filed 3-17-14; 8:45 am]
BILLING CODE 4150-31-P