Findings of Research Misconduct, 15127 [2014-05921]

Download as PDF 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 emcdonald on DSK67QTVN1PROD with NOTICES SUMMARY: VerDate Mar<15>2010 18:34 Mar 17, 2014 Jkt 232001 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, PO 00000 Frm 00033 Fmt 4703 Sfmt 4703 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 burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology. Written comments should be received within 60 days of this notice. Proposed Project Requirements for the Importation of Nonhuman Primates into the United States—Revision—(OMB No. 0920– 0263, expiration date: 4/30/2016)— National Center for Emerging and Zoonotic Infectious Diseases (NCEZID), Division of Global Migration and Quarantine (DGMQ), Centers for Disease Control and Prevention (CDC). E:\FR\FM\18MRN1.SGM 18MRN1

Agencies

[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
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