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Volumn 33, Issue 10, 2007, Pages 1819-1822

Evaluating benefits and harms in intensive care research

Author keywords

[No Author keywords available]

Indexed keywords

ANALYTIC METHOD; CLINICAL OBSERVATION; CLINICAL PRACTICE; CLINICAL PROTOCOL; CLINICAL RESEARCH; HEALTH HAZARD; HEALTH PRACTITIONER; INFORMED CONSENT; INTENSIVE CARE; MEDICAL CARE; MEDICAL DECISION MAKING; MEDICAL ETHICS; MEDICAL RECORD REVIEW; PATIENT CARE; PATIENT PARTICIPATION; RESEARCH ETHICS; RESEARCH SUBJECT; REVIEW; RISK ASSESSMENT; RISK BENEFIT ANALYSIS; RISK REDUCTION; SCIENCE; WELLBEING;

EID: 34748863659     PISSN: 03424642     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00134-007-0818-5     Document Type: Review
Times cited : (3)

References (13)
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  • 2
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  • 3
    • 23044476283 scopus 로고    scopus 로고
    • Will ethical requirements bring critical care research to a halt?
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    • Truog, R.D.1
  • 4
    • 17044390881 scopus 로고    scopus 로고
    • Is clinical research and ethics a zero sum game?
    • Weijer C (2005) Is clinical research and ethics a zero sum game? Critical Care Med 33:912-913
    • (2005) Critical Care Med , vol.33 , pp. 912-913
    • Weijer, C.1
  • 5
    • 0004167304 scopus 로고    scopus 로고
    • U.S. National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research Website: Date accessed: June 3, 2007
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    • The Belmont Report
  • 6
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    • Website: Date accessed: June 3, 2007
    • World Medical Association. Declaration of Helsinki. Website: http://www.wma.net/e/policy/b3.htm. Date accessed: June 3, 2007
    • Declaration of Helsinki
  • 7
    • 0141797654 scopus 로고    scopus 로고
    • A critique of clinical equipoise: Therapeutic misconception in the ethics of clinical trials
    • Miller FG, Brody H (2003) A critique of clinical equipoise: therapeutic misconception in the ethics of clinical trials. Hastings Center Report 33:19-28
    • (2003) Hastings Center Report , vol.33 , pp. 19-28
    • Miller, F.G.1    Brody, H.2
  • 9
    • 2942711455 scopus 로고    scopus 로고
    • When are research risks reasonable in relation to anticipated benefits?
    • Weijer C, Miller PB (2004) When are research risks reasonable in relation to anticipated benefits? Nat Med 10:570-573
    • (2004) Nat Med , vol.10 , pp. 570-573
    • Weijer, C.1    Miller, P.B.2
  • 10
    • 0034737962 scopus 로고    scopus 로고
    • What makes clinical research ethical?
    • Emanuel EJ, Wendler D, Grady C (2000) What makes clinical research ethical? JAMA 283:2701-2711
    • (2000) JAMA , vol.283 , pp. 2701-2711
    • Emanuel, E.J.1    Wendler, D.2    Grady, C.3
  • 11
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    • U.S. National Bioethics Advisory Commission (NBAC) NBAC, Bethesda, MD, Website: Date accessed: June 4, 2007
    • U.S. National Bioethics Advisory Commission (NBAC) (2000) Ethical and policy issues in research involving human participants. NBAC, Bethesda, MD, pp 69-96. Website: http://bioethics.georgetown.edu/nbac/human/overvol1.html. Date accessed: June 4, 2007
    • (2000) Ethical and Policy Issues in Research Involving Human Participants , pp. 69-96
  • 13
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    • Risk in emergency research using a waiver of/exception from consent: Implications of a structured approach for IRB review
    • McRae AD, Ackroyd-Stolarz S, Weijer C (2005) Risk in emergency research using a waiver of/exception from consent: implications of a structured approach for IRB review. Acad Emerg Med 12:1104-1112
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.