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Volumn 178, Issue 7, 2008, Pages 871-873

The effect of privacy legislation on observational research

Author keywords

[No Author keywords available]

Indexed keywords

CANADA; DATA BASE; DISEASE REGISTRY; HUMAN; MEDICAL ETHICS; MEDICAL INFORMATION; MEDICAL RECORD; MEDICAL RESEARCH; MEDICOLEGAL ASPECT; NOTE; PRIVACY; PROFESSIONAL SECRECY;

EID: 41649087324     PISSN: 08203946     EISSN: 14882329     Source Type: Journal    
DOI: 10.1503/cmaj.061353     Document Type: Note
Times cited : (20)

References (15)
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    • Impracticability of informed consent in the Registry of the Canadian Stroke Network
    • Tu JV, Willison DJ, Silver FL, et al. Impracticability of informed consent in the Registry of the Canadian Stroke Network. N Engl J Med 2004;350:1414-21.
    • (2004) N Engl J Med , vol.350 , pp. 1414-1421
    • Tu, J.V.1    Willison, D.J.2    Silver, F.L.3
  • 3
    • 41649117874 scopus 로고    scopus 로고
    • Office of the Privacy Comissioner of Canada. Commissioner's findings: CIBC's privacy practices failed in cases of misdirected faxes. Ottawa: The Office; 2005. Available: www.privcom.gc.ca/incidents/2005/050418_01_e.asp (accesed 2008 Jan 22).
    • Office of the Privacy Comissioner of Canada. Commissioner's findings: CIBC's privacy practices failed in cases of misdirected faxes. Ottawa: The Office; 2005. Available: www.privcom.gc.ca/incidents/2005/050418_01_e.asp (accesed 2008 Jan 22).
  • 4
    • 41649109665 scopus 로고    scopus 로고
    • Background legal research and analysis in support of CIHR's recommendations with respect to the Personal Information Protection and Electronic Documents Act (PIPEDA)
    • Canadian Institutes of Health Research, Ottawa;
    • Canadian Institutes of Health Research. Background legal research and analysis in support of CIHR's recommendations with respect to the Personal Information Protection and Electronic Documents Act (PIPEDA). The Insititutes: Ottawa; 2001. p. 38-9.
    • (2001) The Insititutes , pp. 38-39
  • 5
    • 0037129628 scopus 로고    scopus 로고
    • Commentary: Don't waive consent lightly - involve the public
    • Manning D. Commentary: Don't waive consent lightly - involve the public. BMJ 2002;324:1213.
    • (2002) BMJ , vol.324 , pp. 1213
    • Manning, D.1
  • 6
    • 17244382963 scopus 로고    scopus 로고
    • A feasibility study of signed consent for the collection of patient identifiable information for a national paediatric clinical audit database
    • McKinney PA, Jones S, Parslow R, et al. A feasibility study of signed consent for the collection of patient identifiable information for a national paediatric clinical audit database. BMJ 2005;330:877-9.
    • (2005) BMJ , vol.330 , pp. 877-879
    • McKinney, P.A.1    Jones, S.2    Parslow, R.3
  • 7
    • 85044704248 scopus 로고    scopus 로고
    • The requirement for prior consent to participate on survey response rates: A population-based survey in Grampian
    • Angus VC, Entwistle VA, Emslie MJ, et al. The requirement for prior consent to participate on survey response rates: a population-based survey in Grampian. BMC Health Serv Res 2003;3:21.
    • (2003) BMC Health Serv Res , vol.3 , pp. 21
    • Angus, V.C.1    Entwistle, V.A.2    Emslie, M.J.3
  • 8
    • 0034538696 scopus 로고    scopus 로고
    • Selection bias from requiring patients to give consent to examine data for health services research
    • Woolf SH, Rothemich SF, Johnson RE, et al. Selection bias from requiring patients to give consent to examine data for health services research. Arch Fam Med 2000;9:1111-8.
    • (2000) Arch Fam Med , vol.9 , pp. 1111-1118
    • Woolf, S.H.1    Rothemich, S.F.2    Johnson, R.E.3
  • 9
    • 0032915887 scopus 로고    scopus 로고
    • Medical records and privacy: Empirical effects of legislation
    • McCarthy DB, Shatin D, Drinkard CR, et al. Medical records and privacy: empirical effects of legislation. Health Serv Res 1999;34:417-25.
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    • McCarthy, D.B.1    Shatin, D.2    Drinkard, C.R.3
  • 10
    • 0031796369 scopus 로고    scopus 로고
    • The impact of requiring patient authorization for use of data in medical records research
    • Yawn BP, Yawn RA, Geier GR, et al. The impact of requiring patient authorization for use of data in medical records research. J Fam Pract 1998;47:361-5.
    • (1998) J Fam Pract , vol.47 , pp. 361-365
    • Yawn, B.P.1    Yawn, R.A.2    Geier, G.R.3
  • 11
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    • Consent, confidentiality, and the threat to public health surveillance
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    • Verity, C.1    Nicoll, A.2
  • 12
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    • Data protection, informed consent, and research
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    • (2004) BMJ , vol.328 , pp. 1029-1030
    • Peto, J.1    Fletcher, O.2    Gilham, C.3
  • 13
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    • Canadian Institutes of Health Research. Best practices for protecting privacy in health research (September 2005). The Institutes: Ottawa; 2005. Available: www.cihr-irsc.gc.ca/e/29072.html (accesed 2008 Jan 22).
    • Canadian Institutes of Health Research. Best practices for protecting privacy in health research (September 2005). The Institutes: Ottawa; 2005. Available: www.cihr-irsc.gc.ca/e/29072.html (accesed 2008 Jan 22).
  • 14
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    • Institute for Clinical Evaluative Sciences. Privacy code: protecting personal health information at ICES. Toronto: The Institute; 2005. Available: www.ices.on.ca/file/ACF20B.pdf (accesed 2008 Jan 22).
    • Institute for Clinical Evaluative Sciences. Privacy code: protecting personal health information at ICES. Toronto: The Institute; 2005. Available: www.ices.on.ca/file/ACF20B.pdf (accesed 2008 Jan 22).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.