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Volumn 198, Issue 3, 2013, Pages 134-135

Clinical registries: The urgent need to address ethical hurdles

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUSTRALIA; DISEASE REGISTRY; HEALTH CARE DELIVERY; HEALTH CARE MANAGEMENT; HEALTH CARE QUALITY; INFORMATION PROCESSING; INFORMED CONSENT; MEDICAL ETHICS; MEDICAL INFORMATICS; MEDICAL INFORMATION SYSTEM; MEDICAL RESEARCH; PATIENT INFORMATION; PATIENT SAFETY; PROFESSIONAL STANDARD; PUBLIC HEALTH SERVICE; QUALITY CONTROL PROCEDURES; SWEDEN; UNITED STATES;

EID: 84874582985     PISSN: 0025729X     EISSN: 13265377     Source Type: Journal    
DOI: 10.5694/mja12.10648     Document Type: Article
Times cited : (9)

References (14)
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    • Evans, S.M.1    Bohensky, M.2    Cameron, P.A.3    McNeil, J.4
  • 4
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    • Swedish Association of Local Authorities and Regions
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    • Swedish Association of Local Authorities and Regions. National healthcare quality registries in Sweden. Stockholm: SALAR, 2007. http://www.kvalitetsregister.se/om_kvalitetsregister/quality_registries (accessed Jan 2013).
    • (2013) National Healthcare Quality Registries In Sweden
  • 5
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    • The American Heart Association's recommendations for expanding the applications of existing and future clinical registries: A policy statement from the American Heart Association
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    • Bufalino, V.J.1    Masoudi, F.A.2    Stranne, S.K.3
  • 6
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    • Use of 13 disease registries in 5 countries demonstrates the potential to use outcome data to improve health care's value
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    • Larsson, S.1    Lawyer, P.2    Garellick, G.3
  • 7
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    • Difficulties in establishing long-term trauma outcomes data collections. Could trauma outcomes be routinely monitored in New South Wales, Australia: Piloting a 3 month follow-up?
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    • Mitchell, R.1    Watson, W.L.2    Curtis, K.3
  • 8
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  • 10
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.