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Volumn 3, Issue 1, 2012, Pages

Health outcomes of interest in observational data: Issues in identifying definitions in the literature

Author keywords

Claims database; Drug safety surveillance; Electronic health record database; Health outcome; Health outcome of interest; Literature search; Outcome definition; Outcomes research; Outcomes studies; Surveillance

Indexed keywords

ALGORITHM; ARTICLE; MEDICAL RESEARCH; MEDICAL SOCIETY; OBSERVATIONAL STUDY; OUTCOME ASSESSMENT; PRIORITY JOURNAL; PUBLICATION;

EID: 84861340620     PISSN: None     EISSN: 18771319     Source Type: Journal    
DOI: 10.1016/j.ehrm.2011.11.003     Document Type: Article
Times cited : (18)

References (12)
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  • 3
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    • Varas-Lorenzo, C.1    Rodriguez, L.A.G.2    Maguire, A.3    Castellsague, J.4    Perez-Gutthann, S.5
  • 4
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    • Framework for evaluating public health surveillance systems for early detection of outbreaks: Recommendations from the CDC Working Group
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    • Buehler JW, Hopkins RS, Overhage JM, Sosin DM, Tong V. Framework for evaluating public health surveillance systems for early detection of outbreaks: recommendations from the CDC Working Group. MMWR Recomm Rep. 2004;53(RR-5):1-11.
    • (2004) MMWR Recomm Rep. , vol.53 , pp. 1-11
    • Buehler, J.W.1    Hopkins, R.S.2    Overhage, J.M.3    Sosin, D.M.4    Tong, V.5
  • 7
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    • Advancing the science for active surveillance: Rationale and design for the observational medical outcomes partnership
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    • (2010) Ann Intern Med. , vol.153 , Issue.9 , pp. 600-606
    • Stang, P.E.1    Ryan, P.B.2    Racoosin, J.A.3
  • 8
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    • Department of Health and Human Services, Food and Drug Administration. 21 CFR 310 Section III D4: Safety Reporting Requirements for Human Drug and Biological Products. March 14,. Accessed November 8, 2011
    • Department of Health and Human Services, Food and Drug Administration. 21 CFR 310 Section III D4: Safety Reporting Requirements for Human Drug and Biological Products. March 14, 2003. Available at: http://www.fda.gov/OHRMS/ DOCKETS/98fr/03-5204.pdf. Accessed November 8, 2011.
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  • 9
    • 34848826898 scopus 로고    scopus 로고
    • For the Vaccine Safety Datalink Rapid Cycle Analysis Team. Real-time vaccine safety surveillance for the early detection of adverse events
    • Lieu TA, Kulldorff M, Davis RL, et al., for the Vaccine Safety Datalink Rapid Cycle Analysis Team. Real-time vaccine safety surveillance for the early detection of adverse events. Med Care. 2007;45(Suppl. 2): S89-S95.
    • (2007) Med Care. , vol.45 , Issue.SUPPL. 2
    • Lieu, T.A.1    Kulldorff, M.2    Davis, R.L.3
  • 10
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    • US Food and Drug Administration, eHealth Foundation, and the Brookings Institute The Sentinel Initiative: Structure, Function and Scope. Washington, DC; December 16,. Accessed November 8, 2011
    • US Food and Drug Administration, eHealth Foundation, and the Brookings Institute. The Sentinel Initiative: Structure, Function and Scope. Washington, DC; December 16, 2008. Available at: http://www.fda.gov/oc/initiatives/ criticalpath/transcript121608.pdf. Accessed November 8, 2011.
    • (2008)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.