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Volumn 7, Issue 3, 2009, Pages 98-99

Electronic patient-reported outcomes for collecting sensitive information from patients

Author keywords

[No Author keywords available]

Indexed keywords

ACCESS TO INFORMATION; CANCER PATIENT; COMPUTER INTERFACE; ELECTRONIC DATA INTERCHANGE; ELECTRONIC MEDICAL RECORD; FEASIBILITY STUDY; INFORMATION PROCESSING; NOTE; OUTCOME ASSESSMENT; PATIENT INFORMATION; REGISTRATION; SELF REPORT; SEXUAL DYSFUNCTION; SEXUALITY; COMPUTER; FEMALE; HUMAN; METHODOLOGY; STANDARD; UTILIZATION REVIEW;

EID: 68249138821     PISSN: 15446794     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Note
Times cited : (21)

References (11)
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  • 2
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  • 4
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    • Coons SJ, Gwaltney CJ, Hays RD, et al. Recommendations on evidence needed to support measurement equivalence between electronic and paper-based patient-reported outcome (PRO) measures: ISPOR ePRO Good Research Practices Task Force Report. Value in Health 2008. [published online ahead of print: November 11, 2008].
  • 5
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  • 6
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    • PRO-CTCAE Investigators, version 6, March 27, National Cancer Institute Wiki, Accessed April 2, 2009
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    • (2009) White paper on barriers and strategies for implementation of a patient-reported version of the CTCAE
  • 7
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  • 8
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    • Longitudinal analysis of sexual function reported by men in the Prostate Cancer Prevention Trial
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  • 9
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.