Near misses and research subjects

Quality and Safety in Health Care

Volumn 15, Issue 4, 2006, Pages 228-229

  Murff, H J ^a   Dittus, R S ^b  

^a VETERANS AFFAIRS MEDICAL CENTER   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL PROTOCOL; CLINICAL RESEARCH; CLINICAL TRIAL; HEALTH PROGRAM; HOSPITAL INFECTION; HUMAN; INFORMED CONSENT; MEDICAL CARE; NOTE; PATIENT SAFETY; UNITED STATES;

ATTITUDE OF HEALTH PERSONNEL; HUMAN EXPERIMENTATION; HUMANS; MEDICAL ERRORS; ORGANIZATIONAL CULTURE; RESEARCH SUBJECTS; RISK MANAGEMENT; SENTINEL SURVEILLANCE;

EID: 33747283791     PISSN: 14753898     EISSN: None     Source Type: Journal    
DOI: 10.1136/qshc.2006.018176     Document Type: Note

References (6)

1. Cassel C, Stock MC, Wood AJ, et al. Report of Johns Hopkins University External Review Committee, 8 August, 2001.
2. Steinbrook R. Improving protection for research subjects. N Engl J Med 2002;346:1425-30.
3. Burke JP. Infection control - a problem for patient safety. N Engl J Med 2003;348:651-6.
4. Shaw R, Drever F, Hughes H, et al. Adverse events and near miss reporting in the NHS. Qual Saf Health Care 2005;14:279-83.
5. Murff HJ, Byrne DW, Harris PA, et al. "Near-miss" reporting system development and implications for human subjects protection. In: Henriksen K, Battles JB, Marks ES, Lewin DI, eds. Advances in patient safety: from research to implementation. Volume 3. Implementation issues. AHRQ Publication No 05-0021 -3. Rockville, MD: Agency for Healthcare Research and Quality (AHRQ), 2005.
6. Murff HJ, Pichet JW, Byrne DW, et al. Research participant safety and system factors in general clinical research centers. IRB: Ethics and Human Research 2006 (in press).