Systematic review of medication safety assessment methods

被引:94
作者
Meyer-Massetti, Carla [1 ,2 ]
Cheng, Christine M. [2 ]
Schwappach, David L. B. [1 ,3 ]
Paulsen, Lynn [4 ]
Ide, Brigid [5 ]
Meier, Christoph R. [6 ,7 ,8 ]
Guglielmo, B. Joseph
机构
[1] Swiss Patient Safety Fdn, CH-8032 Zurich, Switzerland
[2] Univ Calif San Francisco, Sch Pharm, Dept Clin Pharm, Medicat Outcomes Ctr, San Francisco, CA 94143 USA
[3] Univ Bern, Inst Social & Prevent Med, Div Social & Behav Hlth Res, Bern, Switzerland
[4] UCSF Med Ctr, Dept Pharmaceut Serv, San Francisco, CA USA
[5] UCSF Med Ctr, Patient Safety & Qual Serv, San Francisco, CA USA
[6] Univ Basel, Pharmacoepidemiol Unit, Basel, Switzerland
[7] Univ Basel, Dept Pharmaceut Sci, Basel Pharmacoepidemiol Unit, Div Clin Pharm & Epidemiol, Basel, Switzerland
[8] Univ Basel Hosp, CH-4031 Basel, Switzerland
关键词
Drugs; adverse reactions; Economics; Errors; medication; Methodology; Quality assurance; Reports; ADVERSE DRUG EVENTS; PHYSICIAN ORDER ENTRY; INTENSIVE-CARE-UNIT; PATIENT SAFETY; TRIGGER-TOOL; ERRORS; SURVEILLANCE; HOSPITALS; HARM; IDENTIFICATION;
D O I
10.2146/ajhp100019
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose. The accuracy, efficiency, and efficacy of four commonly recommended medication safety assessment methodologies were systematically reviewed. Methods. Medical literature databases were systematically searched for any comparative study conducted between January 2000 and October 2009 in which at least two of the four methodologies-incident report review, direct observation, chart review, and trigger tool-were compared with one another. Any study that compared two or more methodologies for quantitative accuracy (adequacy of the assessment of medication errors and adverse drug events) efficiency (effort and cost), and efficacy and that provided numerical data was included in the analysis. Results. Twenty-eight studies were included in this review. Of these, 22 compared two of the methodologies, and 6 compared three methods. Direct observation identified the greatest number of reports of drug-related problems (DRPs), while incident report review identified the fewest. However, incident report review generally showed a higher specificity compared to the other methods and most effectively captured severe DRPs. In contrast, the sensitivity of incident report review was lower when compared with trigger tool. While trigger tool was the least labor-intensive of the four methodologies, incident report review appeared to be the least expensive, but only when linked with concomitant automated reporting systems and targeted follow-up. Conclusion. All four medication safety assessment techniques incident report review, chart review, direct observation, and trigger tool have different strengths and weaknesses. Overlap between different methods in identifying DRPs is minimal. While trigger tool appeared to be the most effective and labor-efficient method, incident report review best identified high-severity DRPs.
引用
收藏
页码:227 / 240
页数:14
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