Computerized Surveillance of Adverse Drug Events in Hospital Patients

作者：David C. Classen · 发表于：JAMA · 年份：1991 · DOI：10.1001/jama.1991.03470200059035 · 被引用次数：643 · 研究领域：Pharmacovigilance and Adverse Drug Reactions、Pharmaceutical Practices and Patient Outcomes、Patient Safety and Medication Errors

Objective. —To develop a new method to improve the detection and characterization of adverse drug events (ADEs) in hospital patients. Design. —Prospective study of all patients admitted to our hospital over an 18-month period. Setting. —LDS Hospital, Salt Lake City, Utah, a 520-bed tertiary care center affiliated with the University of Utah School of Medicine, Salt Lake City. Patients. —We developed a computerized ADE monitor, and computer programs were written using an integrated hospital information system to allow for multiple source detection of potential ADEs occurring in hospital patients. Signals of potential ADEs, both voluntary and automated, included sudden medication stop orders, antidote ordering, and certain abnormal laboratory values. Each day, a list of all potential ADEs from these sources was generated, and a pharmacist reviewed the medical records of all patients with possible ADEs for accuracy and causality. Verified ADEs were characterized as mild, moderate, or severe and as type A (dose-dependent or predictable) or type B (idiosyncratic or allergic) reactions, and causality was further measured using a standardized scoring method. Outcome Measure. —The number and characterization of ADEs detected. Results. —Over 18 months, we monitored 36 653 hospitalized patients. There were 731 verified ADEs identified in 648 patients, 701 ADEs were characterized as moderate or severe, and 664 were classified as type A reactions. During this same period, only nine ADEs ...