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Qual Saf Health Care 14:221-226 doi:10.1136/qshc.2002.002972/10.1136/qshc.2002.002972
  • Classic paper

Computerized surveillance of adverse drug events in hospital patients*

  1. D C Classen1,
  2. S L Pestotnik1,
  3. R S Evans1,
  4. J P Burke1
  1. 1Department of Clinical Epidemiology, LDS Hospital, Salt Lake City, Utah, and the Division of Infectious Diseases, Medicine, University of Utah School of Medicine, Salt Lake City, USA
  1. Correspondence to:
 Dr D C Classen
 Department of Clinical Epidemiology, LDS Hospital, Eighth Avenue and C Street, Salt Lake City, UT 84143, USA

    Abstract

    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 were identified using traditional detection methods. Physicians, pharmacists, and nurses voluntarily reported 92 of the 731 ADEs detected using this automated system. The other 631 ADEs were detected from automated signals, the most common of which were diphenhydramine hydrochloride and naloxone hydrochloride use, high serum drug levels, leukopenia, and the use of phytonadione and antidiarrheals. The most common symptoms and signs were pruritus, nausea and/or vomiting, rash, and confusion-lethargy. The most common drug classes involved were analgesics, anti-infectives, and cardiovascular agents.

    Conclusion: We believe that screening for ADEs with a computerized hospital information system offers a potential method for improving the detection and characterization of these events in hospital patients.

    Footnotes

    • * This is a reprint of a paper that appeared in JAMA, 1991, Volume 266, pages 2847–51.

    • This study was supported in part by grant HS06028 from the Agency for Health Care Policy and Research, Bethesda, Md.

    • We appreciate the tireless and enthusiastic help of Sheron B Bass, RN, for assistance in the identification and monitoring of patients experiencing adverse drug events.