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Incidence of adverse drug events and potential adverse drug events: implications for prevention.
Bates DW, Cullen DJ, Laird N, et al; for the ADE Prevention Group. JAMA. 1995;274:29-34.
 
The authors report on their seminal 1993 study of adverse drug events (ADEs) at the Massachusetts General Hospital and Brigham and Women’s Hospital in Boston. Using 11 intensive and general care units at the two hospitals, the authors prospectively identified actual and potential ADEs by contemporaneous chart review, provider interview, and voluntary incident reporting. The authors report an adjusted rate of ADEs of 6.5 per 100 admissions, 1.8 per 100 considered preventable. Among preventable ADEs, none were fatal, but 43% were judged serious and 20% life threatening. The authors break down ADEs by drug class and by the stage at which the error occurred (ordering, transcription, dispensing, or administration). This study has become the basis for the rationale for implementing computerized physician order entry systems (CPOE), barcoded medication administration systems, and other systems designed to reduce preventable medication errors at each stage.
 
icon indicating hyperlink to external website PubMed citation

 
Resource Type:  Journal Article > Study

Setting of Care:  Hospitals > General Hospitals

Target Audience:  Health Care Providers

Safety Target:  Medication Safety > Medication Errors/Preventable Adverse Drug Events

Error Types:  Epidemiology of Errors and Adverse Events

   Near Miss

Origin/Sponsor:  North America > United States of America
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