-
Observational Study
Factors associated with adverse events resulting from medical errors in the emergency department: two work better than one.
- Yonathan Freund, Hélène Goulet, Jérôme Bokobza, Aurélie Ghanem, Serge Carreira, Delphine Madec, Gaëlle Leroux, Patrick Ray, Jacques Boddaert, Bruno Riou, and Pierre Hausfater.
- Service d'Accueil des Urgences, Hôpital Pitié-Salpêtrière, Paris, France.
- J Emerg Med. 2013 Aug 1;45(2):157-62.
BackgroundThe Emergency Department (ED) is an environment at risk for medical errors.ObjectiveOur aim was to determine the factors associated with the adverse events resulting from medical errors in the ED among patients who were admitted.MethodsThis was a prospective observational study. For a 1-month period, we included all ED patients who were subsequently admitted to the medical ward. Detection of medical errors was made by the admitting physician and then validated by two experts who reviewed all available data and medical charts pertaining to the patient's hospital stay, including the first review from the ward physician. Related adverse events resulting from medical errors were then classified by type and severity. Adverse events were defined as medical errors that needed an intervention or caused harm to the patient. Univariate analysis examined relationships between characteristics of both patients and physicians and the risk of adverse events.ResultsFrom 197 analyzed patients, 130 errors were detected, of these, 34 were categorized as adverse events among 19 patients (10%). Seventy-six percent of these were categorized as proficiency errors. The only factors associated with a lower risk of adverse events were the transition of care involving a handoff within the ED (0% vs. 19%; p = 0.03) and the involvement of a resident (junior doctor) in addition to the senior physician (37% vs. 67%; p < 0.01).ConclusionsIn our study, the involvement of more than one physician was associated with a lower risk of adverse events.Copyright © 2013 Elsevier Inc. All rights reserved.
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