Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/24231
Title: A multicenter record review of in-hospital adverse drug events requiring a higher level of care
Authors: MARQUET, Kristel 
CLAES, Neree 
DE TROY, Elke 
KOX, Gaby 
DROOGMANS, Martijn 
VLEUGELS, Arthur 
Issue Date: 2017
Publisher: TAYLOR & FRANCIS LTD
Source: ACTA CLINICA BELGICA, 72(3), p. 156-162
Abstract: Objective: Adverse drug events (ADEs) are a worldwide concern, particularly when leading to a higher level of care. This study defines a higher level of care as an unplanned (re)admission to an intensive care unit or an intervention by a Medical Emergency Team. The objectives are to describe the incidence and preventability of ADEs leading to a higher level of care, to assess the types of drug involved, and to identify the risk factors. Methods: A three-stage retrospective review was performed in six Belgian hospitals. Patient records were assessed by a trained clinical team consisting of a nurse, a physician, and a clinical pharmacist. Descriptive statistics, univariate, and multiple logistic regressions were used. Results: In this study, 830 patients were detected for whom a higher level of care had been needed. In 160 (19.3%) cases, an ADE had occurred; 134 (83.8%) of these were categorized as preventable adverse drug events (pADEs). The overall incidence rate of patients transferred to a higher level of care because of a pADE was 33.9 (95% CI: 28.5-39.3) per 100,000 patient days at risk. Antibiotics and antithrombotic agents accounted both for one-fifth of all pADEs. Multivariate analysis indicated American Society of Anaesthesiologists physical status score as a risk factor for pADEs. Conclusions: The high number of pADE with patient harm shows that there is a need for structural improvement of pharmacotherapeutic care. Detection of these pADEs can be the basis for the implementation of these improvements.
Notes: [Marquet, Kristel; Claes, Neree; De Troy, Elke; Kox, Gaby; Droogmans, Martijn; Vleugels, Arthur] Hasselt Univ, Fac Med & Life Sci, Agoralaan,Bldg D,Room C53, BE-3590 Diepenbeek, Belgium. [De Troy, Elke; Droogmans, Martijn] Jessa Hosp, Hasselt, Belgium. [Claes, Neree] Antwerp Management Sch, Hlth Care Management, Antwerp, Belgium. [Vleugels, Arthur] Katholieke Univ Leuven, Ctr Hlth Serv & Nursing Res, Leuven, Belgium.
Keywords: adverse drug events; adverse drug reaction; preventable adverse drug event; drug safety; intensive care unit; record review;Adverse drug events; Adverse drug reaction; Preventable adverse drug event; Drug safety; Intensive care unit; Record review
Document URI: http://hdl.handle.net/1942/24231
ISSN: 1784-3286
e-ISSN: 2295-3337
DOI: 10.1080/17843286.2017.1283759
ISI #: 000400986600002
Rights: © Acta Clinica Belgica 2017
Category: A1
Type: Journal Contribution
Validations: ecoom 2018
Appears in Collections:Research publications

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