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. 2015;2(4):387-395.
doi: 10.1007/s40801-015-0045-2. Epub 2015 Oct 23.

Prevalence of Drug-Related Emergency Department Visits at a Teaching Hospital in Malaysia

Affiliations

Prevalence of Drug-Related Emergency Department Visits at a Teaching Hospital in Malaysia

Abubakar Ibrahim Jatau et al. Drugs Real World Outcomes. 2015.

Abstract

Background: Data on the prevalence of adverse drug event (ADE)-related emergency department (ED) visits in developing countries are limited. Malaysia is located in South-East Asia, and, to our knowledge, no information exists on ADE-related ED visits.

Objective: The objective of this study was to determine the prevalence, preventability, severity, and outcome of drug-related ED visits.

Methodology: A cross-sectional study was conducted in consenting patients who visited the ED of Hospital Universiti Sains Malaysia over a 6-week period. The ED physician on duty determined whether or not the visit was drug related according to set criteria. Other relevant information was extracted from the patient's medical folder by a clinical pharmacist.

Results: Of the 434 consenting patients, 133 (30.6 %; 95 % confidence interval [CI] 26-35 %) visits were determined to be ADE related; 55.5 % were considered preventable, 11.3 % possibly preventable, and 33.1 % not preventable. Severity was classed as mild in 1.5 %, moderate in 67.7 %, and severe in 30.8 %. The most common ADEs reported were drug therapeutic failure (55.6 %) and adverse drug reactions (32.3 %). The most frequently implicated drugs were antidiabetics (n = 31; 23.3 %), antihypertensives (n = 28; 21.1 %), antibiotics (n = 13; 9.8 %), and anti-asthmatics (n = 11; 8.3 %). A total of 93 patients (69.9 %) were admitted to the ED for observation, 25 (18.8 %) were discharged immediately after consultation, and 15 (11.3 %) were admitted to the ward through the ED.

Conclusion: The prevalence of ADE-related ED visits was high; more than one-half of the events were considered preventable and one-third was classed as severe. As such, preventive measures will minimize future occurrences and increase patient safety.

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Conflict of interest statement

Compliance with Ethical Standards The study was approved by the ethics committee of Universiti Sultan Zainal Abidin (UniSZA) and Universiti Sains Malaysia (USM) and has been performed in accordance with the ethical standards of the Declaration of Helsinki. Informed consent was obtained from all individual participants included in the study. Conflict of interest Pharm Abubakar Ibrahim Jatau, Dr Myat Moe Thwe Aung, Dr Tuan Hairulnizam Tuan Kamauzan and Prof Ab Fatah Ab Rahman all declare that they have no conflict of interest. Funding No specific funding was received for this research.

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