An observational study of drug administration errors in a Malaysian hospital (study of drug administration errors)

S S Chua1, M H Tea, M H A Rahman

  • 1Department of Pharmacy, Faculty of Medicine, University of Malaysia, Kuala Lumpur, Malaysia. chuass@um.edu.my

Abstract

Insights

Drug administration errors, particularly incorrect timing, are frequent in Malaysian hospitals, similar to developed nations. Establishing a non-punitive reporting system is crucial for developing effective risk management protocols.

Area of Science:

  • Pharmacovigilance
  • Patient Safety
  • Healthcare Quality Improvement

Background:

  • Drug administration errors are a significant patient safety concern, often reaching patients due to lower interception rates compared to prescribing errors.
  • Understanding the frequency and types of these errors is vital for targeted interventions.

Purpose of the Study:

  • To determine the frequency and types of drug administration errors in a Malaysian hospital ward.
  • To compare error rates with international data and identify specific error patterns.

Main Methods:

  • A prospective study employing direct, undisguised observation of drug administrations over 15 days in a hospital ward.
  • Systematic recording of observed administrations and comparison with prescribed medications.

Main Results:

  • An overall drug administration error rate of 11.4% was observed, with incorrect timing being the most common error (25.2%).
  • Potentially life-threatening errors accounted for 10.4% of all administration errors.
  • Intravenous drug administration carried a significantly higher risk of error (21.3%) compared to oral routes (7.9%).

Conclusions:

  • Drug administration error rates in Malaysia are comparable to those in developed countries.
  • Incorrect timing represents the most prevalent type of drug administration error.
  • Implementing a non-punitive medication error reporting system is recommended to facilitate the development of robust risk management strategies.

Related Concept Videos

Pharmacovigilance01:19

Pharmacovigilance

Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
Errors occurring during blood pressure monitoring01:25

Errors occurring during blood pressure monitoring

Blood pressure monitoring is a crucial clinical procedure in diagnosing and managing various cardiovascular conditions. Despite its significance, the accuracy of blood pressure measurements can be compromised by multiple factors, potentially leading to either falsely high or low readings. These inaccuracies are critical as they can significantly impact patient care. So, it is vital to understand these challenges deeply and adopt strategic approaches to minimize errors.
Several factors...
Pharmaceutical Poisoning: Potential Scenarios01:26

Pharmaceutical Poisoning: Potential Scenarios

Pharmaceutical poisoning can occur through various channels, impacting an estimated 2 million hospitalized patients in the U.S. annually with serious adverse drug responses. These scenarios encompass both therapeutic uses, such as drug toxicity, where even standard dosages can lead to severe central nervous system depression, and non-therapeutic exposures, including accidental ingestion by children, and environmental and occupational exposures.Unintentional poisonings often involve exploratory...
Drug Dosing: Geriatric Patients01:15

Drug Dosing: Geriatric Patients

Elderly individuals encompass a diverse population with varying degrees of age-related physiological changes. Defining the elderly presents challenges, as the geriatric population is often arbitrarily categorized as individuals older than 65. However, many individuals in this group lead active and healthy lives, with an increasing number surpassing 85 years and falling into the older elderly category. Physiological changes associated with aging impact performance capacity and homeostatic...
Systematic Error: Methodological and Sampling Errors01:15

Systematic Error: Methodological and Sampling Errors

In the case of systematic errors, the sources can be identified, and the errors can be subsequently minimized by addressing these sources. According to the source, systematic errors can be divided into sampling, instrumental, methodological, and personal errors.
Sampling errors originate from improper sampling methods or the wrong sample population. These errors can be minimized by refining the sampling strategy. Defective instruments or faulty calibrations are the sources of instrumental...
Drug Toxicity: Risk factors01:24

Drug Toxicity: Risk factors

Adverse Drug Reactions (ADRs) are potential complications that arise during pharmacotherapy, influenced by multiple risk factors. Age plays a significant role; both neonates and the elderly are at heightened risk due to their respective immature and diminished metabolic and elimination processes. Gender also impacts ADRs, with females experiencing a 1.5 to 1.7-fold greater risk than males, which may be linked to pharmacokinetic, pharmacodynamic, and hormonal differences. Notably, neonates, the...