Related Experiment Video
Updated: Aug 6, 2026

12:08
Diagonal Method to Measure Synergy Among Any Number of Drugs
Published on: June 21, 2018
Adverse drug event trigger tool: a practical methodology for measuring medication related harm
J D Rozich1, C R Haraden, R K Resar
1Luther Midelfort, Mayo Health System, Eau Claire, WI 54703, USA. rozich.john@mayo.edu
Quality & Safety in Health Care
|June 7, 2003
Summary
Adverse drug events (ADEs) are a frequent patient safety risk. A new "trigger tool" method significantly improves ADE detection rates compared to traditional reporting, enhancing patient safety.
Area of Science:
- Pharmacovigilance
- Patient Safety
- Health Informatics
Background:
- Adverse drug events (ADEs) are a leading cause of healthcare-related injuries.
- Traditional methods for detecting ADEs (chart audits, voluntary reporting) are often ineffective and costly.
- Existing computerized ADE detection methods are effective but require expensive, customized software.
Purpose of the Study:
- To describe a novel, low-cost "trigger tool" for detecting ADEs.
- To evaluate the effectiveness of this adapted technique in identifying medication errors and adverse clinical events.
Main Methods:
- Utilized a modified automated technique, termed the "trigger tool", for ADE detection.
- Focused on a "low tech" approach, adapting existing automated methods.
- Compared the trigger tool's performance against traditional reporting methodologies.
Main Results:
- The trigger tool significantly increases the rate of ADE detection.
- Detection rates were approximately 50-fold higher compared to traditional reporting methods.
- This method offers a more cost-effective approach to identifying drug-related adverse events.
Conclusions:
- The trigger tool is a highly effective and efficient method for detecting ADEs.
- This low-cost, adaptable technique can substantially improve patient safety by identifying medication errors.
- Healthcare systems can benefit from implementing this tool to enhance pharmacovigilance.
Related Concept Videos
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...
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...
Therapeutic Drug Monitoring: Affecting Factors
Therapeutic Drug Monitoring (TDM) is the clinical practice of measuring specific drug levels in a patient's blood or body tissues to manage and optimize therapy. TDM is crucial for drugs with narrow therapeutic windows, like warfarin and phenytoin, where incorrect doses can lead to treatment failure or severe side effects. This monitoring ensures the dosage administered is within a safe and effective range. The factors affecting therapeutic drug monitoring include:Patient-Specific Factors:a.
Therapeutic Drug Monitoring: Drug Analysis Methods
Therapeutic Drug Monitoring (TDM) is a clinical practice that measures specific drug levels in a patient's blood or body tissues to tailor drug therapy effectively. This monitoring is critical for managing drugs with narrow therapeutic indices like digoxin and phenytoin, ensuring they are both safe and effective. For instance, monitoring theophylline levels in asthma patients involves precision and sensitivity to adjust doses according to individual responses to therapy, ensuring efficacy and...
Drug Toxicity: Overview
Drug toxicity quantifies the harm a compound causes to an organism, varying by dose and potentially impacting whole systems or specific organs like the liver. Toxic reactions may arise from venomous insect or spider bites, with effects ranging from mild symptoms to severe outcomes such as brain damage or death. Common forms of acute poisoning include ethanol intoxication and overdose of pain or fever medications, with substances like GHB and heroin being particularly lethal at doses close to...
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...
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...

