Related Experiment Video
Updated: May 27, 2026

06:40
The Dyspepsia Educational Tool As a Novel Aid in Dyspepsia Management
Published on: June 29, 2019
Medication safety: using incident data analysis and clinical focus groups to inform educational needs.
Hannah Hesselgreaves1, Anne Watson, Andy Crawford
1NHS Education for Scotland, Glasgow, UK.
Journal of Evaluation in Clinical Practice
|November 11, 2011
Summary
Collective examination of medication incidents by clinical teams enhances reporting systems. Inter-professional learning is key for improving patient safety and addressing educational needs in healthcare.
Area of Science:
- Healthcare quality improvement
- Patient safety research
- Medical education
Background:
- Medication-related safety incidents pose significant risks to patients, policymakers, and clinicians.
- The impact of education on safety-critical healthcare practices is often underestimated.
- Local incident reporting systems provide valuable data on medication safety issues.
Purpose of the Study:
- To foster collaborative discussions among clinical staff regarding medication safety.
- To identify local contextual factors influencing medication incidents.
- To uncover potential educational needs for improving medication safety practices.
Main Methods:
- A mixed-methods pilot study was conducted in three NHS Scotland acute hospitals.
- Phase 1 involved categorical analysis of 1058 medication incident reports.
- Phase 2 utilized three mixed focus groups with clinical staff.
Main Results:
- Analysis of focus group transcripts revealed four major themes and 12 sub-themes related to medication practices.
- Key themes included the medical role and pharmacological education.
- Sub-themes highlighted issues in the skill mix for medicine administration.
Conclusions:
- Traditional risk management through incident report review is insufficient for improving quality.
- Collective examination of medication incident data by local clinical teams can enhance reporting systems.
- Inter-professional learning and collaboration are crucial for healthcare improvement.
Related Concept Videos
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...
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...
Dosage Regimens: Designs and Approaches
Designing a dosage regimen, which refers to the manner of drug administration, is a complex process involving the selection of drug dose, route, and frequency. This process is underpinned by pharmacokinetic parameters derived from tests and population averages. These parameters are then tailored to patient-specific variables such as diagnosis, demographics, and allergy status. Once therapy commences, therapeutic response monitoring is critical and achieved through clinical and physical...
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...
Dosage Regimens: Partial Pharmacokinetic Parameters
It is not uncommon for complete drug pharmacokinetic profiles to remain elusive in pharmacokinetics. This necessitates certain educated assumptions by pharmacokineticists to determine appropriate dosage regimens without comprehensive pharmacokinetic data from animal or human studies. One prevalent assumption is setting the bioavailability factor, denoted as F, to 1 or 100%. This assumption caters to the scenario where a drug doesn't achieve full systemic absorption, resulting in the patient...
Hazard Ratio
The hazard ratio (HR) is a widely used measure in clinical trials to compare the risk of events, such as death or disease recurrence, between two groups over time. It reflects the ratio of hazard rates—the instantaneous risk of the event occurring—between a treatment group and a control group. This measure provides valuable insights into the relative effectiveness of a treatment by assessing how the risk of an event differs between the two groups.
For example, in a clinical trial evaluating a...
For example, in a clinical trial evaluating a...
