Related Experiment Video
Updated: Jul 5, 2025

06:40
The Dyspepsia Educational Tool As a Novel Aid in Dyspepsia Management
Published on: June 29, 2019
6.6K
User-experience testing of an evidence-to-decision framework for selecting essential medicines
Thomas Piggott1,2, Lorenzo Moja3, Carlos A Cuello Garcia1
1Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada.
PLOS Global Public Health
|January 11, 2024
Summary
Essential medicine lists (EMLs) can be strengthened using Evidence-to-Decision (EtD) frameworks and visual abstracts. These tools enhance transparency and efficiency in prioritizing medicines for global health access.
Area of Science:
- Health Policy
- Evidence Synthesis
- Health Economics
Background:
- Essential Medicine Lists (EMLs) are critical for global medicine prioritization, utilized by the WHO and over 130 countries.
- The World Health Organization's (WHO) Expert Committee on the Selection and Use of Essential Medicines employs criteria similar to GRADE Evidence-to-Decision (EtD) frameworks.
- Improving transparency and evidence integration in EML selection is crucial for achieving universal health coverage.
Purpose of the Study:
- To explore the utility of Evidence-to-Decision (EtD) frameworks and visual abstracts as supplementary tools for Essential Medicine List (EML) applications.
- To assess user experience and identify improvements for integrating EtD frameworks and visual abstracts into the EML selection process.
Main Methods:
- User-experience testing interviews were conducted with key EML stakeholders (13 respondents) using Morville's honeycomb model.
- Thematic analysis was applied to 17 interview transcripts to iteratively refine the EtD framework and visual abstract.
- Two specific EML applications (long-acting insulin analogues and immune checkpoint inhibitors) were used as case studies.
Main Results:
- Stakeholders found EtD frameworks and visual abstracts to be useful, findable, and complementary to traditional EML applications.
- These tools were perceived to increase transparency and efficiency in the evidence assessment process for EML committees.
- 'Availability' was identified and added as a key criterion, aligning with WHO EML selection principles.
Conclusions:
- EtD frameworks and visual abstracts are valuable tools for enhancing evidence communication and decision-making in EML applications.
- Adopting EtD frameworks can align EML processes with health practice guidelines, reducing duplication and improving coordination.
- Strengthening EML development with robust, transparent, and evidence-based methods is essential for global health impact and access to medicines.
Related Concept Videos
Preclinical Development: Overview
4.4K
Preclinical development consists of a series of tests that ensure the safety and efficacy of a new therapeutic compound before it is tested in humans. There are four main phases to this process. First, safety pharmacology tests are conducted to ensure the drug does not produce any acutely harmful effects. These tests examine parameters such as bronchoconstriction, cardiac dysrhythmias, blood pressure changes, and ataxia. Next, preliminary toxicological testing is performed to determine the...
4.4K
Clinical Trials: Overview
3.0K
Clinical development focuses on how the drug will interact with the human body and encompasses four key phases of clinical trials, each serving a specific purpose in assessing the safety and effectiveness of new drugs. These phases overlap and build upon one another. Phase I involves a small group of healthy volunteers (typically 20-80 individuals) or, in cases where significant toxicity is expected, patients with the targeted disease, such as cancer or AIDS. The volunteers are tested for...
3.0K
Drug Discovery: Overview
7.9K
Drug discovery is a multifaceted process involving extensive screening, testing, and optimization of lead compounds to identify potential new drugs for therapeutic use. It combines several approaches, including screening large numbers of natural products, chemical modification of known active molecules, identification of new drug targets, and rational design based on biological mechanisms and drug-receptor structure. These approaches are carried out in both academic research laboratories and...
7.9K
Clinical Trials
6.7K
Clinical trials are prospective experimental studies conducted on humans to determine the safety and efficacy of treatments, drugs, diet methods, and medical devices. Using statistics in clinical trials enables researchers to derive reasonable and accurate conclusions from the collected data, allowing them to make wise decisions in uncertain situations. In medical research, statistical methods are crucial for preventing errors and bias.
There are four phases in a clinical trial. A phase one...
There are four phases in a clinical trial. A phase one...
6.7K
Structure-Activity Relationships and Drug Design
726
Drug design is a dynamic field that involves discovering and developing new medications based on specific biological targets. This process heavily relies on structure-activity relationships (SAR) and quantitative structure-activity relationships (QSAR) to guide the design and optimization of efficient drugs.
SAR studies the intricate relationship between a drug's chemical structure and biological activity. It focuses on understanding how modifications to a drug's structure can influence...
SAR studies the intricate relationship between a drug's chemical structure and biological activity. It focuses on understanding how modifications to a drug's structure can influence...
726
Drug Regulation
1.4K
Drug regulation encompasses the management of drug usage by evaluating its safety and efficacy through assessments conducted by regulatory authorities. Regrettably, the history of drug regulation is marred by several catastrophic events. One such incident is the Elixir Sulfanilamide tragedy, in which the toxic compound diethyl glycol was included in a sweet-tasting medication, leading to numerous fatalities. This event prompted the enactment of the Food, Drug, and Cosmetic Act in 1938. Under...
1.4K

