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[Three ways to develop clinical guidelines. ADAPTE and AGREE GRS procedures]
O Y Rebrova1,2,3
1Endocrinology Research Centre.
Developing new clinical guidelines (CG) is resource-intensive. Adoption (translation) or adaptation (modification) of existing CG offers efficient alternatives, especially when resources are limited, promoting evidence-based medicine.
Area of Science:
- Health Services Research
- Medical Informatics
- Evidence-Based Medicine
Background:
- Developing de novo clinical guidelines (CG) is resource-intensive, requiring significant time, expertise, and funding.
- Limited resources in many countries necessitate alternative approaches to CG development.
- Adoption and adaptation are established methods for creating localized CG.
Purpose of the Study:
- To explore alternative strategies for clinical guideline development.
- To compare the resource implications and methodologies of CG adoption and adaptation.
- To highlight the benefits of adaptation for promoting evidence-based medicine.
Main Methods:
- Review of existing methodologies for clinical guideline development, specifically adoption and adaptation.
- Discussion of the ADAPTE procedure for guideline adaptation.
- Mention of assessment tools like AGREE II and AGREE GRS for evaluating methodological quality.
Main Results:
- Adoption involves direct translation of foreign CG, being the simplest method.
- Adaptation modifies existing CG to suit local healthcare contexts, a more complex process.
- Adaptation, while more demanding than adoption, offers a balance between resource saving and promoting evidence-based medicine.
Conclusions:
- De novo CG development is often unnecessary and costly given information exchange.
- Adoption is preferable in resource-scarce settings.
- Adaptation provides a valuable compromise, saving resources and advancing evidence-based medicine practices.
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