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The process of producing a "NICE" guideline.
1Institute of Psychiatry, King's College, London, United Kingdom. davidpgoldberg@yahoo.com
Epidemiologia E Psichiatria Sociale
|January 26, 2011
Summary
This study outlines the process for creating National Institute for Health and Clinical Excellence (NICE) clinical guidelines. It examines stakeholder engagement and adherence to NICE standards within an evidence-based medicine framework.
Area of Science:
- Health Services Research
- Clinical Practice Guidelines
- Evidence-Based Medicine
Background:
- Developing clinical guidelines requires balancing stakeholder interests with rigorous standards.
- The National Institute for Health and Clinical Excellence (NICE) sets demanding benchmarks for guideline development in the UK.
Purpose of the Study:
- To describe the process of preparing a clinical guideline for NICE.
- To analyze the interplay between stakeholder engagement and NICE standards.
- To discuss the strengths and limitations of an evidence-based medicine approach in this context.
Main Methods:
- The paper details the procedural steps involved in NICE guideline preparation.
- It highlights the engagement strategies with diverse stakeholders.
- It addresses the methodologies for meeting NICE's quality and evidence requirements.
Main Results:
- The process necessitates careful management of multiple stakeholder perspectives.
- Adherence to NICE's stringent standards is a critical component.
- The evidence-based medicine approach presents both advantages and challenges.
Conclusions:
- Successful NICE guideline preparation involves navigating complex stakeholder dynamics.
- Meeting high standards is achievable through a structured, evidence-based process.
- Understanding the strengths and limitations of evidence-based medicine is key to effective guideline development.
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