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Public and Patient Involvement at the UK National Institute for Health and Clinical Excellence

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  • Leela Barham

Abstract

The National Institute for Health and Clinical Excellence (NICE) is the arms-length National Health Service (NHS) agency that provides recommendations to the NHS in England and Wales on clinical practice and technologies that should or should not be used in the NHS. NICE aims to ensure that both the public and patients are included in their work and deliberations that lead to recommendations. This article provides an overview of the ways in which the public and patients can engage with NICE based upon a review of the NICE website and relevant literature. It finds that there are a range of both formal and informal mechanisms that provide an opportunity for the public and patients to be involved, but suggests that there are some improvements that could be made to improve transparency, and suggests further work to explore with the public and patients their views of how involvement should be undertaken. Lessons from the NICE experience are likely to be relevant to other countries that have or are adopting health technology assessment. Copyright Adis Data Information BV 2011

Suggested Citation

  • Leela Barham, 2011. "Public and Patient Involvement at the UK National Institute for Health and Clinical Excellence," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 4(1), pages 1-10, January.
    • Handle: RePEc:spr:patien:v:4:y:2011:i:1:p:1-10
    DOI: 10.2165/11586090-000000000-00000
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    References listed on IDEAS

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    1. Milewa, Timothy, 2008. "Representation and legitimacy in health policy formulation at a national level: Perspectives from a study of health technology eligibility procedures in the United Kingdom," Health Policy, Elsevier, vol. 85(3), pages 356-362, March.
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    Cited by:

    1. Paula K. Lorgelly, 2021. "Patient and Public Involvement in Health Economics and Outcomes Research," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 14(4), pages 379-380, July.
    2. Sean Grant & Glen S. Hazlewood & Holly L. Peay & Ann Lucas & Ian Coulter & Arlene Fink & Dmitry Khodyakov, 2018. "Practical Considerations for Using Online Methods to Engage Patients in Guideline Development," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 11(2), pages 155-166, April.
    3. Lopes, Edilene & Carter, Drew & Street, Jackie, 2015. "Power relations and contrasting conceptions of evidence in patient-involvement processes used to inform health funding decisions in Australia," Social Science & Medicine, Elsevier, vol. 135(C), pages 84-91.
    4. Josie Messina & David Grainger, 2012. "A Pilot Study to Identify Areas for Further Improvements in Patient and Public Involvement in Health Technology Assessments for Medicines," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 5(3), pages 199-211, September.
    5. Dmitry Khodyakov & Sean Grant & Brian Denger & Kathi Kinnett & Ann Martin & Holly Peay & Ian Coulter, 2020. "Practical Considerations in Using Online Modified-Delphi Approaches to Engage Patients and Other Stakeholders in Clinical Practice Guideline Development," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 13(1), pages 11-21, February.

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