Literature DB >> 17936401

Representation and legitimacy in health policy formulation at a national level: perspectives from a study of health technology eligibility procedures in the United Kingdom.

Timothy Milewa1.   

Abstract

Decisions about the availability of publicly funded new drugs, treatments and medical devices are of fundamental interest to patients, health technology manufacturers, clinicians and tax or insurance payers. The issue of who can claim to speak for whom in decisions made on behalf of significant proportions of the population may thus be central to the perceived legitimacy of decision-making procedures. This article focuses on the meaning of representation and legitimacy in relation to such decisions within the National Institute for Health and Clinical Excellence (NICE) in the United Kingdom. Interviews with key informants (n=33) indicate potentially fluid and imprecise aspects of representation and legitimacy that are not necessarily addressed by formal structures for engaging and involving stakeholders in decision-making processes. The findings suggest that those charged with managing bodies such as NICE should adopt a flexible approach to engaging and involving stakeholders. The "representation" of relevant stakeholder constituencies in decision-making procedures is not, however, enough. The legitimacy of decision-making arrangements on behalf of wider society also depends upon transparent reasoned debate that affords different interests the opportunity to challenge, test or advance arguments about evidence in a manner that discounts preconceived ideas about the status and authority of protagonists.

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Year:  2007        PMID: 17936401     DOI: 10.1016/j.healthpol.2007.09.001

Source DB:  PubMed          Journal:  Health Policy        ISSN: 0168-8510            Impact factor:   2.980


  9 in total

1.  Listening for prescriptions: a national consultation on pharmaceutical policy issues.

Authors:  Steve Morgan; Colleen M Cunningham
Journal:  Healthc Policy       Date:  2010-11

2.  Evidence, ethics and inclusion: a broader base for NICE.

Authors:  Stephen Wilmot
Journal:  Med Health Care Philos       Date:  2011-05

Review 3.  Public and patient involvement at the UK National Institute for Health and Clinical Excellence.

Authors:  Leela Barham
Journal:  Patient       Date:  2011       Impact factor: 3.883

4.  Involving patients in health technology funding decisions: stakeholder perspectives on processes used in Australia.

Authors:  Edilene Lopes; Jackie Street; Drew Carter; Tracy Merlin
Journal:  Health Expect       Date:  2015-02-21       Impact factor: 3.377

5.  NICE technology appraisals: working with multiple levels of uncertainty and the potential for bias.

Authors:  Patrick Brown; Michael Calnan
Journal:  Med Health Care Philos       Date:  2013-05

6.  Development of an ICF-based eligibility procedure for education in Switzerland.

Authors:  Judith Hollenweger
Journal:  BMC Public Health       Date:  2011-05-31       Impact factor: 3.295

7.  Sex, drugs and gender roles: mapping the use of sex and gender based analysis in pharmaceutical policy research.

Authors:  Devon L Greyson; Annelies Re Becu; Steven G Morgan
Journal:  Int J Equity Health       Date:  2010-11-19

8.  Institutionalizing telemedicine applications: the challenge of legitimizing decision-making.

Authors:  Paolo Zanaboni; Emanuele Lettieri
Journal:  J Med Internet Res       Date:  2011-09-28       Impact factor: 5.428

9.  Decision making in NICE single technological appraisals: How does NICE incorporate patient perspectives?

Authors:  Ferhana Hashem; Michael W Calnan; Patrick R Brown
Journal:  Health Expect       Date:  2017-07-07       Impact factor: 3.377

  9 in total

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