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Cost effectiveness analysis of different approaches of screening for familial hypercholesterolaemia

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Marks, Dalya, Wonderling, David, Thorogood, Margaret, Lambert, Helen, Humphries, Steve E. and Neil, H. A. W.. (2002) Cost effectiveness analysis of different approaches of screening for familial hypercholesterolaemia. BMJ, Vol.324 (No.7349). ISSN 0959-535X

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Official URL: http://dx.doi.org/10.1136/bmj.324.7349.1303

Abstract

Objectives To assess the cost effectiveness of strategies to screen for and treat familial hypercholesterolaemia. Design Cost effectiveness analysis. A care pathway for each patient was delineated and the associated probabilities, benefits, and costs were calculated. Participants Simulated population aged 16­54 years in England and Wales. Interventions Identification and treatment of patients with familial hypercholesterolaemia by universal screening, opportunistic screening in primary care, screening of people admitted to hospital with premature myocardial infarction, or tracing family members of affected patients. Main outcome measure Cost effectiveness calculated as cost per life year gained (extension of life expectancy resulting from intervention) including estimated costs of screening and treatment. Results Tracing of family members was the most cost effective strategy (£3097 (&5066, $4479) per life year gained) as 2.6 individuals need to be screened to identify one case at a cost of £133 per case detected. If the genetic mutation was known within the family then the cost per life year gained (£4914) was only slightly increased by genetic confirmation of the diagnosis. Universal population screening was least cost effective (£13 029 per life year gained) as 1365 individuals need to be screened at a cost of £9754 per case detected. For each strategy it was more cost effective to screen younger people and women. Targeted strategies were more expensive per person screened, but the cost per case detected was lower. Population screening of 16 year olds only was as cost effective as family tracing (£2777 with a clinical confirmation). Conclusions Screening family members of people with familial hypercholesterolaemia is the most cost effective option for detecting cases across the whole population.

Item Type: Journal Article
Subjects: R Medicine > RA Public aspects of medicine
Divisions: Faculty of Medicine > Warwick Medical School
Library of Congress Subject Headings (LCSH): Hypercholesteremia, Medical screening -- Cost effectiveness
Journal or Publication Title: BMJ
Publisher: BMJ Group
ISSN: 0959-535X
Date: 1 June 2002
Volume: Vol.324
Number: No.7349
Identification Number: 10.1136/bmj.324.7349.1303
Status: Peer Reviewed
Access rights to Published version: Restricted or Subscription Access
Funder: Great Britain. National Health Service (NHS), Merck Sharp & Dohme, British Heart Foundation
Grant number: 95/29/04 (NHS), RG2000025 (BHF), RG93008 (BHF)
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Appraisal and evaluation in central government “The Green Book”. London: Stationery Office, 1997. 27 Wilson J, Jungner YG. Principles and practice of mass screening for disease (WHO Public Health Paper 34). Geneva:WHO, 1968. 28 Bhatnagar D, Morgan J, Siddiq S, Mackness MI, Miller JP, Durrington PN. Outcome of case finding among relatives of patients with known hetero­ zygous familial hypercholesterolaemia. BMJ 2000;321:1497­500. 29 Umans­Eckenhausen MAW, Defesche JC, Sijbrands EJG, Scheerder RLJM, Kastelein JJP. Review of first 5 years of screening for familial hypercholesterolaemia in the Netherlands. Lancet 2001;357:165­8. 30 Tengs TO, Adams ME, Pliskin JS, Safran DG, Siegel JE,Weinstein MC, et al. Five­hundred life­saving interventions and their cost­effectiveness. Risk Analysis 1995;15:369­90.
URI: http://wrap.warwick.ac.uk/id/eprint/34566

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