Probabilistic cost-effectiveness analysis of cascade screening for familial hypercholesterolaemia using alternative diagnostic and identification strategies

被引:117
作者
Nherera, L. [2 ]
Marks, D. [3 ]
Minhas, R.
Thorogood, M. [4 ]
Humphries, S. E. [1 ]
机构
[1] Royal Free & Univ Coll London Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JF, England
[2] BMJ Grp, BMJ Evidence Ctr, BMJ Technol Assessment Grp, London, England
[3] London Sch Hyg & Trop Med, Dept Social & Environm Hlth Res, London WC1, England
[4] Univ Warwick, Warwick Med Sch, Coventry, Warwick, England
关键词
GENETIC CAUSES; ATORVASTATIN; SIMVASTATIN; STATINS; UK;
D O I
10.1136/hrt.2010.213975
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective To estimate the probabilistic cost-effectiveness of cascade screening methods in familial hypercholesterolaemia (FH) from the UK NHS perspective. Design Economic evaluation (cost utility analysis) comparing four cascade screening strategies for FH: Using low-density lipoprotein (LDL) cholesterol measurements to diagnose affected relatives (cholesterol method); cascading only in patients with a causative mutation identified and using DNA tests to diagnose relatives (DNA method); DNA testing combined with LDL-cholesterol testing in families with no mutation identified, only in patients with clinically defined 'definite' FH (DNA+DFH method); DNA testing combined with LDL-cholesterol testing in no-mutation families of both 'definite' and 'probable' FH patients (DNA+DFH+PFH). A probabilistic model was constructed to estimate the treatment benefit from statins, with all diagnosed individuals receiving high-intensity statin treatment. Population A cohort of 1000 people suspected of having FH aged 50 years for index cases and 30 years for relatives, followed for a lifetime. Main outcomes Costs, quality-adjusted life-years (QALY) and incremental cost-effectiveness ratios (ICER). Results The DNA+DFH+PFH method was the most cost-effective cascade screening strategy. The ICER was estimated at 3666 pound/QALY. Using this strategy, of the tested relatives 30.6% will be true positives, 6.3% false positives, 61.9% true negatives and 1.1% false negatives. Probabilistic sensitivity analysis showed that this approach is 100% cost-effective using the conventional benchmark for cost-effective treatments in the NHS of between 20 pound 000 and 30 pound 000 per QALY gained. Conclusion Cascade testing of relatives of patients with DFH and PFH is cost-effective when using a combination of DNA testing for known family mutations and LDL-cholesterol levels in the remaining families. The approach is more cost-effective than current primary prevention screening strategies.
引用
收藏
页码:1175 / 1181
页数:7
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