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基于不同诊断和识别策略的家族性高胆固醇血症级联筛查的概率成本效益分析。

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

机构信息

Centre for Cardiovascular Genetics, British Heart Foundation Laboratories, Royal Free and University College London Medicine School, London WC1E 6JF, UK.

出版信息

Heart. 2011 Jul;97(14):1175-81. doi: 10.1136/hrt.2010.213975.

Abstract

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/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 £20,000 and £30,000 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.

摘要

目的

从英国国民保健制度(NHS)的角度评估家族性高胆固醇血症(FH)级联筛查方法的概率成本效益。

设计

经济评估(成本效用分析)比较了 FH 的四种级联筛查策略:使用低密度脂蛋白(LDL)胆固醇测量来诊断受影响的亲属(胆固醇方法);仅在确定致病突变的患者中级联,并使用 DNA 测试来诊断亲属(DNA 方法);在未发现突变的家族中,仅在具有临床定义的“明确”FH 患者中结合 DNA 测试和 LDL-胆固醇测试(DNA+DFH 方法);在“明确”和“可能”FH 患者的无突变家族中结合 DNA 测试和 LDL-胆固醇测试(DNA+DFH+PFH 方法)。构建了一个概率模型来估计他汀类药物的治疗效益,所有确诊的个体都接受高强度他汀类药物治疗。

人群

一个 1000 名疑似 50 岁的 FH 患者的队列作为指数病例,30 岁的亲属作为队列,终生随访。

主要结果

成本、质量调整生命年(QALY)和增量成本效益比(ICER)。

结果

DNA+DFH+PFH 方法是最具成本效益的级联筛查策略。ICER 估计为 3666 英镑/QALY。使用该策略,测试的亲属中有 30.6%是真阳性,6.3%是假阳性,61.9%是真阴性,1.1%是假阴性。概率敏感性分析表明,在 NHS 中,使用传统的成本效益治疗基准(每获得 1 QALY 的成本在 20000 至 30000 英镑之间),该方法 100%具有成本效益。

结论

在使用已知家族突变的 DNA 测试和剩余家族的 LDL-胆固醇水平的组合对 DFH 和 PFH 患者的亲属进行级联测试时,具有成本效益。该方法比当前的初级预防筛查策略更具成本效益。

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