Centre for Cardiovascular Genetics, British Heart Foundation Laboratories, Royal Free and University College London Medicine School, London WC1E 6JF, UK.
Heart. 2011 Jul;97(14):1175-81. doi: 10.1136/hrt.2010.213975.
To estimate the probabilistic cost-effectiveness of cascade screening methods in familial hypercholesterolaemia (FH) from the UK NHS perspective.
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.
A cohort of 1000 people suspected of having FH aged 50 years for index cases and 30 years for relatives, followed for a lifetime.
Costs, quality-adjusted life-years (QALY) and incremental cost-effectiveness ratios (ICER).
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.
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.
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。
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。
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。
成本、质量调整生命年(QALY)和增量成本效益比(ICER)。
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。
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。