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首页> 外文期刊>Heart >Probabilistic cost-effectiveness analysis of cascade screening for familial hypercholesterolaemia using alternative diagnostic and identification strategies
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Probabilistic cost-effectiveness analysis of cascade screening for familial hypercholesterolaemia using alternative diagnostic and identification strategies

机译:使用替代性诊断和鉴定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

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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/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.
机译:目的从英国NHS角度评估级联筛查方法治疗家族性高胆固醇血症(FH)的概率成本效益。 《设计经济评估》(成本效用分析)比较了FH的四种级联筛选策略: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);仅在鉴定出具有致病突变并使用DNA测试来诊断亲属的患者中级联(DNA方法);仅在具有临床定义的“确定的” FH(DN​​A + DFH方法)的患者中,在未发现突变的家庭中进行DNA检测和LDL-胆固醇检测相结合;在“确定的”和“可能的” FH患者(DNA + DFH + PFH)的无突变家族中进行DNA检测与LDL-胆固醇检测相结合。构建了一个概率模型来估计他汀类药物的治疗益处,所有诊断出的个体都接受高强度他汀类药物治疗。人口一千名怀疑患有跳频的人的年龄在索引病例中为50岁,在亲戚中为30岁,其后终生。主要成果成本,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选策略。 ICER估计为£3666 / QALY。使用此策略,被测亲戚中30.6%为真阳性,6.3%假阳性,61.9%真阴性和1.1%假阴性。概率敏感性分析表明,使用NHS中成本效益治疗的常规基准(每QALY获得2万至3万英镑),该方法具有100%的成本效益。结论当结合使用DNA检测来检测其余家庭的已知家庭突变和LDL-胆固醇水平时,对DFH和PFH患者的亲属进行级联检测是经济有效的。该方法比当前的一级预防筛查策略更具成本效益。

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  • 来源
    《Heart》 |2011年第14期|p.1175-1181|共7页
  • 作者单位

    BMJ Technology Assessment Group, BMJ Evidence Centre,BMJ Group, London, UK;

    Department of Social & Environmental Health Research,London School of Hygiene and Tropical Medicine, London, UK;

    BMJ Evidence Centre, BMJ Group, London, UK;

    Warwick Medical School,University of Warwick,Coventry, Warwickshire, UK;

    Centre for Cardiovascular Genetics, British Heart Foundation Laboratories, Royal Free and University College London Medical School, London,UK;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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