Department of Economic and Public Health Evaluation, Haute Autorité de Santé (HAS), 2 avenue du Stade de France, Saint-Denis, France.
BMC Pediatr. 2012 Jun 8;12:60. doi: 10.1186/1471-2431-12-60.
Five diseases are currently screened on dried blood spots in France through the national newborn screening programme. Tandem mass spectrometry (MS/MS) is a technology that is increasingly used to screen newborns for an increasing number of hereditary metabolic diseases. Medium chain acyl-CoA dehydrogenase deficiency (MCADD) is among these diseases. We sought to evaluate the cost-effectiveness of introducing MCADD screening in France.
We developed a decision model to evaluate, from a societal perspective and a lifetime horizon, the cost-effectiveness of expanding the French newborn screening programme to include MCADD. Published and, where available, routine data sources were used. Both costs and health consequences were discounted at an annual rate of 4%. The model was applied to a French birth cohort. One-way sensitivity analyses and worst-case scenario simulation were performed.
We estimate that MCADD newborn screening in France would prevent each year five deaths and the occurrence of neurological sequelae in two children under 5 years, resulting in a gain of 128 life years or 138 quality-adjusted life years (QALY). The incremental cost per year is estimated at €2.5 million, down to €1 million if this expansion is combined with a replacement of the technology currently used for phenylketonuria screening by MS/MS. The resulting incremental cost-effectiveness ratio (ICER) is estimated at €7 580/QALY. Sensitivity analyses indicate that while the results are robust to variations in the parameters, the model is most sensitive to the cost of neurological sequelae, MCADD prevalence, screening effectiveness and screening test cost. The worst-case scenario suggests an ICER of €72 000/QALY gained.
Although France has not defined any threshold for judging whether the implementation of a health intervention is an efficient allocation of public resources, we conclude that the expansion of the French newborn screening programme to MCADD would appear to be cost-effective. The results of this analysis have been used to produce recommendations for the introduction of universal newborn screening for MCADD in France.
目前,法国通过国家新生儿筛查计划在干血斑上筛查五种疾病。串联质谱(MS/MS)是一种越来越多地用于筛查新生儿遗传性代谢疾病的技术。中链酰基辅酶 A 脱氢酶缺乏症(MCADD)就是其中之一。我们旨在评估在法国引入 MCADD 筛查的成本效益。
我们开发了一个决策模型,从社会角度和终身视角评估扩大法国新生儿筛查计划以纳入 MCADD 的成本效益。使用了已发表的和可获得的常规数据源。成本和健康后果均以每年 4%的速度贴现。该模型适用于法国出生队列。进行了单因素敏感性分析和最坏情况情景模拟。
我们估计,在法国进行 MCADD 新生儿筛查每年可预防 5 名儿童死亡和 2 名 5 岁以下儿童发生神经后遗症,从而增加 128 个生命年或 138 个质量调整生命年(QALY)。每年的增量成本估计为 250 万欧元,如果将这项扩展与用 MS/MS 替代目前用于苯丙酮尿症筛查的技术相结合,成本则降至 100 万欧元。增量成本效益比(ICER)估计为 7580 欧元/QALY。敏感性分析表明,尽管结果对参数变化具有稳健性,但该模型对神经后遗症的成本、MCADD 的患病率、筛查效果和筛查测试成本最为敏感。最坏情况情景表明,ICER 为 72000 欧元/QALY。
尽管法国尚未为判断实施卫生干预措施是否为公共资源的有效分配设定任何阈值,但我们得出的结论是,扩大法国新生儿筛查计划以纳入 MCADD 似乎具有成本效益。这项分析的结果已被用于提出在法国开展普遍的 MCADD 新生儿筛查的建议。