Quaglini Silvana, Rognoni Carla, Spazzolini Carla, Priori Silvia G, Mannarino Savina, Schwartz Peter J
Department of Computer Science and Systems, University of Pavia, Italy.
Eur Heart J. 2006 Aug;27(15):1824-32. doi: 10.1093/eurheartj/ehl115. Epub 2006 Jul 13.
A significant number of preventable cardiac deaths in infancy and childhood are due to long QT syndrome (LQTS) and to unrecognized neonatal congenital heart diseases (CHDs). Both carry a serious risk for avoidable mortality and morbidity but effective treatments exist to prevent lethal arrhythmias or to allow early surgical correction before death or irreversible cardiac damage. As an electrocardiogram (ECG) allows recognition of LQTS and of some of the CHDs that have escaped medical diagnosis, and as LQTS also contributes to sudden infant death syndrome, we have analysed the cost-effectiveness of a nationwide programme of neonatal ECG screening. Our primary analysis focused on LQTS alone; a secondary analysis focused on the possibility of identifying some CHDs also.
A decision analysis approach was used, building a decision tree for the strategies 'screening'-'no screening'. Markov processes were used to simulate the natural or clinical histories of the patients. To assess the impact of potential errors in the estimates of the model parameters, a Monte Carlo sensitivity analysis was performed by varying all baseline values by +/-30%. Incremental cost-effectiveness analysis for the primary analysis shows that with the screening programme, the cost per year of life saved is very low: 11,740 euro. The cost for saving one entire life of 70 years would be 820,000 euro. Even by varying model parameters by +/-30%, the cost per year of life saved remains between 7400 euro and 20,400 euro. These figures define 'highly cost-effective' screening programmes. The secondary analysis provides even more cost-effective results.
A programme of neonatal ECG screening performed in a large European country is cost-effective. An ECG performed in the first month of life will allow the early identification of still asymptomatic infants with LQTS and also of infants with some correctable CHDs not recognized by routine neonatal examinations. Appropriate therapy will prevent unnecessary deaths in infants, children, and young adults.
婴儿期和儿童期大量可预防的心脏死亡是由长QT综合征(LQTS)和未被识别的新生儿先天性心脏病(CHD)所致。这两者都对可避免的死亡率和发病率构成严重风险,但存在有效的治疗方法来预防致命性心律失常,或在死亡或不可逆转的心脏损害发生前进行早期手术矫正。由于心电图(ECG)能够识别LQTS以及一些漏诊的CHD,并且LQTS也与婴儿猝死综合征有关,我们分析了一项全国性新生儿心电图筛查计划的成本效益。我们的主要分析仅聚焦于LQTS;次要分析则聚焦于识别一些CHD的可能性。
采用决策分析方法,构建了“筛查”-“不筛查”策略的决策树。使用马尔可夫过程模拟患者的自然病史或临床病史。为评估模型参数估计中潜在误差的影响,通过将所有基线值上下浮动30%进行蒙特卡洛敏感性分析。主要分析的增量成本效益分析表明,通过筛查计划,每年挽救生命的成本非常低:11,740欧元。挽救一个70岁完整生命的成本将为820,000欧元。即使将模型参数上下浮动30%,每年挽救生命的成本仍在7400欧元至20,400欧元之间。这些数字定义了“极具成本效益”的筛查计划。次要分析提供了更具成本效益的结果。
在一个大型欧洲国家实施的新生儿心电图筛查计划具有成本效益。在出生后第一个月进行的心电图检查将有助于早期识别仍无症状的LQTS婴儿以及一些常规新生儿检查未识别出的可矫正CHD婴儿。适当的治疗将预防婴儿、儿童和年轻人的不必要死亡。