Seror V, Leruez-Ville M, Ӧzek A, Ville Y
Aix Marseille Univ, IRD, AP-HM, SSA, VITROME, Marseille, France.
Institut Hospitalier Universitaire (IHU) - Méditerranée Infection, Marseille, France.
BJOG. 2022 Jan;129(2):301-312. doi: 10.1111/1471-0528.16966. Epub 2021 Nov 9.
To assess the cost-effectiveness of prenatal detection of congenital cytomegalovirus (cCMV) following maternal primary infection in the first trimester within standard pregnancy follow-up or involving population-based screening (serological testing at 7 and 12 weeks of gestation), with or without secondary prevention (valaciclovir) in maternal CMV primary infection.
Cost-effectiveness study from the perspective of the French national health insurance system.
Cost-effectiveness based on previously published probability estimates and associated plausible ranges hypothetical population of 1,000,000 pregnant women.
Hypothetical population of 1,000,000 pregnant women.
Cost-effectiveness of detecting fetal cCMV in terms of the total direct medical costs involved and associated expected outcomes.
Detection rates and clinical outcomes at birth.
Moving to a population-based approach for targeting fetal CMV infections would generate high monetary and organizational costs while increasing detection rates from 15% to 94%. This resource allocation would help implementing horizontal equity according to which individuals with similar medical needs should be treated equally. Secondary prevention with valaciclovir had a significant effect on maternal-fetal CMV transmission and clinical outcomes in newborns, with a 58% decrease of severely infected newborns for a 3.5% additional total costs. Accounting for women decision-making (amniocentesis uptake and termination of pregnancy in severe cases) did not impact the cost-effectiveness results.
These findings could fuel thinking on the opportunity of developing clinical guidelines to rule identification of cCMV infection and administration of in-utero treatment. These findings could fuel the development of clinical guidelines on the identification of congenital CMV infection and the administration of treatment in utero.
CMV serological screening followed by valaciclovir prevention may prevent 58% to 71% of severe cCMV cases for 38 € per pregnancy.
评估在标准孕期随访中或采用基于人群的筛查(妊娠7周和12周时进行血清学检测)的情况下,孕早期孕妇初次感染先天性巨细胞病毒(cCMV)后进行产前检测的成本效益,孕妇CMV初次感染时有无二级预防(伐昔洛韦)。
从法国国家医疗保险系统的角度进行成本效益研究。
基于先前发表的概率估计和相关合理范围,对100万孕妇的假设人群进行成本效益分析。
100万孕妇的假设人群。
根据所涉及的总直接医疗成本和相关预期结果,评估检测胎儿cCMV的成本效益。
出生时的检测率和临床结局。
转向基于人群的方法来检测胎儿CMV感染会产生高昂的资金和组织成本,同时将检测率从15%提高到94%。这种资源分配将有助于实现横向公平,即有相似医疗需求的个体应得到平等对待。伐昔洛韦二级预防对母婴CMV传播和新生儿临床结局有显著影响,严重感染新生儿减少58%,总成本增加3.5%。考虑女性的决策(羊膜穿刺术的接受情况和严重情况下的终止妊娠)并不影响成本效益结果。
这些发现可能促使人们思考制定临床指南以规范cCMV感染的识别和宫内治疗管理的机会。这些发现可能推动先天性CMV感染识别和宫内治疗管理临床指南的制定。
CMV血清学筛查后采用伐昔洛韦预防,每次妊娠花费38欧元,可预防58%至71%的严重cCMV病例。