Vintzileos A M, Ananth C V, Fisher A J, Smulian J C, Day-Salvatore D, Beazoglou T
Department of Obstetrics, Gynecology and Reproductive Sciences, University of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School/St. Peter's Medical Center, New Brunswick 08903, USA.
Obstet Gynecol. 1998 Apr;91(4):535-9. doi: 10.1016/s0029-7844(98)00036-2.
To determine 1) the diagnostic accuracy requirements of first-trimester genetic sonography from the cost-benefit point of view and 2) the economic impact of first-trimester genetic sonography for the United States on the basis of the accuracy of previously published studies.
A cost-benefit equation was developed on the basis of the hypothesis that the cost of chorionic villus sampling (CVS) in pregnant women with advanced maternal age (at least 35 years old) should be at least equal to the cost of genetic sonography with CVS used only for those with abnormal ultrasound results. The components of the equation included the diagnostic accuracy of genetic ultrasound (sensitivity and specificity for detecting Down syndrome), the costs of the CVS package and genetic ultrasound, and the lifetime cost of Down syndrome cases.
First-trimester genetic sonography was found to be beneficial if the overall sensitivity for detecting Down syndrome was greater than 70%, and even then, the cost-benefit ratio depended on the corresponding false-positive rate. The required minimum ultrasound sensitivity varied according to the maternal age-specific prevalence of Down syndrome and ranged between 40% (for women 35 years old) to 96% (for women 44 years old). Of eight published cohorts using nuchal translucency thickness for genetic sonography, five had accuracies of genetic ultrasound compatible with net benefits.
The benefits of first-trimester genetic sonography depend on its diagnostic accuracy. First-trimester genetic sonography has the potential for annual savings of 22 million dollars in the United States.
1)从成本效益角度确定孕早期基因超声检查的诊断准确性要求;2)根据先前发表研究的准确性,确定孕早期基因超声检查对美国的经济影响。
基于以下假设建立了一个成本效益方程,即高龄孕妇(至少35岁)的绒毛取样(CVS)成本应至少等于仅对超声检查结果异常者使用CVS进行基因超声检查的成本。该方程的组成部分包括基因超声的诊断准确性(检测唐氏综合征的敏感性和特异性)、CVS套餐和基因超声检查的成本,以及唐氏综合征病例的终生成本。
如果检测唐氏综合征的总体敏感性大于70%,则发现孕早期基因超声检查是有益的,即便如此,成本效益比仍取决于相应的假阳性率。所需的最低超声敏感性根据唐氏综合征的特定产妇年龄患病率而有所不同,范围在40%(35岁女性)至96%(44岁女性)之间。在八项发表的使用颈部半透明厚度进行基因超声检查的队列研究中,五项研究的基因超声检查准确性与净效益相符。
孕早期基因超声检查的益处取决于其诊断准确性。在美国,孕早期基因超声检查每年有可能节省2200万美元。