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孕中期基因超声检查用于产前检测唐氏综合征的经济学评估。

An economic evaluation of second-trimester genetic ultrasonography for prenatal detection of down syndrome.

作者信息

Vintzileos A M, Ananth C V, Fisher A J, Smulian J C, Day-Salvatore D, Beazoglou T, Knuppel R A

机构信息

Division of Maternal-Fetal Medicine, The Center for Perinatal Health Initiatives, University of Medicine and Dentistry of New Jersey, New Brunswick, NJ, USA.

出版信息

Am J Obstet Gynecol. 1998 Nov;179(5):1214-9. doi: 10.1016/s0002-9378(98)70134-6.

Abstract

OBJECTIVE

The objective of this study was to perform an economic evaluation of second-trimester genetic ultrasonography for prenatal detection of Down syndrome. More specifically, we sought to determine the following: (1) the diagnostic accuracy requirements (from the cost-benefit point of view) of genetic ultrasonography versus genetic amniocentesis for women at increased risk for fetal Down syndrome and (2) the possible economic impact of second-trimester genetic ultrasonography for the US population on the basis of the ultrasonographic accuracies reported in previously published studies.

STUDY DESIGN

A cost-benefit equation was developed from the hypothesis that the cost of universal genetic amniocentesis of patients at increased risk for carrying a fetus with Down syndrome should be at least equal to the cost of universal genetic ultrasonography with amniocentesis used only for those with abnormal ultrasonographic results. The main components of the equation included the diagnostic accuracy of genetic ultrasonography (sensitivity and specificity for detecting Down syndrome), the costs of the amniocentesis package and genetic ultrasonography, and the lifetime cost of Down syndrome cases not detected by the genetic ultrasonography. After appropriate manipulation of the equation a graph was constructed, representing the balance between sensitivity and false-positive rate of genetic ultrasonography; this was used to examine the accuracy of previously published studies from the cost-benefit point of view. Sensitivity analyses included individual risks for Down syndrome ranging from 1:261 (risk of a 35-year-old at 18 weeks' gestation) to 1:44 (risk of a 44-year-old at 18 weeks' gestation). This economic evaluation was conducted from the societal perspective.

RESULTS

Genetic ultrasonography was found to be economically beneficial only if the overall sensitivity for detecting Down syndrome was >74%. Even then, the cost-benefit ratio depended on the corresponding false-positive rate. Of the 7 published studies that used multiple ultrasonographic markers for genetic ultrasonography, 6 had accuracies compatible with benefits. The required ultrasonographic accuracy (sensitivity and false-positive rate) varied according to the prevalence of Down syndrome in the population tested.

CONCLUSIONS

The cost-benefit ratio of second-trimester genetic ultrasonography depends on its diagnostic accuracy, and it is beneficial only when its overall sensitivity for Down syndrome is >74%.

摘要

目的

本研究的目的是对孕中期基因超声检查用于产前检测唐氏综合征进行经济学评价。更具体地说,我们试图确定以下内容:(1)从成本效益角度来看,基因超声检查相对于基因羊膜穿刺术对胎儿唐氏综合征风险增加的女性的诊断准确性要求;(2)根据先前发表的研究报告的超声检查准确性,孕中期基因超声检查对美国人群可能产生的经济影响。

研究设计

基于以下假设建立了一个成本效益方程,即对携带唐氏综合征胎儿风险增加的患者进行普遍基因羊膜穿刺术的成本应至少等于进行普遍基因超声检查并仅对超声检查结果异常者进行羊膜穿刺术的成本。该方程的主要组成部分包括基因超声检查的诊断准确性(检测唐氏综合征的敏感性和特异性)、羊膜穿刺术套餐和基因超声检查的成本,以及基因超声检查未检测出的唐氏综合征病例的终身成本。对方程进行适当处理后绘制了一张图表,代表基因超声检查的敏感性和假阳性率之间的平衡;这用于从成本效益角度检查先前发表的研究的准确性。敏感性分析包括唐氏综合征的个体风险范围,从1:261(孕18周时35岁女性的风险)到1:44(孕18周时44岁女性的风险)。本经济学评价是从社会角度进行的。

结果

仅当检测唐氏综合征的总体敏感性>74%时,基因超声检查才具有经济效益。即便如此,成本效益比仍取决于相应的假阳性率。在7项使用多种超声标志物进行基因超声检查的已发表研究中,6项研究的准确性与效益相符。所需的超声检查准确性(敏感性和假阳性率)因所检测人群中唐氏综合征的患病率而异。

结论

孕中期基因超声检查的成本效益比取决于其诊断准确性,只有当它对唐氏综合征的总体敏感性>74%时才具有效益。

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