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孕中期唐氏综合征联合生化与超声筛查

Combined second-trimester biochemical and ultrasound screening for Down syndrome.

作者信息

Benn Peter A, Kaminsky Lillian M, Ying Jun, Borgida Adam F, Egan James F X

机构信息

Division of Human Genetics, Department of Pediatrics, University of Connecticut Health Center, Farmington 06030, USA.

出版信息

Obstet Gynecol. 2002 Dec;100(6):1168-76. doi: 10.1016/s0029-7844(02)02276-7.

Abstract

OBJECTIVE

To evaluate the efficacy of a Down syndrome screening protocol that combines second-trimester maternal serum analytes and the continuous ultrasound measures of nuchal fold thickness and proximal long bone length.

METHODS

Ultrasound measurements of nuchal fold, femur length, and humerus length were reviewed for 72 second-trimester Down syndrome and 7063 unaffected fetuses. Derived statistical variables for these parameters were entered into a multivariable Gaussian model together with the statistical variables used in the "quad" test (maternal serum alpha-fetoprotein, unconjugated estriol, human chorionic gonadotropin, and inhibin A). Maternal age-specific sensitivities, false-positive rates, and positive predictive values were generated together with receiver operating characteristic curves. Overall efficacy of ultrasound screening alone, the quad test, and the combination of the ultrasound and quad test were compared using a 1:270 second-trimester risk cutoff applied to 1999 US births.

RESULTS

Using ultrasound, a sensitivity of 79.9% and false-positive rate of 6.7% may be achieved (positive predictive value: 1 in 42). The quad test has a sensitivity of 81.5% and false-positive rate of 6.9% (positive predictive value: 1 in 42). The combination of the quad test with nuchal fold and long bone measurements may achieve 90% sensitivity and a 3.1% false-positive rate (positive predictive value: 1 in 18).

CONCLUSION

Combining second-trimester serum testing and fetal biometry is a feasible approach to Down syndrome screening, compatible with current obstetric practice. This modality is substantially more effective than either serum screening or ultrasound alone. Efficacy may be comparable to that reported for combined first- and second-trimester (integrated) screening.

摘要

目的

评估一种唐氏综合征筛查方案的有效性,该方案结合了孕中期母体血清分析物以及颈部褶皱厚度和近端长骨长度的连续超声测量。

方法

回顾了72例孕中期唐氏综合征胎儿和7063例未受影响胎儿的颈部褶皱、股骨长度和肱骨长度的超声测量结果。将这些参数的派生统计变量与“四联”试验(母体血清甲胎蛋白、未结合雌三醇、人绒毛膜促性腺激素和抑制素A)中使用的统计变量一起输入多变量高斯模型。生成了特定孕龄的母体敏感性、假阳性率和阳性预测值以及受试者工作特征曲线。使用适用于1999年美国出生人口的1:270孕中期风险临界值,比较了单独超声筛查、四联试验以及超声与四联试验联合筛查的总体有效性。

结果

使用超声检查,敏感性可达79.9%,假阳性率为6.7%(阳性预测值:42分之一)。四联试验的敏感性为81.5%,假阳性率为6.9%(阳性预测值:42分之一)。四联试验与颈部褶皱和长骨测量相结合,敏感性可达90%,假阳性率为3.1%(阳性预测值:18分之一)。

结论

孕中期血清检测与胎儿生物测量相结合是唐氏综合征筛查的一种可行方法,与当前产科实践相兼容。这种方法比单独的血清筛查或超声检查有效得多。其有效性可能与报道的孕早期和孕中期联合(综合)筛查相当。

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