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唐氏综合征的应急筛查——来自FaSTER试验的结果。

Contingent screening for Down syndrome--results from the FaSTER trial.

作者信息

Cuckle Howard S, Malone Fergal D, Wright David, Porter T Flint, Nyberg David A, Comstock Christine H, Saade George R, Berkowitz Richard L, Ferreira Jose C, Dugoff Lorraine, Craigo Sabrina D, Timor Ilan E, Carr Stephen R, Wolfe Honor M, D'Alton Mary E

机构信息

Columbia University, New York, USA.

出版信息

Prenat Diagn. 2008 Feb;28(2):89-94. doi: 10.1002/pd.1913.

Abstract

OBJECTIVE

Comparison of contingent, step-wise and integrated screening policies.

METHODS

Mid-trimester Down syndrome risks were retrospectively calculated from FaSTER trial data. For contingent screening, initial risk was calculated from ultrasound measurement of nuchal translucency (NT), maternal serum pregnancy-associated plasma protein (PAPP)-A and free beta-human chorionic gonadotrophin (hCG) at 11-13 weeks, and classified positive (>1 in 30), borderline (1 in 30-1500) or negative. Borderline risks were recalculated using alpha-fetoprotein, hCG, unconjugated estriol (uE3) and inhibin at 15-18 weeks, and reclassified as positive (>1 in 270) or negative. For step-wise screening, initial negative risks were also recalculated. For integrated screening, a single risk was calculated from NT, PAPP-A and the second trimester markers.

RESULTS

There were 86 Down syndrome and 32,269 unaffected pregancies. The detection rate for contingent screening was 91% and false-positive rate was 4.5%; initial detection rate was 60%, initial false-positive rate was 1.2% and borderline risk was 23%. Step-wise screening had 92% detection rate and 5.1% false-positive rate; integrated screening had 88% and 4.9% respectively.

CONCLUSION

As predicted by modelling, the contingent screening detection rate for a fixed false-positive rate is comparable with step-wise and integrated screening, but substantially reduces the number needing to return for second trimester testing.

摘要

目的

比较偶然、逐步和综合筛查策略。

方法

从FaSTER试验数据中回顾性计算孕中期唐氏综合征风险。对于偶然筛查,初始风险通过在11至13周时超声测量颈部透明带(NT)、母体血清妊娠相关血浆蛋白(PAPP)-A和游离β-人绒毛膜促性腺激素(hCG)来计算,并分类为阳性(>1/30)、临界(1/30 - 1/500)或阴性。临界风险在15至18周时使用甲胎蛋白、hCG、未结合雌三醇(uE3)和抑制素重新计算,并重新分类为阳性(>1/270)或阴性。对于逐步筛查,初始阴性风险也重新计算。对于综合筛查,从NT、PAPP - A和孕中期标志物计算单一风险。

结果

有86例唐氏综合征妊娠和32269例未受影响的妊娠。偶然筛查的检出率为91%,假阳性率为4.5%;初始检出率为60%,初始假阳性率为1.2%,临界风险为23%。逐步筛查的检出率为92%,假阳性率为5.1%;综合筛查分别为88%和4.9%。

结论

如模型预测,对于固定假阳性率,偶然筛查的检出率与逐步和综合筛查相当,但大幅减少了需要返回进行孕中期检测的人数。

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