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单纯性妊娠与胎儿生长受限超声检查:一项初步随机临床试验。

Uncomplicated Pregnancies and Ultrasounds for Fetal Growth Restriction: A Pilot Randomized Clinical Trial.

作者信息

Hammad Ibrahim A, Chauhan Suneet P, Mlynarczyk Malgorzata, Rabie Nader, Goodie Chris, Chang Eugene, Magann Everett F, Abuhamad Alfred Z

机构信息

Department of Obstetrics and Gynecology, Eastern Virginia Medical School, Norfolk, Virginia.

Division of Maternal Fetal Medicine, Department of Obstetrics, Gynecology and Reproductive Sciences, UT Health Science Center, Houston, Texas.

出版信息

AJP Rep. 2016 Mar;6(1):e83-90. doi: 10.1055/s-0035-1567857. Epub 2015 Nov 16.

Abstract

Objective The purpose of this multicenter pilot study was to determine the feasibility of randomizing uncomplicated pregnancies (UPs) to have third trimester ultrasonographic exams (USE) versus routine prenatal care (RPNC) to improve the detection of small for gestational age (SGA; birth weight < 10% for GA). Material and Methods At three referral centers, 50 UPs were randomized after gestational diabetes was ruled out. Women needed to screen, consenting, and loss to follow-up was ascertained, as was the detection rate of SGA in the two groups. Results During the study period at the three centers, there were 7,680 births, of which 64% were uncomplicated. Of the 234 women approached for randomization, 36% declined. We recruited 149 women and had follow-up delivery data on 97%. The antenatal detection rate of SGA in the intervention group was 67% (95% confidence intervals 31-91%) and 9% (0.5-43%) in control. Conclusion The pilot study provides feasibility data for a multicenter randomized clinical trial to determine if third trimester USE, compared with RPNC, improves the detection of SGA and composite neonatal morbidity.

摘要

目的 本多中心试点研究的目的是确定将无并发症妊娠(UP)随机分为接受孕晚期超声检查(USE)与常规产前护理(RPNC)以提高小于胎龄儿(SGA;出生体重<GA的10%)检出率的可行性。材料与方法 在三个转诊中心,排除妊娠期糖尿病后,将50例UP随机分组。对女性进行筛查、获取同意并确定失访情况,同时确定两组中SGA的检出率。结果 在研究期间,三个中心共有7680例分娩,其中64%为无并发症分娩。在234名被邀请参与随机分组的女性中,36%拒绝了。我们招募了149名女性,97%有随访分娩数据。干预组中SGA的产前检出率为67%(95%置信区间31 - 91%),对照组为9%(0.5 - 43%)。结论 该试点研究为多中心随机临床试验提供了可行性数据,以确定与RPNC相比,孕晚期USE是否能提高SGA及复合新生儿发病率的检出率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/750d/4737635/5bd17198ad34/10-1055-s-0035-1567857-i150057-1.jpg

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