Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Weill Cornell Medical College, New York, NY, USA.
J Ultrasound Med. 2013 Sep;32(9):1581-6. doi: 10.7863/ultra.32.9.1581.
The purpose of this study was to evaluate whether the use of customized fetal reference standards improves the prenatal detection of intrauterine growth restriction.
We conducted a retrospective cohort study. Singleton pregnancies with a diagnosis of a small-for-gestational-age (SGA) fetus based on the in utero reference standard of Hadlock et al (Am J Obstet Gynecol 1985; 151:333-337; Radiology 1991; 181:129-133) were identified from our ultrasound database, and customized percentiles were calculated by adjusting for maternal height, weight, ethnicity, parity, and sex.
A total of 300 pregnancies were identified as SGA by both the Hadlock and customized standards, and 60 were identified as SGA by the Hadlock standard only. Small-for-gestational age pregnancies identified by the Hadlock standard only were significantly less likely to have any abnormal sonographic findings, including an elevated head to abdominal circumference ratio (8.3% versus 21.7%; P = .019), oligohydramnios (3.3% versus 13%; P = .027), abnormal umbilical artery Doppler findings (3.4% versus 14.7%; P = .017), maternal hypertensive disease (3.3% versus 12.7%; P = .041), and preterm delivery (6.7% versus 27.7%; P < .001). There was no difference in neonatal intensive care unit admission rates; however, neonates identified as SGA by the Hadlock standard only were less likely to have a postnatal diagnosis of SGA (9.1% versus 78.3%; P < .001) and had a shorter neonatal intensive care unit stay (median, 2 versus 8 days; P < .001).
Using a customized standard, we have identified a population of pregnancies with low rates of antenatal complications and sonographic findings associated with pathologic growth. Adoption of customized standards to improve our antenatal detection rate of intrauterine growth restriction may decrease the need for intervention in healthy but constitutionally small fetuses.
本研究旨在评估使用定制胎儿参考标准是否能提高产前对宫内生长受限的检测率。
我们进行了一项回顾性队列研究。从我们的超声数据库中确定了基于 Hadlock 等(Am J Obstet Gynecol 1985;151:333-337;Radiology 1991;181:129-133)宫内参考标准诊断为胎儿生长受限(small for gestational age,SGA)的单胎妊娠,并通过调整母亲的身高、体重、种族、产次和性别计算定制百分位数。
Hadlock 和定制标准均将 300 例妊娠诊断为 SGA,Hadlock 标准仅将 60 例妊娠诊断为 SGA。Hadlock 标准仅诊断为 SGA 的妊娠发生任何异常超声表现的可能性显著降低,包括头围与腹围比值升高(8.3%对 21.7%;P =.019)、羊水过少(3.3%对 13%;P =.027)、脐动脉多普勒异常(3.4%对 14.7%;P =.017)、母体高血压疾病(3.3%对 12.7%;P =.041)和早产(6.7%对 27.7%;P <.001)。新生儿重症监护病房(neonatal intensive care unit,NICU)入院率无差异;然而,Hadlock 标准仅诊断为 SGA 的新生儿更不可能在产后被诊断为 SGA(9.1%对 78.3%;P <.001),且 NICU 住院时间更短(中位数 2 天对 8 天;P <.001)。
使用定制标准,我们确定了一组产前并发症发生率低且与病理性生长相关的超声表现发生率低的妊娠。采用定制标准来提高我们产前对宫内生长受限的检出率,可能会减少对健康但先天较小胎儿进行干预的需求。