Fetal and Maternal Factors Predictive of Primary Cesarean Delivery at Term in a Low-Risk Population: NICHD Fetal Growth Studies-Singletons

被引:0
|
作者
Mateus, Julio [1 ]
Stevens, Danielle R. [2 ,11 ]
Grantz, Katherine L. [2 ]
Zhang, Cuilin [3 ,4 ,5 ]
Grewal, Jagteshwar [2 ]
Grobman, William A. [6 ]
Owen, John [7 ]
Sciscione, Anthony C. [8 ]
Wapner, Ronald J. [9 ]
Skupski, Daniel [10 ]
Chien, Edward [12 ]
Wing, Deborah A. [13 ,14 ]
Ranzini, Angela C. [15 ,16 ]
Nageotte, Michael P. [17 ]
Newman, Roger B. [18 ]
机构
[1] Atrium Hlth, Div Maternal Fetal Med, Charlotte, NC USA
[2] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Epidemiol Branch, Div Intramural Populat Hlth Res, NIH, Bethesda, MD USA
[3] Natl Univ Singapore, Global Ctr Asian Womens Hlth, Yong Loo Lin Sch Med, Singapore, Singapore
[4] Natl Univ Singapore, Bia Echo Asia Ctr Reprod Longev & Equal ACRLE, Yong Loo Lin Sch Med, Singapore, Singapore
[5] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Obstet & Gynecol, Singapore, Singapore
[6] Ohio State Univ, Dept Obstet & Gynecol, Div Maternal Fetal Med, Coll Med, Columbus, OH USA
[7] Univ Alabama Birmingham, Dept Obstet & Gynecol, Div Maternal Fetal Med, Ctr Womens Reprod Hlth, Birmingham, AL USA
[8] Christiana Hosp, Div Maternal Fetal Med, Dept Obstet & Gynecol, Newark, DE USA
[9] Columbia Univ, Irving Med Ctr, Dept Obstet & Gynecol, Div Maternal Fetal Med, New York, NY USA
[10] New York Presbyterian Queens, Div Maternal Fetal Med, Dept Obstet & Gynecol, Flushing, NY USA
[11] Weill Cornell Med, New York, NY USA
[12] Cleveland Clin Hlth Syst, Dept Obstet & Gynecol, Div Maternal Fetal Med, Cleveland, OH USA
[13] Univ Calif Irvine, Irvine Med Ctr, Dept Obstet & Gynecol, Div Maternal Fetal Med, Orange, CA USA
[14] Miller Childrens Hosp Irvine, Long Beach Mem Med Ctr, Irvine, CA USA
[15] Metrohlth Syst, Dept Obstet & Gynecol, Cleveland, OH USA
[16] Case Western Reserve Univ, Metrohlth Med Ctr, Cleveland, OH USA
[17] Miller Childrens & Womens Hosp, Long Beach, CA USA
[18] Med Univ South Carolina, Div Maternal Fetal Med, Charleston, SC USA
基金
美国国家卫生研究院;
关键词
estimated fetal weight; fetal biometric parameters; maternal factors; primary cesarean delivery; prediction models; NULLIPAROUS WOMEN; HEALTH; PREVENTION; WEIGHT; MODEL; AGE;
D O I
10.1055/s-0044-1788274
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective This study aimed to examine associations of fetal biometric and amniotic fluid measures with intrapartum primary cesarean delivery (PCD) and develop prediction models for PCD based on ultrasound parameters and maternal factors. Study Design Secondary analysis of the National Institute of the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) Fetal Growth Studies-singleton cohort (2009-2013) including patients with uncomplicated pregnancies and intent to deliver vaginally at >= 37 (0/7) weeks. The estimated fetal weight, individual biometric parameters, fetal asymmetry measurements, and amniotic fluid single deepest vertical pocket assessed at the final scan (mean 37.5 +/- 1.9 weeks) were categorized as <10th, 10th to 90th (reference), and >90th percentiles. Logistic regression analyses examined the association between the ultrasound measures and PCD. Fetal and maternal SuperLearner prediction algorithms were constructed for the full and nulliparous cohorts. Results Of the 1,668 patients analyzed, 249 (14.9%) had PCD. The fetal head circumference, occipital-frontal diameter, and transverse abdominal diameter >90th percentile (adjusted odds ratio [aOR] = 2.50, 95% confidence interval [95% CI]: 1.39, 4.51; aOR = 1.86, 95% CI: 1.02, 3.40; and aOR = 2.13, 95% CI: 1.16, 3.89, respectively) were associated with PCD. The fetal model demonstrated poor ability to predict PCD in the full cohort and in nulliparous patients (area under the receiver-operating characteristic curve [AUC] = 0.56, 95% CI: 0.52, 0.61; and AUC = 0.54, 95% CI: 0.49, 0.60, respectively). Conversely, the maternal model had better predictive capability overall (AUC = 0.79, 95% CI: 0.75, 0.82) and in the nulliparous subgroup (AUC = 0.72, 95% CI: 0.67, 0.77). Models combining maternal/fetal factors performed similarly to the maternal model (AUC = 0.78, 95% CI: 0.75, 0.82 in full cohort, and AUC = 0.71, 95% CI: 0.66, 0.76 in nulliparas). Conclusion Although a few fetal biometric parameters were associated with PCD, the fetal prediction model had low performance. In contrast, the maternal model had a fair-to-good ability to predict PCD. Key Points Fetal HC >90th percentile was associated with cesarean delivery. Fetal parameters did not effectively predict PCD. Maternal factors were more predictive of PCD. Maternal/fetal and maternal models performed similarly. Prediction models had lower performance in nulliparas. d lower performance in nulliparas.
引用
收藏
页码:256 / 267
页数:12
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