Department of Epidemiology, Boston University School of Public Health, Boston, MA, 02118, USA.
Department of Epidemiology, Boston University School of Public Health, Boston, MA, 02118, USA.
Disabil Health J. 2022 Apr;15(2):101259. doi: 10.1016/j.dhjo.2021.101259. Epub 2021 Dec 1.
Women with disabilities are at an increased risk for adverse birth outcomes; however, research among women with congenital neuromuscular disabilities (cNMD) is limited.
To describe characteristics and compare birth outcomes among women with and without cNMD.
Data were from the Slone Birth Defects Study (case-control, conducted from 1976 to 2015), which collected information on demographic, reproductive, and lifestyle characteristics. cNMD included spina bifida, cerebral palsy, muscular dystrophy, contractures, or arthrogryposis and were identified by participant report. Those with cNMD were matched to participants without cNMD by interview year and study site. We use modified Poisson regression to estimate relative risks (RR) for low birthweight, macrosomia, preterm birth, and small/large-for-gestational age (SGA/LGA). Given the case-control design and overrepresentation of infants with congenital anomalies, data were weighted to reflect a 3% national prevalence of infants with congenital anomalies.
Women with cNMD (n = 125) were more likely to be white, nulliparous, have a cesarean section, have an unplanned pregnancy, report a pre-pregnancy BMI ≥25 kg/m, smoke during pregnancy, and report genitourinary infections. Women with cNMD had infants with shorter gestational length (mean difference: -7.44 days, 95% CI: -13.94, -0.95) compared to women without cNMD. cNMD was associated with higher risk of preterm birth (RR = 3.98, 95% CI: 1.33, 11.95) and SGA (RR = 2.14, 95% CI: 0.74, 6.15).
Women with cNMD were more likely to deliver preterm and have an SGA infant. These findings highlight disparities faced by women with cNMD and stress the need to provide optimal perinatal and reproductive care.
残疾女性不良生育结局的风险增加;然而,先天性神经肌肉障碍(cNMD)女性的相关研究有限。
描述 cNMD 女性的特征,并比较其与无 cNMD 女性的生育结局。
数据来自斯隆出生缺陷研究(病例对照,1976 年至 2015 年开展),收集了人口统计学、生殖和生活方式特征信息。cNMD 包括脊柱裂、脑瘫、肌肉营养不良、挛缩或关节挛缩症和先天性多发性关节挛缩症,通过参与者报告进行识别。cNMD 女性与无 cNMD 女性按访谈年份和研究地点进行匹配。我们使用修正泊松回归估计低出生体重、巨大儿、早产和小于胎龄儿/大于胎龄儿(SGA/LGA)的相对风险(RR)。鉴于病例对照设计和先天性异常婴儿的比例过高,数据经过加权处理,以反映全国 3%的先天性异常婴儿患病率。
cNMD 女性(n=125)更可能是白人、初产妇、行剖宫产、非计划妊娠、报告孕前 BMI≥25kg/m²、孕期吸烟和报告有泌尿生殖系统感染。与无 cNMD 女性相比,cNMD 女性的婴儿胎龄更短(平均差异:-7.44 天,95%置信区间:-13.94,-0.95)。cNMD 与早产风险增加相关(RR=3.98,95%置信区间:1.33,11.95)和 SGA(RR=2.14,95%置信区间:0.74,6.15)。
cNMD 女性更有可能早产并产下 SGA 婴儿。这些发现突显了 cNMD 女性面临的差异,并强调了提供最佳围产期和生殖护理的必要性。