Birth outcomes among women with congenital neuromuscular disabilities.
Birth outcomes among women with congenital neuromuscular disabilities.
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DOI:
10.1016/j.dhjo.2021.101259
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发表时间:
2022-04
影响因子:
4.5
通讯作者:
Werler MM
中科院分区:
文献类型:
--
作者:
Huezo García M;Parker SE;Petersen JM;Rubenstein E;Werler MM
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 1976–2015), 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 ≥25kg/m2, 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 a SGA infant. These findings highlight disparities faced by women with cNMD and stress the need to provide optimal perinatal and reproductive care.
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