Cahen-Peretz Adva, Walfisch Asnat, Friger Michael, Sheiner Eyal
Department of Public Health, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Department of Obstetrics and Gynecology, Soroka University Medical Center, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Eur J Obstet Gynecol Reprod Biol. 2017 May;212:20-24. doi: 10.1016/j.ejogrb.2017.02.010. Epub 2017 Mar 3.
To evaluate whether offspring of women with müllerian anomalies are at an increased risk for long-term pediatric morbidity.
A population-based cohort study compared the incidence of long-term (up to the age of 18 years for offspring) hospitalizations due to cardiovascular, endocrine, neurological, hematological, respiratory and urinary morbidity of offspring to mothers diagnosed with uterine anomalies. Deliveries occurred between the years 1991 and 2013 in a tertiary medical center. Multiple pregnancies, unknown gestational age, gestational age of less than 24 weeks, perinatal mortality, and fetuses with congenital malformations were excluded. Kaplan-Meier survival curves were used to compare cumulative morbidity incidence. Survival analysis for clustered data was performed for each major-system pediatric hospitalization.
During the study period 253,808 deliveries met the inclusion criteria; 0.48% (n=1230) of which occurred in women diagnosed with müllerian anomalies. In the Kaplan-Meier survival curve, children born to mothers with müllerian anomalies did not have a significantly different cumulative incidence of any of the long-term pediatric morbidities, compared with the comparison group. In the multivariable survival analysis for clustered data, after adjustment of maternal clusters, maternal age, gestational age and birthweight, müllerian anomalies did not exhibit an independent association with long-term morbidities of the offspring.
Müllerian anomalies do not appear to have an independent impact on long-term morbidity of the offspring.
评估患有苗勒氏管异常的女性的后代发生长期儿科疾病的风险是否增加。
一项基于人群的队列研究,比较了被诊断为子宫异常的母亲的后代因心血管、内分泌、神经、血液、呼吸和泌尿系统疾病导致的长期(后代至18岁)住院发生率。分娩发生在1991年至2013年期间的一家三级医疗中心。排除多胎妊娠、孕周不明、孕周小于24周、围产期死亡率以及患有先天性畸形的胎儿。采用Kaplan-Meier生存曲线比较累积疾病发生率。对每个主要系统的儿科住院情况进行聚类数据的生存分析。
在研究期间,253,808例分娩符合纳入标准;其中0.48%(n = 1230)发生在被诊断为苗勒氏管异常的女性中。在Kaplan-Meier生存曲线中,与对照组相比,患有苗勒氏管异常的母亲所生子女的任何长期儿科疾病的累积发生率均无显著差异。在聚类数据的多变量生存分析中,在调整了母亲聚类、母亲年龄、孕周和出生体重后,苗勒氏管异常与后代的长期疾病无独立关联。
苗勒氏管异常似乎对后代的长期疾病没有独立影响。