Tennant Peter W G, Glinianaia Svetlana V, Wellesley Diana, Draper Elizabeth S, Kurinczuk Jenny J, Tonks Ann M, Tucker David F, Wreyford Ben, Rankin Judith
Institute of Health & Society, Newcastle University, Newcastle upon Tyne, UK.
Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, UK.
Arch Dis Child Fetal Neonatal Ed. 2014 Sep;99(5):F413-8. doi: 10.1136/archdischild-2014-306027. Epub 2014 May 28.
Partial urorectal septum malformation (pURSM) sequence (or 'persistent cloaca') is a rare congenital anomaly characterised by a joining of the urethral, anal, and genital openings into a single common channel. This study describes the epidemiology of pURSM sequence in England and Wales including prevalence, additional anomalies, and pregnancy outcomes.
All cases of pURSM sequence prospectively notified to seven congenital anomaly registers in England and Wales during 1985-2010, whether delivered as live births, spontaneous fetal deaths (≥20 weeks' gestation), or elective terminations of pregnancy for fetal anomaly (TOPFA, any gestation), formed this population-based cohort. The risks of spontaneous fetal and infant death were examined by Kaplan-Meier analysis. Differences in prevalence over time, and between regions, were examined by multilevel Poisson regression.
117 cases were recorded among 4,251,241 total births. Six (5%) pregnancies resulted in spontaneous fetal deaths, 53 (45%) in TOPFA, and 58 (50%) in live births. The prevalence was 2.8 (95% CI 2.3 to 3.4) per 100,000 total births, increasing significantly over time (p=0.002) and differing significantly between regions (p=0.005). 77 cases (66%) had at least one additional major congenital anomaly outside the perineum, including 67 (57%) renal, 29 (25%) musculoskeletal, 26 (23%) digestive system, and 24 (21%) cardiovascular anomalies. The risks of spontaneous fetal and infant death were estimated as 8.9% (95% CI 4.1 to 18.8) and 26.3% (95% CI 15.1 to 43.4) respectively.
This is the largest study of the epidemiology of pURSM sequence. The information will be valuable for families and health professionals whenever a case of pURSM sequence is diagnosed.
部分尿直肠隔畸形序列征(pURSM,即“永存泄殖腔”)是一种罕见的先天性异常,其特征为尿道、肛门和生殖孔融合成一个单一的共同通道。本研究描述了英格兰和威尔士pURSM序列征的流行病学情况,包括患病率、其他伴随异常以及妊娠结局。
1985年至2010年间前瞻性地向英格兰和威尔士的七个先天性异常登记处报告的所有pURSM序列征病例,无论其分娩方式为活产、自然流产(妊娠≥20周)或因胎儿异常而进行的选择性妊娠终止(TOPFA,任何孕周),均构成了这个基于人群的队列。通过Kaplan-Meier分析来研究自然流产和婴儿死亡的风险。通过多水平泊松回归分析来研究患病率随时间以及地区之间的差异。
在4251241例总出生数中记录了117例病例。6例(5%)妊娠导致自然流产,53例(45%)为TOPFA,58例(50%)为活产。每10万例总出生数中的患病率为2.8(95%可信区间2.3至3.4),随时间显著增加(p = 0.002),且地区间差异显著(p = 0.005)。77例(66%)病例在会阴外至少有一项其他主要先天性异常,包括67例(57%)肾脏异常、29例(25%)肌肉骨骼异常、26例(23%)消化系统异常和24例(21%)心血管异常。自然流产和婴儿死亡的风险估计分别为8.9%(95%可信区间4.1至18.8)和26.3%(95%可信区间15.1至43.4)。
这是关于pURSM序列征流行病学的最大规模研究。每当诊断出pURSM序列征病例时,这些信息对家庭和卫生专业人员都将是有价值的。