The association between early membrane rupture, latency, clinical chorioamnionitis, neonatal infection, and adverse perinatal outcomes in twin pregnancies complicated by preterm prelabour rupture of membranes

被引:1
|
作者
von Dadelszen, P
Kives, S
Delisle, MF
Wilson, RD
Joy, R
Ainsworth, L
Al Kharusi, L
Oskamp, M
Barrett, JFR
Ryan, G
Farine, D
Seaward, RGR
机构
[1] Univ British Columbia, Dept Obstet & Gynaecol, Div Maternal Fetal Med, Vancouver, BC, Canada
[2] Univ Toronto, Dept Obstet & Gynaecol, Div Maternal Fetal Med, Toronto, ON, Canada
[3] British Columbia Res Inst Childrens & Womens Hlth, Clin Res Support Unit, Vancouver, BC, Canada
来源
TWIN RESEARCH | 2003年 / 6卷 / 04期
关键词
D O I
10.1375/136905203322296575
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The objective of this study was to evaluate associations between adverse outcomes in twin pregnancies and preterm prelabour rupture of membranes (PPROM). A chart review of 246 consecutive twin pregnancies with confirmed PPROM was conducted. Regression analysis (beta [natural log of the odds ratio] and odds ratio [OR]) was performed to identify independent predictors. Two hundred and forty-six twin pregnancies, 492 liveborns, and 20 neonatal deaths. Mean (SD) PPROM gestational age (GA): 31.3 (3.8) wk; delivery GA: 32.0 (3.3) wk. PPROM < 30wk was associated with increased parity (OR: 2.66), and log (admission leukocyte count) (OR- 9 99) Shortened latency was associated with PPROM GA (beta = -0.17; and chorioamnionitis (beta = 0.95). Neonatal sepsis was predicted by lower delivery GA (OR: 2.04). Adverse perinatal outcomes were protected against by older GA at PPROM (OR 0.53) and shortened latency (OR 0.73). It was concluded that increased leukocytosis and parity implies an infectious aetiology in earlier PPROM. Increased risk for neonatal sepsis at earlier delivery GA is consistent with gestation-dependent fetal immunocompetence. Early PPROM and long latencies were associated with increased adverse perinatal outcomes.
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收藏
页码:257 / 262
页数:6
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