TY - JOUR
T1 - 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
AU - Von Dadelszen, Peter
AU - Kives, Sari
AU - Delisle, Marie France
AU - Wilson, R. Douglas
AU - Joy, Ruth
AU - Ainsworth, Laurie
AU - Al Kharusi, Lamya
AU - Oskamp, Marilynne
AU - Barrett, Jon F.R.
AU - Ryan, Greg
AU - Farine, Dan
AU - Seaward, P. Gareth R.
N1 - Funding Information:
Supported by the MFM group, Mt Sinai Hospital, Toronto (PvD MFM fellowship salary), the BC Research Institute for Children’s and Women’s Health and BC Women’s Hospital and Health Centre Foundation (PvD clinician scientist salary and establishment award), and the BC Ministry of Health (M-FD fellowship salary). We wish to thank the Medical Records Departments of all three hospitals for their assistance with this study.
PY - 2003/8
Y1 - 2003/8
N2 - 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 (β [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 (β = -0.17) and chorioamnionitis (β = 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.
AB - 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 (β [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 (β = -0.17) and chorioamnionitis (β = 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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U2 - 10.1375/136905203322296575
DO - 10.1375/136905203322296575
M3 - Article
C2 - 14511428
AN - SCOPUS:0041878334
SN - 1832-4274
VL - 6
SP - 257
EP - 262
JO - Twin Research and Human Genetics
JF - Twin Research and Human Genetics
IS - 4
ER -