TY - JOUR
T1 - Preterm prelabor rupture of membranes and outcome of very-low-birth-weight infants in the German Neonatal Network
AU - The German Neonatal Network (GNN)
AU - Hanke, Kathrin
AU - Hartz, Annika
AU - Manz, Maike
AU - Bendiks, Meike
AU - Heitmann, Friedhelm
AU - Orlikowsky, Thorsten
AU - Müller, Andreas
AU - Olbertz, Dirk
AU - Kühn, Thomas
AU - Siegel, Jens
AU - Von Der Wense, Axel
AU - Wieg, Christian
AU - Kribs, Angela
AU - Stein, Anja
AU - Pagel, Julia
AU - Herting, Egbert
AU - Göpel, Wolfgang
AU - Härtel, Christoph
AU - Avenarius, Stefan
AU - Bockenholt, Kai
AU - Bohnhorst, Bettina
AU - Dördelmann, Michael
AU - Ehlers, Silke
AU - Gebauer, Corinna
AU - Gerleve, Hubert
AU - Gortner, Ludwig
AU - Groneck, Peter
AU - Hillebrand, Georg
AU - Hoehn, Thomas
AU - Hubert, Mechthild
AU - Hummler, Helmut
AU - Jenke, Andreas
AU - Jensen, Reinhard
AU - Kannt, Olaf
AU - Küster, Helmut
AU - Laux, Reinhard
AU - Lieser, Ursula
AU - Mögel, Michael
AU - Möller, Jens
AU - Müller, Dirk
AU - Reese, Jochen
AU - Roll, Claudia
AU - Schaible, Thomas
AU - Seeliger, Stefan
AU - Segerer, Hugo
AU - Teig, Norbert
AU - Weller, Ursula
AU - Vochem, Matthias
AU - Wintgens, Jürgen
N1 - Publisher Copyright:
© 2015 Hanke et al.
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2015/4/9
Y1 - 2015/4/9
N2 - Objective: It was the aim of our study to evaluate the independent effect of preterm prelabor rupture of membranes (PPROM) as a cause of preterm delivery on mortality during primary hospital stay and significant morbidities in very-low-birth-weight (VLBW) infants < 32 weeks of gestation. Design: Observational, epidemiological study design. Setting: Population-based cohort, German Neonatal Network (GNN). Population: 6102 VLBW infants were enrolled in GNN from 2009-2012, n=4120 fulfilled criteria for primary analysis (< 32 gestational weeks, no pre-eclampsia, HELLP (highly elevated liver enzymes and low platelets syndrome) or placental abruption as cause of preterm birth). Methods: Multivariable logistic regression analyses included PPROM as potential risk factors for adverse outcomes and well established items such as gestational age in weeks, birth weight, antenatal steroids, center, inborn delivery, multiple birth, gender and being small-for-gestational-age. Results: PPROM as cause of preterm delivery had no independent effect on the risk of early-onset sepsis, clinical sepsis and blood-culture proven sepsis, while gestational age proved to be the most important contributor to sepsis risk. The diagnosis of PPROM was associated with an increased risk for bronchopulmonary dysplasia (BPD; OR: 1.25, 95% CI: 1.02-1.55, p=0.03) but not with other major outcomes. Conclusions: The diagnosis of PPROM per se is not associated with adverse outcome in VLBW infants < 32 weeks apart from a moderately increased risk for BPD. Randomized controlled trials with primary neonatal outcomes are needed to determine which subgroup of VLBW infants benefit from expectant or intentional management of PPROM.
AB - Objective: It was the aim of our study to evaluate the independent effect of preterm prelabor rupture of membranes (PPROM) as a cause of preterm delivery on mortality during primary hospital stay and significant morbidities in very-low-birth-weight (VLBW) infants < 32 weeks of gestation. Design: Observational, epidemiological study design. Setting: Population-based cohort, German Neonatal Network (GNN). Population: 6102 VLBW infants were enrolled in GNN from 2009-2012, n=4120 fulfilled criteria for primary analysis (< 32 gestational weeks, no pre-eclampsia, HELLP (highly elevated liver enzymes and low platelets syndrome) or placental abruption as cause of preterm birth). Methods: Multivariable logistic regression analyses included PPROM as potential risk factors for adverse outcomes and well established items such as gestational age in weeks, birth weight, antenatal steroids, center, inborn delivery, multiple birth, gender and being small-for-gestational-age. Results: PPROM as cause of preterm delivery had no independent effect on the risk of early-onset sepsis, clinical sepsis and blood-culture proven sepsis, while gestational age proved to be the most important contributor to sepsis risk. The diagnosis of PPROM was associated with an increased risk for bronchopulmonary dysplasia (BPD; OR: 1.25, 95% CI: 1.02-1.55, p=0.03) but not with other major outcomes. Conclusions: The diagnosis of PPROM per se is not associated with adverse outcome in VLBW infants < 32 weeks apart from a moderately increased risk for BPD. Randomized controlled trials with primary neonatal outcomes are needed to determine which subgroup of VLBW infants benefit from expectant or intentional management of PPROM.
UR - http://www.scopus.com/inward/record.url?scp=84928919809&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0122564
DO - 10.1371/journal.pone.0122564
M3 - Journal articles
C2 - 25856083
AN - SCOPUS:84928919809
VL - 10
JO - PLoS ONE
JF - PLoS ONE
IS - 4
M1 - e0122564
ER -