TY - JOUR
T1 - Fetal and neonatal outcomes after term and preterm delivery following betamethasone administration
AU - Braun, T.
AU - Sloboda, D.M.
AU - Tutschek, B.
AU - Harder, T.
AU - Challis, John
AU - Dudenhausen, J.W.
AU - Plagemann, A.
AU - Henrich, W.
PY - 2015
Y1 - 2015
N2 - © 2015 Published by Elsevier Ireland Ltd. on behalf of International Federation of Gynecology and Obstetrics. Objective To determine the effects of betamethasone on fetal growth and neonatal outcomes. Methods A retrospective cohort study was performed of deliveries that occurred at Charité University Hospital Berlin, Germany, between January 1996 and December 2008. The betamethasone group included women with preterm labor and symptomatic contractions, cervical insufficiency, preterm premature rupture of membranes, or vaginal bleeding. Women in the control group were matched for gestational age at time of delivery and had not received betamethasone. Fetal growth changes and neonatal anthropometry were compared. Results Among 1799 newborns in the betamethasone group and 42 240 in the control group, betamethasone was associated with significantly lower birth weight (154 g lower on average) after adjusting for confounders (e.g. hypertension, smoking, and maternal weight), sex, and gestational age at delivery (P <0.05). The higher the dose, the greater the difference in mean birth weight versus controls in births before 34+ 0 weeks (≤ 16 mg - 444 g; 24 mg - 523 g; > 24 mg - 811 g), without a detectable improvement in neonatal morbidity or mortality. There was a dose-dependent decline in expected fetal weight gain as estimated by serial ultrasonography examinations 6-8 weeks after betamethasone administration (P <0.05). Conclusion Betamethasone exposure reduces fetal weight gain in a dose-dependent manner without improving neonatal morbidity or mortality.
AB - © 2015 Published by Elsevier Ireland Ltd. on behalf of International Federation of Gynecology and Obstetrics. Objective To determine the effects of betamethasone on fetal growth and neonatal outcomes. Methods A retrospective cohort study was performed of deliveries that occurred at Charité University Hospital Berlin, Germany, between January 1996 and December 2008. The betamethasone group included women with preterm labor and symptomatic contractions, cervical insufficiency, preterm premature rupture of membranes, or vaginal bleeding. Women in the control group were matched for gestational age at time of delivery and had not received betamethasone. Fetal growth changes and neonatal anthropometry were compared. Results Among 1799 newborns in the betamethasone group and 42 240 in the control group, betamethasone was associated with significantly lower birth weight (154 g lower on average) after adjusting for confounders (e.g. hypertension, smoking, and maternal weight), sex, and gestational age at delivery (P <0.05). The higher the dose, the greater the difference in mean birth weight versus controls in births before 34+ 0 weeks (≤ 16 mg - 444 g; 24 mg - 523 g; > 24 mg - 811 g), without a detectable improvement in neonatal morbidity or mortality. There was a dose-dependent decline in expected fetal weight gain as estimated by serial ultrasonography examinations 6-8 weeks after betamethasone administration (P <0.05). Conclusion Betamethasone exposure reduces fetal weight gain in a dose-dependent manner without improving neonatal morbidity or mortality.
U2 - 10.1016/j.ijgo.2015.01.013
DO - 10.1016/j.ijgo.2015.01.013
M3 - Article
C2 - 25872453
VL - 130
SP - 64
EP - 69
JO - International Journal of Gynecology Obstetrics
JF - International Journal of Gynecology Obstetrics
SN - 0020-6695
IS - 1
ER -