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Published Online First: 11 August 2006. doi:10.1136/adc.2006.097170
Archives of Disease in Childhood - Fetal and Neonatal Edition 2007;92:F94-F98
Copyright © 2007 BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health.

ORIGINAL ARTICLE

Effect of oestradiol and progesterone replacement on bronchopulmonary dysplasia in extremely preterm infants

A Trotter1, L Maier2, M Kron3, F Pohlandt1

1 Section of Neonatology and Pediatric Critical Care Medicine, Children’s Hospital, University of Ulm, Ulm, Germany
2 Pharmacy, University of Ulm
3 Department of Biometry and Medical Documentation, University of Ulm

Correspondence to:
A Trotter
Center for Perinatal Medicine, Children’s Hospital, University of Bonn, Sigmund-Freudstr 25, 53105 Bonn, Germany; andreas.trotter{at}web.de

Objective: To study whether postnatal replacement of oestradiol and progesterone may help to prevent bronchopulmonary dysplasia (BPD).

Methods: This randomised placebo-controlled double-blind study enrolled 83 infants of <29 weeks gestational age and 1000 g birth weight requiring mechanical ventilation within 12 h after birth. Oestradiol (2.5 mg/kg/day) and progesterone (22.5 mg/kg/day) were given by continuous intravenous infusion of a standard lipid emulsion (15 ml/kg/day) in the replacement group (ESTRA-PRO). The placebo group received the same lipid emulsion without oestradiol or progesterone. A replacement period of at least 2 weeks but not >4 weeks was strived for and defined as "according to protocol". The primary outcome variable was the incidence of BPD or death.

Results: The median birth weight was 670 g (min–max 400–990 g) and the gestational age 25 weeks (23.1–28.1 weeks). The incidence of BPD or death was 48% in the placebo group and 44% in the ESTRA-PRO group (p = 0.38, one-sided testing, intention to treat analysis). In infants treated according to protocol, 32% (9 of 28) in the placebo group and 14% (3 of 21) in the ESTRA-PRO group developed BPD (p = 0.08).

Conclusion: Replacement of oestradiol and progesterone was not effective for prevention of BPD or death in extremely preterm born infants. Better-powered trials are needed to evaluate this new approach.

Abbreviations: ATP, according to protocol; BPD, bronchopulmonary dysplasia; ESTRA-PRO, oestradiol and progesterone replacement; ITT, intention to treat; ROP, retinopathy of prematurity; VEGF, vascular endothelial growth factor


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