Systemic hydrocortisone to prevent bronchopulmonary dysplasia in preterm infants (the SToP-BPD study); a multicenter randomized placebo controlled trial

Autor: Onland Wes, Offringa Martin, Cools Filip, De Jaegere Anne P, Rademaker Karin, Blom Henry, Cavatorta Eric, Debeer Anne, Dijk Peter H, van Heijst Arno F, Kramer Boris W, Kroon Andre A, Mohns Thilo, van Straaten Henrica L, te Pas Arjan B, Theyskens Claire, van Weissenbruch Mirjam M, van Kaam Anton H
Jazyk: angličtina
Rok vydání: 2011
Předmět:
Zdroj: BMC Pediatrics, Vol 11, Iss 1, p 102 (2011)
Druh dokumentu: article
ISSN: 1471-2431
DOI: 10.1186/1471-2431-11-102
Popis: Abstract Background Randomized controlled trials have shown that treatment of chronically ventilated preterm infants after the first week of life with dexamethasone reduces the incidence of the combined outcome death or bronchopulmonary dysplasia (BPD). However, there are concerns that dexamethasone may increase the risk of adverse neurodevelopmental outcome. Hydrocortisone has been suggested as an alternative therapy. So far no randomized controlled trial has investigated its efficacy when administered after the first week of life to ventilated preterm infants. Methods/Design The SToP-BPD trial is a randomized double blind placebo controlled multicenter study including 400 very low birth weight infants (gestational age < 30 weeks and/or birth weight < 1250 grams), who are ventilator dependent at a postnatal age of 7 - 14 days. Hydrocortisone (cumulative dose 72.5 mg/kg) or placebo is administered during a 22 day tapering schedule. Primary outcome measure is the combined outcome mortality or BPD at 36 weeks postmenstrual age. Secondary outcomes are short term effects on the pulmonary condition, adverse effects during hospitalization, and long-term neurodevelopmental sequelae assessed at 2 years corrected gestational age. Analysis will be on an intention to treat basis. Discussion This trial will determine the efficacy and safety of postnatal hydrocortisone administration at a moderately early postnatal onset compared to placebo for the reduction of the combined outcome mortality and BPD at 36 weeks postmenstrual age in ventilator dependent preterm infants. Trial registration number Netherlands Trial Register (NTR): NTR2768
Databáze: Directory of Open Access Journals