Steroid use for established bronchopulmonary dysplasia: study protocol for a systematic review and meta-analysis.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
15 06 2022
Historique:
entrez: 15 6 2022
pubmed: 16 6 2022
medline: 18 6 2022
Statut: epublish

Résumé

Postnatal steroids during the first few weeks of life have been demonstrated to be effective in decreasing the incidence of bronchopulmonary dysplasia (BPD), a serious chronic respiratory condition affecting preterm infants. However, this preventive option is limited by the concern of neurological side effects. Steroids are used to treat established BPD in an attempt to reduce mortality, and length of stay and home oxygen therapy, both of which associated with high levels of parental stress and healthcare costs. Moreover, a late timing for steroid treatment may show a more favourable safety profile in terms of neurodevelopment outcomes, considering the added postnatal brain maturation of these infants. Here, we report a protocol for a systematic review, which aims to determine the efficacy and long-term safety of postnatal steroids for the treatment of established BPD in preterm infants. MEDLINE, Embase, Cochrane databases and sources of grey literature for conference abstracts and trial registrations will be searched with no time or language restriction. We will include case-control studies, cohort studies and non-randomised or randomised trials that evaluate postnatal steroids for infants diagnosed with moderate or severe established BPD at 36 weeks' postmenstrual age. We will pool data from studies that are sufficiently similar to make this appropriate. Data extraction forms will be developed a priori. Observational studies and non-randomised and randomised clinical trials will be analysed separately. We will combine OR with 95% CI for dichotomous outcomes and the mean difference (95% CI) for continuous outcomes. We will account for the expected heterogeneity by using a random-effects model. We will perform subgroup analysis based on the a priori determined covariate of interest. Systematic reviews are exempted from approval by an ethics committee. Attempts will be sought to publish all results. CRD42021218881.

Identifiants

pubmed: 35705335
pii: bmjopen-2021-059553
doi: 10.1136/bmjopen-2021-059553
pmc: PMC9204409
doi:

Substances chimiques

Dexamethasone 7S5I7G3JQL

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e059553

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Sabina Strashun (S)

University of Limerick Graduate Entry Medical School, Limerick, Ireland.

Joanna Seliga-Siwecka (J)

Neonatal and Intensive Care Department, Medical University of Warsaw, Warszawa, Poland joanna.seliga@wum.edu.pl.

Roberto Chioma (R)

Dipartimento di Scienze Mediche e Chirurgiche, Policlinico Universitario Agostino Gemelli, Roma, Italy.

Kinga Zielińska (K)

Neonatal and Intensive Care Department, Medical University of Warsaw, Warszawa, Poland.

Krzysztof Włodarczyk (K)

Medical University of Warsaw, Warszawa, Poland.

Eduardo Villamor (E)

Department of Pediatrics, Maastricht UMC+, Maastricht, The Netherlands.

Roy K Philip (RK)

University Maternity Hospital Limerick, University of Limerick Graduate Entry Medical School, Limerick, Ireland.

Niazy Al Assaf (NA)

University Maternity Hospital Limerick, University of Limerick Graduate Entry Medical School, Limerick, Ireland.

Maria Pierro (M)

University of Milan, Milano, Italy.

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