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Pulmonary hypertension in preterm neonates with bronchopulmonary dysplasia: a meta-analysis
  1. Dwayne Mascarenhas1,2,
  2. Marwa Al-Balushi1,2,
  3. Aida Al-Sabahi1,2,
  4. Dany E Weisz3,
  5. Amish Jain2,4,
  6. Bonny Jasani1,2
  1. 1 The Hospital for Sick Children, Toronto, Ontario, Canada
  2. 2 Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada
  3. 3 Newborn and Developmental Paediatrics, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada
  4. 4 Mount Sinai Hospital, Toronto, Ontario, Canada
  1. Correspondence to Dr Bonny Jasani; bonny.jasani{at}sickkids.ca

Abstract

Context Knowledge gaps exist on the incidence and risk factors for developing pulmonary hypertension (PH) in preterm infants with bronchopulmonary dysplasia (BPD) and its impact on outcomes.

Objective To systematically review and meta-analyse the incidence, risk factors and short- and long-term outcomes of BPD-PH in preterm infants.

Design PubMed, Embase, Cochrane CENTRAL and CINAHL were searched for studies including infants<37 weeks gestational age (GA) or birth weight<2500 g with BPD-PH versus BPD-no PH from inception until 5 April 2023.

Main outcome measures Incidence, risk factors and short- and long-term outcomes.

Results 44 observational studies evaluating 7677 preterm infants were included. The incidence of PH in mild, moderate and severe BPD was 5%, 18% and 41%, respectively. Small for GA (25 studies; N=5814; OR 1.8; 95% CI 1.3, 2.5), necrotising enterocolitis (22 studies; N=3387; OR 1.6; 95% CI 1.3, 2.2), early PH (four studies; N=820 OR 2.2; 95% CI 1.5, 3.3) and severe BPD (20 studies; N=2587; OR 5.4; 95% CI 3.2, 9.1) were significant risk factors for BPD-PH. Compared with BPD-no PH, the BPD-PH group had significantly higher mortality (22 studies; N=4882; OR 6.4; 95% CI 4.7, 8.6), longer duration of mechanical ventilation, oxygen supplementation, length of hospital stay, need for home oxygen and tracheostomy requirement. The BPD-PH infants also had a significantly higher risk of neurodevelopmental impairment in the motor domain.

Conclusions PH increases across the severity of BPD and is associated with higher odds of mortality and adverse short-term and neurodevelopmental outcomes.

PROSPERO registration number CRD42023413119.

  • Neonatology
  • Paediatrics
  • Respiratory Medicine

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Footnotes

  • X @danyweisz

  • Contributors DM has conceptualised and designed the study, designed the data collection instruments, collected data, carried out the initial analyses, drafted the initial manuscript and critically reviewed and revised the manuscript. As guarantor, DM accepts full responsibility for the finished work and/or the conduct of the study, had access to the data and controlled the decision to publish. MA-B and AA-S designed the data collection instruments, collected data and critically reviewed and revised the manuscript. DEW and AJ designed the data collection instruments, coordinated and supervised data collection and critically reviewed and revised the manuscript for important intellectual content. BJ conceptualised and designed the study, designed the data collection instruments, coordinated and supervised data collection, carried out the initial analyses and critically reviewed and revised the manuscript for important intellectual content. All authors approved the final manuscript as submitted and agree to be accountable for all aspects of the work.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.