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Chorioamnionitis as a risk factor for bronchopulmonary dysplasia: a systematic review and meta-analysis
Lisa Hartling1, Yuanyuan Liang, Thierry Lacaze-Masmonteil
1Department of Pediatrics, Children's Hospital of Eastern Ontario, 401 Smyth Road, Ottawa, Ontario, Canada. tlacaze@cheo.on.ca
Insights
Chorioamnionitis (CA) is associated with bronchopulmonary dysplasia (BPD) in preterm infants, but evidence of publication bias suggests caution. Definitive risk factor status for CA remains unproven.
Area of Science:
- Neonatalogy
- Perinatology
- Pediatric Pulmonology
Background:
- Chorioamnionitis (CA) is an infection of the placenta and fetal membranes.
- Bronchopulmonary dysplasia (BPD) is a chronic lung disease affecting premature infants.
Purpose of the Study:
- To systematically review the association between chorioamnionitis and bronchopulmonary dysplasia in preterm infants.
- To assess the strength of evidence and identify potential confounders.
Main Methods:
- Systematic literature search of multiple databases (Medline, Embase, CINAHL, Science Citation Index, PubMed).
- Inclusion of studies with comparison groups, preterm/low birthweight infants, and primary data.
- Independent screening, data extraction, and quality assessment by two reviewers.
- Random effects modeling for meta-analysis and meta-regression for confounders.
Main Results:
- 59 studies (15,295 patients) were included.
- Pooled unadjusted OR showed CA associated with BPD (OR 1.89).
- Pooled adjusted OR was 1.58, with substantial heterogeneity in both analyses.
- Strong evidence of publication bias was detected.
Conclusions:
- Chorioamnionitis is significantly associated with BPD, though adjusted analyses yield more conservative estimates.
- Substantial heterogeneity and publication bias complicate definitive conclusions.
- Chorioamnionitis cannot be definitively established as a risk factor for BPD despite existing evidence.
Objective:
To conduct a systematic review of the association between chorioamnionitis (CA) and bronchopulmonary dysplasia (BPD) in preterm infants.
Methods:
The authors searched Medline, Embase, CINAHL, Science Citation Index and PubMed, reviewed reference lists and contacted the primary authors of relevant studies. Studies were included if they had a comparison group, examined preterm or low birthweight infants, and provided primary data. Two reviewers independently screened the search results, applied inclusion criteria and assessed methodological quality. One reviewer extracted data and a second reviewer checked data extraction. Studies were combined with an OR using a random effects model. Meta-regression was used to explore potential confounders.
Results:
3587 studies were identified; 59 studies (15 295 patients) were included. The pooled unadjusted OR showed that CA was significantly associated with BPD (OR 1.89, 95% CI 1.56 to 2.3). Heterogeneity was substantial (I(2)=66.2%) and may be partially explained by the type of CA. Infants exposed to CA were significantly younger and lighter at birth. The pooled adjusted OR was 1.58 (95% CI 1.11 to 2.24); heterogeneity was substantial (I(2)=65.1%) which may be due to different variables being controlled in each study. There was strong evidence of publication bias which suggests potential overestimation of the measure of association between CA and BPD.
Conclusions:
Unadjusted and adjusted analyses showed that CA was significantly associated with BPD; however, the adjusted results were more conservative in the magnitude of association. The authors found strong evidence of publication bias. Despite a large body of evidence, CA cannot be definitively considered a risk factor for BPD.
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