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Predictors of bronchopulmonary dysplasia occurrence and severity in extremely preterm infants
Xuejing Liu1,2,3, Wanxian Zhang1,2,3, Fangrui Ding1,2,3
1Department of Neonatology, Tianjin Central Hospital of Obstetrics and Gynecology, Tianjin, China.
Insights
Bronchopulmonary dysplasia (BPD) in extremely preterm infants (EPIs) is linked to prolonged mechanical ventilation, blood transfusions, antibiotics, and PDA. Interventions targeting these factors can prevent severe BPD.
Area of Science:
- Neonatal Medicine
- Pediatric Pulmonology
- Critical Care
Background:
- Bronchopulmonary dysplasia (BPD) is a frequent complication in extremely preterm infants (EPIs).
- Effective preventive strategies for BPD are lacking.
- Identifying risk factors is crucial for early intervention and improved outcomes in EPIs.
Purpose of the Study:
- To identify risk factors associated with the development and severity of BPD in EPIs.
- To inform the development of potential BPD prevention strategies.
- To analyze the impact of various clinical factors on BPD occurrence and progression.
Main Methods:
- Retrospective analysis of medical records from 468 EPIs (2012-2024).
- BPD diagnosis based on 2018 National Institute of Child Health and Human Development criteria.
- Multivariable logistic regression to determine independent risk factors for BPD.
Main Results:
- 29.1% of EPIs developed BPD; risk factors included prolonged invasive mechanical ventilation (IMV), frequent red blood cell transfusions (RBCTs), extended antibiotic exposure, and hemodynamically significant patent ductus arteriosus (hsPDA).
- Prolonged IMV and higher fluid balance on postnatal day 7 were risk factors for moderate-to-severe BPD.
- Higher birth weight was protective; whole blood transfusion increased BPD risk compared to packed RBCTs.
Conclusions:
- Prolonged IMV, frequent RBCTs, fluid overload, excessive antibiotics, and hsPDA contribute to BPD in EPIs.
- Targeting modifiable factors like reducing IMV duration and optimizing fluid balance is key.
- Optimizing transfusion protocols and fluid management can help prevent moderate-to-severe BPD in vulnerable infants.
Background:
Bronchopulmonary dysplasia (BPD) is a common complication in extremely preterm infants (EPIs), and there is currently a lack of effective preventive strategies. Identifying risk factors may facilitate early interventions and improve outcomes.
Objective:
To investigate risk factors for the occurrence and severity of BPD in EPIs and inform potential prevention strategies.
Methods:
We conducted a retrospective analysis of medical records from EPIs admitted to the neonatal intensive care unit at Tianjin Central Hospital of Obstetrics and Gynecology between 2012 and 2024. BPD was diagnosed according to the 2018 revised criteria established by the National Institute of Child Health and Human Development. Multivariable logistic regression was used to identify independent risk factors.
Results:
Among 468 EPIs, 136 (29.1%) developed BPD (mild: 14.1%, moderate: 7.1%, severe: 7.9%). Independent risk factors for BPD included prolonged invasive mechanical ventilation (IMV, OR = 1.10, 95% CI 1.03-1.17), frequent red blood cell transfusions (RBCTs, OR = 1.61, 95% CI 1.30-2.01), extended antibiotic exposure (OR = 1.03, 95% CI 1.01-1.06), and hemodynamically significant patent ductus arteriosus (hsPDA, OR = 2.27, 95% CI 1.22-4.20). Prolonged IMV (OR = 1.16, 95% CI 1.06-1.27) and higher fluid balance (FB) on postnatal day 7 (OR = 1.19, 95% CI 1.05-1.34) were independent risk factors for moderate-to-severe BPD, while higher birth weight (OR = 0.99, 95% CI 0.988-0.998) was found to be a protective factor. Whole blood transfusion was associated with an increased risk of BPD (OR = 4.48, 95% CI 1.92-10.43) and moderate-to-severe BPD (OR = 4.81, 95% CI 1.24-18.63) compared to packed RBCTs. In predicting moderate-to-severe BPD, the duration of IMV (cut-off: 6.5 days) and FB on postnatal day 7 (cut-off: -7.2) demonstrated significant predictive value.
Conclusions:
In conclusion, the occurrence and severity of BPD in EPIs are influenced by prolonged IMV, frequent RBCTs, fluid overload, excessive antibiotic exposure, and hsPDA. Early interventions targeting modifiable factors, such as reducing IMV duration, maintaining an appropriate negative FB on postnatal day 7, and optimizing transfusion protocols, are critical to prevent moderate-to-severe BPD.
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