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Early caffeine therapy for prevention of bronchopulmonary dysplasia in preterm infants
Dalal Taha1, Sharon Kirkby, Ursula Nawab
1Division of Pediatrics/Neonatology, Thomas Jefferson University/Nemours , Philadelphia, PA , USA .
Insights
Early caffeine administration in preterm infants improves survival without bronchopulmonary dysplasia (BPD). While beneficial for respiratory outcomes, early caffeine use may increase the risk of necrotizing enterocolitis (NEC).
Area of Science:
- Neonatal Medicine
- Pediatric Pulmonology
- Clinical Pharmacology
Background:
- Bronchopulmonary dysplasia (BPD) is a significant cause of morbidity in preterm infants.
- Caffeine is commonly used to treat apnea of prematurity and may have other benefits.
Purpose of the Study:
- To investigate the association between early caffeine commencement and survival without BPD in preterm infants.
- To evaluate other neonatal outcomes related to early caffeine use.
Main Methods:
- Retrospective analysis of the Alere Neonatal Database.
- Inclusion criteria: infants weighing ≤1250g, treated with caffeine within the first 10 days of life.
- Comparison of outcomes between early (0-2 days) and delayed (3-10 days) caffeine initiation.
Main Results:
- Early caffeine use was linked to a reduction in BPD (OR 0.69) and BPD or death (OR 0.77).
- Improved respiratory outcomes, reduced severe intraventricular hemorrhage and patent ductus arteriosus, and shorter hospitalization were observed with early caffeine.
- An increased risk of necrotizing enterocolitis (NEC) was associated with early caffeine (OR 1.41).
Conclusions:
- Early caffeine commencement in preterm infants is associated with improved survival without BPD.
- The increased risk of NEC with early caffeine warrants further investigation.
Objective:
To determine if an early commencement of caffeine is associated with improved survival without bronchopulmonary dysplasia (BPD) in preterm infants.
Methods:
Retrospective data analysis from the Alere Neonatal Database for infants weighing ≤1250 g, and treated with caffeine within the first 10 days of life. The neonatal outcomes were compared between the infants who received early caffeine (0-2 days) with the infants who received delayed caffeine (3-10 days).
Results:
A total of 2951 infants met the inclusion criteria (early caffeine 1986, late caffeine 965). The early use of caffeine was associated with reduction in BPD (OR 0.69, 95% CI 0.58-0.82, p < 0.001) and BPD or death (OR 0.77, 95% CI 0.63-0.94, p = 0.01). Other respiratory outcomes also improved with the early commencement of caffeine. The frequency of severe intraventricular hemorrhage and patent ductus arteriosus was lower and the length of hospitalization was shorter in infants receiving early caffeine therapy. However, early use of caffeine was associated with an increase in the risk of nectrotizing enterocolits (NEC) (OR 1.41, 95% CI 1.04-1.91, p = 0.027).
Conclusion:
Early commencement of caffeine was associated with improvement in survival without BPD in preterm infants. The risk of NEC with early caffeine use requires further investigation.
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