Source
Children's Hospital, Brigham and Women's Hospital, Harvard Medical School, Boston, Mass., USA. linda.vanmarter@childrens.harvard.edu
Abstract
BACKGROUND:
Recent improvements in the survival of extremely preterm infants have been accompanied by evolution in the pathogenesis and histopathology of bronchopulmonary dysplasia (BPD). Although oxygen and barotrauma-induced injury remain important contributing factors, pulmonary developmental arrest appears to play an equally important causal role in prolonged respiratory illness, especially among the most immature surviving preterm newborns. To date, clinical trials have failed to demonstrate a substantial benefit of a single treatment or preventive strategy for BPD.
OBJECTIVES:
To evaluate the current evidence in favor of treatments that might prevent BPD.
METHODS:
Review of clinical studies of preventive treatment strategies for BPD.
RESULTS:
High frequency oscillatory ventilation, permissive hypercapnea, and inhaled nitric oxide might offer benefit to infants at risk of BPD. These and other potential preventive therapies for BPD, such as superoxide dismutase, inositol, and alpha(1)-proteinase inhibitor, deserve further study.
CONCLUSIONS:
Although some current treatments offer promise, no preventive therapy for BPD has proven safe and effective, except for intramuscular vitamin A. Additional studies of respiratory technologies, management strategies, and protective molecules are needed.
Copyright (c) 2006 S. Karger AG, Basel.