Literature DB >> 16770070

Progress in discovery and evaluation of treatments to prevent bronchopulmonary dysplasia.

Linda J Van Marter1.   

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.

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Year:  2006        PMID: 16770070     DOI: 10.1159/000092867

Source DB:  PubMed          Journal:  Biol Neonate        ISSN: 0006-3126


  4 in total

1.  Nasal ventilation alters mesenchymal cell turnover and improves alveolarization in preterm lambs.

Authors:  Brent Reyburn; Marlana Li; Drew B Metcalfe; Nicholas J Kroll; Jeremy Alvord; Albert Wint; Mar Janna Dahl; Jiancheng Sun; Li Dong; Zheng-Ming Wang; Christopher Callaway; Robert A McKnight; Laurie Moyer-Mileur; Bradley A Yoder; Donald M Null; Robert H Lane; Kurt H Albertine
Journal:  Am J Respir Crit Care Med       Date:  2008-06-12       Impact factor: 21.405

2.  Melatonin protects against oxidative damage in a neonatal rat model of bronchopulmonary dysplasia.

Authors:  Li Pan; Jian-Hua Fu; Xin-Dong Xue; Wei Xu; Ping Zhou; Bing Wei
Journal:  World J Pediatr       Date:  2009-08-20       Impact factor: 2.764

3.  Mitochondrial dysfunction contributes to alveolar developmental arrest in hyperoxia-exposed mice.

Authors:  Veniamin Ratner; Anatoly Starkov; Dzmitry Matsiukevich; Richard A Polin; Vadim S Ten
Journal:  Am J Respir Cell Mol Biol       Date:  2009-01-23       Impact factor: 6.914

4.  Association between oxidative DNA damage and the expression of 8-oxoguanine DNA glycosylase 1 in lung epithelial cells of neonatal rats exposed to hyperoxia.

Authors:  Linlin Jin; Haiping Yang; Jianhua Fu; Xindong Xue; Li Yao; Lin Qiao
Journal:  Mol Med Rep       Date:  2015-02-12       Impact factor: 2.952

  4 in total

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