Orphan drugs in bronchopulmonary dysplasia

被引:0
|
作者
Greenough, Anne [1 ]
Bhat, Prashanth [2 ,3 ]
机构
[1] Kings Coll Hosp London, Div Asthma Allergy & Lung Biol, London SE5 9RS, England
[2] Kings Coll Hosp London, MRC, London SE5 9RS, England
[3] Kings Coll Hosp London, Asthma UK Ctr Allerg Mech Asthma, Div Asthma Allergy & Lung Biol, London SE5 9RS, England
来源
EXPERT OPINION ON ORPHAN DRUGS | 2013年 / 1卷 / 05期
关键词
antioxidant; bronchopulmonary dysplasia; prematurity; CHRONIC LUNG-DISEASE; RESPIRATORY-DISTRESS-SYNDROME; RANDOMIZED CONTROLLED-TRIAL; HUMAN SUPEROXIDE-DISMUTASE; BIRTH-WEIGHT INFANTS; PREMATURE-INFANTS; N-ACETYLCYSTEINE; PRETERM INFANTS; ISCHEMIC-INJURY; NEBULIZED PENTOXIFYLLINE;
D O I
10.1517/21678707.2013.780968
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Bronchopulmonary dysplasia (BPD) is a common adverse outcome of very premature birth. It has a multifactorial aetiology which includes oxygen toxicity. In this review the potential of antioxidants to reduce BPD is explored. Areas covered: The aim of the review is to determine the potential of agents which reduce oxygen toxicity to prevent BPD development. A literature review was undertaken using PubMed using the terms: BPD, prevention of BPD, antioxidants, superoxide dismutase (SOD), N-acetyl cysteine, allopurinol, melatonin, cimetidine, alpha-1-protease inhibitor, pentoxifylline and macrolides. Expert opinion: There are several therapies which reduce oxygen toxicity that have shown promising results with regard to improving the respiratory outcome of prematurely born infants. However, further work is necessary to identify the optimum antioxidant which reduces BPD and improves long-term respiratory outcome.
引用
收藏
页码:351 / 358
页数:8
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