Perinatal prevention of bronchopulmonary dysplasia

被引:16
作者
Greenough, Anne [1 ]
Ahmed, Na'eem [2 ]
机构
[1] Kings Coll London, Sch Med, Div Asthma Allergy & Lung Biol, London WC2R 2LS, England
[2] Kings Coll Hosp NHS Fdn Trust, London, England
关键词
Bronchopulmonary dysplasia; corticosteroids; methylxanthines; resuscitation; surfactant; INHALED NITRIC-OXIDE; CHRONIC LUNG-DISEASE; RANDOMIZED CONTROLLED-TRIAL; HEALTH-CARE UTILIZATION; PRETERM INFANTS; SUPEROXIDE-DISMUTASE; PULMONARY-FUNCTION; PREMATURE-INFANTS; N-ACETYLCYSTEINE; CAFFEINE THERAPY;
D O I
10.1515/jpm-2012-0084
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Bronchopulmonary dysplasia (BPD), defined as oxygen dependency for at least 28 days after birth, is a common adverse outcome of very premature birth. Affected children require frequent readmissions to hospital in the first 2 years, and although lung growth and remodelling results in progressive improvement in lung function, airflow abnormalities may remain Indeed, the most severely affected experience troublesome respiratory symptoms as adolescents and young adults. As a consequence, many potential preventative strategies have been investigated, and some have resulted in a reduction in BPD but with a negative risk/benefit ratio, for example, postnatal corticosteroids. Others therapies, namely antenatal corticosteroids and postnatal surfactant, have resulted in significant benefits to infants, including reductions in respiratory distress syndrome, necrotising enterocolitis, intraventricular haemorrhage and neonatal death, but have not impacted favourably on the incidence of BPD, perhaps due to the increased survival of very immature infants. In one major trial, it has been shown that BPD can be reduced without adverse effects by caffeine administration. Avoidance of high oxygen concentrations at resuscitation is also a promising approach to reduce BPD.
引用
收藏
页码:119 / 126
页数:8
相关论文
共 95 条
[91]   Impact of a physiologic definition on bronchopulmonary dysplasia rates [J].
Walsh, MC ;
Yao, Q ;
Gettner, P ;
Hale, E ;
Collins, M ;
Hensman, A ;
Everette, R ;
Peters, N ;
Miller, N ;
Muran, G ;
Auten, K ;
Newman, N ;
Rowan, G ;
Grisby, C ;
Arnell, K ;
Miller, L ;
Ball, B ;
McDavid, G .
PEDIATRICS, 2004, 114 (05) :1305-1311
[92]   ASSOCIATION OF UREAPLASMA-UREALYTICUM COLONIZATION WITH CHRONIC LUNG-DISEASE OF PREMATURITY - RESULTS OF A METAANALYSIS [J].
WANG, EEL ;
OHLSSON, A ;
KELLNER, JD .
JOURNAL OF PEDIATRICS, 1995, 127 (04) :640-644
[93]   Volume-targeted versus pressure-limited ventilation in the neonate [J].
Wheeler, Kevin ;
Klingenberg, Claus ;
McCallion, Naomi ;
Morley, Colin J. ;
Davis, Peter G. .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2010, (11)
[94]   Antenatal endotoxin and glucocorticoid effects on lung morphometry in preterm lambs [J].
Willet, KE ;
Jobe, AH ;
Ikegami, M ;
Newnham, J ;
Brennan, S ;
Sly, PD .
PEDIATRIC RESEARCH, 2000, 48 (06) :782-788
[95]   Prophylactic versus selective use of surfactant in preventing morbidity and mortality in preterm infants [J].
Ximena Rojas-Reyes, Maria ;
Morley, Colin J. ;
Soll, Roger .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2012, (03)