The management of evolving bronchopulmonary dysplasia

被引:23
|
作者
Schulzke, Sven M. [1 ]
Pillow, J. Jane [1 ]
机构
[1] Univ Western Australia, Sch Womens & Infants Hlth, Perth, WA 6009, Australia
关键词
infant; premature; bronchopulmonary dysplasia; primary prevention; secondary prevention; intensive care units; neonatal; LOW-BIRTH-WEIGHT; CHRONIC LUNG-DISEASE; PERSISTENT PULMONARY-HYPERTENSION; POSITIVE-PRESSURE VENTILATION; RESPIRATORY-DISTRESS-SYNDROME; VITAMIN-A SUPPLEMENTATION; INHALED NITRIC-OXIDE; PRETERM INFANTS; CONTROLLED-TRIAL; PREVENTION;
D O I
10.1016/j.prrv.2009.12.005
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Bronchopulmonary dysplasia (BPD) is associated with increased mortality and significant long-term cardiorespiratory and neurodevelopmental sequelae. Treatment of evolving BPD in the neonatal intensive care unit (NICU) is challenging due to the complex interplay of contributing risk factors which include preterm birth per se, supplemental oxygen, positive pressure ventilation, patent ductus arterious, and pre- and postnatal infection. Management of evolving BPD requires a multimodal approach including adequate nutrition, careful fluid management, effective and safe pharmacotherapy, and respiratory support aiming at minimal lung injury. Among pharmacological interventions, caffeine has the best risk-benefit profile. Systemic postnatal corticosteroids should be reserved to ventilated infants at highest risk of BPD who cannot be weaned from the ventilator. Several ongoing randomised trials are evaluating optimal oxygen saturation targets in preterm infants. The most beneficial respiratory support strategy to minimise lung injury remains unclear and requires further investigation. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:143 / 148
页数:6
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