Rossor Thomas, Greenough Anne
Division of Asthma, Allergy and Lung Biology, MRC and Asthma UK Centre in Allergic Mechanisms of Asthma, King's College London, London, England, UK.
Expert Rev Respir Med. 2015 Feb;9(1):35-43. doi: 10.1586/17476348.2015.986470. Epub 2014 Nov 26.
Pulmonary hypertension (PH) is a common finding in infants with bronchopulmonary dysplasia (BPD). The aim of this review is to describe recent advances in the diagnosis and treatment of PH and discuss whether they will benefit infants and children with BPD related PH. Echocardiography remains the mainstay of diagnosis but has limitations, further developments in diagnostic techniques and identification of biomarkers are required. There are many potential therapies for PH associated with BPD. Inhaled nitric oxide has been shown to improve short term outcomes only. Sidenafil in resource limited settings was shown in three randomized trials to significantly reduce mortality. The efficacy of other therapies including prostacyclin, PDE3 inhibitors and endothelin receptor blockers has only been reported in case reports or case series. Randomized controlled trials with long term follow up are required to appropriately assess the efficacy of therapies aimed at improving the outcome of children with PH.
肺动脉高压(PH)在支气管肺发育不良(BPD)婴儿中很常见。本综述的目的是描述PH诊断和治疗的最新进展,并讨论它们是否会使患有BPD相关PH的婴幼儿受益。超声心动图仍然是诊断的主要手段,但存在局限性,需要进一步发展诊断技术并鉴定生物标志物。对于与BPD相关的PH有许多潜在的治疗方法。吸入一氧化氮仅显示可改善短期预后。在资源有限的环境中,西地那非在三项随机试验中显示可显著降低死亡率。其他疗法,包括前列环素、磷酸二酯酶3抑制剂和内皮素受体阻滞剂的疗效仅在病例报告或病例系列中有所报道。需要进行长期随访的随机对照试验,以适当评估旨在改善PH儿童预后的治疗方法的疗效。