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儿童期肺动脉高压

Pulmonary hypertension in childhood.

作者信息

Haworth S G

机构信息

Dept of Cardiology, Hospital for Sick Children, London, UK.

出版信息

Eur Respir J. 1993 Jul;6(7):1037-43.

PMID:8370430
Abstract

In the presence of pulmonary hypertension, the pulmonary vasculature fails to remodel after birth. Secondary changes then develop, and do so more rapidly than in the adult lung because the cells are exposed to the insult whilst still relatively undifferentiated. The commonest causes of pulmonary hypertension in newborn and young infants are alveolar hypoxia, and congenital heart disease causing a left-to-right shunt and increased pulmonary blood flow. The initial response of an increase in pulmonary arterial muscularity is common to both, but intimal proliferation can develop rapidly in those with complex congenital heart disease. The structural abnormalities are accompanied by abnormalities in the control of pulmonary vascular reactivity, a problem which is the focus of much current research activity.

摘要

在存在肺动脉高压的情况下,肺血管系统在出生后无法进行重塑。继而会出现继发性变化,且由于细胞在仍相对未分化时就受到损伤,这些变化在新生儿和幼婴中比在成人肺中发展得更快。新生儿和幼婴肺动脉高压最常见的原因是肺泡缺氧,以及导致左向右分流和肺血流量增加的先天性心脏病。肺动脉肌层增厚的初始反应在这两种情况中都很常见,但内膜增殖在患有复杂先天性心脏病的患者中可能迅速发展。结构异常伴随着肺血管反应性控制的异常,这一问题是当前许多研究活动的重点。

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