先天性膈疝合并肺动脉高压的发病机制及其临床诊疗研究进展

Pathogenesis of Pulmonary Hypertension and Clinical Progress in Diagnosis and Treatment of Congenital Diaphragmatic Hernia

先天性膈疝(CDH)是新生儿外科常见危重病。该病预后的主要决定因素是其合并的肺发育不良及肺动脉高压(PH)的严重程度。对该病的临床治疗效果,是衡量新生儿科综合治疗水平的一项重要的指标。本文聚焦目前对CDH合并PH的发病机制及其临床诊疗的研究进展,并综述如下。

Congenital diaphragmatic hernia（CDH） is a common and critical care in neonatal surgery, and the severity of pulmonary hypoplasia（PH） and pulmonary hypertension that CDH combined with was the main factor which determines the prognosis. The clinical effects of integrated treatment with CDH was an important indicator of neonatal standards. This article focuses on the research in the pathogenesis of pulmonary hypertension and clinical progress in diagnosis and treatment with CDH.