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首页> 外文期刊>Pulmonary Circulation >Clinical Classification in Pediatric Pulmonary Arterial Hypertension Associated with Congenital Heart Disease:
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Clinical Classification in Pediatric Pulmonary Arterial Hypertension Associated with Congenital Heart Disease:

机译:先天性心脏病伴发的小儿肺动脉高压的临床分类:

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Congenital heart disease (CHD) is a frequent cause of pediatric pulmonary arterial hypertension (PAH), with diverse etiology and outcome. We aimed to describe phenotypic heterogeneity in pediatric PAH associated with CHD (PAH-CHD), assess the applicability of the Nice CHD classification, and explore whether this classification accurately reflects patient/disease characteristics and survival. All children with CHD from a contemporary cohort of consecutive pediatric PAH patients followed in three major referral centers (Denver, New York, the Netherlands) were characterized and classified on the basis of the latest proposed clinical classification for PAH-CHD (World Symposium on Pulmonary Hypertension, Nice, 2013). According to this classification, 24% of 134 children were classified into group 1, 14% into group 2, 19% into group 3, and 30% into group 4; 11% could not be classified. Types of CHD and hemodynamic profile differed between groups, with the highest right atrial pressure in group 4 (P 0.040). Group 3 children had Down syndrome less frequently (P = 0.011) but other (un)defined syndromes most frequently (P = 0.063) and received most intense PAH-targeted therapy (P = 0.003). With 15 deaths and one lung transplant (12%; median follow-up: 4.3 years), survival differences could not be demonstrated between the groups in the Nice CHD classification. Pediatric PAH-CHD is a heterogeneous condition frequently associated with extracardiac, developmental factors that are believed to affect disease development. The Nice CHD classification identifies groups with specific patient/disease characteristics. However, a substantial proportion of children could not be classified. Group 3 forms a distinct disease entity. Its prognostic value could not be determined because of the low number of events. The Nice CHD classification supports clinical characterization of PAH-CHD; however, further refinement is needed to classify all children with PAH-CHD.
机译:先天性心脏病(CHD)是小儿肺动脉高压(PAH)的常见原因,其病因和预后多种多样。我们旨在描述与冠心病相关的儿科PAH(PAH-CHD)的表型异质性,评估Nice CHD分类的适用性,并探讨该分类是否准确反映了患者/疾病的特征和生存期。根据最近提出的PAH-CHD临床分类(世界肺病专题讨论会),对来自当代连续三个儿科PAH患者队列的儿童进行了分类,并在三个主要的转诊中心(丹佛,纽约,荷兰)进行了分类。高血压,尼斯,2013年)。根据这种分类,在134名儿童中,有24%分为1组,14%属于2组,19%属于3组,30%属于4组。 11%无法分类。各组之间的冠心病类型和血流动力学特征不同,第4组的右心房压力最高(P <0.040)。第三组儿童唐氏综合症的发生频率较低(P = 0.011),而其他(未明确定义的)综合症的发生频率最高(P = 0.063),并且接受了以PAH为靶点的最强治疗(P = 0.003)。有15例死亡和1例肺移植(12%;中位随访时间:4.3年),在尼斯冠心病分类中两组之间均未显示生存差异。小儿PAH-CHD是一种异质性疾病,通常与心外,发展因素相关,据认为会影响疾病的发展。尼斯冠心病分类可识别具有特定患者/疾病特征的人群。但是,很大一部分儿童无法分类。第3组形成独特的疾病实体。由于事件数量少,无法确定其预后价值。 Nice CHD分类支持PAH-CHD的临床表征。但是,需要进一步完善以对所有患有PAH-CHD的儿童进行分类。

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