Update in pulmonary arterial hypertension

被引：2

作者：

Mejia Chew, C. R. ^{[1
]}

Alcolea Batres, S. ^{[2
]}

Rios Blanco, J. J. ^{[1
]}

机构：

[1] Hosp Univ La Paz, Med Interna Serv, Grp Hipertens Pulm La Paz GRUHPAZ, Madrid, Spain

[2] Hosp Univ La Paz, Serv Neumol, Grp Hipertens Pulm La Paz GRUHPAZ, Madrid, Spain

来源：

REVISTA CLINICA ESPANOLA | 2016年 / 216卷 / 08期

关键词：

Pulmonary hypertension; Pulmonary arterial hypertension; Review; Endothelin receptor antagonist; Phosphodiesterase type 5 inhibitors; Prostacyclin analogues; SYSTEMIC-SCLEROSIS; RIGHT HEART; MORTALITY; EPOPROSTENOL; PREDICTORS; MANAGEMENT; RIOCIGUAT; DIAGNOSIS; PRESSURE; GRADIENT;

D O I：

10.1016/j.rce.2016.04.002

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Pulmonary arterial hypertension is a rare and progressive disease that mainly affects the pulmonary arterioles (precapillary), regardless of the triggering aetiology. The prevalence of pulmonary hypertension and pulmonary arterial hypertension in Spain is estimated at 19.2 and 16 cases per million inhabitants, respectively. The diagnosis of pulmonary arterial hypertension is based on haemodynamic criteria (mean pulmonary artery pressure >25 mmHg, pulmonary capillary wedge pressure <15 mmHg and pulmonary vascular resistance >3 Wood units) and therefore requires the implementation of right cardiac catheterisation. Sequential therapy witha single drug has been used in clinical practice. However, recent European guidelines recommend combined initial therapy in some situations. This review conducts a critical update of our knowledge of this disease according to the latest guidelines and recommendations. (C) 2016 Elsevier Espana, S.L.U. and Sociedad Espanola de Medicina Interna (SEMI). All rights reserved.

引用

页码：436 / 444

页数：9

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