Evaluation and management of pulmonary arterial hypertension

被引:59
|
作者
Beshay, Sarah [1 ]
Sahay, Sandeep [1 ]
Humbert, Marc [2 ,3 ,4 ]
机构
[1] Houston Methodist Hosp, Div Pulm & Crit Care Med, Dept Med, Houston, TX 77030 USA
[2] Univ Paris Saclay, Fac Med, Le Kremlin Bicetre, France
[3] Hop Bicetre, AP HP, Dept Resp & Intens Care Med, Pulm Hypertens Natl Referral Ctr, Le Kremlin Bicetre, France
[4] Hop Marie Lannelongue, INSERM UMR S 999, Le Plessis Robinson, France
关键词
Pulmonary hypertension; Pulmonary arterial hypertension; Genetics; Risk stratification; Treatment; Patient perspectives; CALCIUM-CHANNEL BLOCKERS; LONG-TERM RESPONSE; COMBINATION THERAPY; MUTATIONS; PRESSURE; RECEPTOR; REGISTRY; RISK; AMBRISENTAN; METABOLISM;
D O I
10.1016/j.rmed.2020.106099
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Pulmonary arterial hypertension is a devastating progressive disease mediated by different pathophysiologic pathways that result in progressive increase in pulmonary vascular resistance along with right ventricular failure and eventually premature death. Despite significant advances in the understanding of the underlying mechanisms and development of a number of targeted therapies, pulmonary arterial hypertension remains a challenging condition with high morbidity and mortality. New therapies are being actively sought, and early recognition remains of paramount importance. In an effort to improve the detection and management of pulmonary hypertension, the 6th World Symposium on Pulmonary Hypertension came up with most recent statements in 2018. The goal of this review is to summarize some key updates from the proceedings of the Symposium pertaining to different aspects of evaluation and management of patients with pulmonary arterial hypertension.
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页数:5
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