Survival of patients with pulmonary arterial hypertension during therapy PAH-specific drugs

Pulmonary arterial hypertension (PAH) is a life threatening syndrome, which is characterized by a progressive increase in pulmonary vascular resistance (PVR), medium pulmonary artery pressure and functional disorders and morphological changes of pulmonary arteries. Despite the relative abundance of...

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Main Authors: D Yu Platonov, N A Tsareva, S N Avdeev
Format: Article
Language:Russian
Published: IP Morozov P.V. 2017-12-01
Series:Системные гипертензии
Subjects:
Online Access:https://syst-hypertension.ru/2075-082X/article/viewFile/29586/pdf
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author D Yu Platonov
N A Tsareva
S N Avdeev
author_facet D Yu Platonov
N A Tsareva
S N Avdeev
author_sort D Yu Platonov
collection DOAJ
description Pulmonary arterial hypertension (PAH) is a life threatening syndrome, which is characterized by a progressive increase in pulmonary vascular resistance (PVR), medium pulmonary artery pressure and functional disorders and morphological changes of pulmonary arteries. Despite the relative abundance of PAH-specific drugs, the choice of a suitable agent for the treatment of a particular patient remains challenging. One of the most important parameters measured in clinical studies is patient survival or, in some cases, mortality. Survival or mortality as secondary or components of the primary endpoint one way or another has been studied in clinical trials of drugs for the treatment of PAH. For tablets drugs for the treatment of some forms of PAH (sildenafil, riociguat, bosentan, macitentan, ambrisentan) currently available data studies, which studied the survival.
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spelling doaj.art-6a0d946f0827427083657794ffb537402022-12-21T23:47:03ZrusIP Morozov P.V.Системные гипертензии2075-082X2542-21892017-12-01143586426614Survival of patients with pulmonary arterial hypertension during therapy PAH-specific drugsD Yu Platonov0N A Tsareva1S N Avdeev2Regional Clinical Hospital; Tver State Medical University of the Ministry of Health of the Russian FederationResearch Institute of Pulmonology of FMBA of Russia; I.M.Sechenov First Moscow State Medical University of the Ministry of Health of the Russian FederationResearch Institute of Pulmonology of FMBA of Russia; I.M.Sechenov First Moscow State Medical University of the Ministry of Health of the Russian FederationPulmonary arterial hypertension (PAH) is a life threatening syndrome, which is characterized by a progressive increase in pulmonary vascular resistance (PVR), medium pulmonary artery pressure and functional disorders and morphological changes of pulmonary arteries. Despite the relative abundance of PAH-specific drugs, the choice of a suitable agent for the treatment of a particular patient remains challenging. One of the most important parameters measured in clinical studies is patient survival or, in some cases, mortality. Survival or mortality as secondary or components of the primary endpoint one way or another has been studied in clinical trials of drugs for the treatment of PAH. For tablets drugs for the treatment of some forms of PAH (sildenafil, riociguat, bosentan, macitentan, ambrisentan) currently available data studies, which studied the survival.https://syst-hypertension.ru/2075-082X/article/viewFile/29586/pdfpulmonary hypertensionpah-specific therapysurvivalsildenafilriociguatbosentanmacitentanambrisentan
spellingShingle D Yu Platonov
N A Tsareva
S N Avdeev
Survival of patients with pulmonary arterial hypertension during therapy PAH-specific drugs
Системные гипертензии
pulmonary hypertension
pah-specific therapy
survival
sildenafil
riociguat
bosentan
macitentan
ambrisentan
title Survival of patients with pulmonary arterial hypertension during therapy PAH-specific drugs
title_full Survival of patients with pulmonary arterial hypertension during therapy PAH-specific drugs
title_fullStr Survival of patients with pulmonary arterial hypertension during therapy PAH-specific drugs
title_full_unstemmed Survival of patients with pulmonary arterial hypertension during therapy PAH-specific drugs
title_short Survival of patients with pulmonary arterial hypertension during therapy PAH-specific drugs
title_sort survival of patients with pulmonary arterial hypertension during therapy pah specific drugs
topic pulmonary hypertension
pah-specific therapy
survival
sildenafil
riociguat
bosentan
macitentan
ambrisentan
url https://syst-hypertension.ru/2075-082X/article/viewFile/29586/pdf
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AT natsareva survivalofpatientswithpulmonaryarterialhypertensionduringtherapypahspecificdrugs
AT snavdeev survivalofpatientswithpulmonaryarterialhypertensionduringtherapypahspecificdrugs