Clinical guidelines for the diagnosis and treatment of pulmonary hypertension

Pulmonary hypertension (PH) is a group of diseases characterized by progressive increases in pulmonary vascular resistance and pulmonary artery pressure, which results in right ventricular heart failure and sudden death. Based on the current version of the guidelines for PH diagnosis and treatment,...

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Main Authors: I E Chazova, S N Avdeev, N A Tsareva, A V Volkov, T V Martyniuk, S N Nakonechnikov
Format: Article
Language:Russian
Published: "Consilium Medicum" Publishing house 2014-09-01
Series:Терапевтический архив
Subjects:
Online Access:https://ter-arkhiv.ru/0040-3660/article/view/31535
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spelling doaj-51aafcad9f474aeaa23692e0aeb16f972020-11-25T03:12:42Zrus"Consilium Medicum" Publishing houseТерапевтический архив0040-36602309-53422014-09-0186942328551Clinical guidelines for the diagnosis and treatment of pulmonary hypertensionI E ChazovaS N AvdeevN A TsarevaA V VolkovT V MartyniukS N NakonechnikovPulmonary hypertension (PH) is a group of diseases characterized by progressive increases in pulmonary vascular resistance and pulmonary artery pressure, which results in right ventricular heart failure and sudden death. Based on the current version of the guidelines for PH diagnosis and treatment, adopted by the experts of the European Society of Cardiology and the European Respiratory Society in 2009, and on the data of Russian and foreign clinical trials, the Russian experts elaborated clinical guidelines for PH in 2013. The latter consider the current classifications of PH, the specific features of its pathogenesis, and its diagnostic algorithm. The section dealing with drugs for maintenance therapy discusses data on the use of oral anticoagulants, diuretics, cardiac glycosides, and oxygen therapy. PH-specific therapy includes calcium antagonists, prostanoids, endothelin receptor antagonists, and phosphodiesterase type 5 inhibitors. Surgical procedures for PH involve atrial septostomy, thromboendartectomy, and lung or heart-lung transplantation. A treatment algorithm is proposed for PH patients. The current medicinal approaches using specific therapy agents and their combinations offer new promises for the effective treatment of patients with PH and improve its prognosis.https://ter-arkhiv.ru/0040-3660/article/view/31535pulmonary hypertensionclinical guidelines
collection DOAJ
language Russian
format Article
sources DOAJ
author I E Chazova
S N Avdeev
N A Tsareva
A V Volkov
T V Martyniuk
S N Nakonechnikov
spellingShingle I E Chazova
S N Avdeev
N A Tsareva
A V Volkov
T V Martyniuk
S N Nakonechnikov
Clinical guidelines for the diagnosis and treatment of pulmonary hypertension
Терапевтический архив
pulmonary hypertension
clinical guidelines
author_facet I E Chazova
S N Avdeev
N A Tsareva
A V Volkov
T V Martyniuk
S N Nakonechnikov
author_sort I E Chazova
title Clinical guidelines for the diagnosis and treatment of pulmonary hypertension
title_short Clinical guidelines for the diagnosis and treatment of pulmonary hypertension
title_full Clinical guidelines for the diagnosis and treatment of pulmonary hypertension
title_fullStr Clinical guidelines for the diagnosis and treatment of pulmonary hypertension
title_full_unstemmed Clinical guidelines for the diagnosis and treatment of pulmonary hypertension
title_sort clinical guidelines for the diagnosis and treatment of pulmonary hypertension
publisher "Consilium Medicum" Publishing house
series Терапевтический архив
issn 0040-3660
2309-5342
publishDate 2014-09-01
description Pulmonary hypertension (PH) is a group of diseases characterized by progressive increases in pulmonary vascular resistance and pulmonary artery pressure, which results in right ventricular heart failure and sudden death. Based on the current version of the guidelines for PH diagnosis and treatment, adopted by the experts of the European Society of Cardiology and the European Respiratory Society in 2009, and on the data of Russian and foreign clinical trials, the Russian experts elaborated clinical guidelines for PH in 2013. The latter consider the current classifications of PH, the specific features of its pathogenesis, and its diagnostic algorithm. The section dealing with drugs for maintenance therapy discusses data on the use of oral anticoagulants, diuretics, cardiac glycosides, and oxygen therapy. PH-specific therapy includes calcium antagonists, prostanoids, endothelin receptor antagonists, and phosphodiesterase type 5 inhibitors. Surgical procedures for PH involve atrial septostomy, thromboendartectomy, and lung or heart-lung transplantation. A treatment algorithm is proposed for PH patients. The current medicinal approaches using specific therapy agents and their combinations offer new promises for the effective treatment of patients with PH and improve its prognosis.
topic pulmonary hypertension
clinical guidelines
url https://ter-arkhiv.ru/0040-3660/article/view/31535
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AT avvolkov clinicalguidelinesforthediagnosisandtreatmentofpulmonaryhypertension
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