EXPERIENCE OF IDIOPATHIC PULMONARY ARTERIAL HYPERTENSION PATIENTS MANAGEMENT IN URAL FEDERAL DISTRICT: FEATURES OFOUTPATIENT-HOSPITAL INTERACTIONS

Idiopathic pulmonary arterial hypertension (IPAH) is a severe chronic and rapidly progressive disease with increasing pulmonary vascular resistance (PVR) due to the ongoing pathogenic processes in the vascular wall that lead to obstruction of small pulmonary arteries and arterioles. IPAH takes a sma...

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Main Authors: S. V. Shalaev, M. V. Arkhipov, A. L. Iofin, A. N. Bykov, L. V. Evrgafova, O. E. Yakovleva, D. F. Nizamova, V. A. Balina, E. V. Milovanova
Format: Article
Language:Russian
Published: InterMedservice 2019-03-01
Series:Евразийский Кардиологический Журнал
Subjects:
Online Access:https://www.heartj.asia/jour/article/view/318
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author S. V. Shalaev
M. V. Arkhipov
A. L. Iofin
A. N. Bykov
L. V. Evrgafova
O. E. Yakovleva
D. F. Nizamova
V. A. Balina
E. V. Milovanova
author_facet S. V. Shalaev
M. V. Arkhipov
A. L. Iofin
A. N. Bykov
L. V. Evrgafova
O. E. Yakovleva
D. F. Nizamova
V. A. Balina
E. V. Milovanova
author_sort S. V. Shalaev
collection DOAJ
description Idiopathic pulmonary arterial hypertension (IPAH) is a severe chronic and rapidly progressive disease with increasing pulmonary vascular resistance (PVR) due to the ongoing pathogenic processes in the vascular wall that lead to obstruction of small pulmonary arteries and arterioles. IPAH takes a small part in the structure among all forms of pulmonary hypertension (PH), the median survival of patients with IPAH before any PAH-specific therapy became available were about 2,8 years, and the average time from the manifestation of the disease to its diagnosis took 2-3 years. This article is an attempt to present an unified data of adult patients with IPAH in Ural Federal district, and describe PH patients medical care service. The article presents the experience of PH Medical Centers across Ural Federal District.
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spelling doaj.art-6e29b3487a7e4676820d11453954b4b12023-03-13T07:47:34ZrusInterMedserviceЕвразийский Кардиологический Журнал2225-16852305-07482019-03-0101142810.38109/2225-1685-2019-1-14-28317EXPERIENCE OF IDIOPATHIC PULMONARY ARTERIAL HYPERTENSION PATIENTS MANAGEMENT IN URAL FEDERAL DISTRICT: FEATURES OFOUTPATIENT-HOSPITAL INTERACTIONSS. V. Shalaev0M. V. Arkhipov1A. L. Iofin2A. N. Bykov3L. V. Evrgafova4O. E. Yakovleva5D. F. Nizamova6V. A. Balina7E. V. Milovanova8Центр сердца и сосудов при ГБУЗ Тюменской области «Областная клиническая больница № 1»; ФГБОУ ВО «Тюменский государственный медицинский университет» МЗ РФФГБОУ ВО «Уральский государственный медицинский университет Минздрава России»ГБУЗ Свердловской области «Свердловская областная клиническая больница №1»ГБУЗ Свердловской области «Свердловская областная клиническая больница №1»ГБУЗ Свердловской области «Свердловская областная клиническая больница №1»ГБУЗ «Челябинский областной кардиологический диспансер»Центр сердца и сосудов при ГБУЗ Тюменской области «Областная клиническая больница № 1»ГБУЗ Тюменской области «Областная клиническая больница № 1»БУ ХМАО-Югры «Окружной кардиологический диспансер «Центр диагностики и сердечно-сосудистой хирургии»Idiopathic pulmonary arterial hypertension (IPAH) is a severe chronic and rapidly progressive disease with increasing pulmonary vascular resistance (PVR) due to the ongoing pathogenic processes in the vascular wall that lead to obstruction of small pulmonary arteries and arterioles. IPAH takes a small part in the structure among all forms of pulmonary hypertension (PH), the median survival of patients with IPAH before any PAH-specific therapy became available were about 2,8 years, and the average time from the manifestation of the disease to its diagnosis took 2-3 years. This article is an attempt to present an unified data of adult patients with IPAH in Ural Federal district, and describe PH patients medical care service. The article presents the experience of PH Medical Centers across Ural Federal District.https://www.heartj.asia/jour/article/view/318легочная артериальная гипертензия (лаг)идиопатическая легочная гипертензия (илаг)регистрэпидемиологиялечение
spellingShingle S. V. Shalaev
M. V. Arkhipov
A. L. Iofin
A. N. Bykov
L. V. Evrgafova
O. E. Yakovleva
D. F. Nizamova
V. A. Balina
E. V. Milovanova
EXPERIENCE OF IDIOPATHIC PULMONARY ARTERIAL HYPERTENSION PATIENTS MANAGEMENT IN URAL FEDERAL DISTRICT: FEATURES OFOUTPATIENT-HOSPITAL INTERACTIONS
Евразийский Кардиологический Журнал
легочная артериальная гипертензия (лаг)
идиопатическая легочная гипертензия (илаг)
регистр
эпидемиология
лечение
title EXPERIENCE OF IDIOPATHIC PULMONARY ARTERIAL HYPERTENSION PATIENTS MANAGEMENT IN URAL FEDERAL DISTRICT: FEATURES OFOUTPATIENT-HOSPITAL INTERACTIONS
title_full EXPERIENCE OF IDIOPATHIC PULMONARY ARTERIAL HYPERTENSION PATIENTS MANAGEMENT IN URAL FEDERAL DISTRICT: FEATURES OFOUTPATIENT-HOSPITAL INTERACTIONS
title_fullStr EXPERIENCE OF IDIOPATHIC PULMONARY ARTERIAL HYPERTENSION PATIENTS MANAGEMENT IN URAL FEDERAL DISTRICT: FEATURES OFOUTPATIENT-HOSPITAL INTERACTIONS
title_full_unstemmed EXPERIENCE OF IDIOPATHIC PULMONARY ARTERIAL HYPERTENSION PATIENTS MANAGEMENT IN URAL FEDERAL DISTRICT: FEATURES OFOUTPATIENT-HOSPITAL INTERACTIONS
title_short EXPERIENCE OF IDIOPATHIC PULMONARY ARTERIAL HYPERTENSION PATIENTS MANAGEMENT IN URAL FEDERAL DISTRICT: FEATURES OFOUTPATIENT-HOSPITAL INTERACTIONS
title_sort experience of idiopathic pulmonary arterial hypertension patients management in ural federal district features ofoutpatient hospital interactions
topic легочная артериальная гипертензия (лаг)
идиопатическая легочная гипертензия (илаг)
регистр
эпидемиология
лечение
url https://www.heartj.asia/jour/article/view/318
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AT evmilovanova experienceofidiopathicpulmonaryarterialhypertensionpatientsmanagementinuralfederaldistrictfeaturesofoutpatienthospitalinteractions