Implementing the ESC/ERS pulmonary hypertension guidelines: real-life cases from a national referral centre

Pulmonary hypertension (PH) comprises a heterogeneous group of disorders characterised by increased pulmonary vascular resistance that results in progressive right ventricular failure. In order to translate current evidence into routine clinical practice, the European Society of Cardiology (ESC) and...

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Main Authors: D. Montani, D. S. O'Callaghan, X. Jaïs, L. Savale, D. Natali, A. Redzepi, S. Hoette, F. Parent, O. Sitbon, G. Simonneau, M. Humbert
Format: Article
Language:English
Published: European Respiratory Society 2009-12-01
Series:European Respiratory Review
Online Access:http://err.ersjournals.com/cgi/content/full/18/114/272
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spelling doaj-811fbe077c70466990e5c33e872588e92020-11-25T00:57:27ZengEuropean Respiratory SocietyEuropean Respiratory Review0905-91801600-06172009-12-0118114272290Implementing the ESC/ERS pulmonary hypertension guidelines: real-life cases from a national referral centreD. MontaniD. S. O'CallaghanX. JaïsL. SavaleD. NataliA. RedzepiS. HoetteF. ParentO. SitbonG. SimonneauM. HumbertPulmonary hypertension (PH) comprises a heterogeneous group of disorders characterised by increased pulmonary vascular resistance that results in progressive right ventricular failure. In order to translate current evidence into routine clinical practice, the European Society of Cardiology (ESC) and the European Respiratory Society (ERS) have recently jointly proposed evidence-based guidelines for the optimal management of different PH patient groups. This article describes a series of clinical cases of PH due to various aetiologies that were referred to a large national PH expert referral centre. In each case, the assessment and therapeutic approach undertaken is described in the context of the new ECS/ERS guidelines. The routine diagnostic work-up of suspected idiopathic pulmonary arterial hypertension (PAH) and recommended treatments for patients with functional class II, III and IV disease is emphasised. Familial screening and management of heritable PAH is discussed. Appropriate investigation and therapeutic strategies for patients with chronic thromboembolic disease and PH that is associated with congenital heart disease, pulmonary veno-occlusive disease and systemic sclerosis are also highlighted. http://err.ersjournals.com/cgi/content/full/18/114/272
collection DOAJ
language English
format Article
sources DOAJ
author D. Montani
D. S. O'Callaghan
X. Jaïs
L. Savale
D. Natali
A. Redzepi
S. Hoette
F. Parent
O. Sitbon
G. Simonneau
M. Humbert
spellingShingle D. Montani
D. S. O'Callaghan
X. Jaïs
L. Savale
D. Natali
A. Redzepi
S. Hoette
F. Parent
O. Sitbon
G. Simonneau
M. Humbert
Implementing the ESC/ERS pulmonary hypertension guidelines: real-life cases from a national referral centre
European Respiratory Review
author_facet D. Montani
D. S. O'Callaghan
X. Jaïs
L. Savale
D. Natali
A. Redzepi
S. Hoette
F. Parent
O. Sitbon
G. Simonneau
M. Humbert
author_sort D. Montani
title Implementing the ESC/ERS pulmonary hypertension guidelines: real-life cases from a national referral centre
title_short Implementing the ESC/ERS pulmonary hypertension guidelines: real-life cases from a national referral centre
title_full Implementing the ESC/ERS pulmonary hypertension guidelines: real-life cases from a national referral centre
title_fullStr Implementing the ESC/ERS pulmonary hypertension guidelines: real-life cases from a national referral centre
title_full_unstemmed Implementing the ESC/ERS pulmonary hypertension guidelines: real-life cases from a national referral centre
title_sort implementing the esc/ers pulmonary hypertension guidelines: real-life cases from a national referral centre
publisher European Respiratory Society
series European Respiratory Review
issn 0905-9180
1600-0617
publishDate 2009-12-01
description Pulmonary hypertension (PH) comprises a heterogeneous group of disorders characterised by increased pulmonary vascular resistance that results in progressive right ventricular failure. In order to translate current evidence into routine clinical practice, the European Society of Cardiology (ESC) and the European Respiratory Society (ERS) have recently jointly proposed evidence-based guidelines for the optimal management of different PH patient groups. This article describes a series of clinical cases of PH due to various aetiologies that were referred to a large national PH expert referral centre. In each case, the assessment and therapeutic approach undertaken is described in the context of the new ECS/ERS guidelines. The routine diagnostic work-up of suspected idiopathic pulmonary arterial hypertension (PAH) and recommended treatments for patients with functional class II, III and IV disease is emphasised. Familial screening and management of heritable PAH is discussed. Appropriate investigation and therapeutic strategies for patients with chronic thromboembolic disease and PH that is associated with congenital heart disease, pulmonary veno-occlusive disease and systemic sclerosis are also highlighted.
url http://err.ersjournals.com/cgi/content/full/18/114/272
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