Pulmonary arterial hypertension associated with congenital heart disease.

Abstract:

:In the past decade, there have been more patients with congenital heart disease (CHD) surviving to adulthood; whether due to late repair, or complex underlying CHD, many of these patients will be faced with pulmonary arterial hypertension (PAH) associated with CHD (APAH-CHD). In this review, the authors discuss the most commonly encountered forms of APAH-CHD, how to interpret the hemodynamic data, and how to classify the patients into meaningful subgroups that have similar management strategies. The current state of targeted medical treatments available to patients with APAH-CHD is also discussed.

journal_name

Clin Chest Med

authors

Krishnan U,Rosenzweig EB

doi

10.1016/j.ccm.2013.08.011

subject

Has Abstract

pub_date

2013-12-01 00:00:00

pages

707-17

issue

4

eissn

0272-5231

issn

1557-8216

pii

S0272-5231(13)00111-1

journal_volume

34

pub_type

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