Literature DB >> 32622496

Congenital Heart Disease and Pulmonary Hypertension.

Andrew Constantine1, Konstantinos Dimopoulos2, Alexander R Opotowsky3.   

Abstract

Pulmonary hypertension (PH) is common in adults with congenital heart disease and carries fundamental implications for management and prognosis. A high index of suspicion, combined with knowledge of the pathogenesis and pathophysiology of PH, is required to achieve a timely, accurate diagnosis, and appropriate classification and treatment. This article provides a guide on how to approach the adult with congenital heart disease and suspected PH of different types, including current management.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Adult congenital heart disease; Cardiac catheterization; Echocardiography; Eisenmenger syndrome; Postcapillary; Precapillary; Pulmonary hypertension

Mesh:

Year:  2020        PMID: 32622496     DOI: 10.1016/j.ccl.2020.04.008

Source DB:  PubMed          Journal:  Cardiol Clin        ISSN: 0733-8651            Impact factor:   2.213


  3 in total

1.  Clinical and genetic analysis of 2 rare cases of Wiskott-Aldrich syndrome from Chinese minorities: Two case reports.

Authors:  Haifeng Liu; Yanchun Wang; Yangfang Li; Lvyan Tao; Yu Zhang; Xiaoli He; Yuantao Zhou; Xiaoning Liu; Yan Wang; Li Li
Journal:  Medicine (Baltimore)       Date:  2021-04-23       Impact factor: 1.817

2.  The Adult Congenital Heart Disease Anatomic and Physiological Classification: Associations with Clinical Outcomes in Patients with Atrial Arrhythmias.

Authors:  Anastasios Kartas; Andreas S Papazoglou; Diamantis Kosmidis; Dimitrios V Moysidis; Amalia Baroutidou; Ioannis Doundoulakis; Stefanos Despotopoulos; Elena Vrana; Athanasios Koutsakis; Georgios P Rampidis; Despoina Ntiloudi; Sotiria Liori; Tereza Mousiama; Dimosthenis Avramidis; Sotiria Apostolopoulou; Alexandra Frogoudaki; Afrodite Tzifa; Haralambos Karvounis; George Giannakoulas
Journal:  Diagnostics (Basel)       Date:  2022-02-11

3.  A novel de novo heterozygous variant of the KCNQ2 gene: Contribution to early‑onset epileptic encephalopathy in a female infant.

Authors:  Hai-Feng Liu; Ting-Yun Yuan; Jia-Wu Yang; Feng Li; Fan Wang; Hong-Min Fu
Journal:  Mol Med Rep       Date:  2022-07-20       Impact factor: 3.423

  3 in total

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