Abstract

Background

This is a case report of a patient diagnosed with Eisenmenger syndrome in adult life.

Case presentation

The patient had a large secundum atrial septal defect diagnosed incidentally in her twenties, with established pulmonary vascular disease and thus the defect was not closed. Over several years the patient showed signs of progressive disease with premature right ventricular dysfunction, preceding any significant symptomatic decline. Her medical therapy was escalated with the addition of intravenous epoprostenol, resulting in both objective and symptomatic improvement.

Conclusions

Early medical intervention and treatment can positively impact on the outcome of patients with pulmonary arterial hypertension associated with congenital heart disease.

Details

Title
Advanced therapies in Eisenmenger syndrome
Author
Nashat, Heba; Constantine, Andrew; Dimopoulos, Konstantinos  VIAFID ORCID Logo 
Pages
1-5
Section
Case study
Publication year
2020
Publication date
2020
Publisher
BioMed Central
e-ISSN
20567251
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2474440024
Copyright
© 2020. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.