Heart failure in adults with congenital heart disease.
Acute heart failure in congenital heart disease
Heart failure in adult congenital heart disease
Heart transplantation in adult congenital heart disease
Journal
International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291
Informations de publication
Date de publication:
15 06 2022
15 06 2022
Historique:
received:
13
01
2022
revised:
28
02
2022
accepted:
07
03
2022
pubmed:
15
3
2022
medline:
4
5
2022
entrez:
14
3
2022
Statut:
ppublish
Résumé
Heart failure (HF) represents the leading cause of morbidity and mortality in adult patients with congenital heart disease. The nature of underlying congenital heart disease has bearing on timing and severity of HF and impacts on short- and long-term outcomes. HF can be subclinical, underscoring the need for close follow-up at tertiary centres with timely management of target hemodynamic lesions. Drug therapies have an effect in systemic left ventricle failure and are employed in acute HF for symptomatic relief. Data on elective drug therapy for the failing systemic right ventricle and/or Fontan circulation is currently lacking. Drugs such as angiotensin receptor blockers with neprilysin inhibitors or sodium-glucose co-transporter-2 inhibitors may show benefit. Cardiac resynchronization therapy, in appropriately selected patients, is considered a treatment option. Mechanical circulatory support and transplantation remain the last resource in highly selected patients. As the congenital heart disease population continues to grow and age, both outpatient and inpatient service for HF will continue to play a major role in the care of adult patients with congenital heart disease.
Identifiants
pubmed: 35283250
pii: S0167-5273(22)00337-0
doi: 10.1016/j.ijcard.2022.03.018
pii:
doi:
Substances chimiques
Angiotensin Receptor Antagonists
0
Sodium-Glucose Transporter 2 Inhibitors
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
39-45Commentaires et corrections
Type : CommentIn
Type : CommentIn
Informations de copyright
Copyright © 2022 Elsevier B.V. All rights reserved.