Clinical Course of TGA After Arterial Switch Operation in the Current Era.

arterial switch operation long-term outcome re-intervention transposition of the great arteries

Journal

JACC. Advances
ISSN: 2772-963X
Titre abrégé: JACC Adv
Pays: United States
ID NLM: 9918419284106676

Informations de publication

Date de publication:
Feb 2024
Historique:
received: 17 01 2023
revised: 28 08 2023
accepted: 13 10 2023
medline: 28 6 2024
pubmed: 28 6 2024
entrez: 28 6 2024
Statut: epublish

Résumé

The number of patients with an arterial switch operation (ASO) for transposition of the great arteries (TGA) is steadily growing; limited information is available regarding the clinical course in the current era. The purpose was to describe clinical outcome late after ASO in a national cohort, including survival, rates of (re-)interventions, and clinical events. A total of 1,061 TGA-ASO patients (median age 10.7 years [IQR: 2.0-18.2 years]) from a nationwide prospective registry with a median follow-up of 8.0 years (IQR: 5.4-8.8 years) were included. Using an analysis with age as the primary time scale, cumulative incidence of survival, (re)interventions, and clinical events were determined. At the age of 35 years, late survival was 93% (95% CI: 88%-98%). The cumulative re-intervention rate at the right ventricular outflow tract and pulmonary branches was 36% (95% CI: 31%-41%). Other cumulative re-intervention rates at 35 years were on the left ventricular outflow tract (neo-aortic root and valve) 16% (95% CI: 10%-22%), aortic arch 9% (95% CI: 5%-13%), and coronary arteries 3% (95% CI: 1%-6%). Furthermore, 11% (95% CI: 6%-16%) of the patients required electrophysiological interventions. Clinical events, including heart failure, endocarditis, and myocardial infarction occurred in 8% (95% CI: 5%-11%). Independent risk factors for any (re-)intervention were TGA morphological subtype (Taussig-Bing double outlet right ventricle [HR: 4.9, 95% CI: 2.9-8.1]) and previous pulmonary artery banding (HR: 1.6, 95% CI: 1.0-2.2). TGA-ASO patients have an excellent survival. However, their clinical course is characterized by an ongoing need for (re-)interventions, especially on the right ventricular outflow tract and the left ventricular outflow tract indicating a strict lifelong surveillance, also in adulthood.

Sections du résumé

Background UNASSIGNED
The number of patients with an arterial switch operation (ASO) for transposition of the great arteries (TGA) is steadily growing; limited information is available regarding the clinical course in the current era.
Objectives UNASSIGNED
The purpose was to describe clinical outcome late after ASO in a national cohort, including survival, rates of (re-)interventions, and clinical events.
Methods UNASSIGNED
A total of 1,061 TGA-ASO patients (median age 10.7 years [IQR: 2.0-18.2 years]) from a nationwide prospective registry with a median follow-up of 8.0 years (IQR: 5.4-8.8 years) were included. Using an analysis with age as the primary time scale, cumulative incidence of survival, (re)interventions, and clinical events were determined.
Results UNASSIGNED
At the age of 35 years, late survival was 93% (95% CI: 88%-98%). The cumulative re-intervention rate at the right ventricular outflow tract and pulmonary branches was 36% (95% CI: 31%-41%). Other cumulative re-intervention rates at 35 years were on the left ventricular outflow tract (neo-aortic root and valve) 16% (95% CI: 10%-22%), aortic arch 9% (95% CI: 5%-13%), and coronary arteries 3% (95% CI: 1%-6%). Furthermore, 11% (95% CI: 6%-16%) of the patients required electrophysiological interventions. Clinical events, including heart failure, endocarditis, and myocardial infarction occurred in 8% (95% CI: 5%-11%). Independent risk factors for any (re-)intervention were TGA morphological subtype (Taussig-Bing double outlet right ventricle [HR: 4.9, 95% CI: 2.9-8.1]) and previous pulmonary artery banding (HR: 1.6, 95% CI: 1.0-2.2).
Conclusions UNASSIGNED
TGA-ASO patients have an excellent survival. However, their clinical course is characterized by an ongoing need for (re-)interventions, especially on the right ventricular outflow tract and the left ventricular outflow tract indicating a strict lifelong surveillance, also in adulthood.

Identifiants

pubmed: 38939383
doi: 10.1016/j.jacadv.2023.100772
pii: S2772-963X(23)00803-7
pmc: PMC11198364
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100772

Informations de copyright

© 2024 The Authors.

Déclaration de conflit d'intérêts

Support was received from the Netherlands Cardiovascular Research lnitiative: An initiative with support of the Dutch Heart Foundation and Hartekind, CVON2019-002 OUTREACH. The authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Leo J Engele (LJ)

Department of Cardiology, Center for Congenital Heart Disease Amsterdam-Leiden (CAHAL), Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
Netherlands Heart Institute, the Netherlands.

Roel L F van der Palen (RLF)

Division of Pediatric Cardiology, Department of Pediatrics, Center for Congenital Heart Disease Amsterdam-Leiden (CAHAL), Leiden University Medical Center, Leiden, the Netherlands.

Renée S Joosen (RS)

Wilhelmina Children's Hospital, University Medical Centre Utrecht, Utrecht, the Netherlands.

Gertjan T Sieswerda (GT)

Department of Cardiology, University Medical Center Utrecht, Utrecht, the Netherlands.

Paul H Schoof (PH)

Department of Pediatric Cardiac Surgery, Wilhelmina Children's Hospital (Part of University Medical Center Utrecht), Utrecht, the Netherlands.

Joost P van Melle (JP)

Department of Cardiology, University Medical Center Groningen, Groningen, the Netherlands.

Rolf M F Berger (RMF)

Department of Pediatric Cardiology, Centre for Congenital Heart Diseases, Beatrix Children's Hospital, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.

Ryan E Accord (RE)

Department of Cardiothoracic Surgery, University Medical Center Groningen, Groningen, the Netherlands.

Lukas A J Rammeloo (LAJ)

Division of Pediatric Cardiology, Department of Pediatrics, Center for Congenital Heart Disease Amsterdam-Leiden (CAHAL), Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.

Thelma C Konings (TC)

Department of Cardiology, Center for Congenital Heart Disease Amsterdam-Leiden (CAHAL), Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.

Wim A Helbing (WA)

Department of Pediatric Cardiology, Erasmus Medical Center, Rotterdam, the Netherlands.

Jolien W Roos-Hesselink (JW)

Department of Cardiology, Erasmus Medical Center, Rotterdam, the Netherlands.

Pieter C van de Woestijne (PC)

Department of Cardiothoracic Surgery, Erasmus Medical Center, Rotterdam, the Netherlands.

Stefan Frerich (S)

Department of Pediatric Cardiology, Academic Hospital Maastricht, Maastricht, the Netherlands.

Arie P J van Dijk (APJ)

Department of Pediatric Cardiology, Radboud University Medical Center, Nijmegen, the Netherlands.
Department of Cardiology, Radboud University Medical Center, Nijmegen, the Netherlands.

Irene M Kuipers (IM)

Division of Pediatric Cardiology, Department of Pediatrics, Center for Congenital Heart Disease Amsterdam-Leiden (CAHAL), Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.

Mark G H Hazekamp (MGH)

Department of Cardiothoracic Surgery, Center for Congenital Heart Disease Amsterdam-Leiden (CAHAL), Leiden University Medical Center, Leiden, the Netherlands.

Barbara J M Mulder (BJM)

Department of Cardiology, Center for Congenital Heart Disease Amsterdam-Leiden (CAHAL), Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
Netherlands Heart Institute, the Netherlands.

Johannes M P J Breur (JMPJ)

Wilhelmina Children's Hospital, University Medical Centre Utrecht, Utrecht, the Netherlands.

Nico Blom (N)

Division of Pediatric Cardiology, Department of Pediatrics, Center for Congenital Heart Disease Amsterdam-Leiden (CAHAL), Leiden University Medical Center, Leiden, the Netherlands.
Division of Pediatric Cardiology, Department of Pediatrics, Center for Congenital Heart Disease Amsterdam-Leiden (CAHAL), Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.

Monique R M Jongbloed (MRM)

Department of Cardiology, Center for Congenital Heart Disease Amsterdam-Leiden (CAHAL), Leiden University Medical Center, Leiden, the Netherlands.
Department of Anatomy and Embryology, Center for Congenital Heart Disease Amsterdam-Leiden (CAHAL), Leiden University Medical Center, Leiden, the Netherlands.

Berto J Bouma (BJ)

Department of Cardiology, Center for Congenital Heart Disease Amsterdam-Leiden (CAHAL), Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
Netherlands Heart Institute, the Netherlands.

Classifications MeSH