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Arrhythmias in children undergoing orthotopic heart transplantation.
Dogan, Eser; Ergin, Firat; Beyter, Mehmet B; Kasikçi, Gülçin K; Ön, Seyma S; Ay, Oguzhan; Levent, Resit E; Engin, Çagatay; Ülger, Zülal.
Afiliação
  • Dogan E; Department of Pediatric Cardiology, Faculty of Medicine, Ege University, Izmir, Türkiye.
  • Ergin F; Department of Pediatric Cardiology, Faculty of Medicine, Ege University, Izmir, Türkiye.
  • Beyter MB; Department of Pediatric Cardiology, Faculty of Medicine, Ege University, Izmir, Türkiye.
  • Kasikçi GK; Department of Pediatric Cardiology, Faculty of Medicine, Ege University, Izmir, Türkiye.
  • Ön SS; Department of Pediatric Cardiology, Faculty of Medicine, Ege University, Izmir, Türkiye.
  • Ay O; Department of Pediatric Cardiology, Faculty of Medicine, Ege University, Izmir, Türkiye.
  • Levent RE; Department of Pediatric Cardiology, Faculty of Medicine, Ege University, Izmir, Türkiye.
  • Engin Ç; Department of Cardiovascular Surgery, Faculty of Medicine, Ege University, Izmir, Türkiye.
  • Ülger Z; Department of Pediatric Cardiology, Faculty of Medicine, Ege University, Izmir, Türkiye.
Front Cardiovasc Med ; 10: 1323958, 2023.
Article em En | MEDLINE | ID: mdl-38274311
ABSTRACT

Introduction:

Heart transplantation (HT) is the only treatment option in children with heart failure secondary to cardiomyopathies and non-reparable congenital heart diseases.

Methods:

We performed a retrospective clinical data review of all consecutive pediatric patients (aged 2-18 years) who underwent orthotopic HT for advanced heart failure at our institution between January 2007 and January 2023. Clinical, procedural, and follow-up data were collected and comprehensively analyzed.

Results:

We identified 27 children (66.7% males) with a median age of 15 years (IQR 7-16) and a median weight of 45 kg (IQR 22-66) at the time of the intervention. 24 patients (88.8%) were diagnosed with dilated cardiomyopathy, 2 (7.4%) with restrictive cardiomyopathy, and 1 (3.7%) with hypertrophic cardiomyopathy. On a median follow-up of 35.07 months (IQR 13.13-111.87), arrhythmias were detected in 9 (33%) patients. Three patients developed symptomatic sinus node dysfunction at 18, 25, and 38 days and received permanent pacemakers. One patient developed a complete AV block during acute rejection at 76 months and received a temporary pacemaker. Two patients developed chronic sinus tachycardia at 4 and 16 months and were treated with Beta-blockers after eliminating all causes of sinus tachycardia. One patient developed a complete right bundle branch block at 12 months. One patient developed ventricular extrasystole at 10 months and was found to have grade 2 rejection. An Atrial extrasystole was detected in one patient at 96 months. We did not identify significant risk factors for arrhythmias post-HT.

Discussion:

After pediatric HT, early-onset rhythm disturbances, often attributed to surgery-related issues such as sinus node dysfunction, may necessitate invasive treatments like permanent pacemaker therapy. Close monitoring post-transplantation is crucial, and routine follow-up with Holter ECG is necessary to identify potential rhythm disorders even in the absence of symptoms. Rhythm disturbances that develop during follow-up can serve as early indicators of graft rejection and should be carefully evaluated.
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Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Cardiovasc Med Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Cardiovasc Med Ano de publicação: 2023 Tipo de documento: Article