Back to Search Start Over

Pacemaker treatment after Fontan surgery-A Swedish national study.

Authors :
Alenius Dahlqvist J
Sunnegårdh J
Hanséus K
Strömvall Larsson E
Nygren A
Dalén M
Berggren H
Johansson Ramgren J
Wiklund U
Rydberg A
Source :
Congenital heart disease [Congenit Heart Dis] 2019 Jul; Vol. 14 (4), pp. 582-589. Date of Electronic Publication: 2019 Mar 18.
Publication Year :
2019

Abstract

Objective: Fontan surgery is performed in children with univentricular heart defects. Previous data regarding permanent pacemaker implantation frequency and indications in Fontan patients are limited and conflicting. We examined the prevalence of and risk factors for pacemaker treatment in a consecutive national cohort of patients after Fontan surgery in Sweden.<br />Methods: We retrospectively reviewed all Swedish patients who underwent Fontan surgery from 1982 to 2017 (n = 599).<br />Results: After a mean follow-up of 12.2 years, 13% (78/599) of the patients with Fontan circulation had received pacemakers. Patients operated with the extracardiac conduit (EC) type of total cavopulmonary connection had a significantly lower prevalence of pacemaker implantation (6%) than patients with lateral tunnel (LT; 17%). Mortality did not differ between patients with (8%) and without pacemaker (5%). The most common pacemaker indication was sinus node dysfunction (SND) (64%). Pacemaker implantation due to SND was less common among patients with EC. Pacemaker implantation was significantly more common in patients with mitral atresia (MA; 44%), double outlet right ventricle (DORV; 24%) and double inlet left ventricle (DILV; 20%). In contrast, patients with pulmonary atresia with intact ventricular septum and hypoplastic left heart syndrome were significantly less likely to receive a pacemaker (3% and 6%, respectively).<br />Conclusions: Thirteen percent of Fontan patients received a permanent pacemaker, most frequently due to SND. EC was associated with a significantly lower prevalence of pacemaker than LT. Permanent pacemaker was more common in patients with MA, DORV, and DILV.<br /> (© 2019 Wiley Periodicals, Inc.)

Details

Language :
English
ISSN :
1747-0803
Volume :
14
Issue :
4
Database :
MEDLINE
Journal :
Congenital heart disease
Publication Type :
Academic Journal
Accession number :
30883035
Full Text :
https://doi.org/10.1111/chd.12766