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Classic-Pattern Dyssynchrony in Adolescents and Adults With a Fontan Circulation
Assami Rösner1, Tigran Khalapyan2, Håvard Dalen3
1Department of Cardiology, Division of Cardiothoracic and Respiratory Medicine, University Hospital of North Norway, Tromsø, Norway.
Insights
Classic-pattern dyssynchrony (CPD) is found in some Fontan patients and is linked to poorer heart function. This suggests CPD may predict response to cardiac resynchronization therapy in single-ventricle patients.
Area of Science:
- Cardiology
- Pediatric Cardiology
- Cardiac Electrophysiology
Background:
- Single ventricle physiology presents unique challenges in cardiac mechanics.
- Previous research indicated potential dyssynchrony in single ventricle hearts.
- The Fontan procedure, a palliative surgery, creates a univentricular circulation model.
Purpose of the Study:
- To investigate the prevalence of classic-pattern dyssynchrony (CPD) in patients with single-ventricle physiology post-Fontan palliation.
- To determine the relationship between CPD, QRS duration, and myocardial function (systolic and diastolic) in this population.
Main Methods:
- Retrospective cross-sectional study of 101 adolescent and adult patients who underwent Fontan procedure.
- Visual assessment of strain curves for the presence of CPD.
- Echocardiographic evaluation of systolic and diastolic function.
Main Results:
- Fifteen percent of Fontan patients exhibited CPD.
- CPD was more common in patients with two sizable ventricular components (43%) compared to dominant left (6%) or right (9%) ventricles (P=.016).
- Patients with CPD showed significantly longer QRS duration, reduced ejection fraction, and impaired global systolic and diastolic strain compared to those without CPD.
Conclusions:
- Classic-pattern dyssynchrony (CPD) is present in a notable proportion of Fontan survivors.
- CPD is associated with diminished systolic and diastolic myocardial function.
- These findings suggest CPD may be a valuable predictor for cardiac resynchronization therapy in univentricular hearts, warranting further investigation.
Background:
Previous studies have suggested the presence of dyssynchrony in the functionally single ventricle. The aim of this study was to investigate the presence of classic-pattern dyssynchrony (CPD), characterized by typical early and late deformation of opposite walls, and its relation to QRS duration and myocardial function in patients with single-ventricle physiology after Fontan palliation.
Methods:
In a retrospective cross-sectional study, 101 adolescent and adult patients with single-ventricle physiology after the Fontan procedure were investigated. Strain curves were visually assessed for the presence of CPD. Systolic and diastolic function were assessed using echocardiography.
Results:
One hundred one patients were included, with varying anatomic morphology: two sizable ventricular components (n = 21), right dominant (n = 21), left dominant (n = 49), and undefined anatomy (n = 10). Fifteen of 101 Fontan patients had CPD. Forty-three percent of patients with two sizable ventricular masses displayed CPD, mostly with prolonged QRS, while the number of patients with CPD with right-dominant (9%) and left-dominant (6%) morphology was significantly lower (P = .016). Those with CPD displayed significantly (P < .05) larger QRS widths (142 ± 22 vs 112 ± 24 msec), lower ejection fractions (31 ± 14% vs 45 ± 14%), lower global early diastolic strain rates (0.7 ± 0.5 vs 1.2 ± 0.8 sec-1), and global systolic circumferential (-10 ± 5% vs -16 ± 7%) and longitudinal (-9 ± 5% vs -14 ± 5%) strain, respectively.
Conclusions:
CPD is present in a proportion of adolescent and adult patients after Fontan palliation. The presence of CPD is associated with reduced systolic and diastolic function compared with Fontan patients without CPD. Because the presence of CPD appears to be a promising predictor for response to cardiac resynchronization therapy in patients with biventricular circulation, these findings may have important potential for prospective evaluation of cardiac resynchronization therapy in patients with univentricular circulation.
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