Pediatric patients with unrepaired Ebstein's anomaly had significantly higher left ventricular native T1 values compared with age- and sex-matched controls (1026 vs 956 ms, P=0.0004).
Case-Control (n=24)
Does unrepaired Ebstein's anomaly associate with increased left ventricular myocardial fibrosis as measured by CMR T1 mapping in pediatric patients?
Children and adolescents with unrepaired Ebstein's anomaly exhibit an abnormal degree of diffuse left ventricular myocardial fibrosis, which correlates with hypoxemia and disease severity.
Absolute Event Rate: 1026% vs 956%
p-value: p=0.0004
Background: Left ventricular dysfunction in Ebstein’s anomaly (EA) is associated with higher mortality. The health of the left ventricular myocardium in children and adolescents with EA has not been investigated in detail. Methods: Patients with unrepaired EA who had undergone cardiac magnetic resonance imaging including T1 mapping were retrospectively reviewed. Patients were compared with age- and sex-matched controls. EA severity index was calculated using volumetric measurements at end diastole (right atrial+atrialized right ventricular volumes/functional right ventricular+left atrial+left ventricular volumes). Global circumferential and radial strain and as well as strain rate were examined using cardiac magnetic resonance feature tracking. Results: Twelve EA patients and an equal number of controls were included. Functional and atrialized right ventricular end-diastolic volumes were 84±15 and 21±13 mL/m 2 , respectively. Late gadolinium enhancement, confined to the right ventricle, was found in 2 patients (16%). Left ventricular native T1 values and extracellular volume fractions were higher in patients compared with controls (1026±47 versus 956±40 ms, P =0.0004 and 28.5±3.4% versus 22.5±2.6%, P <0.001, respectively). Native T1 times correlated inversely with patients’ age, body surface area, and O 2 saturations (r=−0.63, −0.62, and −0.91, respectively; P =0.02, P =0.02, and P <0.0001, respectively). EA severity index ranged between 0.15 and 0.94 and correlated with T1 values (r=0.76, P =0.003). Native T1 correlated with global circumferential strain (r=0.58, P =0.04) but not ejection fraction (EF). EA patients had reduced maximum oxygen uptake (V o 2 max). V o 2 max correlated inversely with T1 values (r=−0.79, P =0.01). Conclusions: Children and adolescents with EA experience an abnormal degree of diffuse myocardial fibrosis. Its association with O 2 saturation points toward a role of hypoxemia in the pathogenesis of fibrosis. Larger and prospective studies are needed to evaluate the value of T1 mapping for risk stratification and monitoring in EA.
Aly et al. (Mon,) conducted a case-control in Ebstein's anomaly (n=24). Unrepaired Ebstein's anomaly vs. Age- and sex-matched controls was evaluated on Left ventricular native T1 values (p=0.0004). Pediatric patients with unrepaired Ebstein's anomaly had significantly higher left ventricular native T1 values compared with age- and sex-matched controls (1026 vs 956 ms, P=0.0004).
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