Key result
RVP QRS duration over ~170 ms identifies reversible VPD-induced cardiomyopathy with 97% specificity.
Why the study?
A high burden of ventricular premature depolarizations has been associated with reversible LV dysfunction, but many patients maintain normal LV function despite high VPD burden, necessitating a method to identify VPD-induced cardiomyopathy.
Cross-Sectional (n=62)
RVa pacing may identify VPD-induced CMP risk; leaves open whether it predicts reversible dysfunction or guides therapy.
BACKGROUND: A high burden of ventricular premature depolarizations (VPDs) has been associated with potentially reversible left ventricular (LV) dysfunction, termed as VPD-induced cardiomyopathy (CMP). However, many patients maintain normal LV function despite a high VPD burden. The purpose of this study was to identify CMP by right ventricle apex (RVa) pacing method in patients with high VPD burden. METHODS: A total of 62 patients (28 male; mean age = 50 ± 15 years) with idiopathic VPDs undergoing ablation were enrolled. RVa pacing was recorded in all patients during the procedure. The paced QRS duration (QRSd) during RV pacing was measured from the pacing spike to the latest QRS deflection on any surface electrocardiogram lead. Patients were divided into two groups: reversible VPD-induced CMP (Group R; n = 15, 14 males, mean age = 54 ± 14 years) and normal LV function (Group N; n = 47, 23 males, mean age = 54 ± 15 years). RESULTS: The LV ejection fraction (%) was significantly lower in Group R as compared with Group N (Group R, Group N = 36 ± 6, 58 ± 4; P < 0.001); however, LV end-diastolic dimension mm was not significantly different between the two study groups (Group R, Group N = 54 ± 5, 50 ± 6; P = 0.06). Similarly, sinus QRS width (P = 0.10), VPD-burden (P = 0.36), and body surface area (P = 0.75) were not significantly different between Group R and Group N. The QRSd was significantly longer in Group R compared with Group N (177 ± 8 vs 150 ± 14; P < 0.001). Using a QRSd cut-off value of 170.1 ms, VPD-induced CMP was identified with a sensitivity of 73% and a specificity of 97%. CONCLUSION: RVa pacing with transmyocardial conduction time assessment was a useful method for identifying idiopathic VPD-induced CMP. Using a QRSd cut-off value of 170.1 ms, VPD-induced CMP was identified with a sensitivity of 73% and a specificity of 97%.
No takes yet. Share an insight, caveat, or question.
Im et al. (2018) conducted a cross-sectional in Idiopathic ventricular premature depolarizations (VPDs) (n=62). Right ventricle apex (RVa) pacing vs. Normal left ventricular function was evaluated on Paced QRS duration (QRSd) during RV pacing (p=<0.001). Right ventricle apex pacing with a paced QRS duration cut-off of 170.1 ms identified reversible VPD-induced cardiomyopathy with 73% sensitivity and 97% specificity.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: