Background: Early identification of subclinical left ventricular (LV) systolic dysfunction (LVSD) in patients with isolated left bundle branch block (LBBB) and preserved LV ejection fraction (LVEF), termed LBBBpEF, is clinically important. Electrocardiography (ECG) has been proposed as a potential screening tool for detecting subclinical LVSD in LBBBpEF patients, but its effectiveness has not been fully validated. This study investigated the relationships between specific ECG characteristics and subclinical LVSD in LBBBpEF patients.
Methods: The study included 111 patients with LBBBpEF. Two-dimensional speckle-tracking echocardiography was used to derive the LV global longitudinal strain (LV GLS), with LV GLS>-20% indicating subclinical LVSD. The recorded ECG characteristics included heart rate, QRS duration, P-R duration, QRS morphology, T-wave morphology, the presence of QS patterns, and discordant LBBB, among others. The presence of QS patterns was defined as the absence of R-waves in lead V1 (or R-waves < 1 mm with a scale of 10 mm/mV). Discordant LBBB was defined as an inconsistency between the T wave and QRS complex in leads I, V5, and V6.
Results: Among the patients, 52 exhibited subclinical LVSD. Compared with those with normal LV systolic function, patients with subclinical LVSD had longer QRS durations, a higher frequency of QS patterns, and more instances of discordant LBBB. A QRS duration of 153 ms was identified as the optimal cut-off for detecting subclinical LVSD, with a sensitivity of 75.00% and specificity of 72.88%. The combination of QRS duration, the presence of QS patterns, and discordant LBBB produced the highest area under the curve of 0.82. Incorporating the presence of QS patterns and discordant LBBB into the QRS duration model increased the integrated discriminant index from 0.07 to 0.15.
Conclusions: QRS duration, the presence of QS patterns, and discordant LBBB are independent predictors of subclinical LVSD in patients with LBBBpEF. An integrated ECG assessment may offer a straightforward screening method for identifying subclinical LVSD in this population.
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