Isolated very low QRS voltage in the frontal leads predicts recurrence of neurally mediated syncope
The study was prompted by our observation that some patients with neurally mediated syncope (NMS) have an isolated QRS complex, of very low voltage (≤0.3 mV cutoff), in 1 of the frontal leads on the 12-lead electrocardiogram. To prospectively evaluate whether the presence of isolated very low voltag...
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Veröffentlicht in: | Heart rhythm 2019-12, Vol.16 (12), p.1862-1869 |
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Zusammenfassung: | The study was prompted by our observation that some patients with neurally mediated syncope (NMS) have an isolated QRS complex, of very low voltage (≤0.3 mV cutoff), in 1 of the frontal leads on the 12-lead electrocardiogram.
To prospectively evaluate whether the presence of isolated very low voltage (VLV) predicts recurrence of NMS.
We included 205 patients (aged 50 ± 17 years) with a median of 3 syncopal episodes. Tilt testing was performed in all patients and was positive in 87 (42%). The patients were followed for a median of 14 months.
VLV in frontal leads was present in 92 patients (45%). During the follow-up period 60 patients experienced recurrence of syncope. The actuarial total syncope recurrence rate at 1 year was 32% (95% confidence interval [CI 23%–44%) in patients with isolated VLV in frontal plane leads, and 14% (95% CI 8%–24%) in patients without VLV (log-rank test P < .0001). The significant relationship between the presence of isolated VLV in the frontal leads and syncope recurrence was retained in Cox multivariate analysis that included the history of presyncope and syncope as well as the left ventricular end-diastolic diameter. The presence of isolated VLV in frontal leads was associated with a 3-fold increase of the risk of recurrent syncope.
Isolated very low QRS voltage in the frontal leads predicts recurrence of NMS independent of clinical factors that predict recurrence of syncope in such patients. This phenomenon may help generate new diagnostic tools and insights into the pathogenesis of NMS.
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ISSN: | 1547-5271 1556-3871 |
DOI: | 10.1016/j.hrthm.2019.06.006 |