Arrhythmic risk in single or recurrent episodes of unexplained syncope with complete bundle branch block.

Rev Esp Cardiol (Engl Ed)

Departament de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain; Servei de Cardiologia, Hospital Universitari Vall d'Hebron i Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain; Centro de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), Spain.

Published: August 2023

AI Article Synopsis

  • The study compares patients with a single syncopal episode (SSE) and those with recurrent syncopal episodes (RSE) who also have complete bundle branch block (cBBB), focusing on arrhythmic risk and clinical outcomes.
  • Results show that both groups have similar risks for arrhythmic syncope and similar rates of diagnostic yield from electrophysiological studies and implantable cardiac monitors.
  • The findings suggest that there is no clinical reason to treat patients with SSE differently from those with RSE, as they experience comparable outcomes and risks.

Article Abstract

Introduction And Objectives: Patients with a single syncopal episode (SSE) and complete bundle branch block (cBBB) are frequently managed more conservatively than patients with recurrent episodes (RSE). The objective of this study was to analyze if there are differences between patients with single or recurrent unexplained syncope and cBBB in arrhythmic risk, the diagnostic yield of tests, and clinical outcomes.

Methods: Cohort study of consecutive patients with unexplained syncope and cBBB with a median follow-up time of 3 years. The patients were evaluated via a stepwise workup protocol based on electrophysiological study (EPS) and long-term follow-up with an implantable cardiac monitor.

Results: Of the 503 patients included in the study, 238 (47.3%) had had only 1 syncopal episode. The risk of an arrhythmic syncope was similar in both groups (58.8% in SSE vs 57.0% in RSE; P=.68), also after adjustment for possible confounding variables (HR, 1.06; 95%CI, 0.81-1.38; P=.674). No significant differences between the groups were found in the EPS results and implantable cardiac monitor diagnostic yield. A total of 141 (59.2%) patients with SSE and 154 (58.1%) patients with RSE required cardiac device implantation (P=.797). After appropriate treatment, 35 (7%) patients had recurrence of syncope. The recurrence rate and mortality were also similar in both groups.

Conclusions: Patients with cBBB and unexplained syncope are at high risk of an arrhythmic etiology, even after the first syncopal episode. Patients with SSE and RSE have a similar arrhythmic risk and similar outcomes, and therefore there is no clinical justification for not managing them in the same manner.

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http://dx.doi.org/10.1016/j.rec.2022.11.009DOI Listing

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