Syncope in ICD recipients: a single centre experience

Europace. 2023 Mar 30;25(3):940-947. doi: 10.1093/europace/euac281.

Abstract

Aims: There is little evidence of the impact of syncope in implantable cardioverter-defibrillator (ICD) patients in routine community hospital care. This single-centre retrospective study sought to evaluate the incidence and prognostic significance of syncope in consecutive ICD patients.

Methods and results: Data were collected on consecutive patients undergoing first ICD implantation between January 2009 and December 2019. The primary endpoints were the first occurrence of all-cause syncope, all-cause mortality, and all-cause hospitalization. Multivariate Cox proportional hazard models were used to identify risk factors associated with syncope and to analyse the subsequent risk of mortality and hospitalization. 1003 patients (58% primary prevention) were included in the final analysis. During a mean follow-up of 1519 ± 1055 days, 106 (10.6%) experienced syncope, 304 died (30.3%), and 477 (47.5%) were hospitalized for any cause. In an analysis adjusted for baseline variables, the first occurrence of syncope was associated with a significantly increased risk of mortality (HR 2.82, P < 0.001) and the first occurrence of hospitalization (HR 2.46, P = 0.002).

Conclusion: Syncope in ICD recipients is common and associated with a poor prognosis irrespective of baseline variables and ICD programming. The occurrence of syncope is associated with a significant increase in the risk of mortality and hospitalization.

Keywords: Hospital admission; Implantable cardioverter-defibrillator; Programming; Shocks; Syncope.

MeSH terms

  • Defibrillators, Implantable* / adverse effects
  • Humans
  • Prognosis
  • Retrospective Studies
  • Risk Factors
  • Syncope / diagnosis
  • Syncope / epidemiology
  • Syncope / etiology