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Dual-chamber pacing for vasovagal syncope: A systematic review and meta-analysis of randomized controlled trials
Francesco Sbarra1, Gianluca Pagnoni1, Susan Darroudi2
1Cardiologic Unit, Specialistic Medicine Department, Guglielmo da Saliceto Hospital, Piacenza, Italy.
Introduction:
Vasovagal syncope (VVS) is the most common cause of transient loss of consciousness and may be recurrent and disabling. Dual-chamber cardiac pacing has been proposed for patients with cardioinhibitory VVS, but randomized trials have yielded inconsistent results, influenced by patient selection and trial blinding.
Methods:
We conducted a systematic review and meta-analysis of randomized controlled trials evaluating dual-chamber pacing in patients with recurrent cardioinhibitory VVS. PubMed, Embase, and the Cochrane Library were searched from inception to May 2025. Risk ratios (RRs) with 95% confidence intervals (CIs) were pooled using fixed- or random-effects models as appropriate. Prespecified subgroup analyses were performed according to trial blinding status and selection for documented asystolic VVS.
Results:
Six randomized controlled trials including 429 patients were identified, evaluating rate-drop response, closed-loop stimulation, or DDI pacing. Overall, active pacing significantly reduced syncope recurrence compared with control (RR 0.47; 95% CI 0.27-0.82). The treatment effect was larger and statistically significant in open-label trials (RR 0.22; 95% CI 0.11-0.46), whereas blinded trials showed a non-significant trend toward benefit (RR 0.59; 95% CI 0.32-1.08). In patients with documented asystolic VVS, pacing significantly reduced recurrent syncope (RR 0.35; 95% CI 0.22-0.55), while no significant benefit was observed in patients not selected for asystolic episodes.
Conclusion:
Dual-chamber pacing was associated with a lower incidence of syncope recurrence across randomized trials in patients with cardioinhibitory vasovagal syncope. However, blinded studies did not demonstrate a statistically significant benefit, and the observed effect appears to be largely influenced by open-label trial designs.
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