Arrhythmias & electrophysiology

Adverse outcomes in patients with atrial fibrillation and a pacemaker: a cohort study

EuropacePublished Prospective cohort study

Authors' conclusion

Patients with AF and a PM experienced an increased rate of adverse cardiovascular outcomes. However, the PM itself was not independently associated with these outcomes.

Study context

Population
Patients with atrial fibrillation (AF) in two Swiss prospective cohorts, yearly follow-up up to 8 years445 (12.1%) with pacemaker (PM) at baseline
Participants
3,675 patients
Exposure
Pacemaker vs no pacemaker
Outcome
MACE (stroke or TIA, MI, CV death, systemic embolism); HF hospitalization
Follow-up
Median 7 years
Methodological detailsmulticentre, 2 Swiss cohorts (Swiss-AF, Beat-AF), time-updated Cox regression
  • Multicentre
  • 2 Swiss cohorts (Swiss-AF, Beat-AF)
  • Time-updated Cox regression

Main finding

As reported in the abstract

PM

Major adverse cardiovascular events (MACE)
5.97 per 100 patient-years
Heart failure (HF)
5.08 per 100 patient-years

No PM

MACE
3.37 per 100 patient-years
HF
2.61 per 100 patient-years

Major adverse cardiovascular events (MACE)

PM5.97 per 100 patient-years
No PM3.37 per 100 patient-years

Heart failure (HF)

PM5.08 per 100 patient-years
No PM2.61 per 100 patient-years
PM vs No PMAdjusted hazard ratio (95% CI)P value
MACE
1.12(0.95–1.33)
P = 0.183
HF
1.14(0.94–1.37)
P = 0.180

Observational data: associations, not effects.

Secondary outcomes

Individual components of MACE

Consistent results (no independent association with PM)

Original publication

Adverse outcomes in patients with atrial fibrillation and a pacemaker: a cohort study. Europace. Published 28 October 2025. doi:10.1093/europace/euaf275

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