Incidence of heart failure after pacemaker implantation: a nationwide Danish Registry-based follow-up study

Author:

Tayal Bhupendar1ORCID,Fruelund Patricia1,Sogaard Peter1,Riahi Sam1,Polcwiartek Christoffer123,Atwater Brett D3,Gislason Gunnar45675ORCID,Risum Niels8,Torp-Pedersen Christian18,Kober Lars9,Kragholm Kristian Hay12

Affiliation:

1. Department of Cardiology, Aalborg University Hospital, Hobrovej 18-22, Aalborg, Denmark

2. Unit of Epidemiology and Biostatistics, Aalborg University Hospital, Hobrovej 18-22, Aalborg, Denmark

3. Division of Cardiology, Duke University Medical Center, Durham, NC, USA

4. Department of Medicine, Zealand University Hospital, Køge, Denmark

5. Faculty of Health and Medical Science, University of Copenhagen, Copenhagen, Denmark

6. The Danish Heart Foundation, Copenhagen, Denmark

7. National Institute of Public Health, University of Southern Denmark, Denmark

8. Department of Clinical Investigation and Cardiology, Nordsjaellands Hospital, Hillerød, Denmark

9. Department of Cardiology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark

Abstract

Abstract Aims The objective of the current study is to investigate the risk of heart failure (HF) after implantation of a pacemaker (PM) with a right ventricular pacing (RVP) lead in comparison to a matched cohort without a PM and factors associated with this risk. Methods and results All patients without a known history of HF who had a PM implanted with an RVP lead between 2000 and 2014 (n = 27 704) were identified using Danish nationwide registries. An age- and gender-matched control cohort (matched 1:5, n = 138 520) without PM and HF was identified to compare the risk. Outcome was the cumulative incidence of HF including fatal HF within the first 2 years of PM implantation, with all-cause mortality and myocardial infarction (MI) as competing risks. Due to violation of proportional hazards, the follow-up period was divided into three time-intervals: <30 days, 30–180 days, and >180 days–2 years. The cumulative incidence of HF including fatal HF was observed in 2937 (10.6%) PM patients. Risks for the three time-intervals were <30 days [hazard ratio (HR) 5.98, 95% CI 5.19–6.90], 30–180 days (HR 1.84, 95% CI 1.71–1.98), and >180 days (HR 1.11, 95% CI 1.04–1.17). Among patients with a PM device, factors associated with increased risk of HF were male sex (HR 1.33, 95% CI 1.24–1.43), presence of chronic kidney disease (CKD) (HR 1.64, 95% CI 1.29–2.09), and prior MI (1.77, 95% 1.50–2.09). Conclusions Pacemaker with an RVP lead is strongly associated with risk of HF specifically within the first 6 months. Patients with antecedent history of MI and CKD had substantially increased risk.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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