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Estimating Bilateral Atrial Function by Cardiovascular Magnetic Resonance Feature Tracking in Patients with Paroxysmal Atrial Fibrillation
Published on: July 20, 2022
Higher premature atrial complex burden from the Holter examination predicts poor cardiovascular outcome
Ting-Chun Huang1,2, Po-Tseng Lee1,2, Mu-Shiang Huang2,3
1Institute of Clinical Medicine, College of Medicine, National Cheng Kung University, 1 University Road, Tainan City, Taiwan.
Insights
Higher premature atrial complexes (PACs) burden significantly increases the risk of all-cause mortality and cardiovascular death. This dose-response relationship highlights the importance of monitoring PAC burden in patient care.
Area of Science:
- Cardiology
- Electrophysiology
- Public Health
Background:
- Premature atrial complexes (PACs) are linked to adverse cardiovascular events.
- The precise relationship between PAC burden and mortality outcomes requires further elucidation.
Purpose of the Study:
- To investigate the distribution of PAC burden.
- To determine the dose-response effects of PAC burden on all-cause mortality and cardiovascular death.
Main Methods:
- Analysis of 15,893 patients from July 2011 to December 2018.
- Multivariate regression using ln PAC and PAC burden quartiles.
- Cox proportional hazards models and competing risk analysis.
Main Results:
- Older individuals and both genders exhibited similar PAC distribution.
- Increased ln PAC was an independent risk factor for all-cause mortality (HR 1.09) and cardiovascular death (HR 1.13).
- The highest quartile of PAC burden showed a significantly higher risk of all-cause mortality (HR 1.47) compared to the lowest quartile.
Conclusions:
- PAC burden demonstrates a clear dose-response effect on all-cause mortality and cardiovascular death.
- Consistent increased risk associated with high PAC burden was observed across subgroups.
- Findings underscore the prognostic significance of PAC burden in clinical practice.
Abstract:
Premature atrial complexes (PACs) have been suggested to increase the risk of adverse events. The distribution of PAC burden and its dose-response effects on all-cause mortality and cardiovascular death had not been elucidated clearly. We analyzed 15,893 patients in a medical referral center from July 1st, 2011, to December 31st, 2018. Multivariate regression driven by ln PAC (beats per 24 h plus 1) or quartiles of PAC burden were examined. Older group had higher PAC burden than younger group (p for trend < 0.001), and both genders shared similar PACs distribution. In Cox model, ln PAC remained an independent risk factor for all-cause mortality (hazard ratio (HR) = 1.09 per ln PAC increase, 95% CI = 1.06‒1.12, p < 0.001). PACs were a significant risk factor in cause-specific model (HR = 1.13, 95% CI = 1.05‒1.22, p = 0.001) or sub-distribution model (HR = 1.12, 95% CI = 1.04‒1.21, p = 0.004). In ordinal PAC model, 4th quartile group had significantly higher risk of all-cause mortality than those in 1st quartile group (HR = 1.47, 95% CI = 1.13‒1.94, p = 0.005), but no difference in cardiovascular death were found in competing risk analysis. In subgroup analysis, the risk of high PAC burden was consistently higher than in low-burden group across pre-specified subgroups. In conclusion, PAC burden has a dose response effect on all-cause mortality and cardiovascular death.
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