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Published on: June 5, 2019
Heart rate: an accessible risk indicator in adult congenital heart disease
Paul M Hendriks1, Annemien E van den Bosch1, Jan A Kors2
1Department of Cardiology, Erasmus MC, Cardiovascular Institute, Thorax Center, Rotterdam, Netherlands.
Insights
Higher resting heart rate is linked to worse outcomes in adults with congenital heart disease (ACHD). This study found increased mortality and heart failure risk with higher heart rates in ACHD patients.
Area of Science:
- Cardiology
- Adult Congenital Heart Disease (ACHD) Research
Background:
- Elevated resting heart rate is a known risk factor for adverse outcomes in general and cardiovascular populations.
- The prognostic significance of resting heart rate in Adult Congenital Heart Disease (ACHD) requires further investigation.
Purpose of the Study:
- To assess the association between resting heart rate and adverse outcomes in patients with moderate or complex ACHD.
Main Methods:
- Prospective observational cohort study including 556 ACHD patients.
- Resting 12-lead ECGs were used to determine heart rate via the Modular ECG Analysis System (MEANS).
- Primary endpoint: all-cause mortality; Secondary endpoint: composite of mortality and heart failure. Survival analysis utilized Kaplan-Meier and Cox proportional hazards models.
Main Results:
- A total of 556 patients (median age 32 years) were included, with a mean heart rate of 69±13 bpm.
- Over a median follow-up of 10.1 years, 6.5% died and 14.9% reached the secondary endpoint.
- Higher heart rates were significantly associated with lower survival and heart failure-free survival, even after adjusting for clinical factors (Mortality HR 1.57 per 10 bpm; Mortality/HF HR 1.33 per 10 bpm).
Conclusions:
- Resting heart rate is a significant independent predictor of mortality and heart failure in ACHD patients.
- Elevated heart rate identifies individuals at higher risk within the ACHD population.
Background:
Higher resting heart rate has been described as a risk factor for adverse outcome in healthy individuals and cardiovascular patients. The aim of this study was to evaluate resting heart rate as risk factor in adult congenital heart disease (ACHD).
Methods:
In this prospective observational cohort study, patients with moderate or complex ACHD were included at routine outpatient visit. Standard 12-lead ECGs were obtained in rest. Heart rate was obtained from the ECG automatically by the Modular ECG Analysis System (MEANS). The primary endpoint was all-cause mortality and the secondary endpoint was a composite of all-cause mortality and heart failure. Survival was derived using the Kaplan-Meier estimator. Subgroups based on heart rate tertiles were compared by the log-rank test. Cox proportional hazards models were adjusted for clinical factors including age, sex and diagnosis (moderate vs complex ACHD).
Results:
A total of 556 patients were included (median age 32 years (IQR 24-41), 57.6% male). Mean heart rate was 69±13 bpm. Negative chronotropic medication was used by 74 (13.3%) patients. During a median follow-up of 10.1 (IQR 9.6-10.5) years, 36 patients (6.5%) died and 83 (14.9%) reached the secondary endpoint. Patients with higher heart rates had significantly lower survival and heart failure-free survival. After adjusting for clinical factors, heart rate remained associated with mortality (HR 1.57 per 10 bpm, 95% CI 1.26 to 1.96) and mortality or heart failure (HR 1.33 per 10 bpm, 95% CI 1.13 to 1.57).
Conclusion:
Higher heart rate is associated with lower survival and heart failure-free survival in ACHD.
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