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Published on: February 22, 2018
Identifying high risk in adults with congenital heart disease and atrial arrhythmias
Sing-Chien Yap1, Louise Harris, Vijay S Chauhan
1Department of Cardiology, Erasmus Medical Center, Rotterdam, the Netherlands.
Insights
Adults with congenital heart disease (CHD) and atrial arrhythmias face increased mortality. Poor functional class, single-ventricle physiology, pulmonary hypertension, and valvular heart disease predict death, enabling risk stratification for better patient outcomes.
Area of Science:
- Cardiology
- Adult Congenital Heart Disease
- Electrophysiology
Background:
- Atrial arrhythmias increase mortality in adults with congenital heart disease (CHD).
- Risk stratification for mortality in this specific patient group remains poorly understood.
- Identifying predictors of death is crucial for managing adult CHD patients with arrhythmias.
Purpose of the Study:
- To identify predictors of mortality in adult patients with CHD and atrial arrhythmias.
- To develop a risk score for stratifying mortality risk in this population.
Main Methods:
- A cohort of 378 adult patients with CHD and atrial arrhythmias was followed from 1999 to 2009.
- Mortality predictors were identified using survival analysis.
- A risk score was constructed based on independent predictors of death.
Main Results:
- The overall mortality rate was 2.0% per patient-year over a median follow-up of 5.2 years.
- Independent predictors of mortality included poor functional class, single-ventricle physiology, pulmonary hypertension, and valvular heart disease.
- A risk score based on these factors differentiated low- (0.5%), moderate- (1.9%), and high-risk (6.5%) groups for mortality.
Conclusions:
- Specific clinical variables effectively identify high-risk adult patients with CHD and atrial arrhythmias.
- The absence of identified risk factors is associated with excellent survival despite atrial arrhythmias.
- The developed risk score aids in stratifying mortality risk for improved clinical management.
Abstract:
Atrial arrhythmias are associated with an increased mortality risk in adults with congenital heart disease (CHD). However, little is known about risk stratification in the specific group of adult patients with CHD and atrial arrhythmias. We sought to identify predictors of mortality in adult with CHD and atrial arrhythmias and to establish a risk score. The study involved 378 adult patients with CHD (mean age 39 ± 13 years) and atrial arrhythmias who had serial follow-up in a tertiary referral center from 1999 through 2009. During a median follow-up of 5.2 years, there were 40 deaths (11%). Overall mortality rate was 2.0% per patient-year. Common modes of death included heart failure-related death (35%), sudden cardiac death (20%), and perioperative death (18%). Independent predictors of mortality were poor functional class (hazard ratio 3.69, 95% confidence interval [CI] 1.69 to 8.03, p = 0.001), single-ventricle physiology (hazard ratio 3.33, 95% CI 1.51 to 7.35, p = 0.003), pulmonary hypertension (hazard ratio 2.96, 95% CI 1.41 to 6.19, p = 0.004), and valvular heart disease (hazard ratio 2.73, 95% CI 1.33 to 5.59, p = 0.006). A risk score was constructed using these predictors in which patients were assigned 1 point for the presence of each risk factor. Mortality rates in the low-risk (no risk factor), moderate-risk (1 risk factor), and high-risk (>1 risk factor) groups were 0.5%, 1.9%, and 6.5% per patient-year, respectively (log-rank p <0.001). In conclusion, in adult with CHD and atrial arrhythmias specific clinical variables identify patients at high risk for death. Importantly, the absence of any of these risk factors is associated with an excellent survival despite the presence of atrial arrhythmias.
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