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Implantation of Total Artificial Heart in Congenital Heart Disease
Published on: July 18, 2014
Mortality in adults with congenital heart disease
Pavithra Naidu1, Leeanne Grigg1, Dominica Zentner1
1Department of Cardiology, 300 Grattan Street, Parkville, Melbourne, Victoria, Australia.
Insights
Most deaths in adult congenital heart disease patients were cardiac-related, primarily sudden cardiac death and heart failure. Identifying risk factors for sudden death may guide preventative therapies for this vulnerable population.
Area of Science:
- Cardiology
- Adult Congenital Heart Disease (ACHD)
- Mortality Studies
Background:
- The Royal Melbourne Hospital (RMH) maintains a registry of Adult Congenital Heart Disease (ACHD) patients, initiated in 1991.
- Understanding mortality patterns in the growing ACHD population is crucial for clinical management and resource allocation.
Purpose of the Study:
- To retrospectively determine the causes of mortality within the RMH ACHD cohort.
- To analyze the frequency and specific causes of death across different congenital heart defect diagnoses.
Main Methods:
- A retrospective analysis was conducted on deceased patients (n=73) from the RMH ACHD registry (1991-2015).
- Data collected included patient age, gender, underlying congenital heart condition, and cause of death.
- Causes of death were categorized as cardiac or non-cardiac, with specific sub-classifications.
Main Results:
- Between 1991 and 2015, 3.3% of the ACHD cohort died, with a median age at death of 32 years.
- The most frequent underlying conditions were Eisenmenger's syndrome (22%) and pulmonary atresia with VSD (12%).
- Cardiac causes accounted for 67% of deaths, with sudden death (40%) and heart failure (13%) being most common. Sepsis was the leading non-cardiac cause (10%).
Conclusions:
- Cardiac causes, particularly sudden death and heart failure, are the predominant causes of mortality in this ACHD cohort.
- Further research into risk factors for sudden cardiac death is warranted to identify patients who could benefit from interventions like implantable cardioverter-defibrillators.
Aim:
Retrospective ascertainment of the causes of mortality in the adult congenital heart disease (ACHD) cohort of the Royal Melbourne Hospital (RMH).
Methods:
Deceased patients (n=73) of the 2519 ACHD patients in the Royal Melbourne Hospital registry (commenced in 1991) were identified. Retrospective analysis was undertaken. Age, gender of deceased individuals, and frequency and cause of death in different congenital diagnosis groups was explored.
Results:
Between 1991 and 2015, death occurred in 3.3% of the ACHD cohort. Median age at death was 32years (IQR 26-41.5) and 51% were male. The most frequent underlying cardiac conditions were Eisenmenger's syndrome (22%), pulmonary atresia and ventricular septal defect+/-major aorto-pulmonary collateral arteries (12%), Tetralogy of Fallot (10%), transposition of great arteries (TGA) with intact ventricular septum (8%), single ventricle (8%) and congenitally corrected TGA (5%). The cause of death was available from medical records in 60 (82%) of the 73 patients. The majority of deaths were due to cardiac causes (67%) including sudden death (40%), heart failure (13%), and documented ventricular arrhythmias (8%). The most common non-cardiac cause of death was sepsis (10%).
Conclusion:
The majority of deaths in this group were due to cardiac causes with sudden death and heart failure being the most common. Identification of risk factors for sudden death might assist identification of patients who may benefit from preventative therapies including implantable cardiac defibrillator.
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