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Implantation of Total Artificial Heart in Congenital Heart Disease
Published on: July 18, 2014
Infective endocarditis in adults with congenital heart disease remains a lethal disease
Oktay Tutarel1,2, Rafael Alonso-Gonzalez1, Claudia Montanaro1
1Adult Congenital Heart Centre & National Centre for Pulmonary Hypertension, Royal Brompton Hospital and Harefield NHS Foundation Trust, London, UK.
Insights
Infective endocarditis (IE) remains a serious risk for adults with congenital heart disease (ACHD), with high mortality rates. Abscess formation and older age predict worse outcomes in these patients.
Area of Science:
- Cardiology
- Infectious Diseases
- Adult Congenital Heart Disease
Background:
- Infective endocarditis (IE) poses a significant threat to patients with adult congenital heart disease (ACHD).
- Understanding IE incidence and outcomes in ACHD is crucial for improving patient care.
Purpose of the Study:
- To determine the incidence of IE in a contemporary cohort of ACHD patients.
- To identify predictors of outcome and mortality associated with IE in ACHD.
- To describe the contemporary IE landscape in ACHD.
Main Methods:
- Retrospective analysis of all IE episodes in ACHD patients at a tertiary center (1999-2013).
- Diagnosis confirmed using modified Duke criteria.
- Primary endpoint: IE-associated mortality.
Main Results:
- 164 IE episodes in 144 ACHD patients; mean age 32.3 years.
- IE mortality was 6.9%; overall mortality 19.4% over median 6.7 years follow-up.
- Abscess development (OR: 7.23) and age (OR: 1.05) predicted IE-associated mortality.
Conclusions:
- IE continues to be associated with high morbidity and mortality in ACHD patients.
- Early identification of risk factors like abscesses is vital for managing IE in this population.
Objective:
Infective endocarditis (IE) is associated with significant morbidity and mortality. Patients with adult congenital heart disease (ACHD) have an increased risk of developing IE. The aim of this study is to describe the incidence, predictors of outcome and mortality associated with IE in ACHD in a contemporary cohort.
Methods:
All episodes of IE in adults with congenital heart disease referred to our tertiary centre between 1999 and 2013 were included in the study. Patients were identified from the hospital database. The diagnosis of endocarditis was established according to the modified Duke criteria. The primary endpoint of the study was endocarditis-associated mortality.
Results:
There were 164 episodes of IE in 144 patients (male 102, 70.8%). Mean age at presentation was 32.3±22.7 years. Out of these, 43% had a simple, 23% a moderate and 32% a complex lesion. It was at least the second bout of IE in 37 episodes (23%). A predisposing event could be identified in only 26.2% of episodes. Surgical intervention during the same admission was performed in 61 episodes (37.2%). During a median follow-up of 6.7 years (IQR 2.9-11.4), 28 (19.4%) patients died. Out of these, 10 deaths were related to IE (IE mortality 6.9%). On unvariate regression analysis, the development of an abscess (OR: 7.23; 95% CI 1.81 to 28.94, p<0.01) and age (OR: 1.05; 95% CI 1.01 to 1.10, p=0.03) were the only predictors of IE-associated mortality. There was no increase in IE cases at our centre during the period of the study.
Conclusions:
IE-associated morbidity and mortality in a contemporary cohort of ACHD patients is still high in the current era.
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