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Risk factors for cardiac dysfunction in children on treatment for cancer at Kenyatta National Hospital, Nairobi
M Shiroya-Wandabwa1, C Yuko-Jowi, R Nduati
1International Centre for AIDS Programs, Kenya.
Insights
Nearly 30% of pediatric oncology patients on treatment had abnormal cardiac function. High cumulative anthracycline doses above 200 mg/m2 significantly increased the risk of cardiac dysfunction.
Area of Science:
- Cardiology
- Pediatric Oncology
- Clinical Research
Background:
- Cancer treatments, particularly anthracyclines, can lead to cardiac dysfunction in children.
- Early identification and risk factor assessment are crucial for managing cardiotoxicity in pediatric cancer patients.
Purpose of the Study:
- To determine the prevalence of abnormal cardiac function in pediatric oncology patients undergoing treatment.
- To identify risk factors associated with cardiac dysfunction in this vulnerable population.
Main Methods:
- A descriptive cross-sectional study with a nested case-control design was conducted.
- Patients were assessed at Kenyatta National Hospital between February and April 2006.
- Left ventricular dysfunction was defined by ejection fraction (EF) <55% or fractional shortening (FS) <29%.
Main Results:
- The point prevalence of cardiac dysfunction was 29% (95% CI 21.2-37.9) among 111 enrolled patients.
- Cumulative anthracycline dose emerged as a significant risk factor for cardiac dysfunction.
- An attributable risk of 77% for cardiac dysfunction was observed with cumulative anthracycline doses exceeding 200 mg/m2.
Conclusions:
- Serial echocardiography is recommended for early detection of cardiac dysfunction in at-risk pediatric oncology patients.
- Alternative treatment protocols are advised when cumulative anthracycline doses surpass 200 mg/m2 due to high attributable risk.
- Further research is needed to explore other risk factors and the long-term effects of anthracycline therapy.
Objective:
To determine the point prevalence of abnormal cardiac function and to assess the risk factors for cardiac dysfunction in paediatric oncology patients on treatment at Kenyatta National Hospital.
Design:
Descriptive cross-sectional study with a nested case control.
Setting:
Kenyatta National Hospital between February and April 2006.
Main Outcome Measures:
Left ventricular dysfunction if ejection fraction (EF) <55% or fractional shortening (FS) <29% defined cases. Controls had EF >55% or FS >29%.
Results:
One hundred and eleven patients were enrolled of whom 32 had abnormal cardiac function and were classified as cases while 79 had normal cardiac function. About a third, point prevalence 29% (95% CI 21.2-37.9), had cardiac dysfunction. Cumulative anthracycline dose was a risk factor for cardiac dysfunction in this population. Above 200 mg/m2 the attributable risk percentage of cardiac dysfunction was 77%.
Conclusions:
Serial echocardiography should be performed to identify patients at risk. Alternative treatment protocols should be used when the cumulative anthracycline dose exceeds 200 mg/m2 due to the high attributable risk. Studies to further assess the other associated risk factors and long term effects of anthracycline are recommended.
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