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Late reduction in cyclosporine dosage does not improve renal function in pediatric heart transplant recipients
James E Rice1, Anne T Shipp, John B Carlin
1Department of Cardiology, Royal Children's Hospital, Melbourne, Victoria, Australia.
Insights
Cyclosporine (CSA) dosage in pediatric heart transplant recipients showed no significant impact on late renal function. Renal function stabilizes after one year, irrespective of CSA dose adjustments.
Area of Science:
- Pediatric Nephrology
- Cardiology
- Immunosuppression Therapy
Background:
- Pediatric heart transplantation relies on immunosuppressants like cyclosporine (CSA).
- Long-term renal function is a critical concern in these young patients.
- Understanding CSA's impact on kidney health is vital for post-transplant care.
Purpose of the Study:
- To investigate the relationship between cyclosporine (CSA) dosage and long-term renal function in children after heart transplantation.
- To assess if changes in CSA dosage over time affect glomerular filtration rate (GFR).
Main Methods:
- Retrospective analysis of pediatric heart transplant recipients with at least 3 years of follow-up.
- Serial measurement of glomerular filtration rate (GFR) and cyclosporine (CSA) levels.
- Statistical analysis using least squares regression to determine GFR and CSA dosage change rates.
Main Results:
- GFR was moderately reduced at 1 year post-transplant but stabilized thereafter.
- No significant correlation was found between CSA dosage/levels and the rate of GFR change.
- Renal function did not significantly improve or decline beyond the first year, regardless of CSA management.
Conclusions:
- Renal function in pediatric heart transplant recipients on CSA is established by 1 year and remains stable.
- Progressive reduction in CSA dosage does not appear to influence renal function after the initial post-transplant year.
Objective:
To determine the relation between cyclosporine (CSA) dosage and late renal function in pediatric heart transplant recipients.
Methods:
In this retrospective study, pediatric patients were observed for at least 3 years after transplantation, with serial measurement of renal glomerular filtration rate (GFR). Patient variables examined included pre-existing disease (cardiomyopathy or congenital heart disease), age at transplantation, duration of follow-up, and CSA dosage and trough levels at 3 months after transplantation and yearly until the latest follow-up. For each patient, the least squares regression method was used to estimate the average rate of change per year (slope value) for GFR and CSA dosage during follow-up.
Results:
Twenty-five patients who met the study criteria underwent transplantation at a median age of 11.7 years (interquartile range [IQR], 6.8-14.5 years) and were observed for a median of 6.0 years (IQR, 4-7). The median GFR at 1 year after transplantation was 73 ml/min/1.73 m(2) (IQR, 50-89) and at latest follow-up was 75 ml/min/1.73 m(2) (IQR, 57-98). The median CSA dosage and trough level at 1 year after transplantation were 6.1 mg/kg/day and 234 ng/ml, and at latest follow-up were 3.45 mg/kg/day and 141 ng/ml, respectively. The median rate of change in GFR was +1.6 ml/year of observation (95% confidence interval, -0.9, 4.7) and was inversely related to measured GFR at 1 year after transplantation. The rate of change of GFR was unrelated to any other patient variables including CSA dosages and levels at the specified time intervals and the rate of change of CSA dosage.
Conclusions:
Measured GFR in pediatric cardiac transplant recipients treated with CSA is moderately depressed at 12 months after transplantation and does not change significantly during subsequent years. No evidence suggests that the usual progressive reduction in CSA dosage influences renal function beyond 1 year after transplantation.
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