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Updated: May 13, 2026

Quantification of the Immunosuppressant Tacrolimus on Dried Blood Spots Using LC-MS/MS
Published on: November 8, 2015
Prevalence of renal dysfunction in tacrolimus-treated pediatric transplant recipients: a systematic review
Violette M G J Gijsen1, Dennis A Hesselink, Kenneth Croes
1Intensive Care and Department of Pediatric Surgery, Erasmus MC Sophia Children's Hospital, Rotterdam, the Netherlands.
Insights
Pediatric non-renal transplant patients treated with tacrolimus show a high prevalence of chronic kidney disease. Further research is needed to understand risk factors and personalize immunosuppression for these children.
Area of Science:
- Pediatric Nephrology
- Transplant Immunology
- Pharmacology
Background:
- Tacrolimus is a common immunosuppressant after transplantation.
- Renal dysfunction is a known complication in adult transplant recipients.
- Data on renal dysfunction in pediatric non-renal transplant recipients is limited.
Purpose of the Study:
- To systematically review the literature on the prevalence of renal dysfunction in children undergoing non-renal transplantation and treated with tacrolimus.
- To assess the range of reported chronic kidney disease prevalence in pediatric liver and heart/lung transplant recipients.
Main Methods:
- Systematic literature search of PubMed/Medline, Embase, and Google up to April 19, 2012.
- Inclusion of studies on pediatric non-renal transplant recipients treated with tacrolimus.
- Analysis of reported prevalences of mild and severe chronic kidney disease.
Main Results:
- Eighteen relevant studies were identified, focusing on liver, heart, and intestinal transplant recipients.
- Prevalence of mild chronic kidney disease ranged from 0% to 39% (liver) and 22.7% to 40% (heart/lung).
- Prevalence of severe chronic kidney disease ranged from 0% to 71.4% (liver) and 6.8% to 46% (heart/lung).
Conclusions:
- A significant proportion of pediatric non-renal transplant patients on tacrolimus experience chronic kidney disease.
- Wide ranges in reported prevalence suggest potential inclusion bias and varying definitions of renal dysfunction.
- Further research is warranted to determine actual risks, identify risk factors, and individualize tacrolimus therapy.
Abstract:
Renal dysfunction after non-renal transplantation in adult tacrolimus-treated transplant patients is well documented. Little is known about its prevalence in children. Age-related changes in both disposition and effect of tacrolimus as well as renal function may preclude extrapolation of adult data to children. To systematically review the literature on renal dysfunction in non-renal pediatric transplant recipients treated with tacrolimus. PubMed/Medline, Embase, and Google were searched from their inception until April 19, 2012, with the search terms "tacrolimus," "renal function," "transplantation," and "children." Eighteen of 385 retrieved papers were considered relevant. Twelve dealt with liver, four with heart transplant, one with heart and lung transplant, and one with intestinal recipients. Reported prevalences of mild and severe chronic kidney disease ranged from 0% to 39% and 0% to 71.4%, respectively, for liver, and from 22.7% to 40% and 6.8% to 46%, respectively, for heart and/or lung transplant recipients. Ranges remained wide after adjusting for follow-up time and disease severity. Possible explanations are inclusion bias and definitions used for renal dysfunction. A considerable proportion of pediatric non-renal transplant patients who receive tacrolimus-based immunosuppression, appear to suffer from chronic kidney disease. This conclusion warrants further research into the real risk, its risk factors, and individualization of immunosuppressant therapy.
Related Concept Videos
Pharmacokinetics in Pediatric Patients: Drug Excretion
Kidney Transplant I: Introduction
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption
Kidney Transplant II: Surgical Procedure
Pharmacokinetics in Pediatric Patients: Drug Distribution

