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Indications for combined liver and kidney transplantation in children
Srinivas P Chava1, Balbir Singh, Sujoy Pal
1Institute of Liver Studies, Kings College London School of Medicine, King's College Hospital, London, UK.
Insights
Combined liver and kidney transplantation (CLKT) offers encouraging results for pediatric patients with metabolic diseases or congenital abnormalities affecting both organs. Early evaluation is crucial for better outcomes in these complex cases.
Area of Science:
- Nephrology
- Hepatology
- Transplantation Medicine
Background:
- Renal failure is common in patients awaiting liver transplantation (LT), increasing morbidity and mortality.
- Combined liver and kidney transplantation (CLKT) is increasingly performed in adults.
- Pediatric CLKT indications differ from adults, often involving metabolic diseases and congenital abnormalities.
Purpose of the Study:
- To review the indications and outcomes of combined liver and kidney transplantation (CLKT) in pediatric patients.
- To highlight the unique aspects of CLKT in children compared to adults.
Main Methods:
- Review of clinical data for pediatric patients undergoing CLKT.
- Analysis of indications, procedures, and outcomes.
Main Results:
- CLKT in children for metabolic diseases or congenital abnormalities shows generally encouraging results.
- Specific indications in children differ significantly from adult populations.
Conclusions:
- Combined liver and kidney transplantation is a viable option for select pediatric cases.
- Early patient evaluation and listing are critical for optimizing outcomes in children with metabolic diseases or congenital abnormalities requiring CLKT.
Abstract:
A significant number of patients awaiting liver transplantation have associated renal failure and renal dysfunction is associated with increased morbidity and mortality after LT. There has been a recent increase in the number of CLKT in adults. The common indications for CLKT in children are different from those of adults and include metabolic diseases affecting the kidney with or without liver dysfunction and congenital developmental abnormalities affecting both organs. The results are generally encouraging among these groups of patients. Early evaluation and listing of patients before they become severely ill or have major systemic manifestations of their metabolic problem are important.
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