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Updated: Jan 30, 2026

Orthotopic Liver Transplantation in Rats
Published on: July 1, 2012
Impact of Immunosuppression on Executive Functioning After Pediatric Liver Transplantation: An Observational Cohort
Imeke Goldschmidt1, Rolf van Dick2, Christoph Jacobi3
1Department of Paediatric Gastroenterology and Hepatology, Hannover Medical School, Hannover.
Insights
Children
Area of Science:
- Pediatric medicine
- Neuroscience
- Immunology
Background:
- Liver transplantation in children is linked to impaired cognitive function.
- Executive functioning deficits are a concern in this population.
- Understanding factors influencing cognitive outcomes is crucial for intervention.
Purpose of the Study:
- To evaluate the impact of immunosuppressive therapy on executive functioning in pediatric liver transplant recipients.
- To assess executive functioning using the Children's Color Trail Test and PedsQL cognitive module (cogPedsQL).
- To identify potential targets for interventions aimed at enhancing executive function post-transplant.
Main Methods:
- Cross-sectional study of 155 children (aged 2-18) post-liver transplant.
- Executive functioning assessed via Children's Color Trail Test and parent/patient cogPedsQL.
- Comparison of outcomes between different calcineurin inhibitor (CNI) regimens, including a switch to once-daily slow-release tacrolimus (Tac).
Main Results:
- Worse executive functioning correlated with longer ICU stays and time since transplant.
- No significant difference between cyclosporine and tacrolimus users.
- Children on once-daily slow-release tacrolimus showed better performance than those on twice-daily tacrolimus.
- Parent-proxy cogPedsQL improved significantly in children switching to once-daily tacrolimus.
Conclusions:
- Executive functioning may deteriorate over time post-liver transplant, influenced by disease burden.
- Once-daily slow-release tacrolimus may offer advantages over twice-daily administration for executive function.
- Further research is needed to optimize immunosuppressive strategies for cognitive health in pediatric liver transplant survivors.
Objectives:
Children after liver transplantation show increased rates of impaired cognitive functioning. We aimed to assess the potential effects of immunosuppressive therapy on executive functioning measured by the Children's Color Trail Test and the cognitive functioning module of the PedsQL (cogPedsQL) in liver transplanted children to explore potential targets for intervention to improve executive functioning.
Methods:
We performed a cross-sectional study in 155 children (78 girls) aged 10.4 (2-18) years at 5.0 (0.1-17) years after liver transplantation, with follow-up at 6 months in n = 114. Executive functioning was assessed by Children's Color Trail Test (ages 8-16) and by patients and parent-proxy cogPedsQL (ages 5-18/2-18, respectively). Results were correlated with clinical parameters. Stability of results over time was compared between n = 23 patients who for clinical reasons switched from twice daily calcineurin inhibitor (CNI) to once-daily slow-release tacrolimus (Tac) during the study period, and patients with unchanged CNI.
Results:
Worse executive functioning was associated with longer stay in the intensive care unit and longer time elapsed since transplantation. No difference was found between users of cyclosporine and Tac. Children on once-daily slow-release Tac performed better than children on twice-daily Tac. In children who switched from twice-daily CNI to once-daily Tac, parent-proxy cogPedsQL improved significantly compared to stable results in the nonswitch group.
Conclusions:
In addition to a strong impact of disease burden around transplantation, executive functioning appears to deteriorate over time. Although there is no clear-cut advantage of any CNI, once-daily Tac appears to be advantageous compared to twice-daily Tac.
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