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Corticosteroids usage in pediatric liver transplantation: To be or not to be!
1Pediatric Liver Centre, King's College Hospital, London, UK.
Insights
Early steroid withdrawal (SW) or elimination in pediatric liver transplant (LT) recipients is safe for patients and graft survival. Steroids negatively impact growth, and steroid-free regimens are beneficial.
Area of Science:
- Pediatric Gastroenterology and Hepatology
- Transplant Immunology
- Pharmacology
Background:
- Early steroid withdrawal (SW) and steroid-free immunosuppression protocols in pediatric liver transplantation (LT) are being explored.
- Potential risks include acute graft rejection (AGR), chronic graft rejection (CGR), and de novo autoimmune hepatitis (d-AIH).
- Benefits primarily involve improved post-LT growth outcomes.
Purpose of the Study:
- To evaluate the risks and benefits of corticosteroid (CS) therapy in pediatric LT recipients.
- To focus on CGR and d-AIH as key risks and growth effects as benefits.
- To analyze clinical trials examining low-dose CS, SW, or steroid-free regimens.
Main Methods:
- Systematic review and comparison of numerous clinical trials involving pediatric LT patients.
- Analysis of data on graft survival, patient outcomes, growth parameters, and incidence of d-AIH.
- Focus on short-term outcomes and the impact of different CS regimens.
Main Results:
- Early SW or elimination from immunosuppression protocols did not negatively affect short-term patient or graft survival.
- High-dose and prolonged CS therapy negatively impacts growth in LT recipients.
- d-AIH development is not associated with CS therapy; chronic low-dose steroids do not prevent d-AIH.
Conclusions:
- Early SW or steroid-free protocols are safe and beneficial for growth in pediatric LT.
- Minimizing CS use is crucial for optimizing growth outcomes post-transplant.
- Current evidence does not support a preventative role for low-dose steroids against d-AIH.
Abstract:
The theoretical risks of early SW, <3 months post-LT, and complete elimination (steroid-free LT) lie in mainly three areas, namely the risks of AGR, CGR, and the development of d-AIH that has been described in SW post-LT in children. These should be balanced against the benefits of early SW mainly manifested as effects on growth post-LT. In this paper, we focused on the clinical trials that included CS therapy risks and benefits in pediatric LT. Focusing mainly on CGR and d-AIH as risks, and the beneficial effects on growth post-LT with either low-dose CS, SW, or steroid-free regimens. Main conclusions from comparing a large number of studies are: early SW or elimination from immunosuppression protocols was neither harmful to the patient nor to the graft survival rate in the short term, the overall impression is that steroids negatively affect growth in LT recipients when used in high doses and prolonged course, and that development of d-AIH is not associated with CS therapy with evidence that chronic low dose steroids post-LT have no preventative role against d-AIH.
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