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Current practice in the management of paediatric autoimmune liver disease in Europe
Mara Cananzi1, Marianne Hørby Jørgensen2, Gustav Buescher3
1Unit of Paediatric Gastroenterology, Digestive Endoscopy, Hepatology and Care of the Child with Liver Transplantation, Department of Women's and Children's Health, University Hospital of Padova, Padova, Italy.
Insights
Management of paediatric autoimmune liver disease (pAILD) in Europe shows significant variation in treatments and drug availability. More collaborative efforts are needed to ensure equitable, age-appropriate care for children with pAILD.
Area of Science:
- Hepatology
- Paediatric Gastroenterology
- Autoimmune Diseases
Background:
- Paediatric autoimmune liver disease (pAILD) is a rare condition with significant health implications.
- Despite treatment advancements, knowledge gaps and uncertainties persist in pAILD management.
- Real-world approaches to pAILD management in Europe require investigation.
Purpose of the Study:
- To investigate the current real-life approach to paediatric autoimmune liver disease (pAILD) management across Europe.
- To gather information on clinical practices, medications, and drug formulation availability for pAILD treatment.
- To identify variations and potential areas for improvement in European pAILD care.
Main Methods:
- A survey was distributed to members of the European Rare Liver Disease Reference Network (ERN RARE-LIVER) and the European Society for Paediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN) Hepatology Interest Group.
- Data collected included clinical activity, prescribed medications, and availability of paediatric drug formulations.
- Responses were gathered from 36 centres across 22 European countries.
Main Results:
- Predniso(lo)ne is universally used as first-line therapy, often combined with azathioprine.
- Azathioprine and mycophenolate are common second-line treatments, with tacrolimus used as a third-line agent.
- Significant disparities exist in the availability of paediatric drug formulations (predniso(lo)ne, azathioprine, mycophenolate, tacrolimus, ursodeoxycholic acid) across Europe, necessitating the use of compounded or crushed medications.
Conclusions:
- Treatment and monitoring strategies for pAILD in Europe exhibit considerable variability.
- The limited availability of age-appropriate paediatric drug formulations poses a challenge to consistent pAILD management.
- Collaborative initiatives are essential to establish evidence-based guidelines and ensure equitable, age-appropriate treatment for children with pAILD.
Objective:
Paediatric autoimmune liver disease (pAILD) is a rare condition with serious health implications. Notwithstanding treatment advancements, areas of uncertainty and knowledge gaps still exist. We here investigated the real-life approach to pAILD management in Europe.
Methods:
A survey was distributed to members of the European Rare Liver Disease Reference Network (ERN RARE-LIVER) and the European Society for Paediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN) Hepatology Interest Group. Information was gathered regarding clinical activity, medications used, and access to paediatric drug formulations at each site.
Results:
Thirty-six centres from 22 European countries responded to the survey. The majority are exclusively paediatric units (86%). Among participants, 80% follow <50 children with pAILD, of which 25%-50% are <10 years old in 44% of centres. All centres use predniso(lo)ne as first-line therapy, alone (15/36) or with azathioprine (21/36). Azathioprine and mycophenolate are the preferred second-line options in centres using first-line steroid monotherapy (11/15) or combined steroid-azathioprine (19/21), respectively. Tacrolimus is used as third-line agent in 15/36 centres. Proactive measurement of drug metabolites and target levels vary widely among centres. Paediatric predniso(lo)ne formulations are commercially available in 7/22 European countries, azathioprine in 3, mycophenolate in 14, tacrolimus in 15 and ursodeoxycholic acid in 14. When paediatric formulations are unavailable, children are treated with magisterial preparations or 'solid' formulations (crushed or intact).
Conclusions:
Treatment of pAILD in Europe varies widely in terms of medications used and treatment monitoring. Availability of paediatric drug formulations across Europe is limited. Collaborative initiatives are needed to define evidence-based strategies for management of pAILD and to promote an equal, age-appropriate treatment for affected children.
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