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Long-term outcome of autoimmune hepatitis in children
O I Saadah1, A L Smith, W Hardikar
1Department of Gastroenterology and Clinical Nutrition, Royal Children's Hospital, Melbourne, Victoria, Australia.
Insights
Autoimmune hepatitis in children shows a favorable long-term outcome, with a 90% transplant-free survival rate. Most children maintain a normal lifestyle, regardless of initial disease severity.
Area of Science:
- Pediatric Hepatology
- Immunology
- Chronic Liver Disease
Background:
- Autoimmune hepatitis (AIH) is a chronic liver disease with unknown causes.
- Prompt diagnosis and treatment are crucial to prevent cirrhosis.
- Limited data exist on the long-term prognosis of pediatric AIH.
Purpose of the Study:
- To evaluate the long-term outcomes of autoimmune hepatitis in children.
- To correlate outcomes with initial clinical and laboratory findings.
Main Methods:
- Retrospective analysis of 30 pediatric AIH patients (1972-2000).
- Data collected from medical records and patient/physician interviews.
- Mean follow-up of 10 years, with 43% followed for over a decade.
Main Results:
- Hepatomegaly, jaundice, and splenomegaly were common presenting symptoms.
- 36% of patients had cirrhosis at diagnosis.
- A 90% transplant-free survival rate was observed.
- Most patients on therapy maintained a normal lifestyle.
Conclusions:
- Pediatric autoimmune hepatitis demonstrates a favorable long-term prognosis.
- Outcomes are positive irrespective of initial presentation.
- Patients achieve a near-normal lifestyle with appropriate management.
Background And Aim:
Autoimmune hepatitis (AIH) is a chronic disease of unknown etiology, which usually progresses to cirrhosis if not diagnosed and treated promptly. Data on long-term follow up in children with AIH are scant. The aim of this study is to assess the long-term outcome of autoimmune hepatitis in children with respect to clinical and laboratory features at presentation.
Methods:
Data were extracted from the medical records of patients presenting over a 28-year period (1972-2000) to the Royal Children's Hospital, Melbourne, Australia. Additional information was obtained by interviewing patients, and their current physicians. Of the 30 patients (22 females, mean age 9 years) identified, 18 had type I, three had type II, four had autoimmune-polyendocrinopathy syndrome type 1, one had infantile giant-cell hepatitis associated with Coomb's-positive hemolytic anemia, and four were seronegative (antinuclear antibody (ANA), smooth muscle antibody (SMA) and liver-kidney microsomal antibody (LKM)).
Results:
Clinical features at presentation included hepatomegaly (86%), jaundice (66%) and splenomegaly (50%). Initial investigations revealed a median serum bilirubin level of 55 micromol/L (range 6-425), median aspartate aminotransferase level of 678 IU (range 70-2548), and abnormal clotting in 33% of patients. Liver biopsies were performed on all patients at presentation and 11 showed cirrhosis (36%). The mean follow-up period was 10.0 +/- 7.8 years with 43% being followed for > 10 years. Only two patients died and one required transplantation. Fourteen (50%) patients continue to be on low dose prednisolone with azathioprine, two (7%) are on prednisolone alone, and six (21%) are on no therapy. When the cirrhotic and non-cirrhotic patients were compared, the albumin level at presentation was significantly lower in the cirrhotic group (P=0.01). Of the patients who were cirrhotic at presentation, six (54%) remain compensated with a mean follow-up period of 8 years. All 24 patients currently under follow up are engaged in age-appropriate activities including school, part- or full-time work.
Conclusion:
Autoimmune hepatitis has a favorable long-term outcome with a transplant-free survival rate of 90% over a mean period of 10.0 +/- 7.8 years (range: 0.5-23), and a normal or near-normal lifestyle irrespective of presenting clinical, laboratory or histological features.
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