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Updated: Aug 15, 2026

Heterotopic Auxiliary Rat Liver Transplantation With Flow-regulated Portal Vein Arterialization in Acute Hepatic Failure
Published on: September 13, 2014
Growth of long-term survivors of liver transplantation
R M Viner1, J T Forton, T J Cole
1Department of Paediatrics, Addenbrooke's Hospital, Cambridge, UK. R.Viner@ich.ucl.ac.uk
Insights
Children transplanted for liver disease show significant growth catch-up, reaching near-normal final height. Early transplantation and good management improve growth outcomes, though some may experience initial delays.
Area of Science:
- Pediatric Gastroenterology
- Transplant Surgery
- Endocrinology
Background:
- Liver transplantation is a life-saving procedure for children with end-stage liver disease.
- Assessing long-term growth and pubertal development is crucial for survivors' quality of life.
Purpose of the Study:
- To evaluate the growth trajectory and final height outcomes in pediatric liver transplant recipients.
- To identify factors influencing growth and pubertal development post-transplantation.
Main Methods:
- A longitudinal study followed 105 children up to seven years post-liver transplantation.
- Growth parameters, including height standard deviation score (zH), were monitored.
- Factors such as age at transplantation, diagnosis, steroid dosage, and liver function were analyzed.
Main Results:
- Mean height standard deviation score (zH) improved from -1.22 at transplantation to -0.55 at final height.
- Significant catch-up growth and pubertal development were observed over five years post-transplant.
- Early growth and pubertal retardation were noted in the first six months, with recovery thereafter.
- Initial zH, bilirubin levels, and prednisolone dose predicted short-term growth.
- Long-term growth was predicted by initial zH and cumulative prednisolone dose.
Conclusions:
- Pediatric liver transplant recipients can achieve near-normal final height, especially when transplanted earlier.
- Early growth and pubertal delays are often transient, with most patients resuming appropriate development.
- Factors like high steroid doses, poor liver function, and retransplantation are associated with poorer height outcomes.
- Severe short stature at final height is primarily seen in those with pre-existing severe growth retardation at transplantation.
Objective:
To assess growth in survivors of liver transplantation.
Study Design:
Growth was studied in 105 children up to seven years after liver transplantation.
Results:
At transplantation, mean height standard deviation score (zH) was -1.22 but 19% of patients were severely growth retarded (height below 0.4th centile). Growth and pubertal retardation were seen in the first six months after liver transplantation. Significant catch up in growth and puberty continued for more than five years. At five years, mean zH was -0.95 and at seven years -0.84. The mean zH of patients at final height was -0.55. zH at six months was predicted by zH and bilirubin at the time of transplantation and prednisolone dose at six months. At four years, zH was predicted by zH at the time of transplantation and the cumulative prednisolone dose. There was no association between zH and age at transplantation, sex, or diagnosis, although those with biliary atresia and those undergoing transplantation under 2 years of age showed more initial growth delay and subsequent catch up. Average age at menarche was 14.2 years.
Conclusions:
The mean height of the group to have reached final height after liver transplantation was on the 27th centile. Those transplanted earlier in childhood are likely to achieve more normal final heights. High steroid dose, poor liver function, and retransplantation are associated with poorer height outcomes. Persisting severe short stature is largely confined to children with severely retarded growth at the time of transplantation. Transient delay in puberty and menarche occur early after transplantation, although appropriate pubertal progress is resumed after two to three years.
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