Liver transplantation is the standard treatment for patients with end-stage liver diseases and is accompanied by high success rate in patients who cannot be treated by any other method. Nowadays, liver transplantation is routinely performed around the world. Moreover, its success rate, which is assessed as 1-year survival, has increased from 30% in the 1970s to 90% today (
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5). Due to this success rate, the number of liver transplantations is increasing every year. However, demand for liver transplantation is much more than what is available; in a way that more than 17000 patients were in the waiting list for liver transplantation in June 2012 in the U.S. (
6). Overall, children comprise 15-20% of patients in liver transplantation waiting lists. However, because children below 5 years old have the highest mortality rate in comparison with other age groups and liver transplantation is the only acceptable standard treatment, which can save them from death, this group of patients are more important (
7). The first liver transplantation was done by Dr. Starzl on a 3-year-old child in 1963 which finally resulted in death (
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6). In Iran, the first liver transplant on a child was performed in Namazi hospital, Shiraz in 1999 (
8). In general, indications for liver transplantation in children include cholestatic diseases, metabolic disorders, acute liver failure resulting from viral infections or drug consumption, chronic hepatitis, cirrhosis, and malignancies (
4). Nevertheless, biliary atresia is the most prevalent disease, which leads to liver transplantation in children. Although, performing surgery during infancy improves the symptoms of the disease to some extent, 75% of such children will need liver transplantation before the age of 5 because of recurrent cholangitis and biliary cirrhosis (
9). Goss et al. reported the 5-year survival of these patients after the transplantation as 78% (
10). Liver transplantation also plays a major role in congenital metabolic disorders; however, it is only recommended in cases when the disease is only in the liver and is treated by transplantation, such as in Crigler-Najjar syndrome, or when the extra-hepatic enzyme abnormality is repaired, such as in tyrosinemia. Moreover, the extra-hepatic symptoms of the metabolic disorder, such as the nervous complications of Wilson’s disease, should not impede the transplantation (
11). In various studies, 1 and 5-year survival rates have been reported as 90% and 85%, respectively (
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14). Determining the best time for liver transplantation as well as the factors affecting both short-term and long-term survival of liver transplant patients are considered as debatable issues in this field (
15). Although more than a decade has passed from performance of pediatric liver transplantation in Iran, no studies have been conducted on the children’s survival rate and its effective factors after transplantation. In addition, this surgery is one of the most expensive interventions for both the patients and the health system.