Director Pediatric Transplantation
Children's Hospital of Pittsburgh
Since the first successful liver transplantation was performed in a child almost 40 years ago, this option has increasingly become a life-saving therapy for children with liver diseases such as biliary atresia. Interestingly, the next most common indication for liver transplant in children has been metabolic diseases such as tyrosinemia or urea cycle defects. Despite the availability of medical therapy for these diseases, the unpredictable nature of the disease and the potential long-term complications of tumors or neurologic problems has led to the use of liver transplant in these children. Results for liver transplantation have increasingly improved with experienced centers demonstrating high rates of survival exceeding 90% at 1 to 2 years. Of note, this includes caring for children who present in very sick condition with acute liver failure or for children with other conditions such as liver tumors. At Children's Hospital of Pittsburgh we have been very focused not only on successful survival outcome but also on assuring that children who undergo transplantation are achieving a highly improved quality of life. One of the ways that this has been achieved has been by developing new ways of handling immunosuppression, i.e., the medicines that are used to prevent rejection of the transplanted organ.
|"For our family, the experience of going through the transplant was less stressful than going through a metabolic crisis because the outcome was much more predictable. Our life has been improved beyond measure in the last year, we don't look back and we have no regrets." Jay and Oula Haddad, parents of Grace age almost 4, transplanted June 24, 2004|
Immunosuppression, as we noted earlier, remains one of the long-term concerns that posttransplant patients encounter. As opposed to earlier protocols that featured multiple drug regimens, our current immunosuppression relies on single drug therapy with steroid use only if there are episodes of rejection. Currently, approximately 40% of patients may encounter an easily treated rejection episode after liver transplant. Three out of 7 of our recently transplanted MSD patients experienced a mild episode of rejection that did require a brief course of steroids. All of the children are on a single drug (Tacrolimus) to control rejection, except for one child who is currently receiving steroids for rejection.
Infections have historically been an important risk factor for transplantation, but we are seeing an improved infection rate following transplantation. For example, virus infections such as those related to CMV and EBV (cytomegalovirus and Epstein Barr Viral, respectively) have steadily decreased to less than 4% in our experience. A more feared complication, post-transplant lymphoproliferative disorder (PTLD) has similarly decreased to less than 3%. In our MSD patients, no patient has developed CMV disease or PTLD.
Significant neurological recovery has been noted in the long-term patient who underwent transplant and subtle but clear improvements have been reported in several of the recently transplanted patients. These findings are now being objectively quantified by neurodevelopmental testing done pre and post-transplant in subsequent transplant recipients.
Liver transplantation may also prove be a cost effective therapy for MSD that may reduce the long-term cost associated with medical care and treatment for acute metabolic decompensation. Most importantly, the uncertain risk of a devastating neurologic complication can be prevented with a successful liver transplantation. Although these children continue to have MSD genetically, the transplanted liver supplies sufficient enzyme activity to metabolize unrestricted protein diets and maintain branch chain amino acid homeostasis.