The current outcomes and future challenges in pediatric vascularized composite allotransplantation.

TitleThe current outcomes and future challenges in pediatric vascularized composite allotransplantation.
Publication TypeJournal Article
Year of Publication2020
AuthorsAzoury SC, Lin I, Amaral S, Chang B, L Levin S
JournalCurr Opin Organ Transplant
Volume25
Issue6
Pagination576-583
Date Published2020 Dec
ISSN1531-7013
Abstract

PURPOSE OF REVIEW: We review the outcomes and future challenges associated with pediatric vascularized composite allotransplantation, including follow-up data from our bilateral pediatric hand-forearm transplantation.

RECENT FINDINGS: In 2015, the first heterologous pediatric upper extremity hand-forearm transplant was performed at the Children's Hospital of Philadelphia, and in 2019, the first pediatric neck reconstructive transplantation was performed in Poland. The 5-year follow-up of the pediatric upper extremity recipient demonstrates similar growth rates bilaterally, an increase in bone age parallel to chronologic age, and perhaps similar overall growth to nontransplant norms. The pediatric upper extremity recipient continues to make gains in functional independence. He excels academically and participates in various extracurricular activities. Future challenges unique to the pediatric population include ethical issues of informed consent, psychosocial implications, limited donor pool, posttransplant compliance issues, and greater life expectancy and therefore time to inherit the many complications of immunosuppression.

SUMMARY: Currently, we recommend pediatric vascularized composite allotransplantation (VCA) for bilateral upper extremity amputees, preferably on immunosuppression already, and those patients who would have the most potential gain not available through standard reconstructive techniques while being able to comply with postoperative immunosuppression protocols, surveillance, rehabilitation, and follow-up.

DOI10.1097/MOT.0000000000000809
Alternate JournalCurr Opin Organ Transplant
PubMed ID33044345