Volume 23, Issue 5 e13466
ORIGINAL ARTICLE

Pediatric vascularized composite allotransplantation: What is the landscape for obtaining appropriate donors in the United States?

Shaun D. Mendenhall

Corresponding Author

Shaun D. Mendenhall

Division of Plastic and Reconstructive Surgery, Department of Surgery, University of Utah School of Medicine, Salt Lake City, Utah

Correspondence

Shaun D. Mendenhall, Division of Plastic and Reconstructive Surgery, Department of Surgery, University of Utah School of Medicine, Salt Lake City, UT.

Email: [email protected]

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Justin D. Sawyer

Justin D. Sawyer

The Institute for Plastic Surgery, Southern Illinois University School of Medicine, Springfield, Illinois

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Bradford L. West

Bradford L. West

Department of Transplant Nephrology, Springfield Clinic, Springfield, Illinois

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Michael W. Neumeister

Michael W. Neumeister

The Institute for Plastic Surgery, Southern Illinois University School of Medicine, Springfield, Illinois

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Abraham Shaked

Abraham Shaked

Division of Transplant Surgery, Department of Surgery, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania

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Lawrence S. Levin

Lawrence S. Levin

Department of Orthopaedic Surgery, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania

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First published: 12 May 2019
Citations: 7

Abstract

Listing the world's first pediatric bilateral hand transplant patient for a donor posed many challenges including matching the appropriate donor age, bone size, skin tone, and growth potential in an already limited donor population. This study describes the prevalence and distribution of potential pediatric VCA donors in the United States. We assessed the UNOS database from 2008 to 2015 to identify the prevalence of potential pediatric VCA donors. Standard VCA inclusion and exclusion criteria were applied to the dataset for all pediatric solid organ donors. Frequency analyses were performed of characteristics important for VCA matching. The dataset began with 57 300 brain-dead donors and after applying the inclusion and exclusion criteria including age <18, decreased to 4663 (8.1%). The number of pediatric potential VCA donors per UNOS region ranged from 11 to 112/year. The majority of pediatric potential VCA donors were blood type O Whites, with the least common profile being blood type AB of “other” ethnicity. The present study confirmed that pediatric VCA donors are rare and may require longer travel times for procurement and listing at multiple centers in order to find a suitable donor. This will be a limiting factor for the expansion of pediatric VCA.

CONFLICT OF INTEREST

The authors of this manuscript have no conflicts of interest to disclose in relation to this article.

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