Impact of selection of cord blood units from the United States and swiss registries on the cost of banking operations.

Published

Journal Article

BACKGROUND: Over the last 2 decades, cord blood (CB) has become an important source of blood stem cells. Clinical experience has shown that CB is a viable source for blood stem cells in the field of unrelated hematopoietic blood stem cell transplantation. METHODS: Studies of CB units (CBUs) stored and ordered from the US (National Marrow Donor Program (NMDP) and Swiss (Swiss Blood Stem Cells (SBSQ)) CB registries were conducted to assess whether these CBUs met the needs of transplantation patients, as evidenced by units being selected for transplantation. These data were compared to international banking and selection data (Bone Marrow Donors Worldwide (BMDW), World Marrow Donor Association (WMDA)). Further analysis was conducted on whether current CB banking practices were economically viable given the units being selected from the registries for transplant. It should be mentioned that our analysis focused on usage, deliberately omitting any information about clinical outcomes of CB transplantation. RESULTS: A disproportionate number of units with high total nucleated cell (TNC) counts are selected, compared to the distribution of units by TNC available. Therefore, the decision to use a low threshold for banking purposes cannot be supported by economic analysis and may limit the economic viability of future public CB banking. CONCLUSIONS: We suggest significantly raising the TNC level used to determine a bankable unit. A level of 125 × 10(7) TNCs, maybe even 150 × 10(7) TNCs, might be a viable banking threshold. This would improve the return on inventory investments while meeting transplantation needs based on current selection criteria.

Full Text

Duke Authors

Cited Authors

  • Bart, T; Boo, M; Balabanova, S; Fischer, Y; Nicoloso, G; Foeken, L; Oudshoorn, M; Passweg, J; Tichelli, A; Kindler, V; Kurtzberg, J; Price, T; Regan, D; Shpall, EJ; Schwabe, R

Published Date

  • February 2013

Published In

Volume / Issue

  • 40 / 1

Start / End Page

  • 14 - 20

PubMed ID

  • 23637645

Pubmed Central ID

  • 23637645

International Standard Serial Number (ISSN)

  • 1660-3796

Digital Object Identifier (DOI)

  • 10.1159/000345690

Language

  • eng

Conference Location

  • Switzerland