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Analysis of the Effect of Race, Socioeconomic Status, and Center Size on Unrelated National Marrow Donor Program Donor Outcomes: Donor Toxicities Are More Common at Low-Volume Bone Marrow Collection Centers

Authors :
Bronwen E. Shaw
Raquel M. Schears
Rammurti T. Kamble
Brent R. Logan
James Gajewski
Andrew S. Artz
Paul O'Donnell
Miguel Angel Diaz
David F. Stroncek
Deidre M. Kiefer
Muneer H. Abidi
Peiman Hematti
Michael A. Pulsipher
Pintip Chitphakdithai
Jane L. Liesveld
Eric Williams
Kimberley A. Kasow
Christopher E. Dandoy
Tanya L. Pedersen
Bipin N. Savani
Hillard M. Lazarus
Hisham Abdel-Azim
Baldeep Wirk
Richard F. Olsson
John R. Wingard
Galen E. Switzer
Navneet S. Majhail
Gorgun Akpek
Dennis L. Confer
Source :
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid, Consejería de Sanidad de la Comunidad de Madrid
Publication Year :
2015
Publisher :
Elsevier BV, 2015.

Abstract

Previous studies have shown that risks of collection-related pain and symptoms are associated with sex, body mass index, and age in unrelated donors undergoing collection at National Marrow Donor Program centers. We hypothesized that other important factors (race, socioeconomic status [SES], and number of procedures at the collection center) might affect symptoms in donors. We assessed outcomes in 2726 bone marrow (BM) and 6768 peripheral blood stem cell (PBSC) donors collected between 2004 and 2009. Pain/symptoms are reported as maximum levels over mobilization and collection (PBSC) or within 2 days of collection (BM) and at 1 week after collection. For PBSC donors, race and center volumes were not associated with differences in pain/symptoms at any time. PBSC donors with high SES levels reported higher maximum symptom levels 1 week after donation (P = .017). For BM donors, black males reported significantly higher levels of pain (OR, 1.90; CI, 1.14 to 3.19; P = .015). No differences were noted by SES group. BM donors from low-volume centers reported more toxicity (OR, 2.09; CI, 1.26 to 3.46; P = .006). In conclusion, race and SES have a minimal effect on donation-associated symptoms. However, donors from centers performing ≤ 1 BM collection every 2 months have more symptoms after BM donation. Approaches should be developed by registries and low-volume centers to address this issue.

Details

ISSN :
10838791
Volume :
21
Database :
OpenAIRE
Journal :
Biology of Blood and Marrow Transplantation
Accession number :
edsair.doi.dedup.....7c8f06220e89848836f3cd12292164f6