Journal of Clinical Oncology  
Search for:
Limit by:
  Browse by Topic or Issue
Home Search/Browse Subscriptions PDA Services My JCO Customer Service

Journal of Clinical Oncology, 2004 ASCO Annual Meeting Proceedings (Post-Meeting Edition).
Vol 22, No 14S (July 15 Supplement), 2004: 9710
© 2004 American Society of Clinical Oncology
This Article
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Download to citation manager
Right arrowRights & Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Mandel, M.
Right arrow Articles by Inbal, A.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Mandel, M.
Right arrow Articles by Inbal, A.

Abstract

Evaluation of pro-angiogenic and pro-coagulant activity of irradiated and non irradiated stored blood used in transfusion practice

M. Mandel, R. Yeskaraev, A. Achiron, R. Weitzen, T. Livnat, G. Harari, J. Baram and A. Inbal

Blood Bank and Insts.of Thrombosis and Oncology, Sheba Medical Center,Tel Hashomer, Israel; Sheba Medical Center, Tel Hashomer, Israel

9710

Background: Side effects of blood transfusion may be associated with infusion of bioactive substances. It has been previously reported that increase in pro-angiogenic and pro-coagulant parameters was observed in plasma of patients transfused with blood and platelet concentrates, respectively. Irradiation of cellular blood components is currently the only acceptable method for prevention of transfusion-associated GVHD. The aim of this study was to evaluate the pro-angiogenic and pro-coagulant potential of stored non-irradiated and irradiated blood. Methods: Ten units of whole blood, 4 of them irradiated at day 7 of storage (2500 rad), were studied. VEGF, thrombin antithrombin complex (TAT), prothrombin fragments 1+2 (F1+2) and endostatin were measured. K and LDH served as parameters of hemolysis. Results: An increase in VEGF was observed with increase in storage time (p by ANOVA = 0.016 and 0.018 for non irradiated and irradiated units, respectively). An increase was more pronounced in irradiated units (p<0.001). No difference in the endostatin level was observed throughout the study (p = 0.259 and 0.326 by ANOVA for non irradiated and irradiated units, respectively). A statistically significant increase in F1+2 and TAT was observed only in stored irradiated units (p= 0.013 for F1+2 and 0.0109 for TAT by ANOVA) with significant difference between the non-irradiated and irradiated units (p = 0.001 for each F1=2 and TAT). Similarly, a significant increase in thrombin generation in irradiated units was observed using a different method (Thromb Haemost 2000; 83:589). An increase in hemolytic parameters was observed in all the units regardless of irradiation (p=0.007 and 0.002 for K in non-irradiated and irradiated units, respectively; p=0.003 and <0.001 for LDH in non-irradiated and irradiated units, respectively). Conclusions: 1. Storage of blood is associated with an increase in pro-angiogenic factor -VEGF with further rise in its levels by irradiation. 2. Storage of irradiated blood is associated with an increase in thrombin generation resulting in potential pro-coagulant activities of the transfused units.

No significant financial relationships to disclose.






About
JCO
 Editorial
Roster
 Advertising
Information
 Librarians &
Institutions
 Rights &
Permissions

Copyright © 2004 by the American Society of Clinical Oncology, Online ISSN: 1527-7755. Print ISSN: 0732-183X
Terms and Conditions of Use
HighWire Press HighWire Press™ assists in the publication of JCO Online