Additive solution-7 reduces the red blood cell cold storage lesion
Background Transfusion of long‐stored red blood cells (RBCs) is associated with decreased in vivo RBC recovery, delivery of RBC breakdown products, and increased morbidity and mortality. Reducing the burden of this RBC “storage lesion” is a major challenge in transfusion medicine. Additive solution‐...
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| Published in: | Transfusion (Philadelphia, Pa.) Vol. 55; no. 3; pp. 491 - 498 |
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| Main Authors: | , , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
United States
Blackwell Publishing Ltd
01.03.2015
Wiley Subscription Services, Inc |
| Subjects: | |
| ISSN: | 0041-1132, 1537-2995, 1537-2995 |
| Online Access: | Get full text |
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| Summary: | Background
Transfusion of long‐stored red blood cells (RBCs) is associated with decreased in vivo RBC recovery, delivery of RBC breakdown products, and increased morbidity and mortality. Reducing the burden of this RBC “storage lesion” is a major challenge in transfusion medicine. Additive solution‐7 (AS‐7) is a new RBC storage solution designed to improve RBC metabolism by providing phosphate and increasing buffering capacity.
Study Design and Methods
Storage quality in AS‐7 was measured in a prospective, randomized, three‐center trial using units of whole blood from healthy human subjects whose RBCs were stored for up to 56 days in AS‐7 (n = 120) or for 42 days in the control solution AS‐1 (n = 60).
Results
Hemolysis and shedding of protein‐containing microvesicles were significantly reduced in RBCs stored in AS‐7 for 42 and 56 days compared with RBCs stored in AS‐1. Autologous in vivo recoveries of RBCs stored in AS‐7 was 88 ± 5% at 42 days (n = 27) and 82 ± 3% at 56 days (n = 27), exceeding recoveries of RBCs stored in currently used solutions.
Conclusion
Increasing the phosphate, pH range, and buffer capacity of a RBC storage system allowed RBCs to be stored better and longer than currently approved storage systems. AS‐7 ameliorates the long‐term storage lesion resulting in significantly increased viability in vitro and in vivo. |
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| Bibliography: | ArticleID:TRF12867 U.S. Army Medical Research and Materiel Command - No. W81XWH0610766 ark:/67375/WNG-PM8DXP1P-J istex:46B0A65442DF2E75304360BE17FD18B9ACB93066 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Article-2 ObjectType-Feature-1 content type line 23 ObjectType-Undefined-3 |
| ISSN: | 0041-1132 1537-2995 1537-2995 |
| DOI: | 10.1111/trf.12867 |