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The introduction of 7-day platelets: A university hospital experience

✍ Scribed by Shauna N. Hay; Caroline C. Immel; Laura S. McClannan; Mark E. Brecher


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
115 KB
Volume
22
Category
Article
ISSN
0733-2459

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✦ Synopsis


Abstract

Introduction: Recently, the FDA approved the Post Approval Surveillance Study of Platelet Outcomes, Release Tested protocol which allows participating institutions to utilize 7 day platelets following guidelines. As one of the first hospitals to implement a 7‐day protocol, we reviewed our hospital experience with 7‐day Gambro apheresis platelets to determine the impact on inventory. Methods: A review of apheresis platelet transfusions and outdate records was performed. Data were collected prospectively from March to August 2006. This data were compared with a retrospective review for the same time period in 2005. Results: For the 1,503 platelets transfused from March–August 2005, the mean day of issue was 3.44 (SD = 1.060). During the same time period of 2006, 1,688 platelets were transfused with a mean day of issue of 4.02 (SD = 1.083). This difference was statistically significant (P < 0.001). The outdate rate dropped from 2.9% (44/1,547) to 1.3% (22/1,710, P < 0.001). During the study period, ∼59.7% of the platelets were 7‐day platelets. Discussion: Over the 6‐month period, we noted a decrease in outdates from 2.9% to 1.3%. There was a shift toward older platelets (from a mean of day 3.4 to day 4). During the study period, 139 platelets were transfused on days 6 or 7 of storage. Overall, the implementation of 7‐day platelets in a university hospital setting was easily accomplished and has resulted in benefits to our institution by decreasing our outdate rate and to our patients by providing an additional 139 days 6 and 7 apheresis platelets with a potential cost savings of $78,952 (over the 6‐month study). J. Clin. Apheresis, 2007. Β© 2007 Wiley‐Liss, Inc.


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