Exploratory studies of extended storage of apheresis platelets in a platelet additive solution (PAS)

被引:59
|
作者
Slichter, Sherrill J. [1 ,2 ]
Corson, Jill [1 ]
Jones, Mary Kay [1 ]
Christoffel, Todd [1 ]
Pellham, Esther [1 ]
Bailey, S. Lawrence [1 ]
Bolgiano, Doug [1 ]
机构
[1] Puget Sound Blood Ctr, Seattle, WA 98104 USA
[2] Univ Washington, Sch Med, Seattle, WA USA
基金
美国国家卫生研究院;
关键词
POOLED BUFFY-COATS; IN-VITRO; SYNTHETIC MEDIA; HYPERCONCENTRATED PLATELETS; 2ND-GENERATION CONTAINERS; PLASMA; SURVIVAL; VIVO; TRANSFUSION; GLUCOSE;
D O I
10.1182/blood-2013-05-501247
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To evaluate the poststorage viability of apheresis platelets stored for up to 18 days in 80% platelet additive solution (PAS)/20% plasma, 117 healthy subjects donated platelets using the Haemonetics MCS+, COBE Spectra (Spectra), or Trima Accel (Trima) systems. Control platelets from the same subjects were compared with their stored test PAS platelets by radiolabeling their stored and control platelets with either (51)chromium or (111)indium. Trima platelets met Food and Drug Administration poststorage platelet viability criteria for only 7 days vs almost 13 days for Haemonetics platelets; ie, platelet recoveries after these storage times averaged 44 +/- 3% vs 49 +/- 3% and survivals were 5.4 +/- 0.3 vs 4.6 +/- 0.3 days, respectively. The differences in storage duration are likely related to both the collection system and the storage bag. The Spectra and Trima platelets were hyperconcentrated during collection, and PAS was added, whereas the Haemonetics platelets were elutriated with PAS, which may have resulted in less collection injury. When Spectra and Trima platelets were stored in Haemonetics' bags, poststorage viability was significantly improved. Platelet viability is better maintained in vitro than in vivo, allowing substantial increases in platelet storage times. However, implementation will require resolution of potential bacterial overgrowth during storage.
引用
收藏
页码:271 / 280
页数:10
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