Prolonged Holding of Whole Blood at 22 °C Does Not Increase Activation in Platelet Concentrates

Vox Sanguinis ◽  
1997 ◽  
Vol 72 (4) ◽  
pp. 225-228 ◽  
Author(s):  
C. Sanz ◽  
A. Pereira ◽  
A.I. Faúndez ◽  
A. Ordinas
Vox Sanguinis ◽  
1997 ◽  
Vol 72 (4) ◽  
pp. 225-228 ◽  
Author(s):  
C. Sanz ◽  
A. Pereira ◽  
A.I. Faundez ◽  
A. Ordinas

Transfusion ◽  
2003 ◽  
Vol 43 (12) ◽  
pp. 1723-1728 ◽  
Author(s):  
Maria L. Lozano ◽  
Elena Pérez-Ceballos ◽  
Jose Rivera ◽  
Dragica Paunovic ◽  
Maria J. Candela ◽  
...  

2014 ◽  
Vol 39 (4) ◽  
pp. 195
Author(s):  
GhadaM El-Gohary ◽  
AzzaS El-Danasoury ◽  
MahiraI El-Mogy ◽  
Amal Farouk ◽  
GhadaS Neseem

Blood ◽  
1966 ◽  
Vol 27 (4) ◽  
pp. 449-459 ◽  
Author(s):  
FREDERICK A. FLATOW ◽  
EMIL J. FREIREICH

Abstract Platelet concentrates prepared in acidified plasma (pH 6.5-6.7) are superior to concentrates prepared by standard methods, and are 80-90 per cent as effective as platelet rich plasma (PRP). The use of excess citric acid to acidify plasma promotes resuspension of the concentrate by eliminating clumping, which is a major factor in the decreased effectiveness of standard concentrates. Analysis of posttransfusion recovery and survival of platelets reveals no evidence of platelet injury in an acid medium. Acidification of PRP inhibits the aggregation of platelets by adenosine diphosphate (ADP). The presence of endogenous ADP may be an important factor in clumping during standard concentrate preparation. A method of acidification of PRP using citric acid is described which allows preparation of an effective concentrate from fresh whole blood without subjecting the red cells to acid pH. Reconstitution of the acidified platelet poor plasma and its native red cells increases the citrate molarity by less than 6 per cent and results in minimal decrease in pH of the whole blood.


Blood ◽  
1965 ◽  
Vol 25 (4) ◽  
pp. 548-566 ◽  
Author(s):  
SHIRLEY EBBE ◽  
MARIO BALDINI ◽  
JANET DONOVAN

Abstract Four methods for measuring the survival of homologous platelets in rabbits were studied: (1) transfusion of nonradioactive platelet concentrates to thrombocytopenic recipients, (2) transfusion of concentrates of platelets labeled in vitro with Cr51-sodium chromate, (3) transfusion of concentrates of platelets labeled in vivo with P32-orthophosphate and (4) transfusion of whole blood labeled in vivo with P32-orthophosphate. The survival time of platelets in normal rabbits was 3-4 days. From comparison of the 3 methods using platelet concentrates, the following conclusions were drawn. (1) All the platelets in a platelet concentrate were capable of recirculating after transfusion. (2) Labeling with P32 or Cr51 did not damage platelets. (3) About one-third of the Cr51 was immediately eluted from viable platelets after they were transfused. (4) Further exchange of the label in vivo did not occur to a significant degree with either Cr51 or P32. (5) Cr51 did not elute from platelets during storage of the platelets. (6) Studies of rabbit platelets had applicability in predicting the behavior of human platelets.


Transfusion ◽  
2007 ◽  
Vol 47 (4) ◽  
pp. 644-652 ◽  
Author(s):  
Hubert Schrezenmeier ◽  
Gabriele Walther-Wenke ◽  
Thomas H. Müller ◽  
Franz Weinauer ◽  
Adelheid Younis ◽  
...  

Transfusion ◽  
2007 ◽  
Vol 47 (3) ◽  
pp. 410-420 ◽  
Author(s):  
Marie Eve Moreau ◽  
Louis Thibault ◽  
Anik Désormeaux ◽  
Miguel Chagnon ◽  
Réal Lemieux ◽  
...  

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