Literature DB >> 20561450

[Inside quality control for whole blood preservation performed at blood transfusion compatibility testing laboratory].

Yang Yu1, Chun-Ya Ma, Qian Feng, Xin Chen, Xiao-Zhen Guan, Xiao-Juan Zhang, Lin-Feng Chen, Zi-Lin Lin, Ji-Chun Pan, Ting Zhang, Qun Luo, De-Qing Wang.   

Abstract

This study was aimed to establish the technique for preparation and storage of internal quality control pro-ducts by using existing blood sample resources of blood transfusion compatibility testing laboratory. 24 healthy blood donors with group A and RhD-positive were randomly selected, and 4 ml venous blood from these donors were collected, respectively. Based on the use of anticoagulant type, whether to add red blood cell preservation solution and the samples stored at room temperature for 1 or 2 hours daily, 24 specimens were randomly divided into 8 groups by using factorial design methodology. All samples in tube with cap were stored at 4 degrees C, and placed at room temperature for 1 or 2 hours daily. ABO, RhD blood group (recorded on the agglutination strength of the forward and reverse typing), IgM anti-B antibody titer, and free hemoglobin concentration in the supernatant for all samples were detected at 0, 7, 14, 21, 28, 35 days of products preservation. The results indicated that the red blood cell damage from the group used anticoagulants ACD-B and added the MAP red blood cell preservation solution and placed at room temperature 1 hour daily (recorded as A2B2C1 group) was kept minimal, and FHb concentration and FHb increments at each time point were the lowest (p < 0.01), the FHb concentration on 35th day was only (24.5 +/- 84.5) mg/L. There was no significant change of A antigen, D antigen and IgM anti-B antibody response activity and stability in A2B2C1 group during storage for 35 days (p > 0.05). In conclusion, blood transfusion compatibility testing laboratory can use A2B2C1 program established by this study to prepare relatively stable modified whole blood internal quality control products in the existing conditions, which can be effectively preserved and meet the requirements of internal quality control for blood transfusion compatibility testing.

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Year:  2010        PMID: 20561450

Source DB:  PubMed          Journal:  Zhongguo Shi Yan Xue Ye Xue Za Zhi        ISSN: 1009-2137


  1 in total

1.  Establishment and performance assessment of preparation technology of internal quality control products for blood transfusion compatibility testing.

Authors:  Yang Yu; Chunya Ma; Qian Feng; Xin Chen; Xiaozhen Guan; Xiaojuan Zhang; Linfeng Chen; Zilin Lin; Jichun Pan; Ting Zhang; Qun Luo; Deqing Wang
Journal:  Exp Ther Med       Date:  2013-03-07       Impact factor: 2.447

  1 in total

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