Hybrid glycophorin and red blood cell antigen genotyping in Asian American type O blood donors with Mi a phenotype

Transfusion ◽  
2019 ◽  
Vol 59 (12) ◽  
pp. 3767-3775 ◽  
Author(s):  
Xin Lin ◽  
Graciela Rubio ◽  
Jigar Patel ◽  
Sukanta Banerjee ◽  
Tom Frame ◽  
...  
Transfusion ◽  
2015 ◽  
Vol 55 (10) ◽  
pp. 2369-2375 ◽  
Author(s):  
Meghan Delaney ◽  
Samantha Harris ◽  
Askale Haile ◽  
Jill Johnsen ◽  
Gayle Teramura ◽  
...  

Transfusion ◽  
2021 ◽  
Author(s):  
Kelsey Hazegh ◽  
Bradley D. Anawalt ◽  
Larry J. Dumont ◽  
Tamir Kanias

Transfusion ◽  
2013 ◽  
Vol 54 (1) ◽  
pp. 86-97 ◽  
Author(s):  
Seema Kacker ◽  
Paul M. Ness ◽  
William J. Savage ◽  
Kevin D. Frick ◽  
R. Sue Shirey ◽  
...  

2019 ◽  
Vol 34 (6) ◽  
pp. 496-503
Author(s):  
Arwa Z. Al-Riyami ◽  
Ali Al-Marhoobi ◽  
Saif Al-Hosni ◽  
Sabah Al Mahrooqi ◽  
Michael Schmidt ◽  
...  

2015 ◽  
Vol 05 (03) ◽  
pp. 004-008
Author(s):  
Mohammed Saleem E. K. ◽  
Soundarya Mahalingam ◽  
Shamee Shastri ◽  
Kamalakshi G. Bhat

AbstractThe development of red blood cell (RBC) isoimmunization with alloantibodies and autoantibodies complicate transfusion therapy in multiply transfused thalassemia patients. We conducted a study to analyse the frequency in our population. Clinical and antibody profile from 55 multiply transfused thalassemic patients who were receiving transfusions were collected and analyzed prospectively. A commercially available 3 cell antigen panel was used for the antibody screening procedure. If antibody screening with the 3-cell antigen panel was positive, an extended 11-cell antigen panel was used for antibody identification in LISS (Low Ionic Strength Solution). All patients received blood matched for only ABO and Rh (D) antigens. A total of 55 transfusion dependent â thalassemics were included in this study out of which 30 (54.55%) were males and 25(45.45%) females with a male to female ratio of 1.2: 1. Frequency of red cell alloimmunization in this study was found to be 1.8%. None of the patients developed red cell autoimmunization. The alloantibody identified in the the patient who developed alloimmunisation was was anti-K. In conclusion, the transfusion of matched blood is essential for chronically transfused beta thalassemia patients in order to avoid alloimmunization.


2020 ◽  
Vol 320 ◽  
pp. 128376
Author(s):  
Hongmei Wang ◽  
Shengbao Duan ◽  
Mingyuan Wang ◽  
Shuangshi Wei ◽  
Yezhou Chen ◽  
...  

Transfusion ◽  
2007 ◽  
Vol 47 (s1) ◽  
pp. 60S-63S ◽  
Author(s):  
Ghazala Hashmi

Vox Sanguinis ◽  
1979 ◽  
Vol 36 (4) ◽  
pp. 252-256 ◽  
Author(s):  
Gaytha E. McPherson ◽  
Ruth F. Wells ◽  
Elizabeth B. Hajleigh ◽  
F. Carl Grumet

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