Abstract
Background Febrile non-hemolytic transfusion reaction (FNHTR) is the most common type of transfusion reactions, and it could be reduced by transfusing patients with leukocyte-poor blood products. However, FNHTR still occur in certain patients transfused with leukocyte-poor red blood cell (LPR) products. It is examined whether human platelet antigen (HPA) could be a potential membrane antigen that plays a role in FNHTR. Methods A total of 120 inpatient subjects who transfused with LPR (60 in FNHTR group, 60 in control group) were typed for HPA-2, HPA-3, and HPA-15 using sequence specific primer-polymerase chain reaction (SSP-PCR) and electrophoresis. Results HPA-2 unmatched rate between donors and patients in FNHTR group was 18%, and only 3% unmatched rate was observed in control group (p = 0.0082). FNHTR group was further classified according to the imputability. There was a significant difference (p = 0.0041) between FNHTR (probable imputability, infection) group and control group, and more significant difference (p = 0.0008) was seen between FNHTR (probable imputability, febrile neutropenia) group and control group. Conclusions Those results indicated that HPA-2 might play roles on inducing FNHTR in patients suffering from infectious diseases and febrile neutropenia. HPA-2 genotyping between donors and recipients might be worth integrating in pre-transfusion testing to increase transfusion safety.
Original language | English |
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Pages (from-to) | 120-123 |
Number of pages | 4 |
Journal | Clinica Chimica Acta |
Volume | 474 |
DOIs | |
State | Published - 11 2017 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2017 Elsevier B.V.
Keywords
- Febrile non-hemolytic transfusion reaction (FNHTR)
- Human platelet antigen (HPA)
- Leukocyte-poor red blood cell (LPR)
- Sequence specific primer-polymerase chain reaction (SSP-PCR)