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[Analysis of transfusion effect of different platelet matching schemes in patients with platelet transfusion refractoriness].
Liang, Y J; Wang, H; Zhao, P Z; Wang, F; Li, Q; Xu, Y; Wu, Y X; Zhang, D M; He, X H.
Afiliação
  • Liang YJ; Laboratory of Blood Transfusion Technology, Taiyuan Blood Center, Taiyuan 030024, China.
  • Wang H; Laboratory of Blood Transfusion Technology, Taiyuan Blood Center, Taiyuan 030024, China.
  • Zhao PZ; Laboratory of Blood Transfusion Technology, Taiyuan Blood Center, Taiyuan 030024, China.
  • Wang F; Laboratory of Blood Transfusion Technology, Taiyuan Blood Center, Taiyuan 030024, China.
  • Li Q; Laboratory of Blood Transfusion Technology, Taiyuan Blood Center, Taiyuan 030024, China.
  • Xu Y; Laboratory of Blood Transfusion Technology, Taiyuan Blood Center, Taiyuan 030024, China.
  • Wu YX; Laboratory of Blood Transfusion Technology, Taiyuan Blood Center, Taiyuan 030024, China.
  • Zhang DM; Laboratory of Blood Transfusion Technology, Taiyuan Blood Center, Taiyuan 030024, China.
  • He XH; Department of Blood Transfusion, Shanxi Bethune Hospital, Taiyuan 030000, China.
Zhonghua Yi Xue Za Zhi ; 104(11): 865-869, 2024 Mar 19.
Article em Zh | MEDLINE | ID: mdl-38462363
ABSTRACT

Objective:

To analyze the transfusion effect of different platelet matching schemes in patients with platelet transfusion refractoriness (PTR).

Methods:

A total of 94 patients with PTR received by Taiyuan Blood Center from January to December 2021 were retrospectively analyzed, including 26 males and 68 females, aged 53(34,66) years. Platelet antibody screening was performed by enzyme-linked immunosorbent assay (ELISA). For patients with positive human leukocyte antigen (HLA) class Ⅰ antibodies, Luminex platform liquid chip assay was used to identify the specificity of antibodies, and platelets with missing allelic expression antigen corresponding to their specific antibodies were found in the platelet donor gene database established in our laboratory. For patients with negative class HLA-Ⅰ antibody screening, medium and high-resolution HLA-A and B alleles were genotyped by polymerase chain reaction restriction sequence specific oligonucleotide (PCR-SSO), and the compatible platelets were searched from the platelet donor gene database by HLA cross-reactive group genotype matching scheme or directly selected by serological cross-matching. The PCI compliance rate and total transfusion effective rate of different mismatch site groups and different matching scheme groups were statistically analyzed.

Results:

Platelet antibody was detected in 39 of 94 PTR patients with a positive rate of 41.5%, and all of them were HLA-Ⅰ antibodies, and 1 case was accompanied by human platelet antigen (HPA) antibody. A total of 134 times of compatible platelets were supplied to 39 patients with HLA-Ⅰ antibody positive by using antibody avoidance matching method. And the total effective rate of transfusion was 97.8% (131/134); The PCI compliance rates of HLA-A antigen mismatch, HLA-B antigen mismatch and HLA-A and B antigen mismatch groups were 81.6% (31/38), 86.5% (32/37) and 78.6% (22/28), respectively. The total effective rate of transfusion was 97.4% (37/38), 94.6% (35/37) and 100% (28/28), respectively, with no statistical significance (all P>0.05). A total of 118 times of compatible platelets were provided by HLA antigen cross-reaction group genotype matching and serological cross-matching, 90 transfusion effects were collected during follow-up, and the total effective rate was 76.7% (69/90).

Conclusion:

The combination of different platelet matching schemes can improve the PCI compliance rate and the total effective rate of transfusion in PTR patients.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trombocitopenia / Intervenção Coronária Percutânea Limite: Female / Humans / Male Idioma: Zh Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trombocitopenia / Intervenção Coronária Percutânea Limite: Female / Humans / Male Idioma: Zh Ano de publicação: 2024 Tipo de documento: Article