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How I safely transfuse patients with sickle-cell disease and manage delayed hemolytic transfusion reactions
Transfusions can be a life-saving treatment of patients with sickle-cell disease (SCD). However, availability of matched units can be limiting because of distinctive blood group polymorphisms in patients of African descent. Development of antibodies against the transfused red blood cells (RBCs), res...
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| 發表在: | Blood |
|---|---|
| Main Authors: | , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
American Society of Hematology
2018
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6014354/ https://ncbi.nlm.nih.gov/pubmed/29724898 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2018-02-785964 |
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