Chou Stella T
1Division of Hematology, The Children's Hospital of Philadelphia, Philadelphia, PA.
Hematology Am Soc Hematol Educ Program. 2013;2013:439-46. doi: 10.1182/asheducation-2013.1.439.
Transfusion therapy is a key intervention in decreasing morbidity and mortality in patients with sickle cell disease (SCD). Current indications for acute and chronic transfusion therapy have significantly increased the number of RBC units transfused to patients with SCD worldwide. This review summarizes transfusion management for the treatment or prevention of neurologic and perioperative complications, acute chest syndrome, and acute anemia associated with SCD. Despite the recognized benefits of transfusion therapy, it is not without the risks of iron overload, alloimmunization, and delayed hemolytic transfusion reactions. Transfusional iron overload management includes automated RBC exchange, noninvasive imaging to monitor iron burden, and iron chelation with parenteral or oral agents. Although limited and extended RBC antigen matching reduces antibody formation, the prevalence of RBC alloimmunization in patients with SCD remains high. Recent studies demonstrate that RH genetic diversity in patients with SCD contributes to Rh alloimmunization, suggesting that even more refined RBC matching strategies are needed. Advances in molecular blood group typing offer new opportunities to improve RBC matching of donors and recipients and can be of particular benefit to patients with SCD.
输血治疗是降低镰状细胞病(SCD)患者发病率和死亡率的关键干预措施。目前急性和慢性输血治疗的适应证显著增加了全球范围内输注给SCD患者的红细胞单位数量。本综述总结了用于治疗或预防SCD相关神经和围手术期并发症、急性胸部综合征及急性贫血的输血管理。尽管输血治疗的益处已得到认可,但它并非没有铁过载、同种免疫和迟发性溶血性输血反应的风险。输血性铁过载管理包括自动红细胞置换、监测铁负荷的非侵入性成像以及使用肠外或口服药物进行铁螯合。尽管有限和扩展的红细胞抗原匹配可减少抗体形成,但SCD患者中红细胞同种免疫的发生率仍然很高。最近的研究表明,SCD患者的RH基因多样性导致Rh同种免疫,这表明需要更精细的红细胞匹配策略。分子血型分型的进展为改善供体和受体的红细胞匹配提供了新机会,对SCD患者可能特别有益。