Krailadsiri P, Gilcher R, Seghatchian J
National Blood Service, Colindale, London, UK.
Transfus Apher Sci. 2001 Apr;24(2):223-5. doi: 10.1016/s1473-0502(01)00054-4.
With the increasing demand for leukoreduction of blood components and the implementation of universal leukoreduction in several countries, the problems associated with leukocyte filtration of sickle cell trait blood have been revisited. Currently, there is no unified standard practice for sickle cell trait donors. Different blood centers adopt different policies. While some defer these donors from red cell component donation, some do not. Some screen all ethnic African donors for hemoglobin S (Hb S), others do not. Furthermore, there are differences in views of whether sickle cell trait red cells should be considered as equivalent to non-sickle cell trait red cells. Some blood centers do not give red cells from a sickle cell trait donor to the newborn or patients undergoing general anesthesia as a preventative measure. In this presentation, we discuss the epidemiology of the sickle gene, the sickling process, problems associated with leukoreduction of sickle cell trait whole blood and red cells, and some unresolved issues concerning donor referral and the usage of sickle cell trait blood.
随着对血液成分白细胞去除的需求不断增加以及一些国家实施普遍白细胞去除措施,与镰状细胞性状血液白细胞过滤相关的问题再次受到关注。目前,对于镰状细胞性状献血者没有统一的标准做法。不同的血液中心采取不同的政策。一些血液中心不让这些献血者捐献红细胞成分,而另一些则允许。一些血液中心对所有非洲裔献血者进行血红蛋白S(Hb S)筛查,而另一些则不进行。此外,对于镰状细胞性状红细胞是否应被视为等同于非镰状细胞性状红细胞,存在不同观点。一些血液中心为预防起见,不给新生儿或接受全身麻醉的患者输注镰状细胞性状献血者的红细胞。在本报告中,我们将讨论镰状基因的流行病学、镰变过程、与镰状细胞性状全血和红细胞白细胞去除相关的问题,以及一些关于献血者转诊和镰状细胞性状血液使用的未解决问题。