首页> 外文期刊>Asian Journal of Transfusion Science >First Indian study to establish safety of immediate-spin crossmatch for red blood cell transfusion in antibody screen-negative recipients
【24h】

First Indian study to establish safety of immediate-spin crossmatch for red blood cell transfusion in antibody screen-negative recipients

机译:首次印度研究建立了抗体筛选阴性接受者立即旋转交叉匹配对红细胞输注的安全性

获取原文
获取外文期刊封面目录资料

摘要

BACKGROUND AND OBJECTIVES: The US Food and Drug Administration and American Association of Blood Banks approved the type and screen approach in 1980s, long after antibody screen (AS) was introduced in 1950s. The present study omits conventional anti-human globulin (AHG) crossmatch and replaces it with immediate-spin (IS) crossmatch as part of pretransfusion testing in AS-negative patients to study the safety and effectiveness of IS crossmatch in recipients. MATERIALS AND METHODS: This prospective longitudinal study was conducted on over 5000 red cell units transfused to AS-negative patients admitted to the hospital. Pretransfusion testing comprised blood grouping and AS followed by IS crossmatch, at the time of issue of red cell unit. The patients were transfused IS compatible red cell units. AHG crossmatch was performed posttransfusion for all red cell units. Any incompatible AHG crossmatch was followed up as suspected transfusion reaction. RESULTS: A total of 5023 red cell units were transfused to 2402 patients with negative AS. 99.7% IS compatible red cell units were also compatible on posttransfusion AHG crossmatch. Anti-P1 alloantibody was identified in one patient who was transfused two IS crossmatch compatible units but later both units were incompatible on AHG crossmatch. There was no clinical or serological sign of hemolysis in the patient. CONCLUSION: In AS-negative patients, IS crossmatch is as safe as conventional AHG crossmatch and can, therefore, replace conventional AHG crossmatch protocol.
机译:背景与目的:在1950年代引入抗体筛选(AS)的很长时间之后,美国食品药品监督管理局和美国血库协会在1980年代批准了类型和筛选方法。本研究省略了传统的抗人球蛋白(AHG)交叉匹配,并用快速旋转(IS)交叉匹配替代了它,作为AS阴性患者输血前测试的一部分,以研究IS交叉匹配在接受者中的安全性和有效性。材料与方法:这项前瞻性纵向研究是针对5000多个红细胞单位进行的,这些红细胞单位被输往住院的AS阴性患者。输血前测试包括红细胞单位发行时的血型和AS,然后是IS交叉匹配。患者被输注IS兼容的红细胞单位。输血后对所有红细胞单位进行AHG交叉匹配。追踪任何不相容的AHG交叉配比,作为可疑的输血反应。结果:共向2402例AS阴性患者输注了5023个红细胞单元。 99.7%IS兼容的红细胞单位在输血后AHG交叉匹配上也兼容。在一名输了两个IS交叉匹配兼容单位的患者中鉴定了抗P1同种抗体,但后来两个单位在AHG交叉匹配上都不兼容。患者没有溶血的临床或血清学迹象。结论:在AS阴性患者中,IS交叉匹配与常规AHG交叉匹配一样安全,因此可以替代常规AHG交叉匹配方案。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号