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血液成分治疗时代:为最大限度提高献血者安全性并优化血小板质量,实行献血前血小板计数的时机已到。

Era of blood component therapy: time for mandatory pre-donation platelet count for maximizing donor safety and optimizing quality of platelets.

作者信息

Das Sudipta Sekhar, Zaman R U, Biswas Dipak

机构信息

Department of Transfusion Medicine, Apollo Gleneagles Hospitals, Kolkata 700054, India.

出版信息

Transfus Apher Sci. 2013 Dec;49(3):640-3. doi: 10.1016/j.transci.2013.07.007. Epub 2013 Aug 5.

Abstract

Blood bank regulatory agencies including the Drug and Cosmetics Act (DCA) of India do not mandate a predonation platelet count in whole blood donation. Mandating such practice will definitely optimize the quality of random donor platelets (RDP) in terms of platelet yield and patient therapeutic benefit. We observed poor platelet yield in RDP concentrates prepared at our center with a significant number not meeting the DCA guideline of ≥ 4.5 × 10(10) per bag processed from 450 ml of whole blood. Therefore we planned this study to evaluate the pre-donation hematological values in our blood donor population and effect of these values on the quality of platelet concentrates. The prospective study included 221 blood donors eligible for donating 450 ml of whole blood (WB). Following the departmental standard operating procedure (SOP) RDPs were prepared using the 'Top & Bottom' quadruple bag system and automated component extractor. Quality of RDP was assessed as per departmental protocol. All results were recorded and subsequently transcribed to SPSS working sheet. A significant (p<0.001) decrement of donor blood counts has been observed after WB donation. Mean donor Hb and platelets reduced by 0.72 g/dl and 22.1 × 10(6)/ml respectively. Quality of RDPs in terms of platelet yield was significantly better (p<0.001) when donor platelet count was >200 × 10(6)/ml. Although platelet yield significantly correlated with the donor platelet count however quality of RDPs in terms of red cell contamination showed no correlation with the donor hematocrit. Platelet yield in random donor platelets is a concern in Eastern India. A platelet yield of 4.5 × 10(10) per bag as mandated by the DCA of India was only achieved when the donor platelet count was >200 × 10(6)/ml. Posttransfusion platelet recovery (PPR) was unsatisfactory in the transfused patient. Introduction of pre-donation platelet count in whole blood donation will maximize donor safety and optimize patient platelet transfusion management.

摘要

包括印度《药品和化妆品法案》(DCA)在内的血库监管机构并未强制要求在全血捐献前进行血小板计数。强制实施这种做法肯定会在血小板产量和患者治疗效益方面优化随机供者血小板(RDP)的质量。我们观察到在我们中心制备的RDP浓缩物中血小板产量不佳,相当数量的产品未达到DCA每袋≥4.5×10¹⁰(从450毫升全血中制备)的指导标准。因此,我们计划开展这项研究,以评估我们献血人群捐献前的血液学指标,以及这些指标对血小板浓缩物质量的影响。这项前瞻性研究纳入了221名符合捐献450毫升全血(WB)条件的献血者。按照部门标准操作程序(SOP),使用“上下”四联袋系统和自动成分提取器制备RDP。根据部门方案评估RDP的质量。记录所有结果,随后转录到SPSS工作表中。全血捐献后,观察到献血者血细胞计数显著下降(p<0.001)。献血者平均血红蛋白和血小板分别降低了0.72克/分升和22.1×10⁶/毫升。当捐献者血小板计数>200×10⁶/毫升时,RDP在血小板产量方面的质量显著更好(p<0.001)。虽然血小板产量与捐献者血小板计数显著相关,但RDP在红细胞污染方面的质量与捐献者血细胞比容无关。在印度东部,随机供者血小板的产量是一个问题。只有当捐献者血小板计数>200×10⁶/毫升时,才能达到印度DCA规定的每袋4.5×10¹⁰的血小板产量。输血患者的输血后血小板回收率(PPR)不理想。在全血捐献中引入捐献前血小板计数将使供者安全性最大化,并优化患者血小板输血管理。

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