首页> 外文期刊>Transfusion: The Journal of the American Association of Blood Banks >Frequency of glucose-6-phosphate dehydrogenase-deficient red blood cell units in a metropolitan transfusion service
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Frequency of glucose-6-phosphate dehydrogenase-deficient red blood cell units in a metropolitan transfusion service

机译:大城市输血服务中葡萄糖-6-磷酸脱氢酶缺陷的红细胞单位的频率

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Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is characterized by red blood cell (RBC) destruction in response to oxidative stress. Although blood donors are not routinely screened for G6PD deficiency, the transfusion of stored G6PD-deficient RBCs may have serious adverse outcomes. By measuring G6PD enzyme activity of RBC units from a large metropolitan hospital transfusion service, we sought to determine 1) the prevalence of G6PD-deficient RBC units, 2) if G6PD activity changes during storage, and 3) if G6PD activity in segments correlates with its activity in the bags. Study Desing and Methods: Quantitative G6PD activity was measured in 301 randomly selected RBC units and 73 D+C-E- (i.e., R0r or R0R0) RBC units, all stored in additive solutions. G6PD deficiency was defined as activity less than 60% of the normal mean. Results: The frequency of G6PD-deficient units in the general inventory was 0.3% (1/301; 95% confidence interval [CI], 0.01%-2.1%). In contrast, its frequency in D+C-E- RBC units was 12.3% (9/73; 95% CI, 6.4%-22.0%). G6PD activity did not significantly change during the 42-day storage period, and G6PD activity measured in RBC storage bags and attached segments correlated well (r = 0.7-0.9, p ?? 0.001, Spearman rank correlation). Conclusions: Although the frequency of G6PD-deficient RBC units in the transfusion service general inventory was relatively low, it was significantly higher among a subset of R0r or R0R 0 units. The latter are preferentially allocated for transfusion to patients with sickle cell disease to decrease the risk of RBC alloimmunization, possibly allowing more of these units to be inadvertently targeted to these patients. ? 2012 American Association of Blood Banks.
机译:背景:6-磷酸葡萄糖脱氢酶(G6PD)缺乏症的特征是响应氧化应激而破坏红细胞(RBC)。尽管没有定期对献血者进行G6PD缺乏症筛查,但输血储存的G6PD缺陷型RBC可能会产生严重的不良后果。通过测量来自大型都会医院输血服务中心的RBC单位的G6PD酶活性,我们试图确定1)G6PD缺陷型RBC单位的患病率,2)G6PD活性在储存过程中是否发生变化,以及3)节段中G6PD活性是否与它在袋子里的活动。研究目的和方法:在301个随机选择的RBC单位和73个D + C-E-(即R0r或R0R0)RBC单位中测量了定量的G6PD活性,所有这些单位都存储在添加剂溶液中。 G6PD缺乏症定义为活动度低于正常平均值的60%。结果:一般清单中G6PD缺陷单元的频率为0.3%(1/301; 95%置信区间[CI],<0.01%-2.1%)。相反,其以D + C-E-RBC单位的频率为12.3%(9/73; 95%CI,6.4%-22.0%)。 G42PD活性在42天的储存期间没有显着变化,并且在RBC储存袋和附着的部分中测得的G6PD活性相关性很好(r = 0.7-0.9,p≤0.001,Spearman等级相关)。结论:尽管输血服务总清单中G6PD缺陷型RBC单位的频率相对较低,但在R0r或R0R 0单位的子集中明显更高。后者优先分配给镰状细胞疾病患者输血,以降低RBC同种免疫的风险,可能使更多的此类单位无意中针对这些患者。 ? 2012年美国血库协会。

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