Blood Donors' Age, Haemoglobin Type, G6PD Status, and Blood Group Impact Storability of CPDA-1 Banked Whole Blood: A Repeated-Measure Cohort Study in Cape Coast, Ghana.

Q3 Medicine
Advances in Hematology Pub Date : 2020-05-30 eCollection Date: 2020-01-01 DOI:10.1155/2020/4959518
Patrick Adu, Gilbert Appiah Kubi, Amos Kumi, Raphael E K Gbedoho, Festus Ansah Kwakye, Emmanuel Sarpong, Constantine Drai, Samuel Dompreh, Fredrick Afful Sersah, Eric Ofori Gyamerah
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Abstract

Background: The high prevalence of haemoglobin variants and glucose 6-phosphate dehydrogenase disorder (G6PDd) in sub-Saharan Africa means that substantial proportions of donor blood units carry these red cell abnormalities.

Aim: This study investigated the impact that inherited haemoglobin variants and/or G6PD status have on whole blood banked at 4-6°C for 35 days.

Method: This repeated-measure cohort study was undertaken on 103 donor blood units collected into blood bag containing CPDA-1 anticoagulant. On days 0, 7, 14, 21, and 35, full blood count, osmotic-induced haemolysis, and plasma K+ levels were estimated. Also, on day 0, G6PD status, haemoglobin variants, % foetal haemoglobin, and blood group of donor units were determined using methaemoglobin reductase, cellulose acetate electrophoresis, modified Bekte alkali denaturation assay, and slide haemagglutination test, respectively.

Result: Overall, although plasma K+ levels increased during storage, donor units from individuals ≥20 years, G6PD normal, Hb AC, or blood group B had comparatively higher percentage change in plasma K+ during storage. Osmotically induced haemolysis of donor units was significantly decreased in Hb AC (compared with Hb A or AS) donor units on days 7, 14, 21, and 35 (p < 0.0001 in each case). G6PDd donor units had comparatively reduced osmotic-induced lysis compared with G6PD normal units, reaching a statistical significance on day 35 (p = 0.043). Also, Hb AC units had comparatively nonstatistically higher plasma K+ at all time points (compared with Hb A or AS). Furthermore, whereas donor units from individuals ≥20 years showed significantly higher median free haemoglobin on day 21 (compared to donor <20 years), when donor units were stratified per Hb variants, only Hb AS units had median free haemoglobin below the 0.8% threshold after 35 days' storage.

Conclusion: Age of donor, blood group, Hb AC variant, and G6PD status may be important considerations in the storability of whole blood.

献血者的年龄、血红蛋白类型、G6PD状态和血型影响CPDA-1全血库的可储存性:加纳海岸角的重复测量队列研究。
背景:在撒哈拉以南非洲,血红蛋白变异和葡萄糖6-磷酸脱氢酶疾病(G6PDd)的高发率意味着相当大比例的供血单位携带这些红细胞异常。目的:本研究探讨了遗传性血红蛋白变异和/或G6PD状态对4-6°C保存35天全血的影响。方法:采用重复测量的队列研究方法,对103个供血单位采集到含有CPDA-1抗凝血剂的血袋中。在第0、7、14、21和35天,评估全血细胞计数、渗透诱导溶血和血浆K+水平。同时,在第0天,分别用甲基血红蛋白还原酶、醋酸纤维素电泳、改良Bekte碱变性试验和玻片血凝试验测定G6PD状态、血红蛋白变异、%胎儿血红蛋白和供体单位血型。结果:总体而言,尽管血浆K+水平在储存期间升高,但≥20岁、G6PD正常、Hb AC或B型血的供体单位在储存期间血浆K+的变化百分比相对较高。在第7、14、21和35天,Hb AC供体单位的渗透诱导溶血明显减少(与Hb A或AS相比)(每种情况p < 0.0001)。与G6PD正常单位相比,G6PDd供体单位的渗透诱导裂解相对减少,在第35天达到统计学意义(p = 0.043)。此外,Hb AC单位在所有时间点的血浆K+相对较高(与Hb A或AS相比)。此外,与献血者相比,年龄≥20岁的献血者单位在第21天的游离血红蛋白中位数显著高于献血者。结论:献血者年龄、血型、Hb AC变异和G6PD状态可能是影响全血储存能力的重要因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advances in Hematology
Advances in Hematology Medicine-Hematology
CiteScore
3.30
自引率
0.00%
发文量
10
审稿时长
15 weeks
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