1999-2017年丹麦首都地区输血并发症的回顾性研究:潜在“危险”献血者的特征?年代

Have Sb, Hother Ce, V. Jh, Dziegiel Mh, Hansen Mb, Ostrowski Sr
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摘要

目的:我们假设,与其他献血者相比,最常发生并发症的献血者会诱发更多和更严重的免疫输血并发症,即潜在的“危险”。次要目的是人口统计学变量的差异。背景:供体相关机制可能导致异基因输血并发症,并可能是一种危险的治疗不良事件。材料与方法:对1999年1月1日至2017年12月31日丹麦首都地区输血数据进行分析;我们的数据集中包括来自194,432名献血者的2,574,646次输血和9,779次输血并发症。我们根据并发症的数量和并发症的频率将献血者分为三组(潜在“危险”与两个不同定义的对照组,即对照1和对照2),并通过统计分析比较了输血并发症的性质和人口统计学变量。结果:潜在“危险”献血者与对照献血者并发症类型比例无差异,根据ABO血型和RhD血型,红细胞、血浆和血小板并发症比例无差异。然而,与对照组相比,ABO血型B的女性献血者更具潜在的“危险”(分别p<0.001和p<0.01)。与对照组相比,潜在“危险”献血者更年轻(40.36岁,45.24岁和42.84岁,p<0.001)。结论:与对照供者相比,潜在的“危险”输血没有显示出更多/严重的免疫并发症。然而,他们在性别、年龄和血型方面存在差异。进一步研究每个供者并发症频率的差异和人口统计学差异是有必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Retrospective Study of Blood Transfusion Complications in the Capital Region of Denmark from 1999-2017: Characteristics of Potentially “Dangerous” Blood Donors?s
Objectives: We hypothesized that the blood donors most frequently involved in complications would induce more and severe immunologic transfusion complications compared to other donors, i.e. potentially “dangerous”. Secondary aims were differences in demographic variables. Background: Donor-related mechanisms may contribute to allogeneic blood transfusion complications and may represent a dangerous treatment adverse event. Materials and Methods: By analyzing transfusion data from the Capital Region of Denmark from January 1, 1999 to December 31, 2017; 2,574,646 blood transfusions and 9,779 transfusion complications from 194,432 blood donors were included in our dataset. We divided donors into three groups based on the number of complications and complication frequency (potentially “dangerous” vs. two differently defined control groups i.e. control 1 and control 2), and compared the nature of transfusion complications and demographic variables by statistical analysis. Results: There were no differences in the proportion of complication types between the potentially “dangerous” donors and control donors, and no difference in the proportion of complications from RBCs, plasma or platelets according to ABO and RhD blood types. However, more potentially “dangerous” donors were female and had ABO blood type B compared to control donors (p<0.001 and p<0.01, respectively). The potentially “dangerous” donors were younger compared to control donors (40.36 years vs. 45.24 years and 42.84 years, p<0.001). Conclusion: The potentially “dangerous” did not display more/severe immunologic transfusion complications compared to control donors. However, they differed in regards to gender, age and blood type. Further research regarding the differences in complication frequency per donor and demographic variety is warranted.
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