Department of Pathology and Cell Biology, Columbia University College of Physicians and Surgeons, New York Presbyterian Hospital, New York, NY.
Department of Pediatrics, Columbia University College of Physicians and Surgeons, New York Presbyterian Hospital, New York, NY.
Blood. 2022 Dec 22;140(25):2730-2739. doi: 10.1182/blood.2022017288.
Although altruistic regular blood donors are vital for the blood supply, many become iron deficient from donation-induced iron loss. The effects of blood donation-induced iron deficiency on red cell transfusion quality or donor cognition are unknown. In this double-blind, randomized trial, adult iron-deficient blood donors (n = 79; ferritin < 15 μg/L and zinc protoporphyrin >60 μMol/mol heme) who met donation qualifications were enrolled. A first standard blood donation was followed by the gold-standard measure for red cell storage quality: a 51-chromium posttransfusion red cell recovery study. Donors were then randomized to intravenous iron repletion (1 g low-molecular-weight iron dextran) or placebo. A second donation ∼5 months later was followed by another recovery study. Primary outcome was the within-subject change in posttransfusion recovery. The primary outcome measure of an ancillary study reported here was the National Institutes of Health Toolbox-derived uncorrected standard Cognition Fluid Composite Score. Overall, 983 donors were screened; 110 were iron-deficient, and of these, 39 were randomized to iron repletion and 40 to placebo. Red cell storage quality was unchanged by iron repletion: mean change in posttransfusion recovery was 1.6% (95% confidence interval -0.5 to 3.8) and -0.4% (-2.0 to 1.2) with and without iron, respectively. Iron repletion did not affect any cognition or well-being measures. These data provide evidence that current criteria for blood donation preserve red cell transfusion quality for the recipient and protect adult donors from measurable effects of blood donation-induced iron deficiency on cognition. This trial was registered at www.clinicaltrials.gov as NCT02889133 and NCT02990559.
尽管利他主义的定期献血者对血液供应至关重要,但许多人由于献血引起的铁丢失而缺铁。献血引起的缺铁对红细胞输注质量或供者认知的影响尚不清楚。在这项双盲、随机试验中,纳入了符合献血条件的成年缺铁性献血者(n=79;铁蛋白<15μg/L 和锌原卟啉>60μMol/mol 血红素)。首先进行一次标准献血,然后进行红细胞储存质量的金标准测量:51 铬输血后红细胞回收率研究。然后,献血者被随机分为静脉铁补充组(1 g 低分子右旋糖酐铁)或安慰剂组。大约 5 个月后进行第二次献血,然后再次进行回收率研究。主要结局是输血后恢复的个体内变化。这里报告的辅助研究的主要结局测量是美国国立卫生研究院工具包衍生的未经校正标准认知流体综合评分。总体而言,筛查了 983 名献血者;110 名是缺铁性的,其中 39 名被随机分配到铁补充组,40 名分配到安慰剂组。铁补充对红细胞储存质量没有影响:输血后恢复的平均变化分别为 1.6%(95%置信区间-0.5 至 3.8)和-0.4%(-2.0 至 1.2),分别有和没有铁。铁补充组对任何认知或健康指标均无影响。这些数据提供了证据,证明当前的献血标准既可以保持接受者的红细胞输注质量,又可以保护成年献血者免受献血引起的缺铁对认知的可测量影响。该试验在 www.clinicaltrials.gov 上注册,编号为 NCT02889133 和 NCT02990559。