Optimizing Falling Drop Hemoglobin Method by Comparing Capillary Versus Venous Blood and Determining the Stability of the Copper Sulfate Solution.

IF 1.3 Q4 HEMATOLOGY
Journal of hematology Pub Date : 2024-12-01 Epub Date: 2024-12-02 DOI:10.14740/jh1337
Amogh Chariyamane, Tim R Randolph
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引用次数: 0

Abstract

Background: Anemia is a global health issue that affects over 1 billion people and contributes to maternal mortality and birth defects. Low-resource, tropical areas face a dual challenge: high prevalence of anemia and inability to access affordable testing methods. The falling drop hemoglobin method has been developed by our lab to quantify hemoglobin concentration and assess anemia by timing the descent of venous blood in a column of copper sulfate solution, without using electricity or batteries. This research aimed to optimize the falling drop hemoglobin method by evaluating the use of capillary blood to reduce within sample variance and assessing copper sulfate stability to determine shelf life in expected working conditions.

Methods: The falling drop hemoglobin method was performed on both venous and capillary blood samples collected directly from the fingertip by dispensing 44 µL of blood in a copper sulfate column. A microhematocrit was performed on the venous blood sample and converted mathematically to a hemoglobin level to serve as the standard. Copper sulfate stability was assessed for 32 weeks among three solutions: solution prepared fresh on day of testing, solution incubated at room temperature, and solution incubated at 37.7 °C.

Results: Capillary blood yielded higher average descent times and higher standard deviations than venous blood. Collecting precisely 44 µL of capillary blood proved challenging and impractical. In copper sulfate stability testing, freshly prepared solution yielded the highest average descent time. A one-way analysis of variance (ANOVA) test and Tukey's honestly significant difference (HSD) post hoc testing revealed no significant difference between mean descent times of freshly prepared and 37.7 °C solutions (P = 0.26) and between room temperature and 37.7 °C solutions (P = 0.64), but a significant difference between freshly prepared and room temperature solutions (P = 0.04).

Conclusions: This study found that capillary blood did not present a more accurate alternative to venous blood in the falling drop hemoglobin test, and copper sulfate did not degrade over 32 weeks at 37.7 °C. This lends support for the current use of venous blood in the test, and for use of copper sulfate solution in tropical climates, where the test is most necessary, with a shelf life of at least 32 weeks.

通过比较毛细管血和静脉血及测定硫酸铜溶液的稳定性来优化滴下血红蛋白法。
背景:贫血是一个全球性的健康问题,影响着超过10亿人,并导致孕产妇死亡和出生缺陷。资源匮乏的热带地区面临着双重挑战:贫血的高患病率和无法获得负担得起的检测方法。下落血红蛋白法是由我们的实验室开发的,通过测定硫酸铜溶液柱中静脉血下降的时间来定量血红蛋白浓度并评估贫血,而不使用电力或电池。本研究旨在通过评估毛细管血的使用减少样本内方差和评估硫酸铜的稳定性来确定预期工作条件下的保质期,从而优化滴落血红蛋白法。方法:直接采集指尖静脉血和毛细血管血,采用滴血血红蛋白法,用硫酸铜柱配血44µL。在静脉血样本上进行微血细胞比容,并将其数学转换为血红蛋白水平作为标准。在测试当天新鲜制备的溶液、室温孵育的溶液和37.7℃孵育的溶液中,评估硫酸铜32周的稳定性。结果:与静脉血相比,毛细血管血平均下降时间更长,标准差更高。事实证明,精确采集44 μ L的毛细血管血液具有挑战性且不切实际。在硫酸铜稳定性试验中,新鲜配制的溶液平均下降时间最长。单因素方差分析(ANOVA)检验和Tukey诚实显著性差异(HSD)事后检验显示,新鲜制备的溶液与37.7°C溶液的平均下降时间无显著差异(P = 0.26),室温溶液与37.7°C溶液的平均下降时间无显著差异(P = 0.64),新鲜制备的溶液与室温溶液的平均下降时间有显著差异(P = 0.04)。结论:本研究发现,滴落血红蛋白试验中毛细血管血并没有比静脉血更准确的替代方法,在37.7℃下,硫酸铜在32周内没有降解。这为目前测试中使用静脉血提供了支持,也为在热带气候下使用硫酸铜溶液提供了支持,在热带气候下,测试是最必要的,其保质期至少为32周。
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
Journal of hematology
Journal of hematology HEMATOLOGY-
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