Christopher DiPasquale, Robert H Christenson, James G Donnelly, Susan A Evans, Alan H B Wu, Eric G Olson, Roy Barr, Nicolas Kosa, Hattie McKenzie, Melissa Abigania, James W Jacobson
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引用次数: 0
Abstract
Background: Capillary blood testing has potential to improve accessibility and adherence for routine tests. Due to historical challenges with sample volume and quality, capillary blood is rarely used for diagnostic testing. These studies provide objective evidence that miniaturized assays and novel capillary collection technologies can enable equivalent results for important panels.
Methods: The studies evaluated equivalence of capillary blood testing using miniaturized assays and novel collection methods. We verified the performance of 20 miniaturized assays vs their unmodified versions. We then evaluated specimen equivalence across 39 analytes by comparing samples collected with novel capillary technologies vs samples collected with conventional technologies. For 38 analytes, specimen equivalence was evaluated vs conventional venous samples, and vs conventional capillary samples for 2 analytes with biological gradients (glucose and total CO2).
Results: Equivalence of miniaturized assays and novel capillary methods to conventional testing was demonstrated across all analytes. Method comparison of all 20 miniaturized assays highly correlated (Pearson r > 0.95) to unmodified versions of each test. Capillary blood collected with the novel collection procedure produced results equivalent to conventional methods, with 37 analytes performing equivalently to venous serum, glucose to both venous and conventional capillary serum, and total CO2 to conventional capillary serum.
Conclusions: Capillary blood can be utilized for routine bloodwork. Issues with sample volume can be overcome by miniaturizing assays without compromising performance. Issues with sample quality can be overcome by novel capillary collection technologies, which additionally enable non-phlebotomist sample collection in a broad scope of healthcare settings.
背景:毛细管血液检测有可能提高常规检查的可及性和依从性。由于样品体积和质量的历史挑战,毛细管血很少用于诊断测试。这些研究提供了客观证据,证明小型化分析和新型毛细管收集技术可以为重要的面板提供等效的结果。方法:研究采用小型化分析方法和新型采集方法评价毛细管血液检测的等效性。我们验证了20种小型化分析方法与其未修改版本的性能。然后,通过比较新型毛细管技术收集的样品与传统技术收集的样品,我们评估了39种分析物的样品等效性。对38种分析物与常规静脉样品进行了等效性评估,并对2种生物梯度分析物(葡萄糖和总二氧化碳)与常规毛细管样品进行了等效性评估。结果:小型化分析和新型毛细管方法与常规测试的等效性在所有分析物中得到证明。所有20个小型化试验与每个试验的未修改版本高度相关(Pearson r = 0.95)的方法比较。采用新方法采集的毛细血管血液的结果与传统方法相当,其中37种分析物对静脉血清的效果相当,对静脉和传统毛细血管血清的葡萄糖效果相当,对传统毛细血管血清的总二氧化碳效果相当。结论:毛细管血可用于常规血液检查。样品容量的问题可以通过小型化分析而不影响性能来克服。样品质量问题可以通过新型毛细管采集技术来克服,该技术还可以在广泛的医疗保健环境中进行非抽血师样品采集。