A-349 Evaluation of i-STAT® Point of Care Blood Gas Cartridges and Competitor Blood Gas Devices Against Reference Standard for PCO2 and PO2

IF 7.1 2区 医学 Q1 MEDICAL LABORATORY TECHNOLOGY Clinical chemistry Pub Date : 2024-10-02 DOI:10.1093/clinchem/hvae106.343
C Beattie, L Thibodeau
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Abstract

Background The i-STAT System provides laboratory quality results in minutes at the patient’s bedside. Accurate and rapid test results are critical for clinical decision making in the presence of blood gas disorders, including oxygenation and acid-base status, where the partial pressure oxygen (PO2) and partial pressure carbon dioxide (PCO2) are needed. The purpose of this study was to compare the analytical performance of the PO2 and PCO2 tests in the i-STAT G3+ and i-STAT CG8+ cartridges to the theoretical PO2 and PCO2 in prepared reference standards. Two other blood gas instruments, a benchtop device and a laboratory device were also compared to the reference PO2 and PCO2. Methods Venous whole blood samples were contrived using saturation tonometry with U.S. NIST (National Institute of Science and Technology) traceable gas tanks to prepare the reference standards, which were value assigned to theoretical PO2 or PCO2 levels based on the molar composition of the gas mixture used. Eleven levels spanning the reportable range of each PO2 (5 mmHg - 800 mmHg) and PCO2 (5 mmHg - 130 mmHg) were prepared and tested in duplicate on the i-STAT G3+ and i-STAT CG8+ cartridges, benchtop device, and the laboratory device. Passing-Bablok linear regression analysis was performed to evaluate the slope and correlation coefficient, comparing each blood gas device against the reference PO2 and PCO2 values. Study designs followed CLSI (Clinical and Laboratory Standards Institute) EP09C-ED3:2018, Measurement Procedure Comparison and Bias Estimation using Patient Samples, 3rd Edition. Passing-Bablok regression analysis was also performed for the i-STAT cartridges and benchtop device against the laboratory device. Results The regression analysis was performed against the reference standards. For PO2, slopes for the i-STAT cartridges ranged from 0.93 - 0.97, the slope for the benchtop device was 0.99, and the slope for the laboratory device was 0.97. Correlation coefficients for all devices were 1.00. For PCO2, slopes for the i-STAT cartridges ranged from 0.98 - 1.02, the slope for the benchtop device was 0.85, and the slope for the laboratory device was 1.01. Correlation coefficients were 1.00 for the i-STAT cartridges and laboratory device, and 0.99 for the benchtop device. The regression analysis was also performed against the laboratory device. For PO2, slopes for the i-STAT cartridges ranged from 0.96 - 1.00, and the slope for the benchtop device was 1.02. Correlation coefficients for all devices were 1.00. For PCO2, slopes for the i-STAT cartridges ranged from 0.97 - 1.01, and the slope for the benchtop device was 0.85. Correlation coefficients were 1.00 for the i-STAT cartridges and 0.99 for the benchtop device. Conclusions The study demonstrated that the i-STAT G3+ and i-STAT CG8+ cartridges used with the i-STAT System were shown to provide laboratory quality results within 2 minutes, showing good agreement to both reference standards and laboratory quality devices. For PCO2, the i-STAT System was shown to have better agreement to both theoretical reference standards and the laboratory device than the benchtop device. These studies were funded by Abbott Laboratories.
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A-349 对照 PCO2 和 PO2 的参考标准评估 i-STAT® 护理点血气盒和同类血气设备
背景 i-STAT 系统可在病人床旁几分钟内提供高质量的化验结果。在出现血气紊乱(包括氧合和酸碱状态)时,准确而快速的检测结果对临床决策至关重要,此时需要氧分压(PO2)和二氧化碳分压(PCO2)。本研究的目的是将 i-STAT G3+ 和 i-STAT CG8+ 血盒中的 PO2 和 PCO2 测试分析性能与准备好的参考标准中的理论 PO2 和 PCO2 进行比较。另外两台血气仪器(一台台式仪器和一台实验室仪器)也与参考 PO2 和 PCO2 进行了比较。方法 使用饱和度眼压计和美国 NIST(国家科学和技术研究所)可追溯气罐计算静脉全血样本,以制备参考标准,并根据所用混合气体的摩尔成分为理论 PO2 或 PCO2 水平赋值。在每个 PO2(5 mmHg - 800 mmHg)和 PCO2(5 mmHg - 130 mmHg)的可报告范围内制备了 11 个水平,并在 i-STAT G3+ 和 i-STAT CG8+ 气瓶、台式设备和实验室设备上进行了重复测试。将每种血气设备与参考 PO2 和 PCO2 值进行比较后,进行 Passing-Bablok 线性回归分析,以评估斜率和相关系数。研究设计遵循 CLSI(临床和实验室标准协会)EP09C-ED3:2018《使用患者样本的测量程序比较和偏差估计》第三版。还对 i-STAT 血盒和台式设备与实验室设备进行了 Passing-Bablok 回归分析。结果 参照标准进行回归分析。对于 PO2,i-STAT 血盒的斜率在 0.93 - 0.97 之间,台式设备的斜率为 0.99,实验室设备的斜率为 0.97。所有设备的相关系数均为 1.00。对于 PCO2,i-STAT 血盒的斜率范围为 0.98 - 1.02,台式设备的斜率为 0.85,实验室设备的斜率为 1.01。i-STAT 血盒和实验室设备的相关系数为 1.00,台式设备的相关系数为 0.99。还对实验室设备进行了回归分析。对于 PO2,i-STAT 血盒的斜率在 0.96 - 1.00 之间,台式设备的斜率为 1.02。所有设备的相关系数均为 1.00。对于 PCO2,i-STAT 血盒的斜率在 0.97 - 1.01 之间,台式设备的斜率为 0.85。i-STAT 血盒的相关系数为 1.00,台式设备的相关系数为 0.99。结论 该研究表明,与 i-STAT 系统配套使用的 i-STAT G3+ 和 i-STAT CG8+ 血盒可在 2 分钟内提供实验室质量结果,与参考标准和实验室质量设备都显示出良好的一致性。对于 PCO2,i-STAT 系统与理论参考标准和实验室设备的一致性均优于台式设备。这些研究由雅培实验室资助。
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来源期刊
Clinical chemistry
Clinical chemistry 医学-医学实验技术
CiteScore
11.30
自引率
4.30%
发文量
212
审稿时长
1.7 months
期刊介绍: Clinical Chemistry is a peer-reviewed scientific journal that is the premier publication for the science and practice of clinical laboratory medicine. It was established in 1955 and is associated with the Association for Diagnostics & Laboratory Medicine (ADLM). The journal focuses on laboratory diagnosis and management of patients, and has expanded to include other clinical laboratory disciplines such as genomics, hematology, microbiology, and toxicology. It also publishes articles relevant to clinical specialties including cardiology, endocrinology, gastroenterology, genetics, immunology, infectious diseases, maternal-fetal medicine, neurology, nutrition, oncology, and pediatrics. In addition to original research, editorials, and reviews, Clinical Chemistry features recurring sections such as clinical case studies, perspectives, podcasts, and Q&A articles. It has the highest impact factor among journals of clinical chemistry, laboratory medicine, pathology, analytical chemistry, transfusion medicine, and clinical microbiology. The journal is indexed in databases such as MEDLINE and Web of Science.
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