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即时检验分析器用于 C 反应蛋白、脂类研究和糖化血红蛋白的验证。

Verification of point-of-care analysers for C-reactive protein, lipid studies and glycated haemoglobin.

机构信息

Biochemistry, Canterbury Health Laboratories, Christchurch, New Zealand; Te Whatu Ora - Health New Zealand Waitaha Canterbury, Christchurch, New Zealand.

Biochemistry, Canterbury Health Laboratories, Christchurch, New Zealand; Te Whatu Ora - Health New Zealand Waitaha Canterbury, Christchurch, New Zealand.

出版信息

Pathology. 2023 Dec;55(7):989-999. doi: 10.1016/j.pathol.2023.07.004. Epub 2023 Sep 9.

Abstract

Due to increased convenience and faster test results, interest in point-of-care testing (PoCT) has grown significantly. Though PoCT may improve the speed and convenience of testing, the devices need to be fit for their intended purpose. Our aim was to verify the performance of Roche cobas b 101 and Abbott Afinion 2 for C-reactive protein (CRP), lipid studies and glycated haemoglobin (HbA1c), and Siemens Atellica DCA for HbA1c. For all PoCT analysers and measurands, accuracy was assessed by method comparison with central laboratory analysers. Passing-Bablok linear regression was performed, and Bland-Altman plots were generated. The proportion of samples within the Royal College of Pathologists of Australasia Quality Assurance Programs Analytical Performance Specifications (RCPAQAP APS) was assessed. Within-run and between-day imprecision was assessed and compared with manufacturer claims and biological variation or clinical guidelines for desirable imprecision. For CRP, both evaluated PoCT analysers had all samples within the RCPAQAP APS and had optimal imprecision according to biological variation. For lipid studies, the Roche cobas b 101 had most samples within the RCPAQAP APS, with two of 22 cholesterol, one of 22 high-density-lipoprotein-cholesterol (HDL-C) and zero of 22 triglyceride comparisons outside the RCPAQAP APS. The Abbott Afinion 2 had a positive bias with all three measured parameters, although the effect was more limited in the calculated parameters cholesterol:HDL-C ratio, non-HDL-C and low-density-lipoprotein-cholesterol (LDL-C). For HbA1c, all analysers had acceptable imprecision for monitoring with coefficient of variation (CV) <3% and minimal bias at the treatment target (HbA1c 53 mmol/mol or 7.0%). However, significant biases were apparent at higher or lower HbA1c for all analysers. All evaluated analysers were fit for purpose for CRP and for serial monitoring of HbA1c, although bias in some analysers was present at extremes of HbA1c. For lipid studies, the Roche cobas b 101 had fewer results outside the RCPAQAP allowable limits, and better precision. The Abbott Afinion 2 had a positive bias on both the cholesterol and HDL-C, but there is limited clinical impact when calculating cholesterol:HDL-C, LDL-C and non-HDL-C.

摘要

由于便利性和更快的测试结果,人们对即时检测(POCT)的兴趣显著增加。虽然 POCT 可能会提高测试的速度和便利性,但这些设备需要适合其预期用途。我们的目的是验证罗氏 cobas b 101 和雅培 Afinion 2 用于 C 反应蛋白(CRP)、脂质研究和糖化血红蛋白(HbA1c),以及西门子 Atellica DCA 用于 HbA1c 的性能。对于所有 POCT 分析仪和测定物,通过与中心实验室分析仪的方法比较来评估准确性。进行了 Passing-Bablok 线性回归,并生成了 Bland-Altman 图。评估了符合澳大利亚皇家病理学家学院质量保证计划分析性能规格(RCPAQAP APS)的样品比例。评估了批内和日间不精密度,并将其与制造商声明以及生物变异或理想不精密度的临床指南进行了比较。对于 CRP,两种经过评估的 POCT 分析仪的所有样品均在 RCPAQAP APS 范围内,并且根据生物变异,其不精密度最佳。对于脂质研究,罗氏 cobas b 101 的大多数样品均在 RCPAQAP APS 范围内,其中 22 个胆固醇中有 2 个、22 个高密度脂蛋白胆固醇(HDL-C)中有 1 个和 22 个三酰甘油中有 0 个不在 RCPAQAP APS 范围内。雅培 Afinion 2 对所有三个测量参数均有正偏倚,尽管在计算参数胆固醇:HDL-C 比值、非高密度脂蛋白胆固醇和低密度脂蛋白胆固醇(LDL-C)中,这种影响更为有限。对于 HbA1c,所有分析仪的监测精密度均可接受,变异系数(CV)<3%,治疗目标(HbA1c 53 mmol/mol 或 7.0%)的偏差最小。然而,所有分析仪在 HbA1c 较高或较低时均存在明显偏差。所有经过评估的分析仪均适用于 CRP 的测定和 HbA1c 的连续监测,尽管在 HbA1c 的极端值处,某些分析仪存在偏差。对于脂质研究,罗氏 cobas b 101 的结果在 RCPAQAP 允许范围内的较少,且精密度更好。雅培 Afinion 2 对胆固醇和 HDL-C 均有正偏倚,但在计算胆固醇:HDL-C、LDL-C 和非高密度脂蛋白胆固醇时,其临床影响有限。

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