罗氏 Accu-Chek Performa 血糖仪在低血糖浓度下的准确性评估:一项为期九年的回顾性研究

iLABMED Pub Date : 2024-06-17 DOI:10.1002/ila2.49
Zhipeng Zhao, Runqing Li, Xiuying Zhao, Lina Zhang, Tengjiao Wang, Song Yang, Ning Han, Dong Zhu
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引用次数: 0

摘要

目的 评价罗氏 Accu-Chek Performa 血糖仪在<5.55 mmol/L (100 mg/dL) 低血糖浓度下的准确性,为期 9 年。 方法 根据国际标准化组织 (ISO) 15197:2013 规定的可接受性标准,使用 2015 年至 2023 年连续 9 年的年度对比数据,对罗氏 Accu-Chek Performa 血糖仪在低血糖浓度下的准确性进行了评估。通过孵育和糖酵解制备出低糖浓度为<5.55 mmol/L的血液样本。中心实验室使用罗氏 Accu-Chek Performa 血糖仪和生化分析仪检测葡萄糖浓度。 结果 回顾性分析了 2015 年至 2023 年期间 211 台血糖仪在<5.55 mmol/L 低血糖浓度下的 2978 对对比结果。临床使用时间从 1 年到 9 年不等,40.76%(211 台血糖仪中的 86 台)的使用时间超过 2 年。血糖仪测量值与实验室参考值之间的相关系数r为0.98(p < 0.001)。罗氏 Accu-Chek Performa 血糖仪的平均值比生化分析仪的平均值高 0.05 mmol/L(0.9 mg/dL)(Z = -13.82,p < 0.0001)。结果显示,100.00% 的罗氏 Accu-Chek Performa 血糖仪(211 台中的 211 台)符合 ISO 15197:2013 中规定的可接受性标准。在 5.55 毫摩尔/升的低血糖浓度下,99.90%(2978 个数据中的 2975 个)的比较数据对误差分布在 ±0.83 毫摩尔/升(15 毫克/分升)的范围内。Parkes 共识误差网格分析表明,100.00% 的对比数据对(2978 个中的 2978 个)位于 A 区域内。 结论 本研究表明,罗氏 Accu-Chek Performa 血糖仪在测量低血糖范围内的血糖时成功达到了 ISO 15197:2013 的准确度标准。应更加关注血糖监测系统在低血糖范围内的性能,尤其是对于容易发生低血糖并需要精确测量的糖尿病患者。
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Accuracy evaluation of Roche Accu-Chek Performa blood glucose meters at low glucose concentrations: A nine-year retrospective study

Objective

To evaluate the accuracy of Roche Accu-Chek Performa glucose meters at a low glucose concentration of <5.55 mmol/L (100 mg/dL) over a 9-year period.

Methods

The accuracy of the Roche Accu-Chek Performa glucose meters at low glucose concentrations was evaluated using annual comparison data for 9 consecutive years from 2015 to 2023, according to the acceptability criteria specified in International Organization for Standardization (ISO) 15197:2013. Blood samples with low glucose concentrations of <5.55 mmol/L were prepared by incubation and glycolysis. The glucose concentration was detected using Roche Accu-Chek Performa glucose meters and a biochemical analyzer in the central laboratory.

Results

A total of 2978 pairs of comparison results from 211 glucose meters at a low glucose concentration of <5.55 mmol/L were retrospectively analyzed from 2015 to 2023. The clinical use duration spanned from 1 to 9 years and 40.76% (86 out of 211 glucose meters) had been used for more than 2 years. The correlation coefficient r between glucose meter measurements and laboratory reference values was 0.98 (p < 0.001). The mean according to Roche Accu-Chek Performa glucose meters was 0.05 mmol/L (0.9 mg/dL) higher than that of the biochemical analyzer (Z = −13.82, p < 0.0001). The results showed that 100.00% (211 out of 211) of the Roche Accu-Chek Performa glucose meters met the acceptability criteria specified in ISO 15197:2013. At a low glucose concentration of <5.55 mmol/L, 99.90% (2975 out of 2978) of the comparative data pairs in the error distribution fell within the range of ±0.83 mmol/L (15 mg/dL). Parkes consensus error grid analysis showed that 100.00% (2978 out of 2978) of comparative data pairs fell within region A.

Conclusions

This study demonstrated that Roche Accu-Chek Performa glucose meters successfully met the accuracy standards of ISO 15197:2013 for measuring blood glucose within the hypoglycemic range. Greater attention should be given to the performance of blood glucose monitoring systems in the low glycemic range, especially for patients with diabetes who are prone to hypoglycemia and require precise measurements.

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