Lenters-Westra Erna, Singh Priyanka, Vetter Beatrice, English Emma
Department of Clinical Chemistry, Isala, Zwolle, the Netherlands.
European Reference Laboratory for Glycohemoglobin, Isala, Zwolle, the Netherlands.
Clin Chem. 2025 Jul 4;71(7):775-788. doi: 10.1093/clinchem/hvaf059.
Access to Hb A1c testing in low- and middle-income countries (LMICs) can be limited, especially in rural areas. This has led to an increased interest in the potential role of point-of-care testing (POCT) for Hb A1c. The analytical performance of many of these devices is poorly understood but accurate and precise measurement is essential for effective diabetes management.
Verification of the manufacturers' claims, for accuracy, imprecision, and interference from hemoglobin variants, was performed using protocols based on established guidance using Clinical and Laboratory Standards Institute (CLSI) protocols (EP-15-A3 and EP-9-A3), international quality targets and 4 certified International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) and National Glycohemoglobin Standardization Program (NGSP) Secondary Reference Measurement Procedures (SRMP). Each of the 19 POC devices were assessed for performance against both IFCC and NGSP certification criteria.
Out of 19 Hb A1c POC devices, only 5 (26%) met international quality criteria (IFCC and NGSP with at least one SRMP), 5 (26%) only met IFCC criteria, and 9 (47%) did not meet either IFCC or NGSP criteria, despite most of these devices having an IFCC and/or NGSP certificate at the time of the study. Three devices showed clear interference from Hb variants.
This study shows the importance of independent evaluations for assessing the performance of Hb A1c POC devices. The analytical performance of the devices was very poor overall, with 74% not meeting both IFCC and NGSP criteria. These evaluations were performed under ideal conditions; performance may worsen further when used in a clinical setting.
在低收入和中等收入国家(LMICs),尤其是农村地区,糖化血红蛋白(Hb A1c)检测的可及性可能有限。这使得人们对即时检验(POCT)在Hb A1c检测中的潜在作用越来越感兴趣。然而,许多这类设备的分析性能了解不足,但准确和精确的测量对于有效的糖尿病管理至关重要。
根据临床和实验室标准协会(CLSI)协议(EP - 15 - A3和EP - 9 - A3)、国际质量目标以及4种经认证的国际临床化学和检验医学联合会(IFCC)和国家糖化血红蛋白标准化计划(NGSP)二级参考测量程序(SRMP)所确立的指南,通过相关方案对制造商在准确性、不精密度以及血红蛋白变异体干扰方面的声明进行验证。对19种POCT设备逐一评估其是否符合IFCC和NGSP认证标准。
在19种Hb A1c POCT设备中,只有5种(26%)符合国际质量标准(IFCC和NGSP且至少有一种SRMP),5种(26%)仅符合IFCC标准,9种(47%)既不符合IFCC标准也不符合NGSP标准,尽管在研究时这些设备中的大多数都拥有IFCC和/或NGSP证书。有三种设备显示出明显受到血红蛋白变异体的干扰。
本研究表明了独立评估对于评估Hb A1c POCT设备性能的重要性。这些设备的分析性能总体非常差,74%不符合IFCC和NGSP标准。这些评估是在理想条件下进行的;在临床环境中使用时性能可能会进一步恶化。