Pfützner A, Hengesbach C, Demircik F, Schipper C, Forst T, Musholt P B
IKFE - Institute of Clinical Research and Development , Mainz , Germany.
Curr Med Res Opin. 2014 Feb;30(2):185-90. doi: 10.1185/03007995.2013.858617. Epub 2013 Nov 6.
Since 2003, blood glucose meters for patient self testing are approved in Europe based on the accuracy performance criteria as defined by the ISO15197 guideline. A new draft ISO guideline is currently under regulatory review, which suggests more strict accuracy acceptance criteria, and which may not be entirely fulfilled by currently commercialized blood glucose meter systems. In order to investigate the compliance of BGStar and iBGStar and several other blood glucose meters with the new draft ISO guideline, we performed a post-hoc analysis of data obtained from a recently performed ISO-conforming clinical accuracy performance study. This study was performed with 106 patients, clinically presenting with blood glucose levels distributed over the entire measurement range and in line with the glucose distribution requirements as demanded by the guideline. The YSI 2300 STAT Plus analyzer (glucose oxidase) served as reference method. While all tested meters had been in a high degree of compliance with the current ISO criteria, performance was lower when analyzed in accordance with the new acceptance criteria (95% of readings have to be within ±15 mg/dL for values <100 mg/dL, and within ±15% for values ≥100 mg/dL). The following meters met the new criteria: Accu-Chek Aviva (95.5%/98.6%), BGStar (98.5%/97.3%), iBGStar (98.5%/97.3%), FreeStyle Freedom Lite (95.5%/96.6%), and OneTouch Ultra2 (95.5%/96.5%). One meter failed with low blood glucose values (Contour: 90.9%/95.9%). In conclusion, BGStar and iBGStar and several other branded meters met the new draft ISO15197 acceptance criteria, when tested in accordance with the instructions for use and with the ISO accuracy testing protocol in a clinical setting.
自2003年起,用于患者自我检测的血糖仪在欧洲是根据ISO15197指南所定义的准确性性能标准获得批准的。目前一项新的ISO指南草案正在监管审查中,该草案提出了更严格的准确性验收标准,而目前商业化的血糖仪系统可能无法完全满足这些标准。为了调查BGStar和iBGStar以及其他几款血糖仪是否符合新的ISO指南草案,我们对最近进行的一项符合ISO标准的临床准确性性能研究中获得的数据进行了事后分析。这项研究对106名患者进行,这些患者临床上呈现的血糖水平分布在整个测量范围内,并且符合指南所要求的葡萄糖分布要求。YSI 2300 STAT Plus分析仪(葡萄糖氧化酶法)用作参考方法。虽然所有测试的血糖仪都高度符合当前的ISO标准,但按照新的验收标准进行分析时性能较低(对于<100mg/dL的值,95%的读数必须在±15mg/dL范围内;对于≥100mg/dL的值,必须在±15%范围内)。以下血糖仪符合新标准:拜安时活力型(95.5%/98.6%)、BGStar(98.5%/97.3%)、iBGStar(98.5%/97.3%)、稳豪倍优型(95.5%/96.6%)和 OneTouch Ultra2(95.5%/96.5%)。一款血糖仪在低血糖值时未达标(轮廓血糖仪:90.9%/95.9%)。总之,在临床环境中按照使用说明和ISO准确性测试方案进行测试时,BGStar和iBGStar以及其他几款品牌血糖仪符合新的ISO15197验收标准。