Young Joanna K, Ellison John M, Marshall Robert
Clinical Affairs, LifeScan Scotland, Ltd., Inverness, Scotland.
J Diabetes Sci Technol. 2008 Sep;2(5):814-8. doi: 10.1177/193229680800200510.
Improvements to blood glucose monitoring systems aim to simplify the testing process, reduce or eliminate errors, and provide additional information for patients with diabetes. New systems must continue to demonstrate high-quality analytical performance. The new OneTouch Vita System (LifeScan, Inc., Milpitas, CA) offers a no-code testing process and proven technology found in the OneTouch Ultra System. Comparative studies were conducted with the new and established systems to evaluate their precision and accuracy.
Within-run precision in blood, total precision with controls, and system accuracy were evaluated using three lots of OneTouch Vita Test Strips and one lot of OneTouch Ultra Test Strips. Accuracy was tested across a wide glucose range (38-520 mg/dl, 2.1-28.9 mmol/liter) using fingertip blood samples from 139 subjects. Reference plasma glucose values were obtained using the YSI 2300 STAT Plus Glucose & Lactate Analyzer (YSI Inc., Yellow Springs, OH). All studies were designed in accordance with requirements published by the International Organization for Standardization (ISO 15197).
Precision testing (within-run and total) with both systems produced coefficients of variation (CVs) of <5% for all sample types and glucose levels. Within-run precision testing with blood showed CVs of <3.1% and <4.7% for the OneTouch Vita and OneTouch Ultra Systems respectively. Total precision with control samples gave CVs of <3.0% and <3.6% for the two systems. Consensus error grid analysis showed equivalent clinical accuracy with 98.4% (821/834) and 98.2% (273/278) of results within zone A. Both systems met the ISO acceptability requirements for system accuracy.
The OneTouch Vita System provides a simple no-code testing process with performance comparable to the OneTouch Ultra and OneTouch Ultra2 Systems.
血糖监测系统的改进旨在简化检测过程、减少或消除误差,并为糖尿病患者提供更多信息。新系统必须持续展现出高质量的分析性能。新型OneTouch Vita系统(美国加利福尼亚州米尔皮塔斯市LifeScan公司)提供无编码检测流程以及在OneTouch Ultra系统中得到验证的技术。对新系统和现有系统进行了对比研究,以评估它们的精密度和准确性。
使用三批OneTouch Vita测试条和一批OneTouch Ultra测试条评估血液中的批内精密度、质控品的总精密度以及系统准确性。使用来自139名受试者的指尖血样本,在较宽的血糖范围内(38 - 520 mg/dl,2.1 - 28.9 mmol/升)测试准确性。使用YSI 2300 STAT Plus葡萄糖和乳酸分析仪(美国俄亥俄州黄泉市YSI公司)获得参考血浆葡萄糖值。所有研究均按照国际标准化组织(ISO 15197)发布的要求设计。
两种系统的精密度测试(批内和总精密度)对于所有样本类型和血糖水平的变异系数(CV)均<5%。血液的批内精密度测试显示,OneTouch Vita系统和OneTouch Ultra系统的CV分别<3.1%和<4.7%。两种系统的质控品总精密度的CV分别<3.0%和<3.6%。一致性误差网格分析显示临床准确性相当,A区内的结果分别有98.4%(821/834)和98.2%(273/278)。两种系统均符合ISO对系统准确性的可接受性要求。
OneTouch Vita系统提供了简单的无编码检测流程,其性能与OneTouch Ultra和OneTouch Ultra2系统相当。