Suppr超能文献

血糖仪的质量规范:通过胰岛素剂量误差的模拟模型进行评估

Quality specifications for glucose meters: assessment by simulation modeling of errors in insulin dose.

作者信息

Boyd J C, Bruns D E

机构信息

Department of Pathology, University of Virginia Medical School, Charlottesville, VA 22908, USA.

出版信息

Clin Chem. 2001 Feb;47(2):209-14.

Abstract

BACKGROUND

Proposed quality specifications for glucose meters allow results to be in error by 5-10% or more of the "true" concentration. Because meters are used as aids in the adjustment of insulin doses, we aimed to characterize the quantitative effect of meter error on the ability to identify the insulin dose appropriate for the true glucose concentration.

METHODS

Using Monte Carlo simulation, we generated random "true" glucose values within defined intervals. These values were converted to "measured" glucose values using mathematical models of glucose meters having defined imprecision (CV) and bias. For each combination of bias and imprecision, 10,000-20,000 true and measured glucose concentrations were matched with the corresponding insulin doses specified by selected insulin-dosing regimens. Discrepancies in prescribed doses were counted and their frequencies plotted in relation to bias and imprecision.

RESULTS

For meters with a total analytical error of 5%, dosage errors occurred in approximately 8-23% of insulin doses. At 10% total error, 16-45% of doses were in error. Large errors of insulin dose (two-step or greater) occurred >5% of the time when the CV and/or bias exceeded 10-15%. Total dosage error rates were affected only slightly by choices of sliding scale among insulin dosage rules or by the range of blood glucose. To provide the intended insulin dosage 95% of the time required that both the bias and the CV of the glucose meter be <1% or <2%, depending on mean glucose concentrations and the rules for insulin dosing.

CONCLUSIONS

Glucose meters that meet current quality specifications allow a large fraction of administered insulin doses to differ from the intended doses. The effects of such dosage errors on blood glucose and on patient outcomes require study.

摘要

背景

血糖仪的拟议质量规范允许检测结果与“真实”浓度存在5%-10%或更高的误差。由于血糖仪被用作调整胰岛素剂量的辅助工具,我们旨在描述血糖仪误差对识别适合真实血糖浓度的胰岛素剂量能力的定量影响。

方法

使用蒙特卡洛模拟,我们在定义的区间内生成随机的“真实”血糖值。利用具有定义不精密度(CV)和偏差的血糖仪数学模型,将这些值转换为“测量”血糖值。对于偏差和不精密度的每种组合,将10000-20000个真实和测量的血糖浓度与选定胰岛素给药方案指定的相应胰岛素剂量相匹配。计算规定剂量的差异,并将其频率相对于偏差和不精密度进行绘制。

结果

对于总分析误差为5%的血糖仪,约8%-23%的胰岛素剂量出现给药误差。总误差为10%时,16%-45%的剂量存在误差。当CV和/或偏差超过10%-15%时,胰岛素剂量出现大误差(两步或更大)的情况超过5%。总给药误差率仅受胰岛素给药规则中滑动比例选择或血糖范围的轻微影响。要在95%的时间内提供预期的胰岛素剂量,要求血糖仪的偏差和CV均<1%或<2%,具体取决于平均血糖浓度和胰岛素给药规则。

结论

符合当前质量规范的血糖仪会使很大一部分给药的胰岛素剂量与预期剂量不同。这种给药误差对血糖和患者预后的影响需要进行研究。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验