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首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Effects of measurement frequency on analytical quality required for glucose measurements in intensive care units: Assessments by simulation models
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Effects of measurement frequency on analytical quality required for glucose measurements in intensive care units: Assessments by simulation models

机译:测量频率对重症监护病房葡萄糖测量所需分析质量的影响:模拟模型评估

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BACKGROUND: Total error allowances have been proposed for glucose meters used in tight-glucose-control (TGC) protocols. It is unclear whether these proposed quality specifications are appropriate for continuous glucose monitoring (CGM). METHODS: We performed Monte Carlo simulations of patients on TGC protocols. To simulate use of glucose meters, measurements were made hourly. To simulate CGM, glucose measurements were made every 5 min. Glucose was measured with defined bias (varied from -20% to 20%) and imprecision (0% to 20% CV). The measured glucose concentrations were used to alter insulin infusion rates according to established treatment protocols. Changes in true glucose were calculated hourly on the basis of the insulin infusion rate, the modeled patient's insulin sensitivity, and a model of glucose homeostasis. Wemodeled 18 000 patients, equally divided between the hourly and every-5-min measurement schemas and distributed among 45 combinations of bias and imprecision and 2 treatment protocols. RESULTS: With both treatment protocols and both measurement frequencies, higher measurement imprecision increased the rates of hypoglycemia and hyperglycemia and increased glycemic variability (SD). These adverse effects of measurement imprecision were lower at the higher measurement frequency. The rate of hypoglycemia at an imprecision (CV) of 5% with hourly measurements was similar to the rate of hypoglycemia at 10% CV when measurements were made every 5 min. With measurements every 5 min, imprecision up to 10% had minimal effects on hyperglycemia or glycemic variability. Effects of simulated analytical bias on glycemia were unaffected by measurement frequency. CONCLUSIONS: Quality specifications for imprecision of glucose meters are not transferable to CGM.
机译:背景:已经提出了用于严格葡萄糖控制(TGC)协议的血糖仪的总误差容限。尚不清楚这些建议的质量规格是否适合连续葡萄糖监测(CGM)。方法:我们对患者进行了TGC方案的蒙特卡罗模拟。为了模拟血糖仪的使用,每小时进行一次测量。为了模拟CGM,每5分钟进行一次葡萄糖测量。血糖的测量具有明确的偏倚(从-20%到20%不等)和不精确(0%到20%CV)。根据确定的治疗方案,将测得的葡萄糖浓度用于改变胰岛素输注速率。每小时根据胰岛素的输注速度,建模的患者的胰岛素敏感性和葡萄糖稳态模型计算真实葡萄糖的变化。我们对18000名患者进行了建模,将其平均划分为每小时和每5分钟一次的测量方案,并分布在45种偏倚和不精确组合以及2种治疗方案中。结果:在两种治疗方案和两种测量频率下,更高的测量不准确性会增加低血糖和高血糖的发生率,并增加血糖变异性(SD)。测量不精确度的这些不利影响在较高的测量频率下较低。每小时测量的不精确度(CV)为5%时的低血糖发生率类似于每5分钟进行一次测量时10%CV时的低血糖发生率。每隔5分钟进行一次测量,高达10%的不精确度对高血糖症或血糖变异性的影响最小。模拟分析偏倚对血糖的影响不受测量频率的影响。结论:血糖仪不精确的质量规格不能转移到CGM。

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