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Specific validation analysis of stochastic ICING model based estimation of insulin sensitivity profile using clinical data

机译:基于临床数据的基于随机ICING模型的胰岛素敏感性分布评估的特定验证分析

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In this paper the performance of an insulin sensitivity profile estimation method is analysed from the the aspects of clinical applicability. In our previous studies it has been demonstrated that the grey box variant of the ICING (Intensive Control Insulin-Nutrition-Glucose) model may be successfully applied to improve the estimation accuracy of the insulin sensitivity profile of intensive care patients. This may enable the application of the model in the clinical treatment, especially in tight glycaemic control. The sensitivity estimation accuracy itself and the accuracy improvement compared to previous methods are highly variable, it strongly depends on the range of blood glucose concentration. In the present study the insulin sensitivity estimation is analysed from the clinically relevant aspects. Modelling error represented by the difference of measured and computed the blood glucose concentration was considered on the total glucose concentration range (measured in mmol/l) - 0 <; cG <; 20 - of the cohort data set as well as on its four subregions, namely hypoglycaemic (0 <; cG ≤ 4), normoglycaemic (4 <; cG ≤ 6.5), mild-hyperglycaemic (6.5 <; cG ≤ 10), and severe-hyperglycaemic (10 <; cG ≤ 20). The results of the computations indicate that the SDE model was significantly better in the normoglycaemic and mild-hyperglycaemic ranges, somewhat better in the hypoglycaemic range and nearly the same in the severe-hyperglycaemic range. The 97 % of all of the concentration values were in the normoglycaemic and the mild-hyperglycaemic range (5841 values), which amplifies our statement in these ranges, but further study is necessary the ensure the verdict for the hypoglycaemic and severe-hyperglycaemic ranges.
机译:本文从临床适用性的角度分析了胰岛素敏感性分布评估方法的性能。在我们以前的研究中,已经证明了ICING(重症控制胰岛素,营养,葡萄糖)模型的灰盒变体可以成功地用于提高重症监护患者胰岛素敏感性分布的估计准确性。这可以使该模型能够在临床治疗中应用,尤其是在严格的血糖控制中。与以前的方法相比,灵敏度估计的准确性本身和准确性的提高是高度可变的,这在很大程度上取决于血糖浓度的范围。在本研究中,从临床相关方面分析了胰岛素敏感性估计。在总葡萄糖浓度范围(以mmol / l为单位)上考虑以测量和计算的血糖浓度之差表示的建模误差-0 <; cG <;队列数据集的20-及其四个子区域,即降血糖(0 <; cG≤4),降血糖(4 <; cG≤6.5),轻度高血糖(6.5 <; cG≤10)和严重-高血糖(10 <; cG≤20)。计算结果表明,SDE模型在常血糖和轻度高血糖范围内明显更好,在低血糖范围内稍好,在重度高血糖范围内几乎相同。所有浓度值中的97%处于正常血糖范围和轻度高血糖范围(5841值),这扩大了我们在这些范围内的陈述,但需要进一步研究以确保确定低血糖和严重高血糖范围。

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