Volume 24, Issue 7

A method for assessing quality of control from glucose profiles

N. R. Hill

Oxford Centre for Diabetes, Endocrinology and Metabolism, Churchill Hospital, Oxford and London Centre for Paediatric Endocrinology and Metabolism and Institute of Child Health, London, UK

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P. C. Hindmarsh

Oxford Centre for Diabetes, Endocrinology and Metabolism, Churchill Hospital, Oxford and London Centre for Paediatric Endocrinology and Metabolism and Institute of Child Health, London, UK

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R. J. Stevens

Oxford Centre for Diabetes, Endocrinology and Metabolism, Churchill Hospital, Oxford and London Centre for Paediatric Endocrinology and Metabolism and Institute of Child Health, London, UK

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I. M. Stratton

Oxford Centre for Diabetes, Endocrinology and Metabolism, Churchill Hospital, Oxford and London Centre for Paediatric Endocrinology and Metabolism and Institute of Child Health, London, UK

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J. C. Levy

Oxford Centre for Diabetes, Endocrinology and Metabolism, Churchill Hospital, Oxford and London Centre for Paediatric Endocrinology and Metabolism and Institute of Child Health, London, UK

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D. R. Matthews

Oxford Centre for Diabetes, Endocrinology and Metabolism, Churchill Hospital, Oxford and London Centre for Paediatric Endocrinology and Metabolism and Institute of Child Health, London, UK

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First published: 24 April 2007
Citations: 73
: Professor D. Matthews, Oxford Centre for Diabetes, Endocrinology and Metabolism, Churchill Hospital, Old Road, Headington, Oxford OX3 7LJ, UK. E‐mail: david.matthews@ocdem.ox.ac.uk

Abstract

Aim  As the practice of multiple assessments of glucose concentration throughout the day increases for people with diabetes, there is a need for an assessment of glycaemic control weighted for the clinical risks of both hypoglycaemia and hyperglycaemia.

Methods  We have developed a methodology to report the degree of risk which a glycaemic profile represents. Fifty diabetes professionals assigned risk values to a range of 40 blood glucose concentrations. Their responses were summarised and a generic function of glycaemic risk was derived. This function was applied to patient glucose profiles to generate an integrated risk score termed the Glycaemic Risk Assessment Diabetes Equation (GRADE). The GRADE score was then reported by use of the mean value and the relative percent contribution to the weighted risk score from the hypoglycaemic, euglycaemic, hyperglycaemic range, respectively, e.g. GRADE (hypoglycaemia%, euglycaemia%, hyperglycaemia%).

Results  The GRADE scores of indicative glucose profiles were as follows: continuous glucose monitoring profile non‐diabetic subjects GRADE = 1.1, Type 1 diabetes continuous glucose monitoring GRADE = 8.09 (20%, 8%, 72%), Type 2 diabetes home blood glucose monitoring GRADE = 9.97 (2%, 7%, 91%).

Conclusions  The GRADE score of a glucose profile summarises the degree of risk associated with a glucose profile. Values < 5 correspond to euglycaemia. The GRADE score is simple to generate from any blood glucose profile and can be used as an adjunct to HbA1c to report the degree of risk associated with glycaemic variability.

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