Abstract
Objective. To assess the potential of insulin lispro to limit the frequency of severe hypoglycaemia without compromising glycaemic control in a cohort of patients with type 1 diabetes who are at a high risk of severe hypoglycemia. Research design and methods. An open-label, randomised, 12-month comparative crossover study of insulin lispro and regular human insulin was performed in 33 patients with type 1 diabetes with impaired hypoglycaemia awareness. The efficacy of each treatment was evaluated by glycaemic control (HbA1c), eight-point home blood glucose profiles, and the frequency and severity of hypoglycaemic episodes and quality of life. Results. Eighteen (55%) patients experienced one or more episodes of severe hypoglycaemia in the 48 weeks of study. There was a trend to a lower incidence of severe hypoglycaemia during treatment with insulin lispro in comparison with regular human insulin (55 vs 84 episodes, p = 0.087). This resulted principally from a 47% lower incidence of nocturnal severe hypoglycaemia with insulin lispro (25 vs 47 episodes, p = 0.11). The lower frequency of severe hypoglycaemia associated with insulin lispro was not explained by differences in glycated haemoglobin between insulin treatments (HbA1c 9.1% insulin lispro vs 9.3% regular human insulin). Conclusions. In individuals with type 1 diabetes, who have impaired awareness of hypoglycaemia, treatment with insulin lispro may be associated with a lower incidence of severe hypoglycaemia manifested predominantly through less frequent nocturnal episodes. Insulin lispro may have a beneficial role in the management of patients with diabetes at risk of severe hypoglycaemia, although a larger study is required to confirm these findings. Copyright © 2001 John Wiley & Sons, Ltd.
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Ferguson, S. C., Strachan, M. W. J., Janes, J. M., & Frier, B. M. (2001). Severe hypoglycaemia in patients with type 1 diabetes and impaired awareness of hypoglycaemia: A comparative study of insulin lispro and regular human insulin. Diabetes/Metabolism Research and Reviews, 17(4), 285–291. https://doi.org/10.1002/dmrr.202
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