دورية أكاديمية

Real‐world effectiveness and safety of insulin glargine 100 U/mL plus lixisenatide in adults with type 2 diabetes: An international, multicentre, 12‐month, prospective observational study.

التفاصيل البيبلوغرافية
العنوان: Real‐world effectiveness and safety of insulin glargine 100 U/mL plus lixisenatide in adults with type 2 diabetes: An international, multicentre, 12‐month, prospective observational study.
المؤلفون: Malik, Rayaz A., Hwu, Chii‐Min, Jammah, Anwar A., Arteaga‐Díaz, Juan M., Djaballah, Khier, Pilorget, Valerie, Alvarez, Agustina, Vera, Carine, Vikulova, Olga
المصدر: Diabetes, Obesity & Metabolism; Jul2024, Vol. 26 Issue 7, p2811-2819, 9p
مصطلحات موضوعية: TYPE 2 diabetes, INSULIN, INSULIN aspart, GLUCAGON-like peptide-1 receptor, GLYCEMIC control, BLOOD sugar, GLUCAGON-like peptide-1 agonists
مستخلص: Aim: To assess the impact of insulin glargine (100 U/mL) and lixisenatide (iGlarLixi) fixed‐ratio combination therapy on the overall management of glycaemia in patients with type 2 diabetes (T2D), previously inadequately controlled with oral antidiabetic drugs ± basal insulin or glucagon‐like peptide‐1 receptor agonists (GLP‐1 RAs). Materials and Methods: This 12‐month, international, multicentre, prospective, observational study included patients (age ≥ 18 years) with T2D who had initiated iGlarLixi within 1 month prior to study inclusion. Data were collected at study inclusion, month 3, month 6 and month 12 from patient diaries, self‐measured plasma glucose, and questionnaires. The primary endpoint was change in HbA1c from baseline to month 6. Results: Of the 737 eligible participants (mean age: 57.8 [standard deviation: 11.2] years; male: 49%), 685 had baseline and post‐baseline HbA1c data available. The least squares mean change in HbA1c from baseline to month 6 was −1.4% (standard error [95% confidence interval (CI)]: 0.05 [−1.5, −1.3]). The absolute change from baseline at month 12 was −1.7% ± 1.9% (95% CI: −1.9, −1.5). There were 72 hypoglycaemia events reported during the study period, with a very low incidence of severe hypoglycaemia (two participants [rate: 0.003 events per patient‐year]). Conclusions: This real‐world observational study shows that initiation of iGlarLixi in people with T2D inadequately controlled on oral antidiabetic drugs ± basal insulin or GLP‐1 RAs improves glycaemic control with a low incidence of hypoglycaemia. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:14628902
DOI:10.1111/dom.15599