首页> 外文期刊>Diabetic medicine: A journal of the British Diabetic Association >Clinical benefits of switching to insulin degludec irrespective of previous basal insulin therapy in people with Type 1 or Type 2 diabetes: evidence from a European, multicentre, retrospective, non‐interventional study ( EU EU ‐ TREAT TREAT )
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Clinical benefits of switching to insulin degludec irrespective of previous basal insulin therapy in people with Type 1 or Type 2 diabetes: evidence from a European, multicentre, retrospective, non‐interventional study ( EU EU ‐ TREAT TREAT )

机译:切换到胰岛素Degludec的临床益处,无论患有1型或2型糖尿病的基础胰岛素治疗:来自欧洲,多期,回顾性,非介入研究的证据(欧盟欧盟治疗零食)

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Abstract Aims To investigate whether the benefits of switching to insulin degludec observed in the European retrospective chart review study EU ‐ TREAT were dependent on the previous basal insulin used. Methods People with Type 1 or Type 2 diabetes were switched to insulin degludec from other basal insulins ≥6 months before data collection. Participants were stratified into three groups based on their previous basal insulin: insulin glargine 100 units/ml (Type 1: n =888; Type 2: n =259); insulin detemir (Type 1: n =726; Type 2: n =415); and neutral protamine Hagedorn (Type 1: n =53; Type 2: n =95). Their glycaemic control and hypoglycaemia incidence at 6 and 12 months post‐switch vs pre‐switch was then evaluated. Results Significant HbA 1c reductions were achieved in all previous basal insulin groups for participants with Type 1 diabetes [insulin glargine 100 units/ml: ?2.08 mmol/mol (?0.19%); insulin detemir: ?2.40 mmol/mol (?0.22%)] and those with Type 2 diabetes [insulin glargine 100 units/ml: ?5.90 mmol/mol (–0.54%); insulin detemir: ?6.01 mmol/mol (?0.55%); neutral protamine Hagedorn: ?2.73 mmol/mol (?0.25%)] at 6 months, except for the relatively small neutral protamine Hagedorn group in those with Type 1 diabetes [?1.75 mmol/mol (?0.16%)], where statistical significance was not reached. At 6 months in the Type 1 diabetes group, switching to insulin degludec from insulin glargine 100 units/ml resulted in significantly lower hypoglycaemia rates across all hypoglycaemia categories; for the insulin detemir group, this significance was also observed for severe and nocturnal non‐severe hypoglycaemia, while the low number of people in the neutral protamine Hagedorn group resulted in nonsignificant reductions in hypoglycaemia rates. At 6 months in the people with Type 2 diabetes, switching to insulin degludec resulted in significantly lower rates of hypoglycaemia across all categories for all groups. Similar outcomes were observed at 12 months. Conclusions Switching to insulin degludec from other basal insulins can improve glycaemic control and/or reduce hypoglycaemia risk in people with diabetes (although there was a nonsignificant reduction in HbA 1c and hypoglycaemia rates for the neutral protamine Hagedorn group in Type 1 diabetes) under routine care.
机译:摘要旨在调查欧洲回顾性图表研究欧盟治疗中观察到胰岛素Degludec的益处是否依赖于之前使用的基础胰岛素。方法将1型或2型糖尿病的人从其他基础胰岛素≥6个月后切换到胰岛素Degludec,在数据收集之前≥6个月。将参与者分为三组,基于其先前的基础胰岛素:胰岛素龟头100单位/ mL(型1:n = 888; 2型:n = 259);胰岛素DECIMIR(类型1:n = 726; 2型:n = 415);和中性protamine hagedorn(型1:n = 53;型2:n = 95)。然后评价它们在开关后6和12个月的血糖控制和低血糖发病率。结果患有1型糖尿病患者的所有先前基底胰岛素基团中达到了显着的HBA 1C减少[胰岛素龟头100单位/ mL:β2.08mmol/ mol(α0.19%);胰岛素DECIMIR:?2.40mmol / mol(?0.22%)]和2型糖尿病患者[胰岛素冰壶100个单位/ ml:α.5.90mmol/ mol(-0.54%);胰岛素Detemir:?6.01 mmol / mol(?0.55%);中性protamine hagedorn:α.2.73mmol/ mol(Δ0.25%)]在6个月外,除了糖尿病型相对较小的中性protamine hagneorn组除外[α1.75mmol/ mol(Δ0.16%)],其中统计学意义没有达到。在1型糖尿病组的6个月内,从胰岛素Glargine 100单位/ ml切换到胰岛素Degludec,导致所有低血糖类别的低血糖率显着降低;对于胰岛素DETEMIR组,对于严重和夜间非严重低血糖症也观察到这种显着性,而中性Protamine Honageorn组的少数人导致低血糖率的减少。在2型糖尿病的人中6个月,切换到胰岛素Degludec,导致所有群体所有类别的低血糖率明显降低。在12个月内观察到类似的结果。结论从其他基础胰岛素切换到胰岛素Degludec可以改善糖尿病患者的血糖控制和/或降低低血糖风险(尽管在常规护理下,HBA 1C和中性Protamine Honageorn组的HBA 1C和低血糖率降低) 。

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