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首页> 外文期刊>Diabetes therapy >Comparison of Efficacy and Economic Value of Prandilin 25 and Humalog Mix 25 in Patients with Newly Diagnosed Type 2 Diabetes by a Continuous Glucose Monitoring System
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Comparison of Efficacy and Economic Value of Prandilin 25 and Humalog Mix 25 in Patients with Newly Diagnosed Type 2 Diabetes by a Continuous Glucose Monitoring System

机译:连续葡萄糖监测系统比较普兰地林25和Humalog Mix 25在新诊断2型糖尿病患者中的疗效和经济价值

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IntroductionTo determine the clinical efficacy and economic value of insulin lispro 25-Prandilin 25 vs. insulin lispro 25-Humalog mix 25 in treatment of newly diagnosed type 2 diabetes mellitus (T2DM) by a continuous glucose monitoring system (CGMS). MethodsThis was a single-center, randomized, case-crossover clinical trial. Participants were randomly allocated to two groups and underwent two kinds of insulin lispro 25 treatment separated by a 1-day washout period. In total, 81 patients with newly diagnosed T2DM with hemoglobin A1c (HbA1c) above 9% were hospitalized and randomly divided to receive Prandilin 25/Humalog mix 25 or Humalog mix 25/Prandilin 25 treatment. All participants were subjected to metformin therapy simultaneously. Glycemic control was reached after 7–8?days Prandilin 25 or Humalog mix 25 treatment; each patient received continuous glucose monitoring (CGM) for 5 consecutive days (from day 1 to day 5). On day 3 of CGM performance, Prandilin 25 treatment was switched to Humalog mix 25 treatment at the same dosage or vice versa. Parameters representing glycemic variability (GV) and postprandial glucose excursions, including 24-h mean blood glucose (24hMBG), 24-h standard deviation of blood glucose (24hSDBG), 24-h mean amplitude of glycemic excursion (24hMAGE), large amplitude of glycemic excursion (LAGE), incremental area under the curve (AUC) for different glucose levels, and postmeal relative areas under the CGM curve (AUCpp) for 1–4?h of each meal, were calculated for each patient. ResultsNo significant differences were found in the 24hMAGE, 24hMBG, 24hSDBG, LAGE, mean 1-h preprandial blood glucose and the incidence of hypoglycemia between the Prandilin 25 treatment group and Humalog mix 25 treatment group. Similarly, there were no between-treatment differences for AUC and time when blood glucose was below 3.9?mmol/l, between 3.9?mmol/l and 10.0?mmol/l, or above 10.0?mmol/l. Further analysis showed the AUCpp for 1–4?h of each meal for two kinds of treatments were similar. However, the mean estimated cost of Prandilin 25 was only 85% of Humalog mix 25 in one treatment course. ConclusionPrandilin 25 is non-inferior in clinical efficacy compared with Humalog mix 25. In view of the significant difference in the cost of the two kinds of insulin lispro 25, Prandilin 25 is a much more cost-effective anti-diabetes drug for management of T2DM. Trial RegistrationChinese Clinical Trial Register identifier, ChiCTR1800015829.
机译:简介要通过连续葡萄糖监测系统(CGMS)确定赖脯胰岛素25-普兰地林25与赖脯胰岛素25-Humalog混合物25在新诊断的2型糖尿病(T2DM)中的临床疗效和经济价值。方法这是一项单中心,随机,病例交叉的临床试验。将参与者随机分为两组,并接受两种lispro 25胰岛素治疗,间隔1天的清除期。总共有81例新诊断为T2DM且血红蛋白A1c(HbA1c)高于9%的患者入院并随机分为两组,接受普兰地林25 / Humalog混合25或Humalog混合25 / Prandilin 25的治疗。所有参与者同时接受二甲双胍治疗。普兰地林25或Humalog mix 25治疗7-8天后达到了血糖控制。每位患者连续5天(从第1天到第5天)接受连续葡萄糖监测(CGM)。在CGM表现的第3天,将Prandilin 25处理改为相同剂量的Humalog mix 25处理,反之亦然。代表血糖变异性(GV)和餐后血糖波动的参数,包括24小时平均血糖(24hMBG),24小时血糖标准差(24hSDBG),24小时平均血糖波动幅度(24hMAGE),计算每位患者每餐1-4 h的血糖波动(LAGE),曲线下的增量面积(AUC)和CGM曲线下的餐后相对面积(AUCpp)(h)。结果Prandilin 25治疗组和Humalog mix 25治疗组之间在24hMAGE,24hMBG,24hSDBG,LAGE,平均1小时餐前血糖和低血糖发生率方面无显着差异。同样,当血糖低于3.9?mmol / l,3.9?mmol / l至10.0?mmol / l或高于10.0?mmol / l时,AUC和治疗时间之间也没有差异。进一步的分析表明,两种治疗方法每餐1-4小时的AUCpp相似。但是,在一个疗程中,普兰地林25的平均估计成本仅为Humalog mix 25的85%。结论普兰地林25与Humalog mix 25相比在临床疗效上不逊色。鉴于两种赖脯胰岛素25的成本存在显着差异,普兰地林25是治疗T2DM的更具成本效益的抗糖尿病药物。试验注册中国临床试验注册标识,ChiCTR1800015829。

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