Bastyr Edward J, Zhang Shuyu, Mou Jiani, Hackett Andy P, Raymond Stephen A, Chang Annette M
1 Eli Lilly and Company , Indianapolis, Indiana.
2 Indiana University School of Medicine , Indianapolis, Indiana.
Diabetes Technol Ther. 2015 Aug;17(8):571-9. doi: 10.1089/dia.2014.0407. Epub 2015 Mar 31.
This report describes the performance of a wireless electronic diary (e-diary) system for data collection and enhanced patient-investigator interactions during intensive insulin management in diabetes clinical trials.
We implemented a customized electronic communication system featuring an e-diary and a Web portal in three global, randomized, controlled Phase 3 clinical trials testing basal insulin peglispro compared with insulin glargine, both combined with prandial insulin lispro, in patients with type 1 or type 2 diabetes mellitus (T1DM and T2DM, respectively). We collected data during 28 weeks of study e-diary use for the report.
Patients (n=2,938) in 31 countries used e-diaries to transmit 2,439,087 blood glucose (BG) values, 96% of which were associated by the patient with a protocol time point during the 72-h response window. Of 208,192 hypoglycemia events captured, 96% had a BG value, and 95% had treatments and outcomes entered by patients within the 72-h window. Patients recorded administration of 1,964,477 insulin doses; 93% of basal insulin doses were adherent with the investigator prescription. Investigators adjusted 13 basal and 92 bolus insulin prescriptions per patient-year using the e-diary system. After 26 weeks of treatment and e-diary use in the combined study arms, hemoglobin A1c values decreased by 0.6% or 1.6% and fasting BG decreased by 7.8 or 28 mg/dL in patients with T1DM or T2DM, respectively.
The e-diary system enabled comprehensive data collection and facilitated communication between investigators and patients for intensive insulin management in three global clinical trials testing basal insulins.
本报告描述了一种无线电子日记(e - 日记)系统在糖尿病临床试验强化胰岛素管理期间用于数据收集及增强患者与研究者互动方面的表现。
我们在三项全球范围内的随机、对照3期临床试验中实施了一个定制的电子通信系统,该系统具有一个电子日记和一个网络门户,试验比较了聚乙二醇化赖脯胰岛素与甘精胰岛素作为基础胰岛素,二者均与餐时胰岛素赖脯胰岛素联合使用,受试对象为1型或2型糖尿病(分别为T1DM和T2DM)患者。我们在为期28周的研究电子日记使用期间收集数据以撰写本报告。
来自31个国家的2938名患者使用电子日记传输了2439087个血糖(BG)值,其中96%的血糖值由患者在72小时反应窗口内与方案规定的时间点相关联。在记录的208192次低血糖事件中,96%有血糖值,95%的患者在72小时窗口内录入了治疗及结果。患者记录了1964477次胰岛素注射剂量;93%的基础胰岛素剂量符合研究者的处方。研究者使用电子日记系统,每位患者每年调整13次基础胰岛素处方和92次餐时胰岛素处方。在联合研究组进行26周的治疗及使用电子日记后,T1DM或T2DM患者的糖化血红蛋白值分别降低了0.6%或1.6%,空腹血糖分别降低了7.8或28mg/dL。
在三项测试基础胰岛素的全球临床试验中,电子日记系统实现了全面的数据收集,并促进了研究者与患者之间关于强化胰岛素管理的沟通。