The effectiveness of telemonitoring and integrated personalized diabetes management in people with insulin-treated type 2 diabetes mellitus.

IF 5.4 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Thanyalak Saetang, Primploy Greeviroj, Subhanudh Thavaraputta, Prangareeya Santisitthanon, Natnicha Houngngam, Nitchakarn Laichuthai
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引用次数: 0

Abstract

Objective: To evaluate the effectiveness of integrated personalized diabetes management (iPDM) through telemedicine (tele-iPDM) with regard to glycaemic control.

Methods: A 6-month single-centre, open-label, prospective randomized controlled trial enrolled insulin-treated patients with type 2 diabetes, aged 18-65 years with glycated haemoglobin (HbA1c) levels of 7.5%-10.5%. The tele-iPDM group received insulin adjustment by investigators through a cloud-based telemonitoring platform for 6 months (blood glucose monitoring reviewed weekly from Weeks 0 to 12 and then monthly from Weeks 13 to 24). The control group performed self-monitoring and insulin adjustment. The primary outcome was the difference in HbA1c change from baseline between the two groups at 24 weeks. Secondary outcomes included changes in HbA1c at 12 weeks, fasting plasma glucose, body weight, body mass index (BMI), the percentage of individuals achieving HbA1c <7% at 24 weeks, the percentage of individuals with an HbA1c reduction of >0.5% at 24 weeks, and incidences of hypoglycaemic events.

Results: A total of 151 participants were enrolled, with a mean age of 53.36 ± 8.08 years and a mean diabetes duration of 12.38 ± 8.47 years. The baseline HbA1c was 8.47 ± 0.76%. The mean HbA1c decreased from baseline to 12 and 24 weeks in both groups. At 12 weeks, HbA1c reduction from baseline was -1.2% (95%CI -1.42 to -0.98) in the tele-iPDM group and -0.57% (95%CI -0.79 to -0.36) in the control group. The mean difference in HbA1c between the tele-iPDM and usual care groups at 12 weeks was -0.63% (95%CI -0.94 to -0.32; p < 0.001). At 24 weeks, HbA1c reduction from baseline was -1.14% (95%CI -1.38 to -0.89) in the tele-iPDM group and - 0.49% (95%CI -0.73 to -0.25) in the control group. The mean difference in HbA1c between the tele-iPDM and usual care groups was -0.65% (95%CI -0.99 to -0.30; p < 0.001). There were no significant differences in body weight, BMI, or hypoglycaemic events between the two groups.

Conclusion: Telemonitoring can support the iPDM care model in individuals with insulin-treated type 2 diabetes. It improves the efficiency of diabetes care, enhances glycaemic control at 12 weeks, and sustains glycaemic control at 24 weeks.

对接受胰岛素治疗的 2 型糖尿病患者进行远程监测和综合个性化糖尿病管理的有效性。
目的:评估通过远程医疗进行综合个性化糖尿病管理(iPDM)对血糖控制的效果:评估通过远程医疗(tele-iPDM)进行综合个性化糖尿病管理(iPDM)对血糖控制的效果:一项为期 6 个月的单中心、开放标签、前瞻性随机对照试验招募了接受胰岛素治疗的 2 型糖尿病患者,他们的年龄在 18-65 岁之间,糖化血红蛋白(HbA1c)水平在 7.5%-10.5% 之间。远程 iPDM 组接受研究人员通过基于云的远程监测平台进行的胰岛素调整,为期 6 个月(第 0 周至第 12 周每周复查一次血糖监测,第 13 周至第 24 周每月复查一次血糖监测)。对照组进行自我监测和胰岛素调整。主要结果是两组在 24 周时 HbA1c 与基线相比的变化差异。次要结果包括 12 周时 HbA1c 的变化、空腹血浆葡萄糖、体重、体重指数 (BMI)、24 周时 HbA1c 达到 0.5% 的人数百分比以及低血糖事件的发生率:共有 151 人参加,平均年龄为(53.36±8.08)岁,平均糖尿病病程为(12.38±8.47)年。基线 HbA1c 为 8.47 ± 0.76%。从基线到 12 周和 24 周,两组患者的平均 HbA1c 均有所下降。12 周时,远程 iPDM 组的 HbA1c 从基线下降了 -1.2% (95%CI -1.42 至 -0.98),对照组的 HbA1c 从基线下降了 -0.57%(95%CI -0.79 至 -0.36)。12 周时,远程 iPDM 组与常规护理组之间 HbA1c 的平均差异为 -0.63%(95%CI -0.94 至 -0.32;P 结论:远程监控可为 iPD 治疗提供支持:远程监测可为胰岛素治疗的 2 型糖尿病患者的 iPDM 护理模式提供支持。它提高了糖尿病护理的效率,加强了 12 周的血糖控制,并维持了 24 周的血糖控制。
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来源期刊
Diabetes, Obesity & Metabolism
Diabetes, Obesity & Metabolism 医学-内分泌学与代谢
CiteScore
10.90
自引率
6.90%
发文量
319
审稿时长
3-8 weeks
期刊介绍: Diabetes, Obesity and Metabolism is primarily a journal of clinical and experimental pharmacology and therapeutics covering the interrelated areas of diabetes, obesity and metabolism. The journal prioritises high-quality original research that reports on the effects of new or existing therapies, including dietary, exercise and lifestyle (non-pharmacological) interventions, in any aspect of metabolic and endocrine disease, either in humans or animal and cellular systems. ‘Metabolism’ may relate to lipids, bone and drug metabolism, or broader aspects of endocrine dysfunction. Preclinical pharmacology, pharmacokinetic studies, meta-analyses and those addressing drug safety and tolerability are also highly suitable for publication in this journal. Original research may be published as a main paper or as a research letter.
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