Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, ON, Canada; Division of Endocrinology and Metabolism, Department of Medicine, University of Toronto, Toronto, ON, Canada.
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, ON, Canada.
Lancet Diabetes Endocrinol. 2017 Jul;5(7):501-512. doi: 10.1016/S2213-8587(17)30167-5. Epub 2017 May 19.
Closed-loop artificial pancreas systems have been in development for several years, including assessment in numerous varied outpatient clinical trials. We aimed to summarise the efficacy and safety of artificial pancreas systems in outpatient settings and explore the clinical and technical factors that can affect their performance.
We did a systematic review and meta-analysis of randomised controlled trials comparing artificial pancreas systems (insulin only or insulin plus glucagon) with conventional pump therapy (continuous subcutaneous insulin infusion [CSII] with blinded continuous glucose monitoring [CGM] or unblinded sensor-augmented pump [SAP] therapy) in adults and children with type 1 diabetes. We searched Medline, Embase, and the Cochrane Central Register of Controlled Trials for studies published from 1946, to Jan 1, 2017. We excluded studies not published in English, those involving pregnant women or participants who were in hospital, and those testing adjunct medications other than glucagon. The primary outcome was the mean difference in percentage of time blood glucose concentration remained in target range (3·9-10 mmol/L or 3·9-8 mmol/L, depending on the study), assessed by random-effects meta-analysis. This study is registered with PROSPERO, number 2015:CRD42015026854.
We identified 984 reports; after exclusions, 27 comparisons from 24 studies (23 crossover and one parallel design) including a total of 585 participants (219 in adult studies, 265 in paediatric studies, and 101 in combined studies) were eligible for analysis. Five comparisons assessed dual-hormone (insulin and glucagon), two comparisons assessed both dual-hormone and single-hormone (insulin only), and 20 comparisons assessed single-hormone artificial pancreas systems. Time in target was 12·59% higher with artificial pancreas systems (95% CI 9·02-16·16; p<0·0001), from a weighted mean of 58·21% for conventional pump therapy (I=84%). Dual-hormone artificial pancreas systems were associated with a greater improvement in time in target range compared with single-hormone systems (19·52% [95% CI 15·12-23·91] vs 11·06% [6·94 to 15·18]; p=0·006), although six of seven comparisons compared dual-hormone systems to CSII with blinded CGM, whereas 21 of 22 single-hormone comparisons had SAP as the comparator. Single-hormone studies had higher heterogeneity than dual-hormone studies (I 79% vs 66%). Bias assessment characteristics were incompletely reported in 12 of 24 studies, no studies masked participants to the intervention assignment, and masking of outcome assessment was not done in 12 studies and was unclear in 12 studies.
Artificial pancreas systems uniformly improved glucose control in outpatient settings, despite heterogeneous clinical and technical factors.
None.
闭环人工胰腺系统已经开发了好几年,包括在众多不同的门诊临床试验中进行评估。我们旨在总结人工胰腺系统在门诊环境中的疗效和安全性,并探讨可能影响其性能的临床和技术因素。
我们对比较人工胰腺系统(仅胰岛素或胰岛素加胰高血糖素)与传统泵治疗(带盲法连续血糖监测[CGM]或无盲法传感器增强泵[SAP]治疗的连续皮下胰岛素输注[CSII])的随机对照试验进行了系统评价和荟萃分析,纳入了成年和儿童 1 型糖尿病患者。我们检索了 Medline、Embase 和 Cochrane 对照试验中心注册库,检索时间为 1946 年至 2017 年 1 月 1 日。我们排除了未以英文发表的研究、涉及孕妇或住院患者的研究,以及测试除胰高血糖素以外的辅助药物的研究。主要结局是通过随机效应荟萃分析评估的血糖浓度在目标范围内的时间百分比的平均值差异(3.9-10mmol/L 或 3.9-8mmol/L,取决于研究)。这项研究在 PROSPERO 注册,编号为 2015:CRD42015026854。
我们确定了 984 份报告;排除后,24 项研究中的 27 项比较(23 项交叉设计和 1 项平行设计)共纳入 585 名参与者(219 名成年研究参与者,265 名儿科研究参与者,101 名混合研究参与者)符合分析条件。5 项比较评估了双激素(胰岛素和胰高血糖素),2 项比较评估了双激素和单激素(仅胰岛素),20 项比较评估了单激素人工胰腺系统。人工胰腺系统的目标时间提高了 12.59%(95%CI 9.02-16.16;p<0.0001),常规泵治疗的加权平均值为 58.21%(I=84%)。与单激素系统相比,双激素人工胰腺系统与目标范围内时间的更大改善相关(19.52%[95%CI 15.12-23.91]vs11.06%[6.94 至 15.18];p=0.006),尽管七项比较中的六项将双激素系统与带盲法 CGM 的 CSII 进行了比较,而 22 项单激素比较中有 21 项将 SAP 作为比较器。单激素研究的异质性高于双激素研究(I 79% vs 66%)。24 项研究中有 12 项未完整报告偏倚评估特征,没有研究对干预分配进行参与者设盲,12 项研究未进行结局评估设盲,12 项研究的设盲情况不清楚。
尽管存在临床和技术因素的异质性,但人工胰腺系统在门诊环境中普遍改善了血糖控制。
无。