Olivier Patricia, Lawson Margaret L, Huot Celine, Richardson Christine, Nakhla Meranda, Romain Judette
Endocrinology Service, Department of Pediatrics, CHU Sainte-Justine, University of Montreal, Montreal, Quebec, Canada.
Division of Endocrinology & Metabolism, Department of Pediatrics, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, Canada
J Diabetes Sci Technol. 2014 May;8(3):523-8. doi: 10.1177/1932296814524855. Epub 2014 Feb 27.
Uncertainty remains about effectiveness of continuous glucose monitoring (CGM) in pediatric type 1 diabetes (T1D). Success with CGM is related to CGM adherence, which may relate to readiness to make the behavior changes required for effective use. We hypothesize that readiness for change will be greater at initiation of insulin pump therapy than in established pump users, and that this will predict CGM adherence. Our objective was to evaluate the feasibility of a randomized controlled trial (RCT) in children with established T1D comparing simultaneous pump and CGM initiation to standard pump therapy with delayed CGM initiation. We randomized participants to simultaneous pump and CGM initiation or to standard pump therapy with the option of adding CGM 4 months later. CGM adherence was tracked via web-based download and readiness for change assessed with the SOCRATES questionnaire. Of 41 eligible children, 20 agreed to participate; 15 subjects completed the study (7 males; baseline age 11.8 ± 4.0 years; T1D duration 2.7 ± 2.7 years; mean A1C 8.2 ± 0.8%). Six of 8 simultaneous group subjects used CGM > 60% of the time for 4 months compared to 1 of 7 delayed group subjects (P = .02). Using SOCRATES, we could assign 87-100% of subjects to a single motivation stage at baseline and 4 months. This pilot study demonstrates the feasibility of randomizing pump naïve children and adolescents with established T1D to simultaneous pump and CGM initiation versus standard pump therapy with delayed CGM initiation. Lessons from this pilot study were used to inform development of a full-scale multicenter RCT.
持续葡萄糖监测(CGM)在儿童1型糖尿病(T1D)中的有效性仍不确定。CGM的成功与CGM依从性有关,而这可能与做好准备做出有效使用所需的行为改变有关。我们假设,与已使用胰岛素泵的患者相比,在开始胰岛素泵治疗时改变的准备程度更高,并且这将预测CGM依从性。我们的目标是评估一项随机对照试验(RCT)在已确诊T1D儿童中的可行性,该试验比较同时启动泵和CGM与延迟启动CGM的标准泵治疗。我们将参与者随机分为同时启动泵和CGM组或标准泵治疗组,后者可在4个月后选择添加CGM。通过基于网络的下载来跟踪CGM依从性,并使用SOCRATES问卷评估改变的准备程度。在41名符合条件的儿童中,20名同意参与;15名受试者完成了研究(7名男性;基线年龄11.8±4.0岁;T1D病程2.7±2.7年;平均糖化血红蛋白8.2±0.8%)。8名同时启动组受试者中有6名在4个月内使用CGM的时间超过60%,而延迟启动组的7名受试者中只有1名(P = 0.02)。使用SOCRATES,我们可以在基线和4个月时将87%-100%的受试者分配到单一的动机阶段。这项初步研究证明了将初治泵的已确诊T1D儿童和青少年随机分为同时启动泵和CGM组与延迟启动CGM的标准泵治疗组的可行性。这项初步研究的经验教训被用于为一项全面的多中心RCT的开展提供信息。