Zadel Alyssa H, Chiampas Katia, Maktaz Katrina, Keller John G, O'Gara Kathy W, Vargas Leonardo, Tzortzakis Angela, Eimer Micah J, Szmuilowicz Emily D
Division of Cardiology, Northwestern Medicine, Chicago, IL, United States.
Medical College of Wisconsin, Milwaukee, WI, United States.
JMIR Diabetes. 2025 Jun 18;10:e69061. doi: 10.2196/69061.
Continuous glucose monitoring (CGM) is used to assess glycemic trends and guide therapeutic changes for people with diabetes. We aimed to increase patient access to this tool by equipping primary care physicians (PCPs) to accurately interpret and integrate CGM into their practice via a multidisciplinary team approach.
The primary objective of this study was to evaluate the feasibility and effectiveness of integrating CGM into primary care clinics using a multidisciplinary approach that included a clinical pharmacist (PharmD) and a certified diabetes care and education specialist (CDCES).
Eighteen PCPs received a 1-hour video training module from an endocrinologist teaching a systematic stepwise approach to CGM interpretation. Patient inclusion criteria included type 2 diabetes mellitus, ≥18 years old, hemoglobin A1c (HbA1c) ≥8% or concern for hypoglycemia, and no previous CGM use or an endocrinology visit in the past year. Patients saw physician extenders (CDCES or a PharmD) for professional CGM placement and education on nutrition, medication administration, and physical activity goals based on the PCP's recommendations. The CDCES or PharmD reviewed CGM data with patients and collaborated with PCPs to adjust the care plan, informed by the systematic stepwise approach to CGM interpretation. Patients either converted to personal CGM if desired or had a second professional CGM device placed after ≥1 month from the initial professional CGM placement and obtained a postintervention HbA1c measurement at ≥3 months from the initial HbA1c measurement. The primary outcomes were time in range, HbA1c, and average time from referral to the first CGM device placement. Follow-up continued with the CDCES or PharmD until patients met the study discharge criteria of HbA1c level ≤7%. Paired t tests with 1-sided P values were used to assess changes in glucose metrics from the initial to postintervention measurements. The McNemar test was used to determine the significance of change in patients meeting the goal of ≥70% time in the target range of 70-180 mg/dL.
The CGM users (n=46) had a mean (SD) age of 62.39 (14.57) years, and 14/46 participants (30%) were female. The mean (SD) time in range increased by 28.06%, from 43.25% (33.41%) at baseline to 71.31% (25.49%) postintervention (P<.001), due to reduced hyperglycemia. The proportion of CGM users meeting the consensus target of the time in range ≥70% increased from 23.81% to 57.14% (P<.001). Postintervention HbA1c decreased by an average of 2.37%, from 9.68% (1.78%) to 7.31% (1.32%; P<.001).
The integration of CGM into primary care clinics to increase patient access is feasible and effective using a multidisciplinary approach.
连续血糖监测(CGM)用于评估糖尿病患者的血糖趋势并指导治疗调整。我们旨在通过使初级保健医生(PCP)具备准确解读CGM并通过多学科团队方法将其纳入临床实践的能力,来增加患者对该工具的使用机会。
本研究的主要目的是评估采用包括临床药剂师(药学博士)和认证糖尿病护理与教育专家(CDCES)的多学科方法,将CGM纳入初级保健诊所的可行性和有效性。
18名初级保健医生接受了内分泌专家提供的1小时视频培训模块,学习CGM解读的系统逐步方法。患者纳入标准包括2型糖尿病、年龄≥18岁、糖化血红蛋白(HbA1c)≥8%或有低血糖担忧,且过去一年未使用过CGM或未就诊于内分泌科。患者根据初级保健医生的建议,由医生助理(CDCES或药学博士)进行专业的CGM放置,并接受关于营养、药物管理和身体活动目标的教育。CDCES或药学博士与患者一起查看CGM数据,并根据CGM解读的系统逐步方法,与初级保健医生合作调整护理计划。患者如有需要可转换为个人CGM,或在首次专业CGM放置≥1个月后放置第二个专业CGM设备,并在首次HbA1c测量≥3个月后进行干预后HbA1c测量。主要结局指标为血糖达标时间、HbA1c以及从转诊到首次CGM设备放置的平均时间。由CDCES或药学博士继续随访,直至患者达到HbA1c水平≤7%的研究出院标准。采用单侧P值的配对t检验评估从初始测量到干预后测量血糖指标的变化。采用McNemar检验确定血糖在70 - 180 mg/dL目标范围内达标时间≥70%的患者变化的显著性。
CGM使用者(n = 46)的平均(标准差)年龄为62.39(14.57)岁,14/46名参与者(30%)为女性。由于高血糖减少,血糖达标时间平均增加了28.06%,从基线时的43.25%(33.41%)增至干预后的71.31%(25.49%)(P <.001)。达到血糖达标时间≥70%共识目标的CGM使用者比例从23.81%增至57.14%(P <.001)。干预后HbA1c平均下降2.37%,从9.68%(1.78%)降至7.31%(1.32%;P <.001)。
采用多学科方法将CGM纳入初级保健诊所以增加患者使用机会是可行且有效的。