实施连续血糖监测以更好地控制血糖而无需长效胰岛素的案例系列

A. Manov, J. Tam, A. Donepudi, S. S. S. Mayesha, Y. Badi, Prof. Andre Manov
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引用次数: 0

摘要

在我们的病例系列中,我们描述了 6 位病情未得到控制的复杂 2 型糖尿病(2-DM)患者。虽然他们每天至少进行 4 次自我血糖监测(SMBG),但血糖控制仍然不理想。我们的内科住院医师初级保健诊所开始对他们进行连续血糖监测(CGM)。患者接受了饮食、生活方式改变以及如何根据 CGM 的血糖结果调整胰岛素方案等方面的教育,以此作为护理标准。我们的 CGM 团队代表每两周会给他们打电话,监测并回答有关胰岛素调整、血糖监测、饮食、体育锻炼或生活方式的任何问题。CGM 团队成员包括内科和过渡年级的医学住院医师,以及本诊所的一名内分泌科认证医师。此外,CGM 小组的一名成员每月都会到诊所为患者看诊一次。起初,为了达到最佳血糖控制效果,患者开始使用长效和速效胰岛素。最终,胰岛素用量逐渐减少,我们所描述的患者开始使用替代药物,如口服抗糖尿病药物,同时使用或不使用注射用胰高血糖素样肽 GLP-1 受体激动剂。停用胰岛素后,我们对所有患者的餐后五小时 C 肽进行了检测,结果均正常。在开始使用 CGM 的几个月内,患者的血糖控制有了显著改善,而且在停用胰岛素后仍能保持。一些患者还减轻了体重。我们的结论是,在一个主要由内科和过渡年住院医师管理的项目中,不仅在内分泌专科门诊,而且在有内分泌医师资格认证的诊所成员的监督下,都可以在内科住院医师诊所安全启动 CGM。我们还证明,在 2 型糖尿病患者中引入 CGM 而不是 SMBG,有助于他们在使用胰岛素时更好地控制血糖,克服葡萄糖毒性,并最终停用胰岛素,仅使用口服抗糖尿病药物和注射或不注射 GLP 1 受体激动剂来维持出色的血糖控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Case Series on Implementation of Continuous Glucose Monitoring for Better Glycemic Control without Long-acting Insulin
In our case series, we are describing 6 patients with uncontrolled, complicated type 2 Diabetes Mellitus (Type 2-DM). Although they were self-monitoring their blood glucose (SMBG) at least 4 times a day, they continued to have suboptimal glucose control. Continuous glucose monitoring (CGM) was started at our Internal medicine residency primary care clinic. The patients were educated on diet, lifestyle changes, and how to adjust their insulin regimen according to their blood glucose results from the CGM as the standard of care. They were called every two weeks by the representative of our CGM team to monitor and answer any queries regarding insulin adjustment, blood glucose monitoring, diet, physical activity, or lifestyle. The CGM team included Internal medicine and transitional year medical residents and a board-certified endocrinologist who was a member of our clinic. Moreover, the patients were seen at the clinic once every month by a member of the CGM team. Long and rapid-acting Insulins were started to achieve optimal glucose control initially. Eventually, Insulin dosage was gradually reduced, and the patients we described were started on alternate agents like oral antidiabetic agents with or without injectable glucagon-like peptide GLP-1 receptor agonists. The five-hour postprandial C-peptide was checked after discontinuation of insulin in all of our patients and was normal. Within a few months of CGM initiation, there was a significant improvement in the patients’ glucose control which was maintained after stopping the Insulin. Some patients were also able to lose weight. We concluded that CGM could be initiated safely in an internal medicine residency clinic not only at specialized endocrine clinics in a project that was managed primarily by internal medicine and transitional year residents under the supervision of a member of the clinic who was board certified in endocrinologists. We also demonstrated the introduction of CGM instead of SMBG in patients with Type 2-DM helped them to achieve better glycemic control with insulin, overcome glucose toxicity, and eventually stop the insulin and maintain excellent glucose control only with oral antidiabetic agents with or without injectable GLP 1 receptor agonist.
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