National Institute of Medical Sciences and Nutrition Salvador Zubirán, Mexico City, Mexico.
LMC Diabetes & Endocrinology, Concord, Canada.
Ann Med. 2021 Dec;53(1):998-1009. doi: 10.1080/07853890.2021.1925148.
Many patients with type 2 diabetes will ultimately require the inclusion of basal insulin in their treatment regimen. Since most people with type 2 diabetes are managed in the community, it is important that primary care providers understand and correctly manage the initiation and titration of basal insulins, and help patients to self-manage insulin injections. Newer, long-acting basal insulins provide greater stability and flexibility than older preparations and improved delivery systems. Basal insulin is usually initiated at a conservative dose of 10 units/day or 0.1-0.2 units/kg/day, then titrated thereafter over several weeks or months, based on patients' self-measured fasting plasma glucose, to achieve an individualized target (usually 80-130 mg/dL). Through a shared decision-making process, confirmation of appropriate goals and titration methods should be established, including provisions for events that might alter scheduled titration (e.g. travel, dietary change, illness, hospitalization, etc.). Although switching between basal insulins is usually easily accomplished, pharmacokinetic and pharmacodynamic differences between formulations require clinicians to provide explicit guidance to patients. Basal insulin is effective long-term, but overbasalization (continuing to escalate dose without a meaningful reduction in fasting plasma glucose) should be avoided.Key messagesPrimary care providers often initiate basal insulin for people with type 2 diabetes.Basal insulin is recommended to be initiated at 10 units/day or 0.1-0.2 units/kg/day, and doses must be titrated to agreed fasting plasma glucose goals, usually 80-130 mg/dL. A simple rule is to gradually increase the initial dose by 1 unit per day (NPH, insulin detemir, and glargine 100 units/mL) or 2-4 units once or twice per week (NPH, insulin detemir, glargine 100 and 300 units/mL, and degludec) until FPG levels remain consistently within the target range. If warranted, switching between basal insulins can be done using simple regimens.The dose of basal insulin should be increased as required up to approximately 0.5-1.0 units/kg/day in some cases. Overbasalization (continuing to escalate dose without a meaningful reduction in fasting plasma glucose) is not recommended; rather re-evaluation of individual therapy, including consideration of more concentrated basal insulin preparations and/or short-acting prandial insulin as well as other glucose-lowering therapies, is suggested.
许多 2 型糖尿病患者最终需要将基础胰岛素纳入其治疗方案。由于大多数 2 型糖尿病患者在社区中得到管理,因此初级保健提供者了解并正确管理基础胰岛素的起始和滴定以及帮助患者自我管理胰岛素注射非常重要。新型长效基础胰岛素比旧制剂具有更好的稳定性和灵活性,并且具有改进的输送系统。基础胰岛素通常以保守剂量 10 单位/天或 0.1-0.2 单位/千克/天开始,然后根据患者的自我测量空腹血糖在数周或数月内进行滴定,以达到个体化目标(通常为 80-130mg/dL)。通过共同决策过程,应确定适当的目标和滴定方法,包括可能改变预定滴定的事件的规定(例如旅行、饮食改变、疾病、住院等)。尽管基础胰岛素之间的转换通常很容易完成,但制剂之间的药代动力学和药效学差异要求临床医生向患者提供明确的指导。基础胰岛素长期有效,但应避免过度基础化(继续增加剂量而没有显著降低空腹血糖)。
关键信息
初级保健提供者通常为 2 型糖尿病患者启动基础胰岛素。
建议以 10 单位/天或 0.1-0.2 单位/千克/天开始基础胰岛素,并根据商定的空腹血糖目标滴定剂量,通常为 80-130mg/dL。一个简单的规则是逐渐增加初始剂量,每天增加 1 单位(NPH、胰岛素地特胰岛素和甘精胰岛素 100 单位/毫升)或每周增加 1-2 次 2-4 单位(NPH、胰岛素地特胰岛素、甘精胰岛素 100 和 300 单位/毫升以及德谷胰岛素),直到 FPG 水平始终保持在目标范围内。如果需要,可以使用简单的方案在基础胰岛素之间进行转换。
在某些情况下,根据需要将基础胰岛素剂量增加至约 0.5-1.0 单位/千克/天。不建议过度基础化(继续增加剂量而没有显著降低空腹血糖);相反,建议重新评估个体治疗,包括考虑更浓缩的基础胰岛素制剂和/或短效餐时胰岛素以及其他降血糖疗法。