Division of Endocrinology, Metabolism and Molecular Medicine, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Diabetes Technol Ther. 2022 Jul;24(7):525-530. doi: 10.1089/dia.2022.0009. Epub 2022 Jun 6.
The high-dose large-volume insulin injections that may become necessary during pregnancy due to marked pregnancy-induced insulin resistance may result in suboptimal therapeutic effectiveness. Use of U-500 insulin, a concentrated insulin formulation, has been suggested during pregnancy. However, the pharmacokinetic properties of U-500 insulin monotherapy can impede achievement of strict pregnancy glycemic targets. We propose a novel regimen for treatment of severe pregnancy-induced insulin resistance that enables precise delivery of U-500 basal insulin therapy through continuous subcutaneous insulin infusion (CSII) while maintaining the desired kinetics of prandial rapid-acting U-100 insulin therapy. This combination approach, guided by continuous glucose monitoring data, enabled achievement of pregnancy glycemic targets while reducing basal insulin requirements by approximately one-third. We report our method for (1) conversion to U-500 insulin delivery through CSII during pregnancy and (2) conversion from U-500 basal insulin delivery through CSII to U-100 intravenous insulin infusion therapy at delivery, to offer clinicians who encounter similar challenging scenarios a novel approach to diabetes management during pregnancy in the setting of marked insulin resistance.
由于明显的妊娠性胰岛素抵抗,怀孕期间可能需要大剂量、大容量的胰岛素注射,这可能导致治疗效果不理想。在怀孕期间,有人建议使用 U-500 胰岛素,这是一种浓缩的胰岛素制剂。然而,U-500 胰岛素单药治疗的药代动力学特性可能会阻碍严格的妊娠血糖目标的实现。我们提出了一种新的方案来治疗严重的妊娠性胰岛素抵抗,该方案通过持续皮下胰岛素输注(CSII)精确输送 U-500 基础胰岛素治疗,同时保持期望的餐时速效 U-100 胰岛素治疗动力学。这种基于连续血糖监测数据的联合治疗方法使妊娠血糖目标得以实现,同时使基础胰岛素需求减少了约三分之一。我们报告了我们的方法,用于(1)在怀孕期间通过 CSII 转换为 U-500 胰岛素给药,以及(2)在分娩时从 CSII 中的 U-500 基础胰岛素给药转换为 U-100 静脉内胰岛素输注治疗,为遇到类似挑战性情况的临床医生提供了一种新的方法来管理在明显胰岛素抵抗的情况下的妊娠糖尿病。