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J Diabetes Sci Technol. 2011 Jan 1;5(1):120-8. doi: 10.1177/193229681100500117.
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Pre- and postprandial hyperinsulinemia during insulin pump treatment; role of the subcutaneous bolus and basal infusion.胰岛素泵治疗期间的餐前和餐后高胰岛素血症;皮下大剂量注射和基础输注的作用。
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本文引用的文献

1
A prospective evaluation of insulin dosing recommendations in patients with type 1 diabetes at near normal glucose control: Basal dosing.对1型糖尿病患者接近正常血糖控制时胰岛素剂量推荐的前瞻性评估:基础剂量。
J Diabetes Sci Technol. 2007 Jan;1(1):36-41. doi: 10.1177/193229680700100106.
2
Comparison of a luminescent oxygen channeling immunoassay and an ELISA for detecting insulin aspart in human serum.比较发光氧通道免疫测定法和 ELISA 检测人血清中天冬胰岛素
J Pharm Biomed Anal. 2010 Jan 5;51(1):217-24. doi: 10.1016/j.jpba.2009.08.008. Epub 2009 Aug 14.
3
Changes in basal insulin infusion rates with subcutaneous insulin infusion: time until a change in metabolic effect is induced in patients with type 1 diabetes.皮下胰岛素输注时基础胰岛素输注率的变化:1型糖尿病患者诱导代谢效应改变所需的时间。
Diabetes Care. 2009 Aug;32(8):1437-9. doi: 10.2337/dc09-0595. Epub 2009 Jun 1.
4
Comparative effect of human soluble insulin and insulin aspart upon hypoglycaemia-induced alterations in cardiac repolarization.人可溶性胰岛素与门冬胰岛素对低血糖诱导的心脏复极改变的比较效应。
Br J Clin Pharmacol. 2003 Mar;55(3):246-51. doi: 10.1046/j.1365-2125.2003.01726.x.
5
Clinical pharmacokinetics and pharmacodynamics of insulin aspart.门冬胰岛素的临床药代动力学与药效学
Clin Pharmacokinet. 2001;40(9):641-59. doi: 10.2165/00003088-200140090-00002.
6
Comparative pharmacokinetics and pharmacodynamics of the novel rapid-acting insulin analogue, insulin aspart, in healthy volunteers.
Eur J Clin Pharmacol. 1999 May;55(3):199-203. doi: 10.1007/s002280050618.
7
Improved postprandial glycemic control with insulin aspart. A randomized double-blind cross-over trial in type 1 diabetes.门冬胰岛素改善1型糖尿病患者餐后血糖控制:一项随机双盲交叉试验
Diabetes Care. 1999 May;22(5):801-5. doi: 10.2337/diacare.22.5.801.
8
Luminescent oxygen channeling assay (LOCI): sensitive, broadly applicable homogeneous immunoassay method.发光氧通道分析(LOCI):灵敏、广泛适用的均相免疫分析方法。
Clin Chem. 1996 Sep;42(9):1518-26.
9
Studies on the pathogenesis of the dawn phenomenon in insulin-dependent diabetic patients.胰岛素依赖型糖尿病患者黎明现象发病机制的研究。
Metabolism. 1984 May;33(5):458-64. doi: 10.1016/0026-0495(84)90148-3.
10
Comparison of plateau insulin levels achieved by intravenous or subcutaneous insulin infusion: evidence for low rates of subcutaneous degradation.静脉注射或皮下注射胰岛素输注所达到的平台期胰岛素水平比较:皮下降解率低的证据。
Diabetes Care. 1983 Mar-Apr;6(2):118-21. doi: 10.2337/diacare.6.2.118.

基础胰岛素输注速率改变后的药代动力学和药效学探索性研究。

Explorative study of pharmacokinetics and pharmacodynamics after change in basal insulin infusion rate.

作者信息

Ihlo Charlotte A, Lauritzen Torsten, Sturis Jeppe, Skyggebjerg Ole, Christiansen Jens S, Laursen Torben

机构信息

Department of Endocrinology M, Aarhus University Hospital, Aarhus C, Denmark.

出版信息

J Diabetes Sci Technol. 2011 Jan 1;5(1):120-8. doi: 10.1177/193229681100500117.

DOI:10.1177/193229681100500117
PMID:21303634
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3045247/
Abstract

BACKGROUND

The use of insulin pumps is rapidly increasing and new, technologically more advanced pumps are continuously being developed. It is of interest to assess the clinical relevance of the many technical features of these pumps, e.g., the effect on pharmacokinetics and pharmacodynamics with change in infusion rate.

METHOD

The aim of this study was to explore the sequence of pharmacokinetic and pharmacodynamic changes after dose doubling of the basal insulin infusion rate with subcutaneous bolus insulin injections once an hour, continuous subcutaneous insulin infusion, and continuous intravenous insulin infusion. Ten type 1 diabetes mellitus patients were included. The insulin doses were calculated based on the habitual insulin doses. The study was designed as an open-labeled, single-center, randomized, crossover exploratory trial.

RESULTS

Dose doubling of the basal insulin infusion rate with the three different administration protocols did not result in any clinically relevant differences in the time courses of the pharmacokinetic and pharmacodynamic parameters. With all three administration protocols, we observed a time interval of more than 6 hours before a new steady state of insulin was achieved.

CONCLUSIONS

Our results indicate that frequent changes in basal subcutaneous insulin infusion rates are not of significant clinical relevance on a 24-hour basis. Regarding technological features of subcutaneous insulin pumps, no discernable advantages of increasing pump stroke frequency were found. This indicates that pump stroke frequency sophistication might not be of clinical relevance in pumps used for basal subcutaneous insulin infusion.

摘要

背景

胰岛素泵的使用正在迅速增加,并且技术上更先进的新型泵也在不断研发。评估这些泵的众多技术特征的临床相关性很有意义,例如,输注速率变化对药代动力学和药效学的影响。

方法

本研究的目的是探讨在每小时一次皮下推注胰岛素、持续皮下胰岛素输注和持续静脉胰岛素输注的情况下,基础胰岛素输注速率加倍后药代动力学和药效学变化的顺序。纳入了10名1型糖尿病患者。胰岛素剂量根据习惯胰岛素剂量计算。该研究设计为开放标签、单中心、随机、交叉探索性试验。

结果

三种不同给药方案使基础胰岛素输注速率加倍,在药代动力学和药效学参数的时间进程上未产生任何临床相关差异。采用所有三种给药方案时,我们观察到在达到新的胰岛素稳态之前有超过6小时的时间间隔。

结论

我们的结果表明,基础皮下胰岛素输注速率的频繁变化在24小时内没有显著的临床相关性。关于皮下胰岛素泵的技术特征,未发现增加泵冲程频率有明显优势。这表明泵冲程频率的复杂性在用于基础皮下胰岛素输注的泵中可能与临床无关。