In Type 1 diabetic patients with good glycaemic control, blood glucose variability is lower during continuous subcutaneous insulin infusion than during multiple daily injections with insulin glargine

被引:89
作者
Bruttomesso, D. [1 ]
Crazzolara, D. [1 ]
Maran, A. [1 ]
Costa, S. [1 ]
Dal Pos, M. [1 ]
Girelli, A. [2 ]
Lepore, G. [3 ]
Aragona, M. [4 ]
Iori, E. [1 ]
Valentini, U. [2 ]
Del Prato, S. [4 ]
Tiengo, A. [1 ]
Buhr, A. [5 ]
Trevisan, R. [3 ]
Baritussio, A.
机构
[1] Univ Padua, Dept Clin & Expt Med, Div Metab Dis, Padua, Italy
[2] Spedali Civil Brescia, Diabetol Unit, I-25125 Brescia, Italy
[3] Osped Riuniti Bergamo, Diabet Unit, I-24100 Bergamo, Italy
[4] Univ Pisa, Metab Unit, Dept Endocrinol & Metab, Pisa, Italy
[5] Disetron Med Syst AG, Burgdorf, Switzerland
关键词
continuous subcutaneous insulin infusion; glucose variability; multiple daily injections with glargine; treatment satisfaction;
D O I
10.1111/j.1464-5491.2007.02365.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims The superiority of continuous subcutaneous insulin infusion (CSII) over multiple daily injections (MDI) with glargine is uncertain. In this randomized cross-over study, we compared CSII and MDI with glargine in patients with Type 1 diabetes well controlled with CSII. The primary end-point was glucose variability. Methods Thirty-nine patients [38.1 +/- 9.3 years old (mean +/- SD), diabetes duration 16.6 +/- 8.2 years, glycated haemoglobin (HbA(1c)) 7.6 +/- 0.8%], already on CSII for at least 6 months, were randomly assigned to CSII with lispro or MDI with lispro and glargine. After 4 months they were switched to the alternative treatment. During the last month of each treatment blood glucose variability was analysed using glucose standard deviation, mean amplitude of glycaemic excursions (MAGE), lability index and average daily risk range (ADRR). As secondary end-points we analysed blood glucose profile, HbA(1c), number of episodes of hypo- and hyperglycaemia, lipid profile, free fatty acids (FFA), growth hormone and treatment satisfaction. Results During CSII, glucose variability was 5-12% lower than during MDI with glargine. The difference was significant only before breakfast considering glucose standard deviation (P = 0.011), significant overall using MAGE (P = 0.016) and lability index (P = 0.005) and not significant using ADRR. Although HbA(1c) was similar during both treatments, during CSII blood glucose levels were significantly lower, hyperglycaemic episodes were fewer, daily insulin dose was less, FFA were lower and treatment satisfaction was greater than during MDI with glargine. The frequency of hypoglycaemic episodes was similar during both treatments. Conclusions During CSII, glucose variability is lower, glycaemic control better and treatment satisfaction higher than during MDI with glargine.
引用
收藏
页码:326 / 332
页数:7
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