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儿科患者中持续皮下胰岛素输注与甘精胰岛素多次每日注射的长期使用比较。

Long-term use of continuous subcutaneous insulin infusion compared with multiple daily injections of glargine in pediatric patients.

作者信息

García-García Emilio, Galera Rafael, Aguilera Purificación, Cara Gabriel, Bonillo Antonio

机构信息

Department of Pediatrics, "Torrecárdenas" Hospital, Almería, Spain.

出版信息

J Pediatr Endocrinol Metab. 2007 Jan;20(1):37-40. doi: 10.1515/jpem.2007.20.1.37.

Abstract

BACKGROUND

Studies comparing continuous subcutaneous insulin infusion (CSII) and glargine in pediatric patients are scarce and cover only 1 year follow up. Although short-term results are favorable for CSII, there is no clear evidence whether this therapy leads to a sustained improvement of glycemic control.

OBJECTIVE

To evaluate long-term effects and safety of CSII versus multiple daily injections (MDI) of glargine over 2 years of treatment in children and adolescents.

PATIENTS AND METHODS

32 patients (aged 12.5 +/- 2.4 years; 19 females) with intensively treated type 1 diabetes mellitus were eligible. They were divided into two groups, virtually identical at study entry: eight on CSII and 24 on MDI of glargine. Variables at 0, 6, 12, 18 and 24 months were compared between groups by two-sided Mann-Whitney and Fisher tests.

RESULTS

No significant differences were found between groups (CSII vs MDI) throughout the study period. At 24 months hemoglobin A1c was 7.70 +/- 0.64% vs 7.54 +/- 0.74% (p = 0.8); body mass index SDS was 0.33 +/- 0.74 vs 0.40 +/- 1.01 (p = 0.9); total daily insulin requirements were 0.95 +/- 0.10 vs 1.05 +/- 0.18 U/kg (p = 0.4), incidence of severe hypoglycemia was 0.00 +/- 0.00 vs 0.04 +/- 0.14 episodes/patient/year (p = 0.8); and incidence of ketoacidosis was 0.20 +/- 0.27 vs 0.04 +/- 0.14 episodes/patient/year (p = 0.2).

CONCLUSION

CSII and MDI with glargine are equally effective and safe in pediatric patients at 2-year follow-up.

摘要

背景

比较持续皮下胰岛素输注(CSII)和甘精胰岛素在儿科患者中的研究较少,且随访期仅1年。尽管CSII的短期结果良好,但尚无明确证据表明该疗法是否能持续改善血糖控制。

目的

评估在儿童和青少年中,CSII与每日多次注射(MDI)甘精胰岛素相比,在2年治疗期内的长期疗效和安全性。

患者和方法

32例(年龄12.5±2.4岁;19例女性)接受强化治疗的1型糖尿病患者符合条件。他们被分为两组,入组时基本相同:8例接受CSII治疗,24例接受甘精胰岛素MDI治疗。通过双侧曼-惠特尼检验和费舍尔检验比较两组在0、6、12、18和24个月时的变量。

结果

在整个研究期间,两组(CSII与MDI)之间未发现显著差异。24个月时,糖化血红蛋白分别为7.70±0.64%和7.54±0.74%(p = 0.8);体重指数标准差分别为0.33±0.74和0.40±1.01(p = 0.9);每日胰岛素总需求量分别为0.95±0.10和1.05±0.18 U/kg(p = 0.4);严重低血糖发生率分别为0.00±0.00和0.04±0.14次/患者/年(p = 0.8);酮症酸中毒发生率分别为0.20±0.27和0.04±0.14次/患者/年(p = 0.2)。

结论

在2年随访期内,CSII和甘精胰岛素MDI在儿科患者中疗效和安全性相当。

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