Raskin Philip, Bode Bruce W, Marks Jennifer B, Hirsch Irl B, Weinstein Richard L, McGill Janet B, Peterson Gregory E, Mudaliar Sunder R, Reinhardt Rickey R
University of Texas, Southwestern Medical Center, Dallas, Texas 75390-8858, USA.
Diabetes Care. 2003 Sep;26(9):2598-603. doi: 10.2337/diacare.26.9.2598.
Compare the efficacy, safety, and patient satisfaction of continuous subcutaneous insulin infusion (CSII) therapy with multiple daily injection (MDI) therapy for patients with type 2 diabetes.
A total of 132 CSII-naive type 2 diabetic patients were randomly assigned (1:1) to CSII (using insulin aspart) or MDI therapy (bolus insulin aspart and basal NPH insulin) in a multicenter, open-label, randomized, parallel-group, 24-week study. Efficacy was assessed with HbA(1c) and eight-point blood glucose (BG) profiles. Treatment satisfaction was determined with a self-administered questionnaire. Safety assessments included adverse events, hypoglycemic episodes, laboratory values, and physical examination findings.
HbA(1c) values decreased similarly for both groups from baseline (8.2 +/- 1.37% for CSII, 8.0 +/- 1.08% for MDI) to end of study (7.6 +/- 1.22% for CSII, 7.5 +/- 1.22% for MDI). The CSII group showed a trend toward lower eight-point BG values at most time points (only significant 90 min after breakfast; 167 +/- 48 vs. 192 +/- 65 mg/dl for CSII and MDI, respectively; P = 0.019). A total of 93% of CSII-treated subjects preferred the pump to their previous injectable insulin regimen for reasons of convenience, flexibility, ease of use, and overall preference. Safety assessments were comparable for both treatment groups.
Insulin aspart in CSII therapy provided efficacy and safety comparable to MDI therapy for type 2 diabetes. Patients with type 2 diabetes can be trained as outpatients to use CSII and prefer CSII to injections, indicating that pump therapy should be considered when initiating intensive insulin therapy for type 2 diabetes.
比较持续皮下胰岛素输注(CSII)疗法与多次皮下注射(MDI)疗法治疗2型糖尿病患者的疗效、安全性及患者满意度。
在一项多中心、开放标签、随机、平行组、为期24周的研究中,共有132例既往未接受过CSII治疗的2型糖尿病患者被随机(1:1)分配至CSII组(使用门冬胰岛素)或MDI组(门冬胰岛素推注联合中效低精蛋白胰岛素基础治疗)。采用糖化血红蛋白(HbA1c)和八点血糖(BG)谱评估疗效。通过自行填写问卷来确定治疗满意度。安全性评估包括不良事件、低血糖发作、实验室检查值及体格检查结果。
两组患者的HbA1c值从基线(CSII组为8.2±1.37%,MDI组为8.0±1.08%)至研究结束时(CSII组为7.6±1.22%,MDI组为7.5±1.22%)均有相似程度的下降。CSII组在大多数时间点的八点BG值有降低趋势(仅在早餐后90分钟时差异有统计学意义;CSII组和MDI组分别为167±48与192±65mg/dl;P = 0.019)。共有93%接受CSII治疗的受试者因方便、灵活、易用及总体偏好等原因,相较于之前的注射胰岛素方案更喜欢胰岛素泵。两组治疗的安全性评估结果相当。
CSII疗法中的门冬胰岛素治疗2型糖尿病的疗效和安全性与MDI疗法相当。2型糖尿病患者可作为门诊患者接受培训以使用CSII,且相较于注射更倾向于CSII,这表明在开始对2型糖尿病进行强化胰岛素治疗时应考虑胰岛素泵治疗。