[α -葡萄糖苷酶抑制剂米格列醇在医生办公室治疗2型糖尿病]。

H C Fehmann
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引用次数: 0

摘要

背景和方法:1999年10月至2000年8月,根据和67 (6)AMG进行了一项观察性研究。本文对2654例2型糖尿病患者进行了766名内科医生给予的3个月的α -葡萄糖苷酶抑制剂米立醇治疗。“DiaLife”研究的目的是获得关于米格列醇在日常实践中的有效性和安全性的数据。餐前和餐后血糖水平、糖化血红蛋白、甘油三酯、尿糖、微量蛋白尿和体重作为有效性参数。还采用了递增处理方案。副作用由提供护理的医生记录,并通过整体耐受性分析进行评估。结果:男女分布均衡。平均年龄62岁,糖尿病平均病程5年。82%的患者伴有疾病:62%的患者患有高血压,43%患有高脂血症,22%患有冠心病。64%的患者已经在接受糖尿病治疗。处方药以磺脲类和双胍类为主。米格列醇逐渐增加(第一周1 × 50mg /天,第二周2 × 50mg /天,直到第三周3 × 50mg /天),最终剂量为3 × 50mg /天或3 × 100mg /天。HbA1c、餐前和餐后血糖水平均显著降低。HbA1c从8.4%降至7.1%。餐前和餐后血糖水平分别降低- 46 mg/dl和- 59 mg/dl。体重平均下降1.9 kg;这种效果在BMI较高的个体中更为明显。47例患者报告了不良反应,主要发生在胃肠道。米格列醇与其他药物组合用无问题。结论:α -葡萄糖苷酶抑制剂米格列醇是治疗2型糖尿病有效、安全的药物。它是单一和联合治疗的理想工具。它显著减轻了体重。90%的医生认为米格列醇的有效性和安全性为“非常好”或“良好”。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The alpha-glucosidase inhibitor miglitol for the treatment of type 2 diabetes mellitus in the doctor's office].

Background and method: An observational study was carried out according to and 67 (6) AMG from october 1999 until august 2000. 2654 patients with diabetes mellitus type 2 were treated by 766 physicians for 3 months with alpha-glucosidase inhibitor miglitol. The aim of the study "DiaLife" was to obtain data regarding the effectiveness and safety of miglitol in the daily practice. Pre- and postprandial glucose levels, HbA1c, triglycerides, urin glucose, microalbuminuria and body weight were used as parameters of effectiveness. Also an increasing treatment scheme was used. Side effects were documented by the care providing physicians and evaluated by the global tolerability analysis.

Results: Males and females showed a balanced distribution. The average age was 62 years and the average duration of diabetes was 5 years. Concomitant diseases were described for 82% of patients: 62% of patients suffered from hypertension, 43% from hyperlipidemia and 22% from coronary heart disease. 64% of patients were already on treatment for diabetes. The mostly prescribed drugs were sulfonylureas and biguanides. Miglitol was gradually increased (first week 1 x 50 mg daily, second week 2 x 50 mg daily, until the third week 3 x 50 mg daily) and the final dosages were 3 x 50 mg or 3 x 100 mg miglitol daily. HbA1c, pre- and postprandial glucose levels were strongly reduced. The HbA1c decreased from 8.4% to 7,1%. Pre- and postprandial glucose levels were reduced minus 46 mg/dl and minus 59 mg/dl. The average decrease of body weight was 1,9 kg; the effect was augmented in individuals with higher BMI. Adverse effects were reported in 47 patients and occured mainly in the GI tract. There were no problems in the combination of miglitol with other pharmacological substance groups.

Conclusion: The alpha-glucosidase inhibitor miglitol is an efficient and safe drug for the treatment of diabetes mellitus type 2. It is an ideal tool for mono- and combination therapy. It reduces remarkably the body weight. 90% of physicians judged miglitol's efficiency and safety as "very good" or "good".

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