厄贝沙坦片联合精蛋白生物合成人胰岛素注射液治疗老年2型糖尿病肾病的临床研究
[Abstract]:Objective to observe the clinical efficacy and safety of irbesartan tablets combined with protamine biosynthetic human insulin injection in the treatment of elderly patients with type 2 diabetic nephropathy. Methods 100 elderly patients with type 2 diabetic nephropathy were randomly divided into control group (n = 50) and experimental group (n = 50). The control group was subcutaneously injected with human insulin 0.25 U kg~ (-1) D1), bid, before breakfast and dinner. The experimental group was treated with irbesartan for 150 mg,qd, on the basis of control group. The patients in both groups were treated for 3 months. The clinical efficacy, urinary albumin excretion rate (24 h UAER),) and adverse drug reaction (ADR) of serum creatinine (SCr), (24 h UAER),) in serum urea nitrogen (BUN),) were compared between the two groups. Results after treatment, the total effective rates of the experimental group and the control group were 94.00% (47 / 50 cases) and 76.00% (38 / 50 cases), respectively. The difference was statistically significant (P0.05). After treatment, the BUN of the experimental group and the control group were (6.84 卤0.56) and (7.67 卤0.70) mmol L ~ (-1), SCr, respectively (76.49 卤8.05) and (86.39 卤8.04) 渭 mol L ~ (-1), respectively. 24 h UAER were (68.02 卤6.75) and (78.70 卤7.52) mg 24 h ~ (-1), respectively, the difference was statistically significant (P0.05). The adverse drug reactions of the two groups were headache, dizziness, palpitation and cough. The adverse drug reaction rates in the test group and the control group were 16.00% and 22.00%, respectively, with no significant difference (P0.05). Conclusion Irbesartan tablet combined with protamine biosynthetic human insulin injection is effective in the treatment of senile type 2 diabetic nephropathy. It can effectively improve the renal function of the patients without increasing the incidence of adverse drug reactions.
【作者单位】: 杭州市第三人民医院肾内科;
【基金】:浙江省医药卫生计划基金资助项目(2011ZHA003)
【分类号】:R587.2;R692.9
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