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出 处:《武警医学》2014年第10期1021-1023,1028,共4页Medical Journal of the Chinese People's Armed Police Force
摘 要:目的:研究正清风痛宁片治疗IgA肾病中等量蛋白尿的临床疗效。方法选择156例IgA肾病中等量蛋白尿患者(尿蛋白定量1~3 g/24 h),按入院顺序号的奇偶数分组,正清风痛宁片联合缬沙坦治疗组(观察组)78例,缬沙坦治疗组(对照组)78例。治疗剂量:正清风痛宁片每次2片,3次/d,缬沙坦治疗80 mg,1次/d,服药并观察12个月,比较两组患者临床缓解率以及24 h尿蛋白定量、血肌酐、血浆白蛋白、总蛋白、血脂等临床指标的变化,并观察临床不良反应。结果观察12个月,观察组临床缓解率高于对照组,分别为87.2%和56.4%(P<0.01);观察组24 h尿蛋白定量为(0.42±0.36)g/24 h,明显低于对照组[(1.59±0.66)g/24 h],两组相比差异有统计学意义(P<0.05);血浆白蛋白和总蛋白、血肌酐水平、血脂水平以及临床不良反应两组对比差异无统计学意义。结论正清风痛宁片联合缬沙坦治疗IgA肾病中等量蛋白尿,临床缓解率高于单纯缬沙坦治疗,能更有效降低24 h尿蛋白定量,无明显不良反应。Objective To study the safety and efficacy of Zhengqiang Fengtongning Tablets in the treatment of IgA nephropa-thy with moderate amount of proteinuria.Methods 156 patients with IgA nephropathy with moderate amount of proteinuria ( urine pro-tein quantitation:1-3 g/24 h) were randomly divided into two groups.The study group was given Zhengqiang Fengtongning Tablets with valsartan and control group was given valsartan alone for treatment.The dosage of Zhengqiang Fengtongning was 2 tablets, 3 times a day, and valsartan was 80 mg/day.Results After treatment for 6 months, the total effective rate in the study group was significantly higher than that in the control group( 87.2%vs 56.4%, P〈0.01).24 h urinary protein in the study group was significantly lower than that in the control group(1.59 ±0.66, P〈0.05).There were no differences in serum albumine, serum creatinine (Scr) , total protein ( TP) , total cholesterol ( TC) , and incidence of adverse reactions between the two groups.Conclusions Zhengqiang Feng-tongning Tablets combined with valsartan for the treatment of IgA nephropathy with moderate amount of proteinuria is safe and reliable, which is worthy of clinical application.
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