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[参乐胶囊治疗肺脾气虚证IgA肾病的前瞻性、多中心、随机对照试验]

[Prospective, multi-centered, randomized and controlled trial on effect of Shenle Capsule in treating patients with IgA nephropathy of Fei-Pi qi-deficiency syndrome].

作者信息

Chen Xiang-Mei, Chen Yi-Ping, Zhou Zhu-Liang

机构信息

Institute of Nephrology, PLA and Key Laboratory, General Hospital of the PLA, Beijing.

出版信息

Zhongguo Zhong Xi Yi Jie He Za Zhi. 2006 Dec;26(12):1061-5.

Abstract

OBJECTIVE

To observe the effect and safety of Chinese compound Shenle Capsule (SC) in treating IgA nephropathy patients of Fei-Pi qi-deficiency syndrome (FPQD).

METHODS

A prospective, multi-centered, randomized, double-blinded, double-mimetic, controlled trial was conducted in 70 IgA nephropathy patients of FPQD syndrome, who were randomly assigned to two groups treated with SC and fosinopril respectively for 12 weeks. The changes of TCM syndrome score, 24 h urine protein quantity (UP), serum creatinine (SCr), hepatic function before and after treatment and the adverse reaction were observed.

RESULTS

Compared with those before treatment, the level of UP and the TCM syndrome scores decreased significantly in both groups (P < 0.05 or P < 0.01), while the level of albumin increased significantly after treatment, and the level of total cholesterol, triglycerid and renal function remained unchanged (P > 0.05). There was no significant difference in all the above parameters between the two groups. According to the curative criterion for Chinese medicine and Western medicine, the total effective rate was 83.3% and 66.7% respectively in the SC treated patients, 82.4% and 58.8% respectively in the fosinopril treated patients, showing insignificant difference between them. In addition, no severe adverse event was found.

CONCLUSION

SC treatment showed effects similar to that of fosinopril in reducing proteinuria and improving TCM syndrome in IgA nephropathy patients of FPQD syndrome, and could be well tolerated by patients.

摘要

目的

观察中药复方参乐胶囊(SC)治疗IgA肾病肺脾气虚证患者的疗效及安全性。

方法

对70例IgA肾病肺脾气虚证患者进行前瞻性、多中心、随机、双盲、双模拟、对照试验,将患者随机分为两组,分别给予SC和福辛普利治疗12周。观察治疗前后中医证候积分、24小时尿蛋白量(UP)、血清肌酐(SCr)、肝功能变化及不良反应。

结果

与治疗前相比,两组患者UP水平及中医证候积分均显著降低(P<0.05或P<0.01),治疗后白蛋白水平显著升高,总胆固醇、甘油三酯及肾功能水平无变化(P>0.05)。两组上述各项指标比较,差异均无统计学意义。按照中西医治疗标准,SC治疗组患者总有效率分别为83.3%和66.7%,福辛普利治疗组分别为82.4%和58.8%,两组差异无统计学意义。此外,未发现严重不良事件。

结论

SC治疗在降低IgA肾病肺脾气虚证患者蛋白尿及改善中医证候方面与福辛普利疗效相似,且患者耐受性良好。

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