Liao Shengchun, Chen Yurou, Wang Shuting, Wang Chen, Ye Chaoyang
Department of Nephrology, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Institute of Traditional Chinese Medicine Kidney Disease, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Ren Fail. 2024 Dec;46(1):2338566. doi: 10.1080/0886022X.2024.2338566. Epub 2024 Apr 24.
Shenkang injection (SKI) has been widely used in China for many years for the treatment of kidney disease. The objective of this systematic review was to assess the efficacy of Shenkang injection for the treatment of acute kidney injury (AKI).
A search was conducted across seven databases, encompassing data from the inception of each database through October 8, 2023. Randomized controlled trials comparing SKI-treated AKI patients with control subjects were extracted. The main outcome measure was serum creatinine (SCr) levels. Secondary outcomes included blood urea nitrogen (BUN), serum cystatin C (CysC), 24-h urine protein (24 h-Upro) levels, APACHE II score and adverse reactions.
This meta-analysis included eleven studies, and the analysis indicated that, compared with the control group, SKI significantly decreased SCr [WMD = -23.31, 95% CI (-28.06, -18.57); < 0.001]; BUN [WMD = -2.07, 95% CI (-2.56, -1.57); < 0.001]; CysC [WMD = -0.55, 95% CI (-0.78, -0.32), < 0.001]; 24-h urine protein [WMD = -0.43, 95% CI (-0.53, -0.34), < 0.001]; and the APACHE II score [WMD = -3.07, 95% CI (-3.67, -2.48), < 0.001]. There was no difference in adverse reactions between the SKI group and the control group [RR = 1.32, 95% CI (0.66, 2.63), = 0.431].
The use of SKI in AKI patients may reduce SCr, BUN, CysC, 24-h Upro levels, and APACHE II scores in AKI patients. The incidence of adverse reactions did not differ from that in the control group. Additional rigorous clinical trials will be necessary in the future to thoroughly evaluate and establish the effectiveness of SKI in the treatment of AKI.
肾康注射液(SKI)在中国已广泛应用多年用于治疗肾脏疾病。本系统评价的目的是评估肾康注射液治疗急性肾损伤(AKI)的疗效。
在七个数据库中进行检索,涵盖各数据库自创建起至2023年10月8日的数据。提取比较肾康注射液治疗急性肾损伤患者与对照组的随机对照试验。主要结局指标为血清肌酐(SCr)水平。次要结局指标包括血尿素氮(BUN)、血清胱抑素C(CysC)、24小时尿蛋白(24 h-Upro)水平、急性生理与慢性健康状况评分系统II(APACHE II)评分及不良反应。
本荟萃分析纳入11项研究,分析表明,与对照组相比,肾康注射液显著降低了SCr[加权均数差(WMD)=-23.31,95%置信区间(CI)(-28.06,-18.57);P<0.001];BUN[WMD=-2.07,95%CI(-2.56,-1.57);P<0.001];CysC[WMD=-0.55,95%CI(-0.78,-0.32),P<0.001];24小时尿蛋白[WMD=-0.43,95%CI(-0.53,-0.34),P<0.001];以及APACHE II评分[WMD=-3.07,95%CI(-3.67,-2.48),P<0.001]。肾康注射液组与对照组之间的不良反应无差异[相对危险度(RR)=1.32,95%CI(0.66,2.63),P=0.431]。
在急性肾损伤患者中使用肾康注射液可能降低急性肾损伤患者的SCr、BUN、CysC、24小时尿蛋白水平及APACHE II评分。不良反应发生率与对照组无差异。未来有必要进行更多严格的临床试验,以全面评估并确定肾康注射液治疗急性肾损伤的有效性。