Wan Weibo, Zhou Jingjing, Lu Rong, Wang Chaoyang, Hu Shuli, Liu Mei, Xiong Rong, Kuang Jing, Fan Xuepeng
Department of Critical Care, Wuhan First Hospital of Hubei Province, Wuhan 430000, China.
Evid Based Complement Alternat Med. 2022 Jul 6;2022:6232264. doi: 10.1155/2022/6232264. eCollection 2022.
The study aimed to assess the clinical efficacy of Huangkui capsule plus methylprednisolone in the treatment of nephropathy and the effect on urinary protein and serum inflammatory factors in patients.
Between June 2017 and July 2020, 90 patients with nephropathy admitted to our hospital were recruited after assessment of eligibility and assigned via the random number table method (1 : 1) to receive either methylprednisolone tablets (observation group) or methylprednisolone tablets plus Huangkui capsules (experimental group). All eligible patients were also given dipyridamole and valsartan. Outcome measures included clinical efficacy, urine protein, hematuria, serum inflammatory factor levels, and adverse reactions.
A higher clinical efficacy was observed in the experimental group versus the observation group ( < 0.05). Huangkui capsules resulted in significantly lower levels of urine protein and hematuria in the experimental group versus the observation group after treatment ( < 0.05). The serum tumor necrosis factor- (TNF-), interleukin (IL)-6, and monocyte chemoattractant protein-1 (MCP-1) levels in the experimental group were significantly lower than those in the observation group after treatment ( < 0.05). Huangkui capsules plus methylprednisolone were associated with a lower incidence of adverse events versus methylprednisolone ( < 0.05).
The clinical efficacy of Huangkui capsule plus methylprednisolone in the treatment of patients with nephropathy is remarkable. It can effectively mitigate the inflammatory responses and enhance renal function, with reliable clinical safety, so it is worthy of clinical application.
本研究旨在评估黄葵胶囊联合甲泼尼龙治疗肾病的临床疗效以及对患者尿蛋白和血清炎症因子的影响。
2017年6月至2020年7月,选取我院收治的90例肾病患者,经评估合格后通过随机数字表法(1∶1)分为两组,分别给予甲泼尼龙片(观察组)或甲泼尼龙片联合黄葵胶囊(试验组)。所有符合条件的患者均给予双嘧达莫和缬沙坦。观察指标包括临床疗效、尿蛋白、血尿、血清炎症因子水平及不良反应。
试验组临床疗效高于观察组(P<0.05)。治疗后,试验组尿蛋白和血尿水平显著低于观察组(P<0.05)。治疗后,试验组血清肿瘤坏死因子-α(TNF-α)、白细胞介素(IL)-6和单核细胞趋化蛋白-1(MCP-1)水平显著低于观察组(P<0.05)。与甲泼尼龙相比,黄葵胶囊联合甲泼尼龙的不良事件发生率较低(P<0.05)。
黄葵胶囊联合甲泼尼龙治疗肾病患者的临床疗效显著。它能有效减轻炎症反应,增强肾功能,临床安全性可靠,值得临床应用。