机构地区:[1]中国人民解放军南部战区总医院,广东广州510010
出 处:《风湿病与关节炎》2021年第8期10-13,共4页Rheumatism and Arthritis
基 金:广州市科技计划项目(201804010152);广东省科技计划重大专项(2012A080201012)。
摘 要:目的:观察复方土茯苓颗粒降低痰瘀痹阻型痛风患者血尿酸的临床疗效和安全性。方法:将104例痰瘀痹阻型痛风间歇期血尿酸升高患者随机分为治疗组和对照组,每组52例。治疗组给予复方土茯苓颗粒治疗,对照组给予苯溴马隆治疗。2组疗程均为12周。观察2组中西医疗效和安全性。结果:治疗组51例、对照组50例完成试验。治疗4周后,2组血尿酸水平较治疗前均降低(P<0.05);治疗8周后,2组血尿酸水平均低于治疗4周(P<0.05);治疗12周后,2组血尿酸水平与治疗8周比较,差异无统计学意义(P>0.05)。治疗4,8,12周后,2组血尿酸水平比较,差异均无统计学意义(P>0.05)。治疗4,8,12周,治疗组、对照组血尿酸<300μmol·L-1患者的比例分别为31.37%、36.00%,50.98%、54.00%,64.71%、68.00%,组间比较,差异均无统计学意义(P>0.05)。治疗12周后,治疗组显效12例,有效34例,无效5例,总有效率为90.20%;对照组显效10例,有效35例,无效5例,总有效率为90.00%。2组比较,差异无统计学意义(P>0.05)。治疗过程中,2组均无不良事件发生;治疗组急性痛风性关节炎发作患者比例低于对照组(P<0.05)。结论:复方土茯苓颗粒降低痰瘀痹阻型痛风患者血尿酸有效、安全,可为临床治疗提供药物选择和依据。Objective:To observe the clinical efficacy and safety of Fufang Tufuling Keli(复方土茯苓颗粒)in reducing blood uric acid in patients with gouty of phlegm stasis obstruction type.Methods:One hundred and four patients with elevated serum uric acid in the remission stage of gout of phlegm stasis obstruction type were randomly divided into a treatment group and a control group,52 cases in each group.The treatment group was treated with Fufang Tufuling Keli and the control group was treated with benzbromarone.The course of treatment for both groups was 12 weeks.The efficacy and safety of Chinese and Western medicine in the two groups were observed.Results:Fifty-one cases in the treatment group and 50 cases in the control group completed the test.After 4 weeks of treatment,the level of serum uric acid in the two groups decreased compared with that before treatment(P<0.05).After 8 weeks of treatment,the level of serum uric acid in the two groups was lower than that after 4 weeks of treatment(P<0.05).There was no significant difference between 12 weeks of treatment and 8 weeks of treatment(P>0.05).After 4,8 and 12 weeks of treatment,there was no significant difference in the level of serum uric acid between the two groups(P>0.05).After 4,8 and 12 weeks of treatment,the proportions of patients with serum uric acid(<300μmol·L-1)in the treatment group and the control group were 31.37%:36.00%,50.98%:54.00%,and 64.71%:68.00%respectively.The differences between groups were statistically significant(P>0.05).After 12 weeks of treatment,12 cases were markedly effective,34 cases were effective and 5 cases were ineffective in the treatment group and the total effective rate was 90.20%;In the control group,10 cases were markedly effective,35 cases were effective and 5 cases were ineffective.The total effective rate was 90.00%.There was no significant difference between the two groups(P>0.05).During the treatment,no adverse events occurred in both groups;the incidence of acute gouty arthritis in the treatment group was lower
分 类 号:R259[医药卫生—中西医结合]
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