1.北京中医药大学,北京100029
2.中国中医科学院,北京100700
3.中日友好医院中医风湿病科 免疫炎性;疾病北京市重点实验室,北京100029
穆闻君,女,26岁,硕士研究生。研究方向:中医药诊治风湿病。
孔维萍,E-mail:kongweiping75@126.com
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穆闻君,孙文婷,胡丽芳,等.补肾强督清化汤治疗强直性脊柱炎肾虚湿热证临床疗效评估[J].北京中医药,2022,41(8):838-843.
MU Wen-jun,SUN Wen-ting,HU Li-fang,et al.Clinical efficacy evaluation of Qiangdu Qinghua Decoction in treating ankylosing spondylitis with kidney deficiency and damp heat syndrome[J]. Beijing Journal of Traditional Chinese Medicine,2022,41(08):838-843.
穆闻君,孙文婷,胡丽芳,等.补肾强督清化汤治疗强直性脊柱炎肾虚湿热证临床疗效评估[J].北京中医药,2022,41(8):838-843. DOI: 10.16025/j.1674-1307.2022.08.003.
MU Wen-jun,SUN Wen-ting,HU Li-fang,et al.Clinical efficacy evaluation of Qiangdu Qinghua Decoction in treating ankylosing spondylitis with kidney deficiency and damp heat syndrome[J]. Beijing Journal of Traditional Chinese Medicine,2022,41(08):838-843. DOI: 10.16025/j.1674-1307.2022.08.003.
目的,2,探讨补肾强督清化汤治疗强直性脊柱炎(AS)肾虚湿热证临床疗效。,方法,2,采用单盲、随机对照的研究方法,将70例AS肾虚湿热证患者按随机数字表法分为观察组和对照组。观察组予补肾强督清化汤联合塞来昔布治疗,对照组予中药安慰剂联合塞来昔布治疗,疗程均为12周。评价2组患者治疗前后临床症状及体征、中医证候评分、疾病活动度、炎症反应指标,采用AS国际评估委员会的工作小组(ASAS)制定的疗效标准评价体系,即ASAS20、ASAS40、ASAS5/6,Bath AS活动性指数50(BASDAI50)和中医证候评分改善率评估补肾强督清化汤的临床疗效。,结果,2,治疗12周后观察组与对照组ASAS20应答率分别为73.5%、44.1%;ASAS40应答率分别为47.1%、17.6%;ASAS5/6应答率分别为52.9%、23.5%;中医总有效率分别为91.88%、55.88%,上述指标2组差异有统计学意义(,P,<,0.05)。治疗后2组AS患者综合指数(BAS-G)、BASDAI、疾病活动评分-C反应蛋白指标(ASDAS-CRP)、Bath功能指数(BASFI)、夜间痛VAS评分、脊柱痛VAS评分、中医证候评分及实验室指标等与治疗前相比均显著改善,差异有统计学意义(,P,<,0.05);组间比较,观察组BAS-G、BASDAI、BASFI、ASDAS-CRP、夜间痛、中医证候评分均优于对照组,差异有统计学意义(,P,<,0.05)。,结论,2,补肾强督清化汤治疗AS肾虚湿热证,临床疗效显著,优于单纯使用塞来昔布,且不良反应少,安全性高。
Objective,2,To investigate the clinical efficacy of Bushen Qiangdu Qinghua Decoction on ankylosing spondylitis (AS) of kidney deficiency and dampness heat syndrome.,Methods,2,Using a single-blind, randomized controlled study method, 70 patients with kidney deficiency and dampness heat syndrome of AS were randomly divided into observation and control groups according to random number table method. The observation group was treated with Bushen Qiangdu Qinghua Decoction combined with celecoxib, while the control group was treated with Chinese herbal medicine placebo combined with celecoxib. The course of treatment was 2 weeks for both groups. The clinical symptoms and signs, TCM symptom scores, disease activity, inflammatory response indexes of the two groups were evaluated before and after the treatment, and the clinical efficacy of Bushen Qiangdu Qinghua Decoction was assessed using the evaluation system of efficacy criteria developed by the working group of AS International Assessment Committee (ASAS), namely ASAS20, ASAS40, ASAS5/6, BASDAI50 and the improvement rate of TCM symptom scores.,Results,2,After 12 weeks of treatment,the ASAS20 response rate was 73.5% and 44.1% in the observation group and the control group respectively; ASAS40 response rate was 47.1% and 17.6% respectively; ASAS5/6 response rate was 52.9% and 23.5% respectively; the total TCM effective rate was 91.88% and 55.88% respectively, and the differences of above indexes between the two groups were statistically significant (,P,<,0.05). After treatment, BAS-G, BASDAI, ASDAS-CRP, BASFI, nocturnal pain VAS score, spinal pain VAS score, TCM evidence score, laboratory index of AS patients in both groups were significantly improved compared with those before treatment, and the differences were statistically significant (,P,<,0.05); compared two groups, BAS-G, BASDAI, ASDAS-CRP nocturnal pain, TCM symptoms scores in the observation group were better than those in the control group, and the differences were statistically significant (,P,<,0.05).,Conclusion,2,The clinical efficacy of Bushen Qiangdu Qinghua Decoction in the treatment of AS with kidney deficiency and dampness heat syndrome is significantly better than that of celecoxib with less adverse effects and high safety.
补肾强督清化汤强直性脊柱炎肾虚湿热证疗效评价
Bushen Qiangdu Qinghua Decoctionankylosing spondylitiskidney deficiency and dampness heat syndromeefficacy evaluation
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