[Multicenter randomized controlled trial of Yiqi Huoxue formula() for the treatment of ruptured lumbar disc herniation].

Q4 Medicine
Yu Zhu, Zhi-Qiang Wang, Shun Lin, Ying-Ying Yao, Xue-Qiang Shen, Xiao-Chun Li, Feng Yu, Xiao-Yang Xiong, Yi Song, Meng-Fei Chen, Peng-Fei Yu, Hong Jiang, Jin-Tao Liu
{"title":"[Multicenter randomized controlled trial of <i>Yiqi Huoxue</i> formula() for the treatment of ruptured lumbar disc herniation].","authors":"Yu Zhu, Zhi-Qiang Wang, Shun Lin, Ying-Ying Yao, Xue-Qiang Shen, Xiao-Chun Li, Feng Yu, Xiao-Yang Xiong, Yi Song, Meng-Fei Chen, Peng-Fei Yu, Hong Jiang, Jin-Tao Liu","doi":"10.12200/j.issn.1003-0034.20240543","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To observe the clinical symptoms and MRI outcomes of patients with ruptured lumbar disc herniation(LDH) through a multicenter randomized controlled study, and to evaluate the clinical efficacy and safety of <i>Yiqi Huoxue</i> formula() in the treatment of this disease.</p><p><strong>Methods: </strong>A total of 160 outpatients and inpatients with ruptured LDH admitted to 4 medical centers from January 2023 to June 2023 were selected and randomly divided into the <i>Yiqi Huoxue</i> formula group and the control group, with 80 patients in each group. In the <i>Yiqi Huoxue</i> formula group, there were 43 males and 37 females, with an age of (41.03±9.56) years and a disease duration of (10.45±25.37) days, and the patients were treated with <i>Yiqi Huoxue</i> formula. In the control group, there were 34 males and 46 females, with an age of (42.14±8.73) years and a disease duration of (11.31±21.14) days;during the acute phase, patients in this group could take celecoxib capsules orally, and methylcobalamin orally at the same time. The Japanese Orthopaedic Association (JOA) score, Oswestry disability index (ODI), changes in the volume of herniated disc tissue on MRI, herniation rate, and absorption rate were recorded at the time of enrollment and during follow-ups at the 3rd, 6th, and 12th month after treatment.</p><p><strong>Results: </strong>A total of 156 patients completed the clinical follow-up, and 4 patients withdrew midway. The clinical symptoms of all patients who completed the study were relieved to varying degrees, and reabsorption of herniated disc tissue was observed in all patients in the <i>Yiqi Huoxue</i> formula group after treatment. For the JOA score:in the <i>Yiqi Huoxue</i> formula group, it was (10.73±2.76) points before treatment and (24.65±2.19) points at the 12th month after treatment;in the control group, it was (11.01±1.20) points before treatment and (17.07±3.26) points at the 12th month after treatment. For the ODI score:in the <i>Yiqi Huoxue</i> formula group, it was (26.21±3.55) points before treatment and (5.65±2.19) points at the 12th month after treatment;in the control group, it was (27.92±2.51) points before treatment and (9.09±2.15) points at the 12th month after treatment. At the 12th month after treatment, the JOA and ODI scores of both groups were better than those before treatment, and the scores of the <i>Yiqi Huoxue</i> formula group were better than those of the control group, with statistically significant differences (<i>P</i><0.05). In terms of the herniated disc volume and herniation rate on MRI, the <i>Yiqi Huoxue</i> formula group was superior to the control group, with statistically significant differences(<i>P</i><0.05). Reabsorption occurred in 56.96%(45/79) of patients in the <i>Yiqi Huoxue</i> formula group, which was significantly higher than the 37.66%(29/77) in the control group.</p><p><strong>Conclusion: </strong>After treatment with <i>Yiqi Huoxue</i> formula, patients with ruptured LDH show significant improvement in clinical symptoms and a marked reduction in the volume of herniated discs. During the follow-up period, no obvious adverse drug reactions are observed in patients, and no recurrence of symptoms is found at the last follow-up, indicating that the formula has safe and reliable efficacy.</p>","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"38 11","pages":"1112-8"},"PeriodicalIF":0.0000,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zhongguo gu shang = China journal of orthopaedics and traumatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12200/j.issn.1003-0034.20240543","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: To observe the clinical symptoms and MRI outcomes of patients with ruptured lumbar disc herniation(LDH) through a multicenter randomized controlled study, and to evaluate the clinical efficacy and safety of Yiqi Huoxue formula() in the treatment of this disease.

Methods: A total of 160 outpatients and inpatients with ruptured LDH admitted to 4 medical centers from January 2023 to June 2023 were selected and randomly divided into the Yiqi Huoxue formula group and the control group, with 80 patients in each group. In the Yiqi Huoxue formula group, there were 43 males and 37 females, with an age of (41.03±9.56) years and a disease duration of (10.45±25.37) days, and the patients were treated with Yiqi Huoxue formula. In the control group, there were 34 males and 46 females, with an age of (42.14±8.73) years and a disease duration of (11.31±21.14) days;during the acute phase, patients in this group could take celecoxib capsules orally, and methylcobalamin orally at the same time. The Japanese Orthopaedic Association (JOA) score, Oswestry disability index (ODI), changes in the volume of herniated disc tissue on MRI, herniation rate, and absorption rate were recorded at the time of enrollment and during follow-ups at the 3rd, 6th, and 12th month after treatment.

Results: A total of 156 patients completed the clinical follow-up, and 4 patients withdrew midway. The clinical symptoms of all patients who completed the study were relieved to varying degrees, and reabsorption of herniated disc tissue was observed in all patients in the Yiqi Huoxue formula group after treatment. For the JOA score:in the Yiqi Huoxue formula group, it was (10.73±2.76) points before treatment and (24.65±2.19) points at the 12th month after treatment;in the control group, it was (11.01±1.20) points before treatment and (17.07±3.26) points at the 12th month after treatment. For the ODI score:in the Yiqi Huoxue formula group, it was (26.21±3.55) points before treatment and (5.65±2.19) points at the 12th month after treatment;in the control group, it was (27.92±2.51) points before treatment and (9.09±2.15) points at the 12th month after treatment. At the 12th month after treatment, the JOA and ODI scores of both groups were better than those before treatment, and the scores of the Yiqi Huoxue formula group were better than those of the control group, with statistically significant differences (P<0.05). In terms of the herniated disc volume and herniation rate on MRI, the Yiqi Huoxue formula group was superior to the control group, with statistically significant differences(P<0.05). Reabsorption occurred in 56.96%(45/79) of patients in the Yiqi Huoxue formula group, which was significantly higher than the 37.66%(29/77) in the control group.

Conclusion: After treatment with Yiqi Huoxue formula, patients with ruptured LDH show significant improvement in clinical symptoms and a marked reduction in the volume of herniated discs. During the follow-up period, no obvious adverse drug reactions are observed in patients, and no recurrence of symptoms is found at the last follow-up, indicating that the formula has safe and reliable efficacy.

【益气活血方()治疗腰椎间盘突出症破裂的多中心随机对照试验】。
目的:通过多中心随机对照研究,观察腰椎间盘突出症(LDH)患者的临床症状及MRI结果,评价益气活血方()治疗该疾病的临床疗效及安全性。方法:选择2023年1月至2023年6月在4个医疗中心收治的160例门诊和住院的LDH破裂患者,随机分为益气活血方组和对照组,每组80例。益气活血方组男性43例,女性37例,年龄(41.03±9.56)岁,病程(10.45±25.37)天,均予益气活血方治疗。对照组男性34例,女性46例,年龄(42.14±8.73)岁,病程(11.31±21.14)d;本组患者急性期可口服塞来昔布胶囊,同时口服甲钴胺素。记录入组时及治疗后第3、6、12个月随访时的JOA评分、Oswestry失能指数(ODI)、椎间盘突出组织MRI体积变化、突出率、吸收率。结果:156例患者完成临床随访,4例中途退出。所有完成研究的患者临床症状均有不同程度缓解,益气活血方组治疗后均观察到椎间盘突出组织重吸收。JOA评分:益气活血方组治疗前为(10.73±2.76)分,治疗后12个月为(24.65±2.19)分;对照组治疗前为(11.01±1.20)分,治疗后12个月为(17.07±3.26)分。ODI评分:益气活血方组治疗前为(26.21±3.55)分,治疗后12个月为(5.65±2.19)分;对照组治疗前为(27.92±2.51)分,治疗后12个月为(9.09±2.15)分。治疗后12个月,两组患者JOA、ODI评分均优于治疗前,且益气活血方组评分优于对照组,差异有统计学意义(益气活血方组优于对照组),差异有统计学意义(益气活血方组优于对照组),差异有统计学意义(益气活血方组优于对照组,差异有统计学意义,显著高于对照组的37.66%(29/77)。结论:LDH破裂患者经益气活血方治疗后,临床症状明显改善,椎间盘突出体积明显减小。随访期间未见患者出现明显药物不良反应,末次随访未见症状复发,说明该配方疗效安全可靠。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
0.50
自引率
0.00%
发文量
189
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书