Kangwook Lee, S. Ko, Min-Joo Kim, C. Park, Min-seok Cho, Jae-Woo Park
{"title":"Yukgunja-tang for Irritable Bowel Syndrome: A Protocol for a Systematic Review and Meta-Analysis","authors":"Kangwook Lee, S. Ko, Min-Joo Kim, C. Park, Min-seok Cho, Jae-Woo Park","doi":"10.22246/jikm.2023.44.3.285","DOIUrl":null,"url":null,"abstract":"Background: Irritable bowel syndrome (IBS) is a digestive disorder characterized by abdominal discomfort or pain accompanied by a change in stool condition. Owing to its complicated mechanisms, a standard treatment for IBS has not yet been established. Yukgunja-tang (YGT) is a Korean herbal medicine known in Asia to be effective in the treatment of gastrointestinal symptoms. In this study, we will conduct a systematic review of randomized controlled trials (RCTs) to assess the efficacy and safety of YGT in IBS treatment.Methods and analysis: English databases, such as Embase, Medline (via PubMed), Allied and Complementary Medicine Database, and Cochrane Central Register of Controlled Trials, will be searched for articles published up to April 2023. Additional databases, such as five Korean, one Chinese, and one Japanese database, will be included. RCTs and quasi-RCTs will also be included in the assessment of the efficacy of YGT. The overall efficacy rate will be the primary outcome, and data such as IBS quality-of-life measurements, global symptom scores, and adverse events will be the secondary outcomes. Review Manager Version 5.3 will be used for evaluation, and the risk of bias (RoB) will be evaluated using Cochrane Collaboration’s RoB tool. The Grading of Recommendations Assessment, Development, and Evaluation approach will be used to score the quality of evidence.Conclusion: This study will demonstrate the efficacy and safety of YGT for treating patients with IBS.","PeriodicalId":22826,"journal":{"name":"The Journal of Internal Korean Medicine","volume":"34 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Internal Korean Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22246/jikm.2023.44.3.285","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Irritable bowel syndrome (IBS) is a digestive disorder characterized by abdominal discomfort or pain accompanied by a change in stool condition. Owing to its complicated mechanisms, a standard treatment for IBS has not yet been established. Yukgunja-tang (YGT) is a Korean herbal medicine known in Asia to be effective in the treatment of gastrointestinal symptoms. In this study, we will conduct a systematic review of randomized controlled trials (RCTs) to assess the efficacy and safety of YGT in IBS treatment.Methods and analysis: English databases, such as Embase, Medline (via PubMed), Allied and Complementary Medicine Database, and Cochrane Central Register of Controlled Trials, will be searched for articles published up to April 2023. Additional databases, such as five Korean, one Chinese, and one Japanese database, will be included. RCTs and quasi-RCTs will also be included in the assessment of the efficacy of YGT. The overall efficacy rate will be the primary outcome, and data such as IBS quality-of-life measurements, global symptom scores, and adverse events will be the secondary outcomes. Review Manager Version 5.3 will be used for evaluation, and the risk of bias (RoB) will be evaluated using Cochrane Collaboration’s RoB tool. The Grading of Recommendations Assessment, Development, and Evaluation approach will be used to score the quality of evidence.Conclusion: This study will demonstrate the efficacy and safety of YGT for treating patients with IBS.
背景:肠易激综合征(IBS)是一种以腹部不适或疼痛伴大便改变为特征的消化系统疾病。由于其复杂的机制,肠易激综合征的标准治疗尚未建立。柳根子汤(YGT)是亚洲公认的治疗胃肠道症状的韩国草药。在本研究中,我们将对随机对照试验(rct)进行系统综述,以评估YGT治疗IBS的有效性和安全性。方法和分析:将检索到2023年4月前发表的文章,如Embase、Medline(通过PubMed)、联合和补充医学数据库、Cochrane中央对照试验注册库等英文数据库。另外,还将增加5个韩文数据库、1个中文数据库、1个日文数据库。对YGT疗效的评价也将纳入随机对照试验和准随机对照试验。总有效率将是主要结局,IBS生活质量测量、总体症状评分和不良事件等数据将是次要结局。使用Review Manager Version 5.3进行评估,并使用Cochrane Collaboration的RoB工具评估偏倚风险(risk of bias, RoB)。建议分级评估、发展和评价方法将用于对证据质量进行评分。结论:本研究将证明YGT治疗IBS患者的有效性和安全性。