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Bloodletting therapy for primary headache: A systematic review and meta-analysis of randomized controlled trials 放血治疗原发性头痛:随机对照试验的系统回顾和荟萃分析
IF 2.5 4区 医学 Q2 Medicine Pub Date : 2023-10-14 DOI: 10.1016/j.eujim.2023.102312
Shuai Dong, Yi-Ying Wang, Bo Li, Shi-Bing Liang, Hui-Juan Cao

Introduction

Headache is one of the most common symptoms worldwide. This systematic review aimed to assess the effectiveness and safety of bloodletting therapy (BLT) for primary headache.

Methods

Four English databases, four Chinese databases and five trials registries were searched from inception to 2nd Sep 2022. Randomized controlled trials which compared BLT to no treatment or drugs for primary headache were included. BLT as adjunctive treatment of drugs or acupuncture was also included. Two authors extracted data and assessed the quality of trials through the Cochrane risk of bias tool 2.0 independently. Pain intensity was the primary outcome (e.g. Visual analogue scale, VAS). Meta-analysis (using RevMan 5.4.1) with random effect model was conducted when there was no serious statistical heterogeneity among trials (I²≤75 %). GRADE was used to assess the certainty of evidence.

Results

Seventeen trials involving 1123 participants were included. Types of BLT included pricking BLT, wet cupping and bloodletting puncture with plum-blossom needle. The most frequently used BLT acupoint was Tai Yang. Type of comparisons included BLT vs. drugs (n = 3), BLT plus drugs vs. drugs (n = 4) and BLT plus acupuncture vs. acupuncture (n = 10). All included trials were assessed as "high risk of bias". Results showed that BLT plus rizatriptan benzoate tablets was superior to drug alone in reducing VAS (Mean Difference (MD)=-2.07 cm, 95 % Confidence Interval (CI) -2.65 cm to -1.50 cm, P<0.00001) and increasing the number of patients with more than half pain relief (by 39 %). BLT plus acupuncture was superior to acupuncture alone (MD=-0.80 cm, 95 % CI -1.20 cm to -0.41 cm, P<0.00001) for pain relief. However, no difference was found between BLT and drugs on decreasing VAS. The certainty of the overall evidence is very low mainly due to the poor methodological quality and high heterogeneity among trials.

Conclusion

Very low certainty evidence suggests that BLT combined with acupuncture or drugs may be more effective in relieving pain of primary headache and other concomitant symptoms. Current evidence does not support confirmatory conclusions about the safety of BLT.

头痛是世界上最常见的症状之一。本系统综述旨在评估放血疗法(BLT)治疗原发性头痛的有效性和安全性。方法检索4个英文数据库、4个中文数据库和5个试验注册库。将BLT与无治疗或药物治疗原发性头痛进行比较的随机对照试验也包括在内。BLT作为药物或针灸的辅助治疗也包括在内。两位作者通过Cochrane风险偏倚工具2.0独立提取数据并评估试验质量。疼痛强度是主要观察指标(如视觉模拟评分,VAS)。当试验间统计异质性不严重(I²≤75%)时,采用随机效应模型进行meta分析(RevMan 5.4.1)。GRADE用于评估证据的确定性。结果共纳入17项试验,1123名受试者。治疗方法包括刺刺、湿拔罐和梅花针放血穿刺。最常使用的穴位是太阳。比较类型包括BLT与药物(n = 3)、BLT +药物与药物(n = 4)、BLT +针灸与针灸(n = 10)。所有纳入的试验都被评估为“高风险偏倚”。结果显示,BLT联合苯甲酸利扎曲坦片在降低VAS(平均差值(MD)=-2.07 cm, 95%可信区间(CI) -2.65 cm ~ -1.50 cm, P<0.00001)和增加一半以上疼痛缓解的患者数量(39%)方面优于单用药物。在缓解疼痛方面,BLT +针灸优于单独针灸(MD=-0.80 cm, 95% CI -1.20 cm ~ -0.41 cm, P<0.00001)。然而,在降低VAS方面,BLT与药物之间没有差异。总体证据的确定性非常低,主要是由于试验的方法学质量差和异质性高。结论极低确定性证据表明,BLT联合针灸或药物治疗可更有效地缓解原发性头痛及其他伴随症状。目前的证据并不支持关于BLT安全性的确认性结论。
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引用次数: 0
Assessing the quality of complementary, alternative, and integrative medicine website information for cancer: A cross-sectional survey and analysis 评估癌症补充、替代和综合医学网站信息的质量:一项横断面调查和分析
IF 2.5 4区 医学 Q2 Medicine Pub Date : 2023-10-11 DOI: 10.1016/j.eujim.2023.102309
Jeremy Y. Ng, Maheen Raja, Umair Tahir, Harmy Thakar, Sabrina L. Balkaran

Introduction

Patients with cancer frequently utilize complementary, alternative, and integrative medicine (CAIM); prior to this, many seek information about these therapies online. Little is known about the quality of this web-based consumer health information. Our study aimed to address this paucity of research by evaluating the quality of CAIM consumer health information on websites discussing the treatment and/or management of cancer.

Methods

Six search terms were entered into Google across four English-speaking countries (Canada, United States, United Kingdom and Australia) on January 4, 2023. The first 20 results of each search were assessed and included if they contained CAIM consumer health information for the treatment and/or management of cancer. Eligible websites were assessed using the 16-item DISCERN instrument, designed to evaluate information quality.

Results

Of 480 identified websites, 393 were duplicates, and 48 fit the eligibility criteria and were assessed using the DISCERN instrument. Mean summed DISCERN scores across all websites was 48.28 (SD = 14.26), and mean scores of the overall quality of each website was 3.11 (SD = 0.66). Several website quality issues were identified, including a lack of transparency surrounding sources of information, areas of uncertainty regarding treatment, consequences of foregoing treatment, and treatment impacts on quality of life.

Conclusion

Healthcare providers should be aware that patients may use these websites for CAIM information. To facilitate informed decision-making, healthcare providers are encouraged to ask about patients’ usage and interest in CAIM and direct them to credible and trustworthy resources.

癌症患者经常使用补充、替代和综合药物(CAIM);在此之前,许多人在网上寻求有关这些疗法的信息。人们对这种基于网络的消费者健康信息的质量知之甚少。我们的研究旨在通过评估讨论癌症治疗和/或管理的网站上CAIM消费者健康信息的质量来解决这一研究匮乏的问题。方法于2023年1月4日,在四个英语国家(加拿大、美国、英国和澳大利亚)的谷歌中输入六个搜索词。如果每个搜索的前20个结果包含用于癌症治疗和/或管理的CAIM消费者健康信息,则对其进行评估并将其包括在内。符合条件的网站使用旨在评估信息质量的16项DISCERN工具进行评估。结果在480个已确定的网站中,393个是重复的,48个符合资格标准,并使用DISCERN工具进行了评估。所有网站的DISCERN总分平均值为48.28(SD=14.26),每个网站的整体质量平均值为3.11(SD=0.66)。发现了一些网站质量问题,包括信息来源缺乏透明度、治疗的不确定性、上述治疗的后果以及治疗对生活质量的影响。结论医疗保健提供者应意识到患者可能会使用这些网站获取CAIM信息。为了促进知情决策,鼓励医疗保健提供者询问患者对CAIM的使用和兴趣,并引导他们获得可信和值得信赖的资源。
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引用次数: 0
Homeopathy as patient empowerment and an active path toward supportive care for non-metastatic breast cancer: A qualitative study (TOUCAN) 顺势疗法作为非转移性乳腺癌患者赋权和支持性治疗的积极途径:一项定性研究(TOUCAN)
IF 2.5 4区 医学 Q2 Medicine Pub Date : 2023-10-05 DOI: 10.1016/j.eujim.2023.102308
Clair-Antoine Veyrier , Guillaume Roucoux , Laurence Baumann-Coblentz , Jacques Massol , Jean-Claude Karp , Jean-Philippe Wagner , Olivier Chassany , Martin Duracinsky

Introduction

Breast cancer is the leading cause of death among French women, although the survival rate is increasing thanks to therapy and supportive care. Homeopathy is one of most widely used non-conventional supportive approaches in this context. This article aims to describe the ways women with non-metastatic breast cancer integrate homeopathy as supportive care into their conventional therapy regimen.

Methods

Qualitative semi-structured interviews and focus groups were conducted using interview guides. They were audio-recorded and first, partially transcribed to elicit emerging themes to revise the interview guide, and later word-for-word for in-depth analysis using Grounded Theory. Sampling, interviewing, transcription and coding occurred iteratively. The study has been reported according to COREQ guidelines.

Results

Fifty people participated: 28 patients, 13 oncologists, 6 homeopaths, 2 gynecologists and 1 nurse. Homeopathy was rarely present in the conventional patient care pathway. Turning to homeopathy was often the patient's initiative. Homeopathy was included to prevent or deal with adverse events from cancer treatments, while attempting to maximize clinical outcomes. Homeopathy was often used early in the care path if the patient had already consulted a homeopath. For others, the fear of chemotherapy triggered an active search for solutions. Homeopathic use was a form of empowerment and engagement, not only limited to patients who habitually used homeopathy. Most patients were treated by a general practitioner specialized in homeopathy, which was acknowledged by their oncologist.

Conclusion

Homeopathy acted as a gateway toward supportive care in tandem with conventional treatment.

简介癌症是法国女性死亡的主要原因,尽管通过治疗和支持性护理,存活率正在提高。顺势疗法是在这种情况下使用最广泛的非传统支持方法之一。本文旨在描述患有非味觉癌症的女性将顺势疗法作为支持性护理纳入传统治疗方案的方法。方法采用访谈指南进行定性半结构化访谈和焦点小组访谈。它们被录音,首先部分转录,以引出新出现的主题来修改面试指南,然后逐字逐句地使用扎根理论进行深入分析。采样、访谈、转录和编码反复进行。该研究已根据COREQ指南进行了报告。结果50人参与:28名患者,13名肿瘤学家,6名顺势疗法医生,2名妇科医生和1名护士。顺势疗法很少出现在传统的患者护理途径中。求助于顺势疗法往往是患者的主动行动。纳入顺势疗法是为了预防或处理癌症治疗的不良事件,同时试图最大限度地提高临床结果。如果患者已经咨询了顺势疗法,顺势疗法通常在护理过程的早期使用。对其他人来说,对化疗的恐惧引发了对解决方案的积极探索。顺势疗法的使用是一种赋权和参与的形式,不仅限于习惯性使用顺势疗法的患者。大多数患者由专门从事顺势疗法的全科医生进行治疗,这得到了肿瘤学家的认可。结论顺势疗法是支持性护理与传统治疗相结合的途径。
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引用次数: 0
The effect of ear acupressure on sexual functioning among lactating women: A randomized sham controlled trial 耳穴按压对哺乳期妇女性功能的影响:一项随机假对照试验
IF 2.5 4区 医学 Q2 Medicine Pub Date : 2023-10-01 DOI: 10.1016/j.eujim.2023.102285
Zainab Alimoardi , Sanaz Barghamadi , Terry Oleson , Mohammad Hossein Ayati , Mark D. Griffiths , Nasim Bahrami

Introduction

Women often experience more problems in sexual functioning after childbirth. Due to the high prevalence of sexual problems during the lactation period, the World Health Organization suggested measures are needed to improve women's sexual functioning during breastfeeding. The present study investigated the effect of auricular acupressure on sexual functioning among lactating women.

Methods

A randomized, sham-controlled trial was conducted between October 2019 to March 2020 in urban comprehensive health centers of Qazvin, Iran. Seventy-six women who had been lactating between six months and one year postpartum were randomly assigned to auricular acupressure group (n = 38) or sham control group (n = 38) using a balanced block randomization method. The intervention group received ear acupressure in 10 sessions (at four-day intervals) and control group also received the sham intervention at the same intervals. Sexual functioning was the primary outcome of the study (assessed using the Female Sexual Function Index) before and at three time points post-intervention (immediately after, one month after, and two months after). The secondary outcome was sexual quality of life assessed using Sexual Quality of Life-Female Version.

Results

Auricular acupressure had a large effect size on female sexual functioning at all three post-intervention time points: immediately after the intervention (adjusted mean difference [95% CI]: 8.37 [6.27; 10.46] with Cohen's d [95% CI]: 1.81[1.28; 2.34]), one month after the intervention (adjusted mean difference [95% CI]: 8.44 [6.41; 10.48] with Cohen's d [95% CI]: 2.01 [1.46; 2.56]), and two months after the intervention (adjusted mean difference [95% CI]: 7.43 [5.12; 9.71] with Cohen's d [95% CI]: 1.57 [1.06; 2.08]). The intervention significantly increased participants’ sexual quality of life on the Sexual Quality of Life-Female scale by 13.73 points in the intervention group compared to the control group (p<0.001). The effect size of intervention for female sexual quality was large (adjusted Cohen's d [95% CI]: 1.09 [0.58; 1.59]). Weekly frequency of sexual intercourse in the intervention group significantly increased compared to sham control group (p<0.001). These changes were clinically significant for sexual functioning and sexual quality of life.

Conclusion

Auricular acupressure appears to be an effective intervention for improving sexual functioning and sexual quality life of lactating women.

Clinical trial registration

Registered with the code of IRCT20190626044028N1 in the Clinical Trial Registration Center of Iran.

女性在分娩后往往会遇到更多的性功能问题。由于哺乳期间性问题的高发,世界卫生组织建议采取措施改善妇女在哺乳期间的性功能。本研究探讨了耳穴按压对哺乳期妇女性功能的影响。方法于2019年10月至2020年3月在伊朗加兹温市城市综合卫生中心进行随机、假对照试验。采用平衡区随机法,将76例产后6个月至1年哺乳期妇女随机分为耳穴按压组(n = 38)和假对照组(n = 38)。干预组接受10次耳指压治疗(间隔4天),对照组也接受相同间隔的假干预。性功能是研究的主要结果(使用女性性功能指数评估),在干预前和干预后的三个时间点(干预后立即,干预后一个月和干预后两个月)。次要结果是使用女性版性生活质量评估性生活质量。结果穴位按摩在干预后三个时间点对女性性功能的影响均较大:干预后立即(调整平均差值[95% CI]: 8.37 [6.27;10.46] Cohen’s d [95% CI]: 1.81[1.28;2.34]),干预后1个月(调整后平均差异[95% CI]: 8.44 [6.41;10.48] Cohen’s d [95% CI]: 2.01 [1.46;2.56]),干预后2个月(调整后平均差异[95% CI]: 7.43 [5.12;9.71] Cohen's d [95% CI]: 1.57 [1.06;2.08])。干预显著提高了参与者的性生活质量(女性性生活质量量表),干预组比对照组提高了13.73分(p<0.001)。干预对女性性质量的效应量很大(调整后的Cohen's d [95% CI]: 1.09 [0.58;1.59])。干预组每周性交次数明显高于假对照组(p < 0.001)。这些变化对性功能和性生活质量具有临床意义。结论耳穴按摩是改善哺乳期妇女性功能和性生活质量的有效干预手段。临床试验注册在伊朗临床试验注册中心注册,注册代码为IRCT20190626044028N1。
{"title":"The effect of ear acupressure on sexual functioning among lactating women: A randomized sham controlled trial","authors":"Zainab Alimoardi ,&nbsp;Sanaz Barghamadi ,&nbsp;Terry Oleson ,&nbsp;Mohammad Hossein Ayati ,&nbsp;Mark D. Griffiths ,&nbsp;Nasim Bahrami","doi":"10.1016/j.eujim.2023.102285","DOIUrl":"10.1016/j.eujim.2023.102285","url":null,"abstract":"<div><h3>Introduction</h3><p>Women often experience more problems in sexual functioning after childbirth. Due to the high prevalence of sexual problems during the lactation period, the World Health Organization suggested measures are needed to improve women's sexual functioning during breastfeeding. The present study investigated the effect of auricular acupressure on sexual functioning among lactating women.</p></div><div><h3>Methods</h3><p>A randomized, sham-controlled trial was conducted between October 2019 to March 2020 in urban comprehensive health centers of Qazvin, Iran. Seventy-six women who had been lactating between six months and one year postpartum were randomly assigned to auricular acupressure group (<em>n</em> = 38) or sham control group (<em>n</em> = 38) using a balanced block randomization method. The intervention group received ear acupressure in 10 sessions (at four-day intervals) and control group also received the sham intervention at the same intervals. Sexual functioning was the primary outcome of the study (assessed using the Female Sexual Function Index) before and at three time points post-intervention (immediately after, one month after, and two months after). The secondary outcome was sexual quality of life assessed using Sexual Quality of Life-Female Version.</p></div><div><h3>Results</h3><p>Auricular acupressure had a large effect size on female sexual functioning at all three post-intervention time points: immediately after the intervention (adjusted mean difference [95% CI]: 8.37 [6.27; 10.46] with Cohen's <em>d</em> [95% CI]: 1.81[1.28; 2.34]), one month after the intervention (adjusted mean difference [95% CI]: 8.44 [6.41; 10.48] with Cohen's <em>d</em> [95% CI]: 2.01 [1.46; 2.56]), and two months after the intervention (adjusted mean difference [95% CI]: 7.43 [5.12; 9.71] with Cohen's <em>d</em> [95% CI]: 1.57 [1.06; 2.08]). The intervention significantly increased participants’ sexual quality of life on the Sexual Quality of Life-Female scale by 13.73 points in the intervention group compared to the control group (<em>p</em>&lt;0.001). The effect size of intervention for female sexual quality was large (adjusted Cohen's <em>d</em> [95% CI]: 1.09 [0.58; 1.59]). Weekly frequency of sexual intercourse in the intervention group significantly increased compared to sham control group (<em>p</em>&lt;0.001). These changes were clinically significant for sexual functioning and sexual quality of life.</p></div><div><h3>Conclusion</h3><p>Auricular acupressure appears to be an effective intervention for improving sexual functioning and sexual quality life of lactating women.</p></div><div><h3>Clinical trial registration</h3><p>Registered with the code of IRCT20190626044028N1 in the Clinical Trial Registration Center of Iran.</p></div>","PeriodicalId":11932,"journal":{"name":"European Journal of Integrative Medicine","volume":null,"pages":null},"PeriodicalIF":2.5,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49370421","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Clinical effects of Baduanjin qigong exercise on cancer-related fatigue: A systematic review and meta-analysis 八段锦气功治疗癌症性疲劳的临床疗效:系统评价和Meta分析
IF 2.5 4区 医学 Q2 Medicine Pub Date : 2023-10-01 DOI: 10.1016/j.eujim.2023.102283
QianQian Liu, LiuYan Zhan, Xue Yan, Yao Li, SiQi Wei

Introduction

A number of randomized controlled trials have investigated the benefits of Baduanjin qigong on cancer-related fatigue (CRF) in cancer survivors. However, the results of these studies were inconclusive and contradictory, due to the limitations of small sample sizes and different measurement scores. We conducted this systematic review and meta-analysis of the evidence available to critically evaluate the efficacy and safety of Baduanjin qigong in improving CRF in cancer patients.

Methods

Eight databases (The Cochrane Library, PubMed, EMBASE, Web of Science, Chinese Biomedical Database (CBM), China National Knowledge Infrastructure (CNKI), Chinese Scientific Journal Database (VIP), and WanFang Database)) were systematically reviewed from inception to September 2022 for randomized controlled trials (RCTs). Two reviewers critically and independently assessed the risk of bias using the Cochrane Collaboration criteria and independently extracted relevant data using the designed tables. All statistical analyses were performed using Review Manager 5.3.

Results

Thirteen eligible studies were included in this systematic review, including 1010 patients. Baduanjin qigong as an add-on therapy significantly improved fatigue symptom scores (Standardized mean difference -1.43, 95% CI -2.01 to -0.84, P< 0.0001, RCTs= 9, n = 640). We found that different intervention frequencies, intervention durations, and intervention cycles of Baduanjin qigong exercise were effective in relieving fatigue, and the differences in effectiveness were similar for different types of cancer patients. Two RCTs reported no adverse events associated with Baduanjin qigong.

Conclusion

Baduanjin qigong may reduce CRF in cancer patients and may be used as a traditional and complementary medicine option for the clinical management of CRF. However, large and well-designed randomized controlled trials are still needed to confirm these findings.

Registration

PROSPERO CRD42022369410.

Funding

Lanzhou University, China (grant number 561,120,201) and Natural Science Youth Fund of Gansu Province (grant number 23JRRA1110).

一些随机对照试验研究了八段锦气功对癌症幸存者癌症相关疲劳(CRF)的益处。然而,由于样本量小,测量分数不同,这些研究的结果是不确定和矛盾的。我们对现有证据进行了系统回顾和荟萃分析,以批判性地评估八段金气功改善癌症患者CRF的有效性和安全性。方法系统回顾8个数据库(Cochrane Library、PubMed、EMBASE、Web of Science、中国生物医学数据库(CBM)、中国知网(CNKI)、中国科学期刊数据库(VIP)和万方数据库),从数据库建立至2022年9月进行随机对照试验(RCTs)。两位审稿人使用Cochrane协作标准独立评估偏倚风险,并使用设计的表格独立提取相关数据。所有统计分析均使用Review Manager 5.3进行。结果本系统评价纳入13项符合条件的研究,包括1010例患者。八段锦气功作为辅助治疗可显著改善疲劳症状评分(标准化平均差为-1.43,95% CI为-2.01 ~ -0.84,P<0.0001, rct = 9, n = 640)。我们发现八段锦气功运动不同的干预频率、干预时间、干预周期均有缓解疲劳的效果,不同类型癌症患者的效果差异相似。两项随机对照试验未报告八段锦气功相关不良事件。结论八段金气功可降低肿瘤患者的恶性循环,可作为临床治疗恶性循环的一种传统辅助药物。然而,仍然需要大规模和精心设计的随机对照试验来证实这些发现。RegistrationPROSPERO CRD42022369410。资助项目:兰州大学(批准号561,120,201)和甘肃省自然科学青年基金(批准号23JRRA1110)。
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引用次数: 0
Development and multiple visualization methods for the therapeutic effects prediction model of five-flavor Sophora Flavescens enteric-coated capsules in the treatment of active ulcerative colitis: A study on model development and result visualization 五味苦参肠溶胶囊治疗活动性溃疡性结肠炎疗效预测模型的建立及多种可视化方法的研究
IF 2.5 4区 医学 Q2 Medicine Pub Date : 2023-10-01 DOI: 10.1016/j.eujim.2023.102297
Zhi-Jun Bu , Zhi-Rui Huang , Yun-Ru Chen , You-Zhu Su , Yuan-Yuan Jin , Yu-Huan Zhang , Qiu-Ju Wu , Xue-Hui Wang , Yu Wang , Jian-Ping Liu , Zhao-Lan Liu

Introduction

The aim of this study was to develop a Therapeutic Effects Prediction Model (TEPM) for the treatment of active ulcerative colitis (UC) using Five-flavor Sophora Flavescens Enteric-coated Capsules (FSEC). This study also aimed to systematically review various visualization methods for the TEPM results and present the model results of FSEC as an example.

Methods

274 patients were randomly assigned to the training and testing datasets in a 7:3 ratio. We employed Least Absolute Shrinkage and Selection Operator (LASSO) regression to select predictive factors and constructed TEPM using logistic regression to assess the probability of disease remission. We assessed model performance by the area under the curve (AUC) and calibration curve. We utilized interactive nomograms, online calculators, scoring systems, graphical scoring tables, as well as the SHapley Additive exPlanations (SHAP) and Local Interpretable Model-agnostic Explanations (LIME) methods to present the model results.

Results

LASSO regression selected several predictors, including erythrocyte sedimentation rate, age, disease type, microscopic bleeding, pus, bridge, disease location, and pain. The AUC of the testing datasets was 0.699, and the calibration curve showed poor performance. The interactive nomogram, online calculator, and the SHAP method were suitable for datasets with predominantly continuous predictors, while scoring systems, graphical scoring tables, and the LIME method might be more appropriate for datasets with fewer continuous predictors. Physicians, researchers, and policymakers could benefit from detailed visualizations using interactive nomogram, the SHAP method, and the LIME method. Scoring systems, graphical scoring tables, and online calculator were available to the general public and non-experts. Scoring systems, graphical scoring tables, and online calculator could provide an overview of the model prediction results, while interactive nomogram, the SHAP method, and the LIME method were recommended for illustrating the complexity and rationality of the model prediction results.

Conclusion

Our study demonstrated that TEPM could predict the potential of FSEC to induce disease remission in patients with active UC. However, the poor calibration curve might be due to the limited sample size. Larger-scale multicenter studies will be needed in the future. Selecting an appropriate visualization method for TEPM should be based on the datasets, audience, and research objectives.

本研究旨在建立五味苦参肠溶胶囊(FSEC)治疗活动性溃疡性结肠炎(UC)的疗效预测模型。本研究还旨在系统地回顾各种TEPM结果的可视化方法,并以FSEC模型结果为例。方法将274例患者按7:3的比例随机分配到训练组和测试组。我们使用最小绝对收缩和选择算子(LASSO)回归来选择预测因素,并使用逻辑回归构建TEPM来评估疾病缓解的概率。我们通过曲线下面积(AUC)和校准曲线来评估模型的性能。我们利用交互式模态图、在线计算器、评分系统、图形计分表以及SHapley加性解释(SHAP)和局部可解释模型不可知解释(LIME)方法来呈现模型结果。结果slasso回归选择了红细胞沉降率、年龄、疾病类型、显微出血、脓、桥、疾病部位和疼痛等预测因子。测试数据集的AUC为0.699,校准曲线性能较差。交互式模态图、在线计算器和SHAP方法适用于主要具有连续预测因子的数据集,而评分系统、图形计分表和LIME方法可能更适用于具有较少连续预测因子的数据集。医生、研究人员和政策制定者可以从使用交互式nomogram、SHAP方法和LIME方法的详细可视化中受益。计分系统、图形计分表和在线计算器可供普通大众和非专家使用。评分系统、图形评分表和在线计算器可以提供模型预测结果的概览,而交互式nomogram、SHAP法和LIME法可以说明模型预测结果的复杂性和合理性。结论我们的研究表明TEPM可以预测FSEC诱导活动性UC患者疾病缓解的潜力。然而,较差的校准曲线可能是由于有限的样本量。未来需要更大规模的多中心研究。为TEPM选择合适的可视化方法应基于数据集、受众和研究目标。
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引用次数: 0
Chinese herbal medicine for primary dysmenorrhea: A systematic review and network meta-analysis of 54 randomized controlled trials 中药治疗原发性痛经:54项随机对照试验的系统评价和网络荟萃分析
IF 2.5 4区 医学 Q2 Medicine Pub Date : 2023-10-01 DOI: 10.1016/j.eujim.2023.102293
Xinbin Wang , Zhongwen Zhang , Haorui Wang , Ruilin Ma , Lili Wang , Xianhui Zhang , Yi Zhang , Rong Wang

Introduction

Primary dysmenorrhea (PD) is a common gynecological complaint among adolescents and young women. Chinese herbal medicines (CHMs) have been widely used for PD treatment in China. However, the relative advantages of different CHM regimens remain uncertain. This systematic review aimed to compare the efficacy and safety of different CHMs for the treatment of PD using network meta-analysis.

Methods

We searched PubMed, Embase, Web of Science, China National Knowledge Infrastructure (CNKI), and Chinese BioMedical Literature Database (CBM) from their inception to December 17, 2022. Randomized controlled trials (RCTs) comparing CHM or Chinese patent drugs with Prostaglandin Synthetase Inhibitors (PGSIs) were included. Risk of bias was assessed using the Cochrane risk of bias tool. A frequentist framework network meta-analysis was performed using R (4.2.2).

Results

A total of 54 RCTs with 5,345 PD patients were included. Compared with PGSIs, Danggui Sini decoction (mean difference [MD] = -5.92, 95% confidence interval [CI] -8.64 to -3.20) and Xiangfu Siwu Decoction (MD = -4.63, 95%CI -8.37 to -0.89) reduced pain significantly.; Danggui Sini decoction (risk ratio[RR] = 1.31, 95%CI 1.12 to 1.53), Danggui shaoyao san (RR = 1.23, 95%CI 1.05 to 1.44), Siwu decoction (RR = 1.32, 95%CI 1.17 to 1.47), Taohong Siwu Decoction (RR = 1.35, 95%CI 1.14 to 1.61), and Wenjing decoction (RR = 1.33, 95%CI 1.19 to 1.52) showed significantly higher overall response rates, and Wenjing decoction could significantly reduce TCM syndrome scores (MD = -4.14, 95%CI -6.84 to -1.44), compared with PGSIs. No serious adverse events were observed. Siwu decoction and Wenjing decoction ranked as the top treatment options in terms of all outcomes of interest (P-score ranking).

Conclusions

CHMs were associated with improved overall response rate, pain reduction, and alleviation of symptoms compared to conventional treatments for patients with PD, and no serious adverse events were observed. However, the confidence in the conclusions is limited because of the lack of high-quality trials.

引言原发性痛经(PD)是青少年和年轻女性常见的妇科疾病。中草药在中国已被广泛用于帕金森病的治疗。然而,不同CHM方案的相对优势仍不确定。本系统综述旨在使用网络荟萃分析比较不同中药治疗帕金森病的疗效和安全性。方法我们检索了PubMed、Embase、Web of Science、中国知识基础设施(CNKI)和中国生物医学文献数据库(CBM),从它们成立到2022年12月17日。随机对照试验(RCTs)将中药或中成药与前列腺素合成酶抑制剂(PGSI)进行比较。使用Cochrane偏倚风险工具评估偏倚风险。结果共纳入54例随机对照试验,5345例帕金森病患者。与PGSI相比,当归四逆汤(平均差[MD]=5.92,95%可信区间[CI]-8.64--3.20)和香附四物汤(MD=-4.63,95%CI-8.37--0.89)显著减轻疼痛。;当归四逆汤(危险比[RR]=1.31,95%CI 1.12至1.53)、当归烧药散(RR=1.23,95%CI 1.05至1.44)、四物汤(RR=1.32,95%CI 1.17至1.47)、桃红四物汤,温精汤可显著降低中医证候积分(MD=4.14,95%CI-6.84--1.44)。未观察到严重不良事件。在所有感兴趣的结果(P评分排名)方面,四物汤和文静汤是首选治疗方案。结论与常规治疗相比,sCHMs与PD患者的总有效率、疼痛减轻和症状减轻有关,没有观察到严重的不良事件。然而,由于缺乏高质量的试验,对结论的信心有限。
{"title":"Chinese herbal medicine for primary dysmenorrhea: A systematic review and network meta-analysis of 54 randomized controlled trials","authors":"Xinbin Wang ,&nbsp;Zhongwen Zhang ,&nbsp;Haorui Wang ,&nbsp;Ruilin Ma ,&nbsp;Lili Wang ,&nbsp;Xianhui Zhang ,&nbsp;Yi Zhang ,&nbsp;Rong Wang","doi":"10.1016/j.eujim.2023.102293","DOIUrl":"10.1016/j.eujim.2023.102293","url":null,"abstract":"<div><h3>Introduction</h3><p>Primary dysmenorrhea (PD) is a common gynecological complaint among adolescents and young women. Chinese herbal medicines (CHMs) have been widely used for PD treatment in China. However, the relative advantages of different CHM regimens remain uncertain. This systematic review aimed to compare the efficacy and safety of different CHMs for the treatment of PD using network meta-analysis.</p></div><div><h3>Methods</h3><p>We searched PubMed, Embase, Web of Science, China National Knowledge Infrastructure (CNKI), and Chinese BioMedical Literature Database (CBM) from their inception to December 17, 2022. Randomized controlled trials (RCTs) comparing CHM or Chinese patent drugs with Prostaglandin Synthetase Inhibitors (PGSIs) were included. Risk of bias was assessed using the Cochrane risk of bias tool. A frequentist framework network meta-analysis was performed using R (4.2.2).</p></div><div><h3>Results</h3><p>A total of 54 RCTs with 5,345 PD patients were included. Compared with PGSIs, Danggui Sini decoction (mean difference [MD] = -5.92, 95% confidence interval [CI] -8.64 to -3.20) and Xiangfu Siwu Decoction (MD = -4.63, 95%CI -8.37 to -0.89) reduced pain significantly.; Danggui Sini decoction (risk ratio[RR] = 1.31, 95%CI 1.12 to 1.53), Danggui shaoyao san (RR = 1.23, 95%CI 1.05 to 1.44), Siwu decoction (RR = 1.32, 95%CI 1.17 to 1.47), Taohong Siwu Decoction (RR = 1.35, 95%CI 1.14 to 1.61), and Wenjing decoction (RR = 1.33, 95%CI 1.19 to 1.52) showed significantly higher overall response rates, and Wenjing decoction could significantly reduce TCM syndrome scores (MD = -4.14, 95%CI -6.84 to -1.44), compared with PGSIs. No serious adverse events were observed. Siwu decoction and Wenjing decoction ranked as the top treatment options in terms of all outcomes of interest (P-score ranking).</p></div><div><h3>Conclusions</h3><p>CHMs were associated with improved overall response rate, pain reduction, and alleviation of symptoms compared to conventional treatments for patients with PD, and no serious adverse events were observed. However, the confidence in the conclusions is limited because of the lack of high-quality trials.</p></div>","PeriodicalId":11932,"journal":{"name":"European Journal of Integrative Medicine","volume":null,"pages":null},"PeriodicalIF":2.5,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45583358","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Moxibustion for chemotherapy-induced myelosuppression: A systematic review and meta-analysis 艾灸治疗化疗诱导的骨髓抑制:系统回顾和荟萃分析
IF 2.5 4区 医学 Q2 Medicine Pub Date : 2023-10-01 DOI: 10.1016/j.eujim.2023.102304
Xiao-Qing Wang , Yue Qiao , Yuan-Yuan Zhang , Li-Hua Yang , Pei-Bei Duan

Introduction

Myelosuppression is a common treatment-related complication in cancer patients. Moxibustion has been proposed as a potentially effective intervention to alleviate the side effects of chemotherapy-induced myelosuppression. This review aimed to investigate the effectiveness and safety of moxibustion in treating chemotherapy-induced myelosuppression, as well as the most promising modalities and patterns of moxibustion application.

Methods

We included randomised controlled trials (RCTs) focusing on the effectiveness of moxibustion on chemotherapy-induced myelosuppression, including the total effective rate, leukocyte count, hemoglobin level, platelet count, neutrophil count, and quality of life as outcomes. Six English and four Chinese databases were searched. Two researchers independently screened the articles, extracted data, and evaluated the quality of the included studies. The quality was assessed using the revised Cochrane Risk-of-Bias tool (RoB 2.0). Meta-regression and subgroup analyses were used to find the most effective modalities and treatment patterns. In addition, we utilised the Grading of Recommendations Assessment, Development, and Evaluation system to establish a persuasive conclusion. Data were meta-analysed using Stata (version 14.0).

Results

Twenty-one studies were included in this systematic review, including 1887 patients. The overall quality of all included studies was moderate. Meta-analysis of 9 RCTs indicated that moxibustion provided a greater therapeutic benefit in the treatment of chemotherapy-induced myelosuppression (RR=1.22, 95%CI=1.15, 1.29, P<0.001). Moreover, the results of 15 RCTs showed a significant increase in leukocyte count (WMD=0.62, 95% CI=0.08, 1.16, P=0.025); 3 RCTs showed elevated hemoglobin level (WMD=11.72, 95%CI=5.67, 17.76, P<0.001), and 3 RCTs showed increased platelet count (WMD=16.24, 95% CI=10.37, 22.11, P<0.001). Furthermore, the results of 5 RCTs showed a significant favourable effect on the quality of life (WMD=5.54, 95%CI=3.09, 7.98, P<0.001). We also assessed the certainty of the body of evidence and the results showed that the total effective rate was assessed as moderate quality, while others were rated as very low. There was no publication bias in this meta-analysis. In addition, five studies reported adverse effects, and none were serious.

Conclusions

Moxibustion may affect chemotherapy-induced myelosuppression. However, owing to the small number of included studies and their low methodological quality, more large-scale, multi-center, high-quality RCTs on moxibustion for chemotherapy-induced myelosuppression are needed.

Registration

CRD42022336319.

骨髓抑制是癌症患者常见的治疗相关并发症。艾灸已被提出作为一种潜在的有效干预措施,以减轻化疗引起的骨髓抑制的副作用。本文旨在探讨艾灸治疗化疗诱导的骨髓抑制的有效性和安全性,以及艾灸最有前景的应用方式和模式。方法采用随机对照试验(RCTs),观察艾灸对化疗诱导的骨髓抑制的疗效,包括总有效率、白细胞计数、血红蛋白水平、血小板计数、中性粒细胞计数和生活质量。检索了6个英文数据库和4个中文数据库。两位研究者独立筛选文章,提取数据,并评估纳入研究的质量。使用修订后的Cochrane风险偏倚工具(RoB 2.0)评估质量。采用meta回归和亚组分析来寻找最有效的治疗方式和治疗模式。此外,我们利用分级建议评估,发展和评价系统,以建立一个有说服力的结论。使用Stata(14.0版本)对数据进行meta分析。结果本系统综述纳入21项研究,共纳入1887例患者。所有纳入研究的总体质量均为中等。9项随机对照试验的荟萃分析表明,艾灸在化疗诱导的骨髓抑制治疗中提供了更大的治疗效益(RR=1.22, 95%CI=1.15, 1.29, P<0.001)。此外,15项rct结果显示白细胞计数显著增加(WMD=0.62, 95% CI=0.08, 1.16, P=0.025);3项rct显示血红蛋白水平升高(WMD=11.72, 95%CI=5.67, 17.76, P<0.001), 3项rct显示血小板计数升高(WMD=16.24, 95%CI= 10.37, 22.11, P<0.001)。此外,5项随机对照试验的结果显示对生活质量有显著的有利影响(WMD=5.54, 95%CI=3.09, 7.98, P<0.001)。我们还评估了证据体的确定性,结果显示总有效率被评为中等质量,而其他被评为非常低。本荟萃分析无发表偏倚。此外,有五项研究报告了不良反应,但没有一项是严重的。结论艾灸可影响化疗诱导的骨髓抑制。然而,由于纳入的研究数量少,方法学质量低,需要更多大规模、多中心、高质量的艾灸化疗诱导骨髓抑制的随机对照试验。
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引用次数: 0
Effectiveness and safety of the combination of Chinese herbal medicine and acupuncture for women with polycystic ovarian syndrome: A systematic review and meta-analysis of randomized controlled trials 中药结合针灸治疗女性多囊卵巢综合征的有效性和安全性:随机对照试验的系统评价和荟萃分析
IF 2.5 4区 医学 Q2 Medicine Pub Date : 2023-10-01 DOI: 10.1016/j.eujim.2023.102291
Xing-yan Liang , Chun-li Lu , Yu Su , Xin-yan Jin , Mu-lian Wu , Yao Lu , Yu Zhou , Zi-xun Zhuang , Chun Luo , Hong-xia Ma

Introduction

This systematic review aimed to evaluate the effectiveness and safety of Chinese herbal medicine (CHM) plus acupuncture for women with polycystic ovarian syndrome (PCOS).

Methods

We searched for eligible randomized controlled trials (RCTs) in nine Chinese and English databases from their inception to May 7, 2023. The Cochrane “Risk of bias” tool and the Grading of Recommendations Assessment, Development and Evaluation (GRADE) methods were used to assess the methodological quality and the certainty of the evidence. Effectiveness is presented as the risk ratio (RR) or mean difference with 95% confidence interval (CI).

Results

A total of 52 studies were included in this systematic review (n = 4180 participants). The overall quality of the RCTs was reduced by unclear or high risk of bias. The certainty of the evidence ranged from very low certainty to moderate certainty. None of the included studies reported the live birth rate. Among women with PCOS seeking fertility treatment, both CHM and acupuncture had a beneficial effect on the clinical pregnancy rate (CHM plus acupuncture (Intervention A), 9 RCTs, n = 754 participants, RR 1.28, 95% CI 1.10, 1.49; moderate certainty evidence; CHM plus acupuncture plus CMT (Intervention B), 16 RCTs, n = 1269 participants, RR 1.71, 95% CI 1.50, 1.94; moderate certainty evidence) and ovulation rate (Intervention A, 5 RCTs, n = 395 participants, RR 1.31, 95% CI 1.15, 1.49; low certainty evidence; Intervention B, 7 RCTs, n = 729 participants, RR 1.31, 95% CI 1.16, 1.48; low certainty evidence) compared to the control group.

Conclusions

There is currently very low to moderate certainty evidence that CHM plus acupuncture can improve the fertility and clinical symptoms of PCOS patients. Further rigorous, double-blinded, placebo-controlled trials are needed to determine the effectiveness of complex interventions of CHM plus acupuncture for treating PCOS.

本系统综述旨在评价中药联合针灸治疗女性多囊卵巢综合征(PCOS)的有效性和安全性。方法在9个中英文数据库中检索符合条件的随机对照试验(RCTs),检索时间为随机对照试验建立至2023年5月7日。使用Cochrane“偏倚风险”工具和分级推荐评估、发展和评价(GRADE)方法来评估方法学质量和证据的确定性。有效性表示为风险比(RR)或95%置信区间(CI)的平均差值。结果本次系统评价共纳入52项研究(n = 4180名受试者)。随机对照试验的总体质量因不明确或高偏倚风险而降低。证据的确定性从非常低的确定性到中等的确定性不等。纳入的研究均未报告活产率。在寻求生育治疗的PCOS女性中,中西医结合针灸对临床妊娠率均有有益影响(中西医结合针灸(干预a), 9项rct, n = 754名参与者,RR 1.28, 95% CI 1.10, 1.49;中等确定性证据;中医+针灸+ CMT(干预B), 16项随机对照试验,n = 1269名受试者,RR 1.71, 95% CI 1.50, 1.94;中等确定性证据)和排卵率(干预A, 5个rct, n = 395名参与者,RR 1.31, 95% CI 1.15, 1.49;低确定性证据;干预B, 7项rct, n = 729名参与者,RR 1.31, 95% CI 1.16, 1.48;低确定性证据)与对照组相比。结论中西医结合针灸治疗可改善PCOS患者的生育能力和临床症状,目前有极低到中等确定性的证据。需要进一步严格的、双盲的、安慰剂对照试验来确定中药加针灸治疗多囊卵巢综合征的复杂干预措施的有效性。
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引用次数: 0
Scoping review of clinical studies on Chinese herbal medicine against Helicobacter pylori and an exploration of its usage pattern 中药抗幽门螺杆菌临床研究综述及应用模式探讨
IF 2.5 4区 医学 Q2 Medicine Pub Date : 2023-10-01 DOI: 10.1016/j.eujim.2023.102268
Yang Zhang , Xiaoyang Hu , Huafeng Zhang , Yujia Pan , Zongyu Zhang , Tianjiao You , Yaguang Han , Jiali Wei , Wenjuan Shen

Introduction

Helicobacter pylori (H. pylori) is a highly infectious bacterium that can aggravate upper gastrointestinal diseases. With the increasingly serious problem of H. pylori drug resistance, it is important to identify new treatment methods. In recent years, there has been an increasing number of studies on the treatment of H. pylori infection and related diseases with Chinese herbal medicine (CHM). The effectiveness of CHM has also emerged. Therefore, the aim of this scoping review was to systematically identify and summarize the characteristics of randomized controlled trails (RCTs) evaluating CHM for treating H. pylori infection.

Methods

Three Chinese and two English language databases were comprehensively searched. Included studies were RCTs of H. pylori-positive patients evaluating oral CHM with or without Western Medicine (WM) compared to WM alone. A descriptive analysis of study characteristics and association rule mining in R Studio software were used to identify frequent herbal combinations. The Cochrane Collaboration Risk of Bias tool was used to assess study quality.

Results

Included were 165 RCTs, with 168 comparisons, involving 16,817 participants. All the RCTs were conducted in China and 68% were published after 2012. The quality of included studies was moderate. The RCTs evaluated 187 herbs that were used in various combinations in 91 types of CHM formulas. Most RCTs compared CHM plus WM to WM only (n = 103 comparisons). Only 68% of the RCTs evaluated a recommended WM triple or quadruple therapy. Results showed that Banxia Xiexin Decoction, Huangqi Jianzhong Decoction, Huanglian Wendan Decoction and Jinghua Weikang Capsule were commonly used. The association rules showed that golden thread (Coptis chinensis Franch.), debark peony root (Paeonia lactiflora Pall.), milkvetch root (Astragalus mongholicus Bunge), dandelion (Taraxacum mongolicum Hand.-Mazz.), dried tangerine peel (Citrus reticulata Blanco), tangshen (Codonopsis pilosula (Franch.) Nannf.), largehead atractylodes rhizome (Atractylodes macrocephala Koidz.), processing liquorice root (Glycyrrhiza glabra L.), pinellia tuber (Pinellia ternata (Thunb.) Makino) were commonly used clinically.

Conclusion

The findings from this review highlight the potential role of CHM formulas for treating H. Pylori and can be used to inform further clinical trials and systematic reviews.

幽门螺杆菌(helicobacter pylori, H. pylori)是一种传染性极强的细菌,可加重上消化道疾病。随着幽门螺杆菌耐药问题的日益严重,寻找新的治疗方法显得尤为重要。近年来,关于中药治疗幽门螺杆菌感染及相关疾病的研究越来越多。中西医结合的有效性也已显现。因此,本综述的目的是系统地识别和总结评估中西医结合治疗幽门螺杆菌感染的随机对照试验(rct)的特点。方法对3个中文数据库和2个英文数据库进行综合检索。纳入的研究是幽门螺杆菌阳性患者的随机对照试验,评估口服CHM联合或不联合西医(WM)与单独西医(WM)的比较。在R Studio软件中使用研究特征的描述性分析和关联规则挖掘来识别频繁的草药组合。使用Cochrane协作偏倚风险工具评估研究质量。结果纳入165项随机对照试验,168项比较,涉及16817名受试者。所有随机对照试验均在中国进行,其中68%发表于2012年以后。纳入的研究质量一般。随机对照试验评估了187种草药在91种中草药配方中的不同组合。大多数随机对照试验比较了CHM加WM和仅WM (n = 103个比较)。只有68%的随机对照试验评估了推荐的WM三联或四联治疗。结果显示,以半夏泻心汤、黄芪建中汤、黄连温丹汤、经花胃康胶囊为常用。关联规则显示:黄连(Coptis chinensis france .)、牡丹根(Paeonia lactiflora Pall.)、黄芪根(Astragalus mongholicus Bunge .)、蒲公英(Taraxacum mongolicum hand.mazz .)、干陈皮(Citrus reticulata Blanco)、唐参(Codonopsis pilosula .))、大头苍术(苍术)、加工甘草(glycyrhiza glabra L.)、半夏块茎(pinellia ternata (Thunb.))牧野)临床常用。结论本综述的发现突出了中草药方剂治疗幽门螺杆菌的潜在作用,并可用于进一步的临床试验和系统评价。
{"title":"Scoping review of clinical studies on Chinese herbal medicine against Helicobacter pylori and an exploration of its usage pattern","authors":"Yang Zhang ,&nbsp;Xiaoyang Hu ,&nbsp;Huafeng Zhang ,&nbsp;Yujia Pan ,&nbsp;Zongyu Zhang ,&nbsp;Tianjiao You ,&nbsp;Yaguang Han ,&nbsp;Jiali Wei ,&nbsp;Wenjuan Shen","doi":"10.1016/j.eujim.2023.102268","DOIUrl":"10.1016/j.eujim.2023.102268","url":null,"abstract":"<div><h3>Introduction</h3><p>Helicobacter pylori (H. pylori) is a highly infectious bacterium that can aggravate upper gastrointestinal diseases. With the increasingly serious problem of H. pylori drug resistance, it is important to identify new treatment methods. In recent years, there has been an increasing number of studies on the treatment of H. pylori infection and related diseases with Chinese herbal medicine (CHM). The effectiveness of CHM has also emerged. Therefore, the aim of this scoping review was to systematically identify and summarize the characteristics of randomized controlled trails (RCTs) evaluating CHM for treating H. pylori infection.</p></div><div><h3>Methods</h3><p>Three Chinese and two English language databases were comprehensively searched. Included studies were RCTs of H. pylori-positive patients evaluating oral CHM with or without Western Medicine (WM) compared to WM alone. A descriptive analysis of study characteristics and association rule mining in R Studio software were used to identify frequent herbal combinations. The Cochrane Collaboration Risk of Bias tool was used to assess study quality.</p></div><div><h3>Results</h3><p>Included were 165 RCTs, with 168 comparisons, involving 16,817 participants. All the RCTs were conducted in China and 68% were published after 2012. The quality of included studies was moderate. The RCTs evaluated 187 herbs that were used in various combinations in 91 types of CHM formulas. Most RCTs compared CHM plus WM to WM only (n = 103 comparisons). Only 68% of the RCTs evaluated a recommended WM triple or quadruple therapy. Results showed that Banxia Xiexin Decoction, Huangqi Jianzhong Decoction, Huanglian Wendan Decoction and Jinghua Weikang Capsule were commonly used. The association rules showed that golden thread (Coptis chinensis Franch.), debark peony root (Paeonia lactiflora Pall.), milkvetch root (Astragalus mongholicus Bunge), dandelion (Taraxacum mongolicum Hand.-Mazz.), dried tangerine peel (Citrus reticulata Blanco), tangshen (Codonopsis pilosula (Franch.) Nannf.), largehead atractylodes rhizome (Atractylodes macrocephala Koidz.), processing liquorice root (Glycyrrhiza glabra L.), pinellia tuber (Pinellia ternata (Thunb.) Makino) were commonly used clinically.</p></div><div><h3>Conclusion</h3><p>The findings from this review highlight the potential role of CHM formulas for treating H. Pylori and can be used to inform further clinical trials and systematic reviews.</p></div>","PeriodicalId":11932,"journal":{"name":"European Journal of Integrative Medicine","volume":null,"pages":null},"PeriodicalIF":2.5,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43462174","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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European Journal of Integrative Medicine
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