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Effects and safety of scalp acupuncture on swallowing function in patients with post-stroke dysphagia: A meta-analysis 头皮针刺对脑卒中后吞咽困难患者吞咽功能的影响和安全性:一项荟萃分析
IF 1.7 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2025-12-09 DOI: 10.1016/j.eujim.2025.102598
GuanChao Chen , WeiYu Wang , HangYu Li , Hong Zhang

Introduction

This study aimed to evaluate the safety and feasibility of scalp acupuncture (SA) on swallowing function in patients with post-stroke dysphagia (PSD).

Methods

China National Knowledge Infrastructure (CNKI), Wanfang Data, VIP Database, SinoMed, PubMed, Cochrane Library, Embase, and Web of Science were searched from database inception to 26 April 2025. The risk of bias was assessed using Cochrane Risk of Bias 2.0 (RoB 2.0). Statistical analysis was performed using Stata 18.0.

Results

Eighteen eligible papers, involving 1410 patients with PSD, were included. Meta-analysis showed that compared to conventional interventions alone, SA combined with conventional interventions significantly reduced water swallowing test (WST) scores [SMD=-1.00, 95 % CI (-1.35, -0.66), Z=-5.701, P = 0.000], reduced standardized swallowing assessment (SSA) scores [MD=-3.78, 95 % CI (-4.89, -2.68), Z=- 6.692, P = 0.000], increased swallowing quality of life (SWAL-QOL) scores [MD = 33.26, 95 % CI (12.79, 53.73), Z = 3.185, P = 0.001], reduced videofluoroscopic dysphagia scale (VDS) scores [MD = 6.28, 95 % CI (4.01, 8.55), Z = 5.419, P = 0.000], and increased Barthel index (BI) scores [MD = 11.62, 95 % CI (9.76, 13.48), Z = 12.248, P = 0.000]. The WST scores, SSA scores, and SWAL-QOL scores exhibited high heterogeneity. A funnel plot suggested no publication bias in WST scores (t = 0.78, P = 0.457). Sensitivity analysis showed strong robustness in the meta-analysis results for WST scores and SSA scores, while potential sources of heterogeneity were identified in SWAL-QOL scores. The quality of evidence was low for SWAL-QOL scores and high for the remaining scores.

Conclusion

Compared with conventional interventions alone, SA combined with conventional interventions has more advantages in improving the scores in WST, SSA, and SWAL-QOL in the treatment of PSD. However, the reliability of this conclusion is constrained by the low quality of evidence for outcome measures, the lack of regular follow-up, and the unclear risk of adverse events. To consolidate research findings and provide more reliable clinical guidance, future studies should prioritize conducting multicenter double-blind trials that incorporate regular follow-up, objective assessments, and standardized protocols.
本研究旨在评价头皮针刺(SA)对脑卒中后吞咽困难(PSD)患者吞咽功能的安全性和可行性。方法检索自建库至2025年4月26日的中国知网、万方数据、维普数据库、中国医学信息网、PubMed、Cochrane图书馆、Embase和Web of Science数据库。采用Cochrane risk of bias 2.0 (RoB 2.0)评估偏倚风险。采用Stata 18.0进行统计学分析。结果共纳入18篇符合条件的文献,涉及1410例PSD患者。meta分析显示,与单独进行常规干预相比,SA联合常规干预显著降低了水吞咽试验(WST)评分[SMD=-1.00, 95% CI (-1.35, -0.66), Z=-5.701, P = 0.000],降低了标准化吞咽评估(SSA)评分[MD=-3.78, 95% CI (-4.89, -2.68), Z=- 6.692, P = 0.000],提高了吞咽生活质量(swa - qol)评分[MD= 33.26, 95% CI (12.79, 53.73), Z= 3.185, P = 0.001],提高了吞咽质量评分[MD= 33.26, 95% CI (12.79, 53.73), Z= 3.185, P = 0.001]。影像透视吞咽困难量表(VDS)评分降低[MD = 6.28, 95% CI (4.01, 8.55), Z = 5.419, P = 0.000], Barthel指数(BI)评分升高[MD = 11.62, 95% CI (9.76, 13.48), Z = 12.248, P = 0.000]。WST评分、SSA评分和sal - qol评分均表现出较高的异质性。漏斗图显示WST评分无发表偏倚(t = 0.78, P = 0.457)。敏感性分析显示,WST评分和SSA评分的meta分析结果具有很强的稳健性,而sal - qol评分则存在潜在的异质性来源。SWAL-QOL评分的证据质量较低,其余评分的证据质量较高。结论与单纯常规干预相比,SA联合常规干预在提高PSD患者WST、SSA、swa - qol评分方面更有优势。然而,这一结论的可靠性受到结果测量证据质量低、缺乏定期随访和不良事件风险不明确的限制。为了巩固研究成果并提供更可靠的临床指导,未来的研究应优先开展多中心双盲试验,包括定期随访、客观评估和标准化方案。
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引用次数: 0
Using explainable machine learning to identify predictors of Kangaroo mother care implementation in Sierra Leone's healthcare system 使用可解释的机器学习来识别塞拉利昂医疗保健系统中袋鼠妈妈护理实施的预测因素
IF 1.7 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2025-12-09 DOI: 10.1016/j.eujim.2025.102596
Afeez A. Soladoye , David B. Olawade , Joseph E. Origbo , Kobloobase O. Usani , Ayomide Israel Adekoya , Ojima Z. Wada , Augustus Osborne

Introduction

Kangaroo Mother Care (KMC) reduces neonatal mortality and improves thermoregulation and breastfeeding, yet uptake remains inconsistent in Sierra Leone. Predictive and explainable tools could target implementation where the need is most significant and resources are scarce. This study aimed to predict KMC adoption and identify actionable predictors using explainable machine learning.

Methods

We analysed a nationally representative dataset from Sierra Leone comprising 7737 births. The study setting was Sierra Leone's healthcare system, with participants including mothers who delivered in health facilities. Following data preprocessing (imputation, MinMax normalisation, categorical encoding, and SMOTE for class imbalance), forward-backward selection reduced 22 candidate variables to 10 key predictors. Five classifiers were trained using a 70:30 stratified split: K-Nearest Neighbors (KNN), logistic regression (LR), Support Vector Machine (SVM), Random Forest (RF), and XGBoost. The outcome was KMC adoption (binary: received/not received). Performance was evaluated using accuracy, precision, recall, F1-score, and ROC-AUC. Interpretability was achieved through SHAP and LIME for global and local explanations.

Results

XGBoost performed best (accuracy 0.72, precision 0.75, recall 0.81, F1 0.78, ROC AUC 0.7685), followed by Random Forest. Predictors associated with KMC included delivery by caesarean section, type of birth, maternal employment, number of antenatal visits, place of delivery, health insurance coverage, and region, while sampling design variables captured contextual heterogeneity. SHAP and LIME consistently highlighted delivery characteristics and socio-economic factors as primary drivers.

Conclusion

Explainable ensemble models can flag infants likely to receive or miss KMC and indicate modifiable levers for improvement. High recall supports use as a screening aid to prioritise counselling, facility preparedness, and postnatal support. Prospective validation, threshold calibration, and integration within routine health information systems are warranted to translate these insights into sustained increases in KMC coverage in Sierra Leone and similar settings.
袋鼠妈妈护理(KMC)降低了新生儿死亡率,改善了体温调节和母乳喂养,但在塞拉利昂,这种做法仍然不一致。可预测和可解释的工具可以针对需求最大且资源稀缺的地方实施。本研究旨在预测KMC的采用,并使用可解释的机器学习识别可操作的预测因子。方法我们分析了塞拉利昂具有全国代表性的数据集,其中包括7737名新生儿。研究背景是塞拉利昂的医疗保健系统,参与者包括在医疗机构分娩的母亲。在进行数据预处理(imputation、MinMax归一化、分类编码和针对类不平衡的SMOTE)后,向前向后选择将22个候选变量减少到10个关键预测因子。使用70:30分层分割训练五个分类器:k -最近邻(KNN),逻辑回归(LR),支持向量机(SVM),随机森林(RF)和XGBoost。结果是KMC采用(二进制:接收/未接收)。使用准确性、精密度、召回率、f1评分和ROC-AUC对性能进行评估。通过SHAP和LIME实现了全球和局部解释的可解释性。结果xgboost表现最佳(正确率0.72,精密度0.75,召回率0.81,F1 0.78, ROC AUC 0.7685), Random Forest次之。与KMC相关的预测因子包括剖腹产分娩、分娩类型、产妇就业、产前检查次数、分娩地点、健康保险覆盖范围和地区,而抽样设计变量捕获了上下文异质性。SHAP和LIME始终强调交付特点和社会经济因素是主要驱动因素。结论可解释的整体模型可以标记婴儿可能接受或错过KMC,并指出改善的可修改杠杆。高回忆支持使用作为筛选援助,优先咨询,设施准备和产后支持。有必要进行前瞻性验证、阈值校准和常规卫生信息系统的整合,以将这些见解转化为塞拉利昂和类似环境中KMC覆盖率的持续增长。
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引用次数: 0
Prakriti-based differences in olfactory perception and receptor gene expression: An Ayurgenomics approach 嗅觉感知和受体基因表达的prakriti基础差异:Ayurgenomics方法
IF 1.7 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2025-12-09 DOI: 10.1016/j.eujim.2025.102599
Deepika Saini , Heena Saini , Neha Singh , Richa Tripathi , Meera K. Bhojani

Introduction

Ayurgenomics, a pioneering approach integrating Ayurveda and genomics, offers a novel perspective to examine inter-individual variability in terms of health, disease susceptibility, and its recovery. This study explores the relationship between Ayurvedic Prakritis (Vata, Pitta, Kapha) and olfactory perception, alongside its underlying genetic expression patterns, to better understand the biological basis of Prakriti classification. This study aimed to examine differences in olfactory perception and olfactory receptor gene expression among individuals with extreme Prakriti types, as classified by Ayurveda, and to explore potential correlations between these molecular variations and Prakriti-specific phenotypes.

Methods

A total of 400 candidates (staff, students and patients attendant) from All India Institute of Ayurveda were initially screened using the CCRAS-SAS. Out of these, 300 healthy participants were enrolled and later assessed for three extreme Prakriti phenotypes Vata, Pitta, and Kapha. Among them, 28 were identified with Ekdoshaja Prakriti and chosen for olfactory perception analysis and 24 participants were selected for olfactory receptor gene expression profiling. Olfactory performance was assessed using the Sniffin Sticks Test, evaluating domains, T-score, D-score, and I-score. Expression levels of olfactory genes were quantified using Quantitative PCR.

Results

Significant differences in olfactory performance were observed across the three Prakriti phenotypes, where Kapha showed the best T score, Pitta showed the best D and I score, and Kapha and Pitta had the best TDI score. OR6K3 gene expression was significantly downregulated in Pitta and Kapha Prakritis. However, OR10Z1 gene expression was upregulated in Kapha relative to the other two Prakriti. We have taken Vata Prakriti as reference. Although the study was conducted on a relatively small sample size, the findings provide valuable preliminary insights into the association between Prakriti types, olfactory perception, and OR gene expression.

Conclusion

This study reveals that individuals from different Prakriti groups display distinct phenotypic traits in olfactory perception along with specific molecular variations. However, these findings should be interpreted in light of the study’s limitations, including a narrow sample drawn from a single institution and a relatively small number of participants. Further studies with larger and more diverse populations are needed to validate these observations.
阿育吠陀基因组学是一种整合阿育吠陀和基因组学的开创性方法,为研究健康、疾病易感性及其恢复方面的个体间差异提供了一种新的视角。本研究探讨了阿育吠陀Prakritis (Vata, Pitta, Kapha)与嗅觉感知之间的关系,以及其潜在的基因表达模式,以更好地了解Prakriti分类的生物学基础。本研究旨在研究阿育吠陀分类的极端Prakriti类型个体的嗅觉感知和嗅觉受体基因表达差异,并探讨这些分子变异与Prakriti特异性表型之间的潜在相关性。方法采用CCRAS-SAS对全印度阿育吠陀研究所的400名候选人(工作人员、学生和患者)进行初步筛选。在这些人中,300名健康参与者被招募,随后对三种极端的Prakriti表型Vata、Pitta和Kapha进行了评估。其中28人被鉴定为Ekdoshaja Prakriti并选择进行嗅觉感知分析,24人被选择进行嗅觉受体基因表达谱分析。嗅觉性能评估使用嗅嗅棒测试,评估域,t得分,d得分和i得分。采用定量PCR法测定嗅觉基因的表达水平。结果三种Prakriti表型在嗅觉表现上存在显著差异,Kapha的T得分最高,Pitta的D和I得分最高,Kapha和Pitta的TDI得分最高。在Pitta和Kapha Prakritis中,OR6K3基因表达显著下调。然而,OR10Z1基因在Kapha中的表达相对于其他两个Prakriti上调。我们以Vata Prakriti作为参考。虽然这项研究的样本量相对较小,但研究结果为Prakriti类型、嗅觉感知和OR基因表达之间的关系提供了有价值的初步见解。结论本研究揭示了不同Prakriti群体的个体在嗅觉感知方面表现出不同的表型特征和特定的分子变异。然而,这些发现应该根据研究的局限性来解释,包括从单一机构抽取的狭窄样本和相对较少的参与者。需要对更大、更多样化的种群进行进一步的研究来验证这些观察结果。
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引用次数: 0
Cannabidiol (CBD): An acceptable non-hormonal treatment option for women suffering with chronic pelvic pain – a cross-sectional observational study 大麻二酚(CBD):一项横断面观察性研究:慢性盆腔疼痛妇女可接受的非激素治疗选择
IF 1.7 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2025-12-06 DOI: 10.1016/j.eujim.2025.102597
Aisha Anwar , Tara Ajith , Róisín Lewis , Vickie Kimandi , Andrew J Drakeley , Dharani K Hapangama , Nicola Tempest

Introduction

Chronic pelvic pain (CPP) represents a significant health issue among women, profoundly impacting their quality of life. Current treatment modalities primarily include hormonal therapy, analgesics, or surgical interventions, which may have side effects or be unsuitable for women attempting to conceive. The objective of this study is to determine if cannabidiol (CBD) is an acceptable non-hormonal self-management option for women with CPP.

Methods

A prospective, cross sectional observational questionnaire study that included 200 women with CPP who attended the gynaecological department at the Liverpool Women’s Hospital (LWH), UK, over a six-month period. The main outcomes included acceptability of CBD as a non-hormonal treatment option for CPP, current treatments/self-management strategies utilised, and interest in participation in future trials investigating CBD for CPP management.

Results

Sixteen % (n = 32) of the questioned cohort were taking alternative treatments, 16.3 % (n = 26) had tried cannabis (prescribed/illicit), and 21.3 % (n = 34) had tried Hemp/CBD oil as an alternative treatment option. A total of 82.5 % (n = 165) of respondents were willing to try CBD; 73.9 % (n = 139) oral, 69.7 % (n = 131) a skin patch, 72.3 % (n = 136) a balm/gel and 33 % (n = 62) a CBD infused tampon. Most women, 75.5 % (n = 151), revealed their willingness to take part in future trials involving CBD as a treatment option.

Conclusion

CPP remains inadequately treated, leading many women to seek alternative therapies. CBD is considered an acceptable option, with a high proportion of surveyed women reporting current or past use to manage their symptoms.
慢性盆腔疼痛(CPP)是女性中一个重要的健康问题,严重影响她们的生活质量。目前的治疗方式主要包括激素治疗、镇痛药或手术干预,这些方法可能有副作用或不适合尝试怀孕的妇女。本研究的目的是确定大麻二酚(CBD)是否是CPP女性可接受的非激素自我管理选择。方法一项前瞻性、横断面观察性问卷调查研究,包括200名在英国利物浦妇女医院(LWH)妇科就诊的CPP妇女,为期6个月。主要结果包括CBD作为CPP的非激素治疗选择的可接受性,目前使用的治疗/自我管理策略,以及参与未来研究CBD用于CPP管理的试验的兴趣。结果16% (n = 32)的患者正在接受替代治疗,16.3% (n = 26)的患者尝试过大麻(处方/非法),21.3% (n = 34)的患者尝试过大麻/CBD油作为替代治疗方案。共有82.5% (n = 165)的受访者愿意尝试CBD;73.9% (n = 139)使用口服,69.7% (n = 131)使用皮肤贴,72.3% (n = 136)使用香膏/凝胶,33% (n = 62)使用注入CBD的卫生棉条。大多数女性(75.5% (n = 151))表示,她们愿意参加将CBD作为治疗选择的未来试验。结论cpp治疗仍不充分,导致许多妇女寻求替代治疗。CBD被认为是一种可接受的选择,有很高比例的受访妇女报告目前或过去使用CBD来控制她们的症状。
{"title":"Cannabidiol (CBD): An acceptable non-hormonal treatment option for women suffering with chronic pelvic pain – a cross-sectional observational study","authors":"Aisha Anwar ,&nbsp;Tara Ajith ,&nbsp;Róisín Lewis ,&nbsp;Vickie Kimandi ,&nbsp;Andrew J Drakeley ,&nbsp;Dharani K Hapangama ,&nbsp;Nicola Tempest","doi":"10.1016/j.eujim.2025.102597","DOIUrl":"10.1016/j.eujim.2025.102597","url":null,"abstract":"<div><h3>Introduction</h3><div>Chronic pelvic pain (CPP) represents a significant health issue among women, profoundly impacting their quality of life. Current treatment modalities primarily include hormonal therapy, analgesics, or surgical interventions, which may have side effects or be unsuitable for women attempting to conceive. The objective of this study is to determine if cannabidiol (CBD) is an acceptable non-hormonal self-management option for women with CPP.</div></div><div><h3>Methods</h3><div>A prospective, cross sectional observational questionnaire study that included 200 women with CPP who attended the gynaecological department at the Liverpool Women’s Hospital (LWH), UK, over a six-month period. The main outcomes included acceptability of CBD as a non-hormonal treatment option for CPP, current treatments/self-management strategies utilised, and interest in participation in future trials investigating CBD for CPP management.</div></div><div><h3>Results</h3><div>Sixteen % (<em>n</em> = 32) of the questioned cohort were taking alternative treatments, 16.3 % (<em>n</em> = 26) had tried cannabis (prescribed/illicit), and 21.3 % (<em>n</em> = 34) had tried Hemp/CBD oil as an alternative treatment option. A total of 82.5 % (<em>n</em> = 165) of respondents were willing to try CBD; 73.9 % (<em>n</em> = 139) oral, 69.7 % (<em>n</em> = 131) a skin patch, 72.3 % (<em>n</em> = 136) a balm/gel and 33 % (<em>n</em> = 62) a CBD infused tampon. Most women, 75.5 % (<em>n</em> = 151), revealed their willingness to take part in future trials involving CBD as a treatment option.</div></div><div><h3>Conclusion</h3><div>CPP remains inadequately treated, leading many women to seek alternative therapies. CBD is considered an acceptable option, with a high proportion of surveyed women reporting current or past use to manage their symptoms.</div></div>","PeriodicalId":11932,"journal":{"name":"European Journal of Integrative Medicine","volume":"81 ","pages":"Article 102597"},"PeriodicalIF":1.7,"publicationDate":"2025-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145786859","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
The effectiveness and safety of GeloMyrtol® forte in the treatment of acute and chronic bronchitis: A rapid review of clinical studies GeloMyrtol®forte治疗急慢性支气管炎的有效性和安全性:临床研究的快速回顾
IF 1.7 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2025-12-03 DOI: 10.1016/j.eujim.2025.102594
Mohsen Sobh , Mohammad Oli Al Islam , Katrin Vagedes , Rolf Heine , Thomas Breitkreuz , Henrik Szőke , Holger Cramer , Jan Vagedes

Introduction

Bronchitis is a global health burden characterized by symptoms such as cough, sputum production, and respiratory distress. Although the efficacy of GeloMyrtol forte, an herbal product, in treating bronchitis has been evaluated in clinical trials, no reviews have yet been conducted.

Methods

This rapid review included the systematic search of PubMed, Cochrane, CINAHL, and CAMbase from inception to February 2025 for clinical trials that investigated the efficacy of GeloMyrtol forte in treating acute or chronic bronchitis. Two independent reviewers screened the resulting papers for eligibility criteria and extracted the relevant data for data synthesis. The risk of bias in the included randomized controlled trials was assessed using the Revised Cochrane Risk-of-Bias tool (RoB-2).

Results

The systematic search in four databases yielded 28 papers, four of which met the inclusion criteria. These four studies included 1846 patients (511 children) with acute (three studies) or chronic (one study) bronchitis. GeloMyrtol forte reduced cough exacerbations and the need for antibiotics, improved respiratory function and sputum consistency, and led to a statistically significant reduction in symptom duration compared to placebo. Side effects were rare, mainly affecting the gastrointestinal tract, and resolved spontaneously. No study examined the effects of GeloMyrtol forte in pregnancy or lactation.

Conclusions

Oral administration of GeloMyrtol forte reduces the intensity and frequency of the signs and symptoms associated with bronchitis, provided that there is no severe infection and no underlying chronic disease.
支气管炎是一种以咳嗽、咳痰和呼吸窘迫等症状为特征的全球性健康负担。虽然GeloMyrtol forte(一种草药产品)治疗支气管炎的疗效已经在临床试验中进行了评估,但尚未进行任何评论。方法本快速回顾包括系统检索PubMed、Cochrane、CINAHL和CAMbase从成立到2025年2月的临床试验,研究GeloMyrtol治疗急性或慢性支气管炎的疗效。两名独立审稿人筛选结果论文的资格标准,并提取相关数据进行数据综合。纳入的随机对照试验的偏倚风险采用修订后的Cochrane风险偏倚工具(rob2)进行评估。结果系统检索4个数据库共获得28篇论文,其中4篇符合纳入标准。这4项研究纳入了1846例急性(3项研究)或慢性(1项研究)支气管炎患者(511名儿童)。与安慰剂相比,GeloMyrtol forte减少了咳嗽加重和对抗生素的需求,改善了呼吸功能和痰稠度,并导致症状持续时间的统计学显着缩短。副作用罕见,主要影响胃肠道,自行消退。目前还没有研究检验强效gelomytorl对妊娠或哺乳期的影响。结论:在无严重感染和无潜在慢性疾病的情况下,口服强力吉罗洛可降低支气管炎相关体征和症状的强度和频率。
{"title":"The effectiveness and safety of GeloMyrtol® forte in the treatment of acute and chronic bronchitis: A rapid review of clinical studies","authors":"Mohsen Sobh ,&nbsp;Mohammad Oli Al Islam ,&nbsp;Katrin Vagedes ,&nbsp;Rolf Heine ,&nbsp;Thomas Breitkreuz ,&nbsp;Henrik Szőke ,&nbsp;Holger Cramer ,&nbsp;Jan Vagedes","doi":"10.1016/j.eujim.2025.102594","DOIUrl":"10.1016/j.eujim.2025.102594","url":null,"abstract":"<div><h3>Introduction</h3><div>Bronchitis is a global health burden characterized by symptoms such as cough, sputum production, and respiratory distress. Although the efficacy of GeloMyrtol forte, an herbal product, in treating bronchitis has been evaluated in clinical trials, no reviews have yet been conducted.</div></div><div><h3>Methods</h3><div>This rapid review included the systematic search of PubMed, Cochrane, CINAHL, and CAMbase from inception to February 2025 for clinical trials that investigated the efficacy of GeloMyrtol forte in treating acute or chronic bronchitis. Two independent reviewers screened the resulting papers for eligibility criteria and extracted the relevant data for data synthesis. The risk of bias in the included randomized controlled trials was assessed using the Revised Cochrane Risk-of-Bias tool (RoB-2).</div></div><div><h3>Results</h3><div>The systematic search in four databases yielded 28 papers, four of which met the inclusion criteria. These four studies included 1846 patients (511 children) with acute (three studies) or chronic (one study) bronchitis. GeloMyrtol forte reduced cough exacerbations and the need for antibiotics, improved respiratory function and sputum consistency, and led to a statistically significant reduction in symptom duration compared to placebo. Side effects were rare, mainly affecting the gastrointestinal tract, and resolved spontaneously. No study examined the effects of GeloMyrtol forte in pregnancy or lactation.</div></div><div><h3>Conclusions</h3><div>Oral administration of GeloMyrtol forte reduces the intensity and frequency of the signs and symptoms associated with bronchitis, provided that there is no severe infection and no underlying chronic disease.</div></div>","PeriodicalId":11932,"journal":{"name":"European Journal of Integrative Medicine","volume":"81 ","pages":"Article 102594"},"PeriodicalIF":1.7,"publicationDate":"2025-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145733032","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
Acupoint catgut embedding for functional constipation: a meta-analysis and data mining of randomized controlled trials 穴位埋线治疗功能性便秘:随机对照试验的荟萃分析和数据挖掘
IF 1.7 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2025-12-01 DOI: 10.1016/j.eujim.2025.102593
Peijia Li , Fumin Wang , Rudan Zheng , Yuxuan Chao , Qinxiu Zhang

Introduction

Functional constipation (FC) is a common gastrointestinal disorder. Acupoint catgut embedding (ACE) is widely used for FC management. This review aimed to investigate the effectiveness, safety and core acupoint combinations of ACE for FC.

Methods

We searched 9 databases and several registration platforms from inception to July 2025 for randomized controlled trials (RCTs) comparing ACE with conventional drugs, manual acupuncture (MA), or sham ACE. Meta-analysis, risk of bias assessment, and GRADE evaluation of evidence certainty were performed. Gephi-0.9.2 was utilized for visualizing the complex networks.

Results

A total of 27 RCTs (n = 2221) were included. ACE significantly improved complete spontaneous bowel movements (CSBM) compared with MA (MD, 1.12, 95 % CI [0.60, 1.64]) and sham ACE (MD, 1.70, 95 % CI [0.94, 2.46]), with the latter exceeding the minimal clinically important difference (MCID). ACE also demonstrated higher total effective rates compared to conventional drugs. (RR, 1.15, 95 % CI [1.09, 1.21]), MA (RR, 1.17, 95 % CI [1.09, 1.25]) and sham ACE (RR, 1.79, 95 % CI [1.18, 2.70]). Superior total effective rate at follow-up was observed over conventional drugs (RR, 1.46, 95 % CI [1.15, 1.84]) and MA (RR, 1.47, 95 % CI [1.06, 2.03]). Additionally, ACE outperformed conventional drugs in improving stool formation (MD, 0.52, 95 % CI [0.18, 0.86]). ACE exhibited a more significant improvement in quality of life compared to conventional drugs (MD, -6.95, 95 % CI [-10.36, -3.54]), MA (MD, -3.11, 95 % CI [-6.06, -0.16], p = 0.04) and sham ACE (MD, -8.18, 95 % CI [-11.63, -4.73]), and all the differences reached the MCID. Adverse events were minimal and occurred infrequently. The evidence certainty ranged from very low to moderate. Core acupoints included ST25, SP15, ST37, RN4, RN12, BL25, ST36, RN6, SJ6.

Conclusion

ACE may be an effective and safe option for FC, and the analysis of core acupoints provided important treatment direction. Nevertheless, the review highlighted the necessity for well-designed, higher-quality experiments.
功能性便秘(FC)是一种常见的胃肠道疾病。穴位埋线(ACE)被广泛应用于FC治疗。本综述旨在探讨ACE治疗FC的有效性、安全性和核心穴位组合。方法我们检索了9个数据库和多个注册平台,从成立到2025年7月,将ACE与常规药物、手工针灸(MA)或假ACE进行比较的随机对照试验(rct)。进行meta分析、偏倚风险评估和GRADE证据确定性评价。使用Gephi-0.9.2对复杂网络进行可视化。结果共纳入27项rct (n = 2221)。与MA (MD, 1.12, 95% CI[0.60, 1.64])和假ACE (MD, 1.70, 95% CI[0.94, 2.46])相比,ACE显著改善了完全自发排便(CSBM),后者超过了最小临床重要差异(MCID)。与常规药物相比,ACE也显示出更高的总有效率。(RR, 1.15, 95% CI[1.09, 1.21])、MA (RR, 1.17, 95% CI[1.09, 1.25])和假性ACE (RR, 1.79, 95% CI[1.18, 2.70])。随访总有效率优于常规药物(RR, 1.46, 95% CI[1.15, 1.84])和MA (RR, 1.47, 95% CI[1.06, 2.03])。此外,ACE在改善大便形成方面优于常规药物(MD, 0.52, 95% CI[0.18, 0.86])。ACE与常规药物(MD, -6.95, 95% CI[-10.36, -3.54])、MA (MD, -3.11, 95% CI [-6.06, -0.16], p = 0.04)、假药ACE (MD, -8.18, 95% CI[-11.63, -4.73])相比,生活质量的改善更为显著,且差异均达到MCID。不良事件极少且不常发生。证据确定性从极低到中等不等。核心穴位包括ST25、SP15、ST37、RN4、RN12、BL25、ST36、RN6、SJ6。结论ace可能是一种安全有效的治疗方法,对核心穴位的分析提供了重要的治疗方向。然而,这篇综述强调了设计良好、质量更高的实验的必要性。
{"title":"Acupoint catgut embedding for functional constipation: a meta-analysis and data mining of randomized controlled trials","authors":"Peijia Li ,&nbsp;Fumin Wang ,&nbsp;Rudan Zheng ,&nbsp;Yuxuan Chao ,&nbsp;Qinxiu Zhang","doi":"10.1016/j.eujim.2025.102593","DOIUrl":"10.1016/j.eujim.2025.102593","url":null,"abstract":"<div><h3>Introduction</h3><div>Functional constipation (FC) is a common gastrointestinal disorder. Acupoint catgut embedding (ACE) is widely used for FC management. This review aimed to investigate the effectiveness, safety and core acupoint combinations of ACE for FC.</div></div><div><h3>Methods</h3><div>We searched 9 databases and several registration platforms from inception to July 2025 for randomized controlled trials (RCTs) comparing ACE with conventional drugs, manual acupuncture (MA), or sham ACE. Meta-analysis, risk of bias assessment, and GRADE evaluation of evidence certainty were performed. Gephi-0.9.2 was utilized for visualizing the complex networks.</div></div><div><h3>Results</h3><div>A total of 27 RCTs (<em>n</em> = 2221) were included. ACE significantly improved complete spontaneous bowel movements (CSBM) compared with MA (MD, 1.12, 95 % CI [0.60, 1.64]) and sham ACE (MD, 1.70, 95 % CI [0.94, 2.46]), with the latter exceeding the minimal clinically important difference (MCID). ACE also demonstrated higher total effective rates compared to conventional drugs. (RR, 1.15, 95 % CI [1.09, 1.21]), MA (RR, 1.17, 95 % CI [1.09, 1.25]) and sham ACE (RR, 1.79, 95 % CI [1.18, 2.70]). Superior total effective rate at follow-up was observed over conventional drugs (RR, 1.46, 95 % CI [1.15, 1.84]) and MA (RR, 1.47, 95 % CI [1.06, 2.03]). Additionally, ACE outperformed conventional drugs in improving stool formation (MD, 0.52, 95 % CI [0.18, 0.86]). ACE exhibited a more significant improvement in quality of life compared to conventional drugs (MD, -6.95, 95 % CI [-10.36, -3.54]), MA (MD, -3.11, 95 % CI [-6.06, -0.16], <em>p</em> = 0.04) and sham ACE (MD, -8.18, 95 % CI [-11.63, -4.73]), and all the differences reached the MCID. Adverse events were minimal and occurred infrequently. The evidence certainty ranged from very low to moderate. Core acupoints included ST25, SP15, ST37, RN4, RN12, BL25, ST36, RN6, SJ6.</div></div><div><h3>Conclusion</h3><div>ACE may be an effective and safe option for FC, and the analysis of core acupoints provided important treatment direction. Nevertheless, the review highlighted the necessity for well-designed, higher-quality experiments.</div></div>","PeriodicalId":11932,"journal":{"name":"European Journal of Integrative Medicine","volume":"81 ","pages":"Article 102593"},"PeriodicalIF":1.7,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145733035","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
Integrative approaches to eye health and disease 眼科健康和疾病的综合方法
IF 1.7 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2025-12-01 DOI: 10.1016/j.eujim.2025.102587
Mojtaba Heydari , Mohammad Hashem Hashempur
NA
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引用次数: 0
Opinion: A 2025 review of chiropractic spinal manipulation for headaches was bound for null results 观点:2025年的一项关于脊椎按摩治疗头痛的综述注定是无效的
IF 1.7 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2025-11-29 DOI: 10.1016/j.eujim.2025.102591
Zachary E. Scott , Robert J. Trager , Casper Nim , Dean L. Smith

Introduction

A systematic review by Ceballos-Laita et al. in 2025 published in the European Journal of Integrative Medicine (DOI: 10.1016/j.eujim.2025.102462) concluded the effectiveness of chiropractic spinal manipulation for cervicogenic, tension-type, and migraine headaches was uncertain, with very low evidence certainty. We highlight limitations in the review’s methods which were bound to lead to a null result that undermine its validity.

Conclusion

Methodological flaws, including, post-hoc protocol deviations, heterogeneity, inconsistencies and potential bias cast doubt on the review’s findings. Clinicians and stakeholders should interpret its results cautiously, considering existing meta-analyses examining spinal manipulation for specific headache types and populations.
Ceballos-Laita等人于2025年发表在《欧洲中西医结合杂志》(DOI: 10.1016/ j.j eujim.2025.102462)上的一篇系统综述得出结论,脊椎推拿治疗颈源性、紧张型和偏头痛的有效性不确定,证据确定性非常低。我们强调了综述方法的局限性,这些局限性必然会导致无效结果,从而破坏其有效性。方法学上的缺陷,包括事后方案偏差、异质性、不一致性和潜在的偏倚,使人们对综述的发现产生怀疑。临床医生和利益相关者应谨慎解释其结果,考虑到现有的荟萃分析检查脊柱操作对特定头痛类型和人群的影响。
{"title":"Opinion: A 2025 review of chiropractic spinal manipulation for headaches was bound for null results","authors":"Zachary E. Scott ,&nbsp;Robert J. Trager ,&nbsp;Casper Nim ,&nbsp;Dean L. Smith","doi":"10.1016/j.eujim.2025.102591","DOIUrl":"10.1016/j.eujim.2025.102591","url":null,"abstract":"<div><h3>Introduction</h3><div>A systematic review by Ceballos-Laita et al. in 2025 published in the European Journal of Integrative Medicine (DOI: 10.1016/j.eujim.2025.102462) concluded the effectiveness of chiropractic spinal manipulation for cervicogenic, tension-type, and migraine headaches was uncertain, with very low evidence certainty. We highlight limitations in the review’s methods which were bound to lead to a null result that undermine its validity.</div></div><div><h3>Conclusion</h3><div>Methodological flaws, including, post-hoc protocol deviations, heterogeneity, inconsistencies and potential bias cast doubt on the review’s findings. Clinicians and stakeholders should interpret its results cautiously, considering existing meta-analyses examining spinal manipulation for specific headache types and populations.</div></div>","PeriodicalId":11932,"journal":{"name":"European Journal of Integrative Medicine","volume":"81 ","pages":"Article 102591"},"PeriodicalIF":1.7,"publicationDate":"2025-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145733033","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
Stakeholder preferences for traditional Chinese medicine services: A systematic review of discrete choice experiments in integrative healthcare 利益相关者对中医服务的偏好:综合医疗中离散选择实验的系统回顾
IF 1.7 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2025-11-29 DOI: 10.1016/j.eujim.2025.102592
Meiyu Zhu , Daiying Wu , Xiaoting Sun , Tongyu Zhang , Chunmei Zhang

Introduction

Traditional Chinese medicine (TCM) is increasingly being integrated into modern healthcare systems worldwide. Understanding stakeholder preferences for TCM services is essential for developing culturally appropriate, patient-centered models of integrative care. This systematic review aims to synthesize and assess evidence from discrete choice experiments (DCEs) to reveal stakeholder preferences for TCM services.

Methods

A systematic literature review was conducted in PubMed, Embase, Web of Science, CINAHL, PsycINFO, CNKI, Wanfang, and SinoMed databases up to December 2024. Studies were included if they used DCE methodology to examine stakeholder preferences for TCM services among patients, healthcare providers, or the general population. Non-empirical articles and reviews were excluded. Two reviewers independently conducted the screening, data extraction, and quality appraisal. Data were synthesized narratively, and semi-quantitative analyses were used to evaluate the frequency, importance, and significance of each attribute. The review protocol was registered in PROSPERO (CRD420250632293).

Results

A total of 23 studies were included. Attributes were primarily identified through literature review and expert consultation. Service cost and service convenience were the most frequently examined attributes. Among the 124 identified attributes, 87.1 % were statistically significant. Service experience, therapeutic effects, and service model were most often ranked as the most important attributes. Willingness-to-pay (WTP) varied considerably, with the highest values observed for service experience.

Conclusions

Stakeholders place considerable value on cost, convenience, and service quality when choosing TCM services. These findings provide important evidence to support the development of personalized, patient-centered TCM service models and inform health policy and practice to enhance the accessibility and acceptance of TCM.
传统中医(TCM)正日益融入世界各地的现代医疗保健系统。了解利益相关者对中医服务的偏好对于发展文化上合适的、以患者为中心的综合护理模式至关重要。本系统综述旨在综合和评估离散选择实验(DCEs)的证据,以揭示利益相关者对中医服务的偏好。方法采用截至2024年12月的PubMed、Embase、Web of Science、CINAHL、PsycINFO、CNKI、万方、SinoMed等数据库进行系统文献综述。如果研究使用DCE方法来检查患者、医疗保健提供者或一般人群中利益相关者对中医服务的偏好,则纳入研究。非实证文章和综述被排除在外。两名审稿人独立进行筛选、数据提取和质量评估。对数据进行叙述性的综合,并采用半定量分析来评估每个属性的频率、重要性和意义。该审查方案已在PROSPERO注册(CRD420250632293)。结果共纳入23项研究。主要通过文献回顾和专家咨询来确定属性。服务成本和服务便利性是最常被检查的属性。在确定的124个属性中,87.1%具有统计学意义。服务体验、治疗效果和服务模式通常被列为最重要的属性。支付意愿(WTP)差异很大,服务体验的值最高。结论利益相关者在选择中医服务时,更看重成本、便利性和服务质量。这些发现为个性化、以患者为中心的中医服务模式的发展提供了重要证据,并为卫生政策和实践提供了信息,以提高中医的可及性和可接受性。
{"title":"Stakeholder preferences for traditional Chinese medicine services: A systematic review of discrete choice experiments in integrative healthcare","authors":"Meiyu Zhu ,&nbsp;Daiying Wu ,&nbsp;Xiaoting Sun ,&nbsp;Tongyu Zhang ,&nbsp;Chunmei Zhang","doi":"10.1016/j.eujim.2025.102592","DOIUrl":"10.1016/j.eujim.2025.102592","url":null,"abstract":"<div><h3>Introduction</h3><div>Traditional Chinese medicine (TCM) is increasingly being integrated into modern healthcare systems worldwide. Understanding stakeholder preferences for TCM services is essential for developing culturally appropriate, patient-centered models of integrative care. This systematic review aims to synthesize and assess evidence from discrete choice experiments (DCEs) to reveal stakeholder preferences for TCM services.</div></div><div><h3>Methods</h3><div>A systematic literature review was conducted in PubMed, Embase, Web of Science, CINAHL, PsycINFO, CNKI, Wanfang, and SinoMed databases up to December 2024. Studies were included if they used DCE methodology to examine stakeholder preferences for TCM services among patients, healthcare providers, or the general population. Non-empirical articles and reviews were excluded. Two reviewers independently conducted the screening, data extraction, and quality appraisal. Data were synthesized narratively, and semi-quantitative analyses were used to evaluate the frequency, importance, and significance of each attribute. The review protocol was registered in PROSPERO (CRD420250632293).</div></div><div><h3>Results</h3><div>A total of 23 studies were included. Attributes were primarily identified through literature review and expert consultation. Service cost and service convenience were the most frequently examined attributes. Among the 124 identified attributes, 87.1 % were statistically significant. Service experience, therapeutic effects, and service model were most often ranked as the most important attributes. Willingness-to-pay (WTP) varied considerably, with the highest values observed for service experience.</div></div><div><h3>Conclusions</h3><div>Stakeholders place considerable value on cost, convenience, and service quality when choosing TCM services. These findings provide important evidence to support the development of personalized, patient-centered TCM service models and inform health policy and practice to enhance the accessibility and acceptance of TCM.</div></div>","PeriodicalId":11932,"journal":{"name":"European Journal of Integrative Medicine","volume":"81 ","pages":"Article 102592"},"PeriodicalIF":1.7,"publicationDate":"2025-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145836857","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
The efficacy and safety of Shensong Yangxin capsule combination therapy in chronic heart failure combined with atrial fibrillation: A systematic review and meta-analysis 参松养心胶囊联合治疗慢性心力衰竭合并心房颤动的疗效和安全性:一项系统综述和meta分析
IF 1.7 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2025-11-28 DOI: 10.1016/j.eujim.2025.102590
Heng Sun , Zuoying Xing , Genhao Fan , Jinyu Huang , Yucai Hu , Boyong Qiu , Yankun Song , Yongxia Wang

Introduction

In recent years, ShenSong YangXin capsule (SSYX) has gained widespread application in China as an adjunctive therapy for patients with chronic heart failure combined with atrial fibrillation (CHF-AF). However, its efficacy and safety profile remain subject to debate, and there is a notable lack of relevant systematic reviews and meta-analyses on this topic.

Methods

A comprehensive search was conducted across seven databases up to August 25, 2025, identifying eligible randomized controlled trials (RCTs). Meta-analysis, subgroup analysis, and sensitivity analysis were performed using RevMan 5.4 and Stata 15.1. The Risk of Bias 2.0 tool was used to evaluate study quality, and publication bias was assessed with Egger’s test in Stata. Trial sequential analysis and the GRADE framework were utilized to assess the cumulative evidence and certainty of outcomes. The study protocol was prospectively registered with PROSPERO (CRD42023482018).

Results

The meta-analysis included 17 RCTs comprising a total of 1756 patients from China. Results indicated that SSYX combined with conventional medication significantly improved clinical efficacy in patients with CHF-AF [RR 1.18 (95 % CI 1.11, 1.25), p < 0.00001] and reduced the incidence of major adverse cardiovascular events (MACE) [RR 0.31 (95 % CI 0.23, 0.41), p < 0.00001]. Statistically significant improvements were also observed in the following outcomes: B-type natriuretic peptide, N-terminal pro-B-type natriuretic peptide, left ventricular ejection fraction, left ventricular end-diastolic diameter, left ventricular end-systolic diameter, QT dispersion (QTd), ventricular rate, and AF duration. Adverse reactions were reported in 11 trials. According to the GRADE framework, one outcome (MACE) was supported by moderate-certainty evidence, three outcomes (clinical efficacy, QTd, and ventricular rate) were graded as low-certainty, and the remaining six outcomes were assessed as having very low-certainty evidence.

Conclusion

The combination therapy incorporating SSYX showed potential benefits compared to conventional treatment alone in patients with CHF-AF. However, the overall certainty of evidence is limited. Therefore, these findings require careful interpretation and further large-scale, rigorously designed RCTs are warranted to provide more robust evidence regarding the efficacy and safety of SSYX.
近年来,参松养心胶囊(SSYX)作为慢性心力衰竭合并心房颤动(CHF-AF)患者的辅助治疗在国内得到了广泛应用。然而,其有效性和安全性仍然存在争议,并且明显缺乏相关的系统评价和荟萃分析。方法综合检索截至2025年8月25日的7个数据库,筛选符合条件的随机对照试验(rct)。采用RevMan 5.4和Stata 15.1软件进行meta分析、亚组分析和敏感性分析。采用风险偏倚2.0工具评价研究质量,发表偏倚采用Stata的Egger检验。使用试验序列分析和GRADE框架来评估累积证据和结果的确定性。该研究方案已在PROSPERO进行前瞻性注册(CRD42023482018)。结果meta分析纳入17项随机对照试验,共纳入1756例中国患者。结果显示,SSYX联合常规药物显著提高了CHF-AF患者的临床疗效[RR 1.18 (95% CI 1.11, 1.25), p < 0.00001],降低了主要心血管不良事件(MACE)的发生率[RR 0.31 (95% CI 0.23, 0.41), p < 0.00001]。以下结果也有统计学显著改善:b型利钠肽、n端前b型利钠肽、左室射血分数、左室舒张末期内径、左室收缩末期内径、QT离散度(QTd)、心室率和房颤持续时间。11项试验报告了不良反应。根据GRADE框架,一个结果(MACE)被中等确定性证据支持,三个结果(临床疗效、QTd和心室率)被分级为低确定性证据,其余六个结果被评估为具有非常低确定性证据。结论:与常规治疗相比,合并SSYX的联合治疗在CHF-AF患者中具有潜在的益处。然而,证据的总体确定性是有限的。因此,这些发现需要仔细解释,并需要进一步大规模、严格设计的随机对照试验,以提供有关SSYX有效性和安全性的更有力证据。
{"title":"The efficacy and safety of Shensong Yangxin capsule combination therapy in chronic heart failure combined with atrial fibrillation: A systematic review and meta-analysis","authors":"Heng Sun ,&nbsp;Zuoying Xing ,&nbsp;Genhao Fan ,&nbsp;Jinyu Huang ,&nbsp;Yucai Hu ,&nbsp;Boyong Qiu ,&nbsp;Yankun Song ,&nbsp;Yongxia Wang","doi":"10.1016/j.eujim.2025.102590","DOIUrl":"10.1016/j.eujim.2025.102590","url":null,"abstract":"<div><h3>Introduction</h3><div>In recent years, ShenSong YangXin capsule (SSYX) has gained widespread application in China as an adjunctive therapy for patients with chronic heart failure combined with atrial fibrillation (CHF-AF). However, its efficacy and safety profile remain subject to debate, and there is a notable lack of relevant systematic reviews and meta-analyses on this topic.</div></div><div><h3>Methods</h3><div>A comprehensive search was conducted across seven databases up to August 25, 2025, identifying eligible randomized controlled trials (RCTs). Meta-analysis, subgroup analysis, and sensitivity analysis were performed using RevMan 5.4 and Stata 15.1. The Risk of Bias 2.0 tool was used to evaluate study quality, and publication bias was assessed with Egger’s test in Stata. Trial sequential analysis and the GRADE framework were utilized to assess the cumulative evidence and certainty of outcomes. The study protocol was prospectively registered with PROSPERO (CRD42023482018).</div></div><div><h3>Results</h3><div>The meta-analysis included 17 RCTs comprising a total of 1756 patients from China. Results indicated that SSYX combined with conventional medication significantly improved clinical efficacy in patients with CHF-AF [RR 1.18 (95 % CI 1.11, 1.25), <em>p</em> &lt; 0.00001] and reduced the incidence of major adverse cardiovascular events (MACE) [RR 0.31 (95 % CI 0.23, 0.41), <em>p</em> &lt; 0.00001]. Statistically significant improvements were also observed in the following outcomes: B-type natriuretic peptide, N-terminal pro-B-type natriuretic peptide, left ventricular ejection fraction, left ventricular end-diastolic diameter, left ventricular end-systolic diameter, QT dispersion (QTd), ventricular rate, and AF duration. Adverse reactions were reported in 11 trials. According to the GRADE framework, one outcome (MACE) was supported by moderate-certainty evidence, three outcomes (clinical efficacy, QTd, and ventricular rate) were graded as low-certainty, and the remaining six outcomes were assessed as having very low-certainty evidence.</div></div><div><h3>Conclusion</h3><div>The combination therapy incorporating SSYX showed potential benefits compared to conventional treatment alone in patients with CHF-AF. However, the overall certainty of evidence is limited. Therefore, these findings require careful interpretation and further large-scale, rigorously designed RCTs are warranted to provide more robust evidence regarding the efficacy and safety of SSYX.</div></div>","PeriodicalId":11932,"journal":{"name":"European Journal of Integrative Medicine","volume":"81 ","pages":"Article 102590"},"PeriodicalIF":1.7,"publicationDate":"2025-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145733034","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
期刊
European Journal of Integrative Medicine
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