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The effect of reflexology on pain, anxiety, fatigue, and sleep in patients undergoing coronary artery bypass graft surgery: A randomized controlled trial 反射疗法对冠状动脉旁路移植手术患者疼痛、焦虑、疲劳和睡眠的影响:随机对照试验
IF 2.5 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-02-01 DOI: 10.1016/j.eujim.2024.102342
Kubra Gunes , Elif Gezginci , Mustafa Tok

Introduction

Reflexology is a non-pharmacological method that helps normalization of bodily functions by applying pressure to the reflex points on the hands, feet and ears, which correspond to all the organs and glands in the body. This study aimed to evaluate the effect of reflexology on pain, anxiety, fatigue, and sleep in patients undergoing cardiovascular surgery.

Methods

This open-label, randomized parallel-group controlled trial was conducted between September 2020 to May 2021 in a university hospital in Turkey. Seventy eligible patients who underwent cardiovascular surgery were randomized into reflexology group (n = 35) or control group (n = 35). While foot reflexology was applied to the reflexology group for 40 min in the first three days after surgery, no intervention was applied to control group. The primary outcome was pain severity, assessed using the Visual Analog Scale, in the first three postoperative days. The other outcomes were anxiety level assessed using the State-Trait Anxiety Inventory, fatigue level assessed using the Visual Analog Scale in the first three postoperative days, and sleep quality assessed using the Richards-Campbell Sleep Questionnaire in the first four postoperative days.

Results

After applying reflexology on the first, second, and third postoperative days, pain scores (d=-2.736, 95% Cl=-3.388 to -2.084) (d=-7.954, 95% Cl=-9.352 to -6.555) (d=-7.528, 95% Cl=-8.860 to -6.196), anxiety scores (d=-3.462, 95% Cl=-4.202 to -1.721) (d=-6.077, 95% Cl=-7.187 to -4.967) (d=-6.537, 95% Cl=-7.717 to -5.357), and fatigue scores (d=-2.490, 95% Cl=-3.115 to -1.866) (d=-6.245, 95% Cl=-7.380 to -5.109) (d=-8.223, 95% Cl=-9.675 to -6.791, respectively) were statistically significantly lower in reflexology group compared to control group. On the second, third, and fourth postoperative days, sleep scores in reflexology group were statistically significantly higher than control group (d = 3.230, 95% Cl=2.519 to 3.941) (d = 4.280, 95% Cl=3.431 to 5.130) (d = 6.106, 95% Cl=4.992 to 7.221, respectively). During the study period, no adverse events were noted in either groups.

Conclusion

This study showed that applying foot reflexology to patients undergoing cardiovascular surgery reduced pain, anxiety, and fatigue and improved sleep quality. Further studies on reflexology practice are recommended to be conducted with larger sample sizes and different groups.

Trial registration Clinical

Trials.gov NCT04473287.

导言反射疗法是一种非药物疗法,通过按压手、脚和耳朵上的反射点来帮助身体机能恢复正常,这些反射点与身体的所有器官和腺体相对应。本研究旨在评估反射疗法对心血管手术患者的疼痛、焦虑、疲劳和睡眠的影响。方法这项开放标签、随机平行组对照试验于 2020 年 9 月至 2021 年 5 月在土耳其一所大学医院进行。符合条件的 70 名心血管手术患者被随机分为足部反射疗法组(35 人)和对照组(35 人)。足部反射疗法组在术后头三天进行 40 分钟的足部反射疗法,而对照组则不进行任何干预。主要结果是术后前三天的疼痛严重程度,采用视觉模拟量表进行评估。结果在术后第一、第二和第三天进行反射疗法后,疼痛评分(d=-2.736,95% Cl=-3.388 to -2.084)(d=-7.954,95% Cl=-9.352~-6.555)(d=-7.528,95% Cl=-8.860~-6.196)、焦虑评分(d=-3.462,95% Cl=-4.202~-1.721)(d=-6.077,95% Cl=-7.187~-4.967)(d=-6.537,95% Cl=-7.717~-5.357)和疲劳评分(d=-2.490,95% Cl=-3.115至-1.866)(d=-6.245,95% Cl=-7.380至-5.109)(d=-8.223,95% Cl=-9.675至-6.791)与对照组相比,反射疗法组明显降低。术后第二、第三和第四天,反射疗法组的睡眠评分在统计学上明显高于对照组(d=3.230,95% Cl=2.519~3.941)(d=4.280,95% Cl=3.431~5.130)(d=6.106,95% Cl=4.992~7.221)。结论这项研究表明,对接受心血管手术的患者进行足部反射疗法可以减轻疼痛、焦虑和疲劳,并改善睡眠质量。建议对足部反射疗法进行更多的研究,并扩大样本量和分组。
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引用次数: 0
Water knotweed is an important candidate for preclinical trials with its high photoprotection and remarkable bioactive properties 水结草具有高度光保护作用和显著的生物活性,是临床前试验的重要候选植物
IF 2.5 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-02-01 DOI: 10.1016/j.eujim.2024.102340
Emine Bagdatli, Aliye Gediz Erturk

Introduction

Persicaria amphibia L. (water knotweed), an edible plant with pharmaceutical properties, is found in Asia, Europe, North America, and Africa. Despite its worldwide distribution and prominence, scientific literature on the plant's therapeutic properties is scarce. This study aimed to comprehensively investigate the antioxidant activity, DNA binding potential, GC–MS, and fluorescence analysis and photoprotective properties of P. amphibia.

Method

Water and ethanol maceration and Soxhlet extraction samples (Pa1–4) of P. amphibia were prepared. Bioactive properties of the plant were investigated. Qualitative and quantitative chemical markers of the samples were described using UV–Vis., fluorescence, and gas chromatography-mass spectrometry (GC–MS) analyses, and phytochemical screening. Photoprotective properties of the plant were also revealed using Mansur method.

Results

The phenolic and flavonoid contents varied between 22.06 ± 0.49 and 28.92 ± 0.51 μg gallic acid equivalent (GAE)/1 mg and 24.54 ± 1.19 and 34.09 ± 0.61 μg quercetin equivalent (QE)/1 mg, respectively. The fluorescence emission spectra of the samples indicated that the samples may contain berberine alkaloid, and riboflavin and quercetin flavonoids. The sun protection factor (SPF) values revealed that the plant [Pa1 (750 and 1000 μg/mL = 10.22 ± 0.05; 13.29 ± 0.25), Pa2 (500 μg/mL = 7.58 ± 0.04) and Pa4 (1000 μg/mL: 11.86 ± 0.13)] has more photoprotective activity compared with carrot seed oil (500, 750 and 1000 µg/mL = 5.22 ± 0.07; 7.72 ± 0.09 and 9.69 ± 0.14) (P ˃ 0.001). Moreover, the samples exhibited considerable antioxidant activity. All four extracts could generally inhibit lipid peroxidation (Pa1–4 = 83.14 % ± 0.36; 82.05 % ± 0.82; 80.87 % ± 0.23 and 81.38 % ± 1.26) as effectively as the standards of ascorbic acid (81.89 % ± 0.88) and α-tocopherol (85.45 ± 1.37) for 25 µg/mL (P ˃ 0.05). The binding affinities between the plant samples and Calf Thymus DNA (CT-DNA) were also determined. The order of the binding affinity is Pa3 > Pa4 > Pa2 > Pa1.

Conclusion

The P. amphibia plant has a significant amount and variety of phytocomponents. Along with bioactive and sun protection properties, this plant could be a cheap, beneficial, and safe ingredient for cosmetic and pharmaceutical formulations.

简介水节草(Persicaria amphibia L.)是一种具有药用价值的可食用植物,分布于亚洲、欧洲、北美洲和非洲。尽管这种植物分布在世界各地,而且很受重视,但有关其治疗特性的科学文献却很少。本研究旨在通过 GC-MS、荧光分析和光保护特性等方法,全面研究安非拉酮的抗氧化活性、DNA 结合潜力:方法:制备羊栖菜的水、乙醇浸泡和索氏提取样品(Pa1-4)。研究了该植物的生物活性特性。利用紫外可见光、荧光、气相色谱-质谱(GC-MS)分析和植物化学筛选对样品的定性和定量化学标记进行了描述。此外,还使用曼苏尔法揭示了该植物的光保护特性:酚类和类黄酮含量分别为 22.06 ± 0.49 和 28.92 ± 0.51 μg 没食子酸当量(GAE)/1 mg,以及 24.54 ± 1.19 和 34.09 ± 0.61 μg 槲皮素当量(QE)/1 mg。样品的荧光发射光谱表明,样品中可能含有小檗碱、核黄素和槲皮黄酮。防晒系数(SPF)值显示,植物[Pa1(750 和 1000 μg/mL = 10.22 ± 0.05; 13.29 ± 0.25)、Pa2(500 μg/mL = 7.58 ± 0.04)和 Pa4(1000 μg/mL: 11.与胡萝卜籽油(500、750 和 1000 µg/mL = 5.22 ± 0.07; 7.72 ± 0.09 和 9.69 ± 0.14)相比,[P4(1000 μg/mL:11.86 ± 0.13)]具有更强的光保护活性(P ˂ 0.001)。此外,样品还表现出相当高的抗氧化活性。在 25 µg/mL 的浓度下,四种提取物都能有效抑制脂质过氧化(Pa1-4 = 83.14% ± 0.36; 82.05 % ± 0.82; 80.87% ± 0.23 和 81.38% ± 1.26),与抗坏血酸(81.89% ± 0.88)和α-生育酚(85.45 ± 1.37)的标准值相当(P ˃ 0.05)。此外,还测定了植物样本与小牛胸腺 DNA(CT-DNA)之间的结合亲和力。结合亲和力的顺序为 Pa3 > Pa4 > Pa2 > Pa1:结论:P. amphibia 植物含有大量和多种植物成分。除了具有生物活性和防晒特性外,这种植物还是一种廉价、有益、安全的化妆品和药物配方成分。
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引用次数: 0
Chinese medicine practitioners’ consensus on traditional Chinese medicine diagnostic patterns, symptoms, and herbal formulas for COVID-19 survivors: A Delphi study 中医师对COVID-19幸存者的中医诊断模式、症状和中药配方的共识:德尔菲研究
IF 2.5 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-02-01 DOI: 10.1016/j.eujim.2024.102339
Jiayin Ruan , Shucheng Chen , Yuen Shan Ho , Vivian Taam Wong , Mei Yuk Lam , Hector Wing Hong Tsang , Ian Hoyin Cheng , Wing Fai Yeung

Introduction

In April 2022, the “Guidance and recommendations on Chinese Medicine Rehabilitation during COVID-19 recovery stage (pilot version)” (the CM Rehabilitation Guidance) was formulated for Hong Kong COVID-19 survivors. However, no consensus regarding traditional Chinese medicine (TCM) diagnostic patterns, symptoms, and herbal formulas in the Guidance has been reached among Hong Kong Chinese medicine practitioners (CMPs). Thus, this study aimed to establish a consensus among them as a guidance for practice.

Methods

A modified Delphi method was conducted from July 28 to September 14, 2022. Each survey gathered feedback by using a five-point Likert scale and open-ended questions. Descriptive statistics for quantitative data and thematic analysis for qualitative data were used. The consensus was defined as ≥80 % level of agreement with interquartile range (IQR) ≤1.

Results

A total of 13 CMPs with clinical experience in managing COVID-19 survivors participated in the three-round Delphi survey. A final consensus was reached regarding the following: (1) the diagnostic pattern qi deficiency of the lung and spleen (median = 4; IQR = 0; level of agreement = 92.31 %) with six new suggested symptom items; (2) the diagnostic pattern dual deficiency of qi and yin (median = 4; IQR = 0.5; level of agreement = 100 %) with three new suggested symptom items; and (3) the suggested herbal formulas for these two diagnostic patterns after modification.

Conclusions

Through the three-round Delphi survey, we established a modified CM Rehabilitation Guidance for Hong Kong COVID-19 survivors. The modified Guidance based on the views of Hong Kong CMPs with frontline clinical experience in COVID-19 should be more applicable to current COVID-19 survivors.

导言2022年4月,为香港COVID-19幸存者制定了《COVID-19康复阶段中医康复指导及建议(试行版)》(《中医康复指导》)。然而,香港中醫師對指引中的傳統中醫診斷模式、症狀及中藥配方尚未達成共識。因此,本研究旨在建立中醫師之間的共識,以作為執業指引。每项调查均采用五点李克特量表和开放式问题收集反馈意见。定量数据采用描述性统计,定性数据采用主题分析。结果共有 13 名具有管理 COVID-19 幸存者临床经验的 CMPs 参与了三轮德尔菲调查。最终就以下方面达成了共识:(1) 肺脾气虚诊断模式(中位数 = 4;IQR = 0;同意度 = 92.31%),新增 6 个建议症状项目;(2) 气阴两虚诊断模式(中位数 = 4;IQR = 0.结论通过三轮德尔菲调查,我们为香港 COVID-19 存活者制定了经修订的《中药康复指南》。修订后的《指南》以具有 COVID-19 一线临床经验的香港中医师为基础,应更适用于目前的 COVID-19 幸存者。
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引用次数: 0
Acupuncture for HIV/AIDs and its complications: A systematic review and meta-analysis 针灸治疗艾滋病毒/艾滋病及其并发症:系统回顾和荟萃分析
IF 2.5 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-01-03 DOI: 10.1016/j.eujim.2024.102330
Zhi-Jie Wang , Lin-Lin Tan , Yu Zhang , Jia-Qi Yan , Jian-Ping Liu

Introduction

Human immunodeficiency virus (HIV) has spread globally. Both acquired immune deficiency syndromes (AIDs) and its complications pose a serious threat to human health. Acupuncture has been reported as a complement to Western medicine for relieving HIV/AIDs-related symptoms, but systematic reviews on acupuncture for HIV/AIDs and its complications are lacking.

Methods

Six databases were searched for both randomized controlled trials (RCTs) and quasi-randomized controlled trials (q-RCTs) using any types of acupuncture for HIV/AIDs and their complications. The primary outcome included global clinical efficacy assessment (i.e., number of patients with improving symptoms), pain, numbness intensity, sleep quality, depression and severe adverse events (i.e., death or hospitalization), and the secondary outcomes included other HIV/AIDs related outcomes such as immune response markers (CD4+ T-lymphocyte count), biochemical markers, functional outcomes (quality of life, level of physical activity), follow-ups and other adverse outcomes such as nausea, vomiting, and fever. Two reviewers independently applied the inclusion criteria, extracted data and evaluated the risk of bias in the included trials. This systematic review is registered with PROSPERO (CRD42020214490).

Results

Sixteen trials (thirteen RCTs and three q-RCTs) on complications including peripheral neuropathy, gastrointestinal symptoms, inflammation, insomnia and depression were included. The results revealed that manual acupuncture plus moxibustion (RR 1.58, 95 % CI [1.10, 2.28], 1 RCT, n = 60), manual acupuncture only (RR 1.56, 95 % CI [1.20, 2.03], 1 RCT, 1 q-RCT, n = 175) or auricular acupuncture (RR 2.02, 95 % CI [1.35, 3.02], 1 RCT, n = 72) could improve the symptoms in HIV-infected patients; reduce pain and numbness intensity, reduce score of Hamilton Depression Scale andimprove sleep quality. Meanwhile, acupuncture appeared to improve biochemical indicators whilst not increasing the drop-out rate, recurrence, mortality or adverse events. The quality of evidence was moderate quality for sleep quality; low quality for global clinical efficacy assessment rate, pain and numbness intensity; and very low quality for pain and depression.

Conclusions

Acupuncture may be an effective and safe intervention for HIV/AIDs related complications, including peripheral neuropathy, inflammation, insomnia and depression. However, the low quality of the evidence limits the relevance of those findings.

导言:人类免疫缺陷病毒(HIV)已在全球蔓延。获得性免疫缺陷综合征及其并发症对人类健康构成严重威胁。据报道,针灸是西医缓解 HIV/IDs 相关症状的辅助手段,但目前仍缺乏针灸治疗 HIV/IDs 及其并发症的系统综述:方法:在六个数据库中检索了使用任何类型的针灸治疗 HIV/AIDS 及其并发症的随机对照试验 (RCT) 和准随机对照试验 (q-RCT)。主要结果包括总体临床疗效评估(即症状改善的患者人数)、疼痛、麻木强度、睡眠质量、抑郁和严重不良事件(即死亡或住院)、次要结果包括与艾滋病毒/艾滋病及其并发症相关的其他结果,如免疫反应指标(CD4+ T淋巴细胞计数)、生化指标、功能性结果(生活质量、体力活动水平)、随访及其他不良结果,如恶心、呕吐和发烧。两名评审员独立应用纳入标准、提取数据并评估纳入试验的偏倚风险。本系统综述已在 PROSPERO(CRD42020214490)上注册:结果:共纳入16项试验(13项RCT和3项q-RCT),并发症包括周围神经病变、胃肠道症状、炎症、失眠和抑郁。结果显示,徒手针刺加艾灸(RR 1.58,95% CI [1.10,2.28],1 项 RCT,n=60)、仅徒手针刺(RR 1.56,95% CI [1.20,2.03],1 项 RCT,1 项 q-RCT,n=175)或耳针(RR 2.02,95% CI [1.35,3.同时,针灸似乎能改善生化指标,但不会增加辍学率、复发率、死亡率或不良事件。在证据质量方面,研究显示睡眠质量的证据质量为中等;全球临床疗效评估率、疼痛和麻木强度的证据质量为低;疼痛和抑郁的证据质量为极低:针灸可能是治疗艾滋病相关并发症(包括周围神经病变、炎症、失眠和抑郁)的一种有效而安全的干预措施。然而,低质量的证据限制了这些研究结果的相关性。
{"title":"Acupuncture for HIV/AIDs and its complications: A systematic review and meta-analysis","authors":"Zhi-Jie Wang ,&nbsp;Lin-Lin Tan ,&nbsp;Yu Zhang ,&nbsp;Jia-Qi Yan ,&nbsp;Jian-Ping Liu","doi":"10.1016/j.eujim.2024.102330","DOIUrl":"10.1016/j.eujim.2024.102330","url":null,"abstract":"<div><h3>Introduction</h3><p>Human immunodeficiency virus (HIV) has spread globally. Both acquired immune deficiency syndromes (AIDs) and its complications pose a serious threat to human health. Acupuncture has been reported as a complement to Western medicine for relieving HIV/AIDs-related symptoms, but systematic reviews on acupuncture for HIV/AIDs and its complications are lacking.</p></div><div><h3>Methods</h3><p>Six databases were searched for both randomized controlled trials (RCTs) and quasi-randomized controlled trials (q-RCTs) using any types of acupuncture for HIV/AIDs and their complications. The primary outcome included global clinical efficacy assessment (i.e., number of patients with improving symptoms), pain, numbness intensity, sleep quality, depression and severe adverse events (i.e., death or hospitalization), and the secondary outcomes included other HIV/AIDs related outcomes such as immune response markers (CD4+ <em>T</em>-lymphocyte count), biochemical markers, functional outcomes (quality of life, level of physical activity), follow-ups and other adverse outcomes such as nausea, vomiting, and fever. Two reviewers independently applied the inclusion criteria, extracted data and evaluated the risk of bias in the included trials. This systematic review is registered with PROSPERO (CRD42020214490).</p></div><div><h3>Results</h3><p>Sixteen trials (thirteen RCTs and three q-RCTs) on complications including peripheral neuropathy, gastrointestinal symptoms, inflammation, insomnia and depression were included. The results revealed that manual acupuncture plus moxibustion (RR 1.58, 95 % CI [1.10, 2.28], 1 RCT, <em>n</em> = 60), manual acupuncture only (RR 1.56, 95 % CI [1.20, 2.03], 1 RCT, 1 q-RCT, <em>n</em> = 175) or auricular acupuncture (RR 2.02, 95 % CI [1.35, 3.02], 1 RCT, <em>n</em> = 72) could improve the symptoms in HIV-infected patients; reduce pain and numbness intensity, reduce score of Hamilton Depression Scale andimprove sleep quality. Meanwhile, acupuncture appeared to improve biochemical indicators whilst not increasing the drop-out rate, recurrence, mortality or adverse events. The quality of evidence was moderate quality for sleep quality; low quality for global clinical efficacy assessment rate, pain and numbness intensity; and very low quality for pain and depression.</p></div><div><h3>Conclusions</h3><p>Acupuncture may be an effective and safe intervention for HIV/AIDs related complications, including peripheral neuropathy, inflammation, insomnia and depression. However, the low quality of the evidence limits the relevance of those findings.</p></div>","PeriodicalId":11932,"journal":{"name":"European Journal of Integrative Medicine","volume":"67 ","pages":"Article 102330"},"PeriodicalIF":2.5,"publicationDate":"2024-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139104126","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
Network pharmacology, molecular docking and experimental verification reveal the mechanism of Yiguanjian decoction in treating acute liver failure 网络药理学、分子对接和实验验证揭示了益肝煎治疗急性肝衰竭的机理。
IF 2.5 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-01-01 DOI: 10.1016/j.eujim.2023.102326
Shuai Wang , Yu Sun , Chunmei Zhang , Bohao Chen , Mei Zhong , Ruili Du , Yuhang Zhou , Guangdong Tong , Lidan Luo

Introduction: The potential targets and action mechanism of Yiguanjian (YGJ) decoction in treating acute liver failure (ALF) were determined using network pharmacology, molecular docking and cell experiments.

Methods: The Pharmacology of Traditional Chinese Medicine Systems (TCMSP) and BATMAN-TCM databases were used to find YGJ decoction targets. The Genecard database was employed to predict targets associated with ALF. Cytascape software was utilised to visualise and select common targets along with establishing a protein–protein interaction (PPI) network. Core targets were screened and putative function was assessed via gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyzes. Molecular docking was performed using AutodockTools, PyMoL and Discovery Studio software to verify the correlation between the YGJ decoction and selected targets. MTT assay was conducted to determine the effect of the YGJ decoction on the viability of Huh-7 human hepatoma cells. The effects of the YGJ decoction on the expression of putative targets in Huh-7 cells were determined via western blot and quantitative real-time polymerase chain reaction analyzes.

Results: Overall, 9153 YGJ decoction and 576 ALF-related targets were obtained, and 469 YGJ decoction and ALF cross targets were obtained. Of these, 20 key targets, including AKT1, estrogen receptor 1 (ESR1), catalase (CAT), interleukin-1β (IL-1β) and discs large homolog 4 (DLG4), were selected from the PPI network. GO function enrichment analysis revealed that these targets were primarily associated with regulating system processes, cell body, oxidoreductase activity and other processes. An enrichment analysis using the KEGG pathway database revealed that the treatment of ALF using the YGJ decoction was primarily associated with the AGE-RAGE, cGMP-PKG and HIF-1 signalling pathways. Molecular docking indicated that quercetin, stigmasterol and β- sitosterol as well as AKT1, ESR1, CAT, IL-1β and DLG4 exhibited good binding affinity. In vitro experiments revealed that the YGJ decoction significantly reversed lipopolysaccharide (LPS)-induced apoptosis (P < 0.01), inhibited LPS-induced increase in IL-1β and ESR1 levels and upregulated LPS-induced decrease in AKT1, CAT and DLG4 levels (P < 0.05).

Conclusions: The YGJ decoction alleviates ALF by regulating multiple targets and its action mechanism may be associated with ameliorating oxidative stress and inflammation.

引言采用网络药理学、分子对接和细胞实验等方法确定了益肝煎治疗急性肝衰竭(ALF)的潜在靶点和作用机制:方法:利用 TCMSP 和 BATMAN-TCM 数据库寻找 YGJ 水煎剂的靶点。利用Genecard数据库预测与ALF相关的靶点。利用Cytascape软件可视化和选择共同靶点,同时建立蛋白质-蛋白质相互作用(PPI)网络。通过基因本体(GO)和京都基因和基因组百科全书(KEGG)通路富集分析筛选核心靶点并评估推定功能。使用 AutodockTools、PyMoL 和 Discovery Studio 软件进行了分子对接,以验证 YGJ 煎剂与所选靶点之间的相关性。MTT 试验测定了 YGJ 水煎剂对 Huh-7 人肝癌细胞活力的影响。通过 Western 印迹和定量实时聚合酶链反应分析确定了 YGJ 水煎剂对 Huh-7 细胞中推测靶点表达的影响:结果:共获得9153个YGJ煎剂和576个ALF相关靶点,以及469个YGJ煎剂和ALF交叉靶点。其中,从PPI网络中筛选出20个关键靶点,包括AKT1、雌激素受体1(ESR1)、过氧化氢酶(CAT)、白细胞介素-1β(IL-1β)和盘大同源物4(DLG4)。GO 功能富集分析表明,这些靶标主要与调节系统过程、细胞体、氧化还原酶活性和其他过程有关。利用 KEGG 通路数据库进行的富集分析表明,使用 YGJ 水煎剂治疗 ALF 主要与 AGE-RAGE、cGMP-PKG 和 HIF-1 信号通路有关。分子对接表明,槲皮素、豆甾醇、β-谷甾醇以及 AKT1、ESR1、CAT、IL-1β 和 DLG4 具有良好的结合亲和力。体外实验表明,YGJ 水煎剂能显著逆转脂多糖(LPS)诱导的细胞凋亡(P < 0.01),抑制 LPS 诱导的 IL-1β 和 ESR1 水平的升高,上调 LPS 诱导的 AKT1、CAT 和 DLG4 水平的降低(P < 0.05):YGJ煎剂通过调节多个靶点缓解ALF,其作用机制可能与改善氧化应激和炎症有关。
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引用次数: 0
Exploring the perceived benefits of a motivational exercise program (FIT-CANCER) in colorectal cancer patients during chemotherapy treatment: A qualitative study from self-determination theory 探索大肠癌患者在化疗期间对运动激励计划(FIT-CANCER)益处的感知:从自我决定理论出发的定性研究
IF 2.5 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-01-01 DOI: 10.1016/j.eujim.2023.102328
María Romero-Elías , David González-Cutre , Ana Ruiz-Casado , Roberto Ferriz , Natalia Navarro-Espejo , Vicente J. Beltrán-Carrillo

Introduction: Physical activity (PA) is considered an important factor to enhance the survival rate and overall quality of life in colorectal cancer (CRC) patients. However, a small percentage of patients comply with PA recommendations and most of them decrease their PA levels during chemotherapy. Theoretical frameworks could be useful for guiding exercise programs focused on the promotion of patients’ adherence to PA. Nevertheless, few studies have applied self-determination theory (SDT), one of the most prominent motivational theories, to understand exercise motivation in interventions with CRC patients. The aim of this study was to explore the benefits of an SDT-based 6-month exercise program (FIT-CANCER) regarding satisfaction of basic psychological needs and different psychological and behavioural consequences in CRC patients (stage II-III) during adjuvant chemotherapy. Methods: Qualitative data from 16 patients (nine men and seven women; Mage = 64.00, SD = 11.58), six relatives (Mage = 55.00, SD = 15.09) and five healthcare professionals (Mage = 40.40, SD = 9.66) were obtained through semi-structured interviews and field notes (N = 27). Results: Participants perceived that the motivational exercise program satisfied CRC patients’ needs for autonomy, competence, relatedness and novelty, giving rise to positive psychological consequences during chemotherapy treatment, such as enjoyment of exercise, optimism, vitality, sociability and keeping some good memories. The program allowed patients to feel that they were actively doing something important to overcome their cancer, an aspect that could foster their psychological well-being. Participants perceived that patients increased their exercise participation during chemotherapy treatment, even during the COVID-19 pandemic, with an online adaptation of the exercise program, and integrated exercise into their lifestyle. Participants also highlighted the importance of patients belonging to a group undergoing a similar situation and the instructor's knowledge, specialization and empathy. Conclusion: Motivational exercise programs could help improve CRC patients’ psychosocial and behavioural outcomes during chemotherapy treatment.

导言:体力活动(PA)被认为是提高结直肠癌(CRC)患者生存率和整体生活质量的重要因素。然而,只有一小部分患者遵照建议进行体育锻炼,而且大部分患者在化疗期间的体育锻炼水平都有所下降。理论框架有助于指导锻炼计划,重点是促进患者坚持锻炼。然而,很少有研究应用自我决定理论(SDT)(最著名的动机理论之一)来了解 CRC 患者干预过程中的运动动机。本研究旨在探讨基于 SDT 的为期 6 个月的运动计划(FIT-CANCER)在满足辅助化疗期间的 CRC 患者(II-III 期)的基本心理需求以及不同的心理和行为后果方面的益处。研究方法通过半结构式访谈和现场记录(N = 27),获得 16 名患者(9 名男性和 7 名女性;Mage = 64.00,SD = 11.58)、6 名亲属(Mage = 55.00,SD = 15.09)和 5 名医护人员(Mage = 40.40,SD = 9.66)的定性数据。结果参与者认为,激励性运动项目满足了 CRC 患者对自主性、能力、相关性和新奇感的需求,在化疗期间产生了积极的心理影响,如享受运动、乐观、活力、交际和保留一些美好回忆。该计划让患者感到他们正在积极地做一些重要的事情来战胜癌症,这一点可以促进他们的心理健康。参与者认为,患者在化疗期间,甚至在 COVID-19 大流行期间,通过对运动计划进行在线调整,增加了对运动的参与,并将运动融入了他们的生活方式。参加者还强调了患者属于一个情况相似的群体以及指导员的知识、专业和同理心的重要性。结论激励性运动项目有助于改善 CRC 患者在化疗期间的社会心理和行为结果。
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引用次数: 0
Acupuncture for Parkinson's disease-related constipation: A systematic review and meta-analysis 针灸治疗帕金森病相关性便秘:系统回顾和荟萃分析
IF 2.5 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-01-01 DOI: 10.1016/j.eujim.2024.102332
Xin-Xin Feng , Lei Chen , Yong-Yi Xu , Kai Zhou , Kai-Yu Huang

Introduction

The hazard of Parkinson's disease-related constipation (PDC) cannot be ignored. Acupuncture has the potential to become a mainstream treatment option for PDC. This review aimed to investigate the effect of acupuncture on PDC, which might provide evidence-based recommendations for clinical application.

Methods

Six databases were searched for randomized controlled trials (RCTs) about acupuncture for PDC. The primary outcome was response rate. The secondary outcomes were rectal resting pressure, anal resting pressure, anal maximum contraction pressure, rectal sensation threshold, rectal maximum tolerable volume, the Constipation Scoring System (CSS) score, the Patient Assessment of Constipation Quality of Life (PAC-QOL) score, and adverse events (AEs).

Results

Eight trials involving 591 participants were included. The methodological quality was generally low. A significant difference was found in response rate when comparing acupuncture with medicine (95 %CI= 1.09 to 1.54, P = 0.003) or blank control (95 %CI= 1.04 to 1.74, P = 0.02), while no significant difference was observed when comparing acupuncture + medicine with medicine. Acupuncture + medicine did have a significant effect on rectal resting pressure, anal resting pressure, anal maximum contraction pressure, rectal sensation threshold and rectal maximum tolerable volume when compared with medicine, while no significant effect was found when acupuncture was compared with medicine. A significant difference was found in the CSS score when acupuncture was compared with blank and in the PAC-QOL score when acupuncture was compared with sham or blank, while no significant difference was found in the PAC-QOL score when acupuncture was compared with medicine. One study reported mild AEs.

Conclusions

Acupuncture might be an effective treatment for PDC. Due to the limited quality of evidence, high-caliber and multi-center RCTs with large sample sizes should be carried out.

(PROSPERO ID is CRD42023422102)

简介:帕金森病相关性便秘(PDC)的危害不容忽视。针灸有望成为治疗帕金森病的主流方法。本综述旨在研究针灸对 PDC 的影响,从而为临床应用提供循证建议。方法检索了六个数据库中有关针灸治疗 PDC 的随机对照试验(RCT)。主要结果为应答率。次要结果为直肠静止压、肛门静止压、肛门最大收缩压、直肠感觉阈值、直肠最大耐受量、便秘评分系统(CSS)评分、便秘患者生活质量评估(PAC-QOL)评分以及不良事件(AEs)。方法学质量普遍较低。针灸与药物(95%CI= 1.09 至 1.54,P=0.003)或空白对照(95%CI= 1.04 至 1.74,P=0.02)相比,反应率有明显差异,而针灸+药物与药物相比则无明显差异。与药物相比,针灸+药物对直肠静息压、肛门静息压、肛门最大收缩压、直肠感觉阈值和直肠最大耐受量有显著影响,而针灸与药物相比则无显著影响。针灸与空白对照时,CSS 评分有明显差异;针灸与假药或空白对照时,PAC-QOL 评分有明显差异,而针灸与药物对照时,PAC-QOL 评分无明显差异。结论针灸可能是治疗 PDC 的有效方法。由于证据质量有限,应进行高水平、多中心、大样本量的 RCT 研究。
{"title":"Acupuncture for Parkinson's disease-related constipation: A systematic review and meta-analysis","authors":"Xin-Xin Feng ,&nbsp;Lei Chen ,&nbsp;Yong-Yi Xu ,&nbsp;Kai Zhou ,&nbsp;Kai-Yu Huang","doi":"10.1016/j.eujim.2024.102332","DOIUrl":"10.1016/j.eujim.2024.102332","url":null,"abstract":"<div><h3>Introduction</h3><p>The hazard of Parkinson's disease-related constipation (PDC) cannot be ignored. Acupuncture has the potential to become a mainstream treatment option for PDC. This review aimed to investigate the effect of acupuncture on PDC, which might provide evidence-based recommendations for clinical application.</p></div><div><h3>Methods</h3><p>Six databases were searched for randomized controlled trials (RCTs) about acupuncture for PDC. The primary outcome was response rate. The secondary outcomes were rectal resting pressure, anal resting pressure, anal maximum contraction pressure, rectal sensation threshold, rectal maximum tolerable volume, the Constipation Scoring System (CSS) score, the Patient Assessment of Constipation Quality of Life (PAC-QOL) score, and adverse events (AEs).</p></div><div><h3>Results</h3><p>Eight trials involving 591 participants were included. The methodological quality was generally low. A significant difference was found in response rate when comparing acupuncture with medicine (95 %CI= 1.09 to 1.54, <em>P</em> = 0.003) or blank control (95 %CI= 1.04 to 1.74, <em>P</em> = 0.02), while no significant difference was observed when comparing acupuncture + medicine with medicine. Acupuncture + medicine did have a significant effect on rectal resting pressure, anal resting pressure, anal maximum contraction pressure, rectal sensation threshold and rectal maximum tolerable volume when compared with medicine, while no significant effect was found when acupuncture was compared with medicine. A significant difference was found in the CSS score when acupuncture was compared with blank and in the PAC-QOL score when acupuncture was compared with sham or blank, while no significant difference was found in the PAC-QOL score when acupuncture was compared with medicine. One study reported mild AEs.</p></div><div><h3>Conclusions</h3><p>Acupuncture might be an effective treatment for PDC. Due to the limited quality of evidence, high-caliber and multi-center RCTs with large sample sizes should be carried out.</p><p>(PROSPERO ID is CRD42023422102)</p></div>","PeriodicalId":11932,"journal":{"name":"European Journal of Integrative Medicine","volume":"65 ","pages":"Article 102332"},"PeriodicalIF":2.5,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139375274","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
Chinese herbal medicine Er-xian decoction for primary ovarian insufficiency: A systematic review of randomized controlled trials and meta-analyses 中药二仙煎治疗原发性卵巢功能不全:随机对照试验和荟萃分析的系统综述
IF 2.5 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-01-01 DOI: 10.1016/j.eujim.2024.102333
Zhefen Mai , Chunli Lu , Xinyan Jin , Zixun Zhuang , Lingjing Lu , Yu Su , Chun Luo , Xia Han , Shaochuan Huo , Hongxia Ma

Introduction

The limitations of hormone therapy for managing primary ovarian insufficiency (POI) have prompted trialists to evaluate the Chinese herbal medicine, Er-xian decoction (containing Curculiginis Rhizome, Epimrdii Herba, Angelicae Sinensis Radix, Morindae Officinalis Radix, Phellodendri Chinrnsis Cortex and Anemarrhenae Rhizoma) for treating POI. This review was conducted to evaluate the effectiveness and safety of Er-xian decoction alone or in addition to hormone therapy in treating POI.

Methods

We conducted a systematic review of randomized controlled trials (RCTs) that reported on Er-xian decoction alone or in addition to hormone therapy in women with POI. Seven databases were searched from inception to 7 June 2023. The included studies were screened with Endnote X9, and methodological quality was assessed using the Cochrane “Risk of bias” tool v1.0. Effects were calculated as mean difference (MD), standard mean difference (SMD), or relative risk with 95% confidence interval (CI) using Review Manager 5.4.1, and data not suitable for statistical analyses were assessed by qualitative methods.

Results

Fifteen studies involving 1274 participants (13 drop-outs) were included. Er-xian decoction plus hormone therapy significantly lowered the follicle-stimulating hormone level (MD –12.48, 95 %CI –15.90 to –9.06; N = 8; P < 0.001) and luteinizing hormone level (MD –8.20, 95 %CI –11.22 to –5.17; N = 8; P < 0.001) and increased the estrogen level (SMD 2.35, 95 %CI 1.52 to 3.18; N = 8; P < 0.001) compared with hormone therapy. There was no significant difference between Er-xian decoction alone and hormone therapy alone in terms of follicle-stimulating hormone level (MD –0.69; 95 %CI, –7.94 to 6.56; N = 5; P = 0.85), luteinizing hormone level (MD 0.29, 95 %CI –3.96 to 4.54; N = 5; P = 0.89) or estrogen level (SMD 0.16, 95 %CI –0.36 to 0.67; N = 5; P = 0.55). In addition, both Er-xian decoction alone and Er-xian decoction plus hormone therapy effectively improved women's menopausal symptoms. Seven studies reported on the occurrence of adverse events, and no severe events were reported.

Conclusion

The findings suggest Er-xian decoction, with or without hormone therapy, may be an effective treatment for POI. However, limitations in the evidence included a high risk of bias and substantial heterogeneity. Further research should be conducted in well-designed and rigorously executed clinical trials with large samples.

Review registration

INPLASY 2,021,110,107.

引言激素疗法在治疗原发性卵巢功能不全(POI)方面的局限性促使试验者对中药二仙煎剂(含莪术、淫羊藿、当归、巴戟天、黄柏、知母)治疗原发性卵巢功能不全(POI)的有效性和安全性进行评估。本研究旨在评估二仙煎剂单独或与激素疗法联合治疗原发性卵巢功能不全的有效性和安全性。方法我们对报道二仙煎剂单独或与激素疗法联合治疗原发性卵巢功能不全妇女的随机对照试验(RCT)进行了系统回顾。我们检索了从开始到 2023 年 6 月 7 日的七个数据库。使用 Endnote X9 对纳入的研究进行了筛选,并使用 Cochrane "偏倚风险 "工具 v1.0 对方法学质量进行了评估。使用Review Manager 5.4.1以平均差(MD)、标准平均差(SMD)或带95%置信区间(CI)的相对风险计算效应,并通过定性方法评估不适合进行统计分析的数据。二仙煎加用激素治疗可显著降低卵泡刺激素水平(MD -12.48,95%CI -15.90 to -9.06;N = 8;P < 0.001)和促黄体生成素水平(MD -8.20,95%CI -11.22至-5.17;N = 8;P <;0.001),并与激素治疗相比增加了雌激素水平(SMD 2.35,95%CI 1.52至3.18;N = 8;P <;0.001)。在卵泡刺激素水平(MD -0.69;95%CI,-7.94 至 6.56;N = 5;P = 0.85)、促黄体生成素水平(MD 0.29,95%CI -3.96 至 4.54;N = 5;P = 0.89)或雌激素水平(SMD 0.16,95%CI -0.36 至 0.67;N = 5;P = 0.55)方面,单用二仙煎剂与单用激素治疗无明显差异。此外,单用二仙煎剂和二仙煎剂加激素治疗均能有效改善妇女的更年期症状。七项研究报告了不良反应的发生情况,没有严重不良反应的报告。然而,证据的局限性包括偏倚风险高和异质性大。进一步的研究应在精心设计和严格执行的大样本临床试验中进行。
{"title":"Chinese herbal medicine Er-xian decoction for primary ovarian insufficiency: A systematic review of randomized controlled trials and meta-analyses","authors":"Zhefen Mai ,&nbsp;Chunli Lu ,&nbsp;Xinyan Jin ,&nbsp;Zixun Zhuang ,&nbsp;Lingjing Lu ,&nbsp;Yu Su ,&nbsp;Chun Luo ,&nbsp;Xia Han ,&nbsp;Shaochuan Huo ,&nbsp;Hongxia Ma","doi":"10.1016/j.eujim.2024.102333","DOIUrl":"10.1016/j.eujim.2024.102333","url":null,"abstract":"<div><h3>Introduction</h3><p>The limitations of hormone therapy for managing primary ovarian insufficiency (POI) have prompted trialists to evaluate the Chinese herbal medicine, Er-xian decoction (containing <em>Curculiginis Rhizome, Epimrdii Herba, Angelicae Sinensis Radix, Morindae Officinalis Radix, Phellodendri Chinrnsis Cortex</em> and <em>Anemarrhenae Rhizoma</em>) for treating POI. This review was conducted to evaluate the effectiveness and safety of Er-xian decoction alone or in addition to hormone therapy in treating POI.</p></div><div><h3>Methods</h3><p>We conducted a systematic review of randomized controlled trials (RCTs) that reported on Er-xian decoction alone or in addition to hormone therapy in women with POI. Seven databases were searched from inception to 7 June 2023. The included studies were screened with Endnote X9, and methodological quality was assessed using the Cochrane “Risk of bias” tool v1.0. Effects were calculated as mean difference (MD), standard mean difference (SMD), or relative risk with 95% confidence interval (CI) using Review Manager 5.4.1, and data not suitable for statistical analyses were assessed by qualitative methods.</p></div><div><h3>Results</h3><p>Fifteen studies involving 1274 participants (13 drop-outs) were included. Er-xian decoction plus hormone therapy significantly lowered the follicle-stimulating hormone level (MD –12.48, 95 %CI –15.90 to –9.06; <em>N</em> = 8; <em>P</em> &lt; 0.001) and luteinizing hormone level (MD –8.20, 95 %CI –11.22 to –5.17; <em>N</em> = 8; <em>P</em> &lt; 0.001) and increased the estrogen level (SMD 2.35, 95 %CI 1.52 to 3.18; <em>N</em> = 8; <em>P</em> &lt; 0.001) compared with hormone therapy. There was no significant difference between Er-xian decoction alone and hormone therapy alone in terms of follicle-stimulating hormone level (MD –0.69; 95 %CI, –7.94 to 6.56; <em>N</em> = 5; <em>P</em> = 0.85), luteinizing hormone level (MD 0.29, 95 %CI –3.96 to 4.54; <em>N</em> = 5; <em>P</em> = 0.89) or estrogen level (SMD 0.16, 95 %CI –0.36 to 0.67; <em>N</em> = 5; <em>P</em> = 0.55). In addition, both Er-xian decoction alone and Er-xian decoction plus hormone therapy effectively improved women's menopausal symptoms. Seven studies reported on the occurrence of adverse events, and no severe events were reported.</p></div><div><h3>Conclusion</h3><p>The findings suggest Er-xian decoction, with or without hormone therapy, may be an effective treatment for POI. However, limitations in the evidence included a high risk of bias and substantial heterogeneity. Further research should be conducted in well-designed and rigorously executed clinical trials with large samples.</p></div><div><h3>Review registration</h3><p>INPLASY 2,021,110,107.</p></div>","PeriodicalId":11932,"journal":{"name":"European Journal of Integrative Medicine","volume":"65 ","pages":"Article 102333"},"PeriodicalIF":2.5,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139375390","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
Evaluation of the effects of Bauhinia forficata as an adjuvant in the treatment of type 2 diabetes mellitus: Systematic review and meta-analysis 评估紫荆花作为辅助药物治疗 2 型糖尿病的效果:系统综述和荟萃分析
IF 2.5 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-01-01 DOI: 10.1016/j.eujim.2024.102331
Liliana Maria Dimer , Tamy Colonetti , Maria Laura Rodrigues Uggioni , Sarah Dagostin Ferraz , Antonio José Grande , Maria Inês Rosa , Luciane Bisognin Ceretta

Introduction

Type 2 diabetes mellitus (T2DM) is characterized by defects in insulin action and secretion. Bauhinia forficata has been observed to exhibit an effect in diabetes treatment due to its hypoglycemic activity. This systematic review with meta-analysis aimed to assess the effects of using Bauhinia forficata as an adjuvant treatment for individuals with T2DM.

Methods

We conducted a comprehensive search strategy using relevant keywords and their synonyms, focusing on "Bauhinia forficata" and "diabetes mellitus." The search encompassed online databases such as Medline, Embase via OVID, and the Cochrane Library, without imposing language restrictions. We included studies that evaluated individuals diagnosed with T2DM, who were administered Bauhinia forficata, compared to placebo or active control, and who presented glycemia and glycated hemoglobin as outcome measures. Studies not meeting these criteria, as well as literature reviews, animal or in vitro experiments, were excluded. The methodological quality of the included studies was assessed using the Risk of Bias 2 tool. The results were presented through tables and graphs, and forest plots were generated to illustrate the effects of interventions on various outcomes, using RevMan software 5.4.

Results

Four studies met the inclusion criteria, comprising two randomized controlled trials (RCT) and two non-randomized studies of interventions (NRSI). Compared to placebo, Bauhinia forficata significantly improved glycemia (SMD -0.60, 95 % CI -0.15 to -1.05, p = 0.009, 1 RCT, n = 111, low certainty evidence; SMD -0.64, 95 % CI -1.25 to -0.03, p = 0.04, I²=42 %, 2 NSRIs pre-test/post-test, n = 40, very low certainty evidence). However, only the RCT evidence demonstrated significant improvements in HbA1c (SMD -0.48, 95 % CI -0.93, p = 0.03, 1 RCT, n = 111, low certainty evidence; SMD -0.25, 95 %CI -0.69 to 0.19, p-0.27, I²=0 %, 2 NSRIs pretest/post-test, n = 40, very low certainty evidence). No differences were found between Bauhinia forficata and Imperata brasiliensis (glycemia SMD -0.03, 95 % CI -1.01 to 0.95, p = 0.96, 1 RCT, n = 16, very low certainty evidence; HbA1c SMD 0.06, 95 % CI -0.92 to 1.04, p = 0.96, 1 RCT, n = 16, very low certainty evidence).

Conclusions

The findings suggest that Bauhinia forficata may be effective in reducing blood glucose levels; however, this evidence needs to be interpreted with caution.

PROSPERO registration

CRD42022370143.

导言2 型糖尿病(T2DM)的特点是胰岛素作用和分泌缺陷。据观察,洋紫荆具有降血糖活性,可用于治疗糖尿病。本系统综述和荟萃分析旨在评估将紫荆灵作为 T2DM 患者辅助治疗的效果。方法我们使用相关关键词及其同义词进行了全面的检索,重点是 "紫荆 "和 "糖尿病"。检索范围包括 Medline、Embase via OVID 和 Cochrane Library 等在线数据库,没有语言限制。我们纳入了对诊断为 T2DM 的患者进行评估的研究,这些患者服用的是洋紫荆,而不是安慰剂或活性对照组,并以血糖和糖化血红蛋白作为结果测量指标。不符合上述标准的研究以及文献综述、动物或体外实验均被排除在外。采用 "偏倚风险 2 "工具对纳入研究的方法学质量进行了评估。结果四项研究符合纳入标准,包括两项随机对照试验(RCT)和两项非随机干预研究(NRSI)。与安慰剂相比,洋紫荆能显著改善血糖(SMD -0.60,95% CI -0.15至-1.05,p=0.009,1 项随机对照试验,n=111,低确定性证据;SMD -0.64,95% CI -1.25 至-0.03,p=0.04,I²=42%,2 项非随机干预试验前测/后测,n=40,极低确定性证据)。然而,只有 RCT 证据显示 HbA1c 有显著改善(SMD -0.48,95% CI -0.93,p=0.03,1 项 RCT,n=111,低确定性证据;SMD -0.25,95%CI -0.69 至 0.19,p-0.27,I²=0%,2 项 NSRIs 测试前/测试后,n=40,极低确定性证据)。洋紫荆和白茅之间未发现差异(血糖 SMD -0.03,95% CI -1.01 至 0.95,p=0.96,1 项 RCT,n=16,极低确定性证据;HbA1c SMD 0.06,95% CI -0.92 至 1.04,p=0.96,1 项 RCT,n=16,极低确定性证据)。结论研究结果表明,洋紫荆可有效降低血糖水平,但需谨慎解释这一证据。
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引用次数: 0
Effects of aromatherapy on anxiety in patients with cancer: A systematic review and meta-analysis of randomized controlled trials 芳香疗法对癌症患者焦虑的影响:随机对照试验的系统回顾和荟萃分析
IF 2.5 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-01-01 DOI: 10.1016/j.eujim.2023.102323
Ju Hyun Ahn, Myoungsuk Kim

Introduction

Patients with cancer often experience anxiety during cancer diagnosis and treatment, which can negatively impact their treatment outcomes. Although aromatherapy is believed to be effective in reducing anxiety in patients with cancer, the evidence has been limited. This review aimed to investigate the effectiveness of aromatherapy in reducing anxiety in patients with cancer and identify potential moderators of the intervention effects.

Methods

This review was conducted using data from PubMed, Embase, Cumulative Index to Nursing and Allied Health Literature (CINAHL), MEDLINE, Cochrane Library, and Web of Science, Regional Information Sharing Systems (RISS), Korean Information Service System (KISS), KoreaMed, and DBpia until March 16, 2023. The final analysis included 11 comparisons from 10 studies that administered aromatherapy to patients with cancer aged 18 years or older. The intervention effect was calculated by the standardized mean difference (SMD), and moderator analysis was performed using subgroup, meta-analysis of variance, and meta-regression analyses. The risk of bias was assessed using the revised Cochrane risk-of-bias tool for randomized trials.

Results

The overall impact of aromatherapy on anxiety reduction in patients with cancer indicated a large effect size (SMD = -0.97, 95 % confidence interval: -1.60 – -0.35, I2 = 94 %). In the subgroup analysis, the types of delivery methods and duration of the intervention were not found to be moderators causing heterogeneity in the effect sizes between trials. However, it was confirmed that the types of essential oils moderated the effects (Qb = 7.80, df = 2, pb = 0.020). Additionally, continuous moderators were not found to significantly moderate the intervention effect.

Conclusion

This review demonstrates that aromatherapy reduces anxiety in patients with cancer, suggesting the possibility of its application in clinical and community settings. However, considering the limited quantity of randomized controlled trials (RCTs) available for subgroup analysis, which potentially impacts the precision of study outcomes, further research is warranted by incorporating additional RCTs.

导言癌症患者在癌症诊断和治疗过程中经常会感到焦虑,这会对治疗效果产生负面影响。虽然芳香疗法被认为能有效减轻癌症患者的焦虑,但相关证据却很有限。本综述旨在研究芳香疗法在减轻癌症患者焦虑方面的有效性,并确定干预效果的潜在调节因素。方法本综述使用的数据来自 PubMed、Embase、Cumulative Index to Nursing and Allied Health Literature (CINAHL)、MEDLINE、Cochrane Library 和 Web of Science、Regional Information Sharing Systems (RISS)、Korean Information Service System (KISS)、KoreaMed 和 DBpia,截止日期为 2023 年 3 月 16 日。最终分析包括 10 项研究中的 11 项比较,这些研究对 18 岁或以上的癌症患者实施了芳香疗法。干预效果以标准化均值差异(SMD)计算,并使用亚组、方差分析和元回归分析进行调节因子分析。结果芳香疗法对减轻癌症患者焦虑的总体影响显示出较大的效应大小(SMD = -0.97,95% 置信区间:-1.60 -0.35,I2 = 94%)。在亚组分析中,没有发现干预方法的类型和持续时间是导致试验间效应大小异质性的调节因素。然而,研究证实,精油的种类对效果有调节作用(Qb = 7.80,df = 2,pb = 0.020)。结论本综述表明,芳香疗法可以减轻癌症患者的焦虑,这表明芳香疗法有可能应用于临床和社区环境中。然而,考虑到可用于亚组分析的随机对照试验(RCT)数量有限,可能会影响研究结果的精确性,因此有必要通过纳入更多的 RCT 进行进一步研究。
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European Journal of Integrative Medicine
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