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Exploring Korean Medicine professions' perspectives on the applicability of ChatGPT in facial palsy practice: A web-based survey 探讨韩国医学专业人士对ChatGPT在面瘫实践中的适用性的看法:一项基于网络的调查
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-12-01 DOI: 10.1016/j.eujim.2024.102422
Ji-Su Lee , Sung-A Kim , Taegon Kim , Seunghoon Lee , Tae-Hun Kim , Jung Won Kang

Introduction

Since November 2022, when Chat Generative Pre-trained Transformer (ChatGPT) was released, studies have been conducted to explore its potential use in various text-based areas. In the field of Korean Medicine (KM), studies evaluating the feasibility of ChatGPT are mainly focused on the educational domain. This study aimed to 1) identify the current level of ChatGPT-generated responses in answering questions from patients and KM practitioners, specifically exemplified by facial palsy and 2) explore the potential applicability of ChatGPT in KM practice through a perception survey of experts.

Methods

This study evaluates the applicability of ChatGPT concerning facial palsy through a survey of board-certified acupuncturists. The survey comprises two parts: assessing response quality for patients and for KM doctors in clinical practice. Ethical approval was obtained, and a 36-item questionnaire was administered online to 33 participants. Responses were analyzed for quality, relevance, and applicability using a combination of Likert scales and a standardized assessment tool.

Results

Among 33 eligible participants, 30 board-certified acupuncturists agreed to participate (response rate: 90.9 %). Survey results showed that the applicability of ChatGPT was lower for specialized KM practitioner inquiries than for general patient inquiries. Although the responses were considered useful to the readers (part 1: 96.7 %, part 2: 63.3 %) and understandable (part 1: 66.7 %, part 2: 60 %), the proportion of positive evaluations was relatively low in the domains assessing reliability and sufficiency.

Conclusions

Though ChatGPT is generally viewed positively for its potential utility, its direct application in KM clinical practice treating facial palsy at its current level seems challenging. To improve reliability, the information generated by ChatGPT should be critically reviewed by qualified expert medical personnel. To enhance sufficiency, further training of the artificial intelligence model with additional KM information is required.
自2022年11月聊天生成预训练转换器(ChatGPT)发布以来,已经进行了研究,以探索其在各种基于文本的领域的潜在用途。在韩医学领域,评估ChatGPT可行性的研究主要集中在教育领域。本研究旨在1)确定ChatGPT在回答患者和KM从业者的问题时产生的反应的当前水平,特别是以面瘫为例;2)通过对专家的感知调查,探索ChatGPT在KM实践中的潜在适用性。方法通过对执业针灸师的调查,评价ChatGPT在面瘫治疗中的适用性。调查包括两个部分:评估患者的反应质量和临床实践中的KM医生。获得了伦理许可,并对33名参与者进行了一份36项的在线问卷调查。使用李克特量表和标准化评估工具的组合来分析回答的质量、相关性和适用性。结果在33名符合条件的参与者中,有30名针灸师同意参与(回复率:90.9%)。调查结果显示,ChatGPT在专业KM从业者查询中的适用性低于一般患者查询。虽然回答被认为对读者有用(第1部分:96.7%,第2部分:63.3%)和可理解(第1部分:66.7%,第2部分:60%),但在评估可靠性和充分性方面,积极评价的比例相对较低。结论虽然ChatGPT的潜在效用被普遍认为是积极的,但其在KM临床实践中治疗面瘫的直接应用在目前的水平似乎具有挑战性。为提高可靠性,ChatGPT生成的信息应由合格的专业医务人员进行严格审查。为了提高充分性,需要使用额外的KM信息进一步训练人工智能模型。
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引用次数: 0
Efficacy and safety of acupuncture for perimenopausal insomnia: A systematic review and meta-analysis of randomized controlled trials 针灸治疗围绝经期失眠的疗效和安全性:随机对照试验的系统回顾和荟萃分析
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-12-01 DOI: 10.1016/j.eujim.2024.102404
Luquan Qin , Zhiyu Zhang , Chuanfang Zhang , Hua Zhou

Introduction

Acupuncture is widely recognized as an alternative therapy for perimenopausal insomnia (PMI) in China, yet it lacks robust evidence-based support. This systematic review evaluated the efficacy and safety of acupuncture in treating PMI.

Methods

We conducted a comprehensive search for randomized controlled trials (RCTs) evaluating acupuncture for PMI across eight databases (PubMed, Cochrane Library, Web of Science, Embase, CNKI, CSPD, CSTJ, and CBM) from their inception until May 17, 2024. We assessed the risk of bias using the Cochrane risk-of-bias tool for randomized trials (RoB). and performed a random-effects meta-analysis and GRADE assessment.

Results

The meta-analysis included 16 studies with 1,112 participants. We found evidence supporting the effectiveness of acupuncture in improving several outcomes. Acupuncture significantly improved sleep quality compared to sham-acupuncture or waitlist control (Pittsburgh sleep quality index (PSQI) MD -3.94, 95 %CI [-5.52, -2.35], 6 RCTs, 412 participants, moderate certainty) and medication (PSQI MD -2.62, 95 %CI [- 4.11, -1.12], 7 RCTs, 520 participants, low certainty). Clinical improvement rates were higher for acupuncture compared to medication or waitlist (RR 1.38, 95 %CI [1.12, 1.69], P = 0.002, low certainty). Objective measures using wrist actigraphy monitor or polysomnography favoured acupuncture over sham-acupuncture or medication for improving sleep efficiency (SMD 1.00, 95 %CI [0.70, 1.31], 5 RCTs, 330 participants, moderate certainty), total sleep time (SMD 0.84, 95 %CI [0.61, 1.06], 5 RCTs, 330 participants, moderate certainty) and wake after sleep onset (SMD -0.80, 95 %CI [-1.20, -0.40], 4 RCTs, 281 participants, low certainty), but not sleep awakenings (SMD 0.03, 95 %CI [-0.22, 0.27] 4 RCTs, 256 participants, low certainty). The effects of acupuncture on the Kupperman index and follicle-stimulating hormone (FSH) were inconclusive due to insufficient data. Adverse events were infrequent and symptoms were generally mild. There was a lower risk of adverse events from acupuncture compared to medication (RR 0.05, 95 %CI [0.0, 0.83], 3 RCTs, 183 participants, low certainty) and no difference compared to sham acupuncture (RR 1.25, 95 %CI [0.5, 3.1], moderate certainty).

Conclusion

The current body of research suggests acupuncture is an effective and safe treatment option for PMI, offering benefits over Western medication, though the available evidence remains limited.

Registration

PROSPERO CRD42023443190
在中国,针灸被广泛认为是治疗围绝经期失眠(PMI)的一种替代疗法,但缺乏强有力的证据支持。本系统综述评价了针灸治疗PMI的有效性和安全性。方法:我们对8个数据库(PubMed、Cochrane Library、Web of Science、Embase、CNKI、CSPD、CSTJ和CBM)中评估针灸治疗PMI的随机对照试验(rct)进行了全面检索,检索时间从这些数据库建立到2024年5月17日。我们使用Cochrane随机试验风险-偏倚工具(RoB)评估偏倚风险。并进行随机效应荟萃分析和GRADE评估。荟萃分析包括16项研究,1112名参与者。我们发现证据支持针灸在改善几个结果方面的有效性。与假针灸或候补对照相比,针灸显著改善了睡眠质量(匹兹堡睡眠质量指数(PSQI) MD -3.94, 95% CI[-5.52, -2.35], 6项随机对照试验,412名受试者,中等确定性)和药物治疗(PSQI MD -2.62, 95% CI[- 4.11, -1.12], 7项随机对照试验,520名受试者,低确定性)。针灸治疗的临床改良率高于药物治疗或等待治疗(RR 1.38, 95% CI [1.12, 1.69], P = 0.002,低确定性)。使用手腕活动监测仪或多导睡眠图进行的客观测量表明,在改善睡眠效率(SMD为1.00,95% CI[0.70, 1.31], 5项随机对照试验,330名受试者,中等确定性)、总睡眠时间(SMD为0.84,95% CI[0.61, 1.06], 5项随机对照试验,330名受试者,中等确定性)和睡眠后醒来(SMD为-0.80,95% CI[-1.20, -0.40], 4项随机对照试验,281名受试者,低确定性)方面,针灸优于假针灸或药物治疗,但在改善睡眠觉醒(SMD为0.03,95% CI[-0.22, 0.27] 4项随机对照试验,256名参与者,低确定性)。针刺对Kupperman指数和促卵泡激素(FSH)的影响由于资料不足尚无定论。不良事件很少发生,症状一般较轻。与药物治疗相比,针灸的不良事件风险较低(RR 0.05, 95% CI[0.0, 0.83], 3个随机对照试验,183名受试者,低确定性),与假针灸相比无差异(RR 1.25, 95% CI[0.5, 3.1],中等确定性)。目前的研究表明,针灸是一种有效和安全的治疗PMI的选择,提供比西药的好处,尽管现有的证据仍然有限。RegistrationPROSPERO CRD42023443190
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引用次数: 0
Phytochemical profiling of Prunus armeniaca kernel extracts and exploration of their multifaceted antioxidant and antibacterial effects through in vitro and in silico studies 亚美尼亚李核提取物的植物化学特征及其体外和体外抗氧化和抗菌作用的探索
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-12-01 DOI: 10.1016/j.eujim.2024.102421
Mohamed Amine El-Hajjaji , Kawtar Fikri-Benbrahim , Mohammed El Ouassete , Nidal Naceiri Mrabti , Najoua Soulo , Asmae El Ghouizi , Badiaa Lyoussi , Zineb Benziane Ouaritini

Introduction

Prunus armeniaca "Apricot" kernels are considered a by-product widely employed in traditional medicine for treating various ailments due to their potential therapeutic properties. The current investigation sought to assess the properties of aqueous and methanol extracts of Prunus armeniaca kernels (PAK).

Methods

The phytochemical composition of the studied extracts was evaluated using high-performance liquid chromatography with a diode array detector (HPLC-DAD). Total antioxidant capacity (TAC), β-carotene bleaching, reducing power (RP), and 2,2-Diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging assays were used to assess antioxidant activity. Using the disc diffusion method and the microdilution test in 96-well microplates against four bacterial strains, the antimicrobial activity of the aforementioned extracts was evaluated. The potential of several phenolic compounds as bacterial inhibitors was assessed through extensive density functional theory (DFT) calculations and molecular docking analyses.

Results

The phytochemical analysis revealed the identification of several phenolic constituents, with tocopherol (11.61 ± 0.9 mg/g of dry extract) and resveratrol (25.3 ± 0.4 mg/g of dry extract) emerging as the major compounds in the aqueous and methanolic extracts, respectively. Both extracts exhibited remarkable antioxidant activity with IC₅₀ values of 1.47 ± 0.08 and 1.97 ± 0.15 mg/mL (DPPH), EC₅₀ = 3.682 ± 0.123 and 12.415 ± 0.344 mg/mL (RP), TAC values of 6.486 ± 0.275 and 5.323 ± 0.826 mg AAE/g, and β-carotene values of 56 ± 0.553 % and 50 ± 0.645 % respectively. Moreover, the aqueous extract showed the highest antibacterial activity against Staphylococcus aureus with a MIC value of 0.625 mg/mL, and an inhibition zone diameter of 11.5 ± 0.71 mm. The combined analysis of docking results and DFT calculations for various phenolic compounds against Staphylococcus aureus (Glycyl-penicillin-binding protein 2a) and Escherichia coli (DNA Gyrase B) revealed significant interactions and reactivities.

Conclusion

These results clearly indicate that PAK contains a high concentration of bioactive compounds, especially tocopherol and resveratrol, and may serve in the treatment of various diseases thanks to its extracts' promising antioxidant and antimicrobial activities.
亚美尼亚prunus armeniaca“杏”核被认为是一种副产品,由于其潜在的治疗特性,被广泛应用于传统医学中治疗各种疾病。本研究旨在评价亚美尼亚李(Prunus armeniaca)仁(PAK)的水提物和甲醇提物的性质。方法采用高效液相色谱二极管阵列检测器(HPLC-DAD)对所研究提取物的植物化学成分进行鉴定。用总抗氧化能力(TAC)、β-胡萝卜素漂白、还原能力(RP)和2,2-二苯基-1-苦味肼基(DPPH)自由基清除试验来评估抗氧化活性。采用圆盘扩散法和96孔微孔板微量稀释试验对4种细菌进行抑菌活性评价。通过广泛的密度泛函理论(DFT)计算和分子对接分析,评估了几种酚类化合物作为细菌抑制剂的潜力。结果经植物化学分析,鉴定出多种酚类成分,其中水提物和甲醇提物的主要成分分别为生育酚(11.61±0.9 mg/g)和白藜芦醇(25.3±0.4 mg/g)。两种提取物都具有显着的抗氧化活性,IC₅₀值为1.47±0.08和1.97±0.15 mg/mL (DPPH), EC₅₀值为3.682±0.123和12.415±0.344 mg/mL (RP), TAC值为6.486±0.275和5.323±0.826 mg AAE/g, β-胡萝卜素值分别为56±0.553 %和50±0.645 %。水提物对金黄色葡萄球菌的抑菌活性最高,MIC值为0.625 mg/mL,抑菌带直径为11.5±0.71 mm。结合对接结果分析和DFT计算,多种酚类化合物对金黄色葡萄球菌(Glycyl-penicillin-binding protein 2a)和大肠杆菌(Escherichia coli, DNA Gyrase B)具有显著的相互作用和反应性。结论白芷提取物中含有高浓度的生物活性物质,特别是生育酚和白藜芦醇,具有良好的抗氧化和抗菌活性,可用于多种疾病的治疗。
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引用次数: 0
Changes in sperm quality with an antioxidant formula in mild-moderate male infertility: A prospective study 轻、中度男性不育症中抗氧化配方对精子质量的影响:一项前瞻性研究
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-12-01 DOI: 10.1016/j.eujim.2024.102412
Carolyn Ee , Jennifer Hunter , Alan Bensoussan , William Ledger , Andrew Davidson , Paul Fahey , Christopher Nicol , Harleen Kaur , Mitchell Low , Kate Templeman , Mahmoud A. Al-Dabbas , Caroline Smith

Introduction

This study aimed to examine for an association between an antioxidant formula and sperm quality, as well as safety, in males with mild to moderate sub-fertility.

Methods

A prospective, open-label single-arm study examined the association between 24 weeks treatment with a proprietary formula containing 15 vitamins, minerals and antioxidants (including L-carnitine, acetyl-L-carnitine, selenium, folic acid, L-cysteine and Co-enzyme Q10) and sperm quality in healthy males aged 20 – 60 with idiopathic teratospermia, asthenospermia and/or mild-moderate oligospermia. The primary outcome was simultaneous change in sperm concentration, progressive motility and morphology between screening, week 16 and week 24. Secondary outcomes included safety, pregnancy rates, sperm oxidative stress, sperm DNA fragmentation, and serum/plasma nutrient levels.

Results

Sixty-one participants, with a mean age of 35.8 years, were included in the intention-to-treat analysis. No improvement in overall sperm quality was observed (i.e. simultaneous improvement in all three measures) as only two of the three sperm quality measures improved. Mean sperm concentration decreased by 0.24 standard deviations (SD) while mean morphology and motility improved by 0.28 and 0.04 SD respectively, however, these changes did not reach clinical significance (set at ≥ 0.4 SD improvement in means). There were no changes in secondary outcomes apart from an increase in homocysteine and vitamin B12 levels and decrease in high DNA stainability. Fifteen pregnancies were reported (pregnancy rate 29 %). Twenty-one of 62 (33.8 %) participants reported 36 adverse events (AEs), one of which was serious, leading to study withdrawal. Most AEs were of mild intensity and resolved.

Conclusion

Twenty-four weeks of an antioxidant formula was not associated with clinically significant changes in overall sperm quality. The formula was generally safe and well tolerated. Our findings are limited by the single- arm design, and randomised controlled trials are required to confirm or refute our findings.
本研究旨在研究抗氧化配方与轻度至中度生育能力低下男性精子质量和安全性之间的关系。方法一项前瞻性、开放标签单臂研究考察了20 - 60岁特发性畸形精子症、弱精子症和/或轻中度少精子症的健康男性服用含有15种维生素、矿物质和抗氧化剂(包括左旋肉碱、乙酰左旋肉碱、硒、叶酸、l-半胱氨酸和辅酶Q10)的专有配方治疗24周与精子质量的关系。主要终点是精子浓度、进行性运动和形态在筛查第16周和第24周之间的同时变化。次要结局包括安全性、妊娠率、精子氧化应激、精子DNA断裂和血清/血浆营养水平。结果61名参与者被纳入意向治疗分析,平均年龄为35.8岁。没有观察到整体精子质量的改善(即所有三项措施同时改善),因为三项精子质量措施中只有两项得到改善。平均精子浓度下降了0.24个标准差(SD),平均形态和活力分别改善了0.28和0.04个标准差,但这些变化未达到临床意义(平均改善≥0.4个标准差)。除了同型半胱氨酸和维生素B12水平升高和高DNA染色性降低外,次要结果没有变化。报告15例妊娠(妊娠率29%)。62名参与者中有21名(33.8%)报告了36例不良事件(ae),其中1例严重,导致研究退出。大多数ae强度较轻且已消退。结论24周的抗氧化配方与总体精子质量的临床显著变化无关。该配方总体上是安全的,耐受性良好。我们的研究结果受到单臂设计的限制,需要随机对照试验来证实或反驳我们的研究结果。
{"title":"Changes in sperm quality with an antioxidant formula in mild-moderate male infertility: A prospective study","authors":"Carolyn Ee ,&nbsp;Jennifer Hunter ,&nbsp;Alan Bensoussan ,&nbsp;William Ledger ,&nbsp;Andrew Davidson ,&nbsp;Paul Fahey ,&nbsp;Christopher Nicol ,&nbsp;Harleen Kaur ,&nbsp;Mitchell Low ,&nbsp;Kate Templeman ,&nbsp;Mahmoud A. Al-Dabbas ,&nbsp;Caroline Smith","doi":"10.1016/j.eujim.2024.102412","DOIUrl":"10.1016/j.eujim.2024.102412","url":null,"abstract":"<div><h3>Introduction</h3><div>This study aimed to examine for an association between an antioxidant formula and sperm quality, as well as safety, in males with mild to moderate sub-fertility.</div></div><div><h3>Methods</h3><div>A prospective, open-label single-arm study examined the association between 24 weeks treatment with a proprietary formula containing 15 vitamins, minerals and antioxidants (including L-carnitine, acetyl-L-carnitine, selenium, folic acid, L-cysteine and Co-enzyme Q10) and sperm quality in healthy males aged 20 – 60 with idiopathic teratospermia, asthenospermia and/or mild-moderate oligospermia. The primary outcome was simultaneous change in sperm concentration, progressive motility and morphology between screening, week 16 and week 24. Secondary outcomes included safety, pregnancy rates, sperm oxidative stress, sperm DNA fragmentation, and serum/plasma nutrient levels.</div></div><div><h3>Results</h3><div>Sixty-one participants, with a mean age of 35.8 years, were included in the intention-to-treat analysis. No improvement in overall sperm quality was observed (i.e. simultaneous improvement in all three measures) as only two of the three sperm quality measures improved. Mean sperm concentration decreased by 0.24 standard deviations (SD) while mean morphology and motility improved by 0.28 and 0.04 SD respectively, however, these changes did not reach clinical significance (set at ≥ 0.4 SD improvement in means). There were no changes in secondary outcomes apart from an increase in homocysteine and vitamin B12 levels and decrease in high DNA stainability. Fifteen pregnancies were reported (pregnancy rate 29 %). Twenty-one of 62 (33.8 %) participants reported 36 adverse events (AEs), one of which was serious, leading to study withdrawal. Most AEs were of mild intensity and resolved.</div></div><div><h3>Conclusion</h3><div>Twenty-four weeks of an antioxidant formula was not associated with clinically significant changes in overall sperm quality. The formula was generally safe and well tolerated. Our findings are limited by the single- arm design, and randomised controlled trials are required to confirm or refute our findings.</div></div>","PeriodicalId":11932,"journal":{"name":"European Journal of Integrative Medicine","volume":"72 ","pages":"Article 102412"},"PeriodicalIF":1.9,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142748554","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
Effect of clinical control and symptom severity on attitudes towards holistic complementary alternative medicine in individuals with chronic obstructive pulmonary disease: A cross-sectional study 临床控制和症状严重程度对慢性阻塞性肺病患者整体补充替代医学态度的影响:横断面研究
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-11-20 DOI: 10.1016/j.eujim.2024.102415
Züleyha Kılıç, Rabiye Çırpan

Introduction

Many symptoms such as dyspnoea, chronic cough, chronic expectoration experienced in chronic obstructive pulmonary disease (COPD) and the progressive course of the disease negatively affect individuals bio-psychosocially and reduce their quality of life. At this point, it is believed to be important to use pharmacological and evidence-based complementary alternative medicine (CAM) methods together for effective disease management in COPD. The purpose of this study was to investigate the effect of clinical control and symptom severity on attitudes towards holistic, complementary, and alternative medicine in individuals with COPD.

Methods

This descriptive and correlational study was conducted with 150 hospitalised individuals with COPD that met the inclusion criteria for the study. A questionnaire form, the Modified Medical Research Council Dyspnoea Scale (mMRC), the Clinical COPD Questionnaire (CCQ), COPD Assessment Test (CAT), and the Holistic Complementary and Alternative Medicine Questionnaire (HCAMQ) were used to collect the data.

Results

In the study, 38% of the individuals with COPD used CAM, and herbal methods were the most preferred. The mean HCAMQ score was 28.24 ± 5.88. There was a statistically significant positive correlation between HCAMQ and mMRC and Clinical COPD Questionnaire functional status scores (p < 0.05). An increase of one unit in the mMRC scores was correlated with an increase in HCAMQ scores of 1.125 points (p < 0.05).

Conclusion

The present study determined that individuals with COPD had a positive attitude towards CAM, and the positive attitude towards CAM decreased with increasing dyspnoea level and decreasing COPD functional status control.

Funding

None
导言:慢性阻塞性肺疾病(COPD)的许多症状,如呼吸困难、慢性咳嗽、慢性痰多,以及疾病的进展过程都会对患者的社会心理产生负面影响,降低他们的生活质量。因此,将药物治疗与循证补充替代医学(CAM)方法结合使用,对慢性阻塞性肺病患者进行有效的疾病管理显得尤为重要。本研究的目的是调查临床控制和症状严重程度对慢性阻塞性肺病患者对整体、补充和替代医学的态度的影响。方法本研究对符合研究纳入标准的 150 名慢性阻塞性肺病住院患者进行了描述性和相关性研究。研究采用了问卷调查表、改良医学研究委员会呼吸困难量表(mMRC)、慢性阻塞性肺病临床问卷(CCQ)、慢性阻塞性肺病评估测试(CAT)以及整体补充和替代医学问卷(HCAMQ)来收集数据。结果在研究中,38%的慢性阻塞性肺病患者使用了CAM,其中草药方法最受青睐。平均 HCAMQ 得分为 28.24 ± 5.88。HCAMQ 与 mMRC 和临床慢性阻塞性肺病问卷功能状态评分之间存在统计学意义上的正相关(p < 0.05)。本研究表明,慢性阻塞性肺病患者对 CAM 持积极态度,并且随着呼吸困难程度的增加和慢性阻塞性肺病功能状态控制程度的降低,对 CAM 的积极态度也随之降低。
{"title":"Effect of clinical control and symptom severity on attitudes towards holistic complementary alternative medicine in individuals with chronic obstructive pulmonary disease: A cross-sectional study","authors":"Züleyha Kılıç,&nbsp;Rabiye Çırpan","doi":"10.1016/j.eujim.2024.102415","DOIUrl":"10.1016/j.eujim.2024.102415","url":null,"abstract":"<div><h3>Introduction</h3><div>Many symptoms such as dyspnoea, chronic cough, chronic expectoration experienced in chronic obstructive pulmonary disease (COPD) and the progressive course of the disease negatively affect individuals bio-psychosocially and reduce their quality of life. At this point, it is believed to be important to use pharmacological and evidence-based complementary alternative medicine (CAM) methods together for effective disease management in COPD. The purpose of this study was to investigate the effect of clinical control and symptom severity on attitudes towards holistic, complementary, and alternative medicine in individuals with COPD.</div></div><div><h3>Methods</h3><div>This descriptive and correlational study was conducted with 150 hospitalised individuals with COPD that met the inclusion criteria for the study. A questionnaire form, the Modified Medical Research Council Dyspnoea Scale (mMRC), the Clinical COPD Questionnaire (CCQ), COPD Assessment Test (CAT), and the Holistic Complementary and Alternative Medicine Questionnaire (HCAMQ) were used to collect the data.</div></div><div><h3>Results</h3><div>In the study, 38% of the individuals with COPD used CAM, and herbal methods were the most preferred. The mean HCAMQ score was 28.24 ± 5.88. There was a statistically significant positive correlation between HCAMQ and mMRC and Clinical COPD Questionnaire functional status scores (p &lt; 0.05). An increase of one unit in the mMRC scores was correlated with an increase in HCAMQ scores of 1.125 points (p &lt; 0.05).</div></div><div><h3>Conclusion</h3><div>The present study determined that individuals with COPD had a positive attitude towards CAM, and the positive attitude towards CAM decreased with increasing dyspnoea level and decreasing COPD functional status control.</div></div><div><h3>Funding</h3><div>None</div></div>","PeriodicalId":11932,"journal":{"name":"European Journal of Integrative Medicine","volume":"72 ","pages":"Article 102415"},"PeriodicalIF":1.9,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142701095","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
Evolving research methodologies are shaping the future of integrative medicine 不断发展的研究方法正在塑造综合医学的未来
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-11-12 DOI: 10.1016/j.eujim.2024.102420
Jennifer Hunter , Guo-Yan Yang , Nicola Robinson
{"title":"Evolving research methodologies are shaping the future of integrative medicine","authors":"Jennifer Hunter ,&nbsp;Guo-Yan Yang ,&nbsp;Nicola Robinson","doi":"10.1016/j.eujim.2024.102420","DOIUrl":"10.1016/j.eujim.2024.102420","url":null,"abstract":"","PeriodicalId":11932,"journal":{"name":"European Journal of Integrative Medicine","volume":"72 ","pages":"Article 102420"},"PeriodicalIF":1.9,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142701097","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
Hotspots and trends in global antiviral herbal basic research: A visualization analysis 全球抗病毒草药基础研究的热点和趋势:可视化分析
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-11-05 DOI: 10.1016/j.eujim.2024.102419
Liangyu Hu, Chunying Wang, Yang Zhang
Introduction: Viral infections can become public health emergencies due to the possibility of the wide transmission of their associated pathogens and their rapid variation. Moreover, most viruses lack effective therapeutic drugs and vaccines. Herbal medicines have been clinically validated for their broad-spectrum antiviral properties and their ability to leverage their complex compositions to target multiple levels, pathways, and channels. In this study, we seek to assess the current global research landscape and identify current and future directions for research on antiviral herbal medicines to guide future pharmacological developments. Methods: Bibliometric and visualization methods were used to analyze 2134 Chinese-language and 4600 English-language journal articles published between 2017 and 2022 from both Chinese and international databases, and the theme words and foci of highly cited papers were analyzed. Results: It was found that coronaviruses (especially severe acute respiratory syndrome coronavirus 2, SARS-CoV-2), the influenza virus, the hepatitis B virus, and the human immunodeficiency virus were the primary targets for antiviral herbal medicines. Key herbs included Glycyrrhiza glabra, Lonicera japonica, Scutellaria baicalensis, Ephedra sinica, Forsythia suspensa, Agastache rugosa, Astragalus membranaceus, and Poria cocos. The primary active compounds known to be responsible for these antiviral effects are alkaloids, bioflavonoids, flavonoids, sterols, and polyphenols, including curcumin, quercetin, kaempferol, wogonin, stigmasterol, β-glutosterol, luteolin, coumarins, naringenin, gallic acid, berberine, and andrographolide. These compounds work through mechanisms such as inhibiting viral replication, blocking virus–receptor interactions, destroying viruses, regulating the immune response, oxidative stress induction, and cytokine response suppression. Conclusions: The research foci included the pharmacodynamic foundations, molecular dynamics simulation, and virtual screening of active components in herbs use for the treatment of viral diseases such as SARS-CoV-2 using bioinformatics, macromolecular docking, and network pharmacology. Significant gaps remain in interdisciplinary collaboration, especially regarding herb cultivation, processing, sustainable harvesting, and potential drug interactions.
导言:病毒感染可能成为公共卫生突发事件,因为其相关病原体可能广泛传播,而且变异迅速。此外,大多数病毒都缺乏有效的治疗药物和疫苗。中草药的广谱抗病毒特性及其利用复杂成分靶向多层次、多途径和多通道的能力已得到临床验证。在本研究中,我们试图评估当前的全球研究状况,并确定当前和未来的抗病毒中药研究方向,以指导未来的药理学发展。研究方法采用文献计量学和可视化方法分析了2017年至2022年期间发表的2134篇中文期刊论文和4600篇英文期刊论文,分别来自中文和国际数据库,并分析了高被引论文的主题词和病灶。结果发现发现冠状病毒(尤其是严重急性呼吸系统综合征冠状病毒2,SARS-CoV-2)、流感病毒、乙型肝炎病毒和人类免疫缺陷病毒是抗病毒中药的主要靶标。主要药材包括甘草、忍冬、黄芩、麻黄、连翘、黄芪和茯苓。已知具有抗病毒作用的主要活性化合物是生物碱、生物类黄酮、类黄酮、甾醇和多酚,包括姜黄素、槲皮素、山柰酚、木犀草素、豆甾醇、β-谷甾醇、木犀草素、香豆素、柚皮苷、没食子酸、小檗碱和穿心莲内酯。这些化合物通过抑制病毒复制、阻断病毒与受体的相互作用、破坏病毒、调节免疫反应、诱导氧化应激和抑制细胞因子反应等机制发挥作用。结论研究重点包括药效学基础、分子动力学模拟,以及利用生物信息学、大分子对接和网络药理学对治疗 SARS-CoV-2 等病毒性疾病的中草药活性成分进行虚拟筛选。在跨学科合作方面仍存在巨大差距,特别是在草药种植、加工、可持续收获和潜在的药物相互作用方面。
{"title":"Hotspots and trends in global antiviral herbal basic research: A visualization analysis","authors":"Liangyu Hu,&nbsp;Chunying Wang,&nbsp;Yang Zhang","doi":"10.1016/j.eujim.2024.102419","DOIUrl":"10.1016/j.eujim.2024.102419","url":null,"abstract":"<div><div>Introduction: Viral infections can become public health emergencies due to the possibility of the wide transmission of their associated pathogens and their rapid variation. Moreover, most viruses lack effective therapeutic drugs and vaccines. Herbal medicines have been clinically validated for their broad-spectrum antiviral properties and their ability to leverage their complex compositions to target multiple levels, pathways, and channels. In this study, we seek to assess the current global research landscape and identify current and future directions for research on antiviral herbal medicines to guide future pharmacological developments. Methods: Bibliometric and visualization methods were used to analyze 2134 Chinese-language and 4600 English-language journal articles published between 2017 and 2022 from both Chinese and international databases, and the theme words and foci of highly cited papers were analyzed. Results: It was found that coronaviruses (especially severe acute respiratory syndrome coronavirus 2, SARS-CoV-2), the influenza virus, the hepatitis B virus, and the human immunodeficiency virus were the primary targets for antiviral herbal medicines. Key herbs included <em>Glycyrrhiza glabra, Lonicera japonica, Scutellaria baicalensis, Ephedra sinica, Forsythia suspensa, Agastache rugosa, Astragalus membranaceus</em>, and <em>Poria cocos</em>. The primary active compounds known to be responsible for these antiviral effects are alkaloids, bioflavonoids, flavonoids, sterols, and polyphenols, including curcumin, quercetin, kaempferol, wogonin, stigmasterol, β-glutosterol, luteolin, coumarins, naringenin, gallic acid, berberine, and andrographolide. These compounds work through mechanisms such as inhibiting viral replication, blocking virus–receptor interactions, destroying viruses, regulating the immune response, oxidative stress induction, and cytokine response suppression. Conclusions: The research foci included the pharmacodynamic foundations, molecular dynamics simulation, and virtual screening of active components in herbs use for the treatment of viral diseases such as SARS-CoV-2 using bioinformatics, macromolecular docking, and network pharmacology. Significant gaps remain in interdisciplinary collaboration, especially regarding herb cultivation, processing, sustainable harvesting, and potential drug interactions.</div></div>","PeriodicalId":11932,"journal":{"name":"European Journal of Integrative Medicine","volume":"72 ","pages":"Article 102419"},"PeriodicalIF":1.9,"publicationDate":"2024-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142701096","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effectiveness and safety of Qianjinweijing decoction in the treatment of bronchiectasis: A systematic review and meta-analysis 千金味精煎剂治疗支气管扩张症的有效性和安全性:系统回顾和荟萃分析
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-11-02 DOI: 10.1016/j.eujim.2024.102418
Limin Zhang, Jin Su, Xiaozheng Wu, Wen Li, Yunzhi Chen
<div><h3>Introduction</h3><div>Bronchiectasis is a chronic inflammatory airway disease marked by permanent dilation of the bronchi, recurrent infections, and associated complications. The traditional Chinese medicine Qianjinweijing Decoction (QJWJ) has shown promising results in bronchiectasis treatment with few side effects. However, there is a lack of recent comprehensive research evaluating its effectiveness. This review aims to examine the effectiveness and safety of QJWJ in treating bronchiectasis.</div></div><div><h3>Methods</h3><div>We searched 7 databases including China National Knowledge Infrastructure (CNKI), Wanfang Database, VIP Chinese Science Database, China Biology Medicine Disc (Sinomed), PubMed, Embase, and Cochrane Library, for relevant randomized controlled trials (RCTs) until May 2023, in both Chinese and English. Two researchers conducted a comprehensive review of literature, extracting data based on predefined criteria. The risk of bias was assessed using the Cochrane Collaboration tool, and meta-analysis was performed using RevMan 5.4.1 and RStudio software. Quality of evidence was evaluated using GRADEpro (V3.6.) software.</div></div><div><h3>Results</h3><div>This review analysed 35 studies with 2609 patients. The QJWJ group consisted of 1318 patients, while the routine pharmacotherapy (RP) group had 1291 patients. Combining QJWJ and RP in bronchiectasis treatment showed better with clinical effectiveness [risk ratio (RR)=1.17, 95 % confidence interval (CI) (1.13, 1.21), <em>P</em> < 0.00001], the percentage of forced expiratory volume in the first second to the predicted value (FEV<sub>1</sub> %) [mean difference (MD)=3.52, 95 % CI (1.48, 5.55), <em>P</em> = 0.0007], the ratio of forced expiratory volume to forced vital capacity in the first second (FEV<sub>1</sub>/FVC) [MD=6.62, 95 % CI (1.52, 11.72), <em>P</em> = 0.01], peak expiratory flow rate (PEFR) [MD=7.14, 95 % CI (5.15, 9.12), <em>P</em> < 0.00001], white blood cell count (WBC) [MD=-1.42, 95 % CI (-2.53, -0.31), <em>P</em> = 0.01], c-reactive protein (CRP) [MD=-7.2, 95 % CI (-9.3, -5.1), <em>P</em> < 0.00001], and the procalcitonin (PCT) [standardized mean difference (SMD)=-1.39, 95 % CI (-2.02, -0.76), <em>P</em> < 0.0001], without increasing the incidence of adverse reactions [RR=0.79, 95 % CI (0.44, 1.42), <em>P</em> = 0.43]. QJWJ alone also significantly improved bronchiectasis treatment, enhanced clinical effectiveness [RR=1.19, 95 % CI (1.04, 1.36), <em>P</em> = 0.010], FEV<sub>1</sub> % [MD=7.09, 95 % CI (4.5, 9.68), <em>P</em> < 0.00001], and reduced WBC [MD=-2.7, 95 % CI (-3.7, -1.7), <em>P</em> < 0.00001], CRP [MD=-4.22, 95 % CI (-55.32, -3.12), <em>P</em> < 0.00001], without increasing the incidence of adverse reactions [RR=0.20, 95 % CI (0.01, 4.06), <em>P</em> = 0.29].</div></div><div><h3>Conclusion</h3><div>Evidence suggested that QJWJ, used alone or with RP, notably improved bronchiectasis treatment outcomes, enhanced lung fun
导言支气管扩张症是一种慢性气道炎症性疾病,以支气管永久性扩张、反复感染和相关并发症为特征。传统中药千金微晶煎剂(QJWJ)在治疗支气管扩张症方面疗效显著,且副作用小。然而,近期缺乏对其疗效进行全面评估的研究。方法我们检索了7个数据库,包括中国国家知识基础设施(CNKI)、万方数据库、VIP中国科学数据库、中国生物医学文献数据库(Sinomed)、PubMed、Embase和Cochrane图书馆,寻找截至2023年5月的相关中英文随机对照试验(RCT)。两名研究人员对文献进行了全面审查,并根据预先确定的标准提取数据。使用 Cochrane 协作工具评估了偏倚风险,并使用 RevMan 5.4.1 和 RStudio 软件进行了荟萃分析。使用 GRADEpro (V3.6.) 软件对证据质量进行了评估。QJWJ组有1318名患者,而常规药物治疗(RP)组有1291名患者。将 QJWJ 和 RP 联合用于支气管扩张症治疗显示出更好的临床疗效[风险比(RR)=1.17,95 % 置信区间(CI)(1.13,1.21),P < 0.00001]、第一秒用力呼气容积占预测值的百分比(FEV1 %)[平均差(MD)=3.52,95 % CI(1.48,5.55),P = 0.0007]、第一秒用力呼气容积与用力肺活量之比(FEV1/FVC)[MD=6.62,95 % CI(1.52,11.72),P = 0.01]、呼气峰流速(PEFR)[MD=7.14,95 % CI(5.15,9.12),P <;0.00001]、白细胞计数(WBC)[MD=-1.42,95 % CI(-2.53,-0.31),P = 0.01]、c 反应蛋白(CRP)[MD=-7.2,95 % CI(-9.3,-5.1),P< 0.00001]、降钙素原(PCT)[标准化平均差(SMD)=-1.39,95 % CI(-2.02,-0.76),P< 0.0001],同时不增加不良反应的发生率[RR=0.79,95 % CI(0.44,1.42),P=0.43]。单用 QJWJ 也能明显改善支气管扩张症的治疗,提高临床疗效 [RR=1.19, 95 % CI (1.04, 1.36), P = 0.010]、FEV1 % [MD=7.09,95 % CI(4.5,9.68),P <;0.00001],降低WBC[MD=-2.7,95 % CI(-3.7,-1.7),P <;0.00001]、CRP[MD=-4.22,95 % CI(-55.32,-3.12),P <;0.结论有证据表明,单独使用或与 RP 一起使用 QJWJ 可显著改善支气管扩张症的治疗效果,增强肺功能,减轻炎症反应,而不会增加不良反应风险。然而,要加强这一结论,还需要高质量、大样本 RCT 的进一步支持。
{"title":"Effectiveness and safety of Qianjinweijing decoction in the treatment of bronchiectasis: A systematic review and meta-analysis","authors":"Limin Zhang,&nbsp;Jin Su,&nbsp;Xiaozheng Wu,&nbsp;Wen Li,&nbsp;Yunzhi Chen","doi":"10.1016/j.eujim.2024.102418","DOIUrl":"10.1016/j.eujim.2024.102418","url":null,"abstract":"&lt;div&gt;&lt;h3&gt;Introduction&lt;/h3&gt;&lt;div&gt;Bronchiectasis is a chronic inflammatory airway disease marked by permanent dilation of the bronchi, recurrent infections, and associated complications. The traditional Chinese medicine Qianjinweijing Decoction (QJWJ) has shown promising results in bronchiectasis treatment with few side effects. However, there is a lack of recent comprehensive research evaluating its effectiveness. This review aims to examine the effectiveness and safety of QJWJ in treating bronchiectasis.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Methods&lt;/h3&gt;&lt;div&gt;We searched 7 databases including China National Knowledge Infrastructure (CNKI), Wanfang Database, VIP Chinese Science Database, China Biology Medicine Disc (Sinomed), PubMed, Embase, and Cochrane Library, for relevant randomized controlled trials (RCTs) until May 2023, in both Chinese and English. Two researchers conducted a comprehensive review of literature, extracting data based on predefined criteria. The risk of bias was assessed using the Cochrane Collaboration tool, and meta-analysis was performed using RevMan 5.4.1 and RStudio software. Quality of evidence was evaluated using GRADEpro (V3.6.) software.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Results&lt;/h3&gt;&lt;div&gt;This review analysed 35 studies with 2609 patients. The QJWJ group consisted of 1318 patients, while the routine pharmacotherapy (RP) group had 1291 patients. Combining QJWJ and RP in bronchiectasis treatment showed better with clinical effectiveness [risk ratio (RR)=1.17, 95 % confidence interval (CI) (1.13, 1.21), &lt;em&gt;P&lt;/em&gt; &lt; 0.00001], the percentage of forced expiratory volume in the first second to the predicted value (FEV&lt;sub&gt;1&lt;/sub&gt; %) [mean difference (MD)=3.52, 95 % CI (1.48, 5.55), &lt;em&gt;P&lt;/em&gt; = 0.0007], the ratio of forced expiratory volume to forced vital capacity in the first second (FEV&lt;sub&gt;1&lt;/sub&gt;/FVC) [MD=6.62, 95 % CI (1.52, 11.72), &lt;em&gt;P&lt;/em&gt; = 0.01], peak expiratory flow rate (PEFR) [MD=7.14, 95 % CI (5.15, 9.12), &lt;em&gt;P&lt;/em&gt; &lt; 0.00001], white blood cell count (WBC) [MD=-1.42, 95 % CI (-2.53, -0.31), &lt;em&gt;P&lt;/em&gt; = 0.01], c-reactive protein (CRP) [MD=-7.2, 95 % CI (-9.3, -5.1), &lt;em&gt;P&lt;/em&gt; &lt; 0.00001], and the procalcitonin (PCT) [standardized mean difference (SMD)=-1.39, 95 % CI (-2.02, -0.76), &lt;em&gt;P&lt;/em&gt; &lt; 0.0001], without increasing the incidence of adverse reactions [RR=0.79, 95 % CI (0.44, 1.42), &lt;em&gt;P&lt;/em&gt; = 0.43]. QJWJ alone also significantly improved bronchiectasis treatment, enhanced clinical effectiveness [RR=1.19, 95 % CI (1.04, 1.36), &lt;em&gt;P&lt;/em&gt; = 0.010], FEV&lt;sub&gt;1&lt;/sub&gt; % [MD=7.09, 95 % CI (4.5, 9.68), &lt;em&gt;P&lt;/em&gt; &lt; 0.00001], and reduced WBC [MD=-2.7, 95 % CI (-3.7, -1.7), &lt;em&gt;P&lt;/em&gt; &lt; 0.00001], CRP [MD=-4.22, 95 % CI (-55.32, -3.12), &lt;em&gt;P&lt;/em&gt; &lt; 0.00001], without increasing the incidence of adverse reactions [RR=0.20, 95 % CI (0.01, 4.06), &lt;em&gt;P&lt;/em&gt; = 0.29].&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Conclusion&lt;/h3&gt;&lt;div&gt;Evidence suggested that QJWJ, used alone or with RP, notably improved bronchiectasis treatment outcomes, enhanced lung fun","PeriodicalId":11932,"journal":{"name":"European Journal of Integrative Medicine","volume":"72 ","pages":"Article 102418"},"PeriodicalIF":1.9,"publicationDate":"2024-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142701094","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
Reflexology specific guidance for using the template for the intervention description and replication (TIDieR): A delphi study 使用干预描述和复制模板(TIDieR)的反射疗法具体指导:德尔菲研究
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-10-23 DOI: 10.1016/j.eujim.2024.102416
Jacqueline James , Joseph T. Costello , Sally Edwards-Price , Tracey Smith , Amanda McAuley , Barbara E. Scott , Spyridon Dimitrakoulas , Marcia Edwards , Dorothy Kelly , David L. Wayte , Andrea F. Porritt , Amy K. Drahota

Introduction

Reflexology is a holistic, complementary therapy, carried out on the feet, hands, ears, or face. There is no single accepted definition of reflexology, as it encompasses various practices, making it important that research studies articulate exactly what the reflexology intervention entailed.
This study sought to produce reflexology-specific guidance for researchers and practitioners, for use with the Template for the Intervention Description and Replication (TIDieR) checklist, to improve the quality of the documentation of reflexology interventions within the research literature.

Method

This study used the TIDieR checklist as a framework for a three-round Delphi process to gain agreement on what information authors should consider including in their study report to support replication of their intervention. Following the Delphi process two online consolidation meetings were held to agree the wording and examples for the guidance document.

Results

Guidance based on the unique considerations of reflexology interventions was developed for use with the TIDieR checklist.
A diverse group of 43 experts from Europe, North America, Asia, and Australasia, including 40 reflexologists, 9 of whom were also study authors, and 2 methodological specialists contributed to the guidance.
Each Delphi round was completed by 39 to 42 (91 % to 98 %) of the 43 panel members, and 16 (37 %) participated in the consolidation meetings. Consensus was reached on 46 items via the Delphi rounds (36 to be included in the guidance and 10 to be excluded); 38 items failed to reach consensus. The consolidation meetings informed the final wording of the guidance document, covering all the 12 TIDieR domains.

Conclusion

The reflexology-specific guidance strongly advocates for the utilisation of the TIDieR checklist, with elaboration tailored for reflexology as used in various contexts internationally. By serving as a reporting guide for reflexology intervention studies, this tool has the capacity to improve the reporting of reflexology intervention studies, thereby facilitating replicability and promoting greater transparency within the field of reflexology.
导言反射疗法是一种在脚、手、耳朵或面部进行的整体性辅助疗法。本研究旨在为研究人员和从业人员提供针对反射疗法的指导,与干预描述和复制模板(TIDieR)核对表一起使用,以提高研究文献中反射疗法干预的记录质量。方法本研究以 TIDieR 核对表为框架,开展了三轮德尔菲过程,以就作者应考虑在其研究报告中包含哪些信息以支持其干预措施的复制达成一致意见。来自欧洲、北美、亚洲和澳大拉西亚的 43 位专家(包括 40 位反射疗法专家,其中 9 位同时也是研究报告的作者)和 2 位方法论专家组成了一个多元化的小组,为指南的编写做出了贡献。43 位小组成员中有 39 到 42 人(91 % 到 98 %)完成了每轮德尔菲讨论,16 人(37 %)参加了合并会议。德尔菲小组就 46 个项目达成共识(36 个项目纳入指南,10 个项目排除在外);38 个项目未能达成共识。合并会议为指导文件的最终措辞提供了依据,该文件涵盖了 TIDieR 的所有 12 个领域。通过作为反射疗法干预研究的报告指南,该工具能够改进反射疗法干预研究的报告,从而提高反射疗法领域的可复制性和透明度。
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引用次数: 0
Ayurveda interventions for non-specific chronic low back pain— protocol for a systematic review and network meta-analysis 阿育吠陀对非特异性慢性腰背痛的干预--系统综述和网络荟萃分析方案
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-10-19 DOI: 10.1016/j.eujim.2024.102413
Ritu Kumari, Mandip Goyal, Kalpesh Panara

Introduction

Low back pain (570 million prevalent cases worldwide) is the main contributor to the overall burden of musculoskeletal conditions. The most common form of low back pain is non-specific low back pain (NSCLBP) (almost 90 %). There are no treatments that completely cure chronic low back pain. Ayurveda is one of the traditional systems of Indian medicine commonly practiced in Southeast Asian countries. Even though Ayurveda interventions (oral medication or procedure-based treatment or combined therapy) are practiced widely for this condition, there is ambiguity about the hierarchy of treatment. The present review has been planned to compare all the available Ayurveda treatment modalities for NSCLBP in terms of efficacy, and safety, in all the age groups of patients.

Methods

This review will be written in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) and the PRISMA extension for network meta-analyses. Electronic searches will be carried out in PubMed, Scopus, TRIP, Website of Indexing of Indian Medical Journals, the Cochrane Register for Controlled Trials, The Clinical Trials Registry- India, AYUSH research portal, and Digital Helpline for Ayurveda Research Articles, and other pre-print repositories since its inception till 31st March 2024. Randomized controlled trials, randomized cross-over studies, cluster-randomized studies, and nonrandomized studies of interventions (prospective cohort studies, non-randomized clinical trials) will be included. The risk of bias will be assessed with ROB-2, ROBINS-I, and other revised risk of bias tools for cross-over studies and cluster randomised studies recommended by the Cochrane collaboration. To evaluate the credibility of the findings, the Grading of Recommendations Assessment, Development, and Evaluation method for network meta-analysis will be implemented. A narrative approach to synthesize and report qualitative and quantitative data will be used, and where feasible, we will conduct network meta-analyses using STATA software.

Conclusions

This protocol defines a plan of the study that would facilitate the process of recommending treatment for NSCLBP, by providing a treatment hierarchy of Ayurvedic treatment to the policymakers and stakeholders.
导言腰背痛(全球有 5.7 亿发病病例)是造成肌肉骨骼疾病总体负担的主要因素。最常见的腰背痛是非特异性腰背痛(NSCLBP)(近 90%)。目前还没有完全治愈慢性腰背痛的疗法。阿育吠陀是印度的传统医学体系之一,在东南亚国家很普遍。尽管阿育吠陀疗法(口服药物、程序性治疗或综合疗法)被广泛用于治疗这种病症,但在治疗的层次上却存在模糊不清的地方。本综述计划比较所有可用的阿育吠陀治疗 NSCLBP 的方法对所有年龄组患者的疗效和安全性。方法本综述将根据系统综述和荟萃分析首选报告项目(PRISMA)和网络荟萃分析 PRISMA 扩展项目撰写。电子检索将在 PubMed、Scopus、TRIP、印度医学期刊索引网站、Cochrane 对照试验注册中心、印度临床试验注册中心、AYUSH 研究门户网站、阿育吠陀研究文章数字帮助热线和其他预印本资料库中进行,检索时间从开始至 2024 年 3 月 31 日。将纳入随机对照试验、随机交叉研究、群组随机研究和非随机干预研究(前瞻性队列研究、非随机临床试验)。将使用 ROB-2、ROBINS-I 以及 Cochrane 协作组织推荐的用于交叉研究和群组随机研究的其他修订版偏倚风险工具来评估偏倚风险。为了评估研究结果的可信度,将采用网络荟萃分析的建议分级评估、发展和评价方法。我们将采用叙事方法来综合和报告定性与定量数据,在可行的情况下,我们将使用 STATA 软件进行网络荟萃分析。结论本方案确定了一项研究计划,通过向政策制定者和利益相关者提供阿育吠陀疗法的治疗层次结构,促进推荐治疗 NSCLBP 的进程。
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引用次数: 0
期刊
European Journal of Integrative Medicine
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