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Neurophysiological Effects of Dry Needling: A Systematic Review and Meta-analysis 干针的神经生理效应:系统回顾和荟萃分析。
IF 3.7 2区 医学 Q1 REHABILITATION Pub Date : 2026-02-01 DOI: 10.1016/j.apmr.2025.08.019
Gabriel Rabanal-Rodríguez PT, MSc , Marcos José Navarro-Santana PT, PhD , Juan Antonio Valera-Calero PT, PhD , Guido Fabián Gómez-Chiguano PT, PhD , Magdalena Kocot-Kępska MD, PhD, EDPM , César Fernández-de-las-Peñas PT, PhD , Gustavo Plaza-Manzano PT, PhD

Objective

To evaluate the neurophysiological effects associated with dry needling. This review evaluates the influence of dry needling on pain-related biomarkers, conditioned pain modulation, and temporal summation to clarify the potential mechanisms underlying its therapeutic effects.

Data Sources

A literature search across the Physiotherapy Evidence Database, Web of Science, PubMed, Cochrane Library, and Scopus databases until October 2024 was conducted.

Study Selection

Studies were included if they assessed the neurophysiological effects of dry needling in animal or human models. Fourteen results were included in the qualitative synthesis (n=4 in animals, n=10 in humans) and 4 in the quantitative analysis. Selection was performed independently by 2 reviewers.

Data Extraction

Data were extracted independently by 2 reviewers using a standardized form. Neurophysiological outcomes included levels of biomarkers (eg, substance P [SP], cortisol, interleukins, calcitonin gene-related peptide , serotonin, and tumor necrosis factor-α) as well as measures of conditioned pain modulation and temporal summation. The methodological quality was assessed using the Physiotherapy Evidence Database, Cochrane Risk of Bias-2, and Risk of Bias in Nonrandomized Studies of Interventions scales.

Data Synthesis

Dry needling showed increases in microRNA-939, microRNA-25, β-endorphin, interleukin-2 (IL-2), tumor necrosis factor-α, inducible isoform of nitric oxide synthases, hypoxia-inducible factor-1α, cyclooxygenase-2, vascular endothelial growth factor, inflammatory cells, IL-6, and acetylcholinesterase, whereas decreases were observed in Myozenin 2, SP, calcitonin gene-related peptide, acetylcholine, and acetylcholine receptor. The effects on neurophysiological variables related to pain processing are limited, leading to small improvements in conditioned pain modulation (standardized mean differences, 0.36; 95% CI, 0.05-0.67) and no apparent changes in temporal summation (standardized mean difference, −0.08; 95% CI, −0.44 to 0.27).

Conclusions

The application of dry needling can induce significant changes in pain-related biomarker levels in animal and human studies, providing insights into its underlying mechanisms of action and potential clinical effects.
目的:探讨干针对神经生理的影响。这篇综述评估了干针对疼痛相关生物标志物、条件疼痛调节和时间累积的影响,以阐明其治疗效果的潜在机制。数据来源:通过物理治疗证据数据库(PEDro)、Web of Science、PubMed、Cochrane Library和Scopus数据库进行文献检索,直至2024年10月。研究选择:如果研究在动物或人类模型中评估了干针的神经生理效应,则纳入研究。14个结果用于定性合成(动物n=4,人n=10), 4个结果用于定量分析。选择由两名审稿人独立完成。数据提取:数据由两名审稿人使用标准化表格独立提取。神经生理学结果包括生物标志物水平(如P物质、皮质醇、白细胞介素、CGRP、血清素、TNF-α),以及条件性疼痛调节和时间累加的测量。采用PEDro、Cochrane偏倚风险2和非随机干预研究偏倚风险量表评估方法学质量。数据综合:干针组miR-939、miR-25、β-内啡肽、IL-2、TNF-α、iNOS、HIF-1α、COX-2、VEGF、炎症细胞、IL-6、AChE升高,MYOZ2、SP、CGRP、ACh、AChR降低。对与疼痛加工相关的神经生理变量的影响有限,导致条件疼痛调节的微小改善(SMD为0.36,95%为0.05至0.67),时间总和无明显变化(SMD为-0.08,95% ci为-0.44至0.27)。结论:在动物和人体研究中,干针的应用可引起疼痛相关生物标志物水平的显著变化,为其潜在的作用机制和潜在的临床效果提供了新的见解。
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引用次数: 0
Inspiratory Muscle Training Enhances Functional Sitting Balance More Than Usual Care in Individuals With Spinal Cord Injury: A Randomized Controlled Trial 在脊髓损伤患者中,吸气肌训练比常规护理更能提高功能性坐位平衡:一项随机对照试验。
IF 3.7 2区 医学 Q1 REHABILITATION Pub Date : 2026-02-01 DOI: 10.1016/j.apmr.2025.09.017
Kanishka Gambhir MPT , Shambhovi Mitra PhD , Anne E. Palermo PhD

Objective

To evaluate the effect of inspiratory muscle training (IMT) on functional sitting balance (FSB) in individuals with spinal cord injury (SCI).

Design

Rater-masked, parallel, 2-group randomized clinical trial.

Setting

Tertiary care SCI rehabilitation hospital.

Participants

Forty-four participants (N=44) (aged 18-60) with C4-T6 injuries (American Spinal Injury Association Impairment Scale A-C) (cervical-SCI=25, thoracic-SCI=19, American Spinal Injury Association Impairment Scale A=33, B=11, C=0) in their first SCI-specific inpatient rehabilitation were randomly assigned into experimental and control groups.

Interventions

Both groups received standard respiratory care and physiotherapy. The experimental group received additional flow-resistive IMT sessions over 6 weeks.

Main Outcome Measures

FSB was measured using the Function in Sitting Test-SCI, and respiratory function was assessed via maximal inspiratory pressure, sustained maximal inspiratory pressure, and Fatigue Index Test score at baseline, 4 weeks and 6 weeks. Data were analyzed using repeated measures general linear model framework in IBM SPSS version 21.

Results

Analysis showed significant improvements in FSB for both groups (P<.001). Sustained maximal inspiratory pressure, maximal inspiratory pressure, and Fatigue Index Test scores improved only for the experimental group (P<.05). Post-hoc analyses of interaction effects showed significantly greater improvements in all variables in the experimental group.

Conclusions

This study is the first to show that FSB improves more with addition of IMT to standard care in individuals with SCI.
目的:探讨吸气肌训练(IMT)对脊髓损伤(SCI)患者功能性坐位平衡(FSB)的影响。设计:对照、平行、两组随机临床试验。地点:印度德里的三级护理SCI康复医院。对象:44例首次接受sci特异性住院康复的C4-T6损伤(AIS A-C)患者(颈- sci =25,胸- sci =19, AIS A=33, B=11, C=0),年龄18-60岁,随机分为实验组和对照组。干预措施:两组均接受标准的呼吸护理和物理治疗。实验组在六周内接受额外的流动阻力IMT治疗。主要结果测量:FSB使用坐位功能测试(FIST-SCI)测量,呼吸功能通过最大吸气压力(MIP)、持续最大吸气压力(SMIP)和疲劳指数测试(FIT)评分在基线、4周和6周进行评估。数据分析使用IBM SPSS version 21中的重复测量一般线性模型框架。结果:分析显示,两组患者的FSB均有显著改善(结论:本研究首次表明,在脊髓损伤患者的标准护理中加入IMT后,FSB改善更多。
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引用次数: 0
Health Care Utilization in Veterans With Tetraplegia in the First Year After Cervical Spinal Cord Injury: Identifying Opportunities for Dissemination of Treatment Information 脊髓损伤后第一年四肢瘫痪退伍军人的医疗保健利用:确定治疗信息传播的机会。
IF 3.7 2区 医学 Q1 REHABILITATION Pub Date : 2026-02-01 DOI: 10.1016/j.apmr.2025.07.011
Katharine Tam MD , Daniel Eaton MPH , Amanda Mayo MD , Aimee James PhD, MPH , Candace Tefertiller PT, DPT, PhD, NCS , Katherine C. Stenson MD , Catherine Curtin MD , Doug Ota MD , Flora Laurent BA , Michael J. Berger MD, PhD , Jana Dengler MD, MASc, MHSc , Ida K. Fox MD

Objective

To describe Veterans Affairs (VA) utilization patterns by Veterans with tetraplegia during the first year after cervical spinal cord injury (SCI) and explore differences among subpopulations. A secondary objective of this study was to develop a process map to guide targeted clinician education about upper limb treatment information.

Design

Retrospective cohort study using the Veterans Health Administration (VHA) Spinal Cord Injury and Disorders (SCI/D) Registry and the VHA Corporate Data Warehouse.

Setting

Outpatient setting in the VHA.

Participants

Veterans (N=884) with traumatic, C5-C8 neurologic level of injury, and American Spinal Injury Association Impairment Scale A-C classification who received care at a regional VA SCI/D Center between October 1, 2012, and September 30, 2019.

Interventions

Not applicable.

Main Outcome Measures

VA health care utilization as defined by ≥1 VA outpatient visit within the first year of SCI using VHA administrative data. We also examined predictors of care interactions using multivariate logistic regression models.

Results

In total, 489 Veterans (55%) had ≥1 VA outpatient visit in the first year after SCI whereas 395 Veterans (45%) did not receive outpatient VA care within their first year after SCI. Veterans who used VA health care received a median of 41 outpatient visits in the first year after SCI. Veterans had the highest median number of visits and shortest time interval from SCI to initial visit with therapists (physical, occupational, and recreational) compared to other health care providers. No significant predictors of care were identified with adjusted and unadjusted multivariate logistic regression.

Conclusions

Health care utilization patterns of Veterans with tetraplegia identified physical, occupational, and recreational therapists as the health care providers who had visits early and often with these Veterans. Therapists are uniquely positioned in health care systems to facilitate communication of treatment opportunities to persons with tetraplegia.
目的:了解四肢瘫痪退伍军人颈脊髓损伤(SCI)后第一年的退伍军人事务(VA)利用情况,并探讨亚群间的差异。本研究的第二个目的是制定一个过程图,以指导有针对性的临床医生对上肢(UL)治疗信息的教育。设计:回顾性队列研究,利用退伍军人健康管理局(VHA)脊髓损伤和疾病(SCI/D)登记处和VHA公司数据仓库(CDW)设置:VHA门诊设置参与者:884名创伤性、C5-C8神经损伤水平(NLI)和美国脊髓损伤协会(ASIA)损伤量表(AIS) a - c分类的退伍军人,他们在2012年10月1日至2019年9月30日期间在VA区域SCI/D中心接受治疗。干预措施:不适用主要结果测量:根据VHA管理数据,在脊髓损伤的第一年至少有一次VA门诊就诊来定义VA医疗保健利用。我们还使用多元逻辑回归模型检验了护理相互作用的预测因子。结果:489名退伍军人(55%)在脊髓损伤后的一年内至少进行过一次VA门诊治疗,而395名退伍军人(45%)在脊髓损伤后的一年内没有接受过VA门诊治疗。使用VA医疗保健的退伍军人在脊髓损伤后的第一年平均有41次门诊就诊。与其他医疗保健提供者(HCP)相比,退伍军人从脊髓损伤到初次就诊(物理、职业和娱乐)的中位数次数最高,间隔时间最短。经调整和未调整的多因素logistic回归均未发现显著的护理预测因子。结论:四肢瘫痪退伍军人的医疗保健利用模式确定了身体、职业和娱乐治疗师是早期和经常访问四肢瘫痪退伍军人的HCPs。治疗师在医疗保健系统中具有独特的地位,可以促进对四肢瘫痪患者的治疗机会的交流。
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引用次数: 0
Cancer Incidence and Risk in Children and Adolescents With Intellectual Disability in South Korea 韩国智障儿童和青少年的癌症发病率和风险
IF 3.7 2区 医学 Q1 REHABILITATION Pub Date : 2026-02-01 DOI: 10.1016/j.apmr.2025.04.023
Hyun Jung Lee MD, PhD , Jae Young Kim MS , Sung Wook Song MD , Shin-Young Yim MD, PhD

Objective

To evaluate cancer risk and identify distinctive cancer patterns in children and adolescents with intellectual disability (ID) in South Korea, where comprehensive research in this population remains limited.

Design

Retrospective cohort study.

Setting

Nationwide population-based data from the National Health Insurance Service-National Health Information Database (NHIS-NHID) in South Korea (2004-2021).

Participants

This study included individuals (N=75,491) with ID aged 2-18 years and 917,699 age- and sex-matched controls without ID (1:10 matching ratio to maximize statistical power).

Interventions

Not applicable.

Main Outcome Measures

Cancer incidence and associated risk factors, including comorbidities, demographic characteristics, and socioeconomic status, analyzed using Cox proportional hazard models.

Results

Children and adolescents with ID had a significantly higher overall cancer incidence and risk compared to the control group (adjusted hazard ratio [HR]: 1.1; 95% confidence interval [CI]: 1.005-1.204). Those with medical comorbidities faced an even greater risk (adjusted HR: 1.96; 95% CI, 1.75-2.194). Significant risk factors included older age (16-≤18y vs 2-<6y: HR 3.529; 95% CI, 3.321-3.749) and lower socioeconomic status (medical aid vs high-income: HR 0.863; 95% CI, 0.788-0.945). The top 5 cancer sites in the ID group were renal pelvis and ureter; heart, mediastinum, and pleura; acute lymphoblastic leukemia; brain; and ovary.

Conclusions

Children and adolescents with ID in South Korea exhibit a distinct cancer risk profile, with elevated cancer incidence compared to the control group. Tailored cancer prevention, early detection strategies, and health care utilization policies are essential to address these needs of this vulnerable group.
目的:评估韩国智力残疾儿童和青少年(ID)的癌症风险并确定其独特的癌症模式,在韩国对这一人群的全面研究仍然有限。设计:回顾性队列研究设置:来自韩国国民健康保险服务-国民健康信息数据库(NHIS-NHID)的基于全国人口的数据(2004-2021)参与者:本研究包括75,491名年龄在2-18岁的ID患者和917,699名年龄和性别匹配的无ID对照组(1:10匹配比例以最大化统计能力)。干预措施:不适用。主要结局指标:使用Cox比例风险模型分析癌症发病率和相关危险因素,包括合并症、人口统计学特征和社会经济地位。结果:与对照组相比,患有ID的儿童和青少年的总体癌症发病率和风险显著高于对照组(调整后的风险比:1.1;95% ci: 1.005-1.204)。那些有医疗合并症的人面临更大的风险(调整后的HR: 1.96;95% ci: 1.75-2.194)。结论:韩国患有ID的儿童和青少年表现出明显的癌症风险特征,与对照组相比,癌症发病率升高。量身定制的癌症预防、早期检测策略和医疗保健利用政策对于解决这一弱势群体的这些需求至关重要。
{"title":"Cancer Incidence and Risk in Children and Adolescents With Intellectual Disability in South Korea","authors":"Hyun Jung Lee MD, PhD ,&nbsp;Jae Young Kim MS ,&nbsp;Sung Wook Song MD ,&nbsp;Shin-Young Yim MD, PhD","doi":"10.1016/j.apmr.2025.04.023","DOIUrl":"10.1016/j.apmr.2025.04.023","url":null,"abstract":"<div><h3>Objective</h3><div>To evaluate cancer risk and identify distinctive cancer patterns in children and adolescents with intellectual disability (ID) in South Korea, where comprehensive research in this population remains limited.</div></div><div><h3>Design</h3><div>Retrospective cohort study.</div></div><div><h3>Setting</h3><div>Nationwide population-based data from the National Health Insurance Service-National Health Information Database (NHIS-NHID) in South Korea (2004-2021).</div></div><div><h3>Participants</h3><div>This study included individuals (N=75,491) with ID aged 2-18 years and 917,699 age- and sex-matched controls without ID (1:10 matching ratio to maximize statistical power).</div></div><div><h3>Interventions</h3><div>Not applicable.</div></div><div><h3>Main Outcome Measures</h3><div>Cancer incidence and associated risk factors, including comorbidities, demographic characteristics, and socioeconomic status, analyzed using Cox proportional hazard models.</div></div><div><h3>Results</h3><div>Children and adolescents with ID had a significantly higher overall cancer incidence and risk compared to the control group (adjusted hazard ratio [HR]: 1.1; 95% confidence interval [CI]: 1.005-1.204). Those with medical comorbidities faced an even greater risk (adjusted HR: 1.96; 95% CI, 1.75-2.194). Significant risk factors included older age (16-≤18y vs 2-&lt;6y: HR 3.529; 95% CI, 3.321-3.749) and lower socioeconomic status (medical aid vs high-income: HR 0.863; 95% CI, 0.788-0.945). The top 5 cancer sites in the ID group were renal pelvis and ureter; heart, mediastinum, and pleura; acute lymphoblastic leukemia; brain; and ovary.</div></div><div><h3>Conclusions</h3><div>Children and adolescents with ID in South Korea exhibit a distinct cancer risk profile, with elevated cancer incidence compared to the control group. Tailored cancer prevention, early detection strategies, and health care utilization policies are essential to address these needs of this vulnerable group.</div></div>","PeriodicalId":8313,"journal":{"name":"Archives of physical medicine and rehabilitation","volume":"107 2","pages":"Pages 279-286"},"PeriodicalIF":3.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143967904","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Association of Sleep Quality With Activity and Participation in Older Adults 老年人睡眠质量与活动和参与的关系。
IF 3.7 2区 医学 Q1 REHABILITATION Pub Date : 2026-02-01 DOI: 10.1016/j.apmr.2025.05.010
Jessie M. VanSwearingen PhD, PT , Caitlan A. Tighe PhD , Subashan Perera PhD , Daniel E. Forman MD , Daniel J. Buysse MD , Jennifer S. Brach PhD, PT

Objective

To explore the relation of self-reported sleep quality with the International Classification of Functioning domains of activity (eg, physical functioning) and participation (eg, disability).

Design

Descriptive, secondary, cross-sectional data analysis

Setting

General community

Participants

Community-dwelling older adults, volunteers, n=249

Interventions

Not applicable

Main Outcome Measures

The Pittsburgh Sleep Quality Index, self-reported measures of activity and participation by the Late-Life Function and Disability Instrument, the Modified Gait Efficacy Scale for confidence in walking, and performance-based measures of physical functioning (gait speed, 6-minute Walk Test, Figure-of-8 Walk Test, and Short Physical Performance Battery). Measures of function were regressed on sleep quality adjusted for age, sex, and comorbidities.

Results

Older adults with good (Pittsburgh Sleep Quality Index ≤5) compared with poor (>5) sleep quality reported better function and disability across almost all considered domains (P<.05). Effect sizes for self-reported and performance-based measures were comparable and in the small to moderate range.

Conclusions

Among older adults with mild to moderate functional limitations and disability, self-reported sleep quality related broadly to activity and participation. Experimental studies are needed to assess the effects of sleep interventions on activity and participation and understand if sleep quality may represent a novel treatment target in future intervention trials to improve function in older adults.
目的:探讨自我报告睡眠质量与国际活动功能域分类(如身体功能)和参与(如残疾)的关系。设计:描述性、二级、横断面数据分析设置:普通社区参与者:社区居住的老年人,志愿者,n=249干预措施:不适用主要结局测量:。匹兹堡睡眠质量指数(PSQI),通过晚年功能和残疾工具(LLFDI)自我报告的活动和参与测量,步行信心的改进步态功效量表,以及基于性能的身体功能测量(步态速度,六分钟步行,8字步行和短物理性能电池,SPPB)。功能指标根据年龄、性别和合并症调整后的睡眠质量进行回归。结果:睡眠质量好的老年人(PSQI≤5)比睡眠质量差的老年人(PSQI≤5)在几乎所有考虑的领域都报告了更好的功能和残疾(p< 0.05)。自我报告和基于表现的测量的效应大小是相当的,在小到中等范围内。结论:在有轻度至中度功能限制和残疾的老年人中,自我报告的睡眠质量与活动和参与广泛相关。需要实验研究来评估睡眠干预对活动和参与的影响,并了解睡眠质量是否可能成为未来干预试验中改善老年人功能的新治疗目标。
{"title":"Association of Sleep Quality With Activity and Participation in Older Adults","authors":"Jessie M. VanSwearingen PhD, PT ,&nbsp;Caitlan A. Tighe PhD ,&nbsp;Subashan Perera PhD ,&nbsp;Daniel E. Forman MD ,&nbsp;Daniel J. Buysse MD ,&nbsp;Jennifer S. Brach PhD, PT","doi":"10.1016/j.apmr.2025.05.010","DOIUrl":"10.1016/j.apmr.2025.05.010","url":null,"abstract":"<div><h3>Objective</h3><div>To explore the relation of self-reported sleep quality with the International Classification of Functioning domains of activity (eg, physical functioning) and participation (eg, disability).</div></div><div><h3>Design</h3><div>Descriptive, secondary, cross-sectional data analysis</div></div><div><h3>Setting</h3><div>General community</div></div><div><h3>Participants</h3><div>Community-dwelling older adults, volunteers, n=249</div></div><div><h3>Interventions</h3><div>Not applicable</div></div><div><h3>Main Outcome Measures</h3><div>The Pittsburgh Sleep Quality Index, self-reported measures of activity and participation by the Late-Life Function and Disability Instrument, the Modified Gait Efficacy Scale for confidence in walking, and performance-based measures of physical functioning (gait speed, 6-minute Walk Test, Figure-of-8 Walk Test, and Short Physical Performance Battery). Measures of function were regressed on sleep quality adjusted for age, sex, and comorbidities.</div></div><div><h3>Results</h3><div>Older adults with good (Pittsburgh Sleep Quality Index ≤5) compared with poor (&gt;5) sleep quality reported better function and disability across almost all considered domains (<em>P</em>&lt;.05). Effect sizes for self-reported and performance-based measures were comparable and in the small to moderate range.</div></div><div><h3>Conclusions</h3><div>Among older adults with mild to moderate functional limitations and disability, self-reported sleep quality related broadly to activity and participation. Experimental studies are needed to assess the effects of sleep interventions on activity and participation and understand if sleep quality may represent a novel treatment target in future intervention trials to improve function in older adults.</div></div>","PeriodicalId":8313,"journal":{"name":"Archives of physical medicine and rehabilitation","volume":"107 2","pages":"Pages 207-214"},"PeriodicalIF":3.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144141211","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Quality and Outcomes of Acute Stroke Care for People With and Without Aphasia 失语症患者和非失语症患者急性卒中护理的质量和结果。
IF 3.7 2区 医学 Q1 REHABILITATION Pub Date : 2026-02-01 DOI: 10.1016/j.apmr.2025.07.007
Marissa Stone BHlthSc , Sarah J. Wallace PhD , David A. Copland PhD , Dominique A. Cadilhac PhD , Kelvin Hill BAppSC , Tara Purvis PhD , Megan Reyneke BCom , Monique F. Kilkenny PhD

Objective

The study aimed to investigate whether the presence of aphasia was associated with differences in acute stroke care quality and to describe in-hospital outcomes.

Design

Observational cohort study of cross-sectional data from the biennial Stroke Foundation National Stroke Audit of Acute Services (2017, 2019, and 2021). Descriptive statistics and multivariable regression models were used to compare quality of care and in-hospital outcomes by aphasia status (care adjusted for hospital variation; outcomes adjusted for age, sex, prior function, stroke type, stroke severity indicators, and hospital variation).

Setting

Acute hospital services in Australia.

Participants

Patients with stroke and aphasia status recorded (n=11,613) were included in the study. A total of 3122 (26.9%) patients had aphasia documented in clinical notes (aphasia 51% male; median age 78 y; no aphasia 58% male; median age 74 y).

Main Outcome Measures

Quality of care indicators aligned with national evidence-based guidelines. In-hospital outcomes included complications, level of independence, survival, and discharge destination.

Results

Patients with aphasia were less likely to be assessed for mood impairment (23% vs 30%; adjusted odds ratio [aOR], 0.73; 95% confidence interval [CI], 0.65-0.81), receive risk factor education (59% vs 70%; aOR, 0.55; 95% CI, 0.48-0.64), or be involved in care plan development (83% vs 95%; aOR, 0.22; 95% CI, 0.18-0.28). Patients with aphasia were more likely to have a more severe stroke and had more in-hospital complications (aOR, 1.46; 95% CI, 1.30-1.63) and in-hospital deaths (aOR, 2.86; 95% CI, 2.36-3.49). They were less independent at discharge (aOR, 0.48; 95% CI, 0.42-0.56), less often discharged home (aOR, 0.63; 95% CI, 0.56-0.72), and more likely to be discharged to residential care (aOR, 1.52; 95% CI, 1.08-2.15). They were more likely to receive inpatient rehabilitation (aOR, 1.15; 95% CI, 1.01-1.30).

Conclusions

Important differences exist in the quality of acute stroke care received by patients with aphasia. Targeted quality improvement in mood screening and risk factor education is needed.
目的:探讨失语是否与急性脑卒中护理质量差异相关;并描述医院的结果。设计:观察队列研究来自两年一次的卒中基金会国家急性卒中审计(2017年、2019年和2021年)的横断面数据。采用描述性统计和多变量回归模型比较失语症状态下的护理质量和住院结果(根据医院差异调整的护理;根据年龄、性别、既往功能、脑卒中类型和严重程度指标以及医院差异调整结果)。环境:澳大利亚急症医院服务。参与者:有中风和失语记录的患者(n=11,613)被纳入研究。3122例(26.9%)有临床记录的失语症(51%为男性;中位年龄78岁;男性无失语症58%;中位年龄74岁)。主要结果测量:护理质量指标符合国家循证指南。住院结果包括并发症、独立水平、生存和出院目的地。结果:失语患者不太可能被评估为情绪障碍(23%对30%;aOR 0.73 95% CI 0.65, 0.81),接受危险因素教育(59%对70%;aOR 0.55 95% CI 0.48, 0.64),或参与护理计划制定(83%对95%;(or 0.22, 95% CI 0.18, 0.28)。失语症患者更有可能发生更严重的中风,有更多的院内并发症(aOR 1.46 95% CI 1.30, 1.63)和院内死亡(aOR 2.86 95% CI 2.36, 3.49)。出院时独立性较差(aOR 0.48, 95% CI 0.42, 0.56);出院回家次数较少(aOR 0.63, 95% CI 0.56, 0.72);更有可能出院到寄宿护理(aOR 1.52, 95% CI 1.08, 2.15)。他们更有可能接受住院康复治疗(aOR 1.15, 95% CI 1.01, 1.30)。结论:失语症患者的急性脑卒中护理质量存在重要差异。需要有针对性地提高情绪筛查的质量和风险因素教育。
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引用次数: 0
Dysphagia Screening in Acute Stroke: Adaptation and Validation of the Modified Volume-Viscosity Swallowing Test With International Dysphagia Diet Standardization Initiative Standards 急性脑卒中中吞咽困难的筛查:国际吞咽困难饮食标准化倡议标准对改进的体积粘度吞咽试验的适应和验证。
IF 3.7 2区 医学 Q1 REHABILITATION Pub Date : 2026-02-01 DOI: 10.1016/j.apmr.2025.06.006
Muhammed Salman MSc, SLP , Preetie Shetty Akkunje PhD , Radish Kumar Balasubramanium PhD , Zulkifli K. Misri MD

Objective

To adapt and validate the modified Volume-Viscosity Swallowing Test (MV-VST), aligned with the International Dysphagia Diet Standardization Initiative (IDDSI) framework, and to enhance its applicability in diverse dietary contexts, particularly in lower-middle-income countries.

Design

A cross-sectional study.

Setting

The research was carried out at an acute care tertiary hospital.

Participants

Seventy patients (N=70) with acute stroke, aged ≥18 years, with a standard education level and no sensory deficits, were included in the study.

Interventions

Not applicable.

Main Outcome Measures

The study consisted of 2 phases. In phase 1, the MV-VST was adapted using IDDSI guidelines with varied viscosities and volumes and validated by 5 experienced swallow specialists. In phase 2, the test was used to screen swallowing safety, swallowing efficacy, and temporal parameters across different consistencies and volumes. In addition, clinical assessment was performed using standardized test batteries (Functional Oral Intake Scale [FOIS] and Eating Assessment Tool [EAT-10]), and a subset of participants underwent a videofluoroscopic swallow study (VFSS). The primary outcome of MV-VST measured parameters were defined as clinical indicators that predict potential deficits, and their correlations with FOIS, EAT-10, and VFSS. Furthermore, the study examined the reliability and validity of the adapted swallowing screening tool, MV-VST.

Results

Of the 70 participants, 62.8% experienced dysphagia. The MV-VST demonstrated significant correlations with clinical assessments (FOIS and EAT-10), showing high test–retest and interrater reliability (Cronbach’s α=0.994). Sensitivity and specificity were 87.5% and 100% for EAT-10, respectively, and 75% and 100% for VFSS, respectively. The tool demonstrated its ability to predict potential deficits in swallowing safety, efficacy, and temporal aspects, with significant differences observed between participants based on MV-VST outcomes.

Conclusions

The adapted MV-VST, using IDDSI standards, is a reliable and valid tool for the early identification of poststroke dysphagia, facilitating timely intervention. Despite limitations like the single-center design and small sample size, the study underscores the potential of the MV-VST in diverse dietary practices. Future research should focus on larger, multicenter studies and integrating advanced technologies for more precise assessments.
目的:本研究旨在适应和验证改良体积粘度吞咽试验(MV-VST),与国际吞咽困难饮食标准化倡议(IDDSI)框架保持一致,以增强其在不同饮食环境中的适用性,特别是在中低收入国家。设计:采用横断面研究。环境:本研究在一家三级急症医院进行。参与者:70例急性中风患者,年龄在18岁或以上,具有标准教育水平,无感觉缺陷。干预措施:不适用。主要结局指标:研究分为两个阶段。在第一阶段,MV-VST采用了不同粘度和体积的IDDSI指南,并由五位经验丰富的吞咽专家进行了验证。在第二阶段,该测试用于筛选不同浓度和体积的吞咽安全性、吞咽疗效和时间参数。此外,使用标准化测试单元[功能性口服摄入量表(FOIS)和进食评估工具(EAT-10)]进行临床评估,一部分参与者接受了视频透视检查(VFSS)。MV-VST的主要结果测量的参数被定义为预测潜在缺陷的临床指标,以及它们与FOIS、EAT-10和VFSS的相关性。此外,本研究检验了适应性吞咽筛查工具MV-VST的信度和效度。结果:70名参与者中,62.8%经历过吞咽困难。MV-VST与临床评价(FOIS、EAT-10)有显著相关性,重测信度高(Cronbach’s α=0.994)。灵敏度和特异性分别为87.5%和100% (EAT-10), 75%和100% (VFSS)。该工具具有预测吞咽安全性、吞咽疗效和时间方面的潜在缺陷的能力,在参与者之间观察到基于MV-VST结果的显着差异。结论:采用IDDSI标准的改良MV-VST是早期识别PSD的可靠有效工具,有助于及时干预。尽管存在单中心设计和小样本量等局限性,但该研究强调了MV-VST在不同饮食实践中的潜力。未来的研究应该集中在更大的、多中心的研究上,并整合先进的技术来进行更精确的评估。
{"title":"Dysphagia Screening in Acute Stroke: Adaptation and Validation of the Modified Volume-Viscosity Swallowing Test With International Dysphagia Diet Standardization Initiative Standards","authors":"Muhammed Salman MSc, SLP ,&nbsp;Preetie Shetty Akkunje PhD ,&nbsp;Radish Kumar Balasubramanium PhD ,&nbsp;Zulkifli K. Misri MD","doi":"10.1016/j.apmr.2025.06.006","DOIUrl":"10.1016/j.apmr.2025.06.006","url":null,"abstract":"<div><h3>Objective</h3><div>To adapt and validate the modified Volume-Viscosity Swallowing Test (MV-VST), aligned with the International Dysphagia Diet Standardization Initiative (IDDSI) framework, and to enhance its applicability in diverse dietary contexts, particularly in lower-middle-income countries.</div></div><div><h3>Design</h3><div>A cross-sectional study.</div></div><div><h3>Setting</h3><div>The research was carried out at an acute care tertiary hospital.</div></div><div><h3>Participants</h3><div>Seventy patients (N=70) with acute stroke, aged ≥18 years, with a standard education level and no sensory deficits, were included in the study.</div></div><div><h3>Interventions</h3><div>Not applicable.</div></div><div><h3>Main Outcome Measures</h3><div>The study consisted of 2 phases. In phase 1, the MV-VST was adapted using IDDSI guidelines with varied viscosities and volumes and validated by 5 experienced swallow specialists. In phase 2, the test was used to screen swallowing safety, swallowing efficacy, and temporal parameters across different consistencies and volumes. In addition, clinical assessment was performed using standardized test batteries (Functional Oral Intake Scale [FOIS] and Eating Assessment Tool [EAT-10]), and a subset of participants underwent a videofluoroscopic swallow study (VFSS). The primary outcome of MV-VST measured parameters were defined as clinical indicators that predict potential deficits, and their correlations with FOIS, EAT-10, and VFSS. Furthermore, the study examined the reliability and validity of the adapted swallowing screening tool, MV-VST.</div></div><div><h3>Results</h3><div>Of the 70 participants, 62.8% experienced dysphagia. The MV-VST demonstrated significant correlations with clinical assessments (FOIS and EAT-10), showing high test–retest and interrater reliability (Cronbach’s α=0.994). Sensitivity and specificity were 87.5% and 100% for EAT-10, respectively, and 75% and 100% for VFSS, respectively. The tool demonstrated its ability to predict potential deficits in swallowing safety, efficacy, and temporal aspects, with significant differences observed between participants based on MV-VST outcomes.</div></div><div><h3>Conclusions</h3><div>The adapted MV-VST, using IDDSI standards, is a reliable and valid tool for the early identification of poststroke dysphagia, facilitating timely intervention. Despite limitations like the single-center design and small sample size, the study underscores the potential of the MV-VST in diverse dietary practices. Future research should focus on larger, multicenter studies and integrating advanced technologies for more precise assessments.</div></div>","PeriodicalId":8313,"journal":{"name":"Archives of physical medicine and rehabilitation","volume":"107 2","pages":"Pages 215-224"},"PeriodicalIF":3.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144339797","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Concussion Recognition: A Guide for Parents and Coaches 脑震荡识别:家长和教练指南。
IF 3.7 2区 医学 Q1 REHABILITATION Pub Date : 2026-02-01 DOI: 10.1016/j.apmr.2025.09.012
Ruairi Connolly MD, Ann Guernon BS, MS, PhD, Jaclyn Stephens BA, MS, PHD, John Leddy MD, Aoife Murray MD, Julia Drattell LAT, ATC, CES, Jacob McPherson PT, DPT, PhD, Karen McCulloch PT, PhD, MS, Quratulain Khan PhD, Akuadasuo Ezenyilimba PhD, Zainab Al Lawati MD, Will Panenka MD, MSc, Samir Belagaje MD, PhD, Tracey Wallace MS, Noemi Lansang MS, Jennifer Wethe PhD
{"title":"Concussion Recognition: A Guide for Parents and Coaches","authors":"Ruairi Connolly MD,&nbsp;Ann Guernon BS, MS, PhD,&nbsp;Jaclyn Stephens BA, MS, PHD,&nbsp;John Leddy MD,&nbsp;Aoife Murray MD,&nbsp;Julia Drattell LAT, ATC, CES,&nbsp;Jacob McPherson PT, DPT, PhD,&nbsp;Karen McCulloch PT, PhD, MS,&nbsp;Quratulain Khan PhD,&nbsp;Akuadasuo Ezenyilimba PhD,&nbsp;Zainab Al Lawati MD,&nbsp;Will Panenka MD, MSc,&nbsp;Samir Belagaje MD, PhD,&nbsp;Tracey Wallace MS,&nbsp;Noemi Lansang MS,&nbsp;Jennifer Wethe PhD","doi":"10.1016/j.apmr.2025.09.012","DOIUrl":"10.1016/j.apmr.2025.09.012","url":null,"abstract":"","PeriodicalId":8313,"journal":{"name":"Archives of physical medicine and rehabilitation","volume":"107 2","pages":"Pages 365-368"},"PeriodicalIF":3.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145450461","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Safety and Efficacy of Very Early Mobilization in Acute Stroke: A Systematic Review and Meta-analysis 急性脑卒中早期活动的安全性和有效性:一项系统回顾和荟萃分析。
IF 3.7 2区 医学 Q1 REHABILITATION Pub Date : 2026-02-01 DOI: 10.1016/j.apmr.2025.10.021
Xiaoyan Li BS , Yali Kong BS

Objective

To evaluate the safety and efficacy of very early mobilization (VEM) after acute stroke through a comprehensive meta-analysis of cohort studies and randomized controlled trials.

Data Sources

A systematic literature search was conducted in PubMed, Cochrane Library, Embase, Web of Science, Google Scholar, and Semantic Scholar from inception to May 2024.

Study Selection

Studies were included if they compared VEM with standard care in adult patients with stroke and reported outcomes related to functional recovery, mortality, or medical complications. Both randomized controlled trials and observational cohort studies were eligible.

Data Extraction

Two independent reviewers extracted study and participant characteristics, intervention details, comparator information, and outcome measures (functional recovery, complications, mortality, and length of stay). Discrepancies were resolved through discussion. Effect sizes (risk ratios, standardized mean differences) with 95% confidence intervals were calculated, and methodological quality was assessed using the Cochrane Risk of Bias tool for randomized controlled trials and the Newcastle-Ottawa Scale for cohort studies.

Data Synthesis

Twenty-three studies, including 84,936 patients in the VEM group and 32,753 in the standard care group, were analyzed. VEM significantly improved functional independence, as measured by the Barthel Index (a validated scale for activities of daily living; standardized mean difference [SMD]=0.61; 95% CI, 0.25-0.98; P<.01) and the modified Rankin Scale (mRS; a disability scale, with scores of 0-2 indicating functional independence; risk ratio [RR]=1.14; 95% CI, 1.03-1.27). It also reduced the length of hospital stay (SMD=−2.53; 95% CI, −4.45 to −0.60; P<.01), pulmonary infection (RR=0.75; 95% CI, 0.57-0.99; P=.04), and urinary tract infection (RR=0.76; 95% CI, 0.71-0.82; P<.01). No significant effects were observed in National Institutes of Health Stroke Scale (a stroke severity scale) scores, mortality, deep vein thrombosis, neurologic deterioration, or falls.

Conclusions

VEM is safe and effective in enhancing functional recovery, reducing complications, and shortening hospitalization after acute stroke. Further high quality studies are needed to optimize timing and dosage of mobilization, particularly considering stroke severity and subtype.
目的:通过队列研究和随机对照试验(rct)的综合荟萃分析,评价急性脑卒中后早期动员(VEM)的安全性和有效性。数据来源:系统检索PubMed、Cochrane Library、Embase、Web of Science、谷歌Scholar、Semantic Scholar等数据库,检索时间自成立至2024年5月。研究选择:将VEM与成人卒中患者的标准治疗进行比较,并报告与功能恢复、死亡率或医学并发症相关的结果的研究被纳入。随机对照试验和观察性队列研究均符合条件。数据综合:分析了23项研究,包括VEM组84,936例患者和标准治疗组32,753例患者。通过Barthel指数(BI,一种有效的日常生活活动量表;标准化平均差[SMD]: 0.61; 95%可信区间[CI]: 0.25, 0.98; P < 0.01)和改进的Rankin量表(mRS,一种残疾量表,得分0-2表示功能独立性;风险比[RR]: 1.14; 95% CI: 1.03, 1.27)来衡量,VEM显著改善了功能独立性。它还减少了住院时间(LOS; SMD: -2.53; 95% CI: -4.45至-0.60;P < 0.01)、肺部感染(RR: 0.75; 95% CI: 0.57, 0.99; P = 0.04)和尿路感染(RR: 0.76; 95% CI: 0.71, 0.82; P < 0.01)。在美国国立卫生研究院卒中量表(NIHSS;卒中严重程度量表)评分、死亡率、深静脉血栓形成(DVT)、神经系统恶化或跌倒方面未观察到显著影响。结论:VEM对急性脑卒中后功能恢复、减少并发症、缩短住院时间安全有效。需要进一步的高质量研究来优化动员的时间和剂量,特别是考虑到卒中的严重程度和亚型。
{"title":"Safety and Efficacy of Very Early Mobilization in Acute Stroke: A Systematic Review and Meta-analysis","authors":"Xiaoyan Li BS ,&nbsp;Yali Kong BS","doi":"10.1016/j.apmr.2025.10.021","DOIUrl":"10.1016/j.apmr.2025.10.021","url":null,"abstract":"<div><h3>Objective</h3><div>To evaluate the safety and efficacy of very early mobilization (VEM) after acute stroke through a comprehensive meta-analysis of cohort studies and randomized controlled trials.</div></div><div><h3>Data Sources</h3><div>A systematic literature search was conducted in PubMed, Cochrane Library, Embase, Web of Science, Google Scholar, and Semantic Scholar from inception to May 2024.</div></div><div><h3>Study Selection</h3><div>Studies were included if they compared VEM with standard care in adult patients with stroke and reported outcomes related to functional recovery, mortality, or medical complications. Both randomized controlled trials and observational cohort studies were eligible.</div></div><div><h3>Data Extraction</h3><div>Two independent reviewers extracted study and participant characteristics, intervention details, comparator information, and outcome measures (functional recovery, complications, mortality, and length of stay). Discrepancies were resolved through discussion. Effect sizes (risk ratios, standardized mean differences) with 95% confidence intervals were calculated, and methodological quality was assessed using the Cochrane Risk of Bias tool for randomized controlled trials and the Newcastle-Ottawa Scale for cohort studies.</div></div><div><h3>Data Synthesis</h3><div>Twenty-three studies, including 84,936 patients in the VEM group and 32,753 in the standard care group, were analyzed. VEM significantly improved functional independence, as measured by the Barthel Index (a validated scale for activities of daily living; standardized mean difference [SMD]=0.61; 95% CI, 0.25-0.98; <em>P</em>&lt;.01) and the modified Rankin Scale (mRS; a disability scale, with scores of 0-2 indicating functional independence; risk ratio [RR]=1.14; 95% CI, 1.03-1.27). It also reduced the length of hospital stay (SMD=−2.53; 95% CI, −4.45 to −0.60; <em>P</em>&lt;.01), pulmonary infection (RR=0.75; 95% CI, 0.57-0.99; <em>P</em>=.04), and urinary tract infection (RR=0.76; 95% CI, 0.71-0.82; <em>P</em>&lt;.01). No significant effects were observed in National Institutes of Health Stroke Scale (a stroke severity scale) scores, mortality, deep vein thrombosis, neurologic deterioration, or falls.</div></div><div><h3>Conclusions</h3><div>VEM is safe and effective in enhancing functional recovery, reducing complications, and shortening hospitalization after acute stroke. Further high quality studies are needed to optimize timing and dosage of mobilization, particularly considering stroke severity and subtype.</div></div>","PeriodicalId":8313,"journal":{"name":"Archives of physical medicine and rehabilitation","volume":"107 2","pages":"Pages 333-352"},"PeriodicalIF":3.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145534291","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Dual-Site Transcranial Direct Current Stimulation Combined With Exercising Improves Fatigue and Sleep Quality in People With Fibromyalgia: A Randomized Sham-Controlled Clinical Trial 双点经颅直流电刺激联合运动可改善纤维肌痛患者的疲劳和睡眠质量:一项随机假对照临床试验
IF 3.7 2区 医学 Q1 REHABILITATION Pub Date : 2026-02-01 DOI: 10.1016/j.apmr.2025.07.022
Rafael Velasco-Velasco MSc , Juan Avendaño-Coy PhD , Elena Labrador-García PT , Elisabeth Bravo-Esteban PhD , Rubén Arroyo-Fernández PhD

Objective

The study aimed to evaluate the effectiveness of a combined program of unihemispheric concurrent dual-site anodal-transcranial direct current stimulation (UHCDS a-tDCS) + therapeutic exercise (TE) on fatigue and sleep quality in people with fibromyalgia syndrome (FMS).

Design

Double-blind, randomized, sham-controlled trial.

Setting

Primary health care center.

Participants

A total of 90 volunteers diagnosed with fibromyalgia. Nine participants dropped out of the study.

Intervention

Participants were randomly allocated in a 1:1:1 ratio to active UHCDS a-tDCS+TE, sham UHCDS a-tDCS+TE, or control receiving TE. The intervention was delivered in 10 sessions over 6 weeks.

Outcome Measures

Fatigue, sleep quality, and quality of life.

Results

Fatigue score decreased significantly in the active group compared with the sham (−9.8 points; 95% CI, −18.9 to −0.8; P=.028) and control groups (−9.9 points; 95% CI, −18.9 to −0.9; P=.027) at posttreatment and compared with the control group at follow-up (−11.5 points; 95% CI, −20.8 to −2.1; P=.01). Sleep quality improved in active group compared with sham and control groups at posttreatment (sham: −14.4 points; 95% CI, −24.2 to −4.5; P=.002; control: −19.5 points; 95% CI, −29.4 to −9.7; P<.001) and at follow-up (sham: −11.2 points; 95% CI, −21.1 to −1.3; P=.02; control: −15.5 points; 95% CI, −25.3 to −5.6; P<.001). Quality of life enhanced in the active group compared with the other groups, both at posttreatment (sham: −15.2 points; 95% CI, −26.6 to −3.9; P=.005; control: −13.7 points; 95% CI, 25.0 to −2.3; P=.012) and at follow-up (sham: −14.5 points; 95% CI, −25.2 to −3.7; P=.004; control: −17.4 points; 95% CI, −28.1 to −6.6; P<.001). Effect sizes for intergroup comparisons were medium across all outcomes: fatigue (η²=0.10; P=.01), sleep quality (η²=0.12; P<.01), and quality of life (η²=0.13; P<.01). No intergroup differences in any outcome were found between the sham and control groups.

Conclusions

Combining UHCDS a-tDCS with TE can result in clinically significant improvements in fatigue, sleep disorders, and quality of life in people with FMS.
目的:评价UHCDS - tdcs +治疗性运动(TE)联合方案对FMS患者疲劳和睡眠质量的影响。设计:双盲、随机、假对照试验。环境:初级卫生保健中心。参与者:90名被诊断为纤维肌痛的志愿者。9名参与者退出了研究。干预:参与者按1:1:1的比例随机分配到活动UHCDS a- tdcs +TE、假UHCDS a- tdcs +TE或对照组接受TE。干预在6周内分10次进行。结局指标:疲劳、睡眠质量和生活质量。结果:与假手术组相比,运动组的疲劳评分明显降低(-9.8分;95% CI -18.9 ~ -0.8;P =0.028)和对照组(-9.9分;95% CI -18.9 ~ -0.9;P =0.027),随访时与对照组比较(-11.5分;95% CI -20.8 ~ -2.1;p = 0.01)。治疗后,与假手术组和对照组相比,活跃组的睡眠质量有所改善(假手术:-14.4点,95% CI -24.2至-4.5;p = 0.002;对照组:-19.5点,95% CI -29.4至-9.7;结论:UHCDS a-tDCS联合TE可显著改善FMS患者的疲劳、睡眠障碍和生活质量。临床试验注册号:NCT05726149 (clinclintrials .gov)。
{"title":"Dual-Site Transcranial Direct Current Stimulation Combined With Exercising Improves Fatigue and Sleep Quality in People With Fibromyalgia: A Randomized Sham-Controlled Clinical Trial","authors":"Rafael Velasco-Velasco MSc ,&nbsp;Juan Avendaño-Coy PhD ,&nbsp;Elena Labrador-García PT ,&nbsp;Elisabeth Bravo-Esteban PhD ,&nbsp;Rubén Arroyo-Fernández PhD","doi":"10.1016/j.apmr.2025.07.022","DOIUrl":"10.1016/j.apmr.2025.07.022","url":null,"abstract":"<div><h3>Objective</h3><div>The study aimed to evaluate the effectiveness of a combined program of unihemispheric concurrent dual-site anodal-transcranial direct current stimulation (UHCDS a-tDCS) + therapeutic exercise (TE) on fatigue and sleep quality in people with fibromyalgia syndrome (FMS).</div></div><div><h3>Design</h3><div>Double-blind, randomized, sham-controlled trial.</div></div><div><h3>Setting</h3><div>Primary health care center.</div></div><div><h3>Participants</h3><div>A total of 90 volunteers diagnosed with fibromyalgia. Nine participants dropped out of the study.</div></div><div><h3>Intervention</h3><div>Participants were randomly allocated in a 1:1:1 ratio to active UHCDS a-tDCS+TE, sham UHCDS a-tDCS+TE, or control receiving TE. The intervention was delivered in 10 sessions over 6 weeks.</div></div><div><h3>Outcome Measures</h3><div>Fatigue, sleep quality, and quality of life.</div></div><div><h3>Results</h3><div>Fatigue score decreased significantly in the active group compared with the sham (−9.8 points; 95% CI, −18.9 to −0.8; <em>P</em>=.028) and control groups (−9.9 points; 95% CI, −18.9 to −0.9; <em>P</em>=.027) at posttreatment and compared with the control group at follow-up (−11.5 points; 95% CI, −20.8 to −2.1; <em>P</em>=.01). Sleep quality improved in active group compared with sham and control groups at posttreatment (sham: −14.4 points; 95% CI, −24.2 to −4.5; <em>P</em>=.002; control: −19.5 points; 95% CI, −29.4 to −9.7; <em>P</em>&lt;.001) and at follow-up (sham: −11.2 points; 95% CI, −21.1 to −1.3; <em>P</em>=.02; control: −15.5 points; 95% CI, −25.3 to −5.6; <em>P</em>&lt;.001). Quality of life enhanced in the active group compared with the other groups, both at posttreatment (sham: −15.2 points; 95% CI, −26.6 to −3.9; <em>P</em>=.005; control: −13.7 points; 95% CI, 25.0 to −2.3; <em>P</em>=.012) and at follow-up (sham: −14.5 points; 95% CI, −25.2 to −3.7; <em>P</em>=.004; control: −17.4 points; 95% CI, −28.1 to −6.6; <em>P</em>&lt;.001). Effect sizes for intergroup comparisons were medium across all outcomes: fatigue (η²=0.10; <em>P</em>=.01), sleep quality (η²=0.12; <em>P</em>&lt;.01), and quality of life (η²=0.13; <em>P</em>&lt;.01). No intergroup differences in any outcome were found between the sham and control groups.</div></div><div><h3>Conclusions</h3><div>Combining UHCDS a-tDCS with TE can result in clinically significant improvements in fatigue, sleep disorders, and quality of life in people with FMS.</div></div>","PeriodicalId":8313,"journal":{"name":"Archives of physical medicine and rehabilitation","volume":"107 2","pages":"Pages 153-161"},"PeriodicalIF":3.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144862067","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
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Archives of physical medicine and rehabilitation
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