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A reliable and valid assessment of upper limb movement quality after stroke: the observational Drinking Task Assessment. 中风后上肢运动质量的可靠有效评估:饮酒任务评估观察法。
IF 2.5 4区 医学 Q1 REHABILITATION Pub Date : 2024-10-09 DOI: 10.2340/jrm.v56.40362
Minnu Jose, Maria Munoz-Novoa, Margit Alt Murphy

Objective: To develop and evaluate the reliability and validity of a new observational Drinking Task Assessment (DTA) designed to assess quality of movement in task performance after stroke.

Design: Reliability and validity.

Methods: The DTA measures movement time and movement quality (smoothness, trunk, shoulder, elbow, and grasp movements) on a 4-level ordinal scale. Thirty participants with chronic stroke were assessed independently by 2 therapists. Intra-class correlation (ICC), standard error of measurement (SEM) and minimal real difference (MRD), weighted kappa, percentage of agreement, and Svensson method were used for reliability assessment. Motion capture-based kinematics and established clinical scales were used to evaluate validity.

Results: The absolute SEM and MRD for movement time were 0.4 and 1 s (11%), respectively. The ICC (≥ 0.93) and weighted kappa (0.71-1.0) showed good to excellent agreement for intra- and inter-rater reliability. DTA showed strong correlations with Fugl-Meyer Assessment (0.74), Action Research Arm Test (0.93), and kinematic measures of smoothness (0.93), trunk displacement (0.91), elbow extension (0.73), and shoulder movements (0.56), indicating good construct validity.

Conclusions: The new DTA proved to be a reliable and valid tool for assessment of movement quality during task performance after stroke.

目的开发并评估一种新的观察性饮酒任务评估(DTA)的可靠性和有效性,该评估旨在评估中风后任务执行中的运动质量:设计:可靠性和有效性:DTA 采用 4 级顺序量表测量运动时间和运动质量(平滑度、躯干、肩、肘和抓握动作)。由两名治疗师对 30 名慢性中风患者进行独立评估。采用类内相关(ICC)、测量标准误差(SEM)和最小实际差异(MRD)、加权卡帕(kappa)、一致性百分比和斯文森法进行可靠性评估。基于运动捕捉的运动学和已建立的临床量表用于评估有效性:运动时间的绝对 SEM 和 MRD 分别为 0.4 秒和 1 秒(11%)。ICC(≥ 0.93)和加权卡帕(0.71-1.0)显示评分者内部和评分者之间的可靠性达到良好到极佳的一致性。DTA与Fugl-Meyer评估(0.74)、行动研究手臂测试(0.93)以及平滑度(0.93)、躯干位移(0.91)、肘关节伸展(0.73)和肩关节运动(0.56)的运动学测量结果均有很强的相关性,表明其具有良好的建构效度:新的 DTA 被证明是评估脑卒中后任务执行过程中运动质量的可靠且有效的工具。
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引用次数: 0
Time-course for acquiring transfer independence in patients with subacute stroke: a prospective cohort study. 亚急性脑卒中患者获得独立转移的时间过程:一项前瞻性队列研究。
IF 2.5 4区 医学 Q1 REHABILITATION Pub Date : 2024-10-09 DOI: 10.2340/jrm.v56.40055
Shin Kitamura, Yohei Otaka, Shintaro Uehara, Yudai Murayama, Kazuki Ushizawa, Yuya Narita, Naho Nakatsukasa, Daisuke Matsuura, Rieko Osu, Kunitsugu Kondo, Sachiko Sakata

Objective: To clarify the time-course of longitudinal changes in the independence level of subtasks composing bed-wheelchair transfer among patients with stroke.

Design: Single-institution prospective cohort study.

Patients: A total of 137 consecutive post-stroke patients using wheelchair on admission to the subacute rehabilitation wards.

Methods: The independence degree in each of the 25 transfer-related subtasks was assessed using the Bed-Wheelchair Transfer Tasks Assessment Form on a three-level scale every two weeks, from admission to the endpoint (either discharge or when achieving independent transfer). Patients were classified based on admission and endpoint assessment form scores using two-step cluster analysis.

Results: Patients were classified into three clusters. The first cluster included 50 patients who exhibited a greater independence level in all subtasks on admission (52.0-100% of patients performed each subtask independently) and at the endpoint (64.0-100%). The second included 30 patients who showed less independence on admission (0-27.8%) but achieved greater independence levels at the endpoint (44.4-97.2%). The third included 51 patients whose independence level remained low in many subtasks from admission (0-5.8%) until the endpoint (0-29.4%).

Conclusion: The independence level and its changing process during transfer were categorized into three time-courses, each requiring different intervention strategies.

目的明确脑卒中患者在床上-轮椅转移的子任务中独立性水平纵向变化的时间过程:设计:单机构前瞻性队列研究:患者:137例连续入住亚急性康复病房、使用轮椅的脑卒中后患者:从入院到终点(出院或实现独立转移时),每两周使用床-轮椅转移任务评估表对25项转移相关子任务中每项任务的独立程度进行三级评分。根据入院和终点评估表的得分,采用两步聚类分析法对患者进行分类:结果:患者被分为三组。第一组包括 50 名患者,他们在入院时(52.0%-100% 的患者独立完成所有子任务)和终点时(64.0%-100% 的患者独立完成所有子任务)表现出较高的独立性。第二组包括 30 名入院时独立性较差(0-27.8%),但在终点时独立性水平较高(44.4-97.2%)的患者。第三组包括51名患者,他们从入院时(0-5.8%)到终点时(0-29.4%),在许多子任务上的独立性水平一直较低:结论:转运过程中的独立性水平及其变化过程可分为三个时间过程,每个过程都需要不同的干预策略。
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引用次数: 0
Positive effects of lower extremity constraint-induced movement therapy on balance, leg strength and dual-task ability in stroke patients: a longitudinal cohort study. 下肢约束诱导运动疗法对中风患者平衡、腿部力量和双任务能力的积极影响:一项纵向队列研究。
IF 2.5 4区 医学 Q1 REHABILITATION Pub Date : 2024-10-03 DOI: 10.2340/jrm.v56.24168
Annika Sefastsson, Ingela Marklund, Håkan Littbrand, Per Wester, Britt-Marie Stålnacke, Ann Sörlin, Birgitta Langhammer, Per Liv, Xiaolei Hu

Objective: To investigate whether high-intensity lower extremity constraint-induced movement therapy can improve balance, leg strength, and dual-task ability.

Design: A longitudinal cohort study in a real-world outpatient clinic.

Patients: 147 community-dwelling participants in the subacute and chronic poststroke phases.

Methods: Participants received lower extremity constraint-induced movement therapy for 6 hours/day during 2 consecutive weeks, including balance, strength, and functional training. The Berg Balance Scale (BBS), Single-Leg-Stance (SLS) bilaterally, one Repetition Maximum (1RM) in a leg press, symmetry of leg strength (Diff-1RM), Timed Up and Go (TUG), and the TUG Manual test were assessed before, after, and 3 months after lower extremity constraint-induced movement therapy.

Results: Compared with preintervention data, statistically significant improvements after lower extremity constraint-induced movement therapy (p < 0.001) were demonstrated for balance with an absolute value in BBS at 1.9 points (effect size 0.38) and SLS at 2.4 s (effect size 0.24), and for leg strength at 10.2 kg (effect size 0.54) for the affected leg. Diff 1RM decreased significantly at 5.8 kg (effect size 0.39) and improvements on dual-task ability at 2.7 s were significant (effect size 0.14). The effects persisted at the 3-month follow-up.

Conclusions: High-intensity lower extremity constraint-induced movement therapy may be a feasible treatment option for middle-aged stroke patients to affect balance, leg strength, and dual-task ability positively in an out-patient clinical setting.

目的:研究高强度下肢约束诱导运动疗法能否改善平衡能力、腿部力量和双重任务能力:研究高强度下肢约束诱导运动疗法能否改善平衡、腿部力量和双重任务能力:设计:在真实世界的门诊进行纵向队列研究:147名社区居民,处于中风后的亚急性和慢性阶段:参与者在连续两周内每天接受 6 小时的下肢约束诱导运动疗法,包括平衡、力量和功能训练。在接受下肢约束运动疗法之前、之后和3个月后,对参与者进行伯格平衡量表(BBS)、双侧单腿站立(SLS)、压腿一次重复最大值(1RM)、腿部力量对称性(Diff-1RM)、定时上下(TUG)和TUG手动测试的评估:结果:与干预前的数据相比,下肢约束诱导运动疗法后的数据有明显改善(p 结论:高强度下肢约束诱导运动疗法对下肢功能有明显改善:在门诊临床环境中,高强度下肢约束诱导运动疗法对中年卒中患者的平衡、腿部力量和双任务能力有积极影响,是一种可行的治疗方案。
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引用次数: 0
Immersive visualization of movement in patients with hemophilic ankle arthropathy. Multicenter, single-blind, randomized clinical trial. 血友病踝关节病患者运动的沉浸式可视化。多中心、单盲、随机临床试验。
IF 2.5 4区 医学 Q1 REHABILITATION Pub Date : 2024-09-30 DOI: 10.2340/jrm.v56.40775
Roberto Ucero-Lozano, Raúl Pérez-Llanes, Rubén Cuesta-Barriuso, Elena Donoso-Úbeda

Objective: To evaluate the efficacy of immersive movement observation in adult patients with haemophilic ankle arthropathy.

Design: Multicentre, single-blind, randomized clinical trial.

Subjects: 48 patients with haemophilia.

Methods: Patients were randomly allocated to 2 groups (180º immersive video-based visualization of movement and a control group with no intervention). Twenty-eight consecutive 15-min home sessions, 1 per day, of immersive visualization of ankle flexion-extension movement were carried out. Three evaluations were performed: pretreatment (T0), post-intervention (T1), and at 16 weeks' follow-up (T2). The primary variable was joint-pain intensity (visual analogue scale). The secondary variables were conditioned pain modulation (Conditioned Pain Modulation Index), pressure pain threshold (pressure algometer), range of motion (goniometry) and kinesiophobia (Tampa Scale of Kinesiophophia).

Results: There were intergroup differences in pain intensity (F = 37.14; p < 0.001), conditioned pain modulation (F = 5.40; p = 0.006), and dorsal (F = 19.17; p < 0.001) and plantar (F = 9.27; p<0.001) ankle flexion. More than 50% of experimental group patients exhibited changes exceeding the minimum detectable change in pain intensity (MDC = 0.43), and the pressure pain threshold in the extensor carpi radialis longus muscle (MDC = 1.34) and malleolus (MDC = 4.93).

Conclusions: 180º immersive video-based visualization of movement can improve the intensity of pain, conditioned pain modulation, and ankle range of motion in patients with haemophilic ankle arthropathy.

目的评估沉浸式运动观察对血友病踝关节病成年患者的疗效:多中心、单盲、随机临床试验:48名血友病患者:患者被随机分配到两组(180º 沉浸式运动可视化视频组和不进行干预的对照组)。连续进行 28 次 15 分钟的踝关节屈伸运动沉浸式可视化训练,每天 1 次。共进行了三次评估:治疗前(T0)、干预后(T1)和 16 周的随访(T2)。主要变量是关节疼痛强度(视觉模拟量表)。次要变量为条件性疼痛调节(条件性疼痛调节指数)、压痛阈值(压痛计)、活动范围(动态关节角度计)和运动恐惧症(坦帕运动恐惧症量表):结果:疼痛强度存在组间差异(F=37.14;P=0.01):基于 180º 沉浸式视频的可视化运动可以改善嗜血性踝关节病患者的疼痛强度、条件性疼痛调节和踝关节活动范围。
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引用次数: 0
The veracity function: integrity, and comprehensiveness of evidence. 真实性功能:证据的完整性和全面性。
IF 2.5 4区 医学 Q1 REHABILITATION Pub Date : 2024-09-30 DOI: 10.2340/jrm.v56.40350
Antti Malmivaara
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引用次数: 0
Efficacy of a new video observational training method (intensive visual simulation) for motor recovery in the upper limb in subacute stroke: a feasibility and proof-of-concept study. 一种新的视频观察训练方法(强化视觉模拟)对亚急性中风患者上肢运动恢复的疗效:一项可行性和概念验证研究。
IF 2.5 4区 医学 Q1 REHABILITATION Pub Date : 2024-09-25 DOI: 10.2340/jrm.v56.36119
Etienne Ojardias, Ahmed Adham, Hugo Bessaguet, Virginie Phaner, Diana Rimaud, Pascal Giraux

Objective: To demonstrate the feasibility and efficacy  of a new video-observation training method (intensive visual simulation) to improve upper limb function.

Design: Small sample, randomized, evaluator-blind, monocentric study.

Patients: Seventeen early subacute ischaemic stroke patients with complete hemiplegia were  randomly assigned to the therapeutic group (n = 8) or control group (CG, n = 9).

Methods: Thirty sessions of intensive visual simulation combined with corrected visual feedback (therapeutic group) or uncorrected visual feedback (control group) were performed over 6 weeks on top of a standard rehabilitation programme.

Main outcome measure: 400-point hand assessment test (400p-HA).

Secondary outcome measures: Box and Blocks (B&B), Purdue Pegboard test, Minnesota.

Results: The 400p-HA test improved significantly from T0 to 6 months for both groups, with a significant difference between groups at 3 months (MW-UT p = 0.046) and 4 months (MW-UT p = 0.046) in favour of the therapeutic group. One-phase exponential modelling of 400p-HA showed a greater plateau for the therapeutic group (F test p = 0.0021). There was also faster recovery of the ability to perform the B&B tests for the therapeutic group (log-rank test p = 0.03).

Conclusion: This study demonstrated the feasibility and potential efficacy of an intensive visual simulation training programme to improve upper limb  function in subacute stroke patients. A larger study is needed to confirm these results.

目的:证明一种新的视频观察训练方法(强化视觉模拟)对改善上肢功能的可行性和有效性:证明一种新的视频观察训练方法(强化视觉模拟)对改善上肢功能的可行性和有效性:小样本、随机、评估者盲法、单中心研究:17名完全性偏瘫的早期亚急性缺血性中风患者被随机分配到治疗组(8人)或对照组(9人):方法:在标准康复计划的基础上,进行为期 6 周的 30 次强化视觉模拟,并结合校正视觉反馈(治疗组)或未校正视觉反馈(对照组):结果:结果:两组患者的 400p-HA 测试均在 0 至 6 个月期间有明显改善,治疗组在 3 个月(MW-UT p = 0.046)和 4 个月(MW-UT p = 0.046)时差异显著。400p-HA 的单相指数模型显示,治疗组的高原反应更明显(F 检验 p = 0.0021)。治疗组进行 B&B 测试的能力恢复也更快(对数秩检验 p = 0.03):本研究证明了强化视觉模拟训练计划对改善亚急性中风患者上肢功能的可行性和潜在疗效。需要更大规模的研究来证实这些结果。
{"title":"Efficacy of a new video observational training method (intensive visual simulation) for motor recovery in the upper limb in subacute stroke: a feasibility and proof-of-concept study.","authors":"Etienne Ojardias, Ahmed Adham, Hugo Bessaguet, Virginie Phaner, Diana Rimaud, Pascal Giraux","doi":"10.2340/jrm.v56.36119","DOIUrl":"10.2340/jrm.v56.36119","url":null,"abstract":"<p><strong>Objective: </strong>To demonstrate the feasibility and efficacy  of a new video-observation training method (intensive visual simulation) to improve upper limb function.</p><p><strong>Design: </strong>Small sample, randomized, evaluator-blind, monocentric study.</p><p><strong>Patients: </strong>Seventeen early subacute ischaemic stroke patients with complete hemiplegia were  randomly assigned to the therapeutic group (n = 8) or control group (CG, n = 9).</p><p><strong>Methods: </strong>Thirty sessions of intensive visual simulation combined with corrected visual feedback (therapeutic group) or uncorrected visual feedback (control group) were performed over 6 weeks on top of a standard rehabilitation programme.</p><p><strong>Main outcome measure: </strong>400-point hand assessment test (400p-HA).</p><p><strong>Secondary outcome measures: </strong>Box and Blocks (B&B), Purdue Pegboard test, Minnesota.</p><p><strong>Results: </strong>The 400p-HA test improved significantly from T0 to 6 months for both groups, with a significant difference between groups at 3 months (MW-UT p = 0.046) and 4 months (MW-UT p = 0.046) in favour of the therapeutic group. One-phase exponential modelling of 400p-HA showed a greater plateau for the therapeutic group (F test p = 0.0021). There was also faster recovery of the ability to perform the B&B tests for the therapeutic group (log-rank test p = 0.03).</p><p><strong>Conclusion: </strong>This study demonstrated the feasibility and potential efficacy of an intensive visual simulation training programme to improve upper limb  function in subacute stroke patients. A larger study is needed to confirm these results.</p>","PeriodicalId":54768,"journal":{"name":"Journal of Rehabilitation Medicine","volume":"56 ","pages":"jrm36119"},"PeriodicalIF":2.5,"publicationDate":"2024-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11445588/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142332579","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
Effects of mirror therapy in post-traumatic complex regional pain syndrome type-1: a randomized controlled study. 镜像疗法对创伤后 1 型复杂区域疼痛综合征的影响:随机对照研究。
IF 2.5 4区 医学 Q1 REHABILITATION Pub Date : 2024-09-24 DOI: 10.2340/jrm.v56.40417
Elif Can Özdemir, Atilla H Elhan, Ayşe A Küçükdeveci

Objective: To investigate the effects of mirror therapy applied in addition to routine rehabilitation on clinical outcomes in post-traumatic complex regional pain syndrome type 1.

Design: Single-blind randomized controlled trial.

Subjects: Patients with trauma-induced complex regional pain syndrome type 1 of the hand receiving outpatient rehabilitation.

Methods: Patients were randomized into mirror therapy and control groups. All patients received routine physical therapy and rehabilitation for 20 sessions (5 sessions/week, for 4 weeks). The mirror group received additional mirror therapy at each session. The primary outcome was pain intensity by numeric rating scale. Secondary outcomes were grip/pinch strength, hand/wrist circumference, dexterity, hand activities, and health-related quality of life. All assessments were performed before and immediately after the treatment, and 4 weeks later at follow-up.

Results: Forty patients were enrolled, 20 in each group. Both groups revealed statistically significant improvements from therapy regarding pain, grip/pinch strength, wrist circumference, dexterity, and hand activities (p <  0.05). When groups were compared regarding the improvements in assessment parameters, no statistically significant difference was found between the 2 groups in any of the outcomes (p > 0.05).

Conclusion: Mirror therapy applied in addition to routine therapy in post-traumatic complex regional pain syndrome type 1 did not provide extra benefit to the improvement of pain, function, and other clinical outcomes.

目的研究在常规康复治疗的基础上应用镜像疗法对创伤后1型复杂区域疼痛综合征临床疗效的影响:设计:单盲随机对照试验:接受门诊康复治疗的手部创伤后1型复杂区域疼痛综合征患者:将患者随机分为镜像治疗组和对照组。所有患者均接受常规理疗和康复治疗,共 20 次(每周 5 次,共 4 周)。镜疗组在每个疗程中接受额外的镜疗。主要结果是疼痛强度,采用数字评分量表。次要结果为握力/夹力、手/腕围、灵活性、手部活动以及与健康相关的生活质量。所有评估均在治疗前和治疗后立即进行,4周后进行随访:40名患者参加了治疗,每组20人。两组患者在疼痛、握力/夹力、腕围、灵活性和手部活动方面的改善均有统计学意义(P < 0.05)。比较两组在评估参数方面的改善情况,发现两组在任何结果上都没有明显的统计学差异(P > 0.05):结论:在常规治疗的基础上对创伤后复杂性区域疼痛综合征(1 型)患者进行镜像治疗,并不能在改善疼痛、功能和其他临床结果方面带来额外的益处。
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引用次数: 0
Enhancing upper extremity muscle strength in individuals with spinal cord injury using low-intensity blood flow restriction exercise. 利用低强度血流限制运动增强脊髓损伤患者的上肢肌力。
IF 2.5 4区 医学 Q1 REHABILITATION Pub Date : 2024-09-24 DOI: 10.2340/jrm.v56.40608
Babak Shadgan, Mehdi Nourizadeh, Yekta Saremi, Leila Baktash, Stefan Lazarevic

Objectives: This study explores the feasibility and effects of low-intensity blood flow restriction exercise on forearm muscle strength and function in individuals with spinal cord injury.

Study design: Pilot randomized clinical trial.

Patients and methods: Ten male and female adult participants with chronic cervical and thoracic spinal cord injury underwent an 8-week low-intensity blood flow restriction exercise programme that targeted forearm muscles. Each participant's contralateral forearm served as the control. Grip strength was the primary outcome measure, and participants also provided qualitative feedback on their experiences.

Results: The study revealed a significant increase in participants' forearm muscle strength on the experimental side engaged in low-intensity blood flow restriction training, with an average strength gain of 7.5 ± 0.36 kg after 16 exercise sessions (Cohen's d = -6.32, 95% CI -8.34, -6.68). In comparison, the control side, following a conventional high- intensity exercise regimen without BFR, showed a more modest strength increase of 4.4 ± 0.67 kg. A mean Patient's Global Impression of Change score of 2.2 reflected overall improvements in participants' daily activities and health status.

Conclusion: This study highlights the feasibility and effectiveness of low-intensity blood flow restriction exercise as a safe and promising approach to enhancing forearm muscle strength in individuals with spinal cord injury. The observed positive outcomes, coupled with a high level of participant satisfaction, underscore the potential of this innovative method to significantly improve limb muscle strength, thereby contributing to greater functional independence in this population.

研究目的本研究探讨了低强度血流限制运动对脊髓损伤患者前臂肌肉力量和功能的可行性和影响:试验性随机临床试验:10名患有慢性颈椎和胸椎脊髓损伤的成年男性和女性参与者接受了为期8周的低强度血流限制运动计划,该计划以前臂肌肉为目标。每位参与者的对侧前臂作为对照组。握力是主要的结果测量指标,参与者还就自己的体验提供了定性反馈:研究显示,参与低强度血流限制训练的实验侧参与者前臂肌肉力量明显增加,16 次训练后平均力量增加 7.5 ± 0.36 公斤(Cohen's d = -6.32,95% CI -8.34,-6.68)。相比之下,采用传统高强度锻炼方法而不进行 BFR 锻炼的对照组力量增加较少,仅为 4.4 ± 0.67 千克。患者的总体变化印象平均得分为 2.2 分,反映出参与者的日常活动和健康状况总体有所改善:这项研究强调了低强度血流限制运动的可行性和有效性,它是增强脊髓损伤患者前臂肌肉力量的一种安全、有前途的方法。观察到的积极结果以及参与者的高度满意度,凸显了这种创新方法在显著提高肢体肌肉力量方面的潜力,从而有助于提高这类人群的功能独立性。
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引用次数: 0
Efficacy of pulmonary rehabilitation in patients with chronic obstructive pulmonary disease and obstructive sleep apnea; a randomized controlled trial. 慢性阻塞性肺病和阻塞性睡眠呼吸暂停患者的肺康复疗效;随机对照试验。
IF 2.5 4区 医学 Q1 REHABILITATION Pub Date : 2024-09-24 DOI: 10.2340/jrm.v56.23757
Honghua Shen, Yiming Xu, Yin Zhang, Lei Ren, Rui Chen

Objective: To evaluate the efficacy of pulmonary rehabilitation in the outcomes of patients with chronic obstructive pulmonary disease-obstructive sleep apnoea overlap syndrome patients who used positive airway pressure.

Design: Prospective randomized controlled single- blind trial.

Patients: A total of 79 patients with chronic obstructive pulmonary disease-obstructive sleep apnoea overlap syndrome were randomly assigned to either the intervention group (n = 40) or control group (n = 39).

Methods: All patients consistently adhered to positive airway pressure therapy every night from enrolment in the study, while intervention group patients received additional moderate-intensity aerobic exercise for 20 weeks. Pre- and post-intervention measurements included the 6-Minute Walk Test, Barthel Index, body mass index, fat mass, free fat mass, forced expiratory volume in 1 s (FEV1), FEV1%predicted, modified Medical Research Council, and polysomnography parameters.

Results: After 20 weeks, the intervention group exhibited statistically significant improvements in 6MWD, Barthel Index, body mass index, fat mass, and modified Medical Research Council compared with control group (all p < 0.01). In addition, the intervention group showed a significantly lower percentage of total sleep time with oxygen saturation < 90% (p = 0.013) and higher lowest nocturnal oxygen saturation (p = 0.008) than the control group. However, there was no significant difference in FEV1 %predicted between the 2 groups.

Conclusion: Pulmonary rehabilitation incorporating moderate-intensity aerobic exercise could improve physical endurance and motor abilities in individuals with chronic obstructive pulmonary disease-obstructive sleep apnoea overlap syndrome, while also improving anamnestic dyspnoea, body composition, and sleep-disordered breathing.

目的评估肺康复治疗对使用气道正压治疗的慢性阻塞性肺疾病-阻塞性睡眠呼吸暂停重叠综合征患者的疗效:前瞻性随机对照单盲试验:共有79名慢性阻塞性肺疾病-阻塞性睡眠呼吸暂停重叠综合征患者被随机分配到干预组(40人)或对照组(39人):所有患者自加入研究起每晚坚持气道正压治疗,干预组患者则接受为期20周的额外中等强度有氧运动。干预前后的测量包括 6 分钟步行测试、巴特尔指数、体重指数、脂肪量、游离脂肪量、1 秒用力呼气容积(FEV1)、FEV1% 预测值、修正的医学研究委员会和多导睡眠图参数:20 周后,与对照组相比,干预组在 6MWD、Barthel 指数、体重指数、脂肪量和改良医学研究委员会方面均有统计学意义上的显著改善(均为 p 结论:干预组与对照组相比,在 6MWD、Barthel 指数、体重指数、脂肪量和改良医学研究委员会方面均有统计学意义上的显著改善:结合中等强度有氧运动的肺康复治疗可提高慢性阻塞性肺病-阻塞性睡眠呼吸暂停重叠综合征患者的身体耐力和运动能力,同时还能改善呼吸困难、身体成分和睡眠呼吸障碍。
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引用次数: 0
Self-reported mental health in hospitalized patients with COVID-19: A 1-year follow-up. COVID-19住院患者自我报告的心理健康状况:为期一年的随访。
IF 2.5 4区 医学 Q1 REHABILITATION Pub Date : 2024-09-24 DOI: 10.2340/jrm.v56.40654
Linda Ashman Kröönström, David Krabbe, Alexandra Larsson, Lena Rafsten, Annie Palstam, Katharina S Sunnerhagen, Hanna C Persson

Objectives: This study aimed to longitudinally follow self-reported symptoms of depression, anxiety, post-traumatic stress disorder, and fatigue during the first year after hospitalization because of COVID-19.

Design: The study was an observational longitudinal study.

Methods and participants: Between July 2020, and February 2021, 211 patients aged ≥ 18 years, hospitalized ≥ 5 days at 5 hospitals in Region Västra Götaland, who had COVID-19, and were non-contagious (at study enrolment) were included in the baseline assessment. Of these, 168 (79.6%) patients completed mental health questionnaires at a 3-month follow-up, and 172 (83.1%) at a 12-month follow-up. A total of 120 (56.9%) participants who completed at least 1 questionnaire at both the 3- and 12-month follow-ups were analysed; the majority were male (n = 78, 65.0%).

Results: There was an improvement in all patients from 3 to 12 months on the fatigue subscales "reduced activity" (p = 0.02) and "physical fatigue" (p = 0.04). No other significant mental health improvements were found. At 12 months, 34 (28.4%) were classified as having anxiety symptoms, 29 (24.1%) as having depression symptoms, and 40 (33.3%) had symptoms of probable post-traumatic stress disorder.

Conclusions: Participants in the present study did not report full mental health recovery 1 year after hospitalization for COVID-19.

研究目的本研究旨在纵向追踪因COVID-19住院后第一年内自我报告的抑郁、焦虑、创伤后应激障碍和疲劳症状:该研究是一项观察性纵向研究:在 2020 年 7 月至 2021 年 2 月期间,211 名年龄≥ 18 岁、在韦斯特拉-哥特兰地区的 5 家医院住院≥ 5 天、患有 COVID-19 且无传染性(在研究注册时)的患者被纳入基线评估。其中,168 名患者(79.6%)在 3 个月的随访中完成了心理健康问卷调查,172 名患者(83.1%)在 12 个月的随访中完成了心理健康问卷调查。在 3 个月和 12 个月的随访中,共有 120 人(56.9%)至少填写了一份问卷,我们对这 120 人进行了分析,其中大部分为男性(78 人,65.0%):从 3 个月到 12 个月,所有患者在疲劳分量表 "活动减少"(p = 0.02)和 "身体疲劳"(p = 0.04)方面都有所改善。心理健康方面没有其他明显改善。在 12 个月时,34 人(28.4%)被归类为有焦虑症状,29 人(24.1%)有抑郁症状,40 人(33.3%)可能有创伤后应激障碍症状:结论:本研究的参与者在因 COVID-19 住院治疗 1 年后并未完全恢复精神健康。
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Journal of Rehabilitation Medicine
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