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Effectiveness of kinesio tape in people with low back pain. A systematic review with meta-analysis. 肌内效贴治疗腰痛的有效性。荟萃分析的系统综述。
IF 3.4 3区 医学 Q1 REHABILITATION Pub Date : 2026-03-24 DOI: 10.23736/S1973-9087.26.09064-7
Jacqueline Inostroza-Quiroz, Ricardo Solano-López, Claudio Bascour-Sandoval, Diana Buitrago-García, Jeritza Salazar, Sayén Huaiquilaf-Jorquera, Matías Rodríguez, María J Oliveros, Pamela Serón

Background: Low back pain (LBP) is a common musculoskeletal condition. Kinesio Tape (KT) has been proposed as a non-pharmacological treatment, but its effectiveness remains unclear.

Evidence acquisition: A systematic review with meta-analysis was conducted according to PRISMA. Searches were performed in MEDLINE-Ovid, Embase-Ovid, PEDro, CENTRAL, CINAHL, LILACS, and Scopus up to January 2025. Randomized controlled trials (RCTs) evaluating KT in individuals with LBP were included. The primary outcomes were functionality and pain intensity, and the secondary outcomes were range of motion and adverse events.

Evidence synthesis: Fifty-four RCTs involving 3479 participants were included. In acute LBP, KT improved functionality by 14.95% (95% CI: -31.40 to 1.50) compared with no intervention on the Oswestry Disability Index (ODI). In chronic LBP, KT improved functionality by 11.9% (95% CI -18.07 to -5.73) compared to no intervention, and 2.31% (95% CI -5.83 to -1.22) versus placebo, both on ODI, and 0.97 points in the Roland-Morris Questionnaire (95% CI -2.45 to 0.51) versus Micropore®. Physiotherapy improved 5.44% (95% CI -0.76 to 10.12) more than KT on ODI. In pregnant women, KT improved functionality by 1.45 points (95% CI -2.97 to 0.07) versus placebo and by 2.19 points (95% CI -4.35 to -0.03) versus no intervention on the Roland-Morris Questionnaire. In irradiated LBP, KT showed no benefit over placebo. For pain on the Visual Analog Scale, KT in acute LBP reduced pain intensity by 1.61 cm (95% CI: -2.54 to -0.08) compared with no intervention. In chronic LBP, KT was superior to no intervention by 1.93 cm (95% CI -2.17 to -1.69), to placebo 0.70 cm (95% CI -1.39 to -0.02), to Micropore® 1.03 cm (95% CI -1.76 to -0.31), and 0.95 cm (95% CI -2.04 to 0.12) more than physiotherapy. In pregnant women, KT reduced pain by up to 3.01 cm (95% CI -4.39 to -1.62) compared to placebo and by -1.78cm (95% CI -3.34 to -0.22) compared to no intervention. Finally, in LBP irradiated, KT decreased by 0.31cm (95% CI -1.23 to 0.60) more than placebo.

Conclusions: KT may improve functionality and reduce pain in short-term LBP. However, its effects on long-term chronic and irradiated LBP remain limited, and further high-quality trials are needed.

背景:腰痛是一种常见的肌肉骨骼疾病。肌内效贴(KT)已被提议作为一种非药物治疗,但其有效性尚不清楚。证据获取:根据PRISMA进行系统评价和荟萃分析。在MEDLINE-Ovid、Embase-Ovid、PEDro、CENTRAL、CINAHL、LILACS和Scopus中进行了截至2025年1月的检索。纳入评估LBP患者KT的随机对照试验(RCTs)。主要结果是功能和疼痛强度,次要结果是活动范围和不良事件。证据综合:纳入54项随机对照试验,涉及3479名受试者。在急性腰痛患者中,与没有干预的Oswestry残疾指数(ODI)相比,KT改善了14.95%的功能(95% CI: -31.40至1.50)。在慢性LBP中,与不干预相比,KT改善了11.9% (95% CI -18.07至-5.73)的功能,与安慰剂相比,在ODI方面改善了2.31% (95% CI -5.83至-1.22),与Micropore®相比,Roland-Morris问卷调查改善了0.97分(95% CI -2.45至0.51)。物理治疗对ODI的改善比KT多5.44% (95% CI -0.76 ~ 10.12)。在罗兰-莫里斯问卷调查中,与安慰剂相比,KT改善了孕妇的功能1.45分(95% CI -2.97至0.07),与未干预相比,KT改善了功能2.19分(95% CI -4.35至-0.03)。在照射过的LBP中,KT没有比安慰剂更好的效果。对于视觉模拟量表上的疼痛,与没有干预相比,急性腰痛的KT减轻了1.61 cm的疼痛强度(95% CI: -2.54至-0.08)。在慢性腰痛中,KT比无干预高1.93 cm (95% CI -2.17至-1.69),比安慰剂高0.70 cm (95% CI -1.39至-0.02),比Micropore®高1.03 cm (95% CI -1.76至-0.31),比物理治疗高0.95 cm (95% CI -2.04至0.12)。在孕妇中,与安慰剂相比,KT减少了3.01 cm (95% CI -4.39至-1.62),与无干预相比减少了-1.78cm (95% CI -3.34至-0.22)。最后,在LBP照射中,KT比安慰剂减少了0.31cm (95% CI -1.23至0.60)。结论:KT可改善短期LBP的功能和减轻疼痛。然而,它对长期慢性和辐照性腰痛的影响仍然有限,需要进一步的高质量试验。
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引用次数: 0
Identifying candidates for torque-assisted exoskeleton for gait assistance after stroke: a pre-specified subgroup analysis. 确定中风后用于步态辅助的扭矩辅助外骨骼的候选者:预先指定的亚组分析。
IF 3.4 3区 医学 Q1 REHABILITATION Pub Date : 2026-03-24 DOI: 10.23736/S1973-9087.26.09160-4
Won H Chang, Tae-Woo Kim, Hyoung S Kim, Fazah A Hanapiah, Jong W Lee, Seung-Hyeon Han, Chai W Jia, Dae H Kim, Deog Y Kim

Background: Wearable robots show promise for gait assistance in stroke patients, yet the clinical characteristics predicting a positive ambulatory response to exoskeletal assistance remain unclear.

Aim: To identify appropriate candidates for torque-assisted exoskeletal wearable robots in stroke patients.

Design: A subgroup analysis using data from an international, multicenter, randomised controlled trial.

Setting: Inpatient.

Population: Fifty-five early subacute stroke patients who completed four weeks of robot-assisted gait training (RAGT) with the wearable exoskeletal robot (ANGEL LEGS M20, Angel Robotics Co., Ltd.).

Methods: Immediately after RAGT for the four weeks, ambulatory function with the exoskeleton on and off was evaluated using the 10-Meter Walk Test (10MWT), 6-Minute Walk Test (6MWT), and Physiological Cost Index (PCI). At the same time, additional assessments included the Functional Ambulatory Category (FAC), Fugl-Meyer Assessment-Lower Extremity, Motricity Index-Lower Limb, Trunk Control Test, and Berg Balance Score. Participants were classified as good-responder, no-responder, or negative-responder groups based on changes in walking performance with exoskeletal assistance. Univariate and multivariate ordinal logistic regression analyses identified factors associated with responsiveness.

Results: In the good-responder group, 10MWT, 6MWT and PCI showed significant improvements in the robot-on state compared with the robot-off state, respectively (P<0.05). Good responders had significantly lower baseline ambulatory, balance, and lower limb motor function compared to negative-responders (P<0.05). Multivariate analysis identified lower FAC as the only independent predictor of positive response to exoskeletal assistance (P<0.05).

Conclusions: Torque-assisted exoskeletal wearable robots may improve ambulatory function in stroke patients with low ambulatory function.

Clinical rehabilitation impact: To achieve meaningful effects through exoskeleton robots, patient selection must be adjusted according to clinical needs.

背景:可穿戴机器人在中风患者的步态辅助方面显示出前景,但预测外骨骼辅助的积极动态反应的临床特征仍不清楚。目的:为脑卒中患者确定合适的扭矩辅助外骨骼可穿戴机器人。设计:亚组分析使用来自国际、多中心、随机对照试验的数据。背景:住院。研究对象:55名早期亚急性中风患者,使用可穿戴外骨骼机器人(ANGEL LEGS M20, ANGEL Robotics Co., Ltd.)完成了为期四周的机器人辅助步态训练(RAGT)。方法:RAGT 4周后,立即使用10米步行测试(10MWT)、6分钟步行测试(6MWT)和生理成本指数(PCI)评估外骨骼打开和关闭时的行走功能。同时,附加的评估包括功能活动分类(FAC)、Fugl-Meyer下肢评估、下肢运动指数、躯干控制测试和Berg平衡评分。根据外骨骼辅助下行走表现的变化,参与者被分为良好反应组、无反应组或负反应组。单变量和多变量有序逻辑回归分析确定了与响应性相关的因素。结果:在反应良好组中,10MWT、6MWT和PCI在机器人开启状态下比关闭状态下分别有显著改善(p结论:扭矩辅助外骨骼可穿戴机器人可以改善运动功能低下的脑卒中患者的运动功能。临床康复影响:为了通过外骨骼机器人达到有意义的效果,必须根据临床需要调整患者选择。
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引用次数: 0
Validation of the Czech adaptation of Mini-BESTest into clinical practice. 捷克Mini-BESTest的临床应用验证。
IF 3.4 3区 医学 Q1 REHABILITATION Pub Date : 2026-03-18 DOI: 10.23736/S1973-9087.26.09228-2
Klaudia Fabicovic, Klara Novotna, Karla Mothejlova, Jakub Jenicek, Eva Kejhova, Eliska Weissova, Vaclav Kulich, Vladimir Rogalewicz, Yvona Angerova

Background: One of the frequently used standardized tools for balance assessment is the Mini-BESTest. Creating validated versions in national languages is very important for its correct administration and usability in people with acquired brain injury.

Aim: Our intention was to verify the validity of the Czech translation Mini-BESTestCZ and describe experiences with its implementation in clinical practice.

Design: Validation study.

Setting: Department of Rehabilitation Medicine, University Hospital.

Population: Patients after stroke or traumatic brain injury.

Methods: The Mini-BESTest was translated and cross-culturally adapted into Czech according to established guidelines. The validation of this test was performed on a group of individuals with acquired brain damage in comparison with the Berg Balance Scale (BBS) and the Timed Up and Go test (TUG). Subsequently, physiotherapists who used the Mini-BESTestCZ in their practice were also contacted to evaluate their feedback and experiences with implementing the test into clinical practice.

Results: A total of 63 people with acquired brain damage participated in the study. Internal consistency of the Czech version of the Mini-BESTest was excellent, with intra-class correlation coefficient ICC=0.99. There were very high correlations between the Mini-BESTest and the BBS (r=0.86) or the TUG (r=-0.74). These results indicate excellent convergent validity for the Mini-BESTestCZ. Physiotherapists considered items related to reactive postural control to be the most difficult to evaluate, and together with Timed Up and Go with cognitive dual task to be the most difficult for patients to understand.

Conclusions: The Czech version of the Mini-BESTest showed great inter-rater reliability and strong convergent validity with neither floor nor ceiling effects (as compared to the Berg Balance Scale), and can be recommended for the use in research and clinical practice for patients with acquired brain damage in subacute or chronic phase.

Clinical rehabilitation impact: The creation of a validated language version of the Mini-BESTest will contribute to better administration and evaluation of this test, not only for people with neurological disorders. We also describe therapists' practical experiences with administering this test.

背景:平衡评估常用的标准化工具之一是mini - best。为获得性脑损伤患者的正确使用和可用性,创建国家语言的验证版本非常重要。目的:我们的目的是验证捷克语翻译Mini-BESTestCZ的有效性,并描述其在临床实践中的实施经验。设计:验证研究。单位:大学附属医院康复医学科。人群:中风或创伤性脑损伤患者。方法:根据制定的指南,将Mini-BESTest翻译成捷克语并进行跨文化改编。该测试在一组获得性脑损伤患者中进行验证,并与Berg平衡量表(BBS)和定时起身测试(TUG)进行比较。随后,在实践中使用Mini-BESTestCZ的物理治疗师也被联系,以评估他们将测试应用于临床实践的反馈和经验。结果:共有63名获得性脑损伤患者参与了这项研究。捷克版Mini-BESTest的内部一致性很好,类内相关系数ICC=0.99。Mini-BESTest与BBS (r=0.86)或TUG (r=-0.74)有非常高的相关性。结果表明,Mini-BESTestCZ具有良好的收敛效度。物理治疗师认为与反应性姿势控制相关的项目是最难评估的,而与认知双重任务的“计时起来”和“走”一起是患者最难理解的。结论:与Berg平衡量表相比,捷克版Mini-BESTest量表具有较高的量表间信度和较强的收敛效度,无下限效应和上限效应,可推荐用于亚急性期或慢性期获得性脑损伤患者的研究和临床实践。临床康复影响:迷你最佳测试的有效语言版本的创建将有助于更好地管理和评估该测试,不仅对神经系统疾病患者。我们还描述了治疗师管理这个测试的实际经验。
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引用次数: 0
From pain mechanisms to functioning: a rehabilitation perspective on fibromyalgia. 从疼痛机制到功能:纤维肌痛的康复视角。
IF 3.4 3区 医学 Q1 REHABILITATION Pub Date : 2026-03-18 DOI: 10.23736/S1973-9087.26.09490-6
Giovanni Iolascon, Antimo Moretti
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引用次数: 0
Physiatrists and/vs. allied health professionals: echoing from Türkiye. 物理治疗医师和/ vs。联合卫生专业人员:来自<s:1> rkiye的呼应。
IF 3.4 3区 医学 Q1 REHABILITATION Pub Date : 2026-02-01 Epub Date: 2025-12-18 DOI: 10.23736/S1973-9087.25.09323-2
Levent Özçakar, İlker Yağci
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引用次数: 0
Beyond professional boundaries: toward evidence-based, multidisciplinary rehabilitation. 超越专业界限:走向循证、多学科康复。
IF 3.4 3区 医学 Q1 REHABILITATION Pub Date : 2026-02-01 Epub Date: 2026-01-12 DOI: 10.23736/S1973-9087.25.09339-6
Fabio Bracciantini, Melania Salina, Daniela Gaburri, Gino Sedda, Katia Libardi, Susanna Verlini, Claudia Pavarelli, Vincenzo Manigrasso, Valerio Barbari, Gino Petri, Silvia Bielli, Cristina Chiaramoni, Mariaconsiglia Calabrese, Rosario Fiolo, Orazio Meli
{"title":"Beyond professional boundaries: toward evidence-based, multidisciplinary rehabilitation.","authors":"Fabio Bracciantini, Melania Salina, Daniela Gaburri, Gino Sedda, Katia Libardi, Susanna Verlini, Claudia Pavarelli, Vincenzo Manigrasso, Valerio Barbari, Gino Petri, Silvia Bielli, Cristina Chiaramoni, Mariaconsiglia Calabrese, Rosario Fiolo, Orazio Meli","doi":"10.23736/S1973-9087.25.09339-6","DOIUrl":"10.23736/S1973-9087.25.09339-6","url":null,"abstract":"","PeriodicalId":12044,"journal":{"name":"European journal of physical and rehabilitation medicine","volume":" ","pages":"106-107"},"PeriodicalIF":3.4,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145951375","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Effects of different exercise interventions on lipid profiles in patients with stable coronary artery disease: a systematic review and network meta-analysis. 不同运动干预对稳定型冠状动脉疾病患者血脂的影响:系统综述和网络荟萃分析
IF 3.4 3区 医学 Q1 REHABILITATION Pub Date : 2026-02-01 Epub Date: 2026-02-16 DOI: 10.23736/S1973-9087.26.09237-3
Hua Chen, Xiaogang Sheng, Jihui Chen

Introduction: Stable coronary artery disease (SCAD) is frequently accompanied by dyslipidemia, and residual lipid abnormalities persist despite pharmacological therapy. Exercise training has been shown to improve lipid metabolism, but the comparative efficacy of different exercise modalities remains unclear.

Evidence acquisition: We conducted a PRISMA-based network meta-analysis including randomized controlled trials (RCTs) that evaluated exercise interventions in patients with stable coronary artery disease and reported lipid-related outcomes. Risk of bias (RoB 2.0) and GRADE were applied. Pairwise and network meta-analyses estimated effects, with SUCRA rankings, consistency, and publication bias assessments.

Evidence synthesis: Twenty randomized controlled trials (RCTs; N.=2314) were included. Combined aerobic and resistance exercise (CAREX) produced the most pronounced reductions in total cholesterol (TC) (MD=-0.88, 95% CrI -1.36 to -0.37) and triglycerides (TG) (MD=-0.49, 95% CrI -0.74 to -0.23), and outperformed continuous aerobic exercise (CAE) in both outcomes. High-intensity interval training (HIIT) and CAE also significantly reduced TG. Mind-body exercise (MBE) and CAREX significantly increased high-density lipoprotein cholesterol (HDL-C) (MD=0.16, 95% CrI 0.04-0.26; MD=0.11, 95% CrI 0.01-0.22, respectively), with mind-body exercise (MBE) ranked highest for this outcome. No exercise modality significantly improved LDL-C. Certainty of evidence was rated as moderate for HDL-C and TG, and low for TC and LDL-C.

Conclusions: CAREX is most effective for lowering TC and TG, while MBE optimally raises HDL-C. Exercise has limited effects on LDL-C, likely due to statin therapy. CAREX and MBE may be prioritized in secondary prevention for SCAD.

稳定性冠状动脉疾病(SCAD)经常伴有血脂异常,尽管药物治疗,残留的脂质异常仍然存在。运动训练已被证明可以改善脂质代谢,但不同运动方式的比较效果尚不清楚。证据获取:我们进行了一项基于prisma的网络荟萃分析,包括随机对照试验(rct),评估了运动干预对稳定冠状动脉疾病患者的影响,并报告了血脂相关的结果。应用偏倚风险(RoB 2.0)和GRADE。通过SUCRA排名、一致性和发表偏倚评估,两两和网络荟萃分析估计了效果。证据综合:纳入20项随机对照试验(rct; n =2314)。有氧和阻力联合运动(CAREX)产生了最显著的总胆固醇(TC) (MD=-0.88, 95% CrI -1.36至-0.37)和甘油三酯(TG) (MD=-0.49, 95% CrI -0.74至-0.23)的降低,并且在两种结果中都优于连续有氧运动(CAE)。高强度间歇训练(HIIT)和CAE也能显著降低TG。心身运动(MBE)和CAREX显著增加高密度脂蛋白胆固醇(HDL-C) (MD=0.16, 95% CrI 0.04-0.26; MD=0.11, 95% CrI 0.01-0.22),其中心身运动(MBE)在该结果中排名最高。无运动方式显著改善LDL-C。HDL-C和TG的证据确定性为中等,TC和LDL-C的证据确定性为低。结论:CAREX对降低TC和TG最有效,而MBE对升高HDL-C最有效。运动对LDL-C的影响有限,可能是由于他汀类药物的治疗。CAREX和MBE可能优先用于SCAD的二级预防。
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引用次数: 0
Effects of serial thermal brine hand baths on hand osteoarthritis: a randomized, double-blind, sham-controlled trial. 连续热盐水手浴对手部骨关节炎的影响:一项随机、双盲、假对照试验。
IF 3.4 3区 医学 Q1 REHABILITATION Pub Date : 2026-02-01 DOI: 10.23736/S1973-9087.26.09113-6
Philipp Klemm, Katharina Ehnert, Beate Vogtherr, Elena Neumann, Tim Wilhelmi, Pascal van Wjinen, Nils Schulz, Uwe Lange

Background: Balneotherapy is used since ancient times, effects on hand osteoarthritis however are not well elucidated.

Aim: To evaluate therapeutic effects of serial thermal brine hand baths (tbhb) in patients experiencing painful hand osteoarthritis (HOA).

Design: Randomized, double-blind, sham-controlled monocentric clinical trial.

Setting: Outpatient clinic, monocentric.

Population: Patients with painful bilateral painful HOA meeting the 1990 American College of Rheumatology classification criteria with a baseline pain level >30 mm on the Visual Analog Scale (VAS) and radiographic evidence of hand osteoarthritis in posteroanterior X-ray projection, classified as Kellgren and Lawrence grade ≥2.

Methods: Probands were randomized to the intervention group (IG) receiving tbhb or the control group (CG) receiving tap water hand baths (sham). Both hand baths (tbhb and sham) were performed 6 times in 3 weeks with 15 min/bath at a water temperature of 25 °C.

Outcomes: The primary outcome was the change in pain intensity (VAS [mm]) following the intervention. Secondary outcomes were changes in the Australian Canadian Osteoarthritis Hand Index (AUSCAN), grip strength, functional parameters of microcirculation (by O2C method), vascular endothelial growth factor (VEGF) and safety. Outcomes were primarily analysed after the last intervention followed by secondary analysis of the follow-up visits 4 and 12 weeks after intervention and during intervention.

Results: A total of 38 patients successfully completed the trial. Pain intensity significantly decreased due to tbhb (P<0.001), with sustained benefits observed up to 3 months post-intervention. The AUSCAN pain subscore was significantly reduced (P<0.001). There was no significant change in other AUSCAN subscores, nor in grip strength or functional parameters of microcirculation including VEGF due to tbhb. No adverse events due to tbhb were observed.

Conclusions: Thermal brine hand baths represent a simple, effective, and well-tolerated method to achieve pain relief in HOA with results lasting up to 12 weeks after intervention.

Clinical rehabilitation impact: Thermal brine hand baths can be used to reduce pain in HOA.

背景:水疗疗法自古以来就被使用,但对手部骨关节炎的疗效尚未得到很好的阐明。目的:评价连续热盐水手浴(thbhb)治疗疼痛性手骨关节炎(HOA)的疗效。设计:随机、双盲、假对照单中心临床试验。环境:门诊,单中心。人群:疼痛性双侧疼痛性HOA患者符合1990年美国风湿病学会分类标准,视觉模拟评分(VAS)基线疼痛水平bbb30 mm,后前方x线片显示手骨关节炎,分类为Kellgren和Lawrence≥2级。方法:先证者随机分为干预组(IG)和对照组(CG),对照组接受自来水手浴(假)治疗。在25°C的水温下,3周内进行6次手浴(下肢和下肢),每次15分钟。结局:主要结局是干预后疼痛强度(VAS [mm])的变化。次要结果是澳大利亚-加拿大骨关节炎手部指数(AUSCAN)、握力、微循环功能参数(O2C法)、血管内皮生长因子(VEGF)和安全性的变化。主要分析最后一次干预后的结果,然后对干预后4周和12周以及干预期间的随访进行二次分析。结果:38例患者成功完成试验。结论:热盐水手浴是一种简单、有效、耐受性良好的方法,可缓解HOA患者的疼痛,干预后效果持续12周。临床康复影响:热盐水手浴可用于减轻HOA疼痛。
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引用次数: 0
Dynamic suprahyoid muscle ultrasound in acute stroke: a prospective observational study for developing a dysphagia severity score. 急性中风的动态舌骨上肌超声:一项发展吞咽困难严重程度评分的前瞻性观察研究。
IF 3.4 3区 医学 Q1 REHABILITATION Pub Date : 2026-02-01 DOI: 10.23736/S1973-9087.26.09112-4
Joo Hye Sung, Sang-Hwa Lee, Jong-Hee Sohn, Sang-Won Han, Heeji Choi, Seung-Ho Shin, Jae Jun Lee, Chulho Kim

Background: Early identification and appropriate management of dysphagia are critical for improving outcomes of acute ischemic stroke.

Aim: To develop a simple and reliable scoring system to predict the severity of dysphagia in patients with acute ischemic stroke by integrating ultrasound (US) parameters with clinical variables.

Design: Prospective, cross-sectional observational study.

Setting: Inpatient neurology department of a university-affiliated hospital.

Population: A total of 212 patients with acute ischemic stroke were prospectively enrolled in this study. The mild dysphagia group and severe dysphagia group comprised 146 patients and 66 patients, respectively. Group assignment was based on the need for dietary modifications confirmed via retrospective review of dietary status, videofluoroscopic swallowing study results, and the occurrence of aspiration pneumonia during hospitalization.

Methods: Dynamic M-mode US of the suprahyoid muscle (SHM) was performed during swallowing. The following six SHM parameters were obtained: SHM thickness (baseline thickness of the SHM); SHM displacement (peak-to-peak amplitude of SHM movement); SHM difference (SHM displacement - SHM thickness); SHM ratio (SHM displacement/SHM thickness); peak-to-peak time; and total duration. The study population was randomly split into training (70%) and test (30%) sets. Least absolute shrinkage and selection operator and logistic regression analyses were performed to identify significant predictors of severe dysphagia. These predictors were used to develop and validate a simple scoring system.

Results: Brainstem lesion, bilateral lesion, National Institutes of Health Stroke Scale (NIHSS) score, SHM difference, and total duration were identified as key predictors of severe dysphagia. A simple scoring system based on these variables showed excellent discriminative performance. Areas under the receiver-operating characteristic curves (AUCs) of the training set and the test set were 0.963 and 0.935, respectively. A cutoff of ≥3 points yielded sensitivity of 97.9% and specificity of 86.4% for the training set as well as sensitivity of 78.9% and specificity of 95.3% for the test set.

Conclusions: This simple scoring system combining US and clinical parameters enabled early identification of patients at increased risk for severe dysphagia.

Clinical rehabilitation impact: The dysphagia severity prediction score can facilitate timely management of patients with acute ischemic stroke, thus potentially reducing complications and enhancing dysphagia rehabilitation.

背景:早期识别和适当处理吞咽困难对改善急性缺血性卒中的预后至关重要。目的:将超声参数与临床变量相结合,建立一种简单可靠的预测急性缺血性脑卒中患者吞咽困难严重程度的评分系统。设计:前瞻性、横断面观察研究。单位:某大学附属医院神经内科住院。人群:共有212例急性缺血性脑卒中患者被前瞻性纳入本研究。轻度吞咽困难组146例,重度吞咽困难组66例。分组是根据饮食调整的需要进行的,通过对饮食状况、视频透视吞咽研究结果和住院期间吸入性肺炎的发生进行回顾性审查。方法:吞咽时对舌骨上肌(SHM)进行动态m型超声。得到以下六个SHM参数:SHM厚度(SHM的基线厚度);SHM位移(SHM运动的峰间振幅);SHM差(SHM位移- SHM厚度);SHM比(SHM位移/SHM厚度);峰时间;总持续时间。研究人群随机分为训练组(70%)和测试组(30%)。最小绝对收缩、选择算子和逻辑回归分析确定严重吞咽困难的显著预测因子。这些预测因子被用来开发和验证一个简单的评分系统。结果:脑干病变、双侧病变、美国国立卫生研究院卒中量表(NIHSS)评分、SHM差异和总持续时间被确定为严重吞咽困难的关键预测因素。基于这些变量的简单评分系统表现出优异的判别性能。训练集和测试集的接收者-工作特征曲线(auc)下面积分别为0.963和0.935。当截断值≥3点时,训练集的灵敏度为97.9%,特异性为86.4%,测试集的灵敏度为78.9%,特异性为95.3%。结论:这个简单的评分系统结合了美国和临床参数,能够早期识别严重吞咽困难风险增加的患者。临床康复影响:吞咽困难严重程度预测评分有助于对急性缺血性脑卒中患者进行及时处理,从而有可能减少并发症,加强吞咽困难康复。
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引用次数: 0
The Italian version of the International Standards for Neurological Classification of Spinal Cord Injury. 意大利版脊髓损伤神经学分类国际标准。
IF 3.4 3区 医学 Q1 REHABILITATION Pub Date : 2026-02-01 DOI: 10.23736/S1973-9087.26.09447-5
Chiara Pavese, Giorgio Scivoletto, Ernesto Losavio
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引用次数: 0
期刊
European journal of physical and rehabilitation medicine
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