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Automated mechanical peripheral stimulation and postural control in subjects with Parkinson's disease and freezing of gait: a randomized controlled trial. 帕金森病和步态冻结受试者的自动机械外周刺激和姿势控制:一项随机对照试验
Q2 Medicine Pub Date : 2018-10-01
J S Prusch, A F R Kleiner, A P Salazar, C Pinto, R R Marchese, M Galli, A S Pagnussat

Individuals with Parkinson's disease (PD) and freezing of gait (FOG) have impaired postural control. Recent studies using foot sensory stimulation delivered by means of automated mechanical peripheral stimulation (AMPS) have demonstrated improvements of gait in individuals with PD. This study aimed to investigate the effects of AMPS on postural control in individuals with PD and FOG. Thirty-three subjects participated in this randomized controlled trial. Participants were allocated to two groups: AMPS and AMPS SHAM. Subjects underwent eight sessions of real (AMPS) or placebo AMPS (AMPS SHAM) once every three/four days. Postural control was assessed by means of posturography before the first and after the eighth session of treatment. We did not find positive effects of AMPS on center of pressure parameters. Thus, it seems that AMPS has no positive effect in terms of improving static postural control in individuals with PD and FOG.

患有帕金森病(PD)和步态冻结(FOG)的个体姿势控制受损。最近的研究表明,通过自动机械外周刺激(AMPS)提供足部感觉刺激,可以改善PD患者的步态。本研究旨在探讨AMPS对PD和FOG患者姿势控制的影响。33名受试者参加了这项随机对照试验。参与者被分为两组:AMPS组和AMPS SHAM组。受试者每三/四天接受八次真实(AMPS)或安慰剂AMPS (AMPS SHAM)治疗。姿势控制在第一次治疗前和第八次治疗后通过姿势摄影进行评估。我们没有发现AMPS对压力中心参数的积极影响。因此,AMPS在改善PD和FOG患者的静态姿势控制方面似乎没有积极作用。
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引用次数: 0
Is there a correlation between urological and cardiovascular dysfunction in Parkinson's disease? 帕金森病患者的泌尿系统和心血管功能障碍之间是否存在相关性?
Q2 Medicine Pub Date : 2018-10-01
Livia Brusa, C Rocchi, V Ponzo, Paolo Stanzione, E Finazzi, A Attanasio

It is well established that non-motor symptoms are a core feature of Parkinson's disease (PD). A dysregulation of the autonomic nervous system seems to be present in PD, supporting the coexistence of urological and cardiovascular non-motor features. We evaluated whether bladder dysfunctions in patients with PD are linked to blood pressure dysregulation. Twenty-eight mild PD patients, previously submitted to a urodynamic evaluation, underwent 24-hour ambulatory blood pressure and heart rate monitoring to allow assessment of their circadian blood pressure profile; the occurrence of postprandial hypotension and orthostatic hypotension was also investigated. No significant differences in blood pressure control were detected between bladder hyperreflexic and normoreflexic subjects. Our findings support different origins of urological and cardiovascular impairments in PD.

非运动症状是帕金森病(PD)的核心特征。自主神经系统的失调似乎存在于PD中,支持泌尿和心血管非运动特征的共存。我们评估了PD患者的膀胱功能障碍是否与血压失调有关。28名轻度PD患者,先前提交尿动力学评估,接受24小时动态血压和心率监测,以评估他们的昼夜血压谱;同时观察餐后低血压和体位性低血压的发生情况。膀胱高反射性和正常反射性受试者在血压控制方面无显著差异。我们的研究结果支持PD患者泌尿系统和心血管损伤的不同起源。
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引用次数: 0
The dawn of algometry: Paolo Mantegazza's research on pain. 算术的曙光:保罗·曼特加扎对疼痛的研究。
Q2 Medicine Pub Date : 2018-10-01
V Cani

By the 1860s, Paolo Mantegazza was a professor of general pathology at the University of Pavia, where he had graduated in medicine in 1854. There, he founded Italy's first laboratory of experimental pathology and did his first research on pain, the subject of various communications presented to the Istituto Lombardo in Milan. In 1880, Mantegazza published Physiology of Pain, one of the several "physiologies" (of pleasure, of love, of hatred, of woman) that he wrote during his career. In this book, a testament to his scientific versatility, experimental observations supplemented his insights into hygienism and anthropology. This research on pain also led to a dispute between Mantegazza and Cesare Lombroso, which was the start of the two scientists' estrangement.

到19世纪60年代,保罗·曼特加扎是帕维亚大学的普通病理学教授,他于1854年从医学专业毕业。在那里,他建立了意大利第一个实验病理学实验室,并进行了他的第一个关于疼痛的研究,这个主题被提交给米兰的伦巴多研究所(Istituto Lombardo)。1880年,曼特加扎出版了《疼痛生理学》,这是他职业生涯中写的几部“生理学”(关于快乐、爱、恨和女人)之一。在这本书中,实验观察补充了他对卫生学和人类学的见解,证明了他的科学通用性。这项关于疼痛的研究也导致了Mantegazza和Cesare Lombroso之间的争论,这是两位科学家疏远的开始。
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引用次数: 0
From paper to informatics: the Post Soft Care-App, an easy-to-use and fast tool to help therapists identify unmet needs in stroke patients. 从论文到信息学:Post Soft Care-App,一个易于使用和快速的工具,帮助治疗师识别中风患者未满足的需求。
Q2 Medicine Pub Date : 2018-10-01
D De Bartolo, G Morone, A Lupo, F Aloise, A Baricich, D Di Francesco, C Calderone, C Cisari, G Verdecchia, Giorgio Sandrini, C Pistarini, G Antonucci, Nicola Smania, Stefano Paolucci, M Iosa

Even after rehabilitation, post stroke patients remain disabled. The Post Stroke Checklist (PSC) was developed to highlight unmet needs of community-dwelling stroke patients. The present study set out to validate Post Soft Care-App, designed to administer the PSC using smartphones and tablets, in order to monitor unmet needs in chronic patients. Fifty-three patients and fifteen physiotherapists were enrolled. The therapists administered the PSC to patients using the app, and then completed a structured questionnaire on its usability and utility. The Post Soft Care-App highlighted the following unmet needs: increased spasticity (56.6%), reduced independence in activities of daily living (47.2%), reduced mobility (45.3%), absence of secondary prevention (45.3%). Therapists positively evaluated Post Soft Care-App as useful, practical, quick to complete (96.2%), and effective in helping improve communication with patients (75.5%). The Post Soft Care-App can be considered a valid assessment tool for helping therapists to monitor functional outcomes in chronic patients.

即使在康复后,中风患者仍然残疾。卒中后检查表(PSC)是为了突出社区居住卒中患者未满足的需求而开发的。本研究旨在验证Post Soft Care-App,该app旨在通过智能手机和平板电脑管理PSC,以监测慢性病患者未满足的需求。53名患者和15名物理治疗师被纳入研究。治疗师使用该应用程序对患者进行PSC,然后完成一份关于其可用性和实用性的结构化问卷。Post Soft Care-App强调了以下未满足的需求:痉挛增加(56.6%),日常生活活动独立性降低(47.2%),活动能力降低(45.3%),缺乏二级预防(45.3%)。治疗师积极评价Post Soft Care-App有用、实用、快速完成(96.2%),并有效地帮助改善与患者的沟通(75.5%)。后软护理应用程序可以被认为是一个有效的评估工具,帮助治疗师监测慢性患者的功能结果。
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引用次数: 0
Multiple sclerosis and non-dystrophic myotonias: do they share a common pathophysiology? 多发性硬化症和非营养不良性肌强直:它们有共同的病理生理学吗?
Q2 Medicine Pub Date : 2018-10-01
S Portaro, A Naro, M Russo, P Bramanti, P Lauria, Giangaetano D'Aleo, G La Rosa, A Bramanti, Rocco Salvatore Calabrò

Some patients with multiple sclerosis (MS) complain of symptoms, such as myokymia, myotonia, spasms, and stiffness, which have been demonstrated to be due to a concurrent non-dystrophic myotonia, i.e. myotonia congenita or paramyotonia congenita. Beyond the known casual association between MS and non-dystrophic myotonia, a channelopathy representing a primary trait of MS rather than an epiphenomenon of demyelization (i.e., an acquired channelopathy) may exist. Indeed, the finding of MS patients with no genetic evidence of non-dystrophic myotonia but showing a clinical picture resembling this condition would support this hypothesis. Thirty patients with MS and no concurrent diagnosis of myotonia congenita or paramyotonia congenita were submitted to the Fournier protocol. Some of these MS patients presented abnormal muscle excitability with scarce myotonic discharges, but only a few of them had clinical features compatible with myotonia congenita or paramyotonia congenita syndromes. Even though the low number of recruited patients did not allow a robust statistical analysis, our data seemed to indicate the presence of an ion channel dysfunction that is independent of the acquired channelopathies and likely represents a common pathophysiological mechanism underlying a unique channelopathy simultaneously involving the peripheral and the central nervous system in individuals with MS. Confirming the presence of such a primary channelopathy in MS patients is of non-negligible importance, since dysfunction of ion channels may represent a suitable therapeutic target in MS.

一些多发性硬化症(MS)患者主诉的症状,如肌无力、肌强直、痉挛和僵硬,已被证明是由于并发的非营养不良性肌强直,即先天性肌强直或先天性肌副强直。除了已知的MS和非营养不良性肌强直之间的偶然联系之外,可能存在一种通道病,它代表MS的主要特征,而不是脱髓鞘的副现象(即获得性通道病)。事实上,MS患者没有非营养不良性肌强直的遗传证据,但表现出类似于这种情况的临床表现,这一发现支持了这一假设。30例MS患者,没有同时诊断为先天性肌强直或先天性肌强直副缩,被提交到Fournier方案。部分MS患者表现为肌肉兴奋性异常,肌强张性放电稀少,但仅有少数患者具有先天性肌强直综合征或先天性肌副强直综合征的临床特征。尽管招募的患者数量少,无法进行可靠的统计分析,我们的数据似乎表明,存在独立于获得性通道病变的离子通道功能障碍,并且可能代表了MS个体中同时涉及外周和中枢神经系统的独特通道病变的共同病理生理机制。确认MS患者中存在这种原发性通道病变具有不可忽视的重要性,因为离子通道功能障碍可能代表MS中合适的治疗靶点。
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引用次数: 0
Recovery of circadian melatonin rhythm after a melatonin holiday in daytime haemodialysis patients on long-term exogenous melatonin. 长期服用外源性褪黑素的日间血液透析患者褪黑素假期后褪黑素昼夜节律的恢复。
Q2 Medicine Pub Date : 2018-10-01
S Sparla, B C Koch, R Bosma, Elsbeth Nagtegaal

The effects of exogenous melatonin on sleep diminish after its long-term use in haemodialysis patients. Our aim was to determine whether melatonin levels accumulate after chronic (at least three months) use of exogenous melatonin, 5 mg daily, and whether discontinuation of this treatment improves endogenous melatonin production and improves the circadian sleep-wake rhythm. In this case series, stable haemodialysis patients discontinued their chronic exogenous melatonin usage for seven days and melatonin concentrations in saliva were analysed. The primary endpoint was recovery of a normal circadian melatonin rhythm. Secondary endpoints were the effects on melatonin pharmacokinetics and sleep parameters. At day three after discontinuation the normal circadian melatonin rhythm recovered in the two patients who discontinued the treatment for the full week. They also had an effective maximum trough level of melatonin. Discontinuing melatonin seems to result in recovery of the circadian rhythm, based on achievement of effective melatonin thresholds. Further research is necessary to investigate whether sleep parameters improve after a drug holiday.most appropriate treatment.

外源性褪黑素对血液透析患者长期使用后睡眠的影响减弱。我们的目的是确定长期(至少三个月)使用外源性褪黑激素,每天5毫克后褪黑激素水平是否会累积,以及停止这种治疗是否会改善内源性褪黑激素的产生和改善昼夜睡眠-觉醒节律。在这个病例系列中,稳定的血液透析患者停止使用慢性外源性褪黑激素7天,并分析了唾液中褪黑激素的浓度。主要终点是恢复正常的褪黑激素昼夜节律。次要终点是对褪黑素药代动力学和睡眠参数的影响。在停药后的第三天,两名停药一整周的患者的正常褪黑激素昼夜节律恢复。他们也有有效的最大低谷褪黑素水平。停止褪黑素似乎导致昼夜节律的恢复,基于实现有效褪黑素阈值。需要进一步的研究来调查药物假期后睡眠参数是否有所改善。最合适的治疗方法。
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引用次数: 0
TIA patients with higher ABCD3-I scores are prone to a higher incidence of intracranial stenosis, unstable carotid plaques and multiple-vessel involvement. ABCD3-I评分较高的TIA患者颅内狭窄、不稳定颈动脉斑块和多血管受累的发生率较高。
Q2 Medicine Pub Date : 2018-10-01
Q Yu, W Miao, J Han

The ABCD3-I criteria have proved to be effective for use in regular clinical practice to assist in transient ischemic attack (TIA) risk stratification and treatment. In this prospective study we aimed to explore the relationships between risk stratification and arterial stenosis location, carotid plaque morphology and vessel involvement in 90 TIA patients, stratifying risk by ABCD3-I scores. Clinical variables such as total cholesterol, triglyceride, low-density lipoprotein cholesterol, glycosylated hemoglobin, homocysteine and high-sensitive C-reactive protein levels were recorded. The endpoint was subsequent stroke at seven-day follow-up. Ninety patients were divided into three risk groups on the basis of their ABCD3-I scores. The results revealed that patients with higher ABCD3-I scores showed a higher occurrence of intracranial stenosis (P < 0.05), less organized carotid plaques (P < 0.05) and multiple-vessel involvement (P < 0.05).

ABCD3-I标准已被证明在常规临床实践中有效地用于辅助短暂性脑缺血发作(TIA)风险分层和治疗。在这项前瞻性研究中,我们旨在探讨90例TIA患者的风险分层与动脉狭窄位置、颈动脉斑块形态和血管累及之间的关系,并通过ABCD3-I评分对风险进行分层。记录临床变量如总胆固醇、甘油三酯、低密度脂蛋白胆固醇、糖化血红蛋白、同型半胱氨酸和高敏c反应蛋白水平。在7天的随访中,终点是随后的中风。90例患者根据ABCD3-I评分分为3个危险组。结果显示,ABCD3-I评分越高的患者颅内狭窄发生率越高(P < 0.05),颈动脉斑块组织越少(P < 0.05),多支血管受累性越低(P < 0.05)。
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引用次数: 0
Cross-cultural adaptation and validation in the Italian population of the wolf motor function test in patients with stroke. 意大利人群脑卒中患者wolf运动功能测试的跨文化适应和验证。
Q2 Medicine Pub Date : 2018-10-01
A Berardi, L Dhrami, M Tofani, Donatella Valente, J Sansoni, G Galeoto

Motor impairments of the upper extremities affect approximately 60% of stroke patients. Rehabilitation is extremely important and can make it possible to identify which manual function is causing difficulty for the patient and hindering daily activities. The Wolf Motor Function Test (WMFT) was recently highly recommended as one of several outcome measures that assess limitations of activities with a high level of psychometrics and clinical utility. The objective of this study was to translate and culturally adapt the WMFT for the Italian population (WMFT-IT) and examine its reliability and validity in Italian post-stroke adults with chronic hemiplegia or hemiparesis. The original scale was translated into Italian and culturally adapted in accordance with international guidelines. Its internal consistency and stability were examined using the Cronbach's alpha (α) coefficient and the intra-class correlation coefficient (ICC), respectively. Its concurrent validity was evaluated using the Pearson's correlation coefficient to compare the instrument with the Italian version of the Jebsen-Taylor Hand Function Test and the Disabilities of the Arm, Shoulder and Hand outcome measure. All WMFT-IT items were either identical or similar in meaning to the items in the original version. The WMFT-IT was administered to 24 subjects. Cronbach's α was 0.91 and 0.98 for the time and performance subscales respectively, and the ICC for test-retest reliability was 0.99. Pearson's correlation coefficients of the time subscale and the performance subscale both showed significant positive correlations (p <0.01). The WMFT-IT was found to be reliable and a valid outcome measure for assessing function and quality of movement of the upper extremities in post-stroke adults in the Italian population.

大约60%的中风患者有上肢运动障碍。康复是极其重要的,它可以使识别哪些手动功能对患者造成困难和妨碍日常活动成为可能。Wolf运动功能测试(WMFT)最近被强烈推荐为评估活动局限性的几种结果测量方法之一,具有高水平的心理测量学和临床实用性。本研究的目的是翻译和适应意大利人群的WMFT (WMFT- it),并检验其在意大利卒中后慢性偏瘫或偏瘫成人中的可靠性和有效性。最初的规模被翻译成意大利语,并根据国际准则进行文化调整。采用Cronbach’s alpha (α)系数和intra-class correlation coefficient (ICC)分别检验其内部一致性和稳定性。使用Pearson相关系数评估其并发效度,将仪器与意大利版的Jebsen-Taylor手功能测试和手臂、肩膀和手的残疾结果测量进行比较。所有WMFT-IT项目在意义上都与原始版本中的项目相同或相似。对24名受试者进行WMFT-IT测试。时间分量表和绩效分量表的Cronbach’s α分别为0.91和0.98,重测信度的ICC为0.99。时间分量表与绩效分量表的Pearson相关系数均呈显著正相关(p
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引用次数: 0
Automated mechanical peripheral stimulation and postural control in subjects with Parkinson's disease and freezing of gait: a randomized controlled trial. 帕金森病和步态冻结受试者的自动机械外周刺激和姿势控制:一项随机对照试验。
Q2 Medicine Pub Date : 2018-10-01 DOI: 10.11138/FNEUR/2018.33.4.206
J. S. Prusch, A. Kleiner, A. P. Salazar, C. Pinto, R. Marchese, M. Galli, A. Pagnussat
Individuals with Parkinson's disease (PD) and freezing of gait (FOG) have impaired postural control. Recent studies using foot sensory stimulation delivered by means of automated mechanical peripheral stimulation (AMPS) have demonstrated improvements of gait in individuals with PD. This study aimed to investigate the effects of AMPS on postural control in individuals with PD and FOG. Thirty-three subjects participated in this randomized controlled trial. Participants were allocated to two groups: AMPS and AMPS SHAM. Subjects underwent eight sessions of real (AMPS) or placebo AMPS (AMPS SHAM) once every three/four days. Postural control was assessed by means of posturography before the first and after the eighth session of treatment. We did not find positive effects of AMPS on center of pressure parameters. Thus, it seems that AMPS has no positive effect in terms of improving static postural control in individuals with PD and FOG.
患有帕金森病(PD)和步态冻结(FOG)的个体姿势控制受损。最近的研究表明,通过自动机械外周刺激(AMPS)提供足部感觉刺激,可以改善PD患者的步态。本研究旨在探讨AMPS对PD和FOG患者姿势控制的影响。33名受试者参加了这项随机对照试验。参与者被分为两组:AMPS组和AMPS SHAM组。受试者每三/四天接受八次真实(AMPS)或安慰剂AMPS (AMPS SHAM)治疗。姿势控制在第一次治疗前和第八次治疗后通过姿势摄影进行评估。我们没有发现AMPS对压力中心参数的积极影响。因此,AMPS在改善PD和FOG患者的静态姿势控制方面似乎没有积极作用。
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引用次数: 6
Clinical and neuroimaging spectrum of hyperglycemia-associated chorea-ballism: systematic review and exploratory analysis of case reports. 高血糖相关性舞蹈症的临床和神经影像学:系统回顾和病例报告的探索性分析。
Q2 Medicine Pub Date : 2018-10-01
Sergio Alejandro Gómez-Ochoa, Blanca Beatriz Espín-Chico, Gabriel David Pinilla-Monsalve, Bonnie M Kaas, Luis Ernesto Téllez-Mosquera

Hyperglycemia-associated chorea-ballism (HCB) is an infrequent neurological syndrome occurring predominantly in elderly females and in the setting of non-ketotic hyperglycemia (NKH). A systematic review was conducted in accordance with the PRISMA statement. Studies published between 1980 and 2018 that reported demographic, clinical, laboratory and imaging features from patients with HCB were screened. 136 studies describing 286 patients were included in the analysis. The patients included had a median age of 72 years; those with ketotic hyperglycemia (KH) were older (p<0.001). Women and NKH patients were the most frequently affected (63% and 92%, respectively). The median glucose level at admission was 420 mg/dL (IQR 328-535), and was significantly higher in KH (p=0.009). Moreover, the absence of a clear lesion on imaging studies and the finding of bilateral imaging evidence of lesions were each more frequent in the KH group (p=0.036 and p=0.008, respectively). 48 cases (19.4%) presented with bilateral CT/MRI lesions, having higher values of plasma osmolarity compared with the patients with unilateral lesions (p=0.011). Every patient received hypoglycemic treatment, but only 174 (60.84%) were prescribed neuroleptics. 213 patients (84.86%) showed a total recovery, after a median of 14 days (IQR 3-31). Bilateral chorea-ballism was supported by bilateral imaging evidence of involvement in only 60% of the cases (positive predictive value). Patients not prescribed neuroleptics, with negative lentiform nucleus involvement, and age within the third tertile (≥ 78 years) had an odds ratio of 6.6 (CI 95% 1.18-141.10) for a complete clinical recovery. Significant differences were identified between types of hyperglycemia and regarding the clinical and imaging laterality features. Furthermore, the predictor variables evaluated showed potential utility for assessing the prognosis of HCB patients.

高血糖相关性舞蹈症(HCB)是一种罕见的神经系统综合征,主要发生在老年女性和非酮症高血糖(NKH)。根据PRISMA声明进行了系统审查。对1980年至2018年间发表的报告HCB患者人口统计学、临床、实验室和影像学特征的研究进行了筛选。分析纳入了136项研究,涉及286例患者。纳入的患者中位年龄为72岁;酮症高血糖症(KH)患者年龄较大(p
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引用次数: 0
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Functional neurology
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