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[Ethnic features of multipathology in elderly and senile patients of the Republic of Sakha suffering from chronic brain ischemia]. [萨哈共和国老年和老年慢性脑缺血患者的多病理民族特征]。
Q3 Medicine Pub Date : 2023-01-01 DOI: 10.17116/jnevro202312307150
P I Kudrina, A N Bogolepova, A L Ariev
OBJECTIVETo study ethnic characteristics of multipathology in elderly and senile patients with chronic cerebral ischemia living in the Republic of Sakha (Yakutia).MATERIAL AND METHODSThe study included 522 inpatients, aged 60 to 89 years, who were divided into subgroups depending on the stage of chronic cerebral ischemia, ethnicity (Evens, Yakuts and Russians) and age (elderly and senile).RESULTSIn addition to vascular cerebral pathology, comorbidities were identified in patients of older age groups. At the same time, polymorbidity was less pronounced in the Evens, the indigenous inhabitants of the northern regions of Yakutia, than in the Yakuts and representatives of the non-indigenous population - Russians.CONCLUSIONThe relatively rare occurrence of comorbid pathologies in Evens is presumably associated with greater adaptation to the extreme climatic conditions of the North.
目的:探讨萨哈(雅库特)地区老年慢性脑缺血患者的多病理民族特征。材料与方法:研究纳入522例住院患者,年龄60 ~ 89岁,根据慢性脑缺血分期、民族(伊文人、雅库特人和俄罗斯人)和年龄(老年和老年)分为亚组。结果:除了血管性脑病理外,在老年患者中还发现了合并症。与此同时,在雅库特北部地区的土著居民埃文人身上,多病发病率比在雅库特人和非土著人口的代表- -俄罗斯人身上更不明显。结论:Evens相对罕见的共病可能与对北方极端气候条件的更大适应有关。
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引用次数: 0
[Clinical characteristics and short-term outcomes of autoimmune encephalitis in adults]. 成人自身免疫性脑炎的临床特点和短期预后
Q3 Medicine Pub Date : 2023-01-01 DOI: 10.17116/jnevro2023123072103
E O Chekanova, A A Shabalina, M N Zakharova

Objective: To characterize clinical, paraclinical features and short-term outcomes in different types of autoimmune encephalitis (AE) in a one-center cohort of Russian patients, as well as to evaluate the frequency and significance of the joint expression of antineuronal and anti-glial antibodies (Abs) in AE.

Material and methods: Forty-one patients were diagnosed with AE at the Research Center of Neurology from November 2020 to December 2022. Demographic, clinical characteristics, results of laboratory tests, MRI of brain, treatment and outcomes of disease were analyzed. The analysis of Abs to glial antigens (myelin-oligodendrocyte glycoprotein - MOG, glial fibrillar acidic protein - GFAP, aquaporin 4 - AQP-4) was performed by indirect immunofluorescence assay (Euroimmun, Germany).

Results: In 24 (58.5%) patients was established definite AE, confirmed by specific Abs detection; in 2 (4.9%) - definite limbic encephalitis, in 15 (36.6%) - seronegative probable AE (including 3 cases of Hashimoto's encephalitis). GFAP-Abs in cerebrospinal fluid (CSF) were detected only in two patients - with clinical and MRI-picture of autoimmune GFAP-astrocytopathy (A-GFAP-A). GFAP- and MOG-Abs in the blood were detected in 25.7% and 6%, respectively, AQP-4-Abs were not detected. There were no correlations between co-expression with glial Abs and clinical characteristics. Systemic and antithyroid Abs were present in 15% and 31%, respectively. Paraneoplastic AE accounted for 22%. For the first time in the Russian population, 2 cases of A-GFAP-A, 6 cases of AE associated with COVID-19 were described. The most common first syndrome were epileptic seizure (34%), psychiatric (29%) and cognitive (14%) disorders. Relapses of AE was observed in 22%. Inflammatory changes in CSF were detected in 41%, focal changes on MRI in 68%. First-line immune therapy was performed in all patients, 85% of cases received pulse therapy with methylprednisolone. Second-line immune therapy (rituximab or cyclophosphamide intravenously) was performed in 19.5%, 78% of patients achieved significant improvement during treatment (scores ≤2 on the modified Rankin scale).

Conclusions: The results allow us to consider COVID-19 as a trigger of AE. The absence of detection of GFAP-Abs in CSF in patients with other types of AE contributes to the confirmation of the specificity of GFAP-seropositivity of CSF for the diagnosis of A-GFAP-A. The expression of GFAP- and MOG-Abs in AE can serve as confirmation of the immuno-mediated etiology of the disease, which is especially important for the AE diagnosis in the absence of antineuronal Abs.

目的:探讨俄罗斯单中心队列不同类型自身免疫性脑炎(AE)患者的临床、临床旁特征及近期预后,评价AE中抗神经元抗体和抗胶质抗体(Abs)联合表达的频率及意义。材料与方法:于2020年11月至2022年12月在神经病学研究中心诊断为AE的患者41例。分析了人口统计学、临床特征、实验室检查结果、脑MRI、治疗和疾病结局。采用间接免疫荧光法(euroimmune, Germany)分析抗体对胶质抗原(髓鞘-少突胶质细胞糖蛋白- MOG、胶质纤维酸性蛋白- GFAP、水通道蛋白4 - AQP-4)的反应。结果:24例(58.5%)患者确诊AE,经特异性抗体检测证实;2例(4.9%)确诊为边缘脑炎,15例(36.6%)血清阴性可能为AE(包括3例桥本脑炎)。脑脊液(CSF)中的gmap - abs仅在两例患者中检测到-具有自身免疫性gmap -星形细胞病(a - gmap -a)的临床和mri图像。血液中分别检测到25.7%和6%的GFAP-和MOG-Abs,未检测到AQP-4-Abs。与胶质抗体共表达与临床特征无相关性。系统性和抗甲状腺抗体分别占15%和31%。副肿瘤AE占22%。在俄罗斯人群中首次报道了2例a - gap - a和6例与COVID-19相关的AE。最常见的第一症状是癫痫发作(34%)、精神疾病(29%)和认知障碍(14%)。AE复发率为22%。脑脊液炎症改变占41%,MRI灶性改变占68%。所有患者均接受一线免疫治疗,85%的病例接受甲基强的松龙脉冲治疗。19.5%的患者接受了二线免疫治疗(利妥昔单抗或静脉注射环磷酰胺),78%的患者在治疗期间获得显著改善(改良Rankin评分≤2分)。结论:结果允许我们考虑COVID-19是AE的触发因素。其他类型AE患者脑脊液中未检测到GFAP-Abs有助于证实脑脊液gfap -血清阳性诊断A-GFAP-A的特异性。GFAP-和mog -抗体在AE中的表达可以作为疾病免疫介导病因的确认,这对于缺乏抗神经元抗体的AE诊断尤其重要。
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引用次数: 0
[Microbiota markers level in the blood and cerebrospinal fluid of patients with different types of multiple sclerosis and radiologically isolated syndrome]. [不同类型多发性硬化症和放射孤立综合征患者血液和脑脊液中微生物群标记物水平]。
Q3 Medicine Pub Date : 2023-01-01 DOI: 10.17116/jnevro202312307296
M A Omarova, V S Rogovskii, T Sh Sadekov, G I Sadekova, O G Zhilenkova, A N Boyko
OBJECTIVETo assess the level of microbiota markers in the blood and cerebrospinal fluid (CSF) of patients with different types of multiple sclerosis (MS), people with radiologically isolated syndrome (RIS) and control subjects.MATERIAL AND METHODSWe used gas chromatography-mass spectrometry (GC-MS) to evaluate the levels of microbiota markers in 69 patients with different types of MS (27 patients in the acute stage, 35 patients with MS in remission, 7 patients with primary-progressive MS), 10 people with RIS, and 47 control subjects (different diseases of the nervous system of a non-autoimmune or inflammatory nature).RESULTSWe showed a statistically significant increase in the content of various microbiota markers in the CSF of patients with MS compared with the control group. We found no change in the content of these markers in blood of patients with MS. This suggests a change of markers of microbial load at the level of the central nervous system, but not at the level of the whole organism. The greatest number of statistically significant differences with the control group was found in the content of markers in CSF of patients with MS in remission. In the acute stage, on the contrary, we found no statistically significant differences compared to the control group. In particular, in CSF of patients with MS in remission, a statistically significant increase in the content of bacterial plasmalogen (4.5 times), and increase in the level of microbial markers specific to Peptostreptococcus anaerobius, Pseudomonas aeruginosa, Eubacterium, Bifidobacterium, Butirivibrio, Moraxella, Acinetobacter, Propionibacterium acnes, as well as an increase of markers of the Epstein-Barr virus were found. In addition, there was an increase of campesterol, the likely source of which is campesterol-producing microfungi. In the CSF of subjects with RIS there were a statistically significant increase in the level of markers of the Epstein-Barr virus, Propionibacterium acnes, as well as Pseudomonas, Moraxella, and Acinetobacter.CONCLUSIONAn association of MS with polymicrobial infection is possible. It is also likely that there is a certain pattern of increase of microbiota markers in the CSF of patients with MS, but not in blood.
目的:评价不同类型多发性硬化症(MS)患者、放射孤立综合征(RIS)患者和对照组血液和脑脊液(CSF)中微生物群标志物的水平。材料和方法:我们采用气相色谱-质谱联用技术(GC-MS)对69例不同类型MS患者(27例急性期MS患者,35例缓解期MS患者,7例原发性进行性MS患者)、10例RIS患者和47例对照受试者(非自身免疫性或炎症性不同神经系统疾病)的微生物群标志物水平进行了评估。结果:我们发现,与对照组相比,MS患者脑脊液中各种微生物群标记物的含量有统计学意义的增加。我们发现ms患者血液中这些标记物的含量没有变化,这表明中枢神经系统水平的微生物负荷标记物发生了变化,但在整个生物体水平上没有变化。MS缓解期患者脑脊液中标志物含量与对照组差异最大,有统计学意义。在急性期,我们发现与对照组相比没有统计学上的显著差异。特别是缓解期MS患者脑脊液中细菌plasmalogen含量升高(4.5倍),厌氧菌胃链球菌、铜绿假单胞菌、真杆菌、双歧杆菌、Butirivibrio、莫拉氏菌、不动杆菌、痤疮丙酸杆菌特异性微生物标志物水平升高,Epstein-Barr病毒标志物升高,均有统计学意义。此外,油菜甾醇含量也有所增加,其来源可能是产油菜甾醇的微真菌。RIS患者脑脊液中Epstein-Barr病毒、痤疮丙酸杆菌、假单胞菌、莫拉氏菌和不动杆菌标记物水平升高具有统计学意义。结论:多发性硬化症可能与多微生物感染有关。也可能是MS患者脑脊液中微生物群标记物有一定的增加模式,而血液中没有。
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引用次数: 0
[B vitamins and brain dysfunction]. B族维生素和脑功能障碍。
Q3 Medicine Pub Date : 2023-01-01 DOI: 10.17116/jnevro202312307197
D A Iskra, A G Trufanov

An unbalanced diet and some other factors are the reason for the extreme prevalence of hypovitaminosis among the population of both developing and developed countries. The metabolic relationships of B vitamins determine the more frequent occurrence of poly-, rather than monovitamin deficiency. Since B vitamins play an important role in the processes of energy production and in the functioning of neurotransmitter systems, the first symptoms of such polyhypovitaminosis are signs of brain dysfunction: asthenia, depression, anxiety, cognitive disorders. Correct diagnosis of polyhypovitaminosis based on the identification of risk groups of patients and the determination of their subclinical or early manifesting signs of brain dysfunction is the most important task of a practicing physician. Detection of insufficient intake and vitamin content, as well as verification of the onset of symptoms of brain dysfunction and the appointment of adequate therapy can significantly increase the effectiveness of treatment, as well as prevent asthenic, psycho-emotional and cognitive disorders in patients with polyhypovitaminosis.

不平衡的饮食和其他一些因素是发展中国家和发达国家人口中维生素缺乏症极端流行的原因。B族维生素的代谢关系决定了多维生素缺乏症比单维生素缺乏症更容易发生。由于B族维生素在能量产生过程和神经递质系统的功能中起着重要作用,因此这种多维生素缺乏症的最初症状是脑功能障碍的迹象:虚弱、抑郁、焦虑、认知障碍。正确诊断多维生素缺乏症的基础上识别患者的危险人群和确定其亚临床或早期表现的脑功能障碍的迹象是执业医师最重要的任务。检测摄入和维生素含量不足,以及验证脑功能障碍症状的发病和预约适当的治疗,可以显著提高治疗的有效性,并预防多维生素缺乏症患者出现虚弱、心理情绪和认知障碍。
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引用次数: 0
[Tractography in functional neuronavigation]. 功能神经导航中的神经束造影。
Q3 Medicine Pub Date : 2023-01-01 DOI: 10.17116/jnevro202312307112
A Yu Dmitriev, V G Dashyan

The review addresses the combined use of tractography and neuronavigation. Fundamentals of diffusion tensor imaging are given, technical aspects of fiber tracking in general and in depicting separate subcortical tracts are described. Main advantages of the method and possible causes of errors are highlighted. Precision assessment of this technology is given by comparing with results of subcortical neurostimulation. Surgical tactics is described depending on distance between the tumor and subcortical pathways.

本文综述了神经束造影和神经导航的联合应用。给出了扩散张量成像的基本原理,描述了一般纤维跟踪和描绘单独的皮质下束的技术方面。强调了该方法的主要优点和可能产生误差的原因。通过与皮质下神经刺激结果的比较,对该技术的精度进行了评价。手术策略的描述取决于肿瘤和皮层下通路之间的距离。
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引用次数: 0
[Relationship of patients with multiple sclerosis to vaccination against COVID-19]. 多发性硬化症患者与COVID-19疫苗接种的关系
Q3 Medicine Pub Date : 2023-01-01 DOI: 10.17116/jnevro202312307229
E L Turova

Objective: To study the attitude of patients with multiple sclerosis (MS) to vaccination as a method of preventing infectious diseases, in particular, COVID-19.

Material and methods: The data of a survey of 408 patients with MS in the Sverdlovsk region in relation to vaccination against COVID-19, conducted using the original questionnaire, were analyzed.

Results: According to the survey data, 266 (65.2%) patients with MS are positive about vaccination. 222 (54.4%) patients with MS refused vaccination. The most common reasons for refusal were - fear that the vaccine could worsen the state of health - 44.1%, coronavirus infection in the last 6 months - 14.85%, «I was always told that I should not be vaccinated» - 14.4%, a combination of the above answers - 16.65%. The accumulated world experience and our observations demonstrate the important role of vaccination of patients with MS from COVID-19.

Conclusions: It is necessary to rise the awareness of vaccination among patients with MS, since until recently this has been given insufficient attention.

目的:了解多发性硬化症(MS)患者对疫苗接种作为预防传染病,特别是COVID-19的态度。材料和方法:对斯维尔德洛夫斯克地区408例MS患者接种COVID-19疫苗相关调查数据进行分析。结果:调查数据显示,266例(65.2%)MS患者疫苗接种阳性。222例(54.4%)MS患者拒绝接种疫苗。最常见的拒绝原因是-担心疫苗会使健康状况恶化- 44.1%,过去6个月感染冠状病毒- 14.85%,“我总是被告知我不应该接种疫苗”- 14.4%,上述答案的组合- 16.65%。积累的国际经验和我们的观察表明,对COVID-19多发性硬化症患者接种疫苗具有重要作用。结论:有必要提高MS患者的疫苗接种意识,因为直到最近这一点还没有得到足够的重视。
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引用次数: 0
[Improving the effectiveness of pharmacotherapy in comorbid patients with chronic cerebral ischemia on an outpatient basis]. [在门诊基础上提高慢性脑缺血合并症患者药物治疗的有效性]。
Q3 Medicine Pub Date : 2023-01-01 DOI: 10.17116/jnevro202312303151
T L Vizilo, E G Arefieva

Objective: To study the efficacy and safety of sequential therapy with Mexidol (500 mg 1 time/day for 14 days intravenously) and Mexidol FORTE 250 (Mexidol FORTE 250 for 250 mg 3 times/day, 60 days) in patients with chronic cerebral ischemia (CCI) on an outpatient basis.

Material and methods: The open comparative study included 56 patients aged 46-74 years, age - 60.5+7.9 years. In all patients, the diagnosis of CCI was confirmed by clinical and neuroimaging methods. Patients of group 1 (n=28) received basic therapy and Mexidol, group 2 (n=28) received only basic therapy.

Results: Against the background of therapy in patients of group 1, there was a statistically significant improvement in the state of cognitive functions, a decrease in the severity of symptoms of depression and anxiety, manifestations of asthenia. The treatment was characterized by good tolerability, absence of adverse events and cases of drug interactions.

Conclusion: Sequential therapy with Mexidol and Mexidol FORTE 250 drugs provides relief of the main clinical manifestations of CCI, is characterized by good tolerability and safety.

目的:研究门诊慢性脑缺血(CCI)患者顺序治疗墨西哥idol (500 mg 1次/天,静脉注射14天)和墨西哥idol FORTE 250(墨西哥idol FORTE 250, 250 mg 3次/天,60天)的疗效和安全性。材料与方法:开放性比较研究纳入56例患者,年龄46 ~ 74岁,年龄- 60.5+7.9岁。所有患者均通过临床和神经影像学方法确诊CCI。组1 (n=28)患者同时接受基础治疗和Mexidol治疗,组2 (n=28)患者仅接受基础治疗。结果:在治疗背景下,1组患者认知功能状态改善,抑郁、焦虑症状严重程度减轻,乏力表现明显,均有统计学意义。治疗的特点是良好的耐受性,没有不良事件和药物相互作用的情况下。结论:美西多和美西多FORTE 250药物序贯治疗可缓解CCI的主要临床表现,具有良好的耐受性和安全性。
{"title":"[Improving the effectiveness of pharmacotherapy in comorbid patients with chronic cerebral ischemia on an outpatient basis].","authors":"T L Vizilo,&nbsp;E G Arefieva","doi":"10.17116/jnevro202312303151","DOIUrl":"https://doi.org/10.17116/jnevro202312303151","url":null,"abstract":"<p><strong>Objective: </strong>To study the efficacy and safety of sequential therapy with Mexidol (500 mg 1 time/day for 14 days intravenously) and Mexidol FORTE 250 (Mexidol FORTE 250 for 250 mg 3 times/day, 60 days) in patients with chronic cerebral ischemia (CCI) on an outpatient basis.</p><p><strong>Material and methods: </strong>The open comparative study included 56 patients aged 46-74 years, age - 60.5+7.9 years. In all patients, the diagnosis of CCI was confirmed by clinical and neuroimaging methods. Patients of group 1 (<i>n</i>=28) received basic therapy and Mexidol, group 2 (<i>n</i>=28) received only basic therapy.</p><p><strong>Results: </strong>Against the background of therapy in patients of group 1, there was a statistically significant improvement in the state of cognitive functions, a decrease in the severity of symptoms of depression and anxiety, manifestations of asthenia. The treatment was characterized by good tolerability, absence of adverse events and cases of drug interactions.</p><p><strong>Conclusion: </strong>Sequential therapy with Mexidol and Mexidol FORTE 250 drugs provides relief of the main clinical manifestations of CCI, is characterized by good tolerability and safety.</p>","PeriodicalId":24030,"journal":{"name":"Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9215105","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
[Modern principles of therapy for patients with spinal muscular atrophy]. 【脊髓性肌萎缩症的现代治疗原则】。
Q3 Medicine Pub Date : 2023-01-01 DOI: 10.17116/jnevro202312303134
N S Bofanova, A R Eliseeva, V S Onchina

Spinal muscular atrophy (SMA) is a common cause of childhood mortality among hereditary diseases of the central nervous system, which are caused by the processes of degeneration and death of motor neurons of the anterior horns of the spinal cord. An urgent issue of modern neurology is pathogenetic therapy for this group of patients, the purpose of which is to increase the level of motoneuron survival protein. We performed a search on current methods of treating SMA in Web of Science, Scopus, PubMed, Embase by the keywords: spinal muscular atrophy, neuromuscular diseases, pathogenetic therapy. Significant progress has been made in the treatment of SMA over the past 7 years. A major advance is the introduction of disease-modifying therapies using SMN2 splicing modulation or gene replacement therapy. At the moment, there are 3 FDA-approved drugs for pathogenetic therapy: Nusinersen, Risdiplam, Zolgensma. The article compares the drugs, evaluates their safety and effectiveness according to the available literature. Modern drugs for the pathogenetic therapy of SMA are highly effective and reduce the mortality rate. The results of clinical trials predict the emergence of new modern drugs. This suggests a favorable prognosis for the treatment of patients with SMA.

脊髓性肌萎缩症(SMA)是由脊髓前角运动神经元的退化和死亡引起的中枢神经系统遗传性疾病中儿童死亡的常见原因。现代神经病学的一个紧迫问题是对这类患者进行病理治疗,其目的是提高运动神经元存活蛋白的水平。我们在Web of Science, Scopus, PubMed, Embase中检索了目前治疗SMA的方法,关键词:脊髓性肌萎缩症,神经肌肉疾病,病理治疗。在过去7年中,SMA的治疗取得了重大进展。一个主要的进展是引入了使用SMN2剪接调节或基因替代疗法的疾病修饰疗法。目前,fda批准了3种用于病理治疗的药物:Nusinersen, Risdiplam, Zolgensma。本文根据现有文献对两种药物进行比较,评价其安全性和有效性。现代药物对SMA的病理治疗效果显著,降低了死亡率。临床试验的结果预示着新的现代药物的出现。这表明治疗SMA患者预后良好。
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引用次数: 0
[Effectiveness of rehabilitation with virtual reality and biofeedback in recovery of hand function after stroke]. [虚拟现实与生物反馈康复在脑卒中后手功能恢复中的效果]。
Q3 Medicine Pub Date : 2023-01-01 DOI: 10.17116/jnevro202312303268
E V Kostenko, L V Petrova, M Yu Martynov, I V Pogonchenkova

Objective: To evaluate the effectiveness and safety of the rehabilitation glove (RG) with virtual reality (VR) and biofeedback (BFB) on recovery of the hand function in patients during the late recovery period after first hemispheric ischemic stroke (IS).

Material and methods: The study was randomized and controlled. One hundred and six patients (age 58.8±4.3 years, time after stroke onset - 8.7±2.1 months) were included in the final analysis. The intervention group (n=56) received rehabilitation with RG and VR. The control group (n=50) received individualized physical therapy. The primary end points were a change in the Fugl-Meyer scale score (FMA-UE), in the Action Research Arm Test (ARAT), and in the nine holes peg test (NHPT). Secondary end points included changes in MRCS, MAS, MoCA, HADS, modified Barthel index (MBI) and quality of life (EQ-5D-5L).

Results: Improvement of the motor function in the intervention group on FMA-UE scale (an increase of ≥7 points in sections A-D) was observed in 46.4% of patients, on ARAT (an increase of ≥5 points) in 53.6% of patients. There was a significant decrease in time from 36.8±6.3 sec. to 22.0±3.9 sec. on NHPT. A negative correlation was observed between the average ARAT score and anxiety (r=-0.7; p<0.05) and depression (r=-0.67; p<0.05). There was also a significant increase in EQ-5D-5L (VAS) by the end of rehabilitation in both groups with better scores in the intervention group (p=0.03).

Conclusion: Rehabilitation based on VR, RG, and BFB is effective in the rehabilitation of dexterous hand function in patients with first hemispheric IS.

目的:评价虚拟现实(VR)与生物反馈(BFB)结合的康复手套(RG)在第一半球缺血性脑卒中(IS)术后恢复期手部功能恢复中的有效性和安全性。材料与方法:采用随机对照法。106例患者(年龄58.8±4.3岁,卒中发生时间- 8.7±2.1个月)纳入最终分析。干预组56例采用RG和VR进行康复治疗。对照组50例接受个体化物理治疗。主要终点是Fugl-Meyer量表评分(FMA-UE)、行动研究臂测试(ARAT)和九孔钉测试(NHPT)的变化。次要终点包括MRCS、MAS、MoCA、HADS、改良Barthel指数(MBI)和生活质量(EQ-5D-5L)的变化。结果:干预组患者FMA-UE评分(A-D段评分提高≥7分)改善46.4%,ARAT评分提高≥5分(53.6%)。NHPT治疗时间由36.8±6.3秒缩短至22.0±3.9秒。平均ARAT评分与焦虑呈负相关(r=-0.7;公关= -0.67;页= 0.03)。结论:基于VR、RG和BFB的康复是第一半球is患者灵巧手功能康复的有效方法。
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引用次数: 1
[A clinical case of multiple sclerosis with an episode of schizophrenia-like syndrome]. [多发性硬化症伴精神分裂症样综合征发作的临床病例]。
Q3 Medicine Pub Date : 2023-01-01 DOI: 10.17116/jnevro2023123041120
U Sh Kuzmina, A V Tukhvatullin, K Z Bakhtiyarova, M A Kutlubaev, O V Lyutov, T R Gizatullin

The article presents a clinical observation of a schizophrenia-like disorder in a patient with multiple sclerosis (MS). The patient had highly active MS with a relapsing course, the diagnosis was made based on the McDonald 2017 criteria. During the course of a demyelinating disease of the nervous system, the patient developed an episode of psychotic disorders with symptoms of mutism, hallucinations, delusions and impaired thinking, which was quickly stopped in stationary conditions. This case is of particular interest to neurologists and psychiatrists, since psychotic disorders occur in MS patients and cause difficulties in diagnosis and treatment.

本文介绍了一个临床观察精神分裂症样障碍患者多发性硬化症(MS)。患者为高活性MS伴复发病程,根据McDonald 2017标准进行诊断。在神经系统脱髓鞘疾病的过程中,患者出现了一段精神障碍,症状包括失语、幻觉、妄想和思维受损,在固定条件下很快停止。这个病例是神经学家和精神病学家特别感兴趣的,因为精神障碍发生在多发性硬化症患者身上,给诊断和治疗带来了困难。
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引用次数: 0
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Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
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