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1.
Cerebellum ; 2024 Jun 13.
Artigo em Inglês | MEDLINE | ID: mdl-38869768

RESUMO

Given the high morbidity related to the progression of gait deficits in spinocerebellar ataxias (SCA), there is a growing interest in identifying biomarkers that can guide early diagnosis and rehabilitation. Spatiotemporal parameter (STP) gait analysis using inertial measurement units (IMUs) has been increasingly studied in this context. This study evaluated STP profiles in SCA types 3 and 10, compared them to controls, and correlated them with clinical scales. IMU portable sensors were used to measure STPs under four gait conditions: self-selected pace (SSP), fast pace (FP), fast pace checking-boxes (FPCB), and fast pace with serial seven subtractions (FPS7). Compared to healthy subjects, both SCA groups had higher values for step time, variability, and swing time, with lower values for gait speed, cadence, and step length. We also found a reduction in speed gain capacity in both SCA groups compared to controls and an increase in speed dual-task cost in the SCA10 group. However, there were no significant differences between the SCA groups. Swing time, mean speed, and step length were correlated with disease severity, risk of falling and functionality in both clinical groups. In the SCA3 group, fear of falling was correlated with cadence. In the SCA10 group, results of the Montreal cognitive assessment test were correlated with step time, mean speed, and step length. These results show that individuals with SCA3 and SCA10 present a highly variable, short-stepped, slow gait pattern compared to healthy subjects, and their gait quality worsened with a fast pace and dual-task involvement.

2.
BMC Geriatr ; 20(1): 45, 2020 02 06.
Artigo em Inglês | MEDLINE | ID: mdl-32028945

RESUMO

BACKGROUND: Motor and cognitive deficits and consequently mobility problems are common in geriatric patients. The currently available methods for diagnosis and for the evaluation of treatment in this vulnerable cohort are limited. The aims of the ComOn (COgnitive and Motor interactions in the Older populatioN) study are (i) to define quantitative markers with clinical relevance for motor and cognitive deficits, (ii) to investigate the interaction between both motor and cognitive deficits and (iii) to assess health status as well as treatment outcome of 1000 geriatric inpatients in hospitals of Kiel (Germany), Brescia (Italy), Porto (Portugal), Curitiba (Brazil) and Bochum (Germany). METHODS: This is a prospective, explorative observational multi-center study. In addition to the comprehensive geriatric assessment, quantitative measures of reduced mobility and motor and cognitive deficits are performed before and after a two week's inpatient stay. Components of the assessment are mobile technology-based assessments of gait, balance and transfer performance, neuropsychological tests, frailty, sarcopenia, autonomic dysfunction and sensation, and questionnaires to assess behavioral deficits, activities of daily living, quality of life, fear of falling and dysphagia. Structural MRI and an unsupervised 24/7 home assessment of mobility are performed in a subgroup of participants. The study will also investigate the minimal clinically relevant change of the investigated parameters. DISCUSSION: This study will help form a better understanding of symptoms and their complex interactions and treatment effects in a large geriatric cohort.


Assuntos
Acidentes por Quedas , Atividades Cotidianas , Idoso , Brasil , Cognição , Medo , Avaliação Geriátrica , Alemanha , Humanos , Itália , Portugal , Estudos Prospectivos , Qualidade de Vida
3.
Arq Neuropsiquiatr ; 75(8): 570-579, 2017 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-28813088

RESUMO

Corticobasal degeneration (CBD) was originally described as a distinct clinicopathological entity in 1967. Since then, different phenotypic presentations have emerged as possible manifestations of CBD histopathological findings. In addition, pathophysiological findings and the molecular basis have been delineated and several aspects of its cognitive manifestations have been clarified. Thus, not only the spectrum of what is currently designated as CBD has expanded, but overlap with other degenerative and even secondary disorders has made clinical diagnostic certainty even more challenging in the absence of specific and readily-available markers. Cognitive deficits in CBD are now recognized as a frequent initial presentation and may appear up to eight years before the motor symptoms, depending on the phenotypic variant. Characteristic cognitive features of CBD involve language deficits, visuospatial and executive dysfunctions, apraxia, and behavioral disorders. Semantic and episodic memories are usually preserved, while language is often impaired in the early stages.


Assuntos
Gânglios da Base/patologia , Córtex Cerebral/patologia , Disfunção Cognitiva/patologia , Demência/patologia , Doenças Neurodegenerativas/patologia , Afasia/patologia , Atrofia/patologia , Disfunção Cognitiva/diagnóstico , Demência/diagnóstico , Diagnóstico Diferencial , Humanos , Idioma , Doenças Neurodegenerativas/diagnóstico , Doenças Neurodegenerativas/psicologia , Testes Neuropsicológicos , Escalas de Graduação Psiquiátrica , Fala/fisiologia
6.
Cien Saude Colet ; 18(9): 2691-8, 2013 Sep.
Artigo em Português | MEDLINE | ID: mdl-23989576

RESUMO

The article seeks to reflect on the legality of the early manifestation of will, established in Brazil through Resolution No. 1.995/12 of the Federal Council of Medicine in the face of the legislative omission and considering the possible linkage of physicians and relatives of terminally ill patients in drafting the Last Will and Testament. It examines the constitutionality of these policies and, therefore, the constitutionality of the resolution itself in light of the new Brazilian constitutional paradigm.


Assuntos
Diretivas Antecipadas/legislação & jurisprudência , Direito a Morrer/legislação & jurisprudência , Brasil , Humanos
8.
Arq. neuropsiquiatr ; 75(8): 570-579, Aug. 2017. tab, graf
Artigo em Inglês | LILACS | ID: biblio-888318

RESUMO

ABSTRACT Corticobasal degeneration (CBD) was originally described as a distinct clinicopathological entity in 1967. Since then, different phenotypic presentations have emerged as possible manifestations of CBD histopathological findings. In addition, pathophysiological findings and the molecular basis have been delineated and several aspects of its cognitive manifestations have been clarified. Thus, not only the spectrum of what is currently designated as CBD has expanded, but overlap with other degenerative and even secondary disorders has made clinical diagnostic certainty even more challenging in the absence of specific and readily-available markers. Cognitive deficits in CBD are now recognized as a frequent initial presentation and may appear up to eight years before the motor symptoms, depending on the phenotypic variant. Characteristic cognitive features of CBD involve language deficits, visuospatial and executive dysfunctions, apraxia, and behavioral disorders. Semantic and episodic memories are usually preserved, while language is often impaired in the early stages.


RESUMO A degeneração corticobasal (DCB) foi originalmente descrita como uma entidade clínico-patológica distinta em 1967. Desde então, nossa compreensão sobre DCB evoluiu substancialmente. Diferentes apresentações fenotípicas emergiram refletindo possíveis manifestações das anormalidades histopatológicos da DCB. Adicionalmente, dados fisiopatológicos e moleculares foram delineados e aspectos das manifestações cognitivas foram explorados. Assim, não só o espectro do que é atualmente designado DCB foi expandido, mas a sobreposição com outras doenças degenerativas e até mesmo secundárias tornaram o diagnóstico clínico ainda mais desafiador na ausência de marcadores específicos e prontamente disponíveis. Déficits cognitivos na DCB são agora reconhecidos frequentemente como apresentações iniciais e podem surgir até 8 anos antes dos sintomas motores, dependendo da variante fenotípica. O quadro cognitivo envolve característicamente déficits de linguagem, disfunção visuoespacial e executiva, apraxia, e distúrbios comportamentais. Anormalidades da linguagem são frequentemente descritas nos estágios iniciais da DCB.


Assuntos
Humanos , Gânglios da Base/patologia , Córtex Cerebral/patologia , Doenças Neurodegenerativas/patologia , Demência/patologia , Disfunção Cognitiva/patologia , Afasia/patologia , Escalas de Graduação Psiquiátrica , Atrofia/patologia , Fala/fisiologia , Doenças Neurodegenerativas/diagnóstico , Doenças Neurodegenerativas/psicologia , Demência/diagnóstico , Diagnóstico Diferencial , Disfunção Cognitiva/diagnóstico , Idioma , Testes Neuropsicológicos
11.
Ciênc. Saúde Colet. (Impr.) ; 18(9): 2691-2698, Set. 2013.
Artigo em Português | LILACS | ID: lil-684677

RESUMO

O artigo se propõe a refletir acerca da legalidade da manifestação antecipada de vontade, instituída no Brasil por meio da Resolução nº. 1.995/12 do Conselho Federal de Medicina, em face da omissão legislativa e considerando a possível vinculação dos médicos e familiares de pacientes terminais ao Testamento Vital. Analisa a constitucionalidade dessas diretivas e, por conseguinte, a constitucionalidade da própria Resolução à luz do novo paradigma constitucional brasileiro.


The article seeks to reflect on the legality of the early manifestation of will, established in Brazil through Resolution No. 1.995/12 of the Federal Council of Medicine in the face of the legislative omission and considering the possible linkage of physicians and relatives of terminally ill patients in drafting the Last Will and Testament. It examines the constitutionality of these policies and, therefore, the constitutionality of the resolution itself in light of the new Brazilian constitutional paradigm.


Assuntos
Humanos , Diretivas Antecipadas/legislação & jurisprudência , Direito a Morrer/legislação & jurisprudência , Brasil
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