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1.
Braz. j. phys. ther. (Impr.) ; 20(5): 471-476, Sept.-Oct. 2016. tab
Article in English | LILACS | ID: biblio-828292

ABSTRACT

ABSTRACT Objective: To determine the responsiveness of the domain climbing up and going down stairs of the Functional Evaluation Scale for Duchenne Muscular Dystrophy (FES-DMD-D3) in a one-year follow-up study. Method: The study included 26 patients with DMD. Effect Size (ES) and Standardized Response Mean (SRM) described the scale’s responsiveness. Results: For climbing up stairs, ES showed that responsiveness was low in the three-month assessments (0.26; 0.35; 0.13; 0.17), low to moderate in the six-month assessments (0.58; 0.48; 0.33), moderate in the nine-month assessments (0.70; 0.68), and high in the 12-month assessment (0.88). SRM showed that responsiveness was low in the three-month assessments (0.29; 0.38; 0.18; and 0.19), low to moderate in the six-month assessments (0.59; 0.51; 0.36), moderate in the nine-month assessments (0.74 and 0.70), and high in the 12-month assessment (0.89). For going down stairs, ES showed that responsiveness was low in the three- and six-month assessments (0.16; 0.25; 0.09; 0.08 and 0.48; 0.35; 0.18, respectively), low to moderate in the nine-month assessments (0.59; 0.44), and moderate in the 12-month assessment (0.71). SRM showed that responsiveness was low in the three- and six-month assessments (0.25; 0.35; 0.12; 0.09 and 0.47; 0.38; 0.21, respectively), low to moderate in the nine-month assessment (0.62; 0.49), and moderate in the 12-month assessment (0.74). Conclusion: Climbing up stairs should be assessed at intervals of nine months or longer, when responsiveness is moderate to high. Going down stairs should be assessed annually because moderate responsiveness was observed in this period.


Subject(s)
Humans , Muscular Dystrophy, Duchenne/physiopathology , Motor Activity/physiology , Follow-Up Studies , Physical Therapy Modalities/standards
2.
Arq. neuropsiquiatr ; 74(1): 75-80, Jan. 2016. tab, graf
Article in English | LILACS | ID: lil-772610

ABSTRACT

ABSTRACT Objective Hand sensory tests do not consider distinct physiological receptors, nor detect normal range variations concerning developmental or pathological changes. We developed an instrument with a set of tests with timing and scoring for assessing haptic perception, which is the interaction between sensory and motor systems, in surfaces exploration, by moving hands. Method Firstly, group meetings were set for test/manual conception and materials testing. The test/manual were submitted to 30 reviewers in 3 stages (10 reviewers on each stage). Results The Hand Haptic Perception Instrument (HHPI) evaluates hand sensorimotor performance on six domains: depression, elevation, texture, compressibility, weight (barognosis) and form perception. Each domain requires specific materials. Score ranges from 0 to 57, being 0 the worst rating. Conclusion This methodological process allowed the development of six domains and instructions to assess haptic perception. This version of HHPI is a pilot model. Further studies will determine reliability and normality ranges.


RESUMO Objetivo Testes de sensibilidade manual não consideram receptores fisiológicos distintos, tampouco variações do desenvolvimento normal ou patológico. Desenvolvemos um instrumento, com pontuação e tempo de desempenho, para avaliar percepção háptica, que é a interação sensório-motora na exploração de superfícies, pelo movimento das mãos. Método Reuniões de grupo foram estabelecidas para desenvolver os testes/ manual e testar materiais. O instrumento e seu manual foram submetidos a 30 revisores, em 3 estágios (com 10 revisores em cada estágio). Resultados O instrumento de avaliação da percepção háptica manual (IAPHM) avalia o desempenho sensório-motor da mão em seis domínios: depressão, elevação, textura, compressibilidade, peso (barognosia) e percepção de forma. Cada domínio requer materiais específicos. A pontuação vai de 0 a 57, sendo 0 a pior pontuação. Conclusão Esse método permitiu o desenvolvimento do instrumento para avaliar percepção háptica. Essa versão do IAPHM é um modelo piloto. Estudos futuros determinarão confiabilidade e variações de normalidade.


Subject(s)
Humans , Hand/physiology , Mechanoreceptors/physiology , Neurophysiology/methods , Psychomotor Performance/physiology , Touch Perception/physiology , Expert Testimony , Group Processes , Merkel Cells/physiology , Pilot Projects , Reference Values , Stereognosis/physiology
3.
Arq. neuropsiquiatr ; 72(1): 5-11, 01/2014. tab, graf
Article in English | LILACS | ID: lil-697591

ABSTRACT

Objective: During the transitional phase (ambulatory to non-ambulatory), synergies characterize the evolution of Duchenne muscular dystrophy (DMD). This study was performed to describe and quantify compensatory movements while sitting down on/rising from the floor and climbing up/down steps. Method: Eighty videos (5 children × 4 assessments × 4 tasks) were recorded quarterly in the year prior to gait loss. Compensatory movements from the videos were registered based on the Functional Evaluation Scale for DMD. Results: The most frequently observed compensatory movements were upper limb support on lower limbs/floor/handrail during all the tasks and lumbar hyperlordosis, trunk support on handrail, equinus foot, increased base of support, non-alternated descent, and pauses while climbing up/down steps. Conclusion: Climbing up/down steps showed a higher number of compensatory movements than sitting down on/rising from the floor, which seemed to be lost before climbing up/down steps in ambulatory children with DMD. .


Objetivo: Durante a fase de transição (deambulador – não-deambulador), sinergias musculares caracterizam a evolução da distrofia muscular de Duchenne (DMD). Este estudo visou descrever e quantificar os movimentos compensatórios durante o sentar/levantar do solo, subir/descer degraus. Oitenta vídeos (5 crianças × 4 avaliações × 4 tarefas) foram gravados trimestralmente durante o ano que antecedeu a perda da marcha. Método: Os movimentos compensatórios dos vídeos foram registrados utilizando a Escala de Avaliação Funcional para DMD. Resultados: Os movimentos compensatórios mais frequentemente observados foram apoio de membros superiores nos membros inferiores/solo/corrimão durante todas as tarefas funcionais e hiperlordose lombar, apoio de tronco no corrimão, pés equinos, aumento da base de suporte, descida não alternada e pausas ao subir/descer degraus. Subir/descer degraus apresentou um número maior de movimentos compensatórios do que sentar/levantar do solo. Conclusão: Sentar/levantar do solo foram habilidades perdidas antes de subir/descer degraus em crianças com DMD. .


Subject(s)
Child , Female , Humans , Male , Activities of Daily Living , Movement/physiology , Muscular Dystrophy, Duchenne/physiopathology , Walking/physiology , Muscle Weakness/physiopathology , Muscular Dystrophy, Duchenne/rehabilitation , Posture/physiology , Reference Values , Retrospective Studies , Time Factors
4.
Acta fisiátrica ; 18(2): 102-106, jun. 2011.
Article in Portuguese | LILACS | ID: lil-663361

ABSTRACT

O objetivo do presente estudo foi verificar os efeitos do treino de força muscular dos membros superiores a partir da abordagem orientada à tarefa, com relação à força muscular, à funcionalidade e à qualidade de vida de um indivíduo adulto com distrofia miotônica do tipo1. Foi realizado um treino de força muscular submáximo (60% da resistência máxima), na freqüência de três terapias semanais, num período de 16 semanas, constituído de três avaliações, a inicial, a final e a de seguimento de um mês do término do protocolo, com base na Medical Research Council scale (MRC), no Total Muscle Score (TMS), na Medida de Função Motora (MFM) e na versão brasileira do questionário de qualidade de vida SF-36. Com relação à força muscular, houve um incremento de 5% no TMS. Na funcionalidade, a MFM apresentouum acréscimo de 1,04% na avaliação final, o qual se perdurou na avaliação de seguimento. Na SF-36, o participante apresentou um acréscimo de 2,12% na segunda avaliação, retornando à pontuação inicial após um mês do protocolo; porém no domínio de capacidade funcional manteve-se o aumento de 20%. O treino de força muscular submáximo orientado à tarefa mostrou-se benéfico com base na forçamuscular e no domínio de capacidade funcional do questionário de qualidade de vida; porém denotou restrita variação quantitativa no âmbito da funcionalidade.


This study aimed to assess the effects of upper limb strength training using a task-oriented approach with respect to muscle strength, functionality and quality of life in an adult with myotonic dystrophy type1. Submaximal muscular strength training (60% maximum resistance)was performed three times a week for a period of 16 weeks, consisting of three evaluations, an initial, a final, and then a follow-up one month after protocol completion based on the Medical Research Council scale (MRC), Total Muscle Score (TMS), Motor Function Measure (MFM), and the Brazilian version of the quality of life questionnaire SF-36. Regardingmuscle strength, there was an increase of 5% in the TMS. In terms offunctionality, the MFM showed an increase of 1.04% in the final evaluationand remained the same in the follow-up evaluation. In the SF-36, theparticipant had an increase of 2.12% in the second evaluation, returning to the initial score one month after protocol. However, concerning functionalcapacity the same 20% increase was observed. The task-orientedsubmaximal muscle strength training proved to be beneficial based on the information reported about muscle strength and functional capacity in the quality of life questionnaire; nonetheless, a small quantitative variation regarding functionality was seen.


Subject(s)
Humans , Male , Middle Aged , Upper Extremity , Task Performance and Analysis , Myotonic Dystrophy/rehabilitation , Myotonic Dystrophy/therapy , Muscle Strength/physiology , Exercise Therapy , Clinical Protocols , Quality of Life , Surveys and Questionnaires
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