Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 3 de 3
Filtre
1.
Arq. neuropsiquiatr ; 75(3): 142-146, Mar. 2017. tab, graf
Article Dans Anglais | LILACS | ID: biblio-838885

Résumé

ABSTRACT The enzyme glutamic acid decarboxylase (GAD), present in GABAergic neurons and in pancreatic beta cells, catalyzes the conversion of gamma-aminobutyric acid (GABA). The cerebellum is highly susceptible to immune-mediated mechanisms, with the potentially treatable autoimmune cerebellar ataxia associated with the GAD antibody (CA-GAD-ab) being a rare, albeit increasingly detected condition. Few cases of CA-GAD-ab have been described. Methods This retrospective and descriptive study evaluated the clinical characteristics and outcomes of patients with CA-GAD-ab. Result Three patients with cerebellar ataxia, high GAD-ab titers and autoimmune endocrine disease were identified. Patients 1 and 2 had classic stiff person syndrome and insidious-onset cerebellar ataxia, while Patient 3 had pure cerebellar ataxia with subacute onset. Patients received intravenous immunoglobulin therapy with no response in Patients 1 and 3 and partial recovery in Patient 2. Conclusion CA-GAD-ab is rare and its clinical presentation may hamper diagnosis. Clinicians should be able to recognize this potentially treatable autoimmune cerebellar ataxia.


RESUMO A enzima ácido glutâmico descarboxilase (GAD), presente nos neurônios GABAérgicos e células beta do pâncreas, catalisa a conversão do ácido gama-aminobutírico (GABA). O cerebelo é altamente susceptível a mecanismos imunomediados, sendo a ataxia cerebelar associada ao anticorpo anti-GAD (CA-GAD) uma doença potencialmente tratável. Embora rara, sua frequência é crescente, com poucos casos descritos. Métodos Estudo retrospectivo e descritivo avaliando características clínicas e desfechos da CA-GAD. Resultados Três pacientes com CA-GAD, altos títulos de anti-GAD e doença endócrina autoimune foram identificados. Os pacientes 1 e 2 tinham síndrome da pessoa rígida em forma clássica e apresentação insidiosa da ataxia cerebelar, enquanto o paciente 3 tinha ataxia cerebelar pura e apresentação subaguda. Os pacientes 1 e 3 não melhoraram com imunoglobulina intravenosa e o paciente 2 teve recuperação parcial. Conclusão A CA-GAD é rara e pode ter apresentação clínica desafiadora. Os médicos devem ser capazes de reconhecer essa forma potencialmente tratável de ataxia cerebelar autoimune.


Sujets)
Humains , Mâle , Femelle , Adulte , Adulte d'âge moyen , Autoanticorps/sang , Ataxie cérébelleuse/complications , Glutamate decarboxylase/sang , Imagerie par résonance magnétique , Ataxie cérébelleuse/diagnostic , Ataxie cérébelleuse/immunologie , Ataxie cérébelleuse/traitement médicamenteux , Études rétrospectives , Résultat thérapeutique , Immunoglobulines par voie veineuse/usage thérapeutique , Glutamate decarboxylase/immunologie
2.
Clinics ; 66(11): 1917-1922, 2011. ilus, tab
Article Dans Anglais | LILACS | ID: lil-605872

Résumé

OBJECTIVES: The objectives of this study are to compare the sensitivity and specificity of three diagnostic tools for delirium (the Intensive Care Delirium Screening Checklist, the Confusion Assessment Method for Intensive Care Units and the Confusion Assessment Method for Intensive Care Units Flowsheet) in a mixed population of critically ill patients, and to validate the Brazilian Portuguese Confusion Assessment Method for Intensive Care Units. METHODS: The study was conducted in four intensive care units in Brazil. Patients were screened for delirium by a psychiatrist or neurologist using the Diagnostic and Statistical Manual of Mental Disorders. Patients were subsequently screened by an intensivist using Portuguese translations of the three tools. RESULTS: One hundred and nineteen patients were evaluated and 38.6 percent were diagnosed with delirium by the reference rater. The Confusion Assessment Method for Intensive Care Units had a sensitivity of 72.5 percent and a specificity of 96.2 percent; the Confusion Assessment Method for Intensive Care Units Flowsheet had a sensitivity of 72.5 percent and a specificity of 96.2 percent; the Intensive Care Delirium Screening Checklist had a sensitivity of 96.0 percent and a specificity of 72.4 percent. There was strong agreement between the Confusion Assessment Method for Intensive Care Units and the Confusion Assessment Method for Intensive Care Units Flowsheet (kappa coefficient = 0.96) CONCLUSION: All three instruments are effective diagnostic tools in critically ill intensive care unit patients. In addition, the Brazilian Portuguese version of the Confusion Assessment Method for Intensive Care Units is a valid and reliable instrument for the assessment of delirium among critically ill patients.


Sujets)
Femelle , Humains , Mâle , Adulte d'âge moyen , Délire avec confusion/diagnostic , Unités de soins intensifs , Dépistage de masse/effets indésirables , Traductions , Brésil , Maladie grave , Délire avec confusion/épidémiologie , Langage , Dépistage de masse/méthodes , Reproductibilité des résultats , Sensibilité et spécificité
3.
Rev. bras. neurol ; 45(3): 33-38, jul.-set. 2009. graf, tab, ilus
Article Dans Portugais | LILACS | ID: lil-527643

Résumé

A Esclerose Lateral Amiotrófica (ELA) é uma doença inexorável e degenerativa que afeta os neurônios motores superiores e inferiores, levando à morte cerca de dois a quatro anos após o início das primeiras manifestações. A proposta do presente artigo será apresentar, com base naliteratura vigente, um panorama das principais técnicas utilizadas e resultados de estudos acerca da reabilitação física desses pacientes. Os exercícios terapêuticos devem ser prescritos e encarados como uma maneira de melhorar a qualidade de vida dos pacientes, sendo os objetivosdirecionados para um melhor desempenho nas atividades básicas e instrumentais da vida diária. Os profissionais engajados na reabilitação física devem auxiliar os pacientes e os cuidadores na luta diária contra as perdas proporcionadas pela doença, decorrentes do comprometimento damotricidade voluntária.


Amyotrophic Lateral Sclerosis (ALS) is a fatal degenerative disease that affects upper and lower neurons and takes approximately two to four years between the first sign and symptoms to death. The aim of the present study is to present the main interventions used in physicalrehabilitation and their results in patients with ALS. The therapeutic exercises should be prescribed with the objective to improve the patient?s quality of life and enhance the performance during basic and instrumental daily activities. The professionals involved in physical rehabilitationshould aid patients and caregivers to overcome their difficulties, especially those related to voluntary motor impairments.


Sujets)
Maladies neuromusculaires/rééducation et réadaptation , Sclérose latérale amyotrophique/rééducation et réadaptation , Techniques de physiothérapie/effets indésirables
SÉLECTION CITATIONS
Détails de la recherche