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1.
Mult Scler Relat Disord ; 81: 105346, 2024 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-38091806

RESUMO

BACKGROUND: Multiple sclerosis has a broad spectrum of clinical courses. Early identification of patients at greater risk of accumulating disability is essential. OBJECTIVES: Identify groups of patients with similar presentation through a mixture model and predict their trajectories over the years. METHODS: Retrospective study of patients from 1994 to 2019. We performed a latent profile analysis followed by a latent transition analysis based on eight parameters: age, disease duration, EDSS, number of relapses, multi-topographic symptoms, motor impairment, sphincter impairment, and infratentorial lesions. RESULTS: We included 629 patients, regardless of the phenotypical classification. We identified three distinct groups at the beginning and end of the follow-up. The three-classes model disclosed the "No disability regardless disease duration" (NDRDD) class with low EDSS and younger patients, the "Disability within a short disease duration" (DSDD) class with the worse disability besides short illness, and the "Disability within a long disease duration" (DLDD) class that achieved high EDSS over a long disease duration. EDSS, disease duration, and no sphincter impairment had the best entropy to distinguish classes at the initial presentation. Over time, the patients from NDRDD had a 52.1 % probability of changing to DLDD and 7.7 % of changing to DSDD. CONCLUSIONS: We identified three groups of clinical presentations and their evolution over time based on considered prognostic factors. The most likely transition is from NDRDD to DLDD.


Assuntos
Pessoas com Deficiência , Esclerose Múltipla Recidivante-Remitente , Esclerose Múltipla , Humanos , Esclerose Múltipla/diagnóstico , Estudos Retrospectivos , Fatores de Tempo , Avaliação da Deficiência , Progressão da Doença , Esclerose Múltipla Recidivante-Remitente/diagnóstico
2.
Mult Scler ; 25(8): 1150-1161, 2019 07.
Artigo em Inglês | MEDLINE | ID: mdl-29761736

RESUMO

BACKGROUND: Neuromyelitis optica leads to severe disability. Preventive treatment includes steroids and immunosuppressants, and indications are based on retrospective and observational studies. METHODS: We analyzed 158 patients with neuromyelitis optica regarding disease course, prognostic factors, and treatment response to azathioprine, a widely available low-cost drug. Disability accumulation was used as an endpoint to treatment response. RESULTS: Eight patients with monophasic and 150 with relapsing disease with a median 7 years of disease duration and 4.6 years of follow-up were evaluated. All relapsing patients received preventive treatment, 100 with azathioprine. Only 30% reached Expanded Disability Status Scale (EDSS) 6, and 69% of patients presented no disability accumulation along follow-up. The time under azathioprine and prednisone use were inversely correlated to the hazard of disability accumulation (hazard ratio (HR) = 0.981 and 0.986, respectively; p < 0.01). Each month under azathioprine use reduced disability accumulation by 2.6% (HR = 0.974, p < 0.01), corresponding to an 80% decrease in EDSS progression over 5 years. INTERPRETATION: We report less disability accumulation than previous series on patients with neuromyelitis optica, two-thirds presenting no disability accumulation along follow-up. Continued azathioprine used from early disease onset was strongly associated to maintenance of neurological function and should be offered as a viable option for low-income scenarios.


Assuntos
Azatioprina/efeitos adversos , Progressão da Doença , Imunossupressores/efeitos adversos , Neuromielite Óptica/tratamento farmacológico , Índice de Gravidade de Doença , Adulto , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Neuromielite Óptica/diagnóstico , Neuromielite Óptica/epidemiologia , Neuromielite Óptica/fisiopatologia
3.
Arq Neuropsiquiatr ; 73(4): 304-8, 2015 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-25992520

RESUMO

OBJECTIVE: To describe the clinical activities at the Neuroimmunology Clinic of the Universidade Federal de São Paulo (UNIFESP) from 1994 to 2013. METHOD: The final diagnosis of all patients that attended the center was reviewed and established upon specific guidelines for each disease. The number of total appointments and extra clinical activities (reports and prescriptions) were also analyzed, as are part of routine activities. RESULTS: 1,599 patients attended the Clinic from 1994 to 2013: 816 with multiple sclerosis (MS), 172 with clinical isolated syndromes, 178 with neuromyelitis optica (NMO), 216 with other demyelinating disease, 20 with metabolic disorder, 42 with a vascular disease and 155 with other or undetermined diagnosis. A mean 219 outpatient visits and 65 extra clinical activities were performed monthly. CONCLUSION: We identified that 15% of patients seen have NMO. As patients with NMO have a more severe disease than MS, this data may be important for planning local health care policies.


Assuntos
Esclerose Múltipla/epidemiologia , Neuromielite Óptica/epidemiologia , Idade de Início , Brasil/epidemiologia , Estudos Transversais , Doenças Desmielinizantes/diagnóstico , Doenças Desmielinizantes/epidemiologia , Hospitais Universitários/estatística & dados numéricos , Humanos , Doenças Metabólicas/diagnóstico , Doenças Metabólicas/epidemiologia , Esclerose Múltipla/diagnóstico , Neuromielite Óptica/diagnóstico , Fatores de Tempo , Doenças Vasculares/diagnóstico , Doenças Vasculares/epidemiologia
4.
Arq. neuropsiquiatr ; 73(4): 304-308, 04/2015. tab, graf
Artigo em Inglês | LILACS | ID: lil-745749

RESUMO

Objective To describe the clinical activities at the Neuroimmunology Clinic of the Universidade Federal de São Paulo (UNIFESP) from 1994 to 2013. Method The final diagnosis of all patients that attended the center was reviewed and established upon specific guidelines for each disease. The number of total appointments and extra clinical activities (reports and prescriptions) were also analyzed, as are part of routine activities. Results 1,599 patients attended the Clinic from 1994 to 2013: 816 with multiple sclerosis (MS), 172 with clinical isolated syndromes, 178 with neuromyelitis optica (NMO), 216 with other demyelinating disease, 20 with metabolic disorder, 42 with a vascular disease and 155 with other or undetermined diagnosis. A mean 219 outpatient visits and 65 extra clinical activities were performed monthly. Conclusion We identified that 15% of patients seen have NMO. As patients with NMO have a more severe disease than MS, this data may be important for planning local health care policies. .


Objetivo Descrever a casuística de pacientes atendidos no setor de Neuroimunologia da Universidade Federal de São Paulo (UNIFESP) de 1994 a 2013. Método Analisamos o diagnóstico final de todos os pacientes atendidos de 1999 a 2013, sendo o diagnóstico revisado na última consulta e estabelecido de acordo com os critérios específicos para cada doença. O volume de atendimentos clínicos e não clínicos (relatórios e receitas) foram contabilizados para avaliar a carga de trabalho da equipe. Resultados 1.599 pacientes foram avaliados: 816 com esclerose múltipla (EM), 172 com síndromes clínicas isoladas, 178 com neuromielite óptica (NMO), 216 com outras doenças desmielinizantes, 20 com doenças metabólicas, 42 com doenças vasculares e 155 com outros diagnósticos ou diagnósticos indefinidos. Identificamos uma média de 219 consultas e 65 solicitações de relatórios por mês. Conclusão Identificamos que 15% dos pacientes atendidos tem NMO. Por ser uma doença mais incapacitante que a EM estes dados podem ser importantes para o planejamento de políticas de saúde locais. .


Assuntos
Humanos , Esclerose Múltipla/epidemiologia , Neuromielite Óptica/epidemiologia , Idade de Início , Brasil/epidemiologia , Estudos Transversais , Doenças Desmielinizantes/diagnóstico , Doenças Desmielinizantes/epidemiologia , Hospitais Universitários/estatística & dados numéricos , Doenças Metabólicas/diagnóstico , Doenças Metabólicas/epidemiologia , Esclerose Múltipla/diagnóstico , Neuromielite Óptica/diagnóstico , Fatores de Tempo , Doenças Vasculares/diagnóstico , Doenças Vasculares/epidemiologia
7.
Arq. neuropsiquiatr ; 65(4b): 1233-1236, dez. 2007. ilus, tab
Artigo em Inglês | LILACS | ID: lil-477778

RESUMO

Glossopharyngeal neuralgia with syncope as a sign of neck cancer is a very rare condition. A review of the literature revealed only 29 cases formerly reported. We present the first Brazilian case of such association. A 68-year-old man presented with paroxysmal excruciating pain over the right side of the neck, sometimes followed by syncope. Given the suspicion of recurrent tumor from a previously treated neck malignancy, a computed tomography scan was performed and a right parapharyngeal tumor was shown. Pain and syncope were successfully controlled with carbamazepine and the patient underwent palliative radiotherapy.


Neuralgia glossofaríngea com síncope como um sinal de câncer do pescoço é uma condição muito rara. Uma revisão da literatura revelou apenas 29 casos relatados anteriormente. Apresentamos o primeiro caso brasileiro de tal associação. Um homem de 68 anos se apresentou com dores paroxísticas insuportáveis no lado direito do pescoço, algumas vezes seguidas de síncope. Dada a suspeita de recidiva tumoral derivada de uma malignidade cervical tratada previamente, realizou-se um exame de tomografia computadorizada que evidenciou um tumor parafaríngeo direito. As dores e as síncopes foram controladas satisfatoriamente com carbamazepina e o paciente foi submetido à radioterapia paliativa.


Assuntos
Idoso , Humanos , Masculino , Doenças do Nervo Glossofaríngeo/etiologia , Recidiva Local de Neoplasia/complicações , Neoplasias Faríngeas/complicações , Síncope/etiologia , Anticonvulsivantes/uso terapêutico , Carbamazepina/uso terapêutico , Doenças do Nervo Glossofaríngeo/diagnóstico , Doenças do Nervo Glossofaríngeo/tratamento farmacológico , Recidiva Local de Neoplasia/diagnóstico , Cuidados Paliativos , Neoplasias Faríngeas/diagnóstico , Neoplasias Faríngeas/radioterapia , Síncope/diagnóstico , Síncope/tratamento farmacológico , Tomografia Computadorizada por Raios X
8.
Arq Neuropsiquiatr ; 65(4B): 1233-6, 2007 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-18345437

RESUMO

Glossopharyngeal neuralgia with syncope as a sign of neck cancer is a very rare condition. A review of the literature revealed only 29 cases formerly reported. We present the first Brazilian case of such association. A 68-year-old man presented with paroxysmal excruciating pain over the right side of the neck, sometimes followed by syncope. Given the suspicion of recurrent tumor from a previously treated neck malignancy, a computed tomography scan was performed and a right parapharyngeal tumor was shown. Pain and syncope were successfully controlled with carbamazepine and the patient underwent palliative radiotherapy.


Assuntos
Doenças do Nervo Glossofaríngeo/etiologia , Recidiva Local de Neoplasia/complicações , Neoplasias Faríngeas/complicações , Síncope/etiologia , Idoso , Anticonvulsivantes/uso terapêutico , Carbamazepina/uso terapêutico , Doenças do Nervo Glossofaríngeo/diagnóstico , Doenças do Nervo Glossofaríngeo/tratamento farmacológico , Humanos , Masculino , Recidiva Local de Neoplasia/diagnóstico , Cuidados Paliativos , Neoplasias Faríngeas/diagnóstico , Neoplasias Faríngeas/radioterapia , Síncope/diagnóstico , Síncope/tratamento farmacológico , Tomografia Computadorizada por Raios X
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