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1.
Neurol Neurochir Pol ; 55(2): 212-222, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-33856686

RESUMEN

INTRODUCTION: The aim of this study was to report the course and outcome of SARS-CoV-2 infection in multiple sclerosis (MS) patients treated with disease-modifying therapies (DMTs) in Poland. A major concern for neurologists worldwide is the course and outcome of SARS-CoV-2 infection in patients with MS treated with different DMTs. Although initial studies do not suggest an unfavourable course of infection in this group of patients, the data is limited. MATERIALS AND METHODS: This study included 396 MS patients treated with DMTs and confirmed SARS-CoV-2 infection from 28 Polish MS centres. Information concerning patient demographics, comorbidities, clinical course of MS, current DMT use, as well as symptoms of SARS-CoV-2 infection, need for pharmacotherapy, oxygen therapy, and/or hospitalisation, and short-term outcomes was collected up to 30 January 2021. Additional data about COVID-19 cases in the general population in Poland was obtained from official reports of the Polish Ministry of Health. RESULTS: There were 114 males (28.8%) and 282 females (71.2%). The median age was 39 years (IQR 13). The great majority of patients with MS exhibited relapsing-remitting course (372 patients; 93.9%). The median EDSS was 2 (SD 1.38), and the mean disease duration was 8.95 (IQR 8) years. Most of the MS patients were treated with dimethyl fumarate (164; 41.41%). Other DMTs were less frequently used: interferon beta (82; 20.70%), glatiramer acetate (42; 10.60%), natalizumab (35;8.84%), teriflunomide (25; 6.31%), ocrelizumab (20; 5.05%), fingolimod (16; 4.04), cladribine (5; 1.26%), mitoxantrone (3; 0.76%), ozanimod (3; 0.76%), and alemtuzumab (1; 0.25%). The overall hospitalisation rate due to COVID-19 in the cohort was 6.81% (27 patients). Only one patient (0.3%) died due to SARS-CoV-2 infection, and three (0.76%) patients were treated with mechanical ventilation; 106 (26.8%) patients had at least one comorbid condition. There were no significant differences in the severity of SARS-CoV-2 infection regarding patient age, duration of the disease, degree of disability (EDSS), lymphocyte count, or type of DMT used. CONCLUSIONS AND CLINICAL IMPLICATIONS: Most MS patients included in this study had a favourable course of SARS-CoV-2 infection. The hospitalisation rate and the mortality rate were not higher in the MS cohort compared to the general Polish population. Continued multicentre data collection is needed to increase the understanding of SARS-CoV-2 infection impact on the course of MS in patients treated with DMTs.


Asunto(s)
COVID-19 , Esclerosis Múltiple Recurrente-Remitente , Esclerosis Múltiple , Adulto , Femenino , Humanos , Factores Inmunológicos , Inmunosupresores , Masculino , Esclerosis Múltiple/tratamiento farmacológico , Esclerosis Múltiple/epidemiología , Polonia/epidemiología , SARS-CoV-2
2.
Clin Neurol Neurosurg ; 184: 105453, 2019 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-31376776

RESUMEN

OBJECTIVES: Fingolimod is indicated for the treatment of relapsing-remitting multiple sclerosis (RRMS) patients with highly aggressive disease characterized by frequent relapses and active magnetic resonance imaging. Its efficacy has been demonstrated in three large phase III trials, used in the regulatory submissions throughout the world. Fingolimod in licensed in Europe since 2011 but with a growing number of disease-modifying drugs (DMD) becoming available for RRMS, it is important to gather real-world evidence data regarding long-term effectiveness in treated patients with MS. The aim of this study was to assess fingolimod effectiveness in a real life Polish group of RRMS patients receiving fingolimod as second line treatment. PATIENTS AND METHODS: The observational study with retrospective data collection was performed at 13 sites that were asked to document eligible patients in consecutive chronological order to avoid selection bias. Demographic and clinical data from 253 adult patients with RRMS treated with fingolimod were analyzed. RESULTS: Mean treatment time with fingolimod was 42 months. Relapses reduction during 3 years treatment period was observed (2.0 v 0.2) and majority of patients were free of relapses. Mean EDSS score was stable during the time of observation. The proportion of patients who were free from any clinical disease activity, i.e. without relapses and disability progression, was over 70%. During the first and second year of observation significant reduction of new MRI lesions was observed. CONCLUSION: In the Polish group of patients with RRMS treated with fingolimod, the majority of them showed freedom from relapses, disability progression and reduction of new MRI lesions. Switching from injectable immunomodulatory drugs to fingolimod is associated with fewer relapses and lower disability progression.


Asunto(s)
Clorhidrato de Fingolimod/uso terapéutico , Inmunosupresores/uso terapéutico , Esclerosis Múltiple Recurrente-Remitente/tratamiento farmacológico , Adulto , Personas con Discapacidad/rehabilitación , Progresión de la Enfermedad , Femenino , Humanos , Masculino , Persona de Mediana Edad , Polonia , Recurrencia
3.
Neurol Neurochir Pol ; 39(2): 120-4, 2005.
Artículo en Polaco | MEDLINE | ID: mdl-15871057

RESUMEN

BACKGROUND AND PURPOSE: Stenosis of internal carotid arteries is one of the leading causes of ischemic stroke. Surgical restoration of arterial patency is the primary therapeutic method, aimed to prevent future ischemic stroke. This treatment mode is mainly reserved for patients with recurrent stenoses of internal carotid artery. Endarterectomy of internal carotid artery poses some risk of complications, and neurological complications are among the most dangerous ones. The purpose of the study was to assess early neurologic complications after surgical reopening of the affected arteries. MATERIAL AND METHODS: The study included 119 patients being operated because of critical stenosis of an internal carotid artery in the Department of General and Vascular Surgery of the Provincial Specialist Hospital in Olsztyn between 1999 and 2003. The main indications for surgical treatment were episodes of sustained cerebral ischemia and stenosis of an internal carotid artery exceeding 70%, documented with the ultrasound or angiographic examination. RESULTS: Neurologic complications occurred in 16 patients (12%). Ischemic stroke occurred in 6 cases, transient ischemic attacks in 4 cases, acute cerebral hyperemia in one case and four patients suffered from transient cranial nerve palsy. The most important risk factors of complications were: a previous episode of cerebral ischemia, significant stenosis of a contralateral artery, nicotinism, arterial hypertension and coronary artery disease. Females are exposed to a significantly greater risk of complications. CONCLUSIONS: Surgical reopening of internal carotid arteries is a relatively safe therapeutic method with a modest risk of neurological complications, with the most dangerous and potentially lethal ischemic stroke occurring relatively rarely.


Asunto(s)
Estenosis Carotídea/cirugía , Enfermedades del Sistema Nervioso Central/etiología , Endarterectomía Carotidea/efectos adversos , Adulto , Anciano , Anciano de 80 o más Años , Enfermedades de los Nervios Craneales/etiología , Femenino , Humanos , Ataque Isquémico Transitorio/etiología , Masculino , Persona de Mediana Edad , Factores de Riesgo , Factores Sexuales , Accidente Cerebrovascular/etiología , Resultado del Tratamiento
4.
Neurol Neurochir Pol ; 37(3): 713-20, 2003.
Artículo en Polaco | MEDLINE | ID: mdl-14593764

RESUMEN

A sporadic case of a 31 year-old woman with genetically confirmed diagnosis of LHON was presented. Both her optic nerves were affected, with a 5-year interval between the onset in one eye and the loss of vision in the second one. Besides optic atrophy clinical and laboratory signs of multiple sclerosis were found. A review of the literature suggests that the G3460A mutation present in this case rarely coexists with a MS-like clinical phenotype.


Asunto(s)
Expresión Génica/genética , Esclerosis Múltiple/genética , Atrofia Óptica Hereditaria de Leber/genética , Mutación Puntual/genética , Adulto , ADN Mitocondrial/genética , Femenino , Humanos , Imagen por Resonancia Magnética , Atrofia Óptica Hereditaria de Leber/patología , Fenotipo
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