ABSTRACT
Multiple sclerosis has become an ever-increasing challenge to neurologists. With the release of the latest medications on the market, Brazilian neurologists feel divided between following their patients' evolution in accordance with the strict rules established by the Brazilian Ministry of Health regarding drug distribution, or following disease progression and worsening in accordance with the evidence in the literature. Therefore, a systematic review of the main published treatment guidelines was conducted and an escalating therapy proposed for guiding multiple sclerosis patient treatment in Brazil.
Subject(s)
Multiple Sclerosis/drug therapy , Academies and Institutes , Consensus , Evidence-Based Medicine , Guidelines as Topic , HumansABSTRACT
ABSTRACT Multiple sclerosis has become an ever-increasing challenge to neurologists. With the release of the latest medications on the market, Brazilian neurologists feel divided between following their patients’ evolution in accordance with the strict rules established by the Brazilian Ministry of Health regarding drug distribution, or following disease progression and worsening in accordance with the evidence in the literature. Therefore, a systematic review of the main published treatment guidelines was conducted and an escalating therapy proposed for guiding multiple sclerosis patient treatment in Brazil.
RESUMO A esclerose múltipla vem se tornando um desafio crescente para os neurologistas. Com o lançamento de novos medicamentos no mercado, os neurologistas brasileiros se encontram divididos entre, apesar da evolução dos seus pacientes, seguir as regras restritas estabelecidas pelo Ministério da Saúde para distribuição de medicamentos, ou ao contrário, considerar a progressão e piora da doença, em concordância com as evidências da literatura. Devido a este impasse foi realizada uma revisão sistemática sobre as principais orientações de tratamento publicadas e foi proposto um escalonamento terapêutico para orientar o tratamento dos pacientes com esclerose múltipla no Brasil.
Subject(s)
Humans , Multiple Sclerosis/drug therapy , Guidelines as Topic , Evidence-Based Medicine , Consensus , Academies and InstitutesABSTRACT
OBJECTIVE: To describe familial forms of demyelinating diseases from an MS referral center in Río de Janeiro State, Brazil. METHODS: A descriptive, cross-sectional study was done to identify familial IIDD cases in Hospital da Lagoa, a public hospital where 75% of patients with IIDD who live in Rio de Janeiro state, located in the Southeast region of Brazil, are referred. The diagnoses of all consecutive patients followed in 2011 were reviewed to apply new diagnostic criteria (Wingerchuk et al., 2008). The diagnosis of IIDD was confirmed based on clinical history, neurological examination, MRI of the skull and spinal cord, CSF analysis and investigation of IgG NMO antibodies. The cases that had at least one other relative with IIDD were selected for the study. RESULTS: Familial forms were found only in the multiple sclerosis (MS) and neuromyelitis optica syndrome (NMOSD) categories. 23 MS families were identified, 60.86% with first degree kinship. It has a Caucasian preponderance, 90% of whom were white. The frequency of early onset was 15% and 20% of the MSf cases have progressive primary course. CONCLUSION: The frequency of familial cases of IIDD was 6.12% among MS patients and 2.8% in NMO spectrum syndromes.
Subject(s)
Family Health , Multiple Sclerosis/epidemiology , Neuromyelitis Optica/epidemiology , Adolescent , Adult , Brazil/epidemiology , Cross-Sectional Studies , Disability Evaluation , Female , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Neurologic Examination , Young AdultABSTRACT
BACKGROUND: It is recognized that there is a particular geographic and ethnic distribution of neuromyelitis optica (NMO) among Caucasian and non-Caucasian populations. OBJECTIVE: To review the diagnoses of patients whom were enrolled in the South Atlantic Project, a Brazilian multiple sclerosis (MS) survey performed from 1995-1998, and to identify NMO and MS case frequencies. METHODS: We reviewed the data from a 10-year follow-up of MS patients. To apply the current diagnostic criteria, the neurologists were asked to collect clinical and laboratory data from the medical records of study patients treated from 1999-2009. RESULTS: The spectrum of inflammatory demyelinating disease in 322 patients (67% white; 33% African-Brazilian) was: 49 (15%) with NMO; 14 (4%) with NMO syndromes; 10 (3%) with acute disseminated encephalomyelitis (ADEM); one isolated tumefactive brain lesion; 249 (77%) with MS (151 with relapsing-remitting MS (RRMS), 70 with secondary progressive MS (SPMS) and 27 with primary progressive MS (PPMS)). Disability was more severe in NMO and PPMS. One-third of the NMO patients had died. CONCLUSIONS: The frequency of NMO was 6.8% in São Paulo and 20.5% in Rio de Janeiro, and mainly seen in persons of African descent, which strengthens the hypothesis of there being an ethnic association of this disease. We recommend that epidemiological studies on MS that were performed previously be reviewed again, to ensure more accurate diagnoses.
Subject(s)
Multiple Sclerosis/pathology , Neuromyelitis Optica/diagnosis , Adolescent , Adult , Child , Cross-Sectional Studies , Disease Progression , Female , Follow-Up Studies , Humans , Male , Middle Aged , Multiple Sclerosis/complications , Neuromyelitis Optica/etiology , Young AdultABSTRACT
BACKGROUND: The visual evoked potential (VEP) is used in the evaluation of multiple sclerosis (MS) patients, showing a delay in P100 wave latency with no changes in amplitude in 60-100% of cases. In the last decade, the recurrent form of neuromyelitis optica (NMO) has been recognized, and clinically characterized by acute events of transverse myelitis (TM) and optic neuritis (ON), differing from MS in clinical and laboratory criteria. Despite these differences, so far, the VEP parameters described in MS have been used in the evaluation of patients with NMO. The objective of this study was to investigate VEP responses in NMO. METHODS: Patients with NMO underwent pattern-reversal visual stimulation. Nineteen patients were selected for the study. RESULTS: Among the 38 eyes examined, 18 (47.4%) had no visual evoked responses and 13 (34.2%) had a reduction of P100 wave amplitude with normal latency. Only two (5.3%) had the pattern described in MS and five (13.2%) were normal. CONCLUSION: Evaluation of VEP in patients with definite NMO revealed a pattern that is different from that of MS in 81.6% of eyes examined, characterized by the absence of responses, or decreased amplitude with normal latency.
Subject(s)
Evoked Potentials, Visual/physiology , Neuromyelitis Optica/physiopathology , Pattern Recognition, Visual/physiology , Adolescent , Adult , Disability Evaluation , Female , Functional Laterality/physiology , Humans , Immunoglobulin G/analysis , Male , Middle Aged , Photic Stimulation , Vision Tests , Visual Acuity , Young AdultABSTRACT
Os autores apresentam casos raros de variantes da Síndrome de Guillain-Barré (SGB) descritas na literatura como forma faringo-cérvico-braquial e forma parapética cujos diagnósticos só foram confirmados após exaustiva investigaçåo e longo acompanhamento evolutivo. É feiro uma revisåo atualizada do assunto, abordando, em especial, as diferentes formas de apresentaçåo da doença e os critérios diagnósticos para SBG adotados pelo Institute of Neurological and Communicative Disorders and Stroke (NINDS)
Subject(s)
Female , Adult , PolyradiculoneuropathyABSTRACT
Os autores apresentam casos raros de variantes da Sindrome de Guillain-Barre (SGB) descritos na literatura como forma faringo-cervico-branquial e forma paraparetica cujos diagnosticos so foram confirmados apos exaustiva investigacao e longo acompanhamento evolutivo. E feita uma revisao atualizada do assunto, abordando, em especial, as diferentes formas de apresentacao da doenca e os criterios diagnosticos para SGB adotados pelo Institute of Neurological and Communicative Disorders and Stroke (N.I.N.D.S.).
