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2.
Epileptic Disord ; 24(6): 994-1019, 2022 12 01.
Article in English | MEDLINE | ID: mdl-36219093

ABSTRACT

This educational review article aims to provide information on the central nervous system (CNS) infectious and parasitic diseases that frequently cause seizures and acquired epilepsy in the developing world. We explain the difficulties in defining acute symptomatic seizures, which are common in patients with meningitis, viral encephalitis, malaria, and neurocysticercosis, most of which are associated with increased mortality and morbidity, including subsequent epilepsy. Geographic location determines the common causes of infectious and parasitic diseases in a particular region. Management issues encompass prompt treatment of acute symptomatic seizures and the underlying CNS infection, correction of associated predisposing factors, and decisions regarding the appropriate choice and duration of antiseizure therapy. Although healthcare provider education, to recognize and diagnose seizures and epilepsy related to these diseases, is a feasible objective to save lives, prevention of CNS infections and infestations is the only definitive way forward to reduce the burden of epilepsy in developing countries.


Subject(s)
Communicable Diseases , Encephalitis, Viral , Epilepsy , Neurocysticercosis , Communicable Diseases/complications , Encephalitis, Viral/complications , Epilepsy/complications , Epilepsy/etiology , Humans , Neurocysticercosis/complications , Neurocysticercosis/epidemiology , Seizures/complications , Seizures/etiology
3.
Front Neurol ; 13: 833293, 2022.
Article in English | MEDLINE | ID: mdl-35547380

ABSTRACT

Temporal lobe epilepsy (TLE) is the most common type of focal epilepsy and is frequently drug-resistant (DR) to antiseizure medication (ASM), corresponding to approximately one-third of the cases. When left inadequately treated, it can worsen the quality of life, cognitive deficits, and risk of death. The standard treatment for drug-resistant TLE is the surgical removal of the structures involved, with good long-term outcome rates of 60-70 % and a low rate of adverse effects. The goal of successful treatment is sustained seizure freedom. In our study, we evaluated sustained long-term (up to 23 years) surgical outcomes in 621 patients with DR-TLE associated with hippocampal sclerosis, who underwent a temporal lobectomy. We analyzed the main predictive factors that influence the surgical outcome related to seizure control, through a longitudinal and retrospective study, using a multivariable regression model. We found that 73.6% of the patients were free from disabling seizures (Engel Class I), maintained over time in 65% of patients followed up to 23 years after surgery. We found that four independent variables predicted seizure outcomes. The presence of dysmnesic and olfactory aura predicted a less favorable outcome. The history of febrile seizure and the surgical technique predicted a good outcome. Regarding the type of surgical technique, the standard anteromesial temporal lobectomy (ATL) led to significantly better outcomes (78.6% Engel Class I) when compared to the selective amygdalohippocampectomy via subtemporal approach (67.2% Engel Class I; p = 0.002), suggesting that the neuronal networks involved in the epileptogenic zone may be beyond mesial temporal structures. The multivariable regression model with the above-mentioned predictor variables revealed an ExpB = 3.627 (N = 621, p < 0.001), indicating that the model was able to distinguish between patients with a seizure-free. We conclude that epilepsy surgery is a safe procedure, with low rates of postoperative complications and good long-term results.

4.
Seizure ; 90: 145-154, 2021 Aug.
Article in English | MEDLINE | ID: mdl-33608134

ABSTRACT

While most patients with focal epilepsy present with clear structural abnormalities on standard, 1.5 or 3 T MRI, some patients are MRI-negative. For those, quantitative MRI techniques, such as volumetry, voxel-based morphometry, and relaxation time measurements can aid in finding the epileptogenic focus. High-field MRI, just recently approved for clinical use by the FDA, increases the resolution and, in several publications, was shown to improve the detection of focal cortical dysplasias and mild cortical malformations. For those cases without any tissue abnormality in neuroimaging, even at 7 T, scalp EEG alone is insufficient to delimitate the epileptogenic zone. They may benefit from the use of high-density EEG, in which the increased number of electrodes helps improve spatial sampling. The spatial resolution of even low-density EEG can benefit from electric source imaging techniques, which map the source of the recorded abnormal activity, such as interictal epileptiform discharges, focal slowing, and ictal rhythm. These EEG techniques help localize the irritative, functional deficit, and seizure-onset zone, to better estimate the epileptogenic zone. Combining those technologies allows several drug-resistant cases to be submitted to surgery, increasing the odds of seizure freedom and providing a must needed hope for patients with epilepsy.


Subject(s)
Brain , Epilepsies, Partial , Brain/diagnostic imaging , Brain/surgery , Electroencephalography , Humans , Magnetic Resonance Imaging , Treatment Outcome
5.
Neurology ; 87(19): 1968-1974, 2016 Nov 08.
Article in English | MEDLINE | ID: mdl-27733569

ABSTRACT

OBJECTIVE: To evaluate a novel approach to control epileptic drop attacks through a selective posterior callosotomy, sparing all prefrontal interconnectivity. METHODS: Thirty-six patients with refractory drop attacks had selective posterior callosotomy and prospective follow-up for >4 years. Falls, episodes of aggressive behavior, and IQ were quantified. Autonomy in activities of daily living, axial tonus, and speech generated a functional score ranging from 0 to 13. Subjective effect on patient well-being and caregiver burden was also assessed. RESULTS: Median monthly frequency of drop attacks decreased from 150 to 0.5. Thirty patients (83%) achieved either complete or >90% control of the falls. Need for constant supervision decreased from 90% to 36% of patients. All had estimated IQ below 85. Median functional score increased from 7 to 10 (p = 0.03). No patient had decrease in speech fluency or hemiparesis. Caregivers rated the effect of the procedure as excellent in 40% and as having greatly improved functioning in another 50%. Clinical, EEG, imaging, and cognitive variables did not correlate with outcome. CONCLUSIONS: This cohort study with objective outcome assessment suggests that selective posterior callosotomy is safe and effective to control drop attacks, with functional and behavioral gains in patients with intellectual disability. Results are comparable to historical series of total callosotomy and suggest that anterior callosal fibers may be spared. CLASSIFICATION OF EVIDENCE: This study provides Class III evidence that selective posterior callosotomy reduces falls in patients with epileptic drop attacks.


Subject(s)
Corpus Callosum/surgery , Prefrontal Cortex/physiology , Psychosurgery/methods , Syncope/surgery , Activities of Daily Living , Adolescent , Adult , Child , Electroencephalography , Epilepsy/complications , Epilepsy/surgery , Female , Humans , Longitudinal Studies , Male , Multivariate Analysis , Neural Pathways/surgery , Retrospective Studies , Syncope/etiology , Treatment Outcome , Video Recording , Young Adult
6.
Int J Neurosci ; 125(9): 711-5, 2015.
Article in English | MEDLINE | ID: mdl-25364881

ABSTRACT

Ocular myositis (OM) is a rare clinical entity characterized by idiopathic, nonspecific inflammation of primarily or exclusively extraocular muscles (EOM). Presentation usually encompasses painful diplopia, exacerbated by eye movement. We report two cases of idiopathic OM with unique characteristics. The first presented with pseudo-sixth nerve palsy due to medial nucleus inflammation and the second presented with recurrent OM, subsequently affecting both eyes. Knowledge of different patterns of presentation and recurrence are important to manage this rare inflammatory syndrome.


Subject(s)
Myositis/diagnosis , Oculomotor Muscles/physiopathology , Orbital Diseases/diagnosis , Adult , Female , Humans , Male , Myositis/physiopathology , Orbital Diseases/physiopathology , Recurrence , Young Adult
7.
Article in Portuguese | LILACS | ID: biblio-879703

ABSTRACT

Epilepsias refratárias a dois esquemas medicamentosos são consideradas resistentes ao tratamento farmacológico. Nestes casos, o médico deve realizar uma ampla revisão diagnóstica, excluindo outros paroxismos. A cirurgia ressectiva deve ser cogitada nas epilepsias focais. Outras intervenções terapêuticas são possíveis, dependendo da situação específica.


Epilepsy refractory to two drug regimens is labeled as drug resistant. In these cases, the physician should perform a comprehensive diagnosis revision, excluding other paroxysms. Ressective surgery must be cogitated in focal epilepsies. Other therapeutic interventions are possible, depending on the specific situation.


Subject(s)
Epilepsy/diagnosis , Epilepsy/therapy
8.
Article in Portuguese | LILACS | ID: biblio-879755

ABSTRACT

Meningite é uma doença causada pela inflamação das membranas que envolvem o cérebro e a medula espinhal, usualmente consequência da infecção do líquor por vírus ou bactérias. A severidade da doença e o tratamento da meningite diferem conforme a etiologia. Este artigo visa estabelecer um algoritmo para a avaliação e tratamento das principais causas de meningite.


Meningitis is a disease caused by the inflammation of the membranes that involve the brain and spinal cord, usually a consequence of the infection of the cerebrospinal fluid by viruses and bacteria. The severity of the disease and the treatment differ according to the etiology. This article aims to be a guide to the evaluation and treatment of the most common causes of meningitis.


Subject(s)
Meningitis , Therapeutics
9.
Thrombosis ; 2014: 753780, 2014.
Article in English | MEDLINE | ID: mdl-25349734

ABSTRACT

Background. Stroke is a leading cause of mortality and disability in Brazil and around the world. Cardioembolism is responsible for nearly 30% of the origins of ischemic stroke. Methods. We analyzed data of 256 patients with cardioembolic ischemic stroke (according to TOAST classification) who were admitted into the Hospital São Lucas-PUCRS from October 2011 to January 2014. The cardioembolic subtype was divided into six subgroups: arrhythmias, valvular heart disease, coronary artery disease, cardiomyopathy, septal abnormalities, and intracardiac injuries. The prevalence of the most important cardiovascular risk factors and medications in use for prevention of systemic embolism by the time of hospital admission was analyzed in each patient. Results. Among 256 patients aged 60.2 +/- 6.9 years, 132 males, arrhythmias were the most common cause of cardioembolism corresponding to 50.7%, followed by valvular heart disease (17.5%) and coronary artery disease (16%). Hypertension (61.7%) and dyslipidemia (43.7%) were the most common risk factors. Less than 50% of patients with arrhythmias were using oral anticoagulants. Conclusions. Identifying the prevalence of cardioembolic stroke sources subgroups has become an increasingly important role since the introduction of new oral anticoagulants. In this study, arrhythmias (especially atrial fibrillation) were the main cause of cardioembolism.

10.
PLoS One ; 9(4): e95269, 2014.
Article in English | MEDLINE | ID: mdl-24760032

ABSTRACT

BACKGROUND: Attention deficit hyperactivity disorder (ADHD) is a common comorbidity of childhood epilepsy, but the neuroanatomical correlates of ADHD in epilepsy have yet to be comprehensively characterized. METHODS: Children with new and recent-onset epilepsy with (n = 18) and without (n = 36) ADHD, and healthy controls (n = 46) underwent high resolution MRI. Measures of cortical morphology (thickness, area, volume, curvature) and subcortical and cerebellar volumes were compared between the groups using the program FreeSurfer 5.1. RESULTS: Compared to the control group, children with epilepsy and ADHD exhibited diffuse bilateral thinning in the frontal, parietal and temporal lobes, with volume reductions in the brainstem and subcortical structures (bilateral caudate, left thalamus, right hippocampus). There were very few group differences across measures of cortical volume, area or curvature. CONCLUSIONS: Children with epilepsy and comorbid ADHD exhibited a pattern of bilateral and widespread decreased cortical thickness as well as decreased volume of subcortical structures and brainstem. These anatomic abnormalities were evident early in the course of epilepsy suggesting the presence of antecedent neurodevelopmental changes, the course of which remains to be determined.


Subject(s)
Attention Deficit Disorder with Hyperactivity/pathology , Brain/pathology , Epilepsy/pathology , Adolescent , Child , Female , Frontal Lobe/pathology , Humans , Magnetic Resonance Imaging , Male , Temporal Lobe/pathology
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