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1.
Clin Interv Aging ; 17: 1423-1432, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-36187571

RESUMO

Background: Confusion and hallucinations in geriatric patients are frequent symptoms and typically associated with delirium, late-life psychosis or dementia syndromes. A far rarer but well-established differential in patients with rapid cognitive deterioration, acute psychosis, abnormal movements and seizures is autoimmune encephalitis. Exemplified by our case we highlight clinical and economic problems arising in management of geriatric patients with cognitive decline and psychotic symptoms. Case Presentation: A 77-year-old female caucasian patient with an unremarkable medical history was hospitalized after a fall in association with diarrhea and hyponatremia. Upon adequate therapy, disorientation and troubled short-term memory persisted. Within a week the patient developed visual hallucinations. Basic blood and urine samples and imaging (cranial computed tomography and magnetic resonance imaging) were unremarkable. With progressive cognitive decline, amnestic impairment, word finding difficulty and general apathy, psychiatric and neurologic expertise was introduced. Advanced diagnostics did not resolve a final diagnosis; an electroencephalogram showed unspecific generalized slowing. Extended clinical observation revealed visual hallucinations and faciobrachial dystonic seizures. A treatment with anticonvulsants was initiated. Cerebrospinal fluid ultimately tested positive for voltage-gated potassium channel LGl1 (leucine-rich-inactivated-1) antibodies confirming diagnosis of autoimmune anti-LGI1 encephalitis. Immediate immunotherapy (high-dose glucocorticoids and administration of intravenous immunoglobulin G) led to a rapid improvement of the patient's condition. After immunotherapy was tapered, the patient had one relapse and completely recovered with reintroduction of glucocorticoids and initiation of therapy with rituximab. Conclusion: Rapidly progressive dementia in geriatric patients demands a structured and multidisciplinary diagnostic approach. Accurate management and financially supportable care is a major issue in rare diseases such as anti-LGI1-encephalitis. Education and awareness about autoimmune encephalitis of all physicians treating a geriatric population is important in order to involve expertise and establish treatment within reasonable time.


Assuntos
Demência , Encefalite , Encefalite Límbica , Canais de Potássio de Abertura Dependente da Tensão da Membrana , Idoso , Anticonvulsivantes/uso terapêutico , Confusão/complicações , Confusão/tratamento farmacológico , Demência/complicações , Encefalite/diagnóstico , Encefalite/tratamento farmacológico , Feminino , Alucinações/complicações , Alucinações/tratamento farmacológico , Doença de Hashimoto , Humanos , Imunoglobulinas Intravenosas/uso terapêutico , Peptídeos e Proteínas de Sinalização Intracelular/uso terapêutico , Leucina/uso terapêutico , Encefalite Límbica/diagnóstico , Encefalite Límbica/tratamento farmacológico , Canais de Potássio de Abertura Dependente da Tensão da Membrana/uso terapêutico , Rituximab/uso terapêutico , Convulsões/tratamento farmacológico , Convulsões/etiologia
2.
J Neurovirol ; 27(1): 12-25, 2021 02.
Artigo em Inglês | MEDLINE | ID: mdl-33367960

RESUMO

With the growing number of COVID-19 cases in recent times. significant set of patients with extra pulmonary symptoms has been reported worldwide. Here we venture out to summarize the clinical profile, investigations, and radiological findings among patients with SARS-CoV-2-associated meningoencephalitis in the form of a systemic review. This review was carried out based on the existing PRISMA (Preferred Report for Systematic Review and Meta analyses) consensus statement. The data for this review was collected from four databases: Pubmed/Medline, NIH Litcovid, Embase, and Cochrane library and Preprint servers up till 30 June 2020. Search strategy comprised of a range of keywords from relevant medical subject headings which includes "SARS-COV-2," "COVID-19," and "meningoencephalitis." All peer reviewed, case-control, case report, pre print articles satisfying our inclusion criteria were involved in the study. Quantitative data was expressed in mean ± SD, while the qualitative date in percentages. Paired t test was used for analysing the data based on differences between mean and respective values with a p < 0.05 considered to be statistically significant. A total of 61 cases were included from 25 studies after screening from databases and preprint servers, out of which 54 of them had completed investigation profile and were included in the final analysis. Clinical, laboratory findings, neuroimaging abnormalities, and EEG findings were analyzed in detail. This present review summarizes the available evidences related to the occurrence of meningoencephalitis in COVID-19.


Assuntos
COVID-19/fisiopatologia , Tosse/fisiopatologia , Fadiga/fisiopatologia , Febre/fisiopatologia , Meningoencefalite/fisiopatologia , SARS-CoV-2/patogenicidade , Adulto , Idoso , Antivirais/uso terapêutico , Azitromicina/uso terapêutico , COVID-19/diagnóstico por imagem , COVID-19/virologia , Confusão/diagnóstico por imagem , Confusão/tratamento farmacológico , Confusão/fisiopatologia , Confusão/virologia , Tosse/diagnóstico por imagem , Tosse/tratamento farmacológico , Tosse/virologia , Dispneia/diagnóstico por imagem , Dispneia/tratamento farmacológico , Dispneia/fisiopatologia , Dispneia/virologia , Eletroencefalografia , Fadiga/diagnóstico por imagem , Fadiga/tratamento farmacológico , Fadiga/virologia , Feminino , Febre/diagnóstico por imagem , Febre/tratamento farmacológico , Febre/virologia , Humanos , Hidroxicloroquina/uso terapêutico , Masculino , Meningoencefalite/diagnóstico por imagem , Meningoencefalite/tratamento farmacológico , Meningoencefalite/virologia , Pessoa de Meia-Idade , Neuroimagem , SARS-CoV-2/efeitos dos fármacos , Tratamento Farmacológico da COVID-19
3.
BMJ Case Rep ; 13(10)2020 Oct 10.
Artigo em Inglês | MEDLINE | ID: mdl-33040034

RESUMO

Influenza encephalopathy, a rare manifestation of influenza infection in the adult population which is not widely recognised, can present with confusion and focal neurological symptoms, including aphasia. The aim of this report is to illustrate the unique presentation of influenza encephalopathy and discuss the need for close attention to and monitoring of this rare but highly fatal disease.A 28-year-old woman was admitted with acute-onset confusion and incoherent speech. CT of the head was unremarkable. Cerebrospinal fluid analysis showed elevation of protein, but was otherwise unremarkable. A detailed history revealed recent upper respiratory symptoms which prompted a rapid influenza test which was positive and oseltamivir was started. The patient's confusion and aphasia gradually improved and her speech was back to her baseline by the next day.


Assuntos
Afasia/etiologia , Confusão/etiologia , Encefalite Viral/diagnóstico , Vírus da Influenza A Subtipo H1N1/isolamento & purificação , Influenza Humana/diagnóstico , Adulto , Afasia/tratamento farmacológico , Confusão/tratamento farmacológico , Diagnóstico Diferencial , Encefalite Viral/complicações , Encefalite Viral/tratamento farmacológico , Encefalite Viral/virologia , Feminino , Humanos , Influenza Humana/complicações , Influenza Humana/tratamento farmacológico , Influenza Humana/virologia , Oseltamivir/uso terapêutico , Resultado do Tratamento
6.
Ann Pharmacother ; 52(7): 645-649, 2018 07.
Artigo em Inglês | MEDLINE | ID: mdl-29442544

RESUMO

BACKGROUND: Few studies on adult and pediatric patients have shown pyridoxine efficacy as additional therapy for those receiving levetiracetam (LEV) to prevent and mitigate behavioral adverse effects (BAEs). OBJECTIVE: The aim of our study was to analyze the safety and efficacy of pyridoxine supplementation in the prevention of LEV adverse effects, including suicidal ideation. METHODS: This randomized, case-control trial included patients receiving LEV as monotherapy treatment. Patients were subdivided into 2 groups, according to whether they were treated with LEV only (group 1) or LEV with supplemental pyridoxine (group 2). RESULTS: In both cohorts, the most frequent BAEs were irritability/aggression followed by depression and confusion. Those patients (92%) who initiated pyridoxine after 1 month of LEV treatment did not need to change or suspend LEV ( P < 0.001), and BAE improved after 9.06 ± 3.05 days of pyridoxine supplementation. None of the patients complained of symptoms of pyridoxine toxicity, and no new adverse effects of LEV off-label were reported. CONCLUSIONS: In our study, we found pyridoxine to be safe and effective in controlling LEV-induced BAEs in children.


Assuntos
Anticonvulsivantes/efeitos adversos , Comportamento Infantil/efeitos dos fármacos , Levetiracetam/efeitos adversos , Piridoxina/administração & dosagem , Adolescente , Adulto , Agressão/efeitos dos fármacos , Criança , Pré-Escolar , Confusão/tratamento farmacológico , Depressão/tratamento farmacológico , Quimioterapia Combinada , Feminino , Humanos , Humor Irritável/efeitos dos fármacos , Masculino , Resultado do Tratamento
11.
Am J Emerg Med ; 35(4): 665.e1-665.e4, 2017 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-27842924

RESUMO

BACKGROUND: Chemical restraint is often required to control agitation induced by methamphetamine. Dexmedetomidine is an α-2 adrenergic receptor agonist with sedative, analgesic, and sympatholytic properties. Its use in the emergency department (ED) to control methamphetamine-induced agitation has not been reported. OBJECTIVE: To report two cases of methamphetamine-induced agitation successfully sedated with dexmedetomidine in the ED. CASE REPORT: The first case was a 42-year-old man with unstable emotion and violent behaviours after smoking methamphetamine. His agitation did not respond to a large cumulative dose of benzodiazepines (10mg of diazepam and 332mg of midazolam) administered over 48h and sedation was achieved with dexmedetomidine. The second case was a 38-year-old methamphetamine user with unstable emotion and recurrent episodes of agitation despite repeated doses of benzodiazepines, whose agitation was controlled with dexmedetomidine infusion. DISCUSSION: In both cases, dexmedetomidine apparently reduced the dose of benzodiazepines needed to achieve adequate sedation. Transient falls in blood pressure and slowing of the heart rate were noted, which resolved either spontaneously or after reducing the infusion rate without requiring drug treatment. CONCLUSION: Dexmedetomidine can be considered as an adjunct for chemical restraint when standard treatment fails to control the agitation induced by methamphetamine, but patient's hemodynamic state should be monitored closely during administration. Its efficacy and safety in the ED warrant further evaluation with prospective controlled trials.


Assuntos
Inibidores da Captação Adrenérgica/efeitos adversos , Agonistas de Receptores Adrenérgicos alfa 2/uso terapêutico , Sintomas Afetivos/tratamento farmacológico , Agressão , Acatisia Induzida por Medicamentos/tratamento farmacológico , Confusão/tratamento farmacológico , Dexmedetomidina/uso terapêutico , Metanfetamina/efeitos adversos , Adulto , Sintomas Afetivos/induzido quimicamente , Acatisia Induzida por Medicamentos/etiologia , Confusão/induzido quimicamente , Serviço Hospitalar de Emergência , Humanos , Masculino
13.
In. Vicente Peña, Ernesto. Medicina Interna. Diagnóstico y tratamiento. La Habana, ECIMED, 2. ed; 2016. , tab.
Monografia em Espanhol | CUMED | ID: cum-63178
14.
Neurol Sci ; 36 Suppl 1: 71-4, 2015 May.
Artigo em Inglês | MEDLINE | ID: mdl-26017516

RESUMO

HaNDL (transient headache and neurological deficits with cerebrospinal fluid lymphocytosis) syndrome is an infrequent condition included at group 7 "headache attributed to non-vascular intracranial disorder" in the recent International Classification of Headache Disorders (ICHD-3), code 7.3.5. The description states "migraine-like headache episodes (typically 1-12) accompanied by neurological deficits including hemiparaesthesia, hemiparesis and/or dysphasia, but positive visual symptoms only uncommonly, lasting several hours. There is lymphocytic pleocytosis. The disorder resolves spontaneously within 3 months". In this description confusional state is not considered as a main symptom, even if in the literature this aspect is frequently reported. Here, we report the cases of two young boys presenting with confusional state as the main complaint. The possible pathogenesis of the different clinical presentation is discussed.


Assuntos
Confusão/etiologia , Cefaleia/complicações , Linfocitose/complicações , Doenças do Sistema Nervoso/complicações , Aciclovir/uso terapêutico , Adolescente , Ceftriaxona/uso terapêutico , Confusão/tratamento farmacológico , Cefaleia/tratamento farmacológico , Humanos , Linfocitose/líquido cefalorraquidiano , Linfocitose/tratamento farmacológico , Masculino , Doenças do Sistema Nervoso/tratamento farmacológico , Adulto Jovem
15.
Brain Inj ; 28(9): 1223-5, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24910931

RESUMO

BACKGROUND: A 36-year-old immunocompetent woman with a posterior fossa arteriovenous malformation (PF-AVM) and hydrocephalus presented with low fever and mental confusion 4 days after ventriculoperitoneal shunting (VPS). METHODS: Cerebrospinal fluid (CSF) and ventricular catheter tip cultures isolated Corynebacterium sp. Similar to previous cases in the literature, species determination was not possible. However, the antibiotic sensitivity profile of this isolate suggested Corynebacterium jeikeium. Conversion to external ventricular drainage (EVD) was done and intravenous vancomycin was administered for 21 days. RESULTS AND CONCLUSIONS: The patient showed progressive improvement. Since the first CSF shunt infection caused by Corynebacterium sp., 16 other cases in the literatures have been reported. Additionally, this study reports the difficulties in recognizing CSF shunt infection caused by this agent and the possible clinical or laboratory patterns as observed in the literature.


Assuntos
Confusão/microbiologia , Infecções por Corynebacterium/diagnóstico , Corynebacterium/isolamento & purificação , Febre/microbiologia , Hidrocefalia/microbiologia , Derivação Ventriculoperitoneal/efeitos adversos , Adulto , Antibacterianos/administração & dosagem , Cateterismo/efeitos adversos , Confusão/tratamento farmacológico , Confusão/etiologia , Infecções por Corynebacterium/tratamento farmacológico , Drenagem , Feminino , Febre/tratamento farmacológico , Febre/etiologia , Humanos , Hidrocefalia/tratamento farmacológico , Hidrocefalia/etiologia , Resultado do Tratamento , Vancomicina/administração & dosagem
16.
Semin Neurol ; 33(3): 219-30, 2013 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-24057825

RESUMO

The normal vestibular system may be adversely affected by environmental challenges which have characteristics that are unfamiliar or ambiguous in the patterns of sensory stimulation they provide. A disordered vestibular system lends susceptibility even to quotidian environmental experiences as the sufferer becomes dependent on potentially misleading, nonvestibular sensory stimuli. In both cases, the sequelae may be vertigo, incoordination, imbalance, and unpleasant autonomic responses. Common environmental motion conditions include visual vertigo, motion sickness, and motorists' disorientation. The core therapy for visual vertigo, motion sickness, and drivers' disorientation is progressive desensitization within a cognitive framework of reassurance and explanation, plus anxiolytic tactics and autogenic control of autonomic symptoms.


Assuntos
Condução de Veículo/psicologia , Confusão/fisiopatologia , Tontura/etiologia , Enjoo devido ao Movimento/fisiopatologia , Vertigem/etiologia , Terapia Comportamental , Confusão/tratamento farmacológico , Confusão/epidemiologia , Confusão/terapia , Tontura/tratamento farmacológico , Tontura/epidemiologia , Tontura/fisiopatologia , Tontura/terapia , Meio Ambiente , Humanos , Individualidade , Enjoo devido ao Movimento/tratamento farmacológico , Enjoo devido ao Movimento/epidemiologia , Enjoo devido ao Movimento/terapia , Orientação , Vertigem/tratamento farmacológico , Vertigem/epidemiologia , Vertigem/fisiopatologia , Vertigem/terapia , Vestíbulo do Labirinto , Percepção Visual
17.
Zh Nevrol Psikhiatr Im S S Korsakova ; 113(7 Pt 2): 25-31, 2013.
Artigo em Russo | MEDLINE | ID: mdl-23994928

RESUMO

Authors have studied the psychopathological structure, risk factors and predictors of mental confusion in 102 patients with dementia of different etiologies (Alzheimer's disease (AD), cerebrovascular dementia (CVD) and mixed Alzheimer disease/vascular dementia). The high frequency (>40%) of mental confusion in patients with dementia admitted to geriatric departments of a psychiatric hospital has been identified. Mental confusion was most frequently characterized by a syndrome of memory and/or confabulatory confusion. The causes of mental confusion in elderly patients with dementia, including the exacerbation of a somatic pathology and changes in conditions of patient's staying in hospital, have been specified. The frequency of mental confusion is correlated with patient's age: more than 55% of cases has been noted in the group aged over 70 years. Mental confusion develops 6 times more frequent in patients with moderately severe and severe dementia than in those with mild dementia. Timely diagnosis and adequate treatment are predictors of favorable outcome in most patients. Treatment of this syndrome should be strictly differential. Antipsychotic treatment is needed in case of persistent psychotic symptoms and severe behavioral disturbances. Drugs for pathogenetic therapy of dementia have been used in the complex treatment of mental confusion in patients with dementia, in particular AD.


Assuntos
Antipsicóticos/uso terapêutico , Confusão/etiologia , Demência/complicações , Avaliação Geriátrica/métodos , Fatores Etários , Idoso , Idoso de 80 Anos ou mais , Confusão/tratamento farmacológico , Confusão/epidemiologia , Demência/tratamento farmacológico , Demência/psicologia , Feminino , Seguimentos , Humanos , Masculino , Prevalência , Prognóstico , Qualidade de Vida , Federação Russa/epidemiologia
18.
Pediatr Nephrol ; 28(5): 827-30, 2013 May.
Artigo em Inglês | MEDLINE | ID: mdl-23389237

RESUMO

BACKGROUND: Atypical hemolytic uremic syndrome (aHUS) is associated with defective regulation of the complement pathway. Neurological involvement is the most common extrarenal complication and represents a major cause of mortality and morbidity. CASE-DIAGNOSIS/TREATMENT: Two girls aged 11 and 6 years, respectively, developed aHUS and were treated immediately with plasma exchange (PE) and fresh frozen plasma infusion (PI). Although initial improvement in renal function was seen in both cases, the first patient showed progressing thrombotic microangiopathy (TMA) despite daily PE, and neurological manifestations (seizures, vision loss, loss of balance, and confusion) developed after 1 month. The second patient developed cerebral TMA (seizures, vision loss, and nystagmus) 6 days after initial presentation and remained unresponsive to PE/PI. Neurological symptoms were similar in both patients, even though they had different complement protein mutations. Treatment with eculizumab achieved complete control of neurological symptoms within 24 h and gradually normalized hematological and renal parameters in both children. CONCLUSIONS: Based on our two cases, we conclude that eculizumab is a rapid-acting, effective, and life-saving treatment for pediatric patients with aHUS and severe neurological involvement, which works by inhibiting complement-mediated TMA in the kidney and other organs, such as the brain.


Assuntos
Anticorpos Monoclonais Humanizados/uso terapêutico , Síndrome Hemolítico-Urêmica/tratamento farmacológico , Doenças do Sistema Nervoso/tratamento farmacológico , Síndrome Hemolítico-Urêmica Atípica , Criança , Ativação do Complemento/efeitos dos fármacos , Ativação do Complemento/genética , Confusão/tratamento farmacológico , Confusão/etiologia , Feminino , Síndrome Hemolítico-Urêmica/complicações , Síndrome Hemolítico-Urêmica/diagnóstico , Síndrome Hemolítico-Urêmica/genética , Síndrome Hemolítico-Urêmica/imunologia , Humanos , Doenças do Sistema Nervoso/diagnóstico , Doenças do Sistema Nervoso/etiologia , Doenças do Sistema Nervoso/imunologia , Exame Neurológico , Nistagmo Patológico/tratamento farmacológico , Nistagmo Patológico/etiologia , Equilíbrio Postural/efeitos dos fármacos , Convulsões/tratamento farmacológico , Convulsões/etiologia , Transtornos de Sensação/tratamento farmacológico , Transtornos de Sensação/etiologia , Resultado do Tratamento , Transtornos da Visão/tratamento farmacológico , Transtornos da Visão/etiologia
19.
Climacteric ; 16(1): 17-27, 2013 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-22646219

RESUMO

OBJECTIVE: To assess effects of desvenlafaxine (administered as desvenlafaxine succinate) on secondary outcomes of mood, climacteric symptoms, and treatment satisfaction in postmenopausal women with moderate to severe menopausal vasomotor symptoms (VMS). METHODS: A 12-week, multicenter, double-blind, placebo-controlled trial was conducted in postmenopausal women with ≥ 50 moderate to severe hot flushes per week. Participants were randomly assigned to desvenlafaxine 100 mg/day, desvenlafaxine 150 mg/day, or placebo. Secondary outcome efficacy variables included Profile of Mood States (POMS), Greene Climacteric Scale (GCS), and Menopausal Symptoms Treatment Satisfaction Questionnaire (MS-TSQ) scores. Change from baseline in POMS total mood disturbance (TMD) score and subdomain scores were evaluated using analysis of covariance, adjusting for treatment and study site as factors and baseline score. GCS total and subdomain scores were analyzed similarly. Treatment satisfaction was analyzed using the row mean score test. RESULTS: A total of 458 women were enrolled. At week 12, desvenlafaxine 100 mg/day significantly improved POMS TMD scores (p <0.001) and four of six POMS subdomains compared with placebo (all p ≤ 0.005). Women taking desvenlafaxine 100 mg/day experienced significantly greater improvement in GCS total scores (p <0.001) and five of six subdomains (all p ≤ 0.029) compared with placebo. Treatment with desvenlafaxine 100 mg/day resulted in significantly greater treatment satisfaction overall and in six of seven additional MS-TSQ items (all p ≤0.042). Desvenlafaxine 150-mg/day results were similar. CONCLUSIONS: Desvenlafaxine treatment improved mood and climacteric symptoms in postmenopausal women with moderate to severe VMS compared with placebo, and more women were satisfied with desvenlafaxine treatment than with placebo.


Assuntos
Sintomas Afetivos/tratamento farmacológico , Cicloexanóis/uso terapêutico , Menopausa/efeitos dos fármacos , Inibidores da Captação de Neurotransmissores/uso terapêutico , Satisfação do Paciente , Adulto , Idoso , Ira/efeitos dos fármacos , Ansiedade/tratamento farmacológico , Dor nas Costas/tratamento farmacológico , Confusão/tratamento farmacológico , Cicloexanóis/farmacologia , Depressão/tratamento farmacológico , Succinato de Desvenlafaxina , Método Duplo-Cego , Fadiga/tratamento farmacológico , Feminino , Fogachos/tratamento farmacológico , Humanos , Hiperidrose/tratamento farmacológico , Humor Irritável/efeitos dos fármacos , Pessoa de Meia-Idade , Inibidores da Captação de Neurotransmissores/farmacologia , Comportamento Sexual/efeitos dos fármacos , Inquéritos e Questionários
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