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1.
Clin Pract Cases Emerg Med ; 2(1): 75-77, 2018 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-29849295

RESUMO

A 20-year-old male United States Marine Corps recruit was admitted to the emergency department with a two-week history of profound, bilateral upper-extremity weakness and numbness. Initially thought to be the result of his military training, the cause was ultimately determined to be genetic. This case represents a rare cause of a somewhat common presenting symptom: chronic symmetric polyneuropathy.

2.
J Med Toxicol ; 12(4): 386-390, 2016 12.
Artigo em Inglês | MEDLINE | ID: mdl-27456263

RESUMO

Hyperbaric oxygen (HBO) has been advocated for treatment of acute carbon monoxide (CO) poisoning. There exists considerable debate as to whether HBO prevents delayed neurologic sequelae (DNS) due to CO poisoning. Additionally, existing data in the literature supporting HBO efficacy do not identify an optimal number of HBO treatments. We sought to determine in a mouse model whether there is a difference between one versus multiple HBO sessions for the prevention of DNS. Fifty mice were randomized into five groups of ten mice each: (1) control, receiving no CO exposure or treatment; (2) CO poisoned, receiving no treatment (CO group); (3) CO poisoned, receiving normobaric oxygen for 58 min following the end of exposure (CO + NBO group); (4) CO poisoned, followed by one session of HBO(CO + HBO1); and (5) CO poisoned, followed by three HBO treatment sessions, one every 6 h (CO + HBO3). Prior to poisoning, all animals were trained in step-down latency (SDL) and step-up latency (SUL) tasks. One week after exposure and treatment, all five groups were retested to evaluate the retention of this training. There was no difference detected among groups in SDL (p = 0.67 among all groups) when evaluated using a Kruskal-Wallis test. There was a significant difference among groups in SUL (p = 0.027 among all groups) when evaluated using a Kruskal-Wallis test. When individual groups were compared using a Wilcoxon signed-rank test with Bonferroni correction, there were no statistically significant differences in either SDL or SUL. There was no difference between groups treated with either one or three HBO sessions. One possibility to explain this might be that HBO sessions administered some time after a CO exposure may enhance the lipid peroxidation cascade and worsen neurologic outcomes; alternatively, HBO may simply impart no benefit when compared to NBO.


Assuntos
Intoxicação por Monóxido de Carbono/terapia , Oxigenoterapia Hiperbárica/métodos , Oxigênio/uso terapêutico , Animais , Modelos Animais de Doenças , Humanos , Masculino , Testes de Estado Mental e Demência , Camundongos , Avaliação de Resultados em Cuidados de Saúde , Estatísticas não Paramétricas
3.
Pediatr Emerg Care ; 26(8): 576-82, 2010 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-20693856

RESUMO

OBJECTIVES: Recurrent signs and symptoms after initial treatment and control of coagulopathy and thrombocytopenia after American pit viper (crotaline) envenomations have been previously described in patients treated with Crotalidae polyvalent immune Fab antivenom (FabAV). The significance and necessity of treatment of these recurrent abnormalities are uncertain. Our goal was to further characterize recurrent coagulopathy or thrombocytopenia in pediatric patients. METHODS: All cases presenting to our Toxicology Consult Service, which covers 6 hospitals in a metropolitan area, from May 2007 to April 2008 with recurrent coagulopathy after initial control with FabAV were included and retrospectively reviewed. RESULTS: Four cases of pediatric patients are presented who presented with recurrent coagulopathy and/or thrombocytopenia after initial control with FabAV. The patients were all treated with delayed administration of FabAV with variable results. Blood products administered without concurrent FabAV were of limited use. The laboratory abnormalities took up to 18 days to resolve in one case. One patient developed hemodynamically significant spontaneous bleeding. CONCLUSIONS: The cases presented here suggest administration of FabAV may correct delayed coagulopathy associated with crotaline envenomations. The first 3 cases illustrate that in the face of severe derangements in laboratory values, most envenomated patients treated with FabAV do not develop significant bleeding. These cases may respond to additional antivenom alone. However, case 4 illustrates that hemodynamically significant spontaneous bleeding can occur. Until more data are available, readministration of FabAV is a reasonable first-line therapy for delayed coagulopathy associated with crotaline envenomations.


Assuntos
Antivenenos/efeitos adversos , Transtornos da Coagulação Sanguínea/etiologia , Fragmentos de Imunoglobulinas/efeitos adversos , Mordeduras de Serpentes/tratamento farmacológico , Trombocitopenia/etiologia , Adolescente , Animais , Antivenenos/uso terapêutico , Transtornos da Coagulação Sanguínea/diagnóstico , Transtornos da Coagulação Sanguínea/terapia , Transfusão de Componentes Sanguíneos/métodos , Criança , Pré-Escolar , Venenos de Crotalídeos , Crotalus , Feminino , Seguimentos , Humanos , Fragmentos Fab das Imunoglobulinas , Fragmentos de Imunoglobulinas/uso terapêutico , Masculino , Prevenção Secundária , Trombocitopenia/diagnóstico , Trombocitopenia/terapia
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