Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 7 de 7
Filtrar
Más filtros










Base de datos
Intervalo de año de publicación
1.
Brain Stimul ; 3(1): 51-3, 2010 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-20633430

RESUMEN

Right unilateral ultra-brief electroconvulsive therapy (RUL UB ECT) has been shown to be efficacious with minimal cognitive adverse effects in adult patients with major depression. We present the case of a 14-year-old girl with major depressive disorder with catatonic and psychotic features whose symptoms remitted after 12 treatments of RUL UB ECT.


Asunto(s)
Catatonia , Trastorno Depresivo Mayor , Terapia Electroconvulsiva/métodos , Adolescente , Catatonia/psicología , Catatonia/terapia , Trastorno Depresivo Mayor/psicología , Trastorno Depresivo Mayor/terapia , Terapia Electroconvulsiva/instrumentación , Femenino , Humanos , Masculino
2.
Cogn Behav Neurol ; 19(4): 204-7, 2006 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-17159617

RESUMEN

BACKGROUND: The noradrenergic system modulates cognitive flexibility for insight-based problem solving in studies using beta-adrenergic antagonists, which block noradrenergic neurotransmission postsynaptically. However, it is not known whether alpha2-adrenergic agonists, that decrease noradrenergic neurotransmission by presynaptic inhibition, have the same effect. OBJECTIVES: Therefore, we wished to test whether alpha2-adrenergic agonists would have a similar effect on cognitive flexibility. METHODS: Eighteen normal adults were tested on cognitive flexibility, problem solving, verbal and spatial memory tasks after receiving clonidine (0.1 mg), an alpha2-agonist, placebo, or ephedrine (25 mg), a noradrenergic stimulant. RESULTS: Three-way analysis of variance revealed no significant drug effect on cognitive flexibility or problem solving. There was also no significant effect of clonidine on memory. CONCLUSIONS: Therefore, alpha2-agonists do not influence cognitive flexibility in the same manner as beta-antagonists. Better performance on memory with clonidine might be expected based on primate studies demonstrating benefits in working memory using clonidine. This benefit was not observed for the commonly used clinical memory tasks in our study. This may have implications for why clonidine has not demonstrated efficacy for cognitive disorders such as Alzheimer disease, despite its known benefit for working memory in animal models.


Asunto(s)
Agonistas alfa-Adrenérgicos/farmacología , Clonidina/farmacología , Cognición/efectos de los fármacos , Cognición/fisiología , Efedrina/farmacología , Memoria/efectos de los fármacos , Adolescente , Adulto , Análisis de Varianza , Presión Sanguínea/efectos de los fármacos , Femenino , Humanos , Masculino , Solución de Problemas/efectos de los fármacos , Desempeño Psicomotor/efectos de los fármacos , Receptores Adrenérgicos alfa 2/efectos de los fármacos , Receptores Adrenérgicos alfa 2/fisiología , Valores de Referencia , Aprendizaje Verbal/efectos de los fármacos
3.
J Emerg Med ; 31(3): 317-24, 2006 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-16982374

RESUMEN

The management of an agitated, abusive or violent patient is a common and challenging problem in Emergency Medicine. Priorities include measures to ensure the safety of the patient and the emergency staff, including provision of physical restraint of the patient and evaluation for correctable medical causes of such behavior. Medications used in the treatment of such patients include benzodiazepines and antipsychotic agents. The newer atypical antipsychotic agents seem to provide a safe and effective treatment for such patients. The atypical antipsychotic agents may have fewer short-term side effects than older typical antipsychotic agents, such as haloperidol and droperidol. Currently available atypical antipsychotic medications for the treatment of acute agitation include ziprasidone and olanzapine, which can be administered in an intramuscular formulation, and risperidone, which is available in a rapidly dissolvable tablet and liquid formulation.


Asunto(s)
Antipsicóticos/uso terapéutico , Benzodiazepinas/administración & dosificación , Benzodiazepinas/uso terapéutico , Tratamiento de Urgencia/métodos , Agitación Psicomotora/tratamiento farmacológico , Violencia/prevención & control , Algoritmos , Quimioterapia Combinada , Servicio de Urgencia en Hospital , Humanos
4.
Clin Gastroenterol Hepatol ; 4(7): 912-7, 2006 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-16797245

RESUMEN

BACKGROUND AND AIMS: Duloxetine hydrochloride was approved by the Food and Drug Administration in August 2004 for the treatment of major depressive disorder and diabetic peripheral neuropathic pain. Initial product labeling contained a precaution regarding the risk for increases in liver function test results. Recently, postmarketing research has revealed episodes of cholestatic jaundice and increases in transaminase levels to greater than 20 times normal in patients with chronic liver disease. METHODS: In this case report, we describe a patient with non-Hodgkin's lymphoma in remission and depression treated with duloxetine and mirtazapine. RESULTS: Approximately 6 weeks after increasing her duloxetine dose from 30 to 60 mg daily, she became jaundiced and presented with fulminant hepatic failure. Liver function tests immediately before initiating duloxetine were not available, although the patient carried no prior history of chronic liver disease. A complete work-up for alternate causes failed to reveal another explanation for the patient's clinical presentation. A liver biopsy examination showed histologic changes of subacute injury and the patient's clinical course was consistent with drug-induced liver injury. Despite aggressive measures, the patient's condition deteriorated and the decision was made to withdraw care. CONCLUSIONS: This report shows a case of fulminant hepatic failure and death involving duloxetine use. Given recent reports of severe hepatotoxicity associated with the use of duloxetine in patients with pre-existing liver disease, further investigation into the safety of this compound is warranted.


Asunto(s)
Antidepresivos/efectos adversos , Fallo Hepático Agudo/inducido químicamente , Tiofenos/efectos adversos , Clorhidrato de Duloxetina , Resultado Fatal , Femenino , Humanos , Fallo Hepático Agudo/patología , Persona de Mediana Edad
6.
Pharmacotherapy ; 24(8): 1095-8, 2004 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-15338858

RESUMEN

Depression is a common comorbidity in patients with heart failure or implantable cardioverter-defibrillators (ICDs). A 35-year-old woman with depression, nonischemic cardiomyopathy, and a history of cardiac arrest had an ICD implanted. During initial testing, the device failed to internally defibrillate the patient. Venlafaxine, an antidepressant with cardiac sodium channel blocking activity, was identified as a potential contributor to her elevated defibrillation threshold. After the venlafaxine was discontinued, the ICD was able to successfully internally defibrillate the patient. Clinicians should be aware of this potential adverse drug-device interaction. Further studies are needed to determine the clinical significance of venlafaxine therapy in patients with ICDs.


Asunto(s)
Antidepresivos de Segunda Generación/efectos adversos , Ciclohexanoles/efectos adversos , Desfibriladores Implantables , Trastorno Depresivo Mayor/tratamiento farmacológico , Falla de Equipo , Paro Cardíaco/terapia , Adulto , Trastorno Depresivo Mayor/complicaciones , Femenino , Paro Cardíaco/complicaciones , Humanos , Clorhidrato de Venlafaxina
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...