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1.
J Psychopharmacol ; 24(1): 131-3, 2010 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-18801834

RESUMO

Presented is a case study of a seventy five year old man who experienced psychosis and depression related to the onset and termination of amiodarone therapy. The study looks at the pharmacology of amiodarone and the mechanisms that may have led to the emergence of these symptoms. It also raises the issue of making a careful assessment of a patient's life event history in that life events that may not be classically regarded as significant life events may be important in the precipitation of mental illness.


Assuntos
Amiodarona/efeitos adversos , Antiarrítmicos/efeitos adversos , Psicoses Induzidas por Substâncias/etiologia , Idoso , Amiodarona/uso terapêutico , Antiarrítmicos/uso terapêutico , Depressão/induzido quimicamente , Humanos , Masculino , Síndrome de Abstinência a Substâncias/fisiopatologia
2.
Int J Geriatr Psychiatry ; 25(4): 411-8, 2010 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-19946860

RESUMO

OBJECTIVE: Although the evidence base for the use of antipsychotics in older people with schizophrenia is generally of low quality, it tends to support the use of atypical antipsychotics. Only limited information regarding longer term adherence to these apparently more effective drugs is available. The aim of this study was to determine predictors of adherence to risperidone or olanzapine in patients over 60. METHODS: Patients receiving care from old age psychiatrists for their schizophrenia were randomised to treatment with olanzapine or risperidone and were followed for up to 3(1/2) years. Kaplan-Meier curves were generated to assess the univariate effect of randomisation drug on long-term adherence and Cox regression adjusted for baseline variables which may have affected adherence. RESULTS: In total, 60.6% of the 66 patients in the study were still taking their randomised drug by the end of the interval in which they remained under observation (64.7% olanzapine and 56.3% risperidone). This difference was non-significant. No baseline variable was associated with an increased risk of non-adherence, though the delivery form of pre-randomisation drug (oral or depot) was weakly (p = 0.054) associated with patients originally on depot being less likely to be adherent to an atypical drug. CONCLUSIONS: Overall adherence with atypical medication was good with almost two-thirds of the patients remaining on their randomisation drug for the interval in which they were under observation. Patients taken off depot were less likely to be adherent but there was no significant difference in adherence between olanzapine and risperidone. Scrutiny of the survival curves suggested that non-adherence is an early event in treatment and patients adherent at 6 months were likely to remain adherent over a longer time period.


Assuntos
Antipsicóticos/uso terapêutico , Benzodiazepinas/uso terapêutico , Adesão à Medicação , Risperidona/uso terapêutico , Esquizofrenia/tratamento farmacológico , Idoso , Feminino , Humanos , Estimativa de Kaplan-Meier , Estudos Longitudinais , Masculino , Pessoa de Meia-Idade , Olanzapina , Modelos de Riscos Proporcionais
3.
Phys Rev Lett ; 102(17): 173201, 2009 May 01.
Artigo em Inglês | MEDLINE | ID: mdl-19518780

RESUMO

Experimentally determined cross sections for the elastic scattering of positrons by argon and xenon atoms have been found to exhibit a steplike increase at the first inelastic threshold energy--i.e., that for positronium formation. Rather than supporting the existence of a cusplike behavior predicted theoretically, this feature, which is more pronounced for xenon, suggests the existence of an intermediate virtual positronium state which enhances the elastic interaction probability.

4.
J Med Chem ; 38(12): 2130-7, 1995 Jun 09.
Artigo em Inglês | MEDLINE | ID: mdl-7783144

RESUMO

The synthesis and structure-activity relationship (SAR) analysis of a novel series of trialkoxyaryl derivatives, as specific and competitive inhibitors of platelet activating factor (PAF), are described. Molecular modeling comparisons of PAF with the known antagonists Ginkgolide B and L-652731 led to the selection of N-[2-[(3,4,5-trimethoxybenzoyl)oxy]ethyl]-N,N,N-trimethylammonium iodide (1) from the Wellcome registry of compounds and to the synthesis of the lead compound N-[2-[[4-(hexyloxy)-3,5-dimethoxybenzoyl]oxy]ethyl]-N,N,N- trimethylammonium iodide (3, pKb 5.43). Further SAR considerations directed the design to 2-(hexyloxy)-1,3-dimethoxy-5-[4-(4-methylthiazol-5-yl)butyl] benzene (38) (pKb 7.14), a novel, specific, and competitive inhibitor of the PAF receptor in rabbit-washed platelets.


Assuntos
Fator de Ativação de Plaquetas/antagonistas & inibidores , Compostos de Amônio Quaternário/síntese química , Animais , Sítios de Ligação , Plaquetas/efeitos dos fármacos , Plaquetas/metabolismo , Células Cultivadas , Masculino , Inibidores da Agregação Plaquetária/farmacologia , Compostos de Amônio Quaternário/metabolismo , Compostos de Amônio Quaternário/farmacologia , Coelhos , Relação Estrutura-Atividade
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