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1.
Acta Psychiatr Scand ; 137(1): 39-46, 2018 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-29072776

RESUMO

OBJECTIVE: Treatment resistance is a challenge for the management of schizophrenia. It is not always clear whether inadequate response is secondary to medication ineffectiveness, as opposed to medication underexposure due to non-adherence or pharmacokinetic factors. We investigated the prevalence of subtherapeutic antipsychotic plasma levels in patients identified as treatment-resistant by their treating clinician. METHOD: Between January 2012 and April 2017, antipsychotic plasma levels were measured in 99 individuals provisionally diagnosed with treatment-resistant schizophrenia by their treating clinicians, but not prescribed clozapine. Patients were followed up to determine whether they were subsequently admitted to hospital. RESULTS: Thirty-five per cent of plasma levels were subtherapeutic, and of these, 34% were undetectable. Black ethnicity (P = 0.006) and lower dose (P < 0.001) were significantly associated with subtherapeutic/undetectable plasma levels. Individuals with subtherapeutic/undetectable levels were significantly more likely to be admitted to hospital (P = 0.02). CONCLUSION: A significant proportion of patients considered treatment-resistant have subtherapeutic antipsychotic plasma levels, and this is associated with subsequent admission. The presence of subtherapeutic plasma levels may suggest a need to address adherence or pharmacokinetic factors as opposed to commencing clozapine treatment. While antipsychotic levels are not recommended for the routine adjustment of dosing, they may assist with the assessment of potential treatment resistance in schizophrenia.


Assuntos
Antipsicóticos/uso terapêutico , Transtornos Psicóticos/tratamento farmacológico , Esquizofrenia/tratamento farmacológico , Adulto , Negro ou Afro-Americano , Idoso , Antipsicóticos/sangue , Relação Dose-Resposta a Droga , Feminino , Hospitalização/estatística & dados numéricos , Humanos , Estimativa de Kaplan-Meier , Modelos Logísticos , Masculino , Adesão à Medicação , Pessoa de Meia-Idade , Farmacocinética , Falha de Tratamento , Resultado do Tratamento , População Branca , Adulto Jovem
2.
Transl Psychiatry ; 7(2): e1024, 2017 02 07.
Artigo em Inglês | MEDLINE | ID: mdl-28170004

RESUMO

An interaction between external stressors and intrinsic vulnerability is one of the longest standing pathoaetiological explanations for schizophrenia. However, novel lines of evidence from genetics, preclinical studies, epidemiology and imaging have shed new light on the mechanisms that may underlie this, implicating microglia as a key potential mediator. Microglia are the primary immune cells of the central nervous system. They have a central role in the inflammatory response, and are also involved in synaptic pruning and neuronal remodeling. In addition to immune and traumatic stimuli, microglial activation occurs in response to psychosocial stress. Activation of microglia perinatally may make them vulnerable to subsequent overactivation by stressors experienced in later life. Recent advances in genetics have shown that variations in the complement system are associated with schizophrenia, and this system has been shown to regulate microglial synaptic pruning. This suggests a mechanism via which genetic and environmental influences may act synergistically and lead to pathological microglial activation. Microglial overactivation may lead to excessive synaptic pruning and loss of cortical gray matter. Microglial mediated damage to stress-sensitive regions such as the prefrontal cortex and hippocampus may lead directly to cognitive and negative symptoms, and account for a number of the structural brain changes associated with the disorder. Loss of cortical control may also lead to disinhibition of subcortical dopamine-thereby leading to positive psychotic symptoms. We review the preclinical and in vivo evidence for this model and consider the implications this has for treatment, and future directions.


Assuntos
Encéfalo/imunologia , Inflamação/imunologia , Microglia/imunologia , Trauma Psicológico/imunologia , Esquizofrenia/imunologia , Psicologia do Esquizofrênico , Meio Social , Estresse Psicológico/imunologia , Animais , Encéfalo/metabolismo , Encéfalo/patologia , Encéfalo/fisiopatologia , Suscetibilidade a Doenças , Dopamina/metabolismo , Substância Cinzenta/imunologia , Substância Cinzenta/metabolismo , Substância Cinzenta/patologia , Substância Cinzenta/fisiopatologia , Hipocampo/imunologia , Hipocampo/metabolismo , Hipocampo/patologia , Hipocampo/fisiopatologia , Humanos , Neuroglia/imunologia , Plasticidade Neuronal , Trauma Psicológico/metabolismo , Trauma Psicológico/patologia , Trauma Psicológico/fisiopatologia , Esquizofrenia/metabolismo , Esquizofrenia/patologia , Esquizofrenia/fisiopatologia , Estresse Psicológico/metabolismo , Estresse Psicológico/patologia , Estresse Psicológico/fisiopatologia
3.
Psychopharmacology (Berl) ; 232(16): 2951-8, 2015 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-25899791

RESUMO

INTRODUCTION: The beta-adrenoceptor antagonist propranolol is known to reduce peripheral and central activity of noradrenaline. A recent study found that intervention with propranolol diminished negative implicit racial bias. MATERIALS AND METHOD: The current study used functional magnetic resonance imaging (fMRI) in order to determine the neural correlates of this effect. Healthy volunteers (N = 40) of white ethnic origin received a single oral dose (40 mg) of propranolol, in a randomised, double-blind, parallel group, placebo-controlled design, before viewing unfamiliar faces of same and other race. RESULTS AND DISCUSSION: We found significantly reduced activity in the fusiform gyrus and thalamus following propranolol to out-group faces only. Additionally, propranolol lowered the implicit attitude score, without affecting explicit prejudice measure. CONCLUSION: These findings suggest that noradrenaline pathways might modulate racial bias by acting on the processing of categorisation in the fusiform gyrus.


Assuntos
Antagonistas Adrenérgicos beta/farmacologia , Face , Preconceito , Propranolol/farmacologia , Lobo Temporal/efeitos dos fármacos , Negro ou Afro-Americano , Atitude , Método Duplo-Cego , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Estimulação Luminosa , Lobo Temporal/fisiologia , População Branca , Adulto Jovem
4.
Acta Psychiatr Scand ; 130(6): 427-38, 2014 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-25201058

RESUMO

OBJECTIVE: To describe a practical approach to the community management of treatment-resistant schizophrenia (TRS). METHOD: A descriptive review of an approach to the assessment and management of patients with TRS, including the community titration of clozapine treatment, and a report of the management recommendations for the first one hundred patients assessed by the Treatment REview and Assessment Team (TREAT). RESULTS: The standardized model for the community assessment, management and titration of clozapine is described. To date, 137 patients have been referred to this service and 100 patients (72%) attended for assessment. Of these, 33 have been initiated on clozapine while fifteen have had clozapine recommended but have not wished to undertake clozapine treatment. Other management options recommended have included augmentation strategies and long-acting injectable antipsychotics. CONCLUSION: The service had increased the number of patients receiving community assessment and initiation of clozapine by five-fold relative to the rate prior to the establishment of the service. The large number of referrals and high attendance rate indicates that there is clinical demand for the model. Systematic evaluation is required to determine the clinical and cost-effectiveness of this model and its potential application to other clinical settings.


Assuntos
Antipsicóticos/uso terapêutico , Clozapina/uso terapêutico , Serviços Comunitários de Saúde Mental/métodos , Transtornos Psicóticos/tratamento farmacológico , Esquizofrenia/tratamento farmacológico , Adulto , Gerenciamento Clínico , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Falha de Tratamento
6.
Int J Eat Disord ; 17(2): 197-200, 1995 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-7757102

RESUMO

Chewing and spitting out food is thought to be a common symptom among people with eating disorders but it has largely been neglected in recent research and diagnostic criteria. We present two cases where chewing and spitting out food was prominent. In each case the symptom differed in its presentation and in the function it served for the patient.


Assuntos
Bulimia/psicologia , Adulto , Idade de Início , Índice de Massa Corporal , Bulimia/terapia , Terapia Cognitivo-Comportamental , Ingestão de Energia , Feminino , Humanos
7.
Ann Emerg Med ; 16(9): 1037-41, 1987 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-3631668

RESUMO

Human reaction to cold stress and hypothermia involves shivering. Another form of overt shaking, postoperative shivering, has been attributed as a thermoregulatory response to postoperative hypothermia. Analysis of the normal human shivering pattern showed a synchronized, slow amplitude modulation (six to eight cycles/min) over all muscles sampled. In addition, there was a frequency of 8 to 10 Hz associated with each low-frequency amplitude modulation. EMG signals from postoperative patients revealed none of the major patterns seen in thermal-induced shivering. Cold-induced vasodilation also was studied and found to occur simultaneously in all cold-stressed fingers regardless of size or innervation. Thermal shivering and cold-induced vasodilation are considered to be manifestations of central neural oscillators.


Assuntos
Temperatura Baixa , Hipotermia/fisiopatologia , Estremecimento , Vasodilatação , Adolescente , Adulto , Período de Recuperação da Anestesia , Temperatura Corporal , Eletromiografia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Temperatura
10.
W V Dent J ; 47(4): 100-4, 1973 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-4520239
12.
Can Anaesth Soc J ; 15(4): 399-400, 1968 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-5661394
13.
J Am Pharm Assoc ; 8(5): 237-41 passim, 1968 May.
Artigo em Inglês | MEDLINE | ID: mdl-5649192
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