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1.
J Clin Psychopharmacol ; 26(5): 462-6, 2006 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-16974185

RESUMEN

BACKGROUND: Increasing numbers of reports have raised concerns about significant increases in weight and adiposity over both short- and long-term treatment in patients treated with antipsychotics (APs). The management of overweight and obesity in patients treated with APs has included pharmacological interventions, dietary suggestions, and behavioral strategies. Nevertheless, current evidence does not support the use of pharmacological management of this specific type of obesity, and only a limited number of studies have been published regarding prevention and treatment of weight gain with other strategies. OBJECTIVE: The aim of this study was to evaluate the effectiveness of an educational intervention (EI) that combines low-calorie diet with increased physical activity to prevent and treat weight gain in patients treated with APs. METHOD: Data were from 53 subjects whose body mass index (BMI) had increased by more than 7% after starting an AP therapy and who consented to participate in a 12-week educational intervention study aimed at preventing further weight gain and, when possible, at inducing a weight loss. Weight and BMI were measured at baseline (at each of the monthly follow-up visits) and at study completion 12 weeks from entry in the study. RESULTS: Twenty-six patients completed the 12-week program. Completers showed a significant mean body weight decrease of 3.15 kg, with a mean BMI reduction of 1.2 (kg/m) at the end of the 3-month period. CONCLUSIONS: Educational intervention can be an important tool for the management of weight increase in patients treated with APs. A larger prospective and controlled study is now needed to confirm our findings.


Asunto(s)
Antipsicóticos/efectos adversos , Obesidad/terapia , Educación del Paciente como Asunto , Aumento de Peso/efectos de los fármacos , Adulto , Índice de Masa Corporal , Restricción Calórica , Terapia por Ejercicio , Femenino , Humanos , Masculino , Obesidad/inducido químicamente , Obesidad/prevención & control , Cooperación del Paciente
2.
Hum Psychopharmacol ; 20(6): 401-8, 2005 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-15991259

RESUMEN

Cognitive deficits are a fundamental feature of the schizophrenic disorder, but the effect of antipsychotic treatment is still debated. The study assesses the effect of olanzapine on neurocognitive functioning and symptomatology of patients with schizophrenic disorder residual type. Executive function evaluation by the Wisconsin card sorting test (WCST) was performed on 39 patients treated with olanzapine (5-20 mg/day); the efficacy of drug in improving symptomatology, safety and quality of life was also evaluated. After 7 months of treatment, the mean number of WCST categories tended to increase. Correct responses increased with a statistically significant change from the baseline. The total and unique errors decreased significantly. At all post-baseline visits a decrease from baseline in the PANSS total, positive and negative scores was seen. The proportion of patients with less severe illness (CGI), increased over the course of the study with a corresponding decrease of patients with more severe illness. The quality of life scores also tended to improve during treatment. The Simpson Angus scale, Barnes-akathisia and abnormal involuntary movement scale scores decreased consistently. The most common treatment emergent drug related adverse events were weight gain, insomnia, agitation and anxiety. Neurocognitive functioning in terms of executive performance and symptomatology improved in people with schizophrenia residual type.


Asunto(s)
Antipsicóticos/uso terapéutico , Cognición/efectos de los fármacos , Esquizofrenia/tratamiento farmacológico , Adulto , Anciano , Enfermedades de los Ganglios Basales/inducido químicamente , Benzodiazepinas/efectos adversos , Benzodiazepinas/uso terapéutico , Femenino , Humanos , Masculino , Persona de Mediana Edad , Olanzapina , Calidad de Vida , Psicología del Esquizofrénico
3.
Hum Psychopharmacol ; 19(8): 549-58, 2004 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-15378663

RESUMEN

OBJECTIVE: To review studies conducted to evaluate the risk of type 2 diabetes in patients treated with different antipsychotic drugs (AP). METHODS: a MEDLINE search (January 1985-February 2003) was conducted to establish the potential relationship between the exposure to AP (conventional and second generation) and the development of type 2 diabetes. Studies were classified according to their experimental design as prospective and retrospective (incidence and prevalence based). RESULTS: Twenty-one studies were selected: nine prospective and eleven retrospective. DATA SYNTHESIS AND CONCLUSIONS: Patients with schizophrenia treated with different AP have an increased risk of developing type 2 diabetes compared with the general population. The data so far available, however, do not establish whether the increasing risk of developing diabetes is a function of the schizophrenia itself or is induced by the antipsychotic treatment. A number of methodological flaws in the study design and data collection do not allow conclusions to be drawn on the risk between patients treated with conventional drugs versus those treated with new ones.


Asunto(s)
Antipsicóticos/efectos adversos , Diabetes Mellitus Tipo 2/inducido químicamente , Esquizofrenia/tratamiento farmacológico , Antipsicóticos/uso terapéutico , Sesgo , Estudios Transversales , Recolección de Datos/estadística & datos numéricos , Diabetes Mellitus Tipo 2/epidemiología , Humanos , Incidencia , Estudios Prospectivos , Estudios Retrospectivos , Riesgo , Esquizofrenia/epidemiología
4.
Ann Gen Hosp Psychiatry ; 3(1): 2, 2004 Feb 12.
Artículo en Inglés | MEDLINE | ID: mdl-14962351

RESUMEN

BACKGROUND: Fluoxetine was the first molecule of a new generation of antidepressants, the Selective Serotonin Re-uptake Inhibitors (SSRIs). It is recurrently the paradigm for the development of any new therapy in the treatment of depression. Many controlled studies and meta-analyses were performed on Fluoxetine, to improve the understanding of its real impact in the psychiatric area. The main objective of this review is to assess the quality and the results reported in the meta-analyses published on Fluoxetine. METHODS: Published articles on Medline, Embase and Cochrane databases reporting meta-analyses were used as data sources for this review.Articles found in the searches were reviewed by 2 independent authors, to assess if these were original meta-analyses. Only data belonging to the most recent and comprehensive meta-analytic studies were included in this review. RESULTS: Data, based on a group of 9087 patients, who were included in 87 different randomized clinical trials, confirms that fluoxetine is safe and effective in the treatment of depression from the first week of therapy. Fluoxetine's main advantage over previously available antidepressants (TCAs) was its favorable safety profile, that reduced the incidence of early drop-outs and improved patient's compliance, associated with a comparable efficacy on depressive symptoms. In these patients, Fluoxetine has proven to be more effective than placebo from the first week of therapy.Fluoxetine has shown to be safe and effective in the elderly population, as well as during pregnancy. Furthermore, it was not associated with an increased risk of suicide in the overall evaluation of controlled clinical trials.The meta-analysis available on the use of Fluoxetine in the treatment of bulimia nervosa shows that the drug is as effective as other agents with fewer patients dropping out of treatment.Fluoxetine has demonstrated to be as effective as chlomipramine in the treatment of Obsessive-Compulsive-Disorder (OCD). CONCLUSION: Fluoxetine can be considered a drug successfully used in several diseases for its favorable safety/efficacy ratio. As the response rate of mentally ill patients is strictly related to each patient's personal characteristics, any new drug in this area, will have to be developed under these considerations.

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