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2.
Int Clin Psychopharmacol ; 16(2): 111-5, 2001 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-11236069

RESUMEN

Treatment of aggression in schizophrenic patients is a major challenge. We sought to examine the efficacy of augmentation of antipsychotic treatment with pindolol in the amelioration of aggression. Thirty male inpatients meeting DSM-IV criteria for schizophrenia, aged 20-65 years involved in four or more aggressive incidents in the two previous months, were enrolled in a double-blind crossover study. Aggression was evaluated per incident, with the Overt Aggression Scale (OAS). Positive and Negative Syndrome Scale (PANSS) was administered at baseline, crossover and at endpoint. Patients received either pindolol or placebo augmentation 5 mg x three times a day until crossover, then switched. No significant differences were found in the PANSS scores between the placebo and pindolol treatments. OAS scores were significantly reduced for number of aggressive incidents towards objects and other persons during pindolol treatment (0.59 versus 1.46, F = 6.09, P < 0.02; 1.96 versus 3.23, F = 4.17, P < 0.05, respectively). Similar results were obtained for severity of incidents (0.89 versus 3.58, F = 19.42, P < 0.0001; 2.89 versus 6.85, F = 10.11, P < 0.004, respectively). Pindolol, with its dual beta and 5-HT1A blocking effect ameliorated both number and severity of aggressive acts. Influence on severity may be associated with a 5-HT1A antagonistic effect.


Asunto(s)
Agresión/efectos de los fármacos , Pindolol/farmacología , Esquizofrenia/complicaciones , Antagonistas de la Serotonina/farmacología , Administración Oral , Adulto , Anciano , Estudios Cruzados , Método Doble Ciego , Humanos , Masculino , Persona de Mediana Edad , Esquizofrenia/tratamiento farmacológico , Índice de Severidad de la Enfermedad , Resultado del Tratamiento
3.
J Clin Psychiatry ; 61(11): 880-9; quiz 890, 2000 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-11105747

RESUMEN

BACKGROUND: Although treatment of severe mental disorders should strive to optimize quality of life (QOL) for the individual patient, little is known about variations in QOL domains and related psychopathologic and psychosocial factors in patients suffering from schizophrenia, schizoaffective disorder, and/or mood disorders. We hypothesized that QOL in severe mental disorder patients would have a more substantial relationship with psychosocial factors than with illness-associated factors. METHOD: A case-control, cross-sectional design was used to examine QOL of 210 inpatients who met DSM-IV criteria for a severe mental disorder and who were consecutively admitted to closed, open, and rehabilitation wards. Following psychiatric examination, 210 inpatients were assessed using standardized self-report measures of QOL, insight, medication side effects, psychological distress, self-esteem, self-efficacy, coping, expressed emotion, and social support. QOL ratings for patients and a matched control group (175 nonpatients) were compared. Regression and factor analyses were used to compare multidimensional variables between patients with schizophrenia and schizoaffective and mood disorders. RESULTS: In all QOL domains, patients were less satisfied than nonpatient controls. Patients with schizophrenia reported less satisfaction with social relationships and medication when compared with patients with schizoaffective and/or mood disorders. Regression analysis established differential clusters of predictors for each group of patients and for various domains of QOL. On the basis of the results of factor analysis, we propose a distress protection model to enhance life satisfaction for severe mental disorder patients. CONCLUSION: Psychosocial factors rather than psychopathologic symptoms affect subjective QOL of hospitalized patients with severe mental disorders. The findings enable better understanding of the combining effects of psychopathology and psychosocial factors on subjective life satisfaction and highlight targets for more effective intervention and rehabilitation.


Asunto(s)
Estado de Salud , Trastornos Mentales/diagnóstico , Trastornos Mentales/psicología , Inventario de Personalidad/estadística & datos numéricos , Calidad de Vida , Adaptación Psicológica , Adolescente , Adulto , Actitud Frente a la Salud , Estudios de Casos y Controles , Estudios Transversales , Emoción Expresada , Análisis Factorial , Femenino , Indicadores de Salud , Hospitalización , Humanos , Masculino , Persona de Mediana Edad , Trastornos Psicóticos/clasificación , Trastornos Psicóticos/diagnóstico , Trastornos Psicóticos/psicología , Esquizofrenia/clasificación , Esquizofrenia/diagnóstico , Psicología del Esquizofrénico , Autoeficacia , Índice de Severidad de la Enfermedad , Apoyo Social
4.
J Clin Psychopharmacol ; 20(3): 325-7, 2000 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-10831019

RESUMEN

The risk of sudden death during clozapine treatment is controversial. The authors present a review of sudden deaths that occurred at Sha'ar Menashe Mental Health Center between January 1991 and August 1997. The number of cases of deceased inpatients was retrieved from the hospital's computerized database and divided into three groups: sudden death, suicide, and disease-related death. Copies of mandatory reports of sudden death filed with the Ministry of Health were obtained, and the corresponding patient records were reviewed. The rates of sudden death, suicide, and disease-related deaths were calculated for clozapine-treated patients (CTPs) during and after treatment and for patients treated with other psychiatric agents (non-CTPs). Among 561 CTPs, there were 4 sudden deaths during treatment, 2 sudden deaths after treatment, 2 suicides during treatment, and 2 disease-related deaths during treatment. Among 4918 non-CTPs, there were 14 sudden deaths, 5 suicides, and 86 disease-related deaths, all of which occurred during treatment with other psychiatric agents. CTPs who experienced sudden death were 10.37 years younger and healthier than non-CTPs who experienced sudden death. The sudden death rate was 3.8 times higher for CTPs than for non-CTPs, whereas the rate of disease-related death was 5 times higher for non-CTPs than for CTPs. Contrary to expectations, the rate of suicide among patients currently receiving clozapine in this sample was 3.6 times higher than among non-CTPs. Because CTPs who experienced sudden death were also younger and healthier, it seems that treatment with clozapine may present a greater risk for sudden death than treatment with other psychiatric medications. The limited number of sudden death cases and deaths from other causes should be noted so that these findings are considered with caution.


Asunto(s)
Antipsicóticos/efectos adversos , Clozapina/efectos adversos , Muerte Súbita/epidemiología , Muerte Súbita/etiología , Anciano , Humanos , Israel/epidemiología , Masculino , Persona de Mediana Edad , Suicidio/estadística & datos numéricos
5.
Am J Med Genet ; 88(6): 628-33, 1999 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-10581481

RESUMEN

Although aggressive, violent, and dangerous behavior in man has multifactorial causes, genetic factors are estimated by twin and adoption studies to substantially contribute to the development of such conduct. Recently, homozygosity of a low enzyme activity variant of the catechol O-methyltransferase (COMT) gene was reported to be associated with aggressive behavior in a group of schizophrenic patients. We observe a similar tendency in a group of 30 schizophrenic patients who were confined to a maximum-security psychiatric facility for homicide. Significant excess (46.7% versus 21.0%) homozygosity of the low activity COMTmet/met genotype was observed in 30 mostly male (28 of 30) homicidal schizophrenic patients compared with 415 control subjects (Pearson chi(2) = 10.53, P = 0.005, df = 2). No difference in COMT genotype was found between 62 nonviolent schizophrenic patients and the 415 control subjects (chi(2) = 0.963, P > 0.1, df = 2). A trend for excess (46.7% versus 25.8%) homozygosity of the low activity COMTmet/met genotype was also observed when the homicidal schizophrenic subjects were compared directly with the nonviolent schizophrenic patients (chi(2) = 4.03, P = 0.1, df = 2). Similarly, an excess of the low activity COMTmet allele was observed in homicidal versus nonviolent schizophrenic patients (chi(2) = 2.92, P = 0.087, df = 2). Similar results were obtained if only male subjects were examined. No significant difference was found between control (257 Ashkenazi and 152 non-Ashkenazi Jews) COMT genotypes in the two principal ethnic groups examined (chi(2) = 3.79, P > 0.1, df = 2). Finally, no association was observed between homicidal behavior in schizophrenic patients and the dopamine D4 exon III repeat length polymorphism (D4DR) and the serotonin transporter promoter-region polymorphism (5-HTTLPR). Am. J. Med. Genet. (Neuropsychiatr. Genet.) 88:628-633, 1999.


Asunto(s)
Catecol O-Metiltransferasa/genética , Catecol O-Metiltransferasa/metabolismo , Homicidio/psicología , Proteínas de Transporte de Membrana , Proteínas del Tejido Nervioso , Polimorfismo Genético/genética , Esquizofrenia/genética , Adulto , Alelos , Proteínas Portadoras/genética , Femenino , Frecuencia de los Genes , Homocigoto , Humanos , Judíos/genética , Masculino , Glicoproteínas de Membrana/genética , Metionina/genética , Persona de Mediana Edad , Regiones Promotoras Genéticas/genética , Receptores de Dopamina D2/genética , Receptores de Dopamina D4 , Secuencias Repetitivas de Ácidos Nucleicos/genética , Esquizofrenia/enzimología , Proteínas de Transporte de Serotonina en la Membrana Plasmática , Caracteres Sexuales , Violencia/psicología
6.
Aviat Space Environ Med ; 67(1): 61-2, 1996 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-8929205

RESUMEN

We present the case of an aviator with Kleine Levin syndrome (KLS). History, physical examination, and special studies presented confirm the diagnosis of this syndrome. Our patient presented as an atypical case of KLS with respect to the presenting symptoms and to frequency of the episodes (6 years apart). He exhibited only intense somnolence, easy arousability, photophobia, hyperacousis, and a voracious appetite. Following a complete medical work up we recommended that an applicant with such a classical case of KLS be disqualified as a crewmember; however, in cases such as that presented above a limited waiver may be considered. The aeromedical significance of this case is to reinforce the importance of screening candidates and seeking precise diagnosis of a past illness or hospitalization.


Asunto(s)
Medicina Aeroespacial , Síndrome de Kleine-Levin , Personal Militar , Adulto , Evaluación de la Discapacidad , Humanos , Israel , Síndrome de Kleine-Levin/diagnóstico , Síndrome de Kleine-Levin/fisiopatología , Masculino
7.
Chem Phys Lipids ; 57(1): 17-27, 1991.
Artículo en Inglés | MEDLINE | ID: mdl-2060061

RESUMEN

Calcium binding to bile salt monomers and micelles is an important issue with respect to the possible (but rare) precipitation of calcium bile salts in the gallbladder. In the present work the binding of Ca2+ to six bile salts was measured in solutions containing 2 to 100 mM bile salts by means of a calcium-sensitive dye, murexide, which determines the ionic calcium concentration. In solutions containing bile salt at concentration higher than 20 mM most, if not all, of the bound Ca2+ is associated with micellar surfaces. The results were analyzed by employing a model which combines specific binding with electrostatic equations and accounts for the system being a closed one. The analysis of Ca2+ binding data considered explicitly the presence of Na+ ions and yielded intrinsic binding coefficients for Ca2+ and Na+ which were utilized to explain and predict binding results for various concentrations of Ca2+, Na+ and bile salts. The calculations indicate that in saline solutions most of the surface sites were bound by Na+, whereas less than 10% were bound by Ca2+ even in the presence of 8 mM Ca2+. The binding of Ca2+ to bile salt micelles increases with pH. An increase in temperature results in reduced binding affinity of Ca2+ to the bile salt micelles.


Asunto(s)
Ácidos y Sales Biliares/metabolismo , Calcio/metabolismo , Ácidos Cólicos/metabolismo , Electrodos , Concentración de Iones de Hidrógeno , Cinética , Micelas , Modelos Biológicos , Sodio/metabolismo , Temperatura
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