RESUMEN
Objective: The aim of the present study was to investigate the coping strategies, mood characteristics and the association between these aspects in patients diagnosed with multiple sclerosis and healthy subjects. Method: Fifty consecutive patients who were diagnosed with multiple sclerosis according to McDonald criteria and thirty-one healthy subjects were included in the study. In addition to the sociodemographic form, Expanded Disability Status Scale (EDSS), Coping Orientation for Problem Experiences Scale (COPE), and Profile of Mood States (POMS) tests were applied to the participants. Results: Non-functional coping strategies were significantly higher in the secondary-progressive type (p≤0.05). Depression-dejection, fatigue-inertia and total POMS scores were significantly higher in the secondary-progressive type (p≤0.05). Conclusion: The results of our study demonstrate the importance of rehabilitation programs that encourage exercise among patients with multiple sclerosis to increase vigor-activity levels. .
Objetivo: Investigar as estratégias de enfrentamento, as características de humor e a associação entre estes aspectos em pacientes com diagnóstico de esclerose múltipla em comparação a indivíduos saudáveis. Método: Foram incluídos no estudo 50 pacientes com diagnóstico de esclerose múltipla de acordo com os critérios de McDonald e 31 pessoas saudáveis. Além da caracterização sócio-econômica, foram aplicados a todos os pacientes testes para avaliar o Expanded Disability Status Scale (EDSS), o Coping Orientation for Problem Experiences Scale (COPE) e o Profile of Mood States (POMS). Resultados: Escores referentes a estratégias de enfrentamento não funcionais foram significativamente maiores na forma secundariamente progressiva (p≤0.05). Escores relativos a depressão-abatimento, fadiga-inércia e escores totais POMS foram significativamente maiores na forma secundariamente progressiva (p≤0.05). Conclusão: Os resultados deste estudo mostram a importância de programas de reabilitação que encorajem os pacientes com esclerose múltipla a praticar exercícios com maiores níveis de vigor e atividade. .
Asunto(s)
Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Adaptación Psicológica , Afecto , Esclerosis Múltiple/psicología , Estudios de Casos y Controles , Evaluación de la Discapacidad , Depresión/psicología , Esclerosis Múltiple/rehabilitación , Pruebas Psicológicas , Calidad de Vida , Factores Sexuales , Factores Socioeconómicos , Encuestas y CuestionariosRESUMEN
Sneddon syndrome (SS) is rare, arterio-occlusive disorder characterized by generalized livedo racemosa of the skin and various central nervous symptoms due to occlusion of medium-sized arteries of unknown. Seizure, cognitive impairment, hypertension, and history of repetitive miscarriages are the other symptoms seen in this disease. Livedo racemosa involves persisting irreversible skin lesions red or blue in color with irregular margins. Usually, SS occurs in women of childbearing age. Protein S deficiency is an inherited or acquired disorder associated with an increased risk of thrombosis. We present a 33-year-old woman with SS with diffuse livedo racemosa, recurrent cerebrovascular diseases, migraine-type headache, sinus vein thrombosis, and protein S deficiency. Protein S deficiency and with Sneddon syndrome rarely encountered in the literature.