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Carers of patients with a diagnosis of depression, aged 60 or over, were assessed for burden (Burden Interview), emotional distress (SRQ-20) and their perception of patients’ behavioral and mood disturbances (Behavioral and Mood Disturbance Scale - BMD). Socio-demographic information of patients and carers was collected with a standardized form. The reliability of the Burden Interview was assessed through its internal consistency. Construct validity was assessed through the exam of the associations of carers’ burden with their perception of patients’ behavioral and mood disturbances, and the carers’ burden with carers’ distress. Eighty-two carers of elderly patients with depression were included, being forty-eight (58,5%) women. The internal consistency was good, with a Cronbach’s alpha of 0.87. The associations between total scores of the Burden Interview and total scores of the SRQ-20 (r=0.37, p=0.001), and between total scores of the Burden Interview with total scores of BMD (r=0.54, p=0.001) were strong, and similar to other studies that examined those associations, indicating a good construct validity of the Brazilian version of the Burden Interview.
Is one of the mostly used scales for burden assessment in carers of elderly patients with demen- tia. Despite being developed from its authors’ clinical and re- search experience with elderly patients with dementia and their relatives, its items are comprehensive and deal with dimensions common to several mental and physical illnesses. Therefore, the ‘BI’ has been used to assess the burden of carers of elderly patients with dement ia and of elderl y people and adults with other mental and physical diseases, such as people who sur- vived a stroke, people who have chronic illnesses and carers’ burden of subara cnoid hemorr hagic patients. The 22 items reflect respondent’ s areas of concern such as: health, social and personal life, financial situation, emotional well being and interpersonal relationships. Items measure the objective and subjective burden reported by the carer but dif- ferent scores are not obtained. The subjective way in which items are written favors the carer’s emotional answer.
The scale’s last item is a general one, in which the respondent is asked to assess how much he/she considers to be burdened due to his/her caretaker role.
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