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Acta Neurológica Colombiana

Print version ISSN 0120-8748On-line version ISSN 2422-4022

Abstract

ROJAS VILLEGAS, Yessika Milena et al. The caregiver burden of dementia patients in a military population: a descriptive study. Acta Neurol Colomb. [online]. 2020, vol.36, n.4, pp.223-231.  Epub Jan 17, 2021. ISSN 0120-8748.  https://doi.org/10.22379/24224022327.

BACKGROUND:

Dementia affects not only the person with the disease, also the caregiver, who represents a fundamental part in the management of patients with dementia.

OBJECTIVE:

The main objective of the present study was to describe the caregiver burden in a group of caregivers of patients with dementia at the Central Military Hospital, exploring possible associations between the burden and variables dependent on the care subject.

DESIGN:

Longitudinal descriptive study.

CONTEXT:

patients who come to a consultation at the Central Military Hospital between August 2016 and April 2018.

MEASUREMENTS:

Demographic data were obtained from the caregiver and the patient with dementia (binomial: caregiver - patient), the Zarit scale was applied for the measurement of the degree of caregiver burden, and functional assessment of the patient with dementia (using Barthel scale and Clinical Dementia Rating -CDR), hospital admissions of the patient with dementia were recorded during 1 year.

RESULTS:

50 caregivers and 50 patients with dementia were included in the study. 45 (90 %) caregivers were women, with an average age of 60 years (SD: 15 min-max 24-85). The caregiver burden was intense in 33 (66 %) caregivers, the feeling of self-abandonment was the main dimension of the burden reported. The higher burden is associated with the higher clinical deterioration of dementia (CDR = 3, P = 0.008), but not with the functional state on the Barthel scale.

Keywords : Dementia; Social Support; Caregivers; Alzheimer; Mental Status; Dementia Tests (MeSH).

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