The determinants of ALS caregiver burden and the feeling of the patients as being a burden were assessed using the Caregiver Burden Inventory and the Self-Perceived Burden Scale in 60 caregiver-patient couples. Caregiver burden was correlated to their level of depression and quality of life and, differently from other chronic disorders, increased with the worsening of patients' disability. ALS patients have a good objective perception of their impact on caregivers.

Caregiver burden and patients' perception of being a burden in ALS

CHIO', Adriano;CALVO, Andrea;GHIGLIONE, paolo;MUTANI, Roberto
2005-01-01

Abstract

The determinants of ALS caregiver burden and the feeling of the patients as being a burden were assessed using the Caregiver Burden Inventory and the Self-Perceived Burden Scale in 60 caregiver-patient couples. Caregiver burden was correlated to their level of depression and quality of life and, differently from other chronic disorders, increased with the worsening of patients' disability. ALS patients have a good objective perception of their impact on caregivers.
2005
64
1780
1782
Sclerosi laterale amiotrofica; caregiver; burden
A. Chio; A. Gauthier; A. Calvo; P. Ghiglione; R. Mutani
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/43313
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