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.
Titolo: | Caregiver burden and patients' perception of being a burden in ALS | |
Autori Riconosciuti: | ||
Autori: | A. Chio; A. Gauthier; A. Calvo; P. Ghiglione; R. Mutani | |
Data di pubblicazione: | 2005 | |
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. | |
Volume: | 64 | |
Pagina iniziale: | 1780 | |
Pagina finale: | 1782 | |
Digital Object Identifier (DOI): | 10.1212/01.WNL.0000162034.06268.37 | |
Parole Chiave: | Sclerosi laterale amiotrofica; caregiver; burden | |
Rivista: | NEUROLOGY | |
Appare nelle tipologie: | 03A-Articolo su Rivista |
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