Literature DB >> 11055053

[Burden and quality of life in carers of patients with Alzheimer type dementia].

J Garre-Olmo1, M Hernández-Ferrándiz, M Lozano-Gallego, J Vilalta-Franch, A Turón-Estrada, M M Cruz-Reina, G Camps-Rovira, S López-Pousa.   

Abstract

OBJECTIVE: To analyze the factors which affect the burden and quality of life in carers of patients with Alzheimer's disease.
MATERIAL AND METHODS: From a sample of 234 carers of patients in the Unit for Assessment of Memory and Dementia with a diagnosis of probable Alzheimer's disease, according to the scale of National Institute of Neurological and Communicative Disorders and Stroke/Alzheimer's Disease and Related Disorders Association (NINCS-ADRDA), and of minimal or slight severity, according to the Cambridge Mental Disorders of the Elderly Examination (CAMDEX) criteria, we obtained sociodemographic variables and administered the following questionnaires: Neuropsychiatric Inventory (NPI), Rapid Disability Rating Scale (RDRS-2), Quality of Life Questionnaire (QLQ) and Burden Interview (BI).
RESULTS: The sex of the carers, the hours of attention to the basic activities of daily life (BADL) and the Cambridge Cognitive Examination (CAMCOQ), Minimental State Examination (MMSE), QLQ, NPI and RDRS-2 scores were related to the BI score. Multiple regression accepted the scoring for NPI, RDRS-2 and QLQ in the model. The QLQ score was associated with male sex of the patient, the age of the carer, employment status, whether or not he lived with the patient, with the family relationship, the hours of attention to the BADL and the scores on CAMCOG, MMSE, RDRS-2, NPI and BI. The multiple regression model included the age of the carer, the BI score and the hours of attention to the BADL.
CONCLUSION: The non-cognitive symptoms, functional disability and poor perception of quality of life are factors affecting the burden and age of the carer, the hours of attention to the BADL and the burden affecting quality of life.

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Year:  2000        PMID: 11055053

Source DB:  PubMed          Journal:  Rev Neurol        ISSN: 0210-0010            Impact factor:   0.870


  5 in total

1.  [Perception, attitudes and needs of Primary Care professionals as regards the patient with dementia].

Authors:  Gabriel Coll de Tuero; Josep Garre-Olmo; Secundí Lòpez-Pousa; Joan Vilalta; Ester Limon; Carmen Caja
Journal:  Aten Primaria       Date:  2011-03-09       Impact factor: 1.137

Review 2.  Quality of life in caregivers of patients with schizophrenia: a literature review.

Authors:  Alejandra Caqueo-Urízar; José Gutiérrez-Maldonado; Claudia Miranda-Castillo
Journal:  Health Qual Life Outcomes       Date:  2009-09-11       Impact factor: 3.186

3.  Caregiver Burden and its Determinants among the Family Members of Patients with Dementia in Iran.

Authors:  Ibrahim Abdollahpour; Maryam Noroozian; Saharnaz Nedjat; Reza Majdzadeh
Journal:  Int J Prev Med       Date:  2012-08

4.  Development of a caregiver burden questionnaire for the patients with dementia in iran.

Authors:  Ibrahim Abdollahpour; Saharnaz Nedjat; Maryam Noroozian; Banafsheh Golestan; Reza Majdzadeh
Journal:  Int J Prev Med       Date:  2010

5.  Psychosocial Adjustment of In-Home Caregivers of Family Members with Dementia and Parkinson's Disease: A Comparative Study.

Authors:  María Cristina Lopes Dos Santos; María Victoria Navarta-Sánchez; José Antonio Moler; Ignacio García-Lautre; Sagrario Anaut-Bravo; Mari Carmen Portillo
Journal:  Parkinsons Dis       Date:  2020-04-28
  5 in total

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