Literature DB >> 22697366

Determinants of quality of life in Alzheimer's disease: perspective of patients, informal caregivers, and professional caregivers.

Maria Gómez-Gallego1, Jesus Gómez-Amor, Juan Gómez-García.   

Abstract

BACKGROUND: Alzheimer's disease (AD) is a chronic medical condition with symptoms that compromise patients' quality of life (QoL). The identification of the factor predicting QoL in AD is essential to develop more effective interventions. Recent research suggests that these factors could be different for the distinct informants. This study explores the QoL predictors considering three different sources of information: patients, caregivers, and healthcare staff.
METHODS: In this cross-sectional study, a sample of 102 patients, their primary caregivers, and 15 members of the healthcare staff evaluated patients' QoL (QoL-AD Scale). Patients' and caregivers' demographic and clinical data (cognitive function, neuropsychiatric symptoms, depression, and caregivers' burden) were considered as QoL predictors.
RESULTS: In multivariate-adjusted linear regression analyses, we observed that patients' ratings were mainly affected by their mood whereas caregivers' ratings were also negatively influenced by patients' irritability and burden. According to staff ratings, both psychotic symptoms and neuroleptics were associated with lower QoL.
CONCLUSIONS: Our findings suggest that depression is the main variable related to patients' QoL and that more careful management of neuropsychiatric disorders is necessary. Both proxies' ratings are not equivalent to patients' reports in terms of predictors but they are complementary. Thus, a thorough QoL assessment should consider separately the perspective of the different informants.

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Year:  2012        PMID: 22697366     DOI: 10.1017/S1041610212001081

Source DB:  PubMed          Journal:  Int Psychogeriatr        ISSN: 1041-6102            Impact factor:   3.878


  15 in total

1.  Addressing the bias problem in the assessment of the quality of life of patients with dementia: determinants of the accuracy and precision of the proxy ratings.

Authors:  M Gomez-Gallego; J Gomez-Garcia; E Ato-Lozano
Journal:  J Nutr Health Aging       Date:  2015-03       Impact factor: 4.075

2.  Before Hospice: Symptom Burden, Dementia, and Social Participation in the Last Year of Life.

Authors:  Halima Amjad; Scott H Snyder; Jennifer L Wolff; Esther Oh; Quincy M Samus
Journal:  J Palliat Med       Date:  2019-05-06       Impact factor: 2.947

Review 3.  Caregiver Burden in Different Stages of Alzheimer's Disease.

Authors:  Elif Koca; Özlem Taşkapilioğlu; Mustafa Bakar
Journal:  Noro Psikiyatr Ars       Date:  2017-03-01       Impact factor: 1.339

4.  Characteristics Associated with Quality of Life in Long-Term Care Residents with Dementia: A Cross-Sectional Study.

Authors:  Maartje S Klapwijk; Monique A A Caljouw; Marjoleine J C Pieper; Jenny T van der Steen; Wilco P Achterberg
Journal:  Dement Geriatr Cogn Disord       Date:  2016-09-27       Impact factor: 2.959

5.  Comparing the health state preferences of older persons, informal caregivers and healthcare professionals: a vignette study.

Authors:  Cynthia S Hofman; Peter Makai; Jeanet W Blom; Han Boter; Bianca M Buurman; Marcel G M Olde Rikkert; Rogier Donders; René J F Melis
Journal:  PLoS One       Date:  2015-03-04       Impact factor: 3.240

6.  Developing a proxy version of the Adult social care outcome toolkit (ASCOT).

Authors:  Stacey Rand; James Caiels; Grace Collins; Julien Forder
Journal:  Health Qual Life Outcomes       Date:  2017-05-19       Impact factor: 3.186

7.  Disease severity accounts for minimal variance of quality of life in people with dementia and their carers: analyses of cross-sectional data from the MODEM study.

Authors:  Nicolas Farina; Derek King; Clare Burgon; Sharne Berwald; Elizabeth Bustard; Yvonne Feeney; Ruth Habibi; Adelina Comas-Herrera; Martin Knapp; Sube Banerjee
Journal:  BMC Geriatr       Date:  2020-07-06       Impact factor: 3.921

8.  Quality of life in mild dementia: patterns of change in self and caregiver ratings over time.

Authors:  Marcia C Dourado; Maria F de Sousa; Raquel L Santos; José P Simões; Marcela L Nogueira; Tatiana T Belfort; Bianca Torres; Rachel Dias; Jerson Laks
Journal:  Braz J Psychiatry       Date:  2016-01-08       Impact factor: 2.697

9.  Establishing a composite endpoint for measuring the effectiveness of geriatric interventions based on older persons' and informal caregivers' preference weights: a vignette study.

Authors:  Cynthia S Hofman; Peter Makai; Han Boter; Bianca M Buurman; Anton J M de Craen; Marcel G M Olde Rikkert; Rogier A R T Donders; René J F Melis
Journal:  BMC Geriatr       Date:  2014-04-18       Impact factor: 3.921

10.  Perspectives of nursing professionals and older adults differ on aspects of care for older people after a nationwide improvement program.

Authors:  Lisanne Marlieke Verweij; Rik Wehrens; Lieke Oldenhof; Roland Bal; Anneke L Francke
Journal:  BMC Health Serv Res       Date:  2018-05-02       Impact factor: 2.655

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