The DOI matches its Crossref record; 23 of the 23 references it cites were found in a registry or an index.
Burden, depression, and anxiety in caregivers of people with amyotrophic lateral sclerosis
Abstract
Amyotrophic lateral sclerosis (ALS) is a progressive and fatal neurodegenerative disease caused by the degeneration of motor neurons. The burden for ALS caregivers is quite high. There are still few studies that have investigated the emotional impact of ALS care. We conducted a cross-sectional study among 40 ALS caregivers, assessing general worries, burden of care, depression, anxiety, perception of social support, and patients' severity of disease. Caregiver burden, depression, and anxiety were positively related with each other, and all these variables had a negative relation with social support. Patient's loss of physical functions was positively related with caregiver burden, anxiety, and somatic expression of depression. Caregivers expressed worries for their own health conditions. Given these results, we consider the hypothesis of an emotional-somatic impact of ALS care. The implications and limitations are discussed.
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In the citing paper
“Previous research has shown that psychological distress and feelings of burden of ALS caregivers are associated with disease characteristics of the patient (i.e. physical and behavioral problems) but also with characteristics of the caregivers themselves, such as their coping style or whether they find positive meaning in caregiving [7, 9, 11–15].”
In the citing paper
“This effect is consistent with research of burden over time in MND family carers [15-17].”
From Feasibility, acceptability and potential effectiveness of dignity therapy for family carers of people with motor neurone disease (2014) · cites this paper as [15]
In the citing paper
“Moreover, carer burden increases in MND family carers over time as patient function declines [15-17].”
From Feasibility, acceptability and potential effectiveness of dignity therapy for family carers of people with motor neurone disease (2014) · cites this paper as [15]
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El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis
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A longitudinal study on quality of life and depression in ALS patient–caregiver couples
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Clinical diagnosis and management of amyotrophic lateral sclerosis
Hardiman, O. M., van den Berg, L. H., & Kiernan, M. C. (2011) · Nature Reviews Neurology · doi:10.1038/nrneurol.2011.153 · Cited by 618
del-Pino-Casado, R., Priego-Cubero, E., López-Martínez, C., & Orgeta, V. (2021) · PLOS ONE · doi:10.1371/journal.pone.0247143 · Cited by 331
“, 2010 [86] 40 Cross-sectional Multiple sclerosis ZBI STAI Palacio et al.”
BackgroundThe cognitive profile of ALS: a systematic review and meta-analysis update
Beeldman, E., Raaphorst, J., Klein Twennaar, M., de Visser, M., Schmand, B. A., & de Haan, R. J. (2016) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp-2015-310734 · Cited by 313
Caregiver burden in amyotrophic lateral sclerosis: A systematic review
de Wit, J., Bakker, L. A., van Groenestijn, A. V., van den Berg, L. H., Schröder, C., Visser-Meily, J. A., & Beelen, A. (2017) · Palliative Medicine · doi:10.1177/0269216317709965 · Cited by 153
Lillo, P., Mioshi, E., & Hodges, J. R. (2012) · BMC Neurology · doi:10.1186/1471-2377-12-156 · Cited by 157
Metadata
- Authors
- Pagnini, F., Rossi, G., Lunetta, C., Banfi, P., Castelnuovo, G., Corbo, M., & Molinari, E.
- Affiliations
- Università Cattolica del Sacro Cuore (IT)
- Azienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda (IT)
- Corresponding author
- Pagnini, Francesco
- ORCID
- Venue
- Psychology, Health & Medicine
- Publisher
- Informa UK Limited
- Published
- 2010-12
- Volume
- 15
- Issue
- 6
- Pages
- 685-693
- ISSN
- 1354-8506 (ISSN-L)
- 1465-3966
- OpenAlex
- W1985871185
- Cited by
- 139
- References
- 23
- Citations by year
- 2026: 6 · 2025: 11 · 2024: 7 · 2023: 13 · 2022: 6 · 2021: 12 · 2020: 14 · 2019: 3 · 2018: 6 · 2017: 6 · 2016: 11 · 2015: 12 · 2014: 13 · 2013: 5 · 2012: 11
- FWCI
- 14.00
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Psychology Health & Medicine (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Nursing › Research and Theory › Nursing care and research
- Health Sciences › Medicine › Clinical Neurology › Amyotrophic Lateral Sclerosis Research
- Social Sciences › Psychology › Clinical Psychology › Family Caregiving in Mental Illness
- Keywords
- amyotrophic lateral sclerosis, caregiver burden, depression, anxiety, social support, emotional impact of caregiving, somatic symptoms of depression, disease severity
- MeSH terms
- Aged, Amyotrophic Lateral Sclerosis, Anxiety, Cross-Sectional Studies, Depression, Female, Humans, Italy, Male, Middle Aged, Surveys and Questionnaires, Caregivers, Cost of Illness
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