TY - JOUR
T1 - Burden, depression, and anxiety in caregivers of people with amyotrophic lateral sclerosis
AU - Pagnini, Francesco
AU - Rossi, G
AU - Lunetta, C
AU - Banfi, P
AU - Castelnuovo, Gianluca
AU - Corbo, M
AU - Molinari, Enrico
PY - 2010
Y1 - 2010
N2 - 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. © 2010 Taylor & Francis.
AB - 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. © 2010 Taylor & Francis.
KW - burden
KW - burden
UR - http://hdl.handle.net/10807/74784
UR - http://www.scopus.com/inward/record.url?eid=2-s2.0-78650140001&partnerid=40&md5=8303a91120334b49cef2e6fbf56a6d24
U2 - 10.1080/13548506.2010.507773
DO - 10.1080/13548506.2010.507773
M3 - Article
SN - 1354-8506
VL - 15
SP - 685
EP - 693
JO - PSYCHOLOGY, HEALTH & MEDICINE
JF - PSYCHOLOGY, HEALTH & MEDICINE
ER -