Literature DB >> 28631956

Coping strategies and psychological distress in caregivers of patients with Amyotrophic Lateral Sclerosis (ALS).

Mattia Siciliano1,2,3, Gabriella Santangelo1,4, Francesca Trojsi2, Carmela Di Somma1, Manila Patrone1, Cinzia Femiano2, Maria Rosaria Monsurrò2, Luigi Trojano1,5, Gioacchino Tedeschi2.   

Abstract

BACKGROUND: Amyotrophic lateral sclerosis (ALS) causes distress in caregivers. The present study aims to examine the association between coping strategies and psychological distress in caregivers of ALS patients.
METHODS: Coping strategies were assessed in 96 ALS informal caregivers by means of the Coping Inventory for Stressful Situations. Data about caregivers' demographic characteristics, levels of burden, depression and anxiety (psychological distress) were also gathered by standardised questionnaires. Patients' clinical, cognitive and behavioural disturbances were evaluated by ALS specific assessment tools.
RESULTS: Sequential logistic regression analysis showed that emotion-oriented coping strategy was significantly associated with high levels of depressive (p < 0.01) and anxiety (p < 0.05) symptoms and high levels of burden (p < 0.05), after controlling for all other variables. Moreover, a significant relationship of patients' functional dependence levels with burden experienced by caregivers was observed. No relationships were detected between task-oriented and avoidance-oriented coping strategies and caregivers' levels of psychological distress.
CONCLUSIONS: The present study supported the mediating effects of coping strategies on intensity of burden, depression and anxiety experienced by ALS caregivers. These findings suggest that interventions aimed at reducing utilisation of maladaptive coping strategies may improve well-being in ALS caregivers, and, possibly, management of symptoms in ALS patients.

Entities:  

Keywords:  Amyotrophic lateral sclerosis. coping strategies; ECAS; Edinburgh Cognitive and Behavioural ALS Screen; caregiver burden; psychological distress

Mesh:

Year:  2017        PMID: 28631956     DOI: 10.1080/21678421.2017.1285316

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler Frontotemporal Degener        ISSN: 2167-8421            Impact factor:   4.092


  8 in total

1.  Psychological Support for Family Caregivers of Patients With Amyotrophic Lateral Sclerosis at the Time of the Coronavirus Disease 2019 Pandemic: A Pilot Study Using a Telemedicine Approach.

Authors:  Minoo Sharbafshaaer; Daniela Buonanno; Carla Passaniti; Manuela De Stefano; Sabrina Esposito; Fabrizio Canale; Giulia D'Alvano; Marcello Silvestro; Antonio Russo; Gioacchino Tedeschi; Mattia Siciliano; Francesca Trojsi
Journal:  Front Psychiatry       Date:  2022-06-16       Impact factor: 5.435

2.  Inappropriate Metacognitive Status Increases State Anxiety in Genetic Counseling Clients.

Authors:  Yuka Shibata; Masaaki Matsushima; Megumi Takeuchi; Momoko Kato; Ichiro Yabe
Journal:  Front Psychol       Date:  2022-05-12

Review 3.  The Impact of Cognitive and Behavioral Symptoms on ALS Patients and Their Caregivers.

Authors:  Jashelle Caga; Sharpley Hsieh; Patricia Lillo; Kaitlin Dudley; Eneida Mioshi
Journal:  Front Neurol       Date:  2019-03-11       Impact factor: 4.003

4.  Traumatised, angry, abandoned but some empowered: a national survey of experiences of family caregivers bereaved by motor neurone disease.

Authors:  Samar M Aoun; Kerrie Noonan; Geoff Thomas; Bruce Rumbold
Journal:  Palliat Care Soc Pract       Date:  2021-08-30

5.  Analysing the influencing factors on caregivers' burden among amyotrophic lateral sclerosis patients in China: a cross-sectional study based on data mining.

Authors:  Ling Lian; Minying Zheng; Ruojie He; Jianing Lin; Weineng Chen; Zhong Pei; Xiaoli Yao
Journal:  BMJ Open       Date:  2022-09-21       Impact factor: 3.006

6.  Quality of life and mental health in the locked-in-state-differences between patients with amyotrophic lateral sclerosis and their next of kin.

Authors:  Elisa Aust; Katharina Linse; Sven-Thomas Graupner; Markus Joos; Daniel Liebscher; Julian Grosskreutz; Johannes Prudlo; Thomas Meyer; René Günther; Sebastian Pannasch; Andreas Hermann
Journal:  J Neurol       Date:  2022-07-06       Impact factor: 6.682

7.  Group interventions for amyotrophic lateral sclerosis caregivers in Ireland: a randomised controlled trial protocol.

Authors:  Tom Burke; Jennifer Wilson O'Raghallaigh; Sinead Maguire; Miriam Galvin; Mark Heverin; Orla Hardiman; Niall Pender
Journal:  BMJ Open       Date:  2019-09-20       Impact factor: 2.692

Review 8.  Support Needs and Interventions for Family Caregivers of Patients with Amyotrophic Lateral Sclerosis (ALS): A Narrative Review with Report of Telemedicine Experiences at the Time of COVID-19 Pandemic.

Authors:  Giulia D'Alvano; Daniela Buonanno; Carla Passaniti; Manuela De Stefano; Luigi Lavorgna; Gioacchino Tedeschi; Mattia Siciliano; Francesca Trojsi
Journal:  Brain Sci       Date:  2021-12-30
  8 in total

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