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Emotional Burden, Quality of Life, and Coping Styles in Care Givers of Patients with Disorders of Consciousness Living in Italy: Preliminary Data

Published online by Cambridge University Press:  06 December 2016

Caterina Romaniello*
Affiliation:
Santa Viola Hospital, Bologna, Italy Clinical Psychology Service, Villa Bellombra Rehabilitation Hospital, Bologna, Italy
Chiara Simoni
Affiliation:
Villa Bellombra Rehabilitation Hospital, Bologna, Italy
Marina Farinelli
Affiliation:
Clinical Psychology Service, Villa Bellombra Rehabilitation Hospital, Bologna, Italy
Erik Bertoletti
Affiliation:
Santa Viola Hospital, Bologna, Italy
Vincenzo Pedone
Affiliation:
Santa Viola Hospital, Bologna, Italy Villa Bellombra Rehabilitation Hospital, Bologna, Italy
Georg Northoff
Affiliation:
Mind, Brain Imaging and Neuroethics, Institute of Mental Health Research, University of Ottawa, ON, Canada
*
Address for correspondence: Dr. Caterina Romaniello, Ospedale Privato Accreditato Santa Viola, Via della Ferriera, 10, 40133 Bologna, Italy. E-mail: romaniello.caterina@gmail.com

Abstract

The literature about the care givers of patients with Disorders of Consciousness (DOCs) has highlighted the impact on both mental and physical dimensions of quality of life. This study aimed to: (1) describe emotional burden, quality of life, and coping styles in care givers of hospitalized patients with DOCs, compared to Italian normative data; (2) explore the relationships between these variables and their associations with socio-demographic features; and (3) describe their changes over time.

Fifteen care givers of patients with DOCs, mostly middle-aged women, were assessed using the Family Strain Questionnaire, the SF-36 Health Survey, and the Coping Orientation to Problems Experienced – Nuova Versione Italiana. Eleven subjects were also assessed after 6 and 12 months. Data were analysed through descriptive statistics, correlations, and nonparametric tests of group differences.

Compared to the Italian normative data, our sample showed a worse outcome in mental health, social functioning, global mental component, and emotional role functioning. Furthermore, subjects with high emotional burden had more thoughts of death compared to subjects with low emotional burden. Follow-up analyses revealed no variables changed over time.

These results highlight the need for psychological interventions and support, since care givers represent an important part of an all-embracing support and care network for patients with DOCs.

Type
Articles
Copyright
Copyright © Australasian Society for the Study of Brain Impairment 2016 

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