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Coping Style in Glioma Patients and Their Caregiver: Evaluation During Disease Trajectory

Background: Patients with glioma have a poor prognosis and, in a short period of time, have to deal with severe forms of disability, which compromise their psychological distress and quality of life. The caregivers of these patients consequently carry a heavy burden in terms of emotional and patient...

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Autores principales: Guariglia, Lara, Ieraci, Sonia, Villani, Veronica, Tanzilli, Antonio, Benincasa, Dario, Sperati, Francesca, Terrenato, Irene, Pace, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8440902/
https://www.ncbi.nlm.nih.gov/pubmed/34539556
http://dx.doi.org/10.3389/fneur.2021.709132
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author Guariglia, Lara
Ieraci, Sonia
Villani, Veronica
Tanzilli, Antonio
Benincasa, Dario
Sperati, Francesca
Terrenato, Irene
Pace, Andrea
author_facet Guariglia, Lara
Ieraci, Sonia
Villani, Veronica
Tanzilli, Antonio
Benincasa, Dario
Sperati, Francesca
Terrenato, Irene
Pace, Andrea
author_sort Guariglia, Lara
collection PubMed
description Background: Patients with glioma have a poor prognosis and, in a short period of time, have to deal with severe forms of disability, which compromise their psychological distress and quality of life. The caregivers of these patients consequently carry a heavy burden in terms of emotional and patient care. The study aims to evaluate the coping strategies of patients and their caregivers during the course of the disease in order to frame the adaptation process in a rapidly progressing pathology. Methods: A prospective study on 24 dyads of patients affected by malignant glioma and their caregivers was conducted between May 2016 and July 2018. Questionnaires designed to identify the coping style (MINI-MaC Scale) and psychological distress (HADS scores) and assess QOL (EQ-5D) were administered at two time points: at first lines of treatment and at disease recurrence. Results: Patients and their caregiver structure adaptive coping strategies during the disease: a coping style oriented toward a fighting spirit prevails at baseline (Mini-Mac Mean 3.23); fatalism prevails at recurrence (Mini-Mac Mean 3.03). Psychological distress affects the coping style expressed: high levels of anxiety symptoms were found to be significantly associated with a coping style oriented toward anxious preoccupation, helpless–hopeless, and fatalism; low depressive symptoms were inversely correlated with fighting spirit coping style. Patients' and caregivers' perceptions of quality of life were correlated between them and with performance status assessed by clinicians. In a dyadic perspective, the adaptation of a member of the couple varies as a function of the other partner's coping style. Conclusions: Our data are in line with previous literature on cancer patients, demonstrating that coping style is not a persistent dimension of personality, but can change depending on the situation. Despite the disease rapid course, patients and their caregivers can structure adaptive and functional defenses to manage the disease.
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spelling pubmed-84409022021-09-16 Coping Style in Glioma Patients and Their Caregiver: Evaluation During Disease Trajectory Guariglia, Lara Ieraci, Sonia Villani, Veronica Tanzilli, Antonio Benincasa, Dario Sperati, Francesca Terrenato, Irene Pace, Andrea Front Neurol Neurology Background: Patients with glioma have a poor prognosis and, in a short period of time, have to deal with severe forms of disability, which compromise their psychological distress and quality of life. The caregivers of these patients consequently carry a heavy burden in terms of emotional and patient care. The study aims to evaluate the coping strategies of patients and their caregivers during the course of the disease in order to frame the adaptation process in a rapidly progressing pathology. Methods: A prospective study on 24 dyads of patients affected by malignant glioma and their caregivers was conducted between May 2016 and July 2018. Questionnaires designed to identify the coping style (MINI-MaC Scale) and psychological distress (HADS scores) and assess QOL (EQ-5D) were administered at two time points: at first lines of treatment and at disease recurrence. Results: Patients and their caregiver structure adaptive coping strategies during the disease: a coping style oriented toward a fighting spirit prevails at baseline (Mini-Mac Mean 3.23); fatalism prevails at recurrence (Mini-Mac Mean 3.03). Psychological distress affects the coping style expressed: high levels of anxiety symptoms were found to be significantly associated with a coping style oriented toward anxious preoccupation, helpless–hopeless, and fatalism; low depressive symptoms were inversely correlated with fighting spirit coping style. Patients' and caregivers' perceptions of quality of life were correlated between them and with performance status assessed by clinicians. In a dyadic perspective, the adaptation of a member of the couple varies as a function of the other partner's coping style. Conclusions: Our data are in line with previous literature on cancer patients, demonstrating that coping style is not a persistent dimension of personality, but can change depending on the situation. Despite the disease rapid course, patients and their caregivers can structure adaptive and functional defenses to manage the disease. Frontiers Media S.A. 2021-09-01 /pmc/articles/PMC8440902/ /pubmed/34539556 http://dx.doi.org/10.3389/fneur.2021.709132 Text en Copyright © 2021 Guariglia, Ieraci, Villani, Tanzilli, Benincasa, Sperati, Terrenato and Pace. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Guariglia, Lara
Ieraci, Sonia
Villani, Veronica
Tanzilli, Antonio
Benincasa, Dario
Sperati, Francesca
Terrenato, Irene
Pace, Andrea
Coping Style in Glioma Patients and Their Caregiver: Evaluation During Disease Trajectory
title Coping Style in Glioma Patients and Their Caregiver: Evaluation During Disease Trajectory
title_full Coping Style in Glioma Patients and Their Caregiver: Evaluation During Disease Trajectory
title_fullStr Coping Style in Glioma Patients and Their Caregiver: Evaluation During Disease Trajectory
title_full_unstemmed Coping Style in Glioma Patients and Their Caregiver: Evaluation During Disease Trajectory
title_short Coping Style in Glioma Patients and Their Caregiver: Evaluation During Disease Trajectory
title_sort coping style in glioma patients and their caregiver: evaluation during disease trajectory
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8440902/
https://www.ncbi.nlm.nih.gov/pubmed/34539556
http://dx.doi.org/10.3389/fneur.2021.709132
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