Constellation, le dépôt institutionnel de l'Université du Québec à Chicoutimi

Distress experienced by lung cancer patients and their family caregivers in the first year of their cancer journey

Aubin Michèle, Vézina Lucie, Verreault René, Simard Sébastien, Hudon Éveline, Desbiens Jean-François, Fillion Lise, Dumont Serge, Tourigny André et Daneault Serge. (2022). Distress experienced by lung cancer patients and their family caregivers in the first year of their cancer journey. Palliative and Supportive Care, 20, (1), p. 15-21.

Le texte intégral n'est pas disponible pour ce document.

URL officielle: https://doi.org/10.1017/S1478951521000377

Résumé

Objective: Diagnosis of cancer is emotionally threatening not only for patients but also for their family caregivers (FC) who witness and share much of the illness experience. This study compares distress experienced by lung cancer patients and their FC during the year following the diagnosis.

Methods: A prospective cohort study of 206 patients recently diagnosed with inoperable lung cancer (participation rate 79.5%) and 131 FC (participation rate 63.6%) was conducted in an ambulatory oncology clinic in Quebec City (Canada). They completed validated questionnaires regarding their personal and psychological characteristics (Hospital and Anxiety Depression Scale—HADS), in the first months after the diagnosis of lung cancer and after 6 and 12 months. Univariate, bivariate, and linear mixed models were conducted to compare patient and FC distress.

Results: At baseline, 7.8% of patients reported distress (HADS total score >15) and their mean distress score was 7.0 ± 4.9 (range 0–42). In contrast, 33.6% of FC presented significant distress and their mean distress score was 12.0 ± 7.2 ( P < 0.0001). Proportions of patients and FC with distress remained relatively stable at 6 and 12 months, and at every time point, FC reported higher levels of distress compared to their relative with cancer ( P < 0.0001). Comparable trends were found when looking at the mean scores of distress, anxiety, and depression throughout the study.

Significance of results: Being diagnosed with lung cancer and going through its different phases seems to affect more FC than patients. The psychological impact of such diagnosis appears early after the diagnosis and does not significantly change over time. These findings reinforce the importance for oncology teams, to include FC in their systematic distress screening program, in order to help them cope with their own feelings and be able to play their role in patient support and care throughout the cancer journey.

Type de document:Article publié dans une revue avec comité d'évaluation
ISSN:1478-9515
Volume:20
Numéro:1
Pages:p. 15-21
Version évaluée par les pairs:Oui
Date:2022
Nombre de pages:7
Identifiant unique:10.1017/S1478951521000377
Sujets:Sciences sociales et humaines > Sciences sociales > Psychologie
Sciences de la santé > Sciences médicales > Oncologie
Département, module, service et unité de recherche:Départements et modules > Département des sciences de la santé > Module de psychologie
Mots-clés:Cancer supportive care, cohort study, distress, family caregiver, lung cancer, patient, soins, étude de cohorte, détresse, proche aidant, cancer du poumon
Déposé le:14 mai 2024 19:06
Dernière modification:14 mai 2024 19:06
Afficher les statistiques de telechargements

Éditer le document (administrateurs uniquement)

Creative Commons LicenseSauf indication contraire, les documents archivés dans Constellation sont rendus disponibles selon les termes de la licence Creative Commons "Paternité, pas d'utilisation commerciale, pas de modification" 2.5 Canada.

Bibliothèque Paul-Émile-Boulet, UQAC
555, boulevard de l'Université
Chicoutimi (Québec)  CANADA G7H 2B1
418 545-5011, poste 5630