Prioritizing chronic pain self-management amid coexisting chronic illnesses: An exploratory qualitative study.

Chronic disease Chronic illness Chronic pain Health psychology Prioritization Qualitative Self-management

Journal

International journal of nursing studies advances
ISSN: 2666-142X
Titre abrégé: Int J Nurs Stud Adv
Pays: England
ID NLM: 101769252

Informations de publication

Date de publication:
Jun 2024
Historique:
received: 21 09 2023
revised: 04 01 2024
accepted: 05 01 2024
medline: 15 5 2024
pubmed: 15 5 2024
entrez: 15 5 2024
Statut: epublish

Résumé

In Canada, one out of five people lives with chronic pain, a condition frequently co-occurring with other chronic illnesses. As with most chronic illnesses, successful engagement in symptom management is key. In the context of multiple illnesses, self-management involves daily prioritization of symptoms and conditions and decision-making, which can be challenging. Self-management of chronic illnesses can require more complex competence and tasks to address the different implications of each condition. Our research objective was to explore types and processes of self-management symptom prioritization among adults living with chronic pain and other chronic illnesses. This research was carried out as part of a larger study that adopted an explanatory sequential mixed-methods design. This study focused more specifically on the qualitative part of the study. Participants recruited for the qualitative component took part in a semi-structured individual interview online or in-person at the center hospitalier de l'Université de Montréal. In total, 25 participants were interviewed, including 18 women and 7 men. To participate in the qualitative part of the study, participants were selected from the larger study and were eligible if they were 18 years old or older and experiencing pain for more than 3 months and had at least one other chronic illness for which they were receiving treatment or engaged in symptom management. Semi-structured interviews were conducted in-person or virtually and were transcribed verbatim. Reflexive thematic analysis was used to explore patients' narratives, and an open and iterative approach was adopted to code interviews and generate themes. The first theme, focus on symptom prioritization, showed different prioritization processes, including prioritizing a dominant illness, prioritizing multiple illnesses to avoid undesirable consequences, and finally absence of or automatic processes of prioritization. In the second theme, we identified several characteristics of an illness, in this case chronic pain that made it a self-management priority: uncontrollable and disabling nature, omnipresence, unpredictability, unpleasantness, and invisibility to others. In the last theme, we highlighted that some psychosocial factors influenced levels of engagement in self-management and prioritization processes, including social support and the patient-physician relationship. Chronic pain was the medical condition most often prioritized by participants in their self-management tasks. Because of its characteristics, it was the medical condition that had the most negative impact on day-to-day functioning.

Sections du résumé

Background UNASSIGNED
In Canada, one out of five people lives with chronic pain, a condition frequently co-occurring with other chronic illnesses. As with most chronic illnesses, successful engagement in symptom management is key. In the context of multiple illnesses, self-management involves daily prioritization of symptoms and conditions and decision-making, which can be challenging. Self-management of chronic illnesses can require more complex competence and tasks to address the different implications of each condition.
Objective UNASSIGNED
Our research objective was to explore types and processes of self-management symptom prioritization among adults living with chronic pain and other chronic illnesses.
Design UNASSIGNED
This research was carried out as part of a larger study that adopted an explanatory sequential mixed-methods design. This study focused more specifically on the qualitative part of the study.
Settings UNASSIGNED
Participants recruited for the qualitative component took part in a semi-structured individual interview online or in-person at the center hospitalier de l'Université de Montréal.
Participants UNASSIGNED
In total, 25 participants were interviewed, including 18 women and 7 men.
Methods UNASSIGNED
To participate in the qualitative part of the study, participants were selected from the larger study and were eligible if they were 18 years old or older and experiencing pain for more than 3 months and had at least one other chronic illness for which they were receiving treatment or engaged in symptom management. Semi-structured interviews were conducted in-person or virtually and were transcribed verbatim. Reflexive thematic analysis was used to explore patients' narratives, and an open and iterative approach was adopted to code interviews and generate themes.
Findings UNASSIGNED
The first theme, focus on symptom prioritization, showed different prioritization processes, including prioritizing a dominant illness, prioritizing multiple illnesses to avoid undesirable consequences, and finally absence of or automatic processes of prioritization. In the second theme, we identified several characteristics of an illness, in this case chronic pain that made it a self-management priority: uncontrollable and disabling nature, omnipresence, unpredictability, unpleasantness, and invisibility to others. In the last theme, we highlighted that some psychosocial factors influenced levels of engagement in self-management and prioritization processes, including social support and the patient-physician relationship.
Conclusions UNASSIGNED
Chronic pain was the medical condition most often prioritized by participants in their self-management tasks. Because of its characteristics, it was the medical condition that had the most negative impact on day-to-day functioning.

Identifiants

pubmed: 38746792
doi: 10.1016/j.ijnsa.2024.100175
pii: S2666-142X(24)00002-X
pmc: PMC11080447
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100175

Informations de copyright

© 2024 The Author(s).

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Charlotte Moore-Bouchard (C)

Research Centre of the Centre Hospitalier de l'Université de Montréal, Montréal, Canada.
Department of Psychology, Université de Montréal, Montréal, Canada.

Marie-Eve Martel (ME)

Research Centre of the Centre Hospitalier de l'Université de Montréal, Montréal, Canada.

Elise Develay (E)

Research Centre of the Centre Hospitalier de l'Université de Montréal, Montréal, Canada.

José Côté (J)

Research Centre of the Centre Hospitalier de l'Université de Montréal, Montréal, Canada.
Faculty of Nursing, Université de Montréal, Montréal, Canada.

Madeleine Durand (M)

Research Centre of the Centre Hospitalier de l'Université de Montréal, Montréal, Canada.
Department of Medicine, Université de Montréal, Montréal, Canada.

M Gabrielle Pagé (MG)

Research Centre of the Centre Hospitalier de l'Université de Montréal, Montréal, Canada.
Department of Psychology, Université de Montréal, Montréal, Canada.
Department of Anesthesiology and Pain Medicine, Université de Montréal, Montréal, Canada.

Classifications MeSH