The Effects of Systemic Lupus–Related Cognitive Impairments on Activities of Daily Living and Life Role Participation: A Qualitative Framework Study

Author:

Barraclough Michelle1ORCID,Howe Aaron2,Soberanis Ana2,Kakvan Mahta3,Chattu Vijay2,Bani‐Fatemi Ali2,Engel Lisa4ORCID,Vitti Michelle3,Nalder Emily2,Goverover Yael5,Gignac Monique6,Bonilla Dennisse3,Nielsen Wils7,Anderson Nicole3,Tartaglia Carmela2,Nowrouzi‐Kia Behdin8ORCID,Touma Zahi3ORCID

Affiliation:

1. University Health Network, Toronto, Ontario, Canada, and The University of Manchester, NIHR Manchester Biomedical Research Centre, Manchester University NHS Foundation Trust, and Manchester Academic Health Science Centre Manchester UK

2. University of Toronto Toronto Ontario Canada

3. University Health Network, and University of Toronto Lupus Clinic, Toronto Western Hospital Toronto Ontario Canada

4. University of Manitoba, Winnipeg, Manitoba, and Institute for Work and Health Toronto Ontario Canada

5. New York University Steinhardt New York USA

6. University Health Network, University of Toronto, and Institute for Work and Health Toronto Ontario Canada

7. University of Toronto Lupus Clinic and Western Hospital Toronto Ontario Canada

8. University of Toronto and University Health Network Toronto Ontario Canada

Abstract

ObjectiveCognitive impairment (CI) in systemic lupus erythematosus (SLE) negatively impacts health‐related quality of life leading to activity limitations. This qualitative study aimed to (1) explore the effect of SLE‐related CI on activities of daily living and life role participation and (2) describe factors influencing activity restriction and life role participation.MethodsSemistructured, in‐depth interviews of lived experience of CI in SLE were conducted with 24 participants with SLE. Sociodemographic and clinical data, and objective and subjective cognitive function, were collected to characterize participants. A qualitative thematic content analysis was undertaken guided by a framework analytical approach.ResultsParticipants reported problems in multiple cognitive domains, with multiple perceived causes. CI was felt to impact work, social, domestic, and family life, health, and independence. Five overarching themes were represented in the data: (1) characterization of SLE‐reported CI, (2) perceived cause of CI, (3) perceived impact of CI on activities of daily living and life role participation, (4) adaptations for managing CI, and (5) influence of CI adaptations on activities of daily living and life role participation.ConclusionThis study provides a better understanding of the patient experience of CI in SLE, how it impacts their lives, and what coping strategies they employ. It highlights the long‐term challenges those with CI in SLE undergo and provides evidence for the urgent need to implement multidisciplinary treatment options. When managing CI, it may be beneficial to evaluate and understand available psychosocial support resources to help identify and reinforce relevant adaptations to improve health‐related quality of life.

Funder

Arthritis Society

Canadian Institutes of Health Research

Lupus Canada

Lupus Research Alliance

Physicians' Services Incorporated Foundation

Publisher

Wiley

Subject

Rheumatology

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