Evidence map›Paper›PMID 39516010›Full record

ArticleLupus science & medicine2024

Using photovoice to investigate patient experiences of lupus nephritis in Canada.

Francesca S Cardwell, Susan J Elliott, Megan R W Barber, Kim Cheema, Sydney George, Adrian Boucher, Ann Elaine Clarke

Abstract read
In one paragraph

Article in Lupus science & medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Francesca S CardwellDepartment of Geography and Environmental Management, University of Waterloo, Waterloo, Ontario, Canada fcardwell@uwaterloo.ca.ORCID 0000-0002-7393-466X
Susan J ElliottDepartment of Geography and Environmental Management, University of Waterloo, Waterloo, Ontario, Canada.
Megan R W BarberDivision of Rheumatology, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada.
Kim CheemaDivision of Nephrology, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada.
Sydney GeorgeHealth Outcomes and Economics, GSK, Mississauga, Ontario, Canada.
Adrian BoucherHealth Outcomes and Economics, GSK, Mississauga, Ontario, Canada.
Ann Elaine ClarkeDivision of Rheumatology, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveLupus nephritis (LN) is a major cause of morbidity and mortality, affecting up to 60% of patients with systemic lupus erythematosus (SLE). The perspectives of patients with SLE have been explored; however, little is known of the lived experiences of patients with LN.

methodsPatients aged ≥18 years with biopsy-proven pure or mixed International Society of Nephrology/Renal Pathology Society Class III, IV or V LN were purposefully recruited from a Canadian lupus cohort to participate in a photovoice (visual-narrative participatory research method) exercise. Participants took photos of what LN means to them, impacts on daily life and factors impacting LN management. Photos were shared and discussed in focus groups.

results13 individuals with LN participated (92.3% were female; mean (SD) age was 41.7 (14.0) years). The mean (SD) number of photos shared per participant was 4.2 (0.9). Photos (n=54) depicted activities/settings that contribute to well-being (n=15), the participants themselves (n=13), healthcare experiences (n=10), home (n=4), community (n=2), friends (n=2), work (n=2) and other challenges (n=6). All participants described physical and psychosocial impacts of living with LN. Although 12 mentioned activities/settings that contribute to well-being (eg, time in natural environments), participants were consistently reminded of limitations imposed by LN due to physical symptoms, challenges presented by the physical environment and the altered life trajectories experienced. Participants discussed the dual burden of LN and the associated medication journey; side effects and medication-related financial challenges were highlighted by ten and five participants, respectively.

conclusionsParticipants reported a substantial psychosocial burden associated with altered life trajectories, the dual burden of LN and the associated medication journey, and the conflicting role of the physical environment. The need for flexibility (ie, from employers, themselves) is an essential component of navigating altered life trajectories.

Indexed as

Lupus NephritisPhotographyAdultCanadaFemaleFocus GroupsHumansMaleMiddle AgedQuality of LifeLupus Erythematosus, SystemicLupus NephritisQualitative research

Identifiers

PMID39516010
PMCPMC11552595

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.