Evidence map›Paper›PMID 39884714›Full record

ArticleLupus science & medicine2025

Medication-related hospitalisations in patients with SLE.

Michèle Stanciu, Joo-Young Esther Lee, Emily G McDonald, Gregory Clark, Christian A Pineau, Fares Kalache, Louis-Pierre Grenier, Évelyne Vinet, Sasha Bernatsky, Arielle Mendel

Abstract read
In one paragraph

Article in Lupus science & medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

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

10 authors.

Michèle StanciuMcGill University, Montreal, Quebec, Canada.ORCID 0009-0004-1547-7220
Joo-Young Esther LeeCentre for Outcomes Research and Evaluation (CORE), Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.
Emily G McDonaldCentre for Outcomes Research and Evaluation (CORE), Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.
Gregory ClarkDepartment of Emergency Medicine, McGill University Health Centre, Montreal, Quebec, Canada.
Christian A PineauDivision of Rheumatology, McGill University Health Centre, Montreal, Quebec, Canada.
Fares KalacheDivision of Rheumatology, McGill University Health Centre, Montreal, Quebec, Canada.
Louis-Pierre GrenierDivision of Rheumatology, McGill University Health Centre, Montreal, Quebec, Canada.
Évelyne VinetCentre for Outcomes Research and Evaluation (CORE), Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.ORCID 0000-0001-7727-5879
Sasha BernatskyCentre for Outcomes Research and Evaluation (CORE), Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.ORCID 0000-0002-9515-2802
Arielle MendelCentre for Outcomes Research and Evaluation (CORE), Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada arielle.mendel@mcgill.ca.ORCID 0000-0001-9732-616X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesPatients with SLE take multiple medications. Within a large prospective longitudinal SLE cohort, we characterised medication-related hospitalisations and their preventability.

methodsWe identified consecutive admissions to our tertiary hospitals between 2015 and 2020. Two independent adjudicators evaluated if medication-related events contributed to the hospitalisation, considering (1) adverse drug events (ADEs) and (2) events from medication non-adherence, using the Leape and Bates method. We classified ADEs as potentially preventable/ameliorable if we identified modifiable factors. Logistic regressions with generalised estimating equations evaluated associations between participant characteristics and medication-related hospitalisations, accounting for repeat hospitalisations within the same participant.

resultsWe studied 68 hospitalisations among 45 participants (91% female). At first hospitalisation, the median age was 38 years (IQR 26.5-53.0) and median SLE duration was 12 years (IQR 5.5-19.5). One or more ADEs contributed to 20 (29%) hospitalisations (11/23 (48%) ADEs being preventable/ameliorable), and SLE flares associated with medication non-adherence contributed to 7 (10%) hospitalisations. Adjusting for age and sex, current prednisone use (adjusted OR (aOR) 3.7, 95% CI 1.1 to 13.0) or ≥1 current immunosuppressant (aOR 11.5, 95% CI 2.7 to 50.0), renal involvement at SLE diagnosis (aOR 6.5, 95% CI 2.7 to 15.7) and polypharmacy (≥5 medications; aOR 11.3, 95% CI 1.2 to 103.8) were associated with having an ADE-related (vs non-ADE) hospitalisation. Age at SLE diagnosis<18 years (OR 5.9, 95% CI 1.3 to 26.6) was associated with hospitalisation for a flare related to non-adherence.

conclusionForty per cent of SLE hospitalisations were medication-related, while half were potentially preventable/ameliorable. Renal involvement, polypharmacy, prednisone and immunosuppressant use were associated with hospitalisation related to an ADE, highlighting a vulnerable group.

Indexed as

Drug-Related Side Effects and Adverse ReactionsHospitalizationImmunosuppressive AgentsLupus Erythematosus, SystemicAdultFemaleHumansLogistic ModelsLongitudinal StudiesMaleMiddle AgedPolypharmacyPrednisoneProspective StudiesImmunosuppressive AgentsPrednisoneAntirheumatic AgentsOutcome Assessment, Health CareSystemic Lupus Erythematosus

Identifiers

PMID39884714
PMCPMC11784163

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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.