Evidence map›Paper›PMID 39388388›Full record

ArticlePloS one2024

Risk of systemic lupus erythematosus flare after COVID-19 hospitalization: A matched cohort study.

Arthur Mageau, Christel Géradin, Kankoé Sallah, Thomas Papo, Karim Sacre, Jean-François Timsit

Abstract read
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Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

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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

6 authors.

Arthur MageauIAME, UMR 1137 INSERM, Team Descid Université Paris Cité and Université Sorbonne Paris Nord, Paris, France.ORCID 0000-0002-2995-767X
Christel GéradinDépartement de médecine interne, Hôpital Bichat-Claude Bernard, Assistance Publique- Hôpitaux de Paris, Université Paris Cité, Paris, France.
Kankoé SallahINSERM CIC-EC 1425, Hôpital Bichat Claude Bernard, Paris, France.
Thomas PapoDépartement de médecine interne, Hôpital Bichat-Claude Bernard, Assistance Publique- Hôpitaux de Paris, Université Paris Cité, Paris, France.
Karim SacreDépartement de médecine interne, Hôpital Bichat-Claude Bernard, Assistance Publique- Hôpitaux de Paris, Université Paris Cité, Paris, France.ORCID 0000-0002-6544-234X
Jean-François TimsitIAME, UMR 1137 INSERM, Team Descid Université Paris Cité and Université Sorbonne Paris Nord, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo analyze the risk of systemic lupus erythematosus (SLE) flare after admission for COVID-19.

methodsWe performed a matched cohort study using the Assistance Publique-Hôpitaux de Paris Clinical Data Warehouse which collects structured medical, biological and administrative information from 11 million patients in Paris area, France. Each SLE patient hospitalized with a COVID-19 diagnosis code between March 2020 and December 2021 was matched to one SLE control patient with an exact matching procedure using age ±3 years, gender, chronic kidney disease, end-stage renal disease, and serological activity. The main outcome was a lupus flare during the 6 months follow-up. A flare was considered if a) documented by the treating physician in the patient's EHR and b) justifying a change in SLE treatment. The electronic health records (EHRs) were individually checked for data accuracy.

resultsAmong 4,533 SLE patients retrieved from the database, 81 (2.8%) have been admitted for COVID-19 between March 2020 and December 31, 2021, and 79 (n = 79/81,97.5%) were matched to a unique unexposed SLE. During follow-up, a flare occurred in 14 (17.7%) patients from the COVID-19 group as compared to 5 (6.3%) in the unexposed control group, including 4 lupus nephritis in the exposed group and 1 in the control group. After adjusting for HCQ use at index date and history of lupus nephritis, the risk of flare was higher in exposed SLE patients (hazard ratio [95% confidence interval] of 3.79 [1.49-9.65]).

conclusionsCOVID-19 hospitalization is associated with an increased risk of flare in SLE.

Indexed as

COVID-19HospitalizationLupus Erythematosus, SystemicAdultAgedCohort StudiesElectronic Health RecordsFemaleHumansMaleMiddle AgedRisk FactorsSARS-CoV-2

Identifiers

PMID39388388
PMCPMC11466388

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