Evidence map›Paper›PMID 39653548›Full record

ArticleLupus science & medicine2024

Treatment trends of systemic lupus erythematosus from 2007 to 2023 in the USA.

Gabriel Figueroa-Parra, Herbert C Heien, Kenneth J Warrington, Nilay D Shah, Cynthia S Crowson, Rozalina G McCoy, Alí Duarte-García

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. 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. Review
  2. Review
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

7 authors.

Gabriel Figueroa-ParraDivision of Rheumatology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0002-6077-8899
Herbert C HeienRobert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic, Rochester, Minnesota, USA.
Kenneth J WarringtonDivision of Rheumatology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0001-7708-2487
Nilay D ShahRobert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic, Rochester, Minnesota, USA.
Cynthia S CrowsonDivision of Rheumatology, Mayo Clinic, Rochester, Minnesota, USA.
Rozalina G McCoyRobert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic, Rochester, Minnesota, USA.
Alí Duarte-GarcíaDivision of Rheumatology, Mayo Clinic, Rochester, Minnesota, USA duarte.ali@mayo.edu.ORCID 0000-0003-1749-5719

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo characterise the changing trends in the pharmacological management of SLE in the USA between 2007 and 2023 as new treatment options emerged.

methodsIn a retrospective cohort study using data from OptumLabs Data Warehouse, we characterised the annual prevalent (ie, all) and incident (ie, new) use of antimalarials, glucocorticoids and immunosuppressive medications among patients with SLE from 2007 to 2023 and assessed for changing trends over time.

resultsWe identified 19 122 adults with SLE; they were 51.2 (SD 16.1) years of age, 89% were female, 61.3% were White, 18.5% were Black and 13.1% were Hispanic. The proportion of prevalent users of antimalarials has decreased from 79.4% in 2007 to 77.2% in 2023 (p=0.0055), while the proportion of incident users fluctuated between a lowest 5.8% in 2021 and a highest 8.1% in 2008 (p=0.008). The proportion of prevalent users of glucocorticoids increased from 64.6% in 2007 to 66.7% in 2023 (p=0.0132), as did the proportion of incident users (12.4% in 2007 to 21.7% in 2023; p<0.0001). The use of cyclophosphamide (2.0% in 2007 to 0.4% in 2023, p<0.0001) has decreased; the use of mycophenolate mofetil (7.7% in 2007 to 10.3% in 2023, p<0.0001), rituximab (1.4% in 2007 to 2.1% in 2023, p<0.0001) and belimumab (0.8% in 2011 to 6.1% in 2023, p=0.0001) has increased.

conclusionsDespite increasing availability of alternative treatment options, patients with SLE in the USA increasingly rely on glucocorticoid-based therapy. Efforts to improve the use of antimalarials and steroid-sparing immunosuppressants are needed.

Indexed as

AntimalarialsGlucocorticoidsImmunosuppressive AgentsLupus Erythematosus, SystemicAdultAgedAntibodies, Monoclonal, HumanizedFemaleHumansMaleMiddle AgedMycophenolic AcidRetrospective StudiesUnited StatesAntibodies, Monoclonal, HumanizedAntimalarialsbelimumabGlucocorticoidsImmunosuppressive AgentsMycophenolic Acidepidemiologyglucocorticoidshealth services researchsystemic lupus erythematosustreatment

Identifiers

PMID39653548
PMCPMC11629018

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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.