Evidence map›Paper›PMID 34887346›Full record

ArticleRMD open2021

Role of targeted therapies in rheumatic patients on COVID-19 outcomes: results from the COVIDSER study.

Jose María Álvaro Gracia, Carlos Sanchez-Piedra, Javier Manero, María Ester Ruiz-Lucea, Laura López-Vives, Cristina Bohorquez, Julia Martinez-Barrio, Gema Bonilla, Paloma Vela, María Jesús García-Villanueva and 12 more

Open access · goldAbstract read
In one paragraph

Article in RMD open, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 28% of its field
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

5 citing papers in PubMed, 11 citations in OpenAlex.

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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

22 authors at 16 institutions in 1 country.

Jose María Álvaro GraciaDepartment of Rheumatology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Carlos Sanchez-PiedraResearch Unit, Sociedad Española de Reumatología, Madrid, Spain.
Javier ManeroRheumatology Department, Hospital Universitario Miguel Servet, Zaragoza, Aragón, Spain.
María Ester Ruiz-LuceaRheumatology Department, Hospital Universitario Basurto, Bilbao, País Vasco, Spain.
Laura López-VivesRheumatology Department, Hospital San Rafael, Barcelona, Catalunya, Spain.
Cristina BohorquezDepartment of Rheumatology, Hospital Universitario Príncipe de Asturias, Alcala de Henares, Madrid, Spain.
Julia Martinez-BarrioDepartment of Rheumatology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Gema BonillaDepartment of Rheumatology, La Paz University Hospital, Madrid, Spain.
Paloma VelaDepartment of Rheumatology, Hospital General Universitario de Alicante, Alicante, Spain.
María Jesús García-VillanuevaDepartment of Rheumatology, Hospital Universitario Ramon y Cajal, Madrid, Madrid, Spain.
María Teresa Navío-MarcoDepartment of Rheumatology, Hospital Universitario Infanta Leonor, Madrid, Spain.
Marina PavíaDepartment of Rheumatology, Hospital Universitario Puerta de Hierro Majadahonda, Majadahonda, Comunidad de Madrid, Spain.
María GalindoDepartment of Rheumatology, Hospital Universitario 12 de Octubre, Madrid, Comunidad de Madrid, Spain.
Celia ErausquinDepartment of Rheumatology, Hospital Doctor Negrin, Las Palmas GC, Spain.
Miguel A Gonzalez-GayDepartment of Rheumatology, Hospital Universitario Marqués de Valdecilla, Santander, Cantabria, Spain.ORCID 0000-0002-7924-7406
Inigo Rua-FigueroaDepartment of Rheumatology, Hospital Doctor Negrin, Las Palmas GC, Spain.
Jose M Pego-ReigosaDepartment of Rheumatology, University Hospital Complex of Vigo, Vigo, Spain.
Isabel CastrejonDepartment of Rheumatology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Jesús T Sanchez-CostaResearch Unit, Sociedad Española de Reumatología, Madrid, Spain.
Enrique González-DávilaDepartamento de Estadística e Investigación Operativa, Universidad de La Laguna, La Laguna, Islas Canarias, Spain.
Federico Diaz-GonzalezDepartment of Rheumatology, Hospital Universitario de Canarias, La Laguna, Spain federico.diaz.gonzalez@gmail.com.ORCID 0000-0002-4139-9295
COVIDSER study group
Hospital General Universitario Gregorio Marañón · ESHospital Universitario de Gran Canaria Doctor Negrín · ESSociedad Española de Reumatología · ESUniversidad de La Laguna · ESComunidad de Madrid · ESHospital de Basurto · ESHospital General Universitario de Alicante Doctor Balmis · ESHospital Universitario Infanta Leonor · ESHospital Universitario La Paz · ESHospital Universitario Miguel Servet · ESHospital Universitario Príncipe de Asturias · ESHospital Universitario Puerta de Hierro Majadahonda · ESHospital Universitario Ramón y Cajal · ESHospital Universitario San Rafael · ESMarqués de Valdecilla University Hospital · ESUniversity Hospital Complex Of Vigo · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo analyse the effect of targeted therapies, either biological (b) disease-modifying antirheumatic drugs (DMARDs), targeted synthetic (ts) DMARDs and other factors (demographics, comorbidities or COVID-19 symptoms) on the risk of COVID-19 related hospitalisation in patients with inflammatory rheumatic diseases.

methodsThe COVIDSER study is an observational cohort including 7782 patients with inflammatory rheumatic diseases. Multivariable logistic regression was used to estimate ORs and 95% CIs of hospitalisation. Antirheumatic medication taken immediately prior to infection, demographic characteristics, rheumatic disease diagnosis, comorbidities and COVID-19 symptoms were analysed.

resultsA total of 426 cases of symptomatic COVID-19 from 1 March 2020 to 13 April 2021 were included in the analyses: 106 (24.9%) were hospitalised and 19 (4.4%) died. In multivariate-adjusted models, bDMARDs and tsDMARDs in combination were not associated with hospitalisation compared with conventional synthetic DMARDs (OR 0.55, 95% CI 0.24 to 1.25 of b/tsDMARDs, p=0.15). Tumour necrosis factor inhibitors (TNF-i) were associated with a reduced likelihood of hospitalisation (OR 0.32, 95% CI 0.12 to 0.82, p=0.018), whereas rituximab showed a tendency to an increased risk of hospitalisation (OR 4.85, 95% CI 0.86 to 27.2). Glucocorticoid use was not associated with hospitalisation (OR 1.69, 95% CI 0.81 to 3.55). A mix of sociodemographic factors, comorbidities and COVID-19 symptoms contribute to patients' hospitalisation.

conclusionsThe use of targeted therapies as a group is not associated with COVID-19 severity, except for rituximab, which shows a trend towards an increased risk of hospitalisation, while TNF-i was associated with decreased odds of hospitalisation in patients with rheumatic disease. Other factors like age, male gender, comorbidities and COVID-19 symptoms do play a role.

Indexed as

Antirheumatic AgentsCOVID-19Rheumatic DiseasesHumansMaleSARS-CoV-2Sociodemographic FactorsAntirheumatic Agentsbiological therapyCOVID-19health careimmune system diseasesoutcome assessment

Identifiers

PMID34887346
PMCPMC8662584
OpenAlexW4200039900

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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.