Evidence map›Paper›PMID 40044746›Full record

Observational studyScientific reports2025

Impact of SARS-CoV-2 infection therapies on the risk of venous thromboembolism and cardiovascular events from the SEMI-COVID-19 Registry.

Crhistian-Mario Oblitas, Pablo Demelo-Rodríguez, Lucía Barrera-López, Francisco Galeano-Valle, Manuel Rubio-Rivas, Jairo Luque Del Pino, Vicente Giner Galvañ, Diana Paredes-Ruíz, Rosa Fernández-Madera Martínez, Martín Gericó Aseguinolaza and 16 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

26 authors.

Crhistian-Mario OblitasInternal Medicine Department, Hospital Clínico de Santiago, Santiago de Compostela, Spain. crhistian.cao@gmail.com.
Pablo Demelo-RodríguezSchool of Medicine, Universidad Complutense de Madrid, Madrid, Spain.
Lucía Barrera-LópezInternal Medicine Department, Hospital Clínico de Santiago, Santiago de Compostela, Spain.
Francisco Galeano-ValleSchool of Medicine, Universidad Complutense de Madrid, Madrid, Spain.
Manuel Rubio-RivasInternal Medicine Department, Hospital Universitario de Bellvitge, L'Hospitalet de Llobregat, Barcelona, Spain.
Jairo Luque Del PinoInternal Medicine Department, Hospital Costa del Sol, Marbella, Spain.
Vicente Giner GalvañInternal Medicine Department, Hospital Universitario San Juan de Alicante, Alicante, Spain.
Diana Paredes-RuízInternal Medicine Department, Hospital Universitario 12 de Octubre, Madrid, Spain.
Rosa Fernández-Madera MartínezInternal Medicine Department, Hospital de Cabueñes, Gijón, Spain.
Martín Gericó AseguinolazaInternal Medicine Department, Hospital Royo Villanova, Zaragoza, Spain.
Ricardo Gómez-HuelgasInternal Medicine Department, Hospital Regional Universitario de Málaga, Málaga, Spain.
Francisco Arnalich FernándezInternal Medicine Department, Hospital Universitario La Paz, Madrid, Spain.
José David Torres PeñaInternal Medicine Department, Hospital Universitario Reina Sofía, Córdoba, Spain.
José Ignacio Martín GonzálezInternal Medicine Department, Hospital Universitario de Salamanca, Salamanca, Spain.
Manuel Méndez-BailónInternal Medicine Department, Hospital Clínico San Carlos, Madrid, Spain.
Daniel Monge MongeInternal Medicine Department, Hospital Complejo Asistencial de Segovia, Segovia, Spain.
Santiago J Freire CastroInternal Medicine Department, Hospital Universitario de A Coruña, A Coruña, Spain.
Cruz Pastor ValverdeInternal Medicine Department, Hospital Universitario Infanta Cristina, Parla, Spain.
Enrique Rodilla-SalaInternal Medicine Department, Hospital de Sagunto, Valencia, Spain.
Marcos Guzmán GarcíaInternal Medicine Department, Hospital San Juan de La Cruz, Jaén, Spain.
María Rivas-CarmenadoInternal Medicine Department, Hospital Universitario Central de Asturias, Oviedo, Spain.
César-Manuel GalloInternal Medicine Department, Hospital Valle del Nalón, Asturias, Spain.
Marina Amparo Perea RibisInternal Medicine Department, Hospital Francesc de Borja, Valencia, Spain.
José-Manuel Casas-RojoSchool of Medicine, Universidad Complutense de Madrid, Madrid, Spain.
Jesús Millán Núñez-CortésSchool of Medicine, Universidad Complutense de Madrid, Madrid, Spain.
SEMICOVID-19 Network

Funding

Columbia Partnership for Prevention and Control of HIV/AIDS Clinical Trials UnitUM1AI069470 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MAGDALENA ELZBIETA SOBIESZCZYK · 2012 to 2026
$44.8M
Columbia Collaborative HIV/AIDS Clinical Trials UnitU01AI069470 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HAMMER, SCOTT M · 2007 to 2011
$15.4M
NIAID NIH HHS U01 AI069470NIAID NIH HHS UM1 AI069470
6 · The paper itself

Abstract

This study aimed to assess the impact of SARS-CoV-2 therapies on the risk of venous thromboembolism (VTE) and other cardiovascular events. A retrospective, multicenter, observational study included hospitalized patients in Spain due to acute SARS-CoV-2 infection from March 2020 to March 2022. A total of 184,324 hospitalized COVID-19 patients were included, with a mean age of 67.5 (± 16) years of whom 58.4% were male. Among the comorbidities, arterial hypertension was the most common, affecting 52.5% (9618 patients), followed by dyslipidemia in 39.5% (7237 patients), diabetes mellitus in 23.7% (1748 patients), and atrial fibrillation in 10.6% (1948 patients). The overall mortality rate was 17.4% (3183 patients) and 9.9% (1819 patients) required admission to an intensive care unit. Cardiovascular events occurred in 4.08% (748 patients), with VTE occurring in 2.78% (510 patients), myocardial infarction in 0.75% (137 patients), and ischemic stroke in 0.55% (101 patients). Among therapies, beta-lactams were used in 66.7% (12,228 patients), systemic corticosteroids in 56.9% (10,424 patients), and tocilizumab in 11.6% (2128 patients). Multivariate analysis revealed an independent association between VTE and the use of tocilizumab (adjusted OR 2.07; p < 0.01), corticosteroids (adjusted OR 1.44; p = 0.02), and macrolides (adjusted OR 0.58; p < 0.01). None of the therapies were associated with the risk of myocardial infarction or ischemic stroke. In this large national cohort, tocilizumab and corticosteroids exhibited an independent association for the risk of VTE, but not for myocardial infarction or ischemic stroke.

Indexed as

Cardiovascular DiseasesCOVID-19COVID-19 Drug TreatmentVenous ThromboembolismAgedAged, 80 and overComorbidityFemaleHumansMaleMiddle AgedRegistriesRetrospective StudiesRisk FactorsSARS-CoV-2SpainCardiovascular diseaseCOVID-19MortalitySARS-CoV-2Venous thromboembolism

Identifiers

PMID40044746
PMCPMC11882944

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.