Evidence map›Paper›PMID 38762708›Full record

Trial reportJournal of thrombosis and thrombolysis2024

Predictors of bleeding and thrombotic events among patients admitted to the hospital with COVID-19 and elevated D-dimer: insights from the ACTION randomized clinical trial.

Pedro Gabriel Melo de Barros E Silva, Remo H M Furtado, Mariana Silveira de Alcântara Chaud, Ariane Vieira Scarlatelli Macedo, Bruna Bronhara, Lucas Petri Damiani, Lilian Mazza Barbosa, Mayra Akimi Suiama, Eduardo Ramacciotti, Priscilla de Aquino Martins and 39 more

Registry-linked trialAbstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Journal of thrombosis and thrombolysis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04394377 (Randomized Clinical Trial to Evaluate a Routine Full Anticoagulation Strategy in Patients With Coronavirus), which is not on this 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.

NCT04394377 phase4completednot on this map

Randomized Clinical Trial to Evaluate a Routine Full Anticoagulation Strategy in Patients With Coronavirus (COVID-19) - COALIZAO ACTION Trial

TypeinterventionalSponsorBrazilian Clinical Research InstituteRan2020 to 2021Enrolled615ConditionsCoronavirus InfectionArmsGroup 1: Rivaroxaban 20mg/d followed by enoxaparin/unfractionated heparin when needed, Group 2: control group with enoxaparin 40mg/d
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

49 authors.

Pedro Gabriel Melo de Barros E SilvaBrazilian Clinical Research Institute, São Paulo, Brazil.
Remo H M FurtadoBrazilian Clinical Research Institute, São Paulo, Brazil.
Mariana Silveira de Alcântara ChaudHospital Samaritano Paulista, São Paulo, Brazil.
Ariane Vieira Scarlatelli MacedoBrazilian Clinical Research Institute, São Paulo, Brazil.
Bruna BronharaBrazilian Clinical Research Institute, São Paulo, Brazil.
Lucas Petri DamianiBrazilian Clinical Research Institute, São Paulo, Brazil.
Lilian Mazza BarbosaBrazilian Clinical Research Institute, São Paulo, Brazil.
Mayra Akimi SuiamaBrazilian Clinical Research Institute, São Paulo, Brazil.
Eduardo RamacciottiBrazilian Clinical Research Institute, São Paulo, Brazil.
Priscilla de Aquino MartinsHospital Estadual Dr Jayme Santos Neves, Serra, Brazil.
Aryadne Lyrio de OliveiraHospital Estadual Dr Jayme Santos Neves, Serra, Brazil.
Vinicius Santana NunesHospital Estadual Dr Jayme Santos Neves, Serra, Brazil.
Luiz Eduardo Fonteles RittInstituto D'Or de Pesquisa E Ensino, Hospital Cárdio Pulmonar, Salvador, Brazil.
Ana Thereza RochaInstituto D'Or de Pesquisa E Ensino, Hospital Cárdio Pulmonar, Salvador, Brazil.
Lucas TramujasHcor Research Institute, São Paulo, Brazil.
Sueli V SantosHcor Research Institute, São Paulo, Brazil.
Dario Rafael Abregu DiazAcademic Research Organization, Hospital Israelita Albert Einstein, São Paulo, Brazil.
Lorena Souza VianaAcademic Research Organization, Hospital Israelita Albert Einstein, São Paulo, Brazil.
Lívia Maria Garcia MelroHospital Samaritano Paulista, São Paulo, Brazil.
Estêvão Lanna FigueiredoHospital Vera Cruz, Belo Horizonte, Brazil.
Fernando Carvalho NeuenschwanderHospital Vera Cruz, Belo Horizonte, Brazil.
Marianna Deway Andrade DracoulakisHospital Naval Marcílio Dias, Rio de Janeiro, Brazil.
Rodolfo Godinho Souza Dourado LimaHospital Naval Marcílio Dias, Rio de Janeiro, Brazil.
Vicente Cés de Souza DantasHospital Santa Paula, São Paulo, Brazil.
Anne Cristine Silva FernandesHospital Santa Paula, São Paulo, Brazil.
Otávio Celso Eluf GebaraSanta Casa de Misericórdia de Votuporanga, Votuporanga, Brazil.
Mauro Esteves HernandesHospital das Clínicas da Faculdade de Medicina de Botucatu, Botucatu, Brazil.
Diego Aparecido Rios QueirozBrazilian Research in Intensive Care Network-BRICNet, São Paulo, Brazil.
Viviane C VeigaBP-A Beneficência Portuguesa de São Paulo, São Paulo, Brazil.
Manoel Fernandes CanesinHospital Felício Rocho, Belo Horizonte, Brazil.
Leonardo Meira de FariaSanta Casa de Misericórdia da Bahia-Hospital Santa Izabel, Salvador, Brazil.
Gilson Soares Feitosa-FilhoHospital Moinhos de Vento, Porto Alegre, Brazil.
Marcelo Basso GazzanaInstituto Dante Pazzanese de Cardiologia, São Paulo, Brazil.
Idelzuíta Leandro LiporaceHospital de Amor de Barretos (Pio XII), Barretos, Brazil.
Aline de Oliveira TwardowskyHospital de Base de São José Do Rio Preto, São José Do Rio Preto, Brazil.
Lilia Nigro MaiaPain and Intensive Care Department, Federal University of Sao Paulo (UNIFESP), São Paulo, Brazil.
Flávia Ribeiro MachadoBP-A Beneficência Portuguesa de São Paulo, São Paulo, Brazil.
Alexandre de Matos SoeiroInstituto Do Coração (InCor), Hospital das Clinicas da Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Germano Emílio Conceição-SouzaInternational Research Center, Hospital Alemão Oswaldo Cruz, São Paulo, Brazil.
Luciana ArmaganijanBrazilian Clinical Research Institute, São Paulo, Brazil.
Patrícia O GuimarãesAcademic Research Organization, Hospital Israelita Albert Einstein, São Paulo, Brazil.
Regis G RosaBP-A Beneficência Portuguesa de São Paulo, São Paulo, Brazil.
Luciano C P AzevedoAcademic Research Organization, Hospital Israelita Albert Einstein, São Paulo, Brazil.
John H AlexanderDuke Clinical Research Institute, Duke University Medical Center, 2400 Pratt Street, Box 3850, Durham, NC, 27705, USA.
Alvaro AvezumImperial College London, London, UK.
Otávio BerwangerAcademic Research Organization, Hospital Israelita Albert Einstein, São Paulo, Brazil.
Alexandre B CavalcantiHcor Research Institute, São Paulo, Brazil.
Renato D LopesBrazilian Clinical Research Institute, São Paulo, Brazil. renato.lopes@dm.duke.edu.
ACTION Coalition COVID-19 Brazil IV Investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapeutic anticoagulation showed inconsistent results in hospitalized patients with COVID-19 and selection of the best patients to use this strategy still a challenge balancing the risk of thrombotic and hemorrhagic outcomes. The present post-hoc analysis of the ACTION trial evaluated the variables independently associated with both bleeding events (major bleeding or clinically relevant non-major bleeding) and the composite outcomes thrombotic events (venous thromboembolism, myocardial infarction, stroke, systemic embolism, or major adverse limb events). Variables were assessed one by one with independent logistic regressions and final models were chosen based on Akaike information criteria. The model for bleeding events showed an area under the curve of 0.63 (95% confidence interval [CI] 0.53 to 0.73), while the model for thrombotic events had an area under the curve of 0.72 (95% CI 0.65 to 0.79). Non-invasive respiratory support was associated with thrombotic but not bleeding events, while invasive ventilation was associated with both outcomes (Odds Ratio of 7.03 [95 CI% 1.95 to 25.18] for thrombotic and 3.14 [95% CI 1.11 to 8.84] for bleeding events). Beyond respiratory support, creatinine level (Odds Ratio [OR] 1.01 95% CI 1.00 to 1.02 for every 1.0 mg/dL) and history of coronary disease (OR 3.67; 95% CI 1.32 to 10.29) were also independently associated to the risk of thrombotic events. Non-invasive respiratory support, history of coronary disease, and creatinine level may help to identify hospitalized COVID-19 patients at higher risk of thrombotic complications.ClinicalTrials.gov: NCT04394377.

Indexed as

COVID-19Fibrin Fibrinogen Degradation ProductsHemorrhageThrombosisAgedAnticoagulantsFemaleHospitalizationHumansMaleMiddle AgedRisk FactorsSARS-CoV-2AnticoagulantsFibrin Fibrinogen Degradation Productsfibrin fragment DAnticoagulantCOVID-19HaemorrhageThromboembolism

Identifiers

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Registered trials

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.