Evidence map›Paper›PMID 36769576›Full record

ArticleJournal of clinical medicine2023

Enoxaparin Posology According to Prothrombotic Status and Bleeding Risk in Hospitalized Patients with SARS-CoV-2 Pneumonia.

Juan Mora-Delgado, Cristina Lojo-Cruz, Patricia Rubio Marín, Eva María Menor Campos, Alfredo Michán-Doña

Abstract read
In one paragraph

Article in Journal of clinical medicine, 2023. 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
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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

5 authors.

Juan Mora-DelgadoInternal Medicine and Palliative Care Clinical Management Unit, Hospital Universitario de Jerez de la Frontera, Jerez de la Frontera, 11407 Cádiz, Spain.ORCID 0000-0002-7633-9794
Cristina Lojo-CruzInternal Medicine and Palliative Care Clinical Management Unit, Hospital Universitario de Jerez de la Frontera, Jerez de la Frontera, 11407 Cádiz, Spain.
Patricia Rubio MarínInternal Medicine and Palliative Care Clinical Management Unit, Hospital Universitario de Jerez de la Frontera, Jerez de la Frontera, 11407 Cádiz, Spain.ORCID 0000-0003-1843-0431
Eva María Menor CamposInternal Medicine and Palliative Care Clinical Management Unit, Hospital Universitario de Jerez de la Frontera, Jerez de la Frontera, 11407 Cádiz, Spain.
Alfredo Michán-DoñaInternal Medicine and Palliative Care Clinical Management Unit, Hospital Universitario de Jerez de la Frontera, Jerez de la Frontera, 11407 Cádiz, Spain.ORCID 0000-0002-4373-6224

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Some patients with COVID-19 have complex hypercoagulable abnormalities that are related to mortality. The optimal dosage of low molecular weight heparin in hospitalized patients with SARS-CoV-2 pneumonia is still not clear. Our objective is to evaluate the effects of adapting the dosage of low molecular weight heparin to thrombotic and bleeding risk scales in this setting. We performed a cohort, retrospective, observational, and analytical study at the Hospital Universitario of Jerez de la Frontera, with patients admitted with SARS-CoV-2 pneumonia from 1 October 2020 to 31 January 2021. They were classified according to whether they received prophylactic, intermediate, or therapeutic doses of enoxaparin. The primary endpoint was intrahospital mortality. Secondary endpoints were the need for invasive ventilation, thromboembolic events, bleeding, and the usefulness of thrombotic and bleeding scales. After binary logistic regression analysis, considering confounding variables, it was found that the use of enoxaparin at therapeutic doses was associated with lower mortality during admission compared to prophylactic and intermediate doses (RR 0.173; 95% CI, 0.038-0.8;

Indexed as

COVID-19enoxaparinhemorrhagic risklow molecular weight heparinSARS-CoV-2 pneumoniathromboembolic diseasethrombotic risk

Identifiers

PMID36769576
PMCPMC9918225

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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.