Evidence map›Paper›PMID 35716998›Full record

ArticleJournal of vascular surgery. Venous and lymphatic disorders2022

Low-molecular-weight heparin compared with unfractionated heparin in critically ill COVID-19 patients.

Panagiotis Volteas, Panagiotis Drakos, Leor N Alkadaa, Nathaniel A Cleri, Anthony A Asencio, Anthony Oganov, Stefanos Giannopoulos, Jordan R Saadon, Charles B Mikell, Jerry A Rubano and 4 more

Abstract read
In one paragraph

Article in Journal of vascular surgery. Venous and lymphatic disorders, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
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  7. COVID-19 Treatment-Current Status, Advances, and Gap.Pathogens (Basel, Switzerland) · 2022
    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

14 authors.

Panagiotis VolteasDepartment of Surgery, Renaissance School of Medicine, Stony Brook, NY.
Panagiotis DrakosDepartment of Surgery, Renaissance School of Medicine, Stony Brook, NY.
Leor N AlkadaaDepartment of Neurosurgery, Renaissance School of Medicine, Stony Brook, NY.
Nathaniel A CleriDepartment of Neurosurgery, Renaissance School of Medicine, Stony Brook, NY.
Anthony A AsencioDepartment of Neurosurgery, Renaissance School of Medicine, Stony Brook, NY.
Anthony OganovDepartment of Neurosurgery, Renaissance School of Medicine, Stony Brook, NY.
Stefanos GiannopoulosDepartment of Surgery, Renaissance School of Medicine, Stony Brook, NY; Division of Vascular Surgery, Department of Surgery, Renaissance School of Medicine, Stony Brook, NY.
Jordan R SaadonDepartment of Neurosurgery, Renaissance School of Medicine, Stony Brook, NY.
Charles B MikellDepartment of Neurosurgery, Renaissance School of Medicine, Stony Brook, NY.
Jerry A RubanoDepartment of Surgery, Renaissance School of Medicine, Stony Brook, NY.
Nicos LabropoulosDivision of Vascular Surgery, Department of Surgery, Renaissance School of Medicine, Stony Brook, NY.
Apostolos K TassiopoulosDepartment of Surgery, Renaissance School of Medicine, Stony Brook, NY; Division of Vascular Surgery, Department of Surgery, Renaissance School of Medicine, Stony Brook, NY.
Sima MofakhamDepartment of Neurosurgery, Renaissance School of Medicine, Stony Brook, NY. Electronic address: sima.mofakham@stonybrookmedicine.edu.
Mohsen BannazadehDepartment of Surgery, Renaissance School of Medicine, Stony Brook, NY; Division of Vascular Surgery, Department of Surgery, Renaissance School of Medicine, Stony Brook, NY.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThrombosis in COVID-19 worsens mortality. In our study, we sought to investigate how the dose and type of anticoagulation (AC) can influence patient outcomes.

methodsThis is a single-center retrospective analysis of critically ill intubated patients with COVID-19, comparing low-molecular-weight heparin (LMWH) and unfractionated heparin (UFH) at therapeutic and prophylactic doses. Of 218 patients, 135 received LMWH (70 prophylactic, 65 therapeutic) and 83 UFH (11 prophylactic, 72 therapeutic). The primary outcome was mortality. Secondary outcomes were thromboembolic complications confirmed on imaging and major bleeding complications. Cox proportional-hazards regression models were used to determine whether the type and dose of AC were independent predictors of survival. We performed Kaplan-Meier survival analysis to compare the cumulative survivals.

resultsOverall, therapeutic AC, with either LMWH (65% vs 79%, P = .09) or UFH (32% vs 46%, P = .73), conveyed no survival benefit over prophylactic AC. UFH was associated with a higher mortality rate than LMWH (66% vs 28%, P = .001), which was also evident in the multivariable analysis (LMWH vs UFH mortality, hazard ratio: 0.47, P = .001) and in the Kaplan-Meier survival analysis. Thrombotic and bleeding complications did not depend on the AC type (prophylactic LMWH vs UFH: thrombosis P = .49, bleeding P = .075; therapeutic LMWH vs UFH: thrombosis P = .5, bleeding P = .17). When comparing prophylactic with therapeutic AC, the rate of both thrombotic and bleeding complications was higher with the use of LMWH compared with UFH. In addition, transfusion requirements were significantly higher with both therapeutic LMWH and UFH.

conclusionsAmong intubated critically ill COVID-19 intensive care unit patients, therapeutic AC, with either LMWH or UFH, conveyed no survival benefit over prophylactic AC. AC with LMWH was associated with higher cumulative survival compared with AC with UFH.

Indexed as

COVID-19ThrombosisAnticoagulantsCritical IllnessHeparinHeparin, Low-Molecular-WeightHumansRetrospective StudiesAnticoagulantsHeparinHeparin, Low-Molecular-WeightAnticoagulation (AC)COVID-19Low-molecular-weight heparin (LMWH)SARS-CoV-2ThromboprophylaxisUnfractionated heparin (UFH)

Identifiers

PMID35716998
PMCPMC9212478

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.