Evidence map›Paper›PMID 35887713›Full record

ArticleJournal of clinical medicine2022

3D-PAST: Risk Assessment Model for Predicting Venous Thromboembolism in COVID-19.

Yi Lee, Qasim Jehangir, Chun-Hui Lin, Pin Li, Anupam A Sule, Laila Poisson, Venugopal Balijepally, Abdul R Halabi, Kiritkumar Patel, Geetha Krishnamoorthy and 1 more

Abstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Prognostic Nutritional Index as a Potential Biomarker for the Risk of Lower Extremity Deep Venous Thrombosis: A Large Retrospective Study.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    Article
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

11 authors.

Yi LeeDepartment of Medicine, St. Joseph Mercy Oakland Hospital, Pontiac, MI 48341, USA.ORCID 0000-0002-2740-5206
Qasim JehangirDepartment of Medicine, St. Joseph Mercy Oakland Hospital, Pontiac, MI 48341, USA.ORCID 0000-0003-2980-067X
Chun-Hui LinDepartment of Public Health Sciences, Henry Ford Health System, Detroit, MI 48202, USA.ORCID 0000-0002-2133-1453
Pin LiDepartment of Public Health Sciences, Henry Ford Health System, Detroit, MI 48202, USA.
Anupam A SuleDepartment of Medicine, St. Joseph Mercy Oakland Hospital, Pontiac, MI 48341, USA.ORCID 0000-0002-5931-3381
Laila PoissonDepartment of Public Health Sciences, Henry Ford Health System, Detroit, MI 48202, USA.
Venugopal BalijepallySchool of Business Administration, Oakland University, Rochester, MI 48307, USA.
Abdul R HalabiDivision of Cardiology, St. Joseph Mercy Oakland Hospital, Pontiac, MI 48341, USA.
Kiritkumar PatelDivision of Cardiology, St. Joseph Mercy Oakland Hospital, Pontiac, MI 48341, USA.
Geetha KrishnamoorthyDepartment of Medicine, St. Joseph Mercy Oakland Hospital, Pontiac, MI 48341, USA.
Girish B NairWilliam Beaumont School of Medicine, Oakland University, Auburn Hills, MI 48307, USA.ORCID 0000-0002-9696-4263

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypercoagulability is a recognized feature in SARS-CoV-2 infection. There exists a need for a dedicated risk assessment model (RAM) that can risk-stratify hospitalized COVID-19 patients for venous thromboembolism (VTE) and guide anticoagulation. We aimed to build a simple clinical model to predict VTE in COVID-19 patients. This large-cohort, retrospective study included adult patients admitted to four hospitals with PCR-confirmed SARS-CoV-2 infection. Model training was performed on 3531 patients hospitalized between March and December 2020 and validated on 2508 patients hospitalized between January and September 2021. Diagnosis of VTE was defined as acute deep vein thrombosis (DVT) or pulmonary embolism (PE). The novel RAM was based on commonly available parameters at hospital admission. LASSO regression and logistic regression were performed, risk scores were assigned to the significant variables, and cutoffs were derived. Seven variables with assigned scores were delineated as: DVT History = 2; High D-Dimer (>500−2000 ng/mL) = 2; Very High D-Dimer (>2000 ng/mL) = 5; PE History = 2; Low Albumin (<3.5 g/dL) = 1; Systolic Blood Pressure <120 mmHg = 1, Tachycardia (heart rate >100 bpm) = 1. The model had a sensitivity of 83% and specificity of 53%. This simple, robust clinical tool can help individualize thromboprophylaxis for COVID-19 patients based on their VTE risk category.

Indexed as

COVID-19deep vein thrombosispulmonary embolismrisk assessment modelSARS-CoV-2venous thromboembolism

Identifiers

PMID35887713
PMCPMC9325096

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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.