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

COVID-19 SARS-CoV-2 deep vein thrombosis pulmonary embolism risk assessment model venous thromboembolism

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
07 Jul 2022
Historique:
received: 24 03 2022
revised: 25 06 2022
accepted: 04 07 2022
entrez: 27 7 2022
pubmed: 28 7 2022
medline: 28 7 2022
Statut: epublish

Résumé

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.

Identifiants

pubmed: 35887713
pii: jcm11143949
doi: 10.3390/jcm11143949
pmc: PMC9325096
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Yi Lee (Y)

Department of Medicine, St. Joseph Mercy Oakland Hospital, Pontiac, MI 48341, USA.

Qasim Jehangir (Q)

Department of Medicine, St. Joseph Mercy Oakland Hospital, Pontiac, MI 48341, USA.

Chun-Hui Lin (CH)

Department of Public Health Sciences, Henry Ford Health System, Detroit, MI 48202, USA.

Pin Li (P)

Department of Public Health Sciences, Henry Ford Health System, Detroit, MI 48202, USA.

Anupam A Sule (AA)

Department of Medicine, St. Joseph Mercy Oakland Hospital, Pontiac, MI 48341, USA.
Department of Informatics, St. Joseph Mercy Oakland Hospital, Pontiac, MI 48341, USA.

Laila Poisson (L)

Department of Public Health Sciences, Henry Ford Health System, Detroit, MI 48202, USA.

Venugopal Balijepally (V)

School of Business Administration, Oakland University, Rochester, MI 48307, USA.

Abdul R Halabi (AR)

Division of Cardiology, St. Joseph Mercy Oakland Hospital, Pontiac, MI 48341, USA.
William Beaumont School of Medicine, Oakland University, Auburn Hills, MI 48307, USA.

Kiritkumar Patel (K)

Division of Cardiology, St. Joseph Mercy Oakland Hospital, Pontiac, MI 48341, USA.

Geetha Krishnamoorthy (G)

Department of Medicine, St. Joseph Mercy Oakland Hospital, Pontiac, MI 48341, USA.

Girish B Nair (GB)

William Beaumont School of Medicine, Oakland University, Auburn Hills, MI 48307, USA.
Division of Pulmonary and Critical Care Medicine, Beaumont Health System, Royal Oak, MI 48183, USA.

Classifications MeSH