Exploring the utility of a novel point-of-care whole blood thrombin generation assay following trauma: A pilot study.

calibrated kinetics plasma thrombin trauma venous thromboembolism

Journal

Research and practice in thrombosis and haemostasis
ISSN: 2475-0379
Titre abrégé: Res Pract Thromb Haemost
Pays: United States
ID NLM: 101703775

Informations de publication

Date de publication:
Mar 2021
Historique:
received: 05 10 2020
revised: 17 12 2020
accepted: 28 12 2020
entrez: 19 4 2021
pubmed: 20 4 2021
medline: 20 4 2021
Statut: epublish

Résumé

Plasma thrombin generation kinetics as measured by the calibrated automated thrombogram (CAT) assay is a predictor of symptomatic venous thromboembolism after trauma. We hypothesized that data from a new prototype assay for measurement of thrombin generation kinetics in fresh whole blood (near patient testing of thrombin generation), will correlate with the standard CAT assay in the same patients, making it a potential tool in the future care of trauma patients. Patients were enrolled from June 2018 to February 2020. Within 12 hours of injury, blood samples were collected simultaneously for both assays. Variables compared and correlated between assays were lag time, peak height, time to peak, and endogenous thrombin potential. Data are presented as median with interquartile range (IQR). Spearman and Pearson correlations were estimated and tested between both assays; a A total of 64 trauma patients had samples analyzed: injury severity score = 17 (IQR), 10-26], hospital length of stay = 7.5 (IQR), 2-18) days, age = 52 (IQR, 35-63) years, 71.9% male, and 42.2% of patients received a transfusion within 24 hours of injury. Thrombin generation parameters between plasma and whole blood were compared and found that all parameters of the two assays correlate in trauma patients. In this pilot study, we have found that a novel point-of-care whole blood thrombin generation assay yields results with modest but statistically significant correlations to those of a standard plasma thrombin generation assay. This finding supports studying this device in a larger, adequately powered study.

Identifiants

pubmed: 33870025
doi: 10.1002/rth2.12483
pii: S2475-0379(22)01340-1
pmc: PMC8035795
doi:

Types de publication

Journal Article

Langues

eng

Pagination

395-402

Subventions

Organisme : NHLBI NIH HHS
ID : R38 HL150086
Pays : United States

Informations de copyright

© 2021 The Authors. Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis (ISTH).

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Auteurs

Michael J Ferrara (MJ)

Mayo Clinic Rochester MN USA.

Taleen A MacArthur (TA)

Mayo Clinic Rochester MN USA.

Saulius Butenas (S)

University of Vermont Colchester VT USA.

Kenneth G Mann (KG)

University of Vermont Colchester VT USA.

Joseph M Immermann (JM)

Mayo Clinic Rochester MN USA.

Grant M Spears (GM)

Mayo Clinic Rochester MN USA.

Kent R Bailey (KR)

Mayo Clinic Rochester MN USA.

Rosemary A Kozar (RA)

Shock Trauma Center University of Maryland School of Medicine Baltimore MD USA.

Stephanie F Heller (SF)

Mayo Clinic Rochester MN USA.

Erica A Loomis (EA)

Mayo Clinic Rochester MN USA.

Daniel Stephens (D)

Mayo Clinic Rochester MN USA.

Myung S Park (MS)

Mayo Clinic Rochester MN USA.

Classifications MeSH