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Activated partial thromboplastin time and anti-Ila monitoring in argatroban anticoagulation in COVID-19 patients on venovenous extracorporeal membrane oxygenation

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00843989%3A_____%2F25%3AE0111701" target="_blank" >RIV/00843989:_____/25:E0111701 - isvavai.cz</a>

  • Result on the web

    <a href="https://journals.sagepub.com/doi/10.1177/10760296251341315" target="_blank" >https://journals.sagepub.com/doi/10.1177/10760296251341315</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1177/10760296251341315" target="_blank" >10.1177/10760296251341315</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Activated partial thromboplastin time and anti-Ila monitoring in argatroban anticoagulation in COVID-19 patients on venovenous extracorporeal membrane oxygenation

  • Original language description

    Unfractionated heparin has long been considered the standard anticoagulation in ECMO, despite some pitfalls such as heparin resistance, heparin induced thrombocytopenia (HIT), etc Recently, some centres started to increasingly use argatroban for this purpose, typically using activated partial thromboplastin time (aPTT) for its monitoring. Direct monitoring of the efficacy of argatroban using Anti-IIa is not yet an established method, although it might be more appropriate as it targets the same pathway.An observational study was performed in adult veno-venous ECMO patients hospitalized with SARS-CoV-2 infection anticoagulated with argatroban to an aPTT target of 40-60 s and Anti-IIa target of 0.4-0.6 µg/mL. Bleeding and thrombotic complications were monitored.Forty-four VV ECMO patients were included, with an overall hospital mortality of approx. 50%. No life-threatening thrombotic events were recorded. The risk of bleeding complications significantly increased with aPTT above 52.7 s and with Anti-IIa values over 0.78 µg/mL. Using the above cut-offs for both the aPTT and Anti-IIa and their combination, the negative predictive value for bleeding was approximately 90%.It seems that the generally recommended limits for Anti-IIa of 1.5 µg/mL may be high. However, further data are needed to confirm lower limits.Trial Registration:retrospectively registered in ClinicalTrials.gov, NCT06038682.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30221 - Critical care medicine and Emergency medicine

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Clinical and applied thrombosis/hemostasis

  • ISSN

    1076-0296

  • e-ISSN

    1938-2723

  • Volume of the periodical

    31

  • Issue of the periodical within the volume

    article 10760296251341315

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    10

  • Pages from-to

    1-10

  • UT code for WoS article

    001492873100001

  • EID of the result in the Scopus database

    2-s2.0-105005846028