Kristina Brisudova

Dr. Kristina Brisudova


Research Focus & Metrics

Academic Career Length

5Years (2022-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
13 June 2024 in Pharmaceuticals
Verified
Journal Article
Open access
PDF file
LSLucia Stanciakova
Lucia Stanciakova
KBKristina Brisudova
Kristina Brisudova
ISIngrid Skornova
Ingrid Skornova
TBTomáš Bolek
Tomáš Bolek
MSMatej Samos
Matej Samos
JSJuraj Sokol
Juraj Sokol
Venous thromboembolism (VTE) represents one of the leading causes of death during pregnancy. The greatest risk for it is the presence of medical or family history of VTE, stillbirth, cesarean section and selected thrombophilia. Appropriate thromboprophylaxis has the potential to decrease the risk of VTE in at-risk pregnant patients by 60–70%. Based on this, the authors reviewed the PubMed, Web of Science and Scopus databases to identify the possibilities of thromboprophylaxis in pregnant patients with a high risk of VTE. Moreover, they summarized its management in specific situations, such as cesarean delivery or neuraxial blockade. Currently, low-molecular-weight heparins (LMWH) are the preferred drugs for anticoagulant thromboprophylaxis in the course of pregnancy and postpartum due to easy administration and a lower rate of adverse events.

28 October 2022 in Journal of Clinical Medicine
Verified
Journal Article
Open access
PDF file
MSMatej Samos
Matej Samos
TBTomáš Bolek
Tomáš Bolek
LSLucia Stanciakova
Lucia Stanciakova
MPMartin Péč
Martin Péč
KBKristina Brisudova
Kristina Brisudova
PKPeter Kubisz
Peter Kubisz
Direct oral anticoagulants (DOAC) are currently the drug of choice for drug prevention of stroke or systemic embolism in patients with atrial fibrillation (AF). However, repeated ischemic stroke or systemic embolism and bleeding while on DOAC is still a challenging clinical phenomenon in the management of future long-term anticoagulation. It is not known whether tailoring the DOAC therapy to achieve optimal therapeutic drug levels could improve the clinical course of DOAC therapy. To be able to tailor the therapy, it is necessary to have a valid laboratory method for DOAC level assessment, to be aware of factors influencing DOAC levels and to have clinical options to tailor the treatment. Furthermore, the data regarding clinical efficacy/safety of tailored DOAC regimes are still lacking. This article reviews the current data on tailored direct oral anticoagulation in patients with AF.