Detailed Information on Publication Record
2023
Use of fondaparinux in patients with heparin-induced thrombocytopenia on veno-venous extracorporeal membrane oxygenation: A three-patient case series report
RYCHLÍČKOVÁ, Jitka, Vladimír ŠRÁMEK and Pavel SUKBasic information
Original name
Use of fondaparinux in patients with heparin-induced thrombocytopenia on veno-venous extracorporeal membrane oxygenation: A three-patient case series report
Authors
RYCHLÍČKOVÁ, Jitka (203 Czech Republic, guarantor, belonging to the institution), Vladimír ŠRÁMEK (203 Czech Republic, belonging to the institution) and Pavel SUK (203 Czech Republic, belonging to the institution)
Edition
Frontiers in Medicine, Lausanne, FRONTIERS MEDIA SA, 2023, 2296-858X
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30104 Pharmacology and pharmacy
Country of publisher
Switzerland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 3.900 in 2022
RIV identification code
RIV/00216224:14110/23:00130657
Organization unit
Faculty of Medicine
UT WoS
000945810700001
Keywords in English
fondaparinux; pharmacokinetics; heparin-induced thrombocytopenia; extracorporeal membrane oxygenation; pharmacoeconomics
Tags
International impact, Reviewed
Změněno: 27/4/2023 10:17, Mgr. Tereza Miškechová
Abstract
V originále
Heparin-induced thrombocytopenia is a life-threatening immune-mediated complication of unfractionated heparin therapy. Fondaparinux is a therapeutic alternative, but it has limited evidence for its use in patients on extracorporeal membrane oxygenation (ECMO). We present a series of three adult patients with COVID-19 on ECMO who were diagnosed with heparin-induced thrombocytopenia after 7-12 days of unfractionated heparin treatment and were switched to fondaparinux. Fondaparinux was initiated with an intravenous loading dose of 5 mg, followed by a dose of 2.5 mg subcutaneously every 8-12 h. Dosage was adjusted according to daily measured anti-Xa concentration with a target range of 0.4-0.7 mg/L. The total duration of treatment with fondaparinux and ECMO ranged from 13 to 26 days. One major bleeding episode unrelated to fondaparinux therapy was observed, and the transfusions requirement was also low in all patients. The ECMO circuit was changed once in each patient. This series provides a deep insight into the use of fondaparinux over an extended period of time in patients on ECMO. Based on the presented data, fondaparinux can be considered a reasonable and affordable anticoagulant in patients without a high risk of bleeding.