RYCHLÍČKOVÁ, Jitka, Vladimír ŠRÁMEK a Pavel SUK. Use of fondaparinux in patients with heparin-induced thrombocytopenia on veno-venous extracorporeal membrane oxygenation: A three-patient case series report. Frontiers in Medicine. Lausanne: FRONTIERS MEDIA SA, 2023, roč. 10, February 2023, s. 1-7. ISSN 2296-858X. Dostupné z: https://dx.doi.org/10.3389/fmed.2023.1112770.
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Základní údaje
Originální název Use of fondaparinux in patients with heparin-induced thrombocytopenia on veno-venous extracorporeal membrane oxygenation: A three-patient case series report
Autoři RYCHLÍČKOVÁ, Jitka (203 Česká republika, garant, domácí), Vladimír ŠRÁMEK (203 Česká republika, domácí) a Pavel SUK (203 Česká republika, domácí).
Vydání Frontiers in Medicine, Lausanne, FRONTIERS MEDIA SA, 2023, 2296-858X.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30104 Pharmacology and pharmacy
Stát vydavatele Švýcarsko
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 3.900 v roce 2022
Kód RIV RIV/00216224:14110/23:00130657
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.3389/fmed.2023.1112770
UT WoS 000945810700001
Klíčová slova anglicky fondaparinux; pharmacokinetics; heparin-induced thrombocytopenia; extracorporeal membrane oxygenation; pharmacoeconomics
Štítky 14110122, 14110516, rivok
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Tereza Miškechová, učo 341652. Změněno: 27. 4. 2023 10:17.
Anotace
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.
VytisknoutZobrazeno: 23. 6. 2024 10:28