2021
DOI: 10.1016/j.ijcard.2021.02.081
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Fondaparinux versus enoxaparin in the contemporary management of non-ST-elevation acute coronary syndromes. Insights from a multicenter registry

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Cited by 6 publications
(5 citation statements)
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“…There was a significant 43% reduction in the adjusted risk of bleeding in the fondaparinux group with fewer clinically relevant major and non-major “actionable” bleeding events versus the enoxaparin group. 43 Furthermore, greater reductions in bleeding were observed in the exploratory analyses with fondaparinux among patients undergoing a transradial approach. The study demonstrated a significant interaction between treatment and vascular access on the multiplicative scale ( P interaction = .0056), but not on an additive scale ( P = .457).…”
Section: Recent Advances In the Use Of Fondaparinux Sodiummentioning
confidence: 94%
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“…There was a significant 43% reduction in the adjusted risk of bleeding in the fondaparinux group with fewer clinically relevant major and non-major “actionable” bleeding events versus the enoxaparin group. 43 Furthermore, greater reductions in bleeding were observed in the exploratory analyses with fondaparinux among patients undergoing a transradial approach. The study demonstrated a significant interaction between treatment and vascular access on the multiplicative scale ( P interaction = .0056), but not on an additive scale ( P = .457).…”
Section: Recent Advances In the Use Of Fondaparinux Sodiummentioning
confidence: 94%
“…The study demonstrated a significant interaction between treatment and vascular access on the multiplicative scale ( P interaction = .0056), but not on an additive scale ( P = .457). 43 Another inference is that considering the current aggressive antithrombotic treatment, higher doses of enoxaparin increase bleeding while fondaparinux 2.5 mg dose may provide a sweet spot of anticoagulant activity in such situations.…”
Section: Recent Advances In the Use Of Fondaparinux Sodiummentioning
confidence: 99%
“…Low-molecular-weight or unfractionated heparin, an indirect inhibitor of factor X by its action on antithrombin, is commonly used in acute coronary syndrome, regardless of diabetes status, for its benefits on survival and major adverse cardiovascular events [108]. An alternative drug, fondaparinux, which also acts on factor X, has a better safety profile [109] but does not have any action on thrombin [110]. Newer oral anticoagulants that include factor Xa inhibitors such as rivaroxaban, apixaban, and edoxaban, and thrombin inhibitors such as bivalirudin, represent other options that target the different aspects of secondary haemostasis.…”
Section: Current Therapeutic Options In Diabetes: Anticoagulantsmentioning
confidence: 99%
“…Результаты анализа другого проспек тивного многоцентрового регистра ARIAMAndalucia, в который в 2015-2017 гг. были включены 2 094 боль ных с ИМбпST (медиана возраста 64 года, 27,7 % женщи ны), госпитализированных в отделения кардиореанима ции, также демонстрируют, что фондапаринукс исполь зуют реже, чем эноксапарин (18 и 82 % соответственно), при этом наблюдалось увеличение частоты использова ния фондапаринукса на протяжении всего периода ис следования (р для тренда <0,0001) [23]. Частота на значения фондапаринукса в РФ при ИМбпST несколь ко меньше, чем в Европе и США.…”
Section: парентеральная антикоагулянтная терапия при лечении больных ...unclassified