Fondaparinux sodium
Research article published in Drugs of today (Barcelona, Spain : 1998) (2002)
Abstract
Fondaparinux (Org-31540 / SR-90107A) is a new drug chemically synthesized for treatment and prophylaxis of thromboembolic disease. Fondaparinux is a selective inhibitor of activated factor X. Its structure is the copy of the heparin pentasaccharide sequence, the shortest chain required for antithrombin inhibition of activated factor X without antithrombin action. Fondaparinux has no effect on coagulation tests and does not bind to platelet factor 4 or promote heparin-induced thrombocytopenia. Fondaparinux inhibits thrombin generation and the growth of thrombi in in vitro and in vivo models. Phase I trials have shown a 100% bioavailability after subcutaneous (s.c.) administration, a rapid onset of action and an approximate half-life of 13.5 h. Fondaparinux is cleared as an active substance by the kidneys. In elderly patients, renal clearance is reduced and the half-life is longer. The phase II Pentathlon trial demonstrated significant dose-dependent reductions in the frequency of venous thromboembolism in total hip-replacement patients and the optimal dose was determined to be 2.5 mg s.c./24 h. Four phase III trials have evaluated fondaparinux starting 6 hours after surgery compared with enoxaparin for prevention of venous thromboembolism following orthopedic surgery in 7,344 patients. The risk of thrombosis was reduced by 50% with fondaparinux and no differences were observed in death or severe bleeding. In a phase II trial, similar efficacy and incidence of major bleeding were seen with fondaparinux s.c. compared with dalteparin s.c. in the treatment of deep venous thrombosis. In patients with acute myocardial infarction, the efficacy of fondaparinux during fibrinolytic therapy was assessed in 326 patients who had acute coronary syndromes of less than a 6 hour duration, showing a slight but statistically not significant advantage for fondaparinux over unfractionated heparin in the coronary angiographies. There is currently no antidote for fondaparinux.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Resumen
Peer-reviewed clinical and outcomes research relevant to medicinal leech therapy and its biology. Indexed in PubMed and verified against the NCBI record.
Por qué esto importa para la hirudoterapia
Esta revisión presenta el fondaparinux, un inhibidor selectivo del factor X activado sintetizado químicamente basado en la secuencia de pentasacárido de heparina, reportando una bioavailability subcutánea del 100%, una vida media aproximada de 13,5 h, eliminación renal, sin efecto en pruebas de coagulación rutinarias, sin unión al factor 4 de plaquetas (sin trombocitopenia inducida por heparina) y datos de fase III de cirugía ortopédica (7.344 pacientes) que muestran un riesgo de trombosis aproximadamente reducido a la mitad versus enoxaparina sin exceso de sangrado severo. En cuanto a la hirudoterapia, el valor es contextual: el fondaparinux es un inhibidor sintético del factor Xa, no una molécula derivada de Hirudo, pero ejemplifica la tradición de descubrimiento de fármacos racional de la ingeniería de anticoagulantes de un solo objetivo precisos — un linaje en el que la hirudina derivada de lombriz (un inhibidor directo de trombina) es un prototipo natural históricamente importante que ayudó a abrir el campo antitrombótico. Aviso: esta es una revisión temprana (2002) de un agente no de lombriz y nota explícitamente que actualmente no hay antídoto para el fondaparinux; no proporciona evidencia directa sobre la terapia con lombriz medicinal.
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Añadido a la biblioteca ASH: May 28, 2026 · Última actualización del sitio: June 18, 2026