Sociedad Americana de Hirudoterapia

Current agents for the treatment of patients with heparin-induced thrombocytopenia

Review published in Curr Opin Pulm Med (2002)

Última actualización: June 18, 2026Revisado por: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Narrative reviewDesarrollo de fármacosEnsayos clínicosWarkentin TE · Current opinion in pulmonary medicine, 2002

Abstract

Several counterintuitive treatment paradoxes complicate the management of immune heparin-induced thrombocytopenia (HIT). For example, simple discontinuation of heparin often fails to prevent subsequent HIT-associated thrombosis. Thus, current treatment guidelines recommend substituting heparin with a rapidly acting alternative anticoagulant (eg, danaparoid, lepirudin, or argatroban) even when HIT is suspected on the basis of thrombocytopenia alone ("isolated HIT"). Another paradox-coumarin (warfarin) anticoagulation-can lead to venous limb gangrene in a patient with HIT-associated deep-vein thrombosis. Thus, warfarin is not recommended during acute thrombocytopenia secondary to HIT. However, warfarin can be given as overlapping therapy with an alternative anticoagulant, provided that (1) initiation of warfarin is delayed until substantial platelet count recovery has occurred (to at least above 100 x 10(9)/L); (2) low initial doses of warfarin are used; (3) at least 5 days of overlapping therapy are given; and (4) the alternative agent is maintained until the platelet count has normalized. It has recently been recognized that HIT antibodies are transient and usually do not recur upon subsequent re-exposure to heparin. This leads to a further paradox-patients with previous HIT can be considered for a brief re-exposure to heparin under exceptional circumstances; for example, heart surgery requiring cardiopulmonary bypass, if HIT antibodies are no longer detectable using sensitive assays. For patients with acute or recent HIT who require urgent heart surgery, other approaches include use of alternative anticoagulants (eg, lepirudin or danaparoid) for cardiopulmonary bypass or antiplatelet agents (eg, tirofiban or epoprostenol) to permit intraoperative use of heparin.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeJournal ArticleReview
Indexed MeSH termsAnticoagulantsAntithrombinsArginineAutoimmune DiseasesChondroitin SulfatesDermatan SulfateDrug CombinationsHeparinHeparan SulfateHirudin TherapyHirudinsHumans

Resumen

Definitive Warkentin review of HIT treatment paradigm including avoidance of warfarin until platelet recovery and use of danaparoid, lepirudin or argatroban as alternatives.

Por qué esto importa para la hirudoterapia

Esta revisión describe las paradojas del manejo de la trombocitopenia inducida por heparin (HIT) y señala que las guías recomiendan sustituir la heparin por un anticoagulante alternativo de acción rápida, enumerando lepirudin junto con danaparoid y argatroban, incluso para el bypass cardiopulmonar. La conexión con la hirudoterapia es que lepirudin es hirudin recombinante, un DTI derivado del anticoagulante de la sanguijuela medicinal, por lo que el artículo muestra que la anticoagulación derivada de la sanguijuela ocupa un nicho clínico reconocido donde la heparin está contraindicada. Advertencia: se trata de una revisión narrativa que resume las guías de tratamiento de otras fuentes en lugar de datos primarios, y se refiere a una proteína de sanguijuela recombinante purificada utilizada como fármaco sistémico, lo cual es distinto de la terapia tópica con Hirudo medicinalis/verbana.

Citación

Current agents for the treatment of patients with heparin-induced thrombocytopenia.

Warkentin TE · Current opinion in pulmonary medicine, 2002

Contexto clínico relacionado

Añadido a la biblioteca ASH: May 27, 2026 · Última actualización del sitio: June 18, 2026

Este sitio web proporciona información educativa y no constituye consejo médico, diagnóstico ni recomendaciones de tratamiento. La terapia con sanguijuelas medicinales conlleva riesgos clínicamente significativos y debe ser realizada únicamente por profesionales calificados bajo protocolos aprobados institucionalmente. La autorización 510(k) de la FDA para sanguijuelas medicinales se limita a indicaciones específicas; las discusiones sobre uso investigativo y fuera de indicación se señalan correspondientemente. Para orientación médica específica, consulte a un profesional de salud calificado.