Американское общество гирудотерапии

Future prospects of prophylaxis for deep vein thrombosis

Review published in Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis (1999)

Последнее обновление: June 18, 2026Рецензент: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Narrative reviewКлинические исследованияРазработка лекарственных препаратовБезопасность и инфекционный контрольФармакология секрета слюнных желёзPini M · Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 1999

Abstract

The last decade has witnessed substantial progress in the prevention and treatment of venous thromboembolism. However, the risk of deep vein thrombosis remains high in trauma patients and those undergoing orthopaedic surgery despite use of the best available prophylaxis. Existing antithrombotics also carry a significant risk of bleeding and other adverse effects, including heparin-induced thrombocytopenia (HIT). More effective and safer anticoagulants are therefore needed. Current approaches for improving the benefit:risk ratio of antithrombotic therapy include the development of indirect thrombin inhibitors with a high anti-Xa:anti-IIa activity ratio, and the use of direct thrombin inhibitors. Novel indirect thrombin inhibitors under investigation include pentasaccharide and the heparinoid danaparoid. These agents may offer reduced bleeding risk compared with conventional therapies, but there is no evidence of greater antithrombotic efficacy. However, due to low cross-reactivity with anti-heparin-platelet factor 4 antibodies, danaparoid and pentasaccharide may prove valuable in the management of HIT. Theoretically, the antithrombotic effect of direct thrombin inhibitors may be greater than that of indirect inhibitors because direct inhibitors are not dependent on endogenous cofactors and are able to inhibit both free and clot-bound thrombin. Direct inhibitors of the active site of thrombin and recombinant variants of hirudin, originally derived from the medicinal leech, are currently under investigation. Early data on lepirudin and desirudin suggest that recombinant hirudins may have clinical applications in thromboprophylaxis for high-risk patients, acute cardiology indications and HIT.

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

Publication typeJournal ArticleReview
Indexed MeSH termsAnticoagulantsForecastingHumansPremedicationThrombinVenous Thrombosis

Резюме

The last decade has witnessed substantial progress in the prevention and treatment of venous thromboembolism.

Почему это важно для гирудотерапии

This review discusses the evolving landscape of antithrombotic prophylaxis for deep vein thrombosis, highlighting limitations of existing therapies including bleeding risk and heparin-induced thrombocytopenia (HIT). Recombinant variants of hirudin, originally derived from the medicinal leech, are discussed as direct thrombin inhibitors under investigation, with early data on lepirudin and desirudin suggesting potential clinical applications in thromboprophylaxis for high-risk patients, acute cardiology indications, and HIT management. The theoretical advantage of direct inhibitors over indirect ones—their ability to inhibit clot-bound thrombin independent of endogenous cofactors—is noted. This is directly relevant to ASH's domain as it addresses clinical translation of leech-derived anticoagulants. The caveat is that this is a review article, and the abstract characterizes the clinical data on recombinant hirudins as "early" and their applications as potential rather than established; no specific trial results are provided.

Цитирование

Future prospects of prophylaxis for deep vein thrombosis

Pini M · Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 1999

Связанный клинический контекст

Добавлено в библиотеку ASH: May 27, 2026 · Последнее обновление сайта: June 18, 2026

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