Американское общество гирудотерапии

Laboratory Monitoring of Parenteral Direct Thrombin Inhibitors

Review published in Seminars in Thrombosis and Hemostasis (2017)

Последнее обновление: June 18, 2026Рецензент: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Narrative reviewРазработка лекарственных препаратовКлинические исследованияVan Cott EM et al. · Seminars in Thrombosis and Hemostasis, 2017

Abstract

Argatroban and bivalirudin are parenteral direct inhibitors of the activity of thrombin, but, unlike heparin, can inhibit both soluble as well as clot-bound thrombin. These agents do not require antithrombin as a cofactor for activity. The parenteral direct thrombin inhibitors (DTIs) can be used in a variety of settings, including heparin-induced thrombocytopenia (HIT) or an allergy to heparin, and patients requiring anticoagulation for an invasive cardiovascular intervention. Both agents have a relatively short half-life in patients without organ system failure and are typically administered by continuous infusion. Argatroban is primarily eliminated by the liver, while bivalirudin is removed by a combination of proteolytic cleavage by thrombin and renal clearance mechanisms. Several laboratory tests are available for monitoring the anticoagulant effects of the DTIs: the activated partial thromboplastin time (aPTT) and the activated clotting time (ACT) are the most commonly used assays, but on occasion, the thrombin time may be useful. Other coagulation assays such as the dilute thrombin time (dTT), chromogenic anti-IIa assays, and the ecarin clotting time (ECT) can be used. The intensity of anticoagulation with DTIs depends on the indication for use. For patients with HIT, the target aPTT is 1.5 to 3.0 and 1.5 to 2.5 times the patient's baseline value for argatroban and bivalirudin, respectively. DTI anticoagulation used during percutaneous coronary intervention can be measured using ACT. Both DTIs may cause an elevation in the international normalized ratio depending on their plasma concentration. This article will review the use of parenteral DTIs and related laboratory assays for assessing the anticoagulant effect of these drugs.

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

Publication typeJournal ArticleReview
Indexed MeSH termsAntithrombinsArginineDrug MonitoringHirudinsHumansInfusions, ParenteralPartial Thromboplastin TimePeptide FragmentsPipecolic AcidsPoint-of-Care SystemsRecombinant ProteinsSulfonamides

Резюме

Authoritative review of laboratory monitoring approaches for parenteral direct thrombin inhibitors argatroban and bivalirudin (aPTT, ACT, thrombin time, ecarin clotting time, chromogenic anti-IIa); discusses indication-specific target ranges.

Почему это важно для гирудотерапии

This review details laboratory monitoring for parenteral direct thrombin inhibitors, focusing on argatroban and bivalirudin in settings such as HIT, heparin allergy, and invasive cardiovascular intervention. It explains that these agents inhibit both soluble and clot-bound thrombin without antithrombin as a cofactor, and discusses aPTT, ACT, dilute thrombin time, chromogenic anti-IIa, and ecarin clotting assays. The abstract does not mention leeches, hirudin, leech saliva, or hirudotherapy, so it offers no defensible connection to ASH's domain or the leech secretome. Its limitation is that it concerns pharmaceutical laboratory assays rather than clinical hirudotherapy outcomes, and no actual leech use is described.

Цитирование

Laboratory Monitoring of Parenteral Direct Thrombin Inhibitors.

Van Cott EM et al. · Seminars in Thrombosis and Hemostasis, 2017

Связанный клинический контекст

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

Этот сайт предоставляет образовательную информацию и не является медицинской консультацией, диагнозом или рекомендацией по лечению. Гирудотерапия сопряжена с клинически значимыми рисками и должна проводиться только квалифицированными клиницистами в рамках институционально утверждённых протоколов. Разрешение FDA 510(k) для медицинских пиявок ограничено определёнными показаниями; обсуждения исследовательского и нелицензионного применения отмечены соответствующим образом. Для индивидуальных медицинских рекомендаций обратитесь к квалифицированному медицинскому специалисту.