Американское общество гирудотерапии

Argatroban Anticoagulation for Heparin Induced Thrombocytopenia After Heartmate 3 Implantation: A Case Series

Case series published in Transplantation Proceedings (2026)

Последнее обновление: June 18, 2026Рецензент: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Research reportКлинические исследованияРазработка лекарственных препаратовPalacios-Castello C et al. · Transplantation Proceedings, 2026

Abstract

BACKGROUND: Heparin-induced thrombocytopenia (HIT) is a rare but potentially fatal immune-mediated complication of heparin therapy. Its incidence is higher after left ventricular assist device (LVAD) implantation compared with other cardiac procedures. While bivalirudin is the most frequently reported alternative anticoagulant in this setting, evidence on argatroban use remains limited. We describe three cases of HIT following HeartMate 3 LVAD implantation, all managed with argatroban. RESULTS: Two patients were successfully transitioned to acenocoumarol (international normalized ratio 2-2.5) and discharged without hemocompatibility-related adverse events, without antiplatelet therapy. The third patient, with multiple thrombophilic disorders (homozygous G20210A prothrombin mutation, low protein C, positive lupus anticoagulant, and mild hyperhomocysteinemia), developed ventilator-associated pneumonia and septic shock, experienced mild bleeding at puncture and tracheostomy sites, and died postoperatively; anticoagulation transition was not achieved. In our cohort, HIT incidence was 10% overall (30 LVADs) and 15% among HeartMate 3 implants (20 LVADs), aligning with prior reports. CONCLUSIONS: Argatroban appears to be an effective and safe alternative anticoagulant for HIT after LVAD implantation, enabling platelet recovery without a significant increase in bleeding or thrombotic events. Differentiating complications attributable to HIT or argatroban from those inherent to LVAD support remains challenging, given the device's intrinsic risks of thrombosis, bleeding, and mortality.

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

Publication typeJournal Article
Indexed MeSH termsHumansPipecolic AcidsArginineSulfonamidesThrombocytopeniaHeparinAnticoagulantsHeart-Assist DevicesMaleMiddle AgedFemaleTreatment Outcome

Резюме

Three-case series of HIT after HeartMate 3 LVAD implantation managed with argatroban; two patients successfully transitioned to acenocoumarol and discharged, with HIT incidence of 15% among HeartMate 3 recipients in the cohort.

Почему это важно для гирудотерапии

This case series describes three patients who developed heparin-induced thrombocytopenia (HIT) after HeartMate 3 left ventricular assist device (LVAD) implantation, all managed with argatroban anticoagulation. Two patients were successfully transitioned to acenocoumarol and discharged without hemocompatibility-related adverse events; the third, who had multiple thrombophilic disorders, developed ventilator-associated pneumonia and septic shock, experienced mild bleeding, and died postoperatively. The article has no direct relevance to ASH's domain: the abstract discusses only argatroban and makes no mention of hirudin, lepirudin, leeches, or any leech-derived therapy. CAVEAT: This is a small three-patient case series with no leech-related content; the connection to hirudotherapy or the leech secretome is absent.

Цитирование

Argatroban Anticoagulation for Heparin Induced Thrombocytopenia After Heartmate 3 Implantation: A Case Series.

Palacios-Castello C et al. · Transplantation Proceedings, 2026

Связанный клинический контекст

Узнайте, как это исследование связано с клинической практикой

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.