Американское общество гирудотерапии

Anticoagulation with Intravenous Direct Thrombin Inhibitors in Pediatric Extracorporeal Membrane Oxygenation: A Systematic Review of the Literature

Systematic review published in Semin Thromb Hemost (2023)

Последнее обновление: June 18, 2026Рецензент: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Systematic reviewРазработка лекарственных препаратовКлинические исследованияKiskaddon AL et al. · Seminars in thrombosis and hemostasis, 2023

Abstract

Although intravenous (IV) direct thrombin inhibitors (DTI) have gained interest in pediatric extracorporeal membrane oxygenation (ECMO), dosing and safety information is limited. The objective of this systematic review was to characterize DTI types, dosing, monitoring, and outcomes (bleeding and thromboembolic) in pediatric ECMO patients managed with IV DTIs. We conducted searches of MEDLINE (Ovid) and Embase (Elsevier) from inception through December 2022. Case reports, retrospective studies, and prospective studies providing per-patients or summary data for patient(s) <18 years of age receiving IV DTI for ECMO anticoagulation were included. Study selection and data extraction were conducted independently by two reviewers. A total of 28 studies: 14 case reports, 13 retrospective studies, and 1 prospective study were included, totaling 329 patients. Bivalirudin was utilized in 318 (96.7%), argatroban in 9 (2.7%), and lepirudin in 2 (0.6%) patients. Infusion dosing included: bivalirudin 0.14 ± 0.37 mg/kg/h, argatroban 0.69 ± 0.73 µg/kg/min, lepirudin 0.14 ± 0.02 mg/kg/h. Laboratory monitoring tests utilized were the activated clotting time, activated partial thromboplastin time (aPTT), diluted thrombin time, and thromboelastography measures. The aPTT was utilized in most patients (95%). Thromboembolism, bleeding, or death were observed in 17%, 17%, and 23% of bivalirudin, argatroban, and lepirudin patients, respectively. Bivalirudin appears to be the most frequently used DTI in pediatric ECMO. Dosing and laboratory monitoring varied, and bleeding and thromboembolic events were reported in 17% of patients. Prospective studies are warranted to establish dosing, monitoring, safety, and efficacy of bivalirudin and other IV DTI in pediatric ECMO.

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

Publication typeSystematic ReviewJournal Article
Indexed MeSH termsHumansChildAntithrombinsExtracorporeal Membrane OxygenationProspective StudiesRetrospective StudiesArgininePipecolic AcidsSulfonamides

Резюме

Systematic review of 28 studies (329 patients) of DTIs in pediatric ECMO. Bivalirudin used in 96.7% of patients, argatroban 2.7%, lepirudin 0.6%; thromboembolism, bleeding, death in 17%, 17%, 23% by drug.

Почему это важно для гирудотерапии

This systematic review characterized intravenous direct thrombin inhibitor (DTI) use in pediatric ECMO, identifying 28 studies totaling 329 patients. The abstract reports that bivalirudin was the most frequently used DTI (96.7%), argatroban in 2.7%, and lepirudin in 0.6% of patients, with bivalirudin infusion dosing of approximately 0.14 mg/kg/h. Thromboembolism, bleeding, or death were observed in 17%, 17%, and 23% of bivalirudin, argatroban, and lepirudin patients, respectively. No defensible connection to hirudotherapy, leech therapy, or the leech secretome exists based on this abstract, which makes no mention of hirudin, leeches, or any derivation thereof. The review is limited by heterogeneous data sources, and the authors call for prospective studies to establish optimal dosing, monitoring, safety, and efficacy.

Цитирование

Anticoagulation with Intravenous Direct Thrombin Inhibitors in Pediatric Extracorporeal Membrane Oxygenation: A Systematic Review of the Literature.

Kiskaddon AL et al. · Seminars in thrombosis and hemostasis, 2023

Связанный клинический контекст

Узнайте, как это исследование связано с клинической практикой

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

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