Amerikanische Gesellschaft für Hirudotherapie

Bivalirudin anticoagulation in neonates and infants undergoing cardiac surgery

Pilot study published in J Cardiothorac Vasc Anesth (2022)

Zuletzt aktualisiert: June 18, 2026Geprüft von: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Research reportArzneimittelentwicklungKlinische StudienHasija S et al. · Journal of cardiothoracic and vascular anesthesia, 2022

Abstract

OBJECTIVES: To determine the dosage of bivalirudin as the anticoagulant for cardiac surgery in neonates and infants. DESIGN: Pilot study. SETTING: Tertiary-care hospital. PARTICIPANTS: Twenty-five neonates and infants with congenital heart disease (CHD) undergoing cardiac surgery. INTERVENTIONS: The children received a 1 mg/kg bivalirudin bolus followed by a 2.5 mg/kg/h infusion as the anticoagulant for cardiac surgery. The dose was adjusted subsequently to maintain an activated clotting time (ACT) >480 s. MEASUREMENTS AND MAIN RESULTS: The mean age and weight were 5.3 months and 5.2 kg, respectively. Out of the 25 children, 16 were cyanotic. Baseline rotational thromboelastometry (ROTEM) (Tem Innovations GmbH, Munich, Germany) analysis revealed an underlying coagulation defect across EXTEM, INTEM, FIBTEM, and ADPTEM parameters. The dose of anticoagulant required was 1 mg/kg, followed by a 2.2 ± 0.4 mg/kg/h infusion. Only 1 child required an additional bolus dose. The ACT remained elevated for 4 hours after discontinuation of infusion. The mean 24-h postoperative chest tube drainage was 92 ± 36 mL. Excessive bleeding occurred in 4 children, 1 of whom required re-exploration. The platelet count remained low for 5 days, and, postoperatively, the prothrombin time and activated partial thromboplastin time remained low for 2 days. CONCLUSIONS: Effective anticoagulation was achieved with bivalirudin in the neonates and infants undergoing cardiac surgery. The dose required to maintain an ACT >480 s was 1.0 mg/kg, followed by 2.2 ± 0.4 mg/kg/h. The ACT remained elevated for 4 h after the discontinuation of bivalirudin infusion, resulting in an increased chest-tube output in some patients. Randomized, controlled trials are needed to further evaluate the safety of bivalirudin in the neonates and infants with complex congenital heart disease undergoing cardiac surgery with cardiopulmonary bypass.

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

Publication typeJournal ArticleResearch Support, Non-U.S. Gov't
Indexed MeSH termsAnticoagulantsCardiac Surgical ProceduresHeart Defects, CongenitalHirudinsHumansInfantInfant, NewbornPeptide FragmentsPilot ProjectsRecombinant Proteins

Zusammenfassung

Pilot study of bivalirudin (1 mg/kg bolus, 2.2 mg/kg/h infusion) in 25 neonates/infants undergoing cardiac surgery; effective anticoagulation with ACT >480 s but elevated ACT post-infusion contributed to bleeding.

Warum dies für die Hirudotherapie relevant ist

This pilot study determined the dosing of bivalirudin for systemic anticoagulation during cardiac surgery in 25 neonates and infants with congenital heart disease, using a 1 mg/kg bolus followed by an infusion titrated to maintain activated clotting time above 480 seconds. The authors report effective anticoagulation at a maintenance dose of 2.2 ± 0.4 mg/kg/h, though ACT remained elevated for four hours after discontinuation, contributing to increased chest-tube output in some patients, with excessive bleeding in 4 children and re-exploration in 1. The abstract does not mention hirudin, leeches, or any leech-derived compound, so no defensible hirudotherapy link exists. The authors describe this as a pilot study and call for randomized controlled trials to further evaluate safety.

Zitation

Bivalirudin anticoagulation in neonates and infants undergoing cardiac surgery.

Hasija S et al. · Journal of cardiothoracic and vascular anesthesia, 2022

Verwandter klinischer Kontext

Zur ASH-Bibliothek hinzugefügt: May 27, 2026 · Letzte Aktualisierung der Website: June 18, 2026

Diese Website stellt Bildungsinformationen bereit und ist weder eine medizinische Beratung noch eine Diagnose oder Behandlungsempfehlung. Die medizinische Blutegeltherapie ist mit klinisch relevanten Risiken verbunden und sollte ausschließlich von qualifizierten Klinikerinnen und Klinikern unter institutionell genehmigten Protokollen durchgeführt werden. Die FDA-510(k)-Zulassung für medizinische Blutegel ist auf bestimmte Indikationen beschränkt; experimentelle und Off-Label-Diskussionen werden entsprechend gekennzeichnet. Für patientenspezifische Beratung wenden Sie sich an eine qualifizierte Gesundheitsfachkraft.