Bivalirudin anticoagulation in neonates and infants undergoing cardiac surgery
Pilot study published in J Cardiothorac Vasc Anesth (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.
Summary
In a pilot study, 25 neonates and infants having cardiac surgery for congenital heart disease received bivalirudin (1 mg/kg bolus, 2.2 mg/kg/h infusion) and achieved effective anticoagulation with ACT above 480 seconds, though elevated post-infusion ACT increased chest-tube drainage in some patients.
Why This Matters for Hirudotherapy
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 authors describe this as a pilot study and call for randomized controlled trials to further evaluate safety. Bivalirudin (formerly Hirulog) is a synthetic peptide anticoagulant designed partly on the C-terminal sequence of hirudin, the anticoagulant of the medicinal leech (Maraganore et al., 1990); this paper studies the drug, not leech therapy.
Citation
Reference (Vancouver style)
Hasija S, Hote MP, Makhija N, Chauhan S, Malhotra P, Khan MA, et al. Bivalirudin anticoagulation in neonates and infants undergoing cardiac surgery. J Cardiothorac Vasc Anesth. 2022;36(10):3841-3846. doi:10.1053/j.jvca.2022.04.044. PMID: 35817672
Bibliographic details (authors, volume, pages, DOI) are taken from the PubMed record.
Added to ASH library: May 27, 2026 · Site last updated: June 18, 2026