Американское общество гирудотерапии

Dose estimation for bivalirudin during pediatric cardiopulmonary bypass

Pharmacokinetic modeling study published in Paediatric Anaesthesia (2021)

Последнее обновление: June 18, 2026Рецензент: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Research reportКлинические исследованияРазработка лекарственных препаратовWolstencroft P et al. · Paediatric anaesthesia, 2021

Abstract

AIM: A typical adult-based bivalirudin regimen during cardiopulmonary bypass uses a loading dose of 1 mg kg-1 and a circuit prime (volume L × 13 mg) with a subsequent intravenous infusion 2.5 mg h-1  kg-1 . Dose in children remains unknown. We wished to determine a practical bivalirudin dosing schedule for children undergoing surgery with cardiopulmonary bypass. METHODS: Published pharmacokinetic parameters in children who were anticoagulated for cardiac catheterization using bivalirudin were compared to adult by scaling for size using allometry. An infusion regimen suitable for children was determined using a bivalirudin target concentration (13 mg L-1 ) common in adults for effect during cardiopulmonary bypass. Predicted bivalirudin infusion rates in children were compared to regimens published as case reports. RESULTS: Current pediatric bivalirudin infusion rates are based on those used in adults with titration during cardiopulmonary bypass to achieve activated clotting times longer than 400 s. Bivalirudin clearance (mL min-1  kg-1 ) can be estimated in children by scaling adult parameters using allometry. Clearance decreases through childhood and higher infusion rates in children would achieve target concentration rapidly without the need to titrate initial infusion rate. An infusion rate of 4.5 mg h-1  kg-1 in a 10 kg infant, 4 mg h-1  kg-1 in a 20 kg child and 3.5 mg h-1  kg-1 in a child 30-40 kg will target an activated clotting time slower than 400 s. Adult regimens could be used in those children heavier than 50 kg. CONCLUSION: Bivalirudin infusion in children should be started after loading dose at rates greater than those used in adults. Dose in neonates remains uncertain because neither pharmacokinetics nor coagulation pharmacodynamics have been adequately characterized.

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

Publication typeJournal Article
Indexed MeSH termsBlood Coagulation TestsCardiopulmonary BypassChildHirudinsHumansInfantInfant, NewbornPeptide FragmentsRecombinant Proteins

Резюме

Pediatric CPB pharmacokinetic modeling identifying weight-based bivalirudin dosing for heparin-incompatible children, with proposed loading dose and maintenance infusion algorithm.

Почему это важно для гирудотерапии

This study estimated a practical bivalirudin dosing schedule for children undergoing surgery with cardiopulmonary bypass by scaling adult pharmacokinetic parameters to children using allometry, targeting a bivalirudin concentration of 13 mg/L. It concludes that children require higher weight-based infusion rates than adults (e.g., 4.5 mg/h/kg in a 10 kg infant) and adult regimens may apply above 50 kg, while neonatal dosing remains uncertain. The abstract does not characterize bivalirudin's relationship to hirudin, leeches, or leech-derived compounds. CAVEAT: No connection to hirudotherapy or the leech secretome is established by this abstract; relevance to ASH's domain is indirect and unstated.

Цитирование

Dose estimation for bivalirudin during pediatric cardiopulmonary bypass.

Wolstencroft P et al. · Paediatric anaesthesia, 2021

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.