Amerikanische Gesellschaft für Hirudotherapie

Dosing lepirudin in patients with heparin-induced thrombocytopenia and normal or impaired renal function: a single-center experience with 68 patients

Clinical study published in Blood (2008)

Zuletzt aktualisiert: June 18, 2026Geprüft von: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Clinical trialKlinische StudienArzneimittelentwicklungTschudi M et al. · Blood, 2008

Abstract

The recommended dose (bolus 0.4 mg/kg followed by 0.15 mg/kg per hour) of lepirudin, a direct thrombin inhibitor licensed for treatment of heparin-induced thrombocytopenia (HIT), is too high. Starting in 2001, we omitted the bolus and reduced maintenance dose by at least one-third. Analyzing 53 HIT patients treated between January 2001 and February 2007, we observed that therapeutic anticoagulation intensity already 4 hours after lepirudin start had been reached with the following initial lepirudin doses (median): 0.078 mg/kg per hour [creatinine clearance (CrCl) more than 60 mL/min], 0.040 mg/kg per hour (CrCl 30-60 mL/min), and 0.013 mg/kg per hour (CrCl < 30 mL/min). The efficacy of this treatment was documented by increasing platelets and decreasing D-dimers. Based on this experience, we derived a lepirudin dosing regimen, which was prospectively evaluated treating 15 HIT patients between March 2007 and February 2008. We show that omitting the initial lepirudin bolus and administering 0.08 mg/kg per hour in patients with CrCl more than 60 mL/min, 0.04 mg/kg per hour in patients with CrCl 30-60 mL/min, and 0.01 to 0.02 mg/kg per hour in those with CrCl less than 30 mL/min is efficacious and safe, as documented by increasing platelet counts, decreasing D-dimer levels, and rare thrombotic (1 of 46) and major bleeding (4 of 46) complications.

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

Publication typeClinical TrialJournal ArticleResearch Support, Non-U.S. Gov't
Indexed MeSH termsAdultAgedAged, 80 and overAnticoagulantsBlood Cell CountBlood PlateletsCreatineDose-Response Relationship, DrugFemaleHeparinHirudinsHumans

Zusammenfassung

Reduced-dose lepirudin protocol omitting the initial bolus and using 0.08, 0.04 or 0.01–0.02 mg/kg/h infusion based on creatinine clearance achieved therapeutic anticoagulation in 68 HIT patients with rare thrombotic (1/46) or major bleeding (4/46) events.

Warum dies für die Hirudotherapie relevant ist

This study examined lepirudin dosing in patients with heparin-induced thrombocytopenia (HIT), finding that the recommended regimen (0.4-mg/kg bolus followed by 0.15 mg/kg/h infusion) was too high. The authors omitted the bolus and reduced maintenance doses by at least one-third, analyzing 53 HIT patients treated between January 2001 and February 2007 and deriving a renal-function-stratified regimen that was prospectively evaluated in 15 additional HIT patients between March 2007 and February 2008. The regimen (0.08 mg/kg/h for CrCl >60, 0.04 for 30–60, 0.01–0.02 for <30 mL/min) proved efficacious and safe, with rare thrombotic (1/46) and major bleeding (4/46) complications. The abstract identifies lepirudin as a direct thrombin inhibitor licensed for HIT treatment but does not mention hirudin, leech saliva, leech therapy, or any leech-derived origin. Although the drug name "lepirudin" suggests a connection, the abstract itself provides no leech-related content, and the relevance to hirudotherapy is not established by the abstract.

Zitation

Dosing lepirudin in patients with heparin-induced thrombocytopenia and normal or impaired renal function: a single-center experience with 68 patients.

Tschudi M et al. · Blood, 2008

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.