Amerikanische Gesellschaft für Hirudotherapie

Anticoagulant use in patients with chronic renal impairment

Review published in American Journal of Cardiovascular Drugs (2005)

Zuletzt aktualisiert: June 18, 2026Geprüft von: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Narrative reviewArzneimittelentwicklungKlinische StudienGrand'Maison A et al. · American Journal of Cardiovascular Drugs, 2005

Abstract

Patients with renal failure have an increased risk of both thrombotic and bleeding complications. A number of antithrombotic drugs undergo renal clearance. Therefore, estimation of renal function is necessary when prescribing these drugs to patients with renal dysfunction. Pharmacokinetic and clinical data in patients with chronic renal impairment are limited for several anticoagulants, and adequate administration information is often absent. Dose adjustment of anticoagulants may be indicated when the creatinine clearance falls below 30 mL/min. Unfractionated heparin, argatroban, and vitamin K antagonists generally do not require dose adjustment with renal dysfunction. However, smaller doses of warfarin may be required to achieve a particular target international normalized ratio. Close monitoring of anticoagulation is recommended when argatroban or high doses of unfractionated heparin are administered in patients with severe chronic renal impairment. Low-molecular weight heparins, danaparoid sodium, hirudins, and bivalirudin all undergo renal clearance. Lower doses and closer anticoagulation monitoring may be advisable when these agents are used in patients with chronic renal failure. We recommend that fondaparinux sodium and ximelagatran (not yet licensed) be avoided in the presence of severe renal impairment and be used with caution in patients with moderate renal dysfunction. While acknowledging the lack of pharmacokinetic data, this review provides specific recommendations for the use of anticoagulants in patients with chronic renal impairment.

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'tReview
Indexed MeSH termsAnticoagulantsArginineAzetidinesBenzylaminesFondaparinuxHeparinHirudinsHumansKidney Failure, ChronicPeptide FragmentsPipecolic AcidsPolysaccharides

Zusammenfassung

Authoritative review covering pharmacokinetics and dose adjustment of recombinant hirudins (lepirudin, desirudin) and bivalirudin in chronic renal impairment — hirudin-class drugs all undergo renal clearance.

Warum dies für die Hirudotherapie relevant ist

This review examines clinical data and administration recommendations for various antithrombotic drugs in patients with chronic renal impairment. It notes that low-molecular-weight heparins, danaparoid sodium, hirudins, and bivalirudin all undergo renal clearance, and recommends lower doses and closer monitoring when these agents are used in chronic renal failure. The abstract lists hirudins and bivalirudin by name among anticoagulants requiring dose adjustment, but does not describe their biological origin, relationship to leech saliva, or any connection to hirudotherapy. The article focuses entirely on systemic pharmaceutical use, with no data on actual leech therapy, so its relevance to ASH is limited and indirect.

Zitation

Anticoagulant use in patients with chronic renal impairment.

Grand'Maison A et al. · American Journal of Cardiovascular Drugs, 2005

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.