Anticoagulation with r-hirudin in regular haemodialysis with heparin-induced thrombocytopenia (HIT II)
First long-term application case series published in Wiener Klinische Wochenschrift (1997)
Abstract
A 69-year-old female patient with renal failure developed heparin-induced thrombocytopenia type II (HIT II) two months after starting haemodialysis therapy with heparin as anticoagulant and a 6-week course of thromboembolism prophylaxis with enoxaparin sodium. The platelet count dropped by 50% as compared with initial values and ex vivo platelet aggregation induced by heparin antibodies (HIPA-test) was detected. Haemodialysis therapy was complicated by a massive thrombosis of dialyzer and ensuing repeated interruptions of treatment. After confirmation of the diagnosis of HIT II haemodialysis therapy was continued with hirudin as anticoagulant. Polysulfone dialyzers and an intravenous bolus of 0.14 mg/kg of recombinant hirudin (r-hirudin) achieved efficient haemodialysis therapy of 4.5 hours, with a minimum therapeutic blood level of hirudin of 0.5 micrograms/mL. More than 50 regular haemodialysis with hirudin anticoagulation were performed without additional problems. The ecarin clotting time (ECT) was used as bedside method to monitor blood levels and for dosage adjustments of hirudin. After the 34th haemodialysis, the frequency (previously 3-4 haemodialyses sessions/week) was reduced to 2 sessions/week. The creatinine clearance increased continuously from initially 2.6 to 10.4 ml/min after the 13th week of hirudin-anticoagulated haemodialysis and the platelet count normalized. In conclusion, we report the first long-term administration of r-hirudin to a patient on regular haemodialysis therapy complicated by heparin-induced thrombocytopenia. The use of hirudin as anticoagulant along with dialyzers impermeable to hirudin offers a novel alternative means of anticoagulation and, even in patients with HIT, enables performing an efficient haemodialysis therapy. Hirudin dosage must be individually adjusted by using bedside drug monitoring of plasma concentrations.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Zusammenfassung
First long-term application of recombinant hirudin (lepirudin) in regular hemodialysis patients with heparin-induced thrombocytopenia (HIT II) — landmark clinical translation.
Warum dies für die Hirudotherapie relevant ist
This case report describes a 69-year-old female hemodialysis patient who developed heparin-induced thrombropenia type II (HIT II) and was successfully transitioned to recombinant hirudin (r-hirudin) anticoagulation using polysulfone dialyzers and an intravenous bolus of 0.14 mg/kg, with more than 50 regular hemodialysis sessions performed without additional problems and platelet counts normalizing. Ecarin clotting time was used for bedside monitoring and dose adjustment. For ASH, this report is relevant because it documents a sustained clinical application of hirudin — the signature anticoagulant of the medicinal leech secretome — in a real-world anticoagulation scenario where heparin was contraindicated. The study is a single case report with no comparative group or controlled dosing protocol, and it concerns recombinant hirudin rather than live leech therapy or crude salivary extract; broader clinical efficacy cannot be inferred from one patient.
Zitation
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