Recombinant hirudin (Lepirndin) provides safe and effective anticoagulation in patients with heparin-induced thrombocytopenia - A prospective study

Citation
A. Greinacher et al., Recombinant hirudin (Lepirndin) provides safe and effective anticoagulation in patients with heparin-induced thrombocytopenia - A prospective study, CIRCULATION, 99(1), 1999, pp. 73-80
Citations number
36
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
CIRCULATION
ISSN journal
00097322 → ACNP
Volume
99
Issue
1
Year of publication
1999
Pages
73 - 80
Database
ISI
SICI code
0009-7322(19990112)99:1<73:RH(PSA>2.0.ZU;2-#
Abstract
Background-The immunological type of heparin-induced thrombocytopenia (HIT) is the most frequent drug-induced thrombocytopenia, This study evaluated t he efficacy of recombinant hirudin (r-hirudin or lepirudin), a potent throm bin inhibitor, for anticoagulation in patients with confirmed HIT. Methods ann Results-Eighty-two patients in this prospective, multicenter st udy received 1 of 4 intravenous r-hirudin regimens: Al, HIT patients with t hrombosis (n=51), 0.4-mg/kg bolus and then 0.15 mg.kg(-1).h(-1); A2, HIT pa tients with thrombosis receiving thrombolysis (n=5), 0.2-mg/kg bolus and th en 0.1 mg.kg(-1).h(-1); B, HIT patients without thrombosis (n=18), 0.1 mg.k g(-1).h(-1) and C, during cardiopulmonary bypass surgery (n=8), 0.25-mg/kg bolus and then 5-mg boluses as needed. Response criteria were increase in p latelet count by greater than or equal to 30% to >10(9)/L and activated par tial thromboplastin time (aPTT) values 1.5 to 3.0 times baseline values ach ieved with a maximum of 2 dose increases, No placebo control was used for e thical reasons, Outcomes of a subset of r-hirudin-treated patients who met predefined inclusion criteria (n=71) were compared with those of a historic al control group (n=120) for combined and individual incidences of death, a mputations, new thromboembolic complications, and incidences of bleeding. P latelet counts increased rapidly in 88.7% of r-hirudin-treated patients wit h acute HIT. In regimens Al and A2, the 25% and 75% quartiles of the aPTT w ere within the target range at all but 1 time point. The incidence of the c ombined end point (death, amputation, new thromboembolic complications) was significantly reduced in r-hirudin patients compared with historical contr ol patients (P=0.014). During first selected treatment, the adjusted hazard ratio for r-hirudin patients versus historical control was 0.279 (95% CI, 0.112 to 0.699; P=0.003). Bleeding rates were similar in both groups. Conclusions-r-Hirudin treatment is associated with a rapid and sustained re covery of platelet counts, sufficient aPTT prolongations, and true clinical benefits for patients with HIT.