Literature DB >> 10603506

Hirudin: Its Biology and Clinical Use.

.   

Abstract

Over a century has passed since the anticoagulant properties of hirudin were identified. Our understanding of this unique and promising 65 amino acid polypeptide has grown steadily, allowing clinical experience to be gained. In acute myocardial infarction, hirudin has been associated with a higher incidence of early and sustained TIMI grade 3 flow, a higher rate of infarct-related artery patency at 18-36 hours with a decreased rate of reocclusion, and a lower incidence of in-hospital death and reinfarction as compared with heparin. hirudin has also been associated with a stable level of articoagulation and an acceptable hemorrhagic complication rate when given in carefully chosen doses. In acute coronary syndromes, the initial results indicate that hirudin can improve the resolution of coronary thrombus and reduce the incidence of recurrent ischemic events. Similarly impressive reductions in thrombotic complications and ischemia have been observed in the early balloon angioplasty experience. Promising results have also been seen with hirudin in preventing deep venous thrombosis following orthopedic surgery. The favorable effects of hirudin as compared with heparin in phase II clinical trials have prompted further investigation in two large phase III trials, TIMI 9 and GUSTO 2. It is hoped that these initial results can be confirmed and that hirudin can be proved to be a safe and effective treatment for thrombotic syndromes of the venous and arterial circulatory systems.

Entities:  

Year:  1994        PMID: 10603506     DOI: 10.1007/BF01061990

Source DB:  PubMed          Journal:  J Thromb Thrombolysis        ISSN: 0929-5305            Impact factor:   2.300


  43 in total

1.  [Purification of hirudin].

Authors:  M JUTISZ; A CHARBONNEL-BERAULT; G MARTINOLI
Journal:  Bull Soc Chim Biol (Paris)       Date:  1963

2.  [Studies on the mechanism of the anticoagulant effect of hirudin].

Authors:  F MARKWARDT
Journal:  Naunyn Schmiedebergs Arch Exp Pathol Pharmakol       Date:  1956

3.  Kinetics of the inhibition of thrombin by hirudin.

Authors:  S R Stone; J Hofsteenge
Journal:  Biochemistry       Date:  1986-08-12       Impact factor: 3.162

4.  Hirudin insensitive thrombin-stimulated platelet release.

Authors:  D S Reinhold; H Gershman
Journal:  Thromb Res       Date:  1985-02-15       Impact factor: 3.944

5.  Inhibition of the thrombin-platelet reaction by hirudin.

Authors:  A Hoffmann; F Markwardt
Journal:  Haemostasis       Date:  1984

6.  Pharmacological studies on the antithrombotic action of hirudin in experimental animals.

Authors:  F Markwardt; J Hauptmann; G Nowak; C Klessen; P Walsmann
Journal:  Thromb Haemost       Date:  1982-06-28       Impact factor: 5.249

7.  The Thrombolysis in Myocardial Infarction (TIMI) trial. Phase I findings.

Authors: 
Journal:  N Engl J Med       Date:  1985-04-04       Impact factor: 91.245

8.  [Use of hirudin in clinical coagulation laboratories].

Authors:  P Walsmann; G Vogel
Journal:  Folia Haematol Int Mag Klin Morphol Blutforsch       Date:  1970

9.  Binding of thrombin to human platelet plasma membranes.

Authors:  S W Tam; T C Detwiler
Journal:  Biochim Biophys Acta       Date:  1978-10-03

10.  The complete covalent structure of hirudin. Localization of the disulfide bonds.

Authors:  J Dodt; U Seemüller; R Maschler; H Fritz
Journal:  Biol Chem Hoppe Seyler       Date:  1985-04
View more
  2 in total

1.  Antithrombotic Therapy during Percutaneous Coronary Intervention.

Authors: 
Journal:  J Thromb Thrombolysis       Date:  1995       Impact factor: 2.300

2.  Thrombin Generation in Patients with Acute Myocardial Infarction Treated with Front-Loaded rt-PA and Recombinant Hirudin (HBW 023).

Authors: 
Journal:  J Thromb Thrombolysis       Date:  1998-07       Impact factor: 2.300

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.