Parenteral anticoagulant agents in PCI

Piera Capranzano, Corrado Tamburino, George D. Dangas

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

Abstract

Unfractionated heparin (UFH) has been the mainstay of anticoagulation in ischemic coronary disease for over a quarter of a century. This chapter examines the data on the use of available anticoagulants in the setting of percutaneous coronary intervention (PCI) for the different clinical presentations of coronary artery disease (CAD), and makes summary recommendations for best clinical practice. Heparin functions as an indirect thrombin inhibitor, exerting its effects through the endogenous serine protease antithrombin (AT) III. Thrombocytopenia is often associated with thrombotic and rarely with hemorrhagic complications. Low molecular weight heparin is produced through the enzymatic or chemical degradation of UFH. Direct thrombin inhibitors (DTI) are small molecules that can bind and inactivate both circulating and clot-bound thrombin. Argatroban is a small, monovalent DTI that binds reversibly to thrombin. Factor Xa inhibitors are the most refined and lowest molecular weight heparin. They contain a pentasaccharide sequence that specifically binds factor Xa.

Original languageEnglish
Title of host publicationInterventional Cardiology
Subtitle of host publicationPrinciples and Practice
Publisherwiley
Pages408-414
Number of pages7
ISBN (Electronic)9781118983652
ISBN (Print)9781118976036
DOIs
StatePublished - 21 Nov 2016

Keywords

  • Argatroban
  • Chemical degradation
  • Coronary artery disease
  • Direct thrombin inhibitors
  • Endogenous serine protease antithrombin
  • Ischemic coronary disease
  • Parenteral anticoagulant agents
  • Percutaneous coronary intervention
  • Thrombocytopenia
  • Unfractionated heparin

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