Article

Elinogrel, an orally and intravenously available ADP-receptor antagonist. How does elinogrel affect a personalized antiplatelet therapy?

Medizinische Klinik III, Kardiologie und Kreislauferkrankungen, Universitätsklinikum Tübingen, Germany.
Hamostaseologie (impact factor: 1.19). 07/2012; 32(3):191-4. DOI:10.5482/ha-1192
Source: PubMed

ABSTRACT The antiplatelet therapy with aspirin and the ADP-receptor blocker clopidogrel is currently the standard medication after coronary intervention or after acute coronary syndrome to prevent recurrent ischemic events and reduce mortality. However, high interindividual response variability to antiplatelet treatment is described in up to 44% of treated patients. A poor response to clopidogrel is caused by multifactorial mechanisms. Individual risk assessment including platelet function testing (PFT) can help to identify high risk patients, although recent randomized trials to investigate effects of PFT-guided therapy have failed to detect an impact on prognostic outcome. Poor response to standard antiplatelet agents can be overcome by switching to alternate substances. Elinogrel is a novel competitive, reversible ADP-receptor antagonist available in oral and intravenous formulation. Additional treatment with elinogrel showed advantages over clopidogrel, including more rapid, less variable, and more complete inhibition of platelet function without significantly increased bleeding complications. This review gives an overview over the investigational drug elinogrel for use in a personalized antiplatelet approach.

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Keywords

ADP-receptor blocker clopidogrel
 
alternate substances
 
antiplatelet therapy
 
antiplatelet treatment
 
Individual risk assessment
 
interindividual response variability
 
investigational drug elinogrel
 
multifactorial mechanisms
 
novel competitive
 
personalized antiplatelet approach
 
platelet function
 
platelet function testing
 
poor response
 
prognostic outcome
 
recent randomized trials
 
recurrent ischemic events
 
reversible ADP-receptor antagonist available
 
risk patients
 
standard antiplatelet agents
 
standard medication
 

K A L Müller