2008
DOI: 10.1097/hco.0b013e3283021ad9
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Antiplatelet and anticoagulant agents: key differences in mechanisms of action, clinical application, and therapeutic benefit in patients with non-ST-segment-elevation acute coronary syndromes

Abstract: Current data indicate that antiplatelet regimens consisting of aspirin, clopidogrel, and a glycoprotein IIb-IIIa inhibitor provide substantial benefit among patients who undergo percutaneous coronary intervention. Optimized antiplatelet and anticoagulant therapy--including aspirin, clopidogrel, a glycoprotein IIb-IIIa inhibitor, and an anticoagulant--may reduce the incidence of subclinical and clinical events.

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Cited by 7 publications
(3 citation statements)
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“…In humans, the PDE3 isoenzyme is mainly found in platelets, vascular smooth muscle, liver, smooth muscle of the airway, T lymphocytes, adipose tissue, and cardiac tissue [8]. The inhibition of PDE3 leads to suppress cAMP degradation with a consequent increase in cAMP in platelets and blood vessels, resulting in inhibition of platelet aggregation and vasodilation, respectively [9,10]. In addition, cilostazol has pleotropic effects, including the improvement of serum lipid profile with lowering triglycerides, the elevation of high‐density lipoprotein cholesterol, and the inhibition of vascular smooth muscle cell growth.…”
Section: Discussionmentioning
confidence: 99%
“…In humans, the PDE3 isoenzyme is mainly found in platelets, vascular smooth muscle, liver, smooth muscle of the airway, T lymphocytes, adipose tissue, and cardiac tissue [8]. The inhibition of PDE3 leads to suppress cAMP degradation with a consequent increase in cAMP in platelets and blood vessels, resulting in inhibition of platelet aggregation and vasodilation, respectively [9,10]. In addition, cilostazol has pleotropic effects, including the improvement of serum lipid profile with lowering triglycerides, the elevation of high‐density lipoprotein cholesterol, and the inhibition of vascular smooth muscle cell growth.…”
Section: Discussionmentioning
confidence: 99%
“…Synergistic platelet inhibition through different platelet activation pathways, by clopidogrel and aspirin, represents a key strategy in current ACS treatment. 17…”
Section: Clinical Use In Acsmentioning
confidence: 99%
“…16 Synergistic platelet inhibition through different platelet activation pathways, by clopidogrel and aspirin, represents a key strategy in current ACS treatment. 17 The rationale for the use of clopidogrel in ACS has been assessed in several trials (Table 1). The CAPRIE trial was the first randomised, blinded, international trial designed to assess the relative efficacy of clopidogrel (75 mg once daily) and aspirin (325 mg once daily) in reducing the risk of a composite outcome cluster of ischaemic stroke, myocardial infarction, or vascular death.…”
Section: Clinical Use In Acsmentioning
confidence: 99%