Anti-thrombotic therapy in non-ST elevation acute coronary syndrome KAA Fox

Platelet activation and thrombin generation are implicated in the pathogenesis of acute coronary syndrome, in the development of major thrombotic complications of the condition, and in the interventional treatments to treat obstructive coronary lesions (principally, percutaneous coronary interventio...

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Main Author: Keith A.A. Fox
Format: Article
Language:English
Published: South African Heart Association 2017-04-01
Series:SA Heart Journal
Subjects:
Online Access:https://www.journals.ac.za/index.php/SAHJ/article/view/2104
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spelling doaj-4f6a91353d394dda87dc6a8ce9c151c52021-08-27T09:59:23ZengSouth African Heart AssociationSA Heart Journal1996-67412071-46022017-04-014149Anti-thrombotic therapy in non-ST elevation acute coronary syndrome KAA FoxKeith A.A. Fox 0University of Edinburgh Platelet activation and thrombin generation are implicated in the pathogenesis of acute coronary syndrome, in the development of major thrombotic complications of the condition, and in the interventional treatments to treat obstructive coronary lesions (principally, percutaneous coronary intervention). Despite treatment with aspirin and heparin there remained a clinically important risk of thrombotic complications both in hospital and following discharge. Newer anti-platelet therapies (thienopyridines and glycoprotein IIb/IIIa inhibitors) reduced platelet mediated complications, but with an increase in bleeding risk. Similarly, low molecular weight heparins reduced thrombotic complcations but with a modest increase in bleeding. Newer anti-thrombins (anti Xa inhibitors and direct thrombin inhibitors) demonstrate similar or improved efficacy, but with reduced bleeding. Insufficient attention has been paid to reducing bleeding complications and recent evidence suggests that major bleeding conveys a significant increase in the risk of death. In addition, clearance of antithrombotic agents by the kidney is impaired in those with renal dysfunction, including in the elderly, and this may contribute to the risks of bleeding. In unselected populations with non-ST elevation ACS more than half the population have a creatinine clearance below 60 ml/min. Reducing the doses of anti-thrombins in patients with renal dysfunction may reduce bleeding complications. The optimal anti-thrombotic strategy in patients with non-ST elevation ACS requires the clinician to consider not only the risk of the patient for thrombotic complcations, but also the hazards of bleeding. Newer anti-thrombotic agents, for the first time, offer potential benefits in bleeding risk with similar or improved efficacy. https://www.journals.ac.za/index.php/SAHJ/article/view/2104anti-thrombotic therapycoronary syndromethrombotic complicationsanti-platelet therapies
collection DOAJ
language English
format Article
sources DOAJ
author Keith A.A. Fox
spellingShingle Keith A.A. Fox
Anti-thrombotic therapy in non-ST elevation acute coronary syndrome KAA Fox
SA Heart Journal
anti-thrombotic therapy
coronary syndrome
thrombotic complications
anti-platelet therapies
author_facet Keith A.A. Fox
author_sort Keith A.A. Fox
title Anti-thrombotic therapy in non-ST elevation acute coronary syndrome KAA Fox
title_short Anti-thrombotic therapy in non-ST elevation acute coronary syndrome KAA Fox
title_full Anti-thrombotic therapy in non-ST elevation acute coronary syndrome KAA Fox
title_fullStr Anti-thrombotic therapy in non-ST elevation acute coronary syndrome KAA Fox
title_full_unstemmed Anti-thrombotic therapy in non-ST elevation acute coronary syndrome KAA Fox
title_sort anti-thrombotic therapy in non-st elevation acute coronary syndrome kaa fox
publisher South African Heart Association
series SA Heart Journal
issn 1996-6741
2071-4602
publishDate 2017-04-01
description Platelet activation and thrombin generation are implicated in the pathogenesis of acute coronary syndrome, in the development of major thrombotic complications of the condition, and in the interventional treatments to treat obstructive coronary lesions (principally, percutaneous coronary intervention). Despite treatment with aspirin and heparin there remained a clinically important risk of thrombotic complications both in hospital and following discharge. Newer anti-platelet therapies (thienopyridines and glycoprotein IIb/IIIa inhibitors) reduced platelet mediated complications, but with an increase in bleeding risk. Similarly, low molecular weight heparins reduced thrombotic complcations but with a modest increase in bleeding. Newer anti-thrombins (anti Xa inhibitors and direct thrombin inhibitors) demonstrate similar or improved efficacy, but with reduced bleeding. Insufficient attention has been paid to reducing bleeding complications and recent evidence suggests that major bleeding conveys a significant increase in the risk of death. In addition, clearance of antithrombotic agents by the kidney is impaired in those with renal dysfunction, including in the elderly, and this may contribute to the risks of bleeding. In unselected populations with non-ST elevation ACS more than half the population have a creatinine clearance below 60 ml/min. Reducing the doses of anti-thrombins in patients with renal dysfunction may reduce bleeding complications. The optimal anti-thrombotic strategy in patients with non-ST elevation ACS requires the clinician to consider not only the risk of the patient for thrombotic complcations, but also the hazards of bleeding. Newer anti-thrombotic agents, for the first time, offer potential benefits in bleeding risk with similar or improved efficacy.
topic anti-thrombotic therapy
coronary syndrome
thrombotic complications
anti-platelet therapies
url https://www.journals.ac.za/index.php/SAHJ/article/view/2104
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