Document Detail


Primary stenting and glycoprotein IIb/IIIa inhibitors in acute myocardial infarction.
MedLine Citation:
PMID:  10426875     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Early patency of the infarct-related vessel improves in-hospital and long-term survival. Mechanical reopening is as effective as or superior to pharmacological therapy in the treatment of acute myocardial infarction. However, in patients treated with primary percutaneous transluminal coronary angioplasty, recurrent ischemia occurs in 10% to 15% before hospital discharge, and angiographic restenosis occurs in 30% to 50% of infarct-related vessel within 6 months. Primary stenting in acute myocardial infarction has been found to be safe and feasible and reduces early and late events. In particular, restenosis rate has been found to be lowered by stent implantation. Use of glycoprotein IIb/IIIa receptor inhibitors alone has resulted in infarct-related vessel patency rates approximately the same as with the use of thrombolytic therapy. Furthermore, glycoprotein IIb/IIIa receptor blockers reduce the occurrence of acute complications during percutaneous transluminal coronary angioplasty. Preliminary results of some ongoing trials showed that the combined therapeutic approach (ie, primary stenting plus glycoprotein IIb/IIIa inhibitors) in patients with acute myocardial infarction reduces both early and late complications of percutaneous transluminal coronary angioplasty. This finding supports the concept that optimal mechanical resolution of the plaque and the inhibition of platelet aggregation are the key of the treatment of the infarct-related vessel.
Authors:
A Colombo; C Briguori
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Publication Detail:
Type:  Journal Article; Review    
Journal Detail:
Title:  American heart journal     Volume:  138     ISSN:  0002-8703     ISO Abbreviation:  Am. Heart J.     Publication Date:  1999 Aug 
Date Detail:
Created Date:  1999-08-30     Completed Date:  1999-08-30     Revised Date:  2006-02-27    
Medline Journal Info:
Nlm Unique ID:  0370465     Medline TA:  Am Heart J     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  S153-7     Citation Subset:  AIM; IM    
Affiliation:
EMO Centro Cuore Columbus, San Raffaele Hospital, Milan, Italy.
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MeSH Terms
Descriptor/Qualifier:
Angioplasty, Transluminal, Percutaneous Coronary
Coronary Angiography
Coronary Vessels / pathology
Feasibility Studies
Humans
Myocardial Infarction / drug therapy,  therapy*
Myocardial Ischemia / etiology
Platelet Aggregation Inhibitors / therapeutic use*
Platelet Glycoprotein GPIIb-IIIa Complex / antagonists & inhibitors*
Platelet Glycoprotein GPIb-IX Complex*
Platelet Membrane Glycoproteins*
Receptors, Antigen, B-Cell / antagonists & inhibitors*
Receptors, Cell Surface / antagonists & inhibitors*
Recurrence
Safety
Stents*
Survival Rate
Thrombolytic Therapy
Vascular Patency
Chemical
Reg. No./Substance:
0/Platelet Aggregation Inhibitors; 0/Platelet Glycoprotein GPIIb-IIIa Complex; 0/Platelet Glycoprotein GPIb-IX Complex; 0/Platelet Membrane Glycoproteins; 0/Receptors, Antigen, B-Cell; 0/Receptors, Cell Surface; 0/glycoprotein receptor GPIb-IX

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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