A risk score system for predicting adverse outcomes and magnitude of benefit with glycoprotein IIb/IIIa inhibitor therapy in patients with unstable angina pectoris

Clinical outcomes of patients with unstable angina are variable. We sought to identify predictors of adverse clinical outcomes in patients with unstable angina and to investigate whether these factors would predict the magnitude of benefit achieved with platelet glycoprotein IIb/IIIa inhibition. We...

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Veröffentlicht in:The American journal of cardiology 2001-09, Vol.88 (5), p.488-492
Hauptverfasser: Sabatine, Marc S, Januzzi, James L, Snapinn, Stephen, Théroux, Pierre, Jang, Ik-Kyung
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container_issue 5
container_start_page 488
container_title The American journal of cardiology
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creator Sabatine, Marc S
Januzzi, James L
Snapinn, Stephen
Théroux, Pierre
Jang, Ik-Kyung
description Clinical outcomes of patients with unstable angina are variable. We sought to identify predictors of adverse clinical outcomes in patients with unstable angina and to investigate whether these factors would predict the magnitude of benefit achieved with platelet glycoprotein IIb/IIIa inhibition. We analyzed 20 variables in the 1,915 patients enrolled in the Platelet Receptor Inhibition for Ischemic Syndrome Management in Patients Limited by Unstable Signs and Symptoms trial. Five independent predictors were identified: age >65 years, prior coronary artery bypass grafting, antecedent aspirin use, antecedent β-blocker use, and ST depressions on the presenting electrocardiogram. A risk score system was created using these predictors in which patients were assigned 1 point for the presence of each risk factor. There was a progressive increase in the rate of the composite end point of death, myocardial infarction, or refractory ischemia at 7 days with an increasing number of risk factors. For patients treated with heparin alone, the composite end point event rate was 6.5% in the group with 0 or 1 predictor, 14.6% in the group with 2 predictors, 22.7% in the group with 3 predictors, and 37.1% in the group with 4 or 5 predictors (p
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For patients treated with heparin alone, the composite end point event rate was 6.5% in the group with 0 or 1 predictor, 14.6% in the group with 2 predictors, 22.7% in the group with 3 predictors, and 37.1% in the group with 4 or 5 predictors (p &lt;0.00001). When dividing patients into low- (0 or 1 point), medium- (2 or 3 points), and high-risk (4 or 5 points) groups, the addition of tirofiban to heparin therapy was associated with no significant benefit in the low-risk group, a 5.2% absolute reduction in the medium-risk group (p = 0.05), and a 16% absolute reduction in the high-risk group (p = 0.0055). 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We sought to identify predictors of adverse clinical outcomes in patients with unstable angina and to investigate whether these factors would predict the magnitude of benefit achieved with platelet glycoprotein IIb/IIIa inhibition. We analyzed 20 variables in the 1,915 patients enrolled in the Platelet Receptor Inhibition for Ischemic Syndrome Management in Patients Limited by Unstable Signs and Symptoms trial. Five independent predictors were identified: age &gt;65 years, prior coronary artery bypass grafting, antecedent aspirin use, antecedent β-blocker use, and ST depressions on the presenting electrocardiogram. A risk score system was created using these predictors in which patients were assigned 1 point for the presence of each risk factor. There was a progressive increase in the rate of the composite end point of death, myocardial infarction, or refractory ischemia at 7 days with an increasing number of risk factors. For patients treated with heparin alone, the composite end point event rate was 6.5% in the group with 0 or 1 predictor, 14.6% in the group with 2 predictors, 22.7% in the group with 3 predictors, and 37.1% in the group with 4 or 5 predictors (p &lt;0.00001). When dividing patients into low- (0 or 1 point), medium- (2 or 3 points), and high-risk (4 or 5 points) groups, the addition of tirofiban to heparin therapy was associated with no significant benefit in the low-risk group, a 5.2% absolute reduction in the medium-risk group (p = 0.05), and a 16% absolute reduction in the high-risk group (p = 0.0055). 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Reticuloendothelial system</subject><subject>Cardiovascular disease</subject><subject>Clinical outcomes</subject><subject>Coronary Angiography</subject><subject>Drug Therapy, Combination</subject><subject>Electrocardiography</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Heparin - administration &amp; dosage</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Myocardial Ischemia - diagnosis</subject><subject>Myocardial Ischemia - etiology</subject><subject>Myocardial Ischemia - prevention &amp; control</subject><subject>Odds Ratio</subject><subject>Pharmacology. 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Blood coagulation. Reticuloendothelial system</topic><topic>Cardiovascular disease</topic><topic>Clinical outcomes</topic><topic>Coronary Angiography</topic><topic>Drug Therapy, Combination</topic><topic>Electrocardiography</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Heparin - administration &amp; dosage</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Myocardial Ischemia - diagnosis</topic><topic>Myocardial Ischemia - etiology</topic><topic>Myocardial Ischemia - prevention &amp; control</topic><topic>Odds Ratio</topic><topic>Pharmacology. 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For patients treated with heparin alone, the composite end point event rate was 6.5% in the group with 0 or 1 predictor, 14.6% in the group with 2 predictors, 22.7% in the group with 3 predictors, and 37.1% in the group with 4 or 5 predictors (p &lt;0.00001). When dividing patients into low- (0 or 1 point), medium- (2 or 3 points), and high-risk (4 or 5 points) groups, the addition of tirofiban to heparin therapy was associated with no significant benefit in the low-risk group, a 5.2% absolute reduction in the medium-risk group (p = 0.05), and a 16% absolute reduction in the high-risk group (p = 0.0055). Thus, we have developed a risk score system using 5 variables that can be used to identify patients at high risk for death and cardiac ischemic events and who experience the greatest benefit from the addition of a glycoprotein IIb/IIIa inhibitor to their treatment regimen.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>11524055</pmid><doi>10.1016/S0002-9149(01)01724-6</doi><tpages>5</tpages></addata></record>
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subjects Adult
Age Distribution
Aged
Angina pectoris
Angina, Unstable - diagnosis
Angina, Unstable - drug therapy
Angina, Unstable - mortality
Biological and medical sciences
Blood. Blood coagulation. Reticuloendothelial system
Cardiovascular disease
Clinical outcomes
Coronary Angiography
Drug Therapy, Combination
Electrocardiography
Female
Follow-Up Studies
Heparin - administration & dosage
Humans
Male
Medical sciences
Middle Aged
Myocardial Ischemia - diagnosis
Myocardial Ischemia - etiology
Myocardial Ischemia - prevention & control
Odds Ratio
Pharmacology. Drug treatments
Platelet Glycoprotein GPIIb-IIIa Complex - antagonists & inhibitors
Predictive Value of Tests
Preventive medicine
Probability
Proportional Hazards Models
Recurrence
Risk Assessment
Risk Factors
Sensitivity and Specificity
Severity of Illness Index
Sex Distribution
Survival Rate
Tirofiban
Treatment Outcome
Tyrosine - administration & dosage
Tyrosine - adverse effects
Tyrosine - analogs & derivatives
title A risk score system for predicting adverse outcomes and magnitude of benefit with glycoprotein IIb/IIIa inhibitor therapy in patients with unstable angina pectoris
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