Media Articles Related to Integrilin (Eptifibatide)
NICE recommends Xarelto as an effective treatment option for reducing risk of secondary events in acute coronary syndrome
Source: Cardiovascular / Cardiology News From Medical News Today [2015.01.23]
The National Institute for Health and Care Excellence (NICE) has issued its Final Appraisal Determination (FAD) recommending Xarelto 2.
Published Studies Related to Integrilin (Eptifibatide)
Upstream clopidogrel use and the efficacy and safety of early eptifibatide treatment in patients with acute coronary syndrome: an analysis from the Early Glycoprotein IIb/IIIa Inhibition in Patients with Non-ST-Segment Elevation Acute Coronary Syndrome (EARLY ACS) trial. [2011.02.22]
CONCLUSIONS: Routine early eptifibatide use, compared with delayed provisional use, may be associated with lower 30-day ischemic risk in non-ST-elevation acute coronary syndrome patients also treated with clopidogrel before angiography. The benefit-risk ratio of intensive platelet inhibition with combined early use of antiplatelet agents needs further evaluation in prospective randomized trials.
Long-term efficacy of high-dose tirofiban versus double-bolus eptifibatide in patients undergoing percutaneous coronary intervention. [2011.01]
BACKGROUND: There is no head-to-head comparison between tirofiban versus eptifibatide in patients undergoing percutaneous coronary intervention (PCI) when added to standard antiaggregating drugs (AAD) to prevent ischemic events within 1 year... CONCLUSION: Head-to-head comparison between eptifibatide and tirofiban in patients undergoing PCI while on double AAD showed that eptifibatide had a lower efficacy on the incidence of composite ischemic events within 1 year, which might be explained by a reduced action on CK-MB pre-PCI.
Comparison of Ecchymosis Rates With Measurement of Automated and Manual Blood Pressures in Patients Receiving Eptifibatide Therapy. [2010.12.01]
CONCLUSIONS:: In 44 post-coronary interventional procedure patients on eptifibatide therapy, ecchymosis occurred in 9% of arms with automated BP measurement and 14% of arms with manual BP measurement during the 24-hour study period. This difference was not statistically significant. No other complications were observed. This study found that the overall incidence of complications from BP measurement was low and not related to whether the device used was an automated or manual BP device in post-coronary interventional procedure patients on eptifibatide therapy. Based on this study and a prior one, the reluctance of clinicians to use automated BP devices in post-procedural coronary intervention patients because of fears of increased tissue bleeding does not appear scientifically justified.
Eptifibatide is noninferior to abciximab in primary percutaneous coronary intervention: results from the SCAAR (Swedish Coronary Angiography and Angioplasty Registry). [2010.08.03]
OBJECTIVES: The aim of this study was to test the noninferiority of eptifibatide relative to abciximab in patients with ST-segment elevation myocardial infarction (STEMI) treated with primary percutaneous coronary intervention (PCI). BACKGROUND: Glycoprotein IIb/IIIa inhibitors are recommended by international guidelines in patients with acute coronary syndromes undergoing PCI. Abciximab is recommended with a higher level of evidence than eptifibatide in patients with STEMI. No large, prospective, randomized trial comparing abciximab and eptifibatide has been published... CONCLUSIONS: This large registry study suggests that eptifibatide is noninferior to abciximab in patients with STEMI undergoing primary PCI with respect to death or MI during 1 year, thereby supporting the use of either drug in clinical practice. Copyright (c) 2010 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.
Randomized comparison of eptifibatide versus abciximab in primary percutaneous coronary intervention in patients with acute ST-segment elevation myocardial infarction: results of the EVA-AMI Trial. [2010.08.03]
OBJECTIVES: The aim of this study was to compare eptifibatide and abciximab as adjuncts to primary percutaneous coronary intervention (PCI). BACKGROUND: The glycoprotein (GP) IIb/IIIa receptor inhibitor abciximab as adjunct to primary PCI in patients with ST-segment elevation myocardial infarctions has been shown to reduce ischemic complications and improve clinical outcomes. So far, no trial has been performed to compare the efficacy of another GP IIb/IIIa receptor inhibitor, eptifibatide, and abciximab in primary PCI... CONCLUSIONS: Eptifibatide as an adjunct to primary PCI is equally as effective as abciximab with respect to STR. (Efficacy of Eptifibatide Compared to Abciximab in Primary Percutaneous Coronary Intervention [PCI] for Acute ST Elevation Myocardial Infarction [STEMI]; NCT00426751). Copyright (c) 2010 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.
Clinical Trials Related to Integrilin (Eptifibatide)
A Safety Study of Eptifibatide in Patients With Sickle Cell Disease [Recruiting]
This study will evaluate the safety of eptifibatide in sickle cell patients and how well it
works during the course of painful crises. The overall hypothesis that we seek to test is
that increased platelet activation and the resultant inflammatory responses are important
contributors to the problems of sickle cell disease. Sickle cell disease has been referred
to both as a condition associated with increased risk of blood clots and increased
inflammation. A painful crisis represents the most common cli nical problem in sickle cell
disease, but the treatment of these crises remains inadequate.
Study of the Combination Therapy of Rt-PA and Eptifibatide to Treat Acute Ischemic Stroke [Recruiting]
The primary goal of this trial is to determine if individuals with acute ischemic stroke
treated with a medium dose of IV rt-PA plus IV eptifibatide started within 3 hours of
symptom onset are more likely to have a better outcome than individuals treated with
standard IV rt-PA alone.
Integrilin and Ilomedin in Combination in Comparison to Standard Treatment in Severe Pneumonia Patients With Severe Sepsis [Recruiting]
This is an investigator sponsored double-blinded, multinational, multi center, randomized
(2: 1 active: placebo), placebo-controlled, phase IIa trial in severe pneumonia patients with
severe sepsis or septic shock, investigating the safety and efficacy of co-administration of
Iloprost and escalating doses of Eptifibatide for continuous intravenous infusion in totally
Combined Approach to Lysis Utilizing Eptifibatide and rt-PA in Acute Ischemic Stroke (CLEAR Stroke) Trial [Completed]
The purpose of this study is determine the effects of using of a combination of two
drugs--integrilin (eptifibatide) and activase (recombinant tissue plasminogen activator,
rt-PA, or recombinant t-PA)--to dissolve blood clots in patients who have a stroke.
EARLY ACS: Early Glycoprotein IIb/IIIa Inhibition in Patients With Non-ST-Segment Elevation Acute Coronary Syndrome (Study P03684AM2) [Recruiting]
The purpose of this study is to see if early INTEGRILIN® (eptifibatide) therapy in patients
with non-ST-segment elevation acute coronary syndrome (ACS) reduces the occurence of death,
heart attack and urgent cardiac intervention (surgery) compared to placebo.
Reports of Suspected Integrilin (Eptifibatide) Side Effects
Cardiogenic Shock (3),
Endotracheal Intubation (3),
Anaphylactic Shock (2),
Peripheral Ischaemia (2),
Blood Culture Positive (2), more >>