Combined glycoprotein IIb/IIIa inhibitor therapy with ticagrelor for patients with acute coronary syndrome

Autor: Chao Chang, Shuan-Li Xin, Zhi-Jiang Xie, Xiu-feng Zhao, Tao Li, Chuan Chen, Feng-Hui Jiao, Hai-Jing Zhou
Rok vydání: 2021
Předmět:
Male
Ticagrelor
Epidemiology
Cardiovascular Procedures
Myocardial Infarction
Disease
Cardiovascular Medicine
030204 cardiovascular system & hematology
Vascular Medicine
Medical Conditions
0302 clinical medicine
Medicine and Health Sciences
Medicine
Drug Interactions
030212 general & internal medicine
Myocardial infarction
Multidisciplinary
Pharmaceutics
Cardiogenic shock
Hematology
Middle Aged
Stroke
Neurology
Cardiovascular Diseases
Cardiology
Female
Research Article
medicine.drug
Acute coronary syndrome
medicine.medical_specialty
Coronary Stenting
Combination therapy
Science
Cerebrovascular Diseases
Hemorrhage
Surgical and Invasive Medical Procedures
Platelet Glycoprotein GPIIb-IIIa Complex
03 medical and health sciences
Signs and Symptoms
Drug Therapy
Internal medicine
Humans
cardiovascular diseases
Acute Coronary Syndrome
Blood Coagulation
Ischemic Stroke
Coagulation Disorders
business.industry
Thrombosis
Cardiovascular Disease Risk
medicine.disease
Medical Risk Factors
Multivariate Analysis
Stent Implantation
Clinical Medicine
business
Glycoprotein IIb/IIIa
Receptor Antagonist Therapy
Mace
Zdroj: PLoS ONE
PLoS ONE, Vol 16, Iss 2, p e0246166 (2021)
ISSN: 1932-6203
DOI: 10.1371/journal.pone.0246166
Popis: This study was to compare the efficacy and safety of combined glycoprotein IIb/IIIa inhibitor (GPI) and ticagrelor versus ticagrelor in patients with acute coronary syndrome (ACS). An observational study was conducted using the Improving Care for Cardiovascular Disease in China-ACS project. Totally, 13,264 patients with ACS and received combination therapy or ticagrelor therapy were analyzed. The primary outcome was the composite of major cardiovascular events (MACE: all-cause mortality, myocardial infarction [MI], stent thrombosis, cardiogenic shock, and ischemic stroke), and secondary outcomes included all-cause mortality, MI, stent thrombosis, cardiogenic shock, and ischemic stroke. The multivariable adjusted analysis indicated that combination therapy was associated with an increased risk of major cardiovascular events (MACE) (P = 0.001), any bleeding (PP = 0.005). Moreover, the multivariable adjusted for propensity score-matched (PSM) analysis suggested that combination therapy produced additional risk of MACE (P = 0.014), any bleeding (PP = 0.005). Moreover, PSM analysis suggested that combination therapy was associated with greater risk of stent thrombosis (P = 0.012) and intracranial bleeding (P = 0.020). Combined GPI and ticagrelor therapies did not have any beneficial effects on MACE, stent thrombosis, intracranial bleeding, any bleeding, or major bleeding.
Databáze: OpenAIRE