A retrospective real world analysis of bleeding events with ticagrelor compared to clopidogrel in ACS patients.
Major bleeding after myocardial infarction portends a poor outcome. A balance is required between potency of platelet inhibition and risk of bleeding. Ticagrelor provides faster and more effective platelet inhibition than Clopidogrel. In the PLATO trial Ticagrelor reduced the incidence of cardiovascular death, myocardial infarction and stroke compared to Clopidogrel after ACS (acute coronary syndrome). Although there was no difference in overall bleeding there was more non-CABG related major bleeding with Ticagrelor. It has since been recommended, in addition to aspirin, in treatment of moderate-high risk ACS by both ESC (European Society of Cardiology) and NICE (National Institute for Clinical Excellence). There has been widespread adoption as first line therapy in UK hospitals. There remains potential concern about bleeding in a "real world" population compromising more high risk patients; particularly more elderly and female, than those in PLATO. The investigators intend to perform a large "real world" comparison of bleeding risk with Ticagrelor compared to Clopidogrel in a UK ACS population. The investigators plan an observational cohort study of patients presenting with ACS at 5 district general hospitals in Merseyside and Cheshire. The investigators will collect data retrospectively on 2500 patients treated with Clopidogrel prior to the guideline change and 2500 treated with Ticagrelor thereafter. The primary end point will be incidence of BARC 3-5 (Bleeding Academic Research Consortium) and PLATO major bleeding.
Study Type
OBSERVATIONAL
Enrollment
5,225
No intervention- purely observational
University Hospital Aintree
Liverpool, United Kingdom
The incidence of major bleeding defined by both BARC (3-5) and PLATO definitions
bleeding event
Time frame: 12 months from treatment starting
Incidence of minor bleeding as defined by BARC and PLATO
Minor bleeding
Time frame: 12 months from treatment starting
Incidence of gastrointestinal bleeding
GI bleeding
Time frame: 12 months from treatment starting
Incidence of intracranial bleeding
intracranial bleeding
Time frame: 12 months from treatment starting
Rate of major adverse cardiovascular events; myocardial infarction, stroke and cardiovascular death
MACE/ischaemic events
Time frame: 12 months from treatment starting
Mortality
all cause mortality
Time frame: 12 months from treatment starting
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