Aspirin Responsiveness and Outcome in Coronary Artery Bypass Graft (CABG) Surgery

University Hospital Basel

Status: Completed

Conditions: Myocardial Ischemia; Thrombosis; Coronary Artery Bypass Graft Triple Vessel; Antithrombotic Drugs [Platelet-aggregation Inhibitors] Causing Adverse Effects in Therapeutic Use

Study type: Observational

Funder types: Other

Identifiers

NCT01174862

288/09

Details and patient eligibility

About

In patients undergoing coronary artery bypass graft (CAGB) surgery, aspirin is commonly prescribed to prevent graft thrombosis and myocardial ischemia. However, there are still a significant number of grafts occluding in the postoperative period. This is partly attributed to reduced aspirin responsiveness, also called "aspirin resistance". At the moment, no standardized definition or laboratory test is available to quantify "aspirin resistance", and strong platelet reactivity in laboratory tests is not necessarily associated with increased thrombotic events. However, there is increasing evidence that reduced aspirin responsiveness in platelet function analyzers is associated with adverse long-term outcome and higher incidence of major adverse events in patients with stable coronary artery disease and in patients undergoing percutaneous coronary intervention. In patients undergoing coronary artery bypass graft surgery, the predictive value of a laboratory finding of reduced aspirin responsiveness remains unclear.

Therefore, the aim of this study is to prospectively evaluate whether the pre- and/or postoperative laboratory finding of reduced aspirin responsiveness defined by MultiplateTM platelet function analyzer is associated with higher incidences of adverse outcome after 30 days and 12 months in patients undergoing CABG surgery.

Enrollment: 304 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• patient undergoing elective CABG surgery
• therapy with aspirin until at least 2 days before surgery
• written informed consent

Exclusion criteria

• missing written consent
• no therapy with aspirin or therapy stopped more than 2 days before surgery
• therapy with clopidogrel more than 3 days before surgery
• emergency surgery
• surgery including more than CABG
• inborn or acquired platelet disorders
• therapy with Selective Serotonin reuptake inhibitors (SSRI)
• severe hepatopathy (spontaneous Quick <70%)
• severe kidney disease (creatinine clearance < 30 ml/min)

Trial design

304 participants in 2 patient groups

Aspirin responder

Description:

Normal aspirin responsiveness in ASPI test (Multiplate)

Aspirin non-responder

Description:

Reduced aspirin responsiveness in ASPI test (Multiplate)