Bleeding Clinical Trial
Official title:
Thrombelastogram and Predicting Microvascular Bleeding in Patients Receiving Antiplatelet Medication Undergoing Cardiac Surgery
Study Objective is to correlate the results of preoperative platelet mapping derived from modified TEG with clinically significant postoperative bleeding and consumption of blood products.
Study Design:
Prospective observational study with blinded assessment of study endpoint variables.
Collection of information concerning study endpoints will be performed by the investigator
blinded to the results of preoperative testing of platelet function. The information will be
collected from 60 patients undergoing cardiac surgery in the Department of Cardiac Surgery
of Sheba Medical Center.
Study endpoints
1. Primary endpoint- resternotomy for bleeding after the surgery.
2. Secondary endpoints- chest tube output during first 24 hours after the surgery;
consumption of blood products during first 3 postoperative days.
;
Observational Model: Cohort, Time Perspective: Prospective
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