Aortic Valve Disease
Conditions
Keywords
Bioprosthesis, Thrombosis, Cerebral emboli, Transcranial Doppler, Platelet function tests
Brief summary
The purpose of this study is to determine if there is any difference in the counts of cerebral emboli and platelet function between two prophylactic treatments of thrombosis currently used at University of Ottawa Heart Institute for the first three months after surgery in low-risk patients undergoing aortic valve replacement with a bioprosthetic valve: 1) daily use of high-dose aspirin \[325 mgs\], and 2) the combination of oral Warfarin \[target INR 2.0 to 3.0\] and low-dose aspirin \[81 mg\].
Detailed description
Background: There are several medications used to prevent blood clotting in patients undergoing surgical replacement of their aortic valves with tissue valves. One of these medications is called warfarin (Coumadin ®) which prevents blood clotting by making the blood "thinner." Another medication is aspirin which prevents the aggregation (clustering) of cells in the blood called platelets. Some clinicians consider that using only aspirin should be enough to protect the patients against the presence of clots in the blood, but others consider that aspirin should be combined with warfarin for better protection. Moreover, physicians express concern over the use of oral anticoagulation due to the possibility of an increased risk of bleeding. The effects of these medications for preventing blood clots traveling to the brain after the surgery are currently unknown. Transcranial doppler ultrasound will be used in these patients to evaluate non-invasively the quantity of fragments of clots circulating in the arteries of the brain. In addition, platelet function will be measured to determine how effective these treatments are for preventing the aggregation of the blood cells called platelets, which may be involved in clot formation. Objective: Our purpose is to determine if there is any difference in the counts of cerebral emboli and platelet function between two prophylactic treatments of thrombosis currently used in our institution for the first three months after surgery in these patients: 1) daily use of high-dose aspirin \[325 mgs\], and 2) the combination of oral Warfarin \[target INR 2.0 to 3.0\] and low-dose aspirin \[81 mg\]. Methods: Patients with low risk profile undergoing primary aortic valve replacement with a bioprosthetic (tissue) valve will be eligible for the study. Patients will receive one of the two prophylactic treatments of thrombosis (1 or 2) depending on the surgeon's preference. Platelet function will be measured before surgery and transcranial doppler within the first 24 hours immediately after the surgery. At the end of one month following surgery, all patients will undergo transcranial doppler and platelet function assessment. The study will be powered on demonstrating the hypothesis of substantial equivalence between the two treatments as regarding the primary outcome (cerebral emboli). Outcome measures: 1. Primary outcome: Bilateral counts of cerebral emboli in the middle cerebral arteries with transcranial doppler ultrasound at one month after surgery 2. Secondary outcomes: Platelet function, incidence of major adverse neurologic and bleeding events at one month following surgery
Interventions
Two standard prophylactic treatments of thrombosis within the first 3 months postsurgery currently used in our institution: a) daily dose of aspirin (325 mgs; b) daily dose of aspirin (81 mg) plus Warfarin for target INR 2.0-2.5
Sponsors
Study design
Eligibility
Inclusion criteria
* Patients undergoing primary aortic valve replacement with bioprosthetic (tissue) valve.
Exclusion criteria
* Emergency surgery or redo operations. * Patients with history of transient ischemic attacks, stroke, or history of carotid stenosis greater than 50% as detected by carotid duplex doppler or angiography. * Patients with COPD who are CO2 retainers. * Patients with LV function less than 50%, or enlarged left ventricle greater than 50 mm as detected by echocardiography or previous history of thromboembolism. * Patients with history of atrial fibrillation or heart rhythm disturbances.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Differences in the Rate of Doppler-detected Cerebral Micro Emboli Between the Two Prophylactic Treatments of Thrombosis | 1 month after surgery | Trans-cranial doppler (TCD) measurements were used to test for the presence of cerebral micro-emboli. Doppler measurements were completed on the neck and throughout the temporal window. In addition, probes were secure to the temporal areas with a headband. Measurements determined presence of air or solid emboli. Each participant at the 1 month visit underwent TCD measurements after 30min of exposure to room air, and again 30min after receiving 100% oxygen through a breathing mask. Results show the comparison of participants on aspirin only vs warfarin + aspirin when TCD was completed both in room air and with 100% oxygen. |
Secondary
| Measure | Time frame |
|---|---|
| Differences in the Degree of Inhibition of Platelet Aggregation Between the Two Prophylactic Treatments of Thrombosis | 1 month after surgery |
| Difference in the Degree of Inhibitor of Platelet Aggregation Between the Two Prophylactic Treatments of Thrombosis | 1 month after surgery |
Countries
Canada
Contacts
Ottawa Heart Institute Research Corporation
Ottawa Heart Institute Research Corporation
Participant flow
Recruitment details
Because all nonexcluded patients completed the study's procedures, the study was stopped after a total of 56 patients were enrolled and followed, with each arm of the study having 28 patients.
Baseline characteristics
| Characteristic | — |
|---|---|
| Age, Continuous | 71.5 years STANDARD_DEVIATION 9.5 |
| Aortic cross clamp time | 81.5 minutes STANDARD_DEVIATION 24 |
| Cardiopulmonary Bypass time | 110 minutes STANDARD_DEVIATION 42 |
| Carotid artery stenosis <70% | 2 Participants |
| Coagulopathy | 0 Participants |
| Diabetes mellitus | 9 Participants |
| Heart Failure | 32 Participants |
| Hypertension | 21 Participants |
| Malignancy | 0 Participants |
| Post operative complications - Bleeding, >3 units PRBCs transfused | 3 Participants |
| Post operative complications - stroke/TIA | 0 Participants |
| Sex: Female, Male Female | 16 Participants |
| Sex: Female, Male Male | 19 Participants |
| Smoking | 4 Participants |
| Thrombocytosis/thrombocytopenia | 0 Participants |
| Type of surgery bAVR + CABG | 12 Participants |
| Type of surgery bAVR only | 16 Participants |
| Type of valve Hancock II | 8 Participants |
| Type of valve Mosaic | 1 Participants |
| Type of valve Perimount | 22 Participants |
| Vertebral artery stenosis | 1 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 28 | 0 / 28 |
| other Total, other adverse events | 0 / 28 | 0 / 28 |
| serious Total, serious adverse events | 0 / 28 | 0 / 28 |