Evaluation of Platelet Aggregability in the Release of CABG in Patients With ACS With DAPT.

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

190 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-07-31

Study Completion Date

2019-01-31

Brief Summary

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The purpose of this study is to assess platelet aggregability by a "point of care" device (Multiplate®) to decrease the release time for coronary artery bypass graft (CABG ) in patients with acute coronary syndrome (ACS) in use of dual antiplatelet therapy.

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Detailed Description

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This open, prospective, randomized study will be included patients with acute coronary syndrome (ACS) and coronary artery bypass graft (CABG) indication in use of double platelet aggregation (aspirin and inhibitor of ADP). The groups to be analyzed will be:

1. Control group: It is composed of patients who will discontinue inhibitor of ADP for 5 days before surgery, and must be operated on the first working day after completing the 5 days without the drug. This group will have aggregability evaluated by platelet function testing (Multiplate®) immediately before the transport to the operating room.
2. Intervention group: It is composed of patients who will be evaluated by platelet function testing (Multiplate®) daily until the value obtained\> 46 AU, when they will be immediately released to CABG, to be held on the first working day after release.

All patients included, after the explanations and signing the informed consent, will initially undergo preoperative examinations as institutional routine. In the immediate period (24 hours) after CABG will be collected on all results of tests to which the patient is submitted in accordance with the institutional routines, and the volume of chest tube bleeding and need for blood transfusions. Clinical data "MACE" will be collected throughout the patient's hospital stay.

Conditions

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Bleeding

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Control Group

Patients who will discontinue inhibitor-ADP for 5 days before surgery, and must be operated on the first working day after completing the 5 days without the drug. This group will have its aggregability evaluated by platelet function testing (Multiplate ADP®) immediately before the transport to the operating room.

Group Type NO_INTERVENTION

No interventions assigned to this group

Intervention Group

Patients will be evaluated by platelet function testing (Multiplate ADP®) daily until the value obtained\> 46 AU, when they will be immediately released to CABG, to be held on the first working day after release.

Group Type ACTIVE_COMPARATOR

Multiplate ADP®

Intervention Type DEVICE

Patients will be evaluated by platelet function testing (Multiplate ADP®) daily until the value obtained\> 46 AU, when they will be immediately released to CABG

Interventions

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Multiplate ADP®

Patients will be evaluated by platelet function testing (Multiplate ADP®) daily until the value obtained\> 46 AU, when they will be immediately released to CABG

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

1. Age\> 18 years;
2. Hospitalization for ACS defined as:

\- Symptoms ischemic unstable pattern, occurring at rest or upon exertion within 72 hours of an unscheduled hospitalization, related to presumed or proven coronary artery, and at least one of the following:
* elevated cardiac biomarkers (troponin I or CK-MB mass) above the 99th percentile.
* Changes in resting electrocardiogram compatible with ischemia or infarction and further evidence of obstructive coronary artery disease:

the resting ECG compatible with ischemia or infarction in at least one of the criteria below:
* ST segment depression of new or presumably new\> 0.5 mm in 2 sequential leads.
* The new ST-segment elevation or presumed new J point in two contínguas leads with value\> 0.2mV in men or\> 0.15mV in women in V2-V3 and / or\> 0.1mV in other leads or new left bundle branch block or presumably again.
* T wave inversion new or presumably new\> 1mm in leads with a broad R wave in two contiguous leads.
* New pathological Q wave or presumably new\> 30 ms duration and\> 1mm deep in 2 contiguous leads or\> 20 ms or QS complex in V2 and V3.
* Peaked new R Wave\> 40 ms in V1 and V2, R / S\> 1 in V1 with positive T wave in the absence of consistent driving change.
* Additional evidence of coronary artery disease in at least one of the criteria below:
* Evidence of myocardial ischemia or new or presumably new in imaging with perfusion.
* Contractility Change in new or presumably new wall.
* Coronary angiography with obstruction\> 70% in epicardial coronary artery.
3. Use of dual antiplatelet therapy (ASA associated with P2Y12 receptor inhibitor);
4. An indication of CABG.
5. Agreement to sign the Informed Consent (IC);

Exclusion Criteria

1. anemia (hematocrit \<30%).
2. Thrombocytopenia (\<100,000 / mm³).
3. Coagulopathy (history of bleeding diathesis or use of oral anticoagulants).
4. Chronic renal failure dialysis or creatinine clearance \<30 ml / min / m2 (estimated by MDRD formula).
5. Active liver disease.
6. combined valvuloplasty or valve replacement surgery ..
7. Angioplasty with stent for less than 30 days or with drug-eluting stents for less than one year.
8. Use of fibrinolytic specific fibrin not less than 48 hours or specific fibrin less than 24 hours of randomization;
9. Any medical condition that in the investigator's opinion present significant risk to the patient or interfere with the interpretation of the safety and efficacy;
10. Patients who are taking part in another clinical study.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No