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| Name | Class |
|---|---|
| Foothills Interventional Cardiology Research Group | UNKNOWN |
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The purpose of this trial is to compare post-conditioning to standard angioplasty (50/50 chance) in patients who present with an acute heart attack and are taken directly for an angioplasty procedure. Post conditioning is a procedure that involves balloon inflation followed by deflation in a series of cycles that appears to show (based on early data) that it can decrease the amount of damage to the heart muscle as compared to standard angioplasty procedures.
Hypothesis: For Subjects undergoing direct PCI for STEMI, post conditioning with cycles of balloon inflation/deflation within the first minute following the re-establishment of coronary blood blow, will decrease the amount of irreversible myocardial damage assessed by delayed enhancement contrast CMR.
In patients who suffer a myocardial infarction, the blood flow usually ceases due to plaque rupture leading to thrombus formation and vessel occlusion. The resultant entity is known as ST Elevation segment myocardial infarction (STEMI) and is a significant health issue in industrialized countries. There are over 50,000 STEMI's every year in Canada and up to 10% of these patients die in hospital and another 10% die within the first year after their heart attack. The more common problem however is not death, but irreparable damage to the left ventricle leading to LV dysfunction and subsequent heart failure and arrythmias. Re-establishing blood flow promptly by administering plasminogen activators (lytics) or mechanically by performing angioplasty is possible and has lowered the mortality rate dramatically.
Although reperfusion is necessary, it gives rise to an entity known as ischemia-reperfusion where acutely re-establishing blood flow and oxygen levels of the heart has detrimental effects. Clinically this is manifested as no-reflow that causes subsequent damage to the left ventricle and decreases the beneficial affect of early reperfusion by PCI. The ischemia-reperfusion effect sets off a molecular cascade of events involving unfavorable interaction between neutrophils, platelets and endothelium, that is fairly well identified. Efforts to pharmacologically block this effect have not proven to be particularly effective.
Post conditioning follows from a concept of pre-conditioning in animals that showed a decrease in myocardial infarct size. Pre-conditioning is not useful as it requires to be performed prior to the development of ischemia/injury. Post conditioning in preliminary studies with animals and one small study in humans have shown promising results for decrease in infarct size. Post conditioning is a procedure of gradual conditioning in which the artery is opened and closed in cycles with inflation/deflation of the culprit artery followed immediately by standard PCI and placement of stent.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Post conditioning | Experimental | Balloon inflations-deflations |
|
| Standard care | Placebo Comparator | No balloon inflations |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Post conditioning | Procedure | 4 cycles of balloon inflation /deflation (post-conditioning) within first minute of opening up artery in primary PCI for STEMI vs usual balloon inflation sequence |
| Measure | Description | Time Frame |
|---|---|---|
| Infarct size as measured by: salvage index = total area at risk - infarct size/total area at risk | 3-5 days post MI |
| Measure | Description | Time Frame |
|---|---|---|
| Corrected TIMI frame count (cTFC) | Immediately post PCI | |
| Myocardial blush score | Immediately post PCI | |
| CK release (under the curve) |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Mouhieddin Traboulsi, MD | University of Calgary, sub-investigator | Study Director |
| Matthias Friedrich, MD | Sub-investigator, Stephenson CMR Centre, FMC; 1403-29th St NW, Calgary; T2N 2T9 | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Foothills Medical Centre | Calgary | Alberta | T2N 2T9 | Canada |
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| ID | Term |
|---|---|
| D009203 | Myocardial Infarction |
| ID | Term |
|---|---|
| D017202 | Myocardial Ischemia |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
| D014652 | Vascular Diseases |
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| ID | Term |
|---|---|
| D057775 | Ischemic Postconditioning |
| ID | Term |
|---|---|
| D013812 | Therapeutics |
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| 1st 48 hours post MI |
| ST segment resolution by 48 hrs compared with admission | 1st 48 hours post MI |
| MRI infarct size | 3-5 days and 6 months |
| MRI maximal transmural extent of irreversible injury | 3-5 days and 6 months |
| CMR regional end-systolic wall stress | 3-5 days and 6 months |
| CMR Myocardial perfusion | 3-5 days and 6 months |
| CMR Myocardial oxygenation | 3-5 days and 6 months |
| Peripheral endothelial function testing (brachial u/s and pulse arterial tonometry) in hospital | 3-5 days post MI |
| CMR quantification of volume of no-reflow | 3-5 days and 6 months |
| D007238 |
| Infarction |
| D007511 | Ischemia |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D009336 | Necrosis |