Intravascular Balloon Lithotripsy in Left Main Stem Percutaneous Coronary Intervention

Inclusion Criteria:

• Subject is ≥ 18 years old.

• Unprotected distal LM (or equivalent) disease defined as:

  1. >70% diameter stenosis (DS) on angiography in the distal LM; or
  2. ≥50% DS in the distal LM with a) non-invasive evidence of ischaemia referable to a hemodynamically significant left main lesion, and/or b) FFR ≤0.80; or
  3. >70% diameter stenosis in either the ostial left anterior descending (LAD) or ostial left circumflex (LCX) that is within 10 mm of the ostium and requires stenting back into the LM (distal LM equivalent); or
  4. >50% diameter stenosis in either the ostial left anterior descending (LAD) or ostial left circumflex (LCX) that is within 10 mm of the ostium and requires stenting back into the LM (distal LM equivalent) with a) non-invasive evidence of ischaemia referable to its myocardial territory and/or b) FFR ≤0.80
• Clinical indication for revascularisation by PCI
• Viability of the treatment vessel as determined by echocardiography, cardiac MRI or other equivalent imaging modality.
• ≥ 270° arc of calcification within at least one stenotic segment demonstrated on intravascular imaging.
• Ability to pass a 0.014" guide wire across the lesion.
• Ability to provide informed consent and comply with all study procedures, including follow-up at 30 days.

• Lesions not related to the distal LM requiring PCI can be treated:

  1. at the time of the study procedure if completed prior to distal LM PCI and the procedure was successful and uncomplicated (defined as a final lesion angiographic diameter stenosis <30% and TIMI 3 flow (visually assessed) for all non-target lesions and vessels without perforation, cardiac arrest or need for defibrillation or cardioversion or hypotension/heart failure requiring mechanical or intravenous hemodynamic support or intubation. In situations where the distal LM lesion is critical, the LM can be ballooned or treated first so long as the study protocol is not deviated.
  2. as a staged procedure either within the same hospital admission or within 30 days. Any staged procedure must be declared at the index procedure otherwise it will be recorded as an event.

Exclusion Criteria:

• Subject is participating in another research study involving an investigational agent (pharmaceutical, biologic, or medical device) that has not reached the primary endpoint.
• Daughter vessel reference diameter < 2.5 mm.
• Use of rotational atherectomy, scoring or cutting balloon, or any investigational device.
• Evidence of aneurysm in target vessel within 10 mm of the target lesion.
• Prior PCI of the LM or PCI of the proximal LAD or proximal LCX within 10 mm of the ostium.
• Prior coronary artery by-pass graft (CABG) surgery.
• Chronic total occlusion (CTO) of the LM, proximal LAD or proximal LCX.
• Untreated pre-procedural haemoglobin < 8 g/dL.
• Renal failure with serum creatinine > 2.5 mg/dL and not on chronic dialysis.
• Uncontrolled diabetes defined as a HbA1c >10%.
• Coagulopathy manifested by platelet count < 50,000/ mL or International Normalized ratio (INR) > 1.7 (INR is only required in patients who have taken warfarin within 2 weeks of enrolment).
• Cardiogenic shock.
• Ongoing ST elevation myocardial infarction (STEMI).
• History of stroke or transient ischemic attack (TIA) within 3 months.
• NYHA class IV heart failure or LVEF < 20%.
• Active peptic ulcer or upper gastrointestinal (GI) bleeding within 6 months.
• Patients with a life expectancy of less than 1 year.
• Visible thrombus (by angiography) at target lesion site.
• Patient has active systemic infection on the day of the index procedure with either fever or requiring intravenous antibiotics.
• Patient has vascular connective tissue disease (e.g. Marfan's syndrome).
• Patient has a hypercoagulable disorder.
• Patient has allergy to imaging contrast media for which they cannot be pre-medicated.
• Allergy to Aspirin.
• Allergy to Clopidogrel, Ticagrelor and Prasugrel.
• Allergy to any component of the drug eluting stent that is planned for use.
• Patient has any other severe comorbidity that is felt to preclude enrolment by the investigator.
• Subject is pregnant or nursing (a negative pregnancy test is required for women of child-bearing potential within 7 days prior to enrolment).