Distrupt Stiffness Trial

Massive Calcifications in the peripheral vessels lead to altered vascular stiffness. This arterial stiffness is an excellent marker for morbidity and mortality and correlates with the progression of cardiovascular disease. Main pathophysiologic principles are altered pulse wave reflections through arterial and aortic stiffness on cardiac functions. Impaired vascular compliance is associated with increased cardiovascular morbidity and leads to a progression of atherosclerotic lesions, impaired ventriculoarterial coupling and ultimately impaired coronary perfusion.

Vascular calcifications are furthermore held responsible for suboptimal vessel expansion and increased risk of complications including dissection and perforation and reduced long-term patency when treated though the endovascular route. Calcium treatment through IVL gives physicians opportunities to tackle this unmet need. IVL treatment is a safe and effective treatment in these heavily calcified lesions proving excellent procedural success compared to PTA driven by a significantly lower rate of major dissections and need for bail-out stent placement. This was evident also in coronary vessels suggesting that calcium fracture is the IVL-related mechanism to enhance vessel compliance and to assists optimal stent expansion.

The influence of this novel strategies with improved hemodynamic capabilities with respect to vasomotion of the vessel wall, vascular function and vascular compliance can be measured by ultrasound, as shown recently. To which extent intravascular lithotripsy has an impact on vessel compliance has not been elucidated so far and could aid to understand the prognostic beneficial effects of intravascular lithotripsy.

The aim of this investigator-initiated trial is thus to investigate the IVL -related beneficial effect of lesion preparation by altering vascular compliance parameters and vasomotion of the vessel wall.

The primary objective is to determine changes in Vessel compliance, function and stiffness and after IVL treatment compared to POBA in symptomatic PAD.

Local vascular compliance as determined through FDC (fractional diameter change) in the distal IEA, CFA, prox. SFA or PA. Measurement of vascular compliance or function in patients is a powerful tool for atherosclerosis research. FDC represents the ratio of the vessel's diameter change between systole and diastole divided by the diastolic diameter. Several interventions are known to decrease cardiovascular risk, including exercise, smoking cessation, or medications with statins improving vascular compliance. Therefore, vascular compliance serves as a ''barometer'' for cardiovascular health that can be used for evaluation of new therapeutic strategies and is prognostic relevant. Moreover numerous studies have proven the prognostic value of vasomotor dysfunction, demonstrating that impaired vasomotor function identifies patients who have increased risk for cardiovascular events. Until now, it is completely unknown if intravascular lithotripsy has an impact on local vascular functions. We have recently shown an impact of paclitaxel coated ballons and mechanical atherothrombectomy on local vascular functions.

Further outcome measures include local and systemic vascular function and stiffness determined through pulse wave velocity (PWV), flow-mediated dilatation (FMD) and augmentation index (augmentation index). Vascular and aortic stiffness, assessed by measurement of PWV, can predict future cardiovascular events and mortality, even after accounting for other established cardiovascular risk factors. During the last years, a large amount of evidence has accumulated demonstrating that arterial stiffness is an important risk factor for cardiovascular disease. FMD represents the percent diameter gain as calculated based on pre-ischemia and post-ischemia (and reactive hyperemia) diameter measurements of the femoral artery. In this context, ischemia is induced through vessel occlusion by means of inflating a blood pressure cuff around the forearm or leg. Standard techniques as determined by Doppler and duplex ultrasonography will quantify tissue perfusion and primary patency. Furthermore, technical success, procedural complications and freedom from target lesion revascularization will be determined.

Peripheral Lithotripsy System The device under investigation is the Peripheral Lithotripsy System (Shockwave Medical, Fremont, California). Miniaturized and arrayed lithotripsy emitters create a localized field effect at the site of the calcium. The Peripheral Lithotripsy System is CE-marked for peripheral arterial disease and for this study, will be used within its indication for use. This included the following: intended for lithotripsy-enhanced balloon dilatation of lesions, including calcified lesions, in the peripheral vasculature, including the iliac, femoral, ilio-femoral and popliteal arteries.

The IVL catheter is delivered across a calcified lesion over an 0.014'' wire and the integrated balloon is expanded to 4atm to facilitate efficient energy transfer.

An electrical discharge from the emitters vaporizes the fluid within the balloon, creating a rapidly expanding and collapsing bubble that generates sonic pressure waves. The waves create a localized field effect that travels through soft vascular tissue, selectively cracking intimal and medial calcium within the vessel wall.

After calcium modification, the integrated balloon may subsequently be used to dilate the lesion at low pressure to maximize luminal gain.