Sponsored by Abiomed, Inc.
Evolving Evidence for Protected PCI With Impella® to Treat High-Risk Complex CAD Patients
PROTECT clinical studies consistently demonstrate MACCE reduction at 90 days.
High-risk intervention is associated with increased morbidity and approximately twofold mortality as compared to patients receiving percutaneous coronary interventions (PCIs).1,2 The criteria as to what defines high risk are still being debated; however, there is consensus that this category of patients includes candidates unsuitable for surgical revascularization due to high-risk clinical presentation, comorbidity, anatomic complexity, or a combination thereof.3 Even though revascularization may be recommended for these patients per current guidelines and appropriate use documents,4 PCI is less likely to be offered in the setting of high surgical risk.5,6 High-risk PCI requires longer procedure time and is associated with an increased risk of hemodynamic instability and increased risk for intraprocedural and postdischarge adverse events, including cardiac arrest,7,8 which also limits the patient’s ability to tolerate interventions required to achieve durable and complete revascularization.
HEMODYNAMIC SUPPORT AND COMPLETE REVASCULARIZATION
Complete revascularization is associated with significantly lower rates of major adverse cardiovascular events (MACE; P < .001), myocardial infarction (MI) (P = .0007), and revascularization (P < .001) as compared with incomplete revascularization.9,10 In addition, revascularization procedures conducted in a single session result in significantly fewer major adverse cerebral and cardiovascular events (MACCE; P = .004) and deaths (P = .006) compared to staged PCI procedures.11 The use of hemodynamic support during PCI in patients with high-risk complex coronary artery disease (CAD) helps maintain hemodynamic stability, which enables complete revascularization.12 Apart from providing hemodynamic stability, an ideal device should increase coronary perfusion, decrease myocardial oxygen consumption, increase cardiac microvascular perfusion, and bridge through myocardial stunning resulting from ischemia during PCI.13-15
The Impella heart pump (Abiomed, Inc.) assists the unloading of the left ventricle, increases coronary perfusion pressure, increases mean arterial pressure, and optimizes end-organ perfusion.16 Impella provides a flow rate ranging from 2.5 L/min to 5.5 L/min, depending on the device and selected performance level, and can be placed either percutaneously or via surgical cutdown in the axillary or femoral artery. A Protected PCI is a PCI supported by the Impella Heart Pump and is indicated for high-risk, complicated CAD patients with or without depressed left ventricular (LV) systolic function. Impella is the most studied mechanical circulatory support device in the history of the FDA, with more than 1,350 patients in the PROTECT clinical studies (PROTECT I, II, and III).
PROTECT I was a prospective, single-arm, multicenter feasibility study of 20 patients that examined the safety and feasibility of the Impella 2.5® device. None of the patients developed hemodynamic compromise during PCI with Impella support. The study demonstrated that Impella 2.5 provides hemodynamic support during high-risk PCI and is safe and easy to implant.17
PROTECT II was a prospective, multicenter, randomized trial that compared Impella 2.5 with an intra-aortic balloon pump (IABP) in patients requiring hemodynamic support during elective or urgent high-risk PCI.18 PROTECT II is the only FDA randomized controlled trial conducted for hemodynamically supported high-risk PCI. The study enrolled 452 patients at 112 sites in the United States and European Union. The primary efficacy endpoint was a composite of 10 major adverse events: death, stroke/transient ischemic attack, MI, repeat revascularization, need for cardiac or vascular operation, acute renal dysfunction, cardiopulmonary resuscitation or ventricular arrhythmia requiring cardioversion, increase in aortic insufficiency by more than one grade, severe hypotension, and failure to achieve angiographic success. The multiple safety endpoints, including this primary endpoint, allowed for a comprehensive evaluation of Impella’s safety profile at 30 days, with a follow-up analysis at 90 days (both prespecified). The primary endpoint analysis showed a significant reduction in major adverse events (MAE) at 90 days (40% vs 51%; P = .023) (Figure 1) as compared to the IABP.18
Other studies from the PROTECT II data set have shown that Impella 2.5 is associated with improved clinical outcomes as compared to IABP at 90-day follow-up:
- 44% lower MACCE (composite of death, stroke, MI, and repeat revascularization) (15.9% vs 28.5%; P = .013) (Figure 2)19
- 22% reduction in MAE (39.5% vs 51.0%; P = .039) for patients with three-vessel disease and impaired LV function20
- 90% reduction in repeat revascularization in patients undergoing rotational atherectomy (3.1% vs 30%; P = .006)21
- Impella support resulted in similar 30-day mortality in patients with and without previous coronary artery bypass grafting (CABG)22
Based on data from PROTECT I, II, and the ongoing cVAD study, FDA granted Impella a first-of-its-kind indication for high-risk PCI patients.23 Further data collected as part of postmarket approval study, inside the cVAD study were presented as PROTECT III during the Transcatheter Cardiovascular Therapeutics (TCT) annual meeting in September 2019.24
PROTECT III is an ongoing, prospective, single-arm FDA postapproval study of Impella (2.5 and CP®) in high-risk PCI.24 The patient population is comparable to the PROTECT II study population. In the interim analysis presented at TCT 2019, 571 Impella CP and 327 Impella 2.5 patients from 45 sites in the United States were enrolled from March 2017 to July 2019. The endpoints were compared with the IABP and the Impella arms from PROTECT II.
In PROTECT III, an analysis of the echocardiography and angiography data was performed by independent core labs, and an independent clinical events committee adjudicated adverse events. The primary endpoint was MACCE at 90 days: death, stroke, MI, and repeat revascularization. PROTECT III included patients with significantly higher baseline and procedural risks. Patients in the PROTECT III study group were older (70.9 vs 67.5 years; P < .001), and more women were treated (26.3% vs 19.4%; P = .044) as compared to the PROTECT II group. However, LV ejection fraction (LVEF) was lower in the PROTECT II patients when compared to the PROTECT III cohort (23.4% vs 32.3%; P < .001). This was due to the expansion of the FDA indication to include patients without depressed ejection fraction. Patients in the PROTECT III group had worse angiographic characteristics with more left main disease (15.7% vs 11.5%; P = .011) and more pre-PCI TIMI 0/1 (14.7% vs. 7.0%; P < .001) as compared to the PROTECT II group. Impella support resulted in physicians treating a greater number of vessels (2.0 vs 1.81; P < .001), more triple-vessel revascularization (29.9% vs 14.4%; P < .001), more atherectomy use (43.3% vs 14.2%; P < .001), and a greater number of vessels treated with atherectomy (2.01 vs 1.44; P < .001) as compared to the PROTECT II group.
The results showed that Protected PCI with Impella decreased MACCE events by 54% in the PROTECT III cohort as compared to the IABP cohort in the PROTECT II trial (16.8% vs 31%; P < .001) (Figure 3).
The PROTECT III interim results validate the results of the PROTECT II randomized controlled trial in real-world clinical practice. A subgroup analysis of PROTECT III demonstrated that Impella support also reduced the incidence of acute kidney injury (5.7% vs 24.5%; P = .0002) as compared to a control group of patients who did not receive Impella support.22,23 Other recent studies show similar renal protection benefits due to Impella support.25-27
In multiple studies and economic models, Protected PCI with Impella has demonstrated significant cost savings and cost-effectiveness with reduced length of stay and reduced readmissions from repeat procedures.28-30 By providing support to the failing heart sooner, clinicians can improve patient outcomes and avoid the longer-term costs associated with alternative resource-intensive therapies and open heart procedures.28
The PROTECT II economic study concluded that for patients with severe LV dysfunction and complex anatomy, Impella-assisted PCI significantly reduced major adverse events at an incremental cost per quality-adjusted life-year (QALY) and is considered to be cost-effective for advanced cardiovascular technologies ($39,000/QALY).28 In the 90 days after initial hospitalization, Impella patients experienced:
- Two fewer days in the hospital (P = .001)28
- A 52% reduction in hospitalizations due to repeat revascularization (P = .024)28
- 50% lower rehospitalization costs compared to IABP (P = .023)28
The cost-effectiveness demonstrated with Impella is consistent with a study of national trends in the utilization of percutaneous ventricular assist devices (pVADs) (including Impella), and other short-term mechanical support, by Stretch et al who observed a correlation between increased utilization of pVADs and decreased costs.30 A systematic review by Maini et al appraised the findings of six cost-effectiveness studies of pVADs.29 Length of stay reductions were observed in all studies, with a clinically relevant observation of fewer days in the intensive care unit, fewer days from readmissions, and two fewer days in the hospital over 90 days (Figure 4).
INDICATIONS FOR PROTECTED PCI
The initial FDA approval for high-risk PCI using the Impella Heart Pump was based on several clinical studies, including PROTECT I and PROTECT II, which enrolled patients undergoing elective and urgent PCI who had advanced comorbidities and the most severe LV dysfunction. Patients were symptomatic and presented with high-risk features, including complex coronary anatomy (mean SYNTAX score, 30 ± 13), depressed LVEF (mean LVEF, 24% ± 6%), and other comorbidities, including previous procedures, with 64% of patients deemed ineligible for CABG. Based on these studies, low EF was initially a requirement for indicated use of Impella with high-risk PCI. However, through the FDA-audited ongoing multicenter, prospective cVAD registry, data were evaluated, analyzed, and presented to the FDA demonstrating that depressed systolic function is only one of many factors that defines the high-risk patient. Patients with complex coronary anatomy or in whom complex procedures are planned (eg, use of ablative technologies such as directional, rotational, orbital, or laser atherectomy), extensive comorbidities including surgical ineligibility, or those at risk for hemodynamic collapse can also be considered high risk and may benefit from a Protected PCI procedure. Based on data from the cVAD Registry, the FDA granted approval to expand the indications for the Impella Heart Pump, eliminating depressed EF as a requirement for on-label use of Impella in Protected PCI. With this postmarket approval, patients with or without depressed LV systolic function in the presence of severe CAD or complex anatomy (eg, left main, multivessel, requiring atherectomy) may be appropriate when a heart team, including a cardiac surgeon, has determined high-risk PCI is the appropriate therapeutic option.
The data supporting this expanded indication included an analysis of 229 consecutive patients with mild to moderately reduced EF. In this cohort, most of the patients were ineligible for CABG due to surgical risk factors. On average, these patients were older, more often female, and had significantly more lesions treated and left main intervention than patients in the cVAD registry cohort with an EF < 35% (n = 464). This comparison demonstrated that high-risk PCI with Impella support was feasible, safe, and achieved favorable outcomes in patients with mild to moderately reduced EF.
SOCIETY GUIDELINES SUPPORT IMPELLA IN HIGH-RISK PCI
Intersocietal clinical guidelines (American College of Cardiology, Heart Failure Society of America, Society for Cardiovascular Angiography and Interventions, and the Society of Thoracic Surgeons) agree the Impella Heart Pump may be beneficial for technically challenging lesions or for prolonged PCI in patients.3 The Interventional Scientific Council of the American College of Cardiology has also published a consensus document detailing the recommended approach to percutaneous mechanical circulatory support in patients undergoing high-risk PCI.31
High-risk PCI presentation is growing and despite the recommendation for percutaneous revascularization, these patients have less chance of receiving PCI due to suboptimal hemodynamic support. Impella allows the heart to rest, providing coronary and peripheral perfusion, enabling the physician to perform a more complete and optimized revascularization. The PROTECT II randomized control trial demonstrated that in high-risk patients, Impella support reduced MACCE at 90 days compared to patients on an IABP. PROTECT III utilizes prospectively collected data representing modern clinical practice for high-risk PCI. Despite a worse procedural and angiographic profile, as compared to the PROTECT II patient population, the clinical outcomes in PROTECT III show a reduction in MACCE compared to the IABP arm and validate the results seen in the PROTECT II study. Results from the PROTECT clinical studies consistently demonstrate a reduction in MACCE at 90 days after Protected PCI with the Impella Heart Pump.
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