Presentation on theme: "Are LVADs Ready To Be Mainstream? Joseph G. Rogers, MD Associate Professor of Medicine Duke University Medical Center J105-0311."— Presentation transcript:
Are LVADs Ready To Be Mainstream? Joseph G. Rogers, MD Associate Professor of Medicine Duke University Medical Center J
Address a large patient population Established safety and efficacy Have a proven track record of clinical success Have an acceptable risk / reward tradeoff Mainstream Therapies
Addressing An Unmet Need The VAD patient population is approaching 100,000 in the United States alone. US population 1 Target population (35-74 age cohort) 1 Diagnosed CHF population 2 All ages NYHA Class IIIB and IV 3 in age cohort Comorbidities estimated in this cohort Target VAD patient population (35-74 years) 301,000, ,100,000 5,520,000 3,744, ,400 (280,800) 93,600 1 US Census Bureau Statistics (2007) 2 Heart and Stroke Statistics, American Heart Association 3 Cardiovascular Round Table research and analysis, The Advisory Board company (2009)
Medical therapy alone can be a poor long-term treatment option for many in the more advanced stages of heart failure. Four major publications show the mortality risk associated with NYHA Class IV heart failure is high, with a 1-year mortality between 60 and 94 percent. 1-4 Heart Failure Has A High Mortality Rate Similar To Aggressive Malignancies Class IV heart failure patients treated with medical therapy alone have mortality rates similar to or greater than aggressive forms of cancer. 5 1 Rose, Gelijns, Moskowitz, et al. NEJM. 345: , Rogers, Butler, Lansman, et al. J Am Coll Cardiol. 50:741-47, Hershberger, Nauman, Walker, et al. J Card Fail. 22:616-24, Gorodeski, Chu, Reese, et al. Circ Heart Fail. 2:320-24, Data on file. Pleasanton, Calif: Thoratec Corp.
HeartMate II is the first and only FDA-approved continuous flow device for both Bridge-to-Transplantation (BTT) and Destination Therapy (DT). HeartMate II ® —A Proven Adjuvant Therapy For Advanced-Stage Heart Failure Bridge-to-Transplantation Non-reversible left heart failure Imminent risk of death Candidate for cardiac transplantation Destination Therapy NYHA Class IIIB or IV heart failure Optimal medical therapy 45 of last 60 days Not a candidate for cardiac transplantation For inpatient and outpatient use
Received European CE Mark in November 2005 Received FDA approval for BTT in April 2008 Received Health Canada approval in May 2009 Received FDA approval for DT in January 2010 Distributed throughout Asia and Australia HeartMate II—Widespread Approval And Adoption FDA approval for BTT April 2008 European CE Mark November 2005 FDA approval for DT January 2010
More than 6,000 patients, spanning over 6,000 patient years across 254 centers worldwide, have now been implanted with the HeartMate II LVAD* Patients supported 2 years: 700 Over 60 patients supported 4 or more years Longest support duration: 6 years Smallest patient: 1.1 BSA Largest patient: 3.2 BSA Age range: 11 – 87 HeartMate II—Most Widely Used, Proven Efficacious, and Durable in Broad Patient Population *As of January 13, 2011
HeartMate II has an unparalleled number of peer- reviewed published studies in highly regarded publications including NEJM and JACC. Data featuring HeartMate II has been published in more than 120* peer-reviewed articles including: 3 New England Journal of Medicine 6 Journal of American College of Cardiology 5 Circulation 35 Journal of Heart and Lung Transplantation 11 Annals of Thoracic Surgery 10 Journal of Thoracic Cardiovascular Surgery HeartMate II—Peer-Reviewed Publications *As of January 2011
Improvements With BTT Results Over Time Miller, Pagani, Russell, et al. NEJM. 357:885-96, Pagani, Miller, Russell, et al. JACC. 54:312-21, Starling, Naka, Boyle, et al. JACC, in press n = 133n = 281n = 169
HeartMate II—Contemporary BTT Outcomes The HeartMate II BTT post-approval study was initiated to assess outcomes in a broader patient care environment outside of a clinical setting, representing real life situations. HeartMate II Group First 169 consecutive HeartMate II patients enrolled in INTERMACS listed, or likely to be listed, for transplant 77 centers enrolled patients from April to August 2008, and were followed for at least 1 year post-implant Endpoints The primary endpoint was survival, and secondary endpoints included adverse events reported upon occurrence and functional status using the 6-minute walk test and EuroQoL scale—determined at baseline and 3, 6, and 12 months post-implant Kirklin JK, Naftel DC, Kormos RL, et al. Second INTERMACS annual report: more than 1,000 primary left ventricular assist device implants. J Heart Lung Transplant. 2010;29:1-10.
The majority of enrolled patients were noted to be INTERMACS 1 or 2. HeartMate II Post-Approval Study Patient Demographics
Operative 30-day survival was 96% and patients achieved 90% successful outcomes at 6 months and 85% at 1 year. HeartMate II Post-Approval Study Actuarial Survival Starling, Naka, Boyle, et al. JACC, in press 2010.
As demonstrated by the EuroQoL instrument, HeartMate II patients experienced early and sustained improvement in quality of life over the course of follow-up, with scores doubling at 12 months post-implant. HeartMate II Post-Approval Study Quality Of Life Starling, Naka, Boyle, et al. JACC, in press 2010.
HeartMate II Adverse Event Rates From The BTT Post- Approval Study Events per patient year. Pagani FD, Miller LW, Russell SD. Extended mechanical circulatory support with a continuous-flow rotary left ventricular assist device. J Am Coll Cardiol. 2009;54: Starling, Naka, Boyle, et al. JACC, in press The HeartMate II post- approval study demonstrated low adverse event rates for stroke and RV failure. Stroke and RV failure rates have improved from the HeartMate II pivotal clinical trial.
Destination Therapy Pivotal Trial Slaughter MS, Rogers JG, Milano CA, et al. Advanced heart failure treated with continuous-flow left ventricular assist device. N Engl J Med. 2009;361(23):
The pivotal HeartMate II Destination Therapy trial demonstrated significant improvements in outcomes compared to randomized patients with pulsatile LVADs 68% survival at 1 year 58% survival at 2 years Survival In The Destination Therapy Pivotal Trial Slaughter MS, Rogers JG, Milano CA, et al. Advanced heart failure treated with continuous- flow left ventricular assist device. N Engl J Med. 2009;361(23): Fang JC. Rise of the machines–left ventricular assist devices as permanent therapy for advanced heart failure. N Engl J Med. 2009;361(23):
Destination Therapy Trial CAP: Overview And Baseline Park SJ. AHA Scientific Sessions, November More than 500 additional DT patients have been enrolled under a continued access protocol (CAP). Mid-trial patients did not vary in baseline characteristics
Improvements In DT Survival Patients enrolled in the mid-trial experienced better survival. * P value adjusted for body surface area Park SJ. AHA Scientific Sessions, November 2010.
Hemorrhagic stroke > 50% reduction 0.03 events per patient year Device-related infections > 35% reduction 0.27 events per patient year Sepsis > 25% reduction 0.27 events per patient year DT CAP Trial Shows Significant Reductions In Adverse Events * p < 0.05 ** p < 0.01 * p < 0.05 ** p < 0.01
HeartMate II therapy stroke rates are similar to other commonly accepted cardiac surgical procedures such as CABG and valve procedures. Stroke Rates Similar To Other Cardiac Surgical Procedures McKhann GM, Grega MA, Borowicz LM, et al. Stroke and encephalopathy after cardiac surgery - an update. Stroke. 2006;37: Boyle AJ, Russell SD, Teuteberg JJ, et al. Low thromboembolism and pump thrombosis with the HeartMate II left ventricular assist device: analysis of outpatient anti-coagulation. J Heart Lung Transplant. 2009;28: Incidence of stroke by cardiac surgical procedure (data collected at Johns Hopkins from 2001 – 2004)
DT CAP Trial Functional Class Improvements Park SJ. AHA Scientific Sessions, November n = 266n = 191n = 158n = 125n = 67 All patients were Class IIIB or IV at baseline.
DT CAP Trial Quality Of Life Improvements m 343 m Park SJ. AHA Scientific Sessions, November 2010.
LVAD Survival Compared To OMM Therapy Park SJ. AHA Scientific Sessions, November 2010.
A range of referral criteria assessments and scoring systems can be utilized to define the right moment to screen a patient for a HeartMate II implant. 1 Appropriate timing for referral is when a patient presents in Class IIIB or IV heart failure and has more than one of the functional or laboratory risk factors. Improved Timing Of Patient Referral For Evaluation Functional Assessment Inability to walk one block without shortness of breath Intolerant or refractory to ACE inhibitor, angiotensin receptor blockers, or beta- blockers One heart failure-related hospital admission in the past 6 months 2 CRT nonresponder High diuretic dose (e.g., 120 mg/d Furosemide) Lab Assessment Serum sodium < 136 mmol/L BUN > 40 mg/dL or Serum Creatinine > 1.8 mg/dL Hemotocrit < 35% 1 Russell SD, Miller LW, Pagani FD. Advanced heart failure: a call to action. Congest Heart Fail. 2008;14: Teuteberg J, Lewis E, Nohria A, et al. Characteristics of patients who die with heart failure and low ejection fraction in the new millennium. J Card Fail. 2006;12(1):47-53.
In Summary HeartMate II: Compelling data from large clinical trials demonstrates efficacy Achieved very high survival rates BTT – 90% 6 months, 85% 1 year DT – 74% 1 year, 64% 2 years Superior to what is anticipated with optimal medical management Substantial and sustained quality of life improvements Acceptable adverse event profile
67 y/o referred for advanced heart failure therapy Ischemic cardiomyopathy EF < 20% with LVEDD = 7.3 cm Cath 1 month prior: 20% pLM, 100% pLAD, stent in pLCX, 50% stenosis pOM1, 60% pRCA with diffuse 50% stenosis throughout. Patent LIMA to LAD, patent SVG to PDA with 50% proximal stenosis Thallium: anterior infarct, no ischemia ICD Co-morbidities: HTN, DM, hyperlipidemia Case Study
Hospitalized once in past 6 months Progressive exertional dyspnea and fatigue (e.g., unable to climb 1 flight of stairs without dyspnea or unhappy with current level of functionality) Occasional nocturnal dyspnea No edema Appetite adequate and no weight change No ICD shocks Meds: ASA 81 mg daily, Clopidogrel 75 mg daily, Furosemide 40 mg daily, Lisinopril 10 mg daily, Metoprolol Tartrate 25 mg twice daily, Simvastatin 20 mg daily, Spironolactone 25 mg daily Case Study
Examination HR=92, BP=96/78 Clear lungs Depressed carotid upstrokes, JVP=12, RRR, No S3 or murmur Trace LE edema Labs: Sodium=134mmol/L, BUN=12 mg/dl, Cr=0.8 mg/dl, BNP=436pg/ml, Albumin=3.5 g/dl Case Study
Questions: Should this patient receive an ICD upgrade to BiV-ICD? Are there opportunities for revascularization? Are the medications optimized? Is this patient an appropriate VAD patient? Case Study