Relationship of background ACEI dose to benefits of candesartan in the CHARM-Added trial.

Slides:



Advertisements
Similar presentations
Cardiac Insufficiency Bisoprolol Study (CIBIS III) Trial
Advertisements

ONgoing Telmisartan Alone and in combination with Ramipril Global Endpoint Trial The telmisartan trial in cardiovascular protection Sponsored by Boehringer.
The Importance of Beta-Blockers in Patients with Heart Failure: A Resynchronization-Defibrillation for Ambulatory Heart Failure Trial (RAFT) Analysis.
EFFECT OF THE DIRECT RENIN INHIBITOR ALISKIREN ON LEFT VENTRICULAR REMODELING FOLLOWING MYOCARDIAL INFARCTION WITH LEFT VENTRICULAR DYSFUNCTION Scott D.
Effects of selective heart rate reduction with ivabradine on left ventricular remodelling and function: results from the SHIFT echocardiography substudy.
McMurray JJV, Young JB, Dunlap ME, Granger CB, Hainer J, Michelson EL et al on behalf of the CHARM investigators Relationship of dose of background angiotensin-converting.
CM-1 ACE Inhibitor Dosing Considerations in CHARM John J.V. McMurray, MD Professor of Medical Cardiology Western Infirmary Glasgow Scotland UK.
Effects of losartan compared with captopril on mortality in patients with symptomatic heart failure: randomized trial -- the Losartan Heart Failure Survival.
CONSENSUS: Cooperative North Scandinavian Enalapril Survival Study Purpose To determine whether the ACE inhibitor enalapril reduces mortality in patients.
CHARM Program: 3 Component trials comparing candesartan with placebo.
חזק בהגנה לבבית Valsartan in Heart Failure
Efficacy and safety of angiotensin receptor blockers: a meta-analysis of randomized trials Elgendy IY et al. Am J Hypertens. 2014; doi:10,1093/ajh/hpu209.
The ONTARGET Trial Reference The ONTARGET investigators. Telmisartan, ramipril, or both in patients at high risk for vascular events. N Engl J Med. 2008;358:15.
analysis from the SHIFT study
HEART FAILURE MANAGEMENT -RAAS BLOCKERS FAZIL BISHARA SR- CARDIOLOGY
Sudden Cardiac Death in Heart Failure Trial Presented at American College of Cardiology Scientific Sessions 2004 Presented by Dr. Gust H. Bardy SCD-HeFTSCD-HeFT.
May 23rd, 2012 Hot topics from the Heart Failure Congress in Belgrade.
COURAGE: Clinical Outcomes Utilizing Revascularization and Aggressive Drug Evaluation Purpose To compare the efficacy of optimal medical therapy (OMT)
ATLAS Clinical Trial Commentary Dr Eric Topol Chairman and Professor, Department of Cardiology Director of the Joseph J Jacobs Center for Thrombosis and.
CHARM-Alternative: Candesartan in Heart failure: Assessment of Reduction in Mortality and morbidity - Alternative Purpose To determine whether the angiotensin.
CHARM-Preserved: Candesartan in Heart failure: Assessment of Reduction in Mortality and morbidity - Preserved Purpose To determine whether the angiotensin.
Massie I-PRESERVE Trial Irbesartan in heart failure with preserved EF Co-PIs: Barry Massie and Peter Carson Executive Committee M. Komajda, R. McKelvie,
Effects on outcomes of heart rate reduction by ivabradine in patients with congestive heart failure: is there an influence of beta-blocker dose? Systolic.
BEAUTI f UL: morBidity-mortality EvAlUaTion of the I f inhibitor ivabradine in patients with coronary disease and left ventricULar dysfunction Purpose.
Randomized, double-blind, multicenter, controlled trial.
CB-1 Background James B. Young, MD Chair, Division of Medicine Cleveland Clinic Foundation.
0902CZR01NL537SS0901 RENAAL Altering the Course of Renal Disease in Hypertensive Patients with Type 2 Diabetes and Nephropathy with the A II Antagonist.
PPAR  activation Clinical evidence. Evolution of clinical evidence supporting PPAR  activation and beyond Surrogate outcomes studies Large.
Update on Valsartan Špinar J.. System renin-angiotensin-aldosteron angiotensinogen angiotensin I angiotensin II aldosteron ANP,BNP thirst resorp. Na +
On behalf of the CHARM Programme Investigators and Committees Candesartan in Heart failure Assessment of Reduction in Mortality and morbidity CHARM.
S ystolic H eart failure treatment with the I f inhibitor ivabradine T rial Main results Swedberg K, et al. Lancet. 2010;376(9744):
Entresto® (sacubitril & valsartan)
RALES: Randomized Aldactone Evaluation Study Purpose To determine whether the aldosterone antagonist spironolactone reduces mortality in patients with.
Aim To determine the effects of a Coversyl- based blood pressure lowering regimen on the risk of recurrent stroke among patients with a history of stroke.
AIRE: Acute Infarction Ramipril Efficacy study Purpose To determine whether the ACE inhibitor ramipril reduces mortality in patients with evidence of heart.
BEST: Beta-blocker Evaluation Survival Trial Purpose To determine whether the β-blocker bucindolol reduces morbidity and mortality in patients with advanced.
SPARCL Stroke Prevention by Aggressive Reduction in Cholesterol Levels trial.
VBWG PROactive: Study design Dormandy JA et al. Lancet. 2005;366: Charbonnel B et al. Diabetes Care. 2004;27: Objective: Assess the effects.
Heart failure: The national burden AHA. Heart disease and stroke statistics–2005 update. Koelling TM et al. Am Heart J. 2004;147:74-8. VBWG Affects 1 million.
Evidence-Based Medicine ACE-Inhibitor and ARB; combination therapy
Review of an article Not all Angiotension-Converting Enzyme (ACE) inhibitors are Equal: Focus on Ramipril and Perindopril DiNicolantonio J, Lavie C, O’Keefe.
The Studies of Oral Enoximone Therapy in Advanced Heart Failure ESSENTIALESSENTIAL Presented at The European Society of Cardiology Congress 2005 Presented.
Influence of background treatment with mineralocorticoid receptor antagonists on ivabradine's effects in patients with chronic heart failure Systolic Heart.
COMET: Carvedilol Or Metoprolol European Trial Purpose To compare the effects of carvedilol (a β 1 -, β 2 - and α 1 -receptor blocker) and short-acting.
Heart rate in heart failure: Heart rate in heart failure: risk marker or risk factor? A subanalysis of the SHIFT trial on behalf of the Investigators M.
ELITE - II Study Design  60 yrs; NYHA II - IV; EF  40 % ACEI naive or  7 days in 3 months prior to entry Standard Rx ( ± Dig / Diuretics ), ß - blocker.
VBWG Growth in heart disease, 2000–2050 Deaths Population Foot DK et al. J Am Coll Cardiol. 2000;35:
OVERTURE FDA Cardiovascular and Renal Drugs Advisory Committee Meeting July 19, 2002 Milton Packer, M.D., FACC Columbia University College of Physicians.
VBWG OASIS-6 The Sixth Organization to Assess Strategies in Acute Ischemic Syndromes trial.
Candesartan in Heart Failure Presented at European Society of Cardiology 2003 CHARM Trial.
Interim Chair, Medicine Brigham and Women’s Hospital Boston, MA
Ischemia Management with Accupril Post Bypass Graft via Inhibition of Angiotensin Converting Enzyme IMAGINEIMAGINE Presented at The European Society of.
SS-1 Candesartan Support Slides. SS-2 Baseline Beta-Blocker Charm Added β-blocker Of patients on β-blockers Mean daily dose of β-blocker CandesartanPlacebo.
European trial on reduction of cardiac events with perindopril in stable coronary artery disease Presented at European Society of Cardiology 2003 EUROPA.
COPERNICUS: Carvedilol Prospective Randomized Cumulative Survival trial Purpose To assess the effect of carvedilol, a β 1 -, β 2 - and α 1 -receptor blocker,
Ten Year Outcome of Coronary Artery Bypass Graft Surgery Versus Medical Therapy in Patients with Ischemic Cardiomyopathy Results of the Surgical Treatment.
Aliskiren and Valsartan for Antihypertensive Therapy Trial
Beyond Current Strategies: Focus on Angiotensin Receptors
CLINICAL DILEMMAS IN HEART FAILURE:
EMPHASIS-HF Extended Follow-up
RAAS Blockade: Focus on ACEI
Avoiding Cardiovascular events through COMbination therapy in Patients LIving with Systolic Hypertension (ACCOMPLISH): Design Randomized, double-blind.
The following slides highlight a report on presentations at a Hotline Session and a Satellite Symposium of the European Society of Cardiology 2003 Congress.
AARDVARK Trial design: Patients with small abdominal aortic aneuryms (AAAs) were randomized in a 1:1:1 fashion to either perindopril 10 mg once daily,
Section III: Neurohormonal strategies in heart failure
PARADIGM-HF Trial design: Participants with NYHA class II-IV and LVEF ≤40% were randomized to LCZ mg twice daily (n = 4,187) vs. enalapril 10 mg.
VALUE Trial design: Hypertensive patients at high cardiovascular risk were randomized to valsartan (n = 7,649) vs. amlodipine (n = 7,596). Results (p =
CIBIS II: Cardiac Insufficiency Bisoprolol Study II
These slides highlight a report from a Hotline Session and a Satellite symposium held at the European Society of Cardiology Congress, 2003 in Vienna Austria,
Treatment Algorithm for Guideline-Directed Medical Therapy Including Novel Therapies (2,9) Green diamonds indicate Class I guideline recommendations, while.
Presentation transcript:

Relationship of background ACEI dose to benefits of candesartan in the CHARM-Added trial

CHARM-Added: Study design McMurray JJV et al. Lancet. 2003;362: Candesartan in Heart failure: Assessment of Reduction in Mortality and morbidity (CHARM)-Added Randomized, double-blind NYHA class II–IV, LVEF ≤40%, stable ACEI dose for ≥30 days N = 2548 Candesartan 32 mg qd n = 1276 Placebo n = 1272 Median follow-up: 41 months Primary outcome: CV death or hospitalization for HF ACEI = angiotensin-converting enzyme inhibitor

CHARM-Added: Baseline characteristics by ACEI dose <FDA maximum dose (n = 2019) ≥FDA maximum dose (n = 529) Male (%) Mean BP (mm Hg) NYHA class (%) II III IV Medical history (%) HF hospitalization MI Angina Hypertension Diabetes / / McMurray JJV et al. Am Heart J. 2006;151:

CHARM-Added: Daily ACEI dose McMurray JJV et al. Am Heart J. 2006;151: *Based on European Society of Cardiology guidelines † Not indicated for heart failure ACEI (86% of patients) Mean dose (mg/day) % on Rx Mean dose (mg/day) Patients (%) Mean dose (mg/day) Patients (%) Enalapril Lisinopril Captopril Ramipril Trandolapril Perindopril † Subgroup analysis, most commonly used ACEIs ≥Recommended (CHARM prespecified)* (n = 1291) ≥Maximum (FDA) (n = 529) All patients (N = 2548)

CHARM-Added: Primary outcome of CV death or HF hospitalization N = 2548 McMurray JJV et al. Am Heart J. 2006;151: Recommended dose of ACEI CHARM prespecified Maximum dose of ACEI FDA 2005 CHARM-Added CHARM-Alternative Pooled results (low LVEF patients) No Yes No Yes Patients (n) Candesartan better Placebo better P value for interaction Hazard ratio (95% Cl)

CHARM-Added: Primary outcome in patients taking a  -blocker McMurray JJV et al. Am Heart J. 2006;151: n = 1413 CV death or HF hospitalization Recommended dose of ACEI CHARM prespecified Maximum dose of ACEI FDA 2005 All patients No Yes No Yes Patients (n) Candesartan better Placebo better P value for interaction Hazard ratio (95% Cl)

Summary: CHARM-Added Candesartan reduced CV death or HF hospitalization in patients taking no ACEI, a moderate ACEI dose, or a high ACEI dose Benefits of candesartan in HF patients were not modified by either ACEI dose or concomitant therapy with a  -blocker ACEIs and angiotensin receptor blockers (ARBs) have distinct and complementary mechanisms of action Combined use of an ACEI and the ARB, candesartan, improved outcomes in patients with HF vs ACE inhibition alone McMurray JJV et al. Am Heart J. 2006;151: