Antithrombotics 201: Aspirin and USPSTF. Presented by: Craig Williams, PharmD., BCPS., FNLA; November, Conflicts of Interest: None

Similar documents
Conflicts of Interest: None. Aspirin, primary prevention and USPSTF. Primary prevention of ASCVD is important

Anti-platelet therapies and dual inhibition in practice

Anticoagulation Management Around Endoscopy: GI Perspective. Nathan Landesman, DO FACOI Flint Gastroenterology Associates October 11, 2017

Antiplatelets and Anticoagulants. Helen Leung, PharmD PGY1 Pharmacy Resident Memorial Hermann-Texas Medical Center

Optimal medical therapy in patients with stable CAD

Disclosure Slide. Controversies in Anticoagulation. Presenter Disclosure Information. Challenges in Anticoagulation

Prostate Biopsy Alerts

3/23/2017. Angelika Cyganska, PharmD Austin T. Wilson, MS, PharmD Candidate Europace Oct;14(10): Epub 2012 Aug 24.

Angelika Cyganska, PharmD Austin T. Wilson, MS, PharmD Candidate 2017

Drug Class Review Newer Oral Anticoagulant Drugs

Post-procedure dose ok after hours. 12 hours (q 24h dosing only) assuming surgical hemostasis; second dose 24 hours after first dose.

9/29/2015. Primary Prevention of Heart Disease: Objectives. Objectives. What works? What doesn t?

Antiplatelet and Anti-Thrombotic Therapy. Ivan Anderson, MD RIHVH Cardiology

Asif Serajian DO FACC FSCAI

Antiplatelet Therapy in Primary CVD Prevention and Stable Coronary Artery Disease. Καρακώστας Γεώργιος Διευθυντής Καρδιολογικής Κλινικής, Γ.Ν.

SESSION 3 11 AM 12:30 PM

ISCHEMIC VASCULAR DISEASE (IVD) MEASURES GROUP OVERVIEW

Updates in Anticoagulation for Atrial Fibrillation and Venous Thromboembolism

SESSION 5 2:20 3:35 PM

5/2/2016. Outpatient Stroke Management Sheila Smith MD May 5, 2016

FACTOR Xa AND PAR-1 BLOCKER : ATLAS-2, APPRAISE-2 & TRACER TRIALS

Xarelto (rivaroxaban)

ACS: What happens after the acute phase? Frans Van de Werf, MD, PhD Leuven, Belgium

Indications of Anticoagulants; Which Agent to Use for Your Patient? Marc Carrier MD MSc FRCPC Thrombosis Program Ottawa Hospital Research Institute

Let s Gi e The So ethi g To Clot About: Controversies in Anticoagulation

7 th Munich Vascular Conference

Is there enough evidence for DAPT after endovascular intervention for PAOD?

THROMBOTIC DISORDERS: The Final Frontier

Pradaxa (dabigatran)

Which drug do you prefer for stable CAD? - P2Y12 inhibitor

Use of Aspirin for primary prevention of cardiovascular disease - USPSTF guideline changes

Eliquis and plavix combination therapy

Does COMPASS Change Practice?

Antithrombotics in Stroke management

Updates in Stroke Management. Jessica A Starr, PharmD, FCCP, BCPS Associate Clinical Professor Auburn University Harrison School of Pharmacy

Drug Class Monograph

DISCLOSURE. What I am Talking About. Rational Use of Antiplatelet Agents. Aspirin. Tom DeLoughery, MD MACP FAWM

Clinical and Economic Value of Rivaroxaban in Coronary Artery Disease

Joshua D. Lenchus, DO, RPh, FACP, SFHM Associate Professor of Medicine and Anesthesiology University of Miami Miller School of Medicine

Low Dose Rivaroxaban Versus Aspirin, in Addition to P2Y12 Inhibition, in Acute Coronary Syndromes (GEMINI-ACS-1)

OUTPATIENT ANTITHROMBOTIC MANAGEMENT POST NON-ST ELEVATION ACUTE CORONARY SYNDROME. TARGET AUDIENCE: All Canadian health care professionals.

Placebo-Controlled Statin Trials

New Antithrombotic and Antiplatelet Drugs in CAD : (Factor Xa inhibitors, Direct Thrombin inhibitors and Prasugrel)

David Stewart, PharmD, BCPS Assistant Professor of Pharmacy Practice East Tennessee State University Bill Gatton College of Pharmacy

Treatment Options and How They Work

Oral Anticoagulation Drug Class Prior Authorization Protocol

CONTRIBUTING FACTORS FOR STROKE:

No relevant financial relationships

Date: / / Hello, my name is [interviewer name], and I'm calling to speak with [participant name]. Is [participant name] available?

Session Objectives. Clopidogrel Resistance. Clopidogrel (Plavix )

Vascular Protection: Preventing Thrombotic Complications of VTE and PAD

Investor Conference Call

Disclosures. Theodore A. Bass MD, FSCAI. The following relationships exist related to this presentation. None

Cangrelor: Is it the new CHAMPION for PCI? Robert Barcelona, PharmD, BCPS Clinical Pharmacy Specialist, Cardiac Intensive Care Unit November 13, 2015

EAU GUIDELINES ON THROMBOPROPHYLAXIS IN UROLOGICAL SURGERY

2013 Hypertension Measure Group Patient Visit Form

Dr Julia Hopyan Stroke Neurologist Sunnybrook Health Sciences Centre

Treatment of Cardiovascular Risk Factors. Kevin M Hayes D.O. F.A.C.C. First Coast Heart and Vascular Center

325 mg aspirin and plavix

Disclosures No relationships (not even to an employer) No off-label uses. Cholesterol Lowering Guidelines: What now?

Timing of Surgery After Percutaneous Coronary Intervention

Disclosure. No relevant financial relationships. Placebo-Controlled Statin Trials

The INR: No Need Anymore? Daniel Blanchard, MD Professor of Medicine Director, Cardiology Fellowship Program UCSD Sulpizio Cardiovascular Center

Disclosures. Prevention of Heart Disease: The New Guidelines. Summary of Talk. Four guidelines. No relevant disclosures.

on Anti-coagulants -- Is It Safe? And When to Stop?

Durlaza. Durlaza (aspirin) Description

When and how to combine antiplatelet agents and anticoagulant?

INR as a Biomarker: Anticoagulation in Atrial Fib, Heart Failure, and Cardiovascular Disease Daniel Blanchard, MD, FACC, FAHA

New Antithrombotic Agents DISCLOSURE

Blood Day for Primary Care

Direct Oral Anticoagulants An Update

Antithrombotics in the elderly. Robert Gabor Kiss FESC FACC Budapest

Placebo-Controlled Statin Trials EXPLAINING THE DECREASE IN DEATHS FROM CHD! PREVENTION OF CARDIOVASCULAR DISEASE IN WOMEN EXPLAINING THE DECREASE IN

ANTITHROMBOTIC/ANTICOAGULANT DRUGS: TECHNOLOGIES AND GLOBAL MARKETS

PCI in Patients with AF Optimizing Oral Anticoagulation Regimen

Using DOACs in CAD Patients in Sinus Ryhthm Results of the ATLAS ACS 2, COMPASS and COMMANDER-HF Trials

Northwestern University Feinberg School of Medicine Calculating the CVD Risk Score: Which Tool for Which Patient?

Placebo-Controlled Statin Trials MANAGEMENT OF HIGH BLOOD CHOLESTEROL MANAGEMENT OF HIGH BLOOD CHOLESTEROL: IMPLICATIONS OF THE NEW GUIDELINES

Management of antithrombotic agents before endoscopy 삼성서울병원소화기내과임상강사이세옥

New Oral Anticoagulants

DEEP VEIN THROMBOSIS (DVT): TREATMENT

Use of Anticoagulants in Geriatrics: Current Evidence and Special Considerations

Platelet inhibition PLUS low-dose anticoagulation a new paradigm for all PAD patients?

Outpatient Treatment of Deep Vein Thrombosis with Low Molecular Weight Heparin (LMWH) Clinical Practice Guideline August 2015

Anticoagulants and antiplatelet therapy in the older patient: Choosing wisely

Update on the NOAC s: 2018 Daniel Blanchard, MD, FACC, FAHA

Afib, Stroke, and DOAC. Albert Luo, MD. Cardiology Lindsey Frischmann, DO. Neurology Xiao Cai, MD. HBS

Dawn Matherne Meyer PhD,RN,FNP-C. Assistant Professor University of California San Diego

Dual Antiplatelet Therapy Made Practical

Learning Objectives. Epidemiology of Acute Coronary Syndrome

Regulatory Hurdles for Drug Approvals

Holy Crap! Why is a Cardiologist Speaking at a GI Meeting? Jonathan A. Rapp, MD, FACC, FSCAI Cardiologist, Mercy Heart Institute Cincinnati, OH

Date: / / Hello, my name is [interviewer name], and I'm calling to speak with [participant name]. Is [participant name] available?

New Antithrombotic Agents

Paolo Gresele Dipartimento di Medicina Sezione di Medicina Interna e Cardiovascolare Università di Perugia

Peri-Procedural Management of Antithrombotic Agents

EvidenceNOW SW Learning Collaborative. Kyle Knierim, MD January 2017

Managing Perioperative Anticoagulation. Edie Shen MD

Nanik Hatsakorzian Pharm.D/MPH

Placebo-Controlled Statin Trials Prevention Of CVD in Women"

Transcription:

Antithrombotics 201: Aspirin and USPSTF Presented by: Craig Williams, PharmD., BCPS., FNLA; November, 2016 Conflicts of Interest: None 1

What percent of patients who die within 30 days of an MI die before reaching the hospital? 1. 10% Deaths within 30 days from MI* 2. 20% 3. 40% 4. 50% 5. 75% 8% 21% 19% 52% Prehospital 24-hours, in -hospital 48 hours, in-hospital 30 days *Guidelines 2006 for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. International Consensus on Science. Circulation 2006;102(8):I-172-203; Part 7: The Era of Repurfusion. Section 1: Acute Coronary Syndromes (AMI) A patient walks into your office and says they just turned 60 years of age and wants your opinion on whether or not to start taking a daily ASA. What would you like to recommend? 2

Some background on aspirin and primary prevention Antithrombotic therapy 1. Anti-platelet therapy 2. anticoagulation 3. thrombolytic Aspirin Clopidogrel (Plavix) Prasugrel (Effient) Ticagrelor (Brilinta) Cangrelor (Kengreal) Aggrenox (ASA+dipyrid.) Vorapaxar (Zontivity) Warfarin (oral) Heparin (IV) LMWH (IV or SQ) Dabigatran (Pradaxa) oral Rivaroxaban (Xarelto) Apixaban (Eliquis) Edoxaban (Savaysa) tpa rpa streptokinase Acute MI Acute stroke Massive PE Prevention of arterial (high pressure) events: MI, stroke Prevention of venous (low pressure) thromboembolism (VTE) DVT, PE, Afib stroke prevention 3

What is the role of the platelet in vasculature? NEJM 2007;357:2482-94 What is the role of the platelet in vasculature? NEJM 2007;357:2482-94 4

The initial platelet plug is important to facilitate endothelial repair and happens through a diverse array of both vascular and platelet receptors Circ 2009;120:2488 So, while still not fully understood, it does make pathophysiologic sense that antiplatelet therapy may benefit atherothrombosis long-term. 5

Key principle to decision making: greater risk=greater benefit The benefit of anti-platelet therapy is greater in higher risk patients and quite low in low risk patients Carlo Patrono, Barry Coller, Garret A. FitzGerald, Jack Hirsh, and Gerald Roth CHEST 2008;133: 1994S-233S. 5% ARR 2 Events prevented per 1000 treated in healthy population The debate in primary prevention: FDA 2014 6

The debate in primary prevention: FDA 2003 FDA committee votes not to approve aspirin for the primary prevention of MI Tue, 09 Dec 2003 21:00:00 Michael O'Riordan Gaithersburg, MD - The evidence supporting the use of aspirin for the primary prevention of MI failed to hold up to the scrutiny of the FDA's Cardiovascular and Renal Drugs Advisory Committee at its most recent December 8, 2003 meeting. The committee voted overwhelmingly 11 votes against and three votes for approval of the petition sought by Bayer Corp to approve aspirin for the reduction of the risk of a first MI in moderate-risk patients, those with a 10-year coronary heart disease risk of < 20% (annual risk ~ 2%) Despite the existing data, which consisted of five major clinical trials, the committee felt the evidence supporting the extended label for aspirin was inconsistent at best or lacking at worst. www.theheart.org Why does the FDA say no : Vascular benefit about offset by major bleeding risk NEJM 2005;353:2373-83 7

So, any use of aspirin for primary prevention is off-label 8

CHEST guidelines. 2012 ADA, 2016 9

19 Pre-existing 2007/2009 USPSTF Aspirin Recommendations The USPSTF recommends the use of aspirin for men age 45 to 79 years when the potential benefit due to a reduction in myocardial infarctions outweighs the potential harm due to an increase in gastrointestinal hemorrhage. (A Recommendation) The USPSTF recommends the use of aspirin for women age 55 to 79 years when the potential benefit of a reduction in ischemic strokes outweighs the potential harm of an increase in gastrointestinal hemorrhage. (A Recommendation) The USPSTF concludes that the current evidence is insufficient to assess the balance of benefits and harms of aspirin for cardiovascular disease prevention in men and women 80 years or older. (I Statement) The USPSTF recommends against the use of aspirin for stroke prevention in women younger than 55 years and for myocardial infarction prevention in men younger than 45 years. (D recommendation) The USPSTF recommends against the routine use of aspirin and nonsteroidal antiinflammatory drugs (NSAIDS) to prevent colorectal cancer in individuals at average risk for colorectal cancer. (D recommendation) 2007 A patient walks into your office and says they just turned 60 years of age and wants your opinion on whether or not to start taking a daily ASA. What would you like to recommend? Answer in 2009: Let s check your CVD risk 10

ATP III: Framingham Point Scores Estimate of 10-Year Risk Age, y Points 20-34 -9 35-39 -4 40-44 0 45-49 3 50-54 6 55-59 8 60-64 10 65-69 11 70-74 12 75-79 13 Systolic BP mm Hg If Untreated If Treated <120 0 0 120-129 0 1 130-139 1 2 140-159 1 2 160 2 3 HDL mg/dl Points 60-1 50-59 0 40-49 1 <40 2 Total Cholesterol Age 20-39 Age 40-49 Age 50-59 Age 60-69 Age 70-79 <160 0 0 0 0 0 160-199 4 3 2 1 0 200-239 7 5 3 1 0 240-279 9 6 4 2 1 280 11 8 5 3 1 Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults. JAMA. 2001;285:2486-2497. Age 20-39 40-49 50-59 60-69 70-79 Nonsmoker 0 0 0 0 0 Smoker 8 5 3 1 1 Point Total 10-Year Risk, % <0 <1 0 1 1 1 2 1 3 1 4 1 5 2 6 2 7 3 8 4 9 5 10 6 11 8 12 10 13 12 14 16 15 20 16 25 17 30 For men: Clinical decision-making with aspirin, 2009: Benefits exceed risks when below the shaded section USPSTF, Annals Int Med 2009;150:396-404 11

For women: Clinical decision-making with aspirin, 2009: Benefits exceed risks when below the shaded section USPSTF, Annals Int Med 2009;150:396-404 So a man or woman needed a Framingham risk score ~ 8-10% for benefits to outweigh risks. Generally, with no major risk factors the 10% threshold was about age 60 for a man and 70 for a woman. But, with significant risk factors, therapy was recommended as young as 45 in men and 55 in women and stopped at age 80 12

Many patients are deciding to take aspirin Guidance was clearly needed and the 2009 guidelines were difficult to operationalize 13

N Engl J Med; March 6, 2003..at least 1 year N Engl J Med; March 6, 2003 14

Lancet, Nov 20, 2010 Average duration of ASA use of 6.0 years Draft RS: For Adults 50-59 years old at increased risk of CVD 30 The USPSTF recommends low-dose aspirin use for the primary prevention of cardiovascular disease (CVD) and colorectal cancer in adults ages 50 to 59 years who have a 10% or greater 10-year CVD risk, are not at increased risk for bleeding, have a life expectancy of at least 10 years, and are willing to take low-dose aspirin daily for at least 10 years. Grade B recommendation 15

Draft RS: For Adults 60-69 years old at increased risk of CVD The decision to use low-dose aspirin to prevent CVD and colorectal cancer in adults ages 60 to 69 years who have a greater than 10% 10-year CVD risk should be an individual one. Persons who are not at increased risk for bleeding, have a life expectancy of at least 10 years, and are willing to take low-dose aspirin daily for at least 10 years are more likely to benefit. Persons who place a higher value on the potential benefits than the potential harms may choose to use low-dose aspirin. 31 Grade C recommendation 32 Draft I Statements The USPSTF concludes that current evidence is insufficient to assess the balance of benefits and harms of aspirin use in adults less than 50 years old. I Statement The USPSTF concludes that current evidence is insufficient to assess the balance of benefits and harms of aspirin use in adults age 70 years and older. I Statement 16

Differences between current recommendation and the draft recommendation Existing RS Age range Men: 45 79 Women: 55 79 Sex Sex specific recommendations CHD/CVD risk Men: 10 year CHD risk 45 59: > 4% 60 69: > 9 % 70 79: > 12% Women: 10 year stroke risk 55 59: >3 % 60 69: >8 % 70 79: >11 % Younger populations D rec: Men < 45, Women < 55 New Draft RS 50 69 No differentiation 10% or greater 10 year CVD risk for 50 69 y/o CHD Framingham Stroke Western Stroke CVD ACC/AHA I rec: Persons < 50 Older populations I rec: Persons > 80 I rec: Persons > 70 CRC Against use of ASA/NSAIDs Integrated into benefit 33 34 Balancing benefits and harms Lifetime Events per 1,000 persons in Women Taking Aspirin CVD Risk MIs Prevented Ischemic Strokes Prevented CRC Cases Prevented Serious GI Bleeding Caused Hemorrhagic Strokes Caused Net Life Years Gained Quality Adjusted Life Years Gained Ages 50 to 59 years 10% 14.8 13.7 13.9 20.9 3.5 21.9 62.1 15% 15.0 14.3 13.5 20.0 3.4 33.4 71.6 20% 15.2 14.4 13.2 18.4 2.9 46.3 83.3 Ages 60 to 69 years 10% 10.1 11.6 10.5 23.0 3.2 1.2 28.4 15% 11.0 12.9 9.3 21.6 3.4 1.7 32.4 20% 11.1 13.0 9.7 21.7 3.3 4.8 36.0 17

35 Balancing benefits and harms Lifetime Events per 1,000 persons in Men Taking Aspirin CVD Risk MIs Prevented Ischemic Strokes Prevented CRC Cases Prevented Serious GI Bleeding Caused Hemorrhagic Strokes Caused Net Life Years Gained Quality Adjusted Life Years Gained Ages 50 to 59 years 10% 22.5 8.4 13.9 28.4 2.3 33.3 58.8 15% 26.7 8.6 12.1 26.0 2.8 39.5 64.4 20% 28.6 9.2 12.2 24.8 2.1 60.5 83.4 Ages 60 to 69 years 10% 15.9 6.6 11.2 31.4 3.1 2.0 18.0 15% 18.6 8.0 10.4 29.8 2.4 9.6 30.9 20% 20.1 8.4 9.1 26.7 2.7 11.6 31.8 36 Guidance on Implementation The decision to start or continue taking aspirin is complex Key considerations: Age related to both benefits and harms, life expectancy needed to gain CRC benefit Baseline CVD risk higher CVD risk increases benefits, aided by using ACC/AHA risk calculator (despite its shortcomings) Risk for bleeding bleeding risk assessment based on patient history Preference for taking daily aspirin very preference sensitive choice 18

Conclusions: USPSTF 2016 A patient walks into your office and says they just turned 60 years of age and wants your opinion on whether or not to start taking a daily ASA. What would you like to recommend? If you have never had a GI bleeding event, let s calculate your 10-year ASCVD risk and: 1.If your 10-year risk of a vascular event is low, then you should not take aspirin 2.If your 10-year risk of a vascular event is > 10% then it is reasonable to take aspirin if you value the CVD benefit over the risk of a major bleed. Conclusions: Other general approaches A patient walks into your office and says they just turned 60 years of age and wants your opinion on whether or not to start taking a daily ASA. What would you like to recommend? 1.The FDA has evaluated the data and declined to give an indication for primary prevention so I m generally going to recommend against 2. Once most American men reach age 50 and women reach age 60, risk is high enough to consider aspirin and they should understand that bleeding risk about equals vascular benefit and that there is a small colon cancer benefit that begins after ~ 5 years 19

Questions Cumulative event rate* (%) 20 16 12 8 4 Aspirin and thienopyridines are equal: Clopidogrel versus aspirin Patients with history of ischemic stroke or MI, or symptomatic PAD n=19,185 followed for 1.9 years ASA Clopidogrel 8.7% RRR (p=0.043) 0.5% ARR* 0 0 3 6 9 12 15 18 21 24 27 30 33 36 Months of follow-up CAPRIE Steering Committee. Lancet 1996; 348: 1329 1339. *events: stroke, MI or vascular death 20