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CME / ABIM MOC / CE

New Guidelines to Prevent SCD: What You Need to Know

  • Authors: Sunil V. Rao, MD; Anne B. Curtis, MD; Gregg Fonarow, MD
  • CME / ABIM MOC / CE Released: 1/25/2018
  • THIS ACTIVITY HAS EXPIRED FOR CREDIT
  • Valid for credit through: 1/25/2019, 11:59 PM EST
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Target Audience and Goal Statement

This activity is intended for cardiologists, emergency medicine physicians, critical care specialists, nurses, and all clinicians interested in preventing sudden cardiac death (SCD).

The goal of this activity is improved risk stratification and better intervention for those patients at high risk for SCD.

Upon completion of this activity, participants will have:

  • Increased knowledge regarding the
    • Latest guidelines on the management of ventricular arrhythmias and prevention of SCD
    • Risk stratification of patients to identify those patients at high risk for SCD
  • Increased competence regarding
    • Effective team-based strategies to implement the latest guidelines into clinical care and optimize SCD prevention for patients at risk


Disclosures

As an organization accredited by the ACCME, Medscape, LLC, requires everyone who is in a position to control the content of an education activity to disclose all relevant financial relationships with any commercial interest. The ACCME defines "relevant financial relationships" as financial relationships in any amount, occurring within the past 12 months, including financial relationships of a spouse or life partner, that could create a conflict of interest.

Medscape, LLC, encourages Authors to identify investigational products or off-label uses of products regulated by the US Food and Drug Administration, at first mention and where appropriate in the content.


Moderator

  • Sunil V. Rao, MD

    Professor of Medicine, Duke University Medical Center; Section Chief, Cardiology, Durham VA Medical Center, Durham North Carolina

    Disclosures

    Disclosure: Sunil V. Rao, MD, has disclosed the following relevant financial relationships:
    Served as an advisor or consultant for: Cardiovascular Systems Inc; Corindus, Inc.; Medtronic, Inc.; Philips Holding USA Inc.; Volcano Corporation

    Dr Rao does not intend to discuss off-label uses of drugs, mechanical devices, biologics, or diagnostics approved by the FDA for use in the United States.

    Dr Rao does not intend to discuss investigational drugs, mechanical devices, biologics, or diagnostics not approved by the FDA for use in the United States.

Panelists

  • Anne B. Curtis, MD, MACP

    SUNY Distinguished Professor; Charles and Mary Bauer Professor and Chair, Department of Medicine, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo; President and CEO, UBMD Internal Medicine, Buffalo, New York

    Disclosures

    Disclosure: Anne B. Curtis, MD, MACP, has disclosed the following relevant financial relationships:
    Served as an advisor or consultant for: Abbott Laboratories; Novartis Pharmaceuticals Corporation; sanofi-aventis
    Served as a speaker or a member of a speakers bureau for: Abbott Laboratories; Medtronic, Inc.

    Dr Curtis does not intend to discuss off-label uses of drugs, mechanical devices, biologics, or diagnostics approved by the FDA for use in the United States.

    Dr Curtis does not intend to discuss investigational drugs, mechanical devices, biologics, or diagnostics not approved by the FDA for use in the United States.

  • Gregg Fonarow, MD

    Eliot Corday Professor of Cardiovascular Medicine; Director, Ahmanson-UCLA Cardiomyopathy Center; Co-Chief, UCLA Division of Cardiology, University of California Los Angeles

    Disclosures

    Disclosure: Gregg Fonarow, MD, has disclosed the following relevant financial relationships:
    Served as an advisor or consultant for: Amgen Inc.; Bayer HealthCare; Janssen Pharmaceuticals; Medtronic, Inc.; Novartis Pharmaceuticals Corporation; St. Jude Medical; ZS Pharma
    Served as a speaker or a member of a speakers bureau for: Novartis Pharmaceuticals Corporation

    Dr Fonarow does not intend to discuss off-label uses of drugs, mechanical devices, biologics, or diagnostics approved by the FDA for use in the United States.

    Dr Fonarow does not intend to discuss investigational drugs, mechanical devices, biologics, or diagnostics not approved by the FDA for use in the United States.

Editor

  • Joy P. Marko, MS, APN-C, CCMEP

    Scientific Director, Medscape, LLC

    Disclosures

    Disclosure: Joy P. Marko, MS, APN-C, CCMEP, has disclosed no relevant financial relationships.

CME Reviewer / Nurse Planner

  • Amy Bernard, MS, BSN, RN-BC

    Lead Nurse Planner, Medscape, LLC

    Disclosures

    Disclosure: Amy Bernard, MS, BSN, RN-BC, has disclosed no relevant financial relationships.


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  • Medscape, LLC designates this enduring material for a maximum of 0.25 AMA PRA Category 1 Credit(s)™ . Physicians should claim only the credit commensurate with the extent of their participation in the activity.

    Medscape, LLC staff have disclosed that they have no relevant financial relationships.

    Successful completion of this CME activity, which includes participation in the evaluation component, enables the participant to earn up to 0.25 MOC points in the American Board of Internal Medicine's (ABIM) Maintenance of Certification (MOC) program. Participants will earn MOC points equivalent to the amount of CME credits claimed for the activity. It is the CME activity provider's responsibility to submit participant completion information to ACCME for the purpose of granting ABIM MOC credit. Aggregate participant data will be shared with commercial supporters of this activity.

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    For Nurses

  • Awarded 0.25 contact hour(s) of continuing nursing education for RNs and APNs; 0.25 contact hours are in the area of pharmacology.

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This activity is designed to be completed within the time designated on the title page; physicians should claim only those credits that reflect the time actually spent in the activity. To successfully earn credit, participants must complete the activity online during the valid credit period that is noted on the title page. To receive AMA PRA Category 1 Credit™, you must receive a minimum score of 70% on the post-test.

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CME / ABIM MOC / CE

New Guidelines to Prevent SCD: What You Need to Know

Authors: Sunil V. Rao, MD; Anne B. Curtis, MD; Gregg Fonarow, MDFaculty and Disclosures
THIS ACTIVITY HAS EXPIRED FOR CREDIT

CME / ABIM MOC / CE Released: 1/25/2018

Valid for credit through: 1/25/2019, 11:59 PM EST

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  • New Guidelines to Prevent SCD: What You Need to Know

  • Slide 1.

    Slide 1.

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  • Key Updates From the New Guidelines[1]

    • The guidelines took a very comprehensive look at every aspect of evaluating patients for the risk of sudden cardiac death (SCD)
    • Patients with heart failure (HF), with a reduced ejection fraction (EF), should be taking guideline-directed medical therapy (GDMT)

  • Slide 5.

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  • Inadequate Vascular Access or at High Risk for Infection[1]

  • Slide 9.

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  • First-Degree Relatives With SCD[1]

    • In patients with refractory HF or with refractory sustained VA or who are nearing the end of life as a result of other illness, clinicians should discuss implantable cardioverter-defibrillator (ICD) shock deactivation (class I)

  • Slide 10.

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  • Shared Decision-Making

    • Discuss options with patients:
      • When considering implantation of a new ICD
      • When thinking about a generator change for an existing ICD
      • To ensure patients understand their risks and physicians understands patients' personal goals and values

  • Slide 11.

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  • Risk Stratification and EF[1]

    • Ejection fraction (EF) has been one of the most important criteria for identifying patients at risk used in the clinical trials
    • In studies in which patients' EFs were good, there often was no defined benefit in the use of ICDs for primary prevention
    • There can be some variability depending on the technique and interpretation
    • When a patient's EF is between 34% and 38% and the cutoff in the guidelines is 35%, clinical judgment must come into play
    • Take into account other potential ways of risk-stratifying that patient
    • Assess using an alternative mechanism such as cardiac magnetic resonance imaging (MRI) or nuclear scanning

  • Slide 13.

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  • SCD Is the First Recognized Clinical Event: Vast Majority of Patients[1]

  • Slide 14.

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  • Determining Risk for Ischemic vs Nonischemic Patients[1]

    • Some patients have hibernating myocardium, which may improve, but it is rare to come out of the range of needing an ICD
    • Revascularization is considered in conjunction with other therapies

  • Slide 15.

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  • 2017 AHA/ACC/HRS Guidelines: Risk for Ventricular Arrhythmias[1]

    • Recommendations regarding whether elective physiologic studies should be done are made regardless of whether it is an ischemic or nonischemic etiology
    • There is a new 2A class recommendation that cardiac MRI with late gadolinium enhancement may be useful for assessing the risk of SCD in patients with nonischemic cardiomyopathy

  • Slide 16.

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  • Primary Prevention of SCD in Patients With NICM[1]

    • There are specific guideline recommendations on when to consider a primary prevention ICD
    • Wait at least 40 days post-MI in an ischemic patient who has had an acute coronary event
    • Wait at least 90 days postrevascularization in patients when considering a primary prevention device in ischemic patients
    • In nonischemic patients, wait for the GDMT to kick in and reassess ventricular function

  • Slide 17.

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  • Primary Prevention of SCD in Patients With Ischemic Heart Disease[1]

  • Slide 18.

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  • WCD: Class IIb Recommendation [2]

    • Patients who have just been revascularized and have that 90-day waiting period, and are being discharged from the hospital, would benefit from use of the WCD

  • Slide 20.

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  • Well-Coordinated Multidisciplinary Teams

  • Slide 21.

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  • This content has been condensed for improved clarity.

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