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CME

Optimizing SCD Prevention: What Do the Guidelines Suggest

  • Authors: Greg C. Fonarow, MD; Barry H. Greenberg, MD
  • CME Released: 11/1/2016
  • THIS ACTIVITY HAS EXPIRED FOR CREDIT
  • Valid for credit through: 11/1/2017, 11:59 PM EST
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Target Audience and Goal Statement

This activity is intended for cardiologists, primary care physicians, critical care specialists, emergency medicine physicians, and all clinicians interested in preventing SCD in at-risk patients.

The goal of this activity is to improve the management of patients at high risk for sudden cardiac arrest (SCA)/sudden cardiac death (SCD) by educating clinicians about SCA/SCD guidelines risk assessment tools and prevention measures.

Upon completion of this activity, participants will:

  1. Have greater competence related to the use of current guidelines for prevention of SCD/SCA in patients who have experienced an MI
  2. Have increased knowledge regarding the role of the care team in integrating new recommendations into clinical practice


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(s)

  • Gregg C. Fonarow, MD

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

    Disclosures

    Disclosure: Gregg Fonarow, MD, has disclosed the following relevant financial relationships:
    Served as an advisor or consultant for: Amgen Inc.; Medtronic, Inc.; Novartis Pharmaceuticals Corporation; St. Jude Medical; ZS Pharma

    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.

Panelist(s)

  • Barry H. Greenberg, MD

    Distinguished Professor of Medicine; Director, Advanced Heart Failure Treatment Program, University of California San Diego, La Jolla, California

    Disclosures

    Disclosure: Barry Greenberg, MD, has disclosed the following relevant financial relationships:
    Served as an advisor or consultant for: Johnson & Johnson Pharmaceutical Research & Development, L.L.C.; Mast Biosurgery; Novartis Pharmaceuticals Corporation; Stealth BioTherapeutics Inc.; Teva Pharmaceuticals USA; Zensun USA Inc.
    Served as a speaker or a member of a speakers bureau for: Novartis Pharmaceuticals Corporation; Otsuka Pharmaceutical Co., Ltd.; Relypsa, Inc.

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

Editor(s)

  • 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(s)

  • Robert Morris, PharmD

    Associate CME Clinical Director, Medscape, LLC

    Disclosures

    Disclosure: Robert Morris, PharmD, has disclosed no relevant financial relationships.


Accreditation Statements


Medscape, LLC is accredited by the American Nurses Credentialing Center (ANCC), the Accreditation Council for Pharmacy Education (ACPE), and the Accreditation Council for Continuing Medical Education (ACCME), to provide continuing education for the healthcare team.

    For Physicians

  • 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.

    Contact This Provider

For questions regarding the content of this activity, contact the accredited provider for this CME/CE activity noted above. For technical assistance, contact [email protected]


Instructions for Participation and Credit

There are no fees for participating in or receiving credit for this online educational activity. For information on applicability and acceptance of continuing education credit for this activity, please consult your professional licensing board.

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.

Follow these steps to earn CME/CE credit*:

  1. Read the target audience, learning objectives, and author disclosures.
  2. Study the educational content online or printed out.
  3. Online, choose the best answer to each test question. To receive a certificate, you must receive a passing score as designated at the top of the test. We encourage you to complete the Activity Evaluation to provide feedback for future programming.

You may now view or print the certificate from your CME/CE Tracker. You may print the certificate but you cannot alter it. Credits will be tallied in your CME/CE Tracker and archived for 6 years; at any point within this time period you can print out the tally as well as the certificates from the CME/CE Tracker.

*The credit that you receive is based on your user profile.

CME

Optimizing SCD Prevention: What Do the Guidelines Suggest

Authors: Greg C. Fonarow, MD; Barry H. Greenberg, MDFaculty and Disclosures
THIS ACTIVITY HAS EXPIRED FOR CREDIT

CME Released: 11/1/2016

Valid for credit through: 11/1/2017, 11:59 PM EST

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  • Optimizing SCD Prevention: What Do the Guidelines Suggest?

  • Slide 1.

    Slide 1.

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  • Risk Is Time-Dependent[4]

    • In the VALIANT trial, the risk of sudden cardiac arrest after myocardial infarction (MI) was examined as a function of time, as well as ejection fraction
    • The greatest risk is in the first few months after MI, and then the risk declines

  • Slide 5.

    Slide 5.

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  • UPDATE: Pharmacologic Treatment for HFrEF[5]

    • Many therapies are designed to prevent progressive remodeling
    • HRS has strong recommendations for the use of an angiotensin-converting enzyme inhibitor (ACEi) or angiotensin receptor blocker (ARB), in combination with beta-blocker therapy, in the post-MI patient population

  • Slide 6.

    Slide 6.

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  • Guidelines Recommend Waiting Period Before Implantation[6]

    • Time is needed to see that patients can tolerate drug therapy
    • For those individuals who are post-MI and who have been revascularized, either percutaneously or surgically; there is a waiting period of 3 months, during which time the neurohormonal blocking agents are initiated and uptitrated
    • For patients who are not revascularized, the guidelines currently recommend a waiting period of greater than 40 days

  • Slide 7.

    Slide 7.

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  • WCD: Window of Vulnerability: Class IIb Recommendation[7]

    • The American Heart Association makes a class IIb recommendation for patient protection during the waiting period window following an MI
    • Physicians and nurses can exert judgment in this patient population during this period of vulnerability

  • Slide 8.

    Slide 8.

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  • WCD: Patient Types[7]

    • A wearable cardioverter-defibrillator (WCD) is a treatment option for patients during the period of time while waiting for optimal dosing
    • Patients can be a candidate for an implantable cardioverter-defibrillator (ICD) should there not be further improvement in their ejection fraction

  • Slide 9.

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  • WEARIT-II: ICD Implantation Rate by Disease Etiology[8]

    • Now clinicians can be much more selective in deciding who needs an ICD
    • Reevaluate patients over a period of time
    • WCD provides assurance during this time that these patients are not going to experience sudden cardiac death (SCD)

  • Slide 10.

    Slide 10.

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  • Heart Rhythm Society Guidelines[6]

    • The Heart Rhythm Society guidelines
      • Emphasize the administration of neurohormonal blocking agents and their uptitration
      • Recommend assessing patients over time to determine if their ejection fraction has improved
      • Recommend considering the use of the implantable ICD
      • Note that the WCD provides a level of safety during the waiting period

  • Slide 11.

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  • Timing Is Everything: WCD[9]

    • We do not want to prematurely put a device into individuals whose ejection fraction may come up to the 35% level or above

  • Slide 12.

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  • Well-Coordinated Multidisciplinary Teams

  • Slide 13.

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This content has been condensed for improved clarity.

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