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Printer-friendly version | This course requires Windows Operating Systems (95/98, NT, 2000, ME, XP), version 5.5 browsers or higher from Microsoft or Netscape.
Certain activities may require additional software to view multimedia, presentation, or printable versions of the content. These activities will be marked as such and will provide links to the required software. That software may be: Macromedia Flash, Adobe Acrobat, Microsoft PowerPoint, Windows Media Player, and Real Networks Real One Player.
| Back to top  | | | ACCREDITATION STATEMENT | This activity has been planned and implemented in accordance with the Essential Areas and Policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint sponsorship of the Elsevier Office of Continuing Medical Education (EOCME) and Excerpta Medica Inc. The EOCME is accredited by the ACCME to provide continuing medical education (CME) for physicians. | Back to top  | | | CREDIT DESIGNATION STATEMENT | The EOCME designates this educational activity for a maximum of 1.0 AMA PRA Category 1 Credit™. Physicians should only claim credit commensurate with the extent of their participation in the activity. | Back to top  | | | DISCLOSURES | As a sponsor accredited by the ACCME, it is the policy of the EOCME to require the disclosure of anyone who is in a position to control the content of an educational activity. All relevant financial relationships with any commercial interests and/or manufacturers must be disclosed to participants at the beginning of each activity. The faculty of this CME activity disclose the following: | Faculty Member | | Manufacturer | | Relationship | | C. Michael Gibson, MS, MD, FACC | | Angel Medical Systems, Archemix, Ascenta Therapeutics, Atrium Medical Corp., Bayer, Biogen Idec, Heartscape Technologies, Momenta Pharmaceuticals, PDL BioPharma, Portola, Schering-Plough, The Medicines Company, Timi3 Systems | | Consultant | | | | UpToDate in Cardiovascular Medicine | | Contributor | | | | Abbott Laboratories, Archemix, AstraZeneca, Baxter, CardioKinetix, Eli Lilly, FoldRx, Genentech, Heartscape Technologies, INO Therapeutics, KAI Pharmaceuticals, Novartis, Nuvelo, POINT Biomedical, Portola, sanofi-aventis U.S., Schering-Plough | | Grants/Research Support | | | | Schering-Plough, The Medicines Company | | Speaker’s Bureau | | | | ActivBiotics, Acusphere, Ascenta Therapeutics, Astra, Bard,
Boston Scientific, Bristol-Myers Squibb, British Biotech, Ciba-Geigy, Corgentech, COR Therapeutics, DVI Guidant, Eli Lilly, Genentech, GlaxoSmithKline, Merck, Millennium, NIH, Nuvelo, PercuSurge, Pfizer, POINT Biomedical, sanofi-aventis U.S., SmithKline Beecham, Sonus, St. Jude Medical, Timi3 Systems | | Past Grants/Research Support/ Speaker’s Bureau | | | | Aventis Pharmaceuticals | | Past Data Safety Monitoring Board Member | | Deborah B. Diercks, MD | | None to disclose | | Grants/Research Support | | | | Eisai, Estellas Pharmaceuticals, sanofi-aventis U.S., The Medicines Company | | Consultant/Advisory Board | | | | Bristol-Myers Squibb, sanofi-aventis U.S., Scios | | Speaker’s Bureau | | Geno J. Merli, MD, FACP | | Boehringer Ingelheim GmbH, Bristol-Myers Squibb, sanofi-aventis U.S. | | Grants/Research Support | | | | Bacchus Vascular, Inc., Bristol-Myers Squibb, sanofi-aventis U.S. | | Consultant | | | | sanofi-aventis U.S. | | Speaker’s Bureau | | Deepak L. Bhatt, MD, FACC, FSCAI, FESC, FACP | | Bristol-Myers Squibb, Eisai, Ethicon, sanofi-aventis U.S., The Medicines Company | | Grants/Research Support | | | | AstraZeneca, Bristol-Myers Squibb, Cardax, Centocor, Cogentus, Daiichi-Sankyo, Eisai, Eli Lilly, GlaxoSmithKline, Johnson & Johnson, McNeil, Medtronic, Millennium, Otsuka, Paringenix, PDL BioPharma, Philips, Portola, sanofi-aventis U.S., Schering-Plough, The Medicines Company, TNS Healthcare, Vertex | | Consultant | | | | Bristol-Myers Squibb, sanofi-aventis U.S., The Medicines Company | | Speaker’s Bureau | | Activity Director | | | | | | Paul Ruest, PhD | | Excerpta Medica | | Nothing to disclose | | Jennifer DiBenedetto | | EOCME | | Nothing to disclose |
| Back to top  | | | RESOLUTION OF CONFLICT OF INTEREST | The EOCME has implemented a process to resolve conflicts of interest for each CME activity. In order to help ensure content objectivity, independence, fair balance, and that the content is aligned with the interest of the public, the EOCME has resolved the conflict by conducting peer review. | Back to top  | | | UNAPPROVED/OFF-LABEL USE DISCLOSURE | The EOCME requires CME faculty to disclose to the participants:
1. When products or procedures being discussed are off-label, unlabeled, experimental, and/or investigational (not US Food and Drug Administration [FDA] approved); and
2. Any limitations on the information that is presented, such as data that are preliminary or that represent ongoing research, interim analyses, and/or unsupported opinion.
Faculty may discuss information about pharmaceutical agents that is outside of FDA-approved labeling. This information is intended solely for CME and is not intended to promote off-label use of these medications. If you have questions, contact the medical affairs department of the manufacturer for the most recent prescribing information. | Back to top  | | | INTENDED AUDIENCE | This activity has been developed for cardiologists, interventional cardiologists, pulmonologists, and emergency medicine physicians. | Back to top  | | | PROGRAM GOALS | Fibrinolysis is the most widely used reperfusion strategy for patients with ST-elevation myocardial infarction (STEMI). As new anticoagulant agents become available, clinicians need to be aware of their benefits and limitations and their recommended place in therapy. The goals of this program are to provide a comprehensive review of recent trials of anticoagulant agents in STEMI patients undergoing fibrinolysis and discuss current guideline recommendations for their use. | Back to top  | | | EDUCATIONAL OBJECTIVES | After completing this educational activity and the post-test, participants should be able to:
- Discuss thrombolytic therapy for myocardial infarction with fibrinolytic agents
- Explain the 2007 American College of Cardiology/American Heart Association (ACC/AHA) guidelines for patients receiving fibrin-specific agents, as well as those receiving streptokinase who are at high risk for thromboembolic events
- Compare direct thrombin inhibitors, factor Xa inhibitors, unfractionated heparin (UFH), and low-molecular-weight heparins (LMWHs) as adjunctive therapy to fibrinolysis
- Explain the overall importance of this clinical initiative
Release Date of Activity: April 2008
Expiration Date of Activity for AMA PRA Credit: April 30, 2010
Estimated Time to Complete This Activity: 1 hour | Back to top  | | | FINANCIAL SUPPORT | This CME activity is supported by an educational grant from sanofi-aventis U.S. | Back to top  | | | CME PLANNING COMMITTEE | C. Michael Gibson, MS, MD, FACC
Deborah B. Diercks, MD
Geno J. Merli, MD, FACP
Deepak L. Bhatt, MD, FACC, FSCAI, FESC, FACP
Paul Ruest, PhD
Jennifer DiBenedetto | Back to top  | | | CME INQUIRIES | For all CME certificate inquiries, please contact Sandy Bakos at s.bakos@elsevier.com | Back to top  | | | SPECIAL NEEDS | We encourage participation by all individuals. If you have any special needs, please contact Wendy Barker at (908) 547-2183 or w.barker@elsevier.com for assistance. | Back to top  | | |
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