Go back to:   
 
 

Performance Improvement
Breast Cancer

Improving the Outcomes of Cardiac Complications in Breast Cancer Patients

Release Date: November 16, 2009
Expiration Date: November 15, 2010

To Start:
Sign-in or register at the bottom to start the performance improvement activity.
 
 

What Is Performance Improvement CME


Traditional educational activities (in the form of live meetings or lectures and other printed or Internet-based CME activities) may make you aware of new information, may illuminate associated health care quality gaps, and may even provide you with the rationale or evidence-based information for improving the care of patients with breast cancer. However, they do not offer any further support in the successful application of the learning in your practice.

This PI-CME activity is a practice-based expert-led initiative that can provide a structured mechanism to identify, implement, and evaluate improvements in your practice that can improve the quality of care for your patients with breast cancer. The activity offers 20 complimentary AMA PRA Category 1 Credit(s)™ should you choose to complete the entire process.

The model for this activity has been provided by the American Medical Association (AMA) and was published in 2004. The AMA defines a PI-CME activity as a structured, self-directed, long-term educational process. The process consists of 3 stages, which are sequentially rolled out over several months. Through this process, you will review past patient charts; determine, make, and evaluate improvements; and then reflect on the progress achieved in the quality of care of your patients.

   
  Follow us on Twitter  

 
   Author Cases For Us
 
   

Disclosures and Important Information


Sponsored by MedCases, LLC

Supported by educational grants from Genentech BioOncology and Sanofi-Aventis.


Release Date: November 16, 2009

Expiration Date: November 15, 2010

Accreditation Statement

MedCases, LLC is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. This activity has been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education.

Credit Designation Statement

MedCases designates this educational activity for a maximum of 20.0 AMA PRA Category 1 Credit(s)™. Physicians should only claim credit commensurate with the extent of their participation in the activity.

Statement of Responsibility

MedCases takes responsibility for the content, quality, and scientific integrity of this CME activity.

Program Chair

Mark D. Pegram, MD, PhD
Professor of Medicine
University of Miami
Division of Hematology/Oncology
Braman Family Breast Cancer Institute
Miami, Florida

Faculty Panel

Harold J. Burstein, MD, PhD
Associate Professor of Medicine
Dana-Farber Cancer Institute
Harvard Medical School
Boston, Massachusetts

Susana M. Campos, MD, MPH
Assistant Professor of Medicine
Dana-Farber Cancer Institute
Harvard Medical School
Boston, Massachusetts

Joyce A. O'Shaughnessy, MD
Co-Chair, Breast Cancer Research
Baylor Sammons Cancer Center
Texas Oncology
U.S. Oncology
Dallas, Texas

Target Audience

This activity is intended for medical oncologists, community oncologists, pathologists, and other allied healthcare professionals involved in managing patients with breast cancer.

Prerequisites

There are no prerequisites.

Statement of Need

The development of effective systemic agents, in addition to advances in research, has introduced several novel approaches and effective treatment options for patients with breast cancer. While these agents have dramatically improved disease-free and overall survival rates, the advent of these new therapies has also been associated with potential toxicity in a subset of patients. As with previous data, reports continue to demonstrate the importance of medical oncologists being aware of potential treatment-related toxicities, as well as the importance of implementing steps for appropriate monitoring, prevention, and management.

In particular, the risk for and management of cardiotoxicity associated with the use of certain systemic agents in the treatment of breast cancer remains an important issue. Considering the widespread use of potentially cardiotoxic agents and the increasingly long-term survival of most patients with early-stage breast cancer, the risk for chemotherapy-induced cardiac dysfunction is a growing concern in the medical oncology community. A greater understanding of the relationship between therapeutic agents and potential adverse cardiac events is therefore needed to effectively treat patients with breast cancer while minimizing treatment-related complications. Such understanding then needs to be applied to improving patient care through effective screening for cardiac risk factors, careful scheduling and selective use of specific agents, appropriate cardiac monitoring, and early intervention when there are signs of heart failure.

Objectives

After completing this activity, you should be able to:

  • Discuss the various mechanisms of cardiac injury attributed to anthracyclines and trastuzumab including the multiple-hit hypothesis responsible for underlying cardiac risks and increased cardiac mortality
  • Describe strategies for early detection of cardiac injury by using biomarkers and routine diagnostic tests of cardiac function
  • Analyze the need for formal baseline cardiovascular disease risk assessment before treatment for breast cancer with either Framingham or Reynolds risk scores
  • Examine feasible alternatives to anthracycline-based chemotherapy that confer lower cardiac risks, including the role of TC and TCH regimens
  • Identify the methods to reduce cardiac injury to myocytes and for the timely treatment of heart failure

Method of Participation

The process you will be following is briefly summarized below. Simple paper- and Internet-based tools have been created to support you in every step of this structured methodology. Members of your staff can assist you with some of the steps.

The entire process should take approximately 6-12 months and will be worth a total of 20 complimentary AMA PRA Category 1 Credits™.

Stage A: Learning from current practice performance assessment

You will complete retrospective patient chart reviews from a "baseline period" of 6 months to abstract data for key performance metrics. You will compare these data with anonymous data from peers and national/state sources, and with recommendations from updated national guidelines and other evidence-based sources, to identify areas for improving the quality of care of your patients.

You will receive 5 complimentary AMA PRA Category 1 Credits™.

Stage B: Learning from application of performance improvement to patient care

You will formulate an improvement plan that could include educational interventions, as well as practice interventions. You will implement and monitor the plan for an "improvement period" of approximately 6 months.

You will receive 5 complimentary AMA PRA Category 1 Credits™. Educational interventions in which you choose to participate will offer additional credits.

Stage C: Learning from evaluation of the performance improvement

You will review patient charts from the "improvement period" and abstract data on key performance metrics. You will compare the improvement period information against the baseline for your practice recorded earlier in Stage A, as well as with anonymous data provided by peers, and will reflect on improvements achieved in patient care and outcomes.

You will receive 5 complimentary AMA PRA Category 1 Credits™. You will receive an additional 5 complimentary AMA PRA Category 1 Credits™ for completing all 3 stages.

Upon completion of each stage, you will be able to save your certificate to your own computer and print it on your own printer.

Important Note — HIPAA Disclaimer

No patient-identifiable data are to be collected or provided and no patient charts are to be submitted. Anonymous data provided by you will be stored in a secure electronic database and cannot be shared with any institutions, third parties, or commercial interests.

Disclosure Statement

As a provider accredited by the Accreditation Council for Continuing Medical Education (ACCME), it is MedCases policy to require the disclosure of the existence of any significant financial interest or any other relationship a faculty member or a provider has with any entity producing, marketing, re-selling, or distributing health care goods or services consumed by, or used on, patients. The following was reported:

Faculty
Mark D. Pegram, MD, PhD Grants/Research Support: sanofi-aventis US
Advisory Board member: Takeda Pharmaceuticals, Wyeth Pharmaceuticals
Harold J. Burstein, MD, PhD Has indicated that he has no significant relationships to disclose
Susana M. Campos, MD, MPH Consultant Fees: Genentech, Inc.
Grants/Research Support: Genentech, Inc.
Speakers' Bureau: Eli Lilly & Company, Genentech, Inc. and GlaxoSmithKline
Joyce A. O'Shaughnessy, MD Speakers' Bureau: Abraxis BioScience Inc., AstraZeneca Pharmaceuticals, Eli Lilly & Company, Genentech, Inc. and sanofi-aventis US
Planning Committee
Ted James, MD; Carolyn Darrow, MPH; and Daryl Lynn Ehrentreu, RPh, MBA indicated that they have not received financial support for consultation, research, or, evaluation, or have a financial interest relevant to this online activity. Sanjay Virmani, MBA has indicated that he is a stockholder for AstraZeneca Pharmaceuticals.

Notice of Off-Label Use Presentations

In accordance with US Food and Drug Administration (FDA) requirements regarding the disclosure of off-label, investigational, or unapproved recommendations for the use of drugs or devices, you are advised that content in this activity does not contain reference(s) to uses of drugs or devices that are off-label, investigational, or unapproved in the United States. The following information is provided for educational purposes and not to endorse off-label use.

Disclaimer

The opinions and recommendations expressed by faculty and other experts whose input is included in this program are their own. This enduring material is produced for educational purposes only. Use of MedCases’ name implies review of educational format design and approach. Please review the complete prescribing information of specific drugs or combination of drugs, including indications, contraindications, warnings and adverse effects before administering pharmacologic therapy to patients.

All information contained within this activity is intended for educational purposes only. Physicians and other health care professionals are encouraged to consult other sources and confirm the information contained in this site because no single reference or service can take the place of medical training, education and experience. Consumers are cautioned that this site is not intended to provide medical advice about any specific medical condition they may have or treatment they may need and they are encouraged to call or see their physician or other health care provider promptly with any health related questions they may have.

The MedCases Web site does not define a standard of care, nor is it intended to dictate an exclusive course of management. Cases are provided for informational and educational purposes only and are not intended as medical advice. This information should not substitute for a visit or consultation with a health care provider.

Privacy Statement

MedCases is committed to maintaining site visitors rights to privacy and confidentiality of personal information. Personal information about site visitors, specific visitor's access and navigation, and information volunteered by site visitors, such as survey information and site registration information, may be used by MedCases to improve the site but will not be shared with or sold to other organizations for commercial purposes without the site visitor's express permission.
Please click here to read MedCases’ detailed privacy policy and other terms of using this web site.

Copyright Information

Copyright © 2009 MedCases, LLC. All rights reserved.

For Further Information

MedCases
4365 US Highway 1, Suite 207
Princeton, NJ 08540
Phone (609) 454-0680
Fax (609) 951-0112
cme@medcases.com

Hardware/Software Requirements and Technical Assistance

This Web-based CME activity is best experienced using a current generation browser, such as Internet Explorer 5.5 or higher. This Web site requires that JavaScript and session cookies be enabled. In addition, you will require the Adobe Acrobat Reader to use the chart review tools.

Detailed Requirements:

  • 128 MB RAM
  • Windows 98 or newer
  • Adobe Flash Player 8 minimum needed
  • Audio playback with speakers for programs that have video content
  • Internet Explorer 5.5 or higher or Mozilla Firefox 1.0 or higher or Apple Safari
  • 1024 x 768 resolution
  • Broadband connection highly recommended

More information about the software described above is available at the links below:

If you need assistance, please email us at info@medcases.com.


Confirmation

By clicking the buttons below, you are confirming that you have reviewed all the above information.

Click the "Begin Stage A" button below to begin stage A.

Please note that you must complete Stage A before beginning Stage B.

Once you have completed Stage A, click the "Begin Stage B" button below to begin stage B.

Please note that you must complete Stage A and Stage B before beginning Stage C.

If you have not completed Stage A, click the "Begin Stage A" button above to complete Stage A.

If you have not completed Stage B, click the "Begin Stage B" button above to complete Stage B.

Once you have completed Stage C, click the "Begin Stage C" button below to begin stage C.