Improving Patient Care:  New Diagnostic Technology for Rapid Detection of Common Infectious Diarrheal Agents
 
CONTINUING MEDICAL EDUCATION INFORMATION
 
Release Date: January 24, 2014
Last Reviewed: January 8, 2014
Expiration Date: January 24, 2015
Time to Complete Activity: 1.75 hours

*This activity expired for credit on January 24, 2015 and is no longer available for credit
 
FACULTY
Kimberle C. Chapin, MD, D(ABMM), FCAP
Professor of Pathology and Medicine
Alpert Brown Medical School
Director of Microbiology and Infectious Disease Molecular Diagnostics
Lifespan Academic Medical Centers
Providence, RI
 
Robert Orenstein, DO, FACP, FIDSA
Associate Professor
Mayo Clinic College of Medicine
Chair - Division of Infectious Diseases
Mayo Clinic in Arizona
Phoenix, AZ
 
Lawrence R. Schiller, MD
Professor of Medicine
Texas A&M University Health Science Center at Dallas
Attending Physician
Program Director, Gastroenterology Fellowship
Baylor University Medical Center
Dallas, TX
 
TARGET AUDIENCE
The target audience for this initiative includes primary care clinicians (family practice and internal medicine physicians), gastroenterologists, infectious disease specialists, travel medicine specialists, nurse practitioners, physician assistants, and other allied healthcare providers interested in and actively engaged in the diagnosis and management of patients with signs and/or symptoms of gastrointestinal infection.
 
STATEMENT OF NEED
Each year, an estimated 211 to 375 million episodes of diarrheal disease occur in the United States, causing significant morbidity and mortality. Patient symptomatology is often insufficient to distinguish among the long list of potential causative bacterial, viral, and parasitic agents. Conventional methods for pathogen detection and identification require multiple specimens for multiple tests, often sent to different laboratories, with turnaround times ranging from a few hours to a week or more. Two new molecular panels were cleared by the U.S. Food and Drug Administration in January 2013. These panels allow same-day, single-specimen testing of common infectious diarrheal pathogens, thereby enabling clinicians to more quickly identify or rule out specific causative pathogens, initiate definitive treatment, and take steps to prevent further spread. This webinar—presented by 3 expert faculty, a gastroenterologist, an infectious disease specialist, and a microbiologist—is designed to increase clinician awareness of these new same-day, single-specimen diagnostic assays. It will also enable clinicians to identify patients who are candidates for testing and interpret test results according to assay performance characteristics and limitations.
 
EDUCATIONAL OBJECTIVES
Upon proper completion of this activity, participants should be better able to:
  • Evaluate the role of new same-day single-specimen diagnostic assays for common infectious diarrheal pathogens in improving time to diagnosis and facilitating treatment decisions.
  • Describe the correct use of new same-day single-specimen diagnostic assays for common infectious diarrheal pathogens in clinical practice, including patient selection, specimen collection and handling, and interpretation of results.
AGENDA
Welcome/Introduction
9 minutes
Chapter 1
The Burden of Infectious Diarrheal Disease
21 minutes
Chapter 2
New Diagnostic Solutions for Infectious Diarrheal Disease
33 minutes
Chapter 3
Using New Gastrointestinal Molecular Panels in Clinical Practice
26 minutes
Case Studies & Concluding Remarks
15 minutes
 
 
FACULTY AND PLANNER DISCLOSURES
In accordance with Accreditation Council for Continuing Medical Education requirements on disclosure, faculty and contributors are asked to disclose any relationships with commercial interests associated with the area of medicine featured in the activity. These relationships are described below.
 
Name of Faculty or Presenter
Reported Financial Relationship
Kimberle C. Chapin, MD, D(ABMM), FCAP
Grant/Research Support: Becton Dickinson, Hologic Corporation, Luminex Corporation
Robert Orenstein, DO, FACP, FIDSA
Nothing to disclose
Lawrence R. Schiller, MD
Speakers’ Bureaus: Abbott/Abbvie, Forest/Ironwood Pharmaceuticals, Santarus, Takeda Pharmaceutical Company
 
 
The planners and managers reported the following financial relationships or relationships to products or devices they or their spouse/life partner have with commercial interests related to the content of this CME activity:
 
Name of Planner or Manager
Reported Financial Relationship
Ashley Marostica, RN, MSN
Nothing to disclose
Amanda Glazar, PhD
Nothing to disclose
 
 
Paradigm Medical Communications, LLC staff members have no financial conflicts to disclose.
 
Physician Accreditation Statement
Paradigm Medical Communications, LLC is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. 
 
Physician Credit Designation
Paradigm Medical Communications, LLC designates this enduring material for a maximum of 1.75 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
 
Physician Assistant Continuing Education
AAPA accepts certificates of participation for educational activities certified for AMA PRA Category 1 Credit™ from organizations accredited by ACCME or a recognized state medical society. Physician assistants may receive a maximum of 1.75 hours of Category 1 Credit for completing this program.
 
Nurse Practitioner Continuing Education

Global Education Group is approved as a provider of nurse practitioner continuing education by the American Association of Nurse Practitioners (AANP): AANP Provider Number 11021. This program has been approved for 1.75 contact hours of continuing education.
 
This program was planned in accordance with AANP CE Standards and Policies and AANP Commercial Support Standard.
 
DISCLOSURE OF COMMERCIAL SUPPORT
This activity is supported by an educational grant from Luminex Corporation.
 
INSTRUCTIONS FOR PARTICIPATION
To receive a CME certificate of participation, participants should:
  • Follow instructions to register or log in with your professional information and complete the pretest.
  • View the online activity in its entirety.
  • Complete and submit the online posttest and evaluation. You must answer 70% of the posttest questions correctly to earn credit. You will have unlimited opportunities to successfully complete the activity.
A certificate of participation will be available for download/printing immediately following your successful completion of the posttest and evaluation.
 
There is no fee required for participation in this activity.
 
HARDWARE/SOFTWARE REQUIREMENTS
This certified CME activity is designed as a self-running Flash presentation. In the event that you need this plug-in, a link to download the required Flash Player has been provided below.
 
Flash Player 10 or later required–download at http://www.adobe.com/support/flashplayer/downloads.html.
 
Supported Browsers:
For Windows: Internet Explorer 7 or higher, Firefox 4.0, Safari 3, Google Chrome, Opera 9.5
For Mac: Safari 3, Firefox 4.0, Google Chrome
For Linux: Firefox 4.0
 
For your convenience, a control bar is located at the bottom of the screen to move forward and backwards through the deck. Click the toggle button with the arrows to view the webinar in full screen. Press the Esc button on your keyboard while in full screen view to return to normal view, and to view the list of chapters.
 
Technical Support: Technical Support: If you have any technical problems or playback issues, please send an email to: contactus@paradigmmc.com.
 
Resolution of Conflict of Interest
Paradigm Medical Communications, LLC (Paradigm) and Global Education Group (Global) require instructors, planners, managers, and other individuals and their spouse/life partner who are in a position to control the content of this activity to disclose any real or apparent conflict of interest they may have as related to the content of this activity. All identified conflicts of interest are thoroughly vetted by Paradigm and Global for fair balance, scientific objectivity of studies mentioned in the materials or used as the basis for content, and appropriateness of patient care recommendations.
 
© 2014 Paradigm Medical Communications, LLC, except where noted. This web presentation may not be reproduced in whole or part without the express written permission of Paradigm Medical Communications, LLC.
 
DISCLAIMER
Participants have an implied responsibility to use the newly acquired information to enhance patient outcomes and their own professional development. The information presented in this activity is not meant to serve as a guideline for patient management. Any procedures, medications, or other courses of diagnosis or treatment discussed in this activity should not be used by clinicians without evaluation of patient conditions and possible contraindications on dangers in use, review of any applicable manufacturer’s product information, and comparison with recommendations of other authorities.
 
This educational activity may contain discussion of published and/or investigational uses of agents that are not indicated by the FDA. Paradigm and Global do not recommend the use of any agent outside of the labeled indications. 
 
The opinions expressed in the educational activity are those of the faculty and do not necessarily represent the views of any organization associated with this activity. Please refer to the official prescribing information for each product for discussion of approved indications, contraindications, and warnings.
 
Contact Us
For information about the accreditation of this program, please contact Paradigm at (845) 398-5100 or contactus@paradigmmc.com.