Using Comparative Effectiveness Research to Improve Patient and Plan Outcomes in Rheumatoid Arthritis: Practical Strategies for Managed Care to Apply EULAR and ACR CER Data
Using Comparative Effectiveness Research to Improve Patient and Plan Outcomes in Rheumatoid Arthritis: Practical Strategies for Managed Care to Apply EULAR and ACR CER Data
William J. Cardarelli, PharmD
Director of Pharmacy
Atrius Health
Harvard Vanguard Medical Associates
Watertown, Massachusetts
Marc C. Levesque, MD
Associate Professor
Division of Rheumatology and Clinical Immunology
University of Pittsburgh
Pittsburgh, Pennsylvania
After completing this activity, participants should be able to:
- Define comparative effectiveness research (CER) and its potential to improve pharmacoeconomic and cost-utility analysis of rheumatoid arthritis (RA) therapy
- Describe the treat-to-target goals of rheumatologists who use CER and other clinical trial data to guide treatment of patients with RA
- Apply CER data presented at EULAR and ACR 2012 to formulary discussions and review
- Improve patient and plan outcomes in RA by translating CER to a patient-centric formulary approach
This activity is designed for managed markets physicians and pharmacists.
This on-demand webcast is available with synchronized slides and audio.
To be eligible for documentation of credit, participants must complete the educational activity, complete the 10-question online post-test with a score of 70% or better, and complete the evaluation form. After successful completion of the post-test and evaluation form online at www.naccme.com, participants may immediately print their documentation of credit.
There is no fee associated with this activity.
This educational activity is a knowledge-based activity.
Participants who have successfully completed the live version of this activity are not eligible to receive credit for these enduring materials.
Release Date: January 8, 2013
Expiration Date: January 8, 2014
Estimated time to complete: 1 hour
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NACCME designates this enduring material for a maximum of 1 AMA PRA Category 1 Credit™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
This activity is approved for 1 contact hour (0.1 CEU) of continuing pharmacy education (UAN 0276-0000-12-050-H01-P).
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Independent Clinical Reviewer: Elinor A. Mody, MD, Director, Women's Orthopedic and Joint Disease Program, Brigham and Women’s Hospital, Assistant Professor, Harvard Medical School, Boston, Massachusetts
The planning committee comprises William J. Cardarelli, PharmD, Marc C. Levesque, MD, and Elinor Mody, MD; and Stephen Chavez, Lindsay Halverson, Mike Kearney, Randy Robbin, John Savage, and Jessica Steuerman.
According to the disclosure policy of NACCME, faculty, editors, managers, and other individuals who are in a position to control content are required to disclose any relevant financial relationships with relevant commercial companies related to this activity. All relevant conflicts of interest that are identified are reviewed for potential conflicts of interest. If a conflict is identified, it is the responsibility of NACCME to initiate a mechanism to resolve the conflict(s). The existence of these interests or relationships is not viewed as implying bias or decreasing the value of the presentation.
All educational materials are reviewed for fair balance, scientific objectivity of studies reported, and levels of evidence.
The faculty has reported the following:
Dr. Levesque: Consultant—Baxter, Genentech, UCB; Grant support—Genentech;Expert witness—Abbott.
Dr. Cardarelli and Dr. Mody disclosed no relevant financial relationships with any commercial interests.
Mr. Chavez, Ms. Halverson, Mr. Robbin, Mr. Savage, and Ms. Steuerman have disclosed no relevant financial relationships with any commercial interests.
Mr. Kearney: Stock Shareholder – Savient Pharmaceuticals, Inc.
NACCME requires faculty to inform participants whenever off-label/unapproved uses of drugs and/or devices are discussed in their presentations.
The faculty have disclosed that no off -label/unapproved uses of drugs and/or devices will be discussed.
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Copyright © 2012 by North American Center for Continuing Medical Education, LLC. All rights reserved. No part of this accredited continuing education activity may be reproduced or transmitted in any form or by any means, electronic or mechanical, without first obtaining permission from North American Center for Continuing Medical Education. The opinions expressed in this educational activity are those of the faculty and are not attributable to NACCME. Clinical judgment must guide each professional in weighing the benefits of treatment against the risk of toxicity. Dosages, indications, and methods of use for products referred to in this activity are not necessarily the same as indicated in the package insert for each product, may reflect the clinical experience of the presenters, and may be derived from the professional literature or other clinical sources. Consult complete prescribing information before administering.
Supported by an educational grant from UCB, Inc.