Tackling the Controversies of Biologic Therapy in Rheumatoid Arthritis and Spondyloarthropathy: Application of Emerging Clinical Data Into Daily Treatment Decisions CME

Paul P. Emery, MA, MD, FRCP, Chair; Josef S. Smolen, MD; Paul Ridker, MD, MPH, FACC, FAHA; Muhammad Asim Khan, MD, MACP, FRCP; Arthur Kavanaugh, MD Author Information and Disclosures

Release Date: March 6, 2008Valid for credit through March 6, 2009

Credits Available
Physicians - maximum of 2.0 AMA PRA Category 1 Credit(s) for physicians

This CME activity is based on transcripts and slides of presentations as delivered by the faculty at the "Tackling the Controversies of Biologic Therapy in Rheumatoid Arthritis and Spondyloarthropathy: Application of Emerging Clinical Data Into Daily Treatment Decisions" symposium held at the Westin Boston Waterfront in Boston, Massachusetts, on November 8, 2007.

To participate in this internet activity: (1) review the target audience, learning objectives, and author disclosures; (2) study the education content; (3) take the post-test and/or complete the evaluation; (4) view/print certificate View details

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Abbott

Learning Objectives
Upon completion of this activity, participants should be better able to
  1. Compare and contrast the efficacy and safety of tumor necrosis factor (TNF) antagonists and other biologic agents in achieving remission and/or modifying the natural history of rheumatoid arthritis (RA), especially in halting radiographic progression of disease, preserving function and quality of life, and improving productivity.
  2. Outline the latest clinical data suggesting that certain TNF antagonists may prevent endothelial dysfunction, the first step in the pathway to atherosclerosis and cardiovascular disease.
  3. Describe the latest clinical data showing the safety and efficacy of TNF antagonists in treating spondyloarthropathy (SpA), including extra-articular manifestations of disease.
  4. Define the benefit/risk ratio for biologic agents used to treat patients with RA.
Authors and Disclosures

Paul P. Emery, MA, MD, FRCP
Disclosure: Grant/Research Support, Consultant, Advisory Board, Honoraria: Abbott


Josef S. Smolen, MD
Disclosure: Grant/Research Support, Consultant, Advisory Board, Honoraria: Abbott, Bristol-Myers Squibb, Centocor, Roche, sanofi-aventis, Schering-Plough, Wyeth, UCB


Paul Ridker, MD, MPH, FACC, FAHA
Disclosure: Grant/Research Support, Consultant: Abbott, Amgen, AstraZeneca, Dade-Behring

Dr Ridker is listed as a coinventor on patents held by the Brigham and Women's Hospital that relate to the use of inflammatory biomarkers in cardiovascular disease.


Muhammad Asim Khan, MD, MACP, FRCP
Disclosure: Consultant, Speakers' Bureau, Advisory Board, Honoraria: Abbott, Amgen, Centocor, Schering-Plough, Wyeth


Arthur Kavanaugh, MD
Disclosure: Grant/Research Support, Honoraria: Abbott, Amgen, Centocor, Biogen Idec, Genentech Inc., Bristol-Myers Squibb


 
Rosalind Franklin University of Medicine and Science
This activity has been planned and implemented in accordance with the Essential Areas and Policies of the Accreditation Council for Continuing Medical Education through the joint sponsorship of The Chicago Medical School at Rosalind Franklin University of Medicine & Science and Scientific Frontiers, Inc. The Chicago Medical School at Rosalind Franklin University of Medicine & Science is accredited by the ACCME to provide continuing medical education for physicians.

The Chicago Medical School at Rosalind Franklin University of Medicine & Science designates this educational activity for a maximum of 2.0 AMA PRA Category 1 Credit(s)™. Physicians should only claim credit commensurate with the extent of their participation in the activity.

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