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Pathways to Improving Outcomes in Pediatric/Adolescent Patients with Atopic Dermatitis - June 2020

Dermatology
Curriculum:
Making A Difference for Your Atopic Dermatitis Patients: Pathways to Improving Outcomes in Atopic Dermatitis and its Comorbidities - Updated June, 2020
Credits:
0.5 AMA PRA Category 1 Credit(s)
Launch Date:
October 10, 2019
Expiration Date:
The accreditation for this activity has expired.

Primary Audience:

Allergists, Dermatologists, Pediatric dermatologists

Relevant Terms:

Atopic Dermatitis, Pediatric Dermatology

Robert Sidbury, M.D., M.P.H.

Robert Sidbury, M.D., M.P.H.
Chief, Division of Dermatology
Seattle Children’s Hospital
Professor, Department of Pediatrics
University of Washington School of Medicine
Seattle, WA

Robert Sidbury MD, MPH got his undergraduate and medical degrees from Duke University, and his Masters in Public Health from Harvard.  He did his internship and residency at UCSF and the Oregon Health and Science University, and completed fellowships at Northwestern University  and Harvard.   He has held faculty positions at Harvard Medical School and the University of Washington School of Medicine where he is currently Professor in the Department of Pediatrics and chief of the division of dermatology.  His clinical and research interests include atopic dermatitis, vascular tumors of infancy, vitamin D, and pediatric health services.   He spends most of his time outside of work playing with his thirteen year old daughter Claire. 

Steven R. Feldman, MD, PhD

Steven R. Feldman, MD, PhD
Department of Dermatology
Wake Forest School of Medicine
Winston-Salem, NC

Steve Feldman received his MD and PhD degrees from Duke University and completed dermatology residency at the University of North Carolina at Chapel Hill and dermatopathology residency at the Medical University of South Carolina.  He is Professor of Dermatology, Pathology, Social Sciences & Health Policy and Molecular Medicine & Translational Science at the Wake Forest School of Medicine.  He leads the Center for Dermatology Research, a health services research center whose mission is to improve the care of patients with skin disease. Dr. Feldman served on the American Academy of Dermatology’s atopic dermatitis guidelines committee.  He has done ground breaking work on patients’ adherence to their medication treatment regimens, the latter leading to the Wake Forest spin off company Causa Research.  Feldman’s clinical work led him to an interest in patient satisfaction.  Feldman created the www.DrScore.com doctor rating/patient satisfaction website.  He has given invited lectures to dermatology groups and organizations around the world including the Pan Arab Dermatology Meeting held in Riyadh, Saudi Arabia, the Iranian Dermatology Society meeting in Tehran, Iran, and the Pan Asian Dermatology Meeting held in Seoul, Korea.  Feldman’s experiences in medicine have led him to try to see how others perceive things, leading to his book Compartments and his recent novella Bent Toward Justice.  Feldman serves on the board of the North Carolina-based Coalition for Peace with Justice.  His research has been published in over 1,000 Medline-reference articles. Feldman also serves as the editor of the Journal of Dermatological Treatment and the Journal of Dermatology and Dermatological Surgery and as chief medical editor of The Dermatologist.

1. Develop strategies for the co-management of atopic dermatitis (AD) and its associated comorbid conditions
2. Identify and manage side effects associated with current AD treatments, including ocular events
3. Tailor treatment regimens for AD based on current guideline recommendations and patient-specific characteristics
4. Facilitate shared decision-making (SDM) for patients with AD through patient engagement and education 

LAUNCH DATE/EXPIRATION DATE
This activity was launched on October 10, 2019 and will expire on October 10, 2020.
 
TARGET AUDIENCE
This activity has been designed to meet the educational needs of allergists, dermatologists, pediatric dermatologists (MD/DOs), and nurse practitioners (NPs), physician assistants (PAs) who manage patients with AD.

ACCREDITATION STATEMENT
This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of Horizon CME and Real CME. Horizon CME is accredited by the ACCME to provide continuing medical education for physicians. 

CREDIT DESIGNATION
Horizon CME designates this enduring material for a maximum of 0.5 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
 
HOW TO CLAIM CREDIT
Statement of credit will be available to print from your user history page.
  • Read the learning objectives and faculty disclosures.
  • Participate in the activity.
  • Complete the post-test and activity evaluation.
  • Physicians who successfully complete the post-test and evaluation will receive CME credit. You must score with an 75% or higher on the post-test to receive credit for this activity.
  • All other participants who successfully complete the post-test and evaluation will receive a certificate of participation.

LEARNER ASSURANCE STATEMENT
Horizon CME requires instructors, planners, managers and other individuals who are in a position to influence the content of this activity to disclose any real or apparent conflict of interest (COI) which may arise as a result of prospective faculty members' relevant relationships with drug or device manufacturer(s). Horizon CME is committed to resolving all conflicts of interest and retaining only those speakers with financial interest conflicts that can be reconciled with the goals and educational integrity of the CME activity.
 
FACULTY DISCLOSURES
Dr. Feldman has served as a Consultant for Abbvie, Alvotech, Advance Medical, Caremark, Celgene, Galderma Laboratories, L.P., Gerson Lehrman Group, Guidepoint Blobal, Janssen, Kikaku, Leo Pharma Inc., Lilly, Medical Quality Enhancement Corporation, Merck & Co., Inc, Mylan, Novartis Pharmaceuticals, Pfizer Inc., Regeneron, Sanofi, Sienna, Sun Pharma, Suncare Research, Ortho Dermatology and Xenoport. He has served as a Speaker for Abbvie, Celgene, Janssen, Leo Pharma Inc., Lilly, Novartis Pharmaceuticals, Pfizer Inc., Regeneron, Sanofi, Sun Pharma, Taro, and Ortho Dermatology. He has received grant support from Abbvie, Celgene, Galderma Laboratories, L.P., Janssen, Novartis Pharmaceuticals, Pfizer, Regeneron, Sanofi, and Taro. He is Founder, Stock holder, Chief Technology Officer for Causa Technologies. He has received Royalties form Informa, UpToDate and Xlibris. He is a majority stock owner in Mecial Quality Enhancement.

Dr. Sidbury 
Dr. Robert Sidbury has served on an Advisory Board for Pfizer. He has served as an investigator for Regeneron and Brickell. He has served as a Consultant for Micreos.
 
Other Contributor/Planner Disclosures
Additional non-faculty contributors and others involved in the planning, development, and editing/review of the content have no relevant financial relationships to disclose.
 
DISCLOSURE OF UNLABELED USE
This educational activity may contain discussion of published and/or investigational uses of agents that are not indicated by the FDA. The planners of this activity 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 the planners.  Please refer to the official prescribing information for each product for discussion of approved indications, contraindications, and warnings.
 
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 or suggested in this activity should not be used by clinicians without evaluation of their patient's conditions and possible contraindications and/or dangers in use, review of any applicable manufacturer's product information, and comparison with recommendations of other authorities.
 
Supporter Acknowledgement
This activity is supported by an independent educational grant from Sanofi Genzyme and Regeneron Pharmaceuticals.


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