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Enabling Multidisciplinary Care Models in Asthma Management

LEARNING OBJECTIVES

  1. Identify patients with severe asthma and initiate timely referral process to specialists to accurately diagnose and define asthma endotypes and optimize treatment plans.
  2. Provide accurate classification of asthma endotypes to guide treatment decisions with biologics.
  3. Apply multidisciplinary care models in the treatment of asthma and deliver patient-centered  care.
  4. Manage comorbidities to improve treatment outcomes and patients’ quality of life.


COURSE INFORMATION    

LAUNCH DATE/EXPIRATION DATE
This activity was launched on September 16, 2024 and will expire on September 16, 2025.

TARGET AUDIENCE
This activity will target groups of asthma specialists (pulmonology and allergy/immunology) and primary care clinicians, including MD, DO, APPs, and Pharmacists.

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 providership of Horizon 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 4.0 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

•    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.
•    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.

 

COURSE FACULTY 

Eileen Wang, MD, MPH
Associate Professor
Division of Allergy and Clinical Immunology
National Jewish Health University of Colorado School of Medicine
Denver, CO
 
Dr. Eileen Wang discloses that she is on a speaker’s bureau for AstraZeneca and Genentech as well as on an advisory board for AstraZeneca and GlaxoSmithKline. In addition to this she conducts research for AstraZeneca, Genentech, GlaxoSmithKline and Sanofi.

 

OTHER CONTRIBUTOR/PLANNER DISCLOSURES
Those others involved in the planning of this activity disclosed no relevant financial relationships with any entity producing, marketing, re-selling, or distributing health care goods or services consumed by, or used on, patients.

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 ACKNOWLEDGMENT
This activity is supported by an independent medical education grant from Regeneron Pharmaceuticals, Inc and Sanofi.