Optimizing Biologic Selection in Severe Asthma: Integrating Guidelines, Equity, and Patient-Centered Care


Maximum Credit Amount: 1.25
Credit Type: ACCME, ANCC
Release: October 11, 2026
Expiration: October 11, 2026
To view the AI Simulation and claim credit, click the "Get CME Credit" to log in or create your free account.
September
17
2026
The Omni Hilton Head
Palmetto Ballroom
7:00 pm - 8:15 pm EST
Sunday
October
11
2026
Allergy Conference
The Seabird Resort
1:00 to 2:00 PM PT
October
18
Southern California
Allergy Conference
The Seabird Resort
Room TBD
Time TBD
To view the AI Simulation and claim credit, click the "Get CME Credit" to log in or create your free account.
Learning Objectives
- Utilize understanding of severe asthma pathophysiology encompassing Type 2 inflammatory pathways, IL-5-mediated mechanisms, and biomarker-based phenotypic classification to guide precision medicine approaches in clinical practice.
- Employ biomarker-driven phenotyping approaches to determine appropriate candidates for biologic therapies, integrating recommendations from the GINA 2025 and CHEST 2025 guidelines along with novel therapeutic agents.
- Implement collaborative decision-making techniques that ensure biologic therapy selections reflect individual patient priorities and preferences within the context of severe asthma management.
- Apply systematic approaches for identifying and addressing comorbid conditions as part of an individualized treatment plan for patients living with severe asthma.
- Recognize social determinants of health that influence severe asthma outcomes.
- Develop actionable strategies to address inequities in care delivery.
Accredited Provider


Joint Accreditation Statement

Physician Credit Designation
Nurse Contact Hours Designation
Global Education Group designates this continuing education activity for 1.25 contact hour(s) including 0.0 pharmacotherapeutic contact hour(s).
Faculty, Staff, and Planners’ Disclosures
Disclosure of Unlabeled Use
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.
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.
Disclosures of Relevant Financial Relationship(s)
Department of Medicine-Allergy/Clinical Immunology
University of Colorado
Aurora, CO
Disclosures
AbbVie, Inc., Alnylam Pharmaceuticals, Inc., Amgen, Inc.,Biogen, Inc., Bristol Myers Squibb Co., Gilead Sciences, Inc., Incyte Corp., Kenvue, Inc., Eli Lilly & Co., Merck & Co., Inc., Pfizer Inc., Regeneron Pharmaceuticals, Inc., Vertex Pharmaceuticals, Inc., Viatris, Inc., Align Technology, Inc., Becton, Dickinson & Co., Boston Scientific Corp., Edwards Lifesciences Corp., GE Healthcare Technologies, Inc., Intuitive Surgical, Inc., Johnson & Johnson, Insulet Corp., ResMed, Inc., Solventum Corp., STERIS Plc, West Pharmaceutical Services, Inc., Quest Diagnostics, Inc., Danaher Corp., Labcorp Holdings, Inc., Revvity, Inc., Bio-Techne Corp., Thermo Fisher Scientific, Inc., Waters Corp., Cardinal Health, Inc., Cencora, Inc., CVS Health Corp., Henry Schein, Inc., McKesson Corp.
Disclosures
AstraZeneca, Bayer, Begin Health, GSK, Kenvue, Lilly, Nasus Pharma, Novartis, Ophelia, Regeneron, Sanofi
HAE Community Endowed Chair, Clinical Service Chief
Division of Allergy & Immunology
University of California, San Diego
San Diego, CA
Consulting Fee (e.g., Advisory Board): ADARx, Astria, Biocryst, Celldex, CSL Behring, Grifols, Intellia, Ionis, Kalvista, Novartis, Pharming, Pharvaris, Sanofi-Regeneron, Takeda
Instructions to Receive Credit
A statement of credit will be issued within four weeks of receipt of a completed activity evaluation form.
Fee Information and Refund/Cancellation Policy
Global Contact Information
System Requirements
Program Overview
Optimizing Biologic Selection in Severe Asthma: Integrating Guidelines, Equity, and Patient-Centered Care is a live CME/CE activity designed to improve clinician competence in biomarker-guided phenotyping, biologic selection, shared decision-making, and equitable severe asthma care. Through expert faculty education and immersive Conversational AI patient simulations, learners will engage in interactive, case-based experiences focused on guideline-concordant treatment selection, comorbidity management, culturally competent communication, and individualized care strategies for patients with severe asthma.
Target Audience
The primary audience for this activity includes pulmonologists, critical care specialists, and allergists/immunologists, as well as nurse practitioners and physician assistants who specialize in the diagnosis and management of severe asthma.
Supporter Acknowledgement

Legal

Stay Informed
We appreciate your ongoing interest and look forward to keeping you informed with the latest details!
Thank you for confirming.
You’ll receive reminder emails for the next LGS CME/CE session, including full access details.
We look forward to your participation.
Earn up to 1.5 AMA PRA Credit
The OX2R Era Is Here. Is Your NT1 Diagnosis?
Phoenix, AZ | October 18, 2026 | 12:00 - 1:15 Phoenix Time
Learning Objectives
- Identify the full NT1 symptom pentad and the systemic clinical burden of orexin deficiency.
- Apply the cataplexy interrogation question at the CPAP non-response encounter.
- Differentiate NT1 from NT2, idiopathic hypersomnia, and common misdiagnoses using the defining diagnostic criterion of cataplexy or CSF hypocretin-1 <110 pg/mL.
- Distinguish NT1 from medication-induced and primary psychiatric EDS using ICSD-3 criteria when psychiatric comorbidity complicates evaluation of excessive daytime sleepiness.
- Apply evidence-based PSG/MSLT diagnostic protocols, including medication washout requirements, SOREMP interpretation, and CSF hypocretin-1 <110 pg/mL as a standalone NT1 diagnostic criterion per ICSD-3.
- Integrate SDoH-informed screening, navigator referral pathways, and telehealth-compatible approaches to reduce diagnostic delay in NT1 across diverse patient populations.
- Individualize NT1 treatment selection using an SDM framework informed by the limitations of current pharmacotherapy and the mechanism of emerging OX2R-directed therapies.
Accredited Provider


Joint Accreditation Statement

Physician Credit Designation
Nurse Contact Hours Designation
Global Education Group designates this continuing education activity for 1.5 contact hour(s) including 0.0 pharmacotherapeutic contact hour(s).
Faculty, Staff, and Planners’ Disclosures
Disclosure of Unlabeled Use
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.
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.
Disclosures of Relevant Financial Relationship(s)
The faculty have the following relevant financial relationships with ineligible companies:
Disclosures
University of California
La Jolla, CA
Disclosures
Volunteer Peer Support Group Facilitator, Wake Up Narcolepsy Oklahoma City, Oklahoma
Disclosures
Instructions to Receive Credit
A statement of credit will be issued within four weeks of receipt of a completed activity evaluation form.
Fee Information and Refund/Cancellation Policy
Global Contact Information
System Requirements
Program Overview
Target Audience
The primary audience for this activity includes pulmonologists, sleep specialists, primary care physicians, internists, hospitalists, nurse practitioners, physician assistants, and respiratory therapists involved in the diagnosis and management of narcolepsy.
Supporter Acknowledgement
Use of artificial intelligence in this activity
How the AI is controlled.
The AI does not search the internet. It does not give you diagnostic or treatment recommendations. Before release, the faculty and the IridiumCE and Global Education Group planners, tested the simulation for accuracy, completeness, balance and freedom from commercial bias on October 12, 2026.
Platform: Patient dialogue is generated using OpenAI's GPT-4.1 model (gpt-4.1-2025-04-14). The patient's video avatar is powered by HeyGen.
Independence. Global, as the accredited provider, is responsible for all content in this activity, including what the AI generates.
Data. All conversation and scores are recorded so we can give personalized feedback, award credit, and evaluate and improve the activity.
Pre-Meeting Simulation: The OX2R Era Is Here. Is Your NT1 Diagnosis?
AI Simulation: The OX2R Era Is Here. Is Your NT1 Diagnosis?