Publication

Eight tips for the implementation of the first licenced peanut allergy oral immunotherapy into clinical practice

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Last modified
  • 05/21/2025
Type of Material
Authors
    Jay Portnoy, Children's Mercy Hospitals and ClinicsChristina E Ciaccio, The University of ChicagoJanet Beausoleil, The Children's Hospital of PhiladelphiaGeorge Du Toit, King’s College London, LondonStanley Fineman, Emory UniversityStanley A Tilles, Aimmune TherapeuticsJune Zhang, Latitude Food Allergy CareClaire Lawrence, Acaster Lloyd Consulting LtdMohamed Yassine, Aimmune TherapeuticsShahzad S Mustafa, University of Rochester School of Medicine and Dentistry
Language
  • English
Date
  • 2022-12-01
Publisher
  • Springer Nature
Publication Version
Copyright Statement
  • © The Author(s) 2022
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 18
Issue
  • 1
Start Page
  • 37
End Page
  • 37
Grant/Funding Information
  • This research was sponsored by Aimmune Therapeutics, a Nestlé Health Science company.
Supplemental Material (URL)
Abstract
  • Background: Shared learnings from the early use of novel therapies can aid in their optimization. The recent introduction of peanut oral immunotherapy (peanut OIT; Palforzia [Peanut (Arachis hypogaea) Allergen Powder-dnfp]) for peanut allergy addresses a significant unmet need but also highlights the requirement for consideration of several factors by both prescribers and patients. Objective: To provide guidance for prescribers of licenced peanut OIT to facilitate treatment delivery and improve outcomes. Methods: Clinicians with experience of licenced peanut OIT (United States n = 6, United Kingdom n = 1) participated in a series of interviews and group discussions designed to elicit tips for successful implementation. Results: Clinicians identified 8 tips that were considered the most relevant, practical, and impactful for prescribers of Peanut (Arachis hypogaea) Allergen Powder-dnfp: (1) preparing to provide treatment, (2) assessing the medical indication for treatment and (3) shared decision making, (4) staff education, (5) establishing office processes, (6) managing patient expectations and using anticipatory guidance, (7) optimising adherence and (8) maintaining flexibility throughout the treatment process. In addition, a range of supporting materials (e.g., checklists and action plans) are provided. Conclusion: The introduction of a novel therapy often requires healthcare providers to modify or adopt practices to effectively employ the treatment. The provision of guidance based upon early real-world experiences of licenced peanut OIT may help inform clinical practice and improve treatment outcomes.
Author Notes
Keywords
Research Categories
  • Health Sciences, Immunology
  • Health Sciences, Medicine and Surgery

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