Eosinophilic granulomatosis with polyangiitis: Patient profiles from a large US allergy practice

Background: Data on the presentation and management of patients with eosinophilic granulomatosis with polyangiitis (EGPA) in private practice are limited. Objective: We sought to characterize the profiles and disease burden of patients with EGPA in a real-world private practice setting. Methods: Thi...

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Main Authors: Michael E. Wechsler, MD, Anna Kovalszki, MD, Jared Silver, MD, PhD, Brian Stone, MD, William McCann, MD, Lynn Huynh, MPH, DrPH, Anamika Khanal, BA, Mingchen Ye, MS, Mei Sheng Duh, MPH, ScD, Arijita Deb, PhD
Format: Article
Language:English
Published: Elsevier 2025-05-01
Series:Journal of Allergy and Clinical Immunology: Global
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Online Access:http://www.sciencedirect.com/science/article/pii/S2772829325000384
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author Michael E. Wechsler, MD
Anna Kovalszki, MD
Jared Silver, MD, PhD
Brian Stone, MD
William McCann, MD
Lynn Huynh, MPH, DrPH
Anamika Khanal, BA
Mingchen Ye, MS
Mei Sheng Duh, MPH, ScD
Arijita Deb, PhD
author_facet Michael E. Wechsler, MD
Anna Kovalszki, MD
Jared Silver, MD, PhD
Brian Stone, MD
William McCann, MD
Lynn Huynh, MPH, DrPH
Anamika Khanal, BA
Mingchen Ye, MS
Mei Sheng Duh, MPH, ScD
Arijita Deb, PhD
author_sort Michael E. Wechsler, MD
collection DOAJ
description Background: Data on the presentation and management of patients with eosinophilic granulomatosis with polyangiitis (EGPA) in private practice are limited. Objective: We sought to characterize the profiles and disease burden of patients with EGPA in a real-world private practice setting. Methods: This was a retrospective, noninterventional, longitudinal study (GSK ID: 217426) of US Allergy Partners network data. For patients with a diagnosis of EGPA, confirmed by 2 or more EGPA clinical features, index was defined as their first visit with an Allergy Partners physician (January 2007–June 2021); postindex lasted until loss of follow-up or study end (December 2021). Patient characteristics at index, physician characteristics at any time, symptoms, treatment characteristics, and clinical outcomes postindex were assessed. Results: Of 52 patients (median follow-up, 3.7 years), 75% were diagnosed with EGPA outside the Allergy Partners network. Each patient received care from a median (Q1-Q3) of 4.0 (3.0-5.0) physician specialties. Most had asthma (92%), rhinitis (75%), and sinusitis (62%) and experienced a mean ± SD of 18.1 ± 4.3 distinct self-reported symptoms. Most (85%) used oral corticosteroids, with 73% (32 of 44) on daily doses of more than 12 mg; 60% used mepolizumab. Overall, 75% of patients (39 of 52) achieved a response (improved/controlled symptoms); 46% (24 of 52) achieved controlled status after worsened, unchanged, or active symptoms, and of these 38% (9 of 24) relapsed. Conclusions: The complex private practice presentation of EGPA, with heterogeneous patient response to standard treatments, highlights a significant disease burden and continued need for optimized treatment strategies within a multidisciplinary team approach.
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spelling doaj-art-70cf86f8a88747639cfef7765f99aa232025-08-20T02:28:38ZengElsevierJournal of Allergy and Clinical Immunology: Global2772-82932025-05-014210043710.1016/j.jacig.2025.100437Eosinophilic granulomatosis with polyangiitis: Patient profiles from a large US allergy practiceMichael E. Wechsler, MD0Anna Kovalszki, MD1Jared Silver, MD, PhD2Brian Stone, MD3William McCann, MD4Lynn Huynh, MPH, DrPH5Anamika Khanal, BA6Mingchen Ye, MS7Mei Sheng Duh, MPH, ScD8Arijita Deb, PhD9National Jewish Health, Denver, Colo; Corresponding author: Michael E. Wechsler, MD, National Jewish Health, 1400 Jackson St, Denver, CO 80230.University of Michigan, Ann Arbor, MichUS Medical Affairs–Respiratory, GSK, Durham, NCAllergy Partners of Western North Carolina, Asheville, NCAllergy Partners of Western North Carolina, Asheville, NCAnalysis Group, Boston, MassAnalysis Group, Boston, MassAnalysis Group, Boston, MassAnalysis Group, Boston, MassGlobal Real-World Evidence & Health Outcomes Research, GSK, Philadelphia, PaBackground: Data on the presentation and management of patients with eosinophilic granulomatosis with polyangiitis (EGPA) in private practice are limited. Objective: We sought to characterize the profiles and disease burden of patients with EGPA in a real-world private practice setting. Methods: This was a retrospective, noninterventional, longitudinal study (GSK ID: 217426) of US Allergy Partners network data. For patients with a diagnosis of EGPA, confirmed by 2 or more EGPA clinical features, index was defined as their first visit with an Allergy Partners physician (January 2007–June 2021); postindex lasted until loss of follow-up or study end (December 2021). Patient characteristics at index, physician characteristics at any time, symptoms, treatment characteristics, and clinical outcomes postindex were assessed. Results: Of 52 patients (median follow-up, 3.7 years), 75% were diagnosed with EGPA outside the Allergy Partners network. Each patient received care from a median (Q1-Q3) of 4.0 (3.0-5.0) physician specialties. Most had asthma (92%), rhinitis (75%), and sinusitis (62%) and experienced a mean ± SD of 18.1 ± 4.3 distinct self-reported symptoms. Most (85%) used oral corticosteroids, with 73% (32 of 44) on daily doses of more than 12 mg; 60% used mepolizumab. Overall, 75% of patients (39 of 52) achieved a response (improved/controlled symptoms); 46% (24 of 52) achieved controlled status after worsened, unchanged, or active symptoms, and of these 38% (9 of 24) relapsed. Conclusions: The complex private practice presentation of EGPA, with heterogeneous patient response to standard treatments, highlights a significant disease burden and continued need for optimized treatment strategies within a multidisciplinary team approach.http://www.sciencedirect.com/science/article/pii/S2772829325000384EGPAbiological productsburden of diseaseeosinophiliaprivate practicesymptoms
spellingShingle Michael E. Wechsler, MD
Anna Kovalszki, MD
Jared Silver, MD, PhD
Brian Stone, MD
William McCann, MD
Lynn Huynh, MPH, DrPH
Anamika Khanal, BA
Mingchen Ye, MS
Mei Sheng Duh, MPH, ScD
Arijita Deb, PhD
Eosinophilic granulomatosis with polyangiitis: Patient profiles from a large US allergy practice
Journal of Allergy and Clinical Immunology: Global
EGPA
biological products
burden of disease
eosinophilia
private practice
symptoms
title Eosinophilic granulomatosis with polyangiitis: Patient profiles from a large US allergy practice
title_full Eosinophilic granulomatosis with polyangiitis: Patient profiles from a large US allergy practice
title_fullStr Eosinophilic granulomatosis with polyangiitis: Patient profiles from a large US allergy practice
title_full_unstemmed Eosinophilic granulomatosis with polyangiitis: Patient profiles from a large US allergy practice
title_short Eosinophilic granulomatosis with polyangiitis: Patient profiles from a large US allergy practice
title_sort eosinophilic granulomatosis with polyangiitis patient profiles from a large us allergy practice
topic EGPA
biological products
burden of disease
eosinophilia
private practice
symptoms
url http://www.sciencedirect.com/science/article/pii/S2772829325000384
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