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Development and Validation of the Risk of Exacerbation in Severe Asthma (RESA) Model

  • Wenjia Chen*
  • , Tae Yoon Lee
  • , David Price
  • , Richard Beasley
  • , Christer Janson
  • , Mariko Koh Siyue
  • , Chandra Prakash Yadav
  • , Hana Müllerová
  • , Pierre Regis Burgel
  • , Trung N. Tran
  • , Benjamin Emmanuel
  • , Eileen Wang
  • , Michael E. Wechsler
  • , David J. Jackson
  • , John Busby
  • , Liam G. Heaney
  • , Paul E. Pfeffer
  • , Bassam Mahboub
  • , Diahn Warng Perng
  • , Borja G. Cosio
  • Luis Perez-de-Llano, Riyad Al-Lehebi, Désirée Larenas-Linnemann, Mona Al-Ahmad, Chin Kook Rhee, Takashi Iwanaga, Enrico Heffler, Giorgio Walter Canonica, Richard Costello, Nikolaos G. Papadopoulos, Andriana I. Papaioannou, Celeste M. Porsbjerg, Carlos A. Torres-Duque, George C. Christoff, Todor A. Popov, Mark Hew, Matthew Peters, Peter G. Gibson, Jorge Maspero, Celine Bergeron, Saraid Cerda, Elvia Angelica Contreras, Mohsen Sadatsafavi
*Corresponding author af dette arbejde

Abstract

Background: Severe asthma (SA) is associated with frequent exacerbations and high treatment costs. Objectives: To develop and validate an individualized risk calculator for severe exacerbations in SA, and evaluate its clinical utility for guiding personalized clinical decisions. Methods: Patients with SA were identified from combined data from the International Severe Asthma Registry (2015-2022) and NOVEL observational longiTudinal studY (2016-2023) across 30 countries and regions. The prediction end point was the 12-month risk of 1 or more or 2 or more severe exacerbations. Using expert input and Bayesian network analysis, 11 routinely measured predictors were identified, measured within the past 12 months. A mixed-effects, zero-inflated negative binomial model was developed, adjusting for between-country variability and biologic drop-in effects. Internal-external cross-validation was performed using the natural clustering by country settings. Results: Data from 9911 patients with SA were used. Essential predictors included age, sex, past 12-month severe exacerbations, asthma control, chronic rhinosinusitis, FEV1 to forced vital capacity ratio, percent predicted FEV1, blood eosinophils, fractional exhaled nitric oxide, and long-term oral corticosteroid and macrolide use. The model also adapted setting-specific baseline risks. In the internal-external cross-validation, across broad geographical and health care variability, the model showed excellent calibration and informative, generalizable discrimination (pooled area under the time-dependent receiver-operating characteristics curve of 0.63 [95% CI, 0.60-0.66] for ≥1 and 0.68 [95% CI, 0.64-0.72] for ≥2 exacerbations). Decision curve analysis showed clear net benefit across risk thresholds. Conclusions: The Risk of Exacerbation in Severe Asthma model quantifies SA exacerbation risk using routinely available predictors and demonstrates potential clinical utility.

OriginalsprogEngelsk
TidsskriftJournal of Allergy and Clinical Immunology: In Practice
Vol/bind14
Udgave nummer7
Sider (fra-til)1589-1600
Antal sider12
ISSN2213-2198
DOI
StatusUdgivet - jul. 2026

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