Risk calculator of the clinical response to antihistamines in chronic urticaria: Development and internal validation

Early detection of CSU patients with low probability of a clinical response with antihistamines could undergo prompt initiation of therapeutic alternatives. The aim of the study was to develop and internally validate a model for predicting the clinical response to antihistamines in adult patients wi...

Full description

Autores:
Sánchez Caraballo, Jorge Mario
Zakzuk Sierra, Josefina
García Gómez, Elizabeth
Velásquez Lopera, Margarita María
Jaimes Barragán, Fabián Alberto
Cardona Villa, Ricardo
Tipo de recurso:
Article of investigation
Fecha de publicación:
2024
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/48110
Acceso en línea:
https://hdl.handle.net/10495/48110
Palabra clave:
Antialérgicos
Anti-Allergic Agents
Anti-Inflammatory Agents
Antiinflamatorios
Chronic Disease
Enfermedad Crónica
Chronic Urticaria
Urticaria Crónica
Histamine Antagonists
Antagonistas de los Receptores Histamínicos
Histamine H1 Antagonists
Antagonistas de los Receptores Histamínicos H1
Omalizumab
Urticaria
https://id.nlm.nih.gov/mesh/D018926
https://id.nlm.nih.gov/mesh/D000893
https://id.nlm.nih.gov/mesh/D002908
https://id.nlm.nih.gov/mesh/D000080223
https://id.nlm.nih.gov/mesh/D006633
https://id.nlm.nih.gov/mesh/D006634
https://id.nlm.nih.gov/mesh/D000069444
https://id.nlm.nih.gov/mesh/D014581
ODS 3: Salud y bienestar. Garantizar una vida sana y promover el bienestar de todos a todas las edades
Rights
openAccess
License
http://creativecommons.org/licenses/by/4.0/
Description
Summary:Early detection of CSU patients with low probability of a clinical response with antihistamines could undergo prompt initiation of therapeutic alternatives. The aim of the study was to develop and internally validate a model for predicting the clinical response to antihistamines in adult patients with chronic spontaneous urticaria (CSU), who consult allergology and dermatology care centers. A cohort of CSU patients, recruited from four participating centers, were followed up for 12 months. Fifteen candidate variables were selected to be included in the multivariate model and then internal validation was done with bootstrap analysis with 1000 simulations. The outcome variable, clinical response to antihistamines, was evaluated with the UAS (Urticaria Activity Score) scale for seven days: "No response to antihistamines" was defined as UAS7 ≥7 points after at least one month with a maximum dose of antihistamines, while "Response to antiH1" was defined as UAS7 ≤6 points for at least three months with the use of antiH1. A total of 790 patients were included. Among the different models analyzed, the model that included age, angioedema, anxiety/depression, time with the disease, NSAIDs (Non-steroidal anti-inflammatory drugs) intolerance, and UAS7 baseline was considered the one with the best performance (accuracy 0.675, HL 0.87, AUC 0.727). The internal validation analyses demonstrated good consistency of the model. In conclusion, this prediction model identifies the probability of response to antihistamines in patients with chronic spontaneous urticaria. The model could be useful for a personalized therapeutic approach according to individual patient risk