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Clinical Evaluation and Outcome Measures of Chronic Spontaneous Urticaria and Chronic Inducible Urticaria

dc.contributor.authorWeller, Karsten
dc.contributor.authorPodder, Indrashis
dc.contributor.authorSalman, Andac
dc.contributor.authorGimenez-Arnau, Anna Maria
dc.contributor.authorNeisinger, Sophia
dc.contributor.authorAltrichter, Sabine
dc.date.accessioned2026-11-05T11:01:42Z
dc.date.issued2025
dc.description.abstractChronic spontaneous urticaria (CSU) and chronic inducible urticaria (CIndU) are debilitating skin diseases characterized by recurrent itchy wheals and/or angioedema, with a considerable negative impact on the patient's quality of life (QoL). Accurate clinical evaluation is important for diagnosis, disease monitoring, and guiding treatment. In CSU, it is primarily based on a detailed history, selected laboratory investigations, and patient-reported outcome measures (PROMs). In CIndU, objective provocation tests and critical threshold testing (CTT) are additionally useful. PROMs have emerged as indispensable tools in assessing disease activity, impact, and control from the patient's perspective. They enhance disease monitoring, support treatment decisions, and facilitate individualized, patient-centered care, and are recommended in routine clinical care and research. Recently, digital tools such as the CRUSE (Chronic Urticaria Self Evaluation) app have further advanced PROM integration, enabling real-time disease tracking and improved clinical workflows. In CIndU, objective provocation tests and CTT help to identify specific triggers and quantify individual stimulus thresholds. A structured approach based on the Assess-Act-Adjust principle facilitates optimal management by linking PROM results, diagnostic tests (eg, CTT), and other data with therapeutic strategies. Its implementation in urticaria care supports personalized medicine, aiming to achieve complete disease control and to normalize the patient's QoL. (c) 2025 Published by Elsevier Inc. on behalf of the American Academy of Allergy, Asthma & Immunology
dc.description.issue9
dc.description.sponsorshipK. Weller reports support for research projects from Novartis, Sanofi, and Takeda outside the submitted work, and personal fees from Biocryst, Biomarin, CSL Behring, Novartis, MOXIE, and Takeda outside the submitted work. He acts as a scientific advisor for MOXIE, which holds the copyright for many disease-specific patient-reported outcome measures (PROMs) in chronic spontaneous urticaria (CSU) and chronic inducible urticaria (CIndU). A. Salman reports speaker and/or advisor fees from AbbVie, Amgen, Bayer, Menarini, Novartis, Pfizer, and Sanofi outside the submitted work. A. M. Gimenez-Arnau is or recently was a speaker and/or advisor for and/or has received research funding from Almirall, Amgen, AstraZeneca, Avene, Blue-Print, Celldex, Escient Pharmaceutials, Genentech, GSK, Harmonic Bio, Incyte, Instituto Carlos III-FEDER, Jaspers, Leo Pharma, Menarini, Mitsubishi Tanabe Pharma, Noucor, Novartis, Sanofi-Regeneron, Septerna, Servier, Thermo Fisher Scientific, and Uriach Pharma. S. Neisinger was a speaker/advisor for Sanofi and Biocryst. S. Altrichter reports support for clinical trials/research funding/honorary support from Allakos, AstraZeneca, ALK, Biocryst, Blueprint, Celltrion, CSL Behring, Incyte, Kalvista, LEOPharma, Lilly, Menarini, Novartis, Phavaris, Sanofi, Takeda, and Thermo-Fisher outside the submitted work. She received nonfinancial support (linguistic translations) from MOXIE, which holds the copyright for many disease-specific PROMs in CSU and CIndU. I. Podder declares that he has no relevant conflicts of interest.
dc.description.volume13
dc.identifier.doi10.1016/j.jaip.2025.07.008
dc.identifier.issn2213-2198
dc.identifier.issn2213-2201
dc.identifier.urihttps://doi.org/10.1016/j.jaip.2025.07.008
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/10782
dc.identifier.wosWOS:001584046500003
dc.language.isoen
dc.publisherELSEVIER
dc.relation.fundingNovartis(Novartis)
dc.relation.fundingSanofi(Sanofi-Aventis)
dc.relation.fundingBiocryst
dc.relation.fundingBiomarin
dc.relation.fundingCSL Behring
dc.relation.fundingMOXIE
dc.relation.fundingTakeda(Takeda Pharmaceutical Company Ltd)
dc.relation.fundingAlmirall(Almirall)
dc.relation.fundingAmgen(Amgen)
dc.relation.fundingAstraZeneca(AstraZeneca)
dc.relation.fundingAvene
dc.relation.fundingBlue-Print
dc.relation.fundingCelldex
dc.relation.fundingEscient Pharmaceutials
dc.relation.fundingGenentech(Roche HoldingGenentech)
dc.relation.fundingGSK(GlaxoSmithKline)
dc.relation.fundingHarmonic Bio
dc.relation.fundingIncyte
dc.relation.fundingInstituto Carlos III-FEDER
dc.relation.fundingJaspers
dc.relation.fundingLeo Pharma(LEO Pharma)
dc.relation.fundingMenarini(Menarini Group)
dc.relation.fundingMitsubishi Tanabe Pharma(Mitsubishi Tanabe Pharma Corporation)
dc.relation.fundingNoucor
dc.relation.fundingSanofi-Regeneron(Regeneron)
dc.relation.fundingSepterna
dc.relation.fundingServier(Servier)
dc.relation.fundingThermo Fisher Scientific
dc.relation.fundingUriach Pharma(Dexcel Pharma)
dc.relation.fundingAllakos
dc.relation.fundingALK
dc.relation.fundingCelltrion
dc.relation.fundingKalvista
dc.relation.fundingLEOPharma(LEO Pharma)
dc.relation.fundingLilly(Eli Lilly)
dc.relation.fundingPhavaris
dc.relation.fundingThermo-Fisher
dc.relation.fundingNovartis
dc.relation.fundingSanofi
dc.relation.fundingTakeda
dc.relation.fundingAlmirall
dc.relation.fundingAmgen
dc.relation.fundingAstraZeneca
dc.relation.fundingGenentech
dc.relation.fundingGSK
dc.relation.fundingLeo Pharma
dc.relation.fundingMenarini
dc.relation.fundingMitsubishi Tanabe Pharma
dc.relation.fundingSanofi-Regeneron
dc.relation.fundingServier
dc.relation.fundingUriach Pharma
dc.relation.fundingLEOPharma
dc.relation.fundingLilly
dc.relation.hasversion10.1016/j.jaip.2025.07.008
dc.relation.ispartofJOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE
dc.subjectUrticaria
dc.subjectSpontaneous
dc.subjectInducible
dc.subjectCSU
dc.subjectCIndU
dc.subjectDisease activity
dc.subjectDisease control
dc.subjectQuality of life
dc.subjectPatient-reported outcome
dc.subjectPROM
dc.subjectProvocation
dc.subjectThreshold testing
dc.subjectEvaluation
dc.subjectDigital
dc.subjectApp
dc.subjectCRUSE
dc.subjectQUALITY-OF-LIFE
dc.subjectMINIMAL IMPORTANT DIFFERENCE
dc.subjectDISEASE-ACTIVITY
dc.subjectCHOLINERGIC URTICARIA
dc.subjectVALIDATION
dc.subjectINSTRUMENT
dc.subjectDIAGNOSIS
dc.subjectVERSION
dc.subjectCOLD
dc.subjectAllergy
dc.subjectImmunology
dc.titleClinical Evaluation and Outcome Measures of Chronic Spontaneous Urticaria and Chronic Inducible Urticaria
dc.typeArticle
oaire.citation.editionScience Citation Index Expanded (SCI-EXPANDED)
oaire.citation.issue9
oaire.citation.volume13
person.identifier.orcid0000-0002-9589-083X
person.identifier.ridHPG-4394-2023
person.identifier.ridAFH-5754-2022

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