Clinical Evaluation and Outcome Measures of Chronic Spontaneous Urticaria and Chronic Inducible Urticaria
| dc.contributor.author | Weller, Karsten | |
| dc.contributor.author | Podder, Indrashis | |
| dc.contributor.author | Salman, Andac | |
| dc.contributor.author | Gimenez-Arnau, Anna Maria | |
| dc.contributor.author | Neisinger, Sophia | |
| dc.contributor.author | Altrichter, Sabine | |
| dc.date.accessioned | 2026-11-05T11:01:42Z | |
| dc.date.issued | 2025 | |
| dc.description.abstract | Chronic 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.issue | 9 | |
| dc.description.sponsorship | K. 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.volume | 13 | |
| dc.identifier.doi | 10.1016/j.jaip.2025.07.008 | |
| dc.identifier.issn | 2213-2198 | |
| dc.identifier.issn | 2213-2201 | |
| dc.identifier.uri | https://doi.org/10.1016/j.jaip.2025.07.008 | |
| dc.identifier.uri | https://openaccess.acibadem.edu.tr/handle/11443/10782 | |
| dc.identifier.wos | WOS:001584046500003 | |
| dc.language.iso | en | |
| dc.publisher | ELSEVIER | |
| dc.relation.funding | Novartis(Novartis) | |
| dc.relation.funding | Sanofi(Sanofi-Aventis) | |
| dc.relation.funding | Biocryst | |
| dc.relation.funding | Biomarin | |
| dc.relation.funding | CSL Behring | |
| dc.relation.funding | MOXIE | |
| dc.relation.funding | Takeda(Takeda Pharmaceutical Company Ltd) | |
| dc.relation.funding | Almirall(Almirall) | |
| dc.relation.funding | Amgen(Amgen) | |
| dc.relation.funding | AstraZeneca(AstraZeneca) | |
| dc.relation.funding | Avene | |
| dc.relation.funding | Blue-Print | |
| dc.relation.funding | Celldex | |
| dc.relation.funding | Escient Pharmaceutials | |
| dc.relation.funding | Genentech(Roche HoldingGenentech) | |
| dc.relation.funding | GSK(GlaxoSmithKline) | |
| dc.relation.funding | Harmonic Bio | |
| dc.relation.funding | Incyte | |
| dc.relation.funding | Instituto Carlos III-FEDER | |
| dc.relation.funding | Jaspers | |
| dc.relation.funding | Leo Pharma(LEO Pharma) | |
| dc.relation.funding | Menarini(Menarini Group) | |
| dc.relation.funding | Mitsubishi Tanabe Pharma(Mitsubishi Tanabe Pharma Corporation) | |
| dc.relation.funding | Noucor | |
| dc.relation.funding | Sanofi-Regeneron(Regeneron) | |
| dc.relation.funding | Septerna | |
| dc.relation.funding | Servier(Servier) | |
| dc.relation.funding | Thermo Fisher Scientific | |
| dc.relation.funding | Uriach Pharma(Dexcel Pharma) | |
| dc.relation.funding | Allakos | |
| dc.relation.funding | ALK | |
| dc.relation.funding | Celltrion | |
| dc.relation.funding | Kalvista | |
| dc.relation.funding | LEOPharma(LEO Pharma) | |
| dc.relation.funding | Lilly(Eli Lilly) | |
| dc.relation.funding | Phavaris | |
| dc.relation.funding | Thermo-Fisher | |
| dc.relation.funding | Novartis | |
| dc.relation.funding | Sanofi | |
| dc.relation.funding | Takeda | |
| dc.relation.funding | Almirall | |
| dc.relation.funding | Amgen | |
| dc.relation.funding | AstraZeneca | |
| dc.relation.funding | Genentech | |
| dc.relation.funding | GSK | |
| dc.relation.funding | Leo Pharma | |
| dc.relation.funding | Menarini | |
| dc.relation.funding | Mitsubishi Tanabe Pharma | |
| dc.relation.funding | Sanofi-Regeneron | |
| dc.relation.funding | Servier | |
| dc.relation.funding | Uriach Pharma | |
| dc.relation.funding | LEOPharma | |
| dc.relation.funding | Lilly | |
| dc.relation.hasversion | 10.1016/j.jaip.2025.07.008 | |
| dc.relation.ispartof | JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE | |
| dc.subject | Urticaria | |
| dc.subject | Spontaneous | |
| dc.subject | Inducible | |
| dc.subject | CSU | |
| dc.subject | CIndU | |
| dc.subject | Disease activity | |
| dc.subject | Disease control | |
| dc.subject | Quality of life | |
| dc.subject | Patient-reported outcome | |
| dc.subject | PROM | |
| dc.subject | Provocation | |
| dc.subject | Threshold testing | |
| dc.subject | Evaluation | |
| dc.subject | Digital | |
| dc.subject | App | |
| dc.subject | CRUSE | |
| dc.subject | QUALITY-OF-LIFE | |
| dc.subject | MINIMAL IMPORTANT DIFFERENCE | |
| dc.subject | DISEASE-ACTIVITY | |
| dc.subject | CHOLINERGIC URTICARIA | |
| dc.subject | VALIDATION | |
| dc.subject | INSTRUMENT | |
| dc.subject | DIAGNOSIS | |
| dc.subject | VERSION | |
| dc.subject | COLD | |
| dc.subject | Allergy | |
| dc.subject | Immunology | |
| dc.title | Clinical Evaluation and Outcome Measures of Chronic Spontaneous Urticaria and Chronic Inducible Urticaria | |
| dc.type | Article | |
| oaire.citation.edition | Science Citation Index Expanded (SCI-EXPANDED) | |
| oaire.citation.issue | 9 | |
| oaire.citation.volume | 13 | |
| person.identifier.orcid | 0000-0002-9589-083X | |
| person.identifier.rid | HPG-4394-2023 | |
| person.identifier.rid | AFH-5754-2022 |
