Evidence map›Paper›PMID 42908253›Full record

ArticleClinical and translational allergy2026

NSAID Tolerance Can Be Restored in NECD Even in the Absence of Complete Remission of Urticaria.

Merve Hormet Igde, Pelin Korkmaz, Semra Demir, Osman Ozan Yegit, Derya Ünal, Merve Dilşad Atasever, Ayşe Feyza Aslan, Leyla Bölek, Selin Ece Güzel, Nevzat Kahveci and 5 more

Abstract read
In one paragraph

Article in Clinical and translational allergy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Merve Hormet IgdeDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0003-1940-3419
Pelin KorkmazDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0002-0225-2485
Semra DemirDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0003-3449-5868
Osman Ozan YegitDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0003-4256-6048
Derya ÜnalDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0001-9741-5939
Merve Dilşad AtaseverDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0003-3996-5929
Ayşe Feyza AslanDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Türkiye.
Leyla BölekDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0001-9844-3624
Selin Ece GüzelDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0002-1421-5964
Nevzat KahveciDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0001-7050-6101
Mehmet Emin SezginDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0002-7654-283X
Şule Çelik KamacıDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0001-7132-2400
Esra KayaDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Türkiye.
Bircan ErdenDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0009-0003-2943-4697
Asli GelincikDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0002-3524-9952

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimData on the course of nonsteroidal anti-inflammatory drug (NSAID) hypersensitivity in NSAID-exacerbated cutaneous disease (NECD) are limited. We aimed to evaluate NSAID tolerance in NECD patients with well-controlled urticaria.

methods142 patients with well-controlled urticaria [Urticaria Control Test (UCT) ≥ 12; Urticaria Activity Score over 7 days (UAS7) ≤ 6] underwent a single blind, placebo-controlled acetylsalicylic acid (ASA) provocation test. Patients were categorized into three groups based on their treatment; omalizumab, antihistamine, or no treatment.

resultsThe median age of the patients was 40 years (IQR 31.5-52), and 79.6% were female. The median disease duration of chronic spontaneous urticaria (CSU) was 4 years (IQR 2-8). The ASA provocation test was positive in 29 patients (20.4%). Positive patients had lower UCT and higher UAS7 scores (both p < 0.001). ASA provocation test positivity was more common in the antihistamine group compared to both the omalizumab (p = 0.001) and untreated groups (p < 0.001). ROC analysis showed that UCT ≤ 15 predicted ASA provocation test positivity with 72.4% sensitivity and 83.2% specificity, while UAS7 ≥ 4 predicted positivity with 72.4% sensitivity and 86.7% specificity. The negative predictive values (NPV) were 92.2% and 92.5%, respectively.

conclusionTo our knowledge, this is the first study to demonstrate, in a large NECD cohort, that NSAID tolerance can be achieved in patients with well-controlled urticaria under different treatment modalities, regardless of complete remission status. UCT ≤ 15 and UAS7 ≥ 4 are useful clinical predictors of provocation test positivity and, given their high NPVs, are particularly valuable for excluding positivity.

Identifiers

PMID42908253
PMCPMC13687787

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