Evidence map›Paper›PMID 42298678›Full record

ArticleAllergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology2026

Declining venom immunotherapy: patient characteristics and clinical outcomes.

Simon Ueberschaar, Axel Trautmann, Johanna Stoevesandt

Abstract read
In one paragraph

Article in Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology, 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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0citing papers 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

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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

3 authors.

Simon UeberschaarDepartment of Dermatology, Venereology, and Allergology, University Hospital Würzburg, Josef-Schneider-Straße 2, 97080, Würzburg, Germany.
Axel TrautmannDepartment of Dermatology, Venereology, and Allergology, University Hospital Würzburg, Josef-Schneider-Straße 2, 97080, Würzburg, Germany.
Johanna StoevesandtDepartment of Dermatology, Venereology, and Allergology, University Hospital Würzburg, Josef-Schneider-Straße 2, 97080, Würzburg, Germany. Stoevesandt_J@ukw.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA largely unknown proportion of Hymenoptera venom-allergic patients do not undergo venom immunotherapy (VIT) despite positive allergy testing and counselling. We aimed to identify factors associated with the refusal of VIT, and evaluate the natural course of venom allergy in untreated individuals.

methodsOut of 1163 candidates for VIT, 271 (23.3%) declined or postponed treatment for at least 12 months. Complete data from 166 of these patients, who were interviewed and counselled during routine follow-up, were available for retrospective evaluation.

resultsPatients declining VIT were significantly more likely to be female (P = 0.012) and had a lower grade of index sting-induced anaphylaxis (P < 0.001) compared to those who accepted treatment. Main reasons for deciding against VIT were that it was considered too time-consuming (39.8%) or perceived as unnecessary (24.1%). A minority of patients (6.6%) declined VIT due to fear of side effects; 7.2% perceived the VIT-associated risk as high to extremely high. Most (69.9%) reported routinely carrying an epinephrine autoinjector. The re-sting rate was 39.2% over a median follow-up of 5 years. Among 65 re-exposed patients, 13 (20%) reported an anaphylactic sting-reaction, with only two cases classified as severe. In no case did a severe relapse occur following a mild index sting reaction.

conclusionIn venom-allergic patients hesitant about VIT, treatment choices should be guided by a shared decision-making process considering risk factors for severe anaphylaxis and the degree of sting exposure, together with the patient's personal needs and preferences.

Indexed as

AnaphylaxisHoney beeNatural courseRisk factorShared decision makingTreatment adherenceVespula

Identifiers

PMID42298678
PMCPMC13270586

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.