Evidence map›Paper›PMID 40212290›Full record

ArticleFrontiers in allergy2025

Basophil activation test and lymphocyte transformation test in cefuroxime-induced anaphylactic reactions.

Andreas Glässner, Diana Dubrall, Gerda Wurpts, Philipp Deck, Günther Weindl, Caspar A Heubach, Amir S Yazdi, Bernhardt Sachs

Abstract read
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Article in Frontiers in allergy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Andreas Glässner *Research Division, Federal Institute for Drugs and Medical Devices (BfArM), Bonn, Germany.
Diana Dubrall *Research Division, Federal Institute for Drugs and Medical Devices (BfArM), Bonn, Germany.
Gerda WurptsDepartment of Dermatology and Allergology, RWTH University Hospital Aachen, Aachen, Germany.
Philipp DeckPharmacology and Toxicology, Pharmaceutical Institute, University of Bonn, Bonn, Germany.
Günther WeindlPharmacology and Toxicology, Pharmaceutical Institute, University of Bonn, Bonn, Germany.
Caspar A HeubachResearch Division, Federal Institute for Drugs and Medical Devices (BfArM), Bonn, Germany.
Amir S YazdiDepartment of Dermatology and Allergology, RWTH University Hospital Aachen, Aachen, Germany.
Bernhardt Sachs *Research Division, Federal Institute for Drugs and Medical Devices (BfArM), Bonn, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Cefuroxime allergy may present as a delayed-type reaction or as an immunoglobulin (Ig)E-mediated immediate-type anaphylactic reaction. The basophil activation test (BAT) is a diagnostic tool for cefuroxime-induced immediate-type reactions, whereas the lymphocyte transformation test (LTT) is typically applied in delayed-type drug allergy. This study aimed to compare the results of the BAT and LTT in 15 patients with cefuroxime-induced anaphylactic reactions considered as confirmed. The pharmacoepidemiological part aimed to analyze spontaneous reports of cefuroxime-associated anaphylactic reactions in the European adverse drug reaction database (EudraVigilance). Methods: In EudraVigilance, 668 reports of cefuroxime-associated anaphylactic reactions for the European Economic Area (EEA) between 2010 and 2023 were analyzed, with 182 (27.2%) of these reports originating from Germany. The BAT and the LTT were performed according to standard protocols. Except for one patient, all BAT were performed prior to the skin tests, whereas all LTT were performed thereafter. Results: Almost all reports were classified as serious (EEA, 99.3%; Germany, 98.9%). In 60.8% (EEA) and 66.9% (Germany) of reports with respective information, the reaction occurred after intravenous administration. BAT was performed in 12 of 15 patients (3/12 positive; sensitivity 25%), while LTT was performed in all 15 patients (7/15 positive; sensitivity 46.7%). Conclusions: Our analysis highlights the importance of cefuroxime-associated anaphylactic reactions, as almost all of the spontaneous reports were classified as serious. Neither a negative BAT nor LTT can rule out a sensitization in cefuroxime-induced anaphylactic reactions.

Indexed as

anaphylactic reactionbasophil activation testcefuroximelymphocyte transformation testspontaneous reports

Identifiers

PMID40212290
PMCPMC11983509

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