Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/35614
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dc.contributor.authorStehlin, Florian-
dc.contributor.authorProsty, Connor-
dc.contributor.authorMulé, Angela-
dc.contributor.authorAl-Otaibi, Ibtihal-
dc.contributor.authorColli, Luca Delli-
dc.contributor.authorGaffar, Judy-
dc.contributor.authorYu, Joshua-
dc.contributor.authorLanoue, Derek-
dc.contributor.authorCopaescu, Ana-Maria-
dc.contributor.authorBen-Shoshan, Moshe-
dc.date2024-
dc.date.accessioned2024-12-11T22:21:16Z-
dc.date.available2024-12-11T22:21:16Z-
dc.date.issued2024-12-03-
dc.identifier.citationThe journal of Allergy and Clinical Immunology. In Practice 2024-12-03en_US
dc.identifier.issn2213-2201-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/35614-
dc.description.abstractIbuprofen is a main cause of drug hypersensitivity reactions in children. The gold standard for diagnosis is the drug provocation test (DPT). We aimed to create a clinical risk-stratification tool to guide this high-risk procedure. We prospectively recruited children with suspected ibuprofen hypersensitivity between January 2017 and March 2024. Using stepwise bidirectional multivariable logistic regression, we calculated a predictive score for a positive ibuprofen DPT. Eighty-two patients with a median age of 5.9 years (IQR: 3.4;11.1) had an ibuprofen DPT. Eighteen (22.0%) had a positive challenge, with an anaphylactic reaction for 11 (61.1%). The I3A score (acronym for Ibuprofen, 3As: Angioedema, Anaphylaxis, Age, Cut-off of 3) encompasses the following items: Angioedema (2 points), Anaphylaxis (1 point), and Age at reaction ≥ 10 years old (1 point). The AUC of the I3A score was 0.84 and the optimal cut-off of <3 conferred a sensitivity of 84.4% % (95% confidence interval [95%CI] 66.7-100.0%) and a specificity of 83.3% (95%CI 75.0-92.2%). The negative predictive value was estimated at 94.7% (95%CI 90.0-100.0%), and the positive predictive value at 60.0% (95%CI 46.2%-76.2%). The relative risk of reacting to challenge in the group I3A 3-4 compared to 0-2 was 11.4 (95CI% 3.62-35.7, p<0.001). Anaphylaxis following DPT was observed in 9/25 [36.0% (95%CI 16.0-56.0%)] in the high-risk group as compared to 2/57 [3.5% (95%CI 0.0-8.8%)] in the low-risk group [relative risk 10.3 (95%CI 2.4-43.5)]. We generated a risk stratification tool to identify children at low-risk of reacting to ibuprofen challenges. Further validation is required in external cohorts.en_US
dc.language.isoeng-
dc.subjectdrug challengeen_US
dc.subjectibuprofenen_US
dc.subjectimmediate hypersensitivity reactionen_US
dc.subjectnon-steroidal anti-inflammatory drugen_US
dc.subjectrisk-stratification scoreen_US
dc.titleGuiding drug provocation testing for ibuprofen hypersensitivity in a pediatric population: Development of the I3A risk-stratification tool.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleThe journal of Allergy and Clinical Immunology. In Practiceen_US
dc.identifier.affiliationDivision of Allergy and Clinical Immunology, Department of Medicine, McGill University Health Center (MUHC), McGill University, Montreal, Quebec, Canada; Division of Immunology and Allergy, Department of Medicine, Lausanne University Hospital, Lausanne, Switzerland; The Research Institute of the McGill University Health Centre, McGill University, McGill University Health Centre (MUHC), Montreal, Quebec, Canada. Electronic address: florian.stehlin@chuv.ch.en_US
dc.identifier.affiliationDivision of Pediatric Allergy and Clinical Immunology, Department of Medicine, McGill University Health Center (MUHC), McGill University, Montreal, Quebec, Canada.en_US
dc.identifier.affiliationDivision of Allergy and Clinical Immunology, Department of Medicine, McGill University Health Center (MUHC), McGill University, Montreal, Quebec, Canada; College of Medicine, Princess Noura Bint Abdulrahman University, Riyadh, Saudi Arabia.en_US
dc.identifier.affiliationDivision of Pediatric Allergy and Clinical Immunology, Department of Medicine, McGill University Health Center (MUHC), McGill University, Montreal, Quebec, Canada.en_US
dc.identifier.affiliationDivision of Ophtalmology, Université de Montréal, Montreal, Quebec, Canada.en_US
dc.identifier.affiliationDepartment of Medicine, McMaster University, Hamilton ON, Canada.en_US
dc.identifier.affiliationDivision of Allergy and Clinical Immunology, Department of Medicine, McGill University Health Center (MUHC), McGill University, Montreal, Quebec, Canada; Department of Medicine, L'Hôpital Montfort, University of Ottawa, Ottawa, ON, Canada.en_US
dc.identifier.affiliationThe Research Institute of the McGill University Health Centre, McGill University, McGill University Health Centre (MUHC), Montreal, Quebec, Canada; Division of Pediatric Allergy and Clinical Immunology, Department of Medicine, McGill University Health Center (MUHC), McGill University, Montreal, Quebec, Canada.en_US
dc.identifier.affiliationInfectious Diseasesen_US
dc.identifier.doi10.1016/j.jaip.2024.11.022en_US
dc.type.contentTexten_US
dc.identifier.pubmedid39637941-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.languageiso639-1en-
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