Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/21520
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dc.contributor.authorMeher-Homji, Zaal-
dc.contributor.authorTam, Constantine S-
dc.contributor.authorSiderov, Jim-
dc.contributor.authorSeymour, John Francis-
dc.contributor.authorHolmes, Natasha E-
dc.contributor.authorChua, Kyra Y L-
dc.contributor.authorPhillips, Elizabeth J-
dc.contributor.authorSlavin, Monica A-
dc.contributor.authorTrubiano, Jason-
dc.date2019-07-01-
dc.date.accessioned2019-08-12T05:01:11Z-
dc.date.available2019-08-12T05:01:11Z-
dc.date.issued2019-07-01-
dc.identifier.citationLeukemia & Lymphoma 2019; 60(14): 3455-3460en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/21520-
dc.description.abstractThe relationship between hematological malignancy and chemotherapy on the prevalence of antibiotic allergy label (AAL) is ill-defined. We performed a multicenter retrospective case-control study comparing AAL rates among cladribine-treated hairy cell leukemia (C-HCL) cases, non-HCL cladribine-treated controls (control-1), and fludarabine-treated controls (control-2). The prevalence of AALs in C-HCL patients was 60%, compared with control-1 (14%, p < .01) and control-2 patients (25%, p < .01). The predominant phenotype was maculopapular exanthem (92%). The drugs implicated in AAL causality in C-HCL patients included beta-lactams (81%), trimethoprim-sulfamethoxazole (58%), and allopurinol (69%). C-HCL patients demonstrate high rates of AAL, potentially due to immune dysregulation, impacting beta-lactam utilization.en
dc.language.isoeng-
dc.subjectHairy cell leukemiaen
dc.subjectallergyen
dc.subjectantibioticsen
dc.subjectcladribineen
dc.subjectmaculopapular exanthemen
dc.titleHigh prevalence of antibiotic allergies in cladribine-treated patients with hairy cell leukemia - lessons for immunopathogenesis and prescribing.en
dc.typeJournal Articleen
dc.identifier.journaltitleLeukemia & Lymphomaen
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Melbourne, Australiaen
dc.identifier.affiliationDepartment of Haematology, Peter MacCallum Cancer Centre, Melbourne, Australiaen
dc.identifier.affiliationPharmacy Department, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Infectious Diseases, Peter MacCallum Cancer Centre, Melbourne, Australiaen
dc.identifier.affiliationDepartment of Infectious Diseases, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Haematology, St Vincents Hospital, Melbourne, Australiaen
dc.identifier.affiliationDepartment of Haematology, Royal Melbourne Hospital, Melbourne, Australiaen
dc.identifier.affiliationDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN, USAen
dc.identifier.doi10.1080/10428194.2019.1633640en
dc.type.contentTexten
dc.identifier.orcid0000-0003-4636-3678en
dc.identifier.orcid0000-0002-9759-5017en
dc.identifier.orcid0000-0003-2188-6835en
dc.identifier.orcid0000-0001-8501-4054en
dc.identifier.orcid0000-0002-8443-314Xen
dc.identifier.orcid0000-0002-5111-6367en
dc.identifier.pubmedid31256738-
dc.type.austinJournal Article-
local.name.researcherChua, Kyra Y L-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
crisitem.author.deptMicrobiology-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptCentre for Antibiotic Allergy and Research-
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