Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/18111
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dc.contributor.authorUrbancic, Karen F-
dc.contributor.authorPisasale, D-
dc.contributor.authorWight, Joel C-
dc.contributor.authorTrubiano, Jason-
dc.date2018-07-21-
dc.date.accessioned2018-07-22T23:26:57Z-
dc.date.available2018-07-22T23:26:57Z-
dc.date.issued2018-07-21-
dc.identifier.citationTransplant infectious disease : an official journal of the Transplantation Society 2018: e12968-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/18111-
dc.description.abstractDapsone may be used for Pneumocystis jirovecii pneumonia (PJP) prophylaxis in haematology patients receiving immunosuppressive therapy or after hematopoietic stem cell transplant (HSCT) in the setting of trimethoprim-sulfamethoxazole (TMP-SMX) adverse drug reaction (ADR) history. Dapsone-induced haematological toxicities such as oxidative haemolysis may limit use in these patients and modern assessments of dapsone allergy cross-reactivity in non-HIV patients with a sulphonamide allergy are largely absent. The aim of this single-centre, retrospective study was to describe dapsone usage in haematology patients requiring PJP prophylaxis, including HSCT recipients, over a 12-month period in terms of indications, incidence of dapsone-attributed oxidative haemolysis, and immune cross-reactivity in those previously labelled with a sulphonamide allergy, as well as describing potential opportunities for first-line TMP-SMX PJP prophylaxis reintroduction. Out of 24 patients meeting the study inclusion criteria, 12 (50%) were receiving dapsone PJP prophylaxis post-HSCT. No cases of breakthrough PJP infection were noted. Sixteen patients (67%) were initiated on dapsone to avoid the perceived risk of further myelosuppression with TMP-SMX and 5 patients (21%) due to prior delayed immune-mediated allergy to TMP-SMX. None experienced rash with dapsone therapy. Six patients (25%) were successfully rechallenged on TMP-SMX, including one patient with prior TMP-SMX-associated rash. Four (17%) patients had confirmed oxidative haemolysis, all resulting in dapsone cessation. Dapsone PJP prophylaxis in haematology patients was effective and safe, with non-life threatening dapsone-related haemolysis noted in a small number. An absence of sulphonamide allergy cross-reactivity was noted, suggesting greater TMP-SMX rechallenges or desensitisation could be considered in those receiving dapsone. This article is protected by copyright. All rights reserved.-
dc.language.isoeng-
dc.subjectPneumocystis jirovecii pneumonia-
dc.subjectadverse drug reactions-
dc.subjectdapsone-
dc.subjecthaematopoietic stem cell transplantation-
dc.titleDapsone safety in haematology patients: pathways to optimising Pneumocystis jirovecii pneumonia prophylaxis in haematology malignancy and transplant recipients.-
dc.typeJournal Articleen_US
dc.identifier.journaltitleTransplant infectious disease : an official journal of the Transplantation Society-
dc.identifier.affiliationPharmacy Department, Austin Health, Heidelberg, Victoria, Australia-
dc.identifier.affiliationDepartment of Infectious Diseases, Austin Health, Heidelberg, Victoria, Australia-
dc.identifier.affiliationCentre for Antibiotic Allergy and Research, Austin Health, Heidelberg, Victoria, Australia-
dc.identifier.affiliationNational Centre for Infections in Cancer, National Health and Medical Research Council Centre of Research Excellence, Peter MacCallum Cancer Centre, Department of Oncology, University of Melbourne, Parkville, VIC, Australia-
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Parkville, VIC, Australia-
dc.identifier.affiliationDepartment of Clinical Haematology, Austin Health, Heidelberg, Victoria, Australia-
dc.identifier.doi10.1111/tid.12968-
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-5111-6367en
dc.identifier.orcid0000-0002-9275-578Xen
dc.identifier.pubmedid30030892-
dc.type.austinJournal Article-
local.name.researcherPisasale, Daisy-
item.languageiso639-1en-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
crisitem.author.deptPharmacy-
crisitem.author.deptPharmacy-
crisitem.author.deptClinical Haematology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptCentre for Antibiotic Allergy and Research-
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