Please use this identifier to cite or link to this item:
https://ahro.austin.org.au/austinjspui/handle/1/18111
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Urbancic, Karen F | - |
dc.contributor.author | Pisasale, D | - |
dc.contributor.author | Wight, Joel C | - |
dc.contributor.author | Trubiano, Jason | - |
dc.date | 2018-07-21 | - |
dc.date.accessioned | 2018-07-22T23:26:57Z | - |
dc.date.available | 2018-07-22T23:26:57Z | - |
dc.date.issued | 2018-07-21 | - |
dc.identifier.citation | Transplant infectious disease : an official journal of the Transplantation Society 2018: e12968 | - |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/18111 | - |
dc.description.abstract | Dapsone 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.iso | eng | - |
dc.subject | Pneumocystis jirovecii pneumonia | - |
dc.subject | adverse drug reactions | - |
dc.subject | dapsone | - |
dc.subject | haematopoietic stem cell transplantation | - |
dc.title | Dapsone safety in haematology patients: pathways to optimising Pneumocystis jirovecii pneumonia prophylaxis in haematology malignancy and transplant recipients. | - |
dc.type | Journal Article | en_US |
dc.identifier.journaltitle | Transplant infectious disease : an official journal of the Transplantation Society | - |
dc.identifier.affiliation | Pharmacy Department, Austin Health, Heidelberg, Victoria, Australia | - |
dc.identifier.affiliation | Department of Infectious Diseases, Austin Health, Heidelberg, Victoria, Australia | - |
dc.identifier.affiliation | Centre for Antibiotic Allergy and Research, Austin Health, Heidelberg, Victoria, Australia | - |
dc.identifier.affiliation | National 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.affiliation | Department of Medicine, University of Melbourne, Parkville, VIC, Australia | - |
dc.identifier.affiliation | Department of Clinical Haematology, Austin Health, Heidelberg, Victoria, Australia | - |
dc.identifier.doi | 10.1111/tid.12968 | - |
dc.type.content | Text | en_US |
dc.identifier.orcid | 0000-0002-5111-6367 | en |
dc.identifier.orcid | 0000-0002-9275-578X | en |
dc.identifier.pubmedid | 30030892 | - |
dc.type.austin | Journal Article | - |
local.name.researcher | Pisasale, Daisy | - |
item.languageiso639-1 | en | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.openairetype | Journal Article | - |
crisitem.author.dept | Pharmacy | - |
crisitem.author.dept | Pharmacy | - |
crisitem.author.dept | Clinical Haematology | - |
crisitem.author.dept | Olivia Newton-John Cancer Wellness and Research Centre | - |
crisitem.author.dept | Infectious Diseases | - |
crisitem.author.dept | Medicine (University of Melbourne) | - |
crisitem.author.dept | Centre for Antibiotic Allergy and Research | - |
Appears in Collections: | Journal articles |
Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.