Please use this identifier to cite or link to this item: http://hdl.handle.net/11054/1006
Title: Safety, clinical effectiveness and trough plasma concentrations of intravenous posaconazole in patients with haematological malignancies and/or undergoing allogeneic haematopoietic stem cell transplantion: off-trial experience.
Authors: Jeong, Wirawan
Haywood, Peter
Shanmuganathan, Naranie
Lindsay, Julian
Urbancic, Karen
Ananda-Rajah, Michelle R.
Chen, Sharon C.A.
Bajel, Ashish
Ritchie, David
Grigg, Andrew
Seymour, John F.
Peleg, Anton Y.
Kong, David C.M.
Slavin, Monica A.
Issue Date: 2016
Publisher: Oxford University Press
Place of publication: Oxford, UK
Publication Title: The Journal of Antimicrobial Chemotherapy
Volume: 71
Issue: 12
Start Page: 3540
End Page: 3547
Abstract: This study describes the safety, clinical effectiveness and trough plasma concentration (Cmin) of intravenous (iv) posaconazole, provided as part of Merck Sharp and Dohme Australia's Named Patient Programme (NPP) in non-clinical trial settings. METHODS: A multicentre, retrospective study on the NPP use of iv posaconazole between July 2014 and March 2015 across seven Australian hospitals. RESULTS: Seventy courses of iv posaconazole were prescribed and evaluated in 61 patients receiving treatment for haematological malignancy. Sixty-one courses were prescribed for prophylaxis against invasive fungal disease (IFD), the majority of which (59) were initiated in patients with gastrointestinal disturbances and/or intolerance to previous antifungals. The median (IQR) duration for prophylaxis was 10 (6-15) days. No breakthrough IFD was observed during or at cessation of iv posaconazole. Nine courses of iv posaconazole were prescribed for treatment of IFD with a median (IQR) duration of 19 (7-30) days. Improvement in signs and symptoms of IFD was observed in five cases at cessation of, and six cases at 30 days post-iv posaconazole. Cmin was measured in 39 courses of iv posaconazole, with the initial level taken [median (IQR)] 4 (3-7) days after commencing iv posaconazole. The median (IQR) of initial Cmin was 1.16 (0.69-2.06) mg/L. No severe adverse events specifically attributed to iv posaconazole were documented, although six courses were curtailed due to potential toxicity. CONCLUSIONS: This non-clinical trial experience suggests that iv posaconazole appeared to be safe and clinically effective for prophylaxis or treatment of IFD in patients receiving treatment for haematological malignancies.
URI: http://hdl.handle.net/11054/1006
ISSN: 0305-7453
DOI: 10.1093/jac/dkw322
Internal ID Number: 00966
Health Subject: ANTIFUNGAL AGENTS
HEMATOLOGIC NEOPLASMS
HUMANS
RETROSPECTIVE STUDIES
TREATMENT OUTCOME
TRIAZOLES
POSACONAZOLE
Type: Journal Article
Article
Appears in Collections:Research Output

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