Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/35637
Title: Management, outcomes and predictors of mortality of Cryptococcus infection in patients without HIV: a multicentre study in 46 hospitals from Australia and New Zealand.
Austin Authors: Coussement, Julien;Heath, Christopher H;Roberts, Matthew B;Lane, Rebekah J;Spelman, Tim;Smibert, Olivia C ;Longhitano, Anthony;Morrissey, C Orla;Nield, Blake;Tripathy, Monica;Davis, Joshua S;Kennedy, Karina J;Lynar, Sarah A;Crawford, Lucy C;Crawford, Simeon J;Smith, Benjamin J;Gador-Whyte, Andrew P;Haywood, Rose;Mahony, Andrew A ;Howard, Julia C;Walls, Genevieve B;O'Kane, Gabrielle M;Broom, Matthew T;Keighley, Caitlin L;Bupha-Intr, Olivia;Cooley, Louise;O'Hern, Jennifer A;Jackson, Justin D;Morris, Arthur J;Bartolo, Caroline;Tramontana, Adrian R;Grimwade, Katherine C;Au Yeung, Victor;Chean, Roy;Woolnough, Emily;Teh, Benjamin W;Slavin, Monica A;Chen, Sharon C-A
Affiliation: Department of Infectious Diseases, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.;Department of Infectious Diseases, Guadeloupe University Hospital, Pointe-a-Pitre, Guadeloupe.
Department of Microbiology, PathWest Laboratory Medicine, and Department of Infectious Diseases, Fiona Stanley Hospital, Murdoch, WA, Australia.;Department of Infectious Diseases, Royal Perth Hospital, Perth, WA, Australia.
Royal Adelaide Hospital, Adelaide, SA, Australia.;Flinders Medical Centre, Bedford Park, SA, Australia.
Auckland City Hospital, Te Toka Tumai, New Zealand.
Department of Health Services Research, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.;Department of Clinical Neuroscience, Karolinska Institute, Stockholm, Sweden.;Burnet Institute, Melbourne, VIC, Australia.;The University of Melbourne Department of Surgery, St. Vincent's Hospital Melbourne, Fitzroy, VIC, Australia.
Austin Health
Monash Health, Clayton, VIC, Australia.
Department of Infectious Diseases, Alfred Health, Melbourne, VIC, Australia.;Department of Infectious Diseases, School of Translational Medicine, Monash University, Melbourne, VIC, Australia.
Royal Prince Alfred Hospital, Camperdown, NSW, Australia.
Gold Coast Hospital and Health Service, Southport, QLD, Australia.
John Hunter Hospital, Newcastle, NSW, Australia.
ACT Pathology, Canberra Health Services, Canberra, ACT, Australia.
Royal Darwin and Palmerston Hospitals, Darwin, NT, Australia.;Menzies School of Health Research, Darwin, NT, Australia.
Royal Darwin and Palmerston Hospitals, Darwin, NT, Australia.
Wollongong Hospital, Wollongong, NSW, Australia.
Eastern Health, Box Hill, VIC, Australia.
St Vincent's Hospital Melbourne, Melbourne, VIC, Australia.
The Prince of Wales Hospital, Sydney, NSW, Australia.
Bendigo Health, Bendigo, VIC, Australia.
Te Whatu Ora Waikato, Hamilton, New Zealand.
Middlemore Hospital, Te Whatu Ora Counties Manukau, Auckland, New Zealand.
Gosford Hospital, Gosford, NSW, Australia.;Wyong Hospital, Hamlyn Terrace, NSW, Australia.
North Shore Hospital, Te Whatu Ora Waitemata, Auckland, New Zealand.;Waitakere Hospital, Te Whatu Ora Waitemata, Auckland, New Zealand.
Southern IML Pathology, Wollongong, NSW, Australia.
Capital, Coast and Hutt Valley District, Wellington, New Zealand.
Royal Hobart Hospital, Hobart, TAS, Australia.
Royal Darwin and Palmerston Hospitals, Darwin, NT, Australia.;Launceston General Hospital, Launceston, TAS, Australia.
Albury Wodonga Health, Albury, VIC, Australia.
Auckland City Hospital, Te Toka Tumai, New Zealand.
Barwon Health, Geelong, VIC, Australia.
Western Health, Footscray, VIC, Australia.;Western Clinical School, Melbourne Medical School, the University of Melbourne, St Albans, VIC, Australia.
Tauranga Hospital, Hauora a Toi Bay of Plenty, Tauranga, New Zealand.;Whakatane Hospital, Hauora a Toi Bay of Plenty, Whakatane, New Zealand.
Ballarat Health Services, Ballarat, VIC, Australia.
Latrobe Regional Hospital, Traralgon, VIC, Australia.
St John of God Midland Public and Private Hospital, Midland, WA, Australia.
Department of Infectious Diseases, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.;Victorian Infectious Diseases Service, Royal Melbourne Hospital, Melbourne, VIC, Australia.
Centre for Infectious Diseases and Microbiology Laboratory Services, Institute of Clinical Pathology and Medical Research, New South Wales Health Pathology, Westmead Hospital, The University of Sydney, Sydney, NSW, Australia.
Issue Date: 18-Dec-2024
Date: 2024
Publication information: Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America 2024-12-18
Abstract: Limited data exist regarding outcomes of cryptococcosis in patients without HIV with few studies having compared outcomes of Cryptococcus gattii, versus C. neoformans, infection. We conducted a retrospective study in 46 Australian and New Zealand hospitals to determine the outcomes of cryptococcosis in patients without HIV diagnosed between 2015 and 2019, and compared outcomes of C. gattii versus C. neoformans infections. Multivariable analysis identified predictors of mortality within one year. Of 426 patients, one-year all-cause mortality was 21%. C. gattii infection was associated with a lower mortality than C. neoformans (adjusted odds ratio [OR]: 0.47, 95% confidence interval [CI]: 0.23-0.95), whilst severe neurological symptoms at presentation was the strongest predictor of death (adjusted OR: 8.46, 95% CI: 2.99-23.98). Almost all (99.5%) patients with central nervous system (CNS) infection received induction antifungal therapy versus 27.7% of isolated pulmonary cryptococcosis. The commonest regimen in CNS disease was liposomal amphotericin B with flucytosine (93.8%, mean duration 31 ± 13 days). Among patients with CNS cryptococcosis, C. gattii infection was associated with higher risk of immune reconstitution inflammatory response (C-IRIS) than C. neoformans (21% versus 3%, p<0.001). Nineteen patients received amphotericin B-based re-induction therapy for suspected relapse but none had microbiological relapse. Serum cryptococcal antigen positivity and lung imaging abnormalities resolved slowly (resolution at one year in 25% and 34% of patients, respectively). Compared with C. neoformans, C. gattii infection demonstrated lower mortality but higher C-IRIS risk in CNS infection. Severe neurological symptoms were the strongest predictor of mortality.
URI: https://ahro.austin.org.au/austinjspui/handle/1/35637
DOI: 10.1093/cid/ciae630
ORCID: 0000-0002-4302-6599
0000-0001-7850-6931
0000-0002-9918-1846
0000-0003-1597-2083
0000-0001-9286-0478
0000-0001-6496-5280
0000-0003-3104-1289
0009-0004-6214-5923
0000-0002-8409-9591
0000-0002-9027-5539
0000-0003-1612-2136
0000-0002-8892-3488
0000-0002-4542-8508
0000-0003-3899-8956
0000-0001-8258-414X
0000-0002-9385-9935
0000-0003-0213-5470
Journal: Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
PubMed URL: 39692570
ISSN: 1537-6591
Type: Journal Article
Subjects: Cryptococcus gattii
Cryptococcus neoformans
antifungal therapy
cryptococcosis
prognosis
Appears in Collections:Journal articles

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