Christopher Heath

Prof. Christopher Heath

orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 April 2020 in mBio
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Journal Article
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NCNancy A. Chow
Nancy A. Chow
JMJose Munoz
Jose Munoz
LGLalitha Gade
Lalitha Gade
EBElizabeth L. Berkow
Elizabeth L. Berkow
XLXiao Li
Xiao Li
Christina CuomoChristina Cuomo
Christina Cuomo
In less than a decade, C. auris has emerged in health care settings worldwide; this species is capable of colonizing skin and causing outbreaks of invasive candidiasis. In contrast to other Candida species, C. auris is unique in its ability to spread via nosocomial transmission and its high rates of drug resistance. As part of the public health response, whole-genome sequencing has played a major role in characterizing transmission dynamics and detecting new C. auris introductions. Through a global collaboration, we assessed genome evolution of isolates of C. auris from 19 countries. Here, we described estimated timing of the expansion of each C. auris clade and of fluconazole resistance, characterized discrete phylogeographic population structure of each clade, and compared genome data to sensitivity measurements to describe how antifungal resistance mechanisms vary across the population. These efforts are critical for a sustained, robust public health response that effectively utilizes molecular epidemiology.

14 October 2021 in Journal of Hematology & Oncology
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Journal Article
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Livio PaganoLivio Pagano
Livio Pagano
JSJon Salmanton-García
Jon Salmanton-García
FMFrancesco Marchesi
Francesco Marchesi
Alessandro BuscaAlessandro Busca
Alessandro Busca
PCPaolo Corradini
Paolo Corradini
NANatasha Ali
Natasha Ali
Background: Patients with hematological malignancies (HM) are at high risk of mortality from SARS-CoV-2 disease 2019 (COVID-19). A better understanding of risk factors for adverse outcomes may improve clinical management in these patients. We therefore studied baseline characteristics of HM patients developing COVID-19 and analyzed predictors of mortality. Methods: The survey was supported by the Scientific Working Group Infection in Hematology of the European Hematology Association (EHA). Eligible for the analysis were adult patients with HM and laboratory-confirmed COVID-19 observed between March and December 2020. Results: The study sample includes 3801 cases, represented by lymphoproliferative (mainly non-Hodgkin lymphoma n = 1084, myeloma n = 684 and chronic lymphoid leukemia n = 474) and myeloproliferative malignancies (mainly acute myeloid leukemia n = 497 and myelodysplastic syndromes n = 279). Severe/critical COVID-19 was observed in 63.8% of patients (n = 2425). Overall, 2778 (73.1%) of the patients were hospitalized, 689 (18.1%) of whom were admitted to intensive care units (ICUs). Overall, 1185 patients (31.2%) died. The primary cause of death was COVID-19 in 688 patients (58.1%), HM in 173 patients (14.6%), and a combination of both COVID-19 and progressing HM in 155 patients (13.1%). Highest mortality was observed in acute myeloid leukemia (199/497, 40%) and myelodysplastic syndromes (118/279, 42.3%). The mortality rate significantly decreased between the first COVID-19 wave (March–May 2020) and the second wave (October–December 2020) (581/1427, 40.7% vs. 439/1773, 24.8%, p value < 0.0001). In the multivariable analysis, age, active malignancy, chronic cardiac disease, liver disease, renal impairment, smoking history, and ICU stay correlated with mortality. Acute myeloid leukemia was a higher mortality risk than lymphoproliferative diseases. Conclusions: This survey confirms that COVID-19 patients with HM are at high risk of lethal complications. However, improved COVID-19 prevention has reduced mortality despite an increase in the number of reported cases.

11 January 2023 in International Journal of Antimicrobial Agents
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Journal Article
Open access
JSJon Salmanton-García
Jon Salmanton-García
WAWing-Yan Au
Wing-Yan Au
MHMartin Hoenigl
Martin Hoenigl
LCLouis Yi Ann Chai
Louis Yi Ann Chai
HBHamid Badali
Hamid Badali
OCOliver A. Cornely
Oliver A. Cornely
Invasive fungal infections (IFIs) in Asia/Pacific are a particular threat to patients with malignancies, uncontrolled diabetes mellitus or undiagnosed/untreated human immunodeficiency virus infection and acquired immunodeficiency syndrome (HIV/AIDS). Adequate and early access to diagnostic tools and antifungals is essential for IFI clinical management and patient survival. Details on institution profile, self-perception on IFI, and access to microscopy, culture, serology, antigen detection, molecular testing, and therapeutic drug monitoring for IFI were collected in a survey. As of June 2022, 235 centres from 40 countries/territories in Asia/Pacific answered the questionnaire. More than half the centres were from six countries: India (25%), China (17%), Thailand (5%), Indonesia, Iran, and Japan (4% each). Candida spp. (93%) and Aspergillus spp. (75%) were considered the most relevant pathogens. Most institutions had access to microscopy (98%) or culture-based approaches (97%). Furthermore, 79% of centres had access to antigen detection, 66% to molecular assays, and 63% to antibody tests. Access to antifungals varied between countries/territories. At least one triazole was available in 93% of the reporting sites (voriconazole [89%] was the most common mould-active azole), whereas 80% had at least one amphotericin B formulation, and 72% had at least one echinocandin. According to the replies provided, the resources available for IFI diagnosis and management vary among Asia/Pacific countries/territories. Economical or geographical factors may play a key role in the incidence and clinical handling of this disease burden. Regional cooperation may be a good strategy to overcome shortcomings.

19 August 2019 in Internal Medicine Journal
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Journal Article
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COChong W. Ong
Chong W. Ong
SCSharon C.‐A. Chen
Sharon C.‐A. Chen
JCJulia E. Clark
Julia E. Clark
CHCatriona L. Halliday
Catriona L. Halliday
SKSarah Kidd
Sarah Kidd
O(on behalf of the Australian and New Zealand Mycoses Interest Group (ANZMIG); and the Hospital Infection Special Interest Group (HICSIG); both of the Australasian Society for Infectious Diseases (ASID).
on behalf of the Australian and New Zealand Mycoses Interest Group (ANZMIG); and the Hospital Infection Special Interest Group (HICSIG); both of the Australasian Society for Infectious Diseases (ASID).

1 January 2019 in Emerging Infectious Diseases
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Journal Article
Open access
CHChristopher Heath
Christopher Heath
JDJohn R. Dyer
John R. Dyer
SPStanley Pang
Stanley Pang
GCGeoffrey W. Coombs
Geoffrey W. Coombs
DGDianne J. Gardam
Dianne J. Gardam
Candida auris Sternal Osteomyelitis Diagnosis in Man from Kenya Visiting Australia, 2015

9 January 2015 in BMC Infectious Diseases
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Journal Article
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PBPeter Boan
Peter Boan
HTHui-Leen Tan
Hui-Leen Tan
JPJulie Pearson
Julie Pearson
GCGeoffrey Coombs
Geoffrey Coombs
CHChristopher Heath
Christopher Heath
JRJames Owen Robinson
James Owen Robinson
Panton Valentine Leukocidin (PVL) has been associated with invasive Staphylococcus aureus soft tissue and pneumonic infections. From September 2007 to January 2009 at Royal Perth Hospital we tested for the PVL gene in S. aureus isolates from an invasive site, a suspected PVL-related soft tissue infection and all MRSA isolates. We could access medical records for 141 PVL positive (PVL + ve) infections and compared these to a control group comprised of 148 PVL negative (PVL-ve) infections. In the PVL + ve group 62 isolates were MRSA (48 were ST93-MRSA-IV) and 79 isolates were methicillin-sensitive S. aureus, and in the PVL-ve group 56 were MRSA (50 were WA-MRSA strains) and 92 were methicillin-sensitive S. aureus. We found the presence of PVL to be significantly associated with younger age, aboriginality, intravenous drug use, community acquisition, shorter length of hospital stay and lower mortality at 1 year. Overall PVL + ve infections more often required surgical intervention (73.0% versus 44.6%, p < 0.001) and were less often polymicrobial (8.5% versus 41.2%, p < 0.001). PVL + ve isolates were more often susceptible to clindamycin (87.9% versus 73.0%, p = 0.002). This study demonstrates that PVL + ve infections are associated with a distinct clinical picture, predominantly pyogenic skin and soft tissue infections often requiring surgery, disproportionately affecting patients who are younger, indigenous or with fewer health-care risk factors.