Literature DB >> 19376667

Initial treatment and outcome of Candida glabrata versus Candida albicans bloodstream infection.

Michael J Klevay1, David L Horn, Dionissios Neofytos, Michael A Pfaller, Daniel J Diekema.   

Abstract

Candida glabrata is a common cause of bloodstream infection (BSI) and exhibits decreased susceptibility to fluconazole. We sought to determine whether patients with C. glabrata infection were at increased risk of inappropriate initial therapy and mortality compared with the more fluconazole-susceptible species Candida albicans by performing a matched case-control study using the Prospective Antifungal Therapy Alliance registry of invasive fungal infections. C. glabrata BSI patients were matched to those with C. albicans BSI by age, sex, and underlying illness after screening all C. glabrata patients entered into the registry from March 2004 through September 2007. Of 161 patients with C. glabrata BSI included and matched to 161 C. albicans patients, those with C. glabrata were less likely to receive an adequate dose of fluconazole as initial therapy (12% versus 52%, P < 0.05) and more likely to receive an echinocandin (44% versus 26%, P < 0.05) or inadequately dosed fluconazole (32% versus 8%, P < 0.05) as initial therapy. Although time to initiation of therapy did not differ by species (P = 0.2), time to receipt of adequate therapy was longer for those with C. glabrata BSI (P < 0.001). Overall, C. glabrata patients were more likely to receive inadequate initial therapy (34% versus 11%, P < 0.05), but 4-week mortality was no different between groups (30% for C. glabrata versus 29% for C. albicans, P = 0.80). We found hematologic malignancy, age greater than 60, the presence of a central venous catheter at diagnosis, mechanical ventilation, and dialysis dependence to be independent predictors of 4-week mortality. The lack of difference in mortality between species may reflect the overriding importance of host variables and/or a difference in virulence by species: further study is needed to investigate these hypotheses.

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Year:  2009        PMID: 19376667     DOI: 10.1016/j.diagmicrobio.2009.03.007

Source DB:  PubMed          Journal:  Diagn Microbiol Infect Dis        ISSN: 0732-8893            Impact factor:   2.803


  15 in total

1.  Frequency of decreased susceptibility and resistance to echinocandins among fluconazole-resistant bloodstream isolates of Candida glabrata.

Authors:  M A Pfaller; M Castanheira; S R Lockhart; A M Ahlquist; S A Messer; R N Jones
Journal:  J Clin Microbiol       Date:  2012-01-25       Impact factor: 5.948

2.  Deletion of ADA2 Increases Antifungal Drug Susceptibility and Virulence in Candida glabrata.

Authors:  Shang-Jie Yu; Ya-Lin Chang; Ying-Lien Chen
Journal:  Antimicrob Agents Chemother       Date:  2018-02-23       Impact factor: 5.191

3.  Management of invasive candidiasis in the intensive care unit.

Authors:  E Geoffrey Playford; Jeff Lipman; Tania C Sorrell
Journal:  Drugs       Date:  2010-05-07       Impact factor: 9.546

4.  Pros and Cons of Extrapolating Animal Data on Antifungal Pharmacodynamics to Humans.

Authors:  Scott W Mueller; Tyree H Kiser
Journal:  Curr Fungal Infect Rep       Date:  2011-03-26

5.  Variation in susceptibility of bloodstream isolates of Candida glabrata to fluconazole according to patient age and geographic location in the United States in 2001 to 2007.

Authors:  M A Pfaller; S A Messer; R J Hollis; L Boyken; S Tendolkar; J Kroeger; D J Diekema
Journal:  J Clin Microbiol       Date:  2009-08-05       Impact factor: 5.948

6.  Transcriptional profiling of Candida glabrata during phagocytosis by neutrophils and in the infected mouse spleen.

Authors:  Yuichi Fukuda; Huei-Fung Tsai; Timothy G Myers; John E Bennett
Journal:  Infect Immun       Date:  2013-02-12       Impact factor: 3.441

7.  Chromatin Loop Formation Induced by a Subtelomeric Protosilencer Represses EPA Genes in Candida glabrata.

Authors:  Eunice López-Fuentes; Grecia Hernández-Hernández; Leonardo Castanedo; Guadalupe Gutiérrez-Escobedo; Katarzyna Oktaba; Alejandro De Las Peñas; Irene Castaño
Journal:  Genetics       Date:  2018-07-12       Impact factor: 4.562

8.  Convergent Evolution of Calcineurin Pathway Roles in Thermotolerance and Virulence in Candida glabrata.

Authors:  Ying-Lien Chen; Jay H Konieczka; Deborah J Springer; Samantha E Bowen; Jing Zhang; Fitz Gerald S Silao; Alice Alma C Bungay; Ursela G Bigol; Marilou G Nicolas; Soman N Abraham; Dawn A Thompson; Aviv Regev; Joseph Heitman
Journal:  G3 (Bethesda)       Date:  2012-06-01       Impact factor: 3.154

9.  Host iron withholding demands siderophore utilization for Candida glabrata to survive macrophage killing.

Authors:  Tracy Nevitt; Dennis J Thiele
Journal:  PLoS Pathog       Date:  2011-03-17       Impact factor: 6.823

10.  Functional genomic analysis of Candida glabrata-macrophage interaction: role of chromatin remodeling in virulence.

Authors:  Maruti Nandan Rai; Sriram Balusu; Neelima Gorityala; Lakshmi Dandu; Rupinder Kaur
Journal:  PLoS Pathog       Date:  2012-08-16       Impact factor: 6.823

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