Geographic and temporal trends in isolation and antifungal susceptibility of Candida parapsilosis: a global assessment from the ARTEMIS DISK Antifungal Surveillance Program, 2001 to 2005
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Outros Autores: | , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1128/JCM.02122-07 http://repositorio.unifesp.br/handle/11600/30464 |
Resumo: | We examined data from the ARTEMIS DISK Antifungal Surveillance Program to describe geographic and temporal trends in the isolation of Candida parapsilosis from clinical specimens and the in vitro susceptibilities of 9,371 isolates to fluconazole and voriconazole. We also report the in vitro susceptibility of bloodstream infection (BSI) isolates of C. parapsilosis to the echinocandins, anidulafungin, caspofungin, and micafungin. C. parapsilosis represented 6.6% of the 141,383 isolates of Candida collected from 2001 to 2005 and was most common among isolates from North America (14.3%) and Latin America (9.9%). High levels of susceptibility to both fluconazole (90.8 to 95.8%) and voriconazole (95.3 to 98.1%) were observed in all geographic regions with the exception of the Africa and Middle East region (79.3 and 85.8% susceptible to fluconazole and voriconazole, respectively). C parapsilosis was most often isolated from blood and skin and/or soft tissue specimens and from patients hospitalized in the medical, surgical, intensive care unit (ICU) and dermatology services. Notably, isolates from the surgical ICU were the least susceptible to fluconazole (86.3%). There was no evidence of increasing azole resistance over time among C. parapsilosis isolates tested from 2001 to 2005. of BSI isolates tested against the three echinocandins, 92, 99, and 100% were inhibited by concentrations of <= 2 mu g/ml of anidulafungin (621 isolates tested), caspofungin (1,447 isolates tested), and micafungin (539 isolates tested), respectively. C. parapsilosis is a ubiquitous pathogen that remains susceptible to the azoles and echinocandins; however, both the frequency of isolation and the resistance of C. parapsilosis to fluconazole and voriconazole may vary by geographic region and clinical service. |
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Geographic and temporal trends in isolation and antifungal susceptibility of Candida parapsilosis: a global assessment from the ARTEMIS DISK Antifungal Surveillance Program, 2001 to 2005We examined data from the ARTEMIS DISK Antifungal Surveillance Program to describe geographic and temporal trends in the isolation of Candida parapsilosis from clinical specimens and the in vitro susceptibilities of 9,371 isolates to fluconazole and voriconazole. We also report the in vitro susceptibility of bloodstream infection (BSI) isolates of C. parapsilosis to the echinocandins, anidulafungin, caspofungin, and micafungin. C. parapsilosis represented 6.6% of the 141,383 isolates of Candida collected from 2001 to 2005 and was most common among isolates from North America (14.3%) and Latin America (9.9%). High levels of susceptibility to both fluconazole (90.8 to 95.8%) and voriconazole (95.3 to 98.1%) were observed in all geographic regions with the exception of the Africa and Middle East region (79.3 and 85.8% susceptible to fluconazole and voriconazole, respectively). C parapsilosis was most often isolated from blood and skin and/or soft tissue specimens and from patients hospitalized in the medical, surgical, intensive care unit (ICU) and dermatology services. Notably, isolates from the surgical ICU were the least susceptible to fluconazole (86.3%). There was no evidence of increasing azole resistance over time among C. parapsilosis isolates tested from 2001 to 2005. of BSI isolates tested against the three echinocandins, 92, 99, and 100% were inhibited by concentrations of <= 2 mu g/ml of anidulafungin (621 isolates tested), caspofungin (1,447 isolates tested), and micafungin (539 isolates tested), respectively. C. parapsilosis is a ubiquitous pathogen that remains susceptible to the azoles and echinocandins; however, both the frequency of isolation and the resistance of C. parapsilosis to fluconazole and voriconazole may vary by geographic region and clinical service.Univ Iowa, Carver Coll Med, Dept Pathol, Iowa City, IA 52242 USAUniv Iowa, Carver Coll Med, Dept Med, Iowa City, IA 52242 USAGiles Sci Inc, Santa Barbara, CA USAUniv Malaya, Kuala Lumpur, MalaysiaUniversidade Federal de São Paulo, São Paulo, BrazilUniv Buenos Aires, Sch Med, Ctr Micol, Buenos Aires, DF, ArgentinaCardiff Univ, Cardiff, S Glam, WalesBaragwanath Hosp, ZA-2013 Johannesburg, South AfricaUniversidade Federal de São Paulo, EPM, São Paulo, BrazilWeb of ScienceAmer Soc MicrobiologyUniv IowaGiles Sci IncUniv MalayaUniversidade Federal de São Paulo (UNIFESP)Univ Buenos AiresCardiff UnivBaragwanath HospPfaller, M. A.Diekema, D. J.Gibbs, D. L.Newell, V. A.Ng, K. P.Colombo, A. [UNIFESP]Finquelievich, J.Barnes, R.Wadula, J.Global Antifungal Surveillance Grp2016-01-24T13:49:35Z2016-01-24T13:49:35Z2008-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion842-849application/pdfhttp://dx.doi.org/10.1128/JCM.02122-07Journal of Clinical Microbiology. Washington: Amer Soc Microbiology, v. 46, n. 3, p. 842-849, 2008.10.1128/JCM.02122-07WOS000254059800002.pdf0095-1137http://repositorio.unifesp.br/handle/11600/30464WOS:000254059800002engJournal of Clinical Microbiologyinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-31T17:10:55Zoai:repositorio.unifesp.br/:11600/30464Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-31T17:10:55Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Geographic and temporal trends in isolation and antifungal susceptibility of Candida parapsilosis: a global assessment from the ARTEMIS DISK Antifungal Surveillance Program, 2001 to 2005 |
title |
Geographic and temporal trends in isolation and antifungal susceptibility of Candida parapsilosis: a global assessment from the ARTEMIS DISK Antifungal Surveillance Program, 2001 to 2005 |
spellingShingle |
Geographic and temporal trends in isolation and antifungal susceptibility of Candida parapsilosis: a global assessment from the ARTEMIS DISK Antifungal Surveillance Program, 2001 to 2005 Pfaller, M. A. |
title_short |
Geographic and temporal trends in isolation and antifungal susceptibility of Candida parapsilosis: a global assessment from the ARTEMIS DISK Antifungal Surveillance Program, 2001 to 2005 |
title_full |
Geographic and temporal trends in isolation and antifungal susceptibility of Candida parapsilosis: a global assessment from the ARTEMIS DISK Antifungal Surveillance Program, 2001 to 2005 |
title_fullStr |
Geographic and temporal trends in isolation and antifungal susceptibility of Candida parapsilosis: a global assessment from the ARTEMIS DISK Antifungal Surveillance Program, 2001 to 2005 |
title_full_unstemmed |
Geographic and temporal trends in isolation and antifungal susceptibility of Candida parapsilosis: a global assessment from the ARTEMIS DISK Antifungal Surveillance Program, 2001 to 2005 |
title_sort |
Geographic and temporal trends in isolation and antifungal susceptibility of Candida parapsilosis: a global assessment from the ARTEMIS DISK Antifungal Surveillance Program, 2001 to 2005 |
author |
Pfaller, M. A. |
author_facet |
Pfaller, M. A. Diekema, D. J. Gibbs, D. L. Newell, V. A. Ng, K. P. Colombo, A. [UNIFESP] Finquelievich, J. Barnes, R. Wadula, J. Global Antifungal Surveillance Grp |
author_role |
author |
author2 |
Diekema, D. J. Gibbs, D. L. Newell, V. A. Ng, K. P. Colombo, A. [UNIFESP] Finquelievich, J. Barnes, R. Wadula, J. Global Antifungal Surveillance Grp |
author2_role |
author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Univ Iowa Giles Sci Inc Univ Malaya Universidade Federal de São Paulo (UNIFESP) Univ Buenos Aires Cardiff Univ Baragwanath Hosp |
dc.contributor.author.fl_str_mv |
Pfaller, M. A. Diekema, D. J. Gibbs, D. L. Newell, V. A. Ng, K. P. Colombo, A. [UNIFESP] Finquelievich, J. Barnes, R. Wadula, J. Global Antifungal Surveillance Grp |
description |
We examined data from the ARTEMIS DISK Antifungal Surveillance Program to describe geographic and temporal trends in the isolation of Candida parapsilosis from clinical specimens and the in vitro susceptibilities of 9,371 isolates to fluconazole and voriconazole. We also report the in vitro susceptibility of bloodstream infection (BSI) isolates of C. parapsilosis to the echinocandins, anidulafungin, caspofungin, and micafungin. C. parapsilosis represented 6.6% of the 141,383 isolates of Candida collected from 2001 to 2005 and was most common among isolates from North America (14.3%) and Latin America (9.9%). High levels of susceptibility to both fluconazole (90.8 to 95.8%) and voriconazole (95.3 to 98.1%) were observed in all geographic regions with the exception of the Africa and Middle East region (79.3 and 85.8% susceptible to fluconazole and voriconazole, respectively). C parapsilosis was most often isolated from blood and skin and/or soft tissue specimens and from patients hospitalized in the medical, surgical, intensive care unit (ICU) and dermatology services. Notably, isolates from the surgical ICU were the least susceptible to fluconazole (86.3%). There was no evidence of increasing azole resistance over time among C. parapsilosis isolates tested from 2001 to 2005. of BSI isolates tested against the three echinocandins, 92, 99, and 100% were inhibited by concentrations of <= 2 mu g/ml of anidulafungin (621 isolates tested), caspofungin (1,447 isolates tested), and micafungin (539 isolates tested), respectively. C. parapsilosis is a ubiquitous pathogen that remains susceptible to the azoles and echinocandins; however, both the frequency of isolation and the resistance of C. parapsilosis to fluconazole and voriconazole may vary by geographic region and clinical service. |
publishDate |
2008 |
dc.date.none.fl_str_mv |
2008-03-01 2016-01-24T13:49:35Z 2016-01-24T13:49:35Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1128/JCM.02122-07 Journal of Clinical Microbiology. Washington: Amer Soc Microbiology, v. 46, n. 3, p. 842-849, 2008. 10.1128/JCM.02122-07 WOS000254059800002.pdf 0095-1137 http://repositorio.unifesp.br/handle/11600/30464 WOS:000254059800002 |
url |
http://dx.doi.org/10.1128/JCM.02122-07 http://repositorio.unifesp.br/handle/11600/30464 |
identifier_str_mv |
Journal of Clinical Microbiology. Washington: Amer Soc Microbiology, v. 46, n. 3, p. 842-849, 2008. 10.1128/JCM.02122-07 WOS000254059800002.pdf 0095-1137 WOS:000254059800002 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Clinical Microbiology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
842-849 application/pdf |
dc.publisher.none.fl_str_mv |
Amer Soc Microbiology |
publisher.none.fl_str_mv |
Amer Soc Microbiology |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1824718189122027520 |