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In Vitro Susceptibilities of Candida spp. to Caspofungin: Four Years of Global Surveillance
Caspofungin is being used increasingly as therapy for invasive candidiasis. Prospective sentinel surveillance for emergence of in vitro resistance to caspofungin among invasive Candida spp. isolates is indicated. We determined the in vitro activity of caspofungin against 8,197 invasive (bloodstream...
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Published in: | Journal of Clinical Microbiology 2006-03, Vol.44 (3), p.760-763 |
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description | Caspofungin is being used increasingly as therapy for invasive candidiasis. Prospective sentinel surveillance for emergence of in vitro resistance to caspofungin among invasive Candida spp. isolates is indicated. We determined the in vitro activity of caspofungin against 8,197 invasive (bloodstream or sterile-site) unique patient isolates of Candida collected from 91 medical centers worldwide from 1 January 2001 to 31 December 2004. We performed antifungal susceptibility testing according to the Clinical and Laboratory Standards Institute (CLSI, formerly NCCLS) M27-A2 method and used a 24-h prominent inhibition endpoint for determination of the MIC. Of 8,197 invasive Candida spp. isolates, species distribution was as follows: 54% Candida albicans, 14% C. glabrata, 14% C. parapsilosis, 11% C. tropicalis, 3% C. krusei, and 4% other Candida spp. Overall, caspofungin was very active against Candida (MIC₅₀/MIC₉₀, 0.03/0.25 [micro]g/ml; 98.2% were inhibited at a MIC of |
doi_str_mv | 10.1128/JCM.44.3.760-763.2006 |
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A ; Boyken, L ; Hollis, R. J ; Messer, S. A ; Tendolkar, S ; Diekema, D. J</creator><creatorcontrib>Pfaller, M. A ; Boyken, L ; Hollis, R. J ; Messer, S. A ; Tendolkar, S ; Diekema, D. J</creatorcontrib><description>Caspofungin is being used increasingly as therapy for invasive candidiasis. Prospective sentinel surveillance for emergence of in vitro resistance to caspofungin among invasive Candida spp. isolates is indicated. We determined the in vitro activity of caspofungin against 8,197 invasive (bloodstream or sterile-site) unique patient isolates of Candida collected from 91 medical centers worldwide from 1 January 2001 to 31 December 2004. We performed antifungal susceptibility testing according to the Clinical and Laboratory Standards Institute (CLSI, formerly NCCLS) M27-A2 method and used a 24-h prominent inhibition endpoint for determination of the MIC. Of 8,197 invasive Candida spp. isolates, species distribution was as follows: 54% Candida albicans, 14% C. glabrata, 14% C. parapsilosis, 11% C. tropicalis, 3% C. krusei, and 4% other Candida spp. Overall, caspofungin was very active against Candida (MIC₅₀/MIC₉₀, 0.03/0.25 [micro]g/ml; 98.2% were inhibited at a MIC of </=0.5 [micro]g/ml and 99.7% were inhibited at a MIC of </=1 [micro]g/ml). Results by species (expressed as MIC₅₀/MIC₉₀ and the percentage inhibited at </=1 [micro]g/ml) were as follows: C. albicans, 0.03/0.06, 99.9; C. glabrata, 0.03/0.06, 99.9; C. parapsilosis, 0.5/0.5, 99.0; C. tropicalis, 0.03/0.06, 99.7; C. krusei, 0.12/0.5, 99.0; and C. guilliermondii, 0.5/1, 94.4. Of the 25 isolates with caspofungin MICs of >1 [micro]g/ml, 12 isolates were C. parapsilosis, 6 isolates were C. guilliermondii, 2 isolates were C. rugosa, and 1 isolate each was C. albicans, C. glabrata, C. krusei, C. lusitaniae, and C. tropicalis. There was no significant change in caspofungin activity over the 4-year study period. Likewise, there was no difference in activity by geographic region. Caspofungin has excellent in vitro activity against invasive clinical isolates of Candida from centers worldwide. Our prospective sentinel surveillance reveals no evidence of emerging caspofungin resistance among invasive clinical isolates of CANDIDA:</description><identifier>ISSN: 0095-1137</identifier><identifier>EISSN: 1098-660X</identifier><identifier>EISSN: 1098-5530</identifier><identifier>DOI: 10.1128/JCM.44.3.760-763.2006</identifier><identifier>PMID: 16517851</identifier><identifier>CODEN: JCMIDW</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>Antifungal Agents - pharmacology ; Biological and medical sciences ; Candida - classification ; Candida - drug effects ; Candida - isolation & purification ; Candida albicans ; Candida rugosa ; Candidiasis - drug therapy ; Candidiasis - microbiology ; Drug Resistance, Fungal ; Echinocandins ; Fundamental and applied biological sciences. Psychology ; Humans ; In Vitro Techniques ; Infectious diseases ; Lipopeptides ; Medical sciences ; Microbial Sensitivity Tests ; Microbiology ; Miscellaneous ; Mycology ; Peptides, Cyclic - pharmacology ; Species Specificity ; Time Factors</subject><ispartof>Journal of Clinical Microbiology, 2006-03, Vol.44 (3), p.760-763</ispartof><rights>2006 INIST-CNRS</rights><rights>Copyright © 2006, American Society for Microbiology 2006</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c614t-5d7550cd9733c599d796738042063781b41776b046592128f94194ee4e4e48683</citedby><cites>FETCH-LOGICAL-c614t-5d7550cd9733c599d796738042063781b41776b046592128f94194ee4e4e48683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1393154/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1393154/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3188,3189,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17594809$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16517851$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pfaller, M. A</creatorcontrib><creatorcontrib>Boyken, L</creatorcontrib><creatorcontrib>Hollis, R. J</creatorcontrib><creatorcontrib>Messer, S. A</creatorcontrib><creatorcontrib>Tendolkar, S</creatorcontrib><creatorcontrib>Diekema, D. J</creatorcontrib><title>In Vitro Susceptibilities of Candida spp. to Caspofungin: Four Years of Global Surveillance</title><title>Journal of Clinical Microbiology</title><addtitle>J Clin Microbiol</addtitle><description>Caspofungin is being used increasingly as therapy for invasive candidiasis. Prospective sentinel surveillance for emergence of in vitro resistance to caspofungin among invasive Candida spp. isolates is indicated. We determined the in vitro activity of caspofungin against 8,197 invasive (bloodstream or sterile-site) unique patient isolates of Candida collected from 91 medical centers worldwide from 1 January 2001 to 31 December 2004. We performed antifungal susceptibility testing according to the Clinical and Laboratory Standards Institute (CLSI, formerly NCCLS) M27-A2 method and used a 24-h prominent inhibition endpoint for determination of the MIC. Of 8,197 invasive Candida spp. isolates, species distribution was as follows: 54% Candida albicans, 14% C. glabrata, 14% C. parapsilosis, 11% C. tropicalis, 3% C. krusei, and 4% other Candida spp. Overall, caspofungin was very active against Candida (MIC₅₀/MIC₉₀, 0.03/0.25 [micro]g/ml; 98.2% were inhibited at a MIC of </=0.5 [micro]g/ml and 99.7% were inhibited at a MIC of </=1 [micro]g/ml). Results by species (expressed as MIC₅₀/MIC₉₀ and the percentage inhibited at </=1 [micro]g/ml) were as follows: C. albicans, 0.03/0.06, 99.9; C. glabrata, 0.03/0.06, 99.9; C. parapsilosis, 0.5/0.5, 99.0; C. tropicalis, 0.03/0.06, 99.7; C. krusei, 0.12/0.5, 99.0; and C. guilliermondii, 0.5/1, 94.4. Of the 25 isolates with caspofungin MICs of >1 [micro]g/ml, 12 isolates were C. parapsilosis, 6 isolates were C. guilliermondii, 2 isolates were C. rugosa, and 1 isolate each was C. albicans, C. glabrata, C. krusei, C. lusitaniae, and C. tropicalis. There was no significant change in caspofungin activity over the 4-year study period. Likewise, there was no difference in activity by geographic region. Caspofungin has excellent in vitro activity against invasive clinical isolates of Candida from centers worldwide. Our prospective sentinel surveillance reveals no evidence of emerging caspofungin resistance among invasive clinical isolates of CANDIDA:</description><subject>Antifungal Agents - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Candida - classification</subject><subject>Candida - drug effects</subject><subject>Candida - isolation & purification</subject><subject>Candida albicans</subject><subject>Candida rugosa</subject><subject>Candidiasis - drug therapy</subject><subject>Candidiasis - microbiology</subject><subject>Drug Resistance, Fungal</subject><subject>Echinocandins</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>Infectious diseases</subject><subject>Lipopeptides</subject><subject>Medical sciences</subject><subject>Microbial Sensitivity Tests</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Mycology</subject><subject>Peptides, Cyclic - pharmacology</subject><subject>Species Specificity</subject><subject>Time Factors</subject><issn>0095-1137</issn><issn>1098-660X</issn><issn>1098-5530</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqFkU9v1DAQxS0EotvCRwBygVvCTPwv5oCEVrQUFXEoRSAOlpM4u66SONhJK749XnbVwglZlmX5N2_85hHyDKFALKvXH9efCsYKWkgBuRS0KAHEA7JCUFUuBHx7SFYAiueIVB6R4xivAZAxzh-TIxQcZcVxRX6cj9lXNwefXS6xsdPsate72dmY-S5bm7F1rcniNBXZ7NM9Tr5bxo0b32SnfgnZd2vCH_Ss97Xpk0q4sa7vzdjYJ-RRZ_ponx7OE3J1-v7L-kN-8fnsfP3uIm8EsjnnreQcmlZJShuuVCuVkLQCVoKgssKaoZSiBia4KpP1TjFUzFq2W5Wo6Al5u9edlnqwbWPHOZheT8ENJvzS3jj978votnrjbzRSRZGzJPDqIBD8z8XGWQ8uDWPnwvolaiElSiXhvyBKRMUVTyDfg03wMQbb3f0GQe_y0yk_zZimOuWXNtW7_FLd87-t3FcdAkvAywNgYmP6LqRBu3jPSa5YBSpx2Z7bus321gWrTRz0dTPcNU3Iiz3SGa_NJiSZq8sSkAICV8BL-hsMFbZq</recordid><startdate>20060301</startdate><enddate>20060301</enddate><creator>Pfaller, M. A</creator><creator>Boyken, L</creator><creator>Hollis, R. J</creator><creator>Messer, S. A</creator><creator>Tendolkar, S</creator><creator>Diekema, D. J</creator><general>American Society for Microbiology</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>M7N</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20060301</creationdate><title>In Vitro Susceptibilities of Candida spp. to Caspofungin: Four Years of Global Surveillance</title><author>Pfaller, M. A ; Boyken, L ; Hollis, R. J ; Messer, S. A ; Tendolkar, S ; Diekema, D. 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Psychology</topic><topic>Humans</topic><topic>In Vitro Techniques</topic><topic>Infectious diseases</topic><topic>Lipopeptides</topic><topic>Medical sciences</topic><topic>Microbial Sensitivity Tests</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Mycology</topic><topic>Peptides, Cyclic - pharmacology</topic><topic>Species Specificity</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pfaller, M. A</creatorcontrib><creatorcontrib>Boyken, L</creatorcontrib><creatorcontrib>Hollis, R. J</creatorcontrib><creatorcontrib>Messer, S. A</creatorcontrib><creatorcontrib>Tendolkar, S</creatorcontrib><creatorcontrib>Diekema, D. 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We performed antifungal susceptibility testing according to the Clinical and Laboratory Standards Institute (CLSI, formerly NCCLS) M27-A2 method and used a 24-h prominent inhibition endpoint for determination of the MIC. Of 8,197 invasive Candida spp. isolates, species distribution was as follows: 54% Candida albicans, 14% C. glabrata, 14% C. parapsilosis, 11% C. tropicalis, 3% C. krusei, and 4% other Candida spp. Overall, caspofungin was very active against Candida (MIC₅₀/MIC₉₀, 0.03/0.25 [micro]g/ml; 98.2% were inhibited at a MIC of </=0.5 [micro]g/ml and 99.7% were inhibited at a MIC of </=1 [micro]g/ml). Results by species (expressed as MIC₅₀/MIC₉₀ and the percentage inhibited at </=1 [micro]g/ml) were as follows: C. albicans, 0.03/0.06, 99.9; C. glabrata, 0.03/0.06, 99.9; C. parapsilosis, 0.5/0.5, 99.0; C. tropicalis, 0.03/0.06, 99.7; C. krusei, 0.12/0.5, 99.0; and C. guilliermondii, 0.5/1, 94.4. Of the 25 isolates with caspofungin MICs of >1 [micro]g/ml, 12 isolates were C. parapsilosis, 6 isolates were C. guilliermondii, 2 isolates were C. rugosa, and 1 isolate each was C. albicans, C. glabrata, C. krusei, C. lusitaniae, and C. tropicalis. There was no significant change in caspofungin activity over the 4-year study period. Likewise, there was no difference in activity by geographic region. Caspofungin has excellent in vitro activity against invasive clinical isolates of Candida from centers worldwide. Our prospective sentinel surveillance reveals no evidence of emerging caspofungin resistance among invasive clinical isolates of CANDIDA:</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>16517851</pmid><doi>10.1128/JCM.44.3.760-763.2006</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antifungal Agents - pharmacology Biological and medical sciences Candida - classification Candida - drug effects Candida - isolation & purification Candida albicans Candida rugosa Candidiasis - drug therapy Candidiasis - microbiology Drug Resistance, Fungal Echinocandins Fundamental and applied biological sciences. Psychology Humans In Vitro Techniques Infectious diseases Lipopeptides Medical sciences Microbial Sensitivity Tests Microbiology Miscellaneous Mycology Peptides, Cyclic - pharmacology Species Specificity Time Factors |
title | In Vitro Susceptibilities of Candida spp. to Caspofungin: Four Years of Global Surveillance |
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