Pharmacokinetics and Antifungal Activity of Echinocandins in Ascites Fluid of Critically Ill Patients
The pharmacokinetics and antifungal activity of the echinocandins anidulafungin (AFG), micafungin (MFG), and caspofungin (CAS) were assessed in ascites fluid and plasma of critically ill adults treated for suspected or proven invasive candidiasis. Ascites fluid was obtained from ascites drains or du...
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Veröffentlicht in: | Antimicrobial agents and chemotherapy 2021-06, Vol.65 (7), p.e0256520-e0256520 |
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creator | Welte, René Oberacher, Herbert Gasperetti, Tiziana Pfisterer, Hartwig Griesmacher, Andrea Santner, Tobias Lass-Flörl, Cornelia Hörtnagl, Caroline Leitner-Rupprich, Sandra Aigner, Maria Lorenz, Ingo Schmid, Stefan Edlinger, Michael Eller, Philipp Dankl, Daniel Joannidis, Michael Bellmann, Romuald |
description | The pharmacokinetics and antifungal activity of the echinocandins anidulafungin (AFG), micafungin (MFG), and caspofungin (CAS) were assessed in ascites fluid and plasma of critically ill adults treated for suspected or proven invasive candidiasis. Ascites fluid was obtained from ascites drains or during paracentesis. The antifungal activity of the echinocandins in ascites fluid was assessed by incubation of Candida albicans and Candida glabrata at concentrations of 0.03 to 16.00 μg/ml. In addition, ascites fluid samples obtained from our study patients were inoculated with the same isolates and evaluated for fungal growth. These patient samples had to be spiked with echinocandins to restore the original concentrations because echinocandins had been lost during sterile filtration. In ascites fluid specimens of 29 patients, echinocandin concentrations were below the simultaneous plasma levels. Serial sampling in 20 patients revealed a slower rise and decline of echinocandin concentrations in ascites fluid than in plasma. Proliferation of C. albicans in ascites fluid was slower than in culture medium and growth of C. glabrata was lacking, even in the absence of antifungals. In CAS-spiked ascites fluid samples, fungal CFU counts moderately declined, whereas spiking with AFG or MFG had no relevant effect. In ascites fluid of our study patients, echinocandin concentrations achieved by therapeutic doses did not result in a consistent eradication of C. albicans or C. glabrata. Thus, therapeutic doses of AFG, MFG, or CAS may result in ascites fluid concentrations preventing relevant proliferation of C. albicans and C. glabrata, but do not warrant reliable eradication. |
doi_str_mv | 10.1128/AAC.02565-20 |
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Ascites fluid was obtained from ascites drains or during paracentesis. The antifungal activity of the echinocandins in ascites fluid was assessed by incubation of Candida albicans and Candida glabrata at concentrations of 0.03 to 16.00 μg/ml. In addition, ascites fluid samples obtained from our study patients were inoculated with the same isolates and evaluated for fungal growth. These patient samples had to be spiked with echinocandins to restore the original concentrations because echinocandins had been lost during sterile filtration. In ascites fluid specimens of 29 patients, echinocandin concentrations were below the simultaneous plasma levels. Serial sampling in 20 patients revealed a slower rise and decline of echinocandin concentrations in ascites fluid than in plasma. Proliferation of C. albicans in ascites fluid was slower than in culture medium and growth of C. glabrata was lacking, even in the absence of antifungals. In CAS-spiked ascites fluid samples, fungal CFU counts moderately declined, whereas spiking with AFG or MFG had no relevant effect. In ascites fluid of our study patients, echinocandin concentrations achieved by therapeutic doses did not result in a consistent eradication of C. albicans or C. glabrata. Thus, therapeutic doses of AFG, MFG, or CAS may result in ascites fluid concentrations preventing relevant proliferation of C. albicans and C. glabrata, but do not warrant reliable eradication.</description><identifier>ISSN: 0066-4804</identifier><identifier>EISSN: 1098-6596</identifier><identifier>DOI: 10.1128/AAC.02565-20</identifier><identifier>PMID: 33972242</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Adult ; Antifungal Agents - pharmacology ; Antifungal Agents - therapeutic use ; Ascites - drug therapy ; Clinical Therapeutics ; Critical Illness ; Echinocandins ; Humans ; Lipopeptides ; Microbial Sensitivity Tests</subject><ispartof>Antimicrobial agents and chemotherapy, 2021-06, Vol.65 (7), p.e0256520-e0256520</ispartof><rights>Copyright © 2021 American Society for Microbiology.</rights><rights>Copyright © 2021 American Society for Microbiology. 2021 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a418t-c59b97ffcbff361cd0119b7b971ae75025b85237080135a5d28d01615c795f253</citedby><cites>FETCH-LOGICAL-a418t-c59b97ffcbff361cd0119b7b971ae75025b85237080135a5d28d01615c795f253</cites><orcidid>0000-0001-5537-3646 ; 0000-0003-2861-3258 ; 0000-0002-2946-7785</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8218616/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8218616/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33972242$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Welte, René</creatorcontrib><creatorcontrib>Oberacher, Herbert</creatorcontrib><creatorcontrib>Gasperetti, Tiziana</creatorcontrib><creatorcontrib>Pfisterer, Hartwig</creatorcontrib><creatorcontrib>Griesmacher, Andrea</creatorcontrib><creatorcontrib>Santner, Tobias</creatorcontrib><creatorcontrib>Lass-Flörl, Cornelia</creatorcontrib><creatorcontrib>Hörtnagl, Caroline</creatorcontrib><creatorcontrib>Leitner-Rupprich, Sandra</creatorcontrib><creatorcontrib>Aigner, Maria</creatorcontrib><creatorcontrib>Lorenz, Ingo</creatorcontrib><creatorcontrib>Schmid, Stefan</creatorcontrib><creatorcontrib>Edlinger, Michael</creatorcontrib><creatorcontrib>Eller, Philipp</creatorcontrib><creatorcontrib>Dankl, Daniel</creatorcontrib><creatorcontrib>Joannidis, Michael</creatorcontrib><creatorcontrib>Bellmann, Romuald</creatorcontrib><title>Pharmacokinetics and Antifungal Activity of Echinocandins in Ascites Fluid of Critically Ill Patients</title><title>Antimicrobial agents and chemotherapy</title><addtitle>Antimicrob Agents Chemother</addtitle><addtitle>Antimicrob Agents Chemother</addtitle><description>The pharmacokinetics and antifungal activity of the echinocandins anidulafungin (AFG), micafungin (MFG), and caspofungin (CAS) were assessed in ascites fluid and plasma of critically ill adults treated for suspected or proven invasive candidiasis. Ascites fluid was obtained from ascites drains or during paracentesis. The antifungal activity of the echinocandins in ascites fluid was assessed by incubation of Candida albicans and Candida glabrata at concentrations of 0.03 to 16.00 μg/ml. In addition, ascites fluid samples obtained from our study patients were inoculated with the same isolates and evaluated for fungal growth. These patient samples had to be spiked with echinocandins to restore the original concentrations because echinocandins had been lost during sterile filtration. In ascites fluid specimens of 29 patients, echinocandin concentrations were below the simultaneous plasma levels. Serial sampling in 20 patients revealed a slower rise and decline of echinocandin concentrations in ascites fluid than in plasma. Proliferation of C. albicans in ascites fluid was slower than in culture medium and growth of C. glabrata was lacking, even in the absence of antifungals. 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Thus, therapeutic doses of AFG, MFG, or CAS may result in ascites fluid concentrations preventing relevant proliferation of C. albicans and C. glabrata, but do not warrant reliable eradication.</description><subject>Adult</subject><subject>Antifungal Agents - pharmacology</subject><subject>Antifungal Agents - therapeutic use</subject><subject>Ascites - drug therapy</subject><subject>Clinical Therapeutics</subject><subject>Critical Illness</subject><subject>Echinocandins</subject><subject>Humans</subject><subject>Lipopeptides</subject><subject>Microbial Sensitivity Tests</subject><issn>0066-4804</issn><issn>1098-6596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc9rHCEUx6U0JJsft56LxwYyG3VWx7kUhmXTBgLJITmL4-iuW0dTdQL739ftpqE5xIv4_PB5vPcF4AtGc4wJv-665RwRymhF0Ccww6jlFaMt-wxmCDFWLThanIDTlLaovGmLjsFJXbcNIQsyA_phI-MoVfhlvc5WJSj9ADufrZn8WjrYqWxfbN7BYOBKbawPqhDWJ2g97JKyWSd44yY77IlltEUindvBW-fgg8xW-5zOwZGRLumL1_sMPN2sHpc_q7v7H7fL7q6SC8xzpWjbt40xqjemZlgNCOO2b0oNS93QMmXPKakbxBGuqaQD4QVhmKqmpYbQ-gx8P3ifp37Ugyq9o3TiOdpRxp0I0or3P95uxDq8CE4wZ5gVwbdXQQy_J52yGG1S2jnpdZiSIHS_aVxOQa8OqIohpajNWxuMxD4ZUZIRf5MRBBX88oDLNBKxDVP0ZRMfsV__H-NN_C-2-g9RZJZs</recordid><startdate>20210617</startdate><enddate>20210617</enddate><creator>Welte, René</creator><creator>Oberacher, Herbert</creator><creator>Gasperetti, Tiziana</creator><creator>Pfisterer, Hartwig</creator><creator>Griesmacher, Andrea</creator><creator>Santner, Tobias</creator><creator>Lass-Flörl, Cornelia</creator><creator>Hörtnagl, Caroline</creator><creator>Leitner-Rupprich, Sandra</creator><creator>Aigner, Maria</creator><creator>Lorenz, Ingo</creator><creator>Schmid, Stefan</creator><creator>Edlinger, Michael</creator><creator>Eller, Philipp</creator><creator>Dankl, Daniel</creator><creator>Joannidis, Michael</creator><creator>Bellmann, Romuald</creator><general>American Society for Microbiology</general><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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5537-3646</orcidid><orcidid>https://orcid.org/0000-0003-2861-3258</orcidid><orcidid>https://orcid.org/0000-0002-2946-7785</orcidid></search><sort><creationdate>20210617</creationdate><title>Pharmacokinetics and Antifungal Activity of Echinocandins in Ascites Fluid of Critically Ill Patients</title><author>Welte, René ; 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Ascites fluid was obtained from ascites drains or during paracentesis. The antifungal activity of the echinocandins in ascites fluid was assessed by incubation of Candida albicans and Candida glabrata at concentrations of 0.03 to 16.00 μg/ml. In addition, ascites fluid samples obtained from our study patients were inoculated with the same isolates and evaluated for fungal growth. These patient samples had to be spiked with echinocandins to restore the original concentrations because echinocandins had been lost during sterile filtration. In ascites fluid specimens of 29 patients, echinocandin concentrations were below the simultaneous plasma levels. Serial sampling in 20 patients revealed a slower rise and decline of echinocandin concentrations in ascites fluid than in plasma. Proliferation of C. albicans in ascites fluid was slower than in culture medium and growth of C. glabrata was lacking, even in the absence of antifungals. In CAS-spiked ascites fluid samples, fungal CFU counts moderately declined, whereas spiking with AFG or MFG had no relevant effect. In ascites fluid of our study patients, echinocandin concentrations achieved by therapeutic doses did not result in a consistent eradication of C. albicans or C. glabrata. Thus, therapeutic doses of AFG, MFG, or CAS may result in ascites fluid concentrations preventing relevant proliferation of C. albicans and C. glabrata, but do not warrant reliable eradication.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>33972242</pmid><doi>10.1128/AAC.02565-20</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-5537-3646</orcidid><orcidid>https://orcid.org/0000-0003-2861-3258</orcidid><orcidid>https://orcid.org/0000-0002-2946-7785</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Antifungal Agents - pharmacology Antifungal Agents - therapeutic use Ascites - drug therapy Clinical Therapeutics Critical Illness Echinocandins Humans Lipopeptides Microbial Sensitivity Tests |
title | Pharmacokinetics and Antifungal Activity of Echinocandins in Ascites Fluid of Critically Ill Patients |
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