Do high MICs predict the outcome in invasive fusariosis?
Abstract Background Invasive fusariosis (IF) affects mostly severely immunocompromised hosts and is associated with poor outcome. Since Fusarium species exhibit high MICs for most antifungal agents, this could explain the poor prognosis. However, a clear-cut correlation between MIC and outcome has n...
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creator | Nucci, Marcio Jenks, Jeffrey Thompson, George R Hoenigl, Martin dos Santos, Marielle Camargo Forghieri, Fabio Rico, Juan Carlos Bonuomo, Valentina López-Soria, Leyre Lass-Flörl, Cornelia Candoni, Anna Garcia-Vidal, Carolina Cattaneo, Chiara Buil, Jochem Rabagliati, Ricardo Roiz, Maria Pia Gudiol, Carlota Fracchiolla, Nicola Campos-Herrero, Maria Isolina Delia, Mario Farina, Francesca Fortun, Jesus Nadali, Gianpaolo Sastre, Enric Colombo, Arnaldo L Pérez Nadales, Elena Alastruey-Izquierdo, Ana Pagano, Livio |
description | Abstract
Background
Invasive fusariosis (IF) affects mostly severely immunocompromised hosts and is associated with poor outcome. Since Fusarium species exhibit high MICs for most antifungal agents, this could explain the poor prognosis. However, a clear-cut correlation between MIC and outcome has not been established.
Objective
To evaluate the correlation between MIC and outcome (6 week death rate) in patients with IF.
Methods
We performed a multicentre retrospective study of patients with IF who received treatment and had MIC levels determined by EUCAST or CLSI for the drug(s) used during treatment. We compared the MIC50 and MIC distribution among survivors and patients who died within 6 weeks from the diagnosis of IF.
Results
Among 88 patients with IF, 74 had haematological diseases. Primary treatment was monotherapy in 52 patients (voriconazole in 27) and combination therapy in 36 patients (liposomal amphotericin B + voriconazole in 23). The MIC50 and range for the five most frequent agents tested were: voriconazole 8 mg/L (range 0.5–64), amphotericin B 2 mg/L (range 0.25–64), posaconazole 16 mg/L (range 0.5–64), itraconazole 32 mg/L (range 4–64), and isavuconazole 32 mg/L (range 8–64). There was no difference in MIC50 and MIC distribution among survivors and patients who died. By contrast, persistent neutropenia and receipt of corticosteroids were strong predictors of 6 week mortality.
Conclusions
Our study did not show any correlation between MIC and mortality at 6 weeks in patients with IF. |
doi_str_mv | 10.1093/jac/dkaa516 |
format | Article |
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Background
Invasive fusariosis (IF) affects mostly severely immunocompromised hosts and is associated with poor outcome. Since Fusarium species exhibit high MICs for most antifungal agents, this could explain the poor prognosis. However, a clear-cut correlation between MIC and outcome has not been established.
Objective
To evaluate the correlation between MIC and outcome (6 week death rate) in patients with IF.
Methods
We performed a multicentre retrospective study of patients with IF who received treatment and had MIC levels determined by EUCAST or CLSI for the drug(s) used during treatment. We compared the MIC50 and MIC distribution among survivors and patients who died within 6 weeks from the diagnosis of IF.
Results
Among 88 patients with IF, 74 had haematological diseases. Primary treatment was monotherapy in 52 patients (voriconazole in 27) and combination therapy in 36 patients (liposomal amphotericin B + voriconazole in 23). The MIC50 and range for the five most frequent agents tested were: voriconazole 8 mg/L (range 0.5–64), amphotericin B 2 mg/L (range 0.25–64), posaconazole 16 mg/L (range 0.5–64), itraconazole 32 mg/L (range 4–64), and isavuconazole 32 mg/L (range 8–64). There was no difference in MIC50 and MIC distribution among survivors and patients who died. By contrast, persistent neutropenia and receipt of corticosteroids were strong predictors of 6 week mortality.
Conclusions
Our study did not show any correlation between MIC and mortality at 6 weeks in patients with IF.</description><identifier>ISSN: 0305-7453</identifier><identifier>EISSN: 1460-2091</identifier><identifier>DOI: 10.1093/jac/dkaa516</identifier><identifier>PMID: 33326585</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Antifungal Agents - therapeutic use ; Fusariosis - drug therapy ; Humans ; Itraconazole ; Microbial Sensitivity Tests ; Retrospective Studies ; Voriconazole - pharmacology</subject><ispartof>Journal of antimicrobial chemotherapy, 2021-03, Vol.76 (4), p.1063-1069</ispartof><rights>The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: journals.permissions@oup.com. 2020</rights><rights>The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-52c6b89e4c85dd62074513d32c2cde817658d98a0cecc49ae5a3facdfe1dccf73</citedby><cites>FETCH-LOGICAL-c357t-52c6b89e4c85dd62074513d32c2cde817658d98a0cecc49ae5a3facdfe1dccf73</cites><orcidid>0000-0001-8651-4405 ; 0000-0002-1653-2824 ; 0000-0003-4031-0778 ; 0000-0002-6959-5263</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1584,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33326585$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nucci, Marcio</creatorcontrib><creatorcontrib>Jenks, Jeffrey</creatorcontrib><creatorcontrib>Thompson, George R</creatorcontrib><creatorcontrib>Hoenigl, Martin</creatorcontrib><creatorcontrib>dos Santos, Marielle Camargo</creatorcontrib><creatorcontrib>Forghieri, Fabio</creatorcontrib><creatorcontrib>Rico, Juan Carlos</creatorcontrib><creatorcontrib>Bonuomo, Valentina</creatorcontrib><creatorcontrib>López-Soria, Leyre</creatorcontrib><creatorcontrib>Lass-Flörl, Cornelia</creatorcontrib><creatorcontrib>Candoni, Anna</creatorcontrib><creatorcontrib>Garcia-Vidal, Carolina</creatorcontrib><creatorcontrib>Cattaneo, Chiara</creatorcontrib><creatorcontrib>Buil, Jochem</creatorcontrib><creatorcontrib>Rabagliati, Ricardo</creatorcontrib><creatorcontrib>Roiz, Maria Pia</creatorcontrib><creatorcontrib>Gudiol, Carlota</creatorcontrib><creatorcontrib>Fracchiolla, Nicola</creatorcontrib><creatorcontrib>Campos-Herrero, Maria Isolina</creatorcontrib><creatorcontrib>Delia, Mario</creatorcontrib><creatorcontrib>Farina, Francesca</creatorcontrib><creatorcontrib>Fortun, Jesus</creatorcontrib><creatorcontrib>Nadali, Gianpaolo</creatorcontrib><creatorcontrib>Sastre, Enric</creatorcontrib><creatorcontrib>Colombo, Arnaldo L</creatorcontrib><creatorcontrib>Pérez Nadales, Elena</creatorcontrib><creatorcontrib>Alastruey-Izquierdo, Ana</creatorcontrib><creatorcontrib>Pagano, Livio</creatorcontrib><title>Do high MICs predict the outcome in invasive fusariosis?</title><title>Journal of antimicrobial chemotherapy</title><addtitle>J Antimicrob Chemother</addtitle><description>Abstract
Background
Invasive fusariosis (IF) affects mostly severely immunocompromised hosts and is associated with poor outcome. Since Fusarium species exhibit high MICs for most antifungal agents, this could explain the poor prognosis. However, a clear-cut correlation between MIC and outcome has not been established.
Objective
To evaluate the correlation between MIC and outcome (6 week death rate) in patients with IF.
Methods
We performed a multicentre retrospective study of patients with IF who received treatment and had MIC levels determined by EUCAST or CLSI for the drug(s) used during treatment. We compared the MIC50 and MIC distribution among survivors and patients who died within 6 weeks from the diagnosis of IF.
Results
Among 88 patients with IF, 74 had haematological diseases. Primary treatment was monotherapy in 52 patients (voriconazole in 27) and combination therapy in 36 patients (liposomal amphotericin B + voriconazole in 23). The MIC50 and range for the five most frequent agents tested were: voriconazole 8 mg/L (range 0.5–64), amphotericin B 2 mg/L (range 0.25–64), posaconazole 16 mg/L (range 0.5–64), itraconazole 32 mg/L (range 4–64), and isavuconazole 32 mg/L (range 8–64). There was no difference in MIC50 and MIC distribution among survivors and patients who died. By contrast, persistent neutropenia and receipt of corticosteroids were strong predictors of 6 week mortality.
Conclusions
Our study did not show any correlation between MIC and mortality at 6 weeks in patients with IF.</description><subject>Antifungal Agents - therapeutic use</subject><subject>Fusariosis - drug therapy</subject><subject>Humans</subject><subject>Itraconazole</subject><subject>Microbial Sensitivity Tests</subject><subject>Retrospective Studies</subject><subject>Voriconazole - pharmacology</subject><issn>0305-7453</issn><issn>1460-2091</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM9LwzAUx4Mobk5P3qUnEaQuaZo2PcmYvwYTL3oO2cury1yXmrQD_3sjmx6FB-_y4cOXDyHnjN4wWvHxSsPYfGgtWHFAhiwvaJrRih2SIeVUpGUu-ICchLCilBaikMdkwDnPCiHFkMg7lyzt-zJ5nk1D0no0FrqkW2Li-g5cg4ndxNvqYLeY1H3Q3rpgw-0pOar1OuDZ_o_I28P96_Qpnb88zqaTeQpclF0qMigWssIcpDCmyGicw7jhGWRgULIyzjCV1BQQIK80Cs1rDaZGZgDqko_I1c7bevfZY-hUYwPgeq036Pqgsryksiq5EBG93qHgXQgea9V622j_pRhVP6lUTKX2qSJ9sRf3iwbNH_vbJgKXO8D17b-mbziSchA</recordid><startdate>20210312</startdate><enddate>20210312</enddate><creator>Nucci, Marcio</creator><creator>Jenks, Jeffrey</creator><creator>Thompson, George R</creator><creator>Hoenigl, Martin</creator><creator>dos Santos, Marielle Camargo</creator><creator>Forghieri, Fabio</creator><creator>Rico, Juan Carlos</creator><creator>Bonuomo, Valentina</creator><creator>López-Soria, Leyre</creator><creator>Lass-Flörl, Cornelia</creator><creator>Candoni, Anna</creator><creator>Garcia-Vidal, Carolina</creator><creator>Cattaneo, Chiara</creator><creator>Buil, Jochem</creator><creator>Rabagliati, Ricardo</creator><creator>Roiz, Maria Pia</creator><creator>Gudiol, Carlota</creator><creator>Fracchiolla, Nicola</creator><creator>Campos-Herrero, Maria Isolina</creator><creator>Delia, Mario</creator><creator>Farina, Francesca</creator><creator>Fortun, Jesus</creator><creator>Nadali, Gianpaolo</creator><creator>Sastre, Enric</creator><creator>Colombo, Arnaldo L</creator><creator>Pérez Nadales, Elena</creator><creator>Alastruey-Izquierdo, Ana</creator><creator>Pagano, Livio</creator><general>Oxford University Press</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><orcidid>https://orcid.org/0000-0001-8651-4405</orcidid><orcidid>https://orcid.org/0000-0002-1653-2824</orcidid><orcidid>https://orcid.org/0000-0003-4031-0778</orcidid><orcidid>https://orcid.org/0000-0002-6959-5263</orcidid></search><sort><creationdate>20210312</creationdate><title>Do high MICs predict the outcome in invasive fusariosis?</title><author>Nucci, Marcio ; Jenks, Jeffrey ; Thompson, George R ; Hoenigl, Martin ; dos Santos, Marielle Camargo ; Forghieri, Fabio ; Rico, Juan Carlos ; Bonuomo, Valentina ; López-Soria, Leyre ; Lass-Flörl, Cornelia ; Candoni, Anna ; Garcia-Vidal, Carolina ; Cattaneo, Chiara ; Buil, Jochem ; Rabagliati, Ricardo ; Roiz, Maria Pia ; Gudiol, Carlota ; Fracchiolla, Nicola ; Campos-Herrero, Maria Isolina ; Delia, Mario ; Farina, Francesca ; Fortun, Jesus ; Nadali, Gianpaolo ; Sastre, Enric ; Colombo, Arnaldo L ; Pérez Nadales, Elena ; Alastruey-Izquierdo, Ana ; Pagano, Livio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-52c6b89e4c85dd62074513d32c2cde817658d98a0cecc49ae5a3facdfe1dccf73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antifungal Agents - therapeutic use</topic><topic>Fusariosis - drug therapy</topic><topic>Humans</topic><topic>Itraconazole</topic><topic>Microbial Sensitivity Tests</topic><topic>Retrospective Studies</topic><topic>Voriconazole - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nucci, Marcio</creatorcontrib><creatorcontrib>Jenks, Jeffrey</creatorcontrib><creatorcontrib>Thompson, George R</creatorcontrib><creatorcontrib>Hoenigl, Martin</creatorcontrib><creatorcontrib>dos Santos, Marielle Camargo</creatorcontrib><creatorcontrib>Forghieri, Fabio</creatorcontrib><creatorcontrib>Rico, Juan Carlos</creatorcontrib><creatorcontrib>Bonuomo, Valentina</creatorcontrib><creatorcontrib>López-Soria, Leyre</creatorcontrib><creatorcontrib>Lass-Flörl, Cornelia</creatorcontrib><creatorcontrib>Candoni, Anna</creatorcontrib><creatorcontrib>Garcia-Vidal, Carolina</creatorcontrib><creatorcontrib>Cattaneo, Chiara</creatorcontrib><creatorcontrib>Buil, Jochem</creatorcontrib><creatorcontrib>Rabagliati, Ricardo</creatorcontrib><creatorcontrib>Roiz, Maria Pia</creatorcontrib><creatorcontrib>Gudiol, Carlota</creatorcontrib><creatorcontrib>Fracchiolla, Nicola</creatorcontrib><creatorcontrib>Campos-Herrero, Maria Isolina</creatorcontrib><creatorcontrib>Delia, Mario</creatorcontrib><creatorcontrib>Farina, Francesca</creatorcontrib><creatorcontrib>Fortun, Jesus</creatorcontrib><creatorcontrib>Nadali, Gianpaolo</creatorcontrib><creatorcontrib>Sastre, Enric</creatorcontrib><creatorcontrib>Colombo, Arnaldo L</creatorcontrib><creatorcontrib>Pérez Nadales, Elena</creatorcontrib><creatorcontrib>Alastruey-Izquierdo, Ana</creatorcontrib><creatorcontrib>Pagano, Livio</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of antimicrobial chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nucci, Marcio</au><au>Jenks, Jeffrey</au><au>Thompson, George R</au><au>Hoenigl, Martin</au><au>dos Santos, Marielle Camargo</au><au>Forghieri, Fabio</au><au>Rico, Juan Carlos</au><au>Bonuomo, Valentina</au><au>López-Soria, Leyre</au><au>Lass-Flörl, Cornelia</au><au>Candoni, Anna</au><au>Garcia-Vidal, Carolina</au><au>Cattaneo, Chiara</au><au>Buil, Jochem</au><au>Rabagliati, Ricardo</au><au>Roiz, Maria Pia</au><au>Gudiol, Carlota</au><au>Fracchiolla, Nicola</au><au>Campos-Herrero, Maria Isolina</au><au>Delia, Mario</au><au>Farina, Francesca</au><au>Fortun, Jesus</au><au>Nadali, Gianpaolo</au><au>Sastre, Enric</au><au>Colombo, Arnaldo L</au><au>Pérez Nadales, Elena</au><au>Alastruey-Izquierdo, Ana</au><au>Pagano, Livio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Do high MICs predict the outcome in invasive fusariosis?</atitle><jtitle>Journal of antimicrobial chemotherapy</jtitle><addtitle>J Antimicrob Chemother</addtitle><date>2021-03-12</date><risdate>2021</risdate><volume>76</volume><issue>4</issue><spage>1063</spage><epage>1069</epage><pages>1063-1069</pages><issn>0305-7453</issn><eissn>1460-2091</eissn><abstract>Abstract
Background
Invasive fusariosis (IF) affects mostly severely immunocompromised hosts and is associated with poor outcome. Since Fusarium species exhibit high MICs for most antifungal agents, this could explain the poor prognosis. However, a clear-cut correlation between MIC and outcome has not been established.
Objective
To evaluate the correlation between MIC and outcome (6 week death rate) in patients with IF.
Methods
We performed a multicentre retrospective study of patients with IF who received treatment and had MIC levels determined by EUCAST or CLSI for the drug(s) used during treatment. We compared the MIC50 and MIC distribution among survivors and patients who died within 6 weeks from the diagnosis of IF.
Results
Among 88 patients with IF, 74 had haematological diseases. Primary treatment was monotherapy in 52 patients (voriconazole in 27) and combination therapy in 36 patients (liposomal amphotericin B + voriconazole in 23). The MIC50 and range for the five most frequent agents tested were: voriconazole 8 mg/L (range 0.5–64), amphotericin B 2 mg/L (range 0.25–64), posaconazole 16 mg/L (range 0.5–64), itraconazole 32 mg/L (range 4–64), and isavuconazole 32 mg/L (range 8–64). There was no difference in MIC50 and MIC distribution among survivors and patients who died. By contrast, persistent neutropenia and receipt of corticosteroids were strong predictors of 6 week mortality.
Conclusions
Our study did not show any correlation between MIC and mortality at 6 weeks in patients with IF.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>33326585</pmid><doi>10.1093/jac/dkaa516</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-8651-4405</orcidid><orcidid>https://orcid.org/0000-0002-1653-2824</orcidid><orcidid>https://orcid.org/0000-0003-4031-0778</orcidid><orcidid>https://orcid.org/0000-0002-6959-5263</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antifungal Agents - therapeutic use Fusariosis - drug therapy Humans Itraconazole Microbial Sensitivity Tests Retrospective Studies Voriconazole - pharmacology |
title | Do high MICs predict the outcome in invasive fusariosis? |
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