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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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Published in:Journal of antimicrobial chemotherapy 2021-03, Vol.76 (4), p.1063-1069
Main Authors: 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
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container_issue 4
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container_title Journal of antimicrobial chemotherapy
container_volume 76
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
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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>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$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. 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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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