Use of isavuconazole in mucormycosis: a systematic review
Mucormycosis is an opportunistic fungal infection which is associated with poor prognosis. Only a few antifungals are available in the arsenal against mucormycosis. The global guidelines for diagnosing and managing mucormycosis recommend high doses of liposomal amphotericin B (LAmB) as the first-lin...
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Published in | BMC infectious diseases Vol. 25; no. 1; pp. 25 - 12 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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BioMed Central Ltd
06.01.2025
BioMed Central BMC |
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Abstract | Mucormycosis is an opportunistic fungal infection which is associated with poor prognosis. Only a few antifungals are available in the arsenal against mucormycosis. The global guidelines for diagnosing and managing mucormycosis recommend high doses of liposomal amphotericin B (LAmB) as the first-line treatment. Isavuconazole is another potential treatment option for mucormycosis.
This systematic review aims to consolidate and analyse existing evidence concerning the efficacy and safety of isavuconazole in treating mucormycosis alone or in combination with LAmB. For data aggregation, comprehensive searches were conducted across various electronic databases, such as PubMed, Science Direct, Trip, Google Scholar, the Cochrane Library, and Open-Gray. Furthermore, we explored the gray literature, employing tailored keywords. The reference lists of the selected articles were scrutinized to identify additional pertinent publications. Articles reporting any studies, case series, or case reports on any form of mucormycosis exclusively involving human subjects published in English were included. There were no time restrictions involved. We extracted crucial data, such as publication year, country, disease form, isavuconazole dosage, frequency, duration, overall outcomes, and reported adverse effects. A total of 31 articles, which included four case series, 24 case reports, one open-label trial, one randomized controlled trial, and one non-interventional registry study, were included in the final analysis. 135 adult patients and 14 children were treated with isavuconazole as primary monotherapy, primary combination therapy, nonprimary monotherapy, or nonprimary combination therapy. The mortality rate following LAmB monotherapy, amphotericin B plus azole, amphotericin B followed with azole, posaconazole only and isavuconazole only was 32%, 6.6%, 13.7%, 17.2% and 24.6%, respectively. The heterogeneity of the studies did not allow for a comparison of the different treatment strategies (primary mono- vs. primary combination, etc.).
The use of isavuconazole in combination therapies during the acute phase via intravenous administration alongside LAmB or other triazoles, followed by long-term monotherapy via the oral route, has yielded promising recovery rates. Adverse events associated with the use of isavuconazole are infrequently reported. |
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AbstractList | BackgroundMucormycosis is an opportunistic fungal infection which is associated with poor prognosis. Only a few antifungals are available in the arsenal against mucormycosis. The global guidelines for diagnosing and managing mucormycosis recommend high doses of liposomal amphotericin B (LAmB) as the first-line treatment. Isavuconazole is another potential treatment option for mucormycosis.Main bodyThis systematic review aims to consolidate and analyse existing evidence concerning the efficacy and safety of isavuconazole in treating mucormycosis alone or in combination with LAmB. For data aggregation, comprehensive searches were conducted across various electronic databases, such as PubMed, Science Direct, Trip, Google Scholar, the Cochrane Library, and Open-Gray. Furthermore, we explored the gray literature, employing tailored keywords. The reference lists of the selected articles were scrutinized to identify additional pertinent publications. Articles reporting any studies, case series, or case reports on any form of mucormycosis exclusively involving human subjects published in English were included. There were no time restrictions involved. We extracted crucial data, such as publication year, country, disease form, isavuconazole dosage, frequency, duration, overall outcomes, and reported adverse effects. A total of 31 articles, which included four case series, 24 case reports, one open-label trial, one randomized controlled trial, and one non-interventional registry study, were included in the final analysis. 135 adult patients and 14 children were treated with isavuconazole as primary monotherapy, primary combination therapy, nonprimary monotherapy, or nonprimary combination therapy. The mortality rate following LAmB monotherapy, amphotericin B plus azole, amphotericin B followed with azole, posaconazole only and isavuconazole only was 32%, 6.6%, 13.7%, 17.2% and 24.6%, respectively. The heterogeneity of the studies did not allow for a comparison of the different treatment strategies (primary mono- vs. primary combination, etc.).Short conclusionThe use of isavuconazole in combination therapies during the acute phase via intravenous administration alongside LAmB or other triazoles, followed by long-term monotherapy via the oral route, has yielded promising recovery rates. Adverse events associated with the use of isavuconazole are infrequently reported. Background Mucormycosis is an opportunistic fungal infection which is associated with poor prognosis. Only a few antifungals are available in the arsenal against mucormycosis. The global guidelines for diagnosing and managing mucormycosis recommend high doses of liposomal amphotericin B (LAmB) as the first-line treatment. Isavuconazole is another potential treatment option for mucormycosis. Main body This systematic review aims to consolidate and analyse existing evidence concerning the efficacy and safety of isavuconazole in treating mucormycosis alone or in combination with LAmB. For data aggregation, comprehensive searches were conducted across various electronic databases, such as PubMed, Science Direct, Trip, Google Scholar, the Cochrane Library, and Open-Gray. Furthermore, we explored the gray literature, employing tailored keywords. The reference lists of the selected articles were scrutinized to identify additional pertinent publications. Articles reporting any studies, case series, or case reports on any form of mucormycosis exclusively involving human subjects published in English were included. There were no time restrictions involved. We extracted crucial data, such as publication year, country, disease form, isavuconazole dosage, frequency, duration, overall outcomes, and reported adverse effects. A total of 31 articles, which included four case series, 24 case reports, one open-label trial, one randomized controlled trial, and one non-interventional registry study, were included in the final analysis. 135 adult patients and 14 children were treated with isavuconazole as primary monotherapy, primary combination therapy, nonprimary monotherapy, or nonprimary combination therapy. The mortality rate following LAmB monotherapy, amphotericin B plus azole, amphotericin B followed with azole, posaconazole only and isavuconazole only was 32%, 6.6%, 13.7%, 17.2% and 24.6%, respectively. The heterogeneity of the studies did not allow for a comparison of the different treatment strategies (primary mono- vs. primary combination, etc.). Short conclusion The use of isavuconazole in combination therapies during the acute phase via intravenous administration alongside LAmB or other triazoles, followed by long-term monotherapy via the oral route, has yielded promising recovery rates. Adverse events associated with the use of isavuconazole are infrequently reported. Keywords: Antifungals, Isavuconazole, Mucormycosis Abstract Background Mucormycosis is an opportunistic fungal infection which is associated with poor prognosis. Only a few antifungals are available in the arsenal against mucormycosis. The global guidelines for diagnosing and managing mucormycosis recommend high doses of liposomal amphotericin B (LAmB) as the first-line treatment. Isavuconazole is another potential treatment option for mucormycosis. Main body This systematic review aims to consolidate and analyse existing evidence concerning the efficacy and safety of isavuconazole in treating mucormycosis alone or in combination with LAmB. For data aggregation, comprehensive searches were conducted across various electronic databases, such as PubMed, Science Direct, Trip, Google Scholar, the Cochrane Library, and Open-Gray. Furthermore, we explored the gray literature, employing tailored keywords. The reference lists of the selected articles were scrutinized to identify additional pertinent publications. Articles reporting any studies, case series, or case reports on any form of mucormycosis exclusively involving human subjects published in English were included. There were no time restrictions involved. We extracted crucial data, such as publication year, country, disease form, isavuconazole dosage, frequency, duration, overall outcomes, and reported adverse effects. A total of 31 articles, which included four case series, 24 case reports, one open-label trial, one randomized controlled trial, and one non-interventional registry study, were included in the final analysis. 135 adult patients and 14 children were treated with isavuconazole as primary monotherapy, primary combination therapy, nonprimary monotherapy, or nonprimary combination therapy. The mortality rate following LAmB monotherapy, amphotericin B plus azole, amphotericin B followed with azole, posaconazole only and isavuconazole only was 32%, 6.6%, 13.7%, 17.2% and 24.6%, respectively. The heterogeneity of the studies did not allow for a comparison of the different treatment strategies (primary mono- vs. primary combination, etc.). Short conclusion The use of isavuconazole in combination therapies during the acute phase via intravenous administration alongside LAmB or other triazoles, followed by long-term monotherapy via the oral route, has yielded promising recovery rates. Adverse events associated with the use of isavuconazole are infrequently reported. Mucormycosis is an opportunistic fungal infection which is associated with poor prognosis. Only a few antifungals are available in the arsenal against mucormycosis. The global guidelines for diagnosing and managing mucormycosis recommend high doses of liposomal amphotericin B (LAmB) as the first-line treatment. Isavuconazole is another potential treatment option for mucormycosis. Mucormycosis is an opportunistic fungal infection which is associated with poor prognosis. Only a few antifungals are available in the arsenal against mucormycosis. The global guidelines for diagnosing and managing mucormycosis recommend high doses of liposomal amphotericin B (LAmB) as the first-line treatment. Isavuconazole is another potential treatment option for mucormycosis.BACKGROUNDMucormycosis is an opportunistic fungal infection which is associated with poor prognosis. Only a few antifungals are available in the arsenal against mucormycosis. The global guidelines for diagnosing and managing mucormycosis recommend high doses of liposomal amphotericin B (LAmB) as the first-line treatment. Isavuconazole is another potential treatment option for mucormycosis.This systematic review aims to consolidate and analyse existing evidence concerning the efficacy and safety of isavuconazole in treating mucormycosis alone or in combination with LAmB. For data aggregation, comprehensive searches were conducted across various electronic databases, such as PubMed, Science Direct, Trip, Google Scholar, the Cochrane Library, and Open-Gray. Furthermore, we explored the gray literature, employing tailored keywords. The reference lists of the selected articles were scrutinized to identify additional pertinent publications. Articles reporting any studies, case series, or case reports on any form of mucormycosis exclusively involving human subjects published in English were included. There were no time restrictions involved. We extracted crucial data, such as publication year, country, disease form, isavuconazole dosage, frequency, duration, overall outcomes, and reported adverse effects. A total of 31 articles, which included four case series, 24 case reports, one open-label trial, one randomized controlled trial, and one non-interventional registry study, were included in the final analysis. 135 adult patients and 14 children were treated with isavuconazole as primary monotherapy, primary combination therapy, nonprimary monotherapy, or nonprimary combination therapy. The mortality rate following LAmB monotherapy, amphotericin B plus azole, amphotericin B followed with azole, posaconazole only and isavuconazole only was 32%, 6.6%, 13.7%, 17.2% and 24.6%, respectively. The heterogeneity of the studies did not allow for a comparison of the different treatment strategies (primary mono- vs. primary combination, etc.).MAIN BODYThis systematic review aims to consolidate and analyse existing evidence concerning the efficacy and safety of isavuconazole in treating mucormycosis alone or in combination with LAmB. For data aggregation, comprehensive searches were conducted across various electronic databases, such as PubMed, Science Direct, Trip, Google Scholar, the Cochrane Library, and Open-Gray. Furthermore, we explored the gray literature, employing tailored keywords. The reference lists of the selected articles were scrutinized to identify additional pertinent publications. Articles reporting any studies, case series, or case reports on any form of mucormycosis exclusively involving human subjects published in English were included. There were no time restrictions involved. We extracted crucial data, such as publication year, country, disease form, isavuconazole dosage, frequency, duration, overall outcomes, and reported adverse effects. A total of 31 articles, which included four case series, 24 case reports, one open-label trial, one randomized controlled trial, and one non-interventional registry study, were included in the final analysis. 135 adult patients and 14 children were treated with isavuconazole as primary monotherapy, primary combination therapy, nonprimary monotherapy, or nonprimary combination therapy. The mortality rate following LAmB monotherapy, amphotericin B plus azole, amphotericin B followed with azole, posaconazole only and isavuconazole only was 32%, 6.6%, 13.7%, 17.2% and 24.6%, respectively. The heterogeneity of the studies did not allow for a comparison of the different treatment strategies (primary mono- vs. primary combination, etc.).The use of isavuconazole in combination therapies during the acute phase via intravenous administration alongside LAmB or other triazoles, followed by long-term monotherapy via the oral route, has yielded promising recovery rates. Adverse events associated with the use of isavuconazole are infrequently reported.SHORT CONCLUSIONThe use of isavuconazole in combination therapies during the acute phase via intravenous administration alongside LAmB or other triazoles, followed by long-term monotherapy via the oral route, has yielded promising recovery rates. Adverse events associated with the use of isavuconazole are infrequently reported. Mucormycosis is an opportunistic fungal infection which is associated with poor prognosis. Only a few antifungals are available in the arsenal against mucormycosis. The global guidelines for diagnosing and managing mucormycosis recommend high doses of liposomal amphotericin B (LAmB) as the first-line treatment. Isavuconazole is another potential treatment option for mucormycosis. This systematic review aims to consolidate and analyse existing evidence concerning the efficacy and safety of isavuconazole in treating mucormycosis alone or in combination with LAmB. For data aggregation, comprehensive searches were conducted across various electronic databases, such as PubMed, Science Direct, Trip, Google Scholar, the Cochrane Library, and Open-Gray. Furthermore, we explored the gray literature, employing tailored keywords. The reference lists of the selected articles were scrutinized to identify additional pertinent publications. Articles reporting any studies, case series, or case reports on any form of mucormycosis exclusively involving human subjects published in English were included. There were no time restrictions involved. We extracted crucial data, such as publication year, country, disease form, isavuconazole dosage, frequency, duration, overall outcomes, and reported adverse effects. A total of 31 articles, which included four case series, 24 case reports, one open-label trial, one randomized controlled trial, and one non-interventional registry study, were included in the final analysis. 135 adult patients and 14 children were treated with isavuconazole as primary monotherapy, primary combination therapy, nonprimary monotherapy, or nonprimary combination therapy. The mortality rate following LAmB monotherapy, amphotericin B plus azole, amphotericin B followed with azole, posaconazole only and isavuconazole only was 32%, 6.6%, 13.7%, 17.2% and 24.6%, respectively. The heterogeneity of the studies did not allow for a comparison of the different treatment strategies (primary mono- vs. primary combination, etc.). The use of isavuconazole in combination therapies during the acute phase via intravenous administration alongside LAmB or other triazoles, followed by long-term monotherapy via the oral route, has yielded promising recovery rates. Adverse events associated with the use of isavuconazole are infrequently reported. |
ArticleNumber | 25 |
Audience | Academic |
Author | Gunathilaka, Shobha Sanjeewani Bandara, Sachithra Ravindi Keragala, Reshani Kaumada Gunathilaka, Kasun Madhumal Wickramage, Sujanthi Senevirathne, Indika Sanjeewa Jayaweera, Asela Sampath |
Author_xml | – sequence: 1 givenname: Shobha Sanjeewani surname: Gunathilaka fullname: Gunathilaka, Shobha Sanjeewani – sequence: 2 givenname: Reshani Kaumada surname: Keragala fullname: Keragala, Reshani Kaumada – sequence: 3 givenname: Kasun Madhumal surname: Gunathilaka fullname: Gunathilaka, Kasun Madhumal – sequence: 4 givenname: Sujanthi surname: Wickramage fullname: Wickramage, Sujanthi – sequence: 5 givenname: Sachithra Ravindi surname: Bandara fullname: Bandara, Sachithra Ravindi – sequence: 6 givenname: Indika Sanjeewa surname: Senevirathne fullname: Senevirathne, Indika Sanjeewa – sequence: 7 givenname: Asela Sampath surname: Jayaweera fullname: Jayaweera, Asela Sampath |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/39762765$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.2147/IDR.S372546 10.1016/j.mmcr.2020.05.008 10.1016/S1473-3099(19)30312-3 10.3390/antibiotics10050487 10.1016/j.amjoto.2015.12.003 10.3389/fmed.2022.844880 10.1016/j.mmcr.2019.10.002 10.1007/s11046-018-0287-0 10.1016/j.idcr.2019.e00591 10.1016/j.ijid.2022.04.009 10.1111/tid.13469 10.1016/S1473-3099(16)00071-2 10.1186/s40360-018-0273-7 10.1016/S0140-6736(15)01159-9 10.2217/fmb-2022-0141 10.1080/08998280.2021.1935138 10.7759/cureus.25124 10.1111/myc.13412 10.1155/2018/6283701 10.1007/s11046-018-0281-6 10.7759/cureus.9610 10.31486/toj.21.0099 10.1097/INF.0000000000002671 10.1016/S0140-6736(21)00219-1 10.1086/599105 10.3111/13696998.2016.1164175 10.1371/journal.ppat.1010858 10.1016/j.mmcr.2019.06.004 10.1002/pbc.27281 10.1016/j.mmcr.2021.06.003 10.1007/s15010-013-0552-6 10.1155/2017/1925070 10.1016/j.mycmed.2020.101046 10.1093/ofid/ofad704 10.3390/jof9020166 10.1016/j.mmcr.2018.11.004 10.1128/JCM.03176-13 10.1155/2019/9839780 10.5005/jp-journals-10071-24443 10.1016/j.envres.2021.111643 |
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References | A Pomorska (10439_CR39) 2019; 184 AA Barg (10439_CR38) 2018; 65 10439_CR28 M Shafiq (10439_CR19) 2018; 10 10439_CR29 M Cornu (10439_CR40) 2018; 19 10439_CR24 D Horn (10439_CR47) 2016; 19 10439_CR22 10439_CR44 10439_CR21 B Spellberg (10439_CR4) 2009; 48 R Soman (10439_CR13) 2022; 120 L Ponce-Rosas (10439_CR23) 2022; 2022 L Ashkenazi-Hoffnung (10439_CR37) 2020; 39 J Ervens (10439_CR26) 2014; 42 Y Ahmed (10439_CR14) 2016; 37 10439_CR17 M Duarte (10439_CR27) 2022; 14 10439_CR16 FM Marty (10439_CR12) 2014; 8 D Peixoto (10439_CR25) 2014; 52 M Risum (10439_CR43) 2021; 10 10439_CR7 MV Batista (10439_CR45) 2023; 9 10439_CR8 10439_CR34 10439_CR9 10439_CR15 10439_CR36 10439_CR31 I Gupta (10439_CR1) 2023; 18 10439_CR30 10439_CR5 X Durà-Miralles (10439_CR18) 2020; 30 10439_CR33 P Sosnowska-Sienkiewicz (10439_CR41) 2022; 9 10439_CR6 10439_CR32 JA Maertens (10439_CR46) 2016; 387 BK Thielen (10439_CR20) 2019; 184 GR Thompson 3rd (10439_CR10) 2022; 65 A Ferdjallah (10439_CR35) 2021; 26 S Saseedharan (10439_CR48) 2023; 27 I Mahalaxmi (10439_CR2) 2021; 201 OA Cornely (10439_CR3) 2019; 19 FM Marty (10439_CR42) 2016; 16 JA Maertens (10439_CR11) 2021; 397 |
References_xml | – ident: 10439_CR9 doi: 10.2147/IDR.S372546 – ident: 10439_CR29 doi: 10.1016/j.mmcr.2020.05.008 – volume: 19 start-page: e405 issue: 12 year: 2019 ident: 10439_CR3 publication-title: Lancet Infect Dis doi: 10.1016/S1473-3099(19)30312-3 – volume: 10 start-page: 487 issue: 5 year: 2021 ident: 10439_CR43 publication-title: Antibiot [Internet] doi: 10.3390/antibiotics10050487 – ident: 10439_CR7 – volume: 37 start-page: 152 issue: 2 year: 2016 ident: 10439_CR14 publication-title: Am J Otolaryngol doi: 10.1016/j.amjoto.2015.12.003 – volume: 8 start-page: 21 year: 2014 ident: 10439_CR12 publication-title: Risk – volume: 9 start-page: 844880 year: 2022 ident: 10439_CR41 publication-title: Front Med doi: 10.3389/fmed.2022.844880 – ident: 10439_CR32 doi: 10.1016/j.mmcr.2019.10.002 – volume: 184 start-page: 81 issue: 1 year: 2019 ident: 10439_CR39 publication-title: Mycopathologia doi: 10.1007/s11046-018-0287-0 – ident: 10439_CR17 doi: 10.1016/j.idcr.2019.e00591 – volume: 120 start-page: 177 year: 2022 ident: 10439_CR13 publication-title: Int J Infect Dis [Internet] doi: 10.1016/j.ijid.2022.04.009 – ident: 10439_CR36 doi: 10.1111/tid.13469 – volume: 16 start-page: 828 issue: 7 year: 2016 ident: 10439_CR42 publication-title: Lancet Infect Dis doi: 10.1016/S1473-3099(16)00071-2 – volume: 10 start-page: e2547 year: 2018 ident: 10439_CR19 publication-title: Cureus – volume: 19 start-page: 81 issue: 1 year: 2018 ident: 10439_CR40 publication-title: BMC Pharmacol Toxicol doi: 10.1186/s40360-018-0273-7 – volume: 387 start-page: 760 issue: 10020 year: 2016 ident: 10439_CR46 publication-title: Lancet [Internet] doi: 10.1016/S0140-6736(15)01159-9 – volume: 18 start-page: 217 issue: 3 year: 2023 ident: 10439_CR1 publication-title: Future Microbiol doi: 10.2217/fmb-2022-0141 – ident: 10439_CR15 doi: 10.1080/08998280.2021.1935138 – ident: 10439_CR28 doi: 10.7759/cureus.25124 – volume: 65 start-page: 186 issue: 2 year: 2022 ident: 10439_CR10 publication-title: Mycoses doi: 10.1111/myc.13412 – ident: 10439_CR31 doi: 10.1155/2018/6283701 – volume: 184 start-page: 121 issue: 1 year: 2019 ident: 10439_CR20 publication-title: Mycopathologia doi: 10.1007/s11046-018-0281-6 – volume: 2022 start-page: 2537186 year: 2022 ident: 10439_CR23 publication-title: Case Rep Infect Dis – ident: 10439_CR16 doi: 10.7759/cureus.9610 – ident: 10439_CR33 doi: 10.31486/toj.21.0099 – volume: 39 start-page: 718 issue: 8 year: 2020 ident: 10439_CR37 publication-title: Pediatr Infect Dis J doi: 10.1097/INF.0000000000002671 – ident: 10439_CR8 – ident: 10439_CR6 – volume: 397 start-page: 499 issue: 10273 year: 2021 ident: 10439_CR11 publication-title: Lancet doi: 10.1016/S0140-6736(21)00219-1 – volume: 14 start-page: e24932 year: 2022 ident: 10439_CR27 publication-title: Cureus – volume: 48 start-page: 1743 issue: 12 year: 2009 ident: 10439_CR4 publication-title: Clin Infect Dis doi: 10.1086/599105 – volume: 19 start-page: 728 issue: 7 year: 2016 ident: 10439_CR47 publication-title: J Med Econ doi: 10.3111/13696998.2016.1164175 – ident: 10439_CR5 doi: 10.1371/journal.ppat.1010858 – ident: 10439_CR24 doi: 10.1016/j.mmcr.2019.06.004 – volume: 65 start-page: e27281 issue: 10 year: 2018 ident: 10439_CR38 publication-title: Pediatr Blood Cancer doi: 10.1002/pbc.27281 – ident: 10439_CR22 doi: 10.1016/j.mmcr.2021.06.003 – volume: 42 start-page: 429 issue: 2 year: 2014 ident: 10439_CR26 publication-title: Infection doi: 10.1007/s15010-013-0552-6 – ident: 10439_CR34 doi: 10.1155/2017/1925070 – volume: 30 start-page: 101046 issue: 4 year: 2020 ident: 10439_CR18 publication-title: J Mycol Med doi: 10.1016/j.mycmed.2020.101046 – ident: 10439_CR44 doi: 10.1093/ofid/ofad704 – volume: 9 start-page: 166 issue: 2 year: 2023 ident: 10439_CR45 publication-title: J Fungi doi: 10.3390/jof9020166 – ident: 10439_CR30 doi: 10.1016/j.mmcr.2018.11.004 – volume: 26 start-page: 863 issue: 8 year: 2021 ident: 10439_CR35 publication-title: J Pediatr Pharmacol Ther JPPT off J PPAG – volume: 52 start-page: 1016 issue: 3 year: 2014 ident: 10439_CR25 publication-title: J Clin Microbiol doi: 10.1128/JCM.03176-13 – ident: 10439_CR21 doi: 10.1155/2019/9839780 – volume: 27 start-page: 260 issue: 4 year: 2023 ident: 10439_CR48 publication-title: Indian J Crit Care Med [Internet] doi: 10.5005/jp-journals-10071-24443 – volume: 201 start-page: 111643 year: 2021 ident: 10439_CR2 publication-title: Environ Res doi: 10.1016/j.envres.2021.111643 |
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Snippet | Mucormycosis is an opportunistic fungal infection which is associated with poor prognosis. Only a few antifungals are available in the arsenal against... Background Mucormycosis is an opportunistic fungal infection which is associated with poor prognosis. Only a few antifungals are available in the arsenal... BackgroundMucormycosis is an opportunistic fungal infection which is associated with poor prognosis. Only a few antifungals are available in the arsenal... Abstract Background Mucormycosis is an opportunistic fungal infection which is associated with poor prognosis. Only a few antifungals are available in the... |
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SubjectTerms | Adult Aged Amphotericin B Amphotericin B - administration & dosage Amphotericin B - therapeutic use Antifungal agents Antifungal Agents - administration & dosage Antifungal Agents - therapeutic use Antifungals Antiparasitic agents Biosynthesis Case reports Child Data management Debridement Dosage and administration Drug dosages Drug therapy Drug Therapy, Combination Female Grey literature Heterogeneity Humans Infections Intravenous administration Isavuconazole Male Middle Aged Mold Mortality Mucormycosis Mucormycosis - drug therapy Nitriles - therapeutic use Observational studies Oral administration Patients Posaconazole Prognosis Pyridines - adverse effects Pyridines - therapeutic use Sterols Systematic Review Treatment Outcome Triazoles - therapeutic use |
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Title | Use of isavuconazole in mucormycosis: a systematic review |
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