Clinical practice update of antifungal prophylaxis in immunocompromised children
Due to the rise in the number and types of immunosuppressed patients, invasive fungal infections (IFI) are an increasing and major cause of morbidity and mortality in immunocompromised adults and children. There is a broad group of pediatric patients at risk for IFI in whom primary and/or secondary...
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Veröffentlicht in: | Revista española de quimioterapia 2019-10, Vol.32 (5), p.410-425 |
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creator | Ramos, J T Romero, C A Belda, S Candel, F J Carazo Gallego, B Fernández-Polo, A Ferreras Antolín, L Garrido Colino, C Navarro, M L Nef, O Olbright, P Rincón-López, E Ruiz Contreras, J Soler-Palacín, P |
description | Due to the rise in the number and types of immunosuppressed patients, invasive fungal infections (IFI) are an increasing and major cause of morbidity and mortality in immunocompromised adults and children. There is a broad group of pediatric patients at risk for IFI in whom primary and/or secondary antifungal prophylaxis (AFP) should be considered despite scant evidence. Pediatric groups at risk for IFI includes extremely premature infants in some settings, while in high-risk children with cancer receiving chemotherapy or undergoing haematopoietic stem cell transplantation (HCT), AFP against yeast and moulds is usually recommended. For solid organ transplanted, children, prophylaxis depends on the type of transplant and associated risk factors. In children with primary or acquired immunodeficiency such as HIV or long-term immunosuppressive treatment, AFP depends on the type of immunodeficiency and the degree of immunosuppression. Chronic granulomatous disease is associated with a particular high-risk of IFI and anti-mould prophylaxis is always indicated. In contrast, AFP is not generally recommended in children with long stay in intensive care units. The choice of AFP is limited by the approval of antifungal agents in different age groups and by their pharmacokinetics characteristics. This document aims to review current available information on AFP in children and to provide a comprehensive proposal for each type of patient. |
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There is a broad group of pediatric patients at risk for IFI in whom primary and/or secondary antifungal prophylaxis (AFP) should be considered despite scant evidence. Pediatric groups at risk for IFI includes extremely premature infants in some settings, while in high-risk children with cancer receiving chemotherapy or undergoing haematopoietic stem cell transplantation (HCT), AFP against yeast and moulds is usually recommended. For solid organ transplanted, children, prophylaxis depends on the type of transplant and associated risk factors. In children with primary or acquired immunodeficiency such as HIV or long-term immunosuppressive treatment, AFP depends on the type of immunodeficiency and the degree of immunosuppression. Chronic granulomatous disease is associated with a particular high-risk of IFI and anti-mould prophylaxis is always indicated. In contrast, AFP is not generally recommended in children with long stay in intensive care units. The choice of AFP is limited by the approval of antifungal agents in different age groups and by their pharmacokinetics characteristics. This document aims to review current available information on AFP in children and to provide a comprehensive proposal for each type of patient.</description><identifier>ISSN: 0214-3429</identifier><identifier>EISSN: 1988-9518</identifier><identifier>PMID: 31507152</identifier><language>eng</language><publisher>Spain: Sociedad Española de Quimioterapia</publisher><subject>Antifungal Agents - therapeutic use ; Candidiasis - prevention & control ; Child ; Drug Monitoring ; Hematopoietic Stem Cell Transplantation - adverse effects ; HIV Infections - complications ; Humans ; Immunocompromised Host ; Immunologic Deficiency Syndromes - complications ; Immunosuppression - adverse effects ; Infant, Extremely Premature ; Infant, Newborn ; Intensive Care Units, Pediatric ; Invasive Fungal Infections - prevention & control ; Neoplasms - drug therapy ; Pneumonia, Pneumocystis - prevention & control ; Primary Prevention - methods ; Review ; Risk Factors ; Secondary Prevention - methods ; Transplant Recipients</subject><ispartof>Revista española de quimioterapia, 2019-10, Vol.32 (5), p.410-425</ispartof><rights>The Author 2019. Published by Sociedad Española de Quimioterapia. This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)(https://creativecommons.org/licenses/by-nc/4.0/).</rights><rights>The Author 2019 2019</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790888/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790888/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31507152$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ramos, J T</creatorcontrib><creatorcontrib>Romero, C A</creatorcontrib><creatorcontrib>Belda, S</creatorcontrib><creatorcontrib>Candel, F J</creatorcontrib><creatorcontrib>Carazo Gallego, B</creatorcontrib><creatorcontrib>Fernández-Polo, A</creatorcontrib><creatorcontrib>Ferreras Antolín, L</creatorcontrib><creatorcontrib>Garrido Colino, C</creatorcontrib><creatorcontrib>Navarro, M L</creatorcontrib><creatorcontrib>Nef, O</creatorcontrib><creatorcontrib>Olbright, P</creatorcontrib><creatorcontrib>Rincón-López, E</creatorcontrib><creatorcontrib>Ruiz Contreras, J</creatorcontrib><creatorcontrib>Soler-Palacín, P</creatorcontrib><creatorcontrib>Fungal Infection Study Group of Spanish Society of Paediatric Infectious Disease (SEIP); Traslational Research Network in Pediatric Infectious Diseases (RITIP)</creatorcontrib><title>Clinical practice update of antifungal prophylaxis in immunocompromised children</title><title>Revista española de quimioterapia</title><addtitle>Rev Esp Quimioter</addtitle><description>Due to the rise in the number and types of immunosuppressed patients, invasive fungal infections (IFI) are an increasing and major cause of morbidity and mortality in immunocompromised adults and children. There is a broad group of pediatric patients at risk for IFI in whom primary and/or secondary antifungal prophylaxis (AFP) should be considered despite scant evidence. Pediatric groups at risk for IFI includes extremely premature infants in some settings, while in high-risk children with cancer receiving chemotherapy or undergoing haematopoietic stem cell transplantation (HCT), AFP against yeast and moulds is usually recommended. For solid organ transplanted, children, prophylaxis depends on the type of transplant and associated risk factors. In children with primary or acquired immunodeficiency such as HIV or long-term immunosuppressive treatment, AFP depends on the type of immunodeficiency and the degree of immunosuppression. Chronic granulomatous disease is associated with a particular high-risk of IFI and anti-mould prophylaxis is always indicated. In contrast, AFP is not generally recommended in children with long stay in intensive care units. The choice of AFP is limited by the approval of antifungal agents in different age groups and by their pharmacokinetics characteristics. This document aims to review current available information on AFP in children and to provide a comprehensive proposal for each type of patient.</description><subject>Antifungal Agents - therapeutic use</subject><subject>Candidiasis - prevention & control</subject><subject>Child</subject><subject>Drug Monitoring</subject><subject>Hematopoietic Stem Cell Transplantation - adverse effects</subject><subject>HIV Infections - complications</subject><subject>Humans</subject><subject>Immunocompromised Host</subject><subject>Immunologic Deficiency Syndromes - complications</subject><subject>Immunosuppression - adverse effects</subject><subject>Infant, Extremely Premature</subject><subject>Infant, Newborn</subject><subject>Intensive Care Units, Pediatric</subject><subject>Invasive Fungal Infections - prevention & control</subject><subject>Neoplasms - drug therapy</subject><subject>Pneumonia, Pneumocystis - prevention & control</subject><subject>Primary Prevention - methods</subject><subject>Review</subject><subject>Risk Factors</subject><subject>Secondary Prevention - methods</subject><subject>Transplant Recipients</subject><issn>0214-3429</issn><issn>1988-9518</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkNlKxEAQRRtRnDj6C9I_EOg13f0iSHCDAX3Q51DpZdKSdEIWcf7e4IY-FdS591DUEcqo0To3kupjlBFGRc4FMxt0Nk2vhAguDD1FG04lUVSyDD2VbUzRQouHEewcrcfL4GD2uA8Y0hzDkvaftB-aQwvvccIx4dh1S-pt3637Lk7eYdvE1o0-naOTAO3kL77nFr3c3jyX9_nu8e6hvN7lAyuKOVcgNGgr-XpicIVS0milrLUiQBDOEU5E4NIRVddM8DWgC-EFq61XYH3Bt-jqyzssdeed9Wkeoa2GMXYwHqoeYvWfpNhU-_6tKpQhWutVcPlX8Nv8-Q3_AGPrZIE</recordid><startdate>20191001</startdate><enddate>20191001</enddate><creator>Ramos, J T</creator><creator>Romero, C A</creator><creator>Belda, S</creator><creator>Candel, F J</creator><creator>Carazo Gallego, B</creator><creator>Fernández-Polo, A</creator><creator>Ferreras Antolín, L</creator><creator>Garrido Colino, C</creator><creator>Navarro, M L</creator><creator>Nef, O</creator><creator>Olbright, P</creator><creator>Rincón-López, E</creator><creator>Ruiz Contreras, J</creator><creator>Soler-Palacín, P</creator><general>Sociedad Española de Quimioterapia</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>5PM</scope></search><sort><creationdate>20191001</creationdate><title>Clinical practice update of antifungal prophylaxis in immunocompromised children</title><author>Ramos, J T ; Romero, C A ; Belda, S ; Candel, F J ; Carazo Gallego, B ; Fernández-Polo, A ; Ferreras Antolín, L ; Garrido Colino, C ; Navarro, M L ; Nef, O ; Olbright, P ; Rincón-López, E ; Ruiz Contreras, J ; Soler-Palacín, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p266t-7a48a8c53214fd67759877ccc4faf4dd0304f35d07bb243677864e42bce7ace63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Antifungal Agents - therapeutic use</topic><topic>Candidiasis - prevention & control</topic><topic>Child</topic><topic>Drug Monitoring</topic><topic>Hematopoietic Stem Cell Transplantation - adverse effects</topic><topic>HIV Infections - complications</topic><topic>Humans</topic><topic>Immunocompromised Host</topic><topic>Immunologic Deficiency Syndromes - complications</topic><topic>Immunosuppression - adverse effects</topic><topic>Infant, Extremely Premature</topic><topic>Infant, Newborn</topic><topic>Intensive Care Units, Pediatric</topic><topic>Invasive Fungal Infections - prevention & control</topic><topic>Neoplasms - drug therapy</topic><topic>Pneumonia, Pneumocystis - prevention & control</topic><topic>Primary Prevention - methods</topic><topic>Review</topic><topic>Risk Factors</topic><topic>Secondary Prevention - methods</topic><topic>Transplant Recipients</topic><toplevel>online_resources</toplevel><creatorcontrib>Ramos, J T</creatorcontrib><creatorcontrib>Romero, C A</creatorcontrib><creatorcontrib>Belda, S</creatorcontrib><creatorcontrib>Candel, F J</creatorcontrib><creatorcontrib>Carazo Gallego, B</creatorcontrib><creatorcontrib>Fernández-Polo, A</creatorcontrib><creatorcontrib>Ferreras Antolín, L</creatorcontrib><creatorcontrib>Garrido Colino, C</creatorcontrib><creatorcontrib>Navarro, M L</creatorcontrib><creatorcontrib>Nef, O</creatorcontrib><creatorcontrib>Olbright, P</creatorcontrib><creatorcontrib>Rincón-López, E</creatorcontrib><creatorcontrib>Ruiz Contreras, J</creatorcontrib><creatorcontrib>Soler-Palacín, P</creatorcontrib><creatorcontrib>Fungal Infection Study Group of Spanish Society of Paediatric Infectious Disease (SEIP); Traslational Research Network in Pediatric Infectious Diseases (RITIP)</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Revista española de quimioterapia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ramos, J T</au><au>Romero, C A</au><au>Belda, S</au><au>Candel, F J</au><au>Carazo Gallego, B</au><au>Fernández-Polo, A</au><au>Ferreras Antolín, L</au><au>Garrido Colino, C</au><au>Navarro, M L</au><au>Nef, O</au><au>Olbright, P</au><au>Rincón-López, E</au><au>Ruiz Contreras, J</au><au>Soler-Palacín, P</au><aucorp>Fungal Infection Study Group of Spanish Society of Paediatric Infectious Disease (SEIP); Traslational Research Network in Pediatric Infectious Diseases (RITIP)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical practice update of antifungal prophylaxis in immunocompromised children</atitle><jtitle>Revista española de quimioterapia</jtitle><addtitle>Rev Esp Quimioter</addtitle><date>2019-10-01</date><risdate>2019</risdate><volume>32</volume><issue>5</issue><spage>410</spage><epage>425</epage><pages>410-425</pages><issn>0214-3429</issn><eissn>1988-9518</eissn><abstract>Due to the rise in the number and types of immunosuppressed patients, invasive fungal infections (IFI) are an increasing and major cause of morbidity and mortality in immunocompromised adults and children. There is a broad group of pediatric patients at risk for IFI in whom primary and/or secondary antifungal prophylaxis (AFP) should be considered despite scant evidence. Pediatric groups at risk for IFI includes extremely premature infants in some settings, while in high-risk children with cancer receiving chemotherapy or undergoing haematopoietic stem cell transplantation (HCT), AFP against yeast and moulds is usually recommended. For solid organ transplanted, children, prophylaxis depends on the type of transplant and associated risk factors. In children with primary or acquired immunodeficiency such as HIV or long-term immunosuppressive treatment, AFP depends on the type of immunodeficiency and the degree of immunosuppression. Chronic granulomatous disease is associated with a particular high-risk of IFI and anti-mould prophylaxis is always indicated. In contrast, AFP is not generally recommended in children with long stay in intensive care units. 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subjects | Antifungal Agents - therapeutic use Candidiasis - prevention & control Child Drug Monitoring Hematopoietic Stem Cell Transplantation - adverse effects HIV Infections - complications Humans Immunocompromised Host Immunologic Deficiency Syndromes - complications Immunosuppression - adverse effects Infant, Extremely Premature Infant, Newborn Intensive Care Units, Pediatric Invasive Fungal Infections - prevention & control Neoplasms - drug therapy Pneumonia, Pneumocystis - prevention & control Primary Prevention - methods Review Risk Factors Secondary Prevention - methods Transplant Recipients |
title | Clinical practice update of antifungal prophylaxis in immunocompromised children |
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