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Optimising Antimicrobial Selection and Duration in the Treatment of Febrile Neutropenia in Children
Febrile neutropenia (FN) is a frequent complication of cancer treatment in children. Owing to the potential for overwhelming bacterial sepsis, the recognition and management of FN requires rapid implementation of evidenced-based management protocols. Treatment paradigms have progressed from hospital...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8019605/ https://www.ncbi.nlm.nih.gov/pubmed/33833534 http://dx.doi.org/10.2147/IDR.S238567 |
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author | Morgan, Jessica E Phillips, Bob Haeusler, Gabrielle M Chisholm, Julia C |
author_facet | Morgan, Jessica E Phillips, Bob Haeusler, Gabrielle M Chisholm, Julia C |
author_sort | Morgan, Jessica E |
collection | PubMed |
description | Febrile neutropenia (FN) is a frequent complication of cancer treatment in children. Owing to the potential for overwhelming bacterial sepsis, the recognition and management of FN requires rapid implementation of evidenced-based management protocols. Treatment paradigms have progressed from hospitalisation with broad spectrum antibiotics for all patients, through to risk adapted approaches to management. Such risk adapted approaches aim to provide safe care through incorporating antimicrobial stewardship (AMS) principles such as implementation of comprehensive clinical pathways incorporating de-escalation strategies with the imperative to reduce hospital stay and antibiotic exposure where possible in order to improve patient experience, reduce costs and diminish the risk of nosocomial infection. This review summarises the principles of risk stratification in FN, the current key considerations for optimising empiric antimicrobial selection including knowledge of antimicrobial resistance patterns and emerging technologies for rapid diagnosis of specific infections and summarises existing evidence on time to treatment, investigations required and duration of treatment. To aid treating physicians we suggest the key features based on current evidence that should be part of any FN management guideline and highlight areas for future research. The focus is on treatment of bacterial infections although fungal and viral infections are also important in this patient group. |
format | Online Article Text |
id | pubmed-8019605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-80196052021-04-07 Optimising Antimicrobial Selection and Duration in the Treatment of Febrile Neutropenia in Children Morgan, Jessica E Phillips, Bob Haeusler, Gabrielle M Chisholm, Julia C Infect Drug Resist Review Febrile neutropenia (FN) is a frequent complication of cancer treatment in children. Owing to the potential for overwhelming bacterial sepsis, the recognition and management of FN requires rapid implementation of evidenced-based management protocols. Treatment paradigms have progressed from hospitalisation with broad spectrum antibiotics for all patients, through to risk adapted approaches to management. Such risk adapted approaches aim to provide safe care through incorporating antimicrobial stewardship (AMS) principles such as implementation of comprehensive clinical pathways incorporating de-escalation strategies with the imperative to reduce hospital stay and antibiotic exposure where possible in order to improve patient experience, reduce costs and diminish the risk of nosocomial infection. This review summarises the principles of risk stratification in FN, the current key considerations for optimising empiric antimicrobial selection including knowledge of antimicrobial resistance patterns and emerging technologies for rapid diagnosis of specific infections and summarises existing evidence on time to treatment, investigations required and duration of treatment. To aid treating physicians we suggest the key features based on current evidence that should be part of any FN management guideline and highlight areas for future research. The focus is on treatment of bacterial infections although fungal and viral infections are also important in this patient group. Dove 2021-03-30 /pmc/articles/PMC8019605/ /pubmed/33833534 http://dx.doi.org/10.2147/IDR.S238567 Text en © 2021 Morgan et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Review Morgan, Jessica E Phillips, Bob Haeusler, Gabrielle M Chisholm, Julia C Optimising Antimicrobial Selection and Duration in the Treatment of Febrile Neutropenia in Children |
title | Optimising Antimicrobial Selection and Duration in the Treatment of Febrile Neutropenia in Children |
title_full | Optimising Antimicrobial Selection and Duration in the Treatment of Febrile Neutropenia in Children |
title_fullStr | Optimising Antimicrobial Selection and Duration in the Treatment of Febrile Neutropenia in Children |
title_full_unstemmed | Optimising Antimicrobial Selection and Duration in the Treatment of Febrile Neutropenia in Children |
title_short | Optimising Antimicrobial Selection and Duration in the Treatment of Febrile Neutropenia in Children |
title_sort | optimising antimicrobial selection and duration in the treatment of febrile neutropenia in children |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8019605/ https://www.ncbi.nlm.nih.gov/pubmed/33833534 http://dx.doi.org/10.2147/IDR.S238567 |
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