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Antibiotherapy in Children with Cystic Fibrosis—An Extensive Review
In cystic fibrosis (CF), the respiratory disease is the main factor that influences the outcome and the prognosis of patients, bacterial infections being responsible for severe exacerbations. The etiology is often multi-microbial and with resistant strains. The aim of this paper is to present curren...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406924/ https://www.ncbi.nlm.nih.gov/pubmed/36010149 http://dx.doi.org/10.3390/children9081258 |
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author | Ciuca, Ioana Mihaiela Dediu, Mihaela Popin, Diana Pop, Liviu Laurentiu Tamas, Liviu Athos Pilut, Ciprian Nicolae Almajan Guta, Bogdan Popa, Zoran Laurentiu |
author_facet | Ciuca, Ioana Mihaiela Dediu, Mihaela Popin, Diana Pop, Liviu Laurentiu Tamas, Liviu Athos Pilut, Ciprian Nicolae Almajan Guta, Bogdan Popa, Zoran Laurentiu |
author_sort | Ciuca, Ioana Mihaiela |
collection | PubMed |
description | In cystic fibrosis (CF), the respiratory disease is the main factor that influences the outcome and the prognosis of patients, bacterial infections being responsible for severe exacerbations. The etiology is often multi-microbial and with resistant strains. The aim of this paper is to present current existing antibiotherapy solutions for CF-associated infections in order to offer a reliable support for individual, targeted, and specific treatment. The inclusion criteria were studies about antibiotherapy in CF pediatric patients. Studies involving adult patients or those with only in vitro results were excluded. The information sources were all articles published until December 2021, in PubMed and ScienceDirect. A total of 74 studies were included, with a total number of 26,979 patients aged between 0–18 years. We approached each pathogen individual, with their specific treatment, comparing treatment solutions proposed by different studies. Preservation of lung function is the main goal of therapy in CF, because once parenchyma is lost, it cannot be recovered. Early personalized intervention and prevention of infection with reputable germs is of paramount importance, even if is an asymmetrical challenge. This research received no external funding. |
format | Online Article Text |
id | pubmed-9406924 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94069242022-08-26 Antibiotherapy in Children with Cystic Fibrosis—An Extensive Review Ciuca, Ioana Mihaiela Dediu, Mihaela Popin, Diana Pop, Liviu Laurentiu Tamas, Liviu Athos Pilut, Ciprian Nicolae Almajan Guta, Bogdan Popa, Zoran Laurentiu Children (Basel) Systematic Review In cystic fibrosis (CF), the respiratory disease is the main factor that influences the outcome and the prognosis of patients, bacterial infections being responsible for severe exacerbations. The etiology is often multi-microbial and with resistant strains. The aim of this paper is to present current existing antibiotherapy solutions for CF-associated infections in order to offer a reliable support for individual, targeted, and specific treatment. The inclusion criteria were studies about antibiotherapy in CF pediatric patients. Studies involving adult patients or those with only in vitro results were excluded. The information sources were all articles published until December 2021, in PubMed and ScienceDirect. A total of 74 studies were included, with a total number of 26,979 patients aged between 0–18 years. We approached each pathogen individual, with their specific treatment, comparing treatment solutions proposed by different studies. Preservation of lung function is the main goal of therapy in CF, because once parenchyma is lost, it cannot be recovered. Early personalized intervention and prevention of infection with reputable germs is of paramount importance, even if is an asymmetrical challenge. This research received no external funding. MDPI 2022-08-20 /pmc/articles/PMC9406924/ /pubmed/36010149 http://dx.doi.org/10.3390/children9081258 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Systematic Review Ciuca, Ioana Mihaiela Dediu, Mihaela Popin, Diana Pop, Liviu Laurentiu Tamas, Liviu Athos Pilut, Ciprian Nicolae Almajan Guta, Bogdan Popa, Zoran Laurentiu Antibiotherapy in Children with Cystic Fibrosis—An Extensive Review |
title | Antibiotherapy in Children with Cystic Fibrosis—An Extensive Review |
title_full | Antibiotherapy in Children with Cystic Fibrosis—An Extensive Review |
title_fullStr | Antibiotherapy in Children with Cystic Fibrosis—An Extensive Review |
title_full_unstemmed | Antibiotherapy in Children with Cystic Fibrosis—An Extensive Review |
title_short | Antibiotherapy in Children with Cystic Fibrosis—An Extensive Review |
title_sort | antibiotherapy in children with cystic fibrosis—an extensive review |
topic | Systematic Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406924/ https://www.ncbi.nlm.nih.gov/pubmed/36010149 http://dx.doi.org/10.3390/children9081258 |
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