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Antibiotherapy in Children with Cystic Fibrosis-An Extensive Review
Ioana Mihaiela Ciuca1,2, Mihaela Dediu1, Diana Popin2
1Pediatric Department, University of Medicine and Pharmacy "Victor Babes" Timisoara, 2 Eftimie Murgu Square, 300041 Timisoara, Romania.
Insights
This review details current antibiotic treatments for pediatric cystic fibrosis (CF) bacterial infections. It emphasizes personalized, early interventions to preserve lung function and improve patient outcomes.
Area of Science:
- Pediatric Pulmonology
- Infectious Diseases
- Pharmacology
Background:
- Respiratory complications are primary drivers of morbidity and mortality in pediatric cystic fibrosis (CF).
- Bacterial infections, often polymicrobial and involving resistant strains, precipitate severe exacerbations in CF patients.
- Effective management of these infections is critical for preserving lung function and improving prognosis.
Purpose of the Study:
- To systematically review and present current antibiotherapy strategies for CF-associated bacterial infections in pediatric patients.
- To provide a comprehensive resource for guiding individualized, targeted treatment decisions.
- To compare and analyze various treatment solutions proposed in existing literature.
Main Methods:
- Systematic literature search of PubMed and ScienceDirect for studies published until December 2021.
- Inclusion criteria focused on antibiotherapy in CF pediatric patients (0-18 years), excluding adult studies or in vitro-only results.
- Analysis of 74 studies encompassing 26,979 patients, examining pathogen-specific treatments.
Main Results:
- Identified and compared diverse antibiotherapy regimens for common CF pathogens.
- Highlighted the importance of pathogen-specific treatment approaches.
- Synthesized information on treatment efficacy and comparative outcomes across studies.
Conclusions:
- Preserving lung function is the paramount therapeutic goal in CF management.
- Early, personalized interventions and infection prevention are crucial, despite challenges.
- This review offers a foundation for evidence-based, tailored antibiotherapy in pediatric CF.
Abstract:
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.
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