Literature DB >> 25102101

Is there a role for antimicrobial stewardship in cystic fibrosis?

Valerie J Waters1, Felix A Ratjen.   

Abstract

There is currently considerable interest in developing antimicrobial stewardship programs in pediatric and adult acute and chronic care hospitals as a method of preserving the activity of existing antimicrobial agents against an increasing number of multidrug-resistant organisms. Cystic fibrosis (CF) is recognized as one of the conditions associated with the highest use of antimicrobials in pediatrics and has thus been identified as a potential target of antimicrobial stewardship programs. The benefits of aggressive antibiotic use to treat pulmonary infections in individuals with CF are well defined and it is not always possible to follow the stewardship principle of narrowing antimicrobial spectrum based on susceptibility testing and treating with short antibiotic courses. However, antimicrobial stewardship still has a role to play in CF. There are practical solutions that can be currently applied. For chronic suppressive antimicrobial therapy, aerosolization is the most effective route, achieving high intrapulmonary concentrations with few systemic toxicities. Given the absence of evidence demonstrating benefit, prolonged intravenous and oral antibiotic courses should generally be avoided. Increasing the number of antibiotics does not necessarily confer a clinical advantage; trials of cycling different antibiotics should be studied as it may have potential benefits both regarding efficacy and development of resistance. Further research is clearly needed in this area to optimize the antibiotic management of this population.

Entities:  

Keywords:  Pseudomonas aeruginosa; antibiotics; cystic fibrosis

Mesh:

Year:  2014        PMID: 25102101     DOI: 10.1513/AnnalsATS.201401-034OI

Source DB:  PubMed          Journal:  Ann Am Thorac Soc        ISSN: 2325-6621


  5 in total

1.  The Rapid Reduction of Infection-Related Visits and Antibiotic Use Among People With Cystic Fibrosis After Starting Elexacaftor-Tezacaftor-Ivacaftor.

Authors:  Aaron C Miller; Logan M Harris; Joseph E Cavanaugh; Mahmoud Abou Alaiwa; David A Stoltz; Douglas B Hornick; Philip M Polgreen
Journal:  Clin Infect Dis       Date:  2022-09-30       Impact factor: 20.999

Review 2.  Current and future treatment options for cystic fibrosis lung disease: latest evidence and clinical implications.

Authors:  Claire Edmondson; Jane C Davies
Journal:  Ther Adv Chronic Dis       Date:  2016-05-01       Impact factor: 5.091

3.  Editorial Commentary: Pseudomonas aeruginosa Eradication: How Do We Measure Success?

Authors:  Edith T Zemanick; Theresa A Laguna
Journal:  Clin Infect Dis       Date:  2015-05-13       Impact factor: 9.079

4.  Update on host-pathogen interactions in cystic fibrosis lung disease.

Authors:  Andreas Hector; Nina Frey; Dominik Hartl
Journal:  Mol Cell Pediatr       Date:  2016-02-23

Review 5.  Five rules for resistance management in the antibiotic apocalypse, a road map for integrated microbial management.

Authors:  Ben Raymond
Journal:  Evol Appl       Date:  2019-05-14       Impact factor: 5.183

  5 in total

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