Literature DB >> 30709744

Antimicrobial susceptibility testing (AST) and associated clinical outcomes in individuals with cystic fibrosis: A systematic review.

Ranjani Somayaji1, Michael D Parkins2, Anand Shah3, Stacey L Martiniano4, Michael M Tunney5, Jennifer S Kahle6, Valerie J Waters7, J Stuart Elborn8, Scott C Bell9, Patrick A Flume10, Donald R VanDevanter11.   

Abstract

BACKGROUND: Antimicrobial susceptibility testing (AST) is a cornerstone of infection management. Cystic fibrosis (CF) treatment guidelines recommend AST to select antimicrobial treatments for CF airway infection but its utility in this setting has never been objectively demonstrated.
METHODS: We conducted a systematic review of primary published articles designed to address two PICO (patient, intervention, comparator, outcome) questions: 1) "For individuals with CF, is clinical response to antimicrobial treatment of bacterial airways infection predictable from AST results available at treatment initiation?" and 2) "For individuals with CF, is clinical response to antimicrobial treatment of bacterial airways infection affected by the method used to guide antimicrobial selection?" Relationships between AST results and clinical response (changes in pulmonary function, weight, signs and symptoms of respiratory tract infection, and time to next event) were assessed for each article and results were compared across articles when possible.
RESULTS: Twenty-five articles describing the results of 20 separate studies, most of which described Pseudomonas aeruginosa treatment, were identified. Thirteen studies described pulmonary exacerbation (PEx) treatment and seven described 'maintenance' of chronic bacterial airways infection. In only three of 16 studies addressing PICO question #1 was there a suggestion that baseline bacterial isolate antimicrobial susceptibility was associated with clinical response to treatment. None of the four studies addressing PICO question #2 suggested that antimicrobial selection methods influenced clinical outcomes.
CONCLUSIONS: There is little evidence that AST predicts the clinical outcome of CF antimicrobial treatment, suggesting a need for careful consideration of current AST use by the CF community.
Copyright © 2019 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

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Year:  2019        PMID: 30709744     DOI: 10.1016/j.jcf.2019.01.008

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  23 in total

1.  Susceptibility of Pseudomonas aeruginosa Recovered from Cystic Fibrosis Patients to Murepavadin and 13 Comparator Antibiotics.

Authors:  Miquel B Ekkelenkamp; Rafael Cantón; María Díez-Aguilar; Michael M Tunney; Deirdre F Gilpin; Francesca Bernardini; Glenn E Dale; J Stuart Elborn; Jumamurat R Bayjanov; Ad Fluit
Journal:  Antimicrob Agents Chemother       Date:  2020-01-27       Impact factor: 5.191

2.  The use of antimicrobial susceptibility testing in pediatric cystic fibrosis pulmonary exacerbations.

Authors:  Jonathan D Cogen; Kathryn B Whitlock; Ronald L Gibson; Lucas R Hoffman; Donald R VanDevanter
Journal:  J Cyst Fibros       Date:  2019-05-28       Impact factor: 5.482

3.  Associating antimicrobial susceptibility testing with clinical outcomes in cystic fibrosis: More rigor and less frequency?

Authors:  Rhonda D Szczesniak; Jonathan D Cogen; Margaret Rosenfeld
Journal:  J Cyst Fibros       Date:  2019-02-26       Impact factor: 5.482

Review 4.  From the soil to the clinic: the impact of microbial secondary metabolites on antibiotic tolerance and resistance.

Authors:  Elena K Perry; Lucas A Meirelles; Dianne K Newman
Journal:  Nat Rev Microbiol       Date:  2021-09-16       Impact factor: 60.633

Review 5.  [Evidence-based treatment of cystic fibrosis].

Authors:  F C Ringshausen; T Hellmuth; A-M Dittrich
Journal:  Internist (Berl)       Date:  2020-12       Impact factor: 0.743

Review 6.  The future of cystic fibrosis care: a global perspective.

Authors:  Scott C Bell; Marcus A Mall; Hector Gutierrez; Milan Macek; Susan Madge; Jane C Davies; Pierre-Régis Burgel; Elizabeth Tullis; Claudio Castaños; Carlo Castellani; Catherine A Byrnes; Fiona Cathcart; Sanjay H Chotirmall; Rebecca Cosgriff; Irmgard Eichler; Isabelle Fajac; Christopher H Goss; Pavel Drevinek; Philip M Farrell; Anna M Gravelle; Trudy Havermans; Nicole Mayer-Hamblett; Nataliya Kashirskaya; Eitan Kerem; Joseph L Mathew; Edward F McKone; Lutz Naehrlich; Samya Z Nasr; Gabriela R Oates; Ciaran O'Neill; Ulrike Pypops; Karen S Raraigh; Steven M Rowe; Kevin W Southern; Sheila Sivam; Anne L Stephenson; Marco Zampoli; Felix Ratjen
Journal:  Lancet Respir Med       Date:  2019-09-27       Impact factor: 30.700

7.  Duration of antibiotic therapy in non-cystic fibrosis bronchiectasis.

Authors:  R Somayaji; C H Goss
Journal:  Curr Pulmonol Rep       Date:  2019-11-26

8.  Pseudomonas aeruginosa aggregates in cystic fibrosis sputum produce exopolysaccharides that likely impede current therapies.

Authors:  Laura K Jennings; Julia E Dreifus; Courtney Reichhardt; Kelly M Storek; Patrick R Secor; Daniel J Wozniak; Katherine B Hisert; Matthew R Parsek
Journal:  Cell Rep       Date:  2021-02-23       Impact factor: 9.423

9.  Pseudomonas aeruginosa antimicrobial susceptibility test (AST) results and pulmonary exacerbation treatment responses in cystic fibrosis.

Authors:  Donald R VanDevanter; Sonya L Heltshe; Jay B Hilliard; Michael W Konstan
Journal:  J Cyst Fibros       Date:  2020-06-04       Impact factor: 5.482

10.  Variation in treatment preferences of pulmonary exacerbations among Australian and New Zealand cystic fibrosis physicians.

Authors:  Grace Currie; Anna Tai; Tom Snelling; André Schultz
Journal:  BMJ Open Respir Res       Date:  2021-07
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