Literature DB >> 32505525

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

Donald R VanDevanter1, Sonya L Heltshe2, Jay B Hilliard3, Michael W Konstan3.   

Abstract

Background Antimicrobial susceptibility testing (AST) of bacterial isolates is a time- and resource-intensive procedure recommended by cystic fibrosis (CF) treatment guidelines for antimicrobial selection for pulmonary exacerbation (PEx) treatment. Methods We studied relationships between Pseudomonas aeruginosa (Pa) isolate AST results, antipseudomonal PEx treatments, and treatment responses as change in weight and percent predicted forced expiratory volume in 1 s (ppFEV1) as well as future antimicrobial treatment hazard for PEx occurring at a CF care center from 1999 through 2018. Treatments were categorized by "Pa coverage" as complete (all Pa isolates susceptible by AST to at least one administered agent), none (no isolates susceptible), incomplete (some, but not all isolates susceptible), and indeterminant (administered antipseudomonals not evaluated by AST). Weight and ppFEV1 responses were compared across Pa coverage categories using unadjusted and adjusted general estimating equations; hazard of future treatment was assessed by Cox and logistic regression. Results Among 3820 antimicrobial PEx treatment events in 413 patients with Pa, 62.6% (2390) had complete Pa coverage; 8.9% (340), 2.4% (99), and 26.2% (1000), had no, incomplete, and indeterminant Pa coverage, respectively. Mean baseline to follow-up weight change was +0.74 kg [95% CI 0.63, 0.86]; ppFEV1 change was +1.60 [1.29, 1.90]. Pa coverage category was not associated with significant differences in weight or ppFEV1 change or with future antimicrobial treatment hazard. Conclusions We did not observe superior responses for AST-defined complete Pa coverage treatments versus lesser coverage treatments, suggesting that AST may be of little utility in choosing antimicrobials for CF PEx treatment.
Copyright © 2020 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cystic fibrosis; Pseudomonas aeruginosa; Pulmonary exacerbation; Susceptibility testing

Mesh:

Substances:

Year:  2020        PMID: 32505525      PMCID: PMC7714709          DOI: 10.1016/j.jcf.2020.05.008

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


  17 in total

1.  Study design considerations for the Standardized Treatment of Pulmonary Exacerbations 2 (STOP2): A trial to compare intravenous antibiotic treatment durations in CF.

Authors:  Sonya L Heltshe; Natalie E West; Donald R VanDevanter; D B Sanders; Valeria V Beckett; Patrick A Flume; Christopher H Goss
Journal:  Contemp Clin Trials       Date:  2017-11-21       Impact factor: 2.226

2.  Antimicrobial resistance in cystic fibrosis: A Delphi approach to defining best practices.

Authors:  Edith Zemanick; Pierre-Régis Burgel; Giovanni Taccetti; Alison Holmes; Felix Ratjen; Catherine A Byrnes; Valerie J Waters; Scott C Bell; Donald R VanDevanter; J Stuart Elborn; Patrick A Flume
Journal:  J Cyst Fibros       Date:  2019-10-31       Impact factor: 5.482

3.  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

4.  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

5.  Approach to treating cystic fibrosis pulmonary exacerbations varies widely across US CF care centers.

Authors:  Nathan C Kraynack; M David Gothard; Lynn M Falletta; John T McBride
Journal:  Pediatr Pulmonol       Date:  2011-04-04

6.  Oral, inhaled, and intravenous antibiotic choice for treating pulmonary exacerbations in cystic fibrosis.

Authors:  Jeffrey S Wagener; Lawrence Rasouliyan; Donald R VanDevanter; David J Pasta; Warren E Regelmann; Wayne J Morgan; Michael W Konstan
Journal:  Pediatr Pulmonol       Date:  2012-08-08

7.  Lung function changes before and after pulmonary exacerbation antimicrobial treatment in cystic fibrosis.

Authors:  Jeffrey S Wagener; Donald R VanDevanter; Michael W Konstan; David J Pasta; Stefanie J Millar; Wayne J Morgan
Journal:  Pediatr Pulmonol       Date:  2019-11-20

8.  IV-treated pulmonary exacerbations in the prior year: An important independent risk factor for future pulmonary exacerbation in cystic fibrosis.

Authors:  Donald R VanDevanter; Nathan J Morris; Michael W Konstan
Journal:  J Cyst Fibros       Date:  2015-10-23       Impact factor: 5.482

Review 9.  Cystic fibrosis pulmonary guidelines: treatment of pulmonary exacerbations.

Authors:  Patrick A Flume; Peter J Mogayzel; Karen A Robinson; Christopher H Goss; Randall L Rosenblatt; Robert J Kuhn; Bruce C Marshall
Journal:  Am J Respir Crit Care Med       Date:  2009-09-03       Impact factor: 21.405

10.  eulerAPE: drawing area-proportional 3-Venn diagrams using ellipses.

Authors:  Luana Micallef; Peter Rodgers
Journal:  PLoS One       Date:  2014-07-17       Impact factor: 3.240

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