Literature DB >> 33693586

Association of Intensity of Antipseudomonal Antibiotic Therapy With Risk of Treatment-Emergent Organisms in Children With Cystic Fibrosis and Newly Acquired Pseudomonas Aeruginosa.

Jonathan D Cogen1,2, Frankline M Onchiri2, Nicole Mayer Hamblett1,2,3, Ronald L Gibson1,2, Wayne J Morgan4, Margaret Rosenfeld1,2.   

Abstract

BACKGROUND: While Pseudomonas aeruginosa (Pa) eradication regimens have contributed to a decline in Pa prevalence in people with cystic fibrosis (CF), this antibiotic exposure might increase the risk of acquisition of drug-resistant organisms. This study evaluated the association between antipseudomonal antibiotic exposure intensity and acquisition risk of drug-resistant organisms among children with CF and new Pa infection.
METHODS: We utilized data from the Early Pseudomonas Infection Control Clinical Trial (EPIC CT), a randomized controlled trial comparing Pa eradication strategies in children with CF and new Pa. The exposure was the number of weeks of oral or inhaled antipseudomonal antibiotics or ever versus never treatment with intravenous antipseudomonal antibiotics during the 18 months of EPIC CT participation. Primary outcomes were risks of acquisition of several respiratory organisms during 5 years of follow-up after EPIC CT estimated using Cox proportional hazards models separately for each specific organism.
RESULTS: Among 249 participants, there was no increased acquisition risk of any organism associated with greater inhaled antibiotic exposure. With each additional week of oral antibiotics, there was an increased hazard of Achromobacter xylosoxidans acquisition (HR, 1.24; 95% CI: 1.02-1.50; P = .03). Treatment with intravenous antibiotics was associated with an increased hazard of acquisition of multidrug-resistant Pa (HR, 2.47; 95% CI: 1.28-4.78; P = .01) and MRSA (HR, 1.57; 95% CI: 1.03-2.40; P = .04).
CONCLUSIONS: Results from this study illustrate the importance of making careful antibiotic choices to balance the benefits of antibiotics in people with CF while minimizing risk of acquisition of drug-resistant organisms.
© The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  zzm321990 Pseudomonas aeruginosazzm321990 ; antibiotics; cystic fibrosis; pulmonary exacerbations

Mesh:

Substances:

Year:  2021        PMID: 33693586      PMCID: PMC9034203          DOI: 10.1093/cid/ciab208

Source DB:  PubMed          Journal:  Clin Infect Dis        ISSN: 1058-4838            Impact factor:   9.079


  21 in total

Review 1.  Pseudomonas aeruginosa chronic colonization in cystic fibrosis patients.

Authors:  Thomas S Murray; Marie Egan; Barbara I Kazmierczak
Journal:  Curr Opin Pediatr       Date:  2007-02       Impact factor: 2.856

2.  Effectiveness of a stepwise Pseudomonas aeruginosa eradication protocol in children with cystic fibrosis.

Authors:  Ana C Blanchard; Eric Horton; Sanja Stanojevic; Louise Taylor; Valerie Waters; Felix Ratjen
Journal:  J Cyst Fibros       Date:  2017-02-09       Impact factor: 5.482

3.  Pseudomonas aeruginosa eradication therapy and risk of acquiring Aspergillus in young children with cystic fibrosis.

Authors:  Sabariah Noor Harun; Nicholas H G Holford; Keith Grimwood; Claire E Wainwright; Stefanie Hennig
Journal:  Thorax       Date:  2019-06-15       Impact factor: 9.139

4.  Diagnostic accuracy of oropharyngeal cultures in infants and young children with cystic fibrosis.

Authors:  M Rosenfeld; J Emerson; F Accurso; D Armstrong; R Castile; K Grimwood; P Hiatt; K McCoy; S McNamara; B Ramsey; J Wagener
Journal:  Pediatr Pulmonol       Date:  1999-11

5.  Treatment of early Pseudomonas aeruginosa infection in patients with cystic fibrosis: the ELITE trial.

Authors:  Felix Ratjen; Anne Munck; Pearl Kho; Gerhild Angyalosi
Journal:  Thorax       Date:  2009-12-08       Impact factor: 9.139

6.  Failure to recover to baseline pulmonary function after cystic fibrosis pulmonary exacerbation.

Authors:  Don B Sanders; Rachel C L Bittner; Margaret Rosenfeld; Lucas R Hoffman; Gregory J Redding; Christopher H Goss
Journal:  Am J Respir Crit Care Med       Date:  2010-05-12       Impact factor: 21.405

7.  Comparison of two treatment regimens for eradication of Pseudomonas aeruginosa infection in children with cystic fibrosis.

Authors:  M Proesmans; F Vermeulen; L Boulanger; J Verhaegen; K De Boeck
Journal:  J Cyst Fibros       Date:  2012-07-02       Impact factor: 5.482

8.  Comparative efficacy and safety of 4 randomized regimens to treat early Pseudomonas aeruginosa infection in children with cystic fibrosis.

Authors:  Miriam M Treggiari; George Retsch-Bogart; Nicole Mayer-Hamblett; Umer Khan; Michal Kulich; Richard Kronmal; Judy Williams; Peter Hiatt; Ronald L Gibson; Terry Spencer; David Orenstein; Barbara A Chatfield; Deborah K Froh; Jane L Burns; Margaret Rosenfeld; Bonnie W Ramsey
Journal:  Arch Pediatr Adolesc Med       Date:  2011-09

9.  Eradication failure of newly acquired Pseudomonas aeruginosa isolates in cystic fibrosis.

Authors:  Malena Cohen-Cymberknoh; Noa Gilead; Silvia Gartner; Sandra Rovira; Hannah Blau; Huda Mussaffi; Joseph Rivlin; Michal Gur; Michal Shteinberg; Lea Bentur; Galit Livnat; Micha Aviram; Elie Picard; Ariel Tenenbaum; Shoshana Armoni; Oded Breuer; David Shoseyov; Eitan Kerem
Journal:  J Cyst Fibros       Date:  2016-05-01       Impact factor: 5.482

10.  Azithromycin for Early Pseudomonas Infection in Cystic Fibrosis. The OPTIMIZE Randomized Trial.

Authors:  Nicole Mayer-Hamblett; George Retsch-Bogart; Margaret Kloster; Frank Accurso; Margaret Rosenfeld; Gary Albers; Philip Black; Perry Brown; AnneMarie Cairns; Stephanie D Davis; Gavin R Graff; Gwendolyn S Kerby; David Orenstein; Rachael Buckingham; Bonnie W Ramsey
Journal:  Am J Respir Crit Care Med       Date:  2018-11-01       Impact factor: 30.528

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