Literature DB >> 18156280

Clinical impact of reducing routine susceptibility testing in chronic Pseudomonas aeruginosa infections in cystic fibrosis.

Christine Etherington1, Melanie Hall, Steven Conway, Daniel Peckham, Miles Denton.   

Abstract

BACKGROUND Susceptibility testing results are not predictive of clinical response to antibiotic therapy in chronic Pseudomonas aeruginosa infections in cystic fibrosis (CF). We assessed the impact of reducing the number of routine susceptibility tests performed on clinical outcome in these cases. METHODS In June 2006, we introduced a protocol whereby susceptibility tests of P. aeruginosa isolates obtained from respiratory samples of people with CF were limited to those taken at the commencement of antibiotic therapy, when there was evidence of clinical failure or routinely if not tested in the previous 3 months. At all other times, isolates were identified and reported as normal but P. aeruginosa isolates were not subjected to susceptibility testing. RESULTS Over a 6 month period, P. aeruginosa was isolated on at least one occasion from 193 patients attending the Adult Cystic Fibrosis Unit. In this period, we reduced the number of routine susceptibility tests by 56% (from a projected 2231 tests on 872 samples to an actual 972 tests on 427 samples). We assessed the response to courses of intravenous antibiotic treatment administered during the 6 month study period in 2006 and for courses administered in the same patients during the same calendar months in 2005. No significant differences in median change of FEV1, FVC, C-reactive protein (CRP), white cell count, weight or duration of intravenous antibiotics were observed. The projected savings of this intervention were 3500 euros in consumables and 170 h (costed at 6500 euros) of laboratory staff time per annum, a total annual saving of 10,000 euros (6500 pounds sterling). CONCLUSIONS For CF units sending regular, routine sputum samples, a reduction in the number of susceptibility tests performed in cases of chronic P. aeruginosa infection can be carried out without impacting on short-term clinical outcomes.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 18156280     DOI: 10.1093/jac/dkm481

Source DB:  PubMed          Journal:  J Antimicrob Chemother        ISSN: 0305-7453            Impact factor:   5.790


  6 in total

1.  Multiple antibiotic-resistant Pseudomonas aeruginosa and lung function decline in patients with cystic fibrosis.

Authors:  Clement L Ren; Michael W Konstan; Ashley Yegin; Lawrence Rasouliyan; Benjamin Trzaskoma; Wayne J Morgan; Warren Regelmann
Journal:  J Cyst Fibros       Date:  2012-03-23       Impact factor: 5.482

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.  Randomized trial of biofilm testing to select antibiotics for cystic fibrosis airway infection.

Authors:  Samuel M Moskowitz; Julia C Emerson; Sharon McNamara; Richard D Shell; David M Orenstein; Daniel Rosenbluth; Marcia F Katz; Richard Ahrens; Douglas Hornick; Patricia M Joseph; Ronald L Gibson; Moira L Aitken; Wade W Benton; Jane L Burns
Journal:  Pediatr Pulmonol       Date:  2010-10-20

4.  Results of antibiotic susceptibility testing do not influence clinical outcome in children with cystic fibrosis.

Authors:  M N Hurley; A H Amin Ariff; C Bertenshaw; J Bhatt; A R Smyth
Journal:  J Cyst Fibros       Date:  2012-03-20       Impact factor: 5.482

5.  Pseudomonas aeruginosa Susceptibility Patterns and Associated Clinical Outcomes in People with Cystic Fibrosis following Approval of Aztreonam Lysine for Inhalation.

Authors:  Claire L Keating; Jonathan B Zuckerman; Pradeep K Singh; Matthew McKevitt; Oksana Gurtovaya; Mark Bresnik; Bruce C Marshall; Lisa Saiman
Journal:  Antimicrob Agents Chemother       Date:  2021-02-17       Impact factor: 5.191

6.  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
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.