Literature DB >> 12917897

Nebulised anti-pseudomonal antibiotics for cystic fibrosis.

G Ryan1, S Mukhopadhyay, M Singh.   

Abstract

BACKGROUND: Persistent infection by Pseudomonas aeruginosa contributes to lung damage, resulting in illness and death in people with cystic fibrosis (CF). Nebulised antibiotics are commonly used to treat this infection.
OBJECTIVES: To examine the evidence that nebulised anti-pseudomonal antibiotic treatment in people with CF reduces frequency of exacerbations of infection, improves lung function, quality of life and survival. To examine adverse effects of nebulised anti-pseudomonal antibiotic treatment. SEARCH STRATEGY: Trials were identified from the Cochrane Cystic Fibrosis and Genetic Disorders Group clinical trials register. Companies that marketed nebulised anti-pseudomonal antibiotics were contacted for information on unpublished trials. Most recent search of the Group's trials register: August 2002. SELECTION CRITERIA: Trials were selected if, nebulised anti-pseudomonal antibiotics treatment was used for four weeks or more in people with CF, allocation to treatment was randomised or quasi-randomised, and there was a placebo or a no placebo control group or another nebulised antibiotic comparison. DATA COLLECTION AND ANALYSIS: For the first version of this review, two reviewers independently selected and judged the quality of, the trials to be included in the review. One reviewer extracted data from these trials and performed all tasks for the updated version of the review. MAIN
RESULTS: Out of 33 trials identified, there were 11, with 873 participants, that met the inclusion criteria. Ten trials with 758 participants compared a nebulised anti-pseudomonal antibiotic with placebo or usual treatment. One of these trials accounted for 68% of the total participants and seven of these trials used a cross-over design. Tobramycin was studied in four trials and follow up ranged from 1 to 32 months. Lung function, measured as forced expired volume in one second (FEV1) was better in the treated group than in control group in nine of these. Resistance to antibiotics increased more in the antibiotic treated group than in placebo group. Tinnitus and voice alteration were more frequent with tobramycin than placebo. One short-term trial of one month, with 115 participants, compared tobramycin and colistin, and showed a trend towards greater improvement in FEV1 in the tobramycin group. REVIEWER'S
CONCLUSIONS: Nebulised anti-pseudomonal antibiotic treatment improves lung function. However, more evidence, from longer duration trials, is needed to determine if this benefit is maintained as well as to determine the significance of development of antibiotic resistant organisms. There is insufficient evidence for recommendations about type of drug and dose regimens.

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Year:  2003        PMID: 12917897     DOI: 10.1002/14651858.CD001021

Source DB:  PubMed          Journal:  Cochrane Database Syst Rev        ISSN: 1361-6137


  11 in total

1.  Nebulized Gentamicin as an Alternative to Nebulized Tobramycin for Tracheitis in Pediatric Patients.

Authors:  Justin K Chen; Brittany L Martin-McNew; Lisa M Lubsch
Journal:  J Pediatr Pharmacol Ther       Date:  2017 Jan-Feb

2.  Evaluation of the Target Inhalation Mode (TIM) breathing maneuver in simulated nebulizer therapy in patients with cystic fibrosis.

Authors:  John Denyer; Ivan Prince; Emma Dixon; Penny Agent; Jennifer Pryor; Margaret Hodson
Journal:  J Aerosol Med Pulm Drug Deliv       Date:  2010-04       Impact factor: 2.849

3.  Tobramycin inhalation powder for P. aeruginosa infection in cystic fibrosis: the EVOLVE trial.

Authors:  Michael W Konstan; David E Geller; Predrag Minić; Florian Brockhaus; Jie Zhang; Gerhild Angyalosi
Journal:  Pediatr Pulmonol       Date:  2010-10-20

4.  Comparative efficacy of two doses of nebulized colistimethate in the eradication of Pseudomonas aeruginosa in children with cystic fibrosis.

Authors:  Marie-Sophie Brochet; Anne-Cathrine McDuff; Jean-François Bussières; Elaine Caron; Geneviève Fortin; Denis Lebel; Jacques-Edouard Marcotte
Journal:  Can Respir J       Date:  2007 Nov-Dec       Impact factor: 2.409

Review 5.  Chronic inflammation in the cystic fibrosis lung: alterations in inter- and intracellular signaling.

Authors:  David Nichols; James Chmiel; Melvin Berger
Journal:  Clin Rev Allergy Immunol       Date:  2008-04       Impact factor: 8.667

Review 6.  Exacerbations in cystic fibrosis: 2 . prevention.

Authors:  Scott C Bell; Philip J Robinson
Journal:  Thorax       Date:  2007-08       Impact factor: 9.139

7.  Management of refractory Pseudomonas aeruginosa infection in cystic fibrosis.

Authors:  Roger Sordé; Albert Pahissa; Jordi Rello
Journal:  Infect Drug Resist       Date:  2011-01-25       Impact factor: 4.003

Review 8.  Guidelines for the management of hospital-acquired pneumonia in the UK: report of the working party on hospital-acquired pneumonia of the British Society for Antimicrobial Chemotherapy.

Authors:  R G Masterton; A Galloway; G French; M Street; J Armstrong; E Brown; J Cleverley; P Dilworth; C Fry; A D Gascoigne; Alan Knox; Dilip Nathwani; Robert Spencer; Mark Wilcox
Journal:  J Antimicrob Chemother       Date:  2008-04-29       Impact factor: 5.790

9.  Making the invisible visible: the availability and desirability of adherence data in routine CF care- findings from a national questionnaire survey.

Authors:  Louisa Robinson; Chin Maguire; Zhe Hui Hoo; Martin J Wildman
Journal:  F1000Res       Date:  2019-11-11

Review 10.  Inhaled anti-pseudomonal antibiotics for long-term therapy in cystic fibrosis.

Authors:  Sherie Smith; Nicola J Rowbotham; Kate H Regan
Journal:  Cochrane Database Syst Rev       Date:  2018-03-30
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