Literature DB >> 22985692

Inhaled aztreonam lysine vs. inhaled tobramycin in cystic fibrosis: a comparative efficacy trial.

Baroukh M Assael1, Tacjana Pressler2, Diana Bilton3, Michael Fayon4, Rainald Fischer5, Raphael Chiron6, Mario LaRosa7, Christiane Knoop8, Noel McElvaney9, Sandra A Lewis10, Mark Bresnik11, A Bruce Montgomery10, Christopher M Oermann12.   

Abstract

BACKGROUND: Open-label, parallel-group, international trial comparing aztreonam for inhalation solution (AZLI) and tobramycin nebulizer solution (TNS) for cystic fibrosis patients with airway Pseudomonas aeruginosa.
METHODS: 273 patients (≥ 6 years); randomized to three 28-day courses (AZLI 75 mg [three-times/day] or TNS 300 mg [twice/day]); 28 off-days separated each course.
RESULTS: 268 patients were treated (AZLI/TNS: 136/132). Mean baseline FEV1 was 52% predicted. Mean relative changes after 1 course (AZLI: 8.35%; TNS: 0.55%; p<0.001) and mean actual changes across 3 courses (AZLI: 2.05%; TNS: -0.66%; p=0.002) indicated AZLI statistical superiority vs. TNS. AZLI-treated patients had fewer respiratory hospitalizations (p=0.044) and respiratory events requiring additional antipseudomonal antibiotics (p=0.004); both treatments were well tolerated. 133 patients received 1 to 3 courses of AZLI treatment in the open-label extension-period (28-day courses separated by 28 days off-treatment); lung function improvements were comparable regardless of whether patients had received TNS or AZLI in the preceding comparative period.
CONCLUSIONS: AZLI demonstrated statistical superiority in lung function and a reduction in acute pulmonary exacerbations compared to TNS over 3 treatment courses (ClinicalTrials.gov: NCT00757237).
Copyright © 2012. Published by Elsevier B.V.

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Year:  2012        PMID: 22985692     DOI: 10.1016/j.jcf.2012.07.006

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


  34 in total

1.  Evaluation of the pharmacokinetics and pharmacodynamics of liposomal amikacin for inhalation in cystic fibrosis patients with chronic pseudomonal infections using data from two phase 2 clinical studies.

Authors:  Olanrewaju O Okusanya; Sujata M Bhavnani; Jeffrey P Hammel; Alan Forrest; Catharine C Bulik; Paul G Ambrose; Renu Gupta
Journal:  Antimicrob Agents Chemother       Date:  2014-03-31       Impact factor: 5.191

Review 2.  Pharmacokinetic and Pharmacodynamic Optimization of Antibiotic Therapy in Cystic Fibrosis Patients: Current Evidences, Gaps in Knowledge and Future Directions.

Authors:  Charlotte Roy; Manon Launay; Sophie Magréault; Isabelle Sermet-Gaudelus; Vincent Jullien
Journal:  Clin Pharmacokinet       Date:  2021-01-24       Impact factor: 6.447

3.  Pragmatic criteria to define chronic pseudomonas aeruginosa infection among adults with cystic fibrosis.

Authors:  Zhe Hui Hoo; Elizabeth Coates; Chin Maguire; Hannah Cantrill; Nadia Shafi; Edward F Nash; Angela McGowan; Stephen J Bourke; William G Flight; Thomas V Daniels; Julia A Nightingale; Mark I Allenby; Rachael Curley; Martin J Wildman
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2018-08-18       Impact factor: 3.267

4.  Sodium nitrite blocks the activity of aminoglycosides against Pseudomonas aeruginosa biofilms.

Authors:  Anna C Zemke; Mark T Gladwin; Jennifer M Bomberger
Journal:  Antimicrob Agents Chemother       Date:  2015-03-23       Impact factor: 5.191

5.  Impact of azithromycin on the clinical and antimicrobial effectiveness of tobramycin in the treatment of cystic fibrosis.

Authors:  Dave P Nichols; Carrie L Happoldt; Preston E Bratcher; Silvia M Caceres; James F Chmiel; Kenneth C Malcolm; Milene T Saavedra; Lisa Saiman; Jennifer L Taylor-Cousar; Jerry A Nick
Journal:  J Cyst Fibros       Date:  2016-12-24       Impact factor: 5.482

Review 6.  Management of Pseudomonas aeruginosa infection in cystic fibrosis patients using inhaled antibiotics with a focus on nebulized liposomal amikacin.

Authors:  Zarmina Ehsan; John P Clancy
Journal:  Future Microbiol       Date:  2015-11-17       Impact factor: 3.165

Review 7.  Current and future treatment options for cystic fibrosis lung disease: latest evidence and clinical implications.

Authors:  Claire Edmondson; Jane C Davies
Journal:  Ther Adv Chronic Dis       Date:  2016-05-01       Impact factor: 5.091

Review 8.  Tackling the increasing complexity of CF care.

Authors:  Gregory S Sawicki; Christopher H Goss
Journal:  Pediatr Pulmonol       Date:  2015-10

Review 9.  Antibiotic management of lung infections in cystic fibrosis. I. The microbiome, methicillin-resistant Staphylococcus aureus, gram-negative bacteria, and multiple infections.

Authors:  James F Chmiel; Timothy R Aksamit; Sanjay H Chotirmall; Elliott C Dasenbrook; J Stuart Elborn; John J LiPuma; Sarath C Ranganathan; Valerie J Waters; Felix A Ratjen
Journal:  Ann Am Thorac Soc       Date:  2014-09

Review 10.  Treatment of Pulmonary Disease of Cystic Fibrosis: A Comprehensive Review.

Authors:  Rosa María Girón Moreno; Marta García-Clemente; Layla Diab-Cáceres; Adrián Martínez-Vergara; Miguel Ángel Martínez-García; Rosa Mar Gómez-Punter
Journal:  Antibiotics (Basel)       Date:  2021-04-23
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