Literature DB >> 28614995

Ease of use of tobramycin inhalation powder compared with nebulized tobramycin and colistimethate sodium: a crossover study in cystic fibrosis patients with pulmonary Pseudomonas aeruginosa infection.

James Greenwood1, Carsten Schwarz2, Urte Sommerwerck3, Edward F Nash4, Michael Tamm5, Weihua Cao6, Paul Mastoridis6, Laurie Debonnett6, Kamal Hamed7.   

Abstract

BACKGROUND: This study assessed the ease of use of tobramycin inhalation powder (TIP) administered via T-326 inhaler versus tobramycin inhalation solution (TIS) and colistimethate sodium (COLI), both administered via nebulizers, for the treatment of chronic pulmonary Pseudomonas aeruginosa infection in patients with cystic fibrosis (CF).
METHODS: A real-world, open-label, crossover, interventional phase IV study was conducted in CF patients aged ⩾6 years with forced expiratory volume in 1 second (FEV1) ⩾25% to ⩽90% predicted. Patients were assigned to one of the three treatment arms in Cycle 1; all patients received TIP in Cycle 2. Each cycle consisted of 28 days on and 28 days off the treatment.
RESULTS: A total of 60 patients [mean (standard deviation) age, 27.6 (8.4) years] were allocated to three treatment arms [TIS/TIP ( n = 14); COLI/TIP ( n = 28); TIP/TIP ( n = 18)] in Cycle 1. The mean total administration time, which included device setup and cleaning, in Cycle 1 versus Cycle 2 for TIS/TIP, COLI/TIP, and TIP/TIP arms were 37.0 versus 5.0 min, 16.4 versus 3.8 min, and 4.2 versus 3.4 min, respectively. The difference in mean total administration time was significantly shorter in Cycle 2 than in Cycle 1 for TIS/TIP ( p = 0.0112) and COLI/TIP ( p = 0.0016) arms. Overall, 12 patients were found to have contaminated devices across the two treatment cycles. In the TIP/TIP arm, no contamination of the T-326 inhaler was observed in either cycle. Treatment satisfaction, assessed by the Treatment Satisfaction Questionnaire for Medication and ACCEPT® questionnaire, was better overall for TIP compared with TIS and COLI. There were no unexpected adverse events and most were mild or moderate in intensity.
CONCLUSION: The T-326 inhaler used to deliver TIP was easy to use, required shorter total administration time, and was much less frequently contaminated than the nebulizers. The safety findings observed for TIP were generally consistent with its established safety profile.

Entities:  

Keywords:  Pseudomonas aeruginosa; T-326 inhaler; device contamination; ease of use; nebulizer; tobramycin

Mesh:

Substances:

Year:  2017        PMID: 28614995      PMCID: PMC5933634          DOI: 10.1177/1753465817710596

Source DB:  PubMed          Journal:  Ther Adv Respir Dis        ISSN: 1753-4658            Impact factor:   4.031


  24 in total

1.  Novel tobramycin inhalation powder in cystic fibrosis subjects: pharmacokinetics and safety.

Authors:  David E Geller; Michael W Konstan; Jeffrey Smith; Sarah B Noonberg; Carol Conrad
Journal:  Pediatr Pulmonol       Date:  2007-04

2.  Adherence to nebulised antibiotics in cystic fibrosis.

Authors:  Gary Latchford; Alistair Duff; Joanne Quinn; Steve Conway; Mark Conner
Journal:  Patient Educ Couns       Date:  2008-10-25

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.  Cystic fibrosis pulmonary guidelines: chronic medications for maintenance of lung health.

Authors:  Patrick A Flume; Brian P O'Sullivan; Karen A Robinson; Christopher H Goss; Peter J Mogayzel; Donna Beth Willey-Courand; Janet Bujan; Jonathan Finder; Mary Lester; Lynne Quittell; Randall Rosenblatt; Robert L Vender; Leslie Hazle; Kathy Sabadosa; Bruce Marshall
Journal:  Am J Respir Crit Care Med       Date:  2007-08-29       Impact factor: 21.405

5.  Inhaled versus nebulised tobramycin: a real world comparison in adult cystic fibrosis (CF).

Authors:  M J Harrison; M McCarthy; C Fleming; C Hickey; C Shortt; J A Eustace; D M Murphy; B J Plant
Journal:  J Cyst Fibros       Date:  2014-05-10       Impact factor: 5.482

6.  Tobramycin inhalation powder manufactured by improved process in cystic fibrosis: the randomized EDIT trial.

Authors:  Ivanka Galeva; Michael W Konstan; Mark Higgins; Gerhild Angyalosi; Florian Brockhaus; Simon Piggott; Karen Thomas; Alexander G Chuchalin
Journal:  Curr Med Res Opin       Date:  2013-06-05       Impact factor: 2.580

7.  Evaluation of dry powder inhalers with a focus on ease of use and user preference in inhaler-naïve individuals.

Authors:  Sofia von Schantz; Nina Katajavuori; Osmo Antikainen; Anne Juppo
Journal:  Int J Pharm       Date:  2016-05-18       Impact factor: 5.875

8.  One-year safety and efficacy of tobramycin powder for inhalation in patients with cystic fibrosis.

Authors:  Michael W Konstan; Patrick A Flume; Ivanka Galeva; Robert Wan; Laurie M Debonnett; Robert J Maykut; Gerhild Angyalosi
Journal:  Pediatr Pulmonol       Date:  2015-12-27

Review 9.  Inhaled therapy in cystic fibrosis: agents, devices and regimens.

Authors:  Penny Agent; Helen Parrott
Journal:  Breathe (Sheff)       Date:  2015-06

Review 10.  Tobramycin Inhalation Powder (TIP): An Efficient Treatment Strategy for the Management of Chronic Pseudomonas Aeruginosa Infection in Cystic Fibrosis.

Authors:  John Lam; Steven Vaughan; Michael D Parkins
Journal:  Clin Med Insights Circ Respir Pulm Med       Date:  2013-11-13
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  4 in total

Review 1.  Cough as an adverse effect on inhalation pharmaceutical products.

Authors:  Rachel Yoon Kyung Chang; Philip Chi Lip Kwok; Sussan Ghassabian; John D Brannan; Heikki O Koskela; Hak-Kim Chan
Journal:  Br J Pharmacol       Date:  2020-08-07       Impact factor: 8.739

Review 2.  Enhancement of lung gene delivery after aerosol: a new strategy using non-viral complexes with antibacterial properties.

Authors:  Angélique Mottais; Tony Le Gall; Yann Sibiril; Julian Ravel; Véronique Laurent; Frédérique d'Arbonneau; Tristan Montier
Journal:  Biosci Rep       Date:  2017-11-17       Impact factor: 3.840

Review 3.  Tobramycin inhalation powder for the treatment of pulmonary Pseudomonas aeruginosa infection in patients with cystic fibrosis: a review based on clinical evidence.

Authors:  Kamal Hamed; Laurie Debonnett
Journal:  Ther Adv Respir Dis       Date:  2017-02-17       Impact factor: 4.031

4.  Assessment of the microbial load of airway clearance devices used by a cohort of children with cystic fibrosis.

Authors:  B Linnane; N H O'Connell; E Obande; S S Dunne; C Clancy; M G Kiernan; D McGrath; K J O'Sullivan; L O'Sullivan; C P Dunne
Journal:  Infect Prev Pract       Date:  2021-06-06
  4 in total

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