Literature DB >> 25496726

Association between the introduction of a new cystic fibrosis inhaled antibiotic class and change in prevalence of patients receiving multiple inhaled antibiotic classes.

Elliott C Dasenbrook1, Michael W Konstan2, Donald R VanDevanter3.   

Abstract

BACKGROUND: In 2010, aztreonam for inhalation solution joined aminoglycosides and colistimethate as a new cystic fibrosis (CF) chronic inhaled antimicrobial therapy. We studied how the introduction of this new inhaled antibiotic class changed the management of US CF patients.
METHODS: The use of inhaled aminoglycosides, colistimethate, and aztreonam among patients followed in the CF Foundation Patient Registry was analyzed by age group, lung disease stage, and microbiologic status both annually, and at individual visits between 2009 and 2012.
RESULTS: The overall prevalence of inhaled antibiotic use did not change during the period, but the prevalence of annual and any visit treatment with >1 inhaled antibiotic class more than doubled. Adults, those with advanced lung disease, and those with >1 Pseudomonas aeruginosa respiratory culture were more likely to receive >1 antibiotic class.
CONCLUSIONS: Inhaled antibiotic management of US CF patients has dramatically changed in association with the introduction of a third inhaled antibiotic class.
Copyright © 2014 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cystic fibrosis; Inhaled antibiotics; Observational research; Patient registry; Pseudomonas aeruginosa

Mesh:

Substances:

Year:  2014        PMID: 25496726      PMCID: PMC4417393          DOI: 10.1016/j.jcf.2014.11.005

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


  8 in total

1.  Spirometric reference values from a sample of the general U.S. population.

Authors:  J L Hankinson; J R Odencrantz; K B Fedan
Journal:  Am J Respir Crit Care Med       Date:  1999-01       Impact factor: 21.405

2.  Applying clinical outcome variables to appropriate aerosolized antibiotics for the treatment of patients with cystic fibrosis.

Authors:  Donald R VanDevanter; Manfred Ballmann; Patrick A Flume
Journal:  Respir Med       Date:  2011-12       Impact factor: 3.415

Review 3.  Cystic fibrosis pulmonary guidelines. Chronic medications for maintenance of lung health.

Authors:  Peter J Mogayzel; Edward T Naureckas; Karen A Robinson; Gary Mueller; Denis Hadjiliadis; Jeffrey B Hoag; Lisa Lubsch; Leslie Hazle; Kathy Sabadosa; Bruce Marshall
Journal:  Am J Respir Crit Care Med       Date:  2013-04-01       Impact factor: 21.405

4.  Shifting patterns of inhaled antibiotic use in cystic fibrosis.

Authors:  Samuel M Moskowitz; Stefanie J Silva; Nicole Mayer-Hamblett; David J Pasta; David R Mink; Jenny A Mabie; Michael W Konstan; Jeffrey S Wagener
Journal:  Pediatr Pulmonol       Date:  2008-09

5.  Pulmonary function between 6 and 18 years of age.

Authors:  X Wang; D W Dockery; D Wypij; M E Fay; B G Ferris
Journal:  Pediatr Pulmonol       Date:  1993-02

Review 6.  Treatment of lung infection in patients with cystic fibrosis: current and future strategies.

Authors:  Gerd Döring; Patrick Flume; Harry Heijerman; J Stuart Elborn
Journal:  J Cyst Fibros       Date:  2012-11-06       Impact factor: 5.482

7.  Outcome measures for clinical trials assessing treatment of cystic fibrosis lung disease.

Authors:  Donald R VanDevanter; Michael W Konstan
Journal:  Clin Investig (Lond)       Date:  2012

8.  eulerAPE: drawing area-proportional 3-Venn diagrams using ellipses.

Authors:  Luana Micallef; Peter Rodgers
Journal:  PLoS One       Date:  2014-07-17       Impact factor: 3.240

  8 in total
  8 in total

Review 1.  Innovating cystic fibrosis clinical trial designs in an era of successful standard of care therapies.

Authors:  Donald R VanDevanter; Nicole Mayer-Hamblett
Journal:  Curr Opin Pulm Med       Date:  2017-11       Impact factor: 3.155

Review 2.  Inhaled Antibiotic Therapy in Chronic Respiratory Diseases.

Authors:  Diego J Maselli; Holly Keyt; Marcos I Restrepo
Journal:  Int J Mol Sci       Date:  2017-05-16       Impact factor: 5.923

3.  An empirical method to cluster objective nebulizer adherence data among adults with cystic fibrosis.

Authors:  Zhe H Hoo; Michael J Campbell; Rachael Curley; Martin J Wildman
Journal:  Patient Prefer Adherence       Date:  2017-03-24       Impact factor: 2.711

4.  Developing Inhaled Antibiotics in Cystic Fibrosis: Current Challenges and Opportunities.

Authors:  Dave P Nichols; Anthony G Durmowicz; Ann Field; Patrick A Flume; Donald R VanDevanter; Nicole Mayer-Hamblett
Journal:  Ann Am Thorac Soc       Date:  2019-05

Review 5.  Cystic Fibrosis: Recent Insights into Inhaled Antibiotic Treatment and Future Perspectives.

Authors:  Giovanni Taccetti; Michela Francalanci; Giovanna Pizzamiglio; Barbara Messore; Vincenzo Carnovale; Giuseppe Cimino; Marco Cipolli
Journal:  Antibiotics (Basel)       Date:  2021-03-22

6.  Ciprofloxacin dry powder inhaler in cystic fibrosis.

Authors:  J Stuart Elborn
Journal:  BMJ Open Respir Res       Date:  2016-01-04

7.  An 8 week open-label interventional multicenter study to explore the lung clearance index as endpoint for clinical trials in cystic fibrosis patients ≥8 years of age, chronically infected with Pseudomonas aeruginosa.

Authors:  Sivagurunathan Sutharsan; Susanne Naehrig; Uwe Mellies; Christian Sieder; Jörg Ziegler
Journal:  BMC Pulm Med       Date:  2020-06-12       Impact factor: 3.317

8.  Rescue therapy within the UK Cystic Fibrosis Registry: An exploration of predictors of intravenous antibiotic use amongst adults with CF.

Authors:  Zhe Hui Hoo; Martin J Wildman; Rachael Curley; Stephen J Walters; Michael J Campbell
Journal:  Respirology       Date:  2017-09-14       Impact factor: 6.424

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.