Literature DB >> 32890021

Treatment of pulmonary exacerbations in cystic fibrosis.

Christabella Ng1, Tejaswi Nadig2, Alan R Smyth1, Patrick Flume2.   

Abstract

PURPOSE OF REVIEW: This review will discuss the challenges of defining a pulmonary exacerbations in cystic fibrosis and the key pathogens, which contribute. It will discuss the treatment options currently available and the importance of preventing pulmonary exacerbations. RECENT
FINDINGS: The basis for treatment of pulmonary exacerbations remains unchanged over the past 15 years and whilst there have been trials exploring alternative antibiotics, there has been little change. However, there are ongoing studies that are expected to establish a platform for identifying best practices. Chronic cystic fibrosis therapies have been shown to reduce pulmonary exacerbations. In the era of new CFTR (cystic fibrosis transmembrane conductance regulator) modulator therapies, the number of pulmonary exacerbations are expected to be even fewer. However, it is unclear whether the other chronic therapies can be discontinued without losing their benefits in reducing exacerbations.
SUMMARY: Although there is no universal definition of a pulmonary exacerbation in cystic fibrosis, proposed definitions have many similarities. We have outlined the current recommendations for treatment of pulmonary exacerbations, including the duration and location of treatments. We have also summarized the key therapies used for prevention of pulmonary exacerbations in cystic fibrosis.

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Year:  2020        PMID: 32890021      PMCID: PMC7958864          DOI: 10.1097/MCP.0000000000000730

Source DB:  PubMed          Journal:  Curr Opin Pulm Med        ISSN: 1070-5287            Impact factor:   2.868


  39 in total

1.  Location and duration of treatment of cystic fibrosis respiratory exacerbations do not affect outcomes.

Authors:  J Michael Collaco; Deanna M Green; Garry R Cutting; Kathleen M Naughton; Peter J Mogayzel
Journal:  Am J Respir Crit Care Med       Date:  2010-06-25       Impact factor: 21.405

2.  Pulmonary exacerbation: towards a definition for use in clinical trials. Report from the EuroCareCF Working Group on outcome parameters in clinical trials.

Authors:  D Bilton; G Canny; S Conway; S Dumcius; L Hjelte; M Proesmans; B Tümmler; V Vavrova; K De Boeck
Journal:  J Cyst Fibros       Date:  2011-06       Impact factor: 5.482

3.  Study design considerations for the Standardized Treatment of Pulmonary Exacerbations 2 (STOP2): A trial to compare intravenous antibiotic treatment durations in CF.

Authors:  Sonya L Heltshe; Natalie E West; Donald R VanDevanter; D B Sanders; Valeria V Beckett; Patrick A Flume; Christopher H Goss
Journal:  Contemp Clin Trials       Date:  2017-11-21       Impact factor: 2.226

4.  Combination antibiotic susceptibility testing to treat exacerbations of cystic fibrosis associated with multiresistant bacteria: a randomised, double-blind, controlled clinical trial.

Authors:  Shawn D Aaron; Katherine L Vandemheen; Wendy Ferris; Dean Fergusson; Elizabeth Tullis; David Haase; Yves Berthiaume; Neil Brown; Pearce Wilcox; Veronica Yozghatlian; Peter Bye; Scott Bell; Francis Chan; Barbara Rose; Alphonse Jeanneret; Anne Stephenson; Mary Noseworthy; Andreas Freitag; Nigel Paterson; Steve Doucette; Colin Harbour; Michel Ruel; Noni MacDonald
Journal:  Lancet       Date:  2005 Aug 6-12       Impact factor: 79.321

5.  Recovery of lung function following a pulmonary exacerbation in patients with cystic fibrosis and the G551D-CFTR mutation treated with ivacaftor.

Authors:  Patrick A Flume; Claire E Wainwright; D Elizabeth Tullis; Sally Rodriguez; Minoo Niknian; Mark Higgins; Jane C Davies; Jeffrey S Wagener
Journal:  J Cyst Fibros       Date:  2017-06-24       Impact factor: 5.482

6.  Approach to treating cystic fibrosis pulmonary exacerbations varies widely across US CF care centers.

Authors:  Nathan C Kraynack; M David Gothard; Lynn M Falletta; John T McBride
Journal:  Pediatr Pulmonol       Date:  2011-04-04

7.  Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR.

Authors:  Claire E Wainwright; J Stuart Elborn; Bonnie W Ramsey; Gautham Marigowda; Xiaohong Huang; Marco Cipolli; Carla Colombo; Jane C Davies; Kris De Boeck; Patrick A Flume; Michael W Konstan; Susanna A McColley; Karen McCoy; Edward F McKone; Anne Munck; Felix Ratjen; Steven M Rowe; David Waltz; Michael P Boyle
Journal:  N Engl J Med       Date:  2015-05-17       Impact factor: 91.245

Review 8.  Macrolide antibiotics for cystic fibrosis.

Authors:  Kevin W Southern; Pierre M Barker; Arturo Solis-Moya; Latifa Patel
Journal:  Cochrane Database Syst Rev       Date:  2012-11-14

9.  Early anti-pseudomonal acquisition in young patients with cystic fibrosis: rationale and design of the EPIC clinical trial and observational study'.

Authors:  Miriam M Treggiari; Margaret Rosenfeld; Nicole Mayer-Hamblett; George Retsch-Bogart; Ronald L Gibson; Judy Williams; Julia Emerson; Richard A Kronmal; Bonnie W Ramsey
Journal:  Contemp Clin Trials       Date:  2009-01-15       Impact factor: 2.226

Review 10.  Neuraminidase inhibitors for the treatment of influenza infection in people with cystic fibrosis.

Authors:  Vanitha A Jagannath; G V Asokan; Zbys Fedorowicz; Tim W R Lee
Journal:  Cochrane Database Syst Rev       Date:  2016-02-24
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  3 in total

1.  Health care costs in a randomized trial of antimicrobial duration among cystic fibrosis patients with pulmonary exacerbations.

Authors:  Laura S Gold; Ryan N Hansen; Donald L Patrick; Ashley Tabah; Sonya L Heltshe; Patrick A Flume; Christopher H Goss; Natalie E West; Don B Sanders; Donald R VanDevanter; Larry Kessler
Journal:  J Cyst Fibros       Date:  2022-03-14       Impact factor: 5.527

Review 2.  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

3.  Lung clearance index to characterize clinical phenotypes of children and adolescents with cystic fibrosis.

Authors:  Simone Gambazza; Federico Ambrogi; Federica Carta; Laura Moroni; Maria Russo; Anna Brivio; Carla Colombo
Journal:  BMC Pulm Med       Date:  2022-04-01       Impact factor: 3.317

  3 in total

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