Literature DB >> 31875166

Duration of antibiotic therapy in non-cystic fibrosis bronchiectasis.

R Somayaji1, C H Goss2,3.   

Abstract

PURPOSE OF REVIEW: a)We conducted a review of the current evidence relating to antibiotic duration in the short and long-term management of non-cystic fibrosis bronchiectasis. RECENT
FINDINGS: b)In non-cystic fibrosis pulmonary exacerbations, evidence is primarily based on expert consensus and recent guidelines recommend antibiotic durations of approximately 14 days. Chronic antibiotics (oral or inhaled) are recommended in patients with frequent exacerbations or with chronic Pseudomonas aeruginosa airways infection. Macrolides are the best studied therapies for long-term use with evidence for effect limited to a 12 month duration. Encouragingly, there are increased efforts to develop registries and conduct larger population level studies to improve patient care.
SUMMARY: c)There is a paucity of evidence for optimal antibiotic strategies in exacerbations and chronic maintenance in persons with non-cystic fibrosis bronchiectasis. Rationally designed studies which utilize a registry and population-based approach will be critical to build evidence-based strategies to optimize management of non-cystic fibrosis bronchiectasis.

Entities:  

Keywords:  FEV1; non-cystic fibrosis bronchiectasis; pulmonary exacerbation; respiratory symptoms; treatment duration

Year:  2019        PMID: 31875166      PMCID: PMC6929711          DOI: 10.1007/s13665-019-00235-w

Source DB:  PubMed          Journal:  Curr Pulmonol Rep


  50 in total

1.  Bacterial colonisation in patients with bronchiectasis: microbiological pattern and risk factors.

Authors:  J Angrill; C Agustí; R de Celis; A Rañó; J Gonzalez; T Solé; A Xaubet; R Rodriguez-Roisin; A Torres
Journal:  Thorax       Date:  2002-01       Impact factor: 9.139

2.  Outcomes of Pseudomonas eradication therapy in patients with non-cystic fibrosis bronchiectasis.

Authors:  Laura White; Ghazi Mirrani; Mark Grover; Judith Rollason; Adam Malin; Jay Suntharalingam
Journal:  Respir Med       Date:  2011-12-26       Impact factor: 3.415

3.  Molecular epidemiological analysis suggests cross-infection with Pseudomonas aeruginosa is rare in non-cystic fibrosis bronchiectasis.

Authors:  Anthony De Soyza; Audrey Perry; Amanda J Hall; Syba S Sunny; Kathy E Walton; Nazim Mustafa; Jane Turton; Dervla T Kenna; Craig Winstanley
Journal:  Eur Respir J       Date:  2013-10-31       Impact factor: 16.671

Review 4.  Inhaled antibiotics for stable non-cystic fibrosis bronchiectasis: a systematic review.

Authors:  Alessandra Monteiro Brodt; Elizabeth Stovold; Linjie Zhang
Journal:  Eur Respir J       Date:  2014-06-12       Impact factor: 16.671

5.  The use of antimicrobial susceptibility testing in pediatric cystic fibrosis pulmonary exacerbations.

Authors:  Jonathan D Cogen; Kathryn B Whitlock; Ronald L Gibson; Lucas R Hoffman; Donald R VanDevanter
Journal:  J Cyst Fibros       Date:  2019-05-28       Impact factor: 5.482

6.  Lung microbiota and bacterial abundance in patients with bronchiectasis when clinically stable and during exacerbation.

Authors:  Michael M Tunney; Gisli G Einarsson; Lan Wei; Maire Drain; Erich R Klem; Chris Cardwell; Madeleine Ennis; Richard C Boucher; Matthew C Wolfgang; J Stuart Elborn
Journal:  Am J Respir Crit Care Med       Date:  2013-05-15       Impact factor: 21.405

7.  Short- and long-term antibiotic treatment reduces airway and systemic inflammation in non-cystic fibrosis bronchiectasis.

Authors:  James D Chalmers; Maeve P Smith; Brian J McHugh; Cathy Doherty; John R Govan; Adam T Hill
Journal:  Am J Respir Crit Care Med       Date:  2012-06-28       Impact factor: 21.405

Review 8.  Prolonged antibiotics for non-cystic fibrosis bronchiectasis in children and adults.

Authors:  Khin Hnin; Chau Nguyen; Kristin V Carson; David J Evans; Michael Greenstone; Brian J Smith
Journal:  Cochrane Database Syst Rev       Date:  2015-08-13

Review 9.  Macrolide therapy in adults and children with non-cystic fibrosis bronchiectasis: a systematic review and meta-analysis.

Authors:  Yong-Hua Gao; Wei-Jie Guan; Gang Xu; Yan Tang; Yang Gao; Zhi-Ya Lin; Zhi-Min Lin; Nan-Shan Zhong; Rong-Chang Chen
Journal:  PLoS One       Date:  2014-03-06       Impact factor: 3.240

10.  Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis.

Authors:  Mark J Hoegger; Anthony J Fischer; James D McMenimen; Lynda S Ostedgaard; Alex J Tucker; Maged A Awadalla; Thomas O Moninger; Andrew S Michalski; Eric A Hoffman; Joseph Zabner; David A Stoltz; Michael J Welsh
Journal:  Science       Date:  2014-08-15       Impact factor: 47.728

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