Literature DB >> 26270620

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

Khin Hnin1, Chau Nguyen, Kristin V Carson, David J Evans, Michael Greenstone, Brian J Smith.   

Abstract

BACKGROUND: The vicious cycle hypothesis for bronchiectasis predicts that bacterial colonisation of the respiratory tract perpetuates inflammatory change. This damages the mucociliary escalator, preventing bacterial clearance and allowing persistence of pro-inflammatory mediators. Conventional treatment with physiotherapy and intermittent antibiotics is believed to improve the condition of people with bronchiectasis, although no conclusive data show that these interventions influence the natural history of the condition. Various strategies have been tried to interrupt this cycle of infection and inflammation, including prolonging antibiotic treatment with the goal of allowing the airway mucosa to heal.
OBJECTIVES: To determine the benefits of prolonged antibiotic therapy in the treatment of patients with bronchiectasis. SEARCH
METHODS: We searched the Cochrane Airways Group Trials Register and reference lists of identified articles. Searches were current as of February 2014. SELECTION CRITERIA: Randomised trials examining the use of prolonged antibiotic therapy (for four or more weeks) in the treatment of bronchiectasis compared with placebo or usual care. DATA COLLECTION AND ANALYSIS: Two review authors independently assessed trial quality and extracted data. We contacted study authors to ask for missing information. MAIN
RESULTS: Eighteen trials met the inclusion criteria, randomly assigning a total of 1157 participants. Antibiotics were given for between four weeks and 83 weeks. Limited meta-analysis was possible because of the diversity of outcomes reported in these trials. Based on the number of participants with at least one exacerbation, the meta-analysis showed significant effects in favour of the intervention (odds ratio (OR) 0.31, 95% confidence interval (CI) 0.19 to 0.52; P value < 0.00001), with events occurring in 271 per 1000 people in the intervention arm (95% CI 126 to 385) and in 546 per 1000 in the control population, based on evidence of moderate quality. A non-statistically significant reduction in hospitalisation favoured the use of prolonged antibiotics with a moderate quality grade of supporting evidence (37 per 1000 in the intervention arm (95% CI 13 to 96) and 87 per 1000 in control (OR 0.40, 95% CI 0.14 to 1.11; P value = 0.08). Drug resistance developed in 36 of 220 participants taking antibiotics compared with 10 of 211 participants given placebo or standard therapy (OR 3.48, 95% CI 1.20 to 10.07; P value = 0.02), translating to natural frequencies of 155 per 1000 in the intervention arm (95% CI 59 to 346) and 50 per 1000 in the control arm. The intervention was well tolerated with no overall significant difference in withdrawal between treatment and placebo groups (OR 0.91, 95% CI 0.56 to 1.49). Diarrhoea was commonly reported as an adverse event, particularly with an oral intervention. AUTHORS'
CONCLUSIONS: Available evidence shows benefit associated with use of prolonged antibiotics in the treatment of patients with bronchiectasis, at least halving the odds of exacerbation (with 275 fewer exacerbations per every 1000 people treated in the antibiotic arm compared with the control arm) and hospitalisation (50 fewer hospitalisations per 1000 people in the antibiotic arm compared with the control arm). However, the risk of emerging drug resistance is increased more than threefold. This review is limited by diversity of trials and by evidence of moderate to low quality. Further randomised controlled trials with adequate power and standardised end points are required.

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Year:  2015        PMID: 26270620      PMCID: PMC6483474          DOI: 10.1002/14651858.CD001392.pub3

Source DB:  PubMed          Journal:  Cochrane Database Syst Rev        ISSN: 1361-6137


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10.  Study protocol, rationale and recruitment in a European multi-centre randomized controlled trial to determine the efficacy and safety of azithromycin maintenance therapy for 6 months in primary ciliary dyskinesia.

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  19 in total

Review 1.  Inhaled Antibiotics for Gram-Negative Respiratory Infections.

Authors:  Eric Wenzler; Dustin R Fraidenburg; Tonya Scardina; Larry H Danziger
Journal:  Clin Microbiol Rev       Date:  2016-07       Impact factor: 26.132

Review 2.  Intermittent prophylactic antibiotics for bronchiectasis.

Authors:  Sally Spencer; Tim Donovan; James D Chalmers; Alexander G Mathioudakis; Melissa J McDonnell; Anthony Tsang; Peter Leadbetter
Journal:  Cochrane Database Syst Rev       Date:  2022-01-05

3.  Duration of antibiotic therapy in non-cystic fibrosis bronchiectasis.

Authors:  R Somayaji; C H Goss
Journal:  Curr Pulmonol Rep       Date:  2019-11-26

4.  Comorbidities and the risk of mortality in patients with bronchiectasis: an international multicentre cohort study.

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Journal:  Lancet Respir Med       Date:  2016-11-16       Impact factor: 30.700

5.  Adverse events in people taking macrolide antibiotics versus placebo for any indication.

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6.  Airway clearance techniques for cystic fibrosis: an overview of Cochrane systematic reviews.

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7.  The Saudi Thoracic Society guidelines for diagnosis and management of noncystic fibrosis bronchiectasis.

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Journal:  Ann Thorac Med       Date:  2017 Jul-Sep       Impact factor: 2.219

Review 8.  Continuous versus intermittent antibiotics for bronchiectasis.

Authors:  Tim Donovan; Lambert M Felix; James D Chalmers; Stephen J Milan; Alexander G Mathioudakis; Sally Spencer
Journal:  Cochrane Database Syst Rev       Date:  2018-06-03

Review 9.  Macrolide antibiotics for bronchiectasis.

Authors:  Carol Kelly; James D Chalmers; Iain Crossingham; Nicola Relph; Lambert M Felix; David J Evans; Stephen J Milan; Sally Spencer
Journal:  Cochrane Database Syst Rev       Date:  2018-03-15

Review 10.  Oral versus inhaled antibiotics for bronchiectasis.

Authors:  Sally Spencer; Lambert M Felix; Stephen J Milan; Rebecca Normansell; Pieter C Goeminne; James D Chalmers; Tim Donovan
Journal:  Cochrane Database Syst Rev       Date:  2018-03-27
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