Efficacy of Pseudomonas aeruginosa eradication regimens in bronchiectasis

Similar documents
Clinical Commissioning Policy: Levofloxacin nebuliser solution for chronic Pseudomonas lung infection in cystic fibrosis (all ages)

Clinical Commissioning Policy Proposition: Levofloxacin nebuliser solution for chronic Pseudomonas lung infection in cystic fibrosis (Adults)

C.S. HAWORTH 1, A. WANNER 2, J. FROEHLICH 3, T. O'NEAL 3, A. DAVIS 4, I. GONDA 3, A. O'DONNELL 5

CCLI. Bronchiectasis Treatment Antibiotics. Charles Haworth. Physician / Patient Conference, Georgetown University, May 2017

Appendix D Clinical specialist statement template

COPD Bronchiectasis Overlap Syndrome.

Inhaled Antibiotics in Non-CF. Dr Michael Loebinger Host Defence Unit Royal Brompton Hospital London, United Kingdom

Eradication regimens for early or recurrent Pseudomonas aeruginosa infection

Pseudomonas aeruginosa eradication guideline

Shared Care Guideline

Nebulised anti-pseudomonal antibiotics for cystic fibrosis (Review)

Bronchiectasis (non-cystic fibrosis), acute exacerbation: antimicrobial prescribing

OPAT FOR INFECTION IN BRONCHIECTASIS

Journal Club The ELITE Trial. Sandra Katalinic, Pharmacy Resident University Hospital of Northern British Columbia April 28, 2010

Is follow up chest X-ray required in children with round pneumonia?

Clinical Study Synopsis

Respiratory Research Newsletter

Dr Conroy Wong. Professor Richard Beasley. Dr Sarah Mooney. Professor Innes Asher

JUERGEN FROEHLICH, JANICE DAHMS, DAVID CIPOLLA,

Long term azithromycin therapy in patients with cystic fibrosis

Bronchiectasis. Introduction. Key points

The Relationship among COPD Severity, Inhaled Corticosteroid Use, and the Risk of Pneumonia.

Guidelines for the use of Nebulised Colistemethate Sodium (Colomycin) Injection () in Pseudomonas aeruginosa Lung Infections in Adults

New Medicine Assessment

LRI Children s Hospital

Clinical Commissioning Policy: Continuous aztreonam lysine for cystic fibrosis (all ages)

Inhalational antibacterial regimens in non-cystic fibrosis patients. Jeff Alder Bayer HealthCare

TRANSPARENCY COMMITTEE OPINION. 15 October Date of Marketing Authorisation (national procedure): 16 April 1997, variation of 18 February 2008

Lower airway microbiota for 'biomarker' measurements of cystic fibrosis disease progression?

Contents. Who should read / have access to this document? What is new in this version?

Dose-dependent effects of tobramycin in an animal model of Pseudomonas sinusitis Am J Rhino Jul-Aug; 21(4):423-7

Barriers and facilitators to vaccination in pregnancy: a qualitative study in Northern Ireland, 2017

INHALED ANTIBIOTICS THERAPY IN NON-CF LUNG DISEASE

without the permission of the author Not to be copied and distributed to others

Nebulised tobramycin for cystic fibrosis. Information for patients Pharmacy

Assessing response to treatment of exacerbations of bronchiectasis in adults

Management of bronchiectasis in adults

Cystic Fibrosis. Cystic Fibrosis. Cystic Fibrosis 5/01/2011 CYSTIC FIBROSIS OF THE PANCREAS AND ITS RELATION TO CELIAC DISEASE. D ANDERSEN.

Bronchiectasis Domiciliary treatment. Prof. Adam Hill Royal Infirmary and University of Edinburgh

TR Protocol Number: TR02-107

Research made simple: What is grounded theory?

Do processing time and storage of sputum influence quantitative bacteriology in bronchiectasis?

The management of bronchiectasis in Europe

roflumilast 500 microgram tablets (Daxas ) SMC No. (635/10) Nycomed Ltd

Technology appraisal guidance Published: 27 March 2013 nice.org.uk/guidance/ta276

National Horizon Scanning Centre. Mannitol dry powder for inhalation (Bronchitol) for cystic fibrosis. April 2008

Treatment of lung infection in patients with cystic fibrosis: Current and future strategies,

Bronchiectasis exacerbations; differences and management. Michael Loebinger Royal Brompton Imperial College

Development of novel inhaled antibiotic regimens in patients with cystic fibrosis (CF) and patients with non-cf bronchiectasis (BE)

Bronchiectasis. What is bronchiectasis? What causes bronchiectasis?

You Can Observe a Lot By Just Watching. Wayne J. Morgan, MD, CM

The team. Medical staff Dr Adam Hill Vacant post- Dr Lithgow Dr Ruzanna Frangulyan Specialist Trainee

Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis (Review)

Cystic Fibrosis the future

Palliative and Supportive Care in Cystic Fibrosis

Arnold L. Smith, MD; Stanley B. Fiel, MD, FCCP; Nicole Mayer-Hamblett, PhD; Bonnie Ramsey, MD; and Jane L. Burns, MD

NON-CF BRONCHIECTASIS IN ADULTS

Citation for published version (APA): Westerman, E. M. (2009). Studies on antibiotic aerosols for inhalation in cystic fibrosis s.n.

Conference Bronchiectasis A Growing Problem

P atients with cystic fibrosis (CF) experience repeated

DRUG: Introduction. `Shared Care Guidelines. They can also be used long term for chronic pulmonary Pseudomonas aeruginosa infection.

Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis(review)

HPV vaccine acceptance in male adolescents

What is Cystic Fibrosis? CYSTIC FIBROSIS. Genetics of CF

Annual Surveillance Summary: Pseudomonas aeruginosa Infections in the Military Health System (MHS), 2017

ivlewbel: Uses heteroscedasticity to estimate mismeasured and endogenous regressor models

Nebulised hypertonic saline for cystic fibrosis.

Early Pseudomonas Infection Control (EPIC) Clinical Study. Overview for Families

Issues of validity and reliability in qualitative research

Care of bladder cancer patients diagnosed in Northern Ireland 2010 & 2011 (Summary)

Macrolide therapy in cystic fibrosis: new developments in clinical use

Cystic Fibrosis Panel Applications (Dornase Alfa) Contents

4.6 Small airways disease

Bronchiectasis it s effects on the NZ population and what we can do to address this

Controlled trial of cycled antibiotic prophylaxis to prevent initial Pseudomonas aeruginosa infection in children with cystic fibrosis

Bronchial reactions to the inhalation of high-dose tobramycin in cystic fibrosis

Azithromycin may antagonize inhaled tobramycin when targeting P. aeruginosa in cystic fibrosis

How To Assess Severity and Prognosis

A randomised clinical trial of nebulised tobramycin or colistin in cystic fibrosis

The role of serum Pseudomonas aeruginosa antibodies in the diagnosis and follow-up of cystic fibrosis

Digoxin use after diagnosis of colorectal cancer and survival: a population-based cohort study.

Inhaled Hypertonic Saline In Adults Hospitalized For Exacerbation Of Cystic Fibrosis Lung Disease: A Retrospective Study For peer review only

Chronic Obstructive Pulmonary Disease (COPD) Treatment Guidelines

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

European Medicines Agency decision

The Bacteriology of Bronchiectasis in Australian Indigenous children

Treatment of early Pseudomonas aeruginosa infection in patients with cystic fibrosis: the ELITE trial

Implementation of a successful eradication protocol for Burkholderia Cepacia complex in cystic fibrosis patients

Cystic Fibrosis: Pulmonary Exacerbations Management Guidelines

Surveillance report Published: 6 April 2016 nice.org.uk. NICE All rights reserved.

Microbiological surveillance in lung disease in ataxia telangiectasia

Pulmonary Exacerbations:

Clinical Study Synopsis

Unconscious Gender Bias in Academia: from PhD Students to Professors

Mechanisms of postural threat: the Achilles heel of postural control?

Role of long term antibiotics in chronic respiratory diseases

Smith, J., & Noble, H. (2014). Bias in research. Evidence-Based Nursing, 17(4), DOI: /eb

Bronchiectasis. Grant Waterer. Professor of Medicine, University of Western Australia Adjunct Professor of Medicine, Northwestern University, Chicago

Research priorities in bronchiectasis: a consensus statement from the EMBARC Clinical Research Collaboration

The Adult Cystic Fibrosis Airway Microbiota Is Stable over Time and Infection Type, and Highly Resilient to Antibiotic Treatment of Exacerbations

Transcription:

Efficacy of Pseudomonas aeruginosa eradication regimens in bronchiectasis Vallières, E., Tumelty, K., Tunney, M. M., Hannah, R., Hewitt, O., Elborn, J. S., & Downey, D. G. (2017). Efficacy of Pseudomonas aeruginosa eradication regimens in bronchiectasis. European Respiratory Journal, 49(4). DOI: 10.1183/13993003.00851-2016 Published in: European Respiratory Journal Document Version: Peer reviewed version Queen's University Belfast - Research Portal: Link to publication record in Queen's University Belfast Research Portal Publisher rights 2017 ERS. This work is made available online in accordance with the publisher s policies. Please refer to any applicable terms of use of the publisher. General rights Copyright for the publications made accessible via the Queen's University Belfast Research Portal is retained by the author(s) and / or other copyright owners and it is a condition of accessing these publications that users recognise and abide by the legal requirements associated with these rights. Take down policy The Research Portal is Queen's institutional repository that provides access to Queen's research output. Every effort has been made to ensure that content in the Research Portal does not infringe any person's rights, or applicable UK laws. If you discover content in the Research Portal that you believe breaches copyright or violates any law, please contact openaccess@qub.ac.uk. Download date:13. Apr. 2018

Efficacy of Pseudomonas aeruginosa Eradication Regimens in Bronchiectasis Emilie Vallières 1, 3-4, Karen Tumelty 4, Michael M. Tunney 2-4, Rosemary Hannah 4, Oonagh Hewitt 4, J. Stuart Elborn 1, 3-4, Damian G. Downey 3-4 1 Queen`s University Belfast, School of Medicine, Dentistry and Biomedical Sciences, Belfast, UK 2 Queen`s University Belfast, School of Pharmacy, Belfast, UK 3 CF and Airways Microbiology Research Group, Queen`s University Belfast, Belfast, UK 4 Belfast City Hospital, Belfast Health and Social Care Trust, Belfast, UK Patients with bronchiectasis and chronic infection with Pseudomonas aeruginosa have more frequent pulmonary exacerbations and hospital admissions, reduced quality of life and survival, in comparison to those who are P. aeruginosa free [1]. Guidelines published by the British Thoracic Society recommend treatment to eradicate P. aeruginosa when first isolated in respiratory tract samples of people with bronchiectasis [2]. However, the best regimen to achieve eradication and how successful eradication is determined are not known. At the Northern Ireland Regional Respiratory Centre (Belfast, United Kingdom), the preferred eradication regimen is a combination of oral ciprofloxacin (for 6 weeks), and nebulised colistimethate sodium (for 3 months)[3]. However, this regimen is varied, according to patient experience (e.g. drug allergy and/or intolerance), clinician judgement and the antimicrobial susceptibility profile of the P. aeruginosa isolate. Therefore, the aims of this study were to determine if the eradication regimens used differed in their efficacy, in order to optimise and standardise clinical practice. Adult patients with bronchiectasis who underwent treatment aimed at P. aeruginosa eradication between 1 January 2007 and 31 December 2014 were identified from the clinical database. Historical data were collected from medical notes. P. aeruginosa eradication was considered successful if all (and at least 3) bacteriologic cultures from respiratory samples collected during the 6-month period following the eradication attempt were negative for P. aeruginosa. Patients who remained on chronic (>3 months) nebulised antibiotics were excluded from the analysis, as this treatment could suppress bacterial growth and overestimate eradication success rate.. In order to select patients with recent acquisition of P.

aeruginosa, we included only those who had never grown P. aeruginosa or those who were free of this bacteria for at least 2 years (and documented by 5 or more negative samples) before the eradication trial. All patients had a second confirmatory sample collected prior to initiation of eradication therapy. Sixty-four (64) patients who had at least one eradication attempt were identified. Their mean (SD) age was 64 (1.6) years, 58% (n=37) were male, and 63% (n=39/62) of patients were receiving azithromycin 500 mg thrice weekly. Forced expiratory volume in one second (FEV 1) was 1.70 (0.15) litres and Forced vital capacity 2.89 (0.19) litres. Eighty-four percent of patients (n=54) received an eradication regimen that included nebulised colistimethate sodium (table 1). The most frequent regimen used was the combination of nebulised colistimethate sodium with oral ciprofloxacin, prescribed for at least 3 weeks (n=27, 42%). Overall, the eradication success rate at 6 months was 52% (n=33) and 70% (n=23) of these patients remained P. aeruginosa free for at least 1 year. Treatment combinations including nebulised colistimethate sodium were more effective (n=31/54, 57%) than those with systemic antibiotics alone (n=2/10, 20%) (Student t-test, p=0.04). Intravenous anti-pseudomonal antibiotics (n=9/18, 50%) were not superior to oral ciprofloxacin (n=21/35, 60%) in the subgroup of patients who also received nebulised antibiotics as part of their regimen (table 1). Additionally, prolonged courses of oral ciprofloxacin (> 3 weeks) were no more efficient than shorter treatment periods (n=15/27, 56% vs n=6/8, 75%). The study population was stratified according to eradication outcome (success versus failure). Demographic and clinical data of both groups were compared in order to identify factors that could have impacted eradication outcome. Age, gender, lung function and duration of infection prior to eradication

were similar between groups. However, chronic azithromycin use was more frequent amongst patients who successfully cleared P. aeruginosa infection (75% vs 47%, p=0.04). This study suggests that eradication regimens combining nebulised and systemic antibiotics are more efficient for P. aeruginosa eradication than treatment without inhaled antibiotic. This finding supports results recently published by Orriols et al. [4]. In that study, the authors randomised 35 patients who recently acquired P. aeruginosa infection to receive 2 weeks of intravenous antibiotics (ceftazidime and tobramycin), followed by either 3 months of nebulised tobramycin or placebo. They found that the interval for recurrence of P. aeruginosa infection was extended in the tobramycin group and that the treatment arm had a reduced number of exacerbations and hospitalisations during the follow-up period. However, one third of patients in the tobramycin group experienced bronchospasm. In our cohort, respiratory symptoms associated with nebulised colistimethate sodium were infrequent as only 2 patients had to discontinue the inhaled treatment prematurely. Although consistent with our findings, results from Orriols study must be interpreted cautiously due to the small sample size and limitations in study design and reporting. The potential benefit conferred by azithromycin on P. aeruginosa eradication needs further investigation. Azithromycin may contribute to biofilm disruption, and may augment the action of antipseudomonal antibiotics [5-7]. In conclusion, this study suggests the superiority of a combination of systemic (oral or intravenous) and inhaled antibiotics in the initial eradication treatment of P. aeruginosa infection in bronchiectasis patients, in comparison to systemic antibiotics only. Considering the literature gap addressing P. aeruginosa eradication in this population, these findings should inform the design of appropriate randomised clinical trials, to determine the best therapeutic approach, including the role of macrolides, in the treatment of new infections with P. aeruginosa in people with bronchiectasis.

Table 1: Frequency and efficacy of antibiotics used as first-line eradication regimens. Treatment Nebulised colistimethate sodium (3 months) & Cipro ( 3 weeks) Cipro (>3 weeks) IVs (2weeks) Cipro + IVs Nil else No nebulised colistimethate sodium Cipro IVs Cipro + IVs Patients, n 8 27 13 5 1 6 2 2 Success, n (%) 6 (75) 15 (55.5) 7 (54) 2 (40) 1 (100) 1 (17) 0 (0) 1 (50) Total 31/54 (57%) 2/10 (20%) 1. Finch, S., et al., A Comprehensive Analysis of the Impact of Pseudomonas aeruginosa Colonization on Prognosis in Adult Bronchiectasis. Ann Am Thorac Soc, 2015. 12(11): p. 1602-11. 2. Pasteur, M.C., D. Bilton, and A.T. Hill, British Thoracic Society guideline for non-cf bronchiectasis. Thorax, 2010. 65 Suppl 1: p. i1-58. 3. Valerius, N.H., C. Koch, and N. Hoiby, Prevention of chronic Pseudomonas aeruginosa colonisation in cystic fibrosis by early treatment. Lancet, 1991. 338(8769): p. 725-6. 4. Orriols, R., et al., Eradication Therapy against Pseudomonas aeruginosa in Non-Cystic Fibrosis Bronchiectasis. Respiration, 2015. 90(4): p. 299-305. 5. Wagner, T., et al., Effects of azithromycin on clinical isolates of Pseudomonas aeruginosa from cystic fibrosis patients. Chest, 2005. 128(2): p. 912-9. 6. Lutz, L., et al., Macrolides decrease the minimal inhibitory concentration of anti-pseudomonal agents against Pseudomonas aeruginosa from cystic fibrosis patients in biofilm. BMC Microbiol, 2012. 12: p. 196. 7. Ichimiya, T., et al., The influence of azithromycin on the biofilm formation of Pseudomonas aeruginosa in vitro. Chemotherapy, 1996. 42(3): p. 186-91.