Effect of long term treatment with azithromycin on clinical status and lung function parameters in cystic fibrosis patients colonised by pseudomonas aeruginosa

A. Vracaric, P. Minic (Uzice, Belgrade, Republic Of Serbia)

Source: Annual Congress 2009 - Cystic fibrosis: advances in clinical research
Session: Cystic fibrosis: advances in clinical research
Session type: Thematic Poster Session
Number: 1268
Disease area: Respiratory infections

Congress or journal article abstract

Abstract

Background: The macrolide antibiotic azithromycin has anti-inflammatory properties potentially benefitial in cystic fibrosis patients.
Objectives:The purpose of our study was to show effect of 6-month long treatment with azithromycin on clinical status of CF patients.Another aim was to demonstrate improvement of lung function during this treatment.
Design: 30 CF patients colonised by Pseudomonas aeruginosa were included. One group of 15 patients received azithromycin 250/500mg three times a week for 6 months. The second was control group. Groups were matched as far as possible for age, clinical status and lung function. After 6 months we compared clinical status (body mass index (BMI), sputum microbiology, acute exacerbations and Chrispin-Norman chest radiograph score) and lung function between the groups.
Methods:Clinical status was evaluated monthly.Standard CF treatments were continued.Acute exacerbations were treated by iv antibiotics.
Results:Sputum microbiology was unchanged in both groups at the end of treatment. Increase in BMI was noted in the macrolide treated group (p<0,05).Increase in Chrispin-Norman score was registered in the second group (p<0,01).The frequency of pulmonary exacerbations was significantly lower in the azithromycin treated group (0,47 vs. 1,27; p<0,01).Pulmonary function improved in the first group: increase of FEV1, MMEF75/25, MEF50, MEF25 (p<0,01) and decrease of sRtot, ITGV and TLC (p<0,01) were registered.
Conclusions:Our data suggest that long term oral azithromycin treatment is associated with improvements in clinical status and lung function parameters of CF patients.


Rating: 0
You must login to grade this presentation.

Share or cite this content

Citations should be made in the following way:
A. Vracaric, P. Minic (Uzice, Belgrade, Republic Of Serbia). Effect of long term treatment with azithromycin on clinical status and lung function parameters in cystic fibrosis patients colonised by pseudomonas aeruginosa. Eur Respir J 2009; 34: Suppl. 53, 1268

You must login to share this Presentation/Article on Twitter, Facebook, LinkedIn or by email.

Member's Comments

No comment yet.
You must Login to comment this presentation.


Related content which might interest you:
Efficacy of low-dose, long-term clarithromycin administration in improving the clinical course in cystic fibrosis patients with chronic P. aeruginosa airway colonization
Source: Eur Respir J 2003; 22: Suppl. 45, 514s
Year: 2003

Pseudomonas aeruginosa in patients with cystic fibrosis - a comparison of early eradication and conventional therapy
Source: Eur Respir J 2004; 24: Suppl. 48, 385s
Year: 2004

Epidemiological-molecular study of colonization by pseudomonas aeruginosa in cystic fibrosis patients
Source: Eur Respir J 2002; 20: Suppl. 38, 379s
Year: 2002

The clinical impact of nebulised antibiotics in adults with bronchiectasis and chronic pseudomonas aeruginosa
Source: Virtual Congress 2020 – Non-tuberculous mycobacterial infections and bronchiectasis
Year: 2020


Daily versus weekly azithromycin in cystic fibrosis patients
Source: Eur Respir J 2007; 30: 487-495
Year: 2007



Azithromycin in chronic respiratory infections with pseudomonas aeruginosa in patients without cystic fibrosis
Source: Annual Congress 2008 - Mechanisms of respiratory infections: interaction between the pathogen and the host
Year: 2008


The efficacy of early eradication therapy in prevention of chronic pseudomonas aeruginosa infection in cystic fibrosis
Source: Eur Respir J 2006; 28: Suppl. 50, 486s
Year: 2006

Evaluating the Leeds criteria for Pseudomonas aeruginosa infection in a cystic fibrosis centre
Source: Eur Respir J 2006; 27: 937-943
Year: 2006



Chronic but not intermittent infection with Pseudomonas aeruginosa is associated with global changes of the lung microbiome in cystic fibrosis
Source: Eur Respir J, 50 (4) 1701086; 10.1183/13993003.01086-2017
Year: 2017



Highly concentrated aerosolized tobramycin in the treatment of patients with cystic fibrosis and Pseudomonas aeruginosa infection
Source: Eur Respir J 2005; 26: Suppl. 49, 620s
Year: 2005

Long-term evaluation of the response to aggressive treatment at the first colonization of P.aeruginosa in cystic fibrosis (CF)
Source: Eur Respir J 2001; 18: Suppl. 33, 126s
Year: 2001

Omics-based tracking of Pseudomonas aeruginosa persistence in “eradicated” cystic fibrosis patients
Source: Eur Respir J, 57 (4) 2000512; 10.1183/13993003.00512-2020
Year: 2021



Burkholderia cepacia infection in adult cystic fibrosis patients: Its impact on lung function and survival
Source: Annual Congress 2010 - New aspects of cystic fibrosis
Year: 2010

Usefulness of long term treatment with azithromycin in patients with bronchiectasis (non cystic fibrosis)
Source: Annual Congress 2010 - Treatment and risk factors in lower respiratory tract infections
Year: 2010


Efficacy of ciprofloxacin against resistant mucoid or non-mucoid P. aeruginosa isolated from non-cystic fibrosis bronchiectasis (NCFB) patients considering lung pharmacokinetics after ciprofloxacin DPI treatment
Source: International Congress 2014 – Antibiotics, antifungals and other therapeutic options
Year: 2014


Novel approaches to the treatment of Pseudomonas aeruginosa infections in cystic fibrosis},
Source: Eur Respir J 2012; 40: 1014-1023
Year: 2012



Bacterial infection and lung function in patients with cystic fibrosis
Source: Eur Respir J 2005; 26: Suppl. 49, 615s
Year: 2005

Effects of long-term azithromycin treatment in patients with non-cystic fibrosis stable bronchiectasis
Source: Annual Congress 2007 - Infectious lung and pleural diseases
Year: 2007


Influence of the lung microbiome on antibiotic susceptibility of cystic fibrosis pathogens
Source: Eur Respir Rev, 28 (152) 190041; 10.1183/16000617.0041-2019
Year: 2019



The independent contribution of Pseudomonas aeruginosa infection to long-term clinical outcomes in bronchiectasis
Source: Eur Respir J, 51 (2) 1701953; 10.1183/13993003.01953-2017
Year: 2018