Literature DB >> 29474110

Chronic Azithromycin Use in Cystic Fibrosis and Risk of Treatment-Emergent Respiratory Pathogens.

Jonathan D Cogen1, Frankline Onchiri2, Julia Emerson1, Ronald L Gibson1, Lucas R Hoffman1, David P Nichols1, Margaret Rosenfeld1.   

Abstract

RATIONALE: Azithromycin has been shown to improve lung function and reduce the number of pulmonary exacerbations in patients with cystic fibrosis. Concerns remain, however, regarding the potential emergence of treatment-related respiratory pathogens.
OBJECTIVES: To determine whether chronic azithromycin use (defined as three-times weekly administration) is associated with increased rates of detection of eight specific respiratory pathogens.
METHODS: We performed a new-user, propensity score-matched retrospective cohort study utilizing data from the Cystic Fibrosis Foundation Patient Registry. Incident azithromycin users were propensity score matched 1:1 with contemporaneous nonusers. Kaplan-Meier curves and Cox proportional hazards regression were used to evaluate the association between chronic azithromycin use and incident respiratory pathogen detection. Analyses were performed separately for each pathogen, limited to patients among whom that pathogen had not been isolated in the 2 years before cohort entry.
RESULTS: After propensity score matching, the mean age of the cohorts was approximately 12 years. Chronic azithromycin users had a significantly lower risk of detection of new methicillin-resistant Staphylococcus aureus, nontuberculous mycobacteria, and Burkholderia cepacia complex compared with nonusers. The risk of acquiring the remaining five pathogens was not significantly different between users and nonusers.
CONCLUSIONS: Using an innovative new-user, propensity score-matched study design to minimize indication and selection biases, we found in a predominantly pediatric cohort that chronic azithromycin users had a lower risk of acquiring several cystic fibrosis-related respiratory pathogens. These results may ease concerns that chronic azithromycin exposure increases the risk of acquiring new respiratory pathogens among pediatric patients with cystic fibrosis.

Entities:  

Keywords:  cystic fibrosis; macrolides; methicillin-resistant Staphylococcus aureus; microbiology

Mesh:

Substances:

Year:  2018        PMID: 29474110      PMCID: PMC6850787          DOI: 10.1513/AnnalsATS.201801-012OC

Source DB:  PubMed          Journal:  Ann Am Thorac Soc        ISSN: 2325-6621


  42 in total

1.  Macrolide treatment for Mycobacterium abscessus and Mycobacterium massiliense infection and inducible resistance.

Authors:  Go-Eun Choi; Sung Jae Shin; Choul-Jae Won; Ki-Nam Min; Taegwon Oh; Mi-Young Hahn; Keehoon Lee; Soo Hyun Lee; Charles L Daley; Seonwoo Kim; Byeong-Ho Jeong; Kyeongman Jeon; Won-Jung Koh
Journal:  Am J Respir Crit Care Med       Date:  2012-08-09       Impact factor: 21.405

2.  Long term effects of azithromycin in patients with cystic fibrosis: A double blind, placebo controlled trial.

Authors:  A Clement; A Tamalet; E Leroux; S Ravilly; B Fauroux; J-P Jais
Journal:  Thorax       Date:  2006-06-29       Impact factor: 9.139

3.  Anti-inflammatory effects of azithromycin in cystic fibrosis airway epithelial cells.

Authors:  Cristina Cigana; Elena Nicolis; Matteo Pasetto; Baroukh Maurice Assael; Paola Melotti
Journal:  Biochem Biophys Res Commun       Date:  2006-10-02       Impact factor: 3.575

4.  Comparative activity of azithromycin against clinical isolates of mycobacteria.

Authors:  B Watt; A Rayner; G Harris
Journal:  J Antimicrob Chemother       Date:  1996-09       Impact factor: 5.790

Review 5.  Cystic fibrosis pulmonary guidelines. Chronic medications for maintenance of lung health.

Authors:  Peter J Mogayzel; Edward T Naureckas; Karen A Robinson; Gary Mueller; Denis Hadjiliadis; Jeffrey B Hoag; Lisa Lubsch; Leslie Hazle; Kathy Sabadosa; Bruce Marshall
Journal:  Am J Respir Crit Care Med       Date:  2013-04-01       Impact factor: 21.405

6.  Long term azithromycin in children with cystic fibrosis: a randomised, placebo-controlled crossover trial.

Authors:  A Equi; I M Balfour-Lynn; A Bush; M Rosenthal
Journal:  Lancet       Date:  2002-09-28       Impact factor: 79.321

7.  Burkholderia cepacia in cystic fibrosis. Variable disease course.

Authors:  D D Frangolias; E Mahenthiralingam; S Rae; J M Raboud; A G Davidson; R Wittmann; P G Wilcox
Journal:  Am J Respir Crit Care Med       Date:  1999-11       Impact factor: 21.405

8.  Association between respiratory tract methicillin-resistant Staphylococcus aureus and survival in cystic fibrosis.

Authors:  Elliott C Dasenbrook; William Checkley; Christian A Merlo; Michael W Konstan; Noah Lechtzin; Michael P Boyle
Journal:  JAMA       Date:  2010-06-16       Impact factor: 56.272

9.  Azithromycin in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa: a randomized controlled trial.

Authors:  Lisa Saiman; Bruce C Marshall; Nicole Mayer-Hamblett; Jane L Burns; Alexandra L Quittner; Debra A Cibene; Sarah Coquillette; Ann Yunker Fieberg; Frank J Accurso; Preston W Campbell
Journal:  JAMA       Date:  2003-10-01       Impact factor: 56.272

Review 10.  Does antibiotic exposure increase the risk of methicillin-resistant Staphylococcus aureus (MRSA) isolation? A systematic review and meta-analysis.

Authors:  Evelina Tacconelli; Giulia De Angelis; Maria A Cataldo; Emanuela Pozzi; Roberto Cauda
Journal:  J Antimicrob Chemother       Date:  2007-11-06       Impact factor: 5.790

View more
  9 in total

Review 1.  Update in Cystic Fibrosis 2018.

Authors:  Bonnie W Ramsey; Gregory P Downey; Christopher H Goss
Journal:  Am J Respir Crit Care Med       Date:  2019-05-15       Impact factor: 21.405

Review 2.  Delivering macrolide antibiotics to heal a broken heart - And other inflammatory conditions.

Authors:  Vincent J Venditto; David J Feola
Journal:  Adv Drug Deliv Rev       Date:  2022-03-30       Impact factor: 17.873

Review 3.  [Evidence-based treatment of cystic fibrosis].

Authors:  F C Ringshausen; T Hellmuth; A-M Dittrich
Journal:  Internist (Berl)       Date:  2020-12       Impact factor: 0.743

Review 4.  Ubiquitination and deubiquitination emerge as players in idiopathic pulmonary fibrosis pathogenesis and treatment.

Authors:  Shuang Li; Jing Zhao; Dong Shang; Daniel J Kass; Yutong Zhao
Journal:  JCI Insight       Date:  2018-05-17

5.  Azithromycin Exhibits Activity Against Pseudomonas aeruginosa in Chronic Rat Lung Infection Model.

Authors:  Manoj Kumar; Madhvi Rao; Tarun Mathur; Tarani Kanta Barman; Vattan Joshi; Tridib Chaira; Smita Singhal; Manisha Pandya; Souhaila Al Khodor; Dilip J Upadhyay; Nobuhisa Masuda
Journal:  Front Microbiol       Date:  2021-04-23       Impact factor: 5.640

6.  Use of proton pump inhibitors is associated with lower hemoglobin levels in people with cystic fibrosis.

Authors:  Alex H Gifford; Julie L Sanville; Meghana Sathe; Sonya L Heltshe; Christopher H Goss
Journal:  Pediatr Pulmonol       Date:  2021-04-26

7.  Azithromycin and the microbiota of cystic fibrosis sputum.

Authors:  Nicole Acosta; Christina S Thornton; Michael G Surette; Ranjani Somayaji; Laura Rossi; Harvey R Rabin; Michael D Parkins
Journal:  BMC Microbiol       Date:  2021-03-30       Impact factor: 3.605

8.  Metabolomic Analysis by Nuclear Magnetic Resonance Spectroscopy as a New Approach to Understanding Inflammation and Monitoring of Pharmacological Therapy in Children and Young Adults With Cystic Fibrosis.

Authors:  Paolo Montuschi; Vincenzina Lucidi; Debora Paris; Enza Montemitro; Rugia Shohreh; Nadia Mores; Dominique Melck; Giuseppe Santini; Fabio Majo; Andrea Motta
Journal:  Front Pharmacol       Date:  2018-06-18       Impact factor: 5.810

Review 9.  Systems Biology and Bile Acid Signalling in Microbiome-Host Interactions in the Cystic Fibrosis Lung.

Authors:  David F Woods; Stephanie Flynn; Jose A Caparrós-Martín; Stephen M Stick; F Jerry Reen; Fergal O'Gara
Journal:  Antibiotics (Basel)       Date:  2021-06-24
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.