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PedAM

Pediatric Disease Annotations & Medicines




Disease cystic fibrosis
Symptom C0854135|pseudomonas aeruginosa infection
Sentences 29
PubMedID- 21942255 All approved antimicrobial agents for administration by inhalation are indicated for pseudomonas aeruginosa infections in patients with cystic fibrosis.
PubMedID- 20941353 Such within-species polymicrobial infection have been reported mainly in chronic and/or open infections (pseudomonas aeruginosa infections of lung in cystic fibrosis patients and of burn wounds , staphylococcus epidermidis joint prosthesis infection , lung tuberculosis , .
PubMedID- 20137079 Feasibility study to inform the design of a randomised controlled trial to eradicate pseudomonas aeruginosa infection in individuals with cystic fibrosis.
PubMedID- 20442386 Context: azithromycin is recommended as therapy for cystic fibrosis (cf) patients with chronic pseudomonas aeruginosa infection, but there has not been sufficient evidence to support the benefit of azithromycin in other patients with cf.
PubMedID- 24737619 Why is a healthy person protected from pseudomonas aeruginosa infections, while individuals with cystic fibrosis or damaged epithelium are particularly susceptible to this opportunistic pathogen.
PubMedID- 25027418 pseudomonas aeruginosa infection is a hallmark of lung disease in cystic fibrosis.
PubMedID- 26534255 Adherence to inhaled antibiotics for the treatment of chronic pseudomonas aeruginosa infection in patients with cystic fibrosis: a systematic literature review.
PubMedID- 23910799 pseudomonas aeruginosa infections are commonly associated with cystic fibrosis, pneumonias, neutropenia and burns.
PubMedID- 22496040 Background: accelerated lung function decline in cystic fibrosis (cf) is associated with mucoid pseudomonas aeruginosa infection.
PubMedID- 22762867 Comparison of two treatment regimens for eradication of pseudomonas aeruginosa infection in children with cystic fibrosis.
PubMedID- 20837573 Early pseudomonas aeruginosa infection in individuals with cystic fibrosis: is susceptibility testing justified.
PubMedID- 24510624 Colistimethate sodium dry powder for inhalation: a review of its use in the treatment of chronic pseudomonas aeruginosa infection in patients with cystic fibrosis.
PubMedID- 24068273 pseudomonas aeruginosa infection in patients with cystic fibrosis: scientific evidence regarding clinical impact, diagnosis, and treatment.
PubMedID- 24194436 Tobramycin inhalation powder: a review of its use in the treatment of chronic pseudomonas aeruginosa infection in patients with cystic fibrosis.
PubMedID- 23802816 Rationale: the efficacy of inhaled tobramycin on chronic pseudomonas aeruginosa infections in patients with cystic fibrosis (cf) has been established in clinical trials.
PubMedID- 19996339 Rationale: antibiotic therapy for early pseudomonas aeruginosa infection in patients with cystic fibrosis (cf) is effective, but the optimal therapeutic regimen and duration for early treatment remains unclear.
PubMedID- 23152277 Objectives: to compare biofilm antimicrobial susceptibility testing-driven therapy to conventional antimicrobial susceptibility testing-driven therapy in the treatment of pseudomonas aeruginosa infection in people with cystic fibrosis.
PubMedID- 20729233 Background: initial pulmonary pseudomonas aeruginosa infection in patients with cystic fibrosis (cf) is currently treated with intensive antibiotic therapy.
PubMedID- 25417708 Levofloxacin inhalation solution for the treatment of chronic pseudomonas aeruginosa infection among patients with cystic fibrosis.
PubMedID- 24091166 Background: inhaled tobramycin therapy has been shown to be efficacious in clinical trials for the eradication of initial pseudomonas aeruginosa infection in children with cystic fibrosis (cf).
PubMedID- 26438797 pseudomonas aeruginosa infections persist in patients with cystic fibrosis (cf) and drive lung disease progression.
PubMedID- 24995163 Liposomal ciprofloxacin has been further developed by aradigm corporation for pseudomonas aeruginosa infections in patients with cystic fibrosis and non-cystic fibrosis bronchiectasis.
PubMedID- 21883670 Initial pseudomonas aeruginosa infection in patients with cystic fibrosis: characteristics of eradicated and persistent isolates.
PubMedID- 23550133 2011), and chronic pseudomonas aeruginosa infection associated with cystic fibrosis involves selection against virulence factors required for an acute infection (smith et al.
PubMedID- 23680696 Hydrogen cyanide concentrations in the breath of adult cystic fibrosis patients with and without pseudomonas aeruginosa infection.
PubMedID- 21893650 Comparative efficacy and safety of 4 randomized regimens to treat early pseudomonas aeruginosa infection in children with cystic fibrosis.
PubMedID- 22401602 Challenges with current inhaled treatments for chronic pseudomonas aeruginosa infection in patients with cystic fibrosis.
PubMedID- 22857271 Regulatory aspects of phase 3 endpoints for new inhaled antibiotics for cystic fibrosis patients with chronic pseudomonas aeruginosa infections.
PubMedID- 22084956 Economic burden of pseudomonas aeruginosa infection in patients with cystic fibrosis.

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