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Updated: May 23, 2025

Antibiotic Efficacy Testing in an Ex vivo Model of Pseudomonas aeruginosa and Staphylococcus aureus Biofilms in the Cystic Fibrosis Lung
Published on: January 22, 2021
Therapeutic Drug Monitoring of Beta-Lactams in Cystic Fibrosis: Unattained Target in Standard Antibiotic Dosing
Eliska Maraczek Markova1,2, Nela Stastna3,4, Libor Fila3
1Department of Clinical Pharmacy, Hospital Pharmacy, University Hospital Brno, Brno, Czech Republic.
Abstract:
Acute exacerbations of cystic fibrosis (CF) diminish quality of life and, if inadequately treated, can be life-threatening. The pathophysiological alterations associated with CF result in modified antibiotic pharmacokinetics. Moreover, the viscous mucus in the lungs limits pathogen exposure to drugs, rendering successful antibiotic treatment challenging. A 23-year-old female patient with CF was repeatedly admitted for intravenous antibiotic therapy for acute exacerbation of Pseudomonas aeruginosa infection. In the context of altered pharmacokinetics in CF, therapeutic drug monitoring of meropenem and piperacillin revealed consistently low plasma levels of both drugs. Targeted plasma levels were ultimately achieved through continuous high-dose infusions, based on therapeutic drug monitoring and subsequent dose adjustments.
Insights
Treating cystic fibrosis (CF) exacerbations requires optimized antibiotic dosing. Therapeutic drug monitoring helped achieve effective meropenem and piperacillin levels in a CF patient with Pseudomonas aeruginosa infection.
Area of Science:
- Pharmacology
- Infectious Diseases
- Pulmonology
Background:
- Acute exacerbations of cystic fibrosis (CF) significantly impact patient quality of life and can be life-threatening.
- CF pathophysiology alters antibiotic pharmacokinetics, complicating treatment.
- Viscous lung mucus in CF reduces drug penetration, posing challenges for effective antibiotic therapy.
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07:46Use of Artificial Sputum Medium to Test Antibiotic Efficacy Against Pseudomonas aeruginosa in Conditions More Relevant to the Cystic Fibrosis Lung
Published on: June 5, 2012
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