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The Emergence of Multidrug-resistant in Cystic Fibrosis Patients on Inhaled Antibiotics

Overview
Journal Lung India
Specialty Pulmonary Medicine
Date 2017 Nov 4
PMID 29098998
Citations 11
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Abstract

Introduction: Multidrug-resistant Pseudomonas aeruginosa (MDR-PA) is an important and growing issue in the care of patients with cystic fibrosis (CF), and a major cause of morbidity and mortality.

Objective: The objective of the study was to describe the frequency of MDR-PA recovered from the lower respiratory samples of pediatric and adult CF patients, and its antibiotic resistance pattern to commonly used antimicrobial agents including β-lactams, aminoglycosides, and fluoroquinolones.

Materials And Methods: The lower respiratory isolates of P. aeruginosa were obtained from inpatients and outpatients CF clinics from a tertiary care teaching hospital for the period from October 2014 to September 2015. The identification and antimicrobial susceptibility for all the isolates were performed by using the BD Phoenix™ and E-test in compliance with Clinical and Laboratory Standards Institute (CLSI) guidelines.

Results: A total of 61 P. aeruginosa samples were isolated from thirty CF patients from twenty families. Twelve sputum samples were positive for MDR-PA (seven nonmucoid and five mucoid isolates) from five CF patients (five families) with moderate-to-very severe lung disease given MDR-PA frequency of 19.7%. The median age of the study group was 20 (range 10-30) years. Three CF patients were on chronic inhaled tobramycin and two on nebulized colistin. The antimicrobial patterns of isolates MDR-PA showed the highest rate of resistance toward each gentamycin, amikacin, and cefepime (100%), followed by 91.7% to ciprofloxacin, 75% to tobramycin, 58.3% to meropenem, and 50% to piperacillin-tazobactam. None of the isolates were resistant to colistin during the study period.

Conclusion: The study results emphasize that the emergence of a significant problem in the clinical isolates of P. aeruginosa in CF patients that dictate appropriate attention to the antibiotic management after proper surveillance.

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References
1.
Knibbs L, Johnson G, Kidd T, Cheney J, Grimwood K, Kattenbelt J . Viability of Pseudomonas aeruginosa in cough aerosols generated by persons with cystic fibrosis. Thorax. 2014; 69(8):740-5. PMC: 4112489. DOI: 10.1136/thoraxjnl-2014-205213. View

2.
OSullivan B, Flume P . The clinical approach to lung disease in patients with cystic fibrosis. Semin Respir Crit Care Med. 2009; 30(5):505-13. DOI: 10.1055/s-0029-1238909. View

3.
Banjar H . Morbidity and mortality data of cystic fibrosis patients. Saudi Med J. 2003; 24(7):730-5. View

4.
Hogardt M, Hoboth C, Schmoldt S, Henke C, Bader L, Heesemann J . Stage-specific adaptation of hypermutable Pseudomonas aeruginosa isolates during chronic pulmonary infection in patients with cystic fibrosis. J Infect Dis. 2006; 195(1):70-80. DOI: 10.1086/509821. View

5.
Ren C, Konstan M, Yegin A, Rasouliyan L, Trzaskoma B, Morgan W . Multiple antibiotic-resistant Pseudomonas aeruginosa and lung function decline in patients with cystic fibrosis. J Cyst Fibros. 2012; 11(4):293-9. PMC: 4089904. DOI: 10.1016/j.jcf.2012.02.005. View