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Changes in Antibiotic Resistance of Children with Cystic Fibrosis and Impact on Clinical Outcomes

Year 2025, Volume: 27 Issue: 2, 165 - 171, 30.08.2025
https://doi.org/10.18678/dtfd.1647114

Abstract

Aim: Antibiotics have an important role in the treatment of cystic fibrosis (CF) lung disease. Antibiotic resistance, especially multidrug resistance (MDR), increases in CF. This study aimed to determine whether there is a change in antibiotic resistance of pathogens isolated from the respiratory tract specimens of CF patients and to evaluate the relationship between the antibiotic resistance and patients’ clinical status and pulmonary function.
Material and Methods: Thirty-nine CF patients with identified microorganisms in respiratory tract specimens from August 2010 through December 2016 were included in the study. 333 respiratory cultures taken from 39 CF patients were analyzed retrospectively.
Results: Methicillin-sensitive S. aureus (MSSA) was isolated from 122 (31.0%) cultures, P. aeruginosa from 97 (24.7%), and methicillin-resistant S. aureus (MRSA) from 22 (5.6%). The prevalence of MSSA (p=0.020) and MRSA (p=0.010) increased from 2010 to 2016, while the prevalence of P. aeruginosa and other microorganisms did not increase. MDR-S. aureus and MDR-P. aeruginosa prevalence did not change, but MRSA prevalence increased over the years (p=0.001). There was a significant relation between the antibiotic resistance and acute pulmonary exacerbations, pulmonary examination findings, loss in weight and height percentile. As the antibiotic resistance increased, FEV1, FVC, FEV1/FVC, PEF, and FEF25-75 were significantly decreased. The use of long-term azithromycin or inhaled antibiotics was not associated with antibiotic resistance.
Conclusion: In CF patients, resistance to antibiotics increased over the years. It is important to obtain respiratory tract cultures regularly and initiate rational antibiotic treatment based on culture results.

References

  • Ratjen F, Döring G. Cystic fibrosis. Lancet. 2003;361(9358):681-9.
  • Balfour-Lynn IM, Elborn S. Respiratory disease: infection. In: Hodson M, Geddes D, Bush A; eds. Cystic fibrosis. 3rd ed. London: Edward Arnold Pub, 2007; 137-57.
  • Sagel SD, Gibson RL, Emerson J, McNamara S, Burns JL, Wagener JS, et al. Impact of Pseudomonas and Staphylococcus infection on inflammation and clinical status in young children with cystic fibrosis. J Pediatr. 2009;154(2):183-8.
  • Jones AM. Patient registry data highlights international differences in survival in cystic fibrosis. Thorax. 2023;78(3):223-4.
  • Fainardi V, Neglia C, Muscarà M, Spaggiari C, Tornesello M, Grandinetti R, et al. Multidrug-resistant bacteria in children and adolescents with cystic fibrosis. Children (Basel). 2022;9(9):1330.
  • Bonyadi P, Saleh NT, Dehghani M, Yamini M, Amini K. Prevalence of antibiotic resistance of Pseudomonas aeruginosa in cystic fibrosis infection: A systematic review and meta-analysis. Microb Pathog. 2022;165:105461.
  • Xu X, Zhang X, Zhang G, Abbasi Tadi D. Prevalence of antibiotic resistance of Staphylococcus aureus in cystic fibrosis infection: a systematic review and meta-analysis. J Glob Antimicrob Resist. 2024;36:419-25.
  • Perikleous EP, Gkentzi D, Bertzouanis A, Paraskakis E, Sovtic A, Fouzas S. Antibiotic resistance in patients with cystic fibrosis: Past, present, and future. Antibiotics (Basel). 2023;12(2):217.
  • Fuchs HJ, Borowitz DS, Christiansen DH, Morris EM, Nash ML, Ramsey BW, et al. Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. The Pulmozyme Study Group. N Engl J Med. 1994;331(10):637-42.
  • VanDevanter DR, Hamblett NM, Simon N, McIntosh J, Konstan MW. Evaluating assumptions of definition-based pulmonary exacerbation endpoints in cystic fibrosis clinical trials. J Cyst Fibros. 2021;20(1):39-45.
  • Lee TW, Brownlee KG, Conway SP, Denton M, Littlewood JM. Evaluation of a new definition for chronic Pseudomonas aeruginosa infection in cystic fibrosis patients. J Cyst Fibros. 2003;2(1):29-34.
  • Aslanhan U, Cakir E, Pur Ozyigit L, Kucuksezer UC, Gelmez YM, Yuksel M, et al. Pseudomonas aeruginosa colonization in cystic fibrosis: Impact on neutrophil functions and cytokine secretion capacity. Pediatr Pulmonol. 2021;56(6):1504-13.
  • Cakir E, Gedik AH, Yuksel M, Iraz M. 82 Contribution of early and repeated nasopharyngeal aspirate cultures in pediatric cystic fibrosis. J Cyst Fibros. 2015;14(Suppl 1):S78.
  • Magiorakos AP, Srinivasan A, Carey RB, Carmeli Y, Falagas ME, Giske CG, et al. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect. 2012;18(3):268-81.
  • Graham BL, Steenbruggen I, Miller MR, Barjaktarevic IZ, Cooper BG, Hall GL, et al. Standardization of Spirometry 2019 Update. An Official American Thoracic Society and European Respiratory Society Technical Statement. Am J Respir Crit Care Med. 2019;200(8):e70-e88.
  • Li D, Schneider-Futschik EK. Current and emerging inhaled antibiotics for chronic pulmonary Pseudomonas aeruginosa and Staphylococcus aureus infections in cystic fibrosis. Antibiotics (Basel). 2023;12(3):484.
  • Langton Hewer SC, Smyth AR. Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis. Cochrane Database Syst Rev. 2009;(4):CD004197.
  • Davies G. Does newborn screening improve early lung function in cystic fibrosis?. Paediatr Respir Rev. 2022;42:17-22.
  • Rosenfeld M, Emerson J, Williams-Warren J, Pepe M, Smith A, Montgomery AB, et al. Defining a pulmonary exacerbation in cystic fibrosis. J Pediatr. 2001;139(3):359-65.
  • Goss CH, Heltshe SL, West NE, Skalland M, Sanders DB, Jain R, et al. A randomized clinical trial of antimicrobial duration for cystic fibrosis pulmonary exacerbation treatment. Am J Respir Crit Care Med. 2021;204(11):1295-305.
  • Southern KW, Solis-Moya A, Kurz D, Smith S. Macrolide antibiotics (including azithromycin) for cystic fibrosis. Cochrane Database Syst Rev. 2024;2(2):CD002203.
  • Walicka-Serzysko K, Postek M, Borawska-Kowalczyk U, Milczewska J, Sands D. Pulmonary function tests in the evaluation of early lung disease in cystic fibrosis. J Clin Med. 2023;12(14):4735.

Kistik Fibrozisli Çocuklarda Antibiyotik Direncindeki Değişimler ve Klinik Sonuçlar Üzerindeki Etkisi

Year 2025, Volume: 27 Issue: 2, 165 - 171, 30.08.2025
https://doi.org/10.18678/dtfd.1647114

Abstract

Amaç: Antibiyotikler, kistik fibrozis (KF) akciğer hastalığının tedavisinde önemli bir role sahiptir. KF'de antibiyotik direnci, özellikle çoklu ilaç direnci (ÇİD) artmaktadır. Bu çalışmanın amacı, KF hastalarının solunum yolu örneklerinden izole edilen mikroorganizmaların antibiyotik direncinde bir değişiklik olup olmadığını belirlemek ve antibiyotik direnci ile hastaların klinik durumu ve akciğer fonksiyonları arasındaki ilişkiyi değerlendirmektir.
Gereç ve Yöntemler: Ağustos 2010 ile Aralık 2016 tarihleri arasında solunum yolu örneklerinde mikroorganizma tespit edilen 39 KF hastası çalışmaya dahil edildi. 39 KF hastasından alınan 333 solunum kültürü geriye dönük olarak analiz edildi.
Bulgular: Metisiline duyarlı S. aureus (MSSA) 122 (%31,0), P. aeruginosa 97 (%24,7) ve metisiline dirençli S. aureus (MRSA) 22 (%5,6) kültürden izole edildi. MSSA (p=0,020) ve MRSA (p=0,010) prevalansı 2010'dan 2016'ya artarken, P. aeruginosa ve diğer mikroorganizmaların prevalansı artmamıştı. ÇİD-S. aureus ve ÇİD-P. aeruginosa prevalansı değişmemiş, ancak MRSA prevalansı yıllar içinde artmıştı (p=0,001). Antibiyotik direnci ile akut pulmoner alevlenme, akciğerde dinleme bulgularının varlığı, kilo ve boy persentil kaybı arasında anlamlı ilişki saptandı. Antibiyotik direnci arttıkça FEV1, FVC, FEV1/FVC, PEF, FEF25-75 anlamlı olarak azalmıştı. Uzun süreli azitromisin veya inhale antibiyotik kullanımı ile antibiyotik direnci arasında ilişkili bulunmadı.
Sonuç: KF hastalarında antibiyotiklere karşı direnç yıllar içinde artmıştır. Düzenli olarak solunum yolu kültürlerinin alınması ve kültür sonuçlarına göre akılcı antibiyotik tedavisinin planlanması önemlidir.

References

  • Ratjen F, Döring G. Cystic fibrosis. Lancet. 2003;361(9358):681-9.
  • Balfour-Lynn IM, Elborn S. Respiratory disease: infection. In: Hodson M, Geddes D, Bush A; eds. Cystic fibrosis. 3rd ed. London: Edward Arnold Pub, 2007; 137-57.
  • Sagel SD, Gibson RL, Emerson J, McNamara S, Burns JL, Wagener JS, et al. Impact of Pseudomonas and Staphylococcus infection on inflammation and clinical status in young children with cystic fibrosis. J Pediatr. 2009;154(2):183-8.
  • Jones AM. Patient registry data highlights international differences in survival in cystic fibrosis. Thorax. 2023;78(3):223-4.
  • Fainardi V, Neglia C, Muscarà M, Spaggiari C, Tornesello M, Grandinetti R, et al. Multidrug-resistant bacteria in children and adolescents with cystic fibrosis. Children (Basel). 2022;9(9):1330.
  • Bonyadi P, Saleh NT, Dehghani M, Yamini M, Amini K. Prevalence of antibiotic resistance of Pseudomonas aeruginosa in cystic fibrosis infection: A systematic review and meta-analysis. Microb Pathog. 2022;165:105461.
  • Xu X, Zhang X, Zhang G, Abbasi Tadi D. Prevalence of antibiotic resistance of Staphylococcus aureus in cystic fibrosis infection: a systematic review and meta-analysis. J Glob Antimicrob Resist. 2024;36:419-25.
  • Perikleous EP, Gkentzi D, Bertzouanis A, Paraskakis E, Sovtic A, Fouzas S. Antibiotic resistance in patients with cystic fibrosis: Past, present, and future. Antibiotics (Basel). 2023;12(2):217.
  • Fuchs HJ, Borowitz DS, Christiansen DH, Morris EM, Nash ML, Ramsey BW, et al. Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. The Pulmozyme Study Group. N Engl J Med. 1994;331(10):637-42.
  • VanDevanter DR, Hamblett NM, Simon N, McIntosh J, Konstan MW. Evaluating assumptions of definition-based pulmonary exacerbation endpoints in cystic fibrosis clinical trials. J Cyst Fibros. 2021;20(1):39-45.
  • Lee TW, Brownlee KG, Conway SP, Denton M, Littlewood JM. Evaluation of a new definition for chronic Pseudomonas aeruginosa infection in cystic fibrosis patients. J Cyst Fibros. 2003;2(1):29-34.
  • Aslanhan U, Cakir E, Pur Ozyigit L, Kucuksezer UC, Gelmez YM, Yuksel M, et al. Pseudomonas aeruginosa colonization in cystic fibrosis: Impact on neutrophil functions and cytokine secretion capacity. Pediatr Pulmonol. 2021;56(6):1504-13.
  • Cakir E, Gedik AH, Yuksel M, Iraz M. 82 Contribution of early and repeated nasopharyngeal aspirate cultures in pediatric cystic fibrosis. J Cyst Fibros. 2015;14(Suppl 1):S78.
  • Magiorakos AP, Srinivasan A, Carey RB, Carmeli Y, Falagas ME, Giske CG, et al. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect. 2012;18(3):268-81.
  • Graham BL, Steenbruggen I, Miller MR, Barjaktarevic IZ, Cooper BG, Hall GL, et al. Standardization of Spirometry 2019 Update. An Official American Thoracic Society and European Respiratory Society Technical Statement. Am J Respir Crit Care Med. 2019;200(8):e70-e88.
  • Li D, Schneider-Futschik EK. Current and emerging inhaled antibiotics for chronic pulmonary Pseudomonas aeruginosa and Staphylococcus aureus infections in cystic fibrosis. Antibiotics (Basel). 2023;12(3):484.
  • Langton Hewer SC, Smyth AR. Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis. Cochrane Database Syst Rev. 2009;(4):CD004197.
  • Davies G. Does newborn screening improve early lung function in cystic fibrosis?. Paediatr Respir Rev. 2022;42:17-22.
  • Rosenfeld M, Emerson J, Williams-Warren J, Pepe M, Smith A, Montgomery AB, et al. Defining a pulmonary exacerbation in cystic fibrosis. J Pediatr. 2001;139(3):359-65.
  • Goss CH, Heltshe SL, West NE, Skalland M, Sanders DB, Jain R, et al. A randomized clinical trial of antimicrobial duration for cystic fibrosis pulmonary exacerbation treatment. Am J Respir Crit Care Med. 2021;204(11):1295-305.
  • Southern KW, Solis-Moya A, Kurz D, Smith S. Macrolide antibiotics (including azithromycin) for cystic fibrosis. Cochrane Database Syst Rev. 2024;2(2):CD002203.
  • Walicka-Serzysko K, Postek M, Borawska-Kowalczyk U, Milczewska J, Sands D. Pulmonary function tests in the evaluation of early lung disease in cystic fibrosis. J Clin Med. 2023;12(14):4735.
There are 22 citations in total.

Details

Primary Language English
Subjects Pediatric Chest Diseases
Journal Section Research Article
Authors

Mukaddes Kılıç Sağlam 0000-0002-7231-5461

Canan Baydemir 0000-0002-1521-7793

Zeynep Seda Uyan 0000-0002-7540-3467

Early Pub Date July 20, 2025
Publication Date August 30, 2025
Submission Date February 27, 2025
Acceptance Date June 20, 2025
Published in Issue Year 2025 Volume: 27 Issue: 2

Cite

APA Kılıç Sağlam, M., Baydemir, C., & Uyan, Z. S. (2025). Changes in Antibiotic Resistance of Children with Cystic Fibrosis and Impact on Clinical Outcomes. Duzce Medical Journal, 27(2), 165-171. https://doi.org/10.18678/dtfd.1647114
AMA Kılıç Sağlam M, Baydemir C, Uyan ZS. Changes in Antibiotic Resistance of Children with Cystic Fibrosis and Impact on Clinical Outcomes. Duzce Med J. August 2025;27(2):165-171. doi:10.18678/dtfd.1647114
Chicago Kılıç Sağlam, Mukaddes, Canan Baydemir, and Zeynep Seda Uyan. “Changes in Antibiotic Resistance of Children With Cystic Fibrosis and Impact on Clinical Outcomes”. Duzce Medical Journal 27, no. 2 (August 2025): 165-71. https://doi.org/10.18678/dtfd.1647114.
EndNote Kılıç Sağlam M, Baydemir C, Uyan ZS (August 1, 2025) Changes in Antibiotic Resistance of Children with Cystic Fibrosis and Impact on Clinical Outcomes. Duzce Medical Journal 27 2 165–171.
IEEE M. Kılıç Sağlam, C. Baydemir, and Z. S. Uyan, “Changes in Antibiotic Resistance of Children with Cystic Fibrosis and Impact on Clinical Outcomes”, Duzce Med J, vol. 27, no. 2, pp. 165–171, 2025, doi: 10.18678/dtfd.1647114.
ISNAD Kılıç Sağlam, Mukaddes et al. “Changes in Antibiotic Resistance of Children With Cystic Fibrosis and Impact on Clinical Outcomes”. Duzce Medical Journal 27/2 (August2025), 165-171. https://doi.org/10.18678/dtfd.1647114.
JAMA Kılıç Sağlam M, Baydemir C, Uyan ZS. Changes in Antibiotic Resistance of Children with Cystic Fibrosis and Impact on Clinical Outcomes. Duzce Med J. 2025;27:165–171.
MLA Kılıç Sağlam, Mukaddes et al. “Changes in Antibiotic Resistance of Children With Cystic Fibrosis and Impact on Clinical Outcomes”. Duzce Medical Journal, vol. 27, no. 2, 2025, pp. 165-71, doi:10.18678/dtfd.1647114.
Vancouver Kılıç Sağlam M, Baydemir C, Uyan ZS. Changes in Antibiotic Resistance of Children with Cystic Fibrosis and Impact on Clinical Outcomes. Duzce Med J. 2025;27(2):165-71.