Применение ингаляционных антибиотиков как одна из мер борьбы с резистентностью бактерий (на примере кистозного фиброза)
https://doi.org/10.58838/2075-1230-2024-102-1-82-86
Аннотация
В представленном обзоре анализируется 33 источника литературы по эффективности ингаляционных антибиотиков у пациентов с кистозным фиброзом и определению их влияния на резистентность бактерий.
Об авторе
А. В. ТахтамышеваДНР
Тахтамышева Анна Валентиновна, врач-терапевт
283005, г. Донецк, ул. Диккенса, 1
Список литературы
1. Клинические рекомендации по ведению пациентов с кистозным фиброзом (муковисцидозом). Москва; 2021. URL: https://cr.minzdrav.gov.ru/recomend/372_2 [Дата обращения 10 декабря 2023г.]
2. Кузовлев А. Н., Мороз В. В., Голубев А. М., Половников С. Г. Ингаляционные антибиотики в лечении тяжелой нозокомиальной пневмонии / // Общая реаниматология. – 2013. – Т. 9. – № 6. – С. 61-70. https://doi.org/10.15360/1813-9779-2013-6-61
3. Чукина М. А., Лукина М. В., Андрущишина Т. Б., и др. Ингаляционное применение амикацина у пациентов с нозокомиальной пневмонией в отделении интенсивной терапии // Вестник Смоленской государственной медицинской академии. – 2019. – Т. 18. – № 1. – С. 137-144.
4. Bassetti M., Luyt C.E., Nicolau D.P., Pugin J. Characteristics of an ideal nebulized antibiotic for the treatment of pneumonia in the intubated patient // Ann Intensive Care. – 2016. – Vol.6, № 1. – Р.35. https://doi.org/10.1186/s13613-016-0140-x PMID: 27090532
5. Choi J., Novak K., Thompson R. Evaluation of Inhaled Tobramycin in Early Eradication of Pseudomonas aeruginosa in Infants With Cystic Fibrosis // J Pediatr Pharmacol Ther. – 2020. – Vol 25, №8. – Р.709-716. https://doi.org/10.5863/1551-6776-25.8.709 PMID: 33214782
6. ClinicalTrials.gov: NCT01270347 Trial of Aeroquin Versus Tobramycin Inhalation Solution (TIS) in Cystic Fibrosis (CF) Patients (TIS) Available at: https://ichgcp.net/clinical-trials-registry/NCT01270347 [Accessed 15 Dec 2022].
7. Daniels T., Mills N., Whitaker P. Nebuliser systems for drug delivery in cystic fibrosis // Cochrane Database Syst Rev. – 2013. – Vol.30, № 4. – Р.CD007639. https://doi.org/10.1002/14651858 PMID:23633344
8. Dasenbrook E.C., Konstan M.W., VanDevanter D.R. Association between the introduction of a new cystic fibrosis inhaled antibiotic class and change in prevalence of patients receiving multiple inhaled antibiotic classes // J Cyst Fibros. – 2015. – Vol.14, №3. – Р.370-5. https://doi.org/10.1016/j.jcf.2014.11.005 PMID: 25496726
9. Dezube R., Jennings M.T., Rykiel M., Diener-West M., Boyle M.P., Chmiel J.F., Dasenbrook E.C. Eradication of persistent methicillin-resistant Staphylococcus aureus infection in cystic fibrosis // J Cyst Fibros. – 2019. – Vol.18, №3. – Р.357-363. https://doi.org/10.1016/j.jcf.2018.07.005 PMID: 30131297
10. Ekkelenkamp M.B., Díez-Aguilar M., Tunney M.M., Elborn J.S., Fluit A.C., Cantón R. Establishing Antimicrobial Susceptibility Testing Methods and Clinical Breakpoints for Inhaled Antibiotic Therapy // Open Forum Infect Dis. // 2022. – Vol.9,№4. – Р.ofac082. https://doi.org/10.1093/ofid/ofac082 PMID: 35265731
11. Elborn J.S., Flume P.A., Cohen F., Loutit J., VanDevanter D.R. Safety and efficacy of prolonged levofloxacin inhalation solution (APT-1026) treatment for cystic fibrosis and chronic Pseudomonas aeruginosa airway infection // J Cyst Fibros. – 2016. – Vol.15, №5. – Р.634-40. https://doi.org/10.1016/j.jcf.2016.01.005 PMID: 26935334
12. Goetz D., Ren C.L. Review of Cystic Fibrosis // Pediatr Ann. – 2019. – Vol.48,№4. –Р.e154-e161. https://doi.org/10.3928/19382359-20190327-01 PMID: 30986316
13. Hatziagorou E., Orenti A., Drevinek P., Kashirskaya N., Mei-Zahav M., De Boeck K; ECFSPR. Electronic address: ECFS-Patient.Registry@uz.kuleuven. ac.be; ECFSPR. Changing epidemiology of the respiratory bacteriology of patients with cystic fibrosis-data from the European cystic fibrosis society patient registry // J Cyst Fibros. –2020. – Vol.19, № 3. – Р.376-383. https://doi.org/10.1016/j.jcf.2019.08.006 PMID: 31492646
14. Henriette Zweijpfenning S.M., Chiron R., Essink S., Schildkraut J., Akkerman O.W., Aliberti S., Altenburg J., Arets B., van Braeckel E., Delaere B., Gohy S., Haarman E., Lorent N., McKew G., Morgan L., Wagner D., van Ingen J., Hoefsloot W. Safety and Outcomes of Amikacin Liposome Inhalation Suspension for Mycobacterium abscessus Pulmonary Disease: A NTM-NET study // Chest. – 2022. – Vol.162, №1. –Р.76-81. https://doi.org/10.1016/j.chest.2022.01.015 PMID: 35063454
15. Hoo Z.H., Curley R., Campbell M.J., Walters S.J., Hind D., Wildman MJ. Accurate reporting of adherence to inhaled therapies in adults with cystic fibrosis: methods to calculate "normative adherence" // Patient Prefer Adherence. – 2016. – Vol. 23, №10. –Р.887-900. https://doi.org/10.2147/PPA.S105530 PMID: 27284242
16. Jennings M.T., Boyle M.P., Weaver D., Callahan K.A., Dasenbrook E.C. Eradication strategy for persistent methicillin-resistant Staphylococcus aureus infection in individuals with cystic fibrosis--the PMEP trial: study protocol for a randomized controlled trial // Trials. –2014. –№ 15. – Р.223. https://doi.org/10.1186/1745-6215-15-223 PMID: 24925006
17. Jones L.A., Doucette L., Dellon E.P., Esther C.R., McKinzie C.J. Use of inhaled imipenem/cilastatin in pediatric patients with cystic fibrosis: A case series // J Cyst Fibros. – 2019. – Vol.18, №4. – e42-e44. https://doi.org/10.1016/j.jcf.2019.04.017 PMID: 31060800
18. Karampitsakos T., Papaioannou O., Kaponi M., Kozanidou A., Hillas G., Stavropoulou E., Bouros D., Dimakou K. Low penetrance of antibiotics in the epithelial lining fluid. The role of inhaled antibiotics in patients with bronchiectasis // Pulm Pharmacol Ther. – 2020. – №60. – Р.101885. https://doi.org/10.1016/j.pupt.2019.101885 PMID: 31891761.
19. Kiefer A., Bogdan C., Melichar V.O. Successful eradication of newly acquired MRSA in six of seven patients with cystic fibrosis applying a short-term local and systemic antibiotic scheme // BMC Pulm Med. – 2018. – Vol.18, №1. –Р.20. https://doi.org/10.1186/s12890-018-0588-6 PMID: 29370836
20. Kuzovlev, A. N. Inhaled Antibiotics in Reanimatology: Problem State and Development Prospects (Review) / A. N. Kuzovlev, A. V. Grechko // General Reanimatology. – 2017. – Vol. 13. – № 5. – P. 69-84. https://doi.org/10.15360/1813-9779-2017-5-69-84
21. Langton Hewer S.C., Smyth A.R. Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis // Cochrane Database Syst Rev. – 2017. – Vol. 4, №4. – Р.CD004197. https://doi.org/10.1002/14651858.CD004197.pub5 PMID: 28440853
22. Lebeaux D., Chauhan A., Rendueles O., Beloin C. From in vitro to in vivo Models of Bacterial Biofilm-Related Infections // Pathogens. –2013. – Vol 2, № 2. – Р.288-356. https://doi.org/10.3390/pathogens2020288 PMID: 25437038
23. Lebeaux D., Ghigo J.M., Beloin C. Biofilm-related infections: bridging the gap between clinical management and fundamental aspects of recalcitrance toward antibiotics // Microbiol Mol Biol Rev. – 2014. – Vol.78, 3. –Р. 510-43. https://doi.org/10.1128/MMBR.00013-14 PMID: 25184564
24. Møller R., Nielsen B.U., Faurholt-Jepsen D., Katzenstein T.L., Skov M., Philipsen L.KD, Pressler T., Johansen H.K, Qvist T. Use of inhaled antibiotics among Danish patients with cystic fibrosis // Pediatr Pulmonol. – 2022. – Vol.57, №7. – Р.1726-1734. https://doi.org/10.1002/ppul.25942 PMID: 35478387
25. Quon B.S., Goss C.H., Ramsey B.W. Inhaled antibiotics for lower airway infections // Ann Am Thorac Soc. – 2014. – Vol.11, № 3. – Р.425-34. https://doi.org/10.1513/AnnalsATS.201311-395FR PMID: 24673698
26. Riveiro V., Casal A., Álvarez-Dobaño J.M., Lourido T., Suárez-Artime P., Rodríguez-García C., Ferreiro L., Toubes M.E., Valdés L. Response to inhaled ceftazidime in patients with non-cystic fibrosis bronchiectasis and chronic bronchial infection unrelated to Pseudomonas aeruginosa.– Clin Respir J. – 2022. – Vol. 16, №11.
27. Stockmann C., Sherwin C.M., Ampofo K., Spigarelli M.G. Development of levofloxacin inhalation solution to treat Pseudomonas aeruginosa in patients with cystic fibrosis // Ther Adv Respir Dis. – 2014. – Vol.8, № 1. – Р. 13-21. https://doi.org/10.1177/1753465813508445 PMID: 24334337
28. Tiddens H.A., Bos A.C., Mouton J.W., Devadason S., Janssens H.M. Inhaled antibiotics: dry or wet? // Eur Respir J. – 2014. – Vol.44, № 5. – Р.1308-18. https://doi.org/10.1183/09031936.00090314 PMID: 25323242.
29. Vázquez-Espinosa E., Girón R.M., Gómez-Punter R.M., García-Castillo E., Valenzuela C., Cisneros C., Zamora E., García-Pérez F..J, Ancochea J. Long-term safety and efficacy of tobramycin in the management of cystic fibrosis // Ther Clin Risk Manag. – 2015. –№ 11. – Р.407-15. https://doi.org/10.2147/TCRM.S75208 PMID: 25792839
30. Wang M., Ridderberg W., Hansen C.R., Høiby N., Jensen-Fangel S., Olesen H.V., Skov M., Lemming L.E., Pressler T., Johansen H.K., Nørskov-Lauritsen N. Early treatment with inhaled antibiotics postpones next occurrence of Achromobacter in cystic fibrosis // J Cyst Fibros. – 2013. – Vol.12, № 6. – Р. 638-43. https://doi.org/10.1016/j.jcf.2013.04.013 PMID: 23727271
31. Weldrick P.J., Hardman M.J., Paunov V.N. Enhanced Clearing of Wound-Related Pathogenic Bacterial Biofilms Using Protease-Functionalized Antibiotic Nanocarriers // ACS Appl Mater Interfaces. – 2019. – Vol.11, 47. – Р.43902-43919. https://doi.org/10.1021/acsami.9b16119 PMID: 31718141
32. White L., Mirrani G., Grover M., Rollason J., Malin A., Suntharalingam J. Outcomes of Pseudomonas eradication therapy in patients with non-cystic fibrosis bronchiectasis // Respir Med. – 2012. – Vol. 106, № 3. – Р.356-60. https://doi.org/10.1016/j.rmed.2011.11.018 PMID: 22204744.
33. Zobell J.T., Epps K.L., Young D.C., Montague M., Olson J., Ampofo K., Chin M.J., Marshall B.C., Dasenbrook E. Utilization of antibiotics for methicillin-resistant Staphylococcus aureus infection in cystic fibrosis // Pediatr Pulmonol. – 2015. – Vol. 50, №6. – Р. 552-9. https://doi.org/10.1002/ppul.23132 PMID: 25559432
Рецензия
Для цитирования:
Тахтамышева А.В. Применение ингаляционных антибиотиков как одна из мер борьбы с резистентностью бактерий (на примере кистозного фиброза). Туберкулез и болезни легких. 2024;102(1):82-86. https://doi.org/10.58838/2075-1230-2024-102-1-82-86
For citation:
Takhtamysheva A.V. Treatment with Inhaled Antibiotics as One of the Measures to Combat Bacterial Resistance (Cystic Fibrosis is Used as an Example). Tuberculosis and Lung Diseases. 2024;102(1):82-86. (In Russ.) https://doi.org/10.58838/2075-1230-2024-102-1-82-86