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A Drug Monograph; Cefiderocol

Yıl 2023, Cilt: 7 Sayı: 1, 9 - 25, 30.04.2023
https://doi.org/10.34084/bshr.1279754

Öz

Increasing antimicrobial resistance day by day necessitates the search for new antimicrobials. Carbapenem resistance, especially in gram-negative bacteria, has reached alarming levels and has become a global public health problem due to the lack of safe alternative treatment options. Cefiderocol is a novel injectable siderophore cephalosporin that hijacks the bacterial iron transport machinery to facilitate cell entry and achieve high periplasmic concentrations. The cephalosporin moiety is the active antimicrobial component, structurally resembling a hybrid between ceftazidime and cefepime. Like other β-lactam agents, the principal bactericidal activity of cefiderocol occurs via inhibition of bacterial cell wall synthesis by binding of penicillin-binding proteins and inhibiting peptidoglycan synthesis, leading to cell death. Cefiderocol has been shown to be stable against hydrolysis by both serine and metallo-ß-lactamases in four Ambler classes, classes A, B, C, and D. Also, efflux pump-mediated resistance and porin mutations have limited effects on cefiderocol. It has broad in vitro activity against gram-negative bacteria, including multidrug-resistant organisms such as carbapenem-resistant Enterobacterales, carbapenem-resistant Pseudomonas aeruginosa, Acinetobacter baumannii, Stenotrophomonas maltophilia and Burkholderia cepacia. It has proven efficacy in the treatment of complicated cases such as complex urinary tract infections, including pyelonephritis, complex intra-abdominal infections, hospital-acquired bacterial pneumonia therapy, and ventilator-associated bacterial pneumonia. It was approved by the US Food and Drug Administration for the treatment of complicated urinary tract infections and nosocomial pneumonia, ventilator-associated bacterial pneumonia. The recommended dose of cefiderecol for complicated urinary tract infections is 2 grams every 8 hours for 7-14 days, 2 grams every 8 hours for 5-14 days for complicated intra-abdominal infections, and it is recommended to be administered as a 3-hour infusion. Cefiderocol is primarily renally excreted unchanged and clearance correlates with creatinine clearance. Dosage adjustment is thus required for both augmented renal clearance and in patients with moderate to severe renal impairment. In vitro and in vivo pharmacodynamic studies have reported that as with other cephalosporins the pharmacodynamic index that best predicts clinical outcome is the percentage of time that free drug concentrations exceed the minimum inhibitory concentration (%fT> MIC). Cefiderocol appears to be well tolerated with side-effect profiles similar to other cephalosporins. Cefiderocol displays favorable pharmacokinetic/pharmacodynamic properties and an acceptable safety profile, suggesting that cefiderocol may be a viable option for treating infections caused by bacteria resistant to other antibiotics.

Kaynakça

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  • 2. Organization WH. WHO Publishes List of Bacteria for Which New Antibiotics Are Ur- gently Needed. Saudi Med J. 2017;38(4):444-445. Accessed March 7, 2023. https://www. who.int/news/item/27-02-2017-who-publishes-list-of-bacteria-for-which-new-antibio- tics-are-urgently-needed
  • 3. Antibiotic resistance threats in the United States, 2019. Published online November 2019. doi:10.15620/CDC:82532
  • 4. Meletis G. Carbapenem resistance: overview of the problem and future perspectives. Ther Adv Infect Dis. 2016;3(1):15-21. doi:10.1177/2049936115621709
  • 5. Bush K, Courvalin P, Dantas G, et al. Tackling antibiotic resistance. Nat Rev Microbiol. 2011;9(12):894-896. doi:10.1038/NRMICRO2693
  • 6. Gülay Z. Beta-Laktamlara ve Karbapenemlere Direnç. Hastan İnfeksiyonları Derg. 2001;5:210-229.
  • 7. McCreary EK, Heil EL, Tamma PD. New perspectives on antimicrobial agents: Cefide- rocol. Antimicrob Agents Chemother. 2021;65(8):e0217120. doi:10.1128/AAC.02171-20
  • 8. Matuschek E, Longshaw C, Takemura M, Yamano Y, Kahlmeter G. Cefiderocol: EUCAST criteria for disc diffusion and broth microdilution for antimicrobial susceptibility testing. J Antimicrob Chemother. 2022;77(6):1662-1669. doi:10.1093/jac/dkac080
  • 9. European Medicines Agency Fetcroja 1 g powder for concentrate for solution for infusi- on: EU summary of product characteristics. 2020. https://www.ema.europa.eu/. Accessed 11 May 2021. https://www.ema.europa.eu/en/documents/product-information/fetcro-ja-epar-product-information_en.pdf
  • 10. Sato T, Yamawaki K. Cefiderocol: Discovery, Chemistry, and In Vivo Profiles of a Novel Siderophore Cephalosporin. Clin Infect Dis. 2019;69(Suppl 7):S538-S543. doi:10.1093/ cid/ciz826
  • 11. Ito A, Nishikawa T, Matsumoto S, et al. Siderophore Cephalosporin Cefiderocol Utilizes Ferric Iron Transporter Systems for Antibacterial Activity against Pseudomonas aeru- ginosa. Antimicrob Agents Chemother. 2016;60(12):7396. doi:10.1128/AAC.01405-16
  • 12. Aoki T, Yoshizawa H, Yamawaki K, et al. Cefiderocol (S-649266), A new siderophore cephalosporin exhibiting potent activities against Pseudomonas aeruginosa and other gram-negative pathogens including multi-drug resistant bacteria: Structure activity rela- tionship. Eur J Med Chem. 2018;155:847-868. doi:10.1016/j.ejmech.2018.06.014
  • 13. El-Lababidi RM, Rizk JG. Cefiderocol: A Siderophore Cephalosporin. Ann Pharmacot- her. 2020;54(12):1215-1231. doi:10.1177/1060028020929988
  • 14. Ito A, Sato T, Ota M, et al. In vitro antibacterial properties of cefiderocol, a novel side- rophore cephalosporin, against gram-negative bacteria. Antimicrob Agents Chemother. 2018;62(1). doi:10.1128/AAC.01454-17
  • 15. Abdul-Mutakabbir JC, Alosaimy S, Morrisette T, Kebriaei R, Rybak MJ. Cefiderocol: A Novel Siderophore Cephalosporin against Multidrug-Resistant Gram-Negative Pat- hogens. Pharmacotherapy. 2020;40(12):1228-1247. doi:10.1002/phar.2476
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  • 18. Katsube T, Wajima T, Echols R, et al. Intrapulmonary Pharmacokinetics of Cefiderocol in Hospitalized and Ventilated Patients Receiving Standard of Care Antibiotics for Bacteri- al Pneumonia. Open Forum Infect Dis. 2020;7(Supplement_1):S668-S668. doi:10.1093/ ofid/ofaa439.1493
  • 19. Nakamura R, Ito-Horiyama T, Takemura M, et al. In Vivo Pharmacodynamic Study of Cefiderocol, a Novel Parenteral Siderophore Cephalosporin, in Murine Thigh and Lung Infection Models. Antimicrob Agents Chemother. 2019;63(9). doi:10.1128/AAC.02031- 18
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Bir İlaç Monografı; Sefiderokol

Yıl 2023, Cilt: 7 Sayı: 1, 9 - 25, 30.04.2023
https://doi.org/10.34084/bshr.1279754

Öz

Gün geçtikçe artan antibimikrobiyal direnç yeni antimikrobiyaller arayışını zorunlu kılmaktadır. Özellikle gram negatif bakterilerdeki karbapenem direnci endişe verici seviyelere ulaşmıştır ve güvenli alternatif tedavi seçeneklerinin olmaması nedeniyle küresel bir halk sağlığı sorunu haline gelmiştir. Sefiderokol, hücre girişini kolaylaştırmak ve yüksek periplazmik konsantrasyonlar elde etmek için bakteriyel demir transport mekanizmasını kullanan yeni bir siderofor sefalosporindir. Sefalosporin parçası, yapısal olarak seftazidim ve sefepim arasında hibrite benzeyen aktif antimikrobiyal bileşendir. Temel bakterisidal aktivitesi diğer β-laktam antibiyotikler gibi penisilin bağlayan proteinlere bağlanarak peptidoglikan sentezinin dolayısıyla hücre duvarının inhibisyonu ve hücre ölümüne yol açması ile gerçekleşir. Sefiderokolün sınıf A, B, C ve D olmak üzere dört Ambler sınıfında hem serin hem de metallo-ß-laktamazlar tarafından hidrolize karşı kararlı olduğu gösterilmiştir. Aynı zamanda effluks pompası aracılı direnç ve porin mutasyonları sefiderokol üzerinde sınırlı etkiye sahiptir. Karbapenem dirençli Enterobacterales, karbapenem dirençli Pseudomonas aeruginosa, Acinetobacter baumannii, Stenotrophomonas maltophilia ve Burkholderia cepacia gibi çoklu ilaca dirençli organizmalar dahil olmak üzere gram negatif bakterilere karşı geniş in vitro etkinliğe sahiptir. Piyelonefrit dahil komplike idrar yolu enfeksiyonları, komplike intraabdominal enfeksiyonlar, hastane kökenli bakteriyel pnömoni ve ventilatör ilişkili bakteriyel pnömoni gibi komplike vakaların tedavisinde etkinliği kanıtlanmıştır. ABD Gıda ve İlaç İdaresi tarafından komplike üriner sistem enfeksiyonları ve nozokomiyal pnömoni, ventilatör ilişkili bakteriyel pnömoninin tedavisi için onaylanmıştır. Komplike üriner sistem enfeksiyonları için önerilen sefiderekol dozu 7- 14 gün boyunca her 8 saatte bir 2 gram, komplike intraabdominal enfeksiyonlar için, 5- 14 gün boyunca her 8 saatte bir 2 gramdır ve 3 saatlik infüzyon olarak uygulanması önerilir. Sefiderokol böbrekler tarafından değişmeden atılır ve klerens, kreatinin klerensi ile ilişkilidir. Bu nedenle hem artmış renal klerens için hem de orta ve şiddetli böbrek yetmezliği olan hastalarda doz ayarlaması gereklidir. In vitro ve in vivo farmakodinamik çalışmalar, diğer sefalosporinlerde olduğu gibi, klinik sonucu en iyi tahmin eden farmakodinamik indeksin, serbest ilaç konsantrasyonlarının minimum inhibitör konsantrasyonu aştığı zamanın yüzdesi olduğunu bildirmiştir. Diğer sefalosporinlere benzer yan etki profilleri olmakla beraber iyi tolere ediliyor görünmektedir. Sefiderokol uygun farmakokinetik/farmakodinamik özellikler ve kabul edilebilir bir güvenlik profili sergiler ve bu durum sefiderekolün diğer antibiyotiklere dirençli bakterilerin neden olduğu enfeksiyonların tedavisinde uygun bir seçenek olabileceğini düşündürmektedir.

Destekleyen Kurum

Bu çalışma için herhangi bir kişi veya kurumdan maddi destek alınmamıştır.

Kaynakça

  • 1. Syed YY. Cefiderocol: A Review in Serious Gram-Negative Bacterial Infections. Drugs. 2021;81(13):1559-1571. doi:10.1007/s40265-021-01580-4
  • 2. Organization WH. WHO Publishes List of Bacteria for Which New Antibiotics Are Ur- gently Needed. Saudi Med J. 2017;38(4):444-445. Accessed March 7, 2023. https://www. who.int/news/item/27-02-2017-who-publishes-list-of-bacteria-for-which-new-antibio- tics-are-urgently-needed
  • 3. Antibiotic resistance threats in the United States, 2019. Published online November 2019. doi:10.15620/CDC:82532
  • 4. Meletis G. Carbapenem resistance: overview of the problem and future perspectives. Ther Adv Infect Dis. 2016;3(1):15-21. doi:10.1177/2049936115621709
  • 5. Bush K, Courvalin P, Dantas G, et al. Tackling antibiotic resistance. Nat Rev Microbiol. 2011;9(12):894-896. doi:10.1038/NRMICRO2693
  • 6. Gülay Z. Beta-Laktamlara ve Karbapenemlere Direnç. Hastan İnfeksiyonları Derg. 2001;5:210-229.
  • 7. McCreary EK, Heil EL, Tamma PD. New perspectives on antimicrobial agents: Cefide- rocol. Antimicrob Agents Chemother. 2021;65(8):e0217120. doi:10.1128/AAC.02171-20
  • 8. Matuschek E, Longshaw C, Takemura M, Yamano Y, Kahlmeter G. Cefiderocol: EUCAST criteria for disc diffusion and broth microdilution for antimicrobial susceptibility testing. J Antimicrob Chemother. 2022;77(6):1662-1669. doi:10.1093/jac/dkac080
  • 9. European Medicines Agency Fetcroja 1 g powder for concentrate for solution for infusi- on: EU summary of product characteristics. 2020. https://www.ema.europa.eu/. Accessed 11 May 2021. https://www.ema.europa.eu/en/documents/product-information/fetcro-ja-epar-product-information_en.pdf
  • 10. Sato T, Yamawaki K. Cefiderocol: Discovery, Chemistry, and In Vivo Profiles of a Novel Siderophore Cephalosporin. Clin Infect Dis. 2019;69(Suppl 7):S538-S543. doi:10.1093/ cid/ciz826
  • 11. Ito A, Nishikawa T, Matsumoto S, et al. Siderophore Cephalosporin Cefiderocol Utilizes Ferric Iron Transporter Systems for Antibacterial Activity against Pseudomonas aeru- ginosa. Antimicrob Agents Chemother. 2016;60(12):7396. doi:10.1128/AAC.01405-16
  • 12. Aoki T, Yoshizawa H, Yamawaki K, et al. Cefiderocol (S-649266), A new siderophore cephalosporin exhibiting potent activities against Pseudomonas aeruginosa and other gram-negative pathogens including multi-drug resistant bacteria: Structure activity rela- tionship. Eur J Med Chem. 2018;155:847-868. doi:10.1016/j.ejmech.2018.06.014
  • 13. El-Lababidi RM, Rizk JG. Cefiderocol: A Siderophore Cephalosporin. Ann Pharmacot- her. 2020;54(12):1215-1231. doi:10.1177/1060028020929988
  • 14. Ito A, Sato T, Ota M, et al. In vitro antibacterial properties of cefiderocol, a novel side- rophore cephalosporin, against gram-negative bacteria. Antimicrob Agents Chemother. 2018;62(1). doi:10.1128/AAC.01454-17
  • 15. Abdul-Mutakabbir JC, Alosaimy S, Morrisette T, Kebriaei R, Rybak MJ. Cefiderocol: A Novel Siderophore Cephalosporin against Multidrug-Resistant Gram-Negative Pat- hogens. Pharmacotherapy. 2020;40(12):1228-1247. doi:10.1002/phar.2476
  • 16. Shionogi Inc. FETROJA (cefiderocol) for injection, for intravenous use: US prescribing information. 2020. https://www.fetroja. com/. Accessed 11 May 2021. Metab Clin Exp. Published online 2008. Accessed March 9, 2023. www.fda.gov/medwatch.
  • 17. Bilal M, El Tabei L, Büsker S, Krauss C, Fuhr U, Taubert M. Clinical Pharmacokinetics and Pharmacodynamics of Cefiderocol. Clin Pharmacokinet. 2021;60(12):1495-1508. doi:10.1007/s40262-021-01063-5
  • 18. Katsube T, Wajima T, Echols R, et al. Intrapulmonary Pharmacokinetics of Cefiderocol in Hospitalized and Ventilated Patients Receiving Standard of Care Antibiotics for Bacteri- al Pneumonia. Open Forum Infect Dis. 2020;7(Supplement_1):S668-S668. doi:10.1093/ ofid/ofaa439.1493
  • 19. Nakamura R, Ito-Horiyama T, Takemura M, et al. In Vivo Pharmacodynamic Study of Cefiderocol, a Novel Parenteral Siderophore Cephalosporin, in Murine Thigh and Lung Infection Models. Antimicrob Agents Chemother. 2019;63(9). doi:10.1128/AAC.02031- 18
  • 20. Kohira N, West J, Ito A, et al. In Vitro Antimicrobial Activity of a Siderophore Cepha- losporin, S-649266, against Enterobacteriaceae Clinical Isolates, Including Carbape- nem-Resistant Strains. Antimicrob Agents Chemother. 2016;60(2):729-734. doi:10.1128/ AAC.01695-15
  • 21. Ito A, Kohira N, Bouchillon SK, et al. In vitro antimicrobial activity of S-649266, a ca- techol-substituted siderophore cephalosporin, when tested against non-fermenting Gram-negative bacteria. J Antimicrob Chemother. 2016;71(3):670-677. doi:10.1093/ JAC/DKV402
  • 22. Zhanel GG, Golden AR, Zelenitsky S, et al. Cefiderocol: A Siderophore Cephalosporin with Activity Against Carbapenem-Resistant and Multidrug-Resistant Gram-Negative Bacilli. Drugs. 2019;79(3):271-289. doi:10.1007/s40265-019-1055-2
  • 23. Kawaguchi N, Katsube T, Echols R, Wajima T. Population Pharmacokinetic Analysis of Cefiderocol, a Parenteral Siderophore Cephalosporin, in Healthy Subjects, Subjects with Various Degrees of Renal Function, and Patients with Complicated Urinary Tract Infec- tion or Acute Uncomplicated Pyelonephritis. Antimicrob Agents Chemother. 2018;62(2).doi:10.1128/AAC.01391-17
  • 24. Wu JY, Srinivas P, Pogue JM. Cefiderocol: A Novel Agent for the Management of Multid- rug-Resistant Gram-Negative Organisms. Infect Dis Ther. 2020;9(1):17-40. doi:10.1007/ S40121-020-00286-6
  • 25. Stracquadanio S, Torti E, Longshaw C, Henriksen AS, Stefani S. In vitro activity of ce- fiderocol and comparators against isolates of Gram-negative pathogens from a range of infection sources: SIDERO-WT-2014–2018 studies in Italy. J Glob Antimicrob Resist. 2021;25:390-398. doi:10.1016/j.jgar.2021.04.019
  • 26. Kazmierczak KM, Tsuji M, Wise MG, et al. In vitro activity of cefiderocol, a siderophore cephalosporin, against a recent collection of clinically relevant carbapenem-non-suscep- tible Gram-negative bacilli, including serine carbapenemase- and metallo-β-lactama- se-producing isolates (SIDERO-WT-2014 . Int J Antimicrob Agents. 2019;53(2):177-184. doi:10.1016/j.ijantimicag.2018.10.007
  • 27. Hackel MA, Tsuji M, Yamano Y, Echols R, Karlowsky JA, Sahm DF. In vitro activity of the siderophore cephalosporin, cefiderocol, against carbapenem-nonsusceptible and multidrug-resistant isolates of gram-negative bacilli collected worldwide in 2014 to 2016. Antimicrob Agents Chemother. 2018;62(2). doi:10.1128/AAC.01968-17
  • 28. Iregui A, Khan Z, Landman D, Quale J. Activity of Cefiderocol against Enterobacterales, Pseudomonas aeruginosa, and Acinetobacter baumannii Endemic to Medical Centers in New York City. Microb Drug Resist. 2020;26(7):722-726. doi:10.1089/mdr.2019.0298
  • 29. Dobias J, Dénervaud-Tendon V, Poirel L, Nordmann P. Activity of the novel siderophore cephalosporin cefiderocol against multidrug-resistant Gram-negative pathogens. Eur J Clin Microbiol Infect Dis. 2017;36(12):2319-2327. doi:10.1007/s10096-017-3063-z
  • 30. Karlowsky JA, Hackel MA, Takemura M, Yamano Y, Echols R, Sahm DF. In Vitro Suscep- tibility of Gram-Negative Pathogens to Cefiderocol in Five Consecutive Annual Multina- tional SIDERO-WT Surveillance Studies, 2014 to 2019. Antimicrob Agents Chemother. 2022;66(2):e0199021. doi:10.1128/AAC.01990-21
  • 31. Shortridge D, Streit JM, Mendes R, Castanheira M. In Vitro Activity of Cefiderocol against U.S. and European Gram-Negative Clinical Isolates Collected in 2020 as Part of the SENTRY Antimicrobial Surveillance Program. Lincopan N, ed. Microbiol Spectr. 2022;10(2):e0271221. doi:10.1128/spectrum.02712-21
  • 32. Ito-Horiyama T, Ishii Y, Ito A, et al. Stability of Novel Siderophore Cephalosporin S-649266 against Clinically Relevant Carbapenemases. Antimicrob Agents Chemother. 2016;60(7):4384-4386. doi:10.1128/AAC.03098-15
  • 33. Hackel MA, Tsuji M, Yamano Y, Echols R, Karlowsky JA, Sahma DF. In Vitro Activity of the Siderophore Cephalosporin, Cefiderocol, against a Recent Collection of Clinically Relevant Gram-Negative Bacilli from North America and Europe, Including Carbape- nem-Nonsusceptible Isolates (SIDERO-WT-2014 Study). Antimicrob Agents Chemot- her. 2017;61(9). doi:10.1128/AAC.00093-17
  • 34. Cefiderocol: Rationale for EUCAST Clinical Breakpoints. Published online 2022. Acces- sed March 19, 2023. http://www.eucast.org.
  • 35. Kanazawa S, Sato T, Kohira N, Ito-Horiyama T, Tsuji M, Yamano Y. Susceptibility of Imi- penem-Susceptible but Meropenem-Resistant blaIMP-6-Carrying Enterobacteriaceae to Various Antibacterials, Including the Siderophore Cephalosporin Cefiderocol. Antimic- rob Agents Chemother. 2017;61(7). doi:10.1128/AAC.00576-17
  • 36. Poirel L, Kieffer N, Nordmann P. Stability of cefiderocol against clinically significant bro- ad-spectrum oxacillinases. Int J Antimicrob Agents. 2018;52(6):866-867. doi:10.1016/j. ijantimicag.2018.11.005
  • 37. Ito A, Nishikawa T, Ota M, et al. Stability and low induction propensity of cefiderocol against chromosomal AmpC b-lactamases of Pseudomonas aeruginosa and Enterobacter cloacae. J Antimicrob Chemother. 2018;73(11):3049-3052. doi:10.1093/jac/dky317
  • 38. Jean SS, Harnod D, Hsueh PR. Global Threat of Carbapenem-Resistant Gram-Negative Bacteria. Front Cell Infect Microbiol. 2022;12. doi:10.3389/fcimb.2022.823684
  • 39. Poirel L, Sadek M, Nordmann P. Contribution of PER-Type and NDM-Type β-Lactama- ses to Cefiderocol Resistance in Acinetobacter baumannii. Antimicrob Agents Chemot- her. 2021;65(10):e0087721. doi:10.1128/AAC.00877-21
  • 40. Lan P, Lu Y, Chen Z, et al. Emergence of High-Level Cefiderocol Resistance in Carba- penem-Resistant Klebsiella pneumoniae from Bloodstream Infections in Patients with Hematologic Malignancies in China. Microbiol Spectr. 2022;10(2). doi:10.1128/SPECT- RUM.00084-22
  • 41. Terreni M, Taccani M, Pregnolato M. New antibiotics for multidrug-resistant bacterial strains: Latest research developments and future perspectives. Molecules. 2021;26(9). doi:10.3390/MOLECULES26092671
  • 42. Martínez JL, Baquero F, Andersson DI. Beyond serial passages: New methods for predicting the emergence of resistance to novel antibiotics. Curr Opin Pharmacol. 2011;11(5):439-445. doi:10.1016/j.coph.2011.07.005
  • 43. Mirza HC, İnce Ceviz G. Investigation of In Vitro Activity of Cefiderocol against Ex- tended-Spectrum Beta-Lactamase-Producing and Carbapenem-Resistant Enterobac- teriaceae Isolates. Türk Mikrobiyoloji Cemiy Derg. 2022;52(3):240-245. doi:10.54453/ TMCD.2022.35119
  • 44. Iregui A, Khan Z, Landman D, Quale J. Activity of Cefiderocol Against Enterobacterales, Pseudomonas aeruginosa, and Acinetobacter baumannii Endemic to Medical Centers in New York City. Microb Drug Resist. 2020;26(7):722-726. doi:10.1089/mdr.2019.0298
  • 45. Hackel MA, Tsuji M, Yamano Y, Echols R, Karlowsky JA, Sahm DF. Reproducibility of broth microdilution MICs for the novel siderophore cephalosporin, cefiderocol, determi- ned using iron-depleted cation-adjusted Mueller-Hinton broth. Diagn Microbiol Infect Dis. 2019;94(4):321-325. doi:10.1016/j.diagmicrobio.2019.03.003
  • 46. European Committee on Antimicrobial Susceptibility Testing. Clinical Breakpoints for Cefiderocol Were Set by EUCAST as Follows: Organisms MIC Breakpoint (Mg/L) Disk Content (Μg).; 2020.
  • 47. Gijón Cordero D, Castillo-Polo JA, Ruiz-Garbajosa P, Cantón R. Antibacterial spectrum of cefiderocol. Rev Esp Quimioter. 2022;35 Suppl 2(Suppl 2):20-27. doi:10.37201/req/ s02.03.2022
  • 48. Lee YR, Yeo S. Cefiderocol, a New Siderophore Cephalosporin for the Treatment of Complicated Urinary Tract Infections Caused by Multidrug-Resistant Pathogens: Precli- nical and Clinical Pharmacokinetics, Pharmacodynamics, Efficacy and Safety. Clin Drug Investig. 2020;40(10):901-913. doi:10.1007/s40261-020-00955-x
  • 49. Saisho Y, Katsube T, White S, Fukase H, Shimada J. Pharmacokinetics, Safety, and Tolera- bility of Cefiderocol, a Novel Siderophore Cephalosporin for Gram-Negative Bacteria, in Healthy Subjects. Antimicrob Agents Chemother. 2018;62(3). doi:10.1128/AAC.02163- 17
  • 50. Bassetti M, Echols R, Matsunaga Y, et al. Efficacy and safety of cefiderocol or best ava- ilable therapy for the treatment of serious infections caused by carbapenem-resistant Gram-negative bacteria (CREDIBLE-CR): a randomised, open-label, multicentre, pathogen-focused, descriptive, phase 3 trial. Lancet Infect Dis. 2021;21(2):226-240. doi:10.1016/S1473-3099(20)30796-9
  • 51. Wunderink RG, Matsunaga Y, Ariyasu M, et al. Cefiderocol versus high-dose, exten- ded-infusion meropenem for the treatment of Gram-negative nosocomial pneumonia (APEKS-NP): a randomised, double-blind, phase 3, non-inferiority trial. Lancet Infect Dis. 2021;21(2):213-225. doi:10.1016/S1473-3099(20)30731-3
  • 52. Portsmouth S, van Veenhuyzen D, Echols R, et al. Cefiderocol versus imipenem-cilastatin for the treatment of complicated urinary tract infections caused by Gram-negative uro- pathogens: a phase 2, randomised, double-blind, non-inferiority trial. Lancet Infect Dis. 2018;18(12):1319-1328. doi:10.1016/S1473-3099(18)30554-1
  • 53. Katsube T, Miyazaki S, Narukawa Y, Hernandez-Illas M, Wajima T. Drug-drug interacti- on of cefiderocol, a siderophore cephalosporin, via human drug transporters. Eur J Clin Pharmacol. 2018;74(7):931-938. doi:10.1007/S00228-018-2458-9
  • 54. Azanza Perea JR, Sádaba Díaz de Rada B. Pharmacokinetics/Pharmacodynamics and to- lerability of cefiderocol in the clinical setting. Rev Esp Quimioter. 2022;35 Suppl 2(Suppl 2):28-34. doi:10.37201/req/s02.04.2022
  • 55. Naseer S, Weinstein EA, Rubin DB, et al. US Food and Drug Administration (FDA): Benefit-Risk Considerations for Cefiderocol (Fetroja®). Clin Infect Dis. 2021;72(12):E1103-E1111. doi:10.1093/cid/ciaa1799
Toplam 55 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Tıbbi Mikrobiyoloji
Bölüm Derleme
Yazarlar

Betül Kars 0000-0003-0472-2863

Sevil Öztaş 0000-0002-4134-1587

Mustafa Altındiş 0000-0003-0411-9669

Erken Görünüm Tarihi 10 Mayıs 2023
Yayımlanma Tarihi 30 Nisan 2023
Kabul Tarihi 16 Nisan 2023
Yayımlandığı Sayı Yıl 2023 Cilt: 7 Sayı: 1

Kaynak Göster

AMA Kars B, Öztaş S, Altındiş M. Bir İlaç Monografı; Sefiderokol. J Biotechnol and Strategic Health Res. Nisan 2023;7(1):9-25. doi:10.34084/bshr.1279754
  • Dergimiz Uluslararası hakemli bir dergi olup TÜRKİYE ATIF DİZİNİ, TürkMedline, CrossREF, ASOS index, Google Scholar, JournalTOCs, Eurasian Scientific Journal Index(ESJI), SOBIAD ve ISIindexing dizinlerinde taranmaktadır. TR Dizin(ULAKBİM), SCOPUS, DOAJ için başvurularımızın sonuçlanması beklenmektedir.