Delafloxacin--A novel fluoroquinolone for the treatment of ciprofloxacin-resistantPseudomonas aeruginosain patients with cystic fibrosis

被引:21
|
作者
Millar, Beverley Cherie [1 ,2 ,3 ]
McCaughan, John [4 ]
Rendall, Jacqueline C. [5 ]
Moore, John E. [1 ,2 ,3 ]
机构
[1] Belfast City Hosp, Dept Bacteriol, Northern Ireland Publ Hlth Lab, Belfast BT9 7AD, Antrim, North Ireland
[2] Queens Univ, Sch Med Dent & Biomed Sci, Wellcome Wolfson Inst Expt Med, Belfast, Antrim, North Ireland
[3] Ulster Univ, Sch Biomed Sci, Coleraine, Londonderry, North Ireland
[4] Royal Grp Hosp, Dept Med Microbiol, Belfast, Antrim, North Ireland
[5] Belfast City Hosp, Northern Ireland Reg Adult Cyst Fibrosis Ctr, Level 8, Belfast, Antrim, North Ireland
关键词
antibiotic resistance; ciprofloxacin; cystic fibrosis; delafloxacin; fluoroquinolone; Pseudomonas aeruginosa;
D O I
10.1111/crj.13262
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Introduction Fluoroquinolone antibiotics, namely ciprofloxacin and levofloxacin, play an important role in treating infection in cystic fibrosis (CF) and ciprofloxacin remains the last widely used and orally available antipseudomonal agent. Recently, a new fluoroquinolone, delafloxacin, has been approved by the FDA for the indication of Acute Bacterial Skin and Skin Structure Infections (ABSSSI). This antibiotic is a novel dual-targeting anionic fluoroquinolone and differs from previous agents in its class, as it lacks a protonatable substituent. To date, there are no reports of its use or activity againstPseudomonas aeruginosain CF. Alarmingly, fluoroquinolone resistance is increasing among CFP aeruginosaisolates. The aims of the study were to (a) examine in vitro susceptibility of delafloxacin against a population ofP. aeruginosa(n = 52) isolated from adult CF patients at our CF centre, (b) to compare delafloxacin and ciprofloxacin in vitro susceptibilities against CFP. aeruginosaand (c) to evaluate where delafloxacin may add benefit in treating CFP aeruginosa. Methods In vitro susceptibilities were examined on 52 non-mucoidP. aeruginosaandP. aeruginosaATCC (TM) 27853 reference strain, by employing Etest(R)gradient test strips for delafloxacin (range:0.002 - 32 mg/L) and ciprofloxacin (0.002 - 32 mg/L), as per manufacturer's instructions (Biomerieux). Results MIC range, MIC(50)and MIC(90)for delafloxacin were 0.064 (R) 32 mg/L, 0.56 mg/L and 2.19 mg/L, respectively. For ciprofloxacin, these were 0.047 (R) 32 mg/L, 1.69 mg/L and 8.0 mg/L, respectively. Overall, isolates were statistically more sensitive to delafloxacin (p = 0.0005) than ciprofloxacin. Of note, 4/12 (33.3%) isolates with intermediate resistance to ciprofloxacin were sensitive to delafloxacin. Similarly, 10/28 (35.7%) isolates resistant to ciprofloxacin were sensitive to delafloxacin, with only 17.9% isolates resistant to ciprofloxacin, resistant to delafloxacin. Conclusion Given similar breakpoints of these fluoroquinolones, these data show that delafloxacin has greater activity than ciprofloxacin. While delafloxacin and ciprofloxacin were equally effective with sensitive isolates, the value of delafloxacin was noted with more resistant isolates to ciprofloxacin. While ciprofloxacin should remain the first line fluoroquinolone for treating CFP aeruginosa, delafloxacin shows potential in treating ciprofloxacin-resistantP aeruginosa.
引用
收藏
页码:116 / 120
页数:5
相关论文
共 50 条
  • [1] Ciprofloxacin as antipseudomonal treatment in patients with cystic fibrosis
    Schaad, UB
    Wedgwood, J
    Ruedeberg, A
    Kraemer, R
    Hampel, B
    PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1997, 16 (01) : 106 - 111
  • [2] THE PK/PD INDEX (CMAX/MIC) FOR CIPROFLOXACIN IN PATIENTS WITH CYSTIC FIBROSIS
    Szalek, Edyta
    Kaminska, Agnieszka
    Gozdzik-Spychalska, Joanna
    Grzeskowiak, Edmund
    Batura-Gabryel, Halina
    ACTA POLONIAE PHARMACEUTICA, 2011, 68 (05): : 777 - 783
  • [3] Coagulopathy in two patients with cystic fibrosis treated with ciprofloxacin
    Moore, Gillian C.
    Redfern, Jan
    Shiach, Caroline R.
    Webb, Kevin
    Jones, Andrew M.
    JOURNAL OF CYSTIC FIBROSIS, 2007, 6 (03) : 209 - 211
  • [4] ANAPHYLACTOID REACTIONS TO CIPROFLOXACIN IN CYSTIC-FIBROSIS PATIENTS
    MILLER, MS
    GAIDO, F
    ROURK, MH
    SPOCK, A
    PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1991, 10 (02) : 164 - 165
  • [5] Alginate Lyase and Ciprofloxacin Co-Immobilization on Biopolymeric Microspheres for Cystic Fibrosis Treatment
    Islan, German A.
    Bosio, Valeria E.
    Castro, Guillermo R.
    MACROMOLECULAR BIOSCIENCE, 2013, 13 (09) : 1238 - 1248
  • [7] Ciprofloxacin pharmacokinetics in young cystic fibrosis patients after repeated oral doses
    Odoul, F
    Le Guellec, C
    Giraut, C
    de Gialluly, C
    Marchand, S
    Paintaud, G
    Saux, MC
    Rolland, JC
    Autret-Leca, E
    THERAPIE, 2001, 56 (05): : 519 - 524
  • [8] Gene Polymorphism of Biotransformation Enzymes and Ciprofloxacin Pharmacokinetics in Pediatric Patients with Cystic Fibrosis
    Zyryanov, Sergey K.
    Ushkalova, Elena A.
    Kondratyeva, Elena, I
    Butranova, Olga, I
    Kondakova, Yulia A.
    BIOMEDICINES, 2022, 10 (05)
  • [9] Developing ciprofloxacin dry powder for inhalation: A story of challenges and rational design in the treatment of cystic fibrosis lung infection
    Alhajj, Nasser
    O'Reilly, Niall J.
    Cathcart, Helen
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2022, 613
  • [10] Spotlight on inhaled ciprofloxacin and its potential in the treatment of non-cystic fibrosis bronchiectasis
    Chorepsima, Stamatia
    Kechagias, Konstantinos S.
    Kalimeris, Georgios
    Triarides, Nikolaos A.
    Falagas, Matthew E.
    DRUG DESIGN DEVELOPMENT AND THERAPY, 2018, 12 : 4059 - 4066