Literature DB >> 35394640

Efficacy and Pharmacodynamic Target Attainment for Ceftazidime-Avibactam Off-Label Dose Regimens in Patients with Continuous or Intermittent Venovenous Hemodialysis: Two Case Reports.

Xiao-Shan Zhang1,2, Yu-Zhen Wang1,2, Da-Wei Shi1, Fang-Min Xu1,2, Jun-Hui Yu1,2, Jie Chen3, Guan-Yang Lin1, Chun-Hong Zhang4, Xu-Ben Yu5, Cong-Rong Tang6.   

Abstract

Limited data are available for ceftazidime-avibactam (CZA) dosing in patients receiving renal replacement therapy, especially the data on the dosing in patients receiving intermittent hemodialysis (IHD). In this report, we firstly described a case in which CZA was administered as 2.5 g after each time of IHD, and a dose of 1.25 g was added on the 48th-hour for the 72-h interdialytic interval. Plasma concentrations of CZA measured at different time indicated that > 50% of administered ceftazidime and avibactam were removed during the 4-h hemodialysis. In addition, we described another case on continuous venovenous hemodialysis (CVVHD), in which CZA was administered as 2.5 g q12h in 2-h infusions. The dose regimen for these two cases could achieve trough concentration of ceftazidime higher than fourfold of the MIC and trough concentration of avibactam higher than the threshold of 1 μg/mL during the treatment, and exert efficient antimicrobial effect.
© 2022. The Author(s).

Entities:  

Keywords:  Ceftazidime–avibactam; Continuous venovenous hemodialysis; Dosing regimen; Intermittent hemodialysis; Plasma concentration

Year:  2022        PMID: 35394640     DOI: 10.1007/s40121-022-00621-z

Source DB:  PubMed          Journal:  Infect Dis Ther        ISSN: 2193-6382


  12 in total

1.  Avibactam reverts the ceftazidime MIC90 of European Gram-negative bacterial clinical isolates to the epidemiological cut-off value.

Authors:  Robert K Flamm; Gregory G Stone; Helio S Sader; Ronald N Jones; Wright W Nichols
Journal:  J Chemother       Date:  2013-12-06       Impact factor: 1.714

Review 2.  Dose Selection and Validation for Ceftazidime-Avibactam in Adults with Complicated Intra-abdominal Infections, Complicated Urinary Tract Infections, and Nosocomial Pneumonia.

Authors:  Shampa Das; Jianguo Li; Todd Riccobene; Timothy J Carrothers; Paul Newell; David Melnick; Ian A Critchley; Gregory G Stone; Wright W Nichols
Journal:  Antimicrob Agents Chemother       Date:  2019-03-27       Impact factor: 5.191

3.  In vitro antibacterial activity of the ceftazidime-avibactam (NXL104) combination against Pseudomonas aeruginosa clinical isolates.

Authors:  Premavathy Levasseur; Anne-Marie Girard; Monique Claudon; Herman Goossens; Michael T Black; Kenneth Coleman; Christine Miossec
Journal:  Antimicrob Agents Chemother       Date:  2012-01-03       Impact factor: 5.191

4.  Pneumonia and Renal Replacement Therapy Are Risk Factors for Ceftazidime-Avibactam Treatment Failures and Resistance among Patients with Carbapenem-Resistant Enterobacteriaceae Infections.

Authors:  Ryan K Shields; M Hong Nguyen; Liang Chen; Ellen G Press; Barry N Kreiswirth; Cornelius J Clancy
Journal:  Antimicrob Agents Chemother       Date:  2018-04-26       Impact factor: 5.191

5.  Steady-State Ceftazidime-Avibactam Serum Concentrations and Dosing Recommendations in a Critically Ill Patient Being Treated for Pseudomonas aeruginosa Pneumonia and Undergoing Continuous Venovenous Hemodiafiltration.

Authors:  Paige Soukup; Andrew C Faust; Vindhya Edpuganti; William C Putnam; James A McKinnell
Journal:  Pharmacotherapy       Date:  2019-10-31       Impact factor: 4.705

6.  Determination of avibactam and ceftazidime in human plasma samples by LC-MS.

Authors:  Henrik Sillén; Richard Mitchell; Rebecca Sleigh; Guy Mainwaring; Katherine Catton; Richard Houghton; Karen Glendining
Journal:  Bioanalysis       Date:  2015       Impact factor: 2.681

7.  Antimicrobial activity of ceftazidime-avibactam against Gram-negative organisms collected from U.S. medical centers in 2012.

Authors:  Helio S Sader; Mariana Castanheira; Robert K Flamm; David J Farrell; Ronald N Jones
Journal:  Antimicrob Agents Chemother       Date:  2013-12-30       Impact factor: 5.191

8.  In Vitro Susceptibility of Global Surveillance Isolates of Pseudomonas aeruginosa to Ceftazidime-Avibactam (INFORM 2012 to 2014).

Authors:  Wright W Nichols; Boudewijn L M de Jonge; Krystyna M Kazmierczak; James A Karlowsky; Daniel F Sahm
Journal:  Antimicrob Agents Chemother       Date:  2016-07-22       Impact factor: 5.191

9.  Contemporary diversity of β-lactamases among Enterobacteriaceae in the nine U.S. census regions and ceftazidime-avibactam activity tested against isolates producing the most prevalent β-lactamase groups.

Authors:  Mariana Castanheira; Sarah E Farrell; Kevin M Krause; Ronald N Jones; Helio S Sader
Journal:  Antimicrob Agents Chemother       Date:  2013-11-18       Impact factor: 5.191

10.  Ceftazidime-Avibactam Population Pharmacokinetic Modeling and Pharmacodynamic Target Attainment Across Adult Indications and Patient Subgroups.

Authors:  Jianguo Li; Mark Lovern; Michelle L Green; Joannellyn Chiu; Diansong Zhou; Craig Comisar; Yuan Xiong; Jeremy Hing; Merran MacPherson; James G Wright; Todd Riccobene; Timothy J Carrothers; Shampa Das
Journal:  Clin Transl Sci       Date:  2018-09-28       Impact factor: 4.689

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