Literature DB >> 33434676

Evaluating the emergence of nonsusceptibility among Pseudomonas aeruginosa respiratory isolates from a phase 3 clinical trial for treatment of nosocomial pneumonia (ASPECT-NP).

Matthew G Johnson1, Christopher Bruno2, Mariana Castanheira3, Brian Yu2, Jennifer A Huntington2, Patricia Carmelitano2, Elizabeth G Rhee2, Carisa De Anda2, Mary Motyl2.   

Abstract

The emergence of Gram-negative resistance during antibacterial therapy yields worse clinical outcomes and increased antimicrobial resistance worldwide. We evaluated the emergence of nonsusceptibility to ceftolozane/tazobactam and meropenem among participants with Pseudomonas aeruginosa lower respiratory tract isolates from ASPECT-NP, a phase 3, randomized, double-blind, multicenter study that demonstrated the noninferiority of a ceftolozane/tazobactam 3-g dose q8h versus a meropenem 1-g dose q8h for treatment of ventilated hospital-acquired/ventilator-associated bacterial pneumonia. Molecular resistance mechanisms among postbaseline nonsusceptible P. aeruginosa isolates and clinical outcomes associated with participants with emergence of nonsusceptibility were examined. Baseline susceptible and postbaseline nonsusceptible P. aeruginosa isolate pairs from the same participant underwent molecular typing. Emergence of nonsusceptibility was not observed among the 59 participants with baseline susceptible P. aeruginosa isolates in the ceftolozane/tazobactam arm. Among 58 participants with baseline susceptible P. aeruginosa isolates in the meropenem arm, emergence of nonsusceptibility was observed in 13 (22.4%). Among participants who received ceftolozane/tazobactam and meropenem, respectively, 5.1% and 3.4% had a new infection with a nonsusceptible strain. None of the isolates with emergence of nonsusceptibility to meropenem developed coresistance to ceftolozane/tazobactam. Molecular mechanisms associated with emergence of nonsusceptibility to meropenem were decreased expression or loss of OprD and overexpression of MexXY. Among participants with emergence of nonsusceptibility to meropenem, clinical outcomes were similar to overall clinical outcomes in the ASPECT-NP meropenem arm. Ceftolozane/tazobactam was more stable to emergence of nonsusceptibility versus meropenem; emergence of nonsusceptibility was not observed in any participants with baseline susceptible P. aeruginosa who received ceftolozane/tazobactam in ASPECT-NP.
Copyright © 2021. Published by Elsevier Ltd.

Entities:  

Keywords:  Antibacterial; Antimicrobial resistance; Ceftolozane/tazobactam; Clinical trial; Pneumonia; Pseudomonas aeruginosa

Year:  2021        PMID: 33434676     DOI: 10.1016/j.ijantimicag.2021.106278

Source DB:  PubMed          Journal:  Int J Antimicrob Agents        ISSN: 0924-8579            Impact factor:   5.283


  3 in total

1.  Clinical and microbiological outcomes, by causative pathogen, in the ASPECT-NP randomized, controlled, Phase 3 trial comparing ceftolozane/tazobactam and meropenem for treatment of hospital-acquired/ventilator-associated bacterial pneumonia.

Authors:  Ignacio Martin-Loeches; Jean-François Timsit; Marin H Kollef; Richard G Wunderink; Nobuaki Shime; Martin Nováček; Ülo Kivistik; Álvaro Réa-Neto; Christopher J Bruno; Jennifer A Huntington; Gina Lin; Erin H Jensen; Mary Motyl; Brian Yu; Davis Gates; Joan R Butterton; Elizabeth G Rhee
Journal:  J Antimicrob Chemother       Date:  2022-03-31       Impact factor: 5.758

Review 2.  Ceftolozane-tazobactam in nosocomial pneumonia.

Authors:  F J Candel; J González Del Castillo; A Julián Jiménez; M Matesanz
Journal:  Rev Esp Quimioter       Date:  2022-04-22       Impact factor: 2.515

3.  Socioeconomic burden of pneumonia due to multidrug-resistant Acinetobacter baumannii and Pseudomonas aeruginosa in Korea.

Authors:  Chung-Jong Kim; Kyoung-Ho Song; Jeonghoon Ahn; Hong Bin Kim; Nam-Kyong Choi; Ji Yun Bae; Hee Jung Choi; Younghee Jung; Seung Soon Lee; Ji-Hwan Bang; Eu Suk Kim; Song Mi Moon; Je Eun Song; Yee Gyung Kwak; Shin Hye Chun; Yeon-Sook Kim; Kyung-Hwa Park; Yu Min Kang; Pyoeng Gyun Choe; Shinwon Lee
Journal:  Sci Rep       Date:  2022-08-17       Impact factor: 4.996

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.