Current and future options for the treatment of serious infections due to carbapenem-resistant <i>Pseudomonas aeruginosa</i>

SUMMARY<i>Pseudomonas aeruginosa</i> is a frequent cause of hospital-acquired infections and is notable both for its virulence and its resistance to multiple antibiotics. In the absence of head-to-head clinical trials and availability of all potential options on a global basis, we have systematically analyzed potential antibiotics for carbapenem-resistant <i>P. aeruginosa</i>. Monotherapy with ceftazidime-avibactam, imipenem-cilastatin-relebactam, cefiderocol, or high doses of ceftolozane-tazobactam is generally considered an acceptable option for serious infections due to carbapenem-resistant <i>P. aeruginosa</i>. The role of testing combinations of antimicrobial agents for <i>in vitro</i> susceptibility is uncertain, as is the administration of nebulized colistin or amikacin in patients with ventilator-associated pneumonia. With regard to new therapies, 10 clinical trials are underway or have been completed on bacteriophage therapy for <i>P. aeruginosa</i> infections. However, no phage options are yet widely approved for use. Other new options in clinical trials include beta-lactam antibiotics combined with new beta-lactamase inhibitors and antibody-based therapies.

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Publication Details

Journal
Clinical Microbiology Reviews
Published
2025-10-09
DOI
https://doi.org/10.1128/cmr.00233-24
Citations
1
Primary Topic
Antibiotic Resistance in Bacteria
Type
article
Field-Weighted Citation Impact
0.59
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article

Current and future options for the treatment of serious infections due to carbapenem-resistant Pseudomonas aeruginosa

Keith S. Kaye, David L. Paterson, Juan Pablo Horcajada, Cornelia B. Landersdorfer et al.
1 citations
Clinical Microbiology Reviews
Antibiotic Resistance in Bacteria
0.59
article

Current and future options for the treatment of serious infections due to carbapenem-resistant Pseudomonas aeruginosa

Keith S. Kaye, David L. Paterson, Juan Pablo Horcajada, Cornelia B. Landersdorfer, Dafna Yahav, Andrea Lay‐Hoon Kwa, Antonio Oliver, Ana Cristina Gales, Burcu Isler, María Virginia Villegas, Jason M. Pogue, M. Montero, Ryan K. Shields
article en
1 citations

Abstract

SUMMARY<i>Pseudomonas aeruginosa</i> is a frequent cause of hospital-acquired infections and is notable both for its virulence and its resistance to multiple antibiotics. In the absence of head-to-head clinical trials and availability of all potential options on a global basis, we have systematically analyzed potential antibiotics for carbapenem-resistant <i>P. aeruginosa</i>. Monotherapy with ceftazidime-avibactam, imipenem-cilastatin-relebactam, cefiderocol, or high doses of ceftolozane-tazobactam is generally considered an acceptable option for serious infections due to carbapenem-resistant <i>P. aeruginosa</i>. The role of testing combinations of antimicrobial agents for <i>in vitro</i> susceptibility is uncertain, as is the administration of nebulized colistin or amikacin in patients with ventilator-associated pneumonia. With regard to new therapies, 10 clinical trials are underway or have been completed on bacteriophage therapy for <i>P. aeruginosa</i> infections. However, no phage options are yet widely approved for use. Other new options in clinical trials include beta-lactam antibiotics combined with new beta-lactamase inhibitors and antibody-based therapies.

Clinical Microbiology ReviewsVol. 38(4)
Rutgers, The State University of New Jersey (US), The University of Queensland (AU), National University of Singapore (SG), Universitat Pompeu Fabra (ES), Universidad El Bosque (CO), University of Michigan (US), Sheba Medical Center (IL), Instituto de Salud Carlos III (ES), Princess Alexandra Hospital (AU), Johnson University (US), Rutgers Sexual and Reproductive Health and Rights (NL), Duke-NUS Medical School (SG), CNR de la Résistance aux Antibiotiques (FR), University of Pittsburgh Medical Center (US), Princess Alexandra Hospital (GB), National University Health System (SG), Hospital Universitario Son Espases (ES), Monash University (AU), Universidade Federal de São Paulo (BR)
Openalex Percentile: Top 29%
Antibiotic Resistance in Bacteria
0.59
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