Evidence map›Paper›PMID 29017262›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2017

Ceftolozane-Tazobactam for the Treatment of Multidrug-Resistant Pseudomonas aeruginosa Infections: Clinical Effectiveness and Evolution of Resistance.

Ghady Haidar, Nathan J Philips, Ryan K Shields, Daniel Snyder, Shaoji Cheng, Brian A Potoski, Yohei Doi, Binghua Hao, Ellen G Press, Vaughn S Cooper and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 139 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
139citing papers in PubMed, 3 pooled it
11.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

139 citing papers in PubMed, 3 syntheses or guidelines pooled it, 271 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Real-world use of ceftolozane/tazobactam: a systematic literature review.Antimicrobial resistance and infection control · 2021
    Pooled it
  4. Trial
  5. Trial
  6. Article
  7. L2 β-lactamase contributes to ceftolozane-tazobactam resistance inAntimicrobial agents and chemotherapy · 2026
    Article
  8. Global epidemiology of carbapenem-resistantJAC-antimicrobial resistance · 2026
    Review
  9. Variable phage susceptibility ofbioRxiv : the preprint server for biology · 2026
    Article
  10. Review
  11. A novel mechanism of ceftolozane-tazobactam resistance inbioRxiv : the preprint server for biology · 2026
    Article
  12. Article
  13. New Antibiotics Against Multidrug-Resistant Gram-Negative Bacteria in Lung Transplantation: Clinical Evidence, Safety, and PK/PD Properties.Transplant international : official journal of the European Society for Organ Transplantation · 2026
    Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Clinical Analysis ofJournal of clinical medicine · 2025
    Article
  19. Article
  20. Difficult-to-TreatAntibiotics (Basel, Switzerland) · 2025
    Review

79 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Ghady HaidarDepartment of Medicine, University of Pittsburgh, Pennsylvania.
Nathan J PhilipsDepartment of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pennsylvania.
Ryan K ShieldsDepartment of Medicine, University of Pittsburgh, Pennsylvania.
Daniel SnyderDepartment of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pennsylvania.
Shaoji ChengXDR Pathogen Laboratory, University of Pittsburgh Medical Center, Pennsylvania.
Brian A PotoskiDepartment of Medicine, University of Pittsburgh, Pennsylvania.
Yohei DoiDepartment of Medicine, University of Pittsburgh, Pennsylvania.
Binghua HaoXDR Pathogen Laboratory, University of Pittsburgh Medical Center, Pennsylvania.
Ellen G PressDepartment of Medicine, University of Pittsburgh, Pennsylvania.
Vaughn S CooperDepartment of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pennsylvania.
Cornelius J ClancyDepartment of Medicine, University of Pittsburgh, Pennsylvania.
M Hong NguyenDepartment of Medicine, University of Pittsburgh, Pennsylvania.
University of Pittsburgh · USUniversity of Pittsburgh Medical Center · USAntibiotic Research UK · GB

Funding

Predicting the emergence of antibiotic resistance through multi-omics approaches and Immune System-surveillanU01AI124302 · NIAID · BOSTON COLLEGE · PI BENTO, JOSE, COOPER, VAUGHN · 2016 to 2020
$10.2M
Colistin-resistant Acinetobacter baumanniiR01AI104895 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DOI, YOHEI, ERNST, ROBERT K · 2014 to 2024
$4.2M
Molecular mechanisms of adaptive diversity in Burkholderia biofilmsR01GM110444 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI COOPER, VAUGHN · 2015 to 2019
$1.5M
Caspofungin pharmacokinetics-pharmacodynamics during intra-adbominal candidiasisK08AI114883 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SHIELDS, RYAN K · 2015 to 2019
$858k
Microbiome and host response signatures for pneumonia among lung transplant recipientsR21AI126157 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CLANCY, CORNELIUS J · 2016 to 2017
$468k
Evolution of KPC-K pneumoniae that persist in patients on prolonged antibioticsR21AI111037 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CLANCY, CORNELIUS J · 2015 to 2016
$465k
Candida albicans gene expression during intra-abdominal infectionsR21AI107290 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NGUYEN, M. HONG THI · 2014 to 2015
$450k
Imaging and PK-PD of micafungin at sites of Candida glabrata infection in vivoR21AI121555 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CLANCY, CORNELIUS J · 2016 to 2017
$444k
Chromosomal and plasmid contributions to colistin resistance and virulence in KPC-producing Klebsiella pneumoniaeR21AI128338 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NGUYEN, M. HONG THI · 2017 to 2018
$444k
Mechanisms and implications of fosfomycin resistance in Escherichia coliR21AI123747 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DOI, YOHEI · 2016 to 2017
$417k
BLRD VA I01 BX001955NIAID NIH HHS K08 AI114883NIAID NIH HHS R01 AI104895NIAID NIH HHS R21 AI107290NIAID NIH HHS R21 AI111037NIAID NIH HHS R21 AI121555NIAID NIH HHS R21 AI123747NIAID NIH HHS R21 AI126157NIAID NIH HHS R21 AI128338NIAID NIH HHS U01 AI124302NIGMS NIH HHS R01 GM110444
6 · The paper itself

Abstract

Background: Data on the use of ceftolozane-tazobactam and emergence of ceftolozane-tazobactam resistance during multidrug resistant (MDR)-Pseudomonas aeruginosa infections are limited. Methods: We performed a retrospective study of 21 patients treated with ceftolozane-tazobactam for MDR-P. aeruginosa infections. Whole genome sequencing and quantitative real-time polymerase chain reaction were performed on longitudinal isolates. Results: Median age was 58 years; 9 patients (43%) were transplant recipients. Median simplified acute physiology score-II (SAPS-II) was 26. Eighteen (86%) patients were treated for respiratory tract infections; others were treated for bloodstream, complicated intraabdominal infections, or complicated urinary tract infections. Ceftolozane-tazobactam was discontinued in 1 patient (rash). Thirty-day all-cause and attributable mortality rates were 10% (2/21) and 5% (1/21), respectively; corresponding 90-day mortality rates were 48% (10/21) and 19% (4/21). The ceftolozane-tazobactam failure rate was 29% (6/21). SAPS-II score was the sole predictor of failure. Ceftolozane-tazobactam resistance emerged in 3 (14%) patients. Resistance was associated with de novo mutations, rather than acquisition of resistant nosocomial isolates. ampC overexpression and mutations were identified as potential resistance determinants. Conclusions: In this small study, ceftolozane-tazobactam was successful in treating 71% of patients with MDR-P. aeruginosa infections, most of whom had pneumonia. The emergence of ceftolozane-tazobactam resistance in 3 patients is worrisome and may be mediated in part by AmpC-related mechanisms. More research on treatment responses and resistance during various types of MDR-P. aeruginosa infections is needed to define ceftolozane-tazobactam's place in the armamentarium.

Indexed as

Anti-Bacterial AgentsCephalosporinsPseudomonas aeruginosaPseudomonas InfectionsAdultAgedAged, 80 and overDrug Resistance, Multiple, BacterialFemaleGenome, BacterialHumansMaleMiddle AgedPenicillanic AcidPennsylvaniaRetrospective StudiesAnti-Bacterial AgentsceftolozaneCephalosporinsPenicillanic AcidTazobactamAmpC beta-lactamaseceftolozane-tazobactamMDR Pseudomonasomega loopresistance mechanisms

Identifiers

PMID29017262
PMCPMC5848332
OpenAlexW2591044857

What OpenQuestion holds

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Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.