Evidence map›Paper›PMID 33256752›Full record

ArticleAnnals of clinical microbiology and antimicrobials2020

Clinical syndromes and treatment location predict utility of carbapenem sparing therapies in ceftriaxone-non-susceptible Escherichia coli bloodstream infection.

Ouli Xie, Kathryn Cisera, Lucy Taylor, Carly Hughes, Benjamin Rogers

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Annals of clinical microbiology and antimicrobials, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06422533 (Ceftolozane/Tazobactam vs. Piperacillin/Tazobactam for the Treatment of Bacteremia Due to Enterobacteriaceae and Pseudomonas Aeruginosa in Hemato-oncological Patients With Severe Neutropenia and Fever), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 46% 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.

NCT06422533 naunknown statusnot on this mapstarted 2023, after this paper: background citation

Ceftolozane/Tazobactam vs. Piperacillin/Tazobactam for the Treatment of Bacteremia Due to Enterobacteriaceae and Pseudomonas Aeruginosa in Hemato-oncological Patients With Severe Neutropenia and Fever: Non-inferiority Study

TypeinterventionalSponsorInstituto Nacional de Cancerologia de MexicoRan2023 to 2025Enrolled226ConditionsHematologic Neoplasms, NeutropeniaArmsCeftolozane/tazobactam, Piperacillin/tazobactam
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Exploring the advancements of Australian OPAT.Therapeutic advances in infectious disease
    Review
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

5 authors at 2 institutions in 1 country.

Ouli XieDepartment of Microbiology, Monash Health, Clayton, Victoria, Australia. oulixie87@gmail.com.ORCID http://orcid.org/0000-0002-5032-1932
Kathryn CiseraDepartment of Microbiology, Monash Health, Clayton, Victoria, Australia.
Lucy TaylorDepartment of Infectious Diseases, Monash Health, Clayton, Victoria, Australia.
Carly HughesDepartment of Microbiology, Monash Health, Clayton, Victoria, Australia.
Benjamin RogersDepartment of Infectious Diseases, Monash Health, Clayton, Victoria, Australia. ben.rogers@monash.edu.
Monash Health · AUMonash Medical Centre · AU

Funding

Merck Sharp and Dohme IIS 57091
6 · The paper itself

Abstract

backgroundCefiderocol, ceftazidime-avibactam, ceftolozane-tazobactam, intravenous fosfomycin and plazomicin represent potential carbapenem sparing agents for extended-spectrum-beta-lactamase or AmpC beta-lactamase producing Escherichia coli infection. However, available data is limited in predicting the volume of carbapenem therapy which could be substituted and real-world contraindications.

methodsWe determined the number of carbapenem days of therapy (DOT) which could be substituted and frequent contraindications accounting for antimicrobial susceptibility and site of infection in an unselected cohort with ceftriaxone-non-susceptible E. coli bacteremia at a single health network from 2015 to 2016. Individual patient data was used to calculate DOT and substitution for each agent.

resultsThere were 108 episodes of E. coli bacteremia resulting in 67.2 carbapenem DOT/100 patient-days of antimicrobial therapy administered. Ceftazidime-avibactam could be used to substitute 36.2 DOT/100 patient-days (54%) for inpatient definitive therapy, ceftolozane-tazobactam for 34.7 DOT/100 patient-days (52%), cefiderocol for 27.1 DOT/100 patient-days (40%), fosfomycin for 23.3 DOT /100 patient-days (35%) and plazomicin for 27.1 DOT/100 patient-days (40%). Non-urinary tract source of infection was the most frequent contraindication to fosfomycin (25), plazomicin (26) and cefiderocol (26). Use in outpatient parenteral antimicrobial therapy (OPAT) programs accounted for 40% of DOT, all of which could be substituted if stability data allowed for ceftazidime-avibactam and ceftolozane-tazobactam.

conclusionsAll tested agents could be used to replace a significant volume of carbapenem therapy. Establishing stability of these agents for use in OPAT is required for maximizing their use as carbapenem sparing agents while randomized clinical data is awaited for some of these agents in resistant E. coli bacteremia.

Indexed as

AgedAged, 80 and overAnti-Bacterial AgentsAzabicyclo CompoundsBacteremiaCarbapenemsCeftazidimeCeftriaxoneCephalosporinsDrug CombinationsDrug Resistance, Multiple, BacterialEscherichia coliEscherichia coli InfectionsFemaleHumansMaleAnti-Bacterial Agentsavibactam, ceftazidime drug combinationAzabicyclo CompoundsCarbapenemsCeftazidimeceftolozane, tazobactam drug combinationCeftriaxoneCephalosporinsDrug CombinationsTazobactamBacteremiaCeftriaxoneDrug resistanceEscherichia coli infectionsMeropenem

Identifiers

PMID33256752
PMCPMC7708213
OpenAlexW3109149797

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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.