Evidence map›Paper›PMID 36879495›Full record

ArticleThe Journal of antimicrobial chemotherapy2023

Piperacillin/tazobactam versus cefepime or carbapenems for cefoxitin-non-susceptible Enterobacter cloacae, Klebsiella aerogenes, Citrobacter freundii, Serratia marcescens and Morganella morganii bacteraemia in immunocompromised patients.

Brian Lu, Miranda Wong, David Ha, Mark Bounthavong, Niaz Banaei, Stanley Deresinski, Calvin Diep

Open access · hybridAbstract read
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
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

7 authors at 3 institutions in 1 country.

Brian LuDepartment of Pharmacy, Stanford Health Care, 300 Pasteur Drive, Stanford, CA 94305, USA.ORCID 0000-0002-6381-5499
Miranda WongDepartment of Pharmacy, Stanford Health Care, 300 Pasteur Drive, Stanford, CA 94305, USA.
David HaDepartment of Quality, Patient Safety and Effectiveness, Stanford Health Care, Stanford, CA, USA.
Mark BounthavongDivision of Clinical Pharmacy, UCSD Skaggs School of Pharmacy & Pharmaceutical Sciences, La Jolla, CA, USA.
Niaz BanaeiDivision of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, CA, USA.
Stanley DeresinskiDepartment of Quality, Patient Safety and Effectiveness, Stanford Health Care, Stanford, CA, USA.
Calvin DiepDepartment of Pharmacy, Stanford Health Care, 300 Pasteur Drive, Stanford, CA 94305, USA.
Stanford Health Care · USStanford University · USUniversity of Montana · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe role of piperacillin/tazobactam for treatment of serious infections due to AmpC-producing organisms remains debatable, particularly in immunocompromised patients.

methodsThis was a retrospective cohort study in immunocompromised patients that investigated the effect of definitive treatment with either piperacillin/tazobactam versus cefepime or carbapenems for bacteraemia caused by cefoxitin-non-susceptible Enterobacterales. The primary endpoint was a composite of clinical and microbiological failure. A logistic regression model was constructed to assess the impact of definitive treatment choice on the primary endpoint.

resultsA total of 81 immunocompromised patients with blood cultures positive for cefoxitin-non-susceptible Enterobacterales were included for analysis. There was more microbiological failure in the piperacillin/tazobactam arm compared with the cefepime/carbapenem arm (11.4% versus 0.0%, P = 0.019). Definitive treatment with cefepime or a carbapenem was associated with a decreased odds of clinical or microbiological failure (OR 0.303, 95% CI 0.093-0.991, P = 0.048) when controlling for baseline characteristics.

conclusionsIn immunocompromised patients with bacteraemia due to cefoxitin-non-susceptible Enterobacterales, definitive treatment with piperacillin/tazobactam was associated with an increased risk of microbiological failure and higher odds of clinical or microbiological failure compared with cefepime or carbapenems.

Indexed as

BacteremiaEnterobacter aerogenesMorganella morganiiAnti-Bacterial Agentsbeta-LactamasesCarbapenemsCefepimeCefoxitinCitrobacter freundiiEnterobacter cloacaeHumansMicrobial Sensitivity TestsPiperacillin, Tazobactam Drug CombinationRetrospective StudiesSerratia marcescensAnti-Bacterial Agentsbeta-LactamasesCarbapenemsCefepimeCefoxitinPiperacillin, Tazobactam Drug Combination

Identifiers

PMID36879495
PMCPMC10068414
OpenAlexW4323348299

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.