Evidence map›Paper›PMID 31859352›Full record

Observational studyClinical infectious diseases : an official publication of the Infectious Diseases Society of America2020

Is Piperacillin-Tazobactam Effective for the Treatment of Pyelonephritis Caused by Extended-Spectrum β-Lactamase-Producing Organisms?

Sima L Sharara, Joe Amoah, Zoi D Pana, Patricia J Simner, Sara E Cosgrove, Pranita D Tamma

Open access · greenAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
7.5field-weighted citation impact, top 2% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 citations in OpenAlex.

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  19. Antimicrobial agents and chemotherapy · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Sima L ShararaThe Johns Hopkins University School of Medicine, Department of Medicine, Baltimore, Maryland, USA.
Joe AmoahThe Johns Hopkins University School of Medicine, Department of Pediatrics, Baltimore, Maryland, USA.
Zoi D PanaEuropean University of Cyprus, Department of Medicine, Nicosia, Cyprus.
Patricia J SimnerThe Johns Hopkins University School of Medicine, Department of Pathology, Baltimore, Maryland, USA.
Sara E CosgroveThe Johns Hopkins University School of Medicine, Department of Medicine, Baltimore, Maryland, USA.
Pranita D TammaThe Johns Hopkins University School of Medicine, Department of Pediatrics, Baltimore, Maryland, USA.
Johns Hopkins Medicine · USEuropean University Cyprus · CYJohns Hopkins University · US

Funding

The Use of MALDI TOF for the Rapid Detection of Carbapenemases from Clinical IsolatesK23AI127935 · NIAID · JOHNS HOPKINS UNIVERSITY · PI TAMMA, PRANITA · 2017 to 2020
$734k
NIAID NIH HHS K23 AI127935
6 · The paper itself

Abstract

backgroundLimited data exist regarding the efficacy of piperacillin-tazobactam (TZP) for the management of nonbacteremic pyelonephritis caused by extended-spectrum β-lactamase (ESBL)-producing organisms.

methodsWe conducted a multicenter observational study comparing clinical outcomes of adults hospitalized with ESBL-producing pyelonephritis who were receiving TZP versus carbapenems, using an inverse probability of treatment weighted propensity score analysis. Patients were eligible for inclusion if all of the following criteria were met: (1) urine cultures growing Escherichia coli, Klebsiella pneumoniae, Klebsiella oxytoca, or Proteus mirabilis at ≥50 000 colony-forming units/mL; (2) identification of an ESBL gene; (3) pyuria (≥10 white blood cells per high powered field in the urine); and (4) dysuria and fever plus at least 1 of the following symptoms: emesis, rigors, hypotension, or flank pain.

resultsThere were 186 patients included in the propensity score-weighted cohort; 45 (24%) received TZP and 141 (76%) received a carbapenem. Of these 186 patients, 27% were admitted to the intensive care unit, 48% were immunocompromised, and 45% had underlying urologic abnormalities. There were no differences between the 2 groups in the proportion of patients (20% vs 25%) with recurrent cystitis or pyelonephritis with the same ESBL-producing organism within 30 days (odds ratio, 0.75; 95% confidence interval, .31-1.81; P = .52). There were no differences in the resolution of clinical symptoms by Day 7 or in 30-day mortality. There was 1 (2%) patient in the TZP arm and 11 (8%) patients in the carbapenem arm who had incident carbapenem-resistant organisms isolated within 30 days (P = .09).

conclusionsTZP may be a reasonable alternative to carbapenems for the management of ESBL-producing pyelonephritis and may mitigate the risk of emergence of carbapenem-resistant organisms, compared with carbapenem therapy.

Indexed as

Escherichia coli InfectionsPyelonephritisAdultAnti-Bacterial Agentsbeta-LactamasesHumansKlebsiella pneumoniaeMicrobial Sensitivity TestsPiperacillin, Tazobactam Drug CombinationRetrospective StudiesAnti-Bacterial Agentsbeta-LactamasesPiperacillin, Tazobactam Drug CombinationcarbapenemESBLurinary tract infectionUTI

Identifiers

PMID31859352
PMCPMC7643734
OpenAlexW2995375219

What OpenQuestion holds

Textmetadata
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.