Evidence map›Paper›PMID 32423104›Full record

ArticleAntibiotics (Basel, Switzerland)2020

Multicenter, Observational Cohort Study Evaluating Third-Generation Cephalosporin Therapy for Bloodstream Infections Secondary to

Caroline Derrick, P Brandon Bookstaver, Zhiqiang K Lu, Christopher M Bland, S Travis King, Kayla R Stover, Kathey Rumley, Shawn H MacVane, Jenna Swindler, Scott Kincaid and 12 more

Open access · goldAbstract read
In one paragraph

Article in Antibiotics (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 33% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

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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

22 authors at 14 institutions in 1 country.

Caroline DerrickDepartment of Medicine, University of South Carolina School of Medicine Columbia, SC 29203, USA.
P Brandon BookstaverDepartment of Clinical Pharmacy and Outcomes Sciences, University of South Carolina College of Pharmacy, Columbia, SC 29208, USA.
Zhiqiang K LuDepartment of Clinical Pharmacy and Outcomes Sciences, University of South Carolina College of Pharmacy, Columbia, SC 29208, USA.
Christopher M BlandDepartment of Clinical and Administrative Pharmacy, University of Georgia College of Pharmacy, Savannah, GA 31324, USA.
S Travis KingDepartment of Pharmacy Practice, University of Mississippi School of Pharmacy, Jackson, MS 39216, USA.
Kayla R StoverDepartment of Pharmacy Practice, University of Mississippi School of Pharmacy, Jackson, MS 39216, USA.
Kathey RumleyVidant Medical Center, Greenville, NC 27835, USA.
Shawn H MacVaneDepartment of Pharmacy, Medical University of South Carolina, Charleston, SC 29425, USA.
Jenna SwindlerMcLeod Regional Medical Center, Florence, SC 29506, USA.
Scott KincaidUniversity of Kentucky Healthcare, Lexington, KY 40536, USA.
Trisha BrananCollege of Pharmacy, University of Georgia, Athens, GA 30602, USA.
David CluckDepartment of Pharmacy Practice, Bill Gatton College of Pharmacy, East Tennessee State University, Johnson City, TN 37614, USA.
Benjamin BrittLexington Medical Center, West Columbia, SC 29169, USA.
Kelly E PillingerCarolinas HealthCare System, Charlotte, NC 28203, USA.
Bruce M JonesSt. Joseph's/Candler Health System, Savannah, GA 31405, USA.
Virginia FlemingCollege of Pharmacy, University of Georgia, Athens, GA 30602, USA.
V Paul DiMondiDepartment of Pharmacy Practice, Campbell University College of Pharmacy and Health Sciences, Buies Creek, NC 27506, USA.
Sandy EstradaLee Health, Fort Myers, FL 33901, USA.
Brad CraneBlount Memorial Hospital, Maryville, TN 37804, USA.
Brian OdleDepartment of Pharmacy Practice, Bill Gatton College of Pharmacy, East Tennessee State University, Johnson City, TN 37614, USA.
Majdi N Al-HasanDepartment of Medicine, University of South Carolina School of Medicine Columbia, SC 29203, USA.
Julie Ann JustoDepartment of Clinical Pharmacy and Outcomes Sciences, University of South Carolina College of Pharmacy, Columbia, SC 29208, USA.
University of Georgia · USUniversity of South Carolina · USCampbell University · USEast Tennessee State University · USPrisma Health · USUniversity of Mississippi · USCarolinas Healthcare System · USLee Memorial Health System · USLexington Medical Center · USMedical University of South Carolina · USMemorial Hospital · USOrlando Regional Medical Center · USSt. Joseph’s Candler Hospital · USUniversity of Kentucky HealthCare · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThere is debate on whether the use of third-generation cephalosporins (3GC) increases the risk of clinical failure in bloodstream infections (BSIs) caused by chromosomally-mediated AmpC-producing Enterobacterales (CAE). This study evaluates the impact of definitive 3GC therapy versus other antibiotics on clinical outcomes in BSIs due to Enterobacter, Serratia, or Citrobacter species.

methodsThis multicenter, retrospective cohort study evaluated adult hospitalized patients with BSIs secondary to Enterobacter, Serratia, or Citrobacter species from 1 January 2006 to 1 September 2014. Definitive 3GC therapy was compared to definitive therapy with other non-3GC antibiotics. Multivariable Cox proportional hazards regression evaluated the impact of definitive 3GC on overall treatment failure (OTF) as a composite of in-hospital mortality, 30-day hospital readmission, or 90-day reinfection.

resultsA total of 381 patients from 18 institutions in the southeastern United States were enrolled. Common sources of BSIs were the urinary tract and central venous catheters (78 (20.5%) patients each). Definitive 3GC therapy was utilized in 65 (17.1%) patients. OTF occurred in 22/65 patients (33.9%) in the definitive 3GC group vs. 94/316 (29.8%) in the non-3GC group (p = 0.51). Individual components of OTF were comparable between groups. Risk of OTF was comparable with definitive 3GC therapy vs. definitive non-3GC therapy (aHR 0.93, 95% CI 0.51-1.72) in multivariable Cox proportional hazards regression analysis.

conclusionsThese outcomes suggest definitive 3GC therapy does not significantly alter the risk of poor clinical outcomes in the treatment of BSIs secondary to Enterobacter, Serratia, or Citrobacter species compared to other antimicrobial agents.

Indexed as

AmpCbacteremiabeta-lactamasescarbapenemscephalosporinssepsis

Identifiers

PMID32423104
PMCPMC7277875
OpenAlexW3024112006

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.