Evidence map›Paper›PMID 35146040›Full record

ArticleOpen forum infectious diseases2022

Multicenter Cohort Study of Ceftaroline Versus Daptomycin for Treatment of Methicillin-Resistant

Evan J Zasowski, Trang D Trinh, Kimberly C Claeys, Abdalhamid M Lagnf, Sahil Bhatia, Kenneth P Klinker, Michael P Veve, Sandy J Estrada, Scott T Johns, Adam J Sawyer and 6 more

Open access · goldAbstract read
In one paragraph

Article in Open forum infectious diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 20% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Trial
  2. Review
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  4. Article
  5. Article
  6. Article
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  8. Contemporary Management of Staphylococcus aureus Bacteremia-Controversies in Clinical Practice.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023
    Review
  9. Review
  10. Article
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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

16 authors at 10 institutions in 1 country.

Evan J ZasowskiAnti-Infective Research Laboratory, Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, Michigan, USA.ORCID https://orcid.org/0000-0002-2595-1860
Trang D TrinhAnti-Infective Research Laboratory, Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, Michigan, USA.ORCID https://orcid.org/0000-0002-9928-4714
Kimberly C ClaeysAnti-Infective Research Laboratory, Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, Michigan, USA.ORCID https://orcid.org/0000-0001-6895-604X
Abdalhamid M LagnfAnti-Infective Research Laboratory, Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, Michigan, USA.
Sahil BhatiaAnti-Infective Research Laboratory, Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, Michigan, USA.
Kenneth P KlinkerCollege of Pharmacy, University of Florida, Gainesville, Florida, USA.
Michael P VeveDepartment of Clinical Pharmacy and Translational Science, College of Pharmacy, University of Tennessee Health Science Center, Knoxville, Tennessee, USA.ORCID https://orcid.org/0000-0001-5967-5211
Sandy J EstradaDepartment of Pharmacy, Lee Health, Fort Myers, Florida, USA.ORCID https://orcid.org/0000-0001-6833-9834
Scott T JohnsVeterans Affairs San Diego Healthcare System, San Diego, California, USA.ORCID https://orcid.org/0000-0002-5668-7564
Adam J SawyerHuntsville Hospital, Huntsville, Alabama, USA.ORCID https://orcid.org/0000-0002-7568-6735
Vanthida HuangDepartment of Pharmacy Practice, Midwestern University College of Pharmacy-Glendale, Glendale, Arizona, USA.ORCID https://orcid.org/0000-0001-8028-3554
Brandi LaFranceOur Lady of the Lake Regional Medical Center, Baton Rouge, Louisiana, USA.
Donald P LevineDepartment of Medicine, Division of Infectious Diseases, School of Medicine, Wayne State University, Detroit, Michigan, USA.ORCID https://orcid.org/0000-0003-2252-5820
Keith S KayeDivision of Allergy, Immunology, and Infectious Diseases, Robert Wood Johnson Medical School, Rutgers University, New Brunswick, New Jersey, USA.ORCID https://orcid.org/0000-0003-2051-1732
Susan L DavisDepartment of Pharmacy Services, Henry Ford Health System, Detroit, Michigan, USA.ORCID https://orcid.org/0000-0002-9341-9964
Michael J RybakAnti-Infective Research Laboratory, Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, Michigan, USA.
Eugene Applebaum College of Pharmacy and Health Sciences · USHuntsville Hospital · USLee Memorial Health System · USLincoln Medical Center · USOur Lady of the Lake Regional Medical Center · USRutgers, The State University of New Jersey · USUniversity of Florida · USUniversity of Tennessee Health Science Center · USVA San Diego Healthcare System · USWayne State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundObservational data suggest ceftaroline may be effective for methicillin-resistant

methodsMulticenter, retrospective, observational cohort study of adult patients with MRSA BSI from 2010 to 2017. Patients treated with ≥72 hours of ceftaroline or daptomycin were included. Those clearing BSI before study drug and those with a pneumonia source were excluded. The primary outcome was composite treatment failure, defined as 30-day mortality, BSI duration ≥7 days on study drug, and 60-day MRSA BSI recurrence. Inverse probability of treatment weighted risk difference in composite failure between daptomycin and ceftaroline groups was computed and 15% noninferiority margin applied.

resultsTwo hundred seventy patients were included; 83 ceftaroline and 187 daptomycin. Ceftaroline was noninferior to daptomycin with respect to composite failure (39% daptomycin, 32.5% ceftaroline; weighted risk difference, 7.0% [95% confidence interval, -5.0% to 19.0%]). No differences between treatment groups was observed for 30-day mortality or other secondary efficacy outcomes. Creatine phosphokinase elevation was significantly more common among daptomycin patients (5.3% vs 0%,

conclusionsNo difference in treatment failure or mortality was observed between MRSA BSI treated with ceftaroline or daptomycin. These data support future study of ceftaroline as a primary MRSA BSI treatment and current use of ceftaroline when an alternative to vancomycin and daptomycin is required.

Indexed as

bacteremiainfective endocarditislipoglycopeptideMRSAβ-lactam

Identifiers

PMID35146040
PMCPMC8825758
OpenAlexW4200043871

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.