Evidence map›Paper›PMID 30915685›Full record

ArticleInfectious diseases and therapy2019

Open-Label Randomized Trial of Early Clinical Outcomes of Ceftaroline Fosamil Versus Vancomycin for the Treatment of Acute Bacterial Skin and Skin Structure Infections at Risk of Methicillin-Resistant Staphylococcus aureus.

Kimberly C Claeys, Evan J Zasowski, Trang D Trinh, Anthony M Casapao, Jason M Pogue, Nitin Bhatia, Ryan P Mynatt, Suprat S Wilson, Crystal Arthur, Robert Welch and 15 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Infectious diseases and therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02582203 (Clinical and Economic Outcomes of Ceftaroline Fosamil for the Treatment of Acute Bacterial Skin and Skin Structure Infections Documented or at Risk of Methicillin-Resistant S. Aureus), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 26% 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.

NCT02582203 phase4completednot on this map

Clinical and Economic Outcomes of Ceftaroline Fosamil for the Treatment of Acute Bacterial Skin and Skin Structure Infections Documented or at Risk of Methicillin-Resistant S. Aureus

TypeinterventionalSponsorWayne State UniversityRan2012 to 2016Enrolled174ConditionsSkin Diseases, Infectious, Staphylococcal Skin InfectionsArmsCeftaroline, Vancomycin
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

25 authors at 6 institutions in 1 country.

Kimberly C ClaeysAnti-Infective Research Laboratory, Wayne State University Eugene Applebaum College of Pharmacy and Health Sciences, Detroit, MI, USA.
Evan J ZasowskiAnti-Infective Research Laboratory, Wayne State University Eugene Applebaum College of Pharmacy and Health Sciences, Detroit, MI, USA.
Trang D TrinhAnti-Infective Research Laboratory, Wayne State University Eugene Applebaum College of Pharmacy and Health Sciences, Detroit, MI, USA.
Anthony M CasapaoAnti-Infective Research Laboratory, Wayne State University Eugene Applebaum College of Pharmacy and Health Sciences, Detroit, MI, USA.
Jason M PogueDetroit Medical Center, Detroit, MI, USA.
Nitin BhatiaDetroit Medical Center, Detroit, MI, USA.
Ryan P MynattDetroit Medical Center, Detroit, MI, USA.
Suprat S WilsonDetroit Medical Center, Detroit, MI, USA.
Crystal ArthurDetroit Medical Center, Detroit, MI, USA.
Robert WelchDetroit Medical Center, Detroit, MI, USA.
Robert SherwinDetroit Medical Center, Detroit, MI, USA.
Wasif HafeezDetroit Medical Center, Detroit, MI, USA.
Donald P LevineDetroit Medical Center, Detroit, MI, USA.
Keith S KayeUniversity of Michigan Medical School, Ann Arbor, MI, USA.
George DelgadoSt. John Hospital and Medical Center, Detroit, MI, USA.
Christopher A GiulianoAnti-Infective Research Laboratory, Wayne State University Eugene Applebaum College of Pharmacy and Health Sciences, Detroit, MI, USA.
Robert TaklaSt. John Hospital and Medical Center, Detroit, MI, USA.
Colleen RieckSt. John Hospital and Medical Center, Detroit, MI, USA.
Leonard B JohnsonSt. John Hospital and Medical Center, Detroit, MI, USA.
Kyle P MurrayDetroit Medical Center, Detroit, MI, USA.
James GordonDetroit Medical Center, Detroit, MI, USA.
Kate ReyesHenry Ford Health System, Detroit, MI, USA.
Pamela HartmanHenry Ford Health System, Detroit, MI, USA.
Susan L DavisAnti-Infective Research Laboratory, Wayne State University Eugene Applebaum College of Pharmacy and Health Sciences, Detroit, MI, USA.
Michael J RybakAnti-Infective Research Laboratory, Wayne State University Eugene Applebaum College of Pharmacy and Health Sciences, Detroit, MI, USA. aa1592@wayne.edu.
Detroit Medical Center · USEugene Applebaum College of Pharmacy and Health Sciences · USSt. John Hospital & Medical Center · USHenry Ford Health System · USUniversity of Michigan–Ann Arbor · USWayne State University · US

Funding

A Pharmacologic Approach to Prevent Daptomycin Resistance in VRER01AI121400 · NIAID · WAYNE STATE UNIVERSITY · PI RYBAK, MICHAEL JOSEPH · 2016 to 2020
$1.9M
NIAID NIH HHS R01 AI121400
6 · The paper itself

Abstract

introductionAcute bacterial skin and skin structure infections (ABSSSIs) remain among the most common infectious processes seen in the clinical setting. For patients with complicated ABSSSIs deemed to require intravenous antibiotics, vancomycin remains the mainstay therapy. Ceftaroline has been shown to be non-inferior to vancomycin and may result in faster resolution of signs of infection.

methodsMulticenter, prospective, open-label, randomized trial of ceftaroline versus vancomycin for the treatment of adult patients admitted for management of ABSSSIs from April 2012 to May 2016; 166 patients in the clinically evaluable (CE) group were needed to determine a 20% difference in primary outcome of clinical response at day 2 or 3 of antibiotics. Clinical response was defined as cessation of spread of lesion and improvement in systemic signs/symptoms of infection. A secondary outcome was a ≥ 20% reduction in lesion size at day 2 or 3 of antibiotics.

resultsOne hundred seventy-four patients were enrolled in the intention-to-treat (ITT) group and 108 were CE. Among CE patients, 54 were randomized to ceftaroline and 54 to vancomycin. Baseline characteristics were similar except patients in the ceftaroline arm were older and had a non-significantly higher degree of comorbidities (median Charlson score 2 vs. 4, respectively). Cellulitis was the most common type of ABSSSI (85.2% vs. 79.6%, respectively). Rapid diagnostic testing of available cultures (n = 55) demonstrated high agreement with clinical microbiology for identification of Staphylococcus aureus (100%) and MRSA (100%). There was no significant difference in primary outcome of day 2 or 3 clinical response (50.0% vs. 51.9%).

conclusionEarly clinical response between vancomycin- and ceftaroline-treated ABSSSIs was similar. Patients with ABSSSIs rarely remained hospitalized for > 2-3 days, thus limiting our ability to critically assess clinical outcomes.

trial registrationClinicalTrials.gov identifier, NCT02582203.

fundingAllergan plc.

Indexed as

Acute bacterial skin and skin structure infectionCeftarolineMethicillin-resistant S. aureusVancomycin

Identifiers

PMID30915685
PMCPMC6522568
OpenAlexW2923164219

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.