Evidence map›Paper›PMID 24968051›Full record

ReviewBiomedica : revista del Instituto Nacional de Salud2014

[Resistance to "last resort" antibiotics in Gram-positive cocci: The post-vancomycin era].

Sandra Rincón, Diana Panesso, Lorena Díaz, Lina P Carvajal, Jinnethe Reyes, José M Munita, César A Arias

Abstract readReview
In one paragraph

Review in Biomedica : revista del Instituto Nacional de Salud, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Multidrug-ResistantMicroorganisms · 2024
    Article
  3. AgrA directly binds to the promoter ofAntimicrobial agents and chemotherapy · 2024
    Article
  4. Article
  5. Review
  6. Article
  7. [National surveillance of clinical isolates ofRevista panamericana de salud publica = Pan American journal of public health · 2020
    Article
  8. Characterization andFrontiers in microbiology · 2020
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. 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 2 institutions in 2 countries.

Sandra RincónUnidad de Genética y Resistencia Antimicrobiana (UGRA), Universidad El Bosque, Bogotá, D.C, Colombia.
Diana PanessoUnidad de Genética y Resistencia Antimicrobiana (UGRA), Universidad El Bosque, Bogotá, D.C, Colombia.
Lorena DíazUnidad de Genética y Resistencia Antimicrobiana (UGRA), Universidad El Bosque, Bogotá, D.C, Colombia.
Lina P CarvajalUnidad de Genética y Resistencia Antimicrobiana (UGRA), Universidad El Bosque, Bogotá, D.C, Colombia.
Jinnethe ReyesUniversity of Texas Medical School at Houston, Houston, TX, USA.
José M MunitaClínica Alemana de Santiago, Universidad del Desarrollo, Santiago de Chile, Chile.
César A AriasUnidad de Genética y Resistencia Antimicrobiana (UGRA), Universidad El Bosque, Bogotá, D.C, Colombia.
Universidad El Bosque · COClínica Alemana · CL

Funding

Molecular Mechanisms Of Daptomycin Resistance In EnterococciR01AI093749 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ARIAS, CESAR AUGUSTO · 2011 to 2015
$1.9M
NIAID NIH HHS R01 AI093749
6 · The paper itself

Abstract

New therapeutic alternatives have been developed in the last years for the treatment of multidrug-resistant Gram-positive infections. Infections caused by methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE) are considered a therapeutic challenge due to failures and lack of reliable antimicrobial options. Despite concerns related to the use of vancomycin in the treatment of severe MRSA infections in specific clinical scenarios, there is a paucity of solid clinical evidence that support the use of alternative agents (when compared to vancomycin). Linezolid, daptomycin and tigecycline are antibiotics approved in the last decade and newer cephalosporins (such as ceftaroline and ceftobiprole) and novel glycopeptides (dalvavancin, telavancin and oritavancin) have reached clinical approval or are in the late stages of clinical development. This review focuses on discussing these newer antibiotics used in the "post-vancomycin" era with emphasis on relevant chemical characteristics, spectrum of antimicrobial activity, mechanisms of action and resistance, as well as their clinical utility.

Indexed as

Drug Resistance, Multiple, BacterialAnti-Bacterial AgentsBacterial ProteinsCephalosporinsDaptomycinDrugs, InvestigationalGenes, BacterialGram-Positive Bacterial InfectionsGram-Positive CocciHumansMethicillin-Resistant Staphylococcus aureusMinocyclineStaphylococcal InfectionsTigecyclineVancomycinAnti-Bacterial AgentsBacterial ProteinsCephalosporinsDaptomycinDrugs, InvestigationalMinocyclineTigecyclineVancomycin

Identifiers

PMID24968051
PMCPMC4435674
OpenAlexW3094608764

What OpenQuestion holds

Textmetadata
LicenceTDM
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.