Evidence map›Paper›PMID 29934998›Full record

ReviewIUBMB life2018

Have we realized the full potential of β-lactams for treating drug-resistant TB?

Elizabeth Story-Roller, Gyanu Lamichhane

Abstract readReview
In one paragraph

Review in IUBMB life, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Microbiology spectrum · 2023
    Article
  9. Article
  10. Article
  11. Repurposing β-Lactams for the Treatment ofAntibiotics (Basel, Switzerland) · 2023
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Investigating β-Lactam Drug Targets inACS infectious diseases · 2021
    Article
  20. 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

2 authors.

Elizabeth Story-RollerCenter for Tuberculosis Research Division of Infectious Diseases, Department of Medicine, Johns Hopkins University, Baltimore, MD, USA.
Gyanu LamichhaneCenter for Tuberculosis Research Division of Infectious Diseases, Department of Medicine, Johns Hopkins University, Baltimore, MD, USA.ORCID 0000-0002-2214-0114

Funding

RESEARCH TRAINING IN MICROBIAL DISEASEST32AI007291 · NIAID · JOHNS HOPKINS UNIVERSITY · PI JOEL N BLANKSON, Sara Elizabeth Cosgrove · 1986 to 2026
$9.1M
Development of an Oral Carbapenem Drug for Treatment of Drug Resistant TBR33AI111739 · NIAID · JOHNS HOPKINS UNIVERSITY · PI LAMICHHANE, GYANU · 2016 to 2018
$1.4M
NIAID NIH HHS R33 AI111739NIAID NIH HHS T32 AI007291
6 · The paper itself

Abstract

β-lactams are the most widely used antibiotics and are effective against a spectrum of pathogenic bacteria. Here, we focus on the state-of-the-art understanding of the molecular underpinnings that determine the overall efficacy of β-lactams against TB and include historical perspectives of this antibiotic class against this ancient disease. We summarize literature that describes why earlier generations of β-lactams are ineffective and the potential promise of newer β-lactams that exhibit improved efficacy against TB. Emerging evidence warrants renewed consideration of newer β-lactams in regimens for treatment of drug-resistant TB. © 2018 IUBMB Life, 70(9):881-888, 2018.

Indexed as

Animalsbeta-Lactamase Inhibitorsbeta-Lactam Resistancebeta-LactamsHumansMycobacterium tuberculosisTuberculosisbeta-Lactamase Inhibitorsbeta-Lactamsbeta-lactamdrug resistancemycobacterium tuberculosistuberculosis

Identifiers

PMID29934998
PMCPMC6119476

What OpenQuestion holds

Textmetadata
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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.