Evidence map›Paper›PMID 36159638›Full record

ReviewFrontiers in cellular and infection microbiology2022

How

Amala Bhagwat, Aditi Deshpande, Tanya Parish

Abstract readReview
In one paragraph

Review in Frontiers in cellular and infection microbiology, 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
–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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Tools to develop antibiotic combinations that target drug tolerance inFrontiers in cellular and infection microbiology · 2022
    Review
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

3 authors.

Amala BhagwatCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States.
Aditi DeshpandeCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States.
Tanya ParishCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States.

Funding

The role of Esx-3 in mediating drug resistanceR01AI129360 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI PARISH, TANYA · 2018 to 2022
$1.8M
NIAID NIH HHS R01 AI129360
6 · The paper itself

Abstract

Drug resistance is an increasing problem for the treatment of tuberculosis. The prevalence of clinical isolates with pre-existing resistance needs to be considered in any drug discovery program. Non-specific mechanisms of resistance such as increased efflux or decreased permeability need to be considered both in developing individual drug candidates and when designing novel regimens. We review a number of different approaches to develop new analogs and drug combinations or improve efficacy of existing drugs that may overcome or delay the appearance of clinical resistance. We also discuss the need to fully characterize mechanisms of resistance and cross- resistance to existing drugs to ensure that novel drugs will be clinically effective.

Indexed as

Mycobacterium tuberculosisTuberculosis, Lymph NodeAntitubercular AgentsDrug DiscoveryDrug ResistanceHumansAntitubercular Agentsantibacterialantibiotic resistanceantibiotic tolerancedrug discoveryMycobacterium tuberculosis

Identifiers

PMID36159638
PMCPMC9500310

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.