Evidence map›Paper›PMID 23987891›Full record

ReviewBMC medicine2013

Rapid diagnostics of tuberculosis and drug resistance in the industrialized world: clinical and public health benefits and barriers to implementation.

Francis Drobniewski, Vladyslav Nikolayevskyy, Horst Maxeiner, Yanina Balabanova, Nicola Casali, Irina Kontsevaya, Olga Ignatyeva

Abstract readReview
In one paragraph

Review in BMC medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
–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

29 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Cerebrospinal fluid Gene XPERT (CBNAAT) in children with tuberculous meningitis.Journal of clinical tuberculosis and other mycobacterial diseases · 2021
    Article
  5. Article
  6. Deciphering Within-Host Microevolution ofMicrobiology and molecular biology reviews : MMBR · 2019
    Review
  7. Whole genome sequencing for drug resistance determination inAfrican journal of laboratory medicine · 2019
    Article
  8. Article
  9. Article
  10. Time-and-motion tool for the assessment of working time in tuberculosis laboratories: a multicentre study.The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease · 2018
    Article
  11. Review
  12. Molecular Diagnosis of Tuberculosis.Chonnam medical journal · 2018
    Review
  13. Article
  14. Article
  15. Article
  16. A performance evaluation of MTBDRplus version 2 for the diagnosis of multidrug-resistant tuberculosis.The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease · 2016
    Article
  17. Article
  18. The implications of whole-genome sequencing in the control of tuberculosis.Therapeutic advances in infectious disease · 2016
    Review
  19. 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

7 authors.

Francis DrobniewskiPublic Health England National Mycobacterium Reference Laboratory, 2 Newark Street, London E1 2AT, UK. f.drobniewski@qmul.ac.uk.
Vladyslav Nikolayevskyy
Horst Maxeiner
Yanina Balabanova
Nicola Casali
Irina Kontsevaya
Olga Ignatyeva

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this article, we give an overview of new technologies for the diagnosis of tuberculosis (TB) and drug resistance, consider their advantages over existing methodologies, broad issues of cost, cost-effectiveness and programmatic implementation, and their clinical as well as public health impact, focusing on the industrialized world. Molecular nucleic-acid amplification diagnostic systems have high specificity for TB diagnosis (and rifampicin resistance) but sensitivity for TB detection is more variable. Nevertheless, it is possible to diagnose TB and rifampicin resistance within a day and commercial automated systems make this possible with minimal training. Although studies are limited, these systems appear to be cost-effective. Most of these tools are of value clinically and for public health use. For example, whole genome sequencing of Mycobacterium tuberculosis offers a powerful new approach to the identification of drug resistance and to map transmission at a community and population level.

Indexed as

Drug Resistance, BacterialAntitubercular AgentsGenome, BacterialHumansMolecular Diagnostic TechniquesMycobacterium tuberculosisSequence Analysis, DNATuberculosis, Multidrug-ResistantAntitubercular Agents

Identifiers

PMID23987891
PMCPMC3765611

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.