Evidence map›Paper›PMID 30883637›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2019

Building the Framework for Standardized Clinical Laboratory Reporting of Next-generation Sequencing Data for Resistance-associated Mutations in Mycobacterium tuberculosis Complex.

Jeffrey A Tornheim, Angela M Starks, Timothy C Rodwell, Jennifer L Gardy, Timothy M Walker, Daniela M Cirillo, Lakshmi Jayashankar, Paolo Miotto, Matteo Zignol, Marco Schito

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2019. 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.

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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

10 authors.

Jeffrey A TornheimDivision of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Angela M StarksDivision of Tuberculosis Elimination, National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia.
Timothy C RodwellFoundation for Innovative New Diagnostics, Geneva, Switzerland.
Jennifer L GardySchool of Population and Public Health, University of British Columbia, Canada.
Timothy M WalkerNuffield Department of Medicine, University of Oxford, United Kingdom.
Daniela M CirilloIRCCS San Raffaele Scientific Institute, Milano, Italy.
Lakshmi JayashankarColumbus Technologies, Inc. Contractor to the National Institute of Allergy and Infectious Diseases, US National Institutes of Health, Bethesda, Maryland.
Paolo MiottoIRCCS San Raffaele Scientific Institute, Milano, Italy.
Matteo ZignolGlobal TB Programme, World Health Organization, Geneva, Switzerland.
Marco SchitoCritical Path to Tuberculosis Drug Regimens, Critical Path Institute, Tucson, Arizona.

Funding

Fogarty Global Health Fellows Coordinating CenterR25TW009340 · FIC · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CHI, BENJAMIN H. · 2012 to 2016
$6.9M
Culture-free next generation sequencing for rapid detection of drug-resistant tuberculosisR21AI135756 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI RODWELL, TIMOTHY CHARLES · 2018 to 2019
$500k
FDA HHS U18 FD005320FIC NIH HHS R25 TW009340NIAID NIH HHS R21 AI135756World Health Organization 001
6 · The paper itself

Abstract

Tuberculosis is the primary infectious disease killer worldwide, with a growing threat from multidrug-resistant cases. Unfortunately, classic growth-based phenotypic drug susceptibility testing (DST) remains difficult, costly, and time consuming, while current rapid molecular testing options are limited by the diversity of antimicrobial-resistant genotypes that can be detected at once. Next-generation sequencing (NGS) offers the opportunity for rapid, comprehensive DST without the time or cost burden of phenotypic tests and can provide useful information for global surveillance. As access to NGS expands, it will be important to ensure that results are communicated clearly, consistent, comparable between laboratories, and associated with clear guidance on clinical interpretation of results. In this viewpoint article, we summarize 2 expert workshops regarding a standardized report format, focusing on relevant variables, terminology, and required minimal elements for clinical and laboratory reports with a proposed standardized template for clinical reporting NGS results for Mycobacterium tuberculosis.

Indexed as

Antitubercular AgentsDrug Resistance, Multiple, BacterialGenotypeHigh-Throughput Nucleotide SequencingHumansMicrobial Sensitivity TestsMutationMycobacterium tuberculosisSequence Analysis, DNATuberculosis, Multidrug-ResistantAntitubercular Agentsinterpretationnext-generation sequencingreportingstandardizationtuberculosis

Identifiers

PMID30883637
PMCPMC6792097

What OpenQuestion holds

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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.