Evidence map›Paper›PMID 23090928›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2013

Implementation of genotype MTBDRplus reduces time to multidrug-resistant tuberculosis therapy initiation in South Africa.

Karen R Jacobson, Danie Theron, Emily A Kendall, Molly F Franke, Marinus Barnard, Paul D van Helden, Tommie C Victor, Elizabeth M Streicher, Megan B Murray, Robin M Warren

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03356925 (Feasibility, Accuracy, and Effect of Point-of-care Xpert MTB/RIF Ultra and Xpert MTB/RIF Ultra Testing in Patients Suspected of Having TB), which is not on this map. Cited by 59 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 8 pooled it
3.5field-weighted citation impact, top 7% 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.

NCT03356925 nacompletednot on this mapstarted 2018, after this paper: background citation

Feasibility, Accuracy, and Effect of Point-of-care Xpert MTB/RIF Ultra and Xpert MTB/RIF Ultra Testing in Patients Suspected of Having TB: a Randomised Controlled Trial

TypeinterventionalSponsorUniversity of StellenboschRan2018 to 2022Enrolled1,549ConditionsTuberculosisArmsXpert Ultra Point of Care testing
3 · Its place in the literature

Who cites it

59 citing papers in PubMed, 8 syntheses or guidelines pooled it, 96 citations in OpenAlex.

  1. Pooled it
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  4. Time to treatment for rifampicin-resistant tuberculosis: systematic review and meta-analysis.The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease · 2017
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  17. Rifampicin resistance inNew microbes and new infections · 2021
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  19. Isoniazid Preventive Therapy in Contacts of Multidrug-Resistant Tuberculosis.American journal of respiratory and critical care medicine · 2020
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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 at 7 institutions in 3 countries.

Karen R JacobsonDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA 02114, USA. krjacobson@partners.org
Danie Theron
Emily A Kendall
Molly F Franke
Marinus Barnard
Paul D van Helden
Tommie C Victor
Elizabeth M Streicher
Megan B Murray
Robin M Warren
Stellenbosch University · ZAMedical Research Council · GBBrigham and Women's Hospital · USHarvard University · USLife Groenkloof Hospital · ZAMassachusetts General Hospital · USOffice of Infectious Diseases · US

Funding

Geospatial clustering and molecular and social epidemiology of drug resistant TBK01TW009213 · FIC · MASSACHUSETTS GENERAL HOSPITAL · PI JACOBSON, KAREN R · 2011 to 2015
$715k
FIC NIH HHS 1K01 TW009213FIC NIH HHS K01 TW009213Wellcome Trust 087383
6 · The paper itself

Abstract

backgroundDiagnosis of drug resistance and timely initiation of multidrug-resistant (MDR) tuberculosis therapy are essential to reduce transmission and improve patient outcomes. We sought to determine whether implementation of the rapid MTBDRplus diagnostic shortened the time from specimen collection to patient MDR tuberculosis therapy initiation.

methodsWe conducted a retrospective cohort analysis of 197 MDR tuberculosis patients treated at Brewelskloof, a rural tuberculosis hospital in Western Cape Province, South Africa, between 2007 and 2011.

resultsEighty-nine patients (45%) were tested using conventional liquid culture and drug susceptibility testing (DST) on solid medium and 108 (55%) were tested using the MTBDRplus assay after positive acid-fast bacilli or culture. Median time from sample taken to therapy initiation was reduced from 80 days (interquartile range [IQR] 62-100) for conventional DST to 55 days (IQR 37.5-78) with the MTBDRplus. Although the laboratory processing time declined significantly, operational delays persisted both in the laboratory and the clinical infrastructure for getting patients started on treatment. In multivariate analysis, patients tested using the MTBDRplus test had a reduced risk of starting treatment 60 days or more after sputum collection of 0.52 (P < .0001) compared with patients tested with culture-based DST, after adjustment for smear status and site of disease.

conclusionsUse of MTBDRplus significantly reduced time to MDR tuberculosis treatment initiation. However, DST reporting to clinics was delayed by more than 1 week due, in part, to laboratory operational delays, including dependence on smear and culture positivity prior to MTBDRplus performance. In addition, once MDR tuberculosis was reported, delays in contacting patients and initiating therapy require improvements in clinical infrastructure.

Indexed as

AdultAntitubercular AgentsCohort StudiesFemaleGenotypeHumansMaleMicrobial Sensitivity TestsMiddle AgedMycobacterium tuberculosisRetrospective StudiesSensitivity and SpecificitySouth AfricaTime FactorsTuberculosis, Multidrug-ResistantYoung AdultAntitubercular Agents

Identifiers

PMID23090928
PMCPMC3552527
OpenAlexW2169609545

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.