Evidence map›Paper›PMID 32711457›Full record

ArticleBMC infectious diseases2020

Impact of GeneXpert MTB/RIF® on treatment initiation and outcomes of RIF-resistant and RIF-susceptible TB patients in Vladimir TB dispensary, Russia.

Julia V Ershova, Grigory V Volchenkov, Tatiana R Somova, Tatiana A Kuznetsova, Natalia V Kaunetis, Dorothy Kaminski, Olga V Demikhova, Larisa N Chernousova, Irina A Vasilyeva, Eleanor M Kerr and 2 more

Open access · goldAbstract read
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Article in BMC infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.2field-weighted citation impact, top 39% 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.

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

9 citing papers in PubMed, 12 citations in OpenAlex.

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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

12 authors at 4 institutions in 4 countries.

Julia V ErshovaU.S. Centers for Disease Control and Prevention, Atlanta, GA, USA. jhe3@cdc.gov.ORCID http://orcid.org/0000-0003-3873-7166
Grigory V VolchenkovVladimir Oblast TB Dispensary, Vladimir, Russia.
Tatiana R SomovaVladimir Oblast TB Dispensary, Vladimir, Russia.
Tatiana A KuznetsovaVladimir Oblast TB Dispensary, Vladimir, Russia.
Natalia V KaunetisVladimir Oblast TB Dispensary, Vladimir, Russia.
Dorothy KaminskiU.S. Centers for Disease Control and Prevention, Atlanta, GA, USA.
Olga V DemikhovaCentral Tuberculosis Research Institute, Moscow, Russia.
Larisa N ChernousovaCentral Tuberculosis Research Institute, Moscow, Russia.
Irina A VasilyevaCentral Tuberculosis Research Institute, Moscow, Russia.
Eleanor M KerrEmory University, Atlanta, GA, USA.
J Peter CegielskiU.S. Centers for Disease Control and Prevention, Atlanta, GA, USA.
Ekaterina V KurbatovaU.S. Centers for Disease Control and Prevention, Atlanta, GA, USA.
Centers for Disease Control and Prevention · USVladimir Law Institute · RUCentral Scientific Research Institute of Tuberculosis Russian Academy of Medical Sciences · RUEmory University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe main advantage of GeneXpert MTB/RIF® (Xpert) molecular diagnostic technology is the rapid detection of M.tuberculosis DNA and mutations associated with rifampicin (RIF) resistance for timely initiation of appropriate treatment and, consequently, preventing further transmission of the disease. We assessed time to treatment initiation and treatment outcomes of RIF-resistant and RIF-susceptible TB patients diagnosed and treated in Vladimir TB Dispensary, Russia in 2012, before and after implementation of GeneXpert MTB/RIF® diagnostic technology.

methodsAll adult patients suspected of having TB during February-December 2012 underwent a clinical examination, chest x-ray, microscopy, culture, and phenotypic drug susceptibility testing (DST). Starting August 2012 Xpert diagnostic technology became available in the facility. We used logistic regression to compare treatment outcomes in pre-Xpert and post-Xpert periods. Kaplan-Meier curves and log-rank test were used to compare the time to treatment initiation between the groups.

resultsOf 402 patients screened for TB during February-December 2012, 338 were diagnosed with TB (280 RIF-susceptible, 58 RIF-resistant). RIF-resistant patients in the post-Xpert group started treatment with second-line drugs (SLD) earlier than those in pre-Xpert group (median 11 vs. 37 days, Log-rank p = 0.02). The hazard ratio for time to SLD treatment initiation was significantly higher in post-Xpert group (HR:2.06; 95%CI:1.09,3.89) compared to pre-Xpert group. Among the 53/58 RIF-resistant TB patients with available treatment outcome, 28 (53%) had successful outcomes (cured/completed treatment) including 15/26 (58%) in post-Xpert group versus 13/27 (48%) in pre-Xpert group. The observed difference, however, was not statistically significant (OR:0.69; 95%CI:0.23,2.06). Among RIF-susceptible TB cases time to treatment initiation was not significantly different between the groups (2 vs. 3 days, Log-rank p = 0.73). Of 252/280 RIF-susceptible TB cases with treatment outcome, 199 (79%) cases had successful outcome including 94/114 (82%) in post-Xpert group versus 105/138 (76%) in pre-Xpert group (OR:0.68; 95%CI:0.36,1.26).

conclusionWe observed that availability of Xpert for initial diagnosis significantly reduced the time to SLD treatment for RIF-resistant patients in the Vladimir TB Dispensary. Although implementation of rapid diagnostics did not improve treatment outcomes, early diagnosis of MDR-TB is important for selection of appropriate treatment regimen and prevention of transmission of drug-resistant strains of TB.

Indexed as

Time-to-TreatmentAdolescentAdultAgedAntibiotics, AntitubercularDNA, BacterialDrug Resistance, BacterialFemaleHumansMaleMicrobial Sensitivity TestsMiddle AgedMutationMycobacterium tuberculosisNucleic Acid Amplification TechniquesProspective StudiesAntibiotics, AntitubercularDNA, BacterialRifampinDrug resistanceGeneXpert MTB/RIFRifampicin

Identifiers

PMID32711457
PMCPMC7382080
OpenAlexW3045316490

What OpenQuestion holds

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LicenceCC BY
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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.