Evidence map›Paper›PMID 26714320›Full record

Observational studyPLoS medicine2015

Association between Regimen Composition and Treatment Response in Patients with Multidrug-Resistant Tuberculosis: A Prospective Cohort Study.

Courtney M Yuen, Ekaterina V Kurbatova, Thelma Tupasi, Janice Campos Caoili, Martie Van Der Walt, Charlotte Kvasnovsky, Martin Yagui, Jaime Bayona, Carmen Contreras, Vaira Leimane and 12 more

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in PLoS medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 2 pooled it
5.0field-weighted citation impact, top 4% 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

30 citing papers in PubMed, 2 syntheses or guidelines pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Article
  9. Observational
  10. Mycoplasma genitalium in Symptomatic Male Urethritis: Macrolide Use Is Associated With Increased Resistance.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2020
    Article
  11. Review
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  15. Observational
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  19. Review
  20. Impact of Fluoroquinolone Use on Mortality Among a Cohort of Patients With Suspected Drug-Resistant Tuberculosis.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2017
    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

22 authors at 13 institutions in 9 countries.

Courtney M YuenCenters for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Ekaterina V KurbatovaCenters for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Thelma TupasiTropical Disease Foundation, Manila, Philippines.
Janice Campos CaoiliCenters for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Martie Van Der WaltMedical Research Council, Pretoria, South Africa.
Charlotte KvasnovskyCenters for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Martin YaguiNational Institute of Health, Lima, Peru.
Jaime BayonaPartners In Health, Boston, Massachusetts, United States of America.
Carmen ContrerasSocios en Salud Sucursal, Lima, Peru.
Vaira LeimaneRiga East University Hospital Centre of Tuberculosis and Lung Diseases, Riga, Latvia.
Julia ErshovaCenters for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Laura E ViaNational Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, United States of America.
HeeJin KimKorean Institute of Tuberculosis, Seoul, Republic of Korea.
Somsak AkksilpDepartment of Disease Control, Ministry of Public Health, Bangkok, Thailand.
Boris Y KazennyyOrel Oblast Tuberculosis Dispensary, Orel, Russian Federation.
Grigory V VolchenkovVladimir Oblast Tuberculosis Dispensary, Vladimir, Russian Federation.
Ruwen JouTaiwan Centers for Disease Control, Taipei, Taiwan.
Kai KliimanTartu University Hospital, Tartu, Estonia.
Olga V DemikhovaCentral Tuberculosis Research Institute, Russian Academy of Medical Sciences, Moscow, Russian Federation.
Irina A VasilyevaCentral Tuberculosis Research Institute, Russian Academy of Medical Sciences, Moscow, Russian Federation.
Tracy DaltonCenters for Disease Control and Prevention, Atlanta, Georgia, United States of America.
J Peter CegielskiCenters for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Centers for Disease Control and Prevention · USCentral Scientific Research Institute of Tuberculosis Russian Academy of Medical Sciences · RUEsSALUD · PEKorea National Tuberculosis Association · KRMinistry of Public Health · THNational Institute of Quality · PENational Institutes of Health · USPartners In Health · USRiga East University Hospital · LVSouth African Medical Research Council · ZATartu University Hospital · EETropical Disease Foundation · PHVladimir Law Institute · RU

Funding

International Research in Korea: Clinical Studies of Drug-Resistant TuberculosisZIAAI001067 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BARRY, CLIFTON · 2009 to 2017
$6.9M
6 · The paper itself

Abstract

backgroundFor treating multidrug-resistant tuberculosis (MDR TB), the World Health Organization (WHO) recommends a regimen of at least four second-line drugs that are likely to be effective as well as pyrazinamide. WHO guidelines indicate only marginal benefit for regimens based directly on drug susceptibility testing (DST) results. Recent evidence from isolated cohorts suggests that regimens containing more drugs may be beneficial, and that DST results are predictive of regimen effectiveness. The objective of our study was to gain insight into how regimen design affects treatment response by analyzing the association between time to sputum culture conversion and both the number of potentially effective drugs included in a regimen and the DST results of the drugs in the regimen. METHODS AND

findingsWe analyzed data from the Preserving Effective Tuberculosis Treatment Study (PETTS), a prospective observational study of 1,659 adults treated for MDR TB during 2005-2010 in nine countries: Estonia, Latvia, Peru, Philippines, Russian Federation, South Africa, South Korea, Thailand, and Taiwan. For all patients, monthly sputum samples were collected, and DST was performed on baseline isolates at the US Centers for Disease Control and Prevention. We included 1,137 patients in our analysis based on their having known baseline DST results for at least fluoroquinolones and second-line injectable drugs, and not having extensively drug-resistant TB. These patients were followed for a median of 20 mo (interquartile range 16-23 mo) after MDR TB treatment initiation. The primary outcome of interest was initial sputum culture conversion. We used Cox proportional hazards regression, stratifying by country to control for setting-associated confounders, and adjusting for the number of drugs to which patients' baseline isolates were resistant, baseline resistance pattern, previous treatment history, sputum smear result, and extent of disease on chest radiograph. In multivariable analysis, receiving an average of at least six potentially effective drugs (defined as drugs without a DST result indicating resistance) per day was associated with a 36% greater likelihood of sputum culture conversion than receiving an average of at least five but fewer than six potentially effective drugs per day (adjusted hazard ratio [aHR] 1.36, 95% CI 1.09-1.69). Inclusion of pyrazinamide (aHR 2.00, 95% CI 1.65-2.41) or more drugs to which baseline DST indicated susceptibility (aHR 1.65, 95% CI 1.48-1.84, per drug) in regimens was associated with greater increases in the likelihood of sputum culture conversion than including more drugs to which baseline DST indicated resistance (aHR 1.33, 95% CI 1.18-1.51, per drug). Including in the regimen more drugs for which DST was not performed was beneficial only if a minimum of three effective drugs was present in the regimen (aHR 1.39, 95% CI 1.09-1.76, per drug when three effective drugs present in regimen). The main limitation of this analysis is that it is based on observational data, not a randomized trial, and drug regimens varied across sites. However, PETTS was a uniquely large and rigorous observational study in terms of both the number of patients enrolled and the standardization of laboratory testing. Other limitations include the assumption of equivalent efficacy across drugs in a category, incomplete data on adherence, and the fact that the analysis considers only initial sputum culture conversion, not reversion or long-term relapse.

conclusionsMDR TB regimens including more potentially effective drugs than the minimum of five currently recommended by WHO may encourage improved response to treatment in patients with MDR TB. Rapid access to high-quality DST results could facilitate the design of more effective individualized regimens. Randomized controlled trials are necessary to confirm whether individualized regimens with more than five drugs can indeed achieve better cure rates than current recommended regimens.

Indexed as

AdolescentAdultAgedAged, 80 and overAntitubercular AgentsClinical ProtocolsCohort StudiesDrug Therapy, CombinationGlobal HealthHumansMicrobial Sensitivity TestsMiddle AgedMycobacteriumProportional Hazards ModelsProspective StudiesSputumAntitubercular Agents

Identifiers

PMID26714320
PMCPMC4700973
OpenAlexW2199941204

What OpenQuestion holds

Textmetadata
LicenceCC0
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.