Evidence map›Paper›PMID 29595509›Full record

SynthesisThe Lancet. Respiratory medicine2018

Comparison of different treatments for isoniazid-resistant tuberculosis: an individual patient data meta-analysis.

Federica Fregonese, Shama D Ahuja, Onno W Akkerman, Denise Arakaki-Sanchez, Irene Ayakaka, Parvaneh Baghaei, Didi Bang, Mayara Bastos, Andrea Benedetti, Maryline Bonnet and 48 more

Erratum issuedOpen access · greenAbstract readComparative StudyMeta-Analysis
In one paragraph

Synthesis in The Lancet. Respiratory medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 52 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 3 pooled it
7.7field-weighted citation impact, top 2% 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

52 citing papers in PubMed, 3 syntheses or guidelines pooled it, 108 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Treatment of Drug-Resistant Tuberculosis. An Official ATS/CDC/ERS/IDSA Clinical Practice Guideline.American journal of respiratory and critical care medicine · 2019
    Guideline
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Real-world treatment outcomes of a 6-month fluoroquinolone-containing regimen for isoniazid mono-resistant pulmonary tuberculosis in Korea.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Article
  10. Recent advances in tuberculosis treatment: Towards shorter, safer, and more effective therapies.Journal of clinical tuberculosis and other mycobacterial diseases · 2026
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
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  18. Article
  19. Article
  20. Multidrug-resistant tuberculosis.Nature reviews. Disease primers · 2024
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

58 authors at 20 institutions in 17 countries.

Federica FregoneseMontreal Chest Institute, McGill University Health Center Research Institute, McGill University, Montreal, Canada.
Shama D AhujaBureau of Tuberculosis Control, New York City Department of Health and Mental Hygiene, Queens, NY, USA.
Onno W AkkermanUniversity Medical Centre Groningen, Department of Pulmonary Diseases and Tuberculosis, University of Groningen, Groningen, Netherlands.
Denise Arakaki-SanchezNational Tuberculosis Control Program, Brasilia, Brazil.
Irene AyakakaUganda Tuberculosis Research Consortium, Kampala, Uganda.
Parvaneh BaghaeiClinical Tuberculosis and Epidemiology Research Center, NRITLD, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Didi BangStatens Serum Institut, Copenhagen, Denmark.
Mayara BastosEpidemiology Department, Social Medicine Institute, University of Rio de Janeiro, Brazil.
Andrea BenedettiMontreal Chest Institute, McGill University Health Center Research Institute, McGill University, Montreal, Canada; Department of Epidemiology, Biostatistics & Occupational Health, McGill University, Montreal, Canada.
Maryline BonnetInstitut de Recherche pour le Développement UM233, INSERM U1175, Université de Montpellier, Montpellier, France; Epicentre MSF, Paris, France.
Adithya CattamanchiDivision of Pulmonary and Critical Care Medicine and Curry International Tuberculosis Center, University of California San Francisco, San Francisco, CA, USA.
Peter CegielskiDivision of Global HIV and TB, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Jung-Yien ChienDepartment of Internal Medicine, National Taiwan University Hospital, National Taiwan University College of Medicine, Taipei, Taiwan.
Helen CoxDivision of Medical Microbiology and Institute of Infectious Diseases and Molecular Medicine University of Cape Town, Cape Town, South Africa.
Martin DedicoatHeart of England NHS Foundation Trust, Birmingham, UK.
Connie ErkensKNCV Tuberculosis Foundation, Team The Netherlands and Elimination, The Hague, Netherlands.
Patricio EscalanteDivision of Pulmonary and Critical Care Medicine, Department of Medicine, and Mayo Clinic Center for Tuberculosis, Mayo Clinic, Rochester, USA.
Dennis FalzonGlobal Tuberculosis Programme, World Health Organization, Geneva, Switzerland.
Anthony J Garcia-PratsDesmond Tutu TB Centre, Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Medea GegiaGlobal Tuberculosis Programme, World Health Organization, Geneva, Switzerland.
Stephen H GillespieSchool of Medicine, University of St Andrews North Haugh, St Andrews, UK.
Judith R GlynnDepartment of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK.
Stefan GoldbergDivision of Tuberculosis Elimination, National Center for HIV, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA.
David GriffithThe University of Texas Health Science Center, Tyler, TX, USA.
Karen R JacobsonSection of Infectious Diseases, Department of Medicine Boston University School of Medicine and Boston Medical Center, Boston, MA, USA.
James C JohnstonDepartment of Medicine, University of British Columbia, Vancouver, BC, Canada; British Columbia Centre for Disease Control, Vancouver, BC, Canada.
Edward C Jones-LópezSection of Infectious Diseases, Department of Medicine Boston University School of Medicine and Boston Medical Center, Boston, MA, USA.
Awal KhanDivision of Tuberculosis Elimination, National Center for HIV, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Won-Jung KohSamsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Afranio KritskiAcademic Tuberculosis Program, School of Medicine, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Zhi Yi LanMontreal Chest Institute, McGill University Health Center Research Institute, McGill University, Montreal, Canada; Department of Epidemiology, Biostatistics & Occupational Health, McGill University, Montreal, Canada.
Jae Ho LeeDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul, South Korea.
Pei Zhi LiMontreal Chest Institute, McGill University Health Center Research Institute, McGill University, Montreal, Canada.
Ethel L MacielLaboratory of Epidemiology, Federal University of Espirito Santo, Espírito Santo, Brazil.
Rafael Mello GalliezState Institute of Infectology São Sebastião, Center for Research and Tuberculosis, Faculty of Medicine, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Corinne S C MerleSpecial Programme for Research and Training in Tropical Diseases, World Health Organization, Geneva, Switzerland; Department of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK.
Melinda MunangHeart of England NHS Foundation Trust, Birmingham, UK.
Gopalan NarendranDepartment of Clinical Research, The National Institute for Research in Tuberculosis, Chennai, India.
Viet Nhung NguyenNational Lung Hospital, Ba Dinh, Hanoi, Vietnam; Hanoi Medical University, Hanoi, Vietnam.
Andrew NunnMedical Research Council UK Clinical Trials Unit, University College London, London, UK.
Akihiro OhkadoDepartment of Epidemiology and Clinical Research, the Research Institute of Tuberculosis, Japan Anti-Tuberculosis Association, Tokyo, Japan; Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.
Jong Sun ParkDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul, South Korea.
Patrick P J PhillipsDivision of Pulmonary & Critical Medicine, University of California San Francisco, San Francisco, CA, USA.
Chinnaiyan PonnurajaThe National Institute for Research in Tuberculosis, Chetpet, India.
Randall RevesDenver Public Health Department, Denver, CO, USA.
Kamila RomanowskiBritish Columbia Centre for Disease Control, Vancouver, BC, Canada.
Kwonjune SeungPartners in Health, Boston, MA, USA.
H Simon SchaafDesmond Tutu TB Centre, Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Alena SkrahinaRepublican Scientific and Practical Centre of Pulmonology and Tuberculosis, Ministry of Health, Minsk, Belarus.
Dick van SoolingenNational Tuberculosis Reference Laboratory, National Institute for Public Health and the Environment, Bilthoven, Netherlands.
Payam TabarsiClinical Tuberculosis and Epidemiology Research Center, NRITLD, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Anete TrajmanMontreal Chest Institute, McGill University Health Center Research Institute, McGill University, Montreal, Canada; Epidemiology Department, Social Medicine Institute, University of Rio de Janeiro, Brazil.
Lisa TrieuBureau of Tuberculosis Control, New York City Department of Health and Mental Hygiene, Queens, NY, USA.
Velayutham V BanurekhaDepartment of Clinical Research, The National Institute for Research in Tuberculosis, Chennai, India.
Piret ViikleppEstonian Tuberculosis Registry, National Institute for Health Development, Tallinn, Estonia.
Jann-Yuan WangDepartment of Internal Medicine, National Taiwan University Hospital, National Taiwan University College of Medicine, Taipei, Taiwan.
Takashi YoshiyamaResearch Institute of Tuberculosis, Tokyo, Japan.
Dick MenziesMontreal Chest Institute, McGill University Health Center Research Institute, McGill University, Montreal, Canada. Electronic address: dick.menzies@mcgill.ca.
McGill University Health Centre · CANational Institute of Research in Tuberculosis · INBC Centre for Disease Control · CABoston Medical Center · USHeart of England NHS Foundation Trust · GBJapan Anti Tuberculosis Association · JPLondon School of Hygiene & Tropical Medicine · GBMasih Daneshvari Hospital · IRNational Center for HIV/AIDS Viral Hepatitis STD and TB Prevention · USNational Taiwan University Hospital · TWNew York City Department of Health and Mental Hygiene · USSeoul National University Bundang Hospital · KRStellenbosch University · ZAUniversidade Federal do Rio de Janeiro · BRUniversity of California, San Francisco · USWorld Health Organization · CHCenter for Global Health · USDenver Public Health · USHanoi Medical University · VNInserm · FR

Funding

CIHRIntramural CDC HHS CC999999World Health Organization 001
6 · The paper itself

Abstract

backgroundIsoniazid-resistant, rifampicin-susceptible (INH-R) tuberculosis is the most common form of drug resistance, and is associated with failure, relapse, and acquired rifampicin resistance if treated with first-line anti-tuberculosis drugs. The aim of the study was to compare success, mortality, and acquired rifampicin resistance in patients with INH-R pulmonary tuberculosis given different durations of rifampicin, ethambutol, and pyrazinamide (REZ); a fluoroquinolone plus 6 months or more of REZ; and streptomycin plus a core regimen of REZ.

methodsStudies with regimens and outcomes known for individual patients with INH-R tuberculosis were eligible, irrespective of the number of patients if randomised trials, or with at least 20 participants if a cohort study. Studies were identified from two relevant systematic reviews, an updated search of one of the systematic reviews (for papers published between April 1, 2015, and Feb 10, 2016), and personal communications. Individual patient data were obtained from authors of eligible studies. The individual patient data meta-analysis was performed with propensity score matched logistic regression to estimate adjusted odds ratios (aOR) and risk differences of treatment success (cure or treatment completion), death during treatment, and acquired rifampicin resistance. Outcomes were measured across different treatment regimens to assess the effects of: different durations of REZ (≤6 months vs >6 months); addition of a fluoroquinolone to REZ (fluoroquinolone plus 6 months or more of REZ vs 6 months or more of REZ); and addition of streptomycin to REZ (streptomycin plus 6 months of rifampicin and ethambutol and 1-3 months of pyrazinamide vs 6 months or more of REZ). The overall quality of the evidence was assessed using GRADE methodology.

findingsIndividual patient data were requested for 57 cohort studies and 17 randomised trials including 8089 patients with INH-R tuberculosis. We received 33 datasets with 6424 patients, of which 3923 patients in 23 studies received regimens related to the study objectives. Compared with a daily regimen of 6 months of (H)REZ (REZ with or without isoniazid), extending the duration to 8-9 months had similar outcomes; as such, 6 months or more of (H)REZ was used for subsequent comparisons. Addition of a fluoroquinolone to 6 months or more of (H)REZ was associated with significantly greater treatment success (aOR 2·8, 95% CI 1·1-7·3), but no significant effect on mortality (aOR 0·7, 0·4-1·1) or acquired rifampicin resistance (aOR 0·1, 0·0-1·2). Compared with 6 months or more of (H)REZ, the standardised retreatment regimen (2 months of streptomycin, 3 months of pyrazinamide, and 8 months of isoniazid, rifampicin, and ethambutol) was associated with significantly worse treatment success (aOR 0·4, 0·2-0·7). The quality of the evidence was very low for all outcomes and treatment regimens assessed, owing to the observational nature of most of the data, the diverse settings, and the imprecision of estimates.

interpretationIn patients with INH-R tuberculosis, compared with treatment with at least 6 months of daily REZ, addition of a fluoroquinolone was associated with better treatment success, whereas addition of streptomycin was associated with less treatment success; however, the quality of the evidence was very low. These results support the conduct of randomised trials to identify the optimum regimen for this important and common form of drug-resistant tuberculosis.

fundingWorld Health Organization and Canadian Institutes of Health Research.

Indexed as

Antibiotics, AntitubercularCohort StudiesDrug Administration ScheduleDrug Therapy, CombinationEthambutolFluoroquinolonesHumansObservational Studies as TopicOutcome Assessment, Health CarePyrazinamideRandomized Controlled Trials as TopicReview Literature as TopicRifampinStreptomycinTuberculosis, Multidrug-ResistantAntibiotics, AntitubercularEthambutolFluoroquinolonesPyrazinamideRifampinStreptomycin

Identifiers

PMID29595509
PMCPMC9017096
OpenAlexW2789995925

What OpenQuestion holds

Textmetadata
LicenceTDM
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.