Evidence map›Paper›PMID 39789804›Full record

SynthesisClinical infectious diseases : an official publication of the Infectious Diseases Society of America2025

Safety of Triple-Dose Rifampin in Tuberculosis Treatment: A Systematic Review and Meta-Analysis.

Omri A Arbiv, Thomas Holmes, Marie JeongMin Kim, Marie Yan, Kamila Romanowski, Sarah K Brode, William J Burman, Dick Menzies, James C Johnston

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Safety of Triple-Dose Rifampin in Tuberculosis Treatment: A Systematic Review and Meta-Analysis.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2025
    Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Omri A ArbivFaculty of Medicine, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0002-6024-9030
Thomas HolmesSchool of Medicine, Royal College of Surgeons in Ireland, Dublin, Ireland.
Marie JeongMin KimDepartment of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Marie YanDepartment of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Kamila RomanowskiProvincial TB Services, BC Centre for Disease Control, Vancouver, British Columbia, Canada.ORCID 0000-0002-7027-3579
Sarah K BrodeFaculty of Medicine, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0002-3855-6368
William J BurmanPublic Health Institute at Denver Health, Denver, Colorado, USA.ORCID 0000-0001-6982-1825
Dick MenziesMcGill International TB Centre, McGill University, Montreal, Quebec, Canada.ORCID 0000-0003-1601-4514
James C JohnstonDepartment of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.ORCID 0000-0002-8879-4989

Funding

Canadian Institute of Health ResearchHealth Research British Columbia Health Professional Investigator ProgramUniversity of British Columbia Clinician-Investigator Program
6 · The paper itself

Abstract

backgroundRecent studies suggest that triple-dose rifampin (TDR; ≥30 mg/kg/d) may be unsafe. We updated a systematic review to investigate the safety and efficacy of TDR.

methodsWe searched Embase, MEDLINE, Cochrane CENTRAL, Cochrane Database for Systematic Reviews, and clinicaltrials.gov for randomized, controlled trials from 1 January 1965 to 10 February 2024 that compared standard-dose rifampin (SDR) with TDR and/or double-dose rifampin (DDR) in human tuberculosis treatment. The primary outcome was pooled incidence rate ratio (IRR) of severe adverse events (SevAEs) between participants who received TDR and those who received SDR. Pooled relative risk (RR) of death was a key secondary outcome. Meta-analysis was performed using the inverse variance method. Heterogeneity was assessed using I2, and bias was assessed using Cochrane Risk of Bias 2. The protocol was prospectively registered (osf.io/kfn5a).

resultsOf the 11 315 articles identified, 17 met inclusion criteria, enrolling 2313 SDR participants (17 studies), 2238 receiving DDR (12 studies), and 1199 receiving TDR (11 studies). Six studies had a high risk of bias. There was an increase in pooled SevAEs among participants who received TDR compared with those who received SDR (IRR, 1.48; 95% confidence interval [CI], 1.12-1.96; I2, 23%), driven by hepatic events (IRR, 1.96; 95% CI, 1.21-3.18). Death did not differ between participants who received TDR and SDR (RR, 1.19; 95% CI, .71-1.99). One limitation is that only 2 included studies were blinded.

conclusionsRegimens that used TDR were associated with an increase in SevAEs, raising concerns regarding safety of TDR regimens.

Indexed as

Antitubercular AgentsRifampinTuberculosisHumansRandomized Controlled Trials as TopicAntitubercular AgentsRifampinepidemiologymeta-analysisrifampinsystematic reviewtuberculosis

Identifiers

PMID39789804
PMCPMC12314497

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.