Evidence map›Paper›PMID 34534310›Full record

ArticleThe Journal of antimicrobial chemotherapy2021

Tebipenem as an oral alternative for the treatment of typhoid caused by XDR Salmonella Typhi.

Elli Mylona, Phat Voong Vinh, Sonia Qureshi, Abhilasha Karkey, Sabina Dongol, Tuyen Ha Thanh, Judd Walson, Lluis Ballell, Elena Fernández Álvaro, Farah Qamar and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 36% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Trial
  2. Review
  3. The oral penems and carbapenems.Clinical microbiology reviews · 2025
    Review
  4. Article
  5. Article
  6. Article
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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

11 authors at 6 institutions in 5 countries.

Elli MylonaUniversity of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, UK.
Phat Voong VinhThe Hospital for Tropical Diseases, Wellcome Trust Major Overseas Programme, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Sonia QureshiAga Khan University, Karachi, Pakistan.
Abhilasha KarkeyNepal Academy of Health Sciences, Oxford University Clinical Research Unit, Kathmandu, Nepal.
Sabina DongolNepal Academy of Health Sciences, Oxford University Clinical Research Unit, Kathmandu, Nepal.
Tuyen Ha ThanhThe Hospital for Tropical Diseases, Wellcome Trust Major Overseas Programme, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Judd WalsonDivision of Allergy and Infectious Disease, Center for Emerging and Re-emerging Infectious Diseases, University of Washington School of Medicine, Seattle, WA, USA.
Lluis BallellGSK Global Health, Tres Cantos, Madrid, Spain.
Elena Fernández ÁlvaroGSK Global Health, Tres Cantos, Madrid, Spain.
Farah QamarAga Khan University, Karachi, Pakistan.
Stephen BakerUniversity of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, UK.
Aga Khan University · PKPatan Academy of Health Sciences · NPUniversity of Cambridge · GBHospital for Tropical Diseases · VNOxford University Clinical Research Unit · VNUniversity of Washington · US

Funding

Bill & Melinda Gates FoundationWellcome TrustWellcome Trust 215515/Z/19/Z
6 · The paper itself

Abstract

backgroundAntimicrobial therapy is essential for the treatment of enteric fever, the infection caused by Salmonella serovars Typhi and Paratyphi A. However, an increase in resistance to key antimicrobials and the emergence of MDR and XDR in Salmonella Typhi poses a major threat for efficacious outpatient treatments.

objectivesWe recently identified tebipenem, an oral carbapenem licensed for use for respiratory tract infections in Japan, as a potential alternative treatment for MDR/XDR Shigella spp. Here, we aimed to test the in vitro antibacterial efficacy of this drug against MDR and XDR typhoidal Salmonella.

methodsWe determined the in vitro activity of tebipenem in time-kill assays against a collection of non-XDR and XDR Salmonella Typhi and Salmonella Paratyphi A (non-XDR) isolated in Nepal and Bangladesh. We also tested the efficacy of tebipenem in combination with other antimicrobials.

resultsWe found that both XDR and non-XDR Salmonella Typhi and Salmonella Paratyphi A are susceptible to tebipenem, exhibiting low MICs, and were killed within 8-24 h at 2-4×MIC. Additionally, tebipenem demonstrated synergy with two other antimicrobials and could efficiently induce bacterial killing.

conclusionsSalmonella Paratyphi A and XDR Salmonella Typhi display in vitro susceptibility to the oral carbapenem tebipenem, while synergistic activity with other antimicrobials may limit the emergence of resistance. The broad-spectrum activity of this drug against MDR/XDR organisms renders tebipenem a good candidate for clinical trials.

Indexed as

Salmonella typhiTyphoid FeverAnti-Bacterial AgentsCarbapenemsHumansSalmonellaAnti-Bacterial AgentsCarbapenemstebipenem

Identifiers

PMID34534310
PMCPMC8598285
OpenAlexW3201613395

What OpenQuestion holds

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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.