Evidence map›Paper›PMID 25733500›Full record

Trial reportAntimicrobial agents and chemotherapy2015

Clinically and microbiologically derived azithromycin susceptibility breakpoints for Salmonella enterica serovars Typhi and Paratyphi A.

Christopher M Parry, Nga Tran Vu Thieu, Christiane Dolecek, Abhilasha Karkey, Ruchi Gupta, Paul Turner, David Dance, Rapeephan R Maude, Vinh Ha, Chinh Nguyen Tran and 25 more

Erratum issuedOpen access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Antimicrobial agents and chemotherapy, 2015. 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 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
8.2field-weighted citation impact, top 3% 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

39 citing papers in PubMed, 65 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Article
  5. Review
  6. Antimicrobial Resistance in Sub-Saharan Africa: A Comprehensive Landscape Review.The American journal of tropical medicine and hygiene · 2025
    Review
  7. Azithromycin resistance inJAC-antimicrobial resistance · 2025
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Increased susceptibility to azithromycin of Pseudomonas aeruginosa biofilms using RPMI 1640 testing media.APMIS : acta pathologica, microbiologica, et immunologica Scandinavica · 2024
    Article
  13. The intrinsic macrolide resistome ofAntimicrobial agents and chemotherapy · 2024
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Virulence and antimicrobial resistance factors inFrontiers in veterinary science · 2022
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

35 authors at 15 institutions in 9 countries.

Christopher M ParryWellcome Trust Major Overseas Programme, The Hospital for Tropical Diseases, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam Centre for Tropical Medicine and Global Health, Old Road Campus, University of Oxford, Oxford, United Kingdom Liverpool School of Tropical Medicine, Liverpool, United Kingdom London School of Hygiene and Tropical Medicine, London, United Kingdom School of Tropical Medicine and Global Health, Nagasaki University, Nagasaki, Japan chris.parry@lshtm.ac.uk.
Nga Tran Vu ThieuWellcome Trust Major Overseas Programme, The Hospital for Tropical Diseases, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Christiane DolecekWellcome Trust Major Overseas Programme, The Hospital for Tropical Diseases, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam Centre for Tropical Medicine and Global Health, Old Road Campus, University of Oxford, Oxford, United Kingdom.
Abhilasha KarkeyOxford University Clinical Research Unit, Patan Academy of Health Sciences, Kathmandu, Nepal.
Ruchi GuptaDepartment of Microbiology, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.
Paul TurnerCentre for Tropical Medicine and Global Health, Old Road Campus, University of Oxford, Oxford, United Kingdom Cambodia-Oxford Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia Shoklo Malaria Research Unit, Mae Sot, Thailand.
David DanceCentre for Tropical Medicine and Global Health, Old Road Campus, University of Oxford, Oxford, United Kingdom Lao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit, Mahosot Hospital, Vientiane, Laos.
Rapeephan R MaudeMahidol-Oxford Tropical Medicine Research Unit (MORU), Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Vinh HaThe Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Chinh Nguyen TranThe Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Phuong Le ThiDong Thap Provincial Hospital, Cao Lanh, Dong Thap Province, Vietnam.
Bay Pham Van BeDong Thap Provincial Hospital, Cao Lanh, Dong Thap Province, Vietnam.
La Tran Thi PhiAn Giang Provincial Hospital, Long Xuyen, Vietnam.
Rang Nguyen NgocAn Giang Provincial Hospital, Long Xuyen, Vietnam.
Aniruddha GhoseChittagong Medical College Hospital, Chittagong, Bangladesh.
Sabina DongolOxford University Clinical Research Unit, Patan Academy of Health Sciences, Kathmandu, Nepal.
James I CampbellWellcome Trust Major Overseas Programme, The Hospital for Tropical Diseases, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam Centre for Tropical Medicine and Global Health, Old Road Campus, University of Oxford, Oxford, United Kingdom.
Duy Pham ThanhWellcome Trust Major Overseas Programme, The Hospital for Tropical Diseases, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Tuyen Ha ThanhWellcome Trust Major Overseas Programme, The Hospital for Tropical Diseases, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Catrin E MooreWellcome Trust Major Overseas Programme, The Hospital for Tropical Diseases, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam Cambodia-Oxford Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.
Soeng SonaCambodia-Oxford Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.
Rajni GaindDepartment of Microbiology, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.
Monorama DebDepartment of Microbiology, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.
Ho Van AnhDong Thap Provincial Hospital, Cao Lanh, Dong Thap Province, Vietnam.
Sach Nguyen VanThe Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Hien Tran TinhWellcome Trust Major Overseas Programme, The Hospital for Tropical Diseases, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam Centre for Tropical Medicine and Global Health, Old Road Campus, University of Oxford, Oxford, United Kingdom.
Nicholas P J DayCentre for Tropical Medicine and Global Health, Old Road Campus, University of Oxford, Oxford, United Kingdom Mahidol-Oxford Tropical Medicine Research Unit (MORU), Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Arjen DondorpCentre for Tropical Medicine and Global Health, Old Road Campus, University of Oxford, Oxford, United Kingdom Mahidol-Oxford Tropical Medicine Research Unit (MORU), Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Guy ThwaitesWellcome Trust Major Overseas Programme, The Hospital for Tropical Diseases, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam Centre for Tropical Medicine and Global Health, Old Road Campus, University of Oxford, Oxford, United Kingdom.
Mohamed Abul FaizMahidol-Oxford Tropical Medicine Research Unit (MORU), Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand Centre for Specialized Care and Research, Chittagong, Bangladesh.
Rattanaphone PhetsouvanhCentre for Tropical Medicine and Global Health, Old Road Campus, University of Oxford, Oxford, United Kingdom Lao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit, Mahosot Hospital, Vientiane, Laos.
Paul NewtonCentre for Tropical Medicine and Global Health, Old Road Campus, University of Oxford, Oxford, United Kingdom Lao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit, Mahosot Hospital, Vientiane, Laos London School of Hygiene and Tropical Medicine, London, United Kingdom.
Buddha BasnyatOxford University Clinical Research Unit, Patan Academy of Health Sciences, Kathmandu, Nepal.
Jeremy J FarrarWellcome Trust Major Overseas Programme, The Hospital for Tropical Diseases, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam Centre for Tropical Medicine and Global Health, Old Road Campus, University of Oxford, Oxford, United Kingdom.
Stephen BakerWellcome Trust Major Overseas Programme, The Hospital for Tropical Diseases, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam Centre for Tropical Medicine and Global Health, Old Road Campus, University of Oxford, Oxford, United Kingdom London School of Hygiene and Tropical Medicine, London, United Kingdom.
Hospital for Tropical Diseases · VNDong Thap Hospital · VNPatan Academy of Health Sciences · NPVardhman Mahavir Medical College & Safdarjung Hospital · INAn Giang University · VNLao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit · LAMahidol Oxford Tropical Medicine Research Unit · THMahidol University · THUniversity of Oxford · GBWellcome Trust · GBAngkor Hospital for Children · KHChittagong Medical College · BDLondon School of Hygiene & Tropical Medicine · GBMahosot Hospital · LAOxford University Clinical Research Unit · VN

Funding

Wellcome Trust 089276Wellcome Trust 100087Wellcome Trust 100087/Z/12/Z
6 · The paper itself

Abstract

Azithromycin is an effective treatment for uncomplicated infections with Salmonella enterica serovar Typhi and serovar Paratyphi A (enteric fever), but there are no clinically validated MIC and disk zone size interpretative guidelines. We studied individual patient data from three randomized controlled trials (RCTs) of antimicrobial treatment in enteric fever in Vietnam, with azithromycin used in one treatment arm, to determine the relationship between azithromycin treatment response and the azithromycin MIC of the infecting isolate. We additionally compared the azithromycin MIC and the disk susceptibility zone sizes of 1,640 S. Typhi and S. Paratyphi A clinical isolates collected from seven Asian countries. In the RCTs, 214 patients who were treated with azithromycin at a dose of 10 to 20 mg/ml for 5 to 7 days were analyzed. Treatment was successful in 195 of 214 (91%) patients, with no significant difference in response (cure rate, fever clearance time) with MICs ranging from 4 to 16 μg/ml. The proportion of Asian enteric fever isolates with an MIC of ≤ 16 μg/ml was 1,452/1,460 (99.5%; 95% confidence interval [CI], 98.9 to 99.7) for S. Typhi and 207/240 (86.3%; 95% CI, 81.2 to 90.3) (P < 0.001) for S. Paratyphi A. A zone size of ≥ 13 mm to a 5-μg azithromycin disk identified S. Typhi isolates with an MIC of ≤ 16 μg/ml with a sensitivity of 99.7%. An azithromycin MIC of ≤ 16 μg/ml or disk inhibition zone size of ≥ 13 mm enabled the detection of susceptible S. Typhi isolates that respond to azithromycin treatment. Further work is needed to define the response to treatment in S. Typhi isolates with an azithromycin MIC of >16 μg/ml and to determine MIC and disk breakpoints for S. Paratyphi A.

Indexed as

AdolescentAzithromycinChildFemaleHumansMaleMicrobial Sensitivity TestsSalmonella entericaSerogroupTyphoid FeverYoung AdultAzithromycin

Identifiers

PMID25733500
PMCPMC4394775
OpenAlexW2161214725

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.