Evidence map›Paper›PMID 38842502›Full record

ArticleThe Journal of antimicrobial chemotherapy2024

Clinical characteristics and genome epidemiology of Stenotrophomonas maltophilia in Japan.

Ryota Hase, Aki Sakurai, Masahiro Suzuki, Naoya Itoh, Kayoko Hayakawa, Kohei Uemura, Yasufumi Matsumura, Hideaki Kato, Takuma Ishihara, David van Duin and 3 more

Abstract readMulticenter Study
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–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

11 citing papers in PubMed.

  1. Clinical, microbiological, and molecular characteristics, outcomes, and risk factors for mortality of patients with Stenotrophomonas maltophilia bloodstream infection.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Article
  2. Article
  3. Article
  4. Observational
  5. Highly effective isolation ofMicrobiology spectrum · 2026
    Article
  6. Article
  7. Aztreonam-Avibactam Successfully Treated SevereJournal of blood medicine · 2026
    Article
  8. Article
  9. Multicenter epidemiology ofFrontiers in microbiology · 2025
    Article
  10. A Mortality Prediction Nomogram forInfection and drug resistance · 2025
    Article
  11. 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

13 authors.

Ryota HaseDepartment of Microbiology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.ORCID 0000-0002-3135-1757
Aki SakuraiDepartment of Microbiology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Masahiro SuzukiDepartment of Microbiology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Naoya ItohDivision of Infectious Diseases, Aichi Cancer Center, Nagoya, Aichi, Japan.ORCID 0000-0001-6269-7884
Kayoko HayakawaDisease Control and Prevention Center, National Center for Global Health and Medicine, Shinjuku, Tokyo, Japan.ORCID 0000-0002-5480-4405
Kohei UemuraDepartment of Biostatistics and Bioinformatics, Interfaculty Initiative in Information Studies, The University of Tokyo, Bunkyo, Tokyo, Japan.
Yasufumi MatsumuraDepartment of Clinical Laboratory Medicine, Kyoto University Graduate School of Medicine, Kyoto, Kyoto, Japan.ORCID 0000-0001-8595-8944
Hideaki KatoInfection Prevention and Control Department, Yokohama City University Hospital, Yokohama, Kanagawa, Japan.
Takuma IshiharaInnovative and Clinical Research Promotion Center, Gifu University Hospital, Gifu, Gifu, Japan.
David van DuinDivision of Infectious Diseases, University of North Carolina School of Medicine, Chapel Hill, NC, USA.ORCID 0000-0003-4784-3227
Norio OhmagariDisease Control and Prevention Center, National Center for Global Health and Medicine, Shinjuku, Tokyo, Japan.ORCID 0000-0002-4622-8970
Yohei DoiDepartment of Microbiology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.ORCID 0000-0002-9620-2525
Sho SaitoDisease Control and Prevention Center, National Center for Global Health and Medicine, Shinjuku, Tokyo, Japan.

Funding

Colistin-resistant Acinetobacter baumanniiR01AI104895 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DOI, YOHEI, ERNST, ROBERT K · 2014 to 2024
$4.2M
Mechanisms of cefiderocol resistanceR21AI151362 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DOI, YOHEI · 2020 to 2021
$420k
Japan Society for the Promotion of Science JP19K19450NCGM Intramural Research Fund 22A1007NIAID NIH HHS R01 AI104895NIAID NIH HHS R21 AI151362NIH HHSShionogi & Co., Ltd R01AI104895
6 · The paper itself

Abstract

backgroundStenotrophomonas maltophilia is a carbapenem-resistant Gram-negative pathogen increasingly responsible for difficult-to-treat nosocomial infections.

objectivesTo describe the contemporary clinical characteristics and genome epidemiology of patients colonized or infected by S. maltophilia in a multicentre, prospective cohort.

methodsAll patients with a clinical culture growing S. maltophilia were enrolled at six tertiary hospitals across Japan between April 2019 and March 2022. The clinical characteristics, outcomes, antimicrobial susceptibility and genomic epidemiology of cases with S. maltophilia were investigated.

resultsIn total, 78 patients were included representing 34 infection and 44 colonization cases. The median age was 72.5 years (IQR, 61-78), and males accounted for 53 cases (68%). The most common comorbidity was localized solid malignancy (39%). Nearly half of the patients (44%) were immunosuppressed, with antineoplastic chemotherapy accounting for 31%. The respiratory tract was the most common site of colonization (86%), whereas bacteraemia accounted for most infection cases (56%). The 30 day all-cause mortality rate was 21%, which was significantly higher in infection cases than colonization cases (35% versus 9%; adjusted HR, 3.81; 95% CI, 1.22-11.96). Susceptibility rates to ceftazidime, levofloxacin, minocycline and sulfamethoxazole/trimethoprim were 14%, 65%, 87% and 100%, respectively. The percentage of infection ranged from 13% in the unclassified group to 86% in genomic group 6A. The percentage of non-susceptibility to ceftazidime ranged from 33% in genomic group C to 100% in genomic groups 6 and 7 and genomic group geniculate.

conclusionsIn this contemporary multicentre cohort, S. maltophilia primarily colonized the respiratory tract, whereas patients with bacteraemia had the highest the mortality from this pathogen. Sulfamethoxazole/trimethoprim remained consistently active, but susceptibility to levofloxacin was relatively low. The proportions of cases representing infection and susceptibility to ceftazidime differed significantly based on genomic groups.

Indexed as

Anti-Bacterial AgentsGram-Negative Bacterial InfectionsMicrobial Sensitivity TestsStenotrophomonas maltophiliaAgedBacteremiaCross InfectionFemaleGenome, BacterialHumansJapanMaleMiddle AgedMolecular EpidemiologyProspective StudiesTrimethoprim, Sulfamethoxazole Drug CombinationAnti-Bacterial AgentsTrimethoprim, Sulfamethoxazole Drug Combination

Identifiers

PMID38842502
PMCPMC11290880

What OpenQuestion holds

Textmetadata
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.