Evidence map›Paper›PMID 37824595›Full record

ArticlePLoS neglected tropical diseases2023

Melioidosis Queensland: An analysis of clinical outcomes and genomic factors.

Ian Gassiep, Delaney Burnard, Budi Permana, Michelle J Bauer, Thom Cuddihy, Brian M Forde, Mark D Chatfield, Weiping Ling, Robert Norton, Patrick N A Harris

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. The Genomic Epidemiology of ClinicalPathogens (Basel, Switzerland) · 2024
    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

10 authors at 2 institutions in 1 country.

Ian GassiepThe University of Queensland, Faculty of Medicine, UQ Centre for Clinical Research, Herston, Queensland, Australia.ORCID 0000-0003-3548-6963
Delaney BurnardQueensland Cyber Infrastructure Foundation, Brisbane, Queensland, Australia.
Budi PermanaThe University of Queensland, Faculty of Medicine, UQ Centre for Clinical Research, Herston, Queensland, Australia.
Michelle J BauerThe University of Queensland, Faculty of Medicine, UQ Centre for Clinical Research, Herston, Queensland, Australia.
Thom CuddihyThe University of Queensland, Faculty of Medicine, UQ Centre for Clinical Research, Herston, Queensland, Australia.
Brian M FordeThe University of Queensland, Faculty of Medicine, UQ Centre for Clinical Research, Herston, Queensland, Australia.
Mark D ChatfieldThe University of Queensland, Faculty of Medicine, UQ Centre for Clinical Research, Herston, Queensland, Australia.
Weiping LingThe University of Queensland, Faculty of Medicine, UQ Centre for Clinical Research, Herston, Queensland, Australia.
Robert NortonPathology Queensland, Townsville University Hospital, Townsville, Queensland, Australia.
Patrick N A HarrisThe University of Queensland, Faculty of Medicine, UQ Centre for Clinical Research, Herston, Queensland, Australia.
The University of Queensland · AUQCIF Ltd. · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe clinical and genomic epidemiology of melioidosis varies across regions.

aimTo describe the clinical and genetic diversity of B. pseudomallei across Queensland, Australia.

methodsWhole genome sequencing of clinical isolates stored at the melioidosis reference lab from 1996-2020 was performed and analysed in conjunction with available clinical data.

resultsIsolates from 292 patients were analysed. Bacteraemia was present in 71% and pneumonia in 65%. The case-fatality rate was 25%. Novel sequence types (ST) accounted for 51% of all isolates. No association was identified between the variable virulence factors assessed and patient outcome. Over time, the proportion of First Nation's patients declined from 59% to 26%, and the proportion of patients aged >70 years rose from 13% to 38%.

conclusionThis study describes a genomically diverse and comparatively distinct collection of B. pseudomallei clinical isolates from across Queensland, Australia. An increasing incidence of melioidosis in elderly patients may be an important factor in the persistently high case-fatality in this region and warrants further investigation and directed intervention.

Indexed as

Burkholderia pseudomalleiMelioidosisAgedAustraliaGenomicsHumansQueensland

Identifiers

PMID37824595
PMCPMC10610085
OpenAlexW4387568723

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.