Evidence map›Paper›PMID 37633257›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2024

Clinical and Genomic Characterization of a Cohort of Patients With Klebsiella pneumoniae Bloodstream Infection.

David J Roach, Sushmita Sridhar, Elizabeth Oliver, Sowmya R Rao, Damien M Slater, Wontae Hwang, Kian Hutt Vater, Anupama Dinesh, Firdausi Qadri, Mohammod J Chisti and 7 more

Open access · greenAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 21 citations in OpenAlex.

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  8. Clinical and microbiological epidemiology ofJAC-antimicrobial resistance · 2026
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  11. Parallel single-cell host immune profiling and pathogen genomic characterization inFrontiers in cellular and infection microbiology · 2026
    Observational
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  18. Review
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  20. Genomic characterization ofFrontiers in microbiology · 2025
    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

17 authors at 6 institutions in 2 countries.

David J RoachThe Broad Institute of MIT and Harvard, Boston, Massachusetts, USA.ORCID 0000-0001-5199-0452
Sushmita SridharThe Broad Institute of MIT and Harvard, Boston, Massachusetts, USA.ORCID 0000-0001-7453-7482
Elizabeth OliverDivision of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, USA.
Sowmya R RaoDepartment of Global Health, Boston University, Boston, Massachusetts, USA.
Damien M SlaterDivision of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, USA.
Wontae HwangDivision of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, USA.
Kian Hutt VaterDivision of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, USA.
Anupama DineshDivision of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, USA.
Firdausi QadriDhaka Hospital, International Centre for Diarrheal Disease Research, Bangladesh.
Mohammod J ChistiDhaka Hospital, International Centre for Diarrheal Disease Research, Bangladesh.
Virginia M PierceDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Sarah E TurbettDivision of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID 0000-0002-3603-8110
Roby P BhattacharyyaThe Broad Institute of MIT and Harvard, Boston, Massachusetts, USA.
Colin J WorbyThe Broad Institute of MIT and Harvard, Boston, Massachusetts, USA.ORCID 0000-0002-9132-7249
Ashlee M EarlThe Broad Institute of MIT and Harvard, Boston, Massachusetts, USA.
Regina C LaRocqueDivision of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID 0000-0003-4558-0339
Jason B HarrisDivision of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, USA.
Massachusetts General Hospital · USBroad Institute · USInternational Centre for Diarrhoeal Disease Research · BDBoston University · USHarvard University · USUniversity of Michigan · US

Funding

Viral Genomics: evolution, spread, and host interactionsU19AI110818 · NIAID · BROAD INSTITUTE, INC. · PI SABETI, PARDIS CHRISTINE · 2014 to 2024
$66.5M
INFECTIOUS DISEASE AND BASIC MICROBIOLOGICAL MECHANISMST32AI007061 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Marcia B Goldberg · 1985 to 2026
$12.1M
NIAID NIH HHS T32 AI007061NIAID NIH HHS U19 AI110818NIH HHS T32AI007061-44
6 · The paper itself

Abstract

backgroundThe clinical and microbial factors associated with Klebsiella pneumoniae bloodstream infections (BSIs) are not well characterized. Prior studies have focused on highly resistant or hypervirulent isolates, limiting our understanding of K. pneumoniae strains that commonly cause BSI. We performed a record review and whole-genome sequencing to investigate the clinical characteristics, bacterial diversity, determinants of antimicrobial resistance, and risk factors for in-hospital death in a cohort of patients with K. pneumoniae BSI.

methodsWe identified 562 patients at Massachusetts General Hospital with K. pneumoniae BSIs between 2016 and 2022. We collected data on comorbid conditions, infection source, clinical outcomes, and antibiotic resistance and performed whole-genome sequencing on 108 sequential BSI isolates from 2021 to 2022.

resultsIntra-abdominal infection was the most common source of infection accounting for 34% of all BSIs. A respiratory tract source accounted for 6% of BSIs but was associated with a higher in-hospital mortality rate (adjusted odds ratio, 5.4 [95% confidence interval, 2.2-12.8]; P < .001 for comparison with other sources). Resistance to the first antibiotic prescribed was also associated with a higher risk of death (adjusted odds ratio, 5.2 [95% confidence interval, 2.2-12.4]; P < .001). BSI isolates were genetically diverse, and no clusters of epidemiologically and genetically linked cases were observed. Virulence factors associated with invasiveness were observed at a low prevalence, although an unexpected association between O-antigen type and the source of infection was found.

conclusionsThese observations demonstrate the versatility of K. pneumoniae as an opportunistic pathogen and highlight the need for new approaches for surveillance and the rapid identification of patients with invasive antimicrobial-resistant K. pneumoniae infection.

Indexed as

BacteremiaCross InfectionKlebsiella InfectionsSepsisAnti-Bacterial AgentsGenomicsHospital MortalityHumansKlebsiella pneumoniaeAnti-Bacterial AgentsbacteremiaKlebsiella pneumoniaemortality modelingvirulence factorswhole-genome sequencing

Identifiers

PMID37633257
PMCPMC10810715
OpenAlexW4386187507

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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.