Evidence map›Paper›PMID 37815489›Full record

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

Plasma Microbial Cell-Free DNA Sequencing in Immunocompromised Patients With Pneumonia: A Prospective Observational Study.

Stephen P Bergin, Roy F Chemaly, Sanjeet S Dadwal, Joshua A Hill, Yeon Joo Lee, Ghady Haidar, Alfred Luk, Alexander Drelick, Peter V Chin-Hong, Esther Benamu and 27 more

Registry-linked trialOpen access · hybridAbstract readObservational StudyMulticenter Study
In one paragraph

Observational study 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. It is linked to trial NCT04047719 (Pneumonia in the ImmunoCompromised - Use of the Karius Test for the Detection of Undiagnosed Pathogens), which is not on this map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
10.9field-weighted citation impact, top 1% 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.

NCT04047719 completednot on this map

Pneumonia in the ImmunoCompromised - Use of the Karius Test for the Detection of Undiagnosed Pathogens

TypeobservationalSponsorKarius, Inc.Ran2019 to 2022Enrolled257ConditionsPneumonia, Bacterial, Pneumonia, Viral, Pneumonia Fungal, Pneumonia CavitaryArmsKarius Test
3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
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  11. Plasma Microbial Cell-free DNA Metagenomic Sequencing for Diagnosis of Invasive Fungal Diseases Among High-risk Outpatient and Inpatient Immunocompromised Hosts.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2025
    Article
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  17. Nature communications · 2025
    Observational
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  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

37 authors at 12 institutions in 1 country.

Stephen P BerginDepartment of Medicine, Division of Pulmonary, Allergy, and Critical Care Medicine, Duke University School of Medicine, Durham, North Carolina, USA.
Roy F ChemalyDepartment of Infectious Diseases, Infection Control and Employee Health, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Sanjeet S DadwalDepartment of Medicine, Division of Infectious Diseases, City of Hope National Medical Center, Duarte California, California, USA.
Joshua A HillVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
Yeon Joo LeeInfectious Diseases Service, Memorial Sloan Kettering Cancer Center, NewYork, New York, USA.
Ghady HaidarDepartment of Medicine, Division of Infectious Diseases, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
Alfred LukSection of Infectious Diseases, John W. Deming Department of Medicine, Tulane University School of Medicine, New Orleans, Louisiana, USA.
Alexander DrelickDepartment of Medicine, Weill Cornell Medicine, NewYork, New York, USA.
Peter V Chin-HongDivision of Infectious Diseases, University of California San Francisco, San Francisco, California, USA.
Esther BenamuDivision of Infectious Diseases, University of Colorado, Aurora, Colorado, USA.
Fareed KhawajaDepartment of Infectious Diseases, Infection Control and Employee Health, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Deepa NanayakkaraDepartment of Medicine, Division of Infectious Diseases, City of Hope National Medical Center, Duarte California, California, USA.
Genovefa A PapanicolaouInfectious Diseases Service, Memorial Sloan Kettering Cancer Center, NewYork, New York, USA.
Catherine Butkus SmallDepartment of Medicine, Weill Cornell Medicine, NewYork, New York, USA.
Monica FungDivision of Infectious Diseases, University of California San Francisco, San Francisco, California, USA.
Michelle A BarronDivision of Infectious Diseases, University of Colorado, Aurora, Colorado, USA.
Thomas DavisDepartment of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Micah T McClainDuke Clinical Research Institute, Durham, North Carolina, USA.
Eileen K MaziarzDepartment of Medicine, Division of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina, USA.
Deng B MadutDepartment of Medicine, Division of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina, USA.
Armando D BedoyaDepartment of Medicine, Division of Pulmonary, Allergy, and Critical Care Medicine, Duke University School of Medicine, Durham, North Carolina, USA.
Daniel L GilstrapDepartment of Medicine, Division of Pulmonary, Allergy, and Critical Care Medicine, Duke University School of Medicine, Durham, North Carolina, USA.
Jamie L ToddDepartment of Medicine, Division of Pulmonary, Allergy, and Critical Care Medicine, Duke University School of Medicine, Durham, North Carolina, USA.
Christina E BarkauskasDepartment of Medicine, Division of Pulmonary, Allergy, and Critical Care Medicine, Duke University School of Medicine, Durham, North Carolina, USA.
Robert BigelowDuke Clinical Research Institute, Durham, North Carolina, USA.
Jeffrey D LeimbergerDuke Clinical Research Institute, Durham, North Carolina, USA.
Ephraim L TsalikDepartment of Medicine, Division of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina, USA.
Olivia WolfDuke Clinical Research Institute, Durham, North Carolina, USA.
Mona MugharKarius Inc., Redwood City, California, USA.
Desiree HollemonKarius Inc., Redwood City, California, USA.
Radha DuttaguptaKarius Inc., Redwood City, California, USA.
Daniel S LupuKarius Inc., Redwood City, California, USA.
Sivan BercoviciKarius Inc., Redwood City, California, USA.
Bradley A PerkinsKarius Inc., Redwood City, California, USA.
Timothy A BlauwkampKarius Inc., Redwood City, California, USA.
Vance G FowlerDuke Clinical Research Institute, Durham, North Carolina, USA.
Thomas L HollandDuke Clinical Research Institute, Durham, North Carolina, USA.ORCID 0000-0001-7745-9010
Duke University · USClinical Research Institute · USCity Of Hope National Medical Center · USCornell University · USMemorial Sloan Kettering Cancer Center · USThe University of Texas MD Anderson Cancer Center · USUniversity of California, San Francisco · USUniversity of Colorado Denver · USIndiana University School of MedicineTulane University · USUniversity of Pittsburgh Medical Center · USUniversity of Washington · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Duke Clinical Research InstituteKarius IncNCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundPneumonia is a common cause of morbidity and mortality, yet a causative pathogen is identified in a minority of cases. Plasma microbial cell-free DNA sequencing may improve diagnostic yield in immunocompromised patients with pneumonia.

methodsIn this prospective, multicenter, observational study of immunocompromised adults undergoing bronchoscopy to establish a pneumonia etiology, plasma microbial cell-free DNA sequencing was compared to standardized usual care testing. Pneumonia etiology was adjudicated by a blinded independent committee. The primary outcome, additive diagnostic value, was assessed in the Per Protocol population (patients with complete testing results and no major protocol deviations) and defined as the percent of patients with an etiology of pneumonia exclusively identified by plasma microbial cell-free DNA sequencing. Clinical additive diagnostic value was assessed in the Per Protocol subgroup with negative usual care testing.

resultsOf 257 patients, 173 met Per Protocol criteria. A pneumonia etiology was identified by usual care in 52/173 (30.1%), plasma microbial cell-free DNA sequencing in 49/173 (28.3%) and the combination of both in 73/173 (42.2%) patients. Plasma microbial cell-free DNA sequencing exclusively identified an etiology of pneumonia in 21/173 patients (additive diagnostic value 12.1%, 95% confidence interval [CI], 7.7% to 18.0%, P < .001). In the Per Protocol subgroup with negative usual care testing, plasma microbial cell-free DNA sequencing identified a pneumonia etiology in 21/121 patients (clinical additive diagnostic value 17.4%, 95% CI, 11.1% to 25.3%).

conclusionsNon-invasive plasma microbial cell-free DNA sequencing significantly increased diagnostic yield in immunocompromised patients with pneumonia undergoing bronchoscopy and extensive microbiologic and molecular testing. CLINICAL TRIALS REGISTRATION: NCT04047719.

Indexed as

PneumoniaAdultHumansImmunocompromised HostProspective StudiesSequence Analysis, DNAbronchoscopyhematologic malignancyhematopoietic cell transplantimmunocompromised pneumoniamicrobial cell-free DNA sequencing

Identifiers

PMID37815489
PMCPMC10954333
OpenAlexW4387472467

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Registered trials

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.