Evidence map›Paper›PMID 35025929›Full record

Observational studyPloS one2022

Baseline procalcitonin as a predictor of bacterial infection and clinical outcomes in COVID-19: A case-control study.

Natalie J Atallah, Hailey M Warren, Matthew B Roberts, Ramy H Elshaboury, Monique R Bidell, Ronak G Gandhi, Meagan Adamsick, Maryam K Ibrahim, Rupali Sood, Savo Bou Zein Eddine and 14 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 40 citations in OpenAlex.

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  10. [Bacterial coinfection in the critically-ill COVID-19 patient: incidence, impact and need for antimicrobial therapy].Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia · 2023
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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

24 authors at 6 institutions in 3 countries.

Natalie J AtallahDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA, United States of America.
Hailey M WarrenDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA, United States of America.
Matthew B RobertsDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA, United States of America.
Ramy H ElshabouryDepartment of Pharmacy, Massachusetts General Hospital, Boston, MA, United States of America.
Monique R BidellDepartment of Pharmacy, Massachusetts General Hospital, Boston, MA, United States of America.
Ronak G GandhiDepartment of Pharmacy, Massachusetts General Hospital, Boston, MA, United States of America.
Meagan AdamsickDepartment of Pharmacy, Massachusetts General Hospital, Boston, MA, United States of America.ORCID 0000-0002-7734-0383
Maryam K IbrahimDepartment of Medicine, Massachusetts General Hospital, Boston, MA, United States of America.
Rupali SoodDepartment of Medicine, Massachusetts General Hospital, Boston, MA, United States of America.
Savo Bou Zein EddineDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA, United States of America.ORCID 0000-0003-3301-5367
Matthew J Cobler-LichterDivision of Cardiology, Massachusetts General Hospital, Boston, MA, United States of America.
Natalie J AlexanderDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA, United States of America.
Kyle D TimmerDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA, United States of America.
Christine J AtallahFaculty of Medicine, University of Balamand, Beirut, Lebanon.
Adam L ViensDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA, United States of America.
Vahe S PanossianFaculty of Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
Allison K SchererDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA, United States of America.ORCID 0000-0003-3735-3873
Teddie ProctorFisher Diagnostics, Part of Thermo Fisher Scientific, Middletown, VA, United States of America.
Sherrie SmarttFisher Diagnostics, Part of Thermo Fisher Scientific, Middletown, VA, United States of America.
Alyssa R LetourneauDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA, United States of America.
Molly L ParasDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA, United States of America.
Sascha JohannesB·R·A·H·M·S GmbH, Part of Thermo Fisher Scientific, Hennigsdorf, Germany.
Jan WiemerB·R·A·H·M·S GmbH, Part of Thermo Fisher Scientific, Hennigsdorf, Germany.
Michael K MansourDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA, United States of America.ORCID 0000-0001-8892-8695
Massachusetts General Hospital · USHarvard University · USThermo Fisher Scientific (Germany) · DEThermo Fisher Scientific (United States) · USAmerican University of Beirut Medical Center · LBUniversity of Balamand · LB

Funding

The role of spleen tyrosine kinase (syk) in neutrophil responses to pathogenic fungi.R01AI132638 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI MANSOUR, MICHAEL K · 2018 to 2021
$1.6M
NIAID NIH HHS R01 AI132638
6 · The paper itself

Abstract

purposeCoronavirus disease-2019 (COVID-19) is associated with a wide spectrum of clinical symptoms including acute respiratory failure. Biomarkers that can predict outcomes in patients with COVID-19 can assist with patient management. The aim of this study is to evaluate whether procalcitonin (PCT) can predict clinical outcome and bacterial superinfection in patients infected with severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2).

methodsAdult patients diagnosed with SARS-CoV-2 by nasopharyngeal PCR who were admitted to a tertiary care center in Boston, MA with SARS-CoV-2 infection between March 17 and April 30, 2020 with a baseline PCT value were studied. Patients who were presumed positive for SARS-CoV-2, who lacked PCT levels, or who had a positive urinalysis with negative cultures were excluded. Demographics, clinical and laboratory data were extracted from the electronic medical records.

results324 patient charts were reviewed and grouped by clinical and microbiologic outcomes by day 28. Baseline PCT levels were significantly higher for patients who were treated for true bacteremia (p = 0.0005) and bacterial pneumonia (p = 0.00077) compared with the non-bacterial infection group. Baseline PCT positively correlated with the NIAID ordinal scale and survival over time. When compared to other inflammatory biomarkers, PCT showed superiority in predicting bacteremia.

conclusionsBaseline PCT levels are associated with outcome and bacterial superinfection in patients hospitalized with SARS-CoV-2.

Indexed as

AgedAged, 80 and overBacterial InfectionsBiomarkersBostonCase-Control StudiesCOVID-19FemaleHumansInflammationMaleMiddle AgedProcalcitoninRetrospective StudiesSARS-CoV-2BiomarkersProcalcitonin

Identifiers

PMID35025929
PMCPMC8758006
OpenAlexW4206753136

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.