Evidence map›Paper›PMID 35284543›Full record

ArticleAnnals of translational medicine2022

SARS-Cov-2 pneumonia phenotyping on imaging exams of patients submitted to minimally invasive autopsy.

Marcel Koenigkam-Santos, Danilo Tadao Wada, Maira Nilson Benatti, Li Siyuan, Sabrina Setembre Batah, Andrea Antunes Cetlin, Marcelo Bezerra de Menezes, Alexandre Todorovic Fabro

Open access · diamondAbstract read
In one paragraph

Article in Annals of translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Marcel Koenigkam-SantosDepartment of Medical Images, Hematology and Oncology, Ribeirao Preto Medical School, University of Sao Paulo, Campus Universitario Monte Alegre, Ribeirao Preto, SP, Brazil.
Danilo Tadao WadaDepartment of Medical Images, Hematology and Oncology, Ribeirao Preto Medical School, University of Sao Paulo, Campus Universitario Monte Alegre, Ribeirao Preto, SP, Brazil.
Maira Nilson BenattiDepartment of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Campus Universitario Monte Alegre, Ribeirao Preto, SP, Brazil.
Li SiyuanDepartment of Surgery and Anatomy, Ribeirao Preto Medical School, University of Sao Paulo, Campus Universitario Monte Alegre, Ribeirao Preto, SP, Brazil.
Sabrina Setembre BatahDepartment of Pathology and Legal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Campus Universitario Monte Alegre, Ribeirao Preto, SP, Brazil.
Andrea Antunes CetlinDepartment of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Campus Universitario Monte Alegre, Ribeirao Preto, SP, Brazil.
Marcelo Bezerra de MenezesDepartment of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Campus Universitario Monte Alegre, Ribeirao Preto, SP, Brazil.
Alexandre Todorovic FabroDepartment of Pathology and Legal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Campus Universitario Monte Alegre, Ribeirao Preto, SP, Brazil.
Universidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Correlation between pathology and imaging of the new SARS-Cov-2 disease (COVID-19) is scarce. This study aimed to characterize SARS-Cov-2 pneumonia on imaging of patients submitted to minimally invasive autopsy (MIA). Methods: This unicentric retrospective observational study included 46 consecutive patients with confirmed COVID-19 who underwent MIA. All clinical chest images were reviewed and classified for the presence and grade of viral pneumonia, as well as disease evolution. On CT, phenotypes were described as consistent with mild, moderate, or severe viral pneumonia, with or without radiological signs of organizing pneumonia (OP). In severe pneumonia, CT could also be classified as diffuse progressive OP or radiological diffuse alveolar damage (DAD). Specific features on CT were noted, including fibroproliferative signs that could indicate potential or initial fibrosis. Results: MIA showed a heterogeneous panel of alterations, with a high prevalence of OP and acute fibrinous and organizing pneumonia (AFOP). Also, signs of interstitial fibrosis corresponded to the most prevalent pathological feature. Initial chest radiography (CXR) findings were mainly consistent with moderate or severe viral pneumonia. Most patients showed stability or improvement (reduction of opacities) on imaging. CTs were performed on 15 patients. Consolidations were found in most patients, frequently showing features consistent with an OP phenotype. Fibroproliferative changes were also prevalent on CT. Conclusions: In this study, SARS-Cov-2 pneumonia showed heterogeneous radiological and pathological patterns. Signs of organization and potential or initial fibrosis were prevalent on both imaging and pathology. Imaging phenotyping may help to predict post-infection fibrosing interstitial pneumonitis in COVID-19.

Indexed as

chest radiography (CXR)computed tomographyCOVID-19minimally invasive autopsy (MIA)

Identifiers

PMID35284543
PMCPMC8904976
OpenAlexW4206581272

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.