Evidence map›Paper›PMID 41028085›Full record

ArticleScientific reports2025

Nationwide longitudinal analysis of COVID-19 hospitalisation burden in immunocompromised patients.

Henrique Andrade R Fonseca, Lucas Ferreira Theotonio Dos Santos, Antonio José Cordeiro Mattos, Juares Ednaldo Romero Bianco, Frederico Monfardini, Gustavo Prado Dos Santos, Lívia Dias de Sousa, Maurício Longato, Guilherme Cordeiro, Mariana Martins Sasse and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. 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
–field-weighted citation impact
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.

  1. Article
  2. 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

11 authors.

Henrique Andrade R FonsecaAcademic Research Organization, Instituto Israelita de Ensino e Pesquisa, Hospital Israelita Albert Einstein, Rua Comendador Elias Jafet, 755, 4º andar. 409N Office, São Paulo, SP, 05652-900, Brazil. henrique.fonseca@einstein.br.
Lucas Ferreira Theotonio Dos SantosAcademic Research Organization, Instituto Israelita de Ensino e Pesquisa, Hospital Israelita Albert Einstein, Rua Comendador Elias Jafet, 755, 4º andar. 409N Office, São Paulo, SP, 05652-900, Brazil.
Antonio José Cordeiro MattosAcademic Research Organization, Instituto Israelita de Ensino e Pesquisa, Hospital Israelita Albert Einstein, Rua Comendador Elias Jafet, 755, 4º andar. 409N Office, São Paulo, SP, 05652-900, Brazil.
Juares Ednaldo Romero BiancoAstrazeneca, São Paulo, Brazil.
Frederico MonfardiniAcademic Research Organization, Instituto Israelita de Ensino e Pesquisa, Hospital Israelita Albert Einstein, Rua Comendador Elias Jafet, 755, 4º andar. 409N Office, São Paulo, SP, 05652-900, Brazil.
Gustavo Prado Dos SantosAcademic Research Organization, Instituto Israelita de Ensino e Pesquisa, Hospital Israelita Albert Einstein, Rua Comendador Elias Jafet, 755, 4º andar. 409N Office, São Paulo, SP, 05652-900, Brazil.
Lívia Dias de SousaAstrazeneca, São Paulo, Brazil.
Maurício LongatoNodian, São Paulo, Brazil.
Guilherme CordeiroNodian, São Paulo, Brazil.
Mariana Martins SasseAstrazeneca, São Paulo, Brazil.
Luiz Vicente RizzoAcademic Research Organization, Instituto Israelita de Ensino e Pesquisa, Hospital Israelita Albert Einstein, Rua Comendador Elias Jafet, 755, 4º andar. 409N Office, São Paulo, SP, 05652-900, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The COVID-19 pandemic has caused over 7 million deaths worldwide, with age, underlying conditions, and immunosuppression increasing the incidence of severe outcomes. Despite vaccination, immunocompromised (IC) individuals show lower vaccine response, probably leading to more breakthrough infections. The objective of our study was to evaluate the overall occurrence of intensive care admission and/or death during hospitalisation, stratified by COVID-19 severity and immunological status (IC vs. non-IC individuals). Our study used a nationwide database to compare COVID-19 hospitalisations and outcomes in IC versus non-immunocompromised individuals (non-IC). This is a longitudinal cohort study analysed de-identified COVID-19 data from Brazil's DATASUS system (02 March 2020-31 December 2023). The study included 361,898 subjects, identifying 7484 (2.07%) IC individuals. IC individuals showed higher rates of chronic liver, neurological, and lung diseases, while non-IC individuals had higher obesity rates. Intensive care unit (ICU) admissions (42.6% vs. 38.5%) and mortality (51.1% vs. 35.9%) were greater in IC compared to non-IC individuals. Therefore, IC individuals consistently experienced more ICU admissions and higher mortality across the COVID-19 pandemic years (odds ratios rising from 1.68 in 2020 to 2.39 in 2023), influenced by the prevalence of SARS-Cov-2 variants. Our study shows higher morbidity and mortality in IC individuals during the COVID-19 pandemic, underscoring the need for targeted strategies like early interventions, reinforcing the need for sustained surveillance, targeted vaccination strategies, and prioritised care.

Indexed as

COVID-19HospitalizationImmunocompromised HostAdultAgedAged, 80 and overBrazilFemaleHumansIntensive Care UnitsLongitudinal StudiesMaleMiddle AgedSARS-CoV-2Young AdultCOVID-19ImmunocompromisedIntensive care unitMortalitySARS-CoV-2Vaccines

Identifiers

PMID41028085
PMCPMC12485154

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.