Evidence map›Paper›PMID 41379187›Full record

ArticleArquivos de gastroenterologia2025

THE ROLE OF DIGESTIVE MANIFESTATIONS IN COVID-19 MORTALITY: EVIDENCES FROM BRAZIL'S FIRST EPIDEMIC WAVE.

Elvis Paim Ferreira, Mariana da Silva Arbués, André Castro Lyra, Lourianne Nascimento Cavalcante

Abstract read
In one paragraph

Article in Arquivos de gastroenterologia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Elvis Paim FerreiraFaculdade de Medicina da Bahia - UFBA; Salvador, BA, Brasil.ORCID http://orcid.org/0000-0001-7458-1723
Mariana da Silva ArbuésEscola Bahiana de Medicina e Saúde Pública; Salvador, BA, Brasil.ORCID http://orcid.org/0009-0005-9247-1022
André Castro LyraFaculdade de Medicina da Bahia - UFBA; Salvador, BA, Brasil.ORCID http://orcid.org/0000-0001-9010-8645
Lourianne Nascimento CavalcanteFaculdade de Medicina da Bahia - UFBA; Salvador, BA, Brasil.ORCID http://orcid.org/0000-0003-1110-0931

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextCOVID-19, caused by SARS-CoV-2, is primarily characteri-zed by respiratory symptoms but also significantly affects the gastrointestinal (GI) tract and liver. Emerging evidence suggests that GI and hepatic manifestations may influence disease severity and outcomes. In Brazil, where disparities between public and private healthcare systems are pronounced, understanding these associations is crucial for optimizing patient management. This study aimed to evaluate the frequency and prognostic implications of digestive and hepatic injuries in hospitalized COVID-19 patients.

objectiveTo analyze the frequency of hepatic and gastrointestinal injuries and their association with outcomes (discharge or death).

methodsA retrospective cross-sectional study analyzed 3,555 patients from 50 private hospitals in Brazil (March-December 2020). Inclusion criteria were age ≥18 years, RT-PCR-confirmed COVID-19, and written consent. Demographic data, comorbidities, GI symptoms (diarrhea, nausea/vomiting, abdominal pain), liver enzymes (ALT, AST), and outcomes (discharge, mortality, ICU admission) were collected via REDCap. Statistical analyses included logistic regression to identify mortality predictors.

resultsAmong 3,555 patients (59.9% male, mean age 55.8 years). A total of 42.2% of patients presented with at least one gastrointestinal (GI) symptom at admission. Diarrhea was reported in 15%, nausea or vomiting in 13.6%, and abdominal pain in 6.5%, with symptom overlap among patients. The deceased group exhibited significantly higher alanine aminotransferase (ALT) (p=0.019) and aspartate aminotransferase (AST) (p=0.026) levels, representing 4.2- and 8.4-fold increases, respectively, with a higher AST/ALT ratio in fatal cases (1.69 vs 0.84). COVID-19 patients in Brazilian private hospitals showed hepatic abnormalities (AST 354.1 IU/L vs 42.1 IU/L in deceased vs discharged patients, P=0.026), with diarrhea associated with lower mortality (OR 0.61; 95%CI 0.42-0.88), while chronic liver disease (OR 2.95; 95%CI 1.35-6.41) and hypoalbuminemia (OR 0.22; 95%CI 0.11-0.38) emerged as independent predictors of death.

conclusionHepatic abnormalities and gastrointestinal symptoms are important markers of COVID-19 severity. Diarrhea, liver enzyme alterations, and serum albumin levels were significant predictors of mortality. Future strategies should prioritize hepatic monitoring, nutritional support, and healthcare equity through targeted interventions for high-risk groups, particularly in resource-limited settings.

Indexed as

COVID-19Gastrointestinal DiseasesLiver DiseasesAdultAgedBrazilCross-Sectional StudiesFemaleHospitalizationHumansMaleMiddle AgedPrognosisRetrospective Studies

Identifiers

PMID41379187
PMCPMC12683944

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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 Socratic graph.