ArticleArquivos de gastroenterologia2025
THE ROLE OF DIGESTIVE MANIFESTATIONS IN COVID-19 MORTALITY: EVIDENCES FROM BRAZIL'S FIRST EPIDEMIC WAVE.
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.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
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
Identifiers
What Socratic holds
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 Socratic graph.