# Effectiveness of COVID-19 Vaccines Against Hospitalization and Severe Disease in Children with Diabetes Mellitus During Pandemic and Post-Pandemic Eras

**Authors:** Laura G. Coelho, Lilian M. Diniz, Stella C. Galante, Cristiane S. Dias, Maria Christina L. Oliveira, Enrico A. Colosimo, Ana Cristina Simões e Silva, Fernanda N. Duelis, Maria Eduarda T. Bernardes, Daniela R. Martelli, Fabrício Emanuel S. Oliveira, Hercílio Martelli-Junior, Robert H. Mak, Eduardo A. Oliveira

PMC · DOI: 10.3390/microorganisms14020501 · Microorganisms · 2026-02-20

## TL;DR

This study shows that COVID-19 vaccines are more effective at preventing severe outcomes in children with diabetes compared to those without, both during and after the pandemic.

## Contribution

The study provides novel evidence on the enhanced vaccine effectiveness in children with diabetes during both pandemic and post-pandemic periods.

## Key findings

- Children with diabetes had higher rates of hospitalization, severe illness, and mortality from COVID-19 compared to those without diabetes.
- Vaccine effectiveness against severe disease was significantly higher in children with diabetes during both pandemic and post-pandemic periods.
- The number needed to vaccinate to prevent one severe case was much lower in children with diabetes compared to those without.

## Abstract

Pediatric patients with SARS-CoV-2 infection are at an increased risk of severe disease and adverse outcomes. Nevertheless, comprehensive data on COVID-19 vaccine effectiveness (VE) in children with diabetes during the post-pandemic period remain limited. This study assessed the VE against severe COVID-19 outcomes during both the pandemic and post-pandemic phases in children with and without diabetes mellitus (DM). A cohort study based on population data was carried out, including all patients under 18 years of age with symptomatic SARS-CoV-2 infection as registered in the Brazilian national surveillance systems from February 2020 to June 2025. The main outcomes were hospitalization due to COVID-19 and severe illness, which included admission to the intensive care unit (ICU), need for invasive ventilation, and death. Utilizing a propensity score-matched cohort, we estimated the VE and the number needed to vaccinate (NNV) for a booster dose against these outcomes by comparing vaccinated and unvaccinated individuals, employing conditional logistic regression adjusted for confounding variables. The cohort comprised 3,730,007 pediatric patients with COVID-19, of whom 7675 (0.2%) had DM. At baseline, children with DM exhibited a significantly higher prevalence of hospitalization (11.2% vs. 2.0%), severe COVID-19 (6.4% vs. 0.6%), and mortality (1.9% vs. 0.1%) than those without DM (all p < 0.001). During the pandemic period, the adjusted VE was consistently higher in children with DM. Against severe disease, the VE was 72.8% (95% CI: 12.3–93.2) in the DM cohort compared with 45.7% (28.1–59.0) in the non-DM cohort. This increased effectiveness corresponded to a more favorable NNV; the NNV to prevent one severe case was 24 (95% CI: 12–232) for children with DM versus 243 (168–440) for those without DM. In the post-pandemic period, the VE remained significantly higher in the DM cohort. Against severe disease, the VE was 76.2% (11.5–93.5) for children with DM and 52.9% (32.7–67.1) for those without. The NNV to prevent one severe case was consistently lower in the DM cohort (8 vs. 591). In conclusion, a complete vaccination regimen, including a booster dose, substantially mitigated severe COVID-19 outcomes in children with DM in the pandemic and post-pandemic periods.

## Linked entities

- **Diseases:** diabetes mellitus (MONDO:0005015)

## Full-text entities

- **Diseases:** obesity (MESH:D009765), VE (MESH:D004673), fever (MESH:D005334), respiratory infections (MESH:D012141), injury to (MESH:D014947), cardiopulmonary disease (MESH:D006323), asthma (MESH:D001249), Dyspnea (MESH:D004417), malignancies (MESH:D009369), DM (MESH:D003920), T1D (MESH:D003922), diabetic ketoacidosis (MESH:D016883), heart, lung, kidney, nervous system, and blood diseases (MESH:D009422), severe acute respiratory infection (MESH:D045169), death (MESH:D003643), immunodeficiency (MESH:D007153), hypertension (MESH:D006973), cough (MESH:D003371), infection (MESH:D007239), cardiovascular disease (MESH:D002318), COVID (MESH:D000086382)
- **Chemicals:** glucose (MESH:D005947), NNV (-)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942963/full.md

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Source: https://tomesphere.com/paper/PMC12942963