# Clinical Insights and Severity of Enterovirus D68 Respiratory Infections in Vietnamese Children

**Authors:** Hirono Otomaru, Yurika Kawazoe, Hien Anh Thi Nguyen, Hien Minh Vo, Hoang Huy Le, Michiko Toizumi, Katsumi Mizuta, Duc Anh Dang, Hiroyuki Moriuchi, Lay-Myint Yoshida

PMC · DOI: 10.1093/ofid/ofag102 · Open Forum Infectious Diseases · 2026-02-26

## TL;DR

This study finds that Enterovirus D68 causes more severe respiratory disease in Vietnamese children compared to other viruses, even in those without pre-existing health issues.

## Contribution

The study quantifies the increased risk of severe disease from EVD68 compared to other viruses, stratified by comorbidity status.

## Key findings

- EVD68 was associated with higher risks of wheeze and pneumonia compared to other viruses.
- Severe disease risk from EVD68 was elevated regardless of comorbidity status.
- ICU recovery times were similar between EVD68 and other virus groups.

## Abstract

Enterovirus D68 (EVD68) causes respiratory disease, yet the risk of severe respiratory disease remains incompletely quantified, especially when stratified by comorbidity status. This study aims to describe the clinical features and risk of severe disease in children with EVD68 compared with those with other Rhinoviruses/Enteroviruses, accounting for comorbidity.

We analyzed 1100 pediatric EV-positive cases from surveillance in Vietnam (2019–2022), excluding viral coinfections. EVD68 was confirmed by real-time PCR. We examined clinical features, treatments, and comorbidities. Standardization methods estimated risk differences (RDs) and risk ratios (RRs) stratified by (1) general comorbidity, (2) asthma, and (3) either of these. Time-to-recovery in intensive care unit (ICU) was compared using Kaplan–Meier methods.

EVD68 was detected in 55/1100 cases (5.0%). Children with EVD68 more often had wheeze, pneumonia, oxygen therapy, and ICU admission. For wheeze, EVD68 was associated with similar elevated risk with and without general comorbidity (RR 1.40 in both; RD 0.27). Pneumonia risk was likewise elevated with EVD68 (with comorbidity: RR 1.17; RD 0.12; without: RR 1.73; RD 0.14). By asthma status, EVD68 increased wheeze risk in both groups; however, the excess was smaller in asthma (RR 1.10; RD 0.09) than non-asthma (RR 1.43; RD 0.29), consistent with baseline wheeze susceptibility in asthma. Pneumonia risk was similar regardless of asthma status. During ICU stay, wheeze persisted longest in both groups. Time-to-recovery was similar between groups.

EVD68 infection was associated with a higher risk of severe disease than Rhinoviruses/Enteroviruses, independent of documented comorbidity, indicating substantial risk even among previously healthy children.

EVD68 infection was associated with greater severity than RV/EV, with higher risk of wheeze and pneumonia, independent of documented comorbidities; ICU course was similar. Ongoing surveillance is warranted worldwide.

## Linked entities

- **Diseases:** pneumonia (MONDO:0005249), asthma (MONDO:0004979)

## Full-text entities

- **Genes:** MFSD6 (major facilitator superfamily domain containing 6) [NCBI Gene 54842] {aka MMR2, SLC73A1, hMMR2}, AFP (alpha fetoprotein) [NCBI Gene 174] {aka AFPD, FETA, HPAFP}
- **Diseases:** hypoxemia (MESH:D000860), Infectious Diseases (MESH:D003141), IMCI (MESH:D000081042), allergic or chronic diseases (MESH:D002908), lower (MESH:D017116), convulsions (MESH:D012640), IMCI pneumonia (MESH:D011014), paralysis (MESH:D010243), reactive airway disease (MESH:D000275), Wheeze (MESH:D012135), EV (MESH:D004819), tachypnea (MESH:D059246), chest indrawing (MESH:D013898), asthma (MESH:D001249), lethargy (MESH:D053609), cough (MESH:D003371), AFM (MESH:C000629404), COVID-19 (MESH:D000086382), weakness (MESH:D018908), RV/EV infection (MESH:D007239), difficulty breathing (MESH:D004417), irritability (MESH:D001523), respiratory disease (MESH:D012140), asthmatics (MESH:D013224), altered consciousness (MESH:D003244), ARIs (MESH:C535427), inflammation (MESH:D007249), EVD68 Infection (MESH:D004769), ARI (MESH:D012141)
- **Chemicals:** sialic acid (MESH:D019158), Oxygen (MESH:D010100)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], enterovirus D68 (no rank) [taxon 42789], Homo sapiens (human, species) [taxon 9606], Picornaviridae (family) [taxon 12058], Enterovirus (genus) [taxon 12059], EV [taxon 2844103]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12968390/full.md

## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12968390/full.md

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Source: https://tomesphere.com/paper/PMC12968390