Publication date: Dec 26, 2024
Most studies on long-term sequelae of SARS-CoV-2-infection in children were conducted pre-Omicron and pre-dated vaccination rollout. We examined long-term risk of new-incident multi-systemic sequelae after SARS-CoV-2 Delta/Omicron infection in a multi-ethnic Asian pediatric population. Retrospective cohort study of Singaporean children aged 1- 17 years infected during Delta/Omicron BA. 1/2 transmission, and contemporaneous test-negative groups. Cox-regression was utilized to estimate risks of new-incident sequelae at 31-300 days post-infection. 267,952 SARS-CoV-2-infected children were included, together with 273,517 test-negatives. ≥95% were infected during Omicron. During Delta, 23. 6% of infected cases were fully-vaccinated; during Omicron, 60. 4% were fully-vaccinated. ≥98% had mild infection not requiring hospitalisation. Overall, there was modestly increased risk of long-term respiratory sequelae (adjusted-hazard-ratio,aHR=1. 09[95%CI=1. 01-1. 18]) and specifically bronchitis (aHR=1. 17[95%CI=1. 06-1. 29]) in the SARS-CoV-2-infected group versus test-negatives. During Delta, increased risk of endocrine conditions (eg. diabetes) was observed (aHR=3. 63[95%CI=1. 25-10. 50]); while during Omicron, increased risk of bronchitis (aHR=1. 09[95%CI=1. 02-1. 20]) was observed in COVID-19 cases versus test-negatives. Elevated risk of bronchitis was observed amongst unvaccinated COVID-19 cases (aHR=1. 17[95%CI=1. 06-1. 29]) versus test-negatives, but not in individuals who had received ≥1 vaccine dose. Risks of chronic sequelae following COVID-19 hospitalisation were comparable to those following historical influenza hospitalisation; albeit reduced when compared to respiratory sequelae following historical hospitalisations for respiratory-syncytial-virus (RSV). Evidence of chronic sequelae in organ systems other than the respiratory system was limited in a pediatric cohort predominantly infected with mild SARS-CoV-2 Omicron infection. Risks of chronic sequelae in hospitalized COVID-19 cases did not substantially differ from historical influenza hospitalisations. Elevated risk of bronchitis was observed following SARS-CoV-2 infection in children, versus test-negatives; similarly, increased risk of respiratory sequelae was documented post-RSV hospitalisation, including children under-5.
Concepts | Keywords |
---|---|
300days | children |
Diabetes | COVID-19 |
Hospitalisations | long COVID |
New | Omicron |
Organ | SARS-CoV-2 |
vaccination |
Semantics
Type | Source | Name |
---|---|---|
disease | MESH | complications |
disease | MESH | Delta infection |
disease | MESH | infection |
disease | MESH | bronchitis |
disease | MESH | COVID-19 |
disease | MESH | influenza |
pathway | REACTOME | SARS-CoV-2 Infection |
disease | MESH | Long Covid |