Clinical features of COVID-19 in children with a chronic adenotonsillar disorder

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Abstract

BACKGROUND: COVID-19, caused by SARS-CoV-2, is a highly contagious infectious disease associated with a risk of severe complications. In Russia, the COVID-19 incidence has exceeded 24 million, with new strains raising the incidence in children up to 18%. The prevalence of long COVID is rising. In children, the adaptive immune system, including the lymphoepithelial ring of the throat, plays a key role in determining the severity of COVID-19. The lymphoid tissue of the Waldeyer’s ring is one of the first immune barriers against coronaviruses and other respiratory infections. The high incidence of co-infection worsens the course of the disease. A chronic adenotonsillar disease has incidence of 32%–35% in children. However, impact of this disease on the severity of COVID-19 and the incidence of co-infection in children is poorly understood.

AIM: The aim of the study was to evaluate impact of the chronic adenotonsillar disease on COVID-19 progression and the incidence of co-infections in children.

MATERIALS AND METHODS: Conducted in St. Petersburg from January 2022 to March 2023, the study included 493 children (300 with COVID-19 and 144 with chronic adenotonsillar disease). Patients were divided into four groups to evaluate impact of chronic adenotonsillar disease on COVID-19 progression. Non-parametric statistical methods were used to analyze the clinical data.

RESULTS: Children with both COVID-19 and chronic adenotonsillar disease demonstrated a more severe course of disease compared to those without chronic adenotonsillar disease. The first group showed an increased incidence of bronchitis, bacterial co-infections, longer hospitalization and disease duration, longer fever duration, and higher maximum temperature. Laboratory data showed higher white blood cell counts in patients with COVID-19 and chronic adenotonsillar disease compared to those without chronic adenotonsillar disease.

CONCLUSIONS: Chronic adenotonsillar disease significantly complicates the course of COVID-19 in children. Further research is needed to elucidate the pathophysiological mechanisms and optimize treatment strategies for children with chronic adenotonsillar disease.

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About the authors

Vladislav V. Afanasev

North-Western State Medical University named after I.I. Mechnikov

Author for correspondence.
Email: streetva@gmail.com
ORCID iD: 0009-0006-9039-6265

Postgraduate student

Russian Federation, 41 Kirochnaya St., Saint Petersburg, 191015

References

  1. Baklaushev VP, Kulemzin SV, Gorchakov AA, et al. COVID-19. Etiology, pathogenesis, diagnosis and treatment. Clinical Practice. 2020;11(1):7–20. EDN: COJLTB doi: 10.17816/clinpract26339
  2. McGowan R.J. Coronavirus Disease 2019 (COVID-19) in Children [Internet]. Available from: https://emedicine.medscape.com/article/2500132-overview Accessed: 07.08.2024.
  3. Filimonov SV, Bugrov IA. The olfactory disorder and protective nasal function damage in patients with COVID-19 in near and distant future. Folia Otorhinolaryngologiae et Pathologiae Respiratoriae. 2022;28(4):19–31. EDN: JRYGFF doi: 10.33848/foliorl23103825-2022-28-4-19-31
  4. Filimonov SV, Volkova SA. ENT status in children after COVID-19 caused by SARS-COV-2 virus in the long-term period. Folia Otorhinolaryngologiae et Pathologiae Respiratoriae. 2023;29(4):57–64. EDN: AZMBCM doi: 10.33848/foliorl23103825-2023-29-4-57-54
  5. Russell MW, Mestecky J. Mucosal immunity: The missing link in comprehending SARS-CoV-2 infection and transmission. Front Immunol. 2022;13:957107. doi: 10.3389/fimmu.2022.957107
  6. Lee BR, Harrison CJ, Myers AL, et al. Differences in pediatric SARS-CoV-2 symptomology and Co-infection rates among COVID-19 pandemic waves. J Clin Virol. 2022;154:105220. doi: 10.1016/j.jcv.2022.105220
  7. Bahl A, Mielke N, Johnson S, et al. Severe COVID-19 outcomes in pediatrics: An observational cohort analysis comparing Alpha, Delta, and Omicron variants. Lancet Reg Health Am. 2023;18:100405. doi: 10.1016/j.lana.2022.100405
  8. Han H, Zhou L, Lv J, et al. Bacterial coinfections contribute to severe COVID-19 in winter. Cell Res. 2023;33:562–564. doi: 10.1038/s41422-023-00821-3
  9. Lai H-C, Hsu YL, Lin CH, et al. Bacterial coinfections in hospitalized children with COVID-19 during the SARS-CoV-2 Omicron BA.2 variant pandemic in Taiwan. Front Med (Lausanne). 2023;10:1178041. doi: 10.3389/fmed.2023.1178041
  10. Preobrazhenskaya YuS, Drozdova MV, Ryazantsev SV. Etiological aspects of chronic pathology of the lymphoepithelial pharyngeal ring in children at the present stage. Effektivnaya farmakoterapiya. 2021;17(18):30–34. EDN: PJVOFT doi: 10.33978/2307-3586-2021-17-18-30-34
  11. Xu Q, Milanez-Almeida P, Martins AJ, et al. Adaptive immune responses to SARS-CoV-2 persist in the pharyngeal lymphoid tissue of children. Nat Immunol. 2023;24:186–199. doi: 10.1038/s41590-022-01367-z
  12. Samara P, Athanasopoulos M, Athanasopoulos I. Unveiling the enigmatic adenoids and tonsils: exploring immunology, physiology, microbiome dynamics, and the transformative power of surgery. Microorganisms. 2023;11(7):1624. doi: 10.3390/microorganisms11071624

Supplementary files

Supplementary Files
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1. JATS XML
2. Fig. 1. Distribution of Patients in the Study Groups by Gender. CAP+ and CAP–: with and without Chronic Adenotonsillar Pathology; COVID-19+ and COVID-19–: with and without New Coronavirus Infection

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3. Fig. 2. Prevalence of chronic adenotonsillar pathology by age in groups with COVID-19+ and COVID-19–

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