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Prevalence and associating factors of long COVID in pediatric patients during the Delta and the Omicron variants

Lokanuwatsatien et al., Frontiers in Pediatrics, doi:10.3389/fped.2023.1127582
May 2023  
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PASC 14% Improvement Relative Risk Favipiravir  Lokanuwatsatien et al.  EARLY TREATMENT Is early treatment with favipiravir beneficial for COVID-19? Prospective study of 802 patients in Thailand (Sep 2021 - Mar 2022) Lower PASC with favipiravir (not stat. sig., p=0.34) c19early.org Lokanuwatsatien et al., Frontiers in P.., May 2023 Favorsfavipiravir Favorscontrol 0 0.5 1 1.5 2+
Prospective analysis of 802 COVID-19 pediatric patients in Thailand, showing no significant difference in long COVID with favipiravir treatment in unadjusted results.
Potential risks of favipiravir include the creation of dangerous variants, and mutagenicity, carcinogenicity, teratogenicity, and embryotoxicity1-5.
This study is excluded in the after exclusion results of meta analysis: unadjusted results with no group details.
risk of PASC, 14.0% lower, OR 0.86, p = 0.34, treatment 400, control 402, RR approximated with OR.
Effect extraction follows pre-specified rules prioritizing more serious outcomes. Submit updates
Lokanuwatsatien et al., 24 May 2023, prospective, Thailand, peer-reviewed, 8 authors, study period September 2021 - March 2022. Contact: pichaya_t@tu.ac.th.
This PaperFavipiravirAll
Prevalence and associating factors of long COVID in pediatric patients during the Delta and the Omicron variants
Tananya Lokanuwatsatien, Araya Satdhabudha, Auchara Tangsathapornpong, Pornumpa Bunjoungmanee, Phakatip Sinlapamongkolkul, Chanapai Chaiyakulsil, Paskorn Sritipsukho, Pichaya Tantiyavarong
Frontiers in Pediatrics, doi:10.3389/fped.2023.1127582
Introduction: The number of pediatric COVID-19 infections is increasing; however, the data on long COVID conditions in children is still limited. Our study aimed to find the prevalence of long COVID in children during the Delta and Omicron waves, as well as associated factors. Methods: A single-center prospective cohort study was conducted. We included 802 RT-PCR-confirmed COVID-19 pediatric patients in the Delta and Omicron periods. Long COVID was defined as having symptoms for ≥3 months after infection. Parents and/or patients were interviewed by phone. Multivariable logistic regression was performed to find associated factors with long COVID. Results: The overall prevalence of long COVID was 30.2%. The Delta period had more prevalence than the Omicron (36.3% vs. 23.9%). Common symptoms for patients 0-3 years' old were loss of appetite, rhinorrhea, and nasal congestion. Conversely, patients 3-18 years' old had hair loss, dyspnea on exertion, rhinorrhea, and nasal congestion. However, there was no significant negative impact on daily life. Most symptoms improved after a 6-month follow-up. Factors associated with long COVID-19 conditions were infection during the Omicron period (adjusted OR: 0.54; 95% CI: 0.39-0.74, P < 0.001), fever (adjusted OR: 1.49, 95% CI: 1.01-2.20, P = 0.04) and rhinorrhea (adjusted OR: 1.47, 95% CI: 1.06-2.02, P = 0.02). Conclusion: Infection during the Omicron wave has a lower prevalence of long COVID. The prognosis is often favorable, and most symptoms gradually become less. However, pediatricians may schedule appointments to surveil long COVID in children with fever or rhinorrhea as an initial symptom.
Ethics statement The studies involving human participants were reviewed and approved by The Human Research Ethics Committee of Thammasat University No 1 (Faculty of Medicine). Written informed consent to participate in this study was provided by the participants' legal guardian/next of kin. Author contributions All authors made substantial contributions to the study and manuscript and met the criteria for authorship defined in the author instruction: TL designed the study, collected data, interpreted the results, drafted and revised the manuscript, and approved the final version of the manuscript. AS designed the study, collected data, interpreted the results, revised the manuscript, and approved the final version of the manuscript. AT designed the study, interpreted the results, revised the manuscript, and approved the final version of the manuscript. PB designed the study, interpreted the results, revised the manuscript, and approved the final version of the manuscript. PSi designed the study, collected data, interpreted the results, revised the manuscript, and approved the final version of the manuscript. CC collected data, designed the study, interpreted the results, revised the manuscript, and approved the final version of the manuscript. PSr designed the study, collected data, interpreted the results, revised the manuscript, and approved the final version of the manuscript. PT designed the study, analyzed data, interpreted the results, drafted and revised the..
References
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