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ABSTRACT

Objective: To review the empirical evidence regarding neuropsychiatric illness (long coronavirus disease [COVID]) in children and adolescents post–severe acute respiratory coronavirus disease 2 (SARS-CoV-2) infection.

Data Sources: A search of PubMed, PsycINFO, Cochrane Library, and Google Scholar was conducted from the date of inception until February 2022 using the keywords corona*, COVID-19, SARS-CoV-2, mental health, depression, anxiety, neurological, psychiatric, long COVID, and post-COVID outcomes. Age filters were used to include children and adolescents aged ≤ 18 years.

Study Selection: The search resulted in the identification of 526 articles; 48 articles met the inclusion criteria.

Data Extraction: Results are presented using a narrative review format. Data regarding long COVID in children and adolescents post–SARS-CoV-2 infection were extracted to understand epidemiologic trends, preventive measures, and treatment options.

Results: Studies during the initial phase of the pandemic reported a mixed range of symptoms from case reports or case series. However, multisystem inflammatory syndrome in children (MIS‐C) was widely reported. During the subsequent phases, the emergence of new variants led to a surge of SARS-CoV-2 infections in pediatric populations. There were highly variable, mixed symptom clusters within 60 days post-infection, which resolved in many patients within 6 months. There were prolonged illnesses and impairments in some children and adolescents with long COVID, and many had similar symptoms even though they tested negative for COVID-19.

Conclusions: Long COVID symptoms are both physical and mental in nature among children and adolescents. The impairments have the potential to affect long-term functioning and increase the overall burden on health care delivery. Despite current studies having methodological issues, there is a consensus to provide multidisciplinary and holistic care to those in need.

Prim Care Companion CNS Disord 2022;24(2):21r03218

To cite: Gupta M, Gupta N, Esang M. Long COVID in children and adolescents. Prim Care Companion CNS Disord. 2022;24(2):21r03218.
To share: https://doi.org/10.4088/PCC.21r03218

© Copyright 2022 Physicians Postgraduate Press, Inc.

aClarion Psychiatric Center, Clarion, Pennsylvania
bReynolds Memorial Hospital, Glendale, West Virginia
*Corresponding author: Mayank Gupta, MD, Clarion Psychiatric Center, 2 Hospital Drive, Clarion, PA 16214 ([email protected]).


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After studying this article, you should be able to:

  • Monitor children and adolescents for symptoms of long COVID using multidisciplinary approaches

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In children, coronavirus disease 2019 (COVID-19)  is often asymptomatic (43%–68% of cases) or causes mild symptoms, and life-threatening illness or death from COVID-19 is rare.1 The extensively studied indirect effects of the COVID-19 pandemic on the mental health of children and adolescents have multiple predisposing and perpetuating factors including social isolation, increased screen time, lack of physical activity, heightened perceived risks, and parenting stress.2 These factors attributed to a surge in mental health emergency visits, self-reports of symptoms of anxiety, depression in adolescents, and externalizing disorders among college-aged youth.

During the initial phase of the pandemic, children and adolescents were considered largely spared from the direct effects of COVID-19 infection, with very limited morbidity and mortality.3 According to the American Academy of Pediatrics, less than 1.5% of child cases have resulted in hospitalization. The neuroinvasive potential of coronaviruses has been previously described for severe acute respiratory syndrome coronavirus (SARS‐CoV),4 Middle East respiratory syndrome coronavirus,5 human coronavirus 229E,6 and human coronavirus OC43.7 The increased risk of neuropsychiatric implications may be attributed to viral infiltration of the central nervous system (CNS), dysregulation of the cytokine network, hypercoagulable states, transmigration of peripheral immune cells, and post–SARS-CoV-2 infection autoimmune effects.8

After a positive test for COVID-19, 13.3% of adults had a cluster of symptoms that lasted for at least 4 weeks and 4.5% for at least 8 weeks.9 These symptoms10 of brain fog, cognitive dysfunction, headache, loss of taste and smell, emotional and mood fluctuations, memory loss (both short term and long term), encephalopathy, cerebrovascular disease, sleep disturbance, and hallucinations were termed long COVID (also called post–COVID-19 condition, post-acute sequelae of COVID-19, or chronic COVID syndrome).10,11 The World Health Organization defines long COVID in adults as “people with a history of probable or confirmed SARS-CoV-2 infection, usually 3 months from the onset of COVID-19, with symptoms that last for at least 2 months and cannot be explained by alternative diagnoses.”12(p3) The neurologic and psychiatric manifestations are observed in 20%−35% of adult patients.13–15 There are studies16,17 in adults on the overall epidemiology, risk factors, and preventive measures (vaccinations) and treatments, but the data in children are largely missing.

Despite reports of a significant increase in SARS-CoV-2 infection in children and adolescents, there is very limited information available about long COVID in this group. The highly transmissible Omicron coronavirus variant in children and adolescents makes up about 5% of all COVID-19 hospitalizations, which is up to 4 times higher than that of previous COVID waves.18 The Omicron variant replicates 70 times faster in human airways and has a harder time multiplying in lung tissue than the Delta variant, suggesting why it might cause less severe disease, but clinicians still worry that infected individuals might develop long COVID. In 2020, several studies19–22 started to report neuropsychiatric sequelae post–SARS-CoV-2 infection in adults; however, it was not until 2021 that long COVID cases were reported among children and adolescents.

For children and adolescents, there are many questions regarding long COVID and the prevalence, risk factors, and plausible molecular, immunologic, and psychological mechanisms for its long-term effects. The objective of this article is to review the literature on long COVID in children and adolescents post–SARS-CoV-2 infection to understand epidemiologic trends, preventive measures, and treatment options.

METHODS

A comprehensive search of several databases was conducted from the date of inception to February 2022. The databases included PubMed, PsycINFO, Cochrane Library, and Google Scholar. The search was designed using the following controlled vocabulary and keywords: corona*, COVID-19, SARS-CoV-2, mental health, depression, anxiety, neurological, psychiatric, long COVID, and post-COVID outcomes. Age filters were used to include children and adolescents aged ≤ 18 years. The search was performed in all languages and was limited to human subjects. A manual search of references in included studies was performed to avoid selection bias. Reverse citations were also reviewed to update the material. Research articles that focused exclusively on the association between COVID-19 infection in children and adolescents and mental health in individuals aged ≤ 18 years were selected for review. The inclusion criteria were any published material on individuals aged ≤ 18 with COVID-19 who reported symptoms of any psychiatric manifestations including depression, anxiety, insomnia, or psychosis. After the removal of duplicates, 526 articles were identified, and 48 articles met the inclusion criteria.1–3,11,13,18,23–65

RESULTS

There is limited empirical evidence about neuropsychiatric symptoms post–SARS-CoV-2 in children and adolescents. The studies included in this review are from diverse populations, including the United Kingdom, Sweden, Norway, Denmark, the United States, Italy, France, Tanzania, and Argentina. More recent studies were also included since the Delta and subsequent variants led to a surge in cases among children and adolescents. These were larger studies with a more robust design to fill data gaps during the initial wave.

Table 1 presents salient features of studies included in the review. Most studies included participants from the United States (6) and the United Kingdom (4). Three studies were from France, while 2 were from Italy. Inflammatory disorders post–SARS-CoV-2 infection, namely a multisystem inflammatory syndrome in children (MIS‐C) and Kawasaki-like disease, were reported the most among the studies. The former was reported in 8 articles,34,36–40,44,47 while 243,49 reported the latter. Neuropsychiatric complications were reported in 5,25–28,30 while 3 articles29,48,50 described neurologic disorders. Table 2 provides an overview of the newer studies, which include cohort studies from Denmark51 and the United Kingdom.53,54 An Italian cross-sectional study52 and Norwegian national register–based cohort study55 provided patterns of symptomatology, duration of illness, and overall burden on health care.

DISCUSSION

In adults, there are reports of marked variability in neuropsychiatric symptoms post–SARS-CoV-2.11–16 For example, in a Chinese case series19 of 214 inpatients, neurologic symptoms of stroke, encephalopathy, and myopathy were reported in about one‐third of the sample. Also, a French study20 of 58 COVID-19–positive patients reported neuropsychiatric long COVID symptoms in 33% of the sample. Similarly, an increased prevalence of depression (29%) was reported in another Chinese cross‐sectional study14 of 205 patients. However, another study21 reported neuropsychiatric manifestations in ~22% of 40,469 patients, with a higher prevalence of headache, sleep disorders, encephalopathy, stroke, transient ischemic attack, seizures, anxiety, mood disorders, and suicidal ideation.

A US-based study22 reported neurologic or psychiatric diagnosis in 33.62% of 236,379 subjects in the following period of 6 months. The authors22 reported a similar pattern of a wide range of symptoms, with intracranial hemorrhage, ischemic stroke, parkinsonism, dementia, anxiety disorder, and psychotic disorder the most common. In another study from the United States,23 the same researchers assessed electronic health records of 44,779 patients with COVID-19 and reported an 18% probability of the first diagnosis of psychiatric illness, including anxiety disorders, insomnia, and dementia, during a period of 14–90 days post–SARS-CoV-2 infection. These trends were suggestive of highly variable symptoms with unaccounted impairments in global functioning.

Neuropsychiatric Manifestations of COVID-19 in Children and Adolescents

Toward the end of December 2020, many children did not completely recover from SARS-CoV-2 infection.3,24 There was increased utilization of online medical forums wherein parents were seeking medical expertise for prolonged clinical manifestations post–COVID-19, which was bought to the attention of clinicians and researchers.25 The first few reports include a case series of 5 children with prolonged headaches, difficulty concentrating, brain fog, and memory loss.26 Buonsenso et al25 assessed 510 children and reported the presence of lack of concentration (60.6%); difficulty in remembering information (45.9%), performing daily activities (40%), and processing information (32.7%); and short-term memory issues. In another case series of 1,695 patients,27 neurologic symptoms were reported in 22% of patients, of which 88% presented transient symptoms. The remaining 12% developed life‐threatening conditions, like Guillain‐Barré syndrome (GBS), encephalopathy, demyelination of CNS, stroke, and acute fulminant edema, which were associated with COVID-19. Among the patients with life-threatening neurologic conditions, 40% presented new neurologic deficits at the time of hospital discharge, whereas 26% died.27 Another case28 reported acute-onset neuropsychiatric syndrome post–SARS-CoV-2 infection in 2 children aged 12 and 13 years. The first presented obsessive-compulsive disorder (OCD) symptoms, emotional lability, facial motor tics, and lack of attention 2 months post-infection, and the second presented symptoms of aggressiveness, irritability, inattentiveness, inappetence, facial motor tic, guttural vocal tics, and hyperactivity.28 A French study29 of 5 infants reported neurologic symptoms of axial hypotonia or drowsiness and moaning sounds. In a cross-cultural multicenter study, Lindan et al30 assessed 38 neurologic findings associated with SARS‐CoV‐2 from France, the United Kingdom, the United States, Brazil, Argentina, Peru, India, and Saudi Arabia. The neuroimaging study’s findings were associated with post-infectious immune‐mediated acute disseminated encephalomyelitis‐like changes of the brain, myelitis, and neural enhancement.30 A prospective study31 of 90 children assessed at a median of 112 days post–SARS-CoV-2 infection found 60% of symptoms were associated with functional impairment at 1–7 months.

The COVID-19 pandemic is also associated with MIS‐C, which shares common characteristics with Kawasaki disease.32 MIS‐C33 associated with COVID-19 presented with toxic shock–like symptoms, hypoxia‐ischemia, elevation of inflammatory markers, and increased incidence of end-organ damage, including the heart,34 kidneys, and other organs.35 Most of these patients were treated with intravenous immunoglobulin (IVIG) or steroids, the recommended interventions for Kawasaki disease. Most patients either fully recovered or showed considerable improvement after treatment. Neurologic involvement was also reported in approximately 35% of cases.33,39 Among neurologic symptoms, headaches, meningism, confusion, seizures, muscular weakness, encephalopathy, short-term memory, agitation, and altered mental health status were most common.36 Several single case studies also reported incidences of MIS‐C, wherein some rare neurologic manifestations37–47 including acute cerebrovascular accidents, reversible splenial lesions, GBS,48 benign intracranial hypertension, meningoencephalitis,49 autoimmune encephalitis, acute disseminated encephalomyelitis, cranial nerve palsies,50 increased intracranial pressure,45 and transverse myelitis were recorded in addition to the commonly reported symptoms.

Underlying Mechanisms Responsible for the Neuropsychiatric Outcomes of COVID‐19

The underlying cellular and molecular mechanisms attributing to the neuroinvasiveness and neurovirulence of SARS‐CoV‐2 remain poorly understood. Several theories include the direct neurotropism or neuroinvasive potential of SARS‐CoV‐2. It may also be a consequence of a systemic inflammatory response triggered by the viral infection. Additionally, vascular and prothrombotic effects of SARS‐CoV‐2 on the CNS or peripheral nervous system vasculature might act as a contributing factor. Lastly, immune‐mediated para-infectious or post-infectious autoimmune effect post–SARS-CoV-2 might play an important role.46 Knowledge of the underlying mechanisms associated with neurologic manifestations of COVID‐19 is critical for the development of safe and effective therapeutics. Amid the absence of data and serious limitations in the current body of research, the findings in adults point toward a significant unaccounted impact on the development and health of children.17

Emerging Research, Challenges, and Limitations of Understanding These Findings

At the beginning of the COVID-19 pandemic, parents and clinicians were unclear about the clinical symptomatology and when to seek medical help. However, the increasing global burden of COVID-19 and the presence of delayed neuropsychiatric symptoms has highlighted the potential for a serious public health crisis among children and adolescents. Altogether, these studies highlight the importance of monitoring prolonged neuropsychiatric manifestations in this population.

Recent studies have recognized the challenges in distinguishing long-term symptoms caused by SARS-CoV-2 infection from pandemic-related symptoms. A Danish study51 reported that the long COVID symptoms could not be attributed to the indirect psychological effects of social isolation, but most cases resolve within 1–5 months. An Italian cross-sectional study52 of 129 children who tested positive for SARS-CoV-2 infection found that about 43% experienced at least 1 symptom more than 60 days after their initial infection. The common symptoms were fatigue, muscle and joint pain, headache, insomnia, respiratory problems, and palpitations. A striking and unexpected finding was with asymptomatic or mildly symptomatic children who also developed chronic, persisting symptoms. There are limitations to these results52 given the cross-sectional design of the study and relatively short follow-up period, but they underscore the lack of any clear pattern in these symptoms.

One large cohort study53 in the United Kingdom (CLoCk Study) found that symptoms were reported equally by children who tested positive and who tested negative for COVID-19. Therefore, multidisciplinary approaches were recommended given both physical and mental health symptoms presented concurrently. The calls for holistic approaches for long COVID have been echoed by another UK cohort study,54 as most patients recovered in 56 days. A linked study55 of nationwide register data from Norway in 1.3 million children and adolescents found that those aged 1–5 years utilized primary health care services for a longer period after COVID-19 without increasing burden on health care delivery. The most common symptoms were fatigue and dyspnea with a slight male predominance, and symptoms were more often observed in older children, possibly due to better language abilities.55 The pattern of long COVID is of remitting and relapsing nature.13

There are also many methodological issues within the lower level of supporting evidence. The clinical presentations have marked inter-subject variability; therefore, it is difficult to account for the heterogeneity. Respondent bias is likely since symptoms are reported by the parents or caregivers. There are also concerns about underreporting due to the highly overlapping nature56 of clinical symptomatology. The relapsing and remitting clinical course of SARS-CoV-2 has not been reported or accounted for, which affects the true estimates of long COVID.57 In addition, not having a control group in the studies of children with other illnesses or infections may affect overall results. Finally, the US Centers for Disease Control and Prevention is not tracking mild COVID-19 breakthrough illnesses and so might miss many cases that lead to long COVID.58

Interventions: Prevention, Accommodations, and Treatment Strategies

Researchers have utilized the best available evidence using a modified Delphi process to define long COVID in children as an illness that “occurs in young people with a history of confirmed SARS-CoV-2 infection, with at least one persisting physical symptom for a minimum duration of 12 weeks after initial testing that cannot be explained by an alternative diagnosis.”59(p11) And, interestingly, waxing and waning of symptoms is more widely accepted.60

Long COVID is now a disability under the Americans with Disabilities Act, Section 504, and Section 1557.61 Given the serious nature of these impairments and their overall impact on the functioning of children, the US Department of Education’s Office for Civil Rights and Office of Special Education and Rehabilitative Services has also recognized long COVID as a disability. It comes under 2 Federal laws, Section 504 of the Rehabilitation Act of 1973 (Section 504) and Parts B and C of the Individuals with Disabilities Education Act.62

There are reports of a surge in the COVID-19 rehabilitation clinics and specialist services across various tertiary centers in the United States. The number of patients seeking medical care has increased exponentially since the Delta and Omicron variants emerged.63 In the United Kingdom, there are reportedly 80 clinics run by the National Health Service to treat long COVID–related symptoms with multidisciplinary approaches for both adults and children.64

The experts have called for widespread vaccination as a preventive measure to contain the burden of long COVID in children. UK government data suggest a 13% decrease in self-reported symptoms among those who already had long COVID after the first dose and a further 9% reduction after the second dose.65 In 2021, the US Congress allocated the National Institutes of Health (NIH) $1.15 billion over 4 years to study the long-term health consequences of SARS-CoV-2 infection. The NIH granted the first awards for a long COVID research program called RECOVER, which will collect data on vaccinated children and adolescents—the missing information from current studies.66 These are steps in the right direction to address the knowledge gap and critical issues in the methodology of the research evidence.

CONCLUSION

Long COVID or post–SARS-CoV-2 neuropsychiatric manifestations are widely accepted in adults, and emerging evidence supports its presence in child and adolescent populations. With the emergence of new variants and higher rates of infection among children and adolescents, there is a gap in the information about the true estimates of long COVID. Knowledge of the trends of overall duration, pathophysiology, risk factors, and impairments in social and academic areas is critical to understanding the burden of long COVID in children and adolescents. The role of clinical monitoring with multidisciplinary approaches for physical problems, reasonable academic accommodations, preventive vaccinations, and mental health support are a few strategies to consider amid this rapidly evolving issue.

Submitted: December 15, 2021; accepted March 9, 2022.
Published online: April 26, 2022.
Disclosure of off-label usage: The authors have determined that, to the best of their knowledge, no investigational information about pharmaceutical agents or device therapies that is outside US Food and Drug Administration–approved labeling has been presented in this activity.
Relevant financial relationships: Drs M. Gupta, N. Gupta, and Esang have no personal affiliations or financial relationships with any commercial interest to disclose relative to this article.
Funding/support: None.

Clinical Points

  • Long COVID in children and adolescents is a distinct clinical condition that presents in relapsing and remitting patterns and is recognized cross-culturally with a mixed range of highly variable symptoms within 60 days of SARS-CoV-2 infection.
  • Many who tested negative for COVID-19 also had long COVID symptoms with impairments similar to those who tested positive.
  • Epidemiology, risk factors, and mechanisms are largely unknown, and although most children and adolescents recover from long COVID within 6 months, many suffer from persistent illness and impairments.
  • Vaccinations may play a role in prevention of long COVID in children and adolescents, and multidisciplinary specialized COVID rehabilitation clinics are a step in the right direction.
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  1. Clarion Psychiatric Center, Clarion, Pennsylvania
  2. Corresponding author: Mayank Gupta, MD, Clarion Psychiatric Center, 2 Hospital Drive, Clarion, PA 16214 ([email protected]).
  3. Reynolds Memorial Hospital, Glendale, West Virginia
  4. Clarion Psychiatric Center, Clarion, Pennsylvania
  1. Zimmermann P, Curtis N. Why is COVID-19 less severe in children? a review of the proposed mechanisms underlying the age-related difference in severity of SARS-CoV-2 infections. Arch Dis Child. 2020;106(5):429–439. PubMed CrossRef
  2. Meade J. Mental health effects of the COVID-19 pandemic on children and adolescents: a review of the current research. Pediatr Clin North Am. 2021;68(5):945–959. PubMed CrossRef
  3. Lu X, Zhang L, Du H, et al; Chinese Pediatric Novel Coronavirus Study Team. SARS-CoV-2 infection in children. N Engl J Med. 2020;382(17):1663–1665. PubMed
  4. Xu J, Zhong S, Liu J, et al. Detection of severe acute respiratory syndrome coronavirus in the brain: potential role of the chemokine mig in pathogenesis. Clin Infect Dis. 2005;41(8):1089–1096. PubMed
  5. Kim JE. Neurological complications during treatment of Middle East respiratory syndrome. 2017;13(3):227–233.
  6. Karnik M, Beeraka NM, Uthaiah CA, et al. A review on SARS-CoV-2-induced neuroinflammation, neurodevelopmental complications, and recent updates on the vaccine development. Mol Neurobiol. 2021;58(9):4535–4563. PubMed CrossRef
  7. Dubé M, Le Coupanec A, Wong AHM, et al. Axonal transport enables neuron-to-neuron propagation of human coronovirus OC43. J Virol. 2018;92(17):e004041. PubMed CrossRef
  8. Jasti M, Nalleballe K, Dandu V, et al. A review of pathophysiology and neuropsychiatric manifestations of COVID-19. J Neurol. 2021;268(6):2007–2012. PubMed
  9. Sudre CH, Murray B, Varsavsky T, et al. Attributes and predictors of long COVID. Nat Med. 2021;27(4):626–631. PubMed CrossRef
  10. Xie Q, Liu XB, Xu YM, et al. Understanding the psychiatric symptoms of COVID-19: a meta-analysis of studies assessing psychiatric symptoms in Chinese patients with and survivors of COVID-19 and SARS by using the Symptom Checklist-90-Revised. Transl Psychiatry. 2021;11(1):290. PubMed CrossRef
  11. Troyer EA, Kohn JN, Hong S. Are we facing a crashing wave of neuropsychiatric sequelae of COVID-19? neuropsychiatric symptoms and potential immunologic mechanisms. Brain Behav Immun. 2020;87:34–39. PubMed CrossRef
  12. Soriano JB, Murthy S, Marshall JC, et al. WHO Clinical Case Definition Working Group on post-COVID-19 condition. A clinical case definition of post-COVID-19 condition by a Delphi consensus [published online ahead of print December 21, 2021]. Lancet Infect Dis. 2021:S1473-3099(21)00703-9. PubMed
  13. Davis HE, Assaf GS, Mccorkell L, et al. Characterizing long COVID in an international cohort: 7 months of symptoms and their impact. 2021;38:101019. PubMed
  14. Cattaneo A, Haroon E, Su KP, et al. Why we do need a new gold open access journal called “Brain, Behavior, and Immunity–Health.” Brain Behav Immun. 2020;83:1–2. PubMed
  15. Rogers JP, Chesney E, Oliver D, et al. Psychiatric and neuropsychiatric presentations associated with severe coronavirus infections: a systematic review and meta-analysis with comparison to the COVID-19 pandemic. Lancet Psychiatry. 2020;7(7):611–627. PubMed CrossRef
  16. Varatharaj A, Thomas N, Ellul MA, et al; CoroNerve Study Group. Neurological and neuropsychiatric complications of COVID-19 in 153 patients: a UK-wide surveillance study. Lancet Psychiatry. 2020;7(10):875–882. PubMed CrossRef
  17. Munblit D, Bobkova P, Spiridonova E, et al; Sechenov StopCOVID Research Team. Incidence and risk factors for persistent symptoms in adults previously hospitalized for COVID-19. Clin Exp Allergy. 2021;51(9):1107–1120. PubMed CrossRef
  18. Kozlov M. Does Omicron hit kids harder? scientists are trying to find out [published online ahead of print February 4, 2022]. Nature. 2022. PubMed CrossRef
  19. Mao L, Jin H, Wang M, et al. Neurologic manifestations of hospitalized patients with coronavirus disease 2019 in Wuhan, China. JAMA Neurol. 2020;77(6):683–690. PubMed CrossRef
  20. Helms J, Kremer S, Merdji H, et al. Neurologic features in severe SARS-CoV-2 infection. N Engl J Med. 2020;382(23):2268–2270. PubMed CrossRef
  21. Nalleballe K, Reddy Onteddu S, Sharma R, et al. Spectrum of neuropsychiatric manifestations in COVID-19. Brain Behav Immun. 2020;88:71–74. PubMed CrossRef
  22. Taquet M, Geddes JR, Husain M, et al. 6-month neurological and psychiatric outcomes in 236 379 survivors of COVID-19: a retrospective cohort study using electronic health records. Lancet Psychiatry. 2021;8(5):416–427. PubMed CrossRef
  23. Taquet M, Luciano S, Geddes JR, et al. Bidirectional associations between COVID-19 and psychiatric disorder: retrospective cohort studies of 62,354 COVID-19 cases in the USA. Lancet Psychiatry. 2021;8(2):130–140. PubMed CrossRef
  24. Munblit D, Simpson F, Mabbitt J, et al. Legacy of COVID-19 infection in children: long-COVID will have a lifelong health/economic impact. Arch Dis Child. 2022;107(3):e2.
  25. Buonsenso D, Pujol FE, Munblit D, et al. Clinical characteristics, activity levels and mental health problems in children with long COVID: a survey of 510 children. [published online ahead of print March 9, 2021]. Preprints. 2021. CrossRef
  26. Ludvigsson JF. Case report and systematic review suggest that children may experience similar long-term effects to adults after clinical COVID-19. Acta Paediatr. 2021;110(3):914–921. PubMed
  27. LaRovere KL, Riggs BJ, Poussaint TY, et al. Neurologic involvement in children and adolescents hospitalized in the United States for COVID-19 or multisystem inflammatory syndrome. JAMA Neurol. 2021;78(5):536–547. PubMed CrossRef
  28. Pavone P, Ceccarelli M, Marino S, et al. SARS-CoV-2–related pediatric acute-onset neuropsychiatric syndrome. Lancet Child Adolesc Health. 2021;5(6):e19–e21. PubMed CrossRef
  29. Nathan N, Prevost B, Corvol H. Atypical presentation of COVID-19 in young infants. Lancet. 2020;395(10235):1481. PubMed CrossRef
  30. Lindan CE, Mankad K, Ram D, et al. Neuroimaging manifestations in children with SARS-CoV-2 infection: a multinational, multicentre collaborative study. Lancet Child Adolesc Health. 2021;5(3):167–177. PubMed CrossRef
  31. Ashkenazi-Hoffnung L, Shmueli E, Ehrlich S, et al. Long COVID in children: observations from a designated pediatric clinic. Pediatr Infect Dis J. 2021;40(12):e509–e511. PubMed CrossRef
  32. Chen TH. Neurological involvement associated with COVID-19 infection in children. J Neurol Sci. 2020;418:117096. PubMed CrossRef
  33. Hutchison L, Plichta AM, Lerea Y, et al. Neuropsychiatric symptoms in an adolescent boy with multisystem inflammatory syndrome in children. Psychosomatics. 2020;61(6):739–744. PubMed CrossRef
  34. Belhadjer Z, Méot M, Bajolle F, et al. Acute heart failure in multisystem inflammatory syndrome in children in the context of global SARS-CoV-2 pandemic. Circulation. 2020;142(5):429–436. PubMed CrossRef
  35. Henderson LA, Canna SW, Friedman KG, et al. American College of Rheumatology Clinical Guidance for multisystem inflammatory syndrome in children associated with SARS – CoV-2 and hyperinflammation in pediatric COVID-19: version 1. Arthritis Rheumatol. 2020;72(11):1791–1805. PubMed
  36. Abdel-Mannan O, Eyre M, Löbel U, et al. Neurologic and radiographic findings associated with COVID-19 infection in children. JAMA Neurol. 2020;77(11):1440–1445. PubMed CrossRef
  37. Feldstein LR, Rose EB, Horwitz SM, et al. Multisystem inflammatory syndrome in US children and adolescents [published online ahead of print 2020]. N England J Med. 2020;383(4):334–36.  PubMed CrossRef
  38. Pouletty M, Borocco C, Ouldali N, et al. Paediatric multisystem inflammatory syndrome temporally associated with SARS- CoV-2 mimicking Kawasaki disease (Kawa- COVID-19): a multicentre cohort. Ann Rheum Dis. 2020;79(8):999–1006. PubMed
  39. Dufort EM, Koumans EH, Chow EJ, et al. Multisystem inflammatory syndrome in children in New York State. N Engl J Med. 2020;383:347–358. PubMed
  40. Chiotos K, Bassiri H, Behrens EM, et al. Multisystem inflammatory syndrome in children during the coronavirus 2019 pandemic: a case series. 2020;9(3):393–398. PubMed
  41. Siracusa L, Cascio A, Giordano S, et al. Neurological complications in pediatric patients with SARS-CoV-2 infection: a systematic review of the literature. Ital J Pediatr. 2021;47(1):123. PubMed
  42. Lin JE, Asfour A, Sewell TB, et al. Neurological issues in children with COVID-19. Neurosci Lett. 2021;743:135567. PubMed CrossRef
  43. Verdoni L, Mazza A, Gervasoni A, et al. An outbreak of severe Kawasaki-like disease at the Italian epicentre of the SARS-CoV-2 epidemic: an observational cohort study. Lancet. 2020;395(10239):1771–1778. PubMed
  44. Abel D, Shen MY, Abid Z, et al. Encephalopathy and bilateral thalamic lesions in a child with MIS-C associated with COVID-19. Neurology. 2020;95(16):745–748. PubMed
  45. Baccarella A, Linder A, Spencer R, et al. Increased intracranial pressure in the setting of multisystem inflammatory syndrome in children, associated with COVID-19. Pediatr Neurol. 2021;115:48–49. PubMed CrossRef
  46. Stafstrom CE, Jantzie LL. COVID-19: neurological considerations in neonates and children. Children (Basel). 2020;7(9):133. PubMed CrossRef
  47. Whittaker E, Bamford A, Kenny J, et al. Clinical characteristics of 58 children with a pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2. JAMA. 2020;324(3):259–269.  PubMed CrossRef
  48. Manji HK, George U, Mkopi NP, et al. Case report Guillain-Barré syndrome associated with COVID-19 infection. Pan Afr Med J. 2020;35(suppl 2):118. PubMed
  49. Toubiana J, Poirault C, Corsia A, et al. Kawasaki-like multisystem inflammatory syndrome in children during the COVID-19 pandemic in Paris, France: prospective observational study. BMJ. 2020;369:m2094. PubMed CrossRef
  50. Roussel A, Germanaud D, Bouchoucha Y, et al. Cranial polyneuropathy as the first manifestation of a severe COVID-19 in a child. Pediatr Blood Cancer. 2021;68(3):e28707. PubMed CrossRef
  51. Borch L, Holm M, Knudsen M, et al. Long COVID symptoms and duration in SARS-CoV-2 positive children: a nationwide cohort study. Eur J Pediatr. 2022;9:1–11. PubMed CrossRef
  52. Buonsenso D, Munblit D, De Rose C, et al. Preliminary evidence on long COVID in children. Acta Paediatr. 2021;110(7):2208–2211. PubMed CrossRef
  53. Stephenson T, Pinto Pereira SM, Shafran R, et al; CLoCk Consortium. Physical and mental health 3 months after SARS-CoV-2 infection (long COVID) among adolescents in England (CLoCk): a national matched cohort study. Lancet Child Adolesc Health. 2022;(22):S2352–S4642. PubMed CrossRef
  54. Molteni E, Sudre CH, Canas LS, et al. Illness duration and symptom profile in symptomatic UK school-aged children tested for SARS-CoV-2. Lancet Child Adolesc Health. 2021;5(10):708–718. PubMed CrossRef
  55. Magnusson K, Skyrud KD, Suren P, et al. Health care use in 700,000 children and adolescents for six months after COVID-19: before and after register based cohort study. BMJ. 2022;376:e066809. PubMed CrossRef
  56. Zimmermann P, Pittet LF, Curtis N. How common is long COVID in children and adolescents? Pediatr Infect Dis J. 2021;40(12):e482–e487. PubMed CrossRef
  57. Gurdasani D, Akrami A, Bradley VC, et al. Long COVID in children. Lancet Child Adolesc Health. 2022;6(1):e2. PubMed CrossRef
  58. Bell ML, Catalfamo CJ, Farland LV, et al. Post-acute sequelae of COVID-19 in a non-hospitalized cohort: results from the Arizona CoVHORT. PLoS One. 2021;16(8):e0254347. PubMed CrossRef
  59. Stephenson T, Allin B, Nugawela MD, et al; CLoCk Consortium. Long COVID (post-COVID-19 condition) in children: a modified Delphi process. Arch Dis Child. 2022:archdischild-2021-323624. PubMed CrossRef >
  60. Stephenson T, Shafran R, De Stavola B, et al. Long-COVID - the physical and mental health of children and non-hospitalized young people 3 months after SARS-CoV-2 infection; a national matched cohort study (The CLoCk) Study. BMJ Open. 2021;11(8):e052838. PubMed
  61. Guidance on “Long COVID” as a Disability Under the ADA, Section 504, and Section 1557. HHS.gov website. Accessed February 24, 2022. https://www.hhs.gov/civil-rights/for-providers/civil-rights-covid19/guidance-long-covid-disability/index.html
  62. US Department of Education Issues Resource on Students and Children with Long COVID. Individuals with Disabilities Education Act website. Published July 27, 2021. Accessed February 22, 2022. https://sites.ed.gov/idea/u-s-department-of-education-issues-resource-on-students-and-children-with-long-covid/
  63. Golden H. ‘The scariest thing’: the children living with long COVID. The Guardian website. Published February 2, 2022. Accessed February 24, 2022. https://www.theguardian.com/society/2022/feb/01/children-long-covid-coronavirus
  64. Iacobucci G. Long COVID: “Holistic” approach is best, given range of symptoms, say researchers. BMJ. 2022;376:o336. PubMed CrossRef
  65. Coronavirus (COVID-19) vaccination and self-reported long COVID in the UK: 25 October 2021. GOV.UK website. Accessed February 24, 2022. https://www.gov.uk/government/statistics/coronavirus-covid-19-vaccination-and-self-reported-long-covid-in-the-uk-25-october-2021
  66. RECOVER Builds Large Nationwide Study Population for Research on ‘Long COVID.’ NIH Record website. Published October 1, 2021. Accessed February 24, 2022. https://nihrecord.nih.gov/2021/10/01/recover-builds-large-nationwide-study-population-research-long-covid