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Article

Neurological Manifestations of Acute SARS-CoV-2 Infection in Pediatric Patients: A 3-Year Study on Differences between Pandemic Waves

by
Iolanda Cristina Vivisenco
1,2,
Andreea Lescaie
1,2,*,
Ana Dragomirescu
2,
Ioana Cătălina Ioniță
2,
Irina Florescu
3,
Bogdan Ciocea
3,
Andreea Rodica Grama
1,2,
Maria-Dorina Crăciun
4,5,
Carmen-Daniela Chivu
4,5,
Coriolan Emil Ulmeanu
1,2 and
Viorela Gabriela Nițescu
1,2
1
Discipline of Pediatrics, Faculty of Dentistry, Carol Davila University of Medicine and Pharmacy, 17-23 Plevnei Road, 010221 Bucharest, Romania
2
Department of Pediatrics, Grigore Alexandrescu Clinical Emergency Hospital for Children, 30-32 Iancu de Hunedoara Road, 011743 Bucharest, Romania
3
Department of Neurology, Grigore Alexandrescu Clinical Emergency Hospital for Children, 30-32 Iancu de Hunedoara Road, 011743 Bucharest, Romania
4
Department of Epidemiology, Faculty of Medicine, Carol Davila University of Medicine and Pharmacy, 17-23 Plevnei Road, 010221 Bucharest, Romania
5
Department of Infection Prevention and Control, Grigore Alexandrescu Clinical Emergency Hospital for Children, 30-32 Iancu de Hunedoara Road, 011743 Bucharest, Romania
*
Author to whom correspondence should be addressed.
Viruses 2024, 16(6), 967; https://doi.org/10.3390/v16060967
Submission received: 14 May 2024 / Revised: 4 June 2024 / Accepted: 14 June 2024 / Published: 17 June 2024
(This article belongs to the Special Issue COVID-19 Complications and Co-infections)

Abstract

:
This study analyzed the neurological manifestation profiles of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection across pandemic waves in pediatric patients. The study collected data on patients aged between 0 and 18 years, diagnosed with acute SARS-CoV-2 infection, admitted to a pediatric tertiary hospital between 1 March 2020 and 28 February 2023. This study included 1677 patients. Neurological manifestations were noted in 10% (n = 168) of patients with a median age of 3.2 years (interquartile range: 1–11.92). Neurological manifestations were significantly associated with the pandemic waves (p = 0.006) and age groups (p < 0.001). Seizures were noted in 4.2% of cases and reached an increasing frequency over time (p = 0.001), but were not associated with age groups. Febrile seizures accounted for the majority of seizures. Headache was reported in 2.6% of cases and had similar frequencies across the pandemic waves and age groups. Muscular involvement was noted in 2% of cases, reached a decreasing frequency over time (p < 0.001), and showed different frequencies among the age groups. Neurological manifestations of acute SARS-CoV-2 infection exhibit distinct patterns, depending on the pandemic wave and patient age group. The Wuhan and Omicron waves involved the nervous system more often than the other waves.

1. Introduction

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has received widespread attention from healthcare professionals and researchers worldwide [1,2]. The likelihood of pediatric patients contracting SARS-CoV-2 was lower in comparison to adults, and they generally exhibited either asymptomatic or milder symptoms [3,4,5,6,7]. Nevertheless, there were instances in which children experienced severe and atypical illnesses [4].
The field of neurology has generated significant interest in relation to SARS-CoV-2 infection, with over 5000 original articles and reviews published on this topic [8,9,10,11]. The occurrence of neurological manifestations in coronavirus disease 2019 (COVID-19) was not surprising, as Middle East respiratory syndrome and severe acute respiratory syndrome coronavirus 1 have been associated with a variety of neurological signs and symptoms [12,13,14]. However, SARS-CoV-2 was associated with neurological manifestations that were not commonly reported with other coronaviruses [15].
It was initially believed that neurological manifestations were rare in pediatric patients [16,17,18]. As research has pointed out the range of neurological symptoms, it has become evident that these symptoms occur frequently in children as well, although their types differ substantially from those identified in adults [19,20,21,22,23,24]. It is worth noting that children generally displayed a higher frequency of seizures, whereas adults were more prone to experiencing strokes [19,20,21,22,23,24].
The neurological presentations of SARS-CoV-2 variants may differ [25]. To the best of the authors knowledge, there is a lack of studies investigating all variants of concern for variant-specific neurological manifestations, despite the necessity of such research [26]. Therefore, this study aimed to provide a thorough characterization of the neurological manifestations associated with all SARS-CoV-2 variants of concern reported in the pediatric population.

2. Materials and Methods

2.1. Study Design

This study analyzed patients under 18 years of age diagnosed with acute SARS-CoV-2 infection who were admitted to a pediatric hospital between 1 March 2020, and 28 February 2023. This study conformed to the ethical principles of the Declaration of Helsinki for medical research. The guardians of all the patients provided informed consent for participation in the study. Approval was obtained from the Ethical Committee of the hospital prior to the commencement of the study (8336/20 March 2023).
The electronic medical records of the hospital informatic system were screened using the keywords “COVID-19”, “SARS-CoV-2”, and U07.1 (COVID-19, virus identified) code of the International Statistical Classification of Diseases and Related Health Problems, Tenth Revision, Australian Modification (ICD-AM-10). According to the national COVID-19 case definition adapted from the World Health Organization (WHO), each patient enrolled in the study was mandated to have a confirmed SARS-CoV-2 infection through either a rapid antigen test or polymerase chain reaction (PCR) test [27,28]. Patients diagnosed with COVID-19 within 90 days of an initial positive test were counted as one occurrence to reduce prolonged positive test results.
The medical records of each patient (n = 1714) were subjected to rigorous examination by a panel of two pediatrician investigators to determine whether neurological symptoms were present at the time of admission or during hospitalization. Subsequently, a team of two pediatric neurologists reviewed the association between neurological manifestations and SARS-CoV-2 infection. Consequently, two groups were defined: the first group included patients with at least one new-onset neurological symptom or exacerbation of a pre-existing neurological condition, while the second group included patients without neurological symptoms.
It was impossible to retrospectively establish the exact ages of 37 patients because they were foreign citizens with refugee status. Consequently, these cases were excluded, and it should be noted that none of these patients exhibited any neurological symptoms.
The primary objective of this study was to assess the variation in the frequency of neurological manifestations across the waves of the SARS-CoV-2 pandemic in Romania. The secondary objectives were to identify the frequency and nature of the neurological manifestations in children infected with SARS-CoV-2 and to evaluate their variations across different age groups.

2.2. Data Collection

Data from electronic medical records were recorded on a spreadsheet using a pre-established coding system according to the recommendations of McNett et al. [29]. The extracted information included demographic characteristics, date of admission, pre-existing neurological diseases, clinical manifestations exhibited at the time of admission and throughout the hospitalization period, and paraclinical features (SARS-CoV-2 rapid antigen or PCR test, pressure and composition of cerebrospinal fluid, cerebral imaging studies, and electroencephalogram).
Data regarding the national reports of SARS-CoV-2 genomic sequences were obtained from the Global Data Sharing Initiative [30,31] and the National Institute of Public Health [32]. The national reports of individuals with COVID-19 by age group were obtained from the WHO COVID-19 detailed surveillance data dashboard [33].

2.3. Definitions

The pandemic wave term describes a period within the occurrence of a specific SARS-CoV-2 variant that was detected in over 50% of the genomic sequences analyzed in Romania (Table 1). The first wave of the virus did not receive an official designation from the WHO and has been referred to in previous research as Wuhan, Wild-type, or the original strain. In this study, the Wuhan label was used.
Patients were categorized according to age based on the WHO global reports, which included age groups ranging from 0 to 4, 5 to 9, 10 to 14, and 15 to 19 years [33]. However, since the study center only admitted individuals under the age of 18, no patients aged 19 years were included in the study. As a result, the respective age group was named 15 to 18 years.
The new-onset neurological manifestations included in this study were seizures, headache, muscular involvement, vasovagal syncope, apnea, anosmia, dysgeusia, encephalopathy, idiopathic endocranial hypertension, ischemic stroke, ataxia, peripheral neuropathy, and sleep myoclonus. The case definitions for these manifestations were in accordance with the scientific literature and are provided in Table A1 of Appendix A [34,35,36,37,38,39,40,41,42,43,44,45,46].
Exacerbation of a pre-existing neurological condition was considered to be the manifestation of symptoms associated with the underlying disease in an individual who received treatment for that disease.

2.4. Statistical Analysis

All statistical analyses were performed using the XL-STAT version 2023.5 (Addinsoft, Paris, France) and VassarStats version SCR-010263 (Vassar College, New York, NY, USA) software. The relationships between neurological features and pandemic waves or age groups were assessed using the chi-square test (Yates correction [47]). When the criteria for reporting the chi-square test results were not met, Fisher’s exact two-tailed test (Freeman–Halton extension [48]) was performed. The trend of neurological manifestation frequencies among age groups or pandemic waves was assessed using the Cochran–Armitage test [49,50]. Standardized residual analyses were performed, and the results were reported as z-scores (z) [51]. The significance level was set at a p-value of less than 0.05, with an Alpha risk of 5%.
The study used Pearson correlation analysis to assess whether the number of patients hospitalized monthly at the study center was representative of the Romanian population aged between 0 and 19 years infected with SARS-CoV-2.

3. Results

This study comprised 1677 cases of acute SARS-CoV-2 infection, with a 10% (n = 168) frequency of neurological manifestations. The study sample accurately represented the frequency of COVID-19 in Romania for patients under 19 years of age, showing a strong correlation between the monthly number of hospitalized patients at the study center and the cumulative number of patients in Romania (Table 2).

3.1. All Neurological Manifestations

The age range of patients with neurological manifestations during acute SARS-CoV-2 infection was broad, from 9 days to 17.58 years of age, with a median age of 3.2 years (interquartile range: 1–11.92).
Neurological symptoms appeared within the first 24 h of respiratory or digestive issues in 58% of cases (98/168), between 24 and 48 h in 2% (n = 3), between 48 and 72 h in 8% (n = 14), and after more than 72 h in 9% (n = 15) of cases. Seven patients (4%) did not experience respiratory or digestive issues at the onset of neurological symptoms, and the temporal relationship between these symptoms was not documented in the remaining 18% (n = 31).
The association between neurological manifestations and SARS-CoV-2 waves was statistically significant (p = 0.006); however, no time trend was observed (Table 3). As shown in Figure 1a, the frequency of these manifestations was higher during the Wuhan and Omicron waves.
Neurological symptoms showed a relationship with age groups (p < 0.001; Figure 2a), with the frequency increasing with age (p < 0.001; Table 4). Moreover, neurological manifestations were significantly associated with SARS-CoV-2 waves in patients aged between 0 and 4 years (χ2(3) = 8.05, p = 0.045; Table A2 of the Appendix A).

3.2. Seizures

Seizures were documented in 4.2% (n = 71) of cases, with 54 instances being febrile seizures. Five patients experienced new-onset seizures without fever, of whom only one was subsequently diagnosed with epilepsy, whereas the others had a normal electroencephalogram. Seizures occurred as an exacerbation of pharmacologically controlled epilepsy in 12 (0.7%) cases, three of which developed status epilepticus.
Statistical analysis revealed a notable disparity in the occurrence of seizures across the various waves of the COVID-19 pandemic (p = 0.012), with a higher frequency observed as new waves emerged (p = 0.001; Table 3). Figure 1b shows the trend of seizure frequency, which was lowest in the Wuhan wave (z = −1.96) and highest in the Omicron wave (z = +2.01).
Seizures were not associated with age group, and no trend was observed (Table 4). Analysis of seizures across SARS-CoV-2 waves within each age group showed a significant time trend for patients aged between 0 and 4 years (χ2(1) = 6.32, p = 0.012; Table A2 of Appendix A).

3.3. Febrile Seizures

Of the total number of patients diagnosed with seizures, 54 experienced febrile seizures during the acute SARS-CoV-2 infection. Of these, 37 were diagnosed with simple febrile seizures, 13 with complex febrile seizures, and four with febrile status epilepticus.
The frequency of febrile seizures reached a minimum in the Wuhan wave and a maximum in the Omicron wave. Febrile seizures were significantly associated with SARS-CoV-2 waves (p = 0.010), with a clear trend over time (p = 0.002; Table 3).
Analysis of seizures across SARS-CoV-2 waves within each age group showed a significant time trend for patients aged between 0 and 4 years (χ2(1) = 6.24, p = 0.013; Table A2 of Appendix A).

3.4. Headache

Headache was reported in 43 patients (2.6%), with a similar frequency between the SARS-CoV-2 waves (Table 3). However, it is worth noting that the highest frequency was registered during the Wuhan wave (Figure 1c).
The analysis of headaches across age groups showed that the highest frequency was reported for patients aged between 10 and 14 years (Figure 2c), although a statistically significant difference was not observed (Table 4).

3.5. Muscular Involvement

Muscular involvement was reported in 2% (n = 34) of cases, including myalgia in 23 cases, hypotonia in six, and myositis in five.
A significant correlation was observed between muscular involvement and the various waves of the pandemic (p < 0.001), which also demonstrated a time trend (p < 0.001; Table 3). Notably, the highest frequency of muscular involvement was recorded during the Wuhan wave, whereas the lowest frequency was observed during the Omicron wave (Figure 1d).
The frequency of muscular involvement was significantly different among the age groups (Figure 2d) and increased with age (Table 4).

3.6. Other Neurological Manifestations

Vasovagal syncope occurred in 1.1% (n = 18) of the patients, out of which 10 were triggered by fever. All cases occurred in Wuhan (n = 5) or in Omicron waves (n = 13). An age-repartition analysis revealed that nine patients were in the 0 to 4 age group, two were in the 5 to 9 age group, four were in the 10 to 14 age group, and three were in the 15 to 18 age group.
Apnea was documented in 0.7% (n = 12) of cases, being a solitary event in nine patients and a recurrent occurrence in three. The age of the patients affected by apnea was below 4 months, except for a 1-year-old and a 4-month-old girl with Aicardi syndrome.
Anosmia and dysgeusia were reported in seven patients (0.4%) diagnosed during the Wuhan and Delta waves. The ages of the patients ranged from 8 to 17 years old.
Encephalopathy was documented in 0.4% (n = 7) of the cases and was reported to affect patients aged between 1 month and 5 years.
Idiopathic intracranial hypertension was reported during the Omicron wave in five infants (0.3%) aged between 2 and 9 months.
An ischemic stroke was diagnosed in a 2-month-old male infant born to a mother with thrombophilia and hospitalized for an acute SARS-CoV-2 infection.
Certain neurological disorders were documented in only one patient: ataxia during the Omicron wave in a 13-year-old boy, peripheral neuropathy during the Omicron wave in an 11-year-old girl, and sleep myoclonus during the Delta wave in an 11-year-old boy.
Exacerbations of pre-existing conditions occurred in children with epilepsy (n = 13), myasthenia gravis (n = 1), and multiple sclerosis (n = 1).

4. Discussion

The findings of this study showed that 10% of pediatric patients with acute SARS-CoV-2 infection experienced neurological manifestations. Although the neurological manifestations were consistent across all pandemic waves, the frequency of these manifestations varied based on the wave of the pandemic and the age of the patient. The neurological manifestations described in this study have been documented in scientific literature, including rare cases [52,53,54,55,56,57,58,59,60,61,62,63].
The neurological consequences of COVID-19 according to age have been explored in several studies with varying results [64,65,66]. The literature review revealed inconsistencies in the classification of age and the absence of age groups used in the official WHO reports. However, this study adopted the same age groups as those presented in the WHO’s global reports on COVID-19 to facilitate data comparisons that may arise in future research in this area [33].
The frequency of neurological manifestations in pediatric patients with acute SARS-CoV-2 infection was lower in this study (10%) than in most previous studies (13.5–40%) [19,67,68,69], but was in line with the findings of Antoon et al. [64] (7%). The frequency of neurological manifestations in pediatric patients may vary due to differences in methodologies, such as variations in upper age limits, analyzed period, and inclusion of multisystem inflammatory syndrome.
Proust et al. [70] identified distinct patterns of central nervous system (CNS) cell invasion in Wuhan and Omicron variants, which may explain the different neurological manifestations associated with each variant. To the best of our knowledge, this is the only real-world study currently available to validate the findings of Proust et al. [70] regarding the increased neurological involvement of the Wuhan and Omicron variants compared with the Alpha and Delta variants.
Studies that analyzed the neurological manifestations during the Omicron wave and compared them with previous periods or other SARS-CoV-2 variants found evidence to support the increase in neurological symptoms [66,71,72,73]. In contrast, Antoon et al. [64] noted more neurological manifestations during the Wuhan wave than during the Omicron wave. This difference may be due to the shorter Omicron spread considered by Antoon et al. [64].
Seizures, including de novo status epilepticus, have been frequently reported in pediatric patients with COVID-19 [74,75]. Moreover, some studies have indicated that seizures are the most common neurological manifestations [66]. The reported frequencies varied across studies, ranging from 0.06% to 61.9% [12,66]. The present study showed a striking increase in seizure frequency during the Omicron wave compared to prior waves. This result was unexpected, as Omicron was believed to be less severe than prior variants [10]. According to Cho et al. [76], seizure frequency decreases with age. However, our study revealed that the highest frequency of seizures was observed in the 5–9 age group (7.8%).
This study, as well as others [64,73], discovered that febrile seizures were the most common neurological manifestation among pediatric patients diagnosed with COVID-19. It is worth noting that Kim et al. [77] highlighted the potential of COVID-19 to cause more severe febrile-induced seizures.
Previous studies have reported headache frequencies ranging from 10% to 20% [12,76], while this study found a frequency of 2.6%. This disparity may be attributable to the subjective nature of headaches and the inability of young children to communicate this symptom.
It is important to note that this study revealed a lower frequency of muscular involvement in patients with COVID-19 than previously reported [12,76]. This discrepancy may be attributed to variations in clinical examination techniques.
This study had several strengths. First, although this study is not the first to evaluate the neurological manifestations of SARS-CoV-2 among various waves or age groups, it has the longest study duration among similar studies. Second, this study involved a comprehensive comparison of all the prevailing SARS-CoV-2 variants in Romania. Third, although our study is limited by single center data, it has the merit of including a cohort that reflects the dissemination of COVID-19 in Romania.
This study has certain limitations. The inclusion of only inpatients may lead to underreporting of neurological symptoms in children with mild or asymptomatic COVID-19. Furthermore, the study may underestimate the self-reported symptoms, especially in younger children who cannot communicate subjective sensations. The reported frequencies may also have been influenced by the retrospective and unicentric nature of this study. Additionally, the specific SARS-CoV-2 variant for each patient could not be determined, as they were categorized based on the prevalent variant in Romania during the corresponding period. It should also be noted that the neurological symptoms detailed in this study are not specific to acute infection with SARS-CoV-2.
This study highlights the necessity of conducting multicenter studies with similar methodologies to gain a comprehensive understanding of the age- and variant-specific neurological manifestations of acute SARS-CoV-2 infection. Such studies can contribute to understanding the potential risks associated with long COVID-19 syndrome.

5. Conclusions

Neurological manifestations of acute SARS-CoV-2 infection exhibited distinct patterns depending on the pandemic wave and patient age group. The first and last waves (Wuhan and Omicron) displayed a greater tendency towards neurological manifestations when compared to the other waves. However, the profiles of the neurological manifestations varied between these two waves. While seizures were more prevalent in the Omicron wave, headaches, and muscular involvement were more common in the Wuhan wave. This observation aligns with prior research that has highlighted the distinct mechanisms of neurological involvement associated with the Wuhan and Omicron variants.

Author Contributions

Conceptualization, I.C.V., A.L., C.E.U. and V.G.N.; methodology, I.C.V., A.L. and V.G.N.; software, A.L. and C.-D.C.; validation, I.C.V., V.G.N., I.F., B.C. and M.-D.C.; formal analysis, I.C.V., A.L., A.D., I.C.I. and C.-D.C.; investigation, I.C.V., A.L., A.D., I.C.I., A.R.G., I.F. and B.C.; resources, V.G.N., M.-D.C. and C.E.U.; data curation, I.C.V., I.F., B.C., M.-D.C. and V.G.N.; writing—original draft preparation, A.L., A.D., I.C.I. and A.R.G.; writing—review and editing, I.C.V., I.F., B.C., C.-D.C., M.-D.C., C.E.U. and V.G.N.; visualization, A.L. and V.G.N.; supervision, V.G.N.; project administration, I.C.V. and V.G.N. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki, and approved by the Ethics Committee of Grigore Alexandrescu Clinical Emergency Hospital for Children (protocol number 8336; date of approval: 20 March 2023).

Informed Consent Statement

Informed consent was obtained from the guardians of all the patients involved in the study.

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request due to privacy concerns.

Acknowledgments

Publication of this paper was supported by the University of Medicine and Pharmacy Carol Davila, through the institutional program Publish not Perish.

Conflicts of Interest

The authors declare no conflicts of interest.

Appendix A

Table A1. Definition used for diagnosis of new-onset neurological manifestations during acute SARS-CoV-2 infection.
Table A1. Definition used for diagnosis of new-onset neurological manifestations during acute SARS-CoV-2 infection.
Neurological
Manifestation
Definition
SeizuresA paroxysmal manifestation involving sudden loss of consciousness and uncontrollable movements, or generalized hypotonia. A pediatric neurologist determined the diagnosis through medical history and clinical presentation.
Simple febrile
seizures
A single episode of generalized seizures occurring within a 24-h period and lasting less than 15 min, in the presence of focal signs accompanied by a fever (temperature above 38 °C) in children under 5 years of age without any underlying neurological diseases [34,35].
Complex febrile seizuresSeizures that occur in children with an underlying neurological disease or prolonged (over 15 min), focal, or multiple seizures in a 24-h period in children without any underlying neurological diseases. These seizures are accompanied by a fever [35].
Established status epilepticusContinuous seizures or recurrent seizures without consciousness recovery over a period of 30 min or more in children who do not have fever [36,37,38].
Febrile status
epilepticus
Continuous seizures or recurrent seizures without consciousness recovery over a period of 30 min or more, accompanied by fever [35].
HeadacheA clinical diagnosis was made after the exclusion of any additional underlying disorders other than SARS-CoV-2 infection in patients who reported headaches during medical examination.
Muscular
involvement
Myalgia or hypotonia reported by the patient or detected by the pediatrician during the medical examination.
Vasovagal
syncope
A temporary, non-traumatic loss of consciousness is triggered by certain factors [39].
ApneaInterruption of breathing for a brief period, accompanied by bradycardia, cyanosis, or pallor [40].
AnosmiaPartial or complete loss of smell was reported by the patient or patient guardian during the medical examination.
DysgeusiaTaste disturbances reported by the patient or patient guardian during a medical examination.
EncephalopathyA diffuse brain condition characterized by altered mental status (lethargy, reduced consciousness, or changes in personality) that persist for over 24 h. The diagnosis was established after the exclusion of any underlaying disorder other than SARS-CoV-2 infection [41,42].
Idiopathic
endocranial
hypertension
(suggested)
Signs and symptoms of increased intracranial pressure, with a normal composition of cerebrospinal fluid, and normal brain imaging [43].
Ischemic strokeSudden onset of neurological symptoms such as hemiplegia or any focal neurological signs, followed by the identification of ischemic stroke through cerebral imaging.
AtaxiaThe disruption of posture and movement coordination. The diagnosis was made by a pediatric neurologist through a medical history and clinical presentation [44].
Peripheral
neuropathy
Self-limited symptoms of peripheral motor or sensory nerve fibers were reported during a medical examination [45].
Sleep MyoclonusInvoluntary and benign brief movements that occur during sleep. The diagnosis was made by a pediatric neurologist based on clinical presentation after ruling out other medical conditions [46].
Table A2. Frequency of neurological manifestations and their association with pandemic waves for each age group.
Table A2. Frequency of neurological manifestations and their association with pandemic waves for each age group.
Wuhan
Wave
%, n
Alpha
Wave
%, n
Delta
Wave
%, n
Omicron
Wave
%, n
χ2(3)
(p Value)
χ2(1)
(p Value)
All neurological manifestations
0–4 years 6.6 (9)2.9 (3)5.2 (13)9.1 (71)8.05 (0.045)4.12 (0.043)
5–9 years 14.3 (2)0 (0)7.1 (2)19 (15)3.81 (0.28) *1.35 (0.25) *
10–14 years 22.2 (6)5.3 (1)22.5 (9)23.6 (17)3.22 (0.36) *0.54 (0.46) *
15–18 years 29 (9)8.3 (1)8.6 (3)19.4 (7)5.57 (0.13)1.23 (0.27)
Seizures
0–4 years 1.5 (2)2.9 (3)2.8 (7)5.5 (43)7.23 (0.06)6.32 (0.012)
5–9 years 0 (0)0 (0)7.1 (2)10.1 (8)2.49 (0.48) *2.37 (0.12) *
10–14 years 3.7 (1)0 (0)2.5 (1)4.2 (3)0.94 (0.82) *0.17 (0.68) *
15–18 years 0 (0)0 (0)2.9 (1)0 (0)2.28 (0.52) *0.08 (0.78) *
Febrile seizures
0–4 years 1.5 (2)1.9 (2)2 (5)4.9 (38)7.38 (0.050)6.24 (0.013)
5–18 years 0 (0)0 (0)1.9 (2)2.7 (5)2.93 (0.40) *2.76 (0.10) *
Headache
5–9 years7.1 (1)0 (0)3.6 (1)7.6 (6)1.15 (0.77) *0.24 (0.63) *
10–14 years18.5 (5)5.3 (1)12.5 (5)13.9 (10)1.75 (0.63) *0.03 (0.86) *
15–18 years9.7 (3)8.3 (1)5.7 (2)11.1 (4)NA (0.90) #0.01 (0.93) *
Muscular involvement
0–4 years3.7 (5)1 (1)1.2 (3)0.4 (3)13.72 (0.003) *11.56 (<0.001) *
5–9 years7.1 (1)0 (0)3.6 (1)3.8 (3)0.73 (0.87) *0.09 (0.76) *
10–14 years3.7 (1)0 (0)5 (2)5.6 (4)1.16 (0.76) *0.50 (0.48) *
15–18 years22.6 (7)8.3 (1)0 (0)5.6 (2)11.22 (0.01) *7.33 (0.007) *
Note: * These values should be interpreted with caution as they do not meet the reporting criteria for the chi-square test. # The p-value is derived from the Fisher exact test.

References

  1. Finsterer, J. Neurological complications of COVID-19 in pediatric patients require comprehensive evaluation. J. Neurovirol. 2022, 28, 339–340. [Google Scholar] [CrossRef] [PubMed]
  2. Taheri, L.; Gheiasi, S.F.; Taher, M.; Basirinezhad, M.H.; Shaikh, Z.A.; Dehghan Nayeri, N. Clinical features of COVID-19 in newborns, infants, and children: A systematic review and meta-analysis. Compr. Child Adolesc. Nurs. 2022, 45, 137–155. [Google Scholar] [CrossRef]
  3. Couture, A.; Lyons, B.C.; Mehrotra, M.L.; Sosa, L.; Ezike, N.; Ahmed, F.S.; Brown, C.M.; Yendell, S.; Azzam, I.A.; Katić, B.J.; et al. Severe Acute Respiratory Syndrome Coronavirus 2 Seroprevalence and Reported Coronavirus Disease 2019 Cases in US Children, August 2020–May 2021. Open Forum Infect. Dis. 2022, 9, ofac044. [Google Scholar] [CrossRef] [PubMed]
  4. Parcha, V.; Booker, K.S.; Kalra, R.; Kuranz, S.; Berra, L.; Arora, G.; Arora, P. A retrospective cohort study of 12,306 pediatric COVID-19 patients in the United States. Sci. Rep. 2021, 11, 10231. [Google Scholar] [CrossRef] [PubMed]
  5. Sinaei, R.; Pezeshki, S.; Parvaresh, S.; Sinaei, R. Why COVID-19 is less frequent and severe in children: A narrative review. World J. Pediatr. 2021, 17, 10–20. [Google Scholar] [CrossRef]
  6. Viner, R.M.; Ward, J.L.; Hudson, L.D.; Ashe, M.; Patel, S.V.; Hargreaves, D.; Whittaker, E. Systematic review of reviews of symptoms and signs of COVID-19 in children and adolescents. Arch. Dis. Child. 2021, 106, 802–807. [Google Scholar] [CrossRef] [PubMed]
  7. Williams, N.; Radia, T.; Harman, K.; Agrawal, P.; Cook, J.; Gupta, A. COVID-19 Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in children and adolescents: A systematic review of critically unwell children and the association with underlying comorbidities. Eur. J. Pediatr. 2021, 180, 689–697. [Google Scholar] [CrossRef] [PubMed]
  8. Chan, K.I.P.; Ignacio, K.H.D.; Omar, A.T.; Khu, K.J.O. Top 100 most cited neurologic and neurosurgical articles on COVID-19: A bibliometric analysis. World Neurosurg. 2022, 157, e137–e147. [Google Scholar] [CrossRef] [PubMed]
  9. Crăciun, M.-D.; Nițescu, G.V.; Golumbeanu, M.; Tănase, A.-A.; Pițigoi, D.; Săndulescu, O.; Crăciun, P.; Enciu, B.G.; Bălănescu, R.N.; Ulici, A. mRNA COVID-19 Vaccine Reactogenicity among Healthcare Workers: Results from an Active Survey in a Pediatric Hospital from Bucharest, January–February 2021. Vaccines 2022, 10, 836. [Google Scholar] [CrossRef]
  10. Zhang, Q.; Li, J.; Weng, L. A bibliometric analysis of COVID-19 publications in neurology by using the visual mapping method. Front. Public Health 2022, 10, 937008. [Google Scholar] [CrossRef]
  11. Verrotti, A.; Mazzocchetti, C.; Iannetti, P. Definitive pathognomonic signs and symptoms of paediatric neurological COVID-19 are still emerging. Acta Paediatr. 2021, 110, 1774–1777. [Google Scholar] [CrossRef] [PubMed]
  12. Cavallieri, F.; Sellner, J.; Zedde, M.; Moro, E. Neurologic complications of coronavirus and other respiratory viral infections. Handb. Clin. Neurol. 2022, 189, 331–358. [Google Scholar] [CrossRef] [PubMed]
  13. Correia, A.O.; Feitosa, P.W.G.; Moreira, J.L.d.S.; Nogueira, S.R.; Fonseca, R.B.; Nobre, M.E.P. Neurological manifestations of COVID-19 and other coronaviruses: A systematic review. Neurol. Psychiatry Brain Res. 2020, 37, 27–32. [Google Scholar] [CrossRef] [PubMed]
  14. Kwong, K.C.N.K.; Mehta, P.R.; Shukla, G.; Mehta, A.R. COVID-19, SARS and MERS: A neurological perspective. J. Clin. Neurosci. 2020, 77, 13–16. [Google Scholar] [CrossRef] [PubMed]
  15. Khatoon, F.; Prasad, K.; Kumar, V. COVID-19 associated nervous system manifestations. Sleep Med. 2022, 91, 231–236. [Google Scholar] [CrossRef] [PubMed]
  16. Panda, P.K.; Sharawat, I.K.; Panda, P.; Natarajan, V.; Bhakat, R.; Dawman, L. Neurological complications of SARS-CoV-2 infection in children: A systematic review and meta-analysis. J. Trop. Pediatr. 2021, 67, fmaa070. [Google Scholar] [CrossRef] [PubMed]
  17. Boronat, S. Neurologic care of COVID-19 in children. Front. Neurol. 2020, 11, 613832. [Google Scholar] [CrossRef]
  18. Kim, Y.; Walser, S.A.; Asghar, S.J.; Jain, R.; Mainali, G.; Kumar, A. A comprehensive review of neurologic manifestations of COVID-19 and management of pre-existing neurologic disorders in children. J. Child Neurol. 2021, 36, 324–330. [Google Scholar] [CrossRef]
  19. LaRovere, K.L.; Riggs, B.J.; Poussaint, T.Y.; Young, C.C.; Newhams, M.M.; Maamari, M.; Walker, T.C.; Singh, A.R.; Dapul, H.; Hobbs, C.V.; et al. Neurologic Involvement in Children and Adolescents Hospitalized in the United States for COVID-19 or Multisystem Inflammatory Syndrome. JAMA Neurol. 2021, 78, 536–547. [Google Scholar] [CrossRef]
  20. Li, C.; Verduzco-Gutierrez, M. Neurologic and neuromuscular sequelae of COVID-19. Phys. Med. Rehabil. Clin. N. Am. 2023, 34, 539–549. [Google Scholar] [CrossRef]
  21. Ray, S.T.J.; Abdel-Mannan, O.; Sa, M.; Fuller, C.; Wood, G.K.; Pysden, K.; Yoong, M.; McCullagh, H.; Scott, D.; McMahon, M.; et al. Neurological manifestations of SARS-CoV-2 infection in hospitalised children and adolescents in the UK: A prospective national cohort study. Lancet Child Adolesc. Health 2021, 5, 631–641. [Google Scholar] [CrossRef] [PubMed]
  22. Schober, M.E.; Robertson, C.L.; Wainwright, M.S.; Roa, J.D.; Fink, E.L. COVID-19 and the pediatric nervous system: Global collaboration to meet a global need. Neurocritical Care 2021, 35, 283–290. [Google Scholar] [CrossRef] [PubMed]
  23. Valderas, C.; Méndez, G.; Echeverría, A.; Suarez, N.; Julio, K.; Sandoval, F. COVID-19 and neurologic manifestations: A synthesis from the child neurologist’s corner. World J. Pediatr. 2022, 18, 373–382. [Google Scholar] [CrossRef] [PubMed]
  24. Meppiel, E.; Peiffer-Smadja, N.; Maury, A.; Bekri, I.; Delorme, C.; Desestret, V.; Gorza, L.; Hautecloque-Raysz, G.; Landre, S.; Lannuzel, A.; et al. Neurologic manifestations associated with COVID-19: A multicentre registry. Clin. Microbiol. Infect. 2021, 27, 458–466. [Google Scholar] [CrossRef] [PubMed]
  25. Misra, S.; Kolappa, K.; Prasad, M.; Radhakrishnan, D.; Thakur, K.T.; Solomon, T.; Michael, B.D.; Winkler, A.S.; Beghi, E.; Guekht, A.; et al. Frequency of neurologic manifestations in COVID-19: A systematic review and meta-analysis. Neurology 2021, 97, e2269–e2281. [Google Scholar] [CrossRef] [PubMed]
  26. Stafstrom, C.E. Neurological effects of COVID-19 in infants and children. Dev. Med. Child Neurol. 2022, 64, 818–829. [Google Scholar] [CrossRef] [PubMed]
  27. The National Institute of Public Health. The National Supervision and Control Center of Communicable Diseases. Methodologies. Available online: https://insp.gov.ro/centrul-national-de-supraveghere-si-control-al-bolilor-transmisibile-cnscbt/metodologii/ (accessed on 1 May 2023).
  28. World Health Organization. COVID-19 Case Definition. Available online: https://www.who.int/publications/i/item/WHO-2019-nCoV-Surveillance_Case_Definition-2022.1 (accessed on 1 May 2023).
  29. McNett, M.; Fink, E.L.; Schober, M.; Mainali, S.; Helbok, R.; Robertson, C.L.; Mejia-Mantilla, J.; Kurtz, P.; Righy, C.; Roa, J.D.; et al. The Global Consortium Study of Neurological dysfunction in COVID-19 (GCS-NeuroCOVID): Development of case report forms for global use. Neurocrit. Care 2020, 33, 793–828. [Google Scholar] [CrossRef] [PubMed]
  30. Khare, S.; Gurry, C.; Freitas, L.; Schultz, M.B.; Bach, G.; Diallo, A.; Akite, N.; Ho, J.; Lee, R.T.; Yeo, W.; et al. GISAID’s role in pandemic response. China CDC Wkly. 2021, 3, 1049–1051. [Google Scholar] [CrossRef] [PubMed]
  31. The Global Initiative on Sharing All Influenza Data. COVID-19 Variants Dashboard. Available online: https://gisaid.org/hcov-19-variants-dashboard/ (accessed on 1 May 2023).
  32. The National Institute of Public Health. The National Supervision and Control Center of Communicable Diseases. Weekly COVID-19 Reports. Available online: https://insp.gov.ro/centrul-national-de-supraveghere-si-control-al-bolilor-transmisibile-cnscbt/informari-saptamanale/ (accessed on 1 May 2023).
  33. World Health Organization. WHO Global COVID-19 Detailed Surveillance Dashboard. Available online: https://data.who.int/dashboards/covid19/more-resources?n=c (accessed on 1 May 2023).
  34. Subcommittee on Febrile Seizures; American Academy of Pediatrics. Neurodiagnostic evaluation of the child with a simple febrile seizure. Pediatrics 2011, 127, 389–394. [Google Scholar] [CrossRef]
  35. Eilbert, W.; Chan, C. FFebrile seizures: A review. J. Am. Coll. Emerg. Physicians Open 2022, 3, e12769. [Google Scholar] [CrossRef]
  36. Trinka, E.; Cock, H.; Hesdorffer, D.; Rossetti, A.O.; Scheffer, I.E.; Shinnar, S.; Shorvon, S.; Lowenstein, D.H. A definition and classification of status epilepticus--Report of the ILAE Task Force on Classification of Status Epilepticus. Epilepsia 2015, 56, 1515–1523. [Google Scholar] [CrossRef]
  37. Abend, N.S.; Loddenkemper, T. Pediatric status epilepticus management. Curr. Opin. Pediatr. 2014, 26, 668–674. [Google Scholar] [CrossRef]
  38. Freilich, E.R.; Schreiber, J.M.; Zelleke, T.; Gaillard, W.D. Pediatric status epilepticus: Identification and evaluation. Curr. Opin. Pediatr. 2014, 26, 655–661. [Google Scholar] [CrossRef] [PubMed]
  39. Brignole, M.; Moya, A.; de Lange, F.J.; Deharo, J.-C.; Elliott, P.M.; Fanciulli, A.; Fedorowski, A.; Furlan, R.; Kenny, R.A.; Martín, A.; et al. 2018 ESC Guidelines for the diagnosis and management of syncope. Eur. Heart J. 2018, 39, 1883–1948. [Google Scholar] [CrossRef] [PubMed]
  40. Committee on Fetus and Newborn. American Academy of Pediatrics. Apnea, sudden infant death syndrome, and home monitoring. Pediatrics 2003, 111, 914–917. [Google Scholar] [CrossRef] [PubMed]
  41. Venkatesan, A.; Tunkel, A.R.; Bloch, K.C.; Lauring, A.S.; Sejvar, J.; Bitnun, A.; Stahl, J.-P.; Mailles, A.; Drebot, M.; Rupprecht, C.E.; et al. Case definitions, diagnostic algorithms, and priorities in encephalitis: Consensus statement of the international encephalitis consortium. Clin. Infect. Dis. 2013, 57, 1114–1128. [Google Scholar] [CrossRef] [PubMed]
  42. Garg, R.K.; Paliwal, V.K.; Gupta, A. Encephalopathy in patients with COVID-19: A review. J. Med. Virol. 2021, 93, 206–222. [Google Scholar] [CrossRef]
  43. Friedman, D.I. The pseudotumor cerebri syndrome. Neurol. Clin. 2014, 32, 363–396. [Google Scholar] [CrossRef]
  44. Bodranghien, F.; Bastian, A.; Casali, C.; Hallett, M.; Louis, E.D.; Manto, M.; Mariën, P.; Nowak, D.A.; Schmahmann, J.D.; Serrao, M.; et al. Consensus Paper: Revisiting the Symptoms and Signs of Cerebellar Syndrome. Cerebellum 2016, 15, 369–391. [Google Scholar] [CrossRef] [PubMed]
  45. Lehmann, H.C.; Wunderlich, G.; Fink, G.R.; Sommer, C. Diagnosis of peripheral neuropathy. Neurol. Res. Pract. 2020, 2, 20. [Google Scholar] [CrossRef]
  46. Caviness, J.N. Myoclonus. Continuum 2019, 25, 1055–1080. [Google Scholar] [CrossRef] [PubMed]
  47. Yates, F. Contingency tables involving small numbers and the χ2 test. Suppl. J. R. Stat. Soc. 1934, 1, 217. [Google Scholar] [CrossRef]
  48. Freeman, G.H.; Halton, J.H. Note on an exact treatment of contingency, goodness of fit and other problems of significance. Biometrika 1951, 38, 141–149. [Google Scholar] [CrossRef] [PubMed]
  49. Cochran, W.G. Some methods for strengthening the common χ2 tests. Biometrics 1954, 10, 417. [Google Scholar] [CrossRef]
  50. Armitage, P. Tests for linear trends in proportions and frequencies. Biometrics 1955, 11, 375. [Google Scholar] [CrossRef]
  51. Ahad, N.A.; Okwonu, F.Z.; Apanapudor, J.S.; Arunaye, F.I.; Ojobor, S.A. Chi-square and adjusted standardised residual analysis. ASM Sci. J. 2023, 18, 1–11. [Google Scholar] [CrossRef]
  52. Schiff, J.; Brennan, C. COVID-19 presenting as a bulging fontanelle. Am. J. Emerg. Med. 2021, 43, 81–82. [Google Scholar] [CrossRef]
  53. Sethuraman, C.M.; Holland, J.M.; Priego, G.M.; Khan, F.M.; Johnson, R.M.B.; Keane, M.M.B. Bulging anterior fontanelle caused by severe acute respiratory syndrome coronavirus-2. Pediatr. Infect. Dis. J. 2023, 42, e4–e5. [Google Scholar] [CrossRef]
  54. Tyagi, K.; Rai, P.; Gautam, A.; Kaur, H.; Kapoor, S.; Suttee, A.; Jaiswal, P.K.; Sharma, A.; Singh, G.; Barnwal, R.P. Neurological manifestations of SARS-CoV-2: Complexity, mechanism and associated disorders. Eur. J. Med. Res. 2023, 28, 307. [Google Scholar] [CrossRef]
  55. Wilpert, N.-M.; Marcelino, A.L.d.A.; Knierim, E.; Incoronato, P.; Sanchez-Sendin, E.; Staudacher, O.; Drenckhahn, A.; Bittigau, P.; Kreye, J.; Prüss, H.; et al. Pediatric de novo movement disorders and ataxia in the context of SARS-CoV-2. J. Neurol. 2023, 270, 4593–4607. [Google Scholar] [CrossRef]
  56. Schneider, S.A.; Desai, S.; Phokaewvarangkul, O.; Rosca, E.C.; Sringean, J.; Anand, P.; Bravo, G.; Cardoso, F.; Cervantes-Arslanian, A.M.; Chovatiya, H.; et al. COVID-19-associated new-onset movement disorders: A follow-up study. J. Neurol. 2023, 270, 2409–2415. [Google Scholar] [CrossRef] [PubMed]
  57. Ben Mohamed, D.; Zouari, R.; Ketata, J.; Nabli, F.; Blel, S.; Ben Sassi, S. Myoclonus status revealing COVID 19 infection. Seizure 2023, 104, 12–14. [Google Scholar] [CrossRef]
  58. Roussel, A.; Germanaud, D.; Bouchoucha, Y.; Ouldali, N.; Vedrenne-Cloquet, M.; Castelle, M.; Baruchel, A. Cranial polyneuropathy as the first manifestation of a severe COVID-19 in a child. Pediatr. Blood Cancer 2021, 68, e28707. [Google Scholar] [CrossRef] [PubMed]
  59. Koh, J.S.; De Silva, D.A.; Quek, A.M.L.; Chiew, H.J.; Tu, T.M.; Seet, C.Y.H.; Hoe, R.H.M.; Saini, M.; Hui, A.C.-F.; Angon, J.; et al. Neurology of COVID-19 in Singapore. J. Neurol. Sci. 2020, 418, 117118. [Google Scholar] [CrossRef] [PubMed]
  60. Stafstrom, C.E.; Jantzie, L.L. COVID-19: Neurological considerations in neonates and children. Children 2020, 7, 133. [Google Scholar] [CrossRef] [PubMed]
  61. Gürlevik, S.L.; Günbey, C.; Ozsurekci, Y.; Oygar, P.D.; Kesici, S.; Gocmen, R.; Aydin, O.; Temucin, Ç.; Tufan, E.; Terzi, K.; et al. Neurologic manifestations in children with COVID-19 from a tertiary center in Turkey and literature review. Eur. J. Paediatr. Neurol. 2022, 37, 139–154. [Google Scholar] [CrossRef] [PubMed]
  62. Tamayo-Múnera, C.; Vizcaino, Z.M.I.; Millán, A.L.T.; Niño-Serna, L.; Alzate, C.G.; Diaz, C.A.V.; Salazar, H.D.H.; Tovar, S.L.G.; Baez, M.C.C.; López-Barón, E. Apnea or cyanosis as COVID-19 initial presentation in newborns. J. Infect. Dev. Ctries 2023, 17, 1401–1406. [Google Scholar] [CrossRef] [PubMed]
  63. Vrushabhendra, S.; Kodavooru, G.A.; Kashyape, P.; Pawar, N. Acute ischemic stroke associated with COVID-19 in a pediatric patient: A case report. Dubai Med. J. 2022, 5, 203–205. [Google Scholar] [CrossRef]
  64. Antoon, J.W.; Hall, M.; Howard, L.M.; Herndon, A.; Freundlich, K.L.; Grijalva, C.G.; Williams, D.J. COVID-19 and Acute Neurologic Complications in Children. Pediatrics 2022, 150, e2022058167. [Google Scholar] [CrossRef] [PubMed]
  65. Abbati, G.; Attaianese, F.; Rosati, A.; Indolfi, G.; Trapani, S. Neurological involvement in children with COVID-19 and MIS-C: A retrospective study conducted for more than two years in a pediatric hospital. Children 2022, 9, 1809. [Google Scholar] [CrossRef]
  66. Yang, D.; Kang, H.-C. Neurological symptoms of SARS-CoV-2 infection in pediatric patients. Ann. Child. Neurol. 2022, 30, 111–119. [Google Scholar] [CrossRef]
  67. Riva, A.; Piccolo, G.; Balletti, F.; Binelli, M.; Brolatti, N.; Verrotti, A.; Amadori, E.; Spalice, A.; Giacomini, T.; Mancardi, M.M.; et al. Acute neurological presentation in children with SARS-CoV-2 infection. Front. Pediatr. 2022, 10, 909849. [Google Scholar] [CrossRef] [PubMed]
  68. Flores-Silva, F.D.; García-Grimshaw, M.; Valdés-Ferrer, S.I.; Vigueras-Hernández, A.P.; Domínguez-Moreno, R.; Tristán-Samaniego, D.P.; Michel-Chávez, A.; González-Duarte, A.; Vega-Boada, F.A.; Reyes-Melo, I.; et al. Neurologic manifestations in hospitalized patients with COVID-19 in Mexico City. PLoS ONE 2021, 16, e0247433. [Google Scholar] [CrossRef] [PubMed]
  69. Fink, E.L.; Robertson, C.L.; Wainwright, M.S.; Roa, J.D.; Lovett, M.E.; Stulce, C.; Yacoub, M.; Potera, R.M.; Zivick, E.; Holloway, A.; et al. Prevalence and Risk Factors of Neurologic Manifestations in Hospitalized Children Diagnosed with Acute SARS-CoV-2 or MIS-C. Pediatr. Neurol. 2022, 128, 33–44. [Google Scholar] [CrossRef] [PubMed]
  70. Proust, A.; Queval, C.J.; Harvey, R.; Adams, L.; Bennett, M.; Wilkinson, R.J. Differential effects of SARS-CoV-2 variants on central nervous system cells and blood-brain barrier functions. J. Neuroinflamm. 2023, 20, 184. [Google Scholar] [CrossRef] [PubMed]
  71. Lu, L.; Chen, L.; Wang, P.; Qi, Z.; Chen, Y.; Wu, X.; Liu, X.; Wang, M.; Li, J.; Yan, B.; et al. Neurological complications during the Omicron COVID-19 wave in China: A cohort study. Eur. J. Neurol. 2024, 31, e16096. [Google Scholar] [CrossRef] [PubMed]
  72. Dimopoulou, D.; Dasoula, F.; Liaska, M.; Eleftheriou, I.; Maritsi, D.; Tsolia, M.; Vartzelis, G. Rise of neurologic manifestations during SARS-CoV-2 Omicron wave in children with COVID-19. Pediatr. Infect. Dis. J. 2023, 42, e128–e129. [Google Scholar] [CrossRef] [PubMed]
  73. Iijima, H.; Kubota, M.; Ogimi, C. Change in seizure incidence in febrile children with COVID-19 in the era of Omicron variant of concern. J. Pediatr. Infect. Dis. Soc. 2022, 11, 514–517. [Google Scholar] [CrossRef] [PubMed]
  74. Ludvigsson, J.F. Convulsions in children with COVID-19 during the Omicron wave. Acta Paediatr. 2022, 111, 1023–1026. [Google Scholar] [CrossRef]
  75. Farley, M.; Zuberi, J. COVID-19 precipitating status epilepticus in a pediatric patient. Am. J. Case Rep. 2020, 21, e925776. [Google Scholar] [CrossRef]
  76. Cho, S.-M.; White, N.; Premraj, L.; Battaglini, D.; Fanning, J.; Suen, J.; Bassi, G.L.; Fraser, J.; Robba, C.; Griffee, M.; et al. Neurological manifestations of COVID-19 in adults and children. Brain 2023, 146, 1648–1661. [Google Scholar] [CrossRef] [PubMed]
  77. Kim, L.; Han, J.Y.; Cho, A.; Kim, H. Complex febrile seizures in children with COVID-19 infection. Ann. Child Neurol. 2023, 31, 137–139. [Google Scholar] [CrossRef]
Figure 1. The association between pandemic waves and (a) all neurological manifestations (n = 168), (b) seizures (n = 71), (c) headaches (n = 43), and (d) muscular involvement (n = 34) in the study population (n = 1677).
Figure 1. The association between pandemic waves and (a) all neurological manifestations (n = 168), (b) seizures (n = 71), (c) headaches (n = 43), and (d) muscular involvement (n = 34) in the study population (n = 1677).
Viruses 16 00967 g001
Figure 2. The association between age groups and (a) all neurological manifestations (n = 168), (b) seizures (n = 71), (c) headache (n = 43), and (d) muscular involvement (n = 34) in the study population (n = 1677).
Figure 2. The association between age groups and (a) all neurological manifestations (n = 168), (b) seizures (n = 71), (c) headache (n = 43), and (d) muscular involvement (n = 34) in the study population (n = 1677).
Viruses 16 00967 g002
Table 1. SARS-CoV-2 pandemic waves in Romania.
Table 1. SARS-CoV-2 pandemic waves in Romania.
Pandemic WavePeriod
Wuhan1 March 2020—31 December 2020
Alpha1 January 2021—30 June 2021
Delta1 July 2021—31 December 2021
Omicron1 January 2022—28 February 2023
Table 2. Pearson coefficient of association between the monthly hospitalized patient count at the study center and the national count among age groups.
Table 2. Pearson coefficient of association between the monthly hospitalized patient count at the study center and the national count among age groups.
Age GroupCOVID-19 Patients at
Study Center
COVID-19 Patients at National LevelPearson r
(95% CI)
p Value
Total (n)Monthly Mean
(SD)
Total
(n)
Monthly Mean
(SD)
0–4 years127632.8
(46.3)
881513896.4
(2448.6)
0.88
(0.72–1.05)
<0.001
5–9 years1293.1
(4.6)
762372117.7
(4434.62)
0.76
(0.54–0.99)
<0.001
10–14 years1583.5
(4.7)
1219873388.5
(7378.4)
0.80
(0.59–1.01)
<0.001
15–19 years1142.6
(2.9)
1171023252.8
(5901.2)
0.54
(0.25–0.84)
0.001
All patients167741.9
(56.5)
40347711207.7
(20929)
0.79
(0.58–1.01)
<0.001
Table 3. Neurological manifestation frequency and their association with the pandemic waves.
Table 3. Neurological manifestation frequency and their association with the pandemic waves.
Wuhan Wave
(n = 208)
Alpha Wave
(n = 143)
Delta Wave
(n = 355)
Omicron Wave
(n = 971)
χ2(3)
(p Value)
χ2(1)
(p Value)
All neurological
manifestations
% (n)
12.5 (26)3.5 (5)7.6 (27)11.3 (110)12.31
(0.006)
0.83
(0.36)
Seizures
% (n)
1.4 (3)2.1 (3)3.1 (11)5.6 (54)10.96
(0.012)
10.15 (0.001)
Febrile seizures
% (n)
1 (2)1.4 (2)2 (7)4.4 (43)11.25
(0.010)
9.80
(0.002)
Headache
% (n)
4.3 (9)1.4 (2)2.5 (9)2.4 (23)3.51
(0.32)
1.24
(0.27)
Muscular involvement
% (n)
6.7 (14)1.4 (2)1.7 (6)1.2 (12)26.71
(<0.001) *
18.95
(<0.001) *
Note: * These values should be interpreted with caution as they do not meet the reporting criteria for the chi-square test.
Table 4. Neurological manifestation frequency and their association with the age groups.
Table 4. Neurological manifestation frequency and their association with the age groups.
0–4 Years
(n = 1276)
5–9 Years
(n = 129)
10–14 Years
(n = 158)
15–18 Years
(n = 114)
χ2(3)
(p Value)
χ2(1)
(p Value)
All neurological
manifestations
% (n)
7.5 (96)14.7 (19)20.9 (33)17.5 (20)39.85
(<0.001)
34.25
(<0.001)
Seizures
% (n)
4.3 (55)7.8 (10)3.2 (5)0.9 (1)7.57
(0.056)
1.85
(0.17)
Febrile seizures
% (n)
3.7 (47)4.7 (6)0 (0)0.9 (1)8.99
(0.029) *
6.04
(0.014) *
Headache
% (n)
NA6.2 (8)13.3 (21)8.8 (10)4.23
(0.12) ^
4.23
(0.12)
Muscular involvement
% (n)
0.9 (12)3.9 (5)4.4 (7)8.8 (10)40.51
(<0.001) *
38.78 (<0.001) *
Note: * These values should be interpreted with caution as they do not meet the reporting criteria for the chi-square test. ^ This value represents the chi-square test results with two degrees of freedom, not three as in the other cells.
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Vivisenco, I.C.; Lescaie, A.; Dragomirescu, A.; Ioniță, I.C.; Florescu, I.; Ciocea, B.; Grama, A.R.; Crăciun, M.-D.; Chivu, C.-D.; Ulmeanu, C.E.; et al. Neurological Manifestations of Acute SARS-CoV-2 Infection in Pediatric Patients: A 3-Year Study on Differences between Pandemic Waves. Viruses 2024, 16, 967. https://doi.org/10.3390/v16060967

AMA Style

Vivisenco IC, Lescaie A, Dragomirescu A, Ioniță IC, Florescu I, Ciocea B, Grama AR, Crăciun M-D, Chivu C-D, Ulmeanu CE, et al. Neurological Manifestations of Acute SARS-CoV-2 Infection in Pediatric Patients: A 3-Year Study on Differences between Pandemic Waves. Viruses. 2024; 16(6):967. https://doi.org/10.3390/v16060967

Chicago/Turabian Style

Vivisenco, Iolanda Cristina, Andreea Lescaie, Ana Dragomirescu, Ioana Cătălina Ioniță, Irina Florescu, Bogdan Ciocea, Andreea Rodica Grama, Maria-Dorina Crăciun, Carmen-Daniela Chivu, Coriolan Emil Ulmeanu, and et al. 2024. "Neurological Manifestations of Acute SARS-CoV-2 Infection in Pediatric Patients: A 3-Year Study on Differences between Pandemic Waves" Viruses 16, no. 6: 967. https://doi.org/10.3390/v16060967

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