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Background:
Systematic Review

Changes in Respiratory Viruses’ Activity in Children During the COVID-19 Pandemic: A Systematic Review

Pediatric Emergency Unit, Santobono-Pausilipon Children’s Hospital, 80129 Naples, Italy
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2025, 14(4), 1387; https://doi.org/10.3390/jcm14041387
Submission received: 27 November 2024 / Revised: 15 February 2025 / Accepted: 17 February 2025 / Published: 19 February 2025
(This article belongs to the Section Clinical Pediatrics)

Abstract

:
Background/Objectives: The impact of the coronavirus disease 2019 (COVID-19) pandemic on health was significant worldwide. The measures adopted to limit the spread of the virus had an indirect effect on the epidemiology of other infectious diseases with similar mechanisms of inter-human transmission. The present literature review analyzed the scenario of pediatric acute respiratory infections in the post-lockdown period compared to the pre-pandemic and lockdown periods. The different patterns of viruses’ outbreaks were evaluated according to the type of local COVID-19 restrictive measures and to the type of pathogen. Methods: Relevant scientific literature published between March 2020 and November 2024 was identified by means of electronic keyword searches in the PubMed, Scopus, and Cochrane Library databases. Results: Worldwide implementation of non-pharmacological public health interventions aimed at limiting the COVID-19 pandemic resulted in a measurable effect on the circulation of other common respiratory viruses, significantly affecting their usual seasonality. Most viruses significantly reduced their activity during the lockdown period but returned to or exceeded historical levels after discontinuation of preventive non-pharmacological measures. For many respiratory viruses, particularly respiratory syncytial virus, an off-season increase was reported. Conclusions: The non-pharmacological interventions, which effectively helped limit the COVID-19 pandemic, resulted in relevant epidemiologic changes in most common respiratory viruses. Given the different seasonality and clinical severity observed for some pathogens after lockdown, possible future off-season or more severe epidemics should be expected.

1. Introduction

Acute respiratory infections (ARIs) are the leading infectious diseases among children worldwide and are significantly associated with pediatric hospitalization and death [1,2,3,4]. The application of multiplex reverse transcriptase polymerase chain reaction (RT-PCR) platforms to the analysis of sputum and deep throat swabs has allowed a better characterization of the etiology of viral ARIs. This kind of technique provides molecular detection of several common respiratory viruses and atypical bacterial pathogens with a turnaround time of few hours [5,6]. The identification of viral etiology allows a better understanding of the clinical features of respiratory tract infections and represents a valuable tool for epidemiological surveillance. Even though its impact on therapeutic strategies may appear limited, an early detection of viral pathogens in children with respiratory symptoms could avoid unnecessary antibiotic therapy, decrease the length of hospitalization, and reduce mortality, particularly from multiple infections [7]. Human rhinovirus/enterovirus (HRV), followed by adenovirus (ADV), has been reported as the commonest viral pathogen detected by PCR techniques in hospitalized children [7]. On the other hand, the significant disease burden and impact of respiratory syncytial virus (RSV) at a hospital level is well known [8].
The coronavirus disease 2019 (COVID-19) epidemic had an enormous impact on health worldwide since 2019. Soon after the outbreak, the epidemiology of infectious diseases dramatically changed. During the first pandemic year (pre-vaccine year), preventive interventions were mostly non-pharmacological (social distancing, mask-wearing, shelter-in-place, travel restrictions, school closure, etc.) [9,10]. Nevertheless, in addition to their undeniable impact on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) diffusion, these measures resulted in preventing the spread of several other respiratory pathogens that are transmitted by large droplets from infected to susceptible people [11]. A review including studies up to 2019 analyzed the use of surgical masks during the common peak seasons of respiratory infections [9]. Unexpectedly, the authors observed that mask wearing was ineffective at limiting the spread of influenza [9]. Nevertheless, this finding may be explained by poor study design, insufficiently powered studies arising from low viral circulation in some studies, poor compliance with mask wearing, the quality of the masks used, self-contamination of the mask by hands, and a lack of protection from eye exposure to respiratory droplets [9]. Hand hygiene measures seemed to have a more important protective effect on the spread of respiratory viruses [9].
Routine long-term implementation of most non-pharmacological interventions may be problematic outside hospital settings and in non-pandemic periods. More effectively, the strict measures adopted during the COVID-19 pandemic would be applied in the event of future epidemics from other respiratory viruses. Indeed, large epidemics from respiratory viruses are likely to emerge, probably due to the re-circulation of viruses within immunologically naïve populations of infants born from mothers who have not reinforced their immunity [12].
The aim of this review is to describe the scenario of ARIs in the post-lockdown period compared to the pre-COVID-19 and lockdown periods, and to analyze the different patterns of outbreaks of the most relevant respiratory viruses in children according to the type of local COVID-19 restrictive measures.

2. Materials and Methods

2.1. Search Strategy

We carried out an electronic keyword literature search for English articles published on the epidemiology and clinical spectrum of pediatric ARIs from the beginning of the COVID-19 pandemic (March 2020) up to November 2024. The search strategy followed the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines [13]. The PubMed, Cochrane Library, and Scopus databases were searched for articles with full-text availability using the following query: “respiratory tract infection OR influenza OR respiratory syncytial virus OR rhinovirus OR parainfluenza OR human metapneumovirus OR adenovirus OR bocavirus OR coronavirus OR SARS-CoV-2 AND children”. When available, the filters “humans” and “child: birth-18 years” were applied. The article search and data extraction were carried out in January 2025. The study protocol was not recorded in an official register.

2.2. Study Selection

All duplicates were removed through manual screening. Reference lists from the retrieved articles were manually searched to identify further eligible studies. Four independent reviewers (M.M., E.B., R.R., L.C.) screened the titles and abstracts, and eligibility was assessed in consensus in the event of disagreement among them. The full text of the selected studies underwent a further screening.

2.3. Inclusion and Exclusion Criteria

The inclusion criteria were as follows: (1) studies addressing epidemiology of one or more respiratory viruses in children during and/or after the COVID-19 pandemic; (2) the focus of the research was the impact of the COVID-19 pandemic on pediatric respiratory infections or the changes observed in the epidemiology of respiratory viruses throughout the pandemic years. The exclusion criteria were as follows: (1) irrelevance to the research topic; (2) articles addressing respiratory infections only before the COVID-19 pandemic; (3) articles focusing on specific populations (e.g., oncologic patients, neurologically impaired children); (4) articles mainly focusing on the genomic aspects of respiratory pathogens; (5) unavailability of free full-text.

2.4. Data Extraction

To confirm the relevance of each included study, the authors extracted the following data, which were reported in a data collection form: name of the first author, title, country, year of publication, study design.

2.5. Risk of Bias Assessment

The Newcastle–Ottawa Quality Assessment Scale [14] was used for assessing the risk of bias for each study. Three reviewers (M.M., E.B, A.G.) independently performed the evaluation. According to the assigned score, the studies were classified as low (<5 points), moderate (5–7 points), and high (>7 points) quality.

2.6. Outcomes

The analysis of the included studies considered the prevalence of various respiratory viruses in children during and after the COVID-19 pandemic as the main outcome. The change in this prevalence in relationship with the different phases of the pandemic represented the focus of the review.

3. Results

After screening the databases, a total of 49,498 articles were returned. Of these, 155 articles were assessed for eligibility, and, after the full text evaluation, 148 were ultimately included in the review (Figure 1). A complete list of the included articles, with the first author’s name, country, and study design is reported in Supplementary Table S1. Supplementary Table S2 includes seven articles initially assessed for eligibility but ultimately excluded from the review after full text evaluation.

3.1. Characteristics of Included Studies

Most included studies had a retrospective observational design, with a minority of prospective observational studies (21/148), nine reviews and two commentaries. Approximately half of the included studies (71/137) were single-centered, whereas 66 were performed in multiple centers. The studies were conducted in 41 different countries. Quality was rated as high for 28 studies, and 56 were graded as moderate (Supplementary Table S1).

3.2. ARIs During the First Lockdown

At the beginning of COVID-19 pandemic, the adopted measures implemented to contain the spread of SARS-CoV-2 infection included stay-at-home-orders, school and business closures, travel restrictions, border closures and mandatory face coverings. These measures also affected the circulation of other respiratory viruses in almost all countries [10,15,16,17,18,19,20,21,22,23]. Not only the spread, but also the seasonality of most respiratory pathogens was altered during the first half of 2020 [16].

3.2.1. Respiratory Syncytial Virus

RSV is the most common cause of acute bronchiolitis that may have a severe clinical presentation, particularly in high-risk patients, such as preterm infants or children with comorbidities [24,25]. RSV causes epidemics during the fall and winter seasons in temperate countries, as well as during the hot rainy seasons in tropical climates [24].
The suppression of RSV activity during the COVID-19 pandemic has been reported in almost all countries [11,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40]. The European Centre for Disease Prevention and Control registered a fall in the detection of RSV from 2000 to 2500 cases per week at peak incidence during the previous four seasonal outbreaks (2016–2017, 2017–2018, 2018–2019, 2019–2020) to less than 700 cases per week in 2020–2021 [41]. The reduction in bronchiolitis led to a substantial reduction in pediatric emergency department visits [30] and in pediatric intensive care unit (PICU) admissions for severe cases [30,42,43].
In a study involving seven US pediatric medical centers, RSV detections in 2020 stopped after week 15 [26]. In 2020 no RSV cases were detected in weeks 15–18 (between 5 and 30 April) in either the emergency department or inpatient settings. The decrease in RSV-positive ARIs in the community mitigation period in 2020 compared to the same period in prior surveillance seasons was greater than 70% [26]. Although a multitude of papers on the epidemiology of RSV during COVID-19 are available, very few studies analyzed the clinical spectrum of rare cases of RSV infection during the lockdown [44].

3.2.2. Influenza

Since February 2019, no seasonal influenza epidemic peak has been observed. In Australia, the reduction in influenza virus (IFV) detections in 2020 compared to 2017–2019 was 90% and 93% in children aged 0–4 and 5–14 years, respectively [45]. Another Australian study from Melbourne reported a 77.3% reduction in the proportion of positive IFV-A detections and an 89.4% reduction in the proportion of positive IFV-B detections during the COVID-19 restriction period compared to pre-pandemic data [46]. There were no IFV-A detections from week 14, 2020, and no IFV-B detections from week 17, 2020—2 weeks after the beginning of the initial lockdown. Similarly, levels of IFV transmission were very low in 2020 in a number of countries all over the world [40,47,48,49,50,51]; this was also true in China, where peaks of IFV-A infection appeared in February 2018 and 2019; the 2020 peak of IFV-A infection was reported in December [52].
A study from Korea analyzed the impact of social distancing on influenza activity in the community, collecting data on clinical influenza-like syndrome, laboratory parameters, and hospitalized cases. The authors reported substantially lower overall influenza activity in 2019–2020 compared to recent influenza seasons (2016–2017 and 2018–2019). The epidemic season terminated 8 to 12 weeks earlier, leading to a decrease in the influenza epidemic duration by 6–12 weeks. The influenza activity peak was lower, with 49.8 influenza-like illnesses/1000 visits compared to 71.9–86.2/1000 visits in previous seasons [53].

3.2.3. Other Viral Infections

Most studies from several geographic areas reported a relevant decrease in the detection of respiratory viruses in children with symptoms of ARIs during the pandemic [54,55,56,57,58,59]. A study from Japan reported a drastic reduction in human metapneumovirus (HMPV) and Mycoplasma pneumoniae during the school closure period. In addition, almost no patients with these infections were hospitalized during the same period [54].
In a large study from China investigating the presence of eight viral pathogens (IFV, RSV, human parainfluenza virus, ADV, human coronavirus, human bocavirus, and HRV) in 314 sentinel hospitals, the impact of non-pharmacological interventions was evaluated in three subsequent periods based on the timeline of major interventions for containing the COVID-19 epidemic in China: 23 January to 7 April 2020 (Phase I), when the city of Wuhan was placed under lockdown, 8 April to 31 August 2020 (Phase II), when nationwide non-pharmacological interventions were relaxed but schools remained closed, and 1 September 2020 to 22 January 2021 (Phase III), when schools were re-opened in most provinces [16]. Overall, they observed the largest drop in the annual cumulative positive rate for IFV, with a reduction of 87.6%, followed by 70.6% for HMPV, 47% for ADV, and 32.3% for the parainfluenza virus [16]. Positive rates of almost all viruses rose significantly above historical levels during Phase III.
Interestingly, reports from different geographic settings have highlighted that, unlike most respiratory viruses, the drop in HRV prevalence was less marked when compared to other pathogens [60,61,62,63,64,65,66,67]. Indeed, it has been hypothesized that the social distancing restrictions during the lockdown were more effective at suppressing the other respiratory viruses than HRV, whose transmission was less altered [68]. Findings of this nature were further confirmed on a global scale by a large meta-analysis identifying HRV and RSV as the most prevalent among all respiratory viruses in children aged 0–12 years during the pandemic [69].
Likewise, HRV (human bocavirus) is reported to have been a significantly prevalent agent in pediatric ARIs during the pandemic period, often detected in association with other co-infecting pathogens, mainly RSV and HRV [70]. Similarly, although the positivity rate of ADV after January 2020 was lower than in the previous two years [52], this pathogen was detected to some extent during the pandemic, in contrast to the consistent reduction in other viruses [48,64,65,67].
These data suggest that standard prophylaxis against SARS-CoV-2 has limited effects in eliminating non-enveloped viruses [64].

3.3. ARIs After Lockdown

During the second half of 2020, most viruses returned to or exceeded historical levels. For many of them an off-season increase has been observed. Most available studies on the re-emergence of viral infections after lockdown concerned RSV infection [71,72].

3.3.1. Respiratory Syncytial Virus

The reappearance of RSV after the strict lockdown has been described worldwide [71,72,73,74,75,76,77,78], targeting a wide immunologically naïve population largely consisting of infants born from mothers who did not reinforce their immunity to RSV [35,79,80]. However, the emergence of RSV epidemics appeared in different seasons and on a different scale compared to previous country-by-country trends [81,82,83,84,85]. These differences may be explained by factors such as climate, culture, quarantine methods, personal protective equipment, hygiene measures, and habits [71]. Nevertheless, the possibility that adults act as a reservoir of infection, significantly impacting RSV epidemiology, has been hypothesized [86]. Furthermore, a persistent negative impact of the pandemic on health-care systems in middle-income regions has been recently hypothesized to explain why the rebound in hospitalization rates of RSV-associated ARIs was mainly limited to high-income countries [87].
An increase in RSV cases at the end of winter 2020 and in the early spring was observed throughout New York state and suggested interseasonal RSV resurgence associated with the reduction of COVID-19 preventive efforts [88], as observed in other countries [89,90,91].
In Taiwan, an unexpected outbreak of bronchiolitis occurred between September and December 2020, even though in this country the pre-pandemic peak of bronchiolitis was usually observed in spring and summer [92].
In Spain, schools reopened in September 2020, when bronchiolitis and RSV cases were expected to re-appear [30]. However, despite re-opening schools, cases of bronchiolitis remained limited. Even more surprisingly, RSV diagnoses were nearly zero at least until the end of 2020 [30]. One possible explanation is that SARS-CoV-2 may have displaced other respiratory viruses, probably replacing their ecological niche, with a disproportionate effect on RSV [30]. In Italy, cases of bronchiolitis increased significantly in October 2021, peaked in November and December, and declined rapidly during the second half of December [93,94,95,96]. The leading role of RSV within the resurgence of viral pathogens after COVID-19-related social distancing has been further confirmed, more recently in some studies analyzing pediatric ARIs during the fall–winter of 2022/2023 [97,98,99,100]. These findings, obtained in very different geographical settings, confirm the high relevance that RSV re-gained after significant suppression during the pandemic.
Regarding the age of the affected children, data from a French birth cohort including infants (<1 year of age) admitted to the hospital with respiratory symptoms due to RSV showed an increase in the median age of affected children compared to previous seasons (4.8 months in 2020–2021 compared to 2.2 and 3.1 months in the 2016–2017 and 2019–2020 seasons, respectively) [101]. The older age of RSV-infected children in 2020–2021 was confirmed in other countries [93,102,103,104,105,106]. Furthermore, a shorter duration of RSV epidemics was reported in 2020–2021 compared to pre-COVID-19 seasons both in the Southern and Northern hemispheres [93,107,108].
Data on the clinical severity of RSV in 2020–2021 are conflicting. It is unclear whether children with a first RSV infection at an older age may be less [109,110] or more prone [111,112,113] to a severe clinical presentation. Infants born in the pandemic years were born to mothers with no RSV exposure during pregnancy, and, since neutralizing antibodies to RSV are short-lived, no significant mother-to-child transmission of RSV-specific antibodies can be expected [113]. This would have made it reasonable to expect a more severe clinical presentation of bronchiolitis. In a study from the US, 81% of children hospitalized with bronchiolitis were admitted to the PICU [92]. These data were confirmed by studies from Italy, Mexico, and South Korea reporting moderate to severe symptoms in approximately 50% of admitted patients [114,115,116]. More importantly, another study showed that almost twice as many patients with bronchiolitis were admitted to the PICU during the post-lockdown phase compared to the usual winter spike in cases (in the pre-lockdown period) [117]. Furthermore, the post-lockdown group was older at admission [117,118,119], but no differences in gender or ethnicity were reported [118]. Conversely, national data from New Zealand for children aged 0–4 years showed an increase in PICU discharges for bronchiolitis in 2021, which was 2.8 times higher than the average recorded in 2015–2019 [120]. However, this increase reflects an incidence rate of hospitalized bronchiolitis of 284 per 100,000 children in 2021, which was three times higher than the average of peaks in 2015–2019 [120]. Therefore, these similar increases in the rates of hospitalization and PICU discharges suggests that, despite a higher incidence of the disease, clinical presentation was not more severe than in previous years.
With regard to RSV genomic diversity in the post-COVID-19 period, an Australian study analyzed genome sequencing on RSV-positive specimens collected before (July 2017–March 2020), during, and after (April 2020–March 2021) the implementation of COVID-19 restrictions [121]. The authors found a variable prevalence of the pre-pandemic co-circulation of RSV-A and B subtypes, with RSV-A accounting for 45–79% of cases. Between late 2020 and early 2021 there was a predominance of the RSV-A subtype (>95%), suggesting that RSV-A was the sole sub-type responsible for 2020 RSV outbreaks [122]. In addition, the analysis of the G gene phylogeny demonstrated that RSV circulating during the Australian 2020–2021 epidemic did not cluster with any other RSV virus observed before pandemic. This finding, in line with similar studies carried out in other countries [122,123,124], suggests that pre-pandemic RSV-A and B were largely eliminated during the COVID-19 restrictions allowing the circulation of new lineages [121,125,126].
Similarly, genomic data from pre- and post-pandemic seasons have also shown a shift in the predominant subtype from RSV-A to RSV-B in European and non-European countries [127,128,129]. Indeed, even though with variations in the considered periods among the available studies, during the 2021 season there was a dominance of RSV-A, whereas in 2022/23 RSV-B was more prevalent [127,128,129,130,131].

3.3.2. Influenza

A study from China including a large cohort of pediatric and adult inpatients and outpatients with or without respiratory symptoms showed no significant peak in IFV-A and IFV-B between December 2020 and February 2021 [52]. Nevertheless, during the flu season of 2021–2022, IFV-B emerged as a leading cause of respiratory infections [132]; a broad surveillance program involving adults and children from two cities in Eastern China detected both IFV-A and IFV-B as the most frequent viral pathogens in the 2023 fall–winter season [133]. Similarly, data from several European and non-European countries showed that since April 2021, IFV-A and B increased disproportionately and reached a peak varying between October 2021 and early 2022 [134,135,136,137], even though the higher number of hospitalizations was not apparently associated with higher severity or mortality [138,139].
With regard to IFV subtypes, the pseudo-extinction of B/Yamagata lineage was reported globally during the pandemic [140,141], with no evidence of resumed circulation after the relaxation of COVID-19 control measures [142]. The implications of this shift, likely deriving from differences in susceptible populations, are potentially immense [142]. Nevertheless, a significant impact on vaccination strategies has already been determined with the recent exclusion of a B/Yamagata antigen from the influenza vaccine [143].

3.3.3. Other Viruses

In several studies, HRV outbreaks were reported both in adults and children both immediately after the re-opening of schools [18,144,145,146,147], and, more recently, during the fall of 2023 [148,149]. Reported outbreaks not only suggest that the virus has spread from schools to the broader community, but indicate that, despite occasional detection in children with no or mild respiratory symptoms, HRV may be associated with severe clinical presentation, with a need for oxygen supplementation in a significant proportion of cases [148,150,151]. The impact of the COVID-19 pandemic on HRV epidemiology has been further documented in South Korea, where schools were closed in March and re-opened in May 2020, while the authorities continued to minimize crowding and maintain face masks and hand hygiene policies [152,153]. In such settings, HRV surged after schools reopened and decreased only after the intensification of social distancing rules [152]. These data suggest that early social distancing measures reduced exposure to HRV during the typical transmission season (January–March), resulting in attenuated acquired immunity and a delayed surge in the fall when social distancing was relaxed. It is notable that, despite the large HRV resurgence, transmission of SARS-CoV-2 remained low in South Korean school-aged children, indicating different methods of transmission [154]. In a study from Finland, the increase in the incidence of HRV in children began in early summer 2020, when school-aged children and some day-care-aged children were having summer holidays [155]. The increase in the summer was likely due to the lifting of social restrictions aimed towards the adult population, as bars were opened and restrictions for gatherings were eased [155].
Although far less studied in comparison to other viruses, data on human metapneumovirus (hMPV) transmission throughout the pandemic years were reported by an Australian group that confirmed the susceptibility of such pathogens to the non-pharmacological mitigation measures adopted to combat COVID-19 [156,157]. The authors found that, after a substantial absence in 2020, hMPV incidence in 2021 almost tripled compared to 2017–2019, with children aged 1–4 years being most frequently affected. As with other viruses, the post-lockdown increased incidence was likely linked to a wider cohort of hMPV-naïve children and waning population immunity [156].

4. Discussion

A significant impact of the COVID-19 pandemic on the circulation of common respiratory viruses has been observed worldwide. The non-pharmacological measures implemented during the pandemic deeply modified the usual epidemiology of common childhood respiratory infections, ultimately leading to a significant decrease in the numbers of pediatric hospital admissions because of ARIs compared to non-pandemic years [158,159]. This reduction could be considered to be an unexpected positive consequence of the non-pharmacological measures taken during the COVID-19 pandemic. Another possible explanation is parents’ reluctance to take their children to healthcare facilities during the pandemic due to fear of SARS-CoV-2 exposure, which could have partially contributed to the decline in the number of patients diagnosed with ARIs [160,161]. Importantly, and most relevant for RSV, during the 2020–2021 season in Europe, when RSV activity was overall very low, the only countries with major RSV outbreaks were those whose policies were to keep primary schools and childcare centers opened throughout lockdowns [162].
When COVID-19 mitigation practices became less stringent—and especially with the re-opening of schools—outbreaks of respiratory infections were registered almost worldwide [71,72,73,74,75,76,77,78,134,135,136,137,144,145,146,147]. With the reoccurrence of viral infections, most episodes were registered outside of the typical pre-pandemic season and in an unexpected age range [81,82,83,84,85,102,103,104,105,106]. The mechanism behind this off-season resurgence is still unclear. Furthermore, the resurgence of respiratory viruses followed different dynamics depending on the type of pathogen. For example, IFV and RSV did not produce a seasonal epidemic in the 2020–21 winter season, while other pathogens such as HRV circulated at various levels and intensity [163]. Factors that determine the spread of pathogens include virological features (virulence, fitness, and transmissibility) and immune evasion, as well as seasonal variations, host characteristics (age, co-morbidities, asymptomatic viral carriage, personal hygiene, and proximity to other hosts), and environmental conditions (temperature, humidity, and the contamination of surfaces) [164,165,166,167,168]. In addition to mitigation due to COVID-19 control measures, the reduction in influenza vaccination campaigns may be another important component of the resurgence in respiratory infections.
The most important differences in outbreaks after lockdown were observed for RSV. Even in the same hemisphere, country-by-country differences in its resurgence in the 2020–2021 season were reported [30,93]. In most countries, schools reopened beginning in September 2020. However, opportunities for viral transmission outside of school from other children or within the family remained. Differences in viruses’ circulation may have been due, at least in part, to restrictive measures to contain SARS-CoV-2 outside of school, which differed by country. For example, in the Campania region (southern Italy), measures to control the spread of SARS-CoV-2 were longer and stricter compared to other Italian regions and to other European countries. The lockdown required the closure of all grade schools and the restriction of children’s group activities from March to October 2020. In the following months (between the end of 2020 and the beginning of 2021), schools remained closed again for a long period in response to SARS-CoV-2 regional peaks. Therefore, during the first two years of the pandemic, there were very few cases of children hospitalized because of ARIs due to RSV or other viruses [36]. With the re-opening of social activities, there was an unexpected peak of respiratory infections, emergency department visits and hospital admissions at one pediatric hospital [93]. Another explanation for the discrepancies in peaks between different countries is the change in testing practices, with more systematic tests performed due to the COVID-19 pandemic, including more tests, even for RSV, in older children [113].
Concerns have been raised about potential future epidemics from respiratory viruses, particularly RSV, within pediatric communities that do not encounter these pathogens over a period of two years and are at risk of paying the so-called “immunity debt” [12]. Available data on the clinical severity of respiratory infections in the post-lockdown period are conflicting [109,110,111,112,113]. On the one hand, increased age at the time of initial infection may be expected to entail reduced hospitalizations, given that the RSV burden is most pronounced in neonates and young infants. On the other hand, this was not reflected in a reduction in the number of bronchiolitis cases admitted, at least in some countries [121]. It may be assumed that, by increasing the pool of susceptible children, including those with underlying risk factors, outbreaks might be more severe with regard to hospitalizations and PICU admissions.
The increased age of RSV infected children following the start of the COVID-19 pandemic is noteworthy [101,102,103,104,105,106]. Several explanations have been hypothesized. Due to the absence of RSV activity following the start of the COVID-19 pandemic, a larger number of infants and young children (with a slight upward age shift) were at increased risk for severe RSV infection because they did not have the opportunity to develop immunity against this pathogen.
Nevertheless, discrepancies in the results from different studies prevent a firm conclusion. Indeed, from an epidemiological point of view, not all the studies had the availability of a program of nationwide surveillance for respiratory infections [35,47,118], and sentinelled data were often used [18,22,23]. Secondly, different methodologies were applied, including many retrospective studies [36,48,75,76,149] and a limited minority of prospective observations [57,65,101]. Moreover, the COVID-19 era changed institutional testing strategies compared to previous seasons, with more extensive testing for viruses such as RSV in older children as well [113]. Finally, RSV epidemiology is currently undergoing a revolution with the potential of completely changing the impact of such pathogen on clinical practice: the widespread administration of nirsevimab, the novel monoclonal antibody against RSV, to neonates and infants [169]. Such an intervention, despite varying by geographic area with regard to the start season and the number of immunized children, is likely to dramatically decrease RSV circulation, with an extraordinary impact in terms of saved lives and reduced hospitalizations. Whether this change will entail the increased diffusion of other viral pathogens that will replace RSV in seasonal epidemics is still to be determined and will represent a topic of major interest in the next few years.
The present review has several limitations. First, despite being extended to a significant number of articles, the literature search was limited to three databases and to studies with full text availability. This aspect, together with the huge number of articles screened, may have resulted in the exclusion of some potentially relevant studies. Furthermore, a comprehensive analysis of the genetic characteristics of the respiratory viruses, specifically addressing their changes during and after the COVID-19 pandemic, was not performed. The reported details derive from the few studies included in the selection process, but are far from exhaustive, as a specific literature search or analysis of genomic databases was not carried out.

5. Conclusions

The strict public health measures adopted to combat the COVID-19 pandemic were successful in limiting community transmission of SARS-CoV-2. In addition, these measures resulted in a significant reduction in infections caused by other respiratory viruses, with a consequent reduction in childhood morbidity, including hospital and PICU admissions. On the other hand, the lockdown measures, which effectively resulted in COVID-19 containment, were very restrictive of personal liberties and, in the absence of a pandemic threatening lives and hospital systems, would not be considered reasonable by the general community. After these dramatic public health changes, the characteristics of viral epidemics and their mutations should be extensively and continuously monitored and analyzed. It remains unclear how long it will take for the seasonality of normal winter respiratory viruses (mainly RSV and IFV) to resume globally. Considering the yearly variations in viral infections’ peaks and rates of infection, it is uncertain whether off-season or more severe respiratory infections will occur in the near future.
Future public health strategies should include the implementation of monitoring systems for respiratory viruses, including a careful assessment of the trends and patterns of circulation and co-infection among children. Such a tool could be crucial for providing timely interventions when new outbreaks occur and may guide preventive strategies aimed at limiting future epidemics, such as non-pharmacological measures or anti-viral prophylaxis in high-risk groups. Further research is also needed to better understand which public health interventions are most effective in reducing the diffusion of the different viral pathogens and when these interventions should be applied to obtain the best balance between prevention of viral spread and social acceptability. Finally, further advances in the link between the viral genome, viral phenotype, and viral interaction with host immunity will hopefully pave the way towards the development of new vaccines, particularly aimed at limiting infections in subjects with underlying conditions or with immunocompromised status.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/jcm14041387/s1, Table S1. Main characteristics of the 148 articles included in the Review; Table S2. Articles initially included during the literature screening but then excluded from the final selection.

Author Contributions

Conceptualization, M.M. and A.G.; methodology, V.T. and L.C.; data collection and analysis, M.M., E.B. and R.R.; writing—original draft preparation, M.M. and A.S.C.; writing—review and editing, A.G. and C.E.; supervision, V.T. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Wang, X.; Li, Y.; O’Brien, K.L.; Madhi, S.A.; Widdowson, M.A.; Byass, P.; Omer, S.B.; Abbas, Q.; Ali, A.; Amu, A.; et al. Respiratory Virus Global Epidemiology Network. Global burden of respiratory infections associated with seasonal influenza in children under 5 years in 2018: A systematic review and modelling study. Lancet Glob. Health 2020, 8, e497–e510. [Google Scholar] [CrossRef]
  2. Wang, X.; Li, Y.; Shi, T.; Bont, L.J.; Chu, H.Y.; Zar, H.J.; Wahi-Singh, B.; Ma, Y.; Cong, B.; Sharland, E.; et al. Respiratory Virus Global Epidemiology Network; RESCEU investigators. Global disease burden of and risk factors for acute lower respiratory infections caused by respiratory syncytial virus in preterm infants and young children in 2019: A systematic review and meta-analysis of aggregated and individual participant data. Lancet 2024, 403, 1241–1253. [Google Scholar]
  3. Wang, X.; Li, Y.; Deloria-Knoll, M.; Madhi, S.A.; Cohen, C.; Ali, A.; Basnet, S.; Bassat, Q.; Brooks, W.A.; Chittaganpitch, M.; et al. Respiratory Virus Global Epidemiology Network. Global burden of acute lower respiratory infection associated with human metapneumovirus in children under 5 years in 2018: A systematic review and modelling study. Lancet Glob. Health 2021, 9, e33–e43. [Google Scholar] [CrossRef]
  4. Wang, X.; Li, Y.; Deloria-Knoll, M.; Madhi, S.A.; Cohen, C.; Arguelles, V.L.; Basnet, S.; Bassat, Q.; Brooks, W.A.; Echavarria, M.; et al. Respiratory Virus Global Epidemiology Network. Global burden of acute lower respiratory infection associated with human parainfluenza virus in children younger than 5 years for 2018: A systematic review and meta-analysis. Lancet Glob. Health 2021, 9, e1077–e1087. [Google Scholar] [CrossRef]
  5. Singh, M.; Gupta, A.; Agarwal, A.; Singh, V.; Omar, B. Precision Diagnosis of Viral Respiratory Infections: Unleashing the Power of Multiplex Polymerase Chain Reaction (PCR) for Enhanced Infection Management. Cureus 2024, 16, e73100. [Google Scholar] [CrossRef]
  6. Domnich, A.; Massaro, E.; Icardi, G.; Orsi, A. Multiplex molecular assays for the laboratory-based and point-of-care diagnosis of infections caused by seasonal influenza, COVID-19, and RSV. Expert. Rev. Mol. Diagn. 2024, 24, 997–1008. [Google Scholar] [CrossRef]
  7. Pan, F.; Wang, B.; Zhang, H.; Shi, Y.; Xu, Q. The clinical application of Filmarray respiratory panel in children especially with severe respiratory tract infections. BMC Infect. Dis. 2021, 21, 230. [Google Scholar] [CrossRef]
  8. Furuse, Y.; Tamaki, R.; Suzuki, A.; Kamigaki, T.; Okamoto, M.; Saito-Obata, M.; Nakagawa, E.; Saito, M.; Segubre-Mercado, E.; Tallo, V.; et al. Epidemiological and clinical characteristics of children with acute respiratory viral infections in the Philippines: A prospective cohort study. Clin. Microbiol. Infect. 2021, 27, 1037.e9–1037.e14. [Google Scholar] [CrossRef]
  9. Jefferson, T.; Del Mar, C.B.; Dooley, L.; Ferroni, E.; Al-Ansary, L.A.; Bawazeer, G.A.; van Driel, M.L.; Jones, M.A.; Thorning, S.; Beller, E.M.; et al. Physical interventions to interrupt or reduce the spread of respiratory viruses. Cochrane Database Syst. Rev. 2020, 11, CD006207. [Google Scholar]
  10. Britton, P.N.; Hu, N.; Saravanos, G.; Shrapnel, J.; Davis, J.; Snelling, T.; Dalby-Payne, J.; Kesson, A.M.; Wood, N.; Macartney, K.; et al. COVID-19 public health measures and respiratory syncytial virus. Lancet Child. Adolesc. Health 2020, 4, e42–e43. [Google Scholar] [CrossRef]
  11. Angoulvant, F.; Ouldali, N.; Yang, D.D.; Filser, M.; Gajdos, V.; Rybak, A.; Guedj, R.; Soussan-Banini, V.; Basmaci, R.; Lefevre-Utile, A.; et al. Coronavirus Disease 2019 Pandemic: Impact Caused by School Closure and National Lockdown on Pediatric Visits and Admissions for Viral and Nonviral Infections-a Time Series Analysis. Clin. Infect. Dis. 2021, 72, 319–322. [Google Scholar] [CrossRef]
  12. Cohen, R.; Ashman, M.; Taha, M.K.; Varon, E.; Angoulvant, F.; Levy, C.; Rybak, A.; Ouldali, N.; Guiso, N.; Grimprel, E. Pediatric Infectious Disease Group (GPIP) position paper on the immune debt of the COVID-19 pandemic in childhood, how can we fill the immunity gap? Infect. Dis. Now. 2021, 51, 418–423. [Google Scholar] [CrossRef]
  13. Page, M.J.; McKenzie, J.E.; Bossuyt, P.M.; Boutron, I.; Hoffmann, T.C.; Mulrow, C.D.; Shamseer, L.; Tetzlaff, J.M.; Akl, E.A.; Brennan, S.E.; et al. The PRISMA 2020 statement: An updated guideline for reporting systematic reviews. BMJ 2021, 372, n71. [Google Scholar] [CrossRef] [PubMed]
  14. Ottawa Hospital Research Institute. The Newcastle-Ottawa Scale (NOS) for Assessing the Quality of Nonrandomised Studies in Meta-Analyses. Available online: https://www.ohri.ca/programs/clinical_epidemiology/oxford.asp (accessed on 20 January 2025).
  15. Guadalupe-Fernández, V.; Martínez-Solanas, E.; Sabrià-Sunyé, A.; Ferrer-Mikoly, C.; Martínez-Mateo, A.; Ciruela-Navas, P.; Mendioroz, J.; Basile, L.; Epidemiological Surveillance Network of Catalonia. Investigating epidemiological distribution (temporality and intensity) of respiratory pathogens following COVID-19 de-escalation process in Catalonia, September 2016-June 2021: Analysis of regional surveillance data. PLoS ONE 2024, 19, e0285892. [Google Scholar] [CrossRef]
  16. Li, Z.J.; Yu, L.J.; Zhang, H.Y.; Shan, C.X.; Lu, Q.B.; Zhang, X.A.; Ren, X.; Zhang, C.H.; Wang, Y.F.; Lin, S.H.; et al. Broad Impacts of Coronavirus Disease 2019 (COVID-19) Pandemic on Acute Respiratory Infections in China: An Observational Study. Clin. Infect. Dis. 2022, 75, e1054–e1062. [Google Scholar] [CrossRef]
  17. Armero, G.; Guitart, C.; Soler-Garcia, A.; Melé, M.; Esteva, C.; Brotons, P.; Muñoz-Almagro, C.; Jordan, I.; Launes, C. Non-Pharmacological Interventions During SARS-CoV-2 Pandemic: Effects on Pediatric Viral Respiratory Infections. Arch. Bronconeumol. 2024, 60, 612–618. [Google Scholar] [CrossRef] [PubMed]
  18. Li, Y.; Wu, Z.; Yan, Y.; Shi, Y.; Huang, J.; Du, H.; Du, Q.; Li, Y.; Lin, Y.; Liu, D.; et al. Prevalence of respiratory viruses among hospitalized children with lower respiratory tract infections during the COVID-19 pandemic in Wuhan, China. Int. J. Infect. Dis. 2024, 139, 6–12. [Google Scholar] [CrossRef] [PubMed]
  19. Zhang, G.; Zhang, Y.; Ba, L.; Liu, L.; Su, T.; Sun, Y.; Dian, Z. Epidemiological changes in respiratory pathogen transmission among children with acute respiratory infections during the COVID-19 pandemic in Kunming, China. BMC Infect. Dis. 2024, 24, 826. [Google Scholar] [CrossRef]
  20. Shen, D.P.; Vermeulen, F.; Debeer, A.; Lagrou, K.; Smits, A. Impact of COVID-19 on viral respiratory infection epidemiology in young children: A single-center analysis. Front. Public Health 2022, 10, 931242. [Google Scholar] [CrossRef] [PubMed]
  21. Ma, J.E.; Ma, Q.F.; Wang, W.; Zeng, Y.; Cui, X.H.; Wang, G.L.; Liu, S.Y.; Wang, Z.; Xiao, X.; Xia, Z.N.; et al. Analysis of Common Respiratory Infected Pathogens in 3100 Children after the Coronavirus Disease 2019 Pandemic. Curr. Med. Sci. 2022, 42, 1094–1098. [Google Scholar] [CrossRef] [PubMed]
  22. Wu, R.; Zhang, J.; Mo, L. Analysis of respiratory virus detection in hospitalized children with acute respiratory infection during the COVID-19 pandemic. Virol. J. 2023, 20, 253. [Google Scholar] [CrossRef] [PubMed]
  23. De Maio, F.; Fiori, B.; Bianco, D.M.; Sanguinetti, M.; Sali, M. Respiratory viruses in the pre and post-pandemic periods in an Italian tertiary hospital. Immun. Inflamm. Dis. 2023, 11, e909. [Google Scholar] [CrossRef] [PubMed]
  24. Baldassarre, M.E.; Loconsole, D.; Centrone, F.; Caselli, D.; Martire, B.; Quartulli, L.; Acquafredda, A.; D’Amato, G.; Maffei, G.; Latorre, G.; et al. Hospitalization for bronchiolitis in children aged ≤ 1year, Southern Italy, year 2021: Need for new preventive strategies? Ital. J. Pediatr. 2023, 49, 66. [Google Scholar] [CrossRef] [PubMed]
  25. Chuang, Y.C.; Lin, K.P.; Wang, L.A.; Yeh, T.K.; Liu, P.Y. The Impact of the COVID-19 Pandemic on Respiratory Syncytial Virus Infection: A Narrative Review. Infect. Drug Resist. 2023, 16, 661–675. [Google Scholar] [CrossRef] [PubMed]
  26. Haddadin, Z.; Schuster, J.E.; Spieker, A.J.; Rahman, H.; Blozinski, A.; Stewart, L.; Campbell, A.P.; Lively, J.Y.; Michaels, M.G.; Williams, J.V.; et al. Acute Respiratory Illnesses in Children in the SARS-CoV-2 Pandemic: Prospective Multicenter Study. Pediatrics 2021, 148, e2021051462. [Google Scholar] [CrossRef]
  27. Curatola, A.; Lazzareschi, I.; Bersani, G.; Covino, M.; Gatto, A.; Chiaretti, A. Impact of COVID-19 outbreak in acute bronchiolitis: Lesson from a tertiary Italian Emergency Department. Pediatr. Pulmonol. 2021, 56, 2484–2488. [Google Scholar] [CrossRef]
  28. Guedj, R.; Lorrot, M.; Lecarpentier, T.; Leger, P.L.; Corvol, H.; Carbajal, R. Infant bronchiolitis dramatically reduced during the second French COVID-19 outbreak. Acta Paediatr. 2021, 110, 1297–1299. [Google Scholar] [CrossRef]
  29. Friedrich, F.; Ongaratto, R.; Scotta, M.C.; Veras, T.N.; Stein, R.T.; Lumertz, M.S.; Jones, M.H.; Comaru, T.; Pinto, L.A. Early Impact of Social Distancing in Response to Coronavirus Disease 2019 on Hospitalizations for Acute Bronchiolitis in Infants in Brazil. Clin. Infect. Dis. 2021, 72, 2071–2075. [Google Scholar] [CrossRef] [PubMed]
  30. Torres-Fernandez, D.; Casellas, A.; Mellado, M.J.; Calvo, C.; Bassat, Q. Acute bronchiolitis and respiratory syncytial virus seasonal transmission during the COVID-19 pandemic in Spain: A national perspective from the pediatric Spanish Society (AEP). J. Clin. Virol. 2021, 145, 105027. [Google Scholar] [CrossRef]
  31. Van Brusselen, D.; De Troeyer, K.; Ter Haar, E.; Vander Auwera, A.; Poschet, K.; Van Nuijs, S.; Bael, A.; Stobbelaar, K.; Verhulst, S.; Van Herendael, B.; et al. Bronchiolitis in COVID-19 times: A nearly absent disease? Eur. J. Pediatr. 2021, 180, 1969–1973. [Google Scholar] [CrossRef] [PubMed]
  32. Razanajatovo, N.H.; Randriambolamanantsoa, T.H.; Rabarison, J.H.; Randrianasolo, L.; Ankasitrahana, M.F.; Ratsimbazafy, A.; Raherinandrasana, A.H.; Razafimanjato, H.; Raharinosy, V.; Andriamandimby, S.F.; et al. Epidemiological Patterns of Seasonal Respiratory Viruses during the COVID-19 Pandemic in Madagascar, March 2020-May 2022. Viruses 2022, 15, 12. [Google Scholar] [CrossRef] [PubMed]
  33. Bhardwaj, S.; Choudhary, M.L.; Chadha, M.S.; Kinikar, A.; Bavdekar, A.; Gujar, N.; Dcosta, P.; Kulkarni, R.; Bafna, S.; Salvi, S.; et al. Resurgence of respiratory syncytial virus infection during COVID-19 pandemic in Pune, India. BMC Infect. Dis. 2024, 24, 586. [Google Scholar] [CrossRef] [PubMed]
  34. Yang, M.C.; Su, Y.T.; Chen, P.H.; Tsai, C.C.; Lin, T.I.; Wu, J.R. Changing patterns of infectious diseases in children during the COVID-19 pandemic. Front. Cell. Infect. Microbiol. 2023, 13, 1200617. [Google Scholar] [CrossRef]
  35. Bardsley, M.; Morbey, R.A.; Hughes, H.E.; Beck, C.R.; Watson, C.H.; Zhao, H.; Ellis, J.; Smith, G.E.; Elliot, A.J. Epidemiology of respiratory syncytial virus in children younger than 5 years in England during the COVID-19 pandemic, measured by laboratory, clinical, and syndromic surveillance: A retrospective observational study. Lancet Infect. Dis. 2023, 3, 56–66. [Google Scholar] [CrossRef] [PubMed]
  36. Berdah, L.; Romain, A.S.; Rivière, S.; Schnuriger, A.; Perrier, M.; Carbajal, R.; Lorrot, M.; Guedj, R.; Corvol, H. Retrospective observational study of the influence of the COVID-19 outbreak on infants’ hospitalisation for acute bronchiolitis. BMJ Open 2022, 12, e059626. [Google Scholar] [CrossRef]
  37. Bermúdez Barrezueta, L.; Gutiérrez Zamorano, M.; López-Casillas, P.; Brezmes-Raposo, M.; Sanz Fernández, I.; Pino Vázquez, M.A. Influence of the COVID-19 pandemic on the epidemiology of acute bronchiolitis. Enferm. Infect. Microbiol. Clin. Engl. Ed. 2023, 41, 348–351. [Google Scholar] [CrossRef] [PubMed]
  38. Jiang, X.; Wang, T.; Dai, G.; Sun, H.; Jiang, W.; Chen, Z.; Yan, Y. Clinical characteristics and etiology of children with bronchiolitis before and during the COVID-19 pandemic in Suzhou, China. Front. Pediatr. 2022, 10, 974769. [Google Scholar] [CrossRef]
  39. Kıymet, E.; Böncüoğlu, E.; Şahinkaya, Ş.; Cem, E.; Çelebi, M.Y.; Düzgöl, M.; Kara, A.A.; Arıkan, K.Ö.; Aydın, T.; İşgüder, R.; et al. Distribution of spreading viruses during COVID-19 pandemic: Effect of mitigation strategies. Am. J. Infect. Control 2021, 49, 1142–1145. [Google Scholar] [CrossRef] [PubMed]
  40. Lucion, M.F.; Del Valle Juárez, M.; Pejito, M.N.; Orqueda, A.S.; Romero Bollón, L.; Mistchenko, A.S.; Gentile, Á. Impact of COVID-19 on the circulation of respiratory viruses in a children’s hospital: An expected absence. Arch. Argent. Pediatr. 2022, 120, 99–105. [Google Scholar]
  41. European Centre for Disease Prevention and Control. Surveillance Atlas of Infectious Diseases. Available online: https://atlas.ecdc.europa.eu/public/index.aspx (accessed on 11 December 2024).
  42. Rambaud, J.; Dauger, S.; Morin, L.; Bergounioux, J.; Leger, P.L.; Carbajal, R.; Renolleau, S.; Guedj, R. Bronchiolitis Admissions to Intensive Care During COVID. Pediatrics 2021, 147, e2021050103. [Google Scholar] [CrossRef]
  43. Hassan, M.Z.; Islam, M.A.; Haider, S.; Shirin, T.; Chowdhury, F. Respiratory Syncytial Virus-Associated Deaths among Children under Five before and during the COVID-19 Pandemic in Bangladesh. Viruses 2024, 16, 111. [Google Scholar] [CrossRef]
  44. Giannattasio, A.; Maglione, M.; D’Anna, C.; Muzzica, S.; Angrisani, F.; Acierno, S.; Perrella, A.; Tipo, V. Silent RSV in infants with SARS-CoV-2 infection: A case series. Pediatr. Pulmonol. 2021, 56, 3044–3046. [Google Scholar] [CrossRef] [PubMed]
  45. Victorian Weekly Influenza Report. Victoria State Government Health and Human Services; Victoria State Government Health and Human Services: Melbourne, Australia, 2020. Available online: https://nla.gov.au/nla.obj-2873887268/view (accessed on 11 December 2024).
  46. Abo, Y.N.; Clifford, V.; Lee, L.Y.; Costa, A.M.; Crawford, N.; Wurzel, D.; Daley, A.J. COVID-19 public health measures and respiratory viruses in children in Melbourne. J. Paediatr. Child Health 2021, 57, 1886–1892. [Google Scholar] [CrossRef]
  47. Badar, N.; Salman, M.; Nisar, N.; Mirza, H.A.; Ahad, A.; Ahmad, F.; Daud, B. Unraveling influenza sentinel surveillance in Pakistan 2008-2024: Epidemiological insights during the pre and post pandemic period of COVID-19. J. Infect. Public Health 2024, 17, 102595. [Google Scholar] [CrossRef] [PubMed]
  48. Bhardwaj, S.; Choudhary, M.L.; Jadhav, S.; Vipat, V.; Ghuge, R.; Salvi, S.; Kulkarni, R.; Kinikar, A.; Padbidri, V.; Bafna, S.; et al. A retrospective analysis of respiratory virus transmission before and during the COVID-19 pandemic in Pune the western region of India. Front. Public Health 2022, 10, 936634. [Google Scholar] [CrossRef]
  49. Eisen, A.K.A.; Gularte, J.S.; Demoliner, M.; de Abreu Goés Pereira, V.M.; Heldt, F.H.; Filippi, M.; de Almeida, P.R.; Hansen, A.W.; Fleck, J.D.; Spilki, F.R. Low circulation of Influenza A and coinfection with SARS-CoV-2 among other respiratory viruses during the COVID-19 pandemic in a region of southern Brazil. J. Med. Virol. 2021, 93, 4392–4398. [Google Scholar] [CrossRef]
  50. Monamele, G.C.; Tsafack, D.T.; Bilounga, C.N.; Njankouo Ripa, M.; Nsangou Yogne, C.; Munshili Njifon, H.L.; Nkom, F.; Tamoufe, U.; Esso, L.; Koro Koro, F.; et al. The Detection of Influenza Virus Before and During the COVID-19 Pandemic in Cameroon. Influenza Other Respir. Viruses 2024, 18, e13313. [Google Scholar] [CrossRef]
  51. Knudsen, P.K.; Lind, A.; Klundby, I.; Dudman, S. The incidence of infectious diseases and viruses other than SARS-CoV-2 amongst hospitalised children in Oslo, Norway during the COVID-19 pandemic 2020-2021. J. Clin. Virol. Plus 2022, 2, 100060. [Google Scholar] [CrossRef] [PubMed]
  52. Du, X.; Wu, G.; Zhu, Y.; Zhang, S. Exploring the epidemiological changes of common respiratory viruses since the COVID-19 pandemic: A hospital study in Hangzhou, China. Arch. Virol. 2021, 166, 3085–3092. [Google Scholar] [CrossRef] [PubMed]
  53. Lee, H.; Song, K.H.; Kim, E.S.; Park, J.S.; Jung, J.; Ahn, S.; Jeong, E.K.; Park, H.; Kim, H.B. Impact of Public Health Interventions on Seasonal Influenza Activity During the COVID-19 Outbreak in Korea. Clin. Infect. Dis. 2021, 73, e132–e140. [Google Scholar] [CrossRef] [PubMed]
  54. Fukuda, Y.; Tsugawa, T.; Nagaoka, Y.; Ishii, A.; Nawa, T.; Togashi, A.; Kunizaki, J.; Hirakawa, S.; Iida, J.; Tanaka, T.; et al. Surveillance in hospitalized children with infectious diseases in Japan: Pre- and post-coronavirus disease 2019. J. Infect. Chemother. 2021, 27, 1639–1647. [Google Scholar] [CrossRef]
  55. Zendehrouh, M.; Karimi, A.; Azimi, L. Respiratory Viral Infections Among Children Hospitalized in a Great Referral Hospital in Iran During the Coronavirus Pandemic. Arch. Pediatr. Infect. Dis. 2023, 11, e136943. [Google Scholar] [CrossRef]
  56. Kang, M.; Sarkar, S.; Angurana, S.K.; Singh, P.; Rana, M.; Bora, I.; Chetanya, R.; Singh, B.; Muralidharan, J.; Ratho, R.K. Paradigm shift of respiratory viruses causing lower respiratory tract infection in children during COVID-19 pandemic in India. J. Infect. Dev. Ctries. 2023, 17, 961–970. [Google Scholar] [CrossRef] [PubMed]
  57. Loevinsohn, G.; Hamahuwa, M.; Hardick, J.; Sinywimaanzi, P.; Fenstermacher, K.Z.J.; Munachoonga, P.; Weynand, A.; Monze, M.; Manabe, Y.C.; Gaydos, C.A.; et al. Respiratory viruses in rural Zambia before and during the COVID-19 pandemic. Trop. Med. Int. Health 2022, 27, 647–654. [Google Scholar] [CrossRef]
  58. Al Kindi, H.; Meredith, L.W.; Al-Jardani, A.; Sajina, F.; Al Shukri, I.; Al Haj, R.; Alyaquobi, F.; Al Wahaibi, A.; Al Maani, A. Time trend of respiratory viruses before and during the COVID-19 pandemic in severe acute respiratory virus infection in the Sultanate of Oman between 2017 and 2022. Influenza Other Respir. Viruses 2023, 17, e13233. [Google Scholar] [CrossRef] [PubMed]
  59. Umran, N.; Kalpana, S.; Dhandapani, P. Prevalence of non- SARS CoV-2 respiratory virus infection in children during COVID-19 pandemic in Chennai, South India. Indian J. Pathol. Microbiol. 2024, 67, 611–614. [Google Scholar] [CrossRef] [PubMed]
  60. Nenna, R.; Matera, L.; Pierangeli, A.; Oliveto, G.; Viscido, A.; Petrarca, L.; La Regina, D.P.; Mancino, E.; Di Mattia, G.; Villani, A.; et al. First COVID-19 lockdown resulted in most respiratory viruses disappearing among hospitalised children, with the exception of rhinoviruses. Acta Paediatr. 2022, 111, 1399–1403. [Google Scholar] [CrossRef] [PubMed]
  61. Pun, J.C.S.; Tao, K.P.; Yam, S.L.S.; Hon, K.L.; Chan, P.K.S.; Li, A.M.; Chan, R.W.Y. Respiratory Viral Infection Patterns in Hospitalised Children Before and After COVID-19 in Hong Kong. Viruses 2024, 16, 1786. [Google Scholar] [CrossRef]
  62. Takashita, E.; Kawakami, C.; Momoki, T.; Saikusa, M.; Shimizu, K.; Ozawa, H.; Kumazaki, M.; Usuku, S.; Tanaka, N.; Okubo, I.; et al. Increased risk of rhinovirus infection in children during the coronavirus disease-19 pandemic. Influenza Other Respir. Viruses 2021, 15, 488–494. [Google Scholar] [CrossRef]
  63. Agca, H.; Akalin, H.; Saglik, I.; Hacimustafaoglu, M.; Celebi, S.; Ener, B. Changing epidemiology of influenza and other respiratory viruses in the first year of COVID-19 pandemic. J. Infect. Public Health 2021, 14, 1186–1190. [Google Scholar] [CrossRef] [PubMed]
  64. Kume, Y.; Hashimoto, K.; Chishiki, M.; Norito, S.; Suwa, R.; Ono, T.; Mochizuki, I.; Mashiyama, F.; Ishibashi, N.; Suzuki, S.; et al. Changes in virus detection in hospitalized children before and after the severe acute respiratory syndrome coronavirus 2 pandemic. Influenza Other Respir. Viruses 2022, 16, 837–841. [Google Scholar] [CrossRef] [PubMed]
  65. Engels, G.; Sack, J.; Weissbrich, B.; Hartmann, K.; Knies, K.; Härtel, C.; Streng, A.; Dölken, L.; Liese, J.G.; CoPraKid Study Group. Very Low Incidence of SARS-CoV-2, Influenza and RSV but High Incidence of Rhino-, Adeno- and Endemic Coronaviruses in Children with Acute Respiratory Infection in Primary Care Pediatric Practices During the Second and Third Wave of the SARS-CoV-2 Pandemic. Pediatr. Infect. Dis. J. 2022, 41, e146–e148. [Google Scholar] [CrossRef]
  66. Vittucci, A.C.; Piccioni, L.; Coltella, L.; Ciarlitto, C.; Antilici, L.; Bozzola, E.; Midulla, F.; Palma, P.; Perno, C.F.; Villani, A. The Disappearance of Respiratory Viruses in Children during the COVID-19 Pandemic. Int. J. Environ. Res. Public Health 2021, 18, 9550. [Google Scholar] [CrossRef]
  67. Boyanton, B.L., Jr.; Frenner, R.A.; Ingold, A.; Ambroggio, L.; Kennedy, J.L. SARS-CoV-2 pandemic non-pharmacologic interventions temporally associated with reduced pediatric infections due to Mycoplasma pneumoniae and co-infecting respiratory viruses in Arkansas. Microbiol. Spectr. 2024, 12, e0290823. [Google Scholar] [CrossRef] [PubMed]
  68. Teo, K.W.; Patel, D.; Sisodia, S.; Roland, D.; Gaillard, E.A.; Tang, J.W. Rhinovirus persistence during the COVID-19 pandemic-Impact on pediatric acute wheezing presentations. J. Med. Virol. 2022, 94, 5547–5552. [Google Scholar] [CrossRef] [PubMed]
  69. Dallmeyer, L.K.; Schüz, M.L.; Fragkou, P.C.; Omony, J.; Krumbein, H.; Dimopoulou, D.; Dimopoulou, K.; Skevaki, C. Epidemiology of respiratory viruses among children during the SARS-CoV-2 pandemic: A systematic review and meta-analysis. Int. J. Infect. Dis. 2024, 138, 10–18. [Google Scholar] [CrossRef]
  70. Arunasalam, S.; Pattiyakumbura, T.; Shihab, S.R.; Muthugala, R.; Noordeen, F. Demographic and clinical characteristics of human bocavirus-1 infection in patients with acute respiratory tract infections during the COVID-19 pandemic in the Central Province of Sri Lanka. BMC Infect. Dis. 2023, 23, 425. [Google Scholar] [CrossRef] [PubMed]
  71. Leija-Martínez, J.J.; Esparza-Miranda, L.A.; Rivera-Alfaro, G.; Noyola, D.E. Impact of Nonpharmaceutical Interventions during the COVID-19 Pandemic on the Prevalence of Respiratory Syncytial Virus in Hospitalized Children with Lower Respiratory Tract Infections: A Systematic Review and Meta-Analysis. Viruses 2024, 16, 429. [Google Scholar] [CrossRef] [PubMed]
  72. Davids, M.; Johnstone, S.; Mendes, A.; Brecht, G.; Avenant, T.; du Plessis, N.; de Villiers, M.; Page, N.; Venter, M. Changes in Prevalence and Seasonality of Pathogens Identified in Acute Respiratory Tract Infections in Hospitalised Individuals in Rural and Urban Settings in South Africa; 2018-2022. Viruses 2024, 16, 404. [Google Scholar] [CrossRef]
  73. Wang, H.; Zheng, Y.; de Jonge, M.I.; Wang, R.; Verhagen, L.M.; Chen, Y.; Li, L.; Xu, Z.; Wang, W. Lockdown measures during the COVID-19 pandemic strongly impacted the circulation of respiratory pathogens in Southern China. Sci. Rep. 2022, 12, 16926. [Google Scholar] [CrossRef] [PubMed]
  74. Fafi, I.; Assad, Z.; Lenglart, L.; Valtuille, Z.; Ouldali, N. Evolution of respiratory syncytial virus burden in young children following the COVID-19 pandemic: Influence of concomitant changes in testing practices. Lancet Infect. Dis. 2024, 24, e216–e217. [Google Scholar] [CrossRef]
  75. Gashgarey, D.; Alsuhaibani, M.; Alhuthil, R.; Alhabshan, H.; Alabdulqader, A.; Badran, R.; Balhmar, A.; Aldawood, H.; AlBanyan, E.A.; AlGhamdi, S.; et al. Evolving Epidemiology of Pediatric Respiratory Syncytial Virus (RSV) Cases Around COVID-19 Pandemic: Impact and Clinical Insights, Retrospective Cohort Study. J. Epidemiol. Glob. Health 2024, 14, 319–326. [Google Scholar] [CrossRef]
  76. Nixon, J.C.; Freeman, K.; Baird, R.W. Altered epidemiological patterns of Respiratory Syncytial Virus and influenza detections in a tropical Australian setting 2020 to 2023. Aust. N. Z. J. Public Health 2024, 48, 100172. [Google Scholar] [CrossRef]
  77. Noble, M.; Khan, R.A.; Walker, B.; Bennett, E.; Gent, N. Respiratory syncytial virus-associated hospitalisation in children aged ≤5 years: A scoping review of literature from 2009 to 2021. ERJ Open Res. 2022, 8, 00593-2021. [Google Scholar] [CrossRef] [PubMed]
  78. Bedir Demirdag, T.; Atay Ünal, N.; Tapısız, A.; Kara, N.; Güdeloğlu, E.; Tezer, H.; Bozdayı, G. Distribution and clinical features of viral respiratory infections in children after face-to-face education in 2021-2022 winter period. J. Pediatr. Inf. 2022, 16, e1–e5. [Google Scholar] [CrossRef]
  79. Di Mattia, G.; Nenna, R.; Mancino, E.; Rizzo, V.; Pierangeli, A.; Villani, A.; Midulla, F. During the COVID-19 pandemic where has respiratory syncytial virus gone? Pediatr. Pulmonol. 2021, 56, 3106–3109. [Google Scholar] [CrossRef] [PubMed]
  80. Jiang, W.; Xu, L.; Wang, Y.; Hao, C. Exploring immunity debt: Dynamic alterations in RSV antibody levels in children under 5 years during the COVID-19 pandemic. J. Infect. 2024, 88, 53–56. [Google Scholar] [CrossRef]
  81. Mazela, J.; Jackowska, T.; Czech, M.; Helwich, E.; Martyn, O.; Aleksiejuk, P.; Smaga, A.; Glazewska, J.; Wysocki, J. Epidemiology of Respiratory Syncytial Virus Hospitalizations in Poland: An Analysis from 2015 to 2023 Covering the Entire Polish Population of Children Aged under Five Years. Viruses 2024, 16, 704. [Google Scholar] [CrossRef]
  82. Kahanowitch, R.; Gaviria, S.; Aguilar, H.; Gayoso, G.; Chorvinksy, E.; Bera, B.; Rodríguez-Martínez, C.E.; Gutierrez, M.J.; Nino, G. How did respiratory syncytial virus and other pediatric respiratory viruses change during the COVID-19 pandemic? Pediatr. Pulmonol. 2022, 57, 2542–2545. [Google Scholar] [CrossRef]
  83. Faraguna, M.C.; Lepri, I.; Clavenna, A.; Bonati, M.; Vimercati, C.; Sala, D.; Cattoni, A.; Melzi, M.L.; Biondi, A. The bronchiolitis epidemic in 2021-2022 during the SARS-CoV-2 pandemic: Experience of a third level centre in Northern Italy. Ital. J. Pediatr. 2023, 49, 26. [Google Scholar] [CrossRef] [PubMed]
  84. Wu, Y.; Zhou, J.; Shu, T.; Li, W.; Shang, S.; Du, L. Epidemiological study of post-pandemic pediatric common respiratory pathogens using multiplex detection. Virol. J. 2024, 21, 168. [Google Scholar] [CrossRef] [PubMed]
  85. Nenna, R.; Matera, L.; Licari, A.; Manti, S.; Di Bella, G.; Pierangeli, A.; Palamara, A.T.; Nosetti, L.; Leonardi, S.; Marseglia, G.L.; et al. An Italian Multicenter Study on the Epidemiology of Respiratory Syncytial Virus During SARS-CoV-2 Pandemic in Hospitalized Children. Front. Pediatr. 2022, 10, 930281. [Google Scholar] [CrossRef]
  86. Binns, E.; Koenraads, M.; Hristeva, L.; Flamant, A.; Baier-Grabner, S.; Loi, M.; Lempainen, J.; Osterheld, E.; Ramly, B.; Chakakala-Chaziya, J.; et al. Influenza and respiratory syncytial virus during the COVID-19 pandemic: Time for a new paradigm? Pediatr. Pulmonol. 2022, 57, 38–42. [Google Scholar] [CrossRef] [PubMed]
  87. Cong, B.; Koç, U.; Bandeira, T.; Bassat, Q.; Bont, L.; Chakhunashvili, G.; Cohen, C.; Desnoyers, C.; Hammitt, L.L.; Heikkinen, T.; et al. Changes in the global hospitalisation burden of respiratory syncytial virus in young children during the COVID-19 pandemic: A systematic analysis. Lancet Infect. Dis. 2024, 24, 361–374. [Google Scholar] [CrossRef]
  88. Halabi, K.C.; Saiman, L.; Zachariah, P. The Epidemiology of Respiratory Syncytial Virus in New York City during the Coronavirus Disease-2019 Pandemic Compared with Previous Years. J. Pediatr. 2022, 242, 242–244. [Google Scholar] [CrossRef] [PubMed]
  89. Foley, D.A.; Yeoh, D.K.; Minney-Smith, C.A.; Martin, A.C.; Mace, A.O.; Sikazwe, C.T.; Le, H.; Levy, A.; Moore, H.C.; Blyth, C.C. The Interseasonal Resurgence of Respiratory Syncytial Virus in Australian Children Following the Reduction of Coronavirus Disease 2019-Related Public Health Measures. Clin. Infect. Dis. 2021, 73, e2829–e2830. [Google Scholar] [CrossRef]
  90. Weinberger Opek, M.; Yeshayahu, Y.; Glatman-Freedman, A.; Kaufman, Z.; Sorek, N.; Brosh-Nissimov, T. Delayed respiratory syncytial virus epidemic in children after relaxation of COVID-19 physical distancing measures, Ashdod, Israel, 2021. Euro Surveill. 2021, 26, 2100706. [Google Scholar] [CrossRef]
  91. Agha, R.; Avner, J.R. Delayed Seasonal RSV Surge Observed During the COVID-19 Pandemic. Pediatrics 2021, 148, e2021052089. [Google Scholar] [CrossRef] [PubMed]
  92. Hsu, H.T.; Huang, F.L.; Ting, P.J.; Chang, C.C.; Chen, P.Y. The epidemiological features of pediatric viral respiratory infection during the COVID-19 pandemic in Taiwan. J. Microbiol. Immunol. Infect. 2021, 9, 1101–1107. [Google Scholar] [CrossRef] [PubMed]
  93. Maglione, M.; Pascarella, A.; Botti, C.; Ricci, G.; Morelli, F.; Camelia, F.; Micillo, A.; Calì, C.; Savoia, F.; Tipo, V.; et al. Changing Epidemiology of Acute Viral Respiratory Infections in Hospitalized Children: The Post-Lockdown Effect. Children 2022, 9, 1242. [Google Scholar] [CrossRef] [PubMed]
  94. Camporesi, A.; Morello, R.; Ferro, V.; Pierantoni, L.; Rocca, A.; Lanari, M.; Trobia, G.L.; Sciacca, T.; Bellinvia, A.G.; De Ferrari, A.; et al. Epidemiology, Microbiology and Severity of Bronchiolitis in the First Post-Lockdown Cold Season in Three Different Geographical Areas in Italy: A Prospective, Observational Study. Children 2022, 9, 491. [Google Scholar] [CrossRef]
  95. Manti, S.; Giallongo, A.; Parisi, G.F.; Papale, M.; Presti, S.; Lo Bianco, M.; Spicuzza, L.; Leonardi, S. Impact of COVID-19 Pandemic and Lockdown on the Epidemiology of RSV-Mediated Bronchiolitis: Experience from Our Centre. Children 2022, 9, 1723. [Google Scholar] [CrossRef]
  96. Treggiari, D.; Pomari, C.; Zavarise, G.; Piubelli, C.; Formenti, F.; Perandin, F. Characteristics of Respiratory Syncytial Virus Infections in Children in the Post-COVID Seasons: A Northern Italy Hospital Experience. Viruses 2024, 16, 126. [Google Scholar] [CrossRef]
  97. Stacevičienė, I.; Ivaškevičienė, I.; Burokienė, S.; Steponavičienė, A.; Vaičiūnienė, D.; Tarutytė, G.; Jankauskienė, A. Epidemiological changes of acute respiratory infections in children: A single-center experience after COVID-19 lockdown. PLoS ONE 2024, 19, e0300877. [Google Scholar] [CrossRef]
  98. Falsaperla, R.; Sortino, V.; La Cognata, D.; Barberi, C.; Corsello, G.; Malaventura, C.; Suppiej, A.; Collotta, A.D.; Polizzi, A.; Grassi, P.; et al. Acute Respiratory Tract Infections (ARTIs) in Children after COVID-19-Related Social Distancing: An Epidemiological Study in a Single Center of Southern Italy. Diagnostics 2024, 14, 1341. [Google Scholar] [CrossRef] [PubMed]
  99. Parola, F.; Brach Del Prever, A.; Deut, V.; Costagliola, G.; Guidi, C.; Ragusa, N.; Tuscano, A.; Timeus, F.; Berger, M. Impact of SARS-CoV-2 Pandemic and Lockdown on the HRSV Circulation: Experience of Three Spoke Hospitals in Northern Italy. Viruses 2024, 16, 230. [Google Scholar] [CrossRef] [PubMed]
  100. Lima, A.K.S.; Banho, C.A.; Sacchetto, L.; de Carvalho Marques, B.; Dos Santos, M.G.; Ribeiro, M.R.; Gandolfi, F.A.; Sakomura, T.P.; Estofolete, C.F.; Nogueira, M.L. Seasonal respiratory virus trends in pediatric patients during the COVID-19 pandemic in Brazil. Braz. J. Microbiol. 2023, 54, 1827–1834. [Google Scholar] [CrossRef]
  101. Casalegno, J.S.; Ploin, D.; Cantais, A.; Masson, E.; Bard, E.; Valette, M.; Fanget, R.; Targe, S.C.; Myar-Dury, A.F.; Doret-Dion, M.; et al. Characteristics of the delayed respiratory syncytial virus epidemic, 2020/2021, Rhône Loire, France. Euro Surveill. 2021, 26, 2100630. [Google Scholar] [CrossRef] [PubMed]
  102. Yeoh, D.K.; Foley, D.A.; Minney-Smith, C.A.; Martin, A.C.; Mace, A.O.; Sikazwe, C.T.; Le, H.; Levy, A.; Blyth, C.C.; Moore, H.C. Impact of Coronavirus Disease 2019 public health measures on detections of influenza and respiratory syncytial virus in children during the 2020 Australian winter. Clin. Infect. Dis. 2021, 72, 2199–2202. [Google Scholar] [CrossRef] [PubMed]
  103. McNab, S.; Ha Do, L.A.; Clifford, V.; Crawford, N.W.; Daley, A.; Mulholland, K.; Cheng, D.; South, M.; Waller, G.; Barr, I.; et al. Changing Epidemiology of Respiratory Syncytial Virus in Australia-Delayed Re-Emergence in Victoria Compared to Western Australia/New South Wales (WA/NSW) After Prolonged Lock-Down for Coronavirus Disease 2019 (COVID-19). Clin. Infect. Dis. 2021, 73, 2365–2366. [Google Scholar] [CrossRef]
  104. Fischli, K.; Schöbi, N.; Duppenthaler, A.; Casaulta, C.; Riedel, T.; Kopp, M.V.; Agyeman, P.K.A.; Aebi, C. Postpandemic fluctuations of regional respiratory syncytial virus hospitalization epidemiology: Potential impact on an immunization program in Switzerland. Eur. J. Pediatr. 2024, 183, 5149–5161. [Google Scholar] [CrossRef] [PubMed]
  105. Ren, L.; Lin, L.; Zhang, H.; Wang, Q.; Cheng, Y.; Liu, Q.; Fang, B.; Xie, L.; Wang, M.; Yang, J.; et al. Epidemiological and clinical characteristics of respiratory syncytial virus and influenza infections in hospitalized children before and during the COVID-19 pandemic in Central China. Influenza Other Respir. Viruses 2023, 17, e13103. [Google Scholar] [CrossRef]
  106. Zheng, Z.; Pitzer, V.E.; Shapiro, E.D.; Bont, L.J.; Weinberger, D.M. Estimation of the Timing and Intensity of Reemergence of Respiratory Syncytial Virus Following the COVID-19 Pandemic in the US. JAMA Netw. Open 2021, 4, e2141779. [Google Scholar] [CrossRef]
  107. New South Wales. NSW Respiratory Surveillance Reports—COVID-19 and Influenza. Available online: https://www.health.nsw.gov.au/Infectious/covid-19/Pages/weekly-reports.aspx (accessed on 11 December 2024).
  108. National Institute for Communicable Diseases. Weekly Respiratory Pathogens Surveillance Report. Johannesburg: National Health Laboratory Service. Available online: https://www.nicd.ac.za/covid-19 (accessed on 11 December 2024).
  109. Trigueros Montes, J.B.; Montes, D.; Miele, A.; Baik-Han, W.; Gulati, G.; Lew, L.Q. The Impact of COVID-19 Pandemic on Respiratory Syncytial Virus Infection in Children. Pulm. Med. 2024, 2024, 2131098. [Google Scholar] [CrossRef] [PubMed]
  110. Jiang, W.; Chen, S.; Lv, M.; Zhang, Z.; Wang, Z.; Shao, X.; Hua, S.; Hao, C.; Wang, Y. Are we ready to face the next wave of RSV surge after the COVID-19 Omicron pandemic in China? Front. Cell. Infect. Microbiol. 2023, 13, 1216536. [Google Scholar] [CrossRef] [PubMed]
  111. Mori, T.; Kitano, T.; Kitagawa, D.; Murata, M.; Onishi, M.; Hachisuka, S.; Okubo, T.; Yamamoto, N.; Nishikawa, H.; Onaka, M.; et al. Risk of admission requirement among children with respiratory infection in the post-COVID-19 pandemic era. J. Infect. Public Health 2024, 17, 102570. [Google Scholar] [CrossRef]
  112. Kim, Y.K.; Song, S.H.; Ahn, B.; Lee, J.K.; Choi, J.H.; Choi, S.H.; Yun, K.W.; Choi, E.H. Shift in Clinical Epidemiology of Human Parainfluenza Virus Type 3 and Respiratory Syncytial Virus B Infections in Korean Children Before and During the COVID-19 Pandemic: A Multicenter Retrospective Study. J. Korean Med. Sci. 2022, 37, e215. [Google Scholar] [CrossRef] [PubMed]
  113. Rao, S.; Armistead, I.; Messacar, K.; Alden, N.B.; Schmoll, E.; Austin, E.; Dominguez, S.R. Shifting Epidemiology and Severity of Respiratory Syncytial Virus in Children During the COVID-19 Pandemic. JAMA Pediatr. 2023, 177, 730–732. [Google Scholar] [CrossRef] [PubMed]
  114. Brisca, G.; Mariani, M.; Buratti, S.; Ferretti, M.; Pirlo, D.; Buffoni, I.; Mallamaci, M.; Salvati, P.; Tagliarini, G.; Piccotti, E.; et al. How has the SARS-CoV-2 pandemic changed the epidemiology and management of acute bronchiolitis? Pediatr. Pulmonol. 2023, 58, 1169–1177. [Google Scholar] [CrossRef] [PubMed]
  115. Gastelum-Bernal, M.A.; Mondragón-González, L.I.; Peñuñuri-Ballesteros, J.M.; Félix-Ramos, G.; Gómez-Jiménez, I.A.; Mejía, L.R.C.; Frías-Mendívil, M. Severity and complications in infants with respiratory syncytial virus infection after the SARS-CoV-2 pandemic. Bol. Med. Hosp. Infant. Mex. 2024, 81, 90–96. [Google Scholar] [PubMed]
  116. Kim, Y.E.; Kang, D.; Park, J.S.; Choi, E.H.; Yun, K.W. Clinical Characteristics and Severity of Respiratory Syncytial Virus Infection in Korean Children during the Post-COVID-19 Pandemic Period. Infect. Chemother. 2024, 56, 83–87. [Google Scholar] [CrossRef] [PubMed]
  117. Cardenas, J.; Pringle, C.; Filipp, S.L.; Gurka, M.J.; Ryan, K.A.; Avery, K.L. Changes in Critical Bronchiolitis After COVID-19 Lockdown. Cureus 2022, 14, e25064. [Google Scholar] [CrossRef] [PubMed]
  118. Pruccoli, G.; Castagno, E.; Raffaldi, I.; Denina, M.; Barisone, E.; Baroero, L.; Timeus, F.; Rabbone, I.; Monzani, A.; Terragni, G.M.; et al. The Importance of RSV Epidemiological Surveillance: A Multicenter Observational Study of RSV Infection during the COVID-19 Pandemic. Viruses 2023, 15, 280. [Google Scholar] [CrossRef]
  119. Zven, S.; Dorr, M.; Malloy, A.M.W.; Susi, A.; Nylund, C.M.; Hisle-Gorman, E. Predicting the RSV Surge: Pediatric RSV Patterns of the COVID Pandemic. Pediatr. Infect. Dis. J. 2023, 42, e349–e351. [Google Scholar] [CrossRef]
  120. Public Health Surveillance: Information for New Zealand Public Health Action. Available online: https://www.esr.cri.nz/expertise/public-health/infectious-disease-intelligence-surveillance/#Surveillancereports (accessed on 11 December 2024).
  121. Eden, J.S.; Sikazwe, C.; Xie, R.; Deng, Y.M.; Sullivan, S.G.; Michie, A.; Levy, A.; Cutmore, E.; Blyth, C.C.; Britton, P.N.; et al. Off-season RSV epidemics in Australia after easing of COVID-19 restrictions. Nat. Commun. 2022, 13, 2884. [Google Scholar] [CrossRef] [PubMed]
  122. Virant, M.J.; Luštrek, M.; Kogoj, R.; Petrovec, M.; Uršič, T. Changes in HRSV Epidemiology but Not Circulating Variants in Hospitalized Children due to the Emergence of SARS-CoV-2. Viruses 2023, 15, 1218. [Google Scholar] [CrossRef] [PubMed]
  123. Dolores, A.; Stephanie, G.; Mercedes, S.N.J.; Érica, G.; Mistchenko, A.S.; Mariana, V. RSV reemergence in Argentina since the SARS-CoV-2 pandemic. J. Clin. Virol. 2022, 149, 105126. [Google Scholar] [CrossRef]
  124. Hönemann, M.; Thiem, S.; Bergs, S.; Berthold, T.; Propach, C.; Siekmeyer, M.; Frille, A.; Wallborn, T.; Maier, M.; Pietsch, C. In-Depth Analysis of the Re-Emergence of Respiratory Syncytial Virus at a Tertiary Care Hospital in Germany in the Summer of 2021 after the Alleviation of Non-Pharmaceutical Interventions Due to the SARS-CoV-2 Pandemic. Viruses 2023, 15, 877. [Google Scholar] [CrossRef] [PubMed]
  125. Lee, C.Y.; Wu, T.H.; Fang, Y.P.; Chang, J.C.; Wang, H.C.; Lin, S.J.; Mai, C.H.; Chang, Y.C.; Chou, T.Y. Delayed respiratory syncytial virus outbreak in 2020 in Taiwan was correlated with two novel RSV-A genotype ON1 variants. Influenza Other Respir. Viruses 2022, 16, 511–520. [Google Scholar] [CrossRef] [PubMed]
  126. Jelley, L.; Douglas, J.; O’Neill, M.; Berquist, K.; Claasen, A.; Wang, J.; Utekar, S.; Johnston, H.; Bocacao, J.; Allais, M.; et al. Spatial and temporal transmission dynamics of respiratory syncytial virus in New Zealand before and after the COVID-19 pandemic. Nat. Commun. 2024, 15, 9758. [Google Scholar] [CrossRef] [PubMed]
  127. Pierangeli, A.; Nenna, R.; Fracella, M.; Scagnolari, C.; Oliveto, G.; Sorrentino, L.; Frasca, F.; Conti, M.G.; Petrarca, L.; Papoff, P.; et al. Genetic diversity and its impact on disease severity in respiratory syncytial virus subtype-A and -B bronchiolitis before and after pandemic restrictions in Rome. J. Infect. 2023, 87, 305–314. [Google Scholar] [CrossRef] [PubMed]
  128. Guo, Y.J.; Wang, B.H.; Li, L.; Li, Y.L.; Chu, X.L.; Li, W. Epidemiological and genetic characteristics of respiratory syncytial virus infection in children from Hangzhou after the peak of COVID-19. J. Clin. Virol. 2023, 158, 105354. [Google Scholar] [CrossRef] [PubMed]
  129. Cai, W.; Köndgen, S.; Tolksdorf, K.; Dürrwald, R.; Schuler, E.; Biere, B.; Schweiger, B.; Goerlitz, L.; Haas, W.; Wolff, T.; et al. Atypical age distribution and high disease severity in children with RSV infections during two irregular epidemic seasons throughout the COVID-19 pandemic, Germany, 2021 to 2023. Euro Surveill. 2024, 29, 2300465. [Google Scholar] [CrossRef] [PubMed]
  130. Pierangeli, A.; Midulla, F.; Piralla, A.; Ferrari, G.; Nenna, R.; Pitrolo, A.M.G.; Licari, A.; Marseglia, G.L.; Abruzzese, D.; Pellegrinelli, L.; et al. Sequence analysis of respiratory syncytial virus cases reveals a novel subgroup -B strain circulating in north-central Italy after pandemic restrictions. J. Clin. Virol. 2024, 173, 105681. [Google Scholar] [CrossRef] [PubMed]
  131. Jiang, M.L.; Xu, Y.P.; Wu, H.; Zhu, R.N.; Sun, Y.; Chen, D.M.; Wang, F.; Zhou, Y.T.; Guo, Q.; Wu, A.; et al. Changes in endemic patterns of respiratory syncytial virus infection in pediatric patients under the pressure of nonpharmaceutical interventions for COVID-19 in Beijing, China. J. Med. Virol. 2023, 95, e28411. [Google Scholar] [CrossRef] [PubMed]
  132. Chang, D.; Lin, M.; Song, N.; Zhu, Z.; Gao, J.; Li, S.; Liu, H.; Liu, D.; Zhang, Y.; Sun, W.; et al. The emergence of influenza B as a major respiratory pathogen in the absence of COVID-19 during the 2021-2022 flu season in China. Virol. J. 2023, 20, 189. [Google Scholar] [CrossRef] [PubMed]
  133. Sun, Y.; Dai, L.; Shan, Y.; Yang, Y.; Wu, Y.; Huang, X.; Ma, N.; Huang, Q.; Jiang, M.; Jia, M.; et al. Pathogen characteristics of respiratory infections in the season after the COVID-19 pandemic between August and December 2023: Evidence from direct-to-consumer testing-based surveillance in Guangzhou and Beijing, China. Int. J. Infect. Dis. 2024, 147, 107195. [Google Scholar] [CrossRef]
  134. Luštrek, M.; Cesar, Z.; Suljič, A.; Kogoj, R.; Knap, N.; Virant, M.J.; Uršič, T.; Petrovec, M.; Avšič-Županc, T.; Korva, M. Influenza A, Influenza B, human respiratory syncytial virus and SARSCoV-2 molecular diagnostics and epidemiology in the post COVID-19 era. Respir. Res. 2024, 25, 234. [Google Scholar] [CrossRef] [PubMed]
  135. Kandeel, A.; Fahim, M.; Deghedy, O.; Roshdy, W.H.; Khalifa, M.K.; Shesheny, R.E.; Kandeil, A.; Naguib, A.; Afifi, S.; Mohsen, A.; et al. Resurgence of influenza and respiratory syncytial virus in Egypt following two years of decline during the COVID-19 pandemic: Outpatient clinic survey of infants and children, October 2022. BMC Public Health 2023, 23, 1067. [Google Scholar] [CrossRef] [PubMed]
  136. Ouafi, M.; Dubos, F.; Engelmann, I.; Lazrek, M.; Guigon, A.; Bocket, L.; Hober, D.; Alidjinou, E.K. Rapid syndromic testing for respiratory viral infections in children attending the emergency department during COVID-19 pandemic in Lille, France, 2021-2022. J. Clin. Virol. 2022, 153, 105221. [Google Scholar] [CrossRef]
  137. Juárez, X.; García Causarano, M.F.; Burundarena, C.; Dondoglio, P.; Montoto Piazza, L.; Wenk, G.; Haleblian, E.; Rial, M.J.; Cancellara, A. Children with influenza admitted at a children’s hospital in Argentina in the 2019-2022 period: What has changed after the COVID-19 pandemic? Arch. Argent. Pediatr. 2024, 122, e202310130. [Google Scholar] [PubMed]
  138. Maison, N.; Peck, A.; Illi, S.; Meyer-Buehn, M.; von Mutius, E.; Hübner, J.; von Both, U. The rising of old foes: Impact of lockdown periods on “non-SARS-CoV-2” viral respiratory and gastrointestinal infections. Infection 2022, 50, 519–524. [Google Scholar] [CrossRef]
  139. Kurz, H.; Sever-Yildiz, G.; Kocsisek, C.V.; Resch, E.; Großschädl, C.; Totschnig, L.; Resch, B. Respiratory Syncytial Virus and Influenza During the COVID-19 Pandemic: A Two-center Experience. Pediatr. Infect. Dis. J. 2024, 43, 410–414. [Google Scholar] [CrossRef]
  140. Olsen, S.J.; Winn, A.K.; Budd, A.P.; Prill, M.M.; Steel, J.; Midgley, C.M.; Kniss, K.; Burns, E.; Rowe, T.; Foust, A.; et al. Changes in influenza and other respiratory virus activity during the COVID-19 pandemic-United States, 2020-2021. Am. J. Transplant. 2021, 21, 3481–3486. [Google Scholar] [CrossRef] [PubMed]
  141. Zheng, L.; Qi, J.; Wu, J.; Zheng, M. Changes in Influenza Activity and Circulating Subtypes During the COVID-19 Outbreak in China. Front. Med. 2022, 9, 829799. [Google Scholar] [CrossRef]
  142. Del Riccio, M.; Nunes, M.C.; Cowling, B.J.; Lina, B.; McCauley, J.W.; Meijer, A.; Nohynek, H.; Boudewijns, B.; Caini, S. Post-disappearance scenarios: Policy implications following the potential disappearance of B/Yamagata lineage influenza viruses. Euro Surveill. 2024, 29, 2400196. [Google Scholar] [CrossRef] [PubMed]
  143. World Health Organization (WHO). Recommended Composition of Influenza Virus Vaccines for Use in the 2024-2025 Northern Hemisphere Influenza Season; WHO: Geneva, Switzerland, 2024; Available online: https://www.who.int/publications/m/item/recommended-composition-of-influenza-virus-vaccines-for-use-in-the-2024-2025-northern-hemisphere-influenza-season (accessed on 27 December 2024).
  144. Poole, S.; Brendish, N.J.; Tanner, A.R.; Clark, T.W. Physical distancing in schools for SARS-CoV-2 and the resurgence of rhinovirus. Lancet Respir. Med. 2020, 8, e92–e93. [Google Scholar] [CrossRef] [PubMed]
  145. Park, S.; Michelow, I.C.; Choe, Y.J. Shifting Patterns of Respiratory Virus Activity Following Social Distancing Measures for Coronavirus Disease 2019 in South Korea. J. Infect. Dis. 2021, 224, 1900–1906. [Google Scholar] [CrossRef]
  146. Thongpan, I.; Vichaiwattana, P.; Vongpunsawad, S.; Poovorawan, Y. Upsurge of human rhinovirus infection followed by a delayed seasonal respiratory syncytial virus infection in Thai children during the coronavirus pandemic. Influenza Other Respir. Viruses 2021, 15, 711–720. [Google Scholar] [CrossRef]
  147. Zhang, R.X.; Chen, D.M.; Qian, Y.; Sun, Y.; Zhu, R.N.; Wang, F.; Ding, Y.X.; Guo, Q.; Zhou, Y.T.; Qu, D.; et al. Surges of hospital-based rhinovirus infection during the 2020 coronavirus disease-19 (COVID-19) pandemic in Beijing, China. World J. Pediatr. 2021, 17, 590–596. [Google Scholar] [CrossRef] [PubMed]
  148. Giannattasio, A.; Maglione, M.; Sarno, M.; Botti, C.; Leone, O.; Contieri, M.; Ciccarelli, A.S.; Calì, C.; Savoia, F.; Tipo, V. Rhinovirus in pediatric respiratory infections: More than a simple cold. J. Med. Virol. 2024, 96, e29959. [Google Scholar] [CrossRef] [PubMed]
  149. Presti, S.; Manti, S.; Gambilonghi, F.; Parisi, G.F.; Papale, M.; Leonardi, S. Comparative Analysis of Pediatric Hospitalizations during Two Consecutive Influenza and Respiratory Virus Seasons Post-Pandemic. Viruses 2023, 15, 1825. [Google Scholar] [CrossRef]
  150. Maison, N.; Omony, J.; Rinderknecht, S.; Kolberg, L.; Meyer-Bühn, M.; von Mutius, E.; Hübner, J.; von Both, U. Old foes following news ways?-Pandemic-related changes in the epidemiology of viral respiratory tract infections. Infection 2024, 52, 209–218. [Google Scholar] [CrossRef] [PubMed]
  151. Gil, E.; Roy, S.; Best, T.; Hatcher, J.; Breuer, J. Increasing rhinovirus prevalence in paediatric intensive care patients since the SARS-CoV2 pandemic. J. Clin. Virol. 2023, 166, 105555. [Google Scholar] [CrossRef] [PubMed]
  152. Yoon, Y.; Kim, K.R.; Park, H.; Kim, S.; Kim, Y.J. Stepwise School Opening and an Impact on the Epidemiology of COVID-19 in the Children. J. Korean Med. Sci. 2020, 35, e414. [Google Scholar] [CrossRef] [PubMed]
  153. Cho, H.J.; Rhee, J.E.; Kang, D.; Choi, E.H.; Lee, N.J.; Woo, S.; Lee, J.; Lee, S.W.; Kim, E.J.; Yun, K.W. Epidemiology of Respiratory Viruses in Korean Children Before and After the COVID-19 Pandemic: A Prospective Study from National Surveillance System. J. Korean Med. Sci. 2024, 39, e171. [Google Scholar] [CrossRef] [PubMed]
  154. Kim, E.Y.; Ryu, B.; Kim, E.K.; Park, Y.J.; Choe, Y.J.; Park, H.K.; Jeong, E.K. Children with COVID-19 after Reopening of Schools, South Korea. Pediatr. Infect. Vaccine 2020, 27, 180–183. [Google Scholar] [CrossRef]
  155. Haapanen, M.; Renko, M.; Artama, M.; Kuitunen, I. The impact of the lockdown and the re-opening of schools and day cares on the epidemiology of SARS-CoV-2 and other respiratory infections in children-A nationwide register study in Finland. EClinical Med. 2021, 34, 100807. [Google Scholar] [CrossRef] [PubMed]
  156. Foley, D.A.; Sikazwe, C.T.; Minney-Smith, C.A.; Ernst, T.; Moore, H.C.; Nicol, M.P.; Smith, D.W.; Levy, A.; Blyth, C.C. An unusual resurgence of human metapneumovirus in Western Australia following the reduction of non-pharmaceutical interventions to prevent SARS-CoV-2 transmission. Viruses 2022, 14, 2135. [Google Scholar] [CrossRef] [PubMed]
  157. Foley, D.A.; Yeoh, D.K.; Minney-Smith, C.A.; Shin, C.; Hazelton, B.; Hoeppner, T.; Moore, H.C.; Nicol, M.; Sikazwe, C.; Borland, M.L.; et al. A surge in human metapneumovirus paediatric respiratory admissions in Western Australia following the reduction of SARS-CoV-2 nonpharmaceutical interventions. J. Paediatr. Child. Health 2023, 59, 987–991. [Google Scholar] [CrossRef] [PubMed]
  158. Pelletier, J.H.; Rakkar, J.; Au, A.K.; Fuhrman, D.; Clark, R.S.B.; Horvat, C.M. Trends in US Pediatric Hospital Admissions in 2020 Compared with the Decade Before the COVID-19 Pandemic. J.A.M.A. Netw. Open 2021, 4, e2037227. [Google Scholar] [CrossRef]
  159. Sachs, N.; Goldberg, L.; Levinsky, Y.; Dizitzer, Y.; Vardi, Y.; Krause, I.; Scheuerman, O.; Livni, G.; Bilavsky, E.; Bilavsky-Yarden, H. The Effect of the COVID-19 Pandemic on Pediatric Respiratory Hospitalizations. Isr. Med. Assoc. J. 2023, 25, 171–176. [Google Scholar]
  160. Hartnett, K.P.; Kite-Powell, A.; DeVies, J.; Coletta, M.A.; Boehmer, T.K.; Adjemian, J.; Gundlapalli, A.V. Impact of the COVID-19 Pandemic on Emergency Department Visits-United States, January 1, 2019-May 30, 2020. MMWR Morb. Mortal. Wkly. Rep. 2020, 69, 699–704. [Google Scholar] [CrossRef]
  161. Liu, P.; Xu, M.; Cao, L.; Su, L.; Lu, L.; Dong, N.; Jia, R.; Zhu, X.; Xu, J. Impact of COVID-19 pandemic on the prevalence of respiratory viruses in children with lower respiratory tract infections in China. Virol. J. 2021, 18, 159. [Google Scholar] [CrossRef] [PubMed]
  162. van Summeren, J.; Meijer, A.; Aspelund, G.; Casalegno, J.S.; Erna, G.; Hoang, U.; Lina, B.; de Lusignan, S.; Teirlinck, A.C.; Thors, V.; et al. Low levels of respiratory syncytial virus activity in Europe during the 2020/21 season: What can we expect in the coming summer and autumn/winter? Euro Surveill. 2021, 26, 2100639. [Google Scholar] [CrossRef] [PubMed]
  163. Amaddeo, A.; Cason, C.; Cozzi, G.; Ronfani, L.; Comar, M. Social distancing measures for COVID-19 are changing winter season. Arch. Dis. Child. 2021, 106, e47. [Google Scholar] [CrossRef]
  164. Geoghegan, J.L.; Holmes, E.C. The phylogenomics of evolving virus virulence. Nat. Rev. Genet. 2018, 19, 756–769. [Google Scholar] [CrossRef] [PubMed]
  165. Niese, R.; van der Vlist, D.; Verhagen, M.; de Haan, N.; Stunnenberg, M.; Serafim, F.; Kretzschmar, M.; van der Wal, A.; Vermeulen, L.; Tholen, A. Risk mapping of respiratory viral transmission and disease severity using individual and environmental health parameters: A scoping review and protocol analysis. One Health 2024, 18, 100741. [Google Scholar] [CrossRef] [PubMed]
  166. Murari, A.; Gelfusa, M.; Craciunescu, T.; Gelfusa, C.; Gaudio, P.; Bovesecchi, G.; Rossi, R. Effects of environmental conditions on COVID-19 morbidity as an example of multicausality: A multi-city case study in Italy. Front. Public Health 2023, 11, 1222389. [Google Scholar] [CrossRef] [PubMed]
  167. Ijaz, M.K.; Sattar, S.A.; Nims, R.W.; Boone, S.A.; McKinney, J.; Gerba, C.P. Environmental dissemination of respiratory viruses: Dynamic interdependencies of respiratory droplets, aerosols, aerial particulates, environmental surfaces, and contribution of viral re-aerosolization. PeerJ 2023, 11, e16420. [Google Scholar] [CrossRef] [PubMed]
  168. Klompas, M.; Milton, D.K.; Rhee, C.; Baker, M.A.; Leekha, S. Current Insights into Respiratory Virus Transmission and Potential Implications for Infection Control Programs: A Narrative Review. Ann. Intern. Med. 2021, 174, 1710–1718. [Google Scholar] [CrossRef] [PubMed]
  169. Assad, Z.; Romain, A.S.; Aupiais, C.; Shum, M.; Schrimpf, C.; Lorrot, M.; Corvol, H.; Prevost, B.; Ferrandiz, C.; Giolito, A.; et al. Nirsevimab and Hospitalization for RSV Bronchiolitis. N. Engl. J. Med. 2024, 391, 144–154. [Google Scholar] [CrossRef] [PubMed]
Figure 1. PRISMA flowchart for selection of studies [13].
Figure 1. PRISMA flowchart for selection of studies [13].
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MDPI and ACS Style

Maglione, M.; Tipo, V.; Barbieri, E.; Ragucci, R.; Ciccarelli, A.S.; Esposito, C.; Carangelo, L.; Giannattasio, A. Changes in Respiratory Viruses’ Activity in Children During the COVID-19 Pandemic: A Systematic Review. J. Clin. Med. 2025, 14, 1387. https://doi.org/10.3390/jcm14041387

AMA Style

Maglione M, Tipo V, Barbieri E, Ragucci R, Ciccarelli AS, Esposito C, Carangelo L, Giannattasio A. Changes in Respiratory Viruses’ Activity in Children During the COVID-19 Pandemic: A Systematic Review. Journal of Clinical Medicine. 2025; 14(4):1387. https://doi.org/10.3390/jcm14041387

Chicago/Turabian Style

Maglione, Marco, Vincenzo Tipo, Emiliano Barbieri, Roberta Ragucci, Agnese Sara Ciccarelli, Chiara Esposito, Ludovica Carangelo, and Antonietta Giannattasio. 2025. "Changes in Respiratory Viruses’ Activity in Children During the COVID-19 Pandemic: A Systematic Review" Journal of Clinical Medicine 14, no. 4: 1387. https://doi.org/10.3390/jcm14041387

APA Style

Maglione, M., Tipo, V., Barbieri, E., Ragucci, R., Ciccarelli, A. S., Esposito, C., Carangelo, L., & Giannattasio, A. (2025). Changes in Respiratory Viruses’ Activity in Children During the COVID-19 Pandemic: A Systematic Review. Journal of Clinical Medicine, 14(4), 1387. https://doi.org/10.3390/jcm14041387

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