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Article

Clinical Characterization of Respiratory Syncytial Virus Infection in Adults: A Neglected Disease?

by
Cassia F. Estofolete
1,2,*,
Cecília A. Banho
1,
Alice T. Verro
2,
Flora A. Gandolfi
1,3,
Bárbara F. dos Santos
1,2,
Livia Sacchetto
1,
Beatriz de C. Marques
1,
Nikos Vasilakis
4,5,6,7,8,9 and
Maurício L. Nogueira
1,2,4,*
1
Laboratório de Pesquisas em Virologia, Faculdade de Medicina de São José do Rio Preto (FAMERP), São José do Rio Preto 15090-000, SP, Brazil
2
Hospital de Base of São José do Rio Preto, São José do Rio Preto 15090-000, SP, Brazil
3
Hospital da Criança e Maternidade of São José do Rio Preto, São José do Rio Preto 15091-240, SP, Brazil
4
Department of Pathology, The University of Texas Medical Branch, Galveston, TX 77555, USA
5
Department of Preventive Medicine and Population Health, The University of Texas Medical Branch, Galveston, TX 77555, USA
6
Center for Vector-Borne and Zoonotic Diseases, The University of Texas Medical Branch, Galveston, TX 77555, USA
7
Center for Biodefense and Emerging Infectious Diseases, The University of Texas Medical Branch, Galveston, TX 77555, USA
8
Center for Tropical Diseases, The University of Texas Medical Branch, Galveston, TX 77555, USA
9
Institute for Human Infection and Immunity, The University of Texas Medical Branch, Galveston, TX 77555, USA
*
Authors to whom correspondence should be addressed.
Viruses 2023, 15(9), 1848; https://doi.org/10.3390/v15091848
Submission received: 14 July 2023 / Revised: 14 August 2023 / Accepted: 23 August 2023 / Published: 31 August 2023
(This article belongs to the Section Human Virology and Viral Diseases)

Abstract

:
Lower respiratory tract infections (LRIs) are a significant cause of disability-adjusted life-years (DALYs) across all age groups, especially in children under 9 years of age, and adults over 75. The main causative agents are viruses, such as influenza and respiratory syncytial virus (RSV). Viral LRIs in adults have historically received less attention. This study investigated the incidence of RSV and influenza in adult patients admitted to a referral hospital, as well as the clinical profile of these infections. Molecular testing was conducted on nasopharyngeal samples taken from a respiratory surveillance cohort comprising adult (15–59 years) and elderly (60+ years) hospitalized patients who tested negative for SARS-CoV-2, to determine the prevalence for influenza and RSV. Influenza was found to be less frequent among the elderly. The main symptoms of RSV infections were cough, fever, dyspnea, malaise, and respiratory distress, while headache, nasal congestion, a sore throat, and myalgia were most frequent in influenza. Elderly patients with RSV were not found to have more severe illness than adults under age 60, underscoring the importance of providing the same care to adults with this viral infection.

1. Introduction

In 2019, lower respiratory tract infections (LRIs) were the fourth-leading cause of disability-adjusted life-years (DALYs) across all age groups, with the greatest impact on children aged 0–9 years, followed by adults over the age of 75. Historical data reveal similar trends, with the strongest impact on children and the elderly [1]. Furthermore, an estimated 176,740 people died from LRIs in South America in 2019 alone, and 3,872,414 life-years were lost [2].
Several viral infections cause LRIs [as reviewed in [3]], but three stand out: respiratory syncytial virus (RSV) [4], and influenza A (IAV) and B (IBV) [5], due to their case numbers, and the consequent burden on health systems due to the increased hospitalization and morbidity rates, especially among children under five years of age [4,5]. Moreover, the accurate etiological diagnosis of LRIs presents a further challenge when viral infections present overlapping symptoms [6]. Viral respiratory infections, including RSV and influenza, may manifest as various respiratory syndromes, such as bronchiolitis, wheezing, asthma exacerbation, croup, pneumonia, and pneumonitis [7].
Up until now, the research on LRIs has focused on children under five and the elderly; the host’s age is a major concern, as early severe disease develops in these groups [8]. Within this context, viral LRIs in non-elderly adults have received little attention. With the emergence of SARS-CoV-2, the unprecedented pandemic, and its devastating effects worldwide, even less attention was paid to other non-SARS-CoV-2 pathogens. Brazil had reported 484,323 cases of severe acute respiratory syndrome (SARS) by epidemiological week 47 of 2022 (ending 26 November). Of these cases, 2.2% were caused by influenza, 3.0% by other respiratory viruses, and 42.4% by undefined agents or etiologies. Among them, the age group most frequently affected was the elderly, with 216,706 cases (50.11%), with 4177 being due to influenza, and 1503 caused by other respiratory viruses [9].
To assess the circulation of respiratory viruses other than SARS-CoV-2 in adults during the COVID-19 pandemic, between December 2021 and April 2022, this study investigated the incidence of RSV and influenza in patients admitted to a referral hospital. We also evaluated the clinical characteristics of infections caused by different viral agents.

2. Materials and Methods

2.1. Description of the Cohort

This study analyzed data from a respiratory surveillance hospital cohort in São José do Rio Preto, São Paulo, Brazil, comprising enrolled adults (individuals aged 15–59 years were considered adults) and elderly patients (60+ years) who were hospitalized at the Hospital de Base de São José do Rio Preto with respiratory symptoms. Nasopharyngeal swab samples were obtained from patients presenting respiratory tract infection symptoms between December 2021 and April 2022.

2.2. Sample Preparation

Total RNA was extracted from 100 µL of nasopharyngeal swab samples using an Extracta Kit Fast DNA and RNA Viral Testing kit (MVXA-P096 FAST), according to the manufacturer’s instructions for the Extracta 96 DNA/RNA extractor and purifier (Loccus, Cotia, Brazil). A one-step real-time polymerase chain reaction (RT-qPCR) was performed, using primers and probes targeting the RNA-dependent RNA polymerase (RdRp), envelope (E), and nucleocapsid (N) of the SARS-CoV-2 genome and human RNAse P designed using the GeneFinder COVID-19 PLUS RealAmp Kit. (OSANG Healthcare, Anyang, Republic of Korea).
Samples that yielded negative results for COVID-19 were tested for three different respiratory viruses (IAV, IBV, and RSV), using an Allplex SARS-CoV-2/IAV/IBV/RSV assay (Seegene Inc., Seoul, Republic of Korea), according to the manufacturer’s instructions. All samples that tested positive for COVID-19 were excluded from the study. RT-qPCR was conducted with a QuantStudio 3 Real-Time PCR System (Thermo Fisher Scientific, Waltham, MA, USA). The results were interpreted based on the cycle threshold (Ct), with samples presenting Cq ≤ 40 considered positive. Positive and negative controls included in the GeneFinder COVID-19 Plus RealAmp kit and the Allplex SARS-CoV-2/IAV/IBV/RSV assay were used, in addition to positive samples included as a positive control. All samples that tested negative for SARS-CoV-2, but positive for other viruses, were included (Figure 1).
Demographic and clinical data, such as sex, ethnicity, age, education level, comorbidities, signs/symptoms, and severity were obtained from the participants’ electronic medical records or local reporting forms and subjected to descriptive and inferential analysis. The chi-square test or Fisher’s exact test was used to compare the categorical variables for the groups diagnosed with IAV, IBV, and RSV, with p < 0.05 considered statistically significant. All statical analyses were performed using the SPSS Statistics software package (version 28.0.1.1; IBM Corporation, Armonk, NY, USA).

3. Results

During the specified study period, 110 samples were considered eligible for the study (Figure 1 and Table 1): 36 (32.73%) were positive for the IAV virus, and 9 (8.18%) for IBV, and RSV was most prevalent, with 51 (46.36%; p < 0.001). Although they were not included in the final analysis of this study, coinfection with the three viruses of interest was observed in 14 samples (12.73%).
The patients infected with IAV were predominantly adults (83.33%; p < 0.001), and white (87.88%; p < 0.001), with a mean age of 38.56 years (±19.51). No significant statistical differences were observed with respect to sex, education, or the presence of comorbidities. For patients infected with IBV, no significant differences were noted, although they were predominantly female (77.78%), white (100%) adults (77.78%), with a mean age of 42.89 years (±18.19), and education up through high school (57.14%). No age group or sex was predominant in the RSV patient group, but white ethnicity (90.20%; p < 0.001), education up to elementary school (56.52%; p = 0.004), and the presence of comorbidities (84.78%; p < 0.001) were more prevalent; the mean age was 59.20 years (±18.21) (Supplementary Table S1).
The clinical data were subdivided according to the diagnosis of influenza A/B (Flu) or RSV, as shown in Table 2 and complemented by Supplementary Table S2. Influenza appeared less frequently in the elderly participants. We found a significant difference in the mean ages: RSV-infected patients were older (59.2 years vs. 39.42 years for patients with influenza). No significant differences were found for sex or ethnicity.
Comorbidities were more frequently present in RSV-infected patients (79.59%) than in other groups (p < 0.001). Of these, high blood pressure was most common in both groups (flu = 18.42%; RSV = 38.78%), but less frequent in the patients with influenza (p = 0.024). An additional statistically significant comorbidity was cardiopathy, which was observed more frequently in patients with RSV (p = 0.004). The frequency of comorbidities by infection group is shown in Table 2.
The main symptoms of influenza were (in descending order) coughing (78.38%), fever (59.46%), nasal congestion (56.76%), myalgia (51.35%), and headache (45.95%). In RSV infections, coughing (71.43%), fever (38.1%), dyspnea (38.1%), malaise (35.71%), and respiratory distress (35.71%) were predominant. Group analysis indicated that headache (p = 0.021), nasal congestion (p = 0.003), sore throat (p > 0.001), and myalgia (p = 0.003) were more frequent in the flu group, while potentially severe symptoms, such as respiratory distress (p < 0.001) and dyspnea (p = 0.005), were more frequent in the RSV group, as shown in Table 2. In terms of severity, no significant difference was seen in deaths or the need for intensive care, but ventilatory support was more frequently required in patients with RSV (p < 0.001). These variables also appear in Table 2.
Our subsequent analysis only examined the hospitalized adults; the most frequently identified respiratory agent in this group was IAV (42.25%), followed by RSV (32.39%), coinfections (15.49%), and IBV (9.86%) (p < 0.001) (Table 3). At this stage, the coinfection group was excluded, as it was impossible to define which agent influenced the variables. No differences were observed with regard to sex or ethnicity, while adults with an incomplete primary school education were predominant in the flu group (p = 0.037). Comorbidities were generally more frequent in the RSV group (p = 0.042) (Table 3).
When symptoms were associated with the viral agent, fever (62.50%; p = 0.012), headache (53.13%; p = 0.008), and myalgia (56.25%; p = 0.005) were seen to be more frequent in the flu group, while dyspnea (42.11%; p = 0.003) and respiratory distress (31.58%; p = 0.002) were, again, associated with RSV infection. Ventilatory support was more frequently required in RSV-infected patients (26.09%; p = 0.009), consistent with the higher frequency of dyspnea and respiratory distress (Table 4).
A final analysis compared the clinical manifestations of RSV infection between adults and elderly patients (Table 5). No differences were observed in sex or ethnicity, while elderly patients with an incomplete primary school education were most prevalent (69.23%; p = 0.049), as was the presence of comorbidities (p = 0.001), most notably cardiopathy (p = 0.046) and high blood pressure (p = 0.049). The most common symptoms in adults (in descending order) were coughing (89.47%), dyspnea (42.11%), respiratory distress (31.78%), fever (26.32%), and nasal congestion (26.32%). The elderly patients were more likely to have a cough (56.42%), fever (47.83%), malaise (47.83%), respiratory distress (39.13%), and dyspnea (34.78%). Differences were only observed for coughing (p = 0.037) and diarrhea (p = 0.035), which were more common in the adults. Interestingly, no differences were observed for dyspnea, respiratory distress, ventilatory support, or death.

4. Discussion

This study reports the frequency of IAV, IBV, and RSV as the cause of LRIs in patients hospitalized between December 2021 and April 2022. This is not the typical season for such respiratory infections in the Southern Hemisphere, and the COVID-19 pandemic was still underway in Brazil. We found RSV to be the main causative agent among the respiratory viruses for which we tested, associated with dyspnea, respiratory distress, and the need for ventilator support, while influenza caused disease characterized by milder symptoms. Most notably, no significant differences were reported in how RSV infections manifested among adult and elderly patients.
RSV is recognized as an important cause of respiratory infection, particularly in children and the elderly. In children, RSV may manifest as an upper respiratory tract infection, characterized by nasal congestion, coughing, fever, malaise, poor appetite, and dehydration. About one-third of infants may develop LRIs that cause pneumonia, bronchiolitis, and laryngotracheitis [10]. These patients may present with tachypnea, wheezing, noisy breathing, and even apnea, progressing to respiratory failure and death [10,11]. The presence of fever is not imperative to identifying suspected cases in RSV, nor in influenza, as proposed by the WHO, as it is absent in around 50% of cases in children and elderly patients [12]. RSV is also associated with long-term sequelae, such as asthma, recurrent wheezing, atopy, and allergies, as well as abnormal respiratory function due to airway remodeling [10]. A review of the costs associated with pediatric hospitalizations in the United States from 2014 to 2021 determined that the average cost per RSV hospitalization ranged from USD 10,214 to USD 57,406, depending on the age group [13].
The literature highlights the involvement of RSVs in children, as well as in elderly people and adults with comorbidities, particularly immunosuppression, asthma, chronic obstructive pulmonary disease, and congestive heart failure [14], in whom this virus may represent an important concern. In these individuals, RSV infection may manifest as nasal congestion and coughing, wheezing, ear pain, sinusitis, crackles, infiltrates on chest radiographs, pneumonia, and respiratory distress. As in children, longer-term complications may be observed, such as a permanent decline in the respiratory function [10]. Falsey et al. observed an annual incidence of RSV ranging from 4 to 10% in high-risk adults, with a higher utilization of medical care; in contrast, the annual frequency in the elderly population was 3–7% [15]. A study in a Thai hospital cohort of adults aged 15 years and above reported 69 cases of RSV infection [16]. These patients were mostly above the age of 50 (87%), and all had at least one comorbidity. The most common clinical presentation was community-acquired pneumonia (82.6%), followed by asthma or chronic obstructive pulmonary disease exacerbation, and acute bronchitis. An analysis of the costs of RSV-associated hospitalization in the elderly estimated an average between USD 8241 and USD 16,034 [17,18]. In adults, the average cost was USD 11,124 [18].
In our study, RSV was identified in over 40% of the samples from non-COVID-19-SARS cases, with similar frequencies in the adult and elderly populations (45.1% vs. 54.9%). Dyspnea was observed in around 38%, and respiratory distress in around 35%, highlighting the clinical impacts of the disease. Comorbidities in general were more frequent in the elderly, as expected. Immunosuppression and pulmonary or cardiac disease are also more common in the elderly, and could represent a risk factor for severe RSV infection. However, the analysis of the clinical manifestation and outcomes of RSV infection did not reveal differences in the occurrence of dyspnea, respiratory distress, or the need for ventilatory support between the adult and elderly groups. Even when comorbidities that could potentially raise the risk for severe disease were present, RSV infection manifested with the same potential severity in both adult and elderly patients, causing dyspnea, respiratory distress, and requiring ventilatory support.
Meanwhile, influenza accounted for 40.91% of cases in this study. Adults were more affected than the elderly, especially by IAV. It is important to note that Brazil’s national immunization program recommends flu vaccination for at-risk groups, including the elderly and adults with comorbidities, but not for healthy adults [19]. The mean age of the patients with IAV and IBV was also lower than that of the RSV patients, and the frequency of comorbidities was consistent with age. The clinical symptom data showed that influenza produced milder disease than RSV, with headaches, myalgia, nasal congestion, and sore throat seen most frequently; these symptoms are usually associated with the upper respiratory tract. In contrast, RSV was associated with a higher frequency of dyspnea and respiratory distress. Our data reinforce that RSV represents a higher potential severity than influenza, a finding corroborated by the more frequent need for ventilatory support.
Influenza was the most common infection when only adult patients were analyzed. The infection was also milder compared to RSV, with fever, headache, myalgia, and nasal congestion most frequently manifesting. In general, IAV and IBV infections may be mostly asymptomatic, with some upper respiratory tract symptoms, such as fever, chills, myalgia, malaise, a dry cough, a sore throat, and nasal discharge [20,21]. The US Centers for Disease Control and Prevention (CDC) estimates the rates of hospitalization and death in symptomatic infections at 1% and 0.1%, respectively [22]. Severe influenza may include respiratory complications such as bronchiolitis, bronchitis, pneumonia, bacterial coinfections, respiratory failure, and acute respiratory distress syndrome, or non-respiratory developments, including heart involvement, myositis, aseptic meningitis, encephalomyelitis, and Guillain–Barré syndrome [20,21]. A four-year prospective hospital cohort involving RSV and influenza revealed similar mortality rates in both diseases: 8% and 7%, respectively [15]. Although we found higher rates, we did not find a statistically significant difference between these viruses. Even though influenza may have the potential for severe disease, we found a higher frequency of this outcome in cases of RSV infection (p < 0.001 for respiratory distress, dyspnea, and ventilatory support). Even in adults, 6.25% of infected patients reported dyspnea, 5.56% required ventilatory support, and 2.78% needed intensive care.
Seasonal outbreaks of influenza and RSV tend to occur in both tropical and temperate countries in winter [23,24], but summertime cases, such as the ones seen in our cohort, do not represent an unexplained event, as even influenza and RSV are common in that season. Non-pharmaceutical interventions to control the spread of SARS-CoV-2, such as masking, also effectively limited the transmission of other respiratory agents, such as RSV and influenza. Cases of viral respiratory illnesses rebounded as control measures loosened, even out of season; this effect was also observed in other countries, including Australia, New Zealand, and South Africa [25]. Similarly, a flu outbreak occurred in Rio de Janeiro in November 2021, when lower mean temperatures were observed, alongside a discrepancy between flu vaccine strains and the circulating virus [23].

5. Conclusions

Our findings demonstrate the importance of differential diagnostics for respiratory infections, even during outbreaks and epidemics. Although the literature has adequately described the effects of respiratory agents in children and the elderly, in our cohort, we did not observe different clinical manifestations of RSV infections in adult and elderly patients, suggesting that this disease may have a significant clinical impact in adults in general, and not just in known risk groups. This observation underscores the need to define the agents that cause moderate and severe respiratory infections, especially as preventive and therapeutic options emerge. Previous studies have been supporting clinical trials in newborns and elderly (for example, clinicaltrials.gov: NCT04908683; NCT04908683; NCT05559476; NCT04732871), but they have not been focusing on adults, although these comprise a potential severity group that should be targeted through future vaccination programs. This is highlighted in this study through our demonstration of how dyspnea, respiratory distress, and the need for ventilatory support occurred at similar frequencies in adults and the elderly.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/v15091848/s1, Table S1: General characteristics of each group in the respiratory surveillance cohort, by infectious agent.; Table S2: Clinical characteristics of patients infected by influenza A and B and respiratory syncytial virus in the respiratory surveillance cohort, December 2021–April 2022.

Author Contributions

Conceptualization: C.F.E. and M.L.N.; Methodology: C.F.E., C.A.B., L.S., B.d.C.M. and M.L.N.; Investigation: C.F.E., A.T.V., C.A.B., F.A.G., B.F.d.S., L.S. and B.d.C.M.; Funding acquisition: C.F.E., N.V. and M.L.N.; Project administration: C.F.E. and M.L.N.; Supervision: N.V. and M.L.N.; Writing—original draft: C.F.E., A.T.V., F.A.G., B.F.d.S., N.V. and M.L.N.; Writing—review and editing: C.F.E., N.V. and M.L.N. All authors have read and agreed to the published version of the manuscript.

Funding

This study was supported by the São Paulo Research Foundation (FAPESP) via grant 2013/21719-3 for M.L.N., and 2022/09229-0 for C.F.E., and by INCT Dengue Program grant 465425/2014-3 (M.L.N.). M.L.N. is a Brazilian National Council for Scientific and Technological Development (CNPq) Research Fellow. M.L.N. and N.V. are partly funded by the Centers for Research in Emerging Infectious Diseases (CREID), “The Coordinating Research on Emerging Arboviral Threats Encompassing the Neotropics (CREATE-NEO)” grant U01AI151807 (to N.V.) from the National Institutes of Health (NIH/USA).

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki, and conducted on retrospective samples, with approval by the Institutional Review Board of the School of Medicine of São José do Rio Preto (FAMERP) (protocol code process 31588920.0.0000.5415, approved on 14 May 2020). The FAMERP IRB granted approval for the study, and the consent terms were waived. Confidentiality was ensured through the de-identification of all samples before data entry and analysis.

Informed Consent Statement

The consent terms were waived by the IRB.

Data Availability Statement

De-identified data are available from the authors upon request.

Acknowledgments

We acknowledge colleagues from Hospital de Base de São José do Rio Preto for support during sample and data collection.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Selection flow of samples and distribution of respiratory agents in the hospital cohort.
Figure 1. Selection flow of samples and distribution of respiratory agents in the hospital cohort.
Viruses 15 01848 g001
Table 1. Epidemiological data from 110 patients with samples showing infection with influenza A, influenza B, and respiratory syncytial virus in the respiratory surveillance cohort.
Table 1. Epidemiological data from 110 patients with samples showing infection with influenza A, influenza B, and respiratory syncytial virus in the respiratory surveillance cohort.
Total Samples (N = 110)
N ResponseN Positive or Mean% or s.d.p-ValueX2df
Agent
 RSV1105146.36%<0.00141.7823
 Influenza A1103632.73%
 Influenza B11098.18%
 Coinfection1101412.73%
Sex
 Female1105247.27%0.5670.3271
 Male1105852.73%
Age group
 Mean age11050.3820.42---
 Adult1107164.55%0.0029.3091
 Elderly1103935.45%
Ethnicity
 White1049490.38%<0.001152.5582
 Black10476.73%
 Mixed race10432.88%
Education
 Primary incomplete934043.01%0.1154.3232
 Primary9300.00%
 High school932425.81%
 College932931.18%
Comorbidities976263.92%0.0067.5151
 Cardiopathy971616.49%<0.00143.5571
 Blood pressure973435.05%0.0038.6701
 Hematological disease9733.09%<0.00185.3711
 Down syndrome9722.06%<0.00189.1651
 Liver disease9766.19%<0.00174.4851
 Asthma9711.03%<0.00193.0411
 Diabetes972020.62%<0.00133.4951
 Neurovascular disease9777.22%<0.00171.0211
 Neurological disease9755.15%<0.00178.0311
 Pneumopathy9777.22%<0.00171.0211
 Immunosuppression9711.03%<0.00193.0411
 Kidney disease9777.22%<0.00171.0211
 Obesity9755.15%<0.00178.0311
 Smoker851618.82%<0.00133.0471
 Cancer9799.28%<0.00164.3401
df: degrees of freedom.
Table 2. Clinical characteristics of 96 patients infected with influenza and respiratory syncytial virus in the respiratory surveillance cohort.
Table 2. Clinical characteristics of 96 patients infected with influenza and respiratory syncytial virus in the respiratory surveillance cohort.
FluRSV
N ResponseN Positive or Mean% or s.d.N ResponseN Positive or Mean% or s.d.p-Value
Age group
 Adult (15–59 years)453782.22%512345.10%<0.001
 Elderly (60+ years)45817.78%512854.90%
 Mean age (years)4539.4219.135159.2018.21<0.001
Sex
 Female452146.67%512650.98%0.673
 Male452453.33%512549.02%
Ethnicity
 White413790.24%514690.20%0.894
 Black4137.32%5135.88%
 Mixed race4112.44%5123.92%
Education
 Primary incomplete38718.42%462656.52%0.002
 Primary3800.00%4600.00%
 High school381539.47%46919.57%
 College381642.11%461123.91%
Comorbidities381847.37%493979.59%<0.001
 Cardiopathy3812.63%491428.57%<0.001
 Blood pressure38718.42%491938.78%0.024
 Hematological disease3800.00%4924.08%0.499
 Down syndrome3800.00%4924.08%0.499
 Liver disease3800.00%49612.24%0.300
 Asthma3812.63%4900.00%0.452
 Diabetes38410.53%491326.53%0.044
 Neurovascular disease3800.00%49612.24%0.030
 Neurological disease3800.00%49510.20%0.061
 Pneumopathy3812.63%49510.20%0.215
 Immunosuppression3800.00%4812.08%1
 Kidney disease3800.00%49612.24%0.030
 Obesity3812.63%4936.12%0.623
 Smoker35617.14%41717.07%1
 Cancer38410.53%49510.20%1
Signs and symptoms
 Fever372259.46%421638.10%0.058
 Headache371745.95%42921.43%0.021
 Myalgia371951.35%42819.05%0.003
 Nasal congestion372156.76%421023.81%0.003
 Cough372978.38%423071.43%0.478
 Sore throat371540.54%4249.52%<0.001
 Dyspnea37410.81%421638.10%0.005
 Respiratory distress3712.70%421535.71%<0.001
 Diarrhea3725.41%4249.52%0.679
 Vomiting3700.00%4212.38%1
 Abdominal pain3738.11%4224.76%0.661
 Malaise37821.62%421535.71%0.169
 Loss of smell3712.70%4200.00%0.468
 Loss of taste3712.70%4200.00%0.468
Hospitalization4545100.00%5151100.00%NA
ICU4212.38%5159.80%0.217
Ventilatory support4249.52%502346.00%<0.001
Death43818.60%461532.61%0.132
Table 3. Epidemiological data from 71 adult patients infected with influenza A, influenza B, and respiratory syncytial virus in the respiratory surveillance cohort.
Table 3. Epidemiological data from 71 adult patients infected with influenza A, influenza B, and respiratory syncytial virus in the respiratory surveillance cohort.
Samples from Hospitalized Adults
N ResponseN Positive or Mean% or s.d.p-ValueX2df
Agent
 RSV712332.39%<0.001193
 Influenza A713042.25%
 Influenza B7179.86%
 Coinfection711115.49%
Sex
 Female713143.66%0.2851.1411
 Male714056.34%
Age group
 Mean age713813.20 ---
Ethnicity
 White675886.57%<0.00185.6422
 Black6768.96%
 Mixed race6734.48%
Education
 Primary incomplete631625.40%0.6920.7372
 Primary6300.00%
 High school632031.75%
 College632133.33%
Comorbidities632844.44%<0.0010.7781
 Cardiopathy6334.76%<0.00151.5711
 Blood pressure631523.81%<0.00117.2861
 Hematological disease6323.17%<0.00155.2541
 Down syndrome6323.17%<0.00155.5241
 Liver disease6346.35%<0.00148.0161
 Asthma6300.00%
 Diabetes63914.29%<0.00132.1431
 Neurovascular disease6311.59%<0.00159.0631
 Neurological disease6300.00%
 Pneumopathy6334.76%<0.00151.5711
 Immunosuppression6311.59%<0.00159.0631
 Kidney disease6346.35%<0.00148.0161
 Obesity6334.76%<0.00151.5711
 Smoker531018.87%<0.00120.5471
 Cancer6346.35%<0.00148.0161
Symptoms
 Fever603151.67%0.7960.0671
 Headache602541.67%0.1971.6671
 Myalgia603660.00%0.3021.0671
 Nasal congestion603050.00%101
 Cough604880.00%<0.00121.61
 Sore throat602033.33%0.0106.6671
 Dyspnea601220.00%<0.00121.61
 Respiratory distress60711.67%<0.00135.2671
 Diarrhea6058.33%<0.00141.6671
 Vomiting6000.00%NANANA
 Abdominal pain6046.67%<0.00145.0671
 Malaise601118.33%<0.00124.0671
 Loss of smell6023.33%<0.00152.2671
 Loss of taste6023.33%<0.00152.2671
Hospitalization7171100.00%NANANA
ICU7057.14%<0.00151.4291
Ventilatory support691217.39%<0.00129.3481
Death5735.26%<0.00118.2841
Table 4. Clinical and epidemiological data from 60 adult patients infected with influenza and respiratory syncytial virus in the respiratory surveillance cohort.
Table 4. Clinical and epidemiological data from 60 adult patients infected with influenza and respiratory syncytial virus in the respiratory surveillance cohort.
Flu (A and B)RSV
N ResponseN Positive or Mean% or s.d.N ResponseN Positive or Mean% or s.d.p-Value
Mean age (years)3731.9710.722343.2613.290.001
Sex
 Female371745.95%231147.83%0.887
 Male372054.05%231252.17%
Ethnicity
 White343088.24%231982.61%0.633
 Black3438.82%2328.70%
 Mixed race3412.94%2328.70%
Education
 Primary incomplete30310.00%20840.00%0.037
 Primary3000.00%2000.00%
 High school301343.33%20735.00%
 College301446.67%20525.00%
Comorbidities331030.30%201365.00%0.013
 Cardiopathy3300.00%20315.00%0.049
 Blood pressure33515.15%20525.00%0.475
 Hematological disease3300.00%2015.00%0.377
 Down syndrome3300.00%20210.00%0.138
 Liver disease3300.00%20420.00%0.017
 Asthma3300.00%2000.00%NA
 Diabetes3313.03%20525.00%0.024
 Neurovascular disease3300.00%2015.00%0.377
 Neurological disease3300.00%2000.00%NA
 Pneumopathy3300.00%20210.00%0.138
 Immunosuppression3300.00%2015.00%0.377
 Kidney disease3300.00%20315.00%0.049
 Obesity3313.03%2015.00%1
 Smoker28414.29%17317.65%1
 Cancer3339.09%2015.00%1
Symptoms
 Fever322062.50%19526,32%0.012
 Headache321753.13%19315.79%0.008
 Myalgia321856.25%19315.79%0.005
 Nasal congestion321959.38%19526.32%0.022
 Cough322475.00%191789.47%0.287
 Sore throat321340.63%19315.79%0.065
 Dyspnea3226.25%19842.11%0.003
 Respiratory distress3200.00%19631.58%0.002
 Diarrhea3213.13%19421.05%0.058
 Vomiting3200.00%1900.00%NA
 Abdominal pain3239.38%1915.26%1
 Malaise32618.75%19421.05%1
 Loss of smell3213.13%1900.00%1
 Loss of taste3213.13%1900.00%1
Hospitalization3737100.00%2323100.00%NA
ICU3612.78%23313.04%0.289
Ventilatory support3625.56%23626.09%0.009
Death36616.67%20840.00%0.053
Table 5. Clinical manifestations of RSV in hospitalized adult and elderly patients.
Table 5. Clinical manifestations of RSV in hospitalized adult and elderly patients.
AdultElderly
N ResponseN Positive or Mean% or s.d.N ResponseN Positive or Mean% or s.d.p-Value
Mean age (years)2343.2613.292872.298.74<0.001
Sex
 Female231147.83%281553.57%0.683
 Male231252.17%281346.43%
Ethnicity
 White231982.61%282796.43%0.195
 Black2328.70%2813.57%
 Mixed race2328.70%2800.00%
Education
 Primary incomplete20840.00%261869.23%0.049
 Primary2000.00%2600.00%
 High school20735.00%2627.69%
 College20525.00%26623.08%
Comorbidities201365.00%2626100.00%0.001
 Cardiopathy20315.00%261142.31%0.046
 Blood pressure20525.00%261453.85%0.049
 Hematological disease2015.00%2613.85%1
 Down syndrome20210.00%2600.00%0.184
 Liver disease20420.00%2627.69%0.380
 Asthma2000.00%2600.00%NA
 Diabetes20525.00%26830.77%0.667
 Neurovascular disease2015.00%26519.23%0.212
 Neurological disease2000.00%26519.23%0.059
 Pneumopathy20210.00%26311.54%1
 Immunosuppression2015.00%2600.00%0.435
 Kidney disease20315.00%26311.54%1
 Obesity2015.00%2627.69%1
 Smoker17317.65%26415.38%1
 Cancer2015.00%26415.38%0.369
Signs and Symptoms
 Fever19526.32%231147.83%0.153
 Headache19315.79%23626.09%0.477
 Myalgia19315.79%23521.74%0.709
 Nasal congestion19526.32%23521.74%1
 Cough191789.47%231356.52%0.037
 Sore throat19315.79%2314.35%0.313
 Dyspnea19842.11%23834.78%0.627
 Respiratory distress19631.58%23939.13%0.611
 Diarrhea19421.05%2300.00%0.035
 Vomiting1900.00%2314.35%1
 Abdominal pain1915.26%2314.35%1
 Malaise19421.05%231147.83%0.071
 Loss of smell1900.00%2300.00%NA
 Loss of taste1900.00%2300.00%NA
Hospitalization2323100.00%2828100.00%NA
ICU23313.04%2827.14%0.647
Ventilatory support23626.09%271555.56%0.142
Death20840.00%26726.92%0.348
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Estofolete, C.F.; Banho, C.A.; Verro, A.T.; Gandolfi, F.A.; dos Santos, B.F.; Sacchetto, L.; Marques, B.d.C.; Vasilakis, N.; Nogueira, M.L. Clinical Characterization of Respiratory Syncytial Virus Infection in Adults: A Neglected Disease? Viruses 2023, 15, 1848. https://doi.org/10.3390/v15091848

AMA Style

Estofolete CF, Banho CA, Verro AT, Gandolfi FA, dos Santos BF, Sacchetto L, Marques BdC, Vasilakis N, Nogueira ML. Clinical Characterization of Respiratory Syncytial Virus Infection in Adults: A Neglected Disease? Viruses. 2023; 15(9):1848. https://doi.org/10.3390/v15091848

Chicago/Turabian Style

Estofolete, Cassia F., Cecília A. Banho, Alice T. Verro, Flora A. Gandolfi, Bárbara F. dos Santos, Livia Sacchetto, Beatriz de C. Marques, Nikos Vasilakis, and Maurício L. Nogueira. 2023. "Clinical Characterization of Respiratory Syncytial Virus Infection in Adults: A Neglected Disease?" Viruses 15, no. 9: 1848. https://doi.org/10.3390/v15091848

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