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. 2021 Mar 30;8(7):ofab159. doi: 10.1093/ofid/ofab159

The Global Epidemiology of RSV in Community and Hospitalized Care: Findings From 15 Countries

Lisa Staadegaard 1,, Saverio Caini 1, Sonam Wangchuk 2, Binay Thapa 2, Walquiria Aparecida Ferreira de Almeida 3, Felipe Cotrim de Carvalho 3, Richard Njouom 4, Rodrigo A Fasce 5, Patricia Bustos 6, Jan Kyncl 7,8, Ludmila Novakova 9, Alfredo Bruno Caicedo 10,11, Domenica Joseth de Mora Coloma 10, Adam Meijer 12, Mariëtte Hooiveld 1, Sue Huang 13, Tim Wood 13, Raquel Guiomar 14, Ana Paula Rodrigues 14, Daria Danilenko 15, Kirill Stolyarov 15, Vernon Jian Ming Lee 16,17, Li Wei Ang 16,18, Cheryl Cohen 19,20, Jocelyn Moyes 19,20, Amparo Larrauri 21, Concepción Delgado-Sanz 21, Mai Quynh Le 22, Phuong Vu Mai Hoang 22, Clarisse Demont 23, Mathieu Bangert 23, Jojanneke van Summeren 1, Michel Dückers 1,24,25, John Paget 1
PMCID: PMC8320297  PMID: 34337092

Abstract

Background

Respiratory syncytial virus (RSV) is one of the leading causes of acute respiratory tract infections. To optimize control strategies, a better understanding of the global epidemiology of RSV is critical. To this end, we initiated the Global Epidemiology of RSV in Hospitalized and Community care study (GERi).

Methods

Focal points from 44 countries were approached to join GERi and share detailed RSV surveillance data. Countries completed a questionnaire on the characteristics of their surveillance system.

Results

Fifteen countries provided granular surveillance data and information on their surveillance system. A median (interquartile range) of 1641 (552–2415) RSV cases per season were reported from 2000 and 2020. The majority (55%) of RSV cases occurred in the <1-year-olds, with 8% of cases reported in those aged ≥65 years. Hospitalized cases were younger than those in community care. We found no age difference between RSV subtypes and no clear pattern of dominant subtypes.

Conclusions

The high number of cases in the <1-year-olds indicates a need to focus prevention efforts in this group. The minimal differences between RSV subtypes and their co-circulation implies that prevention needs to target both subtypes. Importantly, there appears to be a lack of RSV surveillance data in the elderly.

Keywords: epidemiology: RSV, respiratory infections, surveillance


Respiratory syncytial virus (RSV) is one of the leading causes of acute respiratory tract infections (ARIs) in both children and adults [1, 2]. The 2016 Global Burden of Disease (GBD) study estimated that RSV is responsible for 24.8 million ARI episodes and 76 600 deaths each year [3]. By the age of 1, ~60%–70% of children have been infected with RSV, and 2%–3% of these infections result in hospitalization, making RSV a leading cause of mortality and morbidity in children age <5, particularly in low- and median-income countries [4, 5]. Although the incidence of RSV infection is generally lower in adults compared with young children [6], RSV has been increasingly recognized as an important cause of respiratory disease in adults. High hospitalization and mortality rates associated with RSV have been reported in the elderly and in high-risk adults [2, 7].

Over 30 potential vaccines and new monoclonal antibodies (mAbs) are currently being evaluated, and new prevention methods are anticipated in the coming years [8]. For an effective implementation of these preventive measures, a clear understanding of the epidemiology of RSV is required. Several studies have previously reported and compared epidemiological metrics on a regional or global level [1, 3, 9]. However, studies transcending the national level do not leverage national surveillance data, and few studies have focused on the overall age distribution of RSV. Though studies have reviewed the epidemiology of RSV subtypes [10], few studies have done so at global level [11].

An important challenge to understand the epidemiology of RSV is a lack of publicly available data [12]. While most influenza-endemic countries have an influenza surveillance system publicly available data, dedicated surveillance systems for RSV are lacking [13]. RSV cases are therefore mostly captured through influenza surveillance systems, which has inherent challenges, and no public platform consolidating these data exists. In 2016, the World Health Organization initiated a pilot study to evaluate the feasibility of incorporating RSV surveillance into the Global Influenza Surveillance and Response System (GISRS) platform [13]. Two studies that emerged from this initiative compared the seasonality of RSV and influenza and described clinical characteristics as well as the performance of case definitions [13, 14].

Although RSV data collected through influenza surveillance systems are not perfectly sensitive or specific for capturing RSV cases [14], they can be a valuable source to predict the timing and duration of RSV epidemics as well as help define risk groups. Therefore, the Global Epidemiology of RSV (GERi) network was launched in 2019 to examine the global epidemiology and timing of RSV epidemics based on virological surveillance data [15]. Here, we describe the surveillance systems used to collect RSV data in 15 countries. Importantly, through access to national surveillance data, we analyze the age distribution of RSV cases overall and examine whether they are differently distributed across care levels or RSV subtypes.

Lastly, to better define the epidemiology of RSV, we explore the role of RSV A and B in terms of overall patterns (dominant seasons), per country, and per level of care.

METHODS

Collection of Surveillance Data

Focal points of 44 countries across the world (usually based at national influenza centers) were approached between January 2019 and January 2020 to identify whether the respective country conducted RSV surveillance, and if so, they were invited to participate in the GERi network. Those who agreed to participate were sent an Excel data collection template and were asked to provide national RSV surveillance data from 2000 onwards. Data requested included: weekly number of RSV cases, age of the cases, number of specimens tested, and, if available, the RSV subtype. In addition, countries were asked to stratify cases by the level of care from which cases were reported.

Initially our data collection template differentiated between 3 levels of care: primary, secondary, and tertiary care. Primary care was defined as day-to-day health care, that is, the first contact and principal point of continuing care within the health care system. This typically includes general practitioners (GPs) or pediatricians. Secondary care was defined as acute care that required treatment for a short period of time, usually being the emergency department (ED) or the intensive care unit (ICU). Lastly, tertiary care was defined as more specialized consultative health care, which usually concerns inpatients and is provided on referral from primary or secondary care providers. We merged secondary and tertiary care into 1 category (referred to henceforth as “hospitalized care”), with primary care referred to as “community care” from this point forward.

Participating countries were also given a questionnaire (Supplementary Data) focused on the functioning of their respective surveillance system(s). In addition, they were asked for supplementary literature outlining their surveillance system(s). Through this mechanism, information on case definitions, definitions of different levels of care, type of laboratory testing, and representativeness of the data were obtained.

Data Analysis

To be included in the analysis, each season was required to contain at least 50 cases. Seasons north of the Tropic of Cancer were defined as ranging from week 27 to week 26 of the next calendar year. For countries south of the Tropic of Cancer, seasons were defined as ranging from week 1 through week 52 of the same calendar year.

The age distribution of RSV cases was investigated by calculating a median and interquartile range (IQR) at the country level, per level of care, and per RSV subtype. Differences in median were tested for significance using a 2-sample Wilcoxon rank sum. At the country level, age was expressed in the form of a relative illness ratio (RIR). The RIR, used to account for different age structures between countries, was calculated as follows:

RIR=(CiCi)/(NiNi)

Here, Ci represents the number of cases in a given age group (i), and Ni represents the population size in a given age group [16]. Age-specific population data were obtained from the United Nations population division [17].

A meta-analysis was performed to pool results on the proportion of specimen testing positive for RSV each season and per country to estimate this proportion per care level using the R package “metafor” [18]. Pooled estimates were calculated using logit transformation and the DerSimonian-Laird estimator for random effects.

Lastly, the distribution of RSV A and B cases across seasons was analyzed for both community and hospitalized care. Differences in proportions were tested using a z test.

The occurrence of RSV A or B dominant seasons was explored using a ≥60% threshold to define a subtype as being dominant. All analyses were performed and figures created using the statistical program R, version 3.6.1 [19].

RESULTS

Structure of RSV Surveillance in Participating Countries

Of the 44 invited countries, 15 countries (Supplementary Figure 1) provided data, and 13 of these completed the questionnaire (Supplementary Data). A summary of questionnaire results can be found in Table 1. Seven countries provided community care surveillance data, 12 provided data from hospitalized care, and 4 provided data on a combination of both. Cases were recorded as part of sentinel surveillance for all 7 countries providing data on community care and 6 out of 12 countries providing data on hospitalized care. The remaining countries recording cases in hospitalized care take a more passive and voluntary approach, where testing is usually driven by diagnostic needs. Definitions of community and hospitalized care largely overlapped on a country level. Most of the community care data are provided by GPs; however, the data from Portugal included emergency room visits. In some countries, data could not be categorized into level of care. The data from the United States, for example, stemmed from national laboratories that receive data from a variety of public health institutions, and some data from Portugal and Cameroon included both out- and inpatients [20].

Table 1.

Description of the RSV Surveillance Systems by Level of Care (eg, Mix, Community, or Hospitalized Care) of the 15 Participating Countries on the Basis of a Questionnaire

Care Levela Regional Stratification Timing Type of Surveillance Care Level Definition Case Definition Methods Detection Representativeness
Cameroon Mix No Year round Sentinel surveillance system in outpatient and hospitalized patients NA Outpatient: ILIHospitalized: SARI Real-time RT-PCR Data from 6 different regions out of 10
Portugal Mix Yes Seasonal (~weeks 40–18) Nonsentinel, laboratory surveillance# Outpatients & hospitalized patients None Real-time RT-PCR + antigen detection No hospitals in the southern region
United States of America Mix Yes Year round Passive national laboratory surveillance (NREVSS) NA NA NA 10 HHS regions, with data from >500 state and local public health laboratories, commercial labs, and hospitals/universities
The Czech Republic Community care No Seasonal (weeks 40–20) Sentinel surveillance GPs for adults and GPs for children ILI/ARI Antigen detection, virus isolation, and other; Biomerieaux 0.37% of GPs and all regions are covered
The Netherlands Community care No Year round Sentinel surveillance—subset of patients; at least 2 per week and GP sentinel practice, 1 of which should be a child age <10 GPs in a sentinel network ILI/ARI Real-time RT-PCR 0.8% of the Dutch population
New Zealand Community care No Seasonal (~weeks 18–40) Sentinel surveillance—subset of patients: all ILIs in Auckland and Wellington and the first patient with ILI from Monday to Wednesday for the rest of NZ GP-based surveillance ILI Real-time RT-PCR: US CDC protocol 80–90 GP practices covering the whole of NZ; previously (<2015) only Auckland region was included
Portugal Community care Yes Seasonal (~weeks 40–18) Sentinel surveillance+ GP at health care centers or patients attending at emergency rooms ILI Real-time RT-PCR All regions
Russian Federation Community care Yes Year round Sentinel surveillance Patients attended a polyclinic ILI Multiplex PCR Facilities in 10 cities, each in every federal district; this population compromises 16.2% of the population
Singapore Community care No Year round Sentinel surveillance+ Government-funded primary clinics (20) & private GPs (30) covering all regions of the country ARI + fever ≥38°C and cough Antigen detection, gel-based RT-PCR, or multiplex syndromic panels All regions are covered
South Africa Community care No Year round Sentinel surveillance# Primary health care clinic in the community ILI Real-time RT-PCR assay, Fast Track Diagnostics Flu/RSV Conducted at 2 clinics in the country
Bhutan Hospitalized care Yes Year round Sentinel surveillance# Hospitalized patients SARI Real-time RT-PCR Nationally
Brazilb Hospitalized care Yes NA NA NA NA NA NA
Chile Hospitalized care No Year round Sentinel surveillance# Cases are in hospitalized patients, may consult at ER SARI Immunofluorescence assay or RT-PCR Cities located in regions with the highest proportion of the population (80%)
The Czech Republic Hospitalized care No Seasonal (weeks 40–20) Nonsentinel/routinely—subset: ~500–700 swabs each epidemic season Local (district) hospitals and regional hospitals + university hospitals NA Antigen detection, virus isolation, and other; Biomerieaux All regions
Ecuador Hospitalized care No Year round Sentinel surveillance# National sentinel surveillance hospitals SARI Antigen detection Nationally
Spainb Hospitalized care No NA NA NA NA NA NA
The Netherlands Hospitalized care No Year round Passive national laboratory surveillance (virologische weekstaten) Testing requested by GPs, clinical
departments in hospitals, and outpatient clinics
NA Rapid antigen test, PCR 14–21 laboratories across the Netherlands, covering 29%–44% of the population
New Zealand Hospitalized care No Seasonal (~weeks 18–40) Sentinel surveillance# Hospital-based surveillance + ICU SARI Real-time RT-PCR 4 hospitals in Auckland (20% of NZ population)
Russian Federation Hospitalized care Yes Year round Sentinel surveillance# Hospitalized patients (special infectious disease hospitals) SARI Multiplex PCR 10 cities, each in every federal district; this population compromises 16.2% of the population
Singapore Hospitalized care No Year round NA Two pediatric departments in public acute care hospitals SARI Antigen detection, gel-based RT-PCR or multiplex syndromic panels All regions are covered
Vietnam Hospitalized care No Year round NA Hospitalized patients SARI Gel-based RT-PCR North of Vietnam only
South Africa Hospitalized care No Year round Sentinel surveillance system# Hospitalized care & tertiary care facilities SARI (>5-y), LRTI (>2 d–<5 y) Real-time RT-PCR assay, Fast Track Diagnostics Flu/RSV Conducted at 7 hospitals in 5 out of 9 provinces

Symbols: #, surveillance aimed at testing all patients fitting the case definition reporting to the included facilities; +, only samples that were negative for influenza were tested for RSV.

Abbreviations: ARI, acute respiratory infection; GP, general practitioner; HHS, US Department of Health & Human Services; ICU, intensive care unit; ILI, influenza-like-illness; LRTI, lower respiratory tract infection; NA, not available; NREVSS, the National Respiratory and Enteric Virus Surveillance System (USA); PCR, polymerase chain reaction; RT-PCR, reverse transcription polymerase chain reaction; SARI, severe acute respiratory infection.

aCare level definitions: community care = day-to-day health care usually provided by the first contact within the health care system, hospitalized care = both acute care received in the emergency department or intensive care unit and more specialized consultative health care usually concerning inpatients, mix = a combination of the 2.

bBrazil and Spain did not return the questionnaire.

The predominant case definition used to capture RSV was influenza-like illness (ILI) in community care and severe acute respiratory infection (SARI) in hospitalized care, with the exception of the Netherlands and Portugal, where ILI was combined with other acute respiratory infection (ARI) in community care. In most countries, RSV is 1 of several respiratory infections tested for by real-time RT-PCR.

The largest variation between countries was seen when comparing representativeness by country. Most of the countries provided data at the national level, with the exception of Chile, Portugal, and New Zealand. Four countries provided regional data (Bhutan, Brazil, Portugal, and the United States). Another factor influencing the representativeness of the data and comparability across countries was testing policy. Where some countries test a predetermined subset of patients (eg, 1 child and 1 adult per week) presenting with ILI or SARI (the Netherlands: community care; New Zealand: community care; and Portugal: mix), others test all patients presenting with ILI or SARI symptoms (Cameroon, the Czech Republic, Portugal: community care; Russian Federation, South Africa, Bhutan, Chile, Ecuador, New Zealand: hospitalized care). In 2 out of 15 countries, specimens collected are first tested for influenza, and testing for other respiratory viruses only occurs if negative for influenza (Portugal and Singapore). However, most surveillance data were collected year-round.

Overview RSV Surveillance Data

Surveillance data shared by the 15 participating countries are summarized in Table 2. Supplementary Figures 2 and 3 show the available national surveillance data over time. Countries provided data for a median (range) of 7 (1–19) seasons, with a median (IQR) of 1641 (552–2415) RSV cases per season. Apart from Brazil, all countries provided a weekly number of specimens tested, with a median (IQR) of 6420 (3473–22 777) specimens tested per season. The majority of cases (97%) were recorded in hospitalized care, both overall and in countries with data available from both community and hospitalized surveillance. For the United States, no age data were available.

Table 2.

Summary of Available Surveillance Data of the 15 Participating Countries; Data Are Summarized on a Country Level and Further Specified for Level of Care (eg, Community or Hospitalized)

Country Seasons, No. Subtyped Data, % Median Cases per Season (IQR) Care Level Cases per Season, Median (IQR) Average % Positive
Africa South Africa 10 (2009–2018) 36 604 (524–824) Community 81 (80–95) 6
Hospitalized 693 (515–824) 14
Cameroon 1 (2018–2019) 0 22 Community 22 13
Hospitalized NA NA
Americas United States of America 14 (2005/2006–2018/2019) 0 18 007 (5510–37 834) Community NA NA
Hospitalized NA NA
Chile 7 (2012–2018) 0 4923 (4846–5490) Community 138 (124–146) 8
Hospitalized 4773 (4722–5361) 17
Ecuador 7 (2012–2018) 0 482 (365–615) Community NA NA
Hospitalized 482 (365–615) 13
Brazil 5 (2014–2018) 0 2208 (1337–2520) Community NA NA
Hospitalized 2208 (1337–2520) NA
Europe Portugal 8 (2011/2012–2018/2019) 14 529 (247–783) Community 13 (7–13) 4
Hospitalized NA NA
The Netherlands 19 (2000/2001–2018/2019) 100 1980 (1766–2219) Community 73 (53–98) 4
Hospitalized 1959 (1732–2195) NA
The Czech Republic 4 (2014/2015–2017/2018) 3 233 (202–345) Community 22 (17–26) 4
Hospitalized 213 (189–319) 3
Spain 13 (2006/2007–2018/2019) 0 2060 (1638–2969) Community NA NA
Hospitalized 2060 (1638–2969) 13
Russian Federation 5 (2014/2015–2018/2019) 0 133 (104–176) Community 66 (48–88) 4
Hospitalized 67 (56–78) 6
South East Asia Bhutan 3 (2015/2016–2017/2018) 0 98 (82–218) Community NA NA
Hospitalized 41 (33.5–64) 38
Western Pacific Singapore 8 (2011–2018) 4 1786 (1647–2076) Community 90 (75–105) 7
Hospitalized 1710 (1574–1968) 10
New Zealand 6 (2013–2018) 39 610 (533–682) Community 101 (82–128) 7
Hospitalized 466 (450–566) 16
Vietnam 2 (2017–2018) 0 39 (26–41) Community 39 (26–41) 10
Hospitalized NA NA
Average Average 7 - 1463 (512–2335) Community 78 (37–110) 8
Hospitalized 747 (435–1807) 17

Abbreviations: IQR, interquartile range; NA, not available.

The percentage of RSV-positive cases varied widely across countries. The proportions are consistent from season to season at a country level in community care, but there was great variation in hospitalized care. Overall, the percentage of positive cases was higher in hospitalized care (SARI; 12%; 95% CI, 11%–13%; I2 = 99%) than in community care (ILI or ARI; 6%; 95% CI, 5%–6%; I2 = 91%). Forest plots on RSV positivity in community and hospitalized care are shown in Supplementary Figures 4 and 5, respectively.

Age Distribution of RSV Cases

The median age of RSV cases was available for 10 countries, and 4 countries provided cases per age category (Table 3). Portugal provided both exact and categorical age data; however, due to the small number of cases with the exact age (105/4902), Table 3 only presents the categorical data. Spain, not presented in Table 3, provided data stratified as <15- and ≥15-year age categories.

Table 3.

Number of Cases, Median Age, and Age Distribution Expressed as a Relative Illness Ratio of RSV Cases per Country

No. of Cases Median Age (IQR), y Age Category
<1 y 1–4 y ≥5 y No. of Years
No. of Cases Median RIR (IQR) No. of Cases Median RIR (IQR) No. of Cases Median RIR (IQR)
Bhutan 320 1.00 (0.42–2.00) 156 28.5 (22.4–29.8) 125 5.6 (4.8–6.5) 39 0.1 (0.1–0.1) 3
Cameroon 35 1.00 (0.33–4.50) 15 NA 11 NA 9 NA 0
Chile 358 0.92 (0.42–1.00) 189 42.8 (42.6–43.1) 137 7.3 (7.1–7.6) 32 0.1 (0.1–0.1) 2
The Czech Republic 141 6.00 (3.00–43.00) 13 NA 46 NA 82 NA 0
Ecuador 3361 0.58 (0.25–1.00) 2179 31.7 (29.0–33.1) 1051 4.0 (3.8–4.6) 131 0.0 (0.0–0.1) 7
The Netherlands 975 14.82 (1.64–55.66) 157 14.3 (11.9 –18.2) 253 6.2 (5.8–7.0) 565 0.6 (0.5–0.6) 13
New Zealand 3996 1.00 (0.25–5.17) 1992 38.4 (35.8–44.5) 994 4.6 (4.0–5.0) 1010 0.3 (0.1–0.3) 7
Russian Federation 781 3.00 (1.00–8.00) 160 13.8 (6.7–16.5) 371 9.4 (9.0–9.5) 250 0.4 (0.3–0.4) 6
South Africa 6646 0.51 (0.21–1.53) 4416 28.9 (16.5–35.0) 1385 2.4 (2.3–2.5) 845 0.1 (0.1–0.2) 10
Vietnam 78 2.00 (1.50–4.00) 10 NA 50 NA 18 NA 0
Countries With Information on Age Provided Only in Categories <5 y ≥5 y No. of Years
No. of Cases Median RIR (IQR) No. of Cases Median RIR (IQR)
Brazil 11 460 <2 y# NA NA 10 318 12.7 (12.6–12.7) 1142 0.1 (0.1–0.1) 5
Portugal 4902 0–4 NA NA 2973 7.3 (0.7–18.6) 1859 0.4 (0.2–0.6) 7
Singapore 716 1–2 NA NA 523 18.6 (18.1–19.9) 193 0.3 (0.1–0.3) 8

Symbol: #, median age category, as exact ages were not available.

Abbreviations: IQR, interquartile range; NA, not available; RIR, relative illness ratio; RSV, respiratory syncytial virus.

Overall, the median age (IQR) was 0.78 (0.3–2.6), but this differed greatly across countries (Table 3). The RIR was consistently higher in the youngest age category compared with the ≥5-year age category, where the RIR remained consistently below 1 (~20–800 fold). For Spain, the RIR showed a similar pattern, with the highest RIR (IQR), 5.4 (4.9–6.2), in the <15-year-old age category, compared with 0.2 (0.1–0.3) in the ≥15-year-old age category. All countries included RSV cases in those aged 65 or older, comprising ~8% of all cases. This proportion ranged from 1% in Chile, Ecuador, Portugal, and South Africa to 20% in Portugal.

As the majority of cases (n = 9287, 55%) were found in the <1-year-old category, we decided to focus on this group. The monthly age distribution for this category in community and hospitalized care is depicted in Figure 1A–B. In hospitalized care (1B), the number of cases peaked in the 1–2-month age group, after which the number of cases declined for older age groups. In this age category and setting, 70% of cases were ≤6 months of age. The sample size for the <1-year-old age category in community care was substantially smaller (n = 422) than in hospitalized care (n = 8864). The age distribution found in hospitalized care did not appear to repeat itself in the community care setting for cases aged <1 year (Figure 1A).

Figure 1.

Figure 1.

A–B, Number of RSV cases per month in the <1-year-old age category in community and hospitalized care. “Age, mo” on the x-axis refers to the age of the child. The overall number of cases in the <1-year-old category was taken to calculate the proportion of cases in a given month. Abbreviation: RSV, respiratory syncytial virus.

Three countries (New Zealand, Russian Federation, and South Africa) provided exact age data for both levels of care, representing 16 934 RSV cases (Supplementary Figure 6). The median age among community care cases (IQR) was 5.5 (1.9–43.6) years, substantially and significantly higher than the median age (IQR) in hospitalized care (0.6 [0.2–1.4] years; P < .001). The same level of significance (P < .001) was found when comparing age per care level on the individual country level.

RSV Subtype Distribution

Six countries (the Czech Republic, the Netherlands, New Zealand, Portugal, Singapore, and South Africa) provided subtyped RSV data. In the Netherlands, Singapore, and South Africa, ≥90% of RSV cases were typed, whereas this was 3%, 14%, and 39% for the Czech Republic, Portugal, and New Zealand, respectively. These countries reported a total of 6148 RSV subtyped cases, of which 3155 were typed as RSV A cases (51%) and 2993 were typed as RSV B cases (49%). There were 34 seasons containing sufficient subtyped RSV cases to be included in the analysis. The distributions of RSV subtypes for these seasons (from 2010 to 2019) stemmed from 5 countries (the Netherlands, New Zealand, Portugal, Singapore, and South Africa) and are summarized in Figure 2. The figure shows a slightly higher median (IQR) for RSV A (54% [38%–65%]) compared with RSV B (46% [35%–62%]).

Figure 2.

Figure 2.

Proportion of RSV A & B cases per season (n = 34; seasons ordered by increasing proportion RSV A) among subtyped results. Countries included were the Netherlands, New Zealand, Portugal, South Africa, and Singapore, and data from both community and hospitalized care are combined. Proportion distribution was calculated by country for all included seasons. The dark line in the middle indicates the median proportion of both RSV A and B per season, and the dark lines on the left and right indicate the interquartile range. Abbreviation: RSV, respiratory syncytial virus.

There were 12 out of 34 seasons where RSV A was dominant and 10 seasons where RSV B was dominant. Subtype dominance reached ≥80% twice in the Netherlands for RSV B for the 2017/2018 and 2018/2019 seasons, once in New Zealand for RSV A in the 2012 season, and once in Portugal for RSV B in the 2014/2015 season.

For 2 countries (New Zealand and South Africa), subtyped RSV data (n = 2180) were available in both community and hospitalized care. Overall the proportion of RSV A was lower in community care (46%, 264/570) compared with hospitalized care (53%, 859/1610; P < .001). At the country level, the proportion of RSV A was 40% (107/269) in community care in South Africa and 54% (232/433) in hospitalized care (P < .001); in New Zealand this difference was 52% (157/301) compared with 53% (627/1177; P = .78) in community and hospitalized care, respectively.

The age distribution of RSV by subtype was available for a total of 4911 cases distributed across 5 countries (the Czech Republic, the Netherlands, New Zealand, Portugal, and South Africa). The global median age for RSV A (IQR) was 0.9 (0.3–4.3) years compared with 0.9 (0.3–5.2) years for RSV B (P = .96). Similar results were seen at the country level, the only exception being the Netherlands, where RSV B cases had a median age (IQR) of 24.4 (1.7–58.2) years compared with 6.4 (1.6–52.8) years for RSV A cases (P = .02) (Supplementary Figure 7).

DISCUSSION

This study describes for the first time age- and care setting–specific surveillance data at a global level. Importantly, it also provides insight into current RSV surveillance practices at a national level. The GERi network currently encompasses 15 countries and includes 112 seasons of RSV surveillance data between 2000 and 2020. We found several differences in data collection practices and demonstrated that the highest incidence of RSV cases requiring medical attention was found in the <1-year-old age category. In addition, our data set contained very few infections in the 65+ age group (8%).

Though it is well established that RSV is an important cause of respiratory disease requiring medical attention in the very young [5], the impact of RSV on the overall population is not well studied. Though the RIR is consistently higher in the <1-year-old age category, the lack of cases in the elderly might reflect that this group is disproportionately captured by the surveillance systems. In our study, only 8% of total surveillance cases were found in the >65-year-old age category (ranging from 1% in Chile, Ecuador, Portugal, and South Africa to 20% in Portugal). Based on previously published population-based RSV estimates, we would expect this age group to represent between 19% and 33% of total surveillance cases in the United States, 37% in the United Kingdom, 25% in Canada, 16% in Thailand, and <1% in Madagascar [21–26]. Studies in the United States have also reported incidence rates of RSV in the elderly that were nearly twice that of influenza A and that RSV had a high disease severity in the elderly [2]. These data suggest that, at least for developed countries with relatively large elderly populations, surveillance systems may not be sufficiently picking up RSV cases in the ≥65-year-old age group. This could be influenced by a variety of factors, including an atypical clinical presentation in older adults or lower viral titers, which might hinder RSV detection by rapid antigen tests [27].

RSV patients in community care were older than those in hospitalized care, underlined by South Africa and New Zealand—in which all ILI as well as SARI cases are tested. Data from both countries show that cases in hospitalized care were substantially younger. This could be due to the previously demonstrated higher risk of hospitalization in younger individuals [28]. The percentage of cases testing positive for RSV was consistently higher in hospitalized patients, suggesting that RSV might play a larger role among other causes of respiratory infections in the hospitalized setting than in the community setting. Several studies found similarly high proportions of RSV positivity among hospitalized patients [29, 30].

No evidence for age differences between RSV subtypes was found. In most seasons analyzed, both RSV subtypes co-circulated (<80% threshold) and no clear pattern per country or from season to season was found. Though the RSV subtype remained unknown for a large subset of cases, this would likely not impact the proportion of RSV A or B per season found in our study. While among subtyped cases the proportion of RSV A was higher in hospitalized care compared with community care, the evidence was limited. A difference in this distribution could indicate an increased severity for those infected with RSV A [11].

The strengths of the GERi network lie in the size of the data set, the global distribution of the countries, the stratification by level of care, and additional information gained through our questionnaire. This study also comes with several limitations. Although surveillance data are an effective way to determine timing and seasonality of epidemics, it is important to note that only medically attended cases are included in the data set. In addition, influenza surveillance systems—a common foundation for RSV testing—commonly use the ILI case definition, which requires a fever, a clinical symptom not universally and globally represented in RSV cases [14]. Another limitation of the GERi network is the diversity in surveillance systems. The information gathered through the questionnaire, in combination with the size of the database, enables a better interpretation of results. Not all regions and Income categories are equally represented in the database. In line with previous studies that have assessed global data sets, high-income countries tend to provide more data and data that have greater detail [31].

Our results have important public health implications as well as implications for the development of future prevention methods. They highlight and support previous findings on the age groups that need to be targeted to prevent and control infections, with <1-year-olds being of greatest importance. The co-circulation of both RSV types also implies that for a prevention method to be effective it should target both types. This is especially relevant, as neither of the types appears to be overly represented in hospitalized cases.

CONCLUSIONS

The GERi network is the most substantial assessment of RSV surveillance data to date. Importantly, we found several differences in RSV surveillance systems across countries, underlining the need to harmonize surveillance activities for RSV around the world to make the data more comparable and to draw firmer conclusions for prevention and control measures. While our analysis found that the incidence of RSV is highest in the <1-year-old age category, more surveillance data in the elderly may be required, especially in developed countries, to support prevention efforts in this age group.

Supplementary Data

Supplementary materials are available at Open Forum Infectious Diseases online. Consisting of data provided by the authors to benefit the reader, the posted materials are not copyedited and are the sole responsibility of the authors, so questions or comments should be addressed to the corresponding author.

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Acknowledgments

The United States: We thank the Division of Viral Diseases (CDC) for sharing the NVRESS data. The Netherlands: We thank the Dutch Working Group for Clinical Virology (NWKV) for the use of virology diagnostic reports (nonsentinel data) and Sofie Mooij (RIVM) for providing the data. We thank the Nivel Primary Care Database team and general practitioners and their patients for their contribution to the national sentinel surveillance. The team of technicians at RIVM currently represented by Sharon van den Brink, Lisa Wijsman, and Gabriel Goderski are thanked for organizing the logistics and performing testing of the sentinel specimens.

Financial support.  Sanofi Pasteur/AstraZeneca.

Potential conflicts of interest.  C.D. and M.B. are Sanofi employees and may hold shares and/or stock options in the company; J.P. reports that Nivel has received RSV research grants from the Foundation for Influenza Epidemiology and Sanofi Pasteur. The remaining authors declare no competing interests. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

Patient consent.  Our study uses routine surveillance data for which no patient consent is required.

Other contributors. Pedro Pechirra,14 Inês Costa,14 Elizaveta Smorodintseva,15 Tze Minn Mak,18 Lin Cui,18 Raymond Tzer-Pin Lin,18 Anne Von Gottberg,19,20 Jesús Oliva Domíngue.21

References

  • 1. Nair  H, Nokes  DJ, Gessner  BD, et al.  Global burden of acute lower respiratory infections due to respiratory syncytial virus in young children: a systematic review and meta-analysis. Lancet  2010; 375:1545–55. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2. Falsey  AR, Hennessey  PA, Formica  MA, et al.  Respiratory syncytial virus infection in elderly and high-risk adults. N Engl J Med  2005; 352:1749–59. [DOI] [PubMed] [Google Scholar]
  • 3. Troeger  C, Blacker  B, Khalil  IA, et al.  Estimates of the global, regional, and national morbidity, mortality, and aetiologies of lower respiratory infections in 195 countries, 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016. Lancet Infect Dis  2018; 18:1191–210. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Obando-Pacheco  P, Justicia-Grande  AJ, Rivero-Calle  I, et al.  Respiratory syncytial virus seasonality: a global overview. J Infect Dis  2018; 217:1356–64. [DOI] [PubMed] [Google Scholar]
  • 5. Shi  T, McAllister  DA, O’Brien  KL, et al. ; RSV Global Epidemiology Network . Global, regional, and national disease burden estimates of acute lower respiratory infections due to respiratory syncytial virus in young children in 2015: a systematic review and modelling study. Lancet  2017; 390:946–58. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Tin Tin Htar  M, Yerramalla  MS, Moïsi  JC, Swerdlow  DL. The burden of respiratory syncytial virus in adults: a systematic review and meta-analysis. Epidemiol Infect  2020; 148:e48. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Fleming  DM, Taylor  RJ, Lustig  RL, et al.  Modelling estimates of the burden of respiratory syncytial virus infection in adults and the elderly in the United Kingdom. BMC Infect Dis  2015; 15:443. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. PATH Vaccine Resource Library. RSV vaccine and mAb snapshot. Available at: https://vaccineresources.org/details.php?i=1562. Accessed 29 April 2020.
  • 9. Li  Y, Reeves  RM, Wang  X, et al. ; RSV Global Epidemiology Network; RESCEU investigators . Global patterns in monthly activity of influenza virus, respiratory syncytial virus, parainfluenza virus, and metapneumovirus: a systematic analysis. Lancet Glob Health  2019; 7:e1031–45. [DOI] [PubMed] [Google Scholar]
  • 10. Papadopoulos  NG, Gourgiotis  D, Javadyan  A, et al.  Does respiratory syncytial virus subtype influences the severity of acute bronchiolitis in hospitalized infants?  Respir Med  2004; 98:879–82. [DOI] [PubMed] [Google Scholar]
  • 11. Shi  T, Denouel  A, Tietjen  AK, et al.  Global disease burden estimates of respiratory syncytial virus-associated acute respiratory infection in older adults in 2015: a systematic review and meta-analysis. J Infect Dis  2019; 222(Suppl 7): S577–83. [DOI] [PubMed] [Google Scholar]
  • 12. Campbell  H, Bont  L, Nair  H. Respiratory syncytial virus (RSV) disease - new data needed to guide future policy. J Glob Health  2015; 5:020101. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13. Chadha  M, Hirve  S, Bancej  C, et al. ; WHO RSV Surveillance Group . Human respiratory syncytial virus and influenza seasonality patterns—early findings from the WHO global respiratory syncytial virus surveillance. Influenza Other Respir Viruses  2020; 14:638–46. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14. Hirve  S, Crawford  N, Palekar  R, Zhang  W; WHO RSV Surveillance Group . Clinical characteristics, predictors, and performance of case definition—interim results from the WHO global respiratory syncytial virus surveillance pilot. Influenza Other Respir Viruses  2020; 14:647–57. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Nivel. The GERI study. Available at: https://www.nivel.nl/en/geri. Accessed 29 April 2020.
  • 16. Lemaitre  M, Carrat  F. Comparative age distribution of influenza morbidity and mortality during seasonal influenza epidemics and the 2009 H1N1 pandemic. BMC Infect Dis  2010; 10:162. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Population Division, United Nations. World population prospects. Available at: https://population.un.org/wpp/Download/Standard/Population/. Accessed 30 April 2020.
  • 18. Viechtbauer  W. Conducting meta-analyses in R with the metafor package. J Stat Softw  2010; 36:1–48. [Google Scholar]
  • 19. R Core Team. R: a language and environment for statistical computing.  2019. Available at: https://www.r-project.org/. Accessed 29 April 2020.
  • 20. Centers for Disease Control and Prevention. National Respiratory and Enteric Virus Surveillance System. Available at: https://www.cdc.gov/surveillance/nrevss/index.html. Accessed 29 April 2020.
  • 21. Matias  G, Taylor  R, Haguinet  F, et al.  Estimates of hospitalization attributable to influenza and RSV in the US during 1997–2009, by age and risk status. BMC Public Health  2017; 17:271. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22. Zhou  H, Thompson  WW, Viboud  CG, et al.  Hospitalizations associated with influenza and respiratory syncytial virus in the United States, 1993–2008. Clin Infect Dis  2012; 54:1427–36. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23. Pitman  RJ, Melegaro  A, Gelb  D, et al.  Assessing the burden of influenza and other respiratory infections in England and Wales. J Infect  2007; 54:530–8. [DOI] [PubMed] [Google Scholar]
  • 24. Schanzer  DL, Saboui  M, Lee  L, et al.  Burden of influenza, respiratory syncytial virus, and other respiratory viruses and the completeness of respiratory viral identification among respiratory inpatients, Canada, 2003-2014. Influenza Other Respir Viruses  2018; 12:113–21. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. Naorat  S, Chittaganpitch  M, Thamthitiwat  S, et al.  Hospitalizations for acute lower respiratory tract infection due to respiratory syncytial virus in Thailand, 2008–2011. J Infect Dis  2013; 208:S238–45. [DOI] [PubMed] [Google Scholar]
  • 26. Rabarison  JH, Tempia  S, Harimanana  A, et al.  Burden and epidemiology of influenza- and respiratory syncytial virus-associated severe acute respiratory illness hospitalization in Madagascar, 2011–2016. Influenza Other Respir Viruses  2018; 13:138–47. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27. Colosia  AD, Yang  J, Hillson  E, et al.  The epidemiology of medically attended respiratory syncytial virus in older adults in the United States: a systematic review. PLoS One  2017; 12:e0182321. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28. Bont  L, Checchia  PA, Fauroux  B, et al.  Defining the epidemiology and burden of severe respiratory syncytial virus infection among infants and children in Western countries. Infect Dis Ther  2016; 5:271–98. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29. Nokes  DJ, Ngama  M, Bett  A, et al.  Incidence and severity of respiratory syncytial virus pneumonia in rural Kenyan children identified through hospital surveillance. Clin Infect Dis  2009; 49:1341–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30. Pale  M, Nacoto  A, Tivane  A, et al.  Respiratory syncytial and influenza viruses in children under 2 years old with severe acute respiratory infection (SARI) in Maputo, 2015. PLoS One  2017; 12:e0186735. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31. Dückers  MLA, Reifels  L, de Beurs  DP, Brewin  CR. The vulnerability paradox in global mental health and its applicability to suicide. Br J Psychiatry  2019; 215:588–93. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

ofab159_suppl_Supplementary_Figure_S1
ofab159_suppl_Supplementary_Figure_S2
ofab159_suppl_Supplementary_Figure_S3
ofab159_suppl_Supplementary_Figure_S4
ofab159_suppl_Supplementary_Figure_S5
ofab159_suppl_Supplementary_Figure_S6
ofab159_suppl_Supplementary_Figure_S7
ofab159_suppl_Supplementary_Materials

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