ORIGINAL RESEARCH article

Front. Public Health, 18 December 2025

Sec. Infectious Diseases: Epidemiology and Prevention

Volume 13 - 2025 | https://doi.org/10.3389/fpubh.2025.1679596

Association between SARS-CoV-2 in wastewater and COVID-19 hospitalizations in three countries, 2022–2024

  • 1. Pfizer Inc., New York, NY, United States

  • 2. Department of Population Health, Hofstra University, Hempstead, NY, United States

  • 3. The Institute for Social and Economic Research and Policy, Columbia University, New York, NY, United States

Abstract

Importance:

As fewer jurisdictions report national COVID-19 hospitalization rates and testing of mild and asymptomatic cases is reduced, there is a need to better understand the relationship between COVID-19 hospitalizations and alternative measures of COVID-19 circulation, such as wastewater surveillance.

Objective:

We described the association between levels of SARS-CoV-2 in wastewater and COVID-19 hospitalization rates at the national level during and after the pandemic and explored whether wastewater virus level can predict COVID-19 hospitalization rates.

Design, setting, and participants:

Retrospective analysis of public health reports of national wastewater surveillance and COVID-19 hospitalizations from Denmark, the Netherlands, and the United States from 2022 to 2024.

Main outcomes and measures:

For each country, we calculated Pearson correlation coefficients and hospitalization multipliers (defined as the hospitalization rate for a given scaled wastewater virus level), for the overall study period and by Omicron subvariant predominance. Additionally, we developed linear regression models using scaled wastewater virus levels to predict concurrent and projected (1–4 weeks) COVID-19 hospitalization rates.

Results:

There was a strong correlation between national SARS-CoV-2 wastewater virus levels and weekly new COVID-19 hospitalization rates per million (0.86 [95% CI, 0.82 to 0.90], 0.80 [95% CI, 0.72 to 0.85], and 0.89 [95% CI, 0.85 to 0.92] in Denmark, the Netherlands, and the United States, respectively). Correlations were consistently strong across all subvariant predominance periods in all three countries (range, 0.72 to 1.0). Results from linear regression models showed that hospitalization rate lagged wastewater SARS-CoV-2 levels by approximately 1 week. Linear regression models best predicted hospitalizations 1 week into the future (range of mean absolute percentage error, MAPE, 11.2 to 22.6%) with decreasing prediction accuracy within the range of 2–4 weeks (range of MAPE, 32.5 to 62.3% at 4 weeks). The median hospitalization multiplier (defined as ratio of weekly hospitalization rate to scaled wastewater SARS-CoV-2 level) were 859.3 (IQR, 621.7 to 1210.4), 178.3 (IQR, 133.7 to 243.7), and 245.9 (IQR, 184.0 to 293.7) for Denmark, the Netherlands, and the United States, respectively, during the study period. Regression models identified significant reduction in hospitalizations for a given wastewater virus level over time in all three countries.

Conclusions and Relevance:

SARS-CoV-2 wastewater virus levels were strongly correlated with COVID-19 hospitalization rates in the upcoming week. Wastewater to hospitalization ratios can be leveraged to enhance public health decision-making and resource allocation.

Introduction

COVID-19 hospitalizations are an important measure of disease severity and an indicator of the public health burden of COVID-19 (1). National COVID-19 hospitalization rates reflect the overall strain on healthcare systems, guiding resource allocation and policy decisions including emergency preparedness (2, 3). Unlike case counts, which can be influenced by testing availability and individual reporting behaviors, hospitalization rates provide a more stable and clinically meaningful measure of disease burden. Monitoring hospitalization rates at the national level enables timely, coordinated responses to surges in severe illness and supports strategic planning for current and future public health threats (2, 3).

Following declaration of an end to the pandemic by the World Health Organization in May 2023, there was decreased reporting of SARS-CoV-2 infections and COVID-19 hospitalizations. This reduction in reporting in the post-pandemic period has increased the need for alternative measures of disease burden, such as wastewater SARS-CoV-2 levels (4). Wastewater surveillance has emerged as an important measure of community-level infection trends independent of the availability of COVID-19 testing, and can provide an early measure of potential increases in more severe illness (5–7). Such early data may aid timely public health decision-making and resource planning, such as allocation of hospital resources. Several studies have demonstrated a strong correlation between wastewater SARS-CoV-2 levels and measures of COVID-19 burden, including hospitalizations (5, 6, 8–23). However, most of these studies reported data at the municipal or sub-national level, or over a relatively short period of a few months (5, 6, 8–11, 14, 15, 18, 19, 22, 24–27). Few studies have examined the use of wastewater as a potential correlate of COVID-19 hospitalizations on a national scale. A study in the United States that assessed wastewater surveillance data from 159 counties in 45 states from June 2021 through January 2023 found that wastewater-based models accurately predicted county-level weekly new COVID-19 admissions in the following 1–4 weeks (13). Two additional studies from the United States each found a strong positive correlation between county wastewater virus levels and reported COVID-19 cases from June 2020 to May 2021 (21) and with reported COVID-19 cases and COVID-19 hospitalizations in the upcoming 2 weeks from January to September 2022 (21, 23). A study of Austria’s wastewater surveillance system covering about 70% of the country’s population from April 2020 through August 2022 found that wastewater viral loads were predictive of COVID-19 hospital occupancy, with an average lead time of 9–12 days, allowing prediction of short-term demand for public health services (12).

Here we describe the association between wastewater SARS-CoV-2 levels and COVID-19 hospitalization rate from 2022 through 2024 and explore whether wastewater virus level can predict current and anticipated COVID-19 hospitalization rates at the aggregate national level.

Methods

Study design

This study was a retrospective analysis of public health reports of national wastewater surveillance and COVID-19 hospitalizations from 2022 through 2024.

Inclusion criteria

We conducted a search for national wastewater surveillance and COVID-19 hospitalization data among 27 countries included in a prior study evaluating under-reporting of SARS-CoV-2 infections (28). These 27 countries were selected based on the availability of COVID-19 case report data: Austria, Belgium, Brazil, Canada, Chile, China, Colombia, Denmark, Finland, France, Germany, Greece, Ireland, Israel, Italy, Japan, Luxembourg, Malaysia, the Netherlands, Portugal, Qatar, Singapore, South Africa, Spain, Sweden, the United Kingdom, and the United States.

Our search yielded three countries—Denmark, the Netherlands, and the United States—that met the criteria for sufficient data for analysis, defined as: (1) availability of ≥24 months of national SARS-CoV-2 wastewater surveillance data starting from January 2022 [e.g., United States (24), Denmark (17, 29), and the Netherlands (30)], and (2) availability of data on weekly new COVID-19 hospital admissions and/or hospital occupancy starting from January 2022 (31–33).

Wastewater SARS-CoV-2 levels

Wastewater SARS-CoV-2 surveillance data were obtained through publicly available country-specific dashboards, reports, and official websites. Countries were included in the wastewater analyses if datasets were downloadable and provided at least 2 years of data starting January 2022. We excluded countries without publicly available national aggregate wastewater values, even if they reported regional or sub-national data. In cases where reported data were not downloadable, the study team contacted publishers of nationally representative wastewater reports.

In Denmark, wastewater SARS-CoV-2 levels are reported as SARS-CoV-2 relative to fecal matter x 107 during January 6, 2022 through September 19, 2024 (29). In the Netherlands, wastewater SARS-CoV-2 levels are reported as average number of SARS-CoV-2 particles x 1011 during January 8, 2022 through September 21, 2024 (30). In the United States, wastewater SARS-CoV-2 levels are defined as the number of standard deviations above the baseline wastewater SARS-CoV-2 level, transformed to the linear scale (reported as National Wastewater Viral Activity Level) during January 1, 2022, through September 21, 2024 (34). All wastewater datasets were downloaded on October 28, 2024.

COVID-19 hospitalizations

Data on COVID-19 hospitalizations were sourced from official public health surveillance reports for all countries with available wastewater surveillance data. Nationally representative measures of hospitalizations were collected, prioritizing data on weekly new hospitalizations expressed as rates per million inhabitants when available. We also supplemented our search of official sources of hospitalization data with data on COVID-19 hospitalization from public repositories including Our World in Data (32).

Hospitalization rates were obtained from the Statens Serum Institut web page for Denmark (29). Netherlands hospitalization rates were obtained from Our World In Data, a publicly available resource that sources hospitalization data from the Netherlands National Coordination Center Patient Distribution (32, 35). In the United States, hospitalization rates were obtained from the Centers for Disease Control and Prevention’s COVID-19 Hospitalization Surveillance Network (COVID-NET) dashboard which monitors laboratory-confirmed, COVID-19-associated hospitalizations (31). All hospitalization datasets were downloaded on October 28, 2024.

Subvariant predominance

For each country, we defined a subvariant predominance period as any consecutive period when a specific subvariant attained 50% or higher prevalence for ≥4 weeks. Subvariant prevalence was sourced from publicly available databases such as covariants.org or national SARS-CoV-2 surveillance reports. For each country, we defined predominance period by major variant of concern (Omicron) and its major subvariants – BA.1, BA.2, BA.4/5, XBB, or JN.1 (Supplementary Table).

Data cleaning and exploratory data analyses

Completeness and consistency of variables were evaluated through exploratory analyses. Variables with differing reporting frequencies (e.g., daily vs. weekly) were standardized by converting daily data into trailing weekly sums. For countries without clear day of the week when data are reported (example, “week 1, 2022”), we assigned the weekly value to the Saturday corresponding to the United States CDC “Epi Week” reporting, a widely adopted standard for public health surveillance reporting (36). All COVID-19 hospitalization data were converted to weekly new hospitalization rate per million population using United Nations population estimates in instances where only raw numbers of hospitalizations were available (37). Across the three countries included in this study, there was one missing data point from Denmark (weekly hospitalization rate for the week of April 4, 2024) and two missing data points from the Netherlands (wastewater virus levels for the weeks corresponding to October 8, 2023 and September 29, 2024). Weeks with missing data were excluded from the analysis.

Scaled wastewater SARS-CoV-2 level

To enable cross-country comparisons, national wastewater SARS-CoV-2 levels were scaled from 0 to 1 by dividing observed levels by the maximum level for each country during the study period. A uniform scale for wastewater SARS-CoV-2 levels partially overcomes the heterogeneity of measurement scales for our data. For example, wastewater SARS-CoV-2 levels were reported as SARS-CoV-2 relative to fecal matter x 107 in Denmark, average number of SARS-CoV-2 particles x 1011 in the Netherlands, and number of standard deviations above the baseline wastewater SARS-CoV-2 level, transformed to the linear scale in the United States.

Statistical analyses

For each country, we calculated descriptive statistics including medians and interquartile ranges for national wastewater virus levels and hospitalization rates for the overall study period and by subvariant predominance. We explored the association between wastewater virus levels and hospitalization rate using line plots, scatterplots, and correlation coefficients. We also assessed different lags between wastewater and hospitalization data for each country overall, and by subvariant predominance, using analysis of peak correlation coefficients (38) within a range of 0–4 weeks lead or lag. For variable combinations with sample sizes ≥8 weeks, we calculated Pearson correlation coefficients along with corresponding 95% confidence intervals (CI) using the cor function in R version 4.1 (39). Data consistency and variability were evaluated to identify appropriate statistical transformations, such as logarithmic scaling.

To explore time trends in the association between hospitalization rates and wastewater virus levels, we calculated two measures: (1) Wastewater to hospitalization ratio – defined as scaled wastewater SARS-CoV-2 level divided by weekly new COVID-19 hospitalization rate per million, which is a measure of the scaled wastewater virus level for a given weekly new COVID-19 hospitalization rate (2) Hospitalization multiplier – defined as the inverse of wastewater to hospitalization ratio. The hospitalization multiplier is a measure of national hospitalization rate for a given scaled wastewater level. For example, a hospitalization multiplier of 100 can be interpreted as a weekly new COVID-19 hospitalization rate that is approximately a hundred times the observed scaled wastewater level. The rationale for a hospitalization multiplier is to generate a simple number that can be applied in real world settings to translate a given scaled wastewater virus level into an expected weekly new COVID-19 hospitalization rate. Medians, interquartile ranges (IQR), and descriptive plots by country and predominant subvariant were generated for these two measures.

We explored whether wastewater SARS-CoV-2 levels were predictive of weekly new COVID-19 hospitalizations by evaluating several country-specific linear regression models using weekly new COVID-19 hospitalization, with or without log-transformation as a response variable, and scaled wastewater SARS-CoV-2 levels, with a lag of 0–4 weeks and log-transformations as the main predictor. We used lags of 0–4 weeks in keeping with previous studies and the available weekly hospitalization rates in all three countries in our study (5, 8, 11, 12). We also explored whether the association between hospitalization and wastewater virus level was consistent over time by including number of days since January 1, 2022 as a covariate in our regression models. We evaluated regression models using Akaike and Bayesian information criteria (AIC and BIC), adjusted R2, as well as mean absolute percent error (MAPE) and root mean square error (RMSE). We chose MAPE as the main model selection criterion because it was both scale and model agnostic.

All identified data sources were downloaded on October 28, 2024, and analyzed using R v4.1. Medians and interquartile ranges were calculated using the R quantile function and the cor function was used for correlation analyses (39).

Results

Denmark

Wastewater SARS-CoV-2 levels (reported as SARS-CoV-2 relative to fecal matter x 107) had a median of 1367.7 × 107 (IQR, 551.3 to 3359.4) during January 6, 2022 through September 19, 2024, with a decreasing trend over time (Table 1; Figure 1A). The highest median wastewater SARS-CoV-2 level was observed during BA.1 predominance (7907.0 × 107; IQR, 7905.4 to 7908.6), followed by BA.2 (7319.2 × 107; IQR, 1210.4 to 17625.7), with the lowest median levels occurring during XBB (1386.4 × 107; IQR, 679.0 to 2396.0) and JN.1 predominance (518.3 × 107; IQR, 196.3 to 925.8). Median weekly new COVID-19 hospitalization rates per million population were 41.0 (IQR, 21.8 to 83.3) for the full study period (Table 1; Figure 1A). The highest COVID-19 hospitalization rates were observed during BA.2 predominance with a median of 163.5 weekly new COVID-19 hospitalizations per million (IQR, 71.9 to 272.0), followed by BA.1 predominance (median 152.1; IQR, 150.9 to 153.2), and lowest during XBB (median 30.2; IQR, 16.6 to 58.1) and JN.1 predominance (median 16.5; IQR, 5.9 to 31.6).

Table 1

CountryVariableDate rangeAll Omicron, median (IQR)By predominanta subvariant, median (IQR)
BA.1BA.2BA.4/5XBBJN.1
DenmarkWeekly new COVID-19 hospitalization rate, per MJanuary 6, 2022, to
September 19, 2024
41.0 (21.8 to 83.3)152.1 (150.9 to 153.2)163.5 (71.9 to 272.0)72.5 (54.8 to 92.6)30.2 (16.6 to 58.1)16.5 (5.9 to 31.6)
Wastewater SARS-CoV-2 levelbJanuary 6, 2022, to
September 19, 2024
1367.7
(551.3 to 3359.4)
7907.0
(7905.4 to 7908.6)
7319.2
(1210.4 to 17625.7)
2386.7
(1516.3 to 3357.3)
1386.4
(679.0 to 2396.0)
518.3
(196.3 to 925.8)
The NetherlandsWeekly new COVID-19 hospitalization rate, per MJanuary 8, 2022, to
May 4, 2024
28.8
(14.5 to 46.9)
57.7
(48.8 to 70.0)
47.9
(19.9 to 71.0)
32.2
(24.9 to 52.8)
23.3
(11.1 to 38.7)
12.9
(7.3 to 33.5)
Wastewater SARS-Cov-2 levelcJanuary 8, 2022, to
September 21, 2024
706.0
(343.0 to 1228.5)
1422.0
(1014.8 to 1663.5)
591.0
(330.0 to 1629.2)
1030.0
(662.0 to 1565.0)
574.0
(266.0 to 1130.0)
586.0
(147.5 to 1072.0)
United StatesWeekly new COVID-19 hospitalization rate, per MJanuary 1, 2022, to
September 21, 2024
45.0
(29.0 to 71.0)
149.0
(66.5 to 277.5)
29.5
(25.0 to 41.0)
77.5
(70.8 to 94.0)
41.0
(22.8 to 48.2)
35.0
(18.0 to 45.0)
Wastewater SARS-CoV-2 leveldJanuary 1, 2022, to
September 21, 2024
5.0
(2.7 to 7.2)
9.2
(3.2 to 18.1)
1.8
(1.3 to 3.3)
6.7
(5.0 to 8.3)
4.3
(2.1 to 5.6)
5.4
(2.3 to 7.8)

COVID-19 hospitalization rate and wastewater SARS-CoV-2 level in Denmark, the Netherlands, and the United States, 2022–2024.

CDC, Centers for Disease Control and Prevention; IQR, interquartile range; M, million. aSubvariant predominance period defined as any consecutive period when a specific subvariant exceeded 50% prevalence for ≥4 weeks as presented in Table 5. bSARS-CoV-2 relative to fecal matter x 107. cAverage number of SARS-CoV-2 particles x 1011. dNational Wastewater Viral Activity Level as defined by the CDC.

Figure 1

The Netherlands

In the Netherlands, wastewater SARS-CoV-2 level (reported as average number of SARS-CoV-2 particles x 1011) had a median of 706.0 (IQR, 343.0 to 1228.5) during January 8, 2022 through September 21, 2024 (Table 1; Figure 1C) (30, 40). Wastewater virus levels were highest during BA.1 predominance (1422.0 × 1011; IQR, 1014.8 to 1663.5), followed by BA.4/5 (1030.0 × 1011; IQR, 662.0 to 1565.0), and were lowest during XBB (574.0 × 1011; IQR, 266.0 to 1130.0), and JN.1 predominance (586.0 × 1011; IQR, 147.5 to 1072.0). Median weekly new COVID-19 hospitalization rate per million was 28.8 (IQR, 14.5 to 46.9) during January 8, 2022, through May 4, 2024 (Table 1; Figure 1C). Hospitalization rates peaked during BA.1 predominance with 57.7 new COVID-19 hospitalizations per million (IQR, 48.8 to 70.0), followed by 47.9 per million (IQR, 19.9 to 71.0) during BA.2 predominance, and were lowest during XBB (23.3 per million; IQR, 11.1 to 38.7) and JN.1 predominance (12.9 per million; IQR, 7.30 to 33.5).

United States

In the United States, wastewater SARS-CoV-2 level is defined as the number of standard deviations above the baseline wastewater SARS-CoV-2 level, transformed to the linear scale (reported as National Wastewater Viral Activity Level) (24). Median wastewater SARS-CoV-2 level was 5.0 (IQR, 2.7 to 7.2) during January 1, 2022, through September 21, 2024 (Table 1; Figure 1E). The highest levels were observed during BA.1 predominance (median, 9.2; IQR, 3.2 to 18.1), followed by BA.4/5 (median, 6.7; IQR, 5.0 to 8.3), JN.1 (median, 5.4; IQR, 2.3 to 7.8), and XBB (median, 4.3; IQR, 2.1 to 5.6). Median weekly new COVID-19 hospitalization rate per million population was 45.0 (IQR, 29.0 to 71.0) during January 1, 2022 through September 21, 2024 (Table 1; Figure 1E) (31). Hospitalization rates peaked during BA.1 predominance (149.0 per million; IQR, 66.5 to 277.5), followed by BA.4/5 (77.5 per million; IQR, 70.8 to 94.0), and were lowest during JN.1 (35.0 per million; IQR, 18.0 to 45.0) and BA.2 predominance 29.5 (25.0 to 41.0).

Hospitalization multipliers

The median hospitalization multipliers using scaled wastewater SARS-CoV-2 level were 859.3 (IQR, 621.7 to 1210.4), 178.3 (IQR, 133.7 to 243.7), and 245.9 (IQR, 184.0 to 293.7) for Denmark, the Netherlands, and the United States, respectively, during the study period (Table 3; for multipliers using unscaled wastewater SARS-CoV-2 level, see Table 4). There was no clear temporal trend in median hospitalization multiplier in Denmark and the Netherlands with a potential trend of decreasing median multipliers over time in the United States (Table 3). In Denmark, median hospitalization multipliers peaked during BA.4/5 predominance (998.5; IQR, 831.2 to 1118.6) and were lowest during BA.1 predominance (613.0; IQR, 608.6 to 617.3). In the Netherlands, median hospitalization multipliers peaked during BA.2 predominance (226.6; IQR, 81.8 to 298.0) and were lowest during BA.4/5 predominance (138.4; IQR, 121.1 to 183.6). In the United States, median hospitalization multipliers peaked at 393.3 (IQR, 360.9 to 485.5) during BA.1 predominance and were lowest during JN.1 predominance at 167.1 (IQR, 144.5 to 184.6). Loess plots (Figures 2, 3) also show no clear temporal trend in wastewater to hospitalization ratio in Denmark and the Netherlands with potential trend of increasing wastewater to hospitalization ratios in the United States.

Figure 2

Figure 3

Correlation analysis

There was a strong correlation (Pearson correlation coefficients ≥0.80) between weekly new COVID-19 hospitalization rate and wastewater SARS-CoV-2 level in all three countries (Table 2). In Denmark, the correlation coefficient was 0.86 (95% CI, 0.82 to 0.90), in the Netherlands it was 0.80 (95% CI, 0.72 to 0.85), and in the United States it was 0.89 (95% CI, 0.85 to 0.92). Correlations were consistently strong across all subvariant predominance periods in all three countries (range, 0.72 to 1.0). Across all Omicron subvariant predominance periods, correlations in the United States remained consistently high (≥0.91), while correlations in Denmark showed more variability, with the strongest correlation during BA.2 (0.94, 95% CI: 0.85 to 0.98) and JN.1 (0.94, 95% CI: 0.89 to 0.97) but a relatively weaker correlation during BA.4/5 (0.72, 95% CI: 0.49 to 0.85). In the Netherlands, correlations were lowest during BA.1 (0.76, 95% CI: 0.12 to 0.95) and highest during JN.1 predominance (0.96, 95% CI: 0.90 to 0.98).

Table 2

CountryMeasureCorrelation coefficient (95% CI)/# of weeks lead or laga
All OmicronBA.1BA.2BA.4/5XBBJN.1
DenmarkCorrelationb0.86 (0.82 to 0.90)NA0.94 (0.85 to 0.98)0.72 (0.49 to 0.85)0.85 (0.73 to 0.92)0.94 (0.89 to 0.97)
Peak correlationc0.88 (0.84 to 0.91)NA0.98 (0.95 to 0.99)0.78 (0.60 to 0.89)0.89 (0.80 to 0.94)0.94 (0.89 to 0.97)
Lead or lagdLag 1 weekNALag 1 weekLag 1 weekLag 2 weeksNo lead or lag
The NetherlandsCorrelation0.80 (0.72 to 0.85)0.76 (0.12 to 0.95)0.91 (0.75 to 0.97)0.81 (0.61 to 0.91)0.90 (0.83 to 0.94)0.96 (0.90 to 0.98)
Peak correlation0.83 (0.76 to 0.88)0.76 (0.12 to 0.95)0.98 (0.93 to 0.99)0.88 (0.75 to 0.95)0.96 (0.92 to 0.98)0.96 (0.90 to 0.98)
Lead or lagLag 1 weekNo lead or lagLag 1 weekLag 1 weekLag 1 weekLag 1 week
United StatesCorrelation0.89 (0.85 to 0.92)1.00 (0.98 to 1.00)0.99 (0.93 to 1.00)0.93 (0.87 to 0.96)0.91 (0.84 to 0.95)0.98 (0.97 to 0.99)
Peak correlation0.89 (0.85 to 0.92)1.00 (0.98 to 1.00)0.99 (0.93 to 1.00)0.93 (0.87 to 0.96)0.94 (0.90 to 0.97)0.98 (0.97 to 0.99)
Lead or lagNo lead or lagNo lead or lagNo lead or lagNo lead or lagLag 2 weeksNo lead or lag

Correlation, peak correlation and lead/lag between wastewater SARS-CoV-2 level and weekly new COVID-19 hospitalization rate per million in Denmark, the Netherlands, and the United States, overall and by predominant subvariant, 2022–2024.

CI, confidence interval. NA, not applicable. aAny subvariant with <8 weeks of available data is excluded from this analysis. bPearson correlation coefficient between wastewater SARS-CoV-2 level and hospitalization rate without lead or lag. cMaximum observed correlation coefficient between wastewater SARS-CoV-2 level and hospitalization rate regardless of lead or lag. dLead or lag (in weeks) between wastewater SARS-CoV-2 and hospitalization that corresponded with peak correlation.

Table 3

CountryMedian (interquartile range)
All OmicronBA.1BA.2BA.4/5JN.1XBB
Denmark859.3
(621.7 to 1210.4)
613.0
(608.6 to 617.3)
757.3
(509.1 to 1623.9)
998.5
(831.2 to 1118.6)
825.3
(629.2 to 1288.1)
831.6
(614.5 to 1132.5)
The Netherlands178.3
(133.7 to 243.7)
191.8
(150.7 to 234.3)
226.6
(181.8 to 298.0)
138.4
(121.1 to 183.6)
224.5
(137 to 312.4)
173.1
(134.2 to 238.6)
United States245.9
(184.0 to 293.7)
393.3
(360.9 to 485.5)
369.4
(291.4 to 430.6)
292.6
(258.0 to 338.2)
167.1
(144.5 to 184.6)
238.7
(193.2 to 267.1)

Multipliers for weekly new COVID-19 hospitalization rate per million using scaled wastewater SARS-CoV-2 level by country and predominant variant.

Table 4

CountryMedian (interquartile range)
All OmicronBA.1BA.2BA.4/5XBBJN.1
Denmark0.027
(0.0195 to 0.038)
0.0192
(0.0191 to 0.0194)
0.0238
(0.016 to 0.0509)
0.0313
(0.0261 to 0.0351)
0.0261
(0.0193 to 0.0355)
0.0259
(0.0197 to 0.0404)
The Netherlands0.0411
(0.0308 to 0.0561)
0.0442
(0.0347 to 0.054)
0.0522
(0.0419 to 0.0686)
0.0319
(0.0279 to 0.0423)
0.0399
(0.0309 to 0.0549)
0.0517
(0.0315 to 0.0719)
United States10.3704
(7.7622 to 12.3878)
16.5874
(15.2219 to 20.4751)
15.5808
(12.2908 to 18.1603)
12.3392
(10.883 to 14.2619)
10.0655
(8.1476 to 11.2632)
7.0483
(6.0947 to 7.785)

Multipliers for weekly new COVID-19 hospitalization rate per million using wastewater SARS-CoV-2 level (unscaled) by country and predominant variant.

Table 5

CountryResponsePredictorsRegression model coefficientsModel accuracy and goodness of fit
Model IDInterceptBeta1Beta2MAPERMSEAICBICAdj. R2CV
DenmarkHospitalization rateWastewater126.3117335.8185101.532036.31831409.15321417.97810.74621469.2126
Wastewater (1-week lag)225.0774341.677895.829834.27181392.91301401.73800.77401313.0483
Log(wastewater)3191.305040.3033135.519443.65781460.68981469.51470.63322015.7790
Log[wastewater (1-week lag)]4190.830840.4189141.239143.28231458.27101467.09590.63951984.1086
Calendar days5140.5708−0.1517120.666958.04361540.43701549.26190.35163506.5445
Log(hospitalization rate)Wastewater63.16044.023696.0077107.0464352.4933361.31820.44290.7216
Wastewater (1-week lag)73.14834.070695.7711108.2213349.6193358.44420.45420.7069
Log(wastewater)85.91450.730135.974235.0474151.4454160.27040.86750.1709
Log[wastewater (1-week lag)]95.91010.733632.498632.9625138.3727147.19760.87930.1558
Log[wastewater (1-week lag)]; calendar days106.09380.6309−0.001022.580314.715868.533480.30000.92720.0948
Log[wastewater (2-week lag)]115.80400.703941.641338.2575195.4880204.29140.81600.2364
Log[wastewater (2-week lag)]; calendar days126.00790.5947−0.001133.458722.5483148.0983159.83620.87010.1684
Log[wastewater (4-week lag)]135.39670.582473.644153.7921304.5415313.30140.57570.5348
Log[wastewater (4-week lag)]; calendar days145.67990.4423−0.001462.334942.6146272.9827284.66260.66540.4250
The Netherlandshospitalization rateWastewater113.167588.697143.117912.6943948.5023956.83970.6370176.8091
Wastewater (1-week lag)212.335291.985438.441111.9178933.4799941.81730.6800158.2523
Log(wastewater)365.240416.512842.342911.4934924.8483933.18570.7024136.6031
Log[wastewater (1-week lag)]466.079617.076841.551010.8213910.5092918.84650.7362121.5412
Calendar days552.6212−0.046473.850717.79381028.87391037.21130.2867327.9935
Log(hospitalization rate)Wastewater62.54263.123645.081632.6910173.9112182.24850.59340.2621
Wastewater (1-week lag)72.51893.213743.782034.5564164.7967173.13410.62340.2452
Log(wastewater)84.54180.664624.413911.319549.266157.60350.85730.0869
Log[wastewater (1-week lag)]94.57900.689019.577510.46193.271311.60860.90310.0593
Log[wastewater (1-week lag)]; calendar days104.71580.6287−0.000616.45537.0263−36.1272−25.01070.93100.0425
Log[wastewater (2-week lag)]114.53950.675722.357713.011248.583756.89570.85830.0871
Log[wastewater (2-week lag)]; calendar days124.70040.6100−0.000719.41649.877916.388127.47090.89300.0667
Log[wastewater (4-week lag)]134.31420.576042.924218.5462168.8394177.10020.59880.2461
Log[Wastewater (4-week lag)]; calendar days144.57170.4869−0.001038.239015.8497146.6682157.68250.67140.2034
United StatesHospitalization rateWastewater1−6.9465277.096431.086123.30011303.14091312.00840.7762602.5052
Wastewater (1-week lag)2−4.8622264.110628.724724.59441318.49381327.36120.7507666.2846
Log(wastewater)3143.963551.781447.556834.95011418.29251427.16000.49651314.0691
Log[wastewater (1-week lag)]4142.776851.325046.660434.79181417.00281425.87030.50101294.4332
Calendar days5100.9702−0.088064.107642.49491473.80381482.67130.25561893.3982
Log(hospitalization rate)Wastewater62.96983.588835.087747.6151142.3462151.21370.67340.1600
Wastewater (1-week lag)72.98003.492634.875446.6866139.7994148.66680.67930.1575
Log(wastewater)85.29030.888228.578727.324498.4463107.31380.76030.1160
Log[wastewater (1-week lag)]95.27710.884627.422827.792289.618898.48630.77470.1089
Log[wastewater (1-week lag)]; calendar days105.68030.8205−0.001011.237814.8143−130.3849−118.56160.95250.0230
Log[wastewater (2-week lag)]115.17480.830928.195925.6548106.9636115.80990.72840.1235
Log[wastewater (2-week lag)]; calendar days125.55140.7676−0.001017.529617.9373−21.3438−9.54870.89140.0497
Log[wastewater (4-week lag)]134.85180.651938.340122.8450173.0608181.86420.50410.2005
Log[wastewater (4-week lag)]; calendar days145.18630.5871−0.000932.513420.2407126.6521138.39000.64740.1440

Linear regression models for weekly new COVID hospitalization rate per million in Denmark, the Netherlands and the United States, 2022–2024.

Hospitalization rate – weekly new COVID-19 hospitalization rate per million; wastewater – wastewater SARS-CoV-2 level, scaled; calendar days – days since January 1, 2022. AIC, Akaike information criterion; Adj. R2, adjusted R2; BIC, Bayesian information criterion; CV, leave-one-out cross-validation statistic; MAPE, mean absolute percent error; NA – not available; RMSE, root mean squared error.

The peak correlation between weekly hospitalization rate and wastewater for Denmark and the Netherlands occurred at a lag of 1 week while peak correlation for the United States had no lead or lag (Table 2). However, linear regression models suggested a 1-week lag between hospitalization rate and wastewater virus levels in all three countries (Table 5).

Regression models

For Denmark, the Netherlands, and the United States, the best fitting regression model used log-transformed weekly new COVID-19 hospitalization rate as response variable with log-transformed wastewater virus level from the previous week and calendar days as covariates (Table 5; Figures 1B,D,F, 4). Model intercepts (6.1, 4.7, and 5.7, for Denmark, the Netherlands and the United States, respectively), regression coefficients for wastewater virus level (0.63, 0.63, and 0.82, for Denmark, the Netherlands and the United States, respectively), and calendar days (−0.0010, −0.0006 and −0.0010 for Denmark, the Netherlands and the United States, respectively) were generally similar across the three countries in our study. These models suggest that (1) log-transformed weekly hospitalization rate increases as the log-transformed previous-week wastewater SARS-CoV-2 level increases, and (2) in all three countries, there was a statistically significant decrease in log-transformed weekly hospitalization rate over time after adjusting for wastewater virus level.

Figure 4

The best fitting regression model was the same for all three countries (model 10 in Table 5, Supplementary Figures 1–3) with high adjusted R2 values (>0.9) and MAPE of 22.6, 16.5 and 11.2% for Denmark, the Netherlands, and the United States, respectively. Increasing the wastewater lag to 2–4 weeks reduced model accuracy but still provided moderately accurate predictions. For example, increasing the wastewater lag to 2 weeks (4 weeks) increased MAPE to 33.5, 19.4, and 17.5% (62.3, 38.2, and 32.5%), in Denmark, the Netherlands and the United States, respectively (models 12 and 14 in Table 5).

Discussion

In this study, we evaluated the association between levels of SARS-CoV-2 in wastewater and COVID-19 hospitalization rates at the national level from January 2022 through September 2024 (encompassing both pandemic and post-pandemic periods) in Denmark, the Netherlands, and the United States. We found a strong positive correlation between wastewater SARS-CoV-2 levels and weekly new COVID-19 hospitalization rates in all three countries with overall correlation coefficients ranging from 0.80 to 0.89. Correlation coefficients ranged from 0.72 to 1.0 during BA.1, BA.2, BA.4/5, XBB, and JN.1 predominance periods. Correlation coefficients were consistently high in the United States (>0.9) during all subvariant predominance periods while there was some variation in correlation coefficients in Denmark (range 0.72 to 0.94) and the Netherlands (range, 0.76 to 0.96). These differences may reflect variation in national testing intensity, hospitalization admission criteria, or the response of health systems during different phases of the pandemic. Taken together, these results suggest that SARS-CoV-2 wastewater virus levels are a reliable predictor of COVID-19 hospitalization rates both during and after the pandemic and regardless of changes in circulating variants, even though the degree of correlation of wastewater to hospitalization dynamically changes during the different waves of infection. These findings align with several studies reporting strong positive correlations between wastewater virus levels and COVID-19 hospitalizations across diverse geographic settings and variant predominance (5, 8, 11–15, 41).

We also observed that the peak correlation between wastewater SARS-CoV-2 levels and weekly hospitalizations occurred with a one-week lag in Denmark and Netherlands while peak correlation coefficients occurred with no lead or lag in the United States. In all three countries, the best fitting linear regression models used a 1-week lag between hospitalization and wastewater virus levels, and included log-transformed, scaled, wastewater virus level and calendar days as predictors and log-transformed hospitalization rate as outcome. This model performed best overall across Omicron sub-variant predominance periods and across geographical regions. Taken together, our findings suggest a lag between wastewater virus level and hospitalization rate of 1 week for Denmark and Netherlands and 0–1 week for the United States. Our results are consistent with previous studies of wastewater SARS-CoV-2 levels and hospitalization, which reported lags of 4 to 12 days (5, 8, 11, 12, 14, 15, 42). The reason for a lag between hospitalization and wastewater SARS-CoV-2 levels likely reflects the natural history of SARS-CoV-2 infection, with virus shedding beginning at the presymptomatic and early symptomatic stage, and severe symptoms that would require hospitalization generally occurring days after initial symptoms begin (43). Another potential reason for a lag between wastewater and hospitalization rates could be reporting delays in hospitalization data.

Hospitalization multipliers (the hospitalization rate for a given scaled wastewater virus level) were highly variable across countries with medians of 859.3 (IQR, 621.7 to 1210.4), 178.3 (IQR, 133.7 to 243.7), and 245.9 (IQR, 184.0 to 293.7) in Denmark, the Netherlands and the United States, respectively. Regression models, however, showed a statistically significant decrease in hospitalization rate relative to wastewater virus levels over time in all three countries during the study period. The trend of decreasing hospitalization rates relative to wastewater virus levels is likely due to an increase in population immunity from immunizations and infection over time (1). Alternatively, the decreasing hospitalization could also be due to improvements in outpatient treatment of infected cases and/or decreasing virulence of recent SARS-CoV-2 variants (2).

This finding is consistent with a study from Florida (USA) that found total COVID-19 hospitalizations relative to wastewater were highest during the initial infection wave in 2020 followed by Delta and Omicron waves (10). Although a subsequent study conducted in California reported that wastewater to hospitalization ratios were relatively consistent across two Omicron waves of infections (a likely Omicron BA.1/BA.2 wave from December 2021 through March 2022 and a likely BA.4/5 wave from April through September 2022) (8). Discrepancies between these studies could be a result of their limited geographic scope or differences in time periods. Namely, while rates of hospitalization have fallen over time, there may not have been dramatic differences in rates of hospitalization between the first two Omicron waves. Regardless, our finding of decreased hospitalizations relative to wastewater virus levels over time in Denmark, the Netherlands, and the United States is likely a result of increasing population immunity to SARS-CoV-2, improved early treatment of COVID-19, or both (44). Hospitalization multipliers are easy to compute and interpret and could serve as a contemporaneous measure of disease burden. A knowledge of historical multipliers for any given country can be applied to the wastewater level today to calculate expected hospitalization burden. In essence, hospitalization multipliers enable public health professionals to rapidly translate wastewater surveillance signals into expected healthcare demand, thereby supporting proactive resource allocation. In summary, wastewater surveillance data offers a population-level signal of infection trends that precedes increases in hospitalizations, and is independent of clinical testing rate, thereby supporting timely public health decision-making and resource planning.

Limitations

This study has several limitations. First, it focused on three countries with publicly available national wastewater surveillance data, limiting the generalizability of the findings. Additional studies from a broader range of countries, particularly low- and middle-income settings, are needed to understand the global association between wastewater surveillance and COVID-19 hospitalizations (45). While scaling SARS-CoV-2 wastewater concentrations to each country’s observed maximum enables within-country temporal comparisons, differences in assay type, viral target regions, sample processing protocols, and normalization strategies limit the interpretation of results across settings. Likewise, differences in hospitalization rates may be due to heterogeneity in hospitalization definitions, availability of testing, population immunity levels, and vaccination coverage across countries during the study period. Additional factors that may explain differences in hospitalization multipliers include differences in population composition such as age, and immune status, differences in vaccine coverage, prior infections and prevailing SARS-CoV-2 variants (38, 46–49). For example, the U. S. reports SARS-CoV-2 wastewater virus levels as deviations from historical baselines, whereas Denmark and the Netherlands use absolute viral load measures relative to fecal content. These discrepancies may partially account for the observed differences in hospitalization multipliers and model coefficients. For example, both regression and correlation analysis found a 1-week lag between wastewater virus levels and hospitalization rate in Denmark and Netherlands while in the United States, regression analysis found a lag of 1 week in contrast to correlation analysis that found no lead or lag. While it is reasonable to assume that the true lag in the United States is somewhere between 0 and 7 days, it is difficult to determine whether the true lag is closer to 7 days.

Second, the aggregation of data at the national level on a weekly time scale may mask regional variations or localized spikes in infections and hospitalizations. In addition, efforts to make wastewater data comparable across jurisdictions do not capture underlying differences in sample collection, laboratory methods, and data aggregation. Developing standardized protocols for wastewater data collection, analysis, and reporting is essential for improving comparability. Similarly, there are subtle differences in how COVID-19 hospitalizations are defined, with the US reporting weekly new COVID-19 hospitalization rate based on a representative sample of the US population, while hospitalization rates in Denmark and the Netherlands were based on total number of weekly new COVID-19 hospitalizations at the national level which may include both patients with COVID-19 as their primary cause of hospitalization and patients with incidental infections (2, 40). In Netherlands, it is reported that only about 54 to 78% of hospitalized SARS-CoV-2-infected patients had COVID-19 as the primary or a secondary reason for admission (40). Another potential source of uncertainty is within country changes in number of wastewater monitoring sites and refinements of laboratory and/or statistical methods. For example, the proportion of the U. S. population served by national wastewater surveillance sites increased from 12% in 2020 to 45% in 2022 (24). In Denmark, the number of sampling sites declined from 202 in April 2022 to 29 in April 2024 with corresponding reduction in population coverage from 85 to 48% (50).

Third, while hospitalization multipliers can provide important information on real-time COVID-19 burden in real world settings, these multipliers are context specific and not generalizable between different settings. Also, hospitalization multipliers do not account for temporal changes in the relationship between wastewater virus level and hospitalization driven by changes in surveillance systems and/or changes in disease severity over time. Thus, hospitalization multipliers should be ideally supplemented with additional epidemiologic data including test positivity rate, emergency department and/or urgent care visits and context-specific modeling.

Fourth, we used linear regression models with a limited number of variables, namely, scaled wastewater virus level and calendar days to predict national COVID-19 hospitalization rate. Our model could potentially be improved with additional epidemiological variables and/or more complex modelling approaches.

Conclusion

SARS-CoV-2 wastewater virus levels were strongly correlated with COVID-19 hospitalization rates in the following week, providing a cost-effective method for real-time COVID-19 tracking in the post-pandemic era as global and national COVID-19 surveillance systems continue to wind down.

Statements

Data availability statement

Publicly available datasets were analyzed in this study. This data can be found at: United States CDC Wastewater Monitoring https://www.cdc.gov/nwss/ US CDC Hospitalization https://www.cdc.gov/covid/php/covid-net/index.html Denmark National Surveillance https://en.ssi.dk/surveillance-and-preparedness/surveillance-in-denmark/covid-19/national-surveillance-of-sars-cov-2-in-wastewater Netherlands wastewater surveillance https://www.rivm.nl/en/coronavirus-covid-19/research/wastewater#sewageresearch Our World in Data https://covid-19.nyc3.digitaloceanspaces.com/public/owid-covid-data.csv.

Author contributions

MM: Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Resources, Supervision, Validation, Writing – original draft, Writing – review & editing. LC: Conceptualization, Data curation, Formal analysis, Investigation, Project administration, Writing – original draft, Writing – review & editing. TB: Conceptualization, Data curation, Investigation, Methodology, Project administration, Writing – original draft, Writing – review & editing. HV: Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Visualization, Writing – original draft, Writing – review & editing. KD: Data curation, Formal analysis, Methodology, Writing – original draft, Writing – review & editing. JY: Conceptualization, Investigation, Methodology, Resources, Writing – original draft, Writing – review & editing. AY: Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Visualization, Writing – original draft, Writing – review & editing. FK: Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Resources, Validation, Visualization, Writing – original draft, Writing – review & editing. JM: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing. JN: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing.

Funding

The author(s) declared that financial support was received for this work and/or its publication. This study was sponsored by Pfizer. Pfizer was involved in the study design, data collection, data interpretation, writing of the manuscript, and decision to submit it for publication.

Conflict of interest

MM, LC, TB, HV, JY, AY, FK, JM, and JN were employed by Pfizer Inc. and declare employment and/or holding stocks and/or options at Pfizer Inc. during the conduct of the study. KD was an employee of Pfizer Inc. at the time of the study and manuscript development.

Generative AI statement

The author(s) declared that Generative AI was not used in the creation of this manuscript.

Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpubh.2025.1679596/full#supplementary-material

References

  • 1.

    NikollaDAOskvarekJ JZocchiMSRahmanNALeubitzAMoghtaderiAet al. 2024;16:e56546. doi: 10.7759/cureus.56546

  • 2.

    TaylorCAPatelKPhamHKirleyPDKawasakiBMeekJet al. COVID-19-Associated Hospitalizations Among U.S. Adults Aged >/=18 Years - COVID-NET, 12 States, October 2023-April 2024. MMWR Morb Mortal Wkly Rep. (2024) 73:869–75. doi: 10.15585/mmwr.mm7339a2

  • 3.

    AllanMLievreMLaurenson-SchaferHde BarrosSJinnaiYAndrewsSet al. The World Health Organization COVID-19 surveillance database. Int J Equity Health. (2022) 21:167. doi: 10.1186/s12939-022-01767-5,

  • 4.

    WHO. Statement on the fifteenth meeting of the IHR (2005) Emergency Committee on the COVID-19 pandemic. Geneva: World Health Organization (2024).

  • 5.

    KirbyAEWaltersMSJenningsWCFugittRLaCrossNMattioliMet al. Using Wastewater Surveillance Data to Support the COVID-19 Response - United States, 2020-2021. MMWR Morb Mortal Wkly Rep. (2021) 70:1242–4. doi: 10.15585/mmwr.mm7036a2,

  • 6.

    McMahanCSSelfSRennertLKalbaughCKriebelDGravesDet al. COVID-19 wastewater epidemiology: a model to estimate infected populations. Lancet Planet Health. (2021) 5:e874–81. doi: 10.1016/S2542-5196(21)00230-8,

  • 7.

    WHO. Environmental surveillance for SARS-CoV-2 to complement other public health surveillance. Geneva: World Health Organization (2024).

  • 8.

    KadonskyKFNaughtonCCSusaMOlsonRSinghGLDaza-TorresMLet al. Expansion of wastewater-based disease surveillance to improve health equity in California's Central Valley: sequential shifts in case-to-wastewater and hospitalization-to-wastewater ratios. Front Public Health. (2023) 11:1141097. doi: 10.3389/fpubh.2023.1141097,

  • 9.

    Daza-TorresMLMontesinos-LopezJCKimMOlsonRBessCWRuedaLet al. Model training periods impact estimation of COVID-19 incidence from wastewater viral loads. Sci Total Environ. (2023) 858:159680. doi: 10.1016/j.scitotenv.2022.159680,

  • 10.

    ZhanQBablerKMSharkeyMEAmiraliABeaverCCBooneMMet al. Relationships between SARS-CoV-2 in Wastewater and COVID-19 Clinical Cases and Hospitalizations, with and without Normalization against Indicators of Human Waste. ACS ES T Water. (2022) 2:1992–2003. doi: 10.1021/acsestwater.2c00045,

  • 11.

    D'AoustPMTianXTowhidSTXiaoAMercierEHegazyNet al. Wastewater to clinical case (WC) ratio of COVID-19 identifies insufficient clinical testing, onset of new variants of concern and population immunity in urban communities. Sci Total Environ. (2022) 853:158547. doi: 10.1016/j.scitotenv.2022.158547,

  • 12.

    SchenkHHeidingerPInsamHKreuzingerNMarktRNägeleFet al. Prediction of hospitalisations based on wastewater-based SARS-CoV-2 epidemiology. Sci Total Environ. (2023) 873:162149. doi: 10.1016/j.scitotenv.2023.162149,

  • 13.

    LiXLiuHGaoLSherchanSPZhouTKhanSJet al. Wastewater-based epidemiology predicts COVID-19-induced weekly new hospital admissions in over 150 USA counties. Nat Commun. (2023) 14:4548. doi: 10.1038/s41467-023-40305-x,

  • 14.

    KanchanSOgdenEKesheriMSkinnerAMilikenELymanDet al. COVID-19 hospitalizations and deaths predicted by SARS-CoV-2 levels in Boise, Idaho wastewater. Sci Total Environ. (2024) 907:167742. doi: 10.1016/j.scitotenv.2023.167742,

  • 15.

    GalaniAAalizadehRKostakisMMarkouAAlygizakisNLytrasTet al. SARS-CoV-2 wastewater surveillance data can predict hospitalizations and ICU admissions. Sci Total Environ. (2022) 804:150151. doi: 10.1016/j.scitotenv.2021.150151,

  • 16.

    KrogsgaardLWBenedettiGGuddeARichterSRRasmussenLDMidgleySEet al. Results from the SARS-CoV-2 wastewater-based surveillance system in Denmark, July 2021 to June 2022. Water Res. (2024) 252:121223. doi: 10.1016/j.watres.2024.121223,

  • 17.

    McManusOChristiansenLENautaMKrogsgaardLWBahrenscheerNSvon KappelgaardLet al. Predicting COVID-19 Incidence Using Wastewater Surveillance Data, Denmark, October 2021-June 2022. Emerg Infect Dis. (2023) 29:1589–97. doi: 10.3201/eid2908.221634,

  • 18.

    ToledoDMRobbinsAAGallagherTLHershbergerKCBarneyRESalmelaSMet al. Wastewater-Based SARS-CoV-2 Surveillance in Northern New England. Microbiol Spectr. (2022) 10:e0220721. doi: 10.1128/spectrum.02207-21,

  • 19.

    RandazzoWCuevas-FerrandoESanjuanRDomingo-CalapPSanchezG. Metropolitan wastewater analysis for COVID-19 epidemiological surveillance. Int J Hyg Environ Health. (2020) 230:113621. doi: 10.1016/j.ijheh.2020.113621,

  • 20.

    SilvaAMenezesDMoreiraFRRSilvaAVFGTorresOAFonsecaPLCet al. Seroprevalence, prevalence, and genomic surveillance: monitoring the initial phases of the SARS-CoV-2 pandemic in Betim, Brazil. Front Microbiol. (2022) 13:799713. doi: 10.3389/fmicb.2022.799713,

  • 21.

    DuvalletCWuFMcElroyKAImakaevMEndoNXiaoAet al. Nationwide trends in COVID-19 cases and SARS-CoV-2 RNA wastewater concentrations in the United States. ACS ES T Water. (2022) 2:1899–909. doi: 10.1021/acsestwater.1c00434,

  • 22.

    ChengLDhiyebiHAVariaMAtanasKSrikanthanNHayatSet al. Omicron COVID-19 case estimates based on previous SARS-CoV-2 wastewater load, Regional Municipality of Peel, Ontario, Canada. Emerg Infect Dis. (2023) 29:1580–8. doi: 10.3201/eid2908.221580,

  • 23.

    VarkilaMRJMontez-RathMESalomonJAYuXBlockGAOwensDKet al. Use of Wastewater Metrics to Track COVID-19 in the US. JAMA Netw Open. (2023) 6:e2325591. doi: 10.1001/jamanetworkopen.2023.25591,

  • 24.

    AdamsCBiasMWelshRMWebbJReeseHDelgadoSet al. The National Wastewater Surveillance System (NWSS): from inception to widespread coverage, 2020-2022, United States. Sci Total Environ. (2024) 924:171566. doi: 10.1016/j.scitotenv.2024.171566,

  • 25.

    SilvaCSTryndyakVPCamachoLOrloffMSPorterAGarnerKet al. Temporal dynamics of SARS-CoV-2 genome and detection of variants of concern in wastewater influent from two metropolitan areas in Arkansas. Sci Total Environ. (2022) 849:157546. doi: 10.1016/j.scitotenv.2022.157546,

  • 26.

    JohanssonMAQuandelacyTMKadaSPrasadPVSteeleMBrooksJTet al. SARS-CoV-2 Transmission From People Without COVID-19 Symptoms. JAMA Netw Open. (2021) 4:e2035057. doi: 10.1001/jamanetworkopen.2020.35057,

  • 27.

    NattinoGCastiglioniSCeredaDDella VallePGPellegrinelliLBertoliniGet al. Association Between SARS-CoV-2 Viral Load in Wastewater and Reported Cases, Hospitalizations, and Vaccinations in Milan, March 2020 to November 2021. JAMA. (2022) 327:1922–4. doi: 10.1001/jama.2022.4908,

  • 28.

    MustaphaM TKVolkmanHJingyanYYehoshuaADi FuscoMMcLaughlinJM (2024). Under-reporting of SARS-CoV-2 infections in 27 countries, 2020–2022. doi: 10.2139/ssrn.5014145

  • 29.

    Statens Serum Institut, Denmark. National surveillance of SARS-CoV-2 in wastewater. Available online at: https://en.ssi.dk/surveillance-and-preparedness/surveillance-in-denmark/covid-19/national-surveillance-of-sars-cov-2-in-wastewater (accessed December 12, 2024).

  • 30.

    National Institute for Public Health and the Environment, Ministry of Health, Welfare and Sport. (2024). Coronavirus monitoring in wastewater. Available online at: https://www.rivm.nl/en/coronavirus-covid-19/research/wastewater#sewageresearch (accessed December 12, 2024).

  • 31.

    Centers for Disease Control and Prevention, United States. The Coronavirus Disease 2019 (COVID-19) Hospitalization Surveillance Network (COVID-NET). (2024). Available online at: https://www.cdc.gov/covid/php/covid-net/index.html (accessed December 12, 2024).

  • 32.

    Our World in Data (OWID)-COVID Data (2024). Available online at: https://covid-19.nyc3.digitaloceanspaces.com/public/owid-covid-data.csv (accessed October 16, 2024).

  • 33.

    Statens Serum Institut, Denmark. COVID-19 Interactive Dashboard. (2024). Available online at: https://experience.arcgis.com/template/099eb5c9acea4e18b411997815be2f98 (accessed December 12, 2024).

  • 34.

    National Wastewater Surveillance System (NWSS). Centers for Disease Control and Prevention. (2024).Available online at: https://www.cdc.gov/nwss/wastewater-surveillance.html (accessed February 14, 2024).

  • 35.

    Netherlands National Coordination Center Patient Distribution. (2024). Actuele data COVID-bezetting. Available online at: https://lcps.nu/datafeed/ (accessed November 30, 2025).

  • 36.

    CDC. (2024). EpiWeek Function. Centers for Disease Control and Prevention. Available online at: https://www.cdc.gov/epiinfo/user-guide/check-code/epiweekfunctions.html (accessed April 30, 2025).

  • 37.

    United Nations. 2024 Revision of World Population Prospects. United Nations. (2024). Available online at: https://population.un.org/wpp/ (accessed December 12, 2024).

  • 38.

    SchenkHRauchWZulliABoehmAB. SARS-CoV-2 surveillance in US wastewater: Leading indicators and data variability analysis in 2023-2024. PLoS One. (2024) 19:e0313927. doi: 10.1371/journal.pone.0313927,

  • 39.

    R Core Team. R: A Language and Environment for Statistical Computing. Geneva: R Core Team (2021).

  • 40.

    GeubbelsEBackerJABakhshi-RaiezFGeubbelsELPEBoogaardJBroekmanEHet al. The daily updated Dutch national database on COVID-19 epidemiology, vaccination and sewage surveillance. Sci Data. (2023) 10:469. doi: 10.1038/s41597-023-02232-w,

  • 41.

    ZhanQSolo-GabrieleHMSharkeyMEAmiraliABeaverCCBooneMMet al. Correlative analysis of wastewater trends with clinical cases and hospitalizations through five dominant variant waves of COVID-19. ACS ES T Water. (2023) 3:2849–62. doi: 10.1021/acsestwater.3c00032,

  • 42.

    LiRPeiSChenBSongYZhangTYangWet al. Substantial undocumented infection facilitates the rapid dissemination of novel coronavirus (SARS-CoV-2). Science. (2020) 368:489–93. doi: 10.1126/science.abb3221,

  • 43.

    PuhachOMeyerBEckerleI. SARS-CoV-2 viral load and shedding kinetics. Nat Rev Microbiol. (2023) 21:147–61. doi: 10.1038/s41579-022-00822-w,

  • 44.

    CDC. (2025). The Changing Threat of COVID-19. Available online at: https://www.cdc.gov/ncird/whats-new/changing-threat-covid-19.html (accessed January 28, 2025).

  • 45.

    AnnanJHendersonRGrayMClarkRGSarinCBlackK. A Review of Wastewater-Based Epidemiology for the SARS-CoV-2 Virus in Rural, Remote, and Resource-Constrained Settings Internationally: Insights for Implementation, Research, and Policy for First Nations in Canada. Int J Environ Res Public Health. (2024) 21:1429. doi: 10.3390/ijerph21111429,

  • 46.

    BianchiFPStefanizziPDi LorenzoACusciannaETafuriSGerminarioCA. Vaccine coverage for recommended vaccines among splenectomised patients in Apulia, South Italy: a retrospective cohort study. BMJ Open. (2023) 13:e069316. doi: 10.1136/bmjopen-2022-069316,

  • 47.

    ComparciniDCicoliniGTotaroMGovernatoriLPastoreFMiniscalcoDet al. Influenza vaccination hesitancy and related factors among pregnant and breastfeeding women: A cross-sectional study. Hum Vaccin Immunother. (2025) 21:2450858. doi: 10.1080/21645515.2025.2450858,

  • 48.

    VosERAvan HagenCCEWongDSmitsGKuijerMWijmenga-MonsuurAJet al. SARS-CoV-2 Seroprevalence Trends in the Netherlands in the Variant of Concern Era: Input for Future Response. Influenza Other Respir Viruses. (2024) 18:e13312. doi: 10.1111/irv.13312,

  • 49.

    ChoiTXieYAl-AlyZ. Rates of hospitalization and death due to COVID-19 in US veterans with SARS-CoV-2 infection in the XBB-, JN.1-, and KP-predominant eras. Open Forum Infect Dis. (2025) 12:ofaf115. doi: 10.1093/ofid/ofaf115,

  • 50.

    GuddeAKrogsgaardLWBenedettiGSchierbechSKBrokhattingenNPetrovicKet al. Predicting hospital admissions due to COVID-19 in Denmark using wastewater-based surveillance. Sci Total Environ. (2025) 966:178674. doi: 10.1016/j.scitotenv.2025.178674,

Summary

Keywords

COVID, hospitalization, vaccine (COVID-19), wastewater, SARS-CoV-2 infection (COVID-19)

Citation

Mustapha MM, Choi LE, Bergroth T, Volkman HR, Devlin K, Yang J, Yehoshua A, Khan FL, McLaughlin JM and Nguyen JL (2025) Association between SARS-CoV-2 in wastewater and COVID-19 hospitalizations in three countries, 2022–2024. Front. Public Health 13:1679596. doi: 10.3389/fpubh.2025.1679596

Received

04 August 2025

Revised

06 November 2025

Accepted

30 November 2025

Published

18 December 2025

Volume

13 - 2025

Edited by

Severino Jefferson Ribeiro Da Silva, University of Toronto, Canada

Reviewed by

Vasco Ricoca Peixoto, New University of Lisbon, Portugal

Eustachio Cuscianna, University of Bari Aldo Moro, Italy

Updates

Copyright

*Correspondence: Mustapha M. Mustapha,

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Outline

Figures

Cite article

Copy to clipboard


Export citation file


Share article

Article metrics