Evolution of illness severity in hospital admissions due to COVID-19
Published by: The Public Health Agency of Canada
Issue: Volume 50-1/2, January/February 2024: Respiratory Syncytial Virus (RSV)
Date published: January/February 2024
ISSN: 1481-8531
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Volume 50-1/2, January/February 2024: Respiratory Syncytial Virus (RSV)
Epidemiologic Study
Evolution of illness severity in hospital admissions due to COVID-19, Québec, Canada, January to April 2022
Ernest Lo1,2, Élise Fortin1,3,4, Rodica Gilca1,4,5, Pierre-Luc Trépanier1, Hany Geagea1, Zhou Zhou1
Affiliations
1 Institut national de santé publique du Québec, Québec, QC
2 Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montréal, QC
3 Département de microbiologie, Infectiologie et immunologie, Faculté de médecine, Université de Montréal, Québec, QC
4 Département de médecine sociale et préventive, Faculté de médecine, Université Laval, Québec, QC
5 Centre de recherche du CHU de Québec, Université Laval, Québec, QC
Correspondence
Suggested citation
Lo E, Fortin É, Gilca R, Trépanier P-L, Geagea H, Zhou Z. Evolution of illness severity in hospital admissions due to COVID-19, Québec, Canada, January to April 2022. Can Commun Dis Rep 2024;50(1/2):63–76. https://doi.org/10.14745/ccdr.v50i12a08
Keywords: COVID-19, hospitalizations, severity, surveillance
Abstract
Background: The coronavirus disease 2019 (COVID-19) severity is influenced by multiple factors, such as age, underlying medical conditions, individual immunity, infecting variant, and clinical practice. The highly transmissible Omicron variants resulted in decreased COVID-19 screening capacity, which limited disease severity surveillance.
Objective: To report on the temporal evolution of disease severity among patients admitted to Québec hospitals due to COVID-19 between January 2, 2022, and April 23, 2022, which corresponded to the peak period of hospitalizations due to Omicron.
Methods: Retrospective population-based cohort study of all hospital admissions due to COVID-19 in Québec, between January 2, 2022, and April 23, 2022. Study period was divided into four-week periods, corresponding roughly to January, February, March and April. Regression using Cox and Poisson generalized estimating equations (GEEs) was used to quantify temporal variations in length of stay and risk of complications (intensive care admission or in-hospital death) through time, using the Omicron peak (January 2022) as reference. Measures were adjusted for age, sex, vaccination status, presence of chronic diseases, and clustering by hospital.
Results: During the study period, 9,178 of all 18,272 (50.2%) patients hospitalized with a COVID-19 diagnosis were admitted due to COVID-19. Of these, 1,026 (11.2%) were admitted to intensive care and 1,523 (16.6%) died. Compared to January, the risk of intensive care admission was 25% and 31% lower in March and April respectively, while in-hospital fatality continuously decreased by 45% lower in April. The average length of stay was temporarily lower in March (9%).
Conclusion: Severity of admissions due to COVID-19 decreased in the first months of 2022, when predominant circulating variants were considered to be of similar severity. Monitoring hospital admissions due to COVID-19 can contribute to disease severity surveillance.
Introduction
When a new severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variant or sublineage appears, efforts are made to rapidly characterize its transmissibility and severity compared to previous variants. The Omicron BA.1 variant was first detected in Québec on December 8, 2021, during the Delta wave of the pandemic, and became predominant by December 12, 2021. Subsequently, the Omicron BA.2 variant appeared on January 1, 2022, and was predominant by March 27, 2022. A peak in hospital admissions due to SARS-CoV-2 (the coronavirus that causes COVID-19) was recorded on January 18, 2022 Footnote 1. Overall, the Omicron variant had higher transmissibility but lower severity compared to the Delta variant Footnote 2Footnote 3Footnote 4Footnote 5Footnote 6, while the Omicron BA.1 and BA.2 sublineages had comparable severity Footnote 5Footnote 7Footnote 8Footnote 9. Such information is essential for public health teams to help them anticipate the evolution of the epidemic, including the new variant’s impact on healthcare resources. In Canada, where the number of hospital beds per inhabitant is low and the workforce has been affected by the COVID-19 pandemic, information on severity will help to determine whether or not public health measures should be applied or maintained Footnote 10Footnote 11.
Severity of COVID-19 cases depends on factors beyond the characteristics of the virus. In times of high incidence, more hospitalizations will occur and the threshold for hospital admission/discharge might change, regardless of virulence Footnote 12. Natural, vaccine-induced, and hybrid immunity have increased in the population since the beginning of the COVID-19 pandemic but will vary according to time since infection or vaccination Footnote 13Footnote 14Footnote 15. Clinical care has also evolved with increasing knowledge and experience in treatment, as well as with the arrival of antiviral treatments Footnote 16Footnote 17. Finally, with the explosion of cases following the emergence of Omicron variants and the availability of rapid tests, accurate estimates of the total number of cases and, consequently, the proportion of severe disease in the general population, were no longer possible. In contrast, all patients admitted to hospital in the province of Québec receive a PCR test for COVID-19, a practice that was consistent throughout the pandemic Footnote 18. Propensity of hospitalization given a certain level of severity in Québec also was not impacted by the adoption of rapid tests. Thus, tracking the evolution of the severity of cases among those admitted to hospital due to COVID-19 represents a potentially interesting alternative for disease severity monitoring.
We aimed to describe the severity of hospital admissions due to COVID-19 in Québec between January 2022 and April 2022, which corresponded to the Omicron BA.1 and BA.2 waves. We measured length of stay, risk of intensive care admission, and risk of in-hospital death, and quantified temporal variations of these measures.
Methods
Study design and population
A retrospective population-based cohort was built using linked data to study all Québec hospitalizations for which COVID-19 led to hospital admission between January 2, 2022, and April 23, 2022 (Centers for Disease Control and Prevention, weeks 1–16). Patients were followed from admission until discharge, death, or final date of data extraction (May 25, 2022).
Data sources and variables
The COVID-19 hospitalizations were identified using the provincial hospital admissions database, which is a real-time version of the provincial hospital discharge database (MED-ECHO) routinely available before the pandemic. For this real-time database, hospital medical archivists reported any presence of COVID-19 during a hospital stay, regardless of other health conditions. Since December 30, 2021, archivists also provided admission diagnosis for all patients with a COVID-19 diagnosis during their hospital stay. Admission and hospital stay diagnoses are recorded according to the International Classification of Diseases 10th Revision (ICD-10). Among all patients with a COVID-19 diagnosis during their hospital stay, those with an admission code related to COVID-19 were identified as admissions due to COVID-19. The list of COVID-19-related diagnostic codes used in provincial surveillance is provided in Appendix, Table A1. In addition to admission diagnosis, admission and discharge dates, age, sex, intensive care admissions, and death while hospitalized are also recorded in this database. The study period was divided into four four-week periods that corresponded to the peak (January) and the tail (February) of the BA.1 wave, the transition towards BA.2 (March), and the beginning and peak of the BA.2 wave (April) (Figure 1). Using a unique identifier, the hospitalization database was linked to:
- The Québec Integrated Chronic Diseases Surveillance System to identify patients with at least one of 31 comorbidities Footnote 19
- The provincial laboratory database to identify patients who had a positive SARS-CoV-2 test more than 90 days before the current admission (interpreted as a reinfection)
- The provincial immunization registry for information on COVID-19 vaccination status (individuals with at least two doses were considered adequately vaccinated)
Analyses
The proportion of admissions due to COVID-19 with an intensive care admission, as well as the proportion of patient deaths, were computed for each time period. The 25th, 50th and 75th percentiles of length of stay were additionally computed, once again for each time period. Although length of stay was censored after 28 days, the estimated percentiles were always less than 28 days and so were unaffected. These proportions and duration were also stratified by age group (0–45, 46–55, 56–65, 66–75 and over 75 years old), sex, vaccination status, history of COVID-19 infection, and presence or absence of comorbidities, respectively.
Regression analyses were used to quantify the association between both length of stay and risk of complications (intensive care admission or death) vs. time period, using the Omicron peak period (January 2022) as reference. Cox proportional hazards regression was used to analyze length of stay, using random effects to model the possible clustering effect of hospitals. General estimating equations using a Poisson distribution and exchangeable correlation matrix were used to analyze risk of intensive care admission and death, accounting for the possible clustering effect of hospitals. For the above regressions, unadjusted and fully adjusted associations with time period are presented. Fully adjusted models used age group, sex, vaccination status, and chronic disease as covariates; no adjustment was made for history of COVID-19 infection because patients hospitalized for a reinfection were too rare (less than 3% of patients hospitalized for COVID-19). To isolate changes in disease severity from patient immunity to the disease, additional models were produced only for patients who had no known history of COVID-19 infection and who were not vaccinated. In subgroup analyses, separate models were also produced for each age group. Finally, after learning that three hospitals had largely underestimated intensive care admissions in early 2022, the fully adjusted regression was done, excluding these three hospitals, in a post hoc sensitivity analysis. All analyses were done using R 4.0.2; mixed effects Cox regression was done using the coxme package Footnote 20, while Poisson GEE was done using the geepack package Footnote 21.
Results
Between January 2, 2022, and April 23, 2022, 9,178 (50.2%) of all 18,272 patients who were hospitalized with a COVID-19 diagnosis were admitted due to COVID-19. Of these, 1,026 (11.2%) were admitted to an intensive care unit and 1,523 (16.6%) died while hospitalized (these outcomes were not mutually exclusive). Slightly over half of patients admitted due to COVID-19 were male (52.8%), and a majority of patients were over 65 years old (72.2%), adequately vaccinated (72.1%), experiencing their first known SARS-CoV-2 infection (98.1%) and had at least one comorbidity (83.7%). These statistics are described per four-week period in Table 1 (see Table A2 and Table A3 for a description of intensive care unit admissions and deaths per four-week period). Patient characteristics were relatively stable over time, except for a higher proportion of older patients and a lower proportion of inadequately vaccinated patients in March and April. In any given group, patients still hospitalized after 28 days represented less than 10% of inpatients.
Variable | January 2 to January 29, 2022 | January 30 to February 26, 2022 | February 27 to March 26, 2022 | March 27 to April 23, 2022 | ||||
---|---|---|---|---|---|---|---|---|
n | % | n | % | n | % | n | % | |
Global | 4,216 | 100.0 | 1,550 | 100.0 | 1,015 | 100.0 | 2,397 | 100.0 |
Admitted to ICU | 565 | 13.4 | 187 | 12.1 | 89 | 8.8 | 185 | 7.7 |
In-hospital death | 844 | 20.0 | 241 | 15.5 | 150 | 14.8 | 288 | 12.0 |
Age group (years) | ||||||||
0–45 | 469 | 11.1 | 247 | 15.9 | 121 | 11.9 | 248 | 10.3 |
44–55 | 254 | 6.0 | 89 | 5.7 | 39 | 3.8 | 68 | 2.8 |
56–65 | 544 | 12.9 | 171 | 11.0 | 103 | 10.1 | 200 | 8.3 |
66–75 | 911 | 21.6 | 316 | 20.4 | 186 | 18.3 | 446 | 18.6 |
Over 75 | 2,038 | 48.3 | 727 | 46.9 | 566 | 55.8 | 1,435 | 59.9 |
Sex | ||||||||
Male | 2,252 | 53.4 | 809 | 52.2 | 538 | 53.0 | 1,243 | 51.9 |
Female | 1,964 | 46.6 | 741 | 47.8 | 477 | 47.0 | 1,154 | 48.1 |
Vaccination | ||||||||
Adequate | 2,864 | 67.9 | 1,027 | 66.3 | 785 | 77.3 | 1,940 | 80.9 |
Inadequate | 1,348 | 32.0 | 519 | 33.5 | 229 | 22.6 | 453 | 18.9 |
Missing information (or Unknown) | 4 | 0.1 | 4 | 0.3 | 1 | 0.1 | 4 | 0.2 |
Prior infection according to laboratory tests | ||||||||
No | 4,151 | 98.5 | 1,520 | 98.1 | 993 | 97.8 | 2,338 | 97.5 |
Yes | 65 | 1.5 | 30 | 1.9 | 22 | 2.2 | 59 | 2.5 |
Comorbidities | ||||||||
None | 521 | 12.4 | 219 | 14.1 | 122 | 12.0 | 236 | 9.8 |
At least one | 3,526 | 83.6 | 1,247 | 80.5 | 846 | 83.3 | 2,066 | 86.2 |
Missing | 169 | 4.0 | 84 | 5.4 | 47 | 4.6 | 95 | 4.0 |
Globally, patients were more frequently admitted to intensive care units in January and February, while length of stay remained relatively stable over time (Figure 1). Patients also died more frequently during the January peak of hospital admissions, with a gradual decrease throughout the following weeks (Figure 1). These time trends were also observed in regression analyses, after adjusting for age, sex, vaccination status, and presence of at least one comorbidity (Table 2). The proportions of patients admitted to intensive care were 25% and 31% lower in March and April (peak of BA.2; Table 1), respectively, as compared with the Omicron peak (January); this trend towards a risk reduction in time was observed in all age groups except for those 0–45 years old (Table 3). Results were similar when excluding the three hospitals that underestimated intensive care admissions (adjusted risk ratios of 0.92, 0.76 and 0.70 for February, March and April, respectively). The proportion of in-hospital deaths decreased continuously and was 45% lower in April, compared to January (Table 2); this trend was driven by patients over 75 years old, as 78% of deaths occurred in this age group (Table A3). In non-vaccinated patients admitted for a first COVID-19 episode, adjusted time trends in risk of intensive care admission and in-hospital death were very similar to those observed in the entire cohort (Table 2). Finally, the probability of remaining in hospital after any given number of days was 9% lower in March (transition towards BA.2) compared to January (BA.1 peak), but this was a temporary decrease (Table 2). No statistically significant change in length of stay was observed for hospitalizations of non-vaccinated patients. Cox regressions stratified by age group had extremely high statistical variability, indicating both increasing or decreasing lengths of stay (Table 3).
Population type by time period | Length of stay | Intensive care admissions | In-hospital deaths | ||||
---|---|---|---|---|---|---|---|
Unadjusted hazard ratio (95% CI) |
Fully adjustedTable 2 footnote a hazard ratio (95% CI) |
Unadjusted proportion ratio (95% CI) |
Fully adjustedTable 2 footnote c proportion ratio (95% CI) |
Unadjusted proportion ratio (95% CI) |
Fully adjustedTable 2 footnote c proportion ratio (95% CI) |
||
Global | |||||||
January 2 to January 29, 2022 | Reference | Reference | Reference | Reference | Reference | Reference | |
January 30 to February 26, 2022 | 1.01 (0.95–1.07) |
1.01 (0.95–1.07) |
0.90 (0.77–1.05) |
0.91 (0.78–1.07) |
0.78 (0.69–0.89) |
0.81 (0.71–0.92) |
|
February 27 to March 26, 2022 | 0.88 (0.82–0.94) |
0.91 (0.84–0.97) |
0.66 (0.53–0.82) |
0.75 (0.61–0.93) |
0.73 (0.63–0.86) |
0.70 (0.60–0.82) |
|
March 27 to April 23, 2022 | 0.99 (0.94–1.04) |
1.03 (0.97–1.08) |
0.57 (0.48–0.67) |
0.69 (0.58–0.80) |
0.60 (0.53–0.68) |
0.55 (0.48–0.62) |
|
Unvaccinated with no previous COVID-19 infection | |||||||
January 2 to January 29, 2022 | Reference | Reference | Reference | Reference | Reference | Reference | |
January 30 to February 26, 2022 | 1.15 (1.01–1.31) |
1.08 (0.95–1.22) |
1.04 (0.82–1.32) |
1.06 (0.83–1.34) |
0.92 (0.69–1.21) |
0.88 (0.68–1.15) |
|
February 27 to March 26, 2022 | 1.03 (0.85–1.25) |
0.96 (0.80–1.17) |
0.74 (0.48–1.12) |
0.73 (0.48–1.12) |
0.66 (0.40–1.07) |
0.74 (0.47–1.17) |
|
March 27 to April 23, 2022 | 0.98 (0.85–1.13) |
0.88 (0.76–1.01) |
0.69 (0.51–0.95) |
0.71 (0.52–0.97) |
0.65 (0.46–0.92) |
0.57 (0.41–0.81) |
|
Age by time period | Length of stay | Intensive care admissions | In-hospital deaths |
---|---|---|---|
Fully adjustedTable 3 footnote c hazard ratio (95% CI) |
Fully adjustedTable 3 footnote c proportion ratio (95% CI) |
Fully adjustedTable 3 footnote c proportion ratio (95% CI) |
|
0–45 years | |||
January 2 to January 29, 2022 | Reference | Reference | Reference |
January 30 to February 26, 2022 | 1.3 (0.93–1.83) |
0.65 (0.40–1.05) |
1.17 (0.29–4.77) |
February 27, 2022, to March 26, 2022 | 1.12 (0.72–1.73) |
0.50 (0.25–1.02) |
0.81 (0.09–7.06) |
March 27, 2022, to April 23, 2022 | 1.2 (0.89–1.87) |
0.77 (0.48–1.24) |
2.20 (0.72–6.68) |
46–55 years | |||
January 2 to January 29, 2022 | Reference | Reference | Reference |
January 30 to February 26, 2022 | 1.08 (0.85–1.37) |
1.19 (0.73–1.93) |
1.47 (0.50–4.31) |
February 27 to March 26, 2022 | 1.62 (1.19–2.22) |
0.93 (0.45–1.95) |
1.44 (0.35–5.96) |
March 27 to April 23, 2022 | 1.07 (0.83–1.38) |
0.26 (0.08–0.83) |
0 |
56–65 years | |||
January 2 to January 29, 2022 | Reference | Reference | Reference |
January 30 to February 26, 2022 | 0.97 (0.84–1.12) |
0.81 (0.58–1.14) |
0.88 (0.52–1.48) |
February 27 to March 26, 2022 | 0.86 (0.71–1.04) |
0.78 (0.50–1.22) |
0.73 (0.36–1.47) |
March 27 to April 23, 2022 | 1.13 (0.98–1.31) |
0.61 (0.42–0.89) |
0.63 (0.36–1.11) |
66–75 years | |||
January 2 to January 29, 2022 | Reference | Reference | Reference |
January 30 to February 26, 2022 | 1.03 (0.9–1.17) |
0.95 (0.73–1.24) |
0.88 (0.66–1.18) |
February 27 to March 26, 2022 | 0.86 (0.73–1.01) |
0.84 (0.58–1.22) |
0.85 (0.59–1.24) |
March 27 to April 23, 2022 | 1.22 (1.08–1.38) |
0.74 (0.56–0.97) |
0.54 (0.39–0.75) |
Over 75 years | |||
January 2 to January 29, 2022 | Reference | Reference | Reference |
January 30 to February 26, 2022 | 0.95 (0.87–1.04) |
1.04 (0.77–1.40) |
0.77 (0.67–0.90) |
February 27 to March 26, 2022 | 0.85 (0.77–0.94) |
0.76 (0.51–1.13) |
0.67 (0.56–0.80) |
March 27 to April 23, 2022 | 0.92 (0.86–0.99) |
0.73 (0.55–0.96) |
0.53 (0.46–0.61) |
Discussion
This study showed a decreasing trend in the risks of intensive care admission and in-hospital death among patients admitted to hospital due to COVID-19 in Québec throughout the first 16 weeks of 2022. No clear trend emerged with respect to temporal variations in the length of hospital stay. Conclusions were similar in sensitivity analyses focusing on unvaccinated patients with no previous documented COVID-19 infection.
Many factors may have contributed to decreasing severity. Patient age, sex and comorbidities have been identified as risk factors for severe outcomes in the early stages of the pandemic Footnote 12Footnote 22Footnote 23Footnote 24, but analyses for these factors were adjusted and/or stratified, as well as controlled for vaccination status. Residual confounding may nevertheless remain. Xia et al. reported a positive association between in-hospital mortality (in all COVID-19-positive inpatients) and the proportion of available beds occupied by COVID-19-positive patients in Québec, during the first three waves of the pandemic Footnote 12. The arrival of the Omicron variant led to the highest number of patients hospitalized with a COVID-19 diagnosis since the beginning of the pandemic Footnote 1. This patient load may also have contributed to the trends observed in our study. However, the last four-week period included the peak of the BA.2 wave, and severity kept decreasing even though an increase would have been expected given the higher number of admissions. It is possible that this phenomenon may still have occurred but was not strong enough to reverse the overall trend. Clinical practices also keep evolving, with antiviral treatments becoming available at the beginning of the study period and with increasing accessibility over time Footnote 17Footnote 25. However, without access to patient load, healthcare worker absenteeism, or antiviral use data, these variables could not be accounted for. Finally, social determinants of health, which represent a well-known driver of inequalities in COVID-19 susceptibility and outcomes, were not accounted for in these analyses Footnote 26. However, the effect of social determinants is likely controlled for in the regression analyses, at least in part, through other covariates, such as comorbidities and vaccination status.
Variant composition also evolved during the study period and could have contributed to observed severity trends. Delta-infected patients were still being admitted to hospital in early January, which could explain a higher in-hospital mortality during the first four-week period, but not the decrease in severity observed for the last two periods Footnote 27. Estimates of the severity of the BA.1 and BA.2 sublineages have suggested a possible lower severity of BA.2 Footnote 5Footnote 7Footnote 8, though differences measured within each study were not statistically significant. Whole genome sequencing data were unavailable for hospitalized patients; therefore, an association between observed severity trends and variant composition could not be confirmed. Other possible factors are that patients from the more recent periods had shorter follow-up and thus less time to experience outcomes (discharge, intensive care unit admission or death), as not all inpatients had been discharged by the end of the study period. However, all patients were followed for at least 28 days, which should be sufficient to capture the majority of outcomes. The practice of PCR testing of all the patients admitted to hospital in Québec Footnote 18 also rules out changes in testing practices as a factor in severity trends.
In the time preceding the study, PCR testing was done in the general population; nevertheless, not all cases, especially if mild or asymptomatic, were necessarily detected. Therefore, reinfection or the presence of previous COVID-19 infection could have gone undetected in some patients. However, this would only affect severity trends if the proportion of undetected reinfections varied over time. Overall, COVID-19 testing quality and coverage in Québec were high before December 2021 and the advent of Omicron. It is possible, however, that the proportion of hospital patients with unmeasured previous COVID infection acquired during or after December 2021 could have contributed to the observed decreasing severity for the month of April, since a previous infection is defined as one that occurs at least three months before the testing date. Finally, it is possible that the “adequate vaccination” criterion used in the regression analyses does not account for the effect of waning vaccine efficacy, which could result in misclassification of patients that were thought to be protected due to vaccine immunity. However, this effect is likely minimal, given that the majority (84%) of adequately vaccinated patients in this study received their last dose within seven months of hospital admission. This seven-month threshold is based on vaccine effectiveness studies Footnote 28. Sensitivity analyses (not shown), where patients receiving their last dose more than seven months after admission to hospital were classified as inadequately vaccinated, showed negligible difference in estimated severity trends.
When Omicron hit the province of Québec in December 2021, screening clinics and laboratories were quickly overloaded. January 2022 marked the end of two years of universal screening. At this time, a new screening strategy was adopted that targeted only certain subpopulations, mostly consisting of the elderly, especially in long-term care facilities, healthcare workers, and patients admitted to hospital Footnote 29. Surveillance of disease severity by following up on COVID-19 cases until hospital admission or death would therefore have been biased given the reasons behind the selection of these groups (e.g., increased vulnerability, higher exposure to disease and to vaccines, and the healthy worker effect). Monitoring severity among inpatients represented an alternative because all inpatients were still tested. Our previous work on disease severity comparing Omicron and Delta variants among inpatients suggested a lower severity of Omicron hospitalizations, concordant with other studies comparing these two variants with different methodologies Footnote 3Footnote 4Footnote 5Footnote 6Footnote 30. Wolter et al. reached convergent conclusions regarding the relative severity of BA.1 and BA.2 sublineages by measuring and comparing the difference in both risk of hospital admission among cases and risk of severe outcomes among inpatients Footnote 8.
The restriction of analyses only to patients admitted due to COVID-19 is an important strength of this study, as about half of all COVID-19-positive inpatients were admitted for other illnesses that can differ in severity from COVID-19. As well, healthcare-associated cases of COVID-19, which are more frequent in periods of high viral circulation, have been related to more severe outcomes Footnote 31Footnote 32. Unfortunately, admission diagnosis was only available from December 30, 2021, which prevented a comparison of Omicron waves with earlier waves. Before January 2022, all COVID-19-positive patients were analyzed, with the finding that median length of stay, proportion admitted to intensive care, and proportion of in-hospital deaths all varied in a similar manner over time, suggesting that length of stay could be used to inform disease severity Footnote 30. This correspondence was not observed in the present analysis, however. Length of stay may be influenced by patient load during peaks and its utility for surveillance of severity is therefore unclear. Also, the results of this study do not provide information on the effect of interventions that aim to prevent hospitalizations. For instance, compared to the general population, hospitalized cases over-represent individuals where vaccines and antivirals have not been successful. Finally, as was previously pointed out by Twohig et al., this surveillance informs the evolution of severity with a delay, as admissions follow case onset by a few days and as a majority of patients have to be discharged before intensive care admissions, in-hospital deaths, and length of stay can be assessed Footnote 22.
Conclusion
Throughout the first months of 2022, the risks of in-hospital death or intensive care admission decreased in individuals admitted due to COVID-19. Many factors, including changing immunity, reinfection prevalence, antiviral usage, and patient load may have contributed to this trend, which occurred during a time when virulence of predominant circulating variants were not excessively different. Hospital admissions due to COVID-19 represent an opportunity for monitoring trends in disease severity.
Authors' statement
- EL — Conceptualization, data analysis, interpretation, writing–original draft, writing–review & editing
- EF — Conceptualization, data analysis, interpretation, writing–original draft, writing–review & editing
- P-LT — Data analysis
- RG — Interpretation, writing–review & editing
- RT — Interpretation, writing–review & editing
- HG — Interpretation, writing–review & editing
- ZZ — Interpretation, writing–review & editing
The contents of this article and the opinions expressed therein are those of the authors and do not necessarily reflect those of the Government of Canada.
Competing interests
The authors have no competing interests to declare.
Funding
RG received funding from Québec Ministry of Health for a hospital surveillance network of respiratory hospitalizations, not related to the present study.
Appendix
Code | Description |
---|---|
A090 | Gastroentérite et colite autre et non précisée d'origine infectieuse |
A099 | Gastroentérite et colite d'origine non précisée |
A418 | Autres sepsies précisées |
A419 | Sepsie, sans précision |
A498 | Autres infections bactériennes, siège non précisé |
A499 | Infection bactérienne, sans précision |
B348 | Autres infections virales, siège non précisé |
B349 | Infection virale, sans précision |
E860 | Déshydratation |
G430 | Migraine sans aura [migraine commune] |
G431 | Migraine avec aura [migraine classique] |
G432 | État de mal migraineux |
G433 | Migraine compliquée |
G438 | Autres migraines |
G439 | Migraine, sans précision |
G441 | Céphalée vasculaire, non classée ailleurs |
G442 | Céphalée dite de tension |
G444 | Céphalée médicamenteuse, non classée ailleurs |
G448 | Autres syndromes précisés d’algies céphaliques |
G933 | Syndrome de fatigue post-virale |
I260 | Embolie pulmonaire, avec mention de coeur pulmonaire aigu |
I269 | Embolie pulmonaire, sans mention de coeur pulmonaire aigu |
J00 | Rhinopharyngite aiguë [rhume banal] |
J010 | Sinusite maxillaire aiguë |
J011 | Sinusite frontale aiguë |
J012 | Sinusite ethmoïdale aiguë |
J013 | Sinusite sphénoïdale aiguë |
J014 | Pansinusite aiguë |
J018 | Autres sinusites aiguës |
J019 | Sinusite aiguë, sans précision |
J020 | Pharyngite à streptocoques |
J028 | Pharyngite aiguë due à d’autres micro-organismes précisés |
J029 | Pharyngite aiguë, sans précision |
J040 | Laryngite aiguë |
J041 | Trachéite aiguë |
J042 | Laryngo-trachéite aiguë |
J050 | Laryngite obstructive aiguë [croup] |
J051 | Épiglottite aiguë |
J060 | Laryngo-pharyngite aiguë |
J068 | Autres infections aiguës des voies respiratoires supérieures, à localisations multiples |
J069 | Infection des voies respiratoires supérieures, sans précision |
J09 | Grippe, due à un virus grippal zoonotique ou pandémique identifié |
J110 | Grippe avec pneumonie, virus non identifié |
J111 | Grippe avec d'autres manifestations respiratoires, virus non identifié |
J118 | Grippe avec d’autres manifestations, virus non identifié |
J120 | Pneumonie adénovirale |
J121 | Pneumonie due au virus respiratoire syncytial [VRS] |
J122 | Pneumonie due aux virus paragrippaux |
J123 | Pneumonie due au métapneumovirus humain |
J128 | Autre pneumonie virale |
J129 | Pneumonie virale, sans précision |
J13 | Pneumonie due à Streptococcus pneumoniae |
J14 | Pneumonie due à Haemophilus influenzae |
J150 | Pneumonie due à Klebsiella pneumoniae |
J151 | Pneumonie due à Pseudomonas |
J152 | Pneumonie due à des staphylocoques |
J153 | Pneumonie due à des streptocoques, groupe B |
J154 | Pneumonie due à d’autres streptocoques |
J155 | Pneumonie due à Escherichia coli |
J156 | Pneumonie due à d’autres bactéries à Gram négatif |
J157 | Pneumonie due à Mycoplasma pneumoniae |
J158 | Autres pneumonies bactériennes |
J159 | Pneumonie bactérienne, sans précision |
J160 | Pneumonie due à Chlamydia |
J168 | Pneumonie due à d’autres micro-organismes infectieux |
J170 | Pneumonie au cours de maladies bactériennes classées ailleurs |
J171 | Pneumonie au cours de maladies virales classées ailleurs |
J172 | Pneumonie au cours de mycoses |
J173 | Pneumonie au cours de maladies parasitaires |
J178 | Pneumonie au cours d’autres maladies classées ailleurs |
J180 | Bronchopneumonie, sans précision |
J181 | Pneumonie lobaire, sans précision |
J182 | Pneumonie hypostatique, sans précision |
J188 | Autre pneumonie, micro-organisme non précisé |
J189 | Pneumonie, sans précision |
J200 | Bronchite aiguë due à Mycoplasma pneumoniae |
J201 | Bronchite aiguë due à Haemophilus influenzae |
J202 | Bronchite aiguë due à des streptocoques |
J203 | Bronchite aiguë due au virus Coxsackie |
J204 | Bronchite aiguë due aux virus paragrippaux |
J205 | Bronchite aiguë due au virus respiratoire syncytial [VRS] |
J206 | Bronchite aiguë due à des rhinovirus |
J207 | Bronchite aiguë due à des virus ECHO |
J2080 | Bronchite aiguë due au métapneumovirus humain |
J2088 | Bronchite aiguë due à d’autres micro-organismes précisés |
J209 | Bronchite aiguë, sans précision |
J210 | Bronchiolite aiguë due au virus respiratoire syncytial [VRS] |
J211 | Bronchiolite aiguë due au métapneumovirus humain |
J218 | Bronchiolite aiguë due à d’autres micro-organismes précisés |
J219 | Bronchiolite aiguë, sans précision |
J22 | Infection aiguë des voies respiratoires inférieures, sans précision |
J398 | Autres maladies des voies respiratoires supérieures précisées |
J399 | Maladie des voies respiratoires supérieures, sans précision |
J40 | Bronchite, non précisée comme aiguë ou chronique |
J440 | Maladie pulmonaire obstructive chronique avec infection aiguë des voies respiratoires inférieures |
J441 | Maladie pulmonaire obstructive chronique avec exacerbation aiguë, sans précision |
J448 | Autres maladies pulmonaires obstructives chroniques précisées |
J449 | Maladie pulmonaire obstructive chronique, sans précision |
J80 | Syndrome de détresse respiratoire de l'adulte |
J90 | Épanchement pleural, non classé ailleurs |
J91 | Épanchement pleural au cours de maladies classées ailleurs |
J960 | Insuffisance respiratoire aiguë |
J9600 | Insuffisance respiratoire aiguë Type I [hypoxique] |
J9601 | Insuffisance respiratoire aiguë Type II [hypercapnique] |
J9609 | Insuffisance respiratoire aiguë, type non précisé |
J961 | Insuffisance respiratoire chronique |
J9610 | Insuffisance respiratoire chronique Type I [hypoxique] |
J9611 | Insuffisance respiratoire chronique Type II [hypercapnique] |
J9619 | Insuffisance respiratoire chronique, type non précisé |
J969 | Insuffisance respiratoire, sans précision |
J9690 | Insuffisance respiratoire, sans précision, type I [hypoxique] |
J9691 | Insuffisance respiratoire, sans précision, Type II [hypercapnique] |
J9699 | Insuffisance respiratoire, sans précision, type non précisé |
J980 | Affections des bronches, non classées ailleurs |
J984 | Autres affections pulmonaires |
J988 | Autres troubles respiratoires précisés |
J989 | Trouble respiratoire, sans précision |
J998 | Troubles respiratoires au cours d’autres maladies classées ailleurs |
K290 | Gastrite hémorragique aiguë |
K291 | Autres gastrites aiguës |
K296 | Autres gastrites |
K297 | Gastrite, sans précision |
K298 | Duodénite |
K299 | Gastroduodénite, sans précision |
K523 | Colite indéterminée |
K528 | Autres gastroentérites et colites non infectieuses précisées |
K529 | Gastroentérite et colite non infectieuses, sans précision |
K591 | Diarrhée fonctionnelle |
P220 | Syndrome de détresse respiratoire du nouveau-né (SDR) |
P221 | Tachypnée transitoire du nouveau-né |
P228 | Autres détresses respiratoires du nouveau-né |
P229 | Détresse respiratoire du nouveau-né, sans précision |
P230 | Pneumonie congénitale due à un agent viral |
P231 | Pneumonie congénitale à Chlamydia |
P232 | Pneumonie congénitale à staphylocoques |
P233 | Pneumonie congénitale due à des streptocoques, groupe B |
P234 | Pneumonie congénitale à Escherichia coli |
P235 | Pneumonie congénitale à Pseudomonas |
P236 | Pneumonie congénitale due à d’autres agents bactériens |
P238 | Pneumonie congénitale due à d’autres micro-organismes |
P239 | Pneumonie congénitale, sans précision |
P280 | Atélectasie primitive du nouveau-né |
P281 | Atélectasies du nouveau-né, autres et sans précision |
P282 | Crises de cyanose du nouveau-né |
P283 | Apnée primitive du sommeil chez le nouveau-né |
P284 | Autres apnées du nouveau-né |
P285 | Insuffisance respiratoire du nouveau-né |
P288 | Autres affections respiratoires précisées chez le nouveau-né |
P289 | Affection respiratoire du nouveau-né, sans précision |
P2918 | Autre dysrythmie cardiaque néonatale |
P358 | Autres maladies virales congénitales |
P359 | Maladie virale congénitale, sans précision |
P368 | Autre sepsie bactérienne du nouveau-né |
P369 | Sepsie bactérienne du nouveau-né, sans précision |
P741 | Déshydratation du nouveau-né |
R000 | Tachycardie, sans précision |
R002 | Palpitations |
R008 | Anomalies des battements cardiaques, autres et non précisées |
R030 | Constatation d’une élévation de la tension artérielle, sans diagnostic d’hypertension |
R031 | Constatation d’une baisse non spécifique de la tension artérielle |
R05 | Toux |
R060 | Dyspnée |
R061 | Stridor |
R062 | Sifflement |
R063 | Respiration périodique |
R064 | Hyperventilation |
R065 | Respiration par la bouche |
R067 | Éternuement |
R068 | Anomalies de la respiration, autres et non précisées |
R070 | Douleur de la gorge |
R071 | Douleur thoracique respiratoire |
R072 | Douleur précordiale |
R073 | Autres douleurs thoraciques |
R074 | Douleur thoracique, sans précision |
R093 | Expectoration anormale |
R098 | Autres symptômes et signes précisés relatifs aux appareils circulatoire et respiratoire |
R100 | Syndrome abdominal aigu |
R1010 | Douleur localisée au quadrant supérieur droit |
R1011 | Douleur localisée au quadrant supérieur gauche |
R1012 | Douleur épigastrique |
R1019 | Douleur localisée à la partie supérieure de l’abdomen, sans précision |
R1030 | Douleur localisée au quadrant inférieur droit |
R1031 | Douleur localisée au quadrant inférieur gauche |
R1032 | Douleur périombilicale |
R1039 | Douleur localisée à la partie inférieure de l’abdomen, sans précision |
R104 | Douleurs abdominales, autres et non précisées |
R110 | Vomissement en jet |
R111 | Nausées seules |
R112 | Vomissements seuls |
R113 | Nausées avec vomissements |
R130 | Dysphagie oro-pharyngée |
R132 | Dysphagie oesophagienne |
R138 | Dysphagie, autre et non précisée |
R508 | Autre fièvre précisée |
R509 | Fièvre, sans précision |
R51 | Céphalée |
R520 | Douleur aiguë |
R529 | Douleur, sans précision |
R53 | Malaise et fatigue |
R5601 | Convulsions fébriles complexes |
R5602 | Convulsions fébriles simples |
R5609 | Convulsions fébriles, sans précision |
R5680 | Trouble convulsif, décrit ainsi |
R5688 | Convulsions, autres et non précisées |
R571 | Choc hypovolémique |
R572 | Choc septique |
R578 | Autre choc |
R579 | Choc, sans précision |
R590 | Adénopathies localisées |
R591 | Adénopathies généralisées |
R599 | Adénopathie, sans précision |
R650 | Syndrome de réponse inflammatoire systémique d’origine infectieuse sans défaillance organique |
R651 | Syndrome de réponse inflammatoire systémique d’origine infectieuse avec défaillance organique aiguë |
R652 | Syndrome de réponse inflammatoire systémique d’origine non infectieuse sans défaillance organique |
R653 | Syndrome de réponse inflammatoire systémique d’origine non infectieuse avec défaillance organique aiguë |
R659 | Syndrome de réponse inflammatoire systémique, non spécifié |
R91 | Résultats anormaux d’imagerie diagnostique du poumon |
U0490 | Syndrome respiratoire aigu sévère [SRAS] suspect |
U0491 | Syndrome respiratoire aigu sévère [SRAS] probable |
U071 | COVID-19 virus identifié |
U071NV | COVID-19 virus identifié avec ventilation |
U071S | COVID-19 virus identifié avec admission aux soins intensifs |
U071SV | COVID-19 virus identifié avec admission aux soins intensifs et ventilation |
U072 | COVID-19, virus non identifié |
U072NV | COVID-19 virus non identifié avec ventilation |
U072S | COVID-19 virus non identifié avec admission aux soins intensifs |
U072SV | COVID-19 virus non identifié admission aux soins intensifs et ventilation |
U073 | Syndrome inflammatoire multisystémique associé à la COVID-19 |
U074 | Affection post-COVID-19 |
Z038 | Mise en observation pour suspicion d'autres maladies et affections |
Z039 | Mise en observation pour suspicion de maladie ou affection, sans précision |
Z048 | Examen et mise en observation pour d'autres raisons précisées |
Z049 | Examen et mise en observation pour une raison non précisée |
Z519 | Soin médical, sans précision |
Variable | January 2 to 29, 2022 | January 30 to February 26, 2022 | February 27 to March 26, 2022 | March 27 to April 23, 2022 | |||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Hospital admissions | ICU | In-hospital deaths | Hospital admissions | ICU | In-hospital deaths | Hospital admissions | ICU | In-hospital deaths | Hospital admissions | ICU | In-hospital deaths | ||||||||||
N | % (95% CI) | N | % (95% CI) | N | % (95% CI) | N | % (95% CI) | N | % (95% CI) | N | % (95% CI) | N | % (95% CI) | N | % (95% CI) | ||||||
Global | 4,216 | 565 | 13.4 [12.4–14.4] |
844 | 20 [18.8–21.2] |
1,550 | 187 | 12.1 [10.4–13.7] |
241 | 15.5 [13.7–17.4] |
1,015 | 89 | 8.8 [7–10.5] |
150 | 14.8 [12.6–17] |
2,397 | 185 | 7.7 [6.6–8.8] |
288 | 12 [10.7–13.3] |
|
Age group (years) | |||||||||||||||||||||
0–45 | 469 | 65 | 13.9 [10.7–17] |
5 | 1.1 [0.1–2] |
247 | 24 | 9.7 [6–13.4] |
3 | 1.2 [0–2.6] |
121 | 7 | 5.8 [1.6–9.9] |
1 | 0.8 [0–2.4] |
248 | 24 | 9.7 [6–13.4] |
5 | 2 [0.3–3.8] |
|
44–55 | 254 | 50 | 19.7 [14.8–24.6] |
11 | 4.3 [1.8–6.8] |
89 | 18 | 20.2 [11.9–28.6] |
5 | 5.6 [0.8–10.4] |
39 | 8 | 20.5 [7.8–33.2] |
2 | 5.1 [0–12.1] |
68 | 4 | 5.9 [0.3–11.5] |
0 | 0 [0–0] | |
56–65 | 544 | 131 | 24.1 [20.5–27.7] |
60 | 11 [8.4–13.7] |
171 | 34 | 19.9 [13.9–25.9] |
16 | 9.4 [5–13.7] |
103 | 18 | 17.5 [10.1–24.8] |
10 | 9.7 [4–15.4] |
200 | 28 | 14 [9.2–18.8] |
15 | 7.5 [3.8–11.2] |
|
66–75 | 911 | 176 | 19.3 [16.8–21.9] |
161 | 17.7 [15.2–20.1] |
316 | 57 | 18 [13.8–22.3] |
51 | 16.1 [12.1–20.2] |
186 | 27 | 14.5 [9.5–19.6] |
28 | 15.1 [9.9–20.2] |
446 | 60 | 13.5 [10.3–16.6] |
43 | 9.6 [6.9–12.4] |
|
Over 75 | 2,038 | 143 | 7 [5.9–8.1] |
607 | 29.8 [27.8–31.8] |
727 | 54 | 7.4 [5.5–9.3] |
166 | 22.8 [19.8–25.9] |
566 | 29 | 5.1 [3.3–6.9] |
109 | 19.3 [16–22.5] |
1,435 | 69 | 4.8 [3.7–5.9] |
225 | 15.7 [13.8–17.6] |
|
Sex | |||||||||||||||||||||
Male | 2,252 | 350 | 15.5 [14–17] |
502 | 22.3 [20.6–24] |
809 | 108 | 13.3 [11–15.7] |
130 | 16.1 [13.5–18.6] |
538 | 55 | 10.2 [7.7–12.8] |
88 | 16.4 [13.2–19.5] |
1,243 | 103 | 8.3 [6.8–9.8] |
166 | 13.4 [11.5–15.2] |
|
Female | 1,964 | 215 | 10.9 [9.6–12.3] |
342 | 17.4 [15.7–19.1] |
741 | 79 | 10.7 [8.4–12.9] |
111 | 15 [12.4–17.5] |
477 | 34 | 7.1 [4.8–9.4] |
62 | 13 [10–16] |
1,154 | 82 | 7.1 [5.6–8.6] |
122 | 10.6 [8.8–12.3] |
|
Vaccination | |||||||||||||||||||||
Adequate | 2,864 | 312 | 10.9 [9.8–12] |
628 | 21.9 [20.4–23.4] |
1,027 | 96 | 9.3 [7.6–11.1] |
171 | 16.7 [14.4–18.9] |
785 | 63 | 8 [6.1–9.9] |
126 | 16.1 [13.5–18.6] |
1,940 | 137 | 7.1 [5.9–8.2] |
246 | 12.7 [11.2–14.2] |
|
Inadequate | 1,348 | 251 | 18.6 [16.5–20.7] |
216 | 16 [14.1–18] |
519 | 89 | 17.1 [13.9–20.4] |
69 | 13.3 [10.4–16.2] |
229 | 26 | 11.4 [7.2–15.5] |
24 | 10.5 [6.5–14.4] |
453 | 47 | 10.4 [7.6–13.2] |
42 | 9.3 [6.6–11.9] |
|
Missing | 4 | 2 | 50 [1–99] |
0 | 0 [0–0] |
4 | 2 | 50 [1–99] |
1 | 25 [0–67.4] |
1 | 0 | 0 [0–0] |
0 | 0 [0–0] |
4 | 1 | 25 [0–67.4] |
0 | 0 [0–0] |
|
Prior infection according to laboratory tests | |||||||||||||||||||||
No | 4,151 | 563 | 13.6 [12.5–14.6] |
837 | 20.2 [18.9–21.4] |
1,520 | 182 | 12 [10.3–13.6] |
239 | 15.7 [13.9–17.6] |
993 | 89 | 9 [7.2–10.7] |
147 | 14.8 [12.6–17] |
2,338 | 185 | 7.9 [6.8–9] |
284 | 12.1 [10.8–13.5] |
|
Yes | 65 | 2 | 3.1 [0–7.3] |
7 | 10.8 [3.2–18.3] |
30 | 5 | 16.7 [3.3–30] |
2 | 6.7 [0–15.6] |
22 | 0 | 0 [0–0] | 3 | 13.6 [0–28] |
59 | 0 | 0 [0–0] | 4 | 6.8 [0.4–13.2] |
|
Comorbidities | |||||||||||||||||||||
None | 521 | 104 | 20 [16.5–23.4] |
38 | 7.3 [5.1–9.5] |
219 | 29 | 13.2 [8.8–17.7] |
13 | 5.9 [2.8–9.1] | 122 | 10 | 8.2 [3.3–13.1] |
7 | 5,7 [1.6–9.9] |
236 | 30 | 12.7 [8.5–17] |
18 | 7.6 [4.2–11] |
|
At least one | 3,526 | 448 | 12.7 [11.6–13.8] |
798 | 22.6 [21.3–24] |
1,247 | 152 | 12.2 [10.4–14] |
225 | 18 [15.9–20.2] |
846 | 77 | 9,1 [7.2–11] |
140 | 16,5 [14–19.1] |
2,066 | 148 | 7,2 [6.1–8.3] |
267 | 12.9 [11.5–14.4] |
|
Missing | 169 | 13 | 7.7 [3.7–11.7] |
8 | 4.7 [1.5–7.9] |
84 | 6 | 7.1 [1.6–12.7] | 3 | 3.6 [0–7.5] |
47 | 2 | 4.3 [0–10] |
3 | 6.4 [0–13.4] |
95 | 7 | 7.4 [2.1–12.6] |
3 | 3.2 [0–6.7] |
|
Variable | January 2 to 29, 2022 | January 30 to February 26, 2022 | February 27 to March 26, 2022 | March 27 to April 23, 2022 | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Hospital admissions | Percentile | Hospital admissions | Percentile | Hospital admissions | Percentile | Hospital admissions | Percentile | |||||||||
25th | 50th | 75th | 25th | 50th | 75th | 25th | 50th | 75th | 25th | 50th | 75th | |||||
Global | 4,216 | 3 | 7 | 15 | 1,550 | 3 | 6 | 14 | 1,015 | 3 | 7 | 16.5 | 2,397 | 3 | 7 | 14 |
Age group (years) | ||||||||||||||||
0–45 | 469 | 1 | 2 | 6 | 247 | 1 | 2 | 4 | 121 | 1 | 2 | 4 | 248 | 1 | 2 | 3 |
44–55 | 254 | 3 | 5 | 9 | 89 | 2 | 4 | 8 | 39 | 3 | 6 | 13.5 | 68 | 2 | 4 | 10.5 |
56–65 | 544 | 4 | 7 | 15 | 171 | 3 | 7 | 14 | 103 | 3.5 | 7 | 17 | 200 | 2 | 4.5 | 12.3 |
66–75 | 911 | 4 | 8 | 17 | 316 | 3 | 7 | 15 | 186 | 4 | 9 | 17.75 | 446 | 3 | 6 | 12 |
Over 75 | 2,038 | 4 | 8 | 17 | 727 | 4 | 9 | 18 | 566 | 4 | 9 | 19 | 1,435 | 4 | 9 | 17 |
Sex | ||||||||||||||||
Male | 2,252 | 3 | 7 | 15 | 809 | 2 | 6 | 13 | 538 | 3 | 7 | 15 | 1,243 | 3 | 7 | 14.5 |
Female | 1,964 | 3 | 7 | 14 | 741 | 3 | 7 | 15 | 477 | 3 | 7 | 17 | 1,154 | 3 | 6 | 13 |
Vaccination | ||||||||||||||||
Adequate | 2,864 | 4 | 7 | 15 | 1,027 | 3 | 7 | 15.5 | 785 | 4 | 8 | 18 | 1,940 | 3 | 7 | 14 |
Inadequate | 1,348 | 3 | 6 | 13 | 519 | 2 | 5 | 11 | 229 | 2 | 4 | 11 | 453 | 2 | 5 | 14 |
Missing | 4 | – | – | – | 4 | – | – | – | 1 | – | – | – | 4 | – | – | – |
Prior infection according to laboratory tests | ||||||||||||||||
No | 4,151 | 3 | 7 | 15 | 1,520 | 3 | 6 | 14 | 993 | 3 | 7 | 16 | 2,338 | 3 | 7 | 14 |
Yes | 65 | 4 | 8 | 11 | 30 | 4 | 8 | 11 | 22 | 2 | 6 | 21.75 | 59 | 3 | 7 | 15 |
Comorbidities | ||||||||||||||||
None | 521 | 2 | 5 | 11 | 219 | 1 | 3 | 10 | 122 | 2 | 4 | 10 | 236 | 1 | 3 | 10 |
At least one | 3,526 | 4 | 7 | 16 | 1,247 | 3 | 7 | 15.5 | 846 | 4 | 8 | 19 | 2,066 | 3 | 7 | 15 |
Missing | 169 | 1 | 2 | 4 | 84 | 1 | 2 | 3 | 47 | 1 | 2 | 4.5 | 95 | 1 | 2 | 3 |
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