Evolution of illness severity in hospital admissions due to COVID-19

CCDR

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

ernest.plo@gmail.com

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)

Figure 1: Time trends in hospital admissions due to COVID-19, median length of stay and frequency of complications, Québec, January 2, 2022, and April 23, 2022

Figure 1

Figure 1 - Text description

Time trends in hospital admissions due to the coronavirus disease 2019 (COVID-19), median length of stay and frequency of complications, January 2, 2022, and April 23, 2022, Québec. 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). Globally, patients were more frequently admitted to intensive care units in January and February, while length of stay remained relatively stable over time. Patients also died more frequently during the January peak of hospital admissions, with a gradual decrease throughout the following weeks.


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.

Table 1: Description of hospital admissions due to COVID-19, by four-week periods, Québec, January 2, 2022, and April 23, 2022
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).

Table 2: Evolution of length of stayTable 2 footnote a, proportions of patients admitted to ICUTable 2 footnote b and in-hospital deathsTable 2 footnote b among hospital admissions due to COVID-19, Québec, January 2, 2022, and April 23, 2022
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)
Table 3: Evolution of length of stayTable 3 footnote a, proportions of patients admitted to ICUTable 3 footnote b and in-hospital deathsTable 3 footnote b among hospital admissions due to COVID-19, by age group, Québec, January 2 and April 23, 2022
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

Table A1: List of COVID-19-related diagnostic codes (ICD-10) used in provincial surveillance, Quebec
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
Table A2: Number of intensive care unit admissions and in-hospital deaths by age group, sex, vaccination status, prior infection and presence of comorbidities
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]
Table A3: Percentiles for the length of stay in hospital (days), by age group, sex, vaccination status, prior infection and presence of comorbidities
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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