Abstract
Background:
The COVID-19 pandemic has disproportionately affected health care workers. We sought to estimate SARS-CoV-2 seroprevalence among hospital health care workers in Quebec, Canada, after the first wave of the pandemic and to explore factors associated with SARS-CoV-2 seropositivity.
Methods:
Between July 6 and Sept. 24, 2020, we enrolled health care workers from 10 hospitals, including 8 from a region with a high incidence of COVID-19 (the Montréal area) and 2 from low-incidence regions of Quebec. Eligible health care workers were physicians, nurses, orderlies and cleaning staff working in 4 types of care units (emergency department, intensive care unit, COVID-19 inpatient unit and non-COVID-19 inpatient unit). Participants completed a questionnaire and underwent SARS-CoV-2 serology testing. We identified factors independently associated with higher seroprevalence.
Results:
Among 2056 enrolled health care workers, 241 (11.7%) had positive SARS-CoV-2 serology. Of these, 171 (71.0%) had been previously diagnosed with COVID-19. Seroprevalence varied among hospitals, from 2.4% to 3.7% in low-incidence regions to 17.9% to 32.0% in hospitals with outbreaks involving 5 or more health care workers. Higher seroprevalence was associated with working in a hospital where outbreaks occurred (adjusted prevalence ratio 4.16, 95% confidence interval [CI] 2.63–6.57), being a nurse or nursing assistant (adjusted prevalence ratio 1.34, 95% CI 1.03–1.74) or an orderly (adjusted prevalence ratio 1.49, 95% CI 1.12–1.97), and Black or Hispanic ethnicity (adjusted prevalence ratio 1.41, 95% CI 1.13–1.76). Lower seroprevalence was associated with working in the intensive care unit (adjusted prevalence ratio 0.47, 95% CI 0.30–0.71) or the emergency department (adjusted prevalence ratio 0.61, 95% CI 0.39–0.98).
Interpretation:
Health care workers in Quebec hospitals were at high risk of SARS-CoV-2 infection, particularly in outbreak settings. More work is needed to better understand SARS-CoV-2 transmission dynamics in health care settings.
The COVID-19 pandemic has disproportionately affected health care workers. In France, Spain, Italy, Germany and the United States, at least 10% of cases reported in spring 2020 were in health care workers.1 In Quebec, 25% (14 177 of 56 565) of all cases declared during the first wave of the pandemic, from March to July 2020, were in health care workers,2 about one-third of whom were working in acute care hospitals.1 The Montréal area was the most affected region in Quebec and Canada during the first wave, reaching a COVID-19 incidence rate of 1336 per 100 000 population.2
The number of COVID-19 cases reported among health care workers underestimated the number of those infected with SARS-CoV-2 during that period, given limited testing leading to undiagnosed asymptomatic or paucisymptomatic infections.3 Seroprevalence studies are an important tool to determine the proportion of people infected with SARS-CoV-2, both in the general population and among health care workers.4 After the first wave in Quebec, SARS-CoV-2 seroprevalence in adults aged 18–69 years was found to be low (3.1% in Montréal and 1.3% in less affected regions), but this proportion could be much higher among health care workers who had to work despite the general shutdown of social and economic activities, especially if they were exposed to major outbreaks.5
Only 2 other Canadian studies provide SARS-CoV-2 seroprevalence estimates among health care workers, and both studies were from a single centre.6,7 Outside Canada, most seroprevalence studies among health care workers include a single site and do not provide a representative estimate for a defined region.8 Several studies have reported a higher seroprevalence among health care workers from units treating patients with COVID-19 (COVID-19 units) compared with other units (non–COVID-19 units), emergency departments or intensive care units.9,10 Other studies have not identified such associations.11,12 In this study, we aimed to assess the seroprevalence of SARS-CoV-2 antibody among hospital health care workers from a variety of settings after the first pandemic wave in Quebec, and to explore factors associated with SARS-CoV-2 seropositivity.
Methods
Population and design
We conducted a cross-sectional seroprevalence study of hospital health care workers between July 6 and Sept. 24, 2020. Targeted health care workers included physicians, nurses, nursing assistants, orderlies and cleaning staff. Included health care workers had to be older than 18 years, be assigned to the unit for the entire shift during which recruitment occurred and provide direct care to patients (or, for cleaning staff, be exposed to their direct environment). We did not exclude people who had a previous positive SARS-CoV-2 test result.
Recruitment and data collection
We recruited health care workers from 10 acute care hospitals receiving patients with COVID-19 in Quebec (Appendix 1, Supplementary Table 1, available at www.cmaj.ca/lookup/doi/10.1503/cmaj.202783/tab-related-content). Eight hospitals are located in Montréal, a region that was more affected (1336 cases per 100 000 people) than the provincial average (662 cases per 100 000 people) during the first wave.2 The other 2 hospitals are located in the Eastern Townships (200 cases per 100 000 people) and Capitale-Nationale (249 cases per 100 000 people) regions.
We recruited participants from 4 types of units, namely emergency departments, intensive care units, COVID-19 inpatient units, and non–COVID-19 inpatient units, targeting 50 health care workers per unit per hospital. We wanted to document seroprevalence in a variety of settings, including some that provided care to patients with COVID-19. When the number of health care workers was large (mostly in emergency departments), hospital sites were authorized to select a limited number of workdays to reduce the number of health care workers eligible for inclusion. A few COVID-19 and non–COVID-19 units did not have enough health care workers to reach the target and we expanded recruitment to an additional unit with similar patient characteristics and work environment. Personal protective equipment was readily available in all units.
For each unit, we obtained a list of health care workers. We invited all health care workers by email, and sent nonresponders 3 reminders, 48 hours apart. We recruited the first consecutive health care workers that were interested in participating (up to 75 health care workers) when the message was sent out.
Participating health care workers completed an online questionnaire containing 18 questions about sociodemographic data, health status and work-related environment, and a question about the occurrence of any symptoms congruent with COVID-19 since Mar. 1, 2020. We asked participants to self-identify their ethnicity, as ethnicity has been associated with seroprevalence.13 The questionnaire was available in English and French. Eligible health care workers also provided serology samples. Participants had to complete both the questionnaire and serology to be included.
Each hospital site investigator also completed a short questionnaire, mainly to describe outbreaks that occurred in participating units. We classified participants as working in a hospital where outbreaks occurred if at least 1 participating unit at their hospital had an outbreak involving 5 or more health care workers as, in such hospitals, outbreaks were often documented or suspected in most or all participating units.
We validated all participant-reported prior COVID-19 illnesses using a provincial database on SARS-CoV-2 polymerase chain reaction (PCR) test results.2 To determine the timing of blood samples in relation to COVID-19 activity in Quebec, we extracted data on the weekly number of COVID-19 cases from the Institut national de santé publique du Québec website.2
Serological tests
Serological testing to detect 2 subunits (S1/S2) of the SARS-CoV-2 spike protein used an indirect chemiluminescence immunoassay with anti-S1/S2 immunoglobulin (Ig) G, (LiaisonXL analyzer and the LIAISON SARS-CoV-2 S1/S2 IgG test from DiaSorin in accordance with the manufacturer’s instructions. Using 20 μL of the sample, the analyzer automatically calculated antibody concentrations, expressed as arbitrary units (AU/mL), and graded the results. The limit of detection was 3.8 AU/mL and results of 15 AU/mL or greater were considered positive. A Quebec-based study reported a sensitivity of 82%–88% (≥ 35 days post-infection) and a specificity of 100% for this immunoassay.14 A subset of sera was analyzed using a second method, the NADAL COVID-19 IgG/IgM test, which detects the anti-S1 receptor binding domain (Nal von Minden, Appendix 1).
Statistical analysis
We tried to recruit 200 health care workers per hospital and 50 health care workers per unit to achieve a precision of ± 2% at the hospital level and ± 4% at the unit level for the 95% confidence interval (CI). We assumed a 20% seroprevalence in the 8 Montréal hospitals (nhospital = 1600, 95% CI 18%–22%; nunit = 400, 95% CI 16%–24%) and a 5% seroprevalence in the 2 hospitals in low-incidence regions (nhospital = 400, 95% CI 3%–7%; nunit = 100, 95% CI 1%–9%).
We estimated seroprevalence for each hospital and compared it according to various participant characteristics. We compared proportions using the χ2 or Fisher test, as appropriate. Univariate analyses identified variables associated with seropositivity that we included in the multivariate analyses. We used log-binomial generalized estimating equation (GEE) regression, which accounted for clustering within units and hospitals,15 to identify factors independently associated with seropositivity, evaluated with adjusted prevalence ratios. We assessed collinearity in the final model. We also calculated assay sensitivity (the proportion of participants with positive serology among participants with PCR-confirmed infection). We performed all statistical analyses with SAS 9.4 software. We set the significance level at 5% and all tests were 2-sided.
Ethics approval
This study was approved by the CHU de Québec-Université Laval ethics committee.
Results
We invited 4409 health care workers to participate (Figure 1). Of these, 2521 (57.2%) signed the consent form, 2223 (50.4%) were eligible to participate, and 2056 (46.6%) had a blood sample drawn and were included in the analyses. The participation rate among units varied from 43.1% to 49.2%. The participation rate was highest among physicians (77.2%), and lower for nurses (44.0%), nursing assistants (36.6%), cleaning staff (46.7%) and orderlies (31.0%).
Blood samples were drawn between July 6 and Sept. 24, 2020, between the first and second waves of the pandemic, when COVID-19 activity was low in Quebec (Figure 2). No outbreaks of COVID-19 were noted on targeted units during the study period.
Health care workers
In total, 1630 (79.3%) of 2056 participants worked in a hospital from a high-incidence region and 426 (20.7%) in a hospital from low-incidence regions (Table 1). Participants worked mainly in emergency departments (28.2%), followed by intensive care units (22.9%), COVID-19 units (21.2%) and non–COVID-19 units (21.3%). Most were nurses (57.8%), between 30 and 49 years old (57.9%), women (76.1%), born in Canada (75.3%) and white (77.6%). Just over one-third of participants reported having had symptoms congruent with COVID-19 after Mar. 1, 2020 (37.4%), and about half had had at least 1 PCR test (54.6%). Most had worked more than 3 days per week in a COVID-19 unit after Mar. 1, 2020 (60.0%), but a lower proportion had worked occasionally or regularly on a unit during a COVID-19 outbreak (41.0%) or had been removed from work after close contact with a confirmed case (13.9%; Table 1).
Table 1:
Characteristic | Category | No. (%) of participants n = 2056 |
No. (%) of participants with positive serology n = 241 |
Seroprevalence, % | p value |
---|---|---|---|---|---|
Regional incidence of COVID-19* | High | 1630 (79.3) | 228 (94.6) | 14.0 | < 0.001 |
Low | 426 (20.7) | 13 (5.4) | 3.1 | ||
Work in a hospital where outbreaks occurred† | Yes | 789 (38.4) | 179 (74.3) | 22.7 | < 0.001 |
No | 1267 (61.6) | 62 (25.7) | 4.9 | ||
Recruitment unit | Emergency department | 600 (29.2) | 47 (19.5) | 7.8 | < 0.001 |
Intensive care unit | 470 (22.9) | 29 (12.0) | 6.2 | ||
COVID-19 unit | 496 (24.1) | 99 (41.1) | 20.0 | ||
Non–COVID-19 unit | 490 (23.8) | 66 (27.4) | 13.5 | ||
Main work unit | Emergency department | 580 (28.2) | 46 (19.1) | 7.9 | < 0.001 |
Intensive care unit | 469 (22.8) | 29 (12.0) | 6.2 | ||
COVID-19 unit | 436 (21.2) | 101 (42.0) | 23.2 | ||
Non–COVID-19 unit | 438 (21.3) | 51 (21.2) | 11.6 | ||
Other‡ | 133 (6.5) | 14 (5.8) | 10.5 | ||
Age group, yr | 18–29 | 427 (20.8) | 41 (17.0) | 9.6 | 0.6 |
30–39 | 643 (31.3) | 78 (32.4) | 12.1 | ||
40–49 | 547 (26.6) | 70 (29.0) | 12.8 | ||
50–59 | 356 (17.3) | 43 (17.8) | 12.1 | ||
≥ 60 | 83 (4.0) | 9 (3.7) | 10.8 | ||
Occupation | Physician | 432 (21.0) | 31 (12.9) | 7.2 | 0.007 |
Nurse | 1189 (57.8) | 141 (58.5) | 11.9 | ||
Nursing assistant | 132 (6.4) | 22 (9.1) | 16.7 | ||
Orderly | 201 (9.8) | 36 (14.9) | 17.9 | ||
Cleaning staff | 102 (5.0) | 11 (4.6) | 10.8 | ||
Sex | Male | 489 (23.8) | 51 (21.2) | 10.4 | 0.3 |
Female | 1564 (76.1) | 189 (78.4) | 12.1 | ||
Missing§ | 3 (0.1) | – | – | ||
Born in Canada | Yes | 1548 (75.3) | 154 (63.9) | 9.9 | < 0.001 |
No | 503 (24.5) | 86 (35.7) | 17.1 | ||
Missing | 5 (0.2) | – | – | ||
Ethnicity | White | 1594 (77.5) | 163 (67.6) | 10.2 | < 0.001 |
Black | 140 (6.8) | 31 (12.9) | 22.1 | ||
Hispanic | 52 (2.5) | 14 (5.8) | 26.9 | ||
Other¶ | 270 (13.1) | 33 (13.7) | 12.2 | ||
Household | 1 adult, no child | 328 (16.0) | 31 (12.9) | 9.5 | 0.009 |
2 adults, no child | 480 (23.3) | 54 (22.4) | 11.3 | ||
≥ 3 adults, no child | 234 (11.4) | 35 (14.5) | 15.0 | ||
1 adult, ≥ 1 children | 155 (7.5) | 27 (11.2) | 17.4 | ||
2 adults, ≥ 1 children | 672 (32.7) | 64 (26.6) | 9.5 | ||
≥3 adults, ≥ 1 children | 187 (9.1) | 30 (12.4) | 16.0 | ||
PCR test for SARS-CoV-2 | Yes, positive result | 193 (9.4) | 171 (71.0) | 88.6 | < 0.001 |
Yes, negative result | 929 (45.2) | 50 (20.7) | 5.4 | ||
No | 932 (45.3) | 20 (8.3) | 2.1 | ||
Missing§ | 2 (0.1) | – | – | ||
COVID-19-congruent symptoms** | Yes | 768 (37.4) | 186 (77.2) | 24.2 | < 0.001 |
No | 1242 (60.4) | 53 (22.0) | 4.3 | ||
Missing§ | 46 (2.2) | – | – | ||
Chronic disease | Yes | 286 (13.9) | 37 (15.4) | 12.9 | 0.5 |
No | 1755 (85.4) | 202 (83.8) | 11.5 | ||
Missing§ | 15 (0.7) | – | – | ||
Experience in the hospital | Less than 1 year | 179 (8.7) | 19 (7.9) | 10.6 | 0.4 |
1 to 4 year | 526 (25.6) | 70 (29.0) | 13.3 | ||
≥ 5 year | 1346 (65.5) | 151 (62.7) | 11.2 | ||
Missing§ | 5 (0.2) | – | – | ||
Primary work shift | Day | 1330 (64.7) | 159 (66.0) | 12.0 | 0.3 |
Evening | 417 (20.3) | 54 (22.4) | 12.9 | ||
Night | 289 (14.1) | 27 (11.2) | 9.3 | ||
Missing§ | 20 (1.0) | – | – | ||
Mean weekly number of workdays | ≤ 2 | 87 (4.2) | 5 (2.1) | 5.7 | 0.09 |
≥ 3 | 1958 (95.2) | 235 (97.5) | 12.0 | ||
Missing§ | 11 (0.5) | – | – | ||
Mean weekly number of workdays in a hot zone†† | ≤ 2 | 743 (36.1) | 60 (24.9) | 8.1 | < 0.001 |
≥ 3 | 1233 (60.0) | 173 (71.8) | 14.0 | ||
Missing§ | 80 (3.9) | – | – | ||
Work at another site | Yes, including long-term care | 100 (4.9) | 16 (6.6) | 16.0 | 0.3 |
Yes, no long-term care | 194 (9.4) | 19 (7.9) | 9.8 | ||
No | 1757 (85.5) | 204 (84.6) | 11.6 | ||
Missing§ | 5 (0.2) | – | – | ||
Worked in a unit affected by a COVID-19 outbreak | Never | 742 (36.1) | 36 (14.9) | 4.9 | < 0.001 |
Rarely | 223 (10.8) | 29 (12.0) | 13.0 | ||
Sometimes | 281 (13.7) | 39 (16.2) | 13.9 | ||
Regularly | 561 (27.3) | 114 (47.3) | 20.3 | ||
Do not know | 245 (11.9) | 22 (9.1) | 10.0 | ||
Missing§ | 4 (0.2) | – | – | ||
Removal from work because of a close contact with a COVID-19 case | Yes, family contact | 44 (2.1) | 12 (5.0) | 27.3 | < 0.001 |
Yes, work contact‡‡ | 212 (10.3) | 81 (33.6) | 38.2 | ||
Yes, other contact | 29 (1.4) | 3 (1.2) | 10.3 | ||
No | 1751 (85.2) | 138 (57.3) | 7.9 | ||
Missing§ | 20 (1.0) | – | – |
Note: PCR = polymerase chain reaction.
Incidence of COVID-19 in the region where the hospital is located (high = Montréal region; low = Capitale-Nationale and Eastern Townships regions).
Hospitals where an outbreak (involving ≥ 5 health care workers) occurred in 1 or more units targeted for recruitment.
Participant works in other type of units or in different units (e.g., roving team).
Missing = Do not know, prefer not to answer or missing value.
Includes Asian (n = 114, seroprevalence 12.3%), Middle Eastern (n = 53, seroprevalence 13.2%), other category (n = 34, seroprevalence 14.7%), answered more than 1 category (n = 46, seroprevalence 8.7%), prefer not to answer/do not know (n = 23, seroprevalence 21.7%). Fewer than 1% of participants (n = 4) preferred not to answer.
Occurrence of any symptom congruent with COVID-19 since Mar. 1, 2020 (i.e., fever, generalized malaise, extreme fatigue, cough, breathing difficulties, sore throat, loss of smell, loss of taste or diarrhea).
Zone where patients are positive for SARS-CoV-2.
Contact with a patient or another health care worker.
Seroprevalence
A total of 241 (11.7%) of 2056 health care workers had positive serology. The seroprevalence was lower in low-incidence regions (3.1%, 95% CI 1.8%–5.4%) than in the high-incidence region (14.0%, 95% CI 12.3%–15.8%; Figure 3). In the high-incidence region, 4 hospitals had outbreaks in 1 or more targeted units that involved 5 or more health care workers. Seroprevalence ranged from 17.9% to 32.0% (mean 23.6%, 95% CI 20.6%–26.7%) in hospitals with outbreaks of COVID-19 compared with 4.7% to 7.4% (mean 6.5%, 95% CI 5.0%–8.4%) in the 4 hospitals without outbreaks.
Seroprevalence was higher in health care workers who mainly worked in inpatient COVID-19 units and non–COVID-19 units than in those who mainly worked in the emergency department or intensive care unit (Table 2). Seroprevalence was strongly associated with the presence or absence of outbreaks in inpatient COVID-19 and non–COVID-19 units. In the 4 hospitals where outbreaks occurred, the mean seroprevalence was 33.4% among workers in inpatient units.
Table 2:
Hospital | Emergency department n = 580 |
Intensive care unit n = 469 |
COVID-19 unit n = 436 |
Non-COVID-10 unit n = 438 |
Other* n = 133 |
|||||
---|---|---|---|---|---|---|---|---|---|---|
|
|
|
|
|
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No. of HCWs | No. (%) with positive serology | No. of HCWs | No. (%) with positive serology | No. of HCWs | No. (%) with positive serology | No. of HCWs | No. (%) with positive serology | No. of HCWs | No. (%) with positive serology | |
A, n = 207 | 50 | 1 (2.0) | 45 | 2 (4.4) | 41 | 2 (4.9) | 46 | 0 (0.0) | 25 | 0 (0.0) |
| ||||||||||
B, n = 219 | 61 | 2 (3.3) | 40 | 1 (2.5) | 52 | 4 (7.7) | 41 | 1 (2.4) | 25 | 0 (0.0) |
| ||||||||||
Low-incidence regions,† n = 426 |
111 | 3 (2.7) | 85 | 3 (3.5) | 93 | 6 (6.4) | 87 | 1 (1.2) | 50 | 0 (0.0) |
| ||||||||||
C, n = 211 | 50 | 2 (4.0) | 52 | 0 (0.0) | 42 | 2 (4.8) | 62 | 6 (9.7) | 5 | 0 (0.0) |
| ||||||||||
D, n = 215 | 60 | 0 (0.0) | 55 | 2 (3.6) | 28 | 3 (10.7) | 62 | 4 (6.4) | 10 | 1 (10.0) |
| ||||||||||
E, n = 198 | 84 | 6 (7.2) | 40 | 0 (0.0) | 28 | 4 (14.3) | 37 | 1 (2.7) | 10 | 2 (20.0) |
| ||||||||||
F, n = 217 | 57 | 6 (10.5) | 60 | 1 (1.7) | 43 | 5 (11.6) | 42 | 3 (7.1) | 15 | 1 (6.7) |
| ||||||||||
G, n = 190 | 55 | 7 (12.7) | 33 | 2 (6.1) | 65 | 13 (20.0) | 23 | 8 (34.8) | 14 | 4 (28.6) |
| ||||||||||
H, n = 221 | 52 | 7 (13.5) | 61 | 4 (6.6) | 50 | 26 (52.0) | 48 | 2 (4.2) | 10 | 1 (10.0) |
| ||||||||||
I, n = 172 | 61 | 9 (14.8) | 28 | 2 (7.1) | 39 | 15 (38.5) | 27 | 8 (29.6) | 17 | 5 (29.4) |
| ||||||||||
J, n = 206 | 51 | 6 (11.8) | 55 | 15 (27.3) | 48 | 27 (56.2) | 50 | 18 (36.0) | 2 | 0 (0.0) |
| ||||||||||
High-incidence region,† n = 1630 |
469 | 43 (9.2) | 384 | 26 (6.8) | 343 | 95 (27.7) | 351 | 50 (14.2) | 83 | 14 (16.9) |
Note: HCW = health care workers.
Participant works in other type of units or in different units (e.g., roving team).
Hospitals A and B are located in regions with low incidence of COVID-19 during the first wave of the pandemic (i.e., Capitale-Nationale and Eastern Townships). Hospitals C through J are located in the Montréal region, which had a high incidence of COVID-19 during the first wave.
Factors associated with seropositivity
Factors associated with seropositivity in unadjusted analyses included regional incidence of COVID-19, working in a hospital where outbreaks occurred, main work unit, occupation and ethnicity (Table 1). Age (p = 0.6) and sex (p = 0.3) did not show a statistically significant association with seropositivity.
In multivariable models (Table 3), compared with participants who mainly worked in an inpatient non–COVID-19 unit, seropositivity was lower among those who worked in the emergency department (adjusted prevalence ratio 0.61, 95% CI 0.39–0.98) or intensive care unit (adjusted prevalence ratio 0.47, 95% CI 0.30–0.71); seropositivity was numerically, but not significantly, higher in those working in an inpatient COVID-19 unit (adjusted prevalence ratio 1.48, 95% CI 0.93–2.36). Being a nurse or nursing assistant (adjusted prevalence ratio 1.34, 95% CI 1.03–1.74) or orderly (adjusted prevalence ratio 1.49, 95% CI 1.12–1.97) was significantly associated with seropositivity compared with physicians, but being a member of the cleaning staff was not (adjusted prevalence ratio 0.88, 95% CI 0.50–1.54). Black or Hispanic ethnicity was also associated with seropositivity compared with being white (adjusted prevalence ratio 1.41, 95% CI 1.13–1.76). Finally, working in a hospital where an outbreak involving 5 or more health care workers occurred in 1 or more units targeted for recruitment was strongly associated with higher seropositivity (adjusted prevalence ratio 4.16, 95% CI 2.63–6.57).
Table 3:
Variable | Seroprevalence | Prevalence ratio | ||
---|---|---|---|---|
|
|
|||
No. of HCWs | No. (%) with positive serology | Crude (95% CI) | Adjusted (95% CI) | |
Main work unit | ||||
| ||||
Intensive care unit | 469 | 29 (6.2) | 0.53 (0.32–0.89) | 0.47 (0.30–0.71) |
| ||||
Emergency department | 580 | 46 (7.9) | 0.68 (0.41–1.14) | 0.61 (0.39–0.98) |
| ||||
Non–COVID-19 unit | 438 | 51 (11.6) | Ref. | Ref. |
| ||||
COVID-19 unit | 436 | 101 (23.2) | 1.99 (1.16–3.41) | 1.48 (0.93–2.36) |
| ||||
Other* | 133 | 14 (10.5) | 0.90 (0.44–1.85) | 1.03 (0.70–1.50) |
| ||||
Occupation | ||||
| ||||
Physician | 432 | 31 (7.2) | Ref. | Ref. |
| ||||
Nurse or nursing assistant | 1321 | 163 (12.3) | 1.72 (1.23–2.41) | 1.34 (1.03–1.74) |
| ||||
Orderly | 201 | 36 (17.9) | 2.50 (1.75–3.55) | 1.49 (1.12–1.97) |
| ||||
Cleaning staff | 102 | 11 (10.8) | 1.50 (0.78–2.89) | 0.88 (0.50–1.54) |
| ||||
Ethnicity | ||||
| ||||
White | 1594 | 163 (10.2) | Ref. | Ref. |
| ||||
Black† | 140 | 31 (22.1) | 2.17 (1.42–3.29) | 1.41 (1.13–1.76) |
| ||||
Hispanic† | 52 | 14 (26.9) | 2.63 (1.67–4.15) | |
| ||||
Other‡,§ | 270 | 33 (12.2) | 1.20 (0.77–1.87) | 0.89 (0.67–1.18) |
| ||||
Work in a hospital where outbreaks occurred¶ | ||||
| ||||
Yes | 789 | 179 (22.7) | 4.64 (3.19–6.75) | 4.16 (2.63–6.57) |
| ||||
No | 1267 | 62 (4.9) | Ref. | Ref. |
| ||||
Mean weekly number of workdays | ||||
| ||||
≤ 2 | 87 | 5 (5.7) | Ref. | Ref. |
| ||||
≥ 3 | 1958 | 235 (12.0) | 2.09 (0.78–5.57) | 1.75 (0.67–4.58) |
| ||||
Mean weekly number of workdays in a hot zone** | ||||
| ||||
≤ 2 | 743 | 60 (8.1) | Ref. | Ref. |
| ||||
≥ 3 | 1233 | 173 (14.0) | 1.74 (1.14–2.65) | 1.07 (0.74–1.56) |
| ||||
Household | ||||
| ||||
No children | 1042 | 120 (11.5) | Ref. | Ref. |
| ||||
1 adult, ≥ 1 children | 155 | 27 (17.4) | 1.51 (0.88–2.59) | 1.22 (0.79–1.89) |
| ||||
2 adults, ≥ 1 children | 672 | 64 (9.5) | 0.83 (0.59–1.16) | 0.83 (0.61–1.12) |
| ||||
≥ 3 adults, ≥ 1 children | 187 | 30 (16.0) | 1.39 (1.02–1.91) | 1.02 (0.76–1.38) |
Note: CI = confidence interval, HCW = health care workers, Ref. = reference category.
Participant works in other type of units or in different units (e.g., roving team).
Merged categories for Black and Hispanic participants for adjusted models because the model failed to converge when they were entered separately.
Includes Asian (n = 114, seroprevalence 12.3%), Middle Eastern (n = 53, seroprevalence 13.2%), other category (n = 34, seroprevalence 14.7%), answered more than 1 category (n = 46, seroprevalence 8.7%), prefer not to answer/do not know (n = 23, seroprevalence 21.7%). Fewer than 1% of participants (n = 4) preferred not to answer.
Conclusions are the same if participants who answered “do not know” or “prefer not to answer” are excluded.
Hospitals where an outbreak (involving ≥ 5 health care workers) occurred in 1 or more units targeted for recruitment.
Zone where patients are positive for SARS-CoV-2.
Laboratory results
Among the 193 participants who reported a PCR-confirmed diagnosis of SARS-CoV-2 infection before blood sampling, 171 (88.6%) had positive serology and 172 (89.1%) reported having had symptoms of COVID-19. Of all 2056 participants, 171 (8.3%) reported a PCR-confirmed diagnosis and had positive serology, 22 (1.1%) had negative serology despite a PCR-confirmed diagnosis, and 70 (3.4%) had positive serology in the absence of a PCR-confirmed diagnosis of SARS-CoV-2 infection. Among the latter, 32 (45.7%) had had COVID-19 symptoms. Among the 1791 participants with negative serology and without a COVID-19 diagnosis a lower percentage (32.2%) reported having had symptoms. Overall, 171 (71%) of 241 participants with positive serology reported a PCR-confirmed diagnosis of SARS-CoV-2 infection.
Of the 193 participants who reported a PCR-confirmed diagnosis, a positive PCR test result was found from the provincial database for 190 (98.4%). Results using the anti-S1–receptor binding domain IgG/IgM assay produced only minor changes in seroprevalence estimates, compared with the main results (Appendix 1, Supplementary Results).
Interpretation
We observed a higher seroprevalence of SARS-CoV-2 infection among health care workers from 8 Montréal hospitals than among those from 2 hospitals in low-incidence regions of Quebec. The seroprevalence observed in this population in Montréal was similar to that in regions severely affected by the pandemic in Europe,11,13,16–18 but was lower than in the epicentres of the pandemic in London and New York.19–21 The seroprevalence in Montréal hospitals was strongly influenced by outbreaks in both COVID-19 and non–COVID-19 inpatient units; the overall seroprevalence among health care workers in these hospitals was much higher than in 4 other Montréal hospitals that were less affected by outbreaks. The seroprevalence in these latter hospitals was higher than in the Montréal community (< 4%).5 These findings highlight the elevated risk of infection for health care workers in hospitals, particularly for those working in outbreak settings. Interestingly, the 4 Montréal hospitals with higher seroprevalence were older hospitals, a factor that has been associated with larger outbreaks.22
Other authors have identified lower seropositivity rates in intensive care units,16,17 which might be explained by the strict infection control measures implemented in these units, including personal protective equipment, and reduced staff mobility. Higher seropositivity rates in inpatient units23 have also been reported in previous seroprevalence studies.9,10,13,20 Several factors may explain this, including a physical environment that favours transmission, particularly in older hospitals (e.g., exiguity of the premises and indoor ventilation), sub-optimal compliance with infection control measures, or presence of contagious patients (for COVID-9 units). In contrast, other studies have not found an increased risk in these units.11,12 In our study, some hospitals in Montréal had a seroprevalence among health care workers similar to that of the community and did not identify any outbreaks among health care workers in targeted care units.
Being a nurse24,25 or orderly9,10 was independently associated with higher seropositivity rates in several other studies. An epidemiological investigation in Quebec also showed that most confirmed cases of COVID-19 in health care workers were among nurses or orderlies, who frequently acquired SARS-CoV-2 in the workplace.1 More frequent and close contact with patients could partly explain this association.10 Black or Hispanic ethnicity was also associated with higher seropositivity in multivariable analysis. Higher seropositivity in these populations has been found in seroprevalence studies in the United Kingdom and the US.10,13,19,21,24 The factors underlying this association are complex,26 unrelated to biological or genetic factors,27 and may reflect a higher seroprevalence in the community or several social factors, such as high population density, housing issues and people’s ability to self-isolate outside of work. More research in the Canadian context is needed to understand the determinants of higher rates of SARS-CoV-2 seroprevalence among Black and Hispanic health care workers.28
In our study, most health care workers with IgG antibodies to SARS-CoV-2 had previously had a PCR-confirmed SARS-CoV-2 infection. Although the total number of participants with SARS-CoV-2 antibodies was about 25% higher than the number with a COVID-19 diagnosis, our data attest to good case identification in Quebec hospitals. International seroprevalence studies have shown the number of people with a positive serology to be as much as twofold higher than those with PCR-confirmed SARS-CoV-2 infection.11,17 Moreover, the elevated sensitivity of the S1/S2 assay after a COVID-19 diagnosis should be emphasized. Our results are consistent with study findings29–32 that describe the stability of concentrations of the anti-spike antibody for at least 6 months. More work is needed to fully understand the duration of humoral immunity and the sensitivity of various serological assays over time.33,34
Limitations
We were unable to determine how SARS-CoV-2 was acquired by health care workers in our study (e.g., community acquisition, workplace acquisition). The 50% participation rate may imply the presence of selection bias. Reassuringly, particularly for groups with a lower participation rate (e.g., nurses and orderlies), we were able to compare the proportion with a previous PCR-confirmed infection both for participants and at the institution level. This proportion was 10% among participants and 9% at the institution level (data not shown), which would suggest a similar SARS-CoV-2 seroprevalence among participants and nonparticipants. Factors associated with seropositivity in our study (e.g., work unit, occupation, ethnicity) were also consistent with those found in large seroprevalence studies.8,10,13,20 The seroprevalence reported in each hospital may not reflect the exact seroprevalence among health care workers, as we targeted only a few specific units. However, the inclusion of 8 Montréal hospitals that collected data in a similar way provides a representative portrait of seroprevalence for each targeted type of unit in this region. External validity of our findings beyond urban regions of Quebec is limited and additional seroprevalence studies are required. Finally, the imperfect sensitivity and specificity of the S1/S2 assay could slightly underestimate or overestimate seroprevalence. This misclassification is likely nondifferential and might bias some study estimators toward the null hypothesis.
Conclusion
This study showed a high SARS-CoV-2 seroprevalence during the first wave of the COVID-19 pandemic. In 8 Montréal hospitals, the seroprevalence among health care workers was 14%, which is significantly higher than rates in 2 hospitals in regions less affected by the first wave of COVID-19. Seroprevalence was strongly associated with the occurrence of outbreaks in the inpatient units of 4 hospitals, highlighting the risk of infection among hospital workers, particularly in outbreak settings and among nurses, nursing assistants and orderlies in particular. Although we could not identify whether infections were acquired in the hospital or assess the effectiveness of infection prevention and control measures, the high seroprevalence in 4 older hospitals may indicate that factors related to the physical environment, including exiguity of the premises and indoor ventilation, should be considered for preventing SARS-CoV-2 outbreaks, as they make implementation of optimal infection prevention and control measures more challenging. More work is needed to understand the mechanisms of transmission among infected health care workers to, ultimately, implement optimal protective measures. The high risk of SARS-CoV-2 infection in hospital workers supports the prioritization of this group for SARS-CoV-2 vaccination in Canada and efforts made to achieve a very high vaccine uptake in this population.
Supplementary Material
Acknowledgements
The authors thank Sophie Auger, Stéphanie Beauchemin, Christina Benjamin, Christine Blaser, France Bouchard, Valérie Boucher, Mathieu Brodeur, Geneviève Cadieux, Sara Carazo, Annie Chamberland, Marie-Laure Dablaka, Anatolie Duca, Catherine Dupont, Jennifer Eastmond, Marcel Émond, Alvine Fansi, Nathalie Gravel, Sandrine Hegg-Deloye, Zineb Laghdir, Catherine Lambert, Nadine Larente, Gregory Léon, Sondra Mandy Sinanan, Dominique Marcoux, Pierre-Henri Minot, Naiana Muntini, Gentiane Perrault-Sullivan, Karène Proulx-Boucher, Josiane Rivard, Jonathan Roger, Molly Ann Rothschild, Nadine Sicard, Denis Talbot, Esther Trudel, Donald Vinh, Cédric Yansouni, Chung Yan Yuen, Daysi Zentner and the McGill University Health Centre COVID Biobank.
Footnotes
Competing interests: Patrice Savard reports grants from Merck, Sunovion and Verity Pharmaceuticals. Yves Longtin reports grants from Merck, GenePOC, Becton Dickinson and Gojo. Matthew Cheng reports grants from the McGill Interdisciplinary Initiative in Infection and Immunity, Consortium Québécois sur la découverte du médicament and Canadian Institutes of Health Research; personal fees from GEn1E Lifesciences and nplexbio; 2 pending patents for methods related to using cell-free DNA; and participation with the Canadian Immunity Task Force. Jean-Michel Leduc reports research funding from Biomérieux. All reported competing interests were outside the submitted work. No other competing interests were declared.
This article has been peer reviewed.
Contributors: Nicholas Brousseau and Gaston De Serres conceived the study. Patrice Savard, Caroline Quach, Yves Longtin, Matthew Cheng and Alex Carignan contributed to the study design. Laurianne Morin and Manale Ouakki conducted the analyses. All of the authors contributed to data analysis and interpretation. Nicholas Brousseau wrote the first draft of the manuscript. All authors contributed to the drafting of the manuscript, critically revised the manuscript for important intellectual content, gave final approval of the version to be published and agreed to be accountable for all aspects of the work.
Funding: This work was supported by Quebec Ministry of Health and Social Services.
Data sharing: All or portions of the data are available to others. Data will be available upon publication and may be accessed by contacting the corresponding author.
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