Abstract
Objectives
Healthcare workers face distinct occupational challenges that affect their personal health, especially during a pandemic. In this study we compare the characteristics and outcomes of Covid-19 patients who are and who are not healthcare workers (HCW).
Methods
We retrospectively analyzed a cohort of 2,842 adult patients with known HCW status and a positive SARS-CoV-2 RT-PCR test presenting to a large academic medical center emergency department (ED) in New York State from March 21 2020 through June 2020. Early in the pandemic we instituted a policy to collect data on patient occupation and exposures to suspected Covid-19. The primary outcome was hospital admission. Secondary outcomes were ICU admission, need for invasive mechanical ventilation (IMV), and mortality. We compared baseline characteristics and outcomes of Covid-19 adult patients based on whether they were or were not HCW using univariable and multivariable analyses.
Results
Of 2,842 adult patients (mean age 53+/-19 years, 53% male) 193 (6.8%) were HCWs and 2,649 (93.2%) were not HCWs. Compared with non-HCW, HCWs were younger (43 vs 53 years, P<0.001), more likely female (118/193 [61%] vs 1211/2649 [46%], P<0.001), and more likely to have a known Covid-19 exposure (161/193 [83%] vs 946/2649 [36%], P<0.001), but had fewer comorbidities. On presentation to the ED, HCW also had lower frequencies of tachypnea (12/193 [6%] vs 426/2649 [16%], P<0.01), hypoxemia (15/193 [8%] vs 564/2649 [21%], P<0.01), bilateral opacities on imaging (38/193 [20%] vs 1189/2649 [45%], P<0.001), and lymphocytopenia (6/193 [3%] vs 532/2649 [20%], P<0.01) compared to non-HCWs. Direct discharges home from the ED were more frequent in HCW 154/193 (80%) vs 1275/2649 (48%) p<0.001). Hospital admissions (38/193 [20%] vs 1264/2694 [47%], P<0.001), ICU admissions (7/193 [3%] vs 321/2694 [12%], P<0.001), need for IMV (6/193 [3%] vs 321/2694 [12%], P<0.001) and mortality (2/193 [1%] vs 219/2694 [8%], P<0.01) were lower than among non-HCW. After controlling for age, sex, comorbidities, presenting vital signs and radiographic imaging, HCW were less likely to be admitted (OR 0.6, 95%CI 0.3–0.9) than non HCW.
Conclusions
Compared with non HCW, HCW with Covid-19 were younger, had less severe illness, and were less likely to be admitted.
Introduction
Illness in healthcare workers (HCWs) is of particular concern in light of the coronavirus disease 19 (Covid-19) pandemic. HCWs are often at risk for increased exposure to infectious diseases compared to the general population in the surrounding community, and they may serve as vectors for transmission of these illnesses [1]. The repeated exposure to pathogens may also alter the course of infectious disease in HCWs compared to that in the general population in the surrounding community. There is currently little literature studying how HCWs with Covid-19 have fared, and whether their course of disease may be different than non-HCWs.
In April 2020 a CDC Morbidity and Mortality Report documented that HCWs made up 3% of COVID-19 cases in the US, however HCW status was only reported in 16% of cases [2]. In states that reported HCW status of all Covid-19 cases, HCWs made up 11% of cases [2]. In our hospital, routine documentation of healthcare worker status and exposure to patients with suspected Covid-19 was added to the emergency department (ED) patient intake form on March 1.
The objectives of the current study were to compare baseline characteristics and subsequent outcomes in adult patients with Covid-19 who were and were not HCW presenting to a large ED, including those admitted to our hospital and those directly discharged from the ED.
Methods
Study design
We conducted a structured, retrospective review of all patients presenting to our ED with confirmed Covid-19 based on a positive SARS-CoV-2 PCR. This study followed the Strengthening of Reporting of Observational Studies in Epidemiology (STROBE) reporting guidelines for cross-sectional studies [3]. We also followed the recommended methodology of Kaji et al. for retrospective chart reviews [4]. The study was approved by the Stony Brook University IRB with waiver of informed consent (IRB # 2020–00201) on March 30, 2020.
Patients and setting
Our hospital is a 650 bed, suburban academic tertiary-care hospital located approximately 60 miles from Manhattan. Patient volume is approximately 110,000 adult and pediatric patients per year. Eligible patients presented from March 1, 2020 to June 30, 2020 and included all patients over 18 years of age with Covid-19 confirmed by a positive SARS-Cov-2 RT-PCR. As the pandemic evolved, we used a variety of FDA licensed RT-PCR tests that became available from the State of New York, private commercial laboratories and finally from our own hospital laboratory. We have not used antibody testing as this is not an accurate picture of who is acutely infected and evaluated in the ED at our institution. In addition, data on how best to interpret antibody testing across ages and timing post infection is lacking. In our ED we instituted a policy to collect data on patient occupation and exposure to suspected Covid-19 beginning March 1. Patients without information regarding whether they were HCW or not were excluded. Patients were specifically asked whether they had been in close contact with any person with influenza-like symptoms or a positive SARS-CoV-test. This was based on patient self-report and was not confirmed by clinicians or researchers.
Data source and collection
Data included in our analysis were either automatically extracted from the electronic medical record (e.g., vital signs and laboratory results) or were abstracted through manual chart review (e.g., symptoms and HCW status). Specific data extracted included demographics, past medical history and comorbidities based on patient report, baseline vital signs, symptoms at presentation, laboratory test results, radiological findings, treatments, and outcomes (e.g., disposition, need for IMV, and mortality).
We defined all study data and variables prior to initiating the study and trained our data abstractors using a library of definitions. Healthcare workers included physicians, nurses, technicians and any other support staff that come into direct contact with patients. Hypoxemia was defined as an oxygen saturation less than 94% while tachypnea was defined as a respiratory rate greater than 24/min. Fever was defines as a temperature greater than 38° C, and lymphocytopenia was defined as a lymphocyte count less than 1000/ml. We periodically monitored data collection and determined the inter-observer agreement on the primary and secondary outcomes on a randomly selected sample of 200 study patients. Interobserver agreement (Kappa statistic) ranged from 0.96 (95% CI, 0.90–0.99) to 1.0.
Study outcomes
The primary outcome was hospital admission. Secondary outcomes were ICU admission, need for invasive mechanical ventilation, and mortality.
Data analysis
Discrete data are summarized as numbers and frequencies for nominal data and compared with Chi-square or Fisher’s exact tests (when sample sizes were less than 5). Continuous data that were normally distributed are summarized as means with standard deviations (SD) and compared with T-tests. Continuous data that were not normally distributed were summarized as medians with interquartile (IQR) ranges and compared with the Mann Whitney U test. For all variables and models, we only used the initial findings at ED presentation. Exploratory multivariable analysis of primary and secondary outcomes was performed using potential predictor variables chosen based on biological plausibility and previous reports such as age, sex, comorbidities, presenting vital signs, chest XR findings, and HCW status. Comparisons between groups were performed using logistic and linear regression for binary and continuous data respectively. Level of significance was defined as a P value of 0.05 or less. Data was analyzed using SPSS for Windows version 27 (IBM, Armonk, NY).
Results
General characteristics
From March 1 to June 30 2020 there were 2,888 Covid-19 infected patients that presented to our ED, of which 2,846 were over 18 years of age. HCW status was unknown in four patients leaving a sample size of 2,842 study patients. Overall, the mean (SD) age for adult patients was 53 (19) years, 1,513 (53%) were male and 1,306 (46%) were white. The total number of patients admitted to the hospital was 1,406 (49%) of which 328 (12%) were admitted to an ICU (either immediately or subsequent to admission to a regular floor). Invasive mechanical ventilation was required in 261/2842 (9.1%) patients and 221/2842 patients (7.8%) died. A de-identified data set and its dictionary may be accessed at the following publicly available websites: https://figshare.com/articles/book/HCW_COVID_19_Codebook_pdf/13283342 and https://figshare.com/articles/dataset/HCW_Data_v3_xlsx/13283141.
Univariable comparisons
A comparison of patient baseline characteristics based on HCW status is presented in Table 1. Compared with non HCW, HCW were younger (43+/-13 vs 53+/-18 years; mean difference 10, 95%CI 8 to 23, P<0.001] more likely female (61% vs. 46%; mean difference 15%, 95%CI 8–23, P<0.001), and less likely Hispanic (12% vs. 36%; mean difference 23%, 95%CI 17–28, P<0.001). HCW were less likely to have comorbidities (33% vs 49%; mean difference 16%, 95%%CI 8–22, P<0.01) but more likely to have reported a known contact with a person with Covid-19 symptoms (83% vs 36%; mean difference 48%, 95%CI 41–53, P<0.001) than non-HCW. While no HCW resided in a skilled nursing facility, 11% of non HCW came from a nursing home.
Table 1. Patients general characteristics.
Data are presented as numbers and percentages in parentheses unless otherwise specified.
| Non HCW | HCW | Difference in % unless otherwise specified (95% CI) | |
|---|---|---|---|
| Total cases | 2649 | 193 | |
| Male gender | 1438 (54) | 75 (39) | 15 (8–23) |
| Mean age (SD) | 53 (18) | 43 (13) | 10 (8–12) |
| Ethnicity | |||
| Hispanic | 941 (36) | 24 (12) | 23 (17–28) |
| Non-Hispanic | 1349 (51) | 151 (78) | -27 (-33 - -20) |
| Unspecified | 359 (13) | 18 (9) | 4 (-1-8) |
| Number of Comorbidities | |||
| 0 | 1357 (51) | 129 (67) | -16 (-22 - -8) |
| 1 | 599 (23) | 45 (23) | 1 (-8–5) |
| >1 | 693 (26) | 19 (10) | 16 (11–20) |
| Comorbidity | |||
| Diabetes | 473 (18) | 21 (11) | 7 (1–11) |
| HTN | 879 (33) | 40 (21) | 13 (6–18) |
| COPD | 131 (5) | 1 (1) | 4 (2–5) |
| Asthma | 173 (7) | 18 (9) | -3 (-8–1) |
| Cancer | 171 (6) | 3 (2) | 5 (2–6) |
| CHF | 137 (5) | 0 (0) | 5 (3–6) |
| CAD | 263 (10) | 3 (2) | 8 (5–10) |
| Immunosuppressed | 131 (5) | 1 (1) | 4 (2–5) |
| CKD | 156 (6) | 3 (2) | 4 (1–6) |
| Place of Origin | |||
| Home | 2346 (89) | 193 (100) | -11 (-13 - -9) |
| Nursing home | 302 (11) | 0 (0) | 11 (9–13) |
| Contact with sick person (COVID19 or Flu-like Symptoms) | 946 (36) | 161 (83) | 48 (-53 - -41) |
A comparison of initial vital signs, laboratory results and radiological findings based on HCW status is presented in Table 2. Compared with non HCW, HCW were less likely to be tachypneic (6% vs 13%; mean difference 7, 95%CI 2–10, P<0.01), hypoxemic (8% vs 22%; mean difference 13%, 95%CI 8–17, P<0.01), have bilateral lung opacities on imaging (20% vs 45%; mean difference 25, 95%CI 18–31, P<0.01), or have lymphopenia (6% vs 20%; mean difference 14, 95%CI 9–17, P<0.01).
Table 2. Signs, imaging and laboratory characteristics on presentation.
Data are presented as numbers and percentages in parentheses unless otherwise specified.
| Non HCW | HCW | Difference in % unless otherwise specified (95% CI) | |
|---|---|---|---|
| Fever>38° C | 426 (16) | 30 (16) | 1 (-5–6) |
| Tachypnea (RR>24/min.) | 335 (13) | 12 (6) | 7 (2–10) |
| Hypoxemia | |||
| >94% | 2065 (79) | 176 (92) | -13 (-17 - -8) |
| 89–93% | 364 (14) | 10 (5) | 9 (4–12) |
| <88% | 200 (8) | 5 (3) | 5 (1–7) |
| Bilateral opacities on imaging | 1189 (45) | 38 (20) | 25 (18–31) |
| Leukopenia<4000/ml | 157 (9) | 9 (13) | -3 (-14–3) |
| Lymphocytopenia <1000/ml | 532 (20) | 12 (6) | 14 (9–17) |
| Creatinine >1.5 mg/dL | 272 (16) | 5 (7) | 9 (-1–14) |
| D-Dimer>750 mg/L | 223 (23) | 5 (10) | 12 (-1–19) |
| CRP >8.2 mg/ml | 650 (45) | 21 (43) | 2 (-13–16) |
| Procalcitonin>0.5 ng/ml | 256 (18) | 6 (13) | 5 (-10–13) |
| AST>40 U/ml | 721 (46) | 30 (50) | -4 (-18–9) |
| Troponin >0.06 ng/ml | 130 (9) | 2 (4) | 5 (-6–9) |
| Mean (SD) length of symptoms prior to ED arrival, days | 6 (7) | 5 (5) | 1.5 (0.5–2.5) |
HCW: Healthcare worker; RR: Respiratory rate; SD: Standard deviation.
HCW were more likely than non HCW to be directly discharged from the ED (154/193 [80%] vs 1275/2649 [48%]; mean difference 32, 95%CI 25–37 [P<0.001]). By comparison, non HCW were more likely to require ICU admission (321/2649 [12%] vs 7/193 [4%]; mean difference 8, 95%CI 4–11, P<0.001), invasive mechanical ventilation (6/193 [10%] vs 255/2649 [3%]; mean difference 7, 95%CI 3–9, P<0.01), and to die (2/193 [8%] vs 219/2649 [1%]; mean difference 7, 95%CI 4–9, P<0.001) than HCW. See Table 3 for complete results.
Table 3. Disposition.
Data are presented as numbers and percentages in parentheses.
| No. (%) | Non HCW | HCW | Difference in % unless otherwise specified (95% CI) |
|---|---|---|---|
| Discharged from ED | 1275 (48) | 154 (80) | -32 (-37 - -25) |
| Admitted to regular floor | 1264 (48) | 38 (20) | 28 (21–34) |
| Direct admit to ICU | 103 (4) | 1 (0.5) | 3 (1–4) |
| Died in ED | 7 (0.3) | 0 (0) | 0.3 (-0.2–0.2) |
| Length of stay | |||
| All | 5.4 (10.1) | 1.4 (4.0) | 4.0 (3.3–4.7) |
| Discharged | 0.05 (0.40) | 0.02 (0.14) | 0.03 (-0.04–0.09) |
| Admitted | 10.5 (12.1) | 6.9 (6.5) | 3.6 (1.4–5.8) |
| Patients requiring IMV | 255 (10) | 6 (3) | 7 (3–9) |
| Patients requiring ICU | 321 (12) | 7 (4) | 8 (4–11) |
| Overall mortality | 219 (8) | 2 (1) | 7 (4–9) |
HCW: Healthcare worker; ED: Emergency department; CIU: Intensive care unit; IMV: Invasive mechanical ventilation.
Multivariable analyses
After controlling for known potential confounders (including age, sex, comorbidities, vital signs, and CXR findings), variables significantly associated with admission included age (OR 1.05/year, 95%CI 1.04–1.06), fever (OR 2.1, 95%CI 1.57–2.81), tachypnea (OR 6.0, 95%CI 3.56–1.53), hypoxemia (OR 1.46, 95%CI 1.39–1.53) and presence of comorbidities (OR 1.75, 95%CI 1.35–2.25 and 4.1, 95%CI 3.0–5.5 for one or more comorbidities respectively). HCW were less likely than non HCW to require hospital admission (OR 0.58, 95%CI 0.36–0.92) even after adjusting for confounders (Table 4).
Table 4. Multivariable predictors of outcomes.
| OR | 95% CI | |
|---|---|---|
| Hospital Admission | ||
| Male sex | 1.09 | 0.88–1.35 |
| Age per year | 1.05 | 1.04–1.06 |
| Non-HCW | Reference | - |
| HCW | 0.58 | 0.36–0.92 |
| Temp > 38° C | 2.10 | 1.57–2.81 |
| Tachypnea >24/min. | 6.00 | 3.56–10.11 |
| Hypoxemia <94% | 1.46 | 1.39–1.53 |
| Any exposure | 0.50 | 0.40–0.63 |
| # comorbidities | ||
| 0 | Reference | - |
| 1 | 1.75 | 1.35–2.25 |
| 2+ | 4.06 | 3.01–5.47 |
| Invasive Mechanical Ventilation | ||
| Male | 2.04 | 1.48–2.81 |
| Age per year | 0.99 | 0.98–1.00 |
| Non-HCW | Reference | - |
| HCW | 0.97 | 0.38–2.45 |
| Temp > 38° C | 1.30 | 0.92–1.83 |
| Tachypnea > 24/min. | 1.24 | 0.96–1.78 |
| Hypoxemia <94% | 1.09 | 1.06–1.12 |
| Any exposure | 1.22 | 0.88–1.68 |
| # comorbidities | ||
| 0 | Reference | - |
| 1 | 1.36 | 0.91–2.04 |
| 2+ | 1.30 | 0.87-1/93 |
| ICU Admission | ||
| Male sex | 1.73 | 1.30–2.29 |
| Age per year | 0.99 | 0.98–1.00 |
| Non-HCW | Reference | - |
| HCW | 0.80 | 0.33–1.91 |
| Temp > 38° C | 1.16 | 0.85–1.60 |
| Tachypnea >24/min. | 1.54 | 1.11–2.13 |
| Hypoxemia | 1.08 | 1.05–1.10 |
| Any exposure | 1.13 | 0.84–1.52 |
| # comorbidities | ||
| 0 | Reference | - |
| 1 | 1.32 | 0.91–1.90 |
| 2+ | 1.40 | 0.97–2.00 |
| Mortality | ||
| Male | 1.97 | 1.38–2.82 |
| Age per year | 1.05 | 1.04–1.07 |
| Non-HCW | Reference | - |
| HCW | 0.94 | 0.21–4.24 |
| Temp > 38° C | 0.77 | 0.48–1.22 |
| Tachypnea >24/min. | 1.45 | 0.97–2.16 |
| Hypoxemia <94% | 1.09 | 1.06–1.12 |
| Any exposure | 0.80 | 0.54–1.19 |
| # comorbidities | ||
| 0 | Reference | - |
| 1 | 1.03 | 0.61–1.76 |
| 2+ | 1.50 | 0.94–2.41 |
Variables associated with ICU admission after adjusting for confounders were male sex (OR 1.73, 95%CI, 1.3–2.3), tachypnea (OR 1.54, 95%CI 1.1–2.13), and hypoxemia (OR 1.08, 95%CI 1.05–1.10). Variables associated with IMV were male sex (OR 2.04, 95%CI, 1.48–2.81) and hypoxemia (OR 1.09, 95%CI, 1.06–1.12). Variables independently associated with mortality included male sex (OR 1.97, 95%CI 1.38–2.82), age (OR 1.05/year, 95%CI 1.04–1.07) and hypoxemia (OR 1.09, 95%CI 1.06–1.12). Being a HCW was not associated with increased risk of ICU admission, IMV, or mortality.
Discussion
Our study identifies some differences in HCWs with Covid-19 presenting to the emergency department compared to non-HCWs. HCW were generally younger and with fewer comorbidities than non HCW. Compared with non HCW, HCW were less severely ill as evidenced by lower rates of tachypnea, hypoxemia, lymphopenia and the presence of bilateral opacities on radiographic imaging. As a result, HCW were less likely to be admitted to the hospital, to require ICU level of care, require invasive mechanical ventilation and to ultimately die than non HCW. This seemingly milder course of disease in HCWs compared to the general population in the surrounding community is reported in other studies of Covid-19 in HCWs [5]. Given the large number of HCW in our catchment area and their potential high risk of exposure to Covid-19 [6], it is reassuring to find low rates of severe illness when compared to the general population. In our study we found that being a HCW was not associated with poor outcomes even after adjusting for age and comorbidities. A possible reason for our outcomes may be due to the universal availability and use of PPE by our health care workers. We assumed that all patients, visitors and employees were potential asymptomatic carriers, and had instituted strict hand sanitizing protocols, masking and face shields for all staff in contact with patients who are not Covid-19 positive at the time of admission.
Certain characteristics of HCWs with COVID-19 may be attributed to common characteristics of HCWs compared with the general population in the surrounding community who are not HCWs. Although men constitute a larger percentage of total HCWs in the United States, women make up the majority of most types of healthcare occupations including registered nurses, home health aides, medical assistants, and physician assistants [7]. This may be reflected by the large majority of HCW Covid-19 cases in female HCWs. The higher frequency of HCW Covid-19 infection in females and those in the age group 16–44 has been repeatedly found in most studies that report this demographic information [2,5,8–15].
Overall, morbidity and mortality studies for HCWs are sparse, however those that exist suggest that HCWs, particularly physicians, tend to live longer than age and sex matched non HCW [16]. While some studies have found that physicians are more likely to have chronic conditions like obesity, metabolic syndromes, hypertension and cardiovascular disease, others have found that they are at lower risk for these illnesses [1]. HCWs are also more likely to have come in contact with a sick person because of the nature of their job [16]. This strongly supports the importance of continued use of appropriate PPE for all HCW. All of these factors have the potential to contribute to an altered course of Covid-19 in HCWs.
Early studies have found that HCWs have made up a large proportion of early cases of Covid-19, presumably acquired in the hospital. However, deaths among HCW are rare, and mostly affect older HCWs. With increasing understanding of the disease, the number of HCW becoming infected has declined [17]. The importance of widespread availability and use of PPE among HCW is further demonstrated in a recent study finding that HCW who had PPE were less likely to become infected than those without PPE [18]. Studies conducted during previous influenza pandemics have also shown low rates of infection with proper use of PPE and that many HCWs who got infected were relatively young as in our study [19].
At the time of the study, data on asymptomatic infection and super spreaders were not known. Reliance on hospital or department of health-based testing and PPE was standard for all HCW. As more information on community spread and on asymptomatic spread is known, HCW will be better able to decrease their risk of acquisition of Covid-19 outside of work. With the availability of PPE and quicker identification and isolation of community Covid-19 cases, we expect further decreases in Covid-19 infection among HCW.
Our study has several notable limitations. Most importantly, our study was retrospective and subject to considerable selection bias and residual confounding. In addition, the number of healthcare workers was relatively limited. We also did not distinguish between various types of healthcare workers based on their specific profession. More data is needed on subsets of HCW such as nurses, physician extenders and other HCW who have direct patient contact on a daily basis. Furthermore, our study is representative of a single large academic center near the epicenter of the Covid-19 pandemic and may be less representative of other centers. We also did not control for ethnicity.
Conclusions
In summary, we found that when compared to adult non-healthcare workers with Covid-19 presenting to the ED, healthcare workers with Covid-19 were more likely to have an identified COVID exposure, present less severely ill, and less likely to be admitted to the hospital. Longer term follow-up of HCW will be needed to better assess the risk of HCW.
Acknowledgments
We would like to thank the Stony Brook University’s Renaissance School of Medicine COVID-19 Data Repository Quality Initiative instituted by the Office of the Dean of the Renaissance School of Medicine and the Department of Biomedical Informatics for their assistance.
Data Availability
The de-identified data base and its dictionary are publicly available at Figshare: https://figshare.com/articles/book/HCW_COVID_19_Codebook_pdf/13283342https://figshare.com/articles/dataset/HCW_Data_v3_xlsx/13283141.
Funding Statement
No funding was received for this study.
References
- 1.Mohanty A., Kabi A., and Mohanty A.P. Health problems in healthcare workers: A review. J Family Med Prim Care. 2019. August; 8(8): 2568–2572. 10.4103/jfmpc.jfmpc_431_19 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.CDC COVID-19 Response Team. Characteristics of Health Care Personnel with COVID-19—United States, February 12–April 9, 2020. CDC Morbidity and Mortality Weekly Report. April 2020. https://cdc.gov/mmwr/volumes/69/wr/mm6915e6.htm. Accessed on August 5, 2020. [DOI] [PMC free article] [PubMed]
- 3.STROBE Guidelines for Cross-Sectional Studies. Enhancing the QUAlity and Transparency Of health Research (EQUATOR) Network October 22, 2019. https://www.equator-network.org/wp-content/uploads/2015/10/STROBE_checklist_v4_cross-sectional.pdf Accessed on May 6, 2020.
- 4.Kaji AH, Schriger D, Green S. Looking Through the Retrospectoscope: Reducing Bias in Emergency Medicine Chart Review Studies. Annals of Emergency Medicine 2014;64(3):292–298. 10.1016/j.annemergmed.2014.03.025 [DOI] [PubMed] [Google Scholar]
- 5.Chou R., Dana T., Buckley D.I., Selph S., Fu R., and Totten A.M. Epidemiology of and Risk Factors for Coronavirus Infection in Health Care Workers. Ann Intern Med. May 2020. 10.7326/M20-1632 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Nguyen LH, Drew DA, Graham MS, et al. Risk of COVID-19 among front-line health-care workers and the general community: a prospective cohort study. Lancet July 31, 2020. 10.1016/S2468-2667(20)30164-X [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.U.S. Department of Health and Human Services, Health Resources and Services Administration, National Center for Health Workforce Analysis. Sex, Race, and Ethnic Diversity of U.S, Health Occupations (2011–2015), Rockville, Maryland. 2017.
- 8.Wang X., Pan Z., and Cheng Z. Association between 2019-nCoV transmission and N95 respirator use. J Hosp Infect. March 2020;105, 104–105. 10.1016/j.jhin.2020.02.021 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Dai Y.H., G.; Xiong H.; Qiu H.; Yuan X. Psychological impact of the corona- virus disease 2019 (COVID-19) outbreak on healthcare workers in China. Medrxiv March 2020. 10.1101/2020.03.03.20030874. [DOI] [Google Scholar]
- 10.Liu M, He P., Liu HG.; et al. (2020). Clinical characteristics of 30 medical workers infected with new coronavirus pneumonia. Prime. March 2020. 10.1007/978-3-030-59354-4_13 [DOI] [PubMed] [Google Scholar]
- 11.Kang L., Ma S., Chen M., Yang J., Wang Y., Li R., et al. Impact on mental health and perceptions of psychological care among medical and nursing staff in Wuhan during the 2019 novel coronavirus disease outbreak: A cross-sectional study. Brain Behav Immun. March 2020. 10.1016/j.bbi.2020.03.028 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Lai J., Ma S., Wang Y., Cai Z., Hu J., Wei N., et al. (2020). Factors Associated With Mental Health Outcomes Among Health Care Workers Exposed to Coronavirus Disease 2019. JAMA Netw Open. March 2020. 3, e203976 10.1001/jamanetworkopen.2020.3976 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Liu J., Ouyang L.; Guo P.; Wu H.; Fu P.; Chen Y.; et al. Epidemiological, clinical character- istics and outcome of medical staff infected with COVID-19 in Wuhan, China: a retrospective case series analysis. medRxiv. March 2020. https://www.medrxiv.org/content/10.1101/2020.03.09.20033118v1. [Google Scholar]
- 14.Kluytmans M.B., A; Pas S.; Bentvelsen R. G.; Bijllaardt W.; Oudheusden A. J. G.; van Rijen M. M. L.; et al. SARS-CoV-2 infection in 86 healthcare workers in two Dutch hospitals in March 2020. medRXiv. March 2020. 10.1101/2020.03.23.20041913. [DOI] [Google Scholar]
- 15.McMichael T.M., Currie D.W., Clark S., Pogosjans S., Kay M., Schwartz N.G., et al. Epidemiology of Covid-19 in a Long-Term Care Facility in King County, Washington. N Engl J Med. March 2020;382, 2005–2011. 10.1056/NEJMoa2005412 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Frank E.B., H.; Burnett C.A. Mortality Rates and Cases Among U.S. Physicians. Am J Prev Med 2000;19(3): 155–159. 10.1016/s0749-3797(00)00201-4 [DOI] [PubMed] [Google Scholar]
- 17.Bielicki JA, Duval X, Gobat N, Goossens H, Koopmans M, Tacconelli E, et al. Monitoring approaches for health-care workers during the COVID-19 pandemic. Lancet Infect Dis 2020;20:e261–67. 10.1016/S1473-3099(20)30458-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Nguyen, L.H., Drew D.A., Joshi A.D., Guo C.G., Wenjie M., et al. Risk of COVID-19 among frontline healthcare workers and the general community: a prospective cohort study. https://ncbi.nlm.nih.gov/pmc/articles/PMC7273299.
- 19.Hudson B, Toop L, Mangin D, Brunton C, Jennings L, Fletcher L. Pandemic influenza A(H1N1)pdm09: risk of infection in primary healthcare workers. Br J Gen Pract 2013; 10.3399/bjgp13X668212 [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The de-identified data base and its dictionary are publicly available at Figshare: https://figshare.com/articles/book/HCW_COVID_19_Codebook_pdf/13283342https://figshare.com/articles/dataset/HCW_Data_v3_xlsx/13283141.