Hostname: page-component-cd9895bd7-gxg78 Total loading time: 0 Render date: 2024-12-27T06:32:30.049Z Has data issue: false hasContentIssue false

Sources of exposure identified through structured interviews of healthcare workers who test positive for severe acute respiratory coronavirus virus 2 (SARS-CoV-2): A prospective analysis at two teaching hospitals

Published online by Cambridge University Press:  15 December 2021

Chanu Rhee*
Affiliation:
Department of Population Medicine, Harvard Medical School/Harvard Pilgrim Health Care Institute, Boston, Massachusetts Division of Infectious Diseases, Department of Medicine, Brigham and Women’s Hospital, Boston, Massachusetts Infection Control Department, Brigham and Women’s Hospital, Boston, Massachusetts
Meghan A. Baker
Affiliation:
Department of Population Medicine, Harvard Medical School/Harvard Pilgrim Health Care Institute, Boston, Massachusetts Division of Infectious Diseases, Department of Medicine, Brigham and Women’s Hospital, Boston, Massachusetts Infection Control Department, Brigham and Women’s Hospital, Boston, Massachusetts
Robert Tucker
Affiliation:
Infection Control Department, Brigham and Women’s Hospital, Boston, Massachusetts
Diane Griesbach
Affiliation:
Occupational Health Services, Brigham and Women’s Hospital, Boston, Massachusetts
Dinah McDonald
Affiliation:
Occupational Health Services, Brigham and Women’s Faulkner Hospital, Boston, Massachusetts
Sarah A. Williams
Affiliation:
Department of Quality and Safety, Brigham and Women’s Hospital, Boston, Massachusetts
Karen Fiumara
Affiliation:
Department of Quality and Safety, Brigham and Women’s Hospital, Boston, Massachusetts
Andrew Resnick
Affiliation:
Department of Quality and Safety, Brigham and Women’s Hospital, Boston, Massachusetts
Michael Klompas
Affiliation:
Department of Population Medicine, Harvard Medical School/Harvard Pilgrim Health Care Institute, Boston, Massachusetts Division of Infectious Diseases, Department of Medicine, Brigham and Women’s Hospital, Boston, Massachusetts Infection Control Department, Brigham and Women’s Hospital, Boston, Massachusetts
*
Author for correspondence: Chanu Rhee, MD, MPH, Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, 401 Park Drive, Suite 401, Boston, MA 02215. E-mail: crhee@bwh.harvard.edu

Abstract

We interviewed 1,208 healthcare workers with positive SARS-CoV-2 tests between October 2020 and June 2021 to determine likely exposure sources. Overall, 689 (57.0%) had community exposures (479 from household members), 76 (6.3%) had hospital exposures (64 from other employees including 49 despite masking), 11 (0.9%) had community and hospital exposures, and 432 (35.8%) had no identifiable source of exposure.

Type
Concise Communication
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction in any medium, provided the original article is properly cited.
Copyright
© The Author(s), 2021. Published by Cambridge University Press on behalf of The Society for Healthcare Epidemiology of America

Healthcare workers (HCWs) are presumed to be at high risk for severe acute respiratory coronavirus virus 2 (SARS-CoV-2) infection. Reference Jacob, Baker and Fridkin1Reference Scohy, Gruson and Simon5 Studies based on self-reports and serologic testing, however, differ on whether HCW infection rates are higher or similar to rates in surrounding communities and how many infections are acquired inside versus outside the hospital. Importantly, many HCW studies were conducted early in the pandemic when personal protective equipment (PPE) was scarce, testing and infection control strategies were still evolving, and vaccines were not yet deployed. We report on a prospective analysis of HCW infections based on structured interviews at two hospitals in Boston, Massachusetts, beginning in October 2020 when coronavirus disease 2019 (COVID-19) infection control policies had matured and PPE supplies had stabilized.

Methods

Setting, employee testing, contact tracing, and exposure evaluation process

We included all employees at Brigham and Women’s Hospital (803-bed academic hospital) and Brigham and Women’s Faulkner Hospital (162-bed community teaching hospital) who tested positive for SARS-CoV-2 between October 1, 2020, and June 1, 2021. These 2 hospitals collectively employ >23,000 people. Employees were required to undergo PCR testing for any symptoms potentially consistent with COVID-19, if they had a known exposure in the community, or if they interacted with a SARS-CoV-2–positive employee with ≥1 party unmasked for ≥15 minutes while that person was potentially infectious (2 days prior to symptom onset or date of positive test if asymptomatic). Employees who cared for SARS-CoV-2–positive patients before they were placed on COVID-19 precautions were identified through the Epic software (Epic, Verona WI) electronic health record trace function and were notified by e-mail. They were required to test if they were within 2 m of the patient for ≥15 minutes unless both parties wore face masks or the employee wore both a mask (or respirator) and eye protection (face shield or goggles). Asymptomatic employees were also permitted to test on or off site at no cost for any other reason.

All positive employees were immediately interviewed by the occupational health department to ask about presence and timing of symptoms, interactions with patients or staff while potentially infectious, and potential exposure sources in the preceding 14 days. Employee contacts were notified by e-mail or phone if the SARS-CoV-2–positive staff member reported that exposure criteria were met (≥1 party unmasked for ≥15 minutes during the infectious period). Each SARS-CoV-2–positive case was then discussed on daily multidisciplinary calls involving Infection Control, Quality and Safety, and Occupational Health staff. The likely exposure source was adjudicated as community, hospital, mixed, or unknown using case definitions that considered known COVID-19 contacts, whether employees worked on site in the preceding 14 days, whether full PPE was used during care for COVID-19 patients (ie, respirator, eye protection, gown, gloves), and whether masks were worn (Table 1).

Table 1. Criteria for Classifying Source of Healthcare Worker Infections

Classification Criteria
Community source
Definite
community
exposure
• Close contact (within 2 m) with someone outside of the hospital for ≥15 minutes who is confirmed to be SARS-CoV-2 positive within the preceding 14 d, absent a similar exposure within the hospital, OR
• Did not work on-site within the 14 d preceding symptom onset
Likely
community
exposure
• Household contact and employee develop symptoms at the same time and no known work-related exposure, OR
• Household contact displaying COVID-19 symptoms but not tested, and no known work-related exposure, OR
• Traveled out of state within 14 d of symptom onset and no known contact with a SARS-CoV-2–positive patient or staff member at work
Hospital source
Patient
exposure with
inappropriate
PPE
• Did not meet criteria for community exposure, AND
• Close contact (within 2 m) for ≥15 minutes within the prior 14 d with a SARS-CoV-2–positive patient from 2 d prior to symptom onset (or positive test if asymptomatic) to the time patient was placed on precautions, in which the employee was not wearing full PPE (respirator, eye protection [face-shield or goggles], gown, and gloves)
Employee
exposure
• Did not meet criteria for community exposure, AND 1 of the following:
Unmasked: Close contact (within 2 m) within the prior 14 d with a SARS-CoV-2–positive employee anytime from 2 d prior to symptom onset to the time the SARS-CoV-2–positive employee left work, in which either employee was not wearing a mask for ≥15 minutes
Masked: As above, but no reported lapses in mask use
Mixed community/hospital source
Mixed
exposures
• Cared for SARS-CoV-2–positive patient(s) without appropriate PPE OR had an employee exposure (with or without lapses in mask use) within the prior 14 d, AND
• Close contact with someone outside the hospital who tested positive with onset of symptoms on the same day or within 24 h prior to the employee or displayed COVID-19 symptoms but not tested
Unknown source
Patient
exposure with
appropriate PPE
• Did not meet criteria for community or hospital exposure, AND
• Employee had close contact (within 2 m) for ≥15 minutes within the prior 14 d with a SARS-CoV-2–positive patient while wearing full PPE (respirator, eye protection (face-shield or goggles), gown, and gloves)
No known
exposures
• No contacts with known or suspected COVID-19 individuals in or out of the hospital within the prior 14 d, and not meeting any of the definitions above

Employees whose only contacts were with COVID-19 patients while wearing full PPE were classified as having an “unknown” exposure source given the evidence that transmission to HCWs wearing full PPE is exceedingly rare. Reference Braun, Moreno and Buys6 Employees whose only known COVID-19 contacts were other employees were classified as “hospital” exposures even if both reported wearing surgical masks given our observations that minor lapses in mask use (ie, uncovered noses, sipping beverages) during HCW-HCW interactions are not uncommon, and data that transmission can occur despite surgical masks. Reference Klompas, Baker and Griesbach7Reference Klompas, Baker and Rhee9

Patient testing and infection control policies

All patients underwent SARS-CoV-2 PCR testing on admission; PCR-negative patients were retested 72 hours later to identify virus potentially incubating on arrival and again every 3 days through day 14 if they required aerosol-generating procedures. Serial testing was also done for all patients on a unit if a hospital-onset case or potential cluster was detected. Liberal retesting was encouraged for any new symptoms concerning for COVID-19. Precautions for patients with suspected or confirmed COVID-19 included respirators, eye protection, gowns, and gloves. Standard precautions for non–COVID-19 patients included surgical masks and eye protection. A universal mask policy for all employees was in effect.

Analysis

We analyzed the distribution of likely exposure sources among SARS-CoV-2–positive employees overall and stratified by vaccination status using the Cochran-Mantel-Haenszel statistic. The hospitals began administering the BNT162b2(Pfizer/BioNTech) and mRNA-1273 (Moderna) vaccines in mid-December; 85% of all staff were vaccinated by June 1. We considered employees vaccinated if they received ≥1 dose of any vaccine ≥14 days before infection given the evidence of at least partial immunity by this point.

All analyses were conducted using Microsoft Excel 365 software (Microsoft, Redmond, WA) and SAS version 9.4 software (SAS Institute, Cary, NC). The study was approved by the Mass General Brigham Institutional Review Board.

Results

During the study period, 12,228 employees underwent 53,422 tests and 1,208 tested positive for SARS-CoV-2 (2.3% positivity rate), including 121 providers (physicians, physician assistants, nurse practitioners), 324 nurses, 166 patient care or medical assistants, 219 other clinical staff, and 378 nonclinical staff. Also, 1,004 (83.1%) employees were symptomatic when tested. Overall, 689 (57.0%) employees had community exposures (548 definite and 141 likely), including 479 with household contacts. In addition, 76 (6.3%) had hospital exposures: 12 from COVID-19 patients before they were diagnosed and placed on COVID-19 precautions, and 64 from other employees including 49 who reported both parties wore masks. Furthermore, 11 (0.9%) had both community and hospital exposures. Importantly, 432 (35.8%) had an unknown source: 97 who cared for COVID patients wearing full PPE, and 335 with no known COVID-19 contacts (Fig. 1).

Fig. 1. Likely sources of exposure for healthcare workers with positive SARS-CoV-2 tests based on structured occupational health interviews.

Of 1,208 SARS-CoV-2–positive employees, 90 (7.5%) tested positive ≥14 days after their first vaccine dose. Exposures sources for these vaccinated employees were respectively similar to unvaccinated SARS-CoV-2–positive employees: community (63.3% vs 56.5%), hospital (0% vs 6.8%), mixed (1.1% vs 0.9%), and unknown (35.6% vs 35.8%) (P = .65).

Discussion

Overall, 57% of HCWs who tested positive for SARS-CoV-2 between October 2020 and June 2021 had a known community exposure, mostly household contacts. An additional 6% had hospital exposures, mostly from other HCWs (23% with unmasked interactions), and 1% had mixed community and hospital exposures. Strikingly, we were unable to identify a clear exposure source in 36% of cases despite detailed interviews. Most had no known COVID-19 contacts; one-quarter cared for COVID-19 patients but with appropriate PPE. Sources of infection were similar for unvaccinated and vaccinated HCWs.

Our findings complement seroprevalence studies demonstrating that most HCW infections are community acquired. Reference Jacob, Baker and Fridkin1,Reference Baker, Nelson and Overton4,Reference Scohy, Gruson and Simon5 Our analysis does suggest, however, that ∼10% of HCW infections with a known source are potentially attributable to the workplace, particularly from peers and patients with occult or not-yet-diagnosed infections.

The high rate of infections without an identifiable source may reflect the large number of asymptomatic SARS-CoV-2 infections and the fact that many cases in the community go untested and undiagnosed. We presume that many of these HCW infections were acquired in the community given that SARS-CoV-2–positive contacts in the hospital, particularly patients, are more likely to be recognized due to extensive testing and contact tracing. However, it is also possible that we underestimated workplace transmission because hospital policy did not require routine surveillance testing for asymptomatic HCWs and because occupational health staff did not routinely alert HCWs about SARS-CoV-2–positive peers if the peer reported both parties wore masks, despite the known possibility of transmission despite surgical masks. Reference Klompas, Baker and Griesbach7Reference Klompas, Baker and Rhee9 Furthermore, our exposure definition required ≥15 minutes of close contact with a SARS-CoV-2–positive individual, but transmissions can occur over shorter intervals. Reference Klompas, Baker and Griesbach7,Reference Klompas, Baker and Rhee9 These policies and exposure definitions may have made it more difficult to identify workplace exposures.

Our findings are largely concordant with a University of Wisconsin study in which whole-genome sequencing was conducted for 95 HCWs and 137 possible patient contacts. These researchers demonstrated that most HCW infections were community-acquired, but one-quarter were work related, mostly from peers or patients in the context of unsuspected clusters rather than from known SARS-CoV-2–positive patients. Reference Braun, Moreno and Buys6 This analysis and ours suggest that although workplace transmission likely accounts for a minority of HCW infections, there is still room to further enhance hospital infection control policies. Such interventions could include reminding HCWs of the risk of infection from asymptomatic colleagues and patients, minimizing high-risk unmasked interactions in breakrooms and workrooms, ensuring tight fit of surgical masks, and broader use of N95 respirators when community incidence rates are high. Reference Klompas, Baker and Griesbach7,Reference Klompas, Rhee and Baker10 Furthermore, the large fraction of HCW infections without an identifiable source in our analysis underscores a potential benefit of conducting broader and more routine genomic sequencing of patient and HCW isolates. This could help to identify occult transmission pathways and areas of vulnerability, or conversely, provide reassurance about the effectiveness of current hospital infection control policies.

Limitations of our study include the focus on 2 well-resourced hospitals, potentially limiting generalizability, and our inability to use whole-genome sequencing to confirm transmission sources. The likelihood of community SARS-CoV-2 acquisition, particularly from unknown sources, may also vary depending on local public health measures such as mask mandates. Interviews are also subject to recall bias and some staff may have been reluctant to acknowledge lapses in mask use or high-risk behaviors. Lastly, our analysis was conducted before the highly transmissible δ (delta) variant began to predominate in the United States; additional research is needed to understand the impact of the δ variant on the adequacy of current infection control measures, particularly as vaccines may have reduced efficacy against this variant. Nonetheless, our findings provide important context to inform ongoing discussions and policies on how best to protect HCWs from SARS-CoV-2.

Acknowledgments

Financial support

This work was funded by the Centers for Disease Control and Prevention (grant no. 6U54CK000484-04-02). The Centers for Disease Control and Prevention had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.

Conflicts of interest

Drs Rhee and Klompas report royalties from UpToDate, unrelated to this work. All other authors have no potential conflicts of interest to declare.

References

Jacob, JT, Baker, JM, Fridkin, SK, et al. Risk factors associated with SARS-CoV-2 seropositivity among US healthcare personnel. JAMA Netw Open 2021;4:e211283.CrossRefGoogle Scholar
Nguyen, LH, Drew, DA, Graham, MS, et al. Risk of COVID-19 among frontline healthcare workers and the general community: a prospective cohort study. Lancet Public Health 2020;5:e475e483.CrossRefGoogle Scholar
Barrett, ES, Horton, DB, Roy, J, et al. Prevalence of SARS-CoV-2 infection in previously undiagnosed health care workers in New Jersey, at the onset of the US COVID-19 pandemic. BMC Infect Dis 2020;20:853.CrossRefGoogle Scholar
Baker, JM, Nelson, KN, Overton, E, et al. Quantification of occupational and community risk factors for SARS-CoV-2 seropositivity among healthcare workers in a large US healthcare system. Ann Intern Med 2021;174:649654.Google Scholar
Scohy, A, Gruson, D, Simon, A, et al. Seroprevalence of SARS-CoV-2 infection in health care workers of a teaching hospital in Belgium: self-reported occupational and household risk factors for seropositivity. Diagn Microbiol Infect Dis 2021;100:115414.CrossRefGoogle ScholarPubMed
Braun, KM, Moreno, GK, Buys, A, et al. Viral sequencing reveals US healthcare personnel rarely become infected with SARS-CoV-2 through patient contact. Clin Infect Dis 2021;73:e1329e1336.CrossRefGoogle Scholar
Klompas, M, Baker, MA, Griesbach, D, et al. Transmission of SARS-CoV-2 from asymptomatic and presymptomatic individuals in healthcare settings despite medical masks and eye protection. Clin Infect Dis 2021;73:16931695.CrossRefGoogle ScholarPubMed
Goldberg, L, Levinsky, Y, Marcus, N, et al. SARS-CoV-2 infection among healthcare workers despite the use of surgical masks and physical distancing—the role of airborne transmission. Open Forum Infect Dis 2021;8:ofab036.CrossRefGoogle Scholar
Klompas, M, Baker, MA, Rhee, C, et al. A SARS-CoV-2 cluster in an acute care hospital. Ann Intern Med 2021;174:794802.CrossRefGoogle Scholar
Klompas, M, Rhee, C, Baker, M. Universal use of N95s in healthcare settings when community COVID-19 rates are high. Clin Infect Dis 2021. doi: 10.1093/cid/ciab539.Google ScholarPubMed
Figure 0

Table 1. Criteria for Classifying Source of Healthcare Worker Infections

Figure 1

Fig. 1. Likely sources of exposure for healthcare workers with positive SARS-CoV-2 tests based on structured occupational health interviews.