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      Severe acute respiratory coronavirus virus 2 (SARS-CoV-2) IgG results among healthcare workers in a rural upstate New York hospital system

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          Abstract

          To the Editor—To better understand the effectiveness of occupational infection control measures during the coronavirus disease 2019 (COVID-19) pandemic, we surveyed and antibody tested employees of Bassett Healthcare Network, located in rural upstate New York, 200 miles northwest of New York City. Employer-sponsored SARS-CoV-2 IgG antibody testing was conducted from May 4 to 29, 2020. Network leadership prioritized employees with a high likelihood of exposure to COVID-19–infected patients. A 21.7% random sample of employees was also included for antibody testing to ensure that our seroprevalence estimate was representative of all network employees. The study questionnaire captured demographics, COVID-19 polymerase chain reaction (PCR) status, potential COVID-19 work and nonwork exposures, and COVID-19 symptoms experienced since January 1, 2020 (based on the Centers for Disease Control and Prevention’s case report form). The recall period for exposure questions (March 1–May 31, 2020) coincided with New York State’s stay-at-home order plus 2 weeks. We compared seroprevalence among employees to that for patients tested during the same period. Employee serology testing was performed by Bassett Medical Center Laboratory using the SARS-CoV-2 IgG Abbott Architect assay (Abbott Laboratories, Abbott Park, IL), with 100% sensitivity and 99.6% specificity. 1 IgG level ≥1.40 was defined as positive. Most serology testing for patients (96%) was conducted by the Mayo Clinic using the VITROS Anti-SARS-CoV-2 IgG Test (Ortho-Clinical Diagnostics, Linden, NJ), with 90.0% sensitivity and 100% specificity. 2 The remaining patient tests were conducted by the in-house laboratory using the Abbott test. We compared questionnaire responses by antibody status using χ2 tests for categorical variables and t tests for continuous variables. Analyses were conducted using SAS version 9.3 software (SAS Institute, Cary, NC). This study was approved by the Mary Imogene Bassett Institutional Review Board. Results Among 764 employees tested, 15 were positive for SARS-CoV-2 IgG antibodies, for a seroprevalence of 2.0%, compared to 4.5% for patients (ie, 34 seropositives among 762 tested). Of the 764 employees tested, 601 (78.7%) completed the study questionnaire. Seroprevalence among all study participants was 12 of 601 (2.0%) and 4 of 130 (3.1%) in the random sample. The mean IgG level was 4.93 (range, 2.10–8.14) among seropositives and 0.06 (range, 0.01–1.17) among seronegatives. One-third of seropositives reported a positive PCR test, 8.3% reported a negative PCR test, and 58.3% had no PCR test. Of the 589 seronegative employees, 47 reported having a PCR test (all negative). Seropositive employees were just as likely as seronegative employees to report having no direct contact with COVID-19 patients (25.0% vs 17.7%; P = 0.46) (Table 1). Seropositive employees were less likely to report involvement in high-risk patient-related tasks, such as COVID-19 testing, although these differences were not statistically significant. Table 1. Comparison of Employees With and Without Previous SARS-CoV-2 Infection (N=601), Bassett Healthcare Network, May 4–29, 2020 Characteristic No. (%) Positive IgG Test (N=12) Negative IgG Test (N=589) Age  Mean y (standard deviation) 41.8 (16.0) 43.7 (13.7)  Range 23–63 19–78 Sex  Female 10 (83.3) 425 (72.4)  Male 2 (16.7) 161 (27.6) Race/ethnicity  Black 1 (8.3) 12 (2.0)  White 10 (83.3) 521 (88.5)  Other 1 (8.3) 44 (7.4) Body mass index, mean (standard deviation) 30.6 (11.1) 29.8 (7.3) Employment a  Full-time 8 (66.7) 512 (88.4)  Part-time/Per diem 4 (33.3) 67 (11.6) Quarantined, yes b 7 (58.3) 67 (11.4)  Diagnosed COVID positive 4 (33.3) 0  Exposed to known case 3 (25.0) 47 (8.0)  Travel 0 7 (1.2) Patient-related tasks  No direct patient contact 3 (25.0) 104 (17.7)  Testing for COVID-19 in a testing site 0 86 (14.6)  Testing for COVID-19 of patients being admitted 0 89 (15.1)  Emergency services 1 (8.3) 131 (22.2)  Bedside care of nonintubated patient 6 (50.0) 302 (51.3)  Intubation or extubation of patient 1 (8.3) 96 (16.3)  Intensive care of intubated patient 3 (25.0) 138 (23.4)  Respiratory therapy 0 42 (7.1)  Patient transport 1 (8.3) 94 (16.0)  Inpatient support—radiology, phlebotomy/IV team, physical/occupational/speech therapy 0 77 (13.1)  Servicing rooms 0 23 (3.9)  Food and nutrition services 0 8 (1.4)  Clinic rooming and patient visits 1 (8.3) 56 (9.5)  Clinic reception/ward clerk/clinic manager 0 26 (4.4)  Other patient care-related 1 (8.3) 62 (10.5)  Temperature monitoring of employees and patients at entrances 0 38 (6.5)  Respirator fit testing 0 19 (3.2) Possible nonwork exposures  Traveled out of region 2 (16.7) 93 (15.9)  Social distancing   Strict/some 11 (91.7) 551 (96.3)   Not very much/none 1 (8.3) 21 (3.7)  Any nonwork contact with a known/suspected COVID-19 patient c 8 (66.7) 213 (37.6)  Had any contact (within 2 m for >15 min) with a known/suspected COVID-19 patient 5 (41.7) 181 (31.6)   Known 4 (80.0) 108 (60.0)   Suspected 1 (20.0) 62 (34.3)  Lived with a known/suspected COVID-19 patient d 5 (41.7) 62 (10.9)   Known 3 (60.0) 11 (17.7)   Suspected 1 (40.0) 24 (38.7) Household includes an essential services person who continued to work outside the home 6 (50.0) 297 (51.4) COVID-19–like illness COVID-19–like illness since January 1, 2020 8 (66.7) 257 (44.9) Symptoms among those reporting COVID-19-like illness  Cough (new onset or worsening of chronic cough) 6 (75.0) 159 (61.9)   Mostly dry cough 4 (80.0) 69 (85.2)  Headache 6 (75.0) 151 (58.8)  Altered sense of smell/taste 5 (62.5) 25 (9.7)  Sore throat 5 (62.5) 152 (59.1)  Fever (documented or subjective) 4 (50.0) 139 (54.5)  Runny nose (rhinorrhea) 4 (50.0) 134 (52.4)  Chills 3 (37.5) 10 (42.8)  Diarrhea 3 (37.5) 54 (21.0)  Exhaustion 3 (37.5) 118 (45.9)  Muscle aches (myalgia) 3 (37.5) 119 (46.3)  Shortness of breath (dyspnea) 3 (37.5) 80 (31.1)  Nausea or vomiting 2 (25.0) 34 (13.2)  Persistent pain or pressure in the chest 1 (12.5) 40 (15.6) Diagnosed with COVID-19 e 3 (37.5) 0 a P = .0448, χ2. b P < .0001, χ2. c Was within 2 m of a known/suspected COVID-19 patient for ≥15 min or lived with a known/suspected COVID-19 patient. d P = .0072, χ2. e P < .0001, χ2. There were no statistically significant differences by serology status among employees reporting travel outside of the region or social distancing practices. Seropositive employees were more likely than seronegative employees to report having a known or suspected COVID-19 case in their household (41.7% vs 10.9%, P = .0072), and they were just as likely as seronegative employees to report living with an essential services worker who continued to work outside the home (50.0% vs 51.4%; P = .53). Although more seropositive employees had contact outside of work with a known or suspected COVID-19 contact, this difference was not statistically significant (41.7% vs 31.6%; P = .13). Two-thirds of the seropositive employees (66.7%) reported a COVID-19–like illness since January 1, 2020, compared with 44.9% of seronegative employees, however this difference was not statistically significant (P = .13). Of the seropositive employees, 4 (33.3%) were asymptomatic. Among the 258 seronegative employees reporting COVID-19–like illness, 56 stated that their symptoms ended in January or February. Seropositive and seronegative employees showed different profiles in symptoms; seropositive employees were more likely to report sore throat, dry cough, and headache. Discussion Our findings among employees in a rural healthcare network show that direct patient care was not associated with increased likelihood of COVID-19 infection and that seropositivity was more likely associated with nonwork exposures. Similar findings have been reported in urban, densely populated settings and larger medical centers. 3-7 Although travel, social-distancing practices, and having an essential-services worker in the household did not differ by antibody status in our study, being exposed to a COVID-19 contact outside of work or in the same household was positively correlated with antibody status. This study is potentially limited by the timing between COVID-19 exposure and the antibody test. Employees tested >2–3 months following COVID-19 infection may no longer have detectable levels of IgG antibodies, thereby underestimating the prevalence of previous employee infection. 8-10 Other limitations include sampling and recall bias. Employee antibody testing was not done entirely at random; therefore, the estimate of seropositivity reported may not be representative of all employees. Also, seropositive employees may have been more likely to accurately recall potential exposures to COVID-19. Finally, due to the low prevalence of seropositivity, statistical comparisons between seropositive and seronegative employees had limited statistical power. During government-mandated shelter-in-place orders, SARS-CoV-2 IgG seroprevalence among employees in a rural healthcare network was lower than for the community at large. In this rural region, healthcare workers were more likely to be exposed to COVID-19 outside of the workplace than on the job. Thus, it is important that healthcare workers maintain high vigilance regarding potential nonwork exposures as well as healthcare-related patient-care exposures.

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          Rapid Decay of Anti–SARS-CoV-2 Antibodies in Persons with Mild Covid-19

          To the Editor: A recent article suggested the rapid decay of anti–SARS-CoV-2 IgG in early infection, 1 but the rate was not described in detail. We evaluated persons who had recovered from Covid-19 and referred themselves to our institution for observational research. Written informed consent was obtained from all the participants, with approval by the institutional review board. Blood samples were analyzed by enzyme-linked immunosorbent assay (ELISA) to detect anti–SARS-CoV-2 spike receptor-binding domain IgG. 2 The ELISA was further modified to precisely quantify serum anti–receptor-binding domain activity in terms of equivalence to the concentration of a control anti–receptor-binding domain monoclonal IgG (CR3022, Creative Biolabs). Infection had been confirmed by polymerase-chain-reaction assay in 30 of the 34 participants. The other 4 participants had had symptoms compatible with Covid-19 and had cohabitated with persons who were known to have Covid-19 but were not tested because of mild illness and the limited availability of testing. Most of the participants had mild illness; 2 received low-flow supplemental oxygen and leronlimab (a CCR5 antagonist), but they did not receive remdesivir. There were 20 women and 14 men. The mean age was 43 years (range, 21 to 68) (see the Supplementary Appendix, available with the full text of this letter at NEJM.org). A total of 31 of the 34 participants had two serial measurements of IgG levels, and the remaining 3 participants had three serial measurements. The first measurement was obtained at a mean of 37 days after the onset of symptoms (range, 18 to 65), and the last measurement was obtained at a mean of 86 days after the onset of symptoms (range, 44 to 119). The initial mean IgG level was 3.48 log10 ng per milliliter (range, 2.52 to 4.41). On the basis of a linear regression model that included the participants’ age and sex, the days from symptom onset to the first measurement, and the first log10 antibody level, the estimated mean change (slope) was −0.0083 log10 ng per milliliter per day (range, −0.0352 to 0.0062), which corresponds to a half-life of approximately 36 days over the observation period (Figure 1A). The 95% confidence interval for the slope was −0.0115 to −0.0050 log10 ng per milliliter per day (half-life, 26 to 60 days) (Figure 1B). The protective role of antibodies against SARS-CoV-2 is unknown, but these antibodies are usually a reasonable correlate of antiviral immunity, and anti–receptor-binding domain antibody levels correspond to plasma viral neutralizing activity. Given that early antibody decay after acute viral antigenic exposure is approximately exponential, 3 we found antibody loss that was quicker than that reported for SARS-CoV-1, 4,5 and our findings were more consistent with those of Long et al. 1 Our findings raise concern that humoral immunity against SARS-CoV-2 may not be long lasting in persons with mild illness, who compose the majority of persons with Covid-19. It is difficult to extrapolate beyond our observation period of approximately 90 days because it is likely that the decay will decelerate. 3 Still, the results call for caution regarding antibody-based “immunity passports,” herd immunity, and perhaps vaccine durability, especially in light of short-lived immunity against common human coronaviruses. Further studies will be needed to define a quantitative protection threshold and rate of decline of antiviral antibodies beyond 90 days.
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            Performance Characteristics of the Abbott Architect SARS-CoV-2 IgG Assay and Seroprevalence in Boise, Idaho

            Coronavirus disease 2019 (COVID-19), the novel respiratory illness caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is associated with severe morbidity and mortality. The rollout of diagnostic testing in the United States was slow, leading to numerous cases that were not tested for SARS-CoV-2 in February and March 2020 and necessitating the use of serological testing to determine past infections. Here, we evaluated the Abbott SARS-CoV-2 IgG test for detection of anti-SARS-CoV-2 IgG antibodies by testing 3 distinct patient populations.
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              Seroprevalence of antibodies against SARS-CoV-2 among health care workers in a large Spanish reference hospital

              Health care workers (HCW) are a high-risk population to acquire SARS-CoV-2 infection from patients or other fellow HCW. This study aims at estimating the seroprevalence against SARS-CoV-2 in a random sample of HCW from a large hospital in Spain. Of the 578 participants recruited from 28 March to 9 April 2020, 54 (9.3%, 95% CI: 7.1–12.0) were seropositive for IgM and/or IgG and/or IgA against SARS-CoV-2. The cumulative prevalence of SARS-CoV-2 infection (presence of antibodies or past or current positive rRT-PCR) was 11.2% (65/578, 95% CI: 8.8–14.1). Among those with evidence of past or current infection, 40.0% (26/65) had not been previously diagnosed with COVID-19. Here we report a relatively low seroprevalence of antibodies among HCW at the peak of the COVID-19 epidemic in Spain. A large proportion of HCW with past or present infection had not been previously diagnosed with COVID-19, which calls for active periodic rRT-PCR testing in hospital settings.
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                Author and article information

                Journal
                Infect Control Hosp Epidemiol
                Infect Control Hosp Epidemiol
                ICE
                Infection Control and Hospital Epidemiology
                Cambridge University Press (New York, USA )
                0899-823X
                1559-6834
                26 October 2020
                : 1-4
                Affiliations
                [1 ]Research Institute, Bassett Medical Center , Cooperstown, New York
                [2 ]Northeast Center for Occupational Health and Safety, Bassett Medical Center , Cooperstown, New York
                Author notes
                Author for correspondence: Wendy M. Brunner, E-mail: wendy.brunner@ 123456bassett.org
                Author information
                https://orcid.org/0000-0002-1866-7925
                Article
                S0899823X20012969
                10.1017/ice.2020.1296
                7684202
                33100252
                9e594ad2-c1a1-4c82-b615-0159b30510df
                © The Society for Healthcare Epidemiology of America 2020

                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 work is properly cited.

                History
                : 08 October 2020
                : 14 October 2020
                : 18 October 2020
                Page count
                Tables: 1, References: 10, Pages: 4
                Categories
                Letter to the Editor

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