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      COVID-19 and health care worker exposure at Chris Hani Baragwanath Academic Hospital

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            Abstract

            Background: Health care workers (HCWs) are at increased risk of coronavirus disease 2019 (COVID-19). Appropriate risk assessments and testing are essential to reduce transmission and avoid workforce depletion.

            Objective: To investigate the risk of COVID-19 infection among HCWs who fulfil the person under investigation case definition or had exposure to a confirmed COVID-19 contact.

            Methods: We conducted a retrospective review of HCWs who were exposed to and/or tested for COVID-19 during the first wave of the pandemic. Data collected included demographics, exposure type, risk level, and COVID-19 test result. Frequency distribution tables, bivariate analyses, univariate and multivariate analyses were conducted.

            Results: Among the 1111 HCWs reviewed, 643 were tested with 35.6% positive results. PUI's accounted for 62.4% of positive cases. Symptomatic HCWs with no known contact were at a greater risk of infection than those with a patient exposure (p═0.001). The risk of testing positive was higher after a patient exposure (p═0.000) compared to a co-worker contact. Patient-facing designations had a higher risk of SARS-CoV-2 infection than non-clinical designations (p═0.013). The exception to this was security personnel who were 28 times more likely to test positive than any other designation (p═0.000).

            Conclusion: There is a higher positivity rate among HCWs than the general population. The presence of symptoms warrants testing. Nosocomial transmission was derived from patients more than co-worker contacts. Precautions in the workplace need to be reinforced to protect the health and safety of HCWs during this pandemic. These findings should assist with preparedness for future pandemics.

            Main article text

            Introduction

            Coronavirus disease 2019 (COVID-19) is caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The World Health Organization (WHO) declared the COVID-19 outbreak as a global public health emergency on 30 January 2020.(1) South Africa's first case was reported on 5 March 2020 and as of 18th September 2022, there were 4 014 442 positive cases and 102 146 deaths reported in South Africa.(2)

            Healthcare workers (HCW) are at an increased risk of acquiring SARS-CoV-2 infection compared to the general population. International data has shown the estimated prevalence of SARS-CoV-2 in HCWs to be 11%.(3) In the UK and the USA, HCWs had up to a 12 fold increased risk of COVID-19 infection compared to the general population (4) and in Scotland, patient-facing HCWs were at a threefold increased risk of hospital admission from COVID-19.(5) The National Institute of Communicable Diseases (NICD) hospital surveillance survey from January 2021, reported that 3.5% of hospital admissions in South Africa were HCWs and 11.2% of them died.(6) It is critical to implement precautions and procedures in the workplace to protect the health and safety of HCWs during this pandemic.

            Furthermore, nosocomial transmission of COVID-19 is a major concern as an amplifier of local transmission. Reports from different countries worldwide, including China,(7) the United Kingdom,(8,9) and the USA,(10) have shown a rapid spread of COVID-19 through health care facilities. In the first wave, a nosocomial outbreak of COVID-19 in Durban, South Africa highlighted these concerns where a single COVID-19 positive patient resulted in 119 confirmed COVID-19 cases, and of these cases, 80 were staff members.(11) Transmission occurs via aerosols that are inhaled or droplets that contain the virus and come into direct contact with mucous membranes.(12,13)

            SARS-CoV-2 has placed unprecedented stress on health care systems worldwide. Chris Hani Baragwanath Academic Hospital (CHBAH) is the third-largest hospital in the world with approximately three thousand two hundred beds (14) and an average nurse to patient ratio of 3:31.(15) Before COVID-19, staff shortages were already a challenge and with quarantine periods and HCWs absent due to illness, ensuring adequate staffing was a major obstacle. The staffing crisis necessitated doctors and nurses from all departments such as Dermatology, Surgery, and Orthopaedics to curtail their usual duties and assist caring for SARS-CoV-2 infected patients and staff. Staff across CHBAH were required to comply with the hospital's Personal Protective Equipment (PPE) policy: (i) cloth masks for all non-clinical staff, (ii) face shield, medical mask, gown and gloves for all clinical staff, (iii) addition of N95 mask for staff performing aerosol-generating procedures.

            While underuse of appropriate risk assessments and testing will result in rapid spread amongst HCWs and patients, overzealous quarantine or under-testing of exposed HCWs may result in unnecessary and unaffordable depletion of an already strained workforce.(16) In order to optimise health care services and protect HCWs during this pandemic, clear guidelines are required to determine if/when an exposed or symptomatic HCWs should be tested and/or self-isolate or continue to work. The Centres for Disease Control and Prevention (CDC) (17) and WHO (18) have published guidelines for the risk assessment and management of exposed and symptomatic HCWs. Based on these guidelines, the South African Department of Health (DOH) has issued guidelines relevant to the South African setting.(19) A questionnaire entitled “risk assessment questionnaire” (RAQ) was used by the CHBAH Occupational Health and Safety (OHS) department to collect relevant information in order to categorise HCWs into high-risk exposure (HRE), low-risk exposure (LRE), or person under investigation (PUI) groups and thereby direct management according to the aforementioned guidelines.

            There is emerging data internationally evaluating risk assessment and testing procedures for HCWs,(20) however, local data is lacking. We undertook to assess the risk of COVID-19 among HCWs at CHBAH who fulfil the COVID-19 PUI case definition or had exposure to a confirmed COVID-19 contact.

            Methods

            Study sampling and study population

            This is a retrospective review of the RAQs of HCWs that were exposed to and/or tested for COVID-19 by the CHBAH OHS department. RAQs over two months, from 1st May 2020 to 1st July 2020 were reviewed. This period was during the first wave of the COVID-19 pandemic and contained an adequate sample size of ═ 1000 RAQs.

            The study population included asymptomatic HCWs exposed to a confirmed positive case and symptomatic HCWs who met the criteria of the PUI definition.

            Risk assessment of HCWs

            A HRE was defined as exposure within one meter to a confirmed COVID-19 case that lasts for more than fifteen minutes without appropriate PPE or failure of PPE and/or direct contact with respiratory secretions.(19) A LRE was defined as an exposure more than one meter away from a COVID-19 confirmed case OR for less than fifteen minutes OR within one meter but wearing appropriate PPE.(19) A PUI was defined as a person with acute respiratory illness with sudden onset (less than or equal to fourteen days) of at least one of the following: a cough, sore throat, shortness of breath, or anosmia/dysgeusia with or without other symptoms.(21) HCWs were managed as per the NICD and South African DOH guidelines. COVID-19 polymerase chain reaction (PCR) tests were done on all PUIs, all HRE on day eight post-exposure to assess early return to work, and HCWs in the LRE group that became symptomatic. HCWs in the PUI and HRE groups were required to self-isolate while HCWs in the LRE group were able to return to work and monitor for symptoms for fourteen days post-exposure.

            Inclusion criteria

            All staff working at CHBAH regardless of designation (including allied staff, security, and cleaning personnel) were included as HCWs. Staff not directly employed by CHBAH, such as medical students and non-­governmental organisation (NGO) staff were excluded as they were not required to report symptoms or exposure to CHBAH OHS but to their respective institutions. RAQs lacking risk category assessment were excluded.

            Statistical analysis

            Each patient received a study number, which was different from the identifiable hospital number. The study number was kept separately from the patient identification data set. Data was entered into an excel spreadsheet.

            The following data was included: age, gender, designation, department, exposure type, risk level, and HCW COVID-19 test result (if tested). Only doctors and nurses were analysed with regard to “department” as other HCWs work in multiple areas.

            Frequency distribution tables showing percentages and numbers were used to describe the categorical variables of age, gender, designation, department, and exposure type. Frequency distribution tables were also used to describe categorical variables with the test result (COVID positive and COVID negative result). Bivariate analyses were conducted using Pearson's Chi-square tests. The univariate and multivariable logistic regression procedure was used to determine the factors associated with positivity. Stata Inc® software version 16 was used and a p-value of less than 0.05 was considered significant. This study was approved by the Human Research Ethics Committee (Medical) of the University of the Witwatersrand.

            Results

            Demographic data

            The sociodemographic characteristics of the 1111 HCWs are presented in Table 1. There was a female predominance (81.4%) and most of the HCWs were in the 30–39 age category (38.6%). The HCWs comprised mostly of nurses (48.5%) and doctors (27.0%). Most HCWs were from Internal Medicine (33.4%) and Obstetrics & Gynaecology (25.4%), followed by Surgery (18.9%) and Paediatrics (12.7%). Reported occupational exposures accounted for 88.8% of exposures, with 49.2% due to co-worker exposure and 39.6% due to patient exposure. Only 1.4% of HCW exposure was due to community exposure (family & travel) and 9.8% of HCWs had no known exposure. More than half of the HCWs (57.9%) met the criteria for testing for SARS-CoV-2.

            Table 1:

            Sociodemographic characteristics of HCWs

            VariablesFrequency (n) n═1111Percent (%)
            Age (in years)
            <3022019.8
            30–3942938.6
            40–4927124.4
            50–6016514.8
            >60262.3
            Gender
            Female90481.4
            Male20718.6
            Designation
            Allied1019.1
            Cleaner363.2
            Doctor30027.0
            Nurse53948.5
            Pharmacist10.09
            Radiographer121.1
            Support & Logistics1029.2
            Security201.8
            Departmentn═839*
            Anaesthesiology101.2
            Emergency354.2
            Internal Medicine28033.4
            Obstetrics & Gynaecology21325.4
            Paediatrics10712.7
            Psychiatry253.0
            Radiology101.2
            Surgery15918.9
            Exposure type
            Co-worker54749.2
            Family141.3
            No known contact1099.8
            Patient44039.6
            Travel10.1
            Tested for SARS-CoV-2
            Yes64357.9
            No46842.1

            *Only Doctors and Nurses included in Department

            All data expressed as frequencies and percentages

            Risk level and COVID-19 test results

            Only 19.0% met the criteria for HRE, whilst 51.1% for LRE and 29.9% fulfilled the definition of a PUI. The positivity rate in the PUI and HRE groups was 43.1% and 25.6% respectively. In the LRE group, 83.1% of HCWs were not tested as they did not fulfil criteria for testing. However, 17.0% of LRE HCWs became symptomatic within 14 days post-exposure and were tested. Of the HCWs in the LRE group that were tested, 32.0% were positive (Table 2). A significant association between test result and risk level was noted (p═0.001).

            Table 2:

            SARS-CoV-2 result and risk level

            VariablesPUI n═332 n (%)HRE n═211 n (%)LRE n═100ϯ n (%)Total n═643 n (%)p-value
            SARS-CoV-2 result
            Positive143 (43.1)54 (25.6)32 (32.0)229 (35.6)0.0001
            Negative189 (56.9)157 (74.4)68 (68.0)414 (64.4)

            *PUI═person under investigation HRE═high risk exposure LRE═low risk exposure

            ϯBecame symptomatic and therefore tested

            Factors associated with increased risk of COVID-19 infection

            A total of 643 participants were tested with 35.6% positive results (Table 3). More than half the HCWs were nurses (53.7%) followed by doctors (24.9%). Staff in the departments of Internal Medicine (38.3%) and Obstetrics & Gynaecology (17.2%) accounted for most of the positive cases followed by staff in the departments of Paediatrics (14.4%) and Surgery (13.9%). Patient contact was reported in 42.4%, followed by co-worker contact (28.4%), no known contact (25.3%), and a family contact (3.9%). The PUI group accounted for 62.4% of the positive cases followed by 23.6% in the HRE group and 14.0% were from the LRE group that became symptomatic and were therefore tested. A significant association was noted between age (p═0.0201), department (p═0.0001), designation (p═0.0001), exposure type (p═0.0001), risk level (p<0.0001) and a positive test result. There was no significant association between gender (p═0.9621) and test result.

            Table 3:

            Distribution of HCW demographics and COVID-19 test result

            VariablesCOVID-19 Positive n═229 n (%)COVID-19 Negative n═414 n (%)p-value
            Age (in years)
            <3026 (11.4)91 (22.0)0.0201
            30–3991 (39.7)152 (36.7)
            40–4965 (28.4)99 (23.9)
            50–6040 (17.5)59 (14.3)
            >607 (3.1)13 (2.0)
            Gender
            Female184 (80.3)332 (80.2)0.9621
            Male45 (19.7)82 (19.8)
            Designation
            Allied16 (7.0)40 (9.7)0.0001
            Cleaner6 (2.6)18 (4.3)
            Doctor57 (24.9)95 (22.9)
            Nurse123 (53.7)213 (51.4)
            Pharmacist0 (0)1 (0.2)
            Radiographer1 (0.4)0 (0)
            Support & Logistics12 (5.2)45 (10.9)
            Security14 (6.1)2 (0.5)
            Department
            Anaesthesiology10 (5.6)0 (0)0.0001
            Emergency6 (3.3)14 (4.5)
            Internal Medicine69 (38.3)122 (39.6)
            Obstetrics & Gynaecology31 (17.2)89 (28.9)
            Paediatrics26 (14.4)28 (9.1)
            Psychiatry12 (6.7)10 (3.2)
            Radiology1 (0.6)0 (0)
            Surgery25 (13.9)45 (14.6)
            Exposure type
            Co-worker65 (28.4)226 (54.6)<0.0001
            Family9 (3.9)5 (1.2)
            No known contact58 (25.3)32 (7.7)
            Patient97 (42.4)151 (36.5)
            Travel0 (0)0 (0)
            Risk level
            PUI143 (62.4)189 (45.7)0.0001
            HRE54 (23.6)157 (37.9)
            LRE32 (14.0)68 (16.4)

            *Only Doctors and Nurses included in Department

            ϯPUI═person under investigation HRE═high risk exposure LRE═low risk exposure

            In a univariate analysis (Table 4) the age groups from 30 to 60 years were at a higher risk of COVID-19 infection, with the highest risk in the 50–60 year age group (p═0.004). Security personnel were more likely to test positive than nurses (p═0.001) while support and logistics staff were less likely to test positive than nurses (p═0.025). The wide confidence interval seen in the security group can be explained by the small sample size. There was no significant difference between nurses’ and doctors’ positivity rates (p═0.850). HCWs in Obstetrics and Gynaecology were less likely to test positive than HCWs in Paediatrics (p═0.004). Symptomatic HCWs who reported no known exposure to COVID-19 were more likely to have a positive COVID-19 test result than those who reported an occupational exposure to a COVID-19 positive patient contact (p═0.000). In terms of occupational exposure, the risk of testing positive for COVID-19 was less after exposure to a co-worker contact as compared to a patient contact (p═0.000). PUIs were more likely to test COVID-19 positive than LREs that became symptomatic (p═0.049).

            Table 4:

            Univariate analysis of sociodemographic characteristics and COVID-19 test result

            COVID-19 Positive
            VariableAOR95%CIp-value
            Age (years)
            <301
            30–392.091.26–3.480.004
            40–492.291.35–3.920.002
            50–602.371.31–4.290.004
            >601.880.68–5.210.222
            Designation
            Nurse1
            Doctor1.030.69–1.540.850
            Allied0.690.37–1.280.246
            Support & Logistics0.460.23–0.900.025
            Cleaner0.570.22–1.490.257
            Security12.122.7–54.20.001
            Department
            Paediatrics1
            Internal Medicine0.610.33–1.120.111
            Surgery0.590.29–1.230.164
            Obstetrics & Gynaecology0.370.19–0.730.004
            Emergency0.460.15–1.370.166
            Psychiatry1.290.47–3.490.613
            Exposure type
            Patient1
            Co-worker0.440.30–0.650.000
            No known exposure2.821.70–4.650.000
            Family2.800.91–8.610.072
            Risk level
            LRE1
            HRE0.730.43–1.230.239
            PUI1.611.00–2.580.049

            *Only Doctors and Nurses included in Department

            ϯPUI═person under investigation HRE═high risk exposure LRE═low risk exposure

            In light of other factors, the adjusted multivariate analysis (Table 5) showed a lower odds of COVID-19 infection in the HRE group as compared to the LRE that became symptomatic (AOR═0.54; 95%CI:0.30–0.99; p═0.049). The odds of COVID-19 infection was higher in age groups 30–39 years (AOR═2.94; 95%CI:1.61–5.35; p═0.000), 40–49 years (AOR═2.75; 95%CI:1.46–5.18; p═0.002) and 50–60 years (AOR═2.161; 95%CI:1.31–5.23; p═0.007) as compared to < 30 years. Symptomatic HCWs with no known exposure were at a greater odds of infection than those with an occupational patient exposure (AOR═2.58; 95%CI:1.45–4.60; p═0.001) and an increased risk of infection was seen with a family exposure as compared to occupational exposure (AOR═3.54; 95%CI:0.97–12.88; p═0.055). Staff working in security were more likely to test COVID-19 positive than nurses (AOR═28.27; 95%CI:5.67–140.93; p═0.000) whilst Support and logistics were less likely (AOR═0.36; 95%CI:0.16–0.80; P═0.013).

            Table 5:

            Multivariate analysis of sociodemographic characteristics and COVID-19 test result

            COVID-19 Positive
            VariableAOR95%CIp-value
            Risk level
            LRE1
            HRE0.540.30–0.990.049
            PUI1.430.84–2.470.186
            Age
            <301
            30–392.941.61–5.350.000
            40–492.751.46–5.180.002
            50–602.611.31–5.230.007
            Exposure type
            Patient1
            Co-worker0.360.23–0.540.000
            No known contact2.581.45–4.600.001
            Family3.540.97–12.880.055
            Department
            Paediatrics1
            Internal Medicine0.570.43–0.970.037
            Surgery0.530.27–1.050.067
            Obstetrics & Gynaecology0.580.31–1.070.081
            Designation
            Nurse1
            Security28.275.67–140.930.000
            Support & Logistics0.360.16–0.800.013
            Allied0.470.19–1.120.088

            *PUI═person under investigation HRE═high risk exposure LRE═low risk exposure

            Discussion

            The WHO declared the COVID-19 outbreak as a global public health emergency on 30 January 2020.(1) HCWs are the frontline response to the COVID-19 pandemic and their occupational health and safety is central to the fight against the outbreak and maintenance of the health workforce. There is increasing evidence showing that HCWs are at a greater risk of SARS-CoV-2 infection than the general population.(3) Our findings show a higher positivity rate of SARS-CoV-2 infection in HCWs (35.6%) compared with the NICD data from the general population in South Africa reported at this time showing a positivity rate of up to 7.5% (22) although different testing strategies may contribute to this discrepancy.

            The majority of HCWs were female (82.7%) however, there was no significant association between gender and COVID-19 result. This concurs with a seroprevalence study in healthy South African blood donors which showed no gender predilection (23) and in the UK and USA where risk estimates of COVID-19 were similar between male and female HCWs.(4) Our results likely reflect the demographics of HCWs employed at CHBAH as well as the superior healthcare-seeking behaviour seen in females.(24)

            We found that HCWs between 50 and 60 years were the most likely age group to test COVID-19 positive. As age is a risk factor for severe disease,(25) HCWs in older age groups should be particularly vigilant with infection prevention control (IPC) protocols and correct PPE. Our findings are in contrast to HCWs in Switzerland where being older than 50 years was associated with a lower seroprevalence. This difference may be explained by age-related declines in humoral immunity affecting the seropositivity versus PCR tests in our study which will not be affected by this.(20)

            Health care worker designation is a significant predictor of COVID-19 positivity in our study as well as other studies in Denmark,(26) Switzerland,(20) Scotland,(5) Ghana,(27) and Cape Town, South Africa.(28) These studies all show that patient-facing designations such as nurses have a higher risk of SARS-CoV-2 infection than non-­patient facing, non-clinical designations such as support & logistics. Furthermore, HCW COVID-19 infections were more likely as a result of a patient contact than a co-worker contact. These findings suggest nosocomial transmission, particularly from patients, to be the major source of COVID-19 infections in HCWs.

            Of particular significance in our study, however, is that security personnel were almost thirty times more likely to test COVID-19 positive than any other designation. Security personnel wear standard PPE (cloth or surgical masks only) compared to clinical staff that were required to wear a face shield and a surgical or N95 mask; are required to check bags and vehicles of all people entering and exiting the hospital; and are in close proximity to those on their shift, HCWs, and patients. Moreover, security personnel may be less aware of the risks of severe COVID-19 infection and this may influence their stringency to follow personal protective measures. These factors likely contributed to this high positivity rate and highlight the necessity of adequate PPE, IPC protocols, and training for all HCWs regardless of designation to reduce transmission.

            HCWs in Internal Medicine showed the highest rates of COVID-19 positive results, however, a multivariate analysis showed that HCWs in Paediatrics had the highest risk of COVID-19 infection. Initial studies have shown that children are less likely to be infected by and transmit SARS-CoV-2 (29) and this may have led to complacency in protective measures in paediatric staff. The nature of the close patient and parent contact in this department and the paucity of symptoms often shown in paediatric populations may further contribute to increase in transmission risk. There is growing data to suggest that Paediatric HCWs are at a greater risk of COVID-19 infection than initially presumed.(30,31)

            One of the strongest predictors of SARS-CoV-2 infection in HCWs is “symptoms”. The risk of COVID-19 was higher in HCWs who were symptomatic but had no known exposure than HCWs exposed to a patient contact. Almost two-thirds of the COVID-19 positive HCWs in our study were in the PUI risk level and symptoms were a stronger predictor of SARS-CoV-2 infection than a positive HRE history. These findings are supported by a meta-analysis showing that symptoms were significantly associated with SARS-CoV-2 infection in HCWs.(3)

            With the rollout of vaccinations in South Africa, HCWs may feel influenced to be less stringent with PPE when treating patients with COVID-19. However, COVID-19 infection is still possible post-vaccination. In Israel, 22 of 4081 (0.54%) HCWs developed COVID-19 within 10 days post-vaccination.(32) Our study highlights the importance of continuously monitoring for symptoms, even post-vaccination.

            There are some limitations to this study. This study was a retrospective review and testing was done only on HCWs who fulfilled criteria based on the South African DOH guidelines. Therefore the true prevalence of asymptomatic infection in LREs was not able to be determined. This testing strategy may have been influenced by resource constraints at the time and limited access to testing. The HCW screening algorithm relied on self-reporting and HCWs might have had a recall bias. A small sample size was noted in certain designations such as security personnel and we recommend future studies to look further into these subgroups. There may be selection bias in this study as it was performed at the start of the pandemic and therefore may not be representative of infection rates later on in the pandemic.

            Conclusion

            Our results show a higher positivity rate of HCWs compared to the general population. Nosocomial transmission was derived from patients more than co-workers and therefore strict PPE and IPC protocols should be adhered to. Symptoms were one of the greatest predictors of infection irrespective of exposure history. Our findings support the amended guidelines where the presence of symptoms is the most important indicator for testing and isolation. Evidence-based HCW screening protocols are required to ensure HCW safety and at the same time adequate staffing. The findings of this study are important in ensuring preparedness of HCWs for future pandemics.

            References

            1. World Health Organization. COVID-19 public health emergency of international concern. [Accessed January 16, 2022]. Available from: https://www.who.int/publications/m/item/covid-19-public-health-emergency-of-international-­concern-(pheic)-global-research-and-innovation-forum#:~:text=On%2030%20January%202020%20following,of%20International%20Concern%20(PHEIC).

            2. Department of Health. COVID-19 online resource and news portal. [Accessed January 18, 2022]. Available from: https://sacoronavirus.co.za.

            3. Gomez-OchoaSA, FrancoOH, RojasLZ, et al. COVID-19 in health-care workers: a living systematic review and meta-analysis of prevalence, risk factors, clinical characteristics, and outcomes. Am J Epidemiol. 2021;190(1):161–175.

            4. NguyenLH, DrewDA, GrahamMS, et al. Risk of COVID-19 among front-line health-care workers and the general community: a prospective cohort study. Lancet Public Health. 2020;5(9):e475–e83.

            5. ShahASV, WoodR, GribbenC, et al. Risk of hospital admission with coronavirus disease 2019 in healthcare workers and their households: nationwide linkage cohort study. BMJ. 2020;371:m3582.

            6. National Institute For Communicable Diseases. COVID-19 sentinel hospital surveillance weekly update on hospitalized HCWs update: week 19, 2021. [Accessed August 3, 2021]. Available from: https://www.nioh.ac.za/wp-content/uploads/2021/05/COVIDHCWReportWeek19of2021-24-May-2021Final.pdf.

            7. WangX, ZhouQ, HeY, et al. Nosocomial outbreak of COVID-19 pneumonia in Wuhan, China. Eur Respir J. 2020;55(6).

            8. JewkesSV, ZhangY, NichollDJ. Nosocomial spread of COVID-19: lessons learned from an audit on a stroke/neurology ward in a UK district general hospital. Clin Med (Lond). 2020;20(5):e173–e177.

            9. RickmanHM, RamplingT, ShawK, et al. Nosocomial transmission of coronavirus disease 2019: a retrospective study of 66 hospital-acquired cases in a London Teaching Hospital. Clin Infect Dis. 2021;72(4):690–693.

            10. AronsMM, HatfieldKM, ReddySC, et al. Presymptomatic SARS-CoV-2 infections and transmission in a skilled nursing facility. N Engl J Med. 2020;382(22):2081–2090.

            11. LesselsR, MoosaY, de OliveiraT. Report into a nosocomial outbreak of coronavirus disease 2019 (COVID-19) at Netcare St. Augustine's Hospital. [Accessed January 16, 2022]. Available from: https://www.krisp.org.za/news.php?id=421.

            12. KatelarisAL, WellsJ, ClarkP, et al. Epidemiologic evidence for airborne transmission of SARS-CoV-2 during church singing, Australia, 2020. Emerg Infect Dis. 2021;27(6):1677–1680.

            13. World Health Organization. Coronavirus disease (COVID-19): how is it transmitted? [Accessed July 30, 2021]. Available from: https://www.who.int/emergencies/diseases/­novel-coronavirus-2019/question-and-answers-hub/q-a-detail/coronavirus-disease-covid-19-how-is-it-transmitted.

            14. Chris Hani Baragwanath Hospital. General information. [Accessed June 7, 2020]. Available from: https://www.­chrishanibaragwanathhospital.co.za/.

            15. News24. Chris Hani Baragwanath Hospital has lowest staff attendance among Gauteng's largest hospitals. [Accessed June 18, 2020]. Available from: https://www.news24.com/news24/southafrica/news/p2-chris-hani-baragwanath-­hospital-has-lowest-staff-attendance-among-gautengs-largest-hospitals-da-20200202.

            16. AgiusR. COVID-19 and health at work. Occup Med (Lond). 2020.

            17. Centers for Disease Control and Prevention. Interim clinical guidance for management of patients with confirmed coronavirus disease (COVID-19). [Accessed December 31, 2021]. Available from: https://www.cdc.gov/­coronavirus/2019-ncov/hcp/return-to-work.html.

            18. World Health Organization. Risk assessment and management of exposure of health care workers in the context of COVID-19. [Accessed June 7, 2020]. Available from: https://apps.who.int/iris/handle/10665/331496.

            19. Department of Health Republic of South Africa. Guidelines for symptom monitoring and management of essential workers for COVID-19 related infection. [Accessed June 7, 2020]. Available from:.

            20. PiccoliaL, FerrariP, PiumattieG, et al. Risk assessment and seroprevalence of SARS-CoV-2 infection in healthcare workers of COVID-19 and non-COVID-19 hospitals in Southern Switzerland. Lancet Reg Health Eur. 2020.

            21. Department of Health and National Institute of Communicable Disease. Clinical management of suspected or confirmed COVID-19 disease. [Accessed June 7, 2020]. Available from: https://www.nicd.ac.za/wp-content/uploads/2020/05/Clinical-management-of-suspected-or-confirmed-COVID-19-Version-4.pdf.

            22. National Institute For Communicable Diseases. COVID-19 testing summary: week 21 2020. [Accessed July 5, 2021]. Available from: https://www.nicd.ac.za/wp-content/uploads/2020/05/NICD-COVID-19-Testing-SummaryWeek-21-2020-007.pdf.

            23. SykesW, MhlangaL, SwanevelderR, et al. Prevalence of anti-SARS-CoV-2 antibodies among blood donors in Northern Cape, KwaZulu-Natal, Eastern Cape, and Free State provinces of South Africa in January 2021. Res Sq. 2021.

            24. ThompsonAE, AnisimowiczY, MiedemaB, et al. The influence of gender and other patient characteristics on health care-seeking behaviour: a QUALICOPC study. BMC Fam Pract. 2016;17:38.

            25. BahardoustM, HeiatM, KhodabandehM, et al. Predictors for the severe coronavirus disease 2019 (COVID-19) infection in patients with underlying liver disease: a retrospective analytical study in Iran. Sci Rep. 2021;11(1):3066.

            26. IversenK, BundgaardH, HasselbalchRB, et al. Risk of COVID-19 in health-care workers in Denmark: an observational cohort study. Lancet Infect Dis. 2020;20(12):1401–1408.

            27. AshinyoME, DubikSD, DutiV, et al. Healthcare workers exposure risk assessment: a survey among frontline workers in designated COVID-19 treatment centers in Ghana. J Prim Care Community Health. 2020;11:2150132720969483.

            28. ReesK, DunlopJL, Patel-AbrahamsS, StruthersH, McIntyreJA. Primary healthcare workers at risk during COVID-19: an analysis of infections in HIV service providers in five districts of South Africa. S Afr Med J. 2021;111(4):309–314.

            29. LiQ, GuanX, WuP, et al. Early transmission dynamics in Wuhan, China, of novel coronavirus-infected pneumonia. N Engl J Med. 2020;382(13):1199–1207.

            30. MorrisCR, SullivanP, MantusG, et al. Prevalence of SARS-CoV-2 antibodies in pediatric healthcare workers. Int J Infect Dis. 2021;105:474–481.

            31. DevrimI, BayramN. Infection control practices in children during COVID-19 pandemic: differences from adults. Am J Infect Control. 2020;48(8):933–939.

            32. AmitS, BeniSA, BiberA, et al. Postvaccination COVID-19 among healthcare workers, Israel. Emerg Infect Dis. 2021;27(4):1220–1222.

            Author and article information

            Journal
            WUP
            Wits Journal of Clinical Medicine
            Wits University Press (5th Floor University Corner, Braamfontein, 2050, Johannesburg, South Africa )
            2618-0189
            2618-0197
            July 2023
            : 5
            : 2
            : 97-104
            Affiliations
            [1 ]Division of Dermatology, Chris Hani Baragwanath Academic Hospital, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa
            [2 ]Department of Internal Medicine, Chris Hani Baragwanath Academic Hospital, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa
            [3 ]School of Public Health, University of the Witwatersrand, Johannesburg, South Africa
            Author notes
            [* ] Correspondence to: drsaraglatt@ 123456gmail.com
            Author information
            https://orcid.org/0000-0003-4758-4149
            https://orcid.org/0000-0002-2486-3498
            https://orcid.org/0000-0002-9760-8770
            https://orcid.org/0000-0002-3382-2372
            https://orcid.org/0000-0003-3838-5359
            Article
            WJCM
            10.18772/26180197.2023.v5n2a3
            953e2ebc-d3e9-4b48-b0cb-16ad15fbc9e1
            WITS

            Distributed under the terms of the Creative Commons Attribution Noncommercial NoDerivatives License https://creativecommons.org/licenses/by-nc-nd/4.0/, which permits noncommercial use and distribution in any medium, provided the original author(s) and source are credited, and the original work is not modified.

            History
            Categories
            Research Article

            General medicine,Medicine,Internal medicine
            South Africa,health care worker exposure,health care workers,COVID-19,risk assessment

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