<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">ODEM</journal-id><journal-title-group><journal-title>Occupational Diseases and Environmental Medicine</journal-title></journal-title-group><issn pub-type="epub">2333-3561</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/odem.2021.91003</article-id><article-id pub-id-type="publisher-id">ODEM-107252</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Prevalence and Pattern of COVID-19 among Healthcare Workers in Rivers State Nigeria
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Datonye</surname><given-names>Dennis Alasia</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Omosivie</surname><given-names>Maduka</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Departments of Internal Medicine, University of Port Harcourt, Port Harcourt, Nigeria</addr-line></aff><aff id="aff2"><addr-line>Preventive and Social Medicine, University of Port Harcourt, Port Harcourt, Nigeria</addr-line></aff><pub-date pub-type="epub"><day>07</day><month>01</month><year>2021</year></pub-date><volume>09</volume><issue>01</issue><fpage>20</fpage><lpage>32</lpage><history><date date-type="received"><day>3,</day>	<month>January</month>	<year>2021</year></date><date date-type="rev-recd"><day>19,</day>	<month>February</month>	<year>2021</year>	</date><date date-type="accepted"><day>22,</day>	<month>February</month>	<year>2021</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Introduction: The evaluation of COVID-19 prevalence among healthcare workers (HCW) within the general population of COVID-19 cases is an important epidemiologic variable. The objective of this study is to describe the prevalence and patterns of COVID-19 infection in HCWs amongst a group of patients receiving care for COVID-19 in Rivers state, Nigeria. 
  Methods: This study was a prospective descriptive study of all consenting patients who received care through hospitals, designated for COVID-19 treatment in Rivers state either as in-patient or out-patient following a laboratory-confirmed diagnosis of COVID-19 based on a positive SARS-CoV-2 RT-PCR from April to September 2020. 
  Results: A total number of 646 COVID-19 patients were enrolled over the study period with 98 (15.2%) HCWs in the patient population. The HCWs with COVID-19 consisted largely of Doctors 47 (47.9%), Nurses 30 (30.6%), and socio-sanitary and hygiene workers 10 (10.2%). There were 46 (46.9%) female HCWs, compared to Non-HCWs with 112 (21.1%), females, p = 0.000. Sixty-eight (69.4%) HCWs had a source of contact for infection established compared to Non-HCWs with an established source of contact in 181 (34.2%), p = 0.000. Eight (8.2%) HCWs had Severe disease compared to 52 (9.8%) Non-HCWs with severe disease, p = 0.670. The case fatality in HCWs was 1% compared to 1.9% in Non-HCWs, p = 0.554. 
  Conclusion: The prevalence of COVID-19 among HCWs in the study location is high with clinical and clinical support staff particularly, doctors and nurses are at higher risk of COVID-19 infection. This calls for action to improve and prevent HCWs infections in hospital settings in addition to improving HCW infection prevention behaviour in the community. The intensification of risk communication, provision of protective equipment (PPE), and training on the appropriate use of PPE; in addition to routine surveillance for infection is recommended.
 
</p></abstract><kwd-group><kwd>SARS-CoV-2 Infection</kwd><kwd> COVID-19</kwd><kwd> Prevalence</kwd><kwd> Healthcare Workers</kwd><kwd> Nigeria</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>The response to the COVID-19 pandemic as declared by the World Health Organisation (WHO) in March 2020 [<xref ref-type="bibr" rid="scirp.107252-ref1">1</xref>], elevated global cognizance of the role of healthcare workers as a critical resource for the world. This acknowledgement was accentuated as healthcare workers (HCWs) became frontline combatants across all pillars of the COVID-19 response with the attendant risk of infection. Healthcare worker infection, therefore, became an issue of concern in the early period of the pandemic response with documentation of alarming rates of HCW infections [<xref ref-type="bibr" rid="scirp.107252-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref3">3</xref>]. A report from the WHO joint mission to China in February 2020 reported 2055 COVID-19 laboratory-confirmed cases of HCW healthcare infections in 476 hospitals across China [<xref ref-type="bibr" rid="scirp.107252-ref2">2</xref>]. Correspondingly Wang et al. [<xref ref-type="bibr" rid="scirp.107252-ref3">3</xref>], reported that 29% of patients with COVID-19 infection were HCWs from a cohort of 138 patients treated in a hospital in Wuhan. The study [<xref ref-type="bibr" rid="scirp.107252-ref3">3</xref>] also referred to the risk of widespread transmission in healthcare settings as evidenced by a super spreader patient who infected over 10 HCWs in the hospital. Similar observations regarding HCW infections were also noted in Spain as of 31st March 2020 with over 9400 HCWs consisting of approximately 15% of all confirmed cases infected with COVID-19 [<xref ref-type="bibr" rid="scirp.107252-ref4">4</xref>]. The WHO Africa region office also reported that over 10,000 HCWs had been infected with COVID-19 in Africa as of July 2020, with an average rate of 10% of infections in some key countries [<xref ref-type="bibr" rid="scirp.107252-ref5">5</xref>].</p><p>The evaluation of healthcare worker’s prevalence among the general population of COVID-19 cases has therefore become an important variable in the epidemiologic analysis of the pandemic; with studies around the world documenting a range of 3% - 19% prevalence of HCWs among the populations infected with SARS-CoV-2 [<xref ref-type="bibr" rid="scirp.107252-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref9">9</xref>]. Wu et al. [<xref ref-type="bibr" rid="scirp.107252-ref10">10</xref>] in a Chinese centre for disease control (CDC) report, documented that 3.8% of 44,672 cases were healthcare workers; while two studies [<xref ref-type="bibr" rid="scirp.107252-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref12">12</xref>] from Italy reported that HCWs accounted for 9% [<xref ref-type="bibr" rid="scirp.107252-ref11">11</xref>] and 9.8% [<xref ref-type="bibr" rid="scirp.107252-ref12">12</xref>] of cases in March 2020. Elimian et al. [<xref ref-type="bibr" rid="scirp.107252-ref13">13</xref>] in descriptive epidemiology of COVID-19 in Nigeria, found that HCWs accounted for 9.3% of all positive cases. A hospital prevalence study from Qatar [<xref ref-type="bibr" rid="scirp.107252-ref6">6</xref>] reported a prevalence of 10.6% among tested HCWs; whereas the USA CDC [<xref ref-type="bibr" rid="scirp.107252-ref7">7</xref>] reported a 19% prevalence of COVID-19 in HCWs among a population of 49,370 people. In addition to the established higher risk of reporting a positive test for COVID-19 among frontline HCWs compared to the general population [<xref ref-type="bibr" rid="scirp.107252-ref14">14</xref>]; patterns of distinctions in disease demographics and epidemiology, clinical trends and outcomes have also been documented in comparisons of HCWs and the general population with COVID-19 [<xref ref-type="bibr" rid="scirp.107252-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref10">10</xref>]. The evaluation of HCW infections and applicable epidemiologic patterns at subnational and national levels is, therefore, an important research focus; as the consequence of HCWs infection is a depletion in the workforce available to confront the pandemic and increase risk of transmission among other HCWs and patients attending hospitals. These shortages in the health workforce result from self-isolation of health workers for periods of at least two weeks and the time lost to ill health thus imposing an increased workload on available staff. Besides, health workplace safety may also be compromised by the risk of hospital-acquired infections from healthcare workers to patients. The objective of this study is to describe the prevalence and patterns of COVID-19 infection in HCWs amongst a group of patients receiving care for COVID-19 through ambulatory and in-patient hospital services in Rivers state, Nigeria.</p></sec><sec id="s2"><title>2. Methodology</title><sec id="s2_1"><title>2.1. Study Location</title><p>The study was conducted in Rivers State, one of Nigeria’s 36 states located in south-south, Nigeria. The state ranks within the top 7 in the number of COVID-19 cases in the country as stated by the Nigerian Centre for disease control (NCDC) since June 2020 [<xref ref-type="bibr" rid="scirp.107252-ref15">15</xref>].</p></sec><sec id="s2_2"><title>2.2. Study Design, and Population</title><p>This study was a prospective descriptive study of all consenting patients who received care through hospitals, designated for COVID-19 treatment in Rivers state either as in-patient or ambulatory (out-patient) following a laboratory-confirmed diagnosis of COVID-19 based on a positive SARS-CoV-2 RT-PCR after presentation with suggestive symptoms or contact tracing of other patients from April to September 2020. The patients were categorised based on their occupation into Healthcare workers and Non-Healthcare workers. The healthcare workers were classified based on the WHO and International Labour Organisation (ILO) International Standard Classification of occupations (ISCO) [<xref ref-type="bibr" rid="scirp.107252-ref16">16</xref>], and their roles in patient management and healthcare services into six groups. Health Professional (HP) Group 1—Medical and dental doctors; Health Professional (HP) Group 2—Nurses; Health and Health Associate Professional (H &amp; HAP) Group 3—(Pharmacist; Laboratory scientist and technologist, clinical psychologist, social support services and medical records information); Health and Health Associate Professional (H &amp; HAP) Group 4—(Water Sanitation &amp; Hygiene (WASH)/Socio-sanitary/Hygienist, Health attendants, Respiratory and anaesthetic technicians); Health and Health Associate Professional (H &amp; HAP) Group 5—(Public Health officers, epidemiology and disease surveillance officers) and Health Management and Health Support Personnel (HM &amp; HSP) Group 6—(Administrative and support staff and hospital managers).</p></sec><sec id="s2_3"><title>2.3. Data Collection</title><p>A data extraction form built on the open data kit (ODK) tool was used to collect data that was subsequently exported to a Microsoft Excel spreadsheet. Data domains included socio-demography, epidemiology, symptomatology, comorbidity, and disease outcome. Disease severity was classified using Nigerian Centre for disease control National COVID-19 case management guideline parameters [<xref ref-type="bibr" rid="scirp.107252-ref17">17</xref>] as severe and non-severe, with severity defined presence of fever &gt; 38˚C or suspected respiratory infection, plus one of respiratory rate &gt; 30 breaths/min; severe respiratory distress; &gt;SpO<sub>2</sub> ≤ 93% on room air &amp; Presence of co-morbid conditions such as diabetes, asthma, hypertension in adults and cough or difficulty in breathing &amp; at least one of the following central cyanosis or SpO<sub>2</sub> &lt; 92%; severe respiratory distress e.g. grunting breathing, very severe chest in-drawing &amp; signs of pneumonia in children. Disease outcome was classified into discharged and died.</p></sec><sec id="s2_4"><title>2.4. Ethical Considerations</title><p>The Ethical approval was obtained from the Research Ethics Committee of the University of Port Harcourt Teaching Hospital, Rivers state before the commencement of the study. Confidentiality was maintained by the removal of patient identifiers from the dataset and ensuring that only researchers involved in this study had access to the extracted data.</p></sec><sec id="s2_5"><title>2.5. Statistical Analysis</title><p>The data was exported from the Microsoft Excel spreadsheet into IBM Statistical Package for Social Sciences (SPSS) version 23 for the data analysis. The proportion of HCWs among the cohort and the distribution of HCWs by professional category was done using basic descriptive statistics and frequencies. The HCWs were then compared with all adult patients aged over 18 years in the cohort for patterns in epidemiologic and clinical variables using both descriptive and inferential analysis. An independent t-test was used for comparison of means for categorical variables. Qualitative variables were compared for proportions in the occurrence of socio-demographic, epidemiological, and clinical characteristics between HCWs and non HCWs using Pearson chi-square test with mantel Hensel correction with relative risk and odds ratio as appropriate. A two-tailed p-value less than 0.05 was considered statistically significant. The population size for the study was time-bound and dependent on the course of the pandemic. This accounts for limitations arising from the sample size.</p></sec></sec><sec id="s3"><title>3. Results</title><p>A total number of 646 patients were enrolled over the study period with 98 (15.2%) HCWs in the patient population.</p><p>The HCWs consisted largely of HP Group 1—Doctors 47 (47.9%), HP Group 2—Nurses 30 (30.6%), H &amp; HAP Group 3—5 (5.1%), H &amp; HAP Group 4—10 (10.2%), H &amp; HAP Group 5—3 (3.1%), HM &amp; SP Group 6—3 (3.03%). The distribution of HCWs is displayed in <xref ref-type="table" rid="table1">Table 1</xref> and <xref ref-type="fig" rid="fig1">Figure 1</xref>.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Distribution of healthcare workers with COVID-19 by professional grouping</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Health Professional Group</th><th align="center" valign="middle" >Specific Profession</th><th align="center" valign="middle" >N</th><th align="center" valign="middle" >Group total</th><th align="center" valign="middle" >Percentage %</th></tr></thead><tr><td align="center" valign="middle" >Health Professional Group 1</td><td align="center" valign="middle" >Doctors</td><td align="center" valign="middle" >47</td><td align="center" valign="middle" >47</td><td align="center" valign="middle" >47.9</td></tr><tr><td align="center" valign="middle" >Health Professional Group 2</td><td align="center" valign="middle" >Nurses</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >30.6</td></tr><tr><td align="center" valign="middle"  rowspan="2"  >Health &amp; Health Associate Professional Group 3</td><td align="center" valign="middle" >Pharmacist</td><td align="center" valign="middle" >1</td><td align="center" valign="middle"  rowspan="2"  >5</td><td align="center" valign="middle"  rowspan="2"  >5.1</td></tr><tr><td align="center" valign="middle" >Laboratory Science/Technologist</td><td align="center" valign="middle" >4</td></tr><tr><td align="center" valign="middle" >Health &amp; Health Associate Professional Group 4</td><td align="center" valign="middle" >WASH/Sociosanitary &amp; Environmental health officer</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >10.2</td></tr><tr><td align="center" valign="middle" >Health &amp; Health Associate Professional Group 5</td><td align="center" valign="middle" >Public Health Surveillance officers</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >3.1</td></tr><tr><td align="center" valign="middle" >Health Management &amp; Support Professional Group 6</td><td align="center" valign="middle" >Administrative staff</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >3.1</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Total</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >98</td><td align="center" valign="middle" >100%</td></tr></tbody></table></table-wrap><p>Age: The mean age of 98 HCWs was 40.22 &#177; 11.17 compared to 530 patients ≥ 18 years with 39.89 &#177; 11.95, p-value = 0.798 (see <xref ref-type="table" rid="table2">Table 2</xref>).</p><p>The age group distribution of HCWs, with comparison to Non-HCWs, is as displayed in <xref ref-type="table" rid="table2">Table 2</xref>. The majority of the HCWs were in the 31 - 40 (40.8%) and 41 - 50 (23.5%) year age groups, there was no significant difference in comparison with non-healthcare workers p = 0.202, χ<sup>2</sup> = 9.777 (see <xref ref-type="table" rid="table2">Table 2</xref>).</p><p>Gender: There were 52 (53.1%) male HCWs and 46 (46.9%) female HCWs, compared to Non HCWs with 418 (78.9%) males and 112 (21.1%), female proportion, p = 0.000, χ<sup>2</sup> = 29.903.</p><p>The pattern of contact source, comorbidity, disease severity, and outcome variables are presented in <xref ref-type="table" rid="table3">Table 3</xref>. Contact source: 68 (69.4%) HCWs had a source of contact for infection established while a source of contact was unknown for 30 (30.6%) HCWs; compared to Non-HCWs with an established source of contact in 181 (34.2%) and 349 (65.8%) with the source of contact unknown, p = 0.000,</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Age group and gender distribution of healthcare workers compared with non-healthcare workers</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Variable</th><th align="center" valign="middle"  colspan="2"  >Healthcare Workers</th><th align="center" valign="middle"  colspan="2"  >Non-Healthcare Workers</th><th align="center" valign="middle"  rowspan="2"  >χ<sup>2 </sup></th><th align="center" valign="middle"  rowspan="2"  >p value</th></tr></thead><tr><td align="center" valign="middle" >Age Group</td><td align="center" valign="middle" >N</td><td align="center" valign="middle" >%</td><td align="center" valign="middle" >N</td><td align="center" valign="middle" >%</td></tr><tr><td align="center" valign="middle" >18 - 30</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >17.3</td><td align="center" valign="middle" >124</td><td align="center" valign="middle" >23.4</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >31 - 40</td><td align="center" valign="middle" >40</td><td align="center" valign="middle" >40.8</td><td align="center" valign="middle" >173</td><td align="center" valign="middle" >32.6</td><td align="center" valign="middle" >9.777</td><td align="center" valign="middle" >0.202</td></tr><tr><td align="center" valign="middle" >41 - 50</td><td align="center" valign="middle" >23</td><td align="center" valign="middle" >23.5</td><td align="center" valign="middle" >131</td><td align="center" valign="middle" >24.7</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >51 - 60</td><td align="center" valign="middle" >9</td><td align="center" valign="middle" >9.2</td><td align="center" valign="middle" >77</td><td align="center" valign="middle" >14.5</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >61 - 70</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >8.2</td><td align="center" valign="middle" >19</td><td align="center" valign="middle" >3.6</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >&gt;70</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.0</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >1.1</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >98</td><td align="center" valign="middle" >100</td><td align="center" valign="middle" >530</td><td align="center" valign="middle" >99.9</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Mean Age (Years)</td><td align="center" valign="middle"  colspan="2"  >40.22 &#177; 11.168</td><td align="center" valign="middle"  colspan="2"  >39.89 &#177; 11.949</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.798.</td></tr><tr><td align="center" valign="middle" >Gender</td><td align="center" valign="middle" >Male (%)</td><td align="center" valign="middle" >Female N (%)</td><td align="center" valign="middle" >Male N (%)</td><td align="center" valign="middle" >Female N (%)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >53.1%</td><td align="center" valign="middle" >46.9%</td><td align="center" valign="middle" >78.9%</td><td align="center" valign="middle" >21.1%</td><td align="center" valign="middle" >29.903</td><td align="center" valign="middle" >0.000</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> The pattern of comorbidity, disease severity, and outcome variables</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Variable</th><th align="center" valign="middle"  colspan="2"  >Healthcare workers N = 98</th><th align="center" valign="middle"  colspan="2"  >Non-Healthcare workers N = 530</th><th align="center" valign="middle"  rowspan="2"  >χ<sup>2</sup></th><th align="center" valign="middle"  rowspan="2"  >p value</th></tr></thead><tr><td align="center" valign="middle" >Yes (%)</td><td align="center" valign="middle" >No (%)</td><td align="center" valign="middle" >Yes (%)</td><td align="center" valign="middle" >No (%)</td></tr><tr><td align="center" valign="middle" >Contact known</td><td align="center" valign="middle" >69.4</td><td align="center" valign="middle" >30.6</td><td align="center" valign="middle" >34.2</td><td align="center" valign="middle" >65.8</td><td align="center" valign="middle" >43.881</td><td align="center" valign="middle" >0.000</td></tr><tr><td align="center" valign="middle" >Comorbidity</td><td align="center" valign="middle" >33.7</td><td align="center" valign="middle" >66.3</td><td align="center" valign="middle" >33.6</td><td align="center" valign="middle" >66.4</td><td align="center" valign="middle" >0.554</td><td align="center" valign="middle" >0.758</td></tr><tr><td align="center" valign="middle" >Hypertension</td><td align="center" valign="middle" >20.4</td><td align="center" valign="middle" >79.2</td><td align="center" valign="middle" >25.7</td><td align="center" valign="middle" >74.3</td><td align="center" valign="middle" >1.531</td><td align="center" valign="middle" >0.465</td></tr><tr><td align="center" valign="middle" >Diabetes</td><td align="center" valign="middle" >10.2</td><td align="center" valign="middle" >89.8</td><td align="center" valign="middle" >7.74</td><td align="center" valign="middle" >92.3</td><td align="center" valign="middle" >1.072</td><td align="center" valign="middle" >0.585</td></tr><tr><td align="center" valign="middle" >Asthma</td><td align="center" valign="middle" >2.0</td><td align="center" valign="middle" >98.0</td><td align="center" valign="middle" >0.9</td><td align="center" valign="middle" >99.1</td><td align="center" valign="middle" >1.282</td><td align="center" valign="middle" >0.525</td></tr><tr><td align="center" valign="middle" >Heart disease</td><td align="center" valign="middle" >2.0</td><td align="center" valign="middle" >98.0</td><td align="center" valign="middle" >0.8</td><td align="center" valign="middle" >99.2</td><td align="center" valign="middle" >0.444</td><td align="center" valign="middle" >0.801</td></tr><tr><td align="center" valign="middle" >Kidney Disease</td><td align="center" valign="middle" >1.0</td><td align="center" valign="middle" >97.0</td><td align="center" valign="middle" >0.6</td><td align="center" valign="middle" >99.4</td><td align="center" valign="middle" >0.643</td><td align="center" valign="middle" >0.725</td></tr><tr><td align="center" valign="middle" >HIV/AID</td><td align="center" valign="middle" >0.0</td><td align="center" valign="middle" >100.0</td><td align="center" valign="middle" >0.4</td><td align="center" valign="middle" >99.6</td><td align="center" valign="middle" >0.737</td><td align="center" valign="middle" >0.692</td></tr><tr><td align="center" valign="middle" >COPD</td><td align="center" valign="middle" >0.0</td><td align="center" valign="middle" >100.0</td><td align="center" valign="middle" >0.4</td><td align="center" valign="middle" >99.6</td><td align="center" valign="middle" >2.554</td><td align="center" valign="middle" >0.466</td></tr><tr><td align="center" valign="middle" >Severe disease</td><td align="center" valign="middle" >8.2</td><td align="center" valign="middle" >91.8</td><td align="center" valign="middle" >9.8</td><td align="center" valign="middle" >91.2</td><td align="center" valign="middle" >0.670</td><td align="center" valign="middle" >0.802</td></tr><tr><td align="center" valign="middle" >Death</td><td align="center" valign="middle" >1.0</td><td align="center" valign="middle" >99.0</td><td align="center" valign="middle" >1.9</td><td align="center" valign="middle" >98.1</td><td align="center" valign="middle" >1.179</td><td align="center" valign="middle" >0.554</td></tr></tbody></table></table-wrap><p>χ<sup>2</sup> = 43.881, odds ratio = 4.43, CI = 2.378 - 7.061. Sixty-one (62.2%) of the HCWs had their source of contact within the hospital while all the Non-HCWs had a source of contact for infection in the community.</p><p>Presence of comorbidity: Thirty three (33.7%) HWCs had at least one comorbidity present while 65 (66.3%) had none; compared to Non-HCWs with 178 (33.5%) who had a comorbidity and 352 (66.4%) with none, p = 0.758, χ<sup>2</sup> = 0.554.</p><p>Disease severity: 8 (8.2) HCWs had severe disease and 90 (91.8%) had non-severe disease compared to Non-HCWs with 52 (9.8%) with severe disease and 478 (91.2%) with non-severe disease, p = 0.670, χ<sup>2</sup> = 0.802.</p><p>Case fatality: One (1.0%), HCW died while 97 (99.0%) were discharged compared to 10 (1.9%) who died and 520 (98.1%), who were discharged, p = 0.554, χ<sup>2</sup> = 1.179.</p><p>Comorbidities: The pattern of comorbidities is as displayed in <xref ref-type="table" rid="table3">Table 3</xref>. The leading comorbidities in HCWs were hypertension 20.4%, diabetes 10.2%, and asthma 2.0%. Hypertension 25.7% and diabetes 7.7% were also the leading comorbidities in non-healthcare workers. There were no significant differences in the proportions of comorbidity in both groups. The pattern of symptoms: The pattern of symptoms is shown in <xref ref-type="table" rid="table4">Table 4</xref> and <xref ref-type="fig" rid="fig2">Figure 2</xref>. The leading symptoms</p><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> The pattern of symptoms among HCWs and Non-HCWs with COVID-19</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  ></th><th align="center" valign="middle"  colspan="2"  >Healthcare N = 98</th><th align="center" valign="middle"  colspan="2"  >Non Healthcare N = 530</th><th align="center" valign="middle"  rowspan="2"  >χ<sup>2 </sup></th><th align="center" valign="middle"  rowspan="2"  >p value</th></tr></thead><tr><td align="center" valign="middle" >N</td><td align="center" valign="middle" >%</td><td align="center" valign="middle" >N</td><td align="center" valign="middle" >%</td></tr><tr><td align="center" valign="middle" >Symptom</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Fever</td><td align="center" valign="middle" >27</td><td align="center" valign="middle" >27.6</td><td align="center" valign="middle" >142</td><td align="center" valign="middle" >26.8</td><td align="center" valign="middle" >0.403</td><td align="center" valign="middle" >0.818</td></tr><tr><td align="center" valign="middle" >Dry Cough</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >13.3</td><td align="center" valign="middle" >102</td><td align="center" valign="middle" >19.2</td><td align="center" valign="middle" >2.287</td><td align="center" valign="middle" >0.319</td></tr><tr><td align="center" valign="middle" >Productive cough</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >5.1</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >5.7</td><td align="center" valign="middle" >0.411</td><td align="center" valign="middle" >0.814</td></tr><tr><td align="center" valign="middle" >Dyspnoea</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >7.1</td><td align="center" valign="middle" >72</td><td align="center" valign="middle" >13.6</td><td align="center" valign="middle" >3.646</td><td align="center" valign="middle" >0.302</td></tr><tr><td align="center" valign="middle" >Anosmia</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >18.4</td><td align="center" valign="middle" >59</td><td align="center" valign="middle" >11.1</td><td align="center" valign="middle" >4.974</td><td align="center" valign="middle" >0.174</td></tr><tr><td align="center" valign="middle" >Headache</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >10.2</td><td align="center" valign="middle" >53</td><td align="center" valign="middle" >10.0</td><td align="center" valign="middle" >0.374</td><td align="center" valign="middle" >0.830</td></tr><tr><td align="center" valign="middle" >Fatigue</td><td align="center" valign="middle" >12</td><td align="center" valign="middle" >12.2</td><td align="center" valign="middle" >51</td><td align="center" valign="middle" >9.62</td><td align="center" valign="middle" >1.029</td><td align="center" valign="middle" >0.598</td></tr><tr><td align="center" valign="middle" >Myalgia</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >10.2</td><td align="center" valign="middle" >48</td><td align="center" valign="middle" >9.1</td><td align="center" valign="middle" >0.510</td><td align="center" valign="middle" >0.775</td></tr><tr><td align="center" valign="middle" >Aguesia</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >10.2</td><td align="center" valign="middle" >34</td><td align="center" valign="middle" >6.4</td><td align="center" valign="middle" >0.2239</td><td align="center" valign="middle" >0.326</td></tr><tr><td align="center" valign="middle" >Others</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >8.2</td><td align="center" valign="middle" >32</td><td align="center" valign="middle" >6.0</td><td align="center" valign="middle" >1.197</td><td align="center" valign="middle" >0.550</td></tr><tr><td align="center" valign="middle" >Diarrhoea</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >4.1</td><td align="center" valign="middle" >22</td><td align="center" valign="middle" >4.2</td><td align="center" valign="middle" >0.553</td><td align="center" valign="middle" >0.759</td></tr><tr><td align="center" valign="middle" >Sore Throat</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >5.1</td><td align="center" valign="middle" >19</td><td align="center" valign="middle" >3.6</td><td align="center" valign="middle" >1.083</td><td align="center" valign="middle" >0.582</td></tr><tr><td align="center" valign="middle" >Rhinorrhoea</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >3.1</td><td align="center" valign="middle" >19</td><td align="center" valign="middle" >3.6</td><td align="center" valign="middle" >0.616</td><td align="center" valign="middle" >0.863</td></tr><tr><td align="center" valign="middle" >Vomiting</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >2.0</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >2.0</td><td align="center" valign="middle" >0.564</td><td align="center" valign="middle" >0.754</td></tr></tbody></table></table-wrap><p>in HCWs were fever (27.6%), anosmia (18.4%), dry cough (13.3%), fatigue (12.2%), headaches (10.2%), and myalgia (10.2%), and ageusia (10.2%). In Non-Healthcare workers, the leading symptoms were fever (26.79%), dry cough (19.2%), shortness of breath (13.6%), anosmia (11.1%), headache (10.0%), fatigue (9.6%), and myalgia (9.1%). There were no significant differences in the proportion of symptom patterns.</p></sec><sec id="s4"><title>4. Discussion</title><p>Healthcare worker infection with SARS-CoV-2 has been a global source of concern since the onset of the pandemic with alarming prevalence rates of HCW infection. The prevalence of HCWs infection in this group of patients seen in hospitals from a Nigerian state was 15.2%. Though is it within the range of 3% - 19% reported globally [<xref ref-type="bibr" rid="scirp.107252-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref9">9</xref>]; it is a source of concern as it is higher than the 9.3% prevalence reported by Elimian et al. [<xref ref-type="bibr" rid="scirp.107252-ref13">13</xref>], in a descriptive study of COVID-19 from all states in Nigeria. The understanding that Rivers state is one of the high burden states for COVID-19 infection may also explain the higher prevalence of HCWs infection above a National average value in this study. The prevalence of HCW infection in this study is similar to 15% reported in Spain [<xref ref-type="bibr" rid="scirp.107252-ref4">4</xref>] and lower than 19% from the USA [<xref ref-type="bibr" rid="scirp.107252-ref7">7</xref>], which were both within the early phases of the pandemic in March and April 2020 respectively. In further comparison with other studies, the prevalence of HCWs with COVID-19 in this study is above 2.8% and 2.5% observed by Shararidad et al. [<xref ref-type="bibr" rid="scirp.107252-ref18">18</xref>] and Giesen et al. [<xref ref-type="bibr" rid="scirp.107252-ref19">19</xref>] from Iran and Spain respectively among hospitalised patients. A systematic review of global studies [<xref ref-type="bibr" rid="scirp.107252-ref8">8</xref>] reported HCW infection prevalence of 3.9% consisting of an estimated 152,888 of 3,912,156 cases as of 8 may 2020; while Wu et al. [<xref ref-type="bibr" rid="scirp.107252-ref10">10</xref>] from China found a prevalence of 3.4%. Two other studies [<xref ref-type="bibr" rid="scirp.107252-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref12">12</xref>], from Italy reported a prevalence of 9% and 9.8% respectively while a study in Qatar [<xref ref-type="bibr" rid="scirp.107252-ref6">6</xref>] found a prevalence of 10%. The prevalence of the above studies, is lower than the finding in this index study. It is therefore evident that HCWs contribute significantly to the burden of COVID-19 in the study location with prevalence rates above what is general observed from many other studies.</p><p>In the professional group of HCWs the most affected by COVID-19 in this study were doctors (47.9%), nurses (30.6%), and WASH/Environmental health, health attendants (10.2%). This shows that medical and clinical staff who have direct contact with patients and support staff who are in contact with the patient's environment are most at risk for infection. This pattern corresponds with the findings of Zheng et al. [<xref ref-type="bibr" rid="scirp.107252-ref20">20</xref>] in a study from the London teaching hospital which found that clinical staff groups had higher infection rates 7.3% compared to non-clinical staff with 2.8%, with medical and dental and nursing and midwifery as the professional groups with the highest rates of infections. A similar pattern was also observed by Sotgui et al. [<xref ref-type="bibr" rid="scirp.107252-ref21">21</xref>] at an Italian forefront hospital in a serologic prevalence study for SARS-CoV-2 with doctors (47.0%), Nurses (26.2%), and socio-sanitary workers (5.5%), having the highest prevalence of SARS-CoV-2 infection. Other studies have also corroborated this pattern as shown in a systematic review of global studies [<xref ref-type="bibr" rid="scirp.107252-ref8">8</xref>] which had nurses (38.6%) and Doctors (31.3%) as the leading professional category in correspondence with the findings of this study. Lombardi et al. [<xref ref-type="bibr" rid="scirp.107252-ref22">22</xref>] in Italy also reported Doctors, Health technicians, Nurses, and Health assistants 10.5%, 9.4%, 8.4%, and 8% were the leading professional groups with SARS-CoV-2 infection. Fusco et al. [<xref ref-type="bibr" rid="scirp.107252-ref11">11</xref>] also reported a higher proportion of nurses (50%) and doctors (23%) in their cohort. Alajmi et al. [<xref ref-type="bibr" rid="scirp.107252-ref6">6</xref>] from a Qatar national surveillance study reported the highest infection rates in Nurses (33.2%) and non-clinical support staff with (31.3%) with physicians consisting 5% of infections. Maskari et al. [<xref ref-type="bibr" rid="scirp.107252-ref23">23</xref>] from Oman reported Nurses with 38% of infections while doctors and paramedics had 13% of infections each with administrative/support staff making up 36%. The pattern of reported by Alajmi [<xref ref-type="bibr" rid="scirp.107252-ref6">6</xref>] and Maskari [<xref ref-type="bibr" rid="scirp.107252-ref23">23</xref>] differs slightly from our pattern with nurses, non-clinical support, and paramedics having higher rates of infections compared to doctors. The variations may be due to a higher proportion of community-acquired infections over hospital-acquired infections documented in those studies. The summary of all studies still shows that clinical workers especially doctors and nurses and support staff with contact to patient environments have a higher risk of infection. Clinical staff are therefore at higher risk and require an emphasis on risk communication prevention messages, provision of PPEs, and surveillance for infection. There were no significant differences in the mean age and age group distribution profile of HCWs and non HCWs in this study, with the mean age of 40.22 years above the national average of or mean of 37.1 years explained by the exclusion of people under 18 in the comparisons. Similar age means and median and age group distribution have also been reported by other studies [<xref ref-type="bibr" rid="scirp.107252-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref23">23</xref>].</p><p>There was a significant difference in the gender distribution between healthcare and non-healthcare workers in this study, with a higher female prevalence among healthcare workers compared to non-healthcare workers, this reflects the high preponderance of females in healthcare occupations in Nigeria especially nursing which accounted for over 30% of the HCWs and doctors. Other studies show a similar trend of female HCWs proportions above general population figures with Fusco et al. [<xref ref-type="bibr" rid="scirp.107252-ref11">11</xref>], Bandyopadhyay [<xref ref-type="bibr" rid="scirp.107252-ref8">8</xref>], Lombardi et al. [<xref ref-type="bibr" rid="scirp.107252-ref22">22</xref>], Maskari et al. [<xref ref-type="bibr" rid="scirp.107252-ref23">23</xref>] reporting proportions of 49%, 71.6%, 62.4%, and 64% respectively.</p><p>In this study, the majority of HCWs (69.4%) with COVID-19 had a source of contact established compared to non-healthcare workers with a predominantly unknown source of disease indicating higher levels of community transmission in Non-HCWs. Also, the majority of HCWs had their contacts within the hospital environment from patients and other healthcare workers. These findings correspond with that of Wang et al. [<xref ref-type="bibr" rid="scirp.107252-ref3">3</xref>] who reported a higher rate of hospital-associated transmission in HCW of 29% compared to 12.3% in hospitalized non-HCWs. This finding shows the need for better infection prevention and control practice and appropriate PPE use among HCWs in this environment to reduce transmission of SARS-CoV-2 among HCWs. There was no significant difference in the presence of comorbidity, the proportion of disease severity, and case fatality in the study among HCWs and non HCWs. Hypertension and diabetes were the leading comorbidities both in HCWs and Non-HCWs. This observation is reassuring as HCWs do not have a higher risk of adverse outcomes compared to the general population. Also, the case fatality among HCWs reported in this study corresponds with global observations from a systematic review by Bandyopadhyay et al. [<xref ref-type="bibr" rid="scirp.107252-ref8">8</xref>] that reported a global case fatality among HCWs at 1 in 100 (1%). The pattern of hypertension and diabetes as the leading comorbid disease condition has also been reported by other studies [<xref ref-type="bibr" rid="scirp.107252-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref23">23</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref24">24</xref>]. Wang et al. [<xref ref-type="bibr" rid="scirp.107252-ref3">3</xref>] reported hypertension and diabetes as the leading comorbid disease conditions, while Maskari et al. [<xref ref-type="bibr" rid="scirp.107252-ref23">23</xref>] reported diabetes as the leading comorbid disease condition over hypertension. The range of comorbidity presence of 22.9% to 46.4% among HCWs reported by Wang et al. [<xref ref-type="bibr" rid="scirp.107252-ref3">3</xref>] and Maskari et al. [<xref ref-type="bibr" rid="scirp.107252-ref23">23</xref>] respectively is comparable to the 33.7% reported in this study.</p><p>The pattern of symptoms among the HCWs in this study was similar and did not differ significantly from non-HCWS, with fever, dry cough, fatigue, headaches, myalgia, anosmia, ageusia, and shortness of breath as the leading symptoms in line with the existing symptom pattern and other studies involving the general population [<xref ref-type="bibr" rid="scirp.107252-ref25">25</xref>] and HCWs [<xref ref-type="bibr" rid="scirp.107252-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref6">6</xref>]. The presence of anosmia among HCWs as the second most common symptom in this study is a finding of interest as anosmia is predictive of less severe disease, reduced hospitalizations’, and lower in-hospital mortality in COVID-19 patients [<xref ref-type="bibr" rid="scirp.107252-ref26">26</xref>] [<xref ref-type="bibr" rid="scirp.107252-ref27">27</xref>].</p></sec><sec id="s5"><title>5. Conclusion</title><p>The study has shown that the prevalence of COVID-19 among HCWs in the study location is high and a cause of epidemiologic concern as HCWs contribute a significant burden of COVID-19 infections. This calls for action to improve and prevent HCWs infections in hospital settings in addition to improving HCW infection prevention behaviour in the community. Clinical and clinical support staff particularly doctors and nurses are at higher risk of COVID-19 infections and require intensification of risk communication, provision of protective equipment (PPE), and training on the appropriate use of PPE; in addition to routine surveillance for infection. There is no risk for the development of more severe disease and higher case fatality among HCWs compared to the general population.</p></sec><sec id="s6"><title>Acknowledgements</title><p>We acknowledge all members of the health team who cared for the patients and the data collectors engaged in the study.</p></sec><sec id="s7"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s8"><title>Cite this paper</title><p>Alasia, D.D. and Maduka, O. (2021) Prevalence and Pattern of COVID-19 among Healthcare Workers in Rivers State Nigeria. Occupational Diseases and Environmental Medicine, 9, 20-32. https://doi.org/10.4236/odem.2021.91003</p></sec></body><back><ref-list><title>References</title><ref id="scirp.107252-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">WHO. WHO Director-General’s Opening Remarks at the Media Briefing on COVID-19—11 March 2020. https://www.who.int/director-general/speeches/detail/who-director-general-s-opening-remarks-at-the-media-briefing-on-covid-19---11-march-2020</mixed-citation></ref><ref id="scirp.107252-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">WHO-China Joint Mission. Report of the WHO-China Joint Mission on Coronavirus Disease 2019 (COVID-19), February 2020. https://www.who.int/docs/default-source/coronaviruse/who-china-joint-mission-on-covid-19-final-report.pdf</mixed-citation></ref><ref id="scirp.107252-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Wang, D., Hu, B., Hu, C., Zhu, F., Liu, X., Zhang, J., et al. (2020) Clinical Characteristics of 138 Hospitalized Patients with 2019 Novel Coronavirus-Infected Pneumonia in Wuhan, China. Journal of the American Medical Association, 323, 1061. https://doi.org/10.1001/jama.2020.1585</mixed-citation></ref><ref id="scirp.107252-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Benavides, L. (2019) The Coronavirus Crisis: Spain’s Health Staff Are Catching the Coronavirus as Protective Gear Runs Short. https://www.npr.org/sections/coronavirus-live-updates/2020/03/31/824654965/spains-health-staff-are-catching-the-coronavirus-as-protective-gear-runs-short</mixed-citation></ref><ref id="scirp.107252-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">WHO Regional Office for Africa (2020) Over 10 000 Health Workers in Africa Infected with COVID-19. WHO Africa News 23rd July 2020. https://www.afro.who.int/news/over-10-000-health-workers-africa-infected-covid-19</mixed-citation></ref><ref id="scirp.107252-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Alajmi, J., Jeremijenkoa, A.M., Abrahama, J.C., Alishaqa, M., Concepciona, E.G., Butta, A.A. and Abou-Samra, A.-B. (2020) COVID-19 Infection among Healthcare Workers in a National Healthcare System: The Qatar Experience. International Journal of Infectious Diseases, 100, 386-389. https://doi.org/10.1016/j.ijid.2020.09.027</mixed-citation></ref><ref id="scirp.107252-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">CDC (2020) COVID-19 Response Team. Characteristics of Health Care Personnel with COVID-19: United States, February 12-April 9, 2020. Morbidity and Mortality Weekly Report, 69, 477-481. https://doi.org/10.15585/mmwr.mm6915e6</mixed-citation></ref><ref id="scirp.107252-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Bandyopadhyay, S., Baticulon, R.E., Kadhum, M., Alser, M., Ojuka, D.K., Badereddin, Y., et al. (2020) Infection and Mortality of Healthcare Workers Worldwide from COVID-19: A Systematic Review. BMJ Global Health, 5, e003097. https://doi.org/10.1101/2020.06.04.20119594</mixed-citation></ref><ref id="scirp.107252-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Ali, S., Noreen, S., Farooq, I., Bugshan, A. and Vohra, F. (2020) Risk Assessment of Healthcare Workers at the Frontline against COVID-19. Pakistan Journal of Medical Sciences, 36, S99-S103. https://doi.org/10.12669/pjms.36.COVID19-S4.2790</mixed-citation></ref><ref id="scirp.107252-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Wu, Z. and MacGoogan, J.M. (2020) Characteristics of and Important Lessons from the Coronavirus Disease 2019 (COVID-19) Outbreak in China Summary of a Report of 72 314 Cases from the Chinese Center for Disease Control and Prevention. JAMA, 323, 1239-1242. https://doi.org/10.1001/jama.2020.2648</mixed-citation></ref><ref id="scirp.107252-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Fusco, F.M., Pisaturo, M., Iodice, V., Bellopede, R., Tambaro, O. and Parrella, G. (2020) COVID-19 among Healthcare Workers in a Specialist Infectious Disease Setting in Naples, Southern Italy: Results of a Cross-Sectional Surveillance Study. Journal of Hospital Infection, 105, 596-600. https://doi.org/10.1016/j.jhin.2020.06.021</mixed-citation></ref><ref id="scirp.107252-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Livingston, E. and Bucher, K. (2020) Coronavirus Disease 2019 (COVID-19) in Italy. JAMA, 323, 1335. https://doi.org/10.1001/jama.2020.4344</mixed-citation></ref><ref id="scirp.107252-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Elimian, K.O., Ochu, C.L., Ilori, E., Oladejo, J., Igumbor, E., Steinhardt, L., Wagai, J., et al. (2020) Descriptive Epidemiology of Coronavirus Disease 2019 in Nigeria, 27 February-6 June 2020. Epidemiology and Infection, 148, e208. https://doi.org/10.1017/S095026882000206X</mixed-citation></ref><ref id="scirp.107252-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Nguyen, L.H., Drew, D.A., Graham, M.S., Joshi, A.D., Guo, G.-C. and Ma, W. (2020) Risk of COVID-19 among Front-Line Health-Care Workers and the General Community: A Prospective Cohort Study. Lancet Public Health, 5, e475-e483.</mixed-citation></ref><ref id="scirp.107252-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Nigerian Centre for Disease Control (NCDC) (2020) COVID-19 in Nigeria: Confirmed COVID-19 Cases by State, 20th November 2020. https://covid19.ncdc.gov.ng</mixed-citation></ref><ref id="scirp.107252-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">WHO (2020) Classifying Health Workers: Mapping Occupations to the International Standard Classification: International Labour Organization, International Standard Classification of Occupations: ISCO-08. https://www.who.int/hrh/statistics/Health_workers_classification.pdf</mixed-citation></ref><ref id="scirp.107252-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Nigerian Centre for Disease Control (NCDC) (2020) National Interim Guidelines for Clinical Management of COVID19. https://covid19.ncdc.gov.ng/media/files/National_Interim_Guidelines_for_Clinical_Management_of_COVID-19_v3.pdf</mixed-citation></ref><ref id="scirp.107252-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Shahriarirad, R., Khodamoradi, Z., Erfani, A., Hosseinpour, H., Ranjbar, K., Emami, Y., Mirahmadizadeh, A., et al. (2020) Epidemiological and Clinical Features of 2019 Novel Coronavirus Diseases (COVID-19) in the South of Iran. BMC Infectious Diseases, 20, 427. https://doi.org/10.1186/s12879-020-05128-x</mixed-citation></ref><ref id="scirp.107252-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Giesen, C., Diez-Izquierdoa, L., Saa-Requejoa, C.M., Lopez-Carrilloa, I., Lopez-Vilelaa, C.A., Seco-Martineza, A. and Prieto, M.T.R. (2020) Epidemiological Characteristics of the COVID-19 Outbreak in a Secondary Hospital in Spain. American Journal of Infection Control, 49, 143-150.</mixed-citation></ref><ref id="scirp.107252-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Zheng, C., Hafezi-Bakhtiari, N., Cooper, V., Davidson, H., Habibi, M., Riley, P. and Breathnach, A. (2020) Characteristics and Transmission Dynamics of COVID-19 in Healthcare Workers at a London Teaching Hospital. Journal of Hospital Infection, 106, 325-329. https://doi.org/10.1016/j.jhin.2020.07.025</mixed-citation></ref><ref id="scirp.107252-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">Sotgiu, G., Barassi, A., Miozzo, M., Saderi, L., Piana, A., Orfeo, N., et al. (2020) SARS-CoV-2 Specific Serological Pattern in Healthcare Workers of an Italian COVID-19 Forefront Hospital. BMC Pulmonary Medicine, 20, 203. https://doi.org/10.1186/s12890-020-01237-0</mixed-citation></ref><ref id="scirp.107252-ref22"><label>22</label><mixed-citation publication-type="other" xlink:type="simple">Lombardi, A., Consonni, D., Carugno, M., Bozzi, G., Mangioni, D., Muscatello, A., et al. (2020) Characteristics of 1573 Healthcare Workers Who Underwent Nasopharyngeal Swab Testing for SARS-CoV-2 in Milan, Lombardy, Italy. Clinical Microbiology and Infection, 26, 1413.e9-1413.e13. https://doi.org/10.1016/j.cmi.2020.06.013</mixed-citation></ref><ref id="scirp.107252-ref23"><label>23</label><mixed-citation publication-type="other" xlink:type="simple">Maskari, Z.L., Blushi, A.A.L., Khamis, F., Tai, A.A.L., Salmi, I.A.L., Harthi, H.A.L., et al. (2020) Characteristic of Healthcare Workers Infected with COVID-19, a Cross-Sectional Observational Study. International Journal of Infectious Diseases, 102, 32-36. https://doi.org/10.1016/j.ijid.2020.10.009</mixed-citation></ref><ref id="scirp.107252-ref24"><label>24</label><mixed-citation publication-type="other" xlink:type="simple">Zhou, F., Yu, T., Du, R., Fan, G., Liu, Y., Liu, Z., et al. (2020) Clinical Course and Risk Factors for Mortality of Adult Inpatients with COVID-19 in Wuhan, China: A Retrospective Cohort Study. The Lancet, 395, 1054-1062. https://doi.org/10.1016/S0140-6736(20)30566-3</mixed-citation></ref><ref id="scirp.107252-ref25"><label>25</label><mixed-citation publication-type="other" xlink:type="simple">Ahmed, A., Ali, A. and Hasan, S. (2020) Comparison of Epidemiological Variations in COVID-19 Patients inside and outside of China—A Meta-Analysis. Frontiers in Public Health, 8, 193. https://doi.org/10.3389/fpubh.2020.00193</mixed-citation></ref><ref id="scirp.107252-ref26"><label>26</label><mixed-citation publication-type="other" xlink:type="simple">Talavera, B., García-Azorína, D., Martínez-Píasa, E., Trigoa, J., Hernández-Péreza, I. and Valle-Pe&amp;#241;acoba, G. (2020) Anosmia Is Associated with Lower In-Hospital Mortality in COVID-19. Journal of the Neurological Sciences, 419, Article ID: 117163. https://doi.org/10.1016/j.jns.2020.117163</mixed-citation></ref><ref id="scirp.107252-ref27"><label>27</label><mixed-citation publication-type="other" xlink:type="simple">Foster, K.J., Jauregui, E., Tajudeen, B., Faraz Bishehsari, F. and Mahdavinia, M. (2020) Smell Loss Is a Prognostic Factor for Lower Severity of Coronavirus Disease 2019. Annals of Allergy, Asthma &amp; Immunology, 125, 475-494. https://doi.org/10.1016/j.anai.2020.07.023</mixed-citation></ref></ref-list></back></article>