Learning Objectives
Identify common health risk factors in the working population that are associated with developing severe COVID-19 illness.
Discuss the “three pillars” of assessment of COVID-19 illness and severity risk among workers and their use in a matrix to guide return-to-work recommendations.
Describe and give examples of the use of the matrix as a practical tool for managing COVID-19 relative risk in workers.
Coronavirus disease (COVID-19) was declared as a pandemic by the World Health Organization (WHO) on March 11, 2020.1 Common symptoms include fever, fatigue, cough, dyspnea, sore throat, headache, anosmia, hypogeusia or ageusia, asthenia, conjunctivitis, and gastrointestinal issues (loss of appetite, diarrhea, nausea, and vomiting). Although a significant number of patients are asymptomatic or have mild clinical symptoms at presentation, a small percentage of cases can progress to uncontrolled inflammatory response with acute respiratory distress syndrome or even multiple organ failure.2–6 Some individuals are at high-risk for developing severe symptoms which are associated with significant morbidity and mortality, including the elderly, certain ethnicities (eg, African Americans) and those affected by health risk factors and chronic diseases.6–8 Specific organ damage has been described in COVID-19 patients, such as acute respiratory distress syndrome,9 cardiovascular injuries (cardiac imbalance, coronary thrombosis, direct myocardial injury, arrhythmias, and venous thromboembolism),10–13 acute liver injury,14,15 acute kidney injury and kidney replacement therapy,16,17 and neurological complications (severe stroke, Guillain–Barre syndrome, acute encephalitis, seizures, and skeletal muscle injury)18 that may represent a higher risk for those with pre-existing chronic health conditions.
In 2020, the global impact of COVID-19 posed unprecedented challenges to health agencies, governments, companies, healthcare systems, academia, and individuals. From the public health perspective, non-pharmaceutical interventions (NPIs) are an important strategy to mitigate the impact by slowing the epidemic spread, reducing peak healthcare demand, and protecting people at higher risk of acquiring the infection.19 According to The Imperial College, physical distancing of people at high-risk groups is particularly effective at reducing severe outcomes. NPIs will need to be maintained until an effective COVID-19 vaccine becomes widely available.19
Based on clinical epidemiology studies, lists of health risk factors and medical conditions that predispose individuals to severe forms of COVID-19 have been developed and published by several health agencies such as WHO,20 CDC,21 NHS,22 and others. Examples of these risk factors include age, obesity, hypertension, and several health conditions such as diabetes—which are all prevalent among workers globally.7 Using the 2017 Global Burden of Disease data, Clark et al7 estimated that 22% of the global population (1.7 billion people) have at least one underlying condition which increases the risk of severe COVID-19 and 4% of the global population (349 million people) are at greatly elevated risk for severe disease and necessitating hospitalization if they contract COVID-19.
For workers at increased risk who cannot work from home, return to work may expose them to COVID-19 going to and from work and at their workplaces. Strategies and guidelines are therefore needed to protect all workers, especially those at increased risk of COVID-19 complications. Governments around the world have generally not provided guidance on how to protect workers at increased risk nor assistance with decision-making about return to work for persons at heightened risk of complications and mortality from COVID-19.23
Occupational medicine specialists in a number of countries have developed medical guidelines to protect the health of workers until an effective preventive treatment or vaccine is available for COVID-19.24–26 Nabeel and Fischman27 proposed a four-step approach to guide return to work of individuals with high risk which includes: (1) assess the risk of exposure in the workplace which depends on the degree of interaction with people and the nature of job tasks; (2) identify the scope of individual risk and stratify the severity or the degree of control of the disease; (3) recommend protective measures in the workplace if work from home is not possible, and (4) advise workers on reduction strategies for modifiable risks (eg, BMI, blood glucose, etc). Coggon et al28 developed a risk model considering age, sex, ethnicity, smoking habits, and comorbidities to support decisions on occupational placement of workers in the UK during the pandemic. Larochelle23 has proposed a framework for medical decisions about returning or continuing to work amidst the pandemic based on the risk of contracting SARS-CoV-2 at the workplace and the individual risk of complications and death if infected (both risks stratified as low, medium, and high). The author suggested that patients with high risk in both domains should be counseled to stop working, those with high risk in one domain and medium risk in the other should mitigate exposure and consider staying out of work, and all patients at work should be counseled to take precautions (use of mask, hand hygiene, and PPE as recommended).
The purpose of this study is to develop a global framework to support physicians, companies, and governments on how to ensure the health and safety of workers at a higher risk of unfavorable outcomes of COVID-19 during the current pandemic, considering individual risk factors, workplace exposure risk, and the level of community transmission of SARS-Cov-2.
METHODS
A review of clinical and epidemiology COVID-19 studies was conducted. The literature search on July 15, 2020 utilized medical databases (PubMed and Scielo) with MESH terms including COVID-19: “covid19” OR “covid 19” OR “sarscov2,” and MESH terms related to risk factors identified as associated with adverse COVID-19 outcomes: “smoking,” “chronic disease,” “diabetes,” “pregnancy,” “immunosuppression,” “neurodegenerative diseases,” “pulmonary disease, chronic obstructive,” “asthma,” “liver diseases,” “obesity,” “hypertension,” “cancer,” “heart disease,” “COPD,” and “asthma”. In addition, a search with MESH terms including COVID-19 and “epidemiology” was conducted. We identified studies which described the prevalence and/or assessed the effects of sociodemographic factors, risk factors, and medical conditions associated with unfavorable COVID-19 related outcomes.
The criteria for high-risk individuals and their management from the United States, Brazil, and India were also reviewed, according to the dashboard provided by the Center for Systems Science and Engineering (CSSE) at Johns Hopkins University (JHU).29 In addition, an internet search for the three most affected countries in Europe (UK, Spain, and Italy) was conducted. The European continent became the epicenter for the pandemic following the first reported cases in China. Among the 10 countries most affected by the COVID-19 pandemic, South Africa was the only country to our knowledge to release a specific recommendation for managing employees at increased risk for COVID-19.
Recommendations from Labor and Health & Safety government agencies regarding the risk of exposure to COVID-19 at workplaces were then reviewed. The risk that a worker may be exposed to in various work settings was quantified and stratified. The third step was to review indicators which quantified the level of transmission in the community and stratify the risk of exposure of the worker in a community. In conclusion, a framework was created which included three pillars of risk based on worker health factors, workplace risk, and community level risk.
RESULTS
The Individual Risk Pillar
The literature review is summarized in Tables 1 and 2 . Seventy-three studies were reviewed, including 66 single country studies and seven reports with data from two or more countries. Almost half, 36 of the studies, were from China, followed by the US (21), Italy (10), Spain (6), France (4), UK and Mexico (3), South Korea (3), and Brazil and the Netherlands (2). The most common study methodology was cohort (33), followed by descriptive studies (22), meta-analysis and/or systematic review (14), case-control (3), and cross-sectional (1).
TABLE 1 -
Summary, Characteristics, and Key Findings of 73 Studies Reviewed
Author
Sample
Methodology
Country
Findings
Aggarwal et al30
4,858
Meta-analysis of studies about association of CVD with severe diseases and increased mortality in COVID-19 patients
China and USA
Previous cardiovascular disease was significantly associated with a higher risk of a severe disease (OR = 3.14; 95% CI 2.32-4.24) and death outcome (OR = 11.08; 95% CI: 2.59–47.32), but not significantly associated with mortality in severe form of COVID-19 (OR = 1.72; 95% CI: 0.97–3.06)
Akalin et al31
36
Cohort of adult kidney-transplant recipients with COVID-19 (median follow-up of 21 days)
USA
96% of patients had radiographic findings suggestive of viral pneumonia. During follow up, 39% needed intubation and mechanical ventilation, 21% needed renal replacement therapy and 28% died
Alberici et al32
20
Cohort of long-term kidney transplant patients with COVID-19 (median follow-up of 7 days)
Italy
At baseline all cases had fever, one had dyspnea; 50% of all cases had bilateral infiltrates Chest X-ray, 35% had unilateral infiltrates and 15% had no infiltrates. During follow up, 87% had radiological worsening and among those 73% needed oxygen therapy. Six patients had acute kidney injury and one needed hemodialysis. Five patients died after a median period of 15 days
Assaad et al33
302
Retrospective cohort study of cancer patients with suspected COVID-19 (median follow-up time of 25 days)
France
18.2% of patients tested positive for SARS-COV-2. 9.9% of patients died during the observation period among all patients, 21% died in the PCR positive group and 10% in the negative group. Detection of SARS-COV-2 on RT-PCR was not associated with an increased death rate. 80% of cancer patients who died had metastatic disease (in both groups). Receiving any cancer treatment on the last 30 days was not associated to increased risk of death.
Bello-Chavolla et al34
51,633
Retrospective cohort of COVID-19 cases
Mexico
Age ≥65 years (HR 2.02, P < 0.001), diabetes (HR 1.34, P < 0.001), early-onset diabetes (<40 years) (HR 2.86, P < 0.001), obesity (HR 1.25, P < 0.001), chronic kidney disease (HR 1.99, P < 0.001), COPD (HR 1.40, P < 0.001), immunosuppression (HR 1.27, P = 0.007) were significantly associated to increased lethality in COVID-19 cases. In patients with diabetes mellitus, mortality was higher in those with concomitant comorbidities (immunosuppression, COPD, CKD, hypertension) and those aged over 65 years. Diabetes mortality was partially mediated by obesity, the effect of obesity represented 49.5% of the total effect of diabetes.
Bezzio et al35
79
Prospective observational cohort study with adults with Inflammatory bowel disease and COVID-19
Italy
55% had COVID-19 pneumonia, 36% were hospitalized, 13% needed mechanical ventilation and 11% died. Active IBD was associated with severe COVID-19 outcomes and all patients were under treatment for a disease flare. Ulcerative Colitis was significantly associated with COVID-19 pneumonia, but not with death. 38% had at least one comorbidity: hypertension (11%), coronary heart disease (6%), COPD (6%), ankylosing spondylitis (3%), rheumatoid arthritis (1%), multiple sclerosis (1%), undifferentiated connective tissue disease (1%), Hypothyroidism 1 (1%). Charlson Comorbidity Index distribution: 0 (54%), 1 (18%), 2 (15%), 3 (8%), 4 (4%), 5 (1%). Risk of COVID-19 pneumonia was significantly associated with age over 65 years (OR 5.87, P = 0.03), ulcerative colitis (OR 2.91, P = 0.03), IBD disease activity (OR 10.25, P = 0.003), and Charlson Comorbidity Index score >1 (OR 2.91, P = 0.04). COVID-19-related death was significantly associated with age over 65 years (OR 19.6, P = 0.002), IBD disease activity (OR 8.45, P = 0.02) and Charlson Comorbidity Index score >1 (OR 16.66, P = 0.01).
Cai et al36
383
Case series of adults with COVID-19 admitted to a hospital
China
Overweight (OR 1.84, P = 0.05) and obesity (OR 3.40, P = 0.007) were significantly associated to severe forms of COVID-19. Comparing obese and normal weight man, the obese were at increased odds of developing severe forms (OR 5.66, P = 0.003).
China CDC37
44,672
Descriptive and exploratory analysis of cases in China until 2/11/2020.
China
Overall case-fatality rate (CFR) was 2.3% but higher for those with underlying medical conditions: cardiovascular diseases (10.5%), diabetes (7.3%), chronic respiratory disease (6.3%), hypertension (6.0%) and cancer (5.6%). CFR was also higher for older age groups (0.2% 0–40 years, 0.4% 40–19 years, 1.3% 50–59 years, 3.6% 60–69 years, 8% 70–80 years, and 14.8% >80 years).
Chen et al38
274
Retrospective case series of patients with COVID-19 (113 who died and 161 who recovered)
China
Male sex was more frequent among deceased patients (73% vs 55%). Deceased patients were significantly older than recovered (media age 68 vs 51) years. Among deceased cases: hypertension (48% vs 24%), diabetes (21% vs 14%), cardiovascular disease (14% vs 4%), chronic lung diseases (10% vs 4%), cancer (4% vs 1%), cerebrovascular disease (4% vs 0%) and chronic kidney disease (4% vs 1%)
Chen et al39
9
Case series (retrospective review of medical records)
China
All nine pregnant women in the third trimester underwent caesarean section. The clinical characteristics of COVID-19 infection during pregnancy were similar to those reported for non-pregnant adults. None of the nine patients developed severe pneumonia or died.
Chhiba et al40
1,526
Retrospective cohort of COVID-19 cases
USA
14.4% of cases has asthma. Asthma was not significantly associated to a higher risk of hospitalization (RR 0.96, P = 0.71). Diabetes (RR 1.16; 95% CI: 1.00–1.36), and obstructive sleep apnea (RR 1.23; 95% CI: 1.01–1.49) were significantly associated to a higher risk hospital admission regardless of asthma status.
Choi et al41
293
Cohort study with COVID-19
South Korea
Among all cases, reported comorbidities were: hypertension (9.9%), diabetes mellitus (7.2%), allergic disease (13.0%), chronic lung disease (5.8%), peripheral vascular disease (4.4%), cancer (2.4%), liver disease (1.7%), congestive heart failure (2.0%), cerebrovascular disease (1.7%), rheumatic disease 2 (0.7%), acute myocardial infarction (0.3%), kidney disease (0,3%). 12.3% cases were classified as the progression group and 87.7% as the improvement/stabilization group. Risk factors significantly associated to poorer outcomes were older age (49.5 vs 27.0 years old, P < 0.001), hypertension (HR 3.56, P < 0.001) and diabetes mellitus (HR 6.59, P < 0.001)
Christensen et al42
448
Retrospective cohort
Denmark
Comorbidities 10 years before COVID-19 data were used to calculate the Charlson Comorbidity Index Score (CCIS), which categorizes comorbidities and calculates a single comorbidity score for a patient (diagnosis considered are: myocardial infarction, heart failure, cerebrovascular disease, peripheral vascular disease, diabetes, dementia, hemi- or paraplegia, rheumatic disease, peptic ulcer, COPD, chronic renal disease, liver disease, cancer, metastatic cancer, HIV/AIDS). The distribution of cases by CCIS was 0: 65.0%, 1–2: 24.8%, 3–4: 6.4% and >4: 3.8%. On the entire sample, 17.8% had severe outcome and 9.3% died. The risk of severe forms significantly increased with CCIS>0: CCIS 1–2: OR 1.76 (95% CI 1.43–2.16), CCIS 3–4: OR 2.36 (95% CI 1.74–3.18) and CCIS >4: OR, 2.67 (95% CI 1.87–3.81). The risk of death also significantly increased with CCIS>0: CCIS 1–2: OR (95% CI 1.57–2.9), CCIS 3–4: OR 3.00 (95% CI 2.06–4.38) and CCIS > 4: OR 3.85 (95% CI 2.51–5.90)
Cummings et al43
257
Prospective observational cohort of critically ill patients.
USA
67% were men and 82% had at least one chronic illness: hypertension (63%), diabetes (36%) and obesity (46%). Older age (HR 1.31, CI 95% 1.09–1.57), hypertension chronic (HR 1.58 CI 95% 0.89–2.81), cardiac disease (HR 1.76 CI 95% 1.08–2.86) and chronic pulmonary disease (COPD or interstitial lung disease) (HR 2.94 CI 95% 1.48–5.84) were significantly associated with in-hospital mortality.
Della Gatta et al44
51
Systematic review of pregnant with COVID-19 reported cases
China
No cases in the first trimester, 2 in the second trimester, 49 in the third trimester. One 30-year-old patient with no comorbidities and diagnosis of at 34 weeks develop server form of COVID-19 and intrauterine fetal demise has occurred. 48 neonates (one set of twins) were in good condition at birth. One neonate was delivered by cesarean 34 weeks of gestational age and died 9 days after delivery and perinatal infection could not be excluded.
Docherty et al45
20,133
Prospective cohort with minimal follow-up time of 2 weeks.
UK
77% had comorbidities: chronic cardiac disease (31%), uncomplicated diabetes (21%), non-asthmatic chronic pulmonary disease (18%) and chronic kidney disease (16%). Increasing age [50–59 years (HR 2.63, P < 0.001); 60–69 years (HR 4.99, P < 0.001); 70–79 years (HR 8.51, P < 0.001); ≥80 years (HR 11.09, P < 0.001)], male sex (female sex was significantly associated with lower mortality—HR 0.81, P < 0.001), chronic cardiac disease (HR 1.16, P < 0.001), chronic non-asthmatic pulmonary disease (HR 1.17, P < 0.001), chronic kidney disease (HR 1.28, P < 0.001), obesity (HR 1.33, P < 0.001), stroke (HR 1.17, P = 0.001), dementia (HR 1.40, P < 0.001), cancer (HR 1.13, P = 0.017), and liver disease (HR 1.51, P < 0.001) were associated with higher mortality.
Du et al46
179
Prospective cohort of patients with COVID-19 pneumonia.
China
Age >65 years (OR 3.765), cardiovascular and cerebrovascular diseases (OR 2.464) were associated with higher mortality.
Ebekozien et al47
64
Preliminary report of observational study among patients with type 1 diabetes and COVID-19 and COVID-19-like symptoms (with test pending or unavailable)
USA
The most common outcome for both groups was diabetic ketoacidosis (45.5% in the confirmed COVID-19 group and 13.3% the suspected or test pending group). Median HbA1c in the COVID-19—like group was 8.0% and in the in the COVID-19—positive was 8.5%. Over 50% of all cases had hyperglycemia, and nearly one-third of patients experienced DKA. Comorbidities among all cases were: obesity (39.4%), hypertension or cardiovascular disease (12.1%), asthma (7.9%), Hashimoto thyroiditis (4.8%) and hyperlipidemia (4.8%)
Fadini et al48
Not available
Meta-analysis of studies reporting the prevalence of diabetes among people infected with the SARS-CoV-2 and its impact on disease severity or progression
Italy and China
A relatively lower prevalence of diabetes among COVID-19 cases has been observed in Italy and China, compared with general population. Pooled rate ratio of diabetes among patients with severe COVID-19 compared with those with the better outcome was 2.26 (95% CI 1.47–3.49) among six studies in China. Among 355 with who died of COVID-19 in Italy, the prevalence of diabetes was 35.5% and the rate ratio among patients who died of SARS-CoV-2 infection compared with the general population was 1.75
Fredi et al49
143
Single-center observational study of patients with rheumatic diseases and confirmed or possible COVID-19 and case control study
Italy
72% of patients with confirmed COVID-19 developed pneumonia and were hospitalized. 10% of patients with confirmed or suspected COVID-19 (10 in those with confirmed COVID-19 and two in those with suspected COVID-19). Deceased patients with confirmed COVID-19 were older than survivors (median age 78.8 years vs 65.5, P = 0.0002). No differences were found in sex, comorbidities, or therapies between the survivors and non-survivors. In the case control study no significant differences were found in duration of hospital stay, comorbidities prevalence, and death rates.
Gao et al50
150
Case control study (75 obese and 75 non-obese COVID-19 patients)
China
Obese cases had lower lymphocyte counts and higher levels of plasma C-reactive protein (early indicators of severe COVID-19), longer hospital stay (median 23 vs 18, P = 0.037) and greater proportion of severe clinical presentation (33.3% vs 14.7%, P = 0.007). Obesity was significantly associated with a higher risk of severe COVID-19 (adjusted OR 3.00, 95% CI 1.22–7.38). There was a clear dose–response relationship between increasing values of BMI and percentage of cases with severe COVID-19: each 1-unit increase in BMI was also associated with a 12% increase in the risk of having severe forms of COVID-19.
García-Pachón et al51
168
Descriptive study of adults with COVID-19 admitted to a hospital
Spain
Prevalence of asthma among COVID-19 cases: 2.4%, COPD prevalence: 7.1%. The prevalence of asthma and COPD was similar to the expected for general population in the country.
Grandbastien et al52
106
Monocentric, retrospective, cohort study of cases admitted to one hospital
France
Among 106 patients with COVID-19, 23 had asthma. Asthma was not significantly associated to more involvement of lung parenchyma on CT scan (OR 0.90, P = 0.786), to a higher risk of being admitted to an ICU (OR 1.065; P = 0.92) and higher risk of exacerbation before and during hospital admission (generalized linear mixed-effect model, P = 0.09)
Grasselli et al53
1,591
Retrospective observational study of 1591 consecutive patients admitted to ICU.
Italy
82% (95% CI 79.98%–83.82%) were men, median age was 63 years, 86% of patients had at least one comorbidity: 49% hypertension, 21% cardiovascular disease (cardiomyopathy and heart failure), 18% hypercholesterolemia, 17% diabetes type, 2, 8% cancer (active neoplasia and neoplasia in remission), 4% COPD, 3% chronic kidney disease, 3% chronic liver disease and 20% others (anemia, asthma, inflammatory bowel disease, epilepsy, chronic respiratory insufficiency, endocrine disorders, connective tissue diseases, neurologic disorders, chronic pancreatitis, immunocompromise, and organ transplant).
Grasselli et al54
3,988
Retrospective cohort of COVID-19 patients admitted to a hospital
Italy
Hospital mortality rate were 12/1000 patients-days and ICU mortality rate was 27/1000. Median age was 63 years old and 79.9% of patients were men. 60.5% at least one comorbidity: hypertension (42.1%), hypercholesterolemia (16.5%), heart disease (16.2%), type 2 diabetes (12.9%), cancer (8.3%), COPD (2.3%), chronic kidney disease (2.2%), and liver disease (2.2%). Older age (HR 1.75; 95% CI 1.60–1.92), male sex (HR 1.57; 95% CI 1.31–1.88), COPD (HR 1.68; 95% CI 1.28–2.19), hypercholesterolemia (HR 1.25; 95% CI 1.02–1.52), and type 2 diabetes (HR 1.18; 95% CI, 1.01–1.39) were independent factors significantly associated to higher mortality rates.
Guan et al55
1,099
Descriptive and exploratory study of cases
China
Mean age was 48.9 years, 57.3% patients were men, 23.7% had at least one coexisting disorder, the most common were hypertension (15%), diabetes (7.4%), coronary heart disease (2.5%), hepatitis B infection (2.1%), cerebrovascular disease (1.4%), COPD (1.1%), cancer (0.9%), chronic renal disease (0.7%), and immunodeficiency (0.1%).
Guan et al56
1,590
Retrospective case study
China
25.1% reported at least one comorbidity. Reported comorbidities were hypertension (16.9%), other cardiovascular diseases (3.7%), cerebrovascular diseases (1.9%), diabetes (8.2%), HBV infection (1.8%), COPD (1.5%), chronic kidney diseases (1.3%), cancer (1.1%), and immunodeficiency (0.2%). No patient reported asthma. At least one comorbidity was more frequent in severe cases than in non-severe cases (32.8% vs 10.3%). Severe clinical presentation was observed in 19.3% of patients with comorbidities versus 4.5% of those without. Among patients with at least one comorbidity the hazard ratio of severe forms was 1.79 (95% CI 1.16–2.77) and 2.59 (95% CI 1.61–4.17) among those with two or more comorbidities. The HR of each comorbidity was: COPD: 2.681 (95% CI 1.424–5.058), diabetes 1.586 (95% CI 1.028–2.449), hypertension 1.575 (95% CI 1.069–2.322), cancer 3.501 (95% CI 1.604–7.643).
Gupta et al57
2,215
Multicenter cohort study of COVID-19 patients admitted to ICUs at 65 hospitals
USA
35.4% of patients died. Older age (80 vs <40 years OR 11.15, 95% CI, 6.19–20.06), male sex (OR 1.50, 95% CI 1.19–1.90), obesity (40 vs <25 OR 1.51, 95% CI 1.01–2.25), coronary artery disease (OR 1.47, 95% CI 1.07–2.02), cancer (OR 2.15, 95% CI 1.35–3.43), liver disease (OR 2.61, 95% CI 1.30–5.25), and CKD (OR 2.43, 95% CI 1.46–4.05) were significantly associated to a higher risk of death.
Haroun-Díaz et al58
80
Case description (assessment of COVID-19 effects on severe asthma patients)
Spain
COVID-19 was confirmed on three patients (3.75%). None of the three cases developed ARDS and did not require ICU admission or oxygen therapy
Hoek et al59
23
Descriptive study of COVID-19 cases in solid organ transplantation recipients
Netherlands
23 SOT recipients: 15 kidney, four heart, three lung, one kidney-after-heart, and one liver. All patients had a baseline immunosuppressive treatment. 83% of patients were hospitalized, 2 among 23 were admitted to an ICU and five patients died of COVID-19. Mortality was higher among patients with higher Clinical Frailty Scale (CFS) scores (5.8 vs 1.92 for survivors).
Huang et al60
6,452
Systematic review, meta-analysis, and meta-regression of diabetes and COVID-19 cases
China
Meta-analysis showed that diabetes was significantly associated with worst outcomes (RR 2.38 P < 0.001), mortality (RR 2.12, P < 0.001), severe disease (RR 2.45, P < 0.001), ARDS (RR 4.64, P = 0.001) and disease progression (RR 3.31, P = 0.04). Meta-regression showed that association between diabetes and worst outcome was affected by age (P = 0.003) and hypertension (P < 0.001).
Ioannidis et al61
226,017
Cross-sectional survey of countries with 800 or more deaths of COVID-19 as of April 24, 2020
13 USA states and 14 countries
Individuals <40 accounted for <1.3% of all COVID-19 deaths in European countries and Canada and 0.4–2.3% in the US states. However, in Mexico and India were a much larger proportion. Patients <65 accounted for 4.5–11.2% of COVID-19 deaths in Canada and European countries, 8.3–22.7% in US States, and were most deaths in India and Mexico. Individuals 80 years or older accounted for the majority of deaths in Europe (except Ireland) and Canada, in the US there was variability across states (39–63%). In Mexico, they accounted for 8.3% of deaths (no data on India). Patients <65 had 30- to 100-fold lower risk of COVID-19 death than those 65 or older in 11 European countries and Canada, 16- to 52-fold lower risk in US locations, and less than 10-fold in India and Mexico.
Kammar-García et al62
13,842
Retrospective cohort
Mexico
38.8% of cases were hospitalized, among those admitted to a hospital 55.5% were admitted to an ICU and 11.4% were intubated. 45.3% had at least one comorbidity, 26% had one comorbidity, 12.9% had two comorbidities, and 6.4% had three or more comorbidities. 95.6% of patients without comorbidities survived while 88.5% of those with one comorbidity, 81.8% of those with two comorbidities, and 73.7% of those with three or more comorbidities survived. Survival was significantly decreased as the number of comorbidities increased (log-rank Mantel-Cox, P < 0.0001). Survival analysis showed that comorbidity determines survival regardless of age. The risk of hospital admission (OR 3.1, 95% CI 2.7–3.7), pneumonia (OR 3.02, 95% CI 2.6–3.5), ICU admission (OR 2, 95% CI 1.5–2.7), and death (HR 3.5, 95% CI 2.9–4.2) was significantly increased in cases with three or more comorbidities than in patients with 1, 2 or no comorbidities.
Kasraeian et al63
87
Systematic review and meta-analysis of cases with COVID-19 pneumonia and pregnancy
China
78% of the pregnant women showed mild or moderate COVID-19. Clinical presentation of COVID-19 pneumonia was similar to the observed among other adult populations. 92% underwent cesarean section. No pregnancy loss was observed. No evidence of vertical transmission was found.
Khalil et al64
2,567
Systematic review and meta-analysis of clinical features and pregnancy outcomes of COVID-19 in pregnancy
USA, China, Spain, Italy, France, Brazil, and Netherlands
73.9% were in the third trimester. 21.8% had preterm birth (before 37 weeks), most of them indicated by a doctor (18.4%). ICU admission was necessary in 7.0% and intubation in 3.4%. Maternal mortality was low (0.9%). At least one comorbidity was reported in 32.5%: obesity 38.2%, smoker 3.3%, asthma 8.8%, hypertension 4.2%, cardiac disease 3.2%. Admission to ICU was significantly associated to comorbidities (beta = 0.007, P < 0.05), maternal age >35 (beta = 0.007, P < 0.01). Positive RT-PCR in neonates’ nasal swab was observed in 1.4%.
Killerby et al65
531
Retrospective study 220 hospitalized and 311 outpatient adults with COVID-19
USA
Age over 65 years (OR 3.4, 95% CI 1.6–7.4), black race (OR 3.2, 95% CI 1.8–5.8), diabetes mellitus (OR 3.1, 95% CI 1.7–5.9), male sex (OR 2.4, 95% CI 1.4–4.1), smoking (OR 2.3, 95% CI 1.2–4.5) and obesity (OR 1.9, 95% CI 1.1–3.3) were significantly associated with hospitalization.
Kumar et al66
16,033
Meta-analysis with studies from three countries
China, USA, France
Calculated pooled prevalence of diabetes: 11.2% (95% CI: 9.5%–13.0%). Calculated pooled odds ratio of association of diabetes mellitus with severe forms was 2.16 (1.74–2.68; P < 0.01). Calculated pooled odds ratio of association of diabetes mellitus with death was 1.90 (1.37–2.64; P < 0.01).
Lee et al67
800
Prospective cohort study of patients with active cancer and symptomatic COVID-19
UK
28% patients died, with death principally attributable to COVID-19 in 93% of patients. The risk of death was significantly associated with older age (median 73 years vs 66 years; P < 0.001) and with higher comorbidities including cardiovascular disease (21% vs 11%, P < 0.001) and hypertension (41% vs 27%; P < 0.001). Chemotherapy, immunotherapy, hormonal therapy, radiotherapy, and targeted therapies were associated to a higher risk of death.
Li et al68
548
Cohort study of severe cases.
China
Fatality rates estimated to be 1.1% in nonsevere cases and 32.5% in severe cases. Age over 65 years old (OR 2.2, 95% CI 1.5–3.5) and hypertension (OR 2.0, 95% CI 1.3–3.2) were significantly associated with severe clinical presentation and age 65 years (HR 1.7, 95% CI 1.1–2.7) or more and hyperglycemia (HR 1.8, 95% CI 1.1–2.8) were associated to death in severe cases.
Liang et al69
710
Retrospective cohort study throughout the country.
China
Age (OR 1.03, 95% CI 1.01–1.05), number of comorbidities (chronic obstructive pulmonary disease, diabetes, hypertension, coronary artery disease, cerebrovascular disease, hepatitis B, cancer, chronic renal disease, immunodeficiency disease, and pregnancy—OR 1.6 95% CI, 1.27–2.00) and cancer history (OR 4.07, 95% CI 1.23–13.43) were significant predictors of critical illness.
Liang et al70
18
Prospective cohort of COVID-19 cases
China
1% of COVID-19 cases had a medical history of cancer. 25% of cancer patients had done surgery or chemotherapy on the last month and 75% were cancer recovered in medical follow up. Patients with cancer had a more severe baseline CT findings, deteriorated significantly faster than those without cancer (median time to severe events 13 days vs 43 days, P < 0.0001) and significantly higher risk or severe outcomes (39% vs 8%, P = 0.0003). Lung cancer patients did not have a higher risk of severe events compared with patients with other cancers.
Mirzaei et al71
252
Systematic review of COVID-19 and HIV co-infection
China, Italy, Spain, Turkey, Uganda, USA
80.9% were men, mean age was 52.7 years and 98% were on antiretroviral therapy. Reported comorbidities: hypertension (39.3%), obesity or hyperlipidemia (19.3%), chronic obstructive pulmonary disease (18.0%), and diabetes (17.2%). 66.5% presented mild to moderate symptoms. Despite death among COVID19-HIV coinfected patients was high (14.3%) data suggest that mortality risk factors are related to older age and other comorbidities and not due to HIV.
Nie et al72
671
Descriptive study
China
22.4% of cases had comorbidities: 10.4% had cardiovascular diseases (of whom 85.7% had hypertension), 1.8% had diabetes, 2.5% had respiratory diseases. Cardiovascular diseases (including hypertension), diabetes and respiratory diseases were not significantly associated to with higher COVID-19 severity. Older age was significantly associated to with higher COVID-19 severity (OR 1.026, P = 0.003). 2 of 3 pregnant patients had severe disease.
Ortiz-Brizuela et al73
309
Prospective cohort study with 140 inpatients and 169 outpatients
Mexico
Compared with outpatients, inpatients were older and had more diabetes (22.9% vs 5.3%, P < 0.001) and hypertension (32.1% vs 9.5%, P < 0.001). Admission to ICU was significantly associated with diabetes (41.4% vs 18%, P = 0.016)
Pachiega et al74
276,703
Observational study
Brazil
83% of deaths cases were over 60 years old and 58.6% were male. Estimated prevalence of comorbidities in deaths was 83% (95% CI: 79–87). Comorbidities observed: chronic heart diseases (35%), diabetes (28.7%), asthma/COPD (8.2%), kidney diseases (5.9%), stroke (5.3%), hypertension (5.1%), obesity (4.4%) immunosuppressive diseases (3.8%), cancer (0.6%)
Palmieri et al75
3,032
Descriptive study patients who died of COVID-19
Italy
368 death cases were <65 years old and 2,644 were >65 years old. 4.1% of cases had no comorbidities, 15% had 1, 21.4% had 2, and 59.6% had 3 or more. Reported prevalence of comorbidities: ischemic heart disease (28.2%), atrial fibrillation (22.5%), heart failure (16.2%), hypertension (68.3%), type 2 diabetes (30.1%), dementia (15.8%), COPD (16.4%), cancer (15.8%), chronic liver disease (4.0%), chronic renal failure (20.4%), dialysis (1.8%), HIV (0.2%), autoimmune diseases (3.8%), obesity (11%). Patients over 65 years had more comorbidities than those <65 years (3.3 ± 1.9 vs 2.5 ± 1.8, P < 0.001). 10.9% patients <65 years had no comorbidities compared with 3.2% patients ≥65 years.
Panepinto et al76
178
Case series describing patients with sickle cell disease and COVID-19
USA
Median age of cases was 26 years old. 6% were asymptomatic, 54% had mild disease, 18% had moderate disease, 17% had severe disease, and 5% had critical disease. 69% were hospitalized, 11% were admitted to an ICU, and 7% died.
Patanavanich et al77
11,590
Meta-analysis
China, Korea, and USA
Smoking was significantly associated with an increased with COVID-19 progression (OR 1.91, P = 0.001). Limitations in various articles suggest that the risk of smoking may be even higher.
Pereira et al78
90
Retrospective study with solid organ transplantation patients and COVID-19
USA
76% of patients were hospitalized. 19% patients did not need oxygen therapy, 29% required nasal cannula, 12% non-rebreather mask, high flow nasal cannula or BIPAP and 35% were intubated and needed mechanical ventilation. 18% of all patients died.
Petrilli et al79
5,279
Prospective cohort study
USA
51.9% cases were admitted to hospital. 62.9% of entire sample reported at least one chronic condition. Observed comorbidities: hypertension (42.7%), diabetes (22.6%), asthma/COPD (14.9%), chronic kidney disease (12.3%), cancer (7.6%), coronary artery disease (13.3%), heart failure (7%), hyperlipidemia (32.5%), and obesity (BMI 30–39: 29.4% and BMI>40: 5.9%). Risk factors significantly associated with hospital admission were: age >75 (OR 37.9, P < 0.001), age 65–74 (OR 8.7, P < 0.001), heart failure (OR 4.4, P < 0.001), male sex (OR 2.8, P < 0.001), chronic kidney disease (OR 2.6, P < 0.001), obesity (BMI 30–39 OR 1.8, P < 0.001; BMI >40 OR 2.4, P < 0.001), hypertension (OR 1.8, P < 0.001) and diabetes (OR 2.2, P < 0.001). Risk factors significantly associated with critical illness were: age (65–74 OR 1.7, P = 0.004; >75 OR 2.3, P < 0.001), male sex (OR 1.5, P < 0.001), heart failure (OR 1.9, P < 0.001), BMI over 40 (OR 1.5, P = 0.03) and diabetes (OR 1.2, P = 0.03)
Richardson et al80
5,700
Descriptive analysis of cases admitted to hospitals in NY.
USA
Comorbidities were observed in 88% of hospitalized patients and the most common were hypertension, obesity, and diabetes.
Rivera-Izquierdo et al81
238
Retrospective case series of patients hospitalized for COVID-19
Spain
25.6% of patients died. No patients under 50 years old died. The risk factors significantly associated with a greater hazard of death were age (3% increase per 1-year increase in age) and diabetes mellitus (HR 2.42, 95% CI 1.43–4.09).
Robilotti et al82
423
Cohort study of cancer patients with COVID-19
USA
40% of cases were admitted to hospital, 20% had severe respiratory illness and 9% needed mechanical ventilation. Case fatality was 12% on the entire sample, 24% for those admitted to a hospital, and 35% for those admitted to an ICU. Age >65 (OR 1.82, P = 0.004), smoking (current/former) (OR 1.60 P = 0.022), race non-white (OR 1.62, P = 0.029), hematologic cancer (OR 2.49, P = 0.003), cardiac disorder (OR 1.86, P = 0.015), chronic kidney disease (OR 1.84, P = 0.003), chronic lymphopenia or corticosteroids (OR 1.85, P = 0.030), ICI (immune checkpoint inhibitors) therapy (OR 2.84, P = 0.013) were associated to a higher risk of hospitalization and severe respiratory illness. Age >65 (OR 1.67, P = 0.024), smoking (current/former) (OR 1.78, P = 0.007), cardiac disorder (OR 2.02, P = 0.002), chronic kidney disease (OR 1.68, P = 0.02), and ICI therapy (OR 2.38 P = 0.005). Receiving chemotherapy on the last month, major surgery and metastatic cancer were not significantly associated to a higher risk of severe forms of COVID-19. Seven pediatric patients had mild presentation and no complication was observed.
Sardu et al83
59
Cohort of COVID-19 pneumonia patients with normal glycemia a and hyperglycemia at baseline
Italy
D-dimer levels were significantly higher in patients with hyperglycemia than in those with normal glycemia (P < 0.001). COVID-19 patients with diabetes and patients with hyperglycemia had a higher risk of severe form of disease than patients without diabetes and normoglycemia. Few patients with hyperglycemia with or without previous DM were free from severe disease compared with patients with normoglycemia without previous diabetes (P < 0.02).
Shi et al84
306
Case-control study 153 patients with COVID-19 patients and diabetes matched with 153 sex and age-matched COVID-19 controls admitted at two tertiary hospitals
China
Patients with diabetes had a higher prevalence of hypertension (56.9% vs 28.8%), cardiovascular disease (20.9% vs 11.1%), and cerebrovascular disease (7.8% vs 1.3%), all P < 0.05. Diabetes patients were more likely to be admitted to ICU (17.6% vs 7.8%, P < 0.05) and to have ARDS (24.8% vs 11.1%), acute cardiac injury (30.7% vs 17.0%), secondary infections (24.2% vs 11.1%), shock (20.9% vs 10.5%), and acute kidney injury (12.4% vs 3.3%), all P < 0.05. For all cases, hypertension, cardiovascular disease and chronic pulmonary disease were independently associated with in-hospital death. Diabetes (HR 1.58, 95% CI 0.84–2.99). After adjustment diabetes was not statistically significantly associated with in-hospital death. Among patients with diabetes, age over 70 years (HR 2.39, 95% CI 1.03–5.56) and hypertension (HR 3.10, 95% CI 1.14–8.44) were associated with in-hospital death.
Stokes et al85
1,320,488
Descriptive (case surveillance)
USA
14% were hospitalized, 2% were admitted to an ICU, and 5% died. Comorbidities reported: cardiovascular disease (32%), diabetes (30%), and chronic lung disease (18%), renal disease (7.6), immunocompromised (5.3%), neurologic/neurodevelopmental disability (4.8%). 45% of patients reporting at least one health condition were hospitalized versus 7.6% among those who did not report underlying conditions. 19.5% of cases with comorbidities died versus 1.6% of those without comorbidities.
Suleyman et al86
463
Case series (retrospective review) of patients from a healthcare System
USA
94% patients had at least one comorbidity: 63.7% hypertension, 39.3% chronic kidney disease and 38.4% diabetes. Male sex (OR 2.0, P = 0.001), severe obesity (OR, 2.0, P = 0.02), and chronic kidney disease (OR, 2.0, P = 0.006) were significantly associated with ICU admission and age >60 years (OR 3.5, P < 0.001), severe obesity (OR 3.2, P < 0.001), CKD (OR 2.4, P < 0.001), and cancer (OR 2.5, P = 0.01) were independently associated with the need for mechanical ventilation.
Sun et al87
244
Retrospective case-control study among patients over 60 years old
China
58.5% in the discharged group and 32.2% in the deceased group were women. Comorbidities prevalence: 21% had diabetes and 14.4% had coronary heart disease. Older age (OR 1.122, P = 0.037) was significantly associated with increased risk for death.
Vila-Córcoles et al88
1,547
Population-based retrospective cohort with adults over 50 years-old
Spain
Among 349 positive cases, the most common reported comorbidities were: hypertension (58.7%), hypercholesterolemia (35%), heart disease (33%), diabetes (26.9%), and obesity (26.1%). A higher incidence of COVID-19 was observed among patients with neurologic disease, atrial fibrillation, chronic renal disease, heart disease, chronic respiratory disease, diabetes, and cancer. An increased risk of acquiring COVID-19 was significantly associated with heart disease (HR: 1.47, P = 0.045) and chronic respiratory disease (HR: 1.75, P = 0.05)
Wang et al89
138
Case series of COVID-19 pneumonia cases
China
46.4% patients had one or more chronic diseases: hypertension (31.2%), diabetes (10.1%), cardiovascular disease (14.5%), cancer (7.2%), cerebrovascular disease (5.1%), COPD (2.9%), chronic kidney disease (5.5%), chronic liver disease (2.9%), HIV infection (1.4%). Patients admitted to ICU care were significantly older (median age 66 vs 51; P < 0.001) and had more underlying diseases: hypertension, diabetes, cardiovascular disease, and cerebrovascular disease.
Wang et al90
1,558
Meta-analysis
China
COVID-19 patients with hypertension (OR 2.29, P < 0.001), diabetes (OR 2.47, P < 0.001), or COPD (OR 5.97, P < 0.001) had a higher risk of exacerbation. Cardiovascular disease (OR 2.93, P < 0.001) and cerebrovascular disease e (OR 3.89, P = 0.002) were significantly associated with severe COVID-19. Liver disease, cancer, and kidney disease were not significantly associated with severe COVID-19.
Williamson et al91
5,683
Cohort study from 2/1 to 4/25/2020 encompassing general population and deaths cases of COVID-19
UK
Death from COVID-19 was significantly associated with older age [60–70 (HR 2.09 95% CI 1.84–2.38), 70–80 (HR 4.77 95% CI 4.23–5.38), >80 (HR 12.64 95% CI 11.19–14.28)], male sex (HR 1.99, 95% CI 1.88–2.10), uncontrolled diabetes (HR 2.36, 5% CI 2.18–2.56), severe asthma (HR 1.25, CI 1.08–1.44), obesity [class I (HR 1.27, 95% CI 1.18–1.36), class II (HR 1.56, 95% CI 1.41–1.73), class III (HR 2.27, 95% CI 1.99–2.58), liver disease (HR 1.61, 95% CI 1.33–1.95), stroke/dementia (HR 1.79, 95% CI 1.67–1.93), other neurological (HR 2.46, 95% CI 2.19–2.76), kidney disease (HR 1.72, 95% CI 1.62–1.83), organ transplant (HR 4.27, 95% CI 3.20–5.70), spleen diseases (HR 1.41, 95% CI 0.93–2.12), Rheumatoid/Lupus/ Psoriasis (HR 1.23, 95% CI 1.12–1.35), other immunosuppressive condition (HR 1.69, 95% CI 1.21–2.34). Ethnicity had a significant effect on the risk of death of COVID-19 for black people (HR 1.71, 95% CI 1.44–2.02) and Asian people (HR 1.62, 95% CI 1.43–1.82)
Wu et al92
201
Retrospective cohort from 12/25/2019 to 1/26/2020
China
41.8% developed ARDS and of those, 52.4% died. Comorbidities prevalence: hypertension (19.4%), diabetes 22 (10.9%), cardiovascular disease 8 (4.0%), liver disease 7 (3.5%), nervous system disease 7 (3.5%), chronic lung disease 5 (2.5%), chronic kidney disease 2 (1.0%), and cancer (0.5%). Age ≥65 years significantly associated with higher risks of developing ARDS (HR 3.26, 95% CI 2.08–5.11) and death (HR 6.17, 95% CI, 3.26–11.67). Compared with patients with and without ARDS, ARDS cases had a higher proportion of hypertension (13.7%, P = 0.02) and diabetes (13.9%, P = 0.002).
Wu et al93
926
Meta-analysis of diabetes and COVID-19 cases
China
A strong association between diabetes and mortality of COVID-19 patients was found: OR 1.75 (95% CI 1.31–2.36, P = 0.0002).
Xu et al94
703
Retrospective observational study of patients admitted to tertiary hospitals in China between 01/10/2020 and 3/13/2020.
China
Death and other adverse outcomes groups were older, more men and had more comorbidities, especially with >2 comorbidities (cardiovascular disease, diabetes, hypertension, COPD, chronic liver disease, chronic kidney disease and malignancy).
Yamada et al95
210
Retrospective cohort of patients with chronic kidney disease and COVID-19
USA
CKD patients had a higher risk of severe disease (RR 2.51, P < 0.001) and death (RR 2.05, P < 0.001) without adjusting age groups. A significant increased risk of mortality was found in CKD patients when stratifying by age groups among age from 60 to 79 (RR 1.80, 95% CI 1.15–2.83), but not in patients age 80 or older (RR 1.15 95% CI 0.71–1.86). Significant higher risk of death was found when CKD was associated to other comorbidities: atrial fibrillation (OR 2.13, 95% CI 1.03–4.43), heart failure (OR 2.09, 95% CI 1.16–3.77), and ischemic heart disease (OR 2.87, 95% CI 1.04–3.36)
Yang et al96
710
Single-centered, retrospective, observational study, of adult patients with COVID-19 admitted to ICU
China
Compared with survivors, non-survivors were older (64.6 vs 51.9) and were more likely to have chronic medical illnesses (53% vs 20%). Comorbidities and risk factors among survivors and non-survivors were chronic cardiac disease (10%), chronic pulmonary disease (8%), cerebrovascular disease (13.5%), diabetes (17%), cancer (4%), dementia (2%), malnutrition (2%), and smoking (4%).
Zaigham and Andersson97
108
Systematic review all case reports and series of COVID-19 and pregnancy
China, Sweden, USA, Korea, and Honduras
Three ICU admissions were reported but no maternal deaths. One neonatal death and one intrauterine death were also reported. Most mothers were discharged with no major complications, severe maternal morbidity, and perinatal deaths were reported. Vertical transmission of the COVID-19 could not be ruled out
Zhang et al98
869
Retrospective cohort, single-center study of COVID-19 cases
China
616 (70.9%) were discharged and 95 patients (10.9%) were transferred to due to worsening disease. Comorbidities reported: hypertension (10.5%), diabetes (2.4%), and COPD/asthma (1.6%). Cases with comorbidities had a significantly higher risk of condition worsening (HR, 2.733, P = 0.001)
Zhao et al99
2,002
Meta-analysis
China
Pooled OR of COPD for the development of severe COVID-19 was 4.38 (95% CI 2.34–8.20). Pooled OR of COPD for death of COVID-19 was 1.93 (95% CI 59–7.43). OR of current smoking the development of severe COVID-19 was 1.98 (95% CI: 1.29–3.05).
Zheng et al100
3,027
Meta-analysis
China
Male sex (OR 1.76, P < 0.00001), age 65 or older (OR 6.06, P < 0.00001), and smoking (OR 2.51, P = 0.0006) were significantly associated with disease progression. Diabetes (OR 3.68, P < 0.00001), hypertension (OR = 2.72, P = 0.0002), cardiovascular disease (OR 5.19, P < 0.00001), respiratory disease (OR 5.15, P < 0.00001) were significantly associated with critical/mortal disease.
Zhou et al101
171
Retrospective, multicenter cohort study of adult inpatients (from 12/29/2019 to 1/31/2020
China
48% patients had comorbidity: hypertension (30%), diabetes (19%), and coronary heart disease (8%). Older age (OR 1.14), coronary heart disease (OR 21.4, P < 0·0001), hypertension (OR 3.05, P = 0.0010), diabetes (OR 2.85, P = 0·0062) were significantly associated with in-hospital death.
Zhu et al102
7,337
28 days retrospective cohort of inpatient cases focusing on the association between plasma glucose levels and outcomes in COVID-19 patients with T2D
China
Prevalence of T2D was similar to the country prevalence. T2D was significantly correlated with ARDS. The in-hospital death rate was significantly higher in patients with T2D relative to the non-diabetic individuals (HR 1.70, P < 0.001). Compared with the poor controlled group, the well-controlled group had less frequent occurrences of ARDS, acute heart injury, acute kidney injury, septic shock, and DIC. Death rate was significantly lower in the well-controlled group.
TABLE 2 -
Overview of Risk Factors and Conditions Studied in the 73 Articles Reviewed
Author
Type of Study
Age
Sex
Race
CVD
HBP
DM
Obesity
Smoking
CRD
CKD
Cancer
HIV
Liver Disease
Pregnancy
Organ Transplantation
Stroke and Other Neurologic
Rheumatic Disease
IBD
SCD
OSA
Association /Score
Aggarwal et al30
Meta-analysis
X
Akalin et al31
Cohort
X
Alberici et al32
Cohort
X
Assaad et al33
Cohort
X
Bello-Chavolla et al34
Cohort
X
X
X
X
X
X
X
Bezzio et al35
Cohort
X
X
X
Cai et al36
Descriptive
X
China CDC37
Descriptive
X
X
X
X
Chen et al38
Descriptive
X
X
X
X
X
X
X
X
X
Chen et al39
Descriptive
X
Chhiba et al40
Cohort
X
X
X
Choi et al41
Cohort
X
X
X
Christensen et al42
Cohort
X
X
Cummings et al43
Cohort
X
X
X
X
Della Gatta et al44
Systematic review
X
Docherty et al45
Cohort
X
X
X
X
X
X
X
X
Du et al46
Cohort
X
X
X
Ebekozien et al47
Descriptive
X
Fadini et al48
Meta-analysis
X
Fredi et al49
Descriptive
X
X
Gao et al 50
Case-control
X
García-Pachón et al51
Descriptive
X
Grandbastien et al52
Cohort
X
Grasselli et al53
Descriptive
X
X
X
X
X
X
X
X
X
X
X
X
Grasselli et al54
Cohort
X
X
X
X
Guan et al55
Descriptive
X
X
X
X
X
X
X
X
Guan et al56
Cohort
X
X
X
X
X
Gupta et al57
Cohort
X
X
X
X
X
X
X
Haroun-Díaz et al58
Descriptive
X
Hoek et al59
Descriptive
X
Huang et al60
Meta-analysis
X
X
X
Ioannidis et al61
Cross-sectional
X
Kammar-García et al62
Cohort
X
Kasraeian et al63
Meta-analysis
X
Khalil et al64
Systematic review
X
Killerby et al65
Cohort
X
X
X
X
X
Kumar et al66
Meta-analysis
X
Lee et al67
Cohort
X
Li et al68
Cohort
X
X
X
Liang et al69
Cohort
X
X
X
X
X
X
X
X
Liang et al70
Cohort
X
Mirzaei et al71
Systematic review
X
Nie et al72
Descriptive
X
Ortiz-Brizuela et al73
Cohort
X
X
X
Pachiega et al74
Descriptive
X
X
X
X
X
X
X
X
X
X
Palmieri et al75
Descriptive
X
X
X
X
X
X
X
X
X
X
X
Panepinto et al76
Descriptive
X
Patanavanich et al77
Meta-analysis
X
Pereira et al78
Descriptive
X
Petrilli et al79
Cohort
X
X
X
X
X
X
X
Richardson et al80
Descriptive
X
X
X
X
X
X
X
X
X
X
X
Rivera-Izquierdo et al81
Cohort
X
X
Robilotti et al82
Cohort
X
Sardu et al83
Cohort
X
Shi et al84
Case-control
X
X
X
Stokes et al85
Descriptive
X
X
X
X
X
X
X
X
Suleyman et al86
Descriptive
Sun et al87
Case-control
X
Vila-Córcoles et al88
Cohort
X
X
X
Wang et al89
Descriptive
X
X
Wang et al90
Meta-analysis
X
X
X
X
X
X
X
Williamson et al91
Cohort
X
X
X
X
X
X
X
X
X
X
X
X
Wu et al92
Cohort
X
X
X
Wu et al93
Meta-analysis
X
Xu et al94
Descriptive
X
X
X
X
X
X
X
X
X
X
Yamada et al95
Cohort
X
Yang et al96
Descriptive
X
X
X
X
X
X
X
Zaigham & Andersson97
Systematic review
X
Zhang et al98
Cohort
X
X
X
X
X
Zhao et al99
Meta-analysis
X
Zheng et al100
Meta-analysis
X
X
X
X
X
X
Zhou et al101
Cohort
X
X
X
X
Zhu et al102
Cohort
X
The descriptive studies examine associations between sociodemographic factors (age, male sex, non-White race/ethnicity), health risks (eg, smoking, BMI), and chronic diseases (eg, cardiovascular, hypertension, diabetes, chronic respiratory diseases, kidney diseases, cancer, immunosuppression, and rheumatic diseases), and adverse COVID-19 outcomes. Despite raising concerns about reported risk factors, descriptive studies do not confirm a causal association of these factors with severe disease and death.103 Cohort studies are more likely to prove etiology; in these studies, significant associations with adverse COVID-19 outcomes included older age (19 studies), male gender (seven studies), non-White race (two studies), cardiovascular diseases (eight studies), hypertension (10 studies), diabetes (17 studies), BMI greater than 30 kg/m2 (three studies), cigarette smoking (one study), chronic respiratory diseases (11 studies), chronic kidney diseases (six studies), cancer (nine studies), immunosuppression (three studies), liver diseases (three studies), pregnancy (one study), organ transplantation (three studies), stroke and other neurologic (three studies), rheumatic diseases (one study), inflammatory bowel disease (one study), obstructive sleep apnea (one study), and association or combination of more than one disease and increasing risk (six studies). Three case-control studies were reviewed and reported associations of age (two studies), hypertension (one study), diabetes (one study), and obesity (one study) with COVID-19 complications. Among the 10 meta-analyses reviewed, conclusions supported significant associations with complications for diabetes (five studies), cardiovascular diseases (three studies), chronic respiratory diseases (three studies), older age (three studies), male sex (two studies), smoking (two studies), hypertension (two studies), pregnancy, stroke, and other neurologic conditions (both one study).
Table 3 presents a summary of guidelines for at-risk individuals published by several countries and legal guidelines and requirements for the management of at-risk workers. Governmental recommendations are generally in line with the published literature, based on age, health risk factors, and chronic medical conditions. However, there are several important differences. Some countries have been more specific and provided more detailed clinical criteria (UK22,108 and South Africa113 ) while others provide only guidelines with few details (India,107 Spain,109 and Brazil105 ). Two countries created empirical risk categories: USA (increased risk and possibly at increased risk)114 and UK (high risk or clinically extremely vulnerable and moderate risk or clinically vulnerable).22 Legal requirements on management of high risk workers for employers differ by country, ranging from general protection measures, as Spain110 and India107 with no specific recommendations, to the United States104 with general recommendation that employers must consider, to the UK108 and Brazil106 with more specific obligations for employers to stringent requirements in South Africa,113 which require employers to have policies and procedures to address the needs of vulnerable employees.
TABLE 3 -
Summary of Criteria and Management Guidelines for at Risk Workers Published by Country Health Authorities
Country
Agencies
Criteria
Management Recommendation
USA
CDC21 OSHA104
• Age >60 years old• Underlying medical conditions at an increased risk: ✓ Cancer ✓ Chronic kidney disease ✓ COPD ✓ Immunocompromised state from solid organ transplant ✓ Obesity ✓ Serious heart conditions (CHF, CAD and cardiomyopathies) ✓ Sickle cell disease ✓ Type 2 diabetes mellitus• Underlying medical conditions possibly at an increased risk ✓ Asthma (moderate-to-severe) ✓ Cerebrovascular disease (affects blood vessels and blood supply to the brain) ✓ Cystic fibrosis ✓ Hypertension or high blood pressure ✓ Immunocompromised state (weakened immune system) from blood or bone marrow transplant, immune deficiencies, HIV, use of corticosteroids, or use of other immune weakening medicines ✓ Neurologic conditions, such as dementia ✓ Liver disease ✓ Pregnancy ✓ Pulmonary fibrosis (having damaged or scarred lung tissues) ✓ Smoking ✓ Thalassemia (a type of blood disorder) ✓ Type 1 diabetes mellitus
Employers should develop plans that consider and address the level(s) of risk associated with different worksitesGeneral protective measures must be implemented (social distancing, use of masks and hand/respiratory hygiene)
Brazil
Ministry of Health105 Secretary of Labor106
Age >60 years oldSevere or decompensated heart diseases (heart failures, CAD, arrhythmias and hypertension)Severe or decompensated lung diseases (COPD, asthma, oxygen-dependent)Immunocompromised stateAdvanced kidney disease (stages 3, 4 or 5)Diabetes (according to physician opinion)High-risk pregnancy
High-risk workers must work from home if possible or measures to reduce exposure must be implementedA list of high-risk employees must be available if requested by labor inspectionGeneral protective measures must be implemented (social distancing, use of masks and hand/respiratory hygiene)
India
Ministry of Health and Family Welfare107
Age >60 years oldDiabetesHypertensionCardiac diseaseChronic lung diseaseCerebrovascular diseaseChronic kidney diseaseImmunosuppressionCancer
High-risk workers must adopt general protective measures (social distancing, use of masks and hand/respiratory hygiene) at workplaces
UK
National Health System22 Health and Safety Executive108
High risk (clinically extremely vulnerable) ✓ Organ transplant ✓ Chemotherapy or antibody treatment for cancer, including immunotherapy ✓ Intense course of radiotherapy (radical radiotherapy) for lung cancer ✓ Targeted cancer treatments that can affect the immune system (such as protein kinase inhibitors or PARP inhibitors) ✓ Blood cancer (leukemia, lymphoma, or myeloma) ✓ Bone marrow or stem cell transplant in the past 6 months or taking immunosuppressant medicine ✓ Severe lung condition (cystic fibrosis, severe asthma or severe COPD) ✓ Severe combined immunodeficiency (SCID) or sickle cell disease ✓ High doses of steroids or immunosuppressant medicine ✓ Serious heart condition and are pregnantModerate risk (clinically vulnerable) ✓ Age 70 or older ✓ Not severe lung disease (asthma, COPD, emphysema or bronchitis) ✓ Heart disease (such as heart failure) ✓ Diabetes ✓ Chronic kidney disease ✓ Liver disease (such as hepatitis) ✓ Neurologic diseases (Parkinson disease, motor neuron disease, multiple sclerosis, or cerebral palsy) ✓ Use of medicine that can affect the immune system (such as low doses of steroids) ✓ Severe obesity (BMI 40 or above) ✓ Pregnancy
Clinically extremely vulnerable workers must not return to work before specific dates.After specific dates, employees can return to work if workplace is COVID-secure. If possible, they should work from home.
Spain
Ministry of Health109 Ministry of Labor110
Risk factors for COVID-19 complications ✓ Older age ✓ Heart diseases and hypertension ✓ Diabetes ✓ COPD ✓ Cancer ✓ Immunosuppression ✓ Pregnancy ✓ Obesity ✓ Smoking ✓ Other chronic diseases
General protective measures must be implemented at all workplaces (communication, social distancing, use of masks, and hand/respiratory hygiene)
Italy
Ministry of Health111 Ministry of Labor and Social Policies112
Risk factors for death of COVID-19 ✓ Older age ✓ Hypertensive heart disease ✓ Diabetes ✓ Coronary heart diseases ✓ Cancer ✓ Organ transplant recipients
High-risk worker, if certified by local health authority may take medical leave during COVID-19 pandemic according to country legislation
South Africa
National Department of Health113
Risk factors for serious complications and severe illness from COVID-19 ✓ 60 years and older ✓ One or more of the underlying commonly encountered chronic medical conditions (of any age) particularly if not well controlled: Chronic lung disease: moderate to severe asthma, chronic obstructive pulmonary disease (COPD), bronchiectasis, idiopathic pulmonary fibrosis, active TB and post-tuberculous lung disease (PTLD) Diabetes (poorly controlled) or with late complications Moderate/severe hypertension (poorly controlled) or with target organ damage Serious heart conditions: heart failure, coronary artery disease, cardiomyopathies, pulmonary hypertension; congenital heart disease Chronic kidney disease being treated with dialysis Chronic liver disease including cirrhosis Severe obesity (BMI of 40 or higher) Immunocompromised as a result of cancer treatment, bone marrow, or organ transplantation, immune deficiencies, poorly controlled HIV or AIDS, prolonged use of corticosteroids and other immune weakening medications >28 weeks pregnant (and especially with any comorbidity)
Employers should have a policy and procedures to address the needs of vulnerable employees.These measures need to consider the work environment and activities and include:Ensuring that potential exposure to the SARS-CoV-2 virus is eliminated or minimizedIf potential exposure cannot be eliminated the employer should explore other ways of temporary workplace accommodation that prevent the risk of infection.If the accommodation is not possible, consider work from home.If the above steps are not possible, adopt leave procedures according to country legislation.
The Workplace Risk Pillar
The workplace in the era of the pandemic is being redesigned to reduce spread of the COVID-19 virus. A significant number of employees are working from home and are concerned about returning to work.115,116 Baker et al117 estimated the number of workers in the United States who are frequently exposed to infection and disease, and therefore COVID-19, in the workplace more than once a month. Approximately 10% of US workers are exposed to disease or infection at least once per week, while 18.4% are exposed to disease or infection at least once per month. The majority of these workers are healthcare workers. Other occupations frequently exposed include police officers, correction officers, fire fighters, office and administrative support staff, educators, and community and social service workers. Mitigating the spread of COVID-19 through workplace policies and procedures is important in the overall strategy to limiting the spread of the pandemic. Understanding the estimated number of workers potentially exposed is useful in developing workplace specific strategies.118
The factors associated with the employee safely returning to the workplace in the context of COVID-19 have been categorized by Rafeemanesh et al118 as: (1) control measures including engineering controls, (2) administrative controls, and (3) personal protective equipment. Control measures include isolation of symptomatic individuals, proper ventilation, barriers between staff and clients/customers, using disposable tools and instruments, continuous cleaning, and disinfection. Administrative controls include preventing entry of sick workers, continuous training of staff on hygiene, reducing staff hours, and restricting staff gatherings. Personal protective equipment includes proper masks/respirators, eye protection, gloves, and special clothing.
Based on evaluation of workplace exposures, different occupations have been associated with a particular level of risk.119 For example, by the nature of their work, healthcare workers are generally at the highest risk of COVID-19 infection whereas an outdoor agricultural worker is generally at low risk because they work independently and at a distance from coworkers (apart from risks associated with commuting and housing).120 The US Occupational Health and Safety Administration has classified risk of occupational exposure from very high, high, medium, and lower risk.104 Very high-risk occupations include healthcare workers performing aerosol-generating procedures and laboratory personnel and morgue workers performing autopsies. High occupational risk of exposure includes healthcare workers, medical transport workers, and mortuary workers who prepare bodies. Medium exposure risk jobs are those requiring contact within 6 ft./2 m with people who might be infected. Low risk jobs include those that do not require contact within 6 ft./2 m of the public or coworkers (Table 4 ).
TABLE 4 -
Occupational Risk Stratification
104
Risk Level
OSHA Designation
Description
Examples
4
Very high
Jobs with high risk of exposure to confirmed or suspected sources of Sars-Cov-2 during medical, laboratory or postmortem procedures
Healthcare personnel carrying out procedures such as intubation, bronchoscopy, dental procedures and invasive sample collection on suspected or confirmed COVID-19 patientsHealthcare personnel collecting or handling specimens from confirmed or suspected COVID-19 patientsMorgue workers performing autopsies on the bodies of people with confirmed or suspected COVID-19
3
High
Jobs with high risk of exposure to known or suspected sources of COVID-19
Healthcare staff (eg, physicians, nurses, physiotherapists, nutritionists, and others who must enter patients’ rooms) providing care to confirmed or suspected COVID-19 patients (except when performing aerosol-generating procedures)Medical transportation workers moving confirmed or suspected COVID-19 patients in enclosed vehicles.Mortuary workers involved in preparing bodies of deceased people who are known to have suspected of confirmed COVID-19 at the time of their death.
2
Medium
Jobs with contact within 6 feet with people who may be infected with SARS-CoV-2, but who are not confirmed or suspected COVID-19 patients (general public)
School workers, high-volume retail workers, and other high-population-density work environments
1
Lower risk (caution)
Jobs that do not require contact with confirmed or suspected COVID-19 patients nor contact within 6 feet of general public
All occupations with minimal contact with the public and other coworkers
The Community Risk Pillar
The third aspect that must be taken in consideration for managing the risk of workers is the level of community transmission of SARS-Cov-2, which reflects how prevalent the disease is in the community.121,122 The risk of acquiring the disease is associated with the prevalence of disease where the individual lives and works.123 To find out the level of community transmission, the physician must be aware of the available information and data which are provided by the World Health Organization, government health agencies around the world, research centers, and other sources. WHO has defined four transmission scenarios for COVID-19124 and provides updated information for all countries as (1) no new cases, (2) sporadic cases, (3) clusters of cases, and (4) community transmission on its website.125 Noticeably, current experience with COVID-19 indicates that in many regions with sporadic cases, aggressive testing strategies may reveal underlying community transmission.126 CDC classifies levels of community transmission as (1) no to minimal community transmission, (2) minimal to moderate community transmission, when there is sustained transmission and potential risk for rapid increase in cases, (3) substantial, controlled transmission, when there is large scale but controlled community transmission, and (4) substantial, uncontrolled transmission, when there is large scale, uncontrolled community transmission, including communal settings.127 EndCoronavirus is an international volunteer coalition with over 4000 scientists, community organizers, citizens, and business owners operating since February 29, 2020. This organization offers guidelines and recommendations with the intent to help governments, communities, healthcare, institutions, families, and individuals to end the pandemic. The coalition's website128 includes data which classifies countries as “winning,” “nearly there,” and “need action.” If available, more precise measures like number of daily cases per 100,000 (low less than 1, moderate 1 to 10, high 11 to 25, and critical more than 25) and percent of positive PCR tests (low less than 3%, moderate 3% to 6%, high greater than 6% to 10%, and critical more than 10%) can be used by the physician to estimate the risk that a worker will be exposed at the community level.129,130 The Johns Hopkins Coronavirus Resource Center (CRC)131 provides updated COVID-19 data and expert guidance by aggregating and analyzing data available from the United States and other countries (cases, testing, contact tracing, and vaccine efforts) to assist policymakers and healthcare professionals worldwide to respond to the pandemic. Their website includes the percentage of positive COVID-19 tests for most countries.
Table 5 summarizes data the physician should consider when defining the level of transmission in a community and determining the risk for a patient. The four levels of community spread listed in Table 5 are based on metrics published by WHO, CDC, Johns Hopkins University, and Harvard Global Health Institute. Other relevant indicators of community transmission such as R0 and herd immunity have not been considered in our model for stratifying the level of community transmission. At this time, there are no definitive reports on how to use such indicators to quantify risk. Additional research is needed to determine if such metrics should be included in worker risk models. Therefore, we recommend healthcare providers continue to focus primarily on metrics used to measure COVID-19 community transmission.
TABLE 5 -
Levels of Community Transmission
1
2
3
4
WHO transmission status
No new cases
Sporadic cases
Clusters of cases
Community transmission
Level of Community Transmission (CDC)
No to minimal community transmission
Minimal to moderate community transmission
Substantial, controlled transmission
Substantial, uncontrolled transmission
Country status at endcoronavirus.org
Winning
Nearly there
Nearly there
Need action
Country or state % of positive tests at coronavirus.jhu.edu/testing
≤ 3%
3%–6%
6%–10%
>10%
Daily new cases per 100,000 people (if available)
<1
1<10
10–25
>25
DISCUSSION
The Individual Risk Pillar
The literature review found a strong association with older age as an independent risk for severe forms and death of COVID-19. The risk for ICU admission and/or death increases exponentially with age which may be explained by immunosenescence,132,133 “inflammaging,”132,133 and reduced mucociliary clearance.134 Male gender has also been reported in most studies as an independent risk factor for death and severe clinical forms of COVID-19, which may be related to a higher prevalence of chronic diseases, higher health risk behaviors, occupational exposure, and sex differences in the expression of angiotensin-converting enzyme 2 (ACE2) and transmembrane serine protease 2 (TMPRSS2) which have both been implicated on virus entry on target cells.135,136 Race and ethnicity have been reported as independent risk factors in four studies (two cohorts and two descriptive) for higher mortality among non-white (Black, Hispanic, and Asian). However, the reason for this observation is not known at this time. Possible explanations include living conditions, health disparities, prevalence of comorbidities, and chronic stress.137
Obesity has been reported in several studies as an independent risk factor for COVID-19 morbidity and mortality. Notably, one study found a clear dose–response gradient between increasing BMI and a greater risk of virus complications,50 which supports a cause and effect relationship. Another study found that obesity represented 49.5% of the total effect of diabetes on COVID-19 mortality.34 Such findings may be related to effects on immunity, occurrence of comorbidities,138 and effects on the respiratory system.139 A consistent finding in our literature review was that smoking is associated with unfavorable COVID-19 outcomes, which can be related to several and probably interactive effects such as structural changes in the respiratory tract, impaired cell-mediated immunity in the alveolus, depletion of interleukin-1 and interleukin-6, reduced activity of natural killer (NK) cell in peripheral blood, reduced level of circulating immunoglobulins, and depressed phagocyte activity.140 However, immunologic abnormalities are reversible and expected to resolve within 6 weeks after stopping smoking140 so all workers must be advised and supported to quit smoking during the COVID-19 pandemic.
Pre-existing cardiovascular disease (CVD) (such as coronary artery disease, cardiomyopathy, valvular diseases, and heart failure), have consistently been reported as a risk for poor COVID-19 outcomes. Of note, a study conducted in China found a very strong association (odds ratio 21.4, P < 0.0001)101 between coronary heart disease and in-hospital death. Hypertension has been reported as an independent risk factor for unfavorable COVID-19 outcomes. It is not clear whether this increased risk is directly related to hypertension or to other associated comorbidities (CVD, diabetes, obesity, and others) or anti-hypertensive medication treatment.141,142 Treatment resistant hypertension is associated with increased inflammatory biomarkers (interleukin-6, interleukin-1β, tumor necrosis factor-α, and high-sensitivity C-reactive protein).143 Hypertension might serve to enhance the systemic inflammatory response observed in patients with COVID-19. However, more research is needed to clarify the pathophysiological relation and associated risk, especially among patients with treatment resistant hypertension.144 There has been initial concern about the safety of angiotensin-converting-enzyme inhibitors (ACE inhibitors) and angiotensin II receptor blockers (ARBs), related to the intensification of ACE2 receptor expression, which could be associated with an increased risk of SARS-CoV-2 infection.145 However, ACE2 receptors may protect against acute respiratory distress syndrome (ARDS) in COVID-19 patients145 and more recent studies suggest that the use of renin-angiotensin-aldosterone system inhibitors is not associated with increased risk of severe forms of COVID-19.146,147
Diabetes is an independent predictor of COVID-19 severity and mortality, which may be due to the inhibition of neutrophil chemotaxis, altered cytokine production, phagocytic cell dysfunction, impaired T cell-mediated immune responses, and ineffective microbial clearance.148 Hyperglycemia can also be a consequence of COVID-19 infection, caused by ACE2-dependent transient damage of pancreatic islets and exocrine tissue. Hyperglycemia and diabetes development during hospital admission have been reported.149 Hyperglycemia at admission, without history of diabetes, was reported by Sardu et al83 as an independent risk factor for poorer outcomes. Current research highlights the importance of glycemic control during the COVID-19 pandemic and protective measures for workers with diabetes.
The respiratory diseases most studied have been COPD and asthma and one study also assessed interstitial lung diseases. COPD has consistently been identified in several studies as an independent risk factor for severe forms of COVID-19. While some studies found a significant association of asthma and poorer outcomes, others did not. Studies that reported a poorer outcome tended to combine asthma and COPD as one category (chronic respiratory diseases). Three studies which were limited to patients with asthma did not find an association with more severe COVID-19 lung involvement and poorer clinical outcomes. A large UK cohort study found a significant association of severe asthma and death of COVID-19.91 Considering that COPD is associated with impaired local and systemic inflammatory response, reduced host immunity, microbiome imbalance, increased mucus production and structural lung damage as well as with increased risk of morbidity and mortality of respiratory infections,150 COPD patients must be considered as high risk for complications from COVID-19. In the absence of additional research, moderate and severe asthma patients must also be considered at a higher risk.
Chronic kidney disease (CKD) has consistently been associated with severe forms of COVID-19 complications in several reports, including six cohort studies. In addition, CKD has an extensively documented association with CVD, and CKD and CVD share common risk factors (diabetes mellitus, obesity, hypertension, smoking, and dyslipidemia).151 Our study suggests that patients who are undergoing treatment for some types of cancers (hematologic cancers and locally advanced and metastatic solid tumors) have more complications and higher death rates from COVID-19. However, this may not be the case for all types of cancer. Workers with cancer must be carefully evaluated to assess their risk level.
In this review, three cohort studies found a significant association of pre-existing chronic liver diseases with more severe COVID-19. Current research suggests that workers with chronic liver disease must be carefully evaluated to determine their risk level for COVID-19 complications and death. The few published studies of patients with rheumatic diseases, have indicated no elevated risk for COVID-19 complications. According to the American College of Rheumatology, there is currently no evidence that rheumatic diseases should be considered as a risk factor for unfavorable COVID-19 outcomes.152 Immunosuppressive treatments must not be interrupted because exacerbation of rheumatic disease may lead to a systemic inflammatory state and organ specific manifestation of the underlying condition (especially kidney and lung) which may increase the risk of COVID complications.153 There is currently insufficient evidence to draw definitive conclusions regarding the level of risk in patients with rheumatic diseases.
Active inflammatory bowel diseases and treatment for a disease flare are associated with COVID-19 complications and death. However, it is not clear if immunosuppressive therapy is also associated with morbidity and mortality. Available research suggests a possible association with concomitant corticosteroid therapy.35 There are few published studies of organ transplantation recipients, but the current evidences suggest that organ transplant patients are at a significantly greater risk of complications and death and must be considered at very high risk for COVID-19 unfavorable outcomes.
We found no evidence that people living with HIV with good clinical and virologic control are at increased risk for severe forms of COVID-19. However, caution is warranted for HIV patients with high viral load, low CD4 cell count, severe disease, and those not using antiretroviral therapy71 who may be at increased risk. Three cohort studies reported a significant association of pre-existing stroke and other neurologic diseases with morbidity and death from COVID-19. Current research strongly suggests that workers with stroke and other neurologic diseases must be considered at higher risk for complications of COVID-19. We found one study which suggested that sickle-cell disease (SCD) patients are at higher risk of COVID-19 complications.76 More studies are necessary, but workers with SCD should be considered at high risk from COVID-19 because infection is the leading cause of morbidity and mortality among SCD patients.154 One study reported a higher risk of hospital admission of patients with obstructive sleep apnea disorder,40 but it is not clear if it is related to other comorbidities (obesity, cardiovascular diseases, and diabetes).
Some studies reported similar risk among pregnant and non-pregnant patients and one cohort reported pregnancy among the risk factors associated with critical COVID-19 illness. Vertical transmission, and its long-term potential consequences cannot currently be excluded. At the present time, pregnancy, especially if associated comorbidities are present (obesity, hypertension, pre-eclampsia, and diabetes), should be considered at higher risk until further studies are available.
Four cohort studies reported that as the number of comorbidities increases, the risk of severe forms of COVID-19 complications also increases while two other cohort studies found that higher Charlson Comorbidity Index Scores were significantly associated with COVID-19 complications. These observations have important implications for physicians since multiple risk factors are frequently observed among workers.155,156
At this time, the knowledge about SARS-CoV-2 is incomplete and the literature in this area is rapidly evolving. However, based on our literature review, relevant risks that can be identified by healthcare providers to determine worker risk for COVID-19 morbidity and mortality include:
Age over 60 years old; there is generally increasing risk with age;
Male sex;
Cardiovascular diseases, like CAD, CHF, cardiomyopathy, and valvular diseases, especially if active and/or not well managed and compensated;
Hypertension, especially if not responsive to treatment with three antihypertensive drug classes (usually a diuretic, a long-acting calcium channel blocker, and a blocker of the renin-angiotensin system) and/or with target organ damage;
Diabetes types 1 and 2, with a greater risk if blood glucose is not within goal and/or with target organ damage;
Obesity (BMI more than 30 kg/m2 ), with greater risk with increasing BMI;
Current smoking;
Chronic respiratory diseases: COPD, interstitial lung diseases, and moderate-to-severe asthma and cystic fibrosis;
Significant chronic kidney disease;
Cancer, especially in cases of hematologic cancers, locally advanced and metastatic solid tumors;
Significant chronic liver disease;
Pregnancy, especially those with associated comorbidities;
Organ transplantation recipients;
HIV patients with high viral load, low CD4 cell count, severe disease, and those not using antiretroviral therapy;
Neurological diseases (eg, stroke with significant functional limitation, etc)
Active inflammatory bowel diseases;
Sickle-cell disease.
Table 6 illustrates the risk modeling we have developed to categorize workers according to individual health risks.
TABLE 6 -
Individual Health Risk Matrix
Severity Levels (Clinical Criteria)
Risk Factors
1
2
3
4
Age
<60
≥60 and <65
≥65 and <70
≥70
Sex
Female
Male
No current evidence
No current evidence
Smoking
Non-smoker
No current evidence
Current smoker
Current smoker
Diabetes
No diabetes
Well managed with diet and oral hypoglycemics without target organ damage
Well managed with diet and insulin without target organ damage
Poorly managed (with hyperglycemia) and/or with target organ damage
BMI
BMI <30
BMI ≥30 and <35
BMI ≥35 and ≤39.9
BMI ≥40 or BMI >35 and ≤39.9 with metabolic syndrome
Hypertension
Normal blood pressure, no treatment
Hypertension diagnosis, well controlled
Hypertension diagnosis, poorly controlled
Resistant hypertension not responsive to treatment with three antihypertensive drug classes and/or with target organ damage
COPD
No disease
Stage 1157
Stage 2157
Stages 3 and 4157
Asthma
No history or past asthma with no symptoms
Mild asthma158,159
Moderate asthma158,159
Severe asthma158,159
Other respiratory diseases
No disease
No current evidence
Interstitial lung disease with only mild to moderate physiologicalImpairment160
Severe interstitial lung disease160 or cystic fibrosis
Cardiomyopathy/Valvular heart disease
No disease or only predisposing etiologic factor
Mild condition without evidence of hemodynamic repercussion
Moderate condition without evidence of hemodynamic repercussion
Moderate condition with evidence of hemodynamic repercussion or Use of blood thinners or severe condition
Congestive heart failure
No disease
Classes I and II and well controlled161
Classes III and well controlled161
Class IV or classes II and III poorly controlled161
Coronary artery disease
No disease
Coronary event >60 days without resulting limitation of physical activity162
Coronary event >60 days with slight limitation of physical activity well controlled with treatment162
Recent (<60 days) and/or with marked limitation or inability to carry on any physical activity162
Renal disease
No disease
Stages 1163
Stages 2 or 3163
Stages 4 or 5; and/or dialysis163
Cancer
No disease
No current evidence
No current evidence
Hematologic cancers, locally advanced and metastatic solid tumors
Liver diseases
No disease
Mild condition
Moderate condition without evidence of liver failure
Severe conditions and/or liver failure (hepatic encephalopathy)
Pregnancy
Non-pregnant
Pregnant <28 weeks
Pregnant ≥28 weeks or 30 days after delivery with no comorbidities
Pregnant ≥28 weeks or 30 days after delivery with comorbidities
Organ transplantation
No transplant
No transplant
No transplant
Organ transplantation recipients
HIV
No disease
HIV with normal CD4 cell count and using antiretroviral therapy
HIV with low CD4 cell count, severe disease and those not using antiretroviral therapy
HIV with low CD4 cell count, severe disease and those not using antiretroviral therapy
Neurological diseases (stroke and others)
No disease
Mild condition
Moderate condition
Severe condition
Inflammatory bowel disease
No disease
Clinical remission (asymptomatic)
Mild or moderate disease with few symptoms164
Severe disease164
Sickle-cell disease
No current evidence
No current evidence
No current evidence
Homozygous sickle cell disease
Although there is an association with several health risks such as cigarette smoking and BMI and elevated risk for COVID-19 complications, there is no current evidence that mitigation of these risk factors results in lower risk of the severity of COVID-19. Nevertheless, it seems prudent to advise workers to modify such risk factors with the hope of attenuating their risk.
Our explanation for differences observed in higher risk worker definitions by official health agencies may be that it is difficult for any government to establish standards and guidance in an evolving science like the COVID-19 pandemic. The different recommendations and legal requirements to manage high-risk workers may reflect the differences in country culture, labor legislation, politics, and social security regulation. Healthcare workers in all countries must comply with local laws and regulations, however, physicians must keep in mind that COVID-19 research is constantly evolving and, similarly, medical decision making, and practice guidelines are also evolving.122
The Workplace Risk Pillar
Some evidence exists that a COVID-19 case may, in some settings, be work-related.165 The risk of exposure to SARS-CoV-2 in the healthcare workplace is based on reported estimates of 150,000 healthcare professionals infected and at least 700 who have died in the United States as of September 2020.166 However, other factors must be considered. In addition, workers may contract the virus during travel to and from their jobs in crowded public or semiprivate transportation.166 Protective measures adopted by the employer are effective to reduce viral dissemination in the workplace167 and the absence of effective workplace controls has been associated with COVID-19 outbreaks in recently opened workplaces.166 When managing a specific case of a high-risk worker, we recommend healthcare providers include an assessment of transportation used by the worker in addition to worksite control measures.
The Community Risk Pillar
Table 5 presents five definitions for the level of COVID-19 transmission in a particular country. These designations may be used by healthcare providers to determine relative risk for managing high-risk workers. The WHO transmission status is available and periodically updated on the internet for almost all countries.125 The CDC level of community transmission is not currently published and relies on a determination by the physician. Other metrics are available on endcoronavirus.org128 and the Johns Hopkins131 websites. It is not currently possible to estimate the future transmission of SARS-CoV-2. Several scenarios of peaks and valleys of COVID-19 incidence have been projected for the post-pandemic period until 2025.168 Such projections depend in part on several factors such as intensity and timing of control measures, the degree of seasonal variation in transmission, the duration of immunity, and the degree of cross-immunity between SARS-CoV-2 and other coronaviruses.168 Precise measures of determining community activity, such as number of daily cases per 100,000 and percent of positive PCR testing should ideally be used by healthcare providers where available. We acknowledge that in several countries such data are not currently available.
Proposed Framework
Table 7 summarizes four workplace options and guidelines for workers returning to work based on COVID-19 relative risk, considering individual, community, and workplace factors: (1) return to the workplace with standard recommendations, (2) return to the workplace with specific additional recommendations, (3) return to the workplace with specific work accommodation, and (4) currently stay out of the workplace. Figure 1 shows the proposed scheme, combining data on individual risk level and the OSHA classification of SARS-CoV-2 infection risk at work at the different levels of community transmission. Notably, community transmission level 3 and 4 have the same recommendations, because level 3 progresses to level 4 with more aggressive testing policies.126
TABLE 7 -
Workplace Guidelines for Workers
A In the workplace with standard recommendations
Frequent hand hygiene (water and soap, alcohol gel available)Use of cloth (fabric) masksRespiratory hygieneCough and sneeze etiquettePhysical distancing (6 feet/3 m at work, cafeteria, etc)
BIn the workplace with specific recommendations
Standard recommendations plus: ✓ Surgical masks and face shield at work ✓ Clean and disinfect frequently touched surfaces ✓ Individual transportation ✓ Encourage optimal management of health condition(s) ✓ Follow-up with Occupational Health service (if available) ✓ Determine if vaccinations are up to date (eg, influenza, pneumonia) ✓ Special precautions in case of contact with suspected or confirmed cases
CIn the workplace with work accommodation
Work from homeorOther work accommodation (such as work at specific location, go to the workplace a few days in the week, isolating the worker in a safer environment to perform work such as plexiglass or enclosure or other accommodations arranged in consultation with an occupational expert)
DOut of workplace
Work from homeorSick leave (disability benefit according to local regulation)orOther leave
FIGURE 1: Proposed worker guidelines based on community, job, and individual risk for COVID-19 morbidity and mortality.
Larochelle23 proposed a matrix for determining the risk for workers of developing severe COVID-19 infection. The matrix was a 3 × 3 matrix with nine possible risk groups and interventions. One axis is the risk of contracting SARS-CoV-2 in the workplace rated as low, medium, and high. The other axis is the risk of death from COVID-19 as low, medium, and high. Each of the nine boxes is assigned as A, B, or C recommendation for how the healthcare professional should advise a patient based on the nine-box risk. For example, a worker who is at high risk of contracting SARS-CoV-2 in the workplace and at high risk of death because of their health risk factors should be advised to consider stopping work if working remotely is not an option. We have expanded the Larochelle matrix23 to include job risk ranked from 1 to 4 where 1 is low risk, for example, workers who can work from home, to 4 for very high job risk for healthcare workers exposed to aerosol transmission from patients potentially infected with SARS-CoV-2. The individual employee risk of morbidity and mortality in the Larochelle model was expanded from 3 to 4 levels where 1 is relatively low risk and 4 is very high risk (see Fig. 1 ). The recommend four steps for using the proposed matrix in clinical practice is described in Fig. 2 and summarized below:
Step 1: Define community transmission level according to Table 5 . If possible, physicians must consider data at the smallest geographic area available (eg, city or state instead of country data). Precise measure of transmission such as percentage of positive tests and daily new cases per 100,000 people, if available, are preferred.
Step 2: Define individual risk level. Using Table 3 , classify each patient according to age and health risks. We suggest healthcare providers assign each worker a risk level and consider the highest level of relative risk for each worker. We acknowledge that comorbidity is common in workers who may have more than one medical conditions at level 2 and/or 3. In such situations, once research indicates that the relative risk increases as the number of comorbidities increase, the physician may assign the worker to level 4.
Step 3: Define job risk level. Use Table 4 and investigate the patient information about job exposure. Beyond the definitions provided by OSHA, we recommend physicians investigate potential exposure on transportation and protective measures implemented by the employer. If the exposure at work is not at the higher levels, if exposure may occur at transportation and/or protective measures are not properly provided by the employer, the healthcare provider should assign the worker as exposed to a higher level. For high risk activities, if recommended PPE are not available, the physician should consider job exposure as very high.
Step 4: Provide recommendations to the worker. Once all the three risk levels (individual, job, and community) are defined, using the proposed matrix (Fig. 1 ), select the recommendation (A, B, C, or D) from the matrix box (Fig. 1 ) and use the recommendations presented in Table 7 as a reference to define the medical management for each patient.
FIGURE 2: Steps in the use of the proposed risk matrix.
Limitations
We acknowledge several limitations of this literature review and proposed framework. We have stratified three different risk levels and there is a certain lack of precision for the definition of each level, that can be counterbalanced by the individual judgment of each physician. The medical literature on COVID-19 is rapidly evolving, so healthcare providers must keep current on research and practice guidelines with new information on risks for morbidity and mortality associated with health risks and chronic conditions. The reviewed studies used to stratify individual risk have been done with the general population and not limited to employed people. Therefore, the health risks for COVID-19 morbidity and mortality may not be applicable for a working population. The metrics to determine community and workplace risk may be incomplete and not applicable to all workers. Numerous medical conditions have not been studied which may contribute to the relative risk of morbidity and mortality from COVID-19. Workplace risk may, in some instances, be better characterized by the number of unusual lapses in protection rather than the usual practices associated with a particular industry. The matrices we developed for relative risk based on community, job and individual risk are empirical and will require prospective validation.
CONCLUSION
A practice tool for healthcare providers has been developed to determine a worker's relative risk of acquiring and the severity of COVID-19 based on individual risk, workplace risk, and community risk. Recommendations for managing workers based on these three risk pillars are illustrated in three matrices.
Acknowledgments
The authors wish to acknowledge Alyssa B. Schultz, PhD for her editing of this manuscript.
REFERENCES
1. Cucinotta D, Vanelli M. WHO Declares COVID-19 a pandemic.
Acta Biomed 2020; 91:157–160.
2. Feng W, Zong W, Wang F, et al. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2): a review.
Mol Cancer 2020; 19:100.
3. Polidoro RB, Hagan RS, de Santis Santiago R, Schmidt NW. Overview: systemic inflammatory response derived from lung injury caused by SARS-CoV-2 infection explains severe outcomes in COVID-19.
Front Immunol 2020; 11:1626.
4. Chakraborty S, Basu A. The COVID-19 pandemic: catching up with the cataclysm.
F1000Res 2020; 9:F1000 Faculty Rev-638.
5. Yuki K, Fujiogi M, Koutsogiannaki S. COVID-19 pathophysiology: a review.
Clin Immunol 2020; 215:108427.
6. Pascarella G, Strumia A, Piliego C, et al. COVID-19 diagnosis and management: a comprehensive review.
J Intern Med 2020; 288:192–206.
7. Clark A, Jit M, Warren-Gash C, et al. Global, regional, and national estimates of the population at increased risk of severe COVID-19 due to underlying health conditions in 2020: a modelling study.
Lancet Glob Health 2020; 8:e1003–e1017.
8. Feng IaW, Zong W, Wang F, Ju S. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2): a review.
Mol Cancer 2020; 19:100.
9. Xie Y, Wang Z, Liao H, Marley G, Wu D, Tang W. Epidemiologic, clinical, and laboratory findings of the COVID-19 in the current pandemic: systematic review and meta-analysis.
BMC Infect Dis 2020; 20:640.
10. Driggin E, Madhavan MV, Bikdeli B, et al. Cardiovascular considerations for patients, Health Care Workers, and Health Systems during the COVID-19 pandemic.
J Am Coll Cardiol 2020; 75:2352–2371.
11. Askin L, Tanriverdi O, Askin HS. The effect of coronavirus disease 2019 on cardiovascular diseases.
Arq Bras Cardiol 2020; 114:817–822.
12. Costa IBSDS, Bittar CS, Rizk SI, et al. The heart and COVID-19: what cardiologists need to know.
Arq Bras Cardiol 2020; 114:805–816.
13. Bansal M. Cardiovascular disease and COVID-19.
Diabetes Metab Syndr 2020; 14:247–250.
14. Cai Q, Huang D, Yu H, et al. Characteristics of liver tests in COVID-19 patients.
J Hepatol 2020; 73:566–574.
15. Xu Z, Shi L, Wang Y, et al. Pathological findings of COVID-19 associated with acute respiratory distress syndrome.
Lancet Respir Med 2020; 8:420–422.
16. Nogueira SÁR, Oliveira SCS, Carvalho AFM, et al. Renal changes and acute kidney injury in covid-19: a systematic review.
Rev Assoc Med Bras 2020; 66:112–117.
17. Fu EL, Janse RJ, de Jong Y, et al. Acute kidney injury and kidney replacement therapy in COVID-19: a systematic review and meta-analysis.
Clin Kidney J 2020; 13:550–563.
18. Aghagoli G, Gallo Marin B, Katchur NJ, Chaves-Sell F, Asaad WF, Murphy SA. Neurological involvement in COVID-19 and potential mechanisms: a review.
Neurocrit Care 2020. 1–10. doi: 10.1007/s12028-020-01049-4.
19. Ferguson NM, Laydon D, Nedjati-Gilani G, et al. WHO Collaborating Centre for Infectious Disease Modelling; MRC Centre for Global Infectious Disease Analysis; Abdul Latif Jameel Institute for Disease and Emergency Analytics; Imperial College London, UK. Report 9 - Impact of non-pharmaceutical interventions (NPIs) to reduce COVID-19 mortality and healthcare demand. Available at:
https://www.imperial.ac.uk/mrc-global-infectious-disease-analysis/covid-19/report-9-impact-of-npis-on-covid-19/ . Accessed June 12, 2020.
20. World Health Organization. Coronavirus disease 2019 (COVID-19) situation report – 51. Available at:
https://www.who.int/docs/default-source/coronaviruse/situation-reports/20200311-sitrep-51-COVID-19.pdf . Accessed July 10, 2020.
21. The United States of America. Centers for Disease Control and Prevention (CDC). People Who Are at Increased Risk for Severe Illness. Available at:
https://www.cdc.gov/coronavirus/2019-ncov/need-extra-precautions/people-at-increased-risk.html . Accessed August 1, 2020.
22. The National Health System. Who's at higher risk from coronavirus. Available at:
https://www.nhs.uk/conditions/coronavirus-covid-19/people-at-higher-risk/whos-at-higher-risk-from-coronavirus/ . Accessed August 1, 2020.
23. Larochelle MR. Is it safer for me to go to work?” Risk stratification for workers during the COVID-9 pandemic.
N Engl Med 2020; 383:e28.
24. Lalloo D, Munna R, Macdonald E. COVID-19 return to work guide for health professionals advising patients and employers. The Society of Occupational Medicine; 2020. Available at:
https://www.som.org.uk/SOM_RTW_guide_health_professionals_COVID-19_FINAL.pdf . Accessed September 22, 2020.
25. Taylor T, Das R, Mueller K, et al. Safely returning America to work: part I: general guidance for employers.
J Occup Environ Med 2020; 62:771–779.
26. Rocha RNM, Fernandes FC, Bezerra JC. ANAMT practical guide on COVID-19 for Occupational Physicians. Available at:
https://www.anamt.org.br/portal/wp-content/uploads/2020/04/GUIA_CORONA_VIRUS_2020_v4.pdf . Accessed September 22, 2020.
27. Nabeel I, Fischman M. What are return to work recommendations for individuals with high risk factors or comorbidities during SARS-CoV-2 pandemic? Available at:
https://acoem.org/COVID-19-Resource-Center/COVID-19-Q-A-Forum/What-are-return-to-work-recommendations-for-individuals-with-high-risk-factors-or-comorbidities-duri . Accessed June 13, 2020.
28. Coggon D, Croft P, Cullinan P, Williams A. Assessment of workers’ personal vulnerability to covid-19 using ’covid-age’.
Occup Med (Lond) 2020; 70:461–464.
29. COVID-19 Dashboard by the Center for Systems Science and Engineering (CSSE) at Johns Hopkins University (JHU). Available at:
https://coronavirus.jhu.edu/map.html . Accessed July 25, 2020.
30. Aggarwal G, Cheruiyot I, Aggarwal S, et al. Association of cardiovascular disease with coronavirus disease 2019 (COVID-19) severity: a meta-analysis.
Curr Probl Cardiol 2020; 45:100617.
31. Akalin E, Azzi Y, Bartash R, et al. Covid-19 and kidney transplantation.
N Engl J Med 2020; 382:2475–2477.
32. Alberici F, Delbarba E, Manenti C, et al. A single center observational study of the clinical characteristics and short-term outcome of 20 kidney transplant patients admitted for SARS-CoV2 pneumonia.
Kidney Int 2020; 97:1083–1088.
33. Assaad S, Avrillon V, Fournier ML, et al. High mortality rate in cancer patients with symptoms of COVID-19 with or without detectable SARS-COV-2 on RT-PCR.
Eur J Cancer 2020; 135:251–259.
34. Bello-Chavolla OY, Bahena-López JP, Antonio-Villa NE, et al. Predicting mortality due to SARS-CoV-2: a mechanistic score relating obesity and diabetes to COVID-19 outcomes in mexico.
J Clin Endocrinol Metab 2020; 105:dgaa346.
35. Bezzio C, Saibeni S, Variola A, et al. Outcomes of COVID-19 in 79 patients with IBD in Italy: an IG-IBD study.
Gut 2020; 69:1213–1217.
36. Cai Q, Chen F, Wang T, et al. Obesity and COVID-19 severity in a designated hospital in Shenzhen, China.
Diabetes Care 2020; 43:1392–1398.
37. The Novel Coronavirus Pneumonia Emergency Response Epidemiology Team. The epidemiological characteristics of an outbreak of 2019 novel coronavirus diseases (COVID-19) – China, 2020.
China CDC Wkly 2020; 2:113–122.
38. Chen T, Wu D, Chen H, et al. Clinical characteristics of 113 deceased patients with coronavirus disease 2019: retrospective study.
BMJ 2020; 368:m1091.
39. Chen H, Guo J, Wang C, et al. Clinical characteristics and intrauterine vertical transmission potential of COVID-19 infection in nine pregnant women: a retrospective review of medical records.
Lancet 2020; 395:809–815.
40. Chhiba KD, Patel GB, Vu THT, et al. Prevalence and characterization of asthma in hospitalized and non-hospitalized patients with COVID-19.
J Allergy Clin Immunol 2020; 146:307.e4–314.e4.
41. Choi MH, Ahn H, Ryu HS, et al. Clinical characteristics and disease progression in early-stage COVID-19 patients in South Korea.
J Clin Med 2020; 9:E1959.
42. Christensen DM, Strange JE, Gislason G, et al. Charlson Comorbidity index score and risk of severe outcome and death in Danish COVID-19 patients.
J Gen Intern Med 2020; 35:2801–2803.
43. Cummings MJ, Baldwin MR, Abrams D, et al. Epidemiology, clinical course, and outcomes of critically ill adults with COVID-19 in New York City: a prospective cohort study.
Lancet 2020; 395:1763–1770.
44. Della Gatta AN, Rizzo R, Pilu G, Simonazzi G. Coronavirus disease 2019 during pregnancy: a systematic review of reported cases.
Am J Obstet Gynecol 2020; 223:36–41.
45. Docherty AB, Harrison EM, Green CA, et al. Features of 20 133 UK patients in hospital with COVID-19 using the ISARIC WHO Clinical Characterization Protocol: prospective observational cohort study.
BMJ 2020; 369:m1985.
46. Du RH, Liang LR, Yang CQ, et al. Predictors of mortality for patients with COVID-19 pneumonia caused by SARS-CoV-2: a prospective cohort study.
Eur Respir J 2020; 55:2000524.
47. Ebekozien OA, Noor N, Gallagher MP, Alonso GT. Type 1 Diabetes and COVID-19: preliminary findings from a multicenter surveillance study in the U S.
Diabetes Care 2020; 43:e83–e85.
48. Fadini GP, Morieri ML, Longato E, Avogaro A. Prevalence and impact of diabetes among people infected with SARS-CoV-2.
J Endocrinol Invest 2020; 43:867–869.
49. Fredi M, Cavazzana I, Moschetti L, Andreoli L, Franceschini F. Brescia Rheumatology COVID-19 Study Grou. COVID-19 in patients with rheumatic diseases in northern Italy: a single-centre observational and case–control study.
Lancet Rheumatol 2020; 2:e549–e556.
50. Gao F, Zheng KI, Wang XB, et al. Obesity is a risk factor for greater COVID-19 severity.
Diabetes Care 2020; 43:e72–e74.
51. García-Pachón E, Zamora-Molina L, Soler-Sempere MJ, et al. Asthma and COPD in hospitalized COVID-19 patients.
Arch Bronconeumol 2020; 56:604–606.
52. Grandbastien M, Piotin A, Godet J, et al. SARS-CoV-2 pneumonia in hospitalized asthmatic patients did not induce severe exacerbation.
J Allergy Clin Immunol Pract 2020; 8:2600–2607.
53. Grasselli G, Greco M, Zanella A, et al. Risk factors associated with mortality among patients with COVID-19 in intensive care units in Lombardy, Italy.
JAMA Intern Med 2020; 180:1345–1355.
54. Grasselli G, Zangrillo A, Zanella A, et al. Baseline characteristics and outcomes of 1591 patients infected with SARS-CoV-2 admitted to icus of the Lombardy Region, Italy.
JAMA 2020; 323:1574–1581.
55. Guan WJ, Ni ZY, Hu Y, et al. Clinical characteristics of Coronavirus disease 2019 in China.
N Engl J Med 2020; 382:1708–1720.
56. Guan WJ, Liang WH, Zhao Y, et al. Comorbidity and its impact on 1590 patients with COVID-19 in China: a nationwide analysis.
Eur Respir J 2020; 55:2000547.
57. Gupta S, Hayek SS, Wang W, et al. Factors associated with death in critically ill patients with Coronavirus Disease 2019 in the US.
JAMA Intern Med 2020; 180:1436–1446.
58. Haroun-Díaz E, de la Torre MV, Ruano FJ, et al. Severe asthma during the COVID-19 pandemic: clinical observations.
J Allergy Clin Immunol Pract 2020; 8:2787–2789.
59. Hoek RAS, Manintveld OC, Betjes MGH, et al. COVID-19 in solid organ transplant recipients: a single-center experience.
Transpl Int 2020; 33:1099–1105.
60. Huang I, Lim MA, Pranata R. Diabetes mellitus is associated with increased mortality and severity of disease in COVID-19 pneumonia - a systematic review, meta-analysis, and meta-regression.
Diabetes Metab Syndr 2020; 14:395–403.
61. Ioannidis JPA, Axfors C, Contopoulos-Ioannidis DG. Population level COVID-19 mortality risk for non-elderly individuals overall and for non-elderly individuals without underlying diseases in pandemic epicenters.
Environ Res 2020; 188:109890.
62. Kammar-García A, Vidal-Mayo JJ, Vera-Zertuche JM, et al. Impact of comorbidities in Mexican Sars-Cov-2-positive patients: a retrospective analysis in a national cohort.
Rev Invest Clin 2020; 72:151–158.
63. Kasraeian M, Zare M, Vafaei H, et al. COVID-19 pneumonia and pregnancy; a systematic review and meta-analysis.
J Matern Fetal Neonatal Med 2020; 19:1–8.
64. Khalil A, Kalafat E, Benlioglu C, et al. SARS-CoV-2 infection in pregnancy: a systematic review and meta-analysis of clinical features and pregnancy outcomes.
Lancet 2020; 25:100446.
65. Killerby ME, Link-Gelles R, Haight SC, et al. Characteristics associated with hospitalization among patients with COVID-19 - metropolitan Atlanta, Georgia, March-April 2020.
MMWR Morb Mortal Wkly Rep 2020; 69:790–794.
66. Kumar A, Arora A, Sharma P, et al. Is diabetes mellitus associated with mortality and severity of COVID-19? A meta-analysis.
Diabetes Metab Syndr 2020; 14:535–545.
67. Lee LYW, Cazier JB, Starkey T, et al. COVID-19 mortality in patients with cancer on chemotherapy or other anticancer treatments: a prospective cohort study.
Lancet 2020; 395:1919–1926.
68. Li X, Xu S, Yu M, et al. Risk factors for severity and mortality in adult COVID-19 inpatients in Wuhan.
J Allergy Clin Immunol 2020; 146:110–118.
69. Liang W, Liang H, Ou L, et al. Development and validation of a clinical risk score to predict the occurrence of critical illness in hospitalized patients with COVID-19.
JAMA Intern Med 2020; 180:1081–1089.
70. Liang W, Guan W, Chen R, et al. Cancer patients in SARS-CoV-2 infection: a nationwide analysis in China.
Lancet Oncol 2020; 21:335–337.
71. Mirzaei H, McFarland W, Karamouzian M, Sharifi H. COVID-19 among people living with HIV: a systematic review.
AIDS Behav 2020. 1–8. doi:10.1007/s10461-020-02983-2.
72. Nie Y, Li J, Huang X, et al. Epidemiological and clinical characteristics of 671 COVID-19 patients in Henan Province, China.
Int J Epidemiol 2020. dyaa081doi: 10.1093/ije/dyaa081.
73. Ortiz-Brizuela E, Villanueva-Reza M, González-Lara MF, et al. Clinical and epidemiological characteristics of patients diagnosed with COVID-19 in a tertiary care center in Mexico City: a prospective cohort study.
Rev Invest Clin 2020; 72:165–177.
74. Pachiega J, Afonso AJDS, Sinhorin GT, et al. Chronic heart diseases as the most prevalent comorbidities among deaths by COVID-19 in Brazil.
Rev Inst Med Trop Sao Paulo 2020; 62:e45.
75. Palmieri L, Vanacore N, Donfrancesco C, et al. Clinical characteristics of hospitalized individuals dying with COVID-19 by age group in Italy.
J Gerontol A Biol Sci Med Sci 2020; 75:1796–1800.
76. Panepinto JA, Brandow A, Mucalo L, et al. Coronavirus disease among persons with Sickle Cell Disease, United States, March 20-May 21, 2020.
Emerg Infect Dis 2020; 26:2473–2476.
77. Patanavanich R, Glantz SA. Smoking is associated with COVID-19 progression: a meta-analysis.
Nicotine Tob Res 2020; 22:1653–1656.
78. Pereira MR, Mohan S, Cohen DJ, et al. COVID-19 in solid organ transplant recipients: initial report from the US epicenter.
Am J Transplant 2020; 20:1800–1808.
79. Petrilli CM, Jones SA, Yang J, et al. Factors associated with hospital admission and critical illness among 5279 people with coronavirus disease 2019 in New York City: prospective cohort study.
BMJ 2020; 369:m1966.
80. Richardson S, Hirsch JS, Narasimhan M, et al. Presenting characteristics, comorbidities, and outcomes among 5700 patients hospitalized with COVID-19 in the New York City area.
JAMA 2020; 323:2052–2059.
81. Rivera-Izquierdo M, Del Carmen Valero-Ubierna M, R-delAmo JL, et al. Sociodemographic, clinical and laboratory factors on admission associated with COVID-19 mortality in hospitalized patients: a retrospective observational study.
PLoS One 2020; 15:e0235107.
82. Robilotti EV, Babady NE, Mead PA, et al. Determinants of COVID-19 disease severity in patients with cancer.
Nat Med 2020; 26:1218–1223.
83. Sardu C, D’Onofrio N, Balestrieri ML, et al. Outcomes in patients with hyperglycemia affected by COVID-19: can we do more on glycemic control?
Diabetes Care 2020; 43:1408–1415.
84. Shi Q, Zhang X, Jiang F, et al. Clinical characteristics and risk factors for mortality of COVID-19 patients with diabetes in Wuhan, China: a two-center, retrospective study.
Diabetes Care 2020; 43:1382–1391.
85. Stokes EK, Zambrano LD, Anderson KN, et al. Coronavirus disease 2019 case surveillance — United States, January 22–May 30, 2020.
MMWR Morb Mortal Wkly Rep 2020; 69:759–765.
86. Suleyman G, Fadel RA, Malette KM, et al. Clinical characteristics and morbidity associated with coronavirus disease 2019 in a series of patients in metropolitan detroit.
JAMA Netw Open 2020; 3:e2012270.
87. Sun H, Ning R, Tao Y, et al. Risk factors for mortality in 244 older adults with COVID-19 in Wuhan, China: a retrospective study.
J Am Geriatr Soc 2020; 68:E19–E23.
88. Vila-Córcoles Á, Ochoa-Gondar O, Torrente-Fraga C, et al. Evaluation of incidence and risk profile for suffering Covid-19 infection by underlying conditions among middle-aged and older adults in Tarragona.
Rev Esp Salud Publica 2020; 94:e202006065.
89. Wang D, Hu B, Hu C, et al. Clinical Characteristics of 138 hospitalized patients with 2019 novel coronavirus–infected pneumonia in Wuhan, China.
JAMA 2020; 323:1061–1069.
90. Wang B, Li R, Lu Z, Huang Y. Does comorbidity increase the risk of patients with COVID-19: evidence from meta-analysis.
Aging 2020; 12:6049–6057.
91. The OpenSAFELY Collaborative: Williamson E, Walker A, Bhaskaran K, Bacon S et al. OpenSAFELY: factors associated with COVID-19-related hospital death in the linked electronic health records of 17 million adult NHS patients. medRxiv 2020.05.06.20092999; doi:
https://doi.org/10.1101/2020.05.06.20092999
92. Wu C, Chen X, Cai Y, et al. Risk factors associated with acute respiratory distress syndrome and death in patients with coronavirus disease 2019 pneumonia in Wuhan, China.
JAMA Intern Med 2020; 180:934–943.
93. Wu ZH, Tang Y, Cheng Q. Diabetes increases the mortality of patients with COVID-19: a meta-analysis.
Acta Diabetol 2020. 1–6. doi: 10.1007/s00592-020-01546-0.
94. Xu PP, Tian RH, Luo S, et al. Risk factors for adverse clinical outcomes with COVID-19 in China: a multicenter, retrospective, observational study.
Theranostics 2020; 10:6372–6383.
95. Yamada T, Mikami T, Chopra N, Miyashita H, Chernyavsky S, Miyashita S. Patients with chronic kidney disease have a poorer prognosis of coronavirus disease 2019 (COVID-19): an experience in New York City.
Int Urol Nephrol 2020; 52:1405–1406.
96. Yang X, Yu Y, Xu J, et al. Clinical course and outcomes of critically ill patients with SARS-CoV-2 pneumonia in Wuhan, China: a single-centered, retrospective, observational study.
Lancet Respir Med 2020; 8:475–481.
97. Zaigham M, Andersson O. Maternal and perinatal outcomes with COVID-19: a systematic review of 108 pregnancies.
Acta Obstet Gynecol Scand 2020; 99:823–829.
98. Zhang J, Wang M, Zhao M, et al. The clinical characteristics and prognosis factors of mild-moderate patients with COVID-19 in a mobile cabin hospital: a retrospective, single-center study.
Front Public Health 2020; 8:264.
99. Zhao Q, Meng M, Kumar R, et al. The impact of COPD and smoking history on the severity of COVID-19: a systemic review and meta-analysis.
J Med Virol 2020; 92:1915–1921.
100. Zheng Z, Peng F, Xu B, et al. Risk factors of critical & mortal COVID-19 cases: a systematic literature review and meta-analysis.
J Infect 2020; 81:e16–e25.
101. Zhou F, Yu T, Du R, et al. Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study [published correction appears in Lancet. 2020 Mar 28;395(10229):1038].
Lancet 2020; 395:1054–1062.
102. Zhu L, She ZG, Cheng X, et al. Association of blood glucose control and outcomes in patients with COVID-19 and pre-existing Type 2 diabetes.
Cell Metab 2020; 31:1068.e3–1077.e3.
103. Manja V, Lakshminrusimha S. Epidemiology and clinical research design, Part 1: study types.
Neoreviews 2014; 15:e558–e569.
104. The United States of America. U.S. Department of Labor. Occupational Safety and Health Administration. Guidance on Preparing Workplaces for COVID-19. Available at:
https://www.osha.gov/Publications/OSHA3990.pdf . Accessed June 13, 2020
105. The Federative Republic of Brazil. Ministério da Saúde. Available at:
https://coronavirus.saude.gov.br/ . Accessed July 31, 2020.
106. The Federative Republic of Brazil. Diário Oficial da União. Portaria Conjunta n° 20. Available at:
https://www.in.gov.br/en/web/dou/-/portaria-conjunta-n-20-de-18-de-junho-de-2020-262408085 . Accessed July 1, 2020.
107. The Republic of India. Ministry of Health and Family Welfare. Directorate General of Health Services (EMR Division). Version 5. 03.07.20. Clinical Management Protocol: COVID-19. Available at:
https://www.mohfw.gov.in/pdf/UpdatedClinicalManagementProtocolforCOVID19dated03072020.pdf . Accessed August 3, 2020.
108. The United Kingdom of Great Britain and Northern Ireland. Health and Safety Executive. Working safely during the coronavirus (COVID-19) outbreak. 6. Protect vulnerable workers. Available at:
https://www.hse.gov.uk/coronavirus/working-safely/protect-people.htm . Accessed August 2, 2020.
109. The Kingdom of Spain. Ministry of Health. General Directorate of Public Health, Quality and Innovation. Scientific and technical information. Coronavirus disease, COVID-19. Available at:
https://www.mscbs.gob.es/profesionales/saludPublica/ccayes/alertasActual/nCov-China/documentos/ITCoronavirus.pdf . Accessed August 10, 2020.
110. The Kingdom of Spain. Ministry of Labor and Social Economy. Guide for workplaces during COVID-19 pandemic. Available at:
http://www.mites.gob.es/ficheros/ministerio/inicio_destacados/Gua_Definitiva.pdf . Accessed August 10, 2020.
112. The Italian Republic. Ministry of Labor and Social Policies. The shared protocol on measures to combat COVID-19 in the workplace has been integrated. Available at:
https://www.lavoro.gov.it/notizie/Pagine/Sicurezza-sul-lavoro-Integrato-il-Protocollo-condiviso-sulle-misure-per-il-contrasto-al-Covid-19-negli-ambienti-di-lavoro.aspx . Accessed August 10, 2020.
113. The Republic of South Africa. Department of Health. Guidance on vulnerable employees and workplace accommodation in relation to COVID-19 (V4: 25 May 2020). Available at:
https://www.saiosh.co.za/news/509605/DOH-COVID-19-Guidance-on-vulnerable-employees-and-workplace-accommodation.htm . Accessed August 10, 2020.
114. The Centers for Disease Control and Prevention. People with Certain Medical Conditions. Available at:
https://www.cdc.gov/coronavirus/2019-ncov/need-extra-precautions/people-with-medical-conditions.html . Accessed on September 7, 2020.
115. International Labour Organization. An employer's guide on managing your workplace during COVID-19. Geneva; 2020. ISBN 9789220320853.
116. Rapp N, O’Keefe B. A blueprint for redesigning the office in the pandemic era.
Fortune 2020. 46–47.
117. Baker MG, Peckham TK, Seixas NS. Estimating the burden of United States workers exposed to infection or disease: a key factor in containing risk of COVID-19 infection.
PLoS One 2020; 15:e0232452.
118. Rafeemanesh E, Ahmadi F, Memarzadeh M. A review of the strategies and studies on the prevention and control of the new coronavirus in workplaces.
Arch Bone Jt Surg 2020; 8:242–246.
119. Barbieri T, Basso G, Scicchitano S. Italian worker at risk during the Covid-19 epidemic.
SSRN Electronic J 2020; DOI: 10.2139/ssrn.3572065.
120. Lan FY, Wei CF, Hsu YT, Christiani DC, Kales SN. Work-related COVID-19 transmission in six Asian countries/areas: a follow-up study.
PLoS One 2020; 15:e0233588.
121. Bauchner H, Fontanarosa P. Thinking of risk in the era of COVID-19.
JAMA 2020; 324:151–153.
122. Fischhoff B. Making decisions in a COVID-19 World.
JAMA 2020; 324:139–140.
123. Kucharski A. The Rules of Contagion: Why Things Spread and Why They Stop. Great Britain: Profile Books; 2020.
124. The World Health Organization. Critical preparedness, readiness and response actions for COVID-19. Available at:
https://www.who.int/publications/i/item/critical-preparedness-readiness-and-response-actions-for-covid-19 . Accessed August 29, 2020.
125. World Health Organization. Situation reports. Available at:
https://www.who.int/emergencies/diseases/novel-coronavirus-2019/situation-reports/. Accessed September 20, 2020.
126. The Centers for Disease Control and Prevention. Framework for implementation of COVID-19 community mitigation measures for lower-resource countries. Available at:
https://www.cdc.gov/coronavirus/2019-ncov/downloads/global-covid-19/community-mitigation-measures.pdf . Accessed August 30, 2020.
127. The Centers for Disease Control and Prevention. implementation of mitigation strategies for communities with local COVID-19 transmission. Available at:
https://www.cdc.gov/coronavirus/2019-ncov/community/community-mitigation.html . Accessed August 29, 2020.
128. Some are winning - some are not. Which countries do best in beating COVID-19? Available at:
https://www.endcoronavirus.org/countries . Accessed September 7, 2020.
129. Rasmussen SA, Khoury MJ, Del Rio C. Precision public health as a key tool in the COVID-19 response.
JAMA 2020; 324:933–934.
130. Harvard Global Health Institute. Pandemic resilience: getting it done. A TTSI Technical Advice Handbook V 2.0; 2020. Available at:
https://ethics.harvard.edu/files/center-for-ethics/files/ttsi_technical_advice_handbook_2.0_june_30_2020_final.pdf . Accessed August 30, 2020.
131. The Johns Hopkins Coronavirus Resource Center. How does testing in the U.S. compare to other countries? Available at:
https://coronavirus.jhu.edu/testing/international-comparison . Accessed September 11, 2020.
132. Perrotta F, Corbi G, Mazzeo G, et al. COVID-19 and the elderly: insights into pathogenesis and clinical decision-making.
Aging Clin Exp Res 2020; 32:1599–1608.
133. Aw D, Silva AB, Palmer DB. Immunosenescence: emerging challenges for an ageing population.
Immunology 2007; 120:435–446.
134. Ho JC, Chan KN, Hu WH, et al. The effect of aging on nasal mucociliary clearance, beat frequency, and ultrastructure of respiratory cilia.
Am J Respir Crit Care Med 2001; 163:983–988.
135. Sharma G, Volgman AS, Michos ED. Sex differences in mortality from COVID-19 pandemic: are men vulnerable and women protected?
JACC Case Rep 2020; 2:1407–1410.
136. Hoffmann M, Kleine-Weber H, Schroeder S, et al. SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor.
Cell 2020; 181:271.e8–280.e8.
137. Chowkwanyun M, Reed AL Jr. Racial health disparities and Covid-19 - caution and context.
N Engl J Med 2020; 383:201–203.
138. Watanabe M, Risi R, Tuccinardi D, Baquero CJ, Manfrini S, Gnessi L. Obesity and SARS-CoV-2: a population to safeguard.
Diabetes Metab Res Rev 2020. e3325.
139. Murugan AT, Sharma G. Obesity and respiratory diseases.
Chron Respir Dis 2008; 5:233–242.
140. Arcavi L, Benowitz NL. Cigarette smoking and infection.
Arch Intern Med 2004; 164:2206–2216.
141. Singh AK, Gupta R, Misra A. Comorbidities in COVID-19: Outcomes in hypertensive cohort and controversies with renin angiotensin system blockers.
Diabetes Metab Syndr 2020; 14:283–287.
142. Shibata S, Arima H, Asayama K, et al. Hypertension and related diseases in the era of COVID-19: a report from the Japanese Society of Hypertension Task Force on COVID-19.
Hypertens Res 2020; 43:1028–1046.
143. Barbaro NR, Fontana V, Modolo R, et al. Increased arterial stiffness in resistant hypertension is associated with inflammatory biomarkers.
Blood Press 2015; 24:7–13.
144. Azevedo RB, Botelho BG, Hollanda JVG, et al. Covid-19 and the cardiovascular system: a comprehensive review.
J Hum Hypertens 2020. 1–8. doi: 10.1038/s41371-020-0387-4.
145. González-Rayas JM, Rayas-Gómez AL, García-González JJ, González-Yáñez JM, Hernández-Hernández JA, López-Sánchez RC. COVID-19 and ACE-inhibitors and angiotensin receptor blockers: the need to differentiate between early infection and acute lung injury.
Rev Colombi Cardiol 2020; 27:129–131.
146. Hippisley-Cox J, Tan PS, Coupland C. Risk of severe COVID-19 disease with ACE inhibitors and angiotensin receptor blockers: cohort study including 8.3 million people.
Heart 2020; 106:1503–1511.
147. Savarese G, Benson L, Sundström J, Lund LH. Association between Renin-Angiotensin-Aldosterone system inhibitor use and COVID-19 Hospitalization and death: a 1,4 million patient Nation-Wide registry analysis.
Eur J Heart Fail 2020; doi: 10.1002/ejhf.2060.
148. Cristelo C, Azevedo C, Marques JM, Nunes R, Sarmento B. SARS-CoV-2 and diabetes: new challenges for the disease.
Diabete Res Clin Pract 2020; 164:108228.
149. Liu F, Long X, Zhang B, Zhang W, Chen X, Zhang Z. ACE2 expression in pancreas may cause pancreatic damage after SARS-CoV-2 infection.
Clin Gastroenterol Hepatol 2020; 18:2128.e2–2130.e2.
150. Lippi G, Henry BM. Chronic obstructive pulmonary disease is associated with severe coronavirus disease 2019 (COVID-19).
Respir Med 2020; 167:105941.
151. Said S, Hernandez GT. The link between chronic kidney disease and cardiovascular disease.
J Nephropathol 2014; 3:99–104.
152. Mikuls TR, Johnson SR, Fraenkel L, et al. American college of rheumatology guidance for the management of rheumatic disease in adult patients during the COVID-19 pandemic: version 2.
Arthritis Rheumatol 2020; 72:1241–1251.
153. Tam LS, Tanaka Y, Handa R, et al. Care for patients with rheumatic diseases during COVID-19 pandemic: a position statement from APLAR.
Int J Rheum Dis 2020; 23:717–722.
154. de Azevedo JTC, Malmegrim KCR. Immune mechanisms involved in sickle cell disease pathogenesis: current knowledge and perspectives.
Immunol Lett 2020; 224:1–11.
155. Cabral GG, Dantas de Souza AC, Barbosa IR, Jerez-Roig J, Souza DLB. Multimorbidity and its impact on workers: a review of longitudinal studies.
Saf Health Work 2019; 10:393–399.
156. Carvalho JN, Roncalli ÂG, Cancela MC, Souza DL. Prevalence of multimorbidity in the Brazilian adult population according to socioeconomic and demographic characteristics.
PLoS One 2017; 12:e0174322.
157. Rabe KF, Hurd S, Anzueto A, et al. Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: GOLD executive summary.
Am J Respir Crit Care Med 2007; 176:532–555.
158. Global Initiative for Asthma. Global strategy for asthma management and prevention. Available at:
https://ginasthma.org/wp-content/uploads/2019/06/GINA-2019-main-report-June-2019-wms.pdf . Accessed October 25, 2020.
159. Reddel HK, FitzGerald JM, Bateman ED, et al. GINA 2019: A fundamental change in asthma management: Treatment of asthma with short-acting bronchodilators alone is no longer recommended for adults and adolescents.
Eur Respir J 2019; 53:1901046.
160. Robbie H, Daccord C, Chua F, Devaraj A. Evaluating disease severity in idiopathic pulmonary fibrosis.
Eur Respir Rev 2017; 26:170051.
161. Inamdar AA, Inamdar AC. Heart failure: diagnosis, management and utilization.
J Clin Med 2016; 5:62.
162. Russell SD, Saval MA, Robbins JL, et al. New York Heart Association functional class predicts exercise parameters in the current era.
Am Heart J 2009; 158: (4 suppl): S24–S30.
163. Parmar MS. Chronic renal disease.
BMJ 2002; 325:85–90.
164. Satsangi J, Silverberg MS, Vermiere S, Colombel J-F. The Montreal classification of inflammatory bowel disease: controversies, consensus, and implications.
Gut 2005; 55:749–753.
165. Taylor MT, Murphy MG, Roseman A. Is an Employee's COVID-19 Case Work-Related and Recordable? OSHA Provides Employers Clarity Through Enforcement Guidance. National Law Review, Volume X, Number 105. Available at:
https://www.natlawreview.com/article/employee-s-covid-19-case-work-related-and-recordableosha-provides-employers-clarity . Accessed September 21, 2020.
166. Michaels D, Wagner GR. Occupational Safety and Health Administration (OSHA) and worker safety during the COVID-19 pandemic.
JAMA 2020; 324:1389–1390.
167. Fellows of the Collegium Ramazzini. 24th Collegium Ramazzini Statement: Prevention of work-related infection in the COVID-19 pandemic.
J Occup Environ Med 2020; 62:e467–e468.
168. Kissler SM, Tedijanto C, Goldstein E, Grad YH, Lipsitch M. Projecting the transmission dynamics of SARS-CoV-2 through the postpandemic period.
Science 2020; 368:860–868.