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Table 5 Comparison of FDA-EUA and COVAM seropositivity and symptom characteristics among those with PCR-confirmed COVID

From: Infection prevention strategies are highly protective in COVID-19 units while main risks to healthcare professionals come from coworkers and the community

Seropositive and PCR-positives

FDA-EUA Assay or COVAM N (%)

FDA-EUA assay serology N (%)

COVAM serology N (%)

p valuea

PCR-positive—total

41

38

41

 

Seropositive

41

38

41

 

Reported to Occ health

41

38

41

 

No symptom reported

4

9.8%

4

10.5%

4

9.8%

0.81

Any symptom reported

37

90.2%

34

89.5%

37

90.2%

0.81

 Symptom type

       

 Fever

31

75.6%

30

78.9%

31

75.6%

0.77

 Non febrile illness

6

14.6%

4

10.5%

6

14.6%

0.84

 Fatigue

31

75.6%

29

76.3%

31

75.6%

0.89

 Chills

30

73.2%

28

73.7%

30

73.2%

0.90

 Myalgia

30

73.2%

28

73.7%

30

73.2%

0.90

 Congestion

21

51.2%

19

50.0%

21

51.2%

0.94

Cough

24

58.5%

23

60.5%

24

58.5%

0.91

 Loss of smell

27

65.9%

26

68.4%

27

65.9%

0.87

 Shortness of breath

15

36.6%

14

36.8%

15

36.6%

0.93

Days between symptoms and serology sample collection

       

 < 14 days

4

9.8%

3

7.9%

4

9.8%

0.96

 15–29 days

7

17.1%

6

15.8%

7

17.1%

 

 30–44 days

7

17.1%

7

18.4%

7

17.1%

 

 45–59 days

17

41.5%

16

42.1%

17

41.5%

 

 60–74 days

1

2.4%

1

2.6%

1

2.4%

 

 ≥ 75 days

1

2.4%

1

2.6%

1

2.4%

 
  1. FDA-EUA, Food and drug administration emergency use authorization; COVAM, coronavirus antigen microarray
  2. ap value = chi square comparing FDA-EUA with COVAM serology