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. 2021 May 19;106(8):2208–2220. doi: 10.1210/clinem/dgab349

Table 1:

Baseline characteristics of patients attending ≥ 3 months following presentation.

Participant characteristics Total Cohort
(n=70)
No Dexamethasone
(n=48)
Dexamethasone
(n=22)
P value No fatigue
(n=26)
Fatigue
(n=44)
P value
Age (years) 55.9
(13.0)
55.6
(13.3)
56.6
(12.6)
.77 61.1
(11.6)
52.8
(12.9)
.009
Sex:
Male 47/70
(67.1%)
33/48
(68.8%)
14/22
(63.6%)
.79 23/26
(88.5%)
24/44 (54.5%) .004
Female 23/70
(32.9%)
15/48
(31.3%)
8/22
(36.4%)
3/26
(11.5%)
20/44 (45.5%)
Ethnicity:
Asian 17/70
(24.3%)
7/48
(14.6%)
10/22
(45.5%)
.006 8/26
(30.8%)
9/44
(20.5%)
.82
Black 7/70
(10.0%)
4/48
(8.3%)
3/22
(13.6%)
3/26
(11.5%)
4/44
(9.1%)
Mixed 2/70
(2.9%)
1/48
(2.1%)
1/22
(4.6%)
1/26
(3.9%)
1/44
(2.3%)
Other – not stated 17/70
(24.3%)
17/48
(35.4%)
0
(0.0%)
5/26
(19.2%)
12/44
(27.3%)
White 27/70
(38.6%)
19/48
(39.6%)
8/22
(36.4%)
9/26
(34.6%)
18/44
(40.9%)
Comorbidities:
Hypertension 24/70
(34.3%)
13/48
(27.1%)
11/22
(50.0%)
.05 6/26
(23.1%)
18/44
(40.9%)
.20
Cardiovascular disease 4/70
(5.7%)
4/48
(8.3%)
0/22
(0.0%)
3/26
(11.5%)
1/44
(2.3%)
Diabetes 20/70
(28.6%)
11/48
(22.9%)
9/22
(40.9%)
7/26
(26.9%)
13/44
(29.5%)
 Type 1 0/30
(0.0%)
0/11
(0.0%)
0/9
(0.0%)
0/7
(0.0%)
0/13
(0.0%)
 Type 2 18/20
(90.0%)
10/11
(90.9%)
8/9
(88.9%)
6/7
(85.7%)
13/13
(100.0%)
 Unspecified 2/20
(10.0%)
1/11
(90.1%)
1/9
(11.1%)
1/7
(14.3%)
0/13
(0.0%)
Obesity (BMI >30kg/m 2 )
 Yes 15/70
(21.4%)
6/48
(12.5%)
9/22
(40.9%)
4/26
(15.4%)
11/44
(25.0%)
 No 30/70
(42.9%)
20/48
(41.7%)
10/22
(45.5%)
17/26
(65.4%)
13/44
(29.5%)
 Unknown 25/70
(35.7%)
22/48
(45.8%)
3/22
(13.6%)
5/26
(19.2%)
20/44
(45.5%)
Smoking status:
Current smoker 2/70
(2.9%)
1/48
(2.1%)
1/22
(4.5%)
.23 2/26
(7.7%)
0/44
(0.0%)
.16
Ex-smoker 6/70
(8.6%)
6/48
(12.5%)
0/22
(0.0%)
3/26
(11.5%)
3/44
(6.8%)
Never-smoked 60/70
(85.7%)
39/48
(81.3%)
21/22
(95.5%)
21/26
(80.8%)
39/44
(88.6%)
Unknown 2/70
(2.9%)
2/48
(4.2%)
0/22
(0.0%)
0/26
(0.0%)
2/44
(4.6%)
Disease outcome:
Hospitalized 54/70
(77.1%)
32/48
(66.7%)
22/22
(100.0%)
NA 17/26
(65.4%)
37/44
(84.1%)
.07
 NIV 5/54
(9.3%)
1/32
(3.1%)
4/22
(18.2%)
0/26
(0.0%)
5/37
(13.5%)
 ITU admission 7/54
(13.00%)
3/32
(9.4%)
4/22
(18.2%)
3/26
(11.5%)
4/37
(10.8%)
Non-hospitalized 16/70
(22.9%)
16/48
(33.3%)
0/22
(0.0%)
9/26
(34.6%)
7/44
(15.9%)
Disease Severity:
Mild 12/70
(17.1%)
12/48
(25.0%)
0/22
(0.0%)
.04 8/26
(30.8%)
4/44
(9.1%)
.03
Moderate 30/70
(42.9%)
19/48
(39.6%)
11/22
(50.0%)
6/26
(23.1%)
24/44
(54.5%)
Severe 21/70
(30.0%)
14/48
(29.2%)
7/22
(31.8%)
9/26
(34.6%)
12/44
(27.3%)
Critical 7/70
(10.0%)
3/48
(6.3%)
4/22
(18.2%)
3/26
(11.5%)
4/44
(9.1%)
Dexamethasone treatment 22/70
(31.4%)
NA 22/22
(100%)
NA 0/26
(0.0%)
22/44
(50.0%)
NA
Cumulative dose dexamethasone treatment (mg) 38.73
(18.49)
NA 38.73
(18.49)
NA NA 38.73
(18.49)
NA
Additional treatments:
 Remdesivir 15/70
(21.4%)
1/48
(2.1%)
14/22
(63.6%)
.05 8/26
(30.8%)
7/44
(15.9%)
.26
 Tocilizumab 1/70
(1.4%)
1/48
(2.1%)
0/22
(0.0%)
1/26
(3.9%)
0/44
(0.0%)
 Conv. Plasma 2/70
(2.9%)
0/48
(0.0%)
2/22
(9.1%)
1/26
(3.9%)
1/44
(2.3%)
 Other 3/70
(4.3%)
1/48
(2.1%)
2/22
(9.1%)
0/26
(0.0%)
3/44
(6.8%)
Duration of admission (days) 5.0
(1.0, 8.0)
4.0
(0.0, 8.0)
6.0
(4.0, 9.8)
<.001 6.5
(3.0, 1.3)
4.0
(0.0, 7.8)
.03
Time since presentation (days) 210.0
(112.0, 261.0)
242.0
(209.5, 287.0)
95.5
(88.8, 113.3)
<.001 215.00
(121.0, 252.3)
209.0
(102.0, 281.0)
.83

Data are means (SD) for continuous variables parametrically distributed and medians (lower quartile, upper quartile) for continuous non-parametrically distributed variables. For categorical data, numbers of patients (percentages) are presented. Continuous data that are parametrically distributed were compared using t-tests, continuous data not parametrically distributed were compared using Mann-Whitney U test. Groups of continuous data parametrically distributed were compared using ANOVA test. Groups of continuous data non-parametrically distributed were compared using Kruskal-Wallis test. Categorical data were compared using Chi-Squared test. NIV: non-invasive ventilation; ITU: intensive therapy unit, Conv Plasma: convalescent plasma; Other: additional treatments include Anakinra (interleukin-1 receptor antagonist), Kaletra (Lopinavir/Ritonavir), Namilumab; NA: not applicable.

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