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. 2021 Jun 28;12:680188. doi: 10.3389/fimmu.2021.680188

Table 1.

Demographics, Presenting Symptoms, Parameters, and Laboratory Investigations Stratified by Remdesivir treatment.

Remdesivir No Remdesivir P-value
N 28 27
Age, years 55 (45-65) 55 (42-65) 0.83
Sex 26 (93%) 16 (59%) 0.0043
Ethnicity
 -Chinese 12 (43%) 22 (81%)
 -South Asian 9 (32%) 1 (4%) 0.0063
 -Other 7 (25%) 4 (15%)
Charlson comorbidity index 0 (0-1) 0 (0-1) 0.87
 -Diabetes 11 (39%) 8 (30%) 0.57
 -Hypertension 16 (57%) 17 (63%) 0.78
Days from symptom onset to desaturation 8 (5-9) 8 (6-9) 0.93
Other experimental therapy
 -Anti-viral† 4 (14%) 18 (67%) <0.0001
 -Immunomodulator‡ 4 (14%) 4 (15%) 1.00
Responders (n=21) Non-responders (n=6)
Doses (Interquartile range; median [days]) 10 – 10; 10 7 – 10; 10
Invasive mechanical ventilation 7 (25%) 10 (37%) 0.39
-Duration (days, range) - 6 (5-27) - 8 (2-30)
Total duration supplemental oxygen (days) 10.5 (8-18) 9 (5-13) 0.090
Duration hospital admission (days) 21.5 (16-27) 17 (13-21) 0.10
Progression to intubation 6 (22%) 10 (37%) 0.372
Death 2 (7%) 1 (4%) 1.00

AData is presented as median and inter-quartile range or n (%) unless otherwise specified. Continuous variables compared with Mann-Whitney, categorical with Fisher’s exact or Chi square as appropriate.

B†Lopinavir/ritonavir in 19, hydroxychloroquine in 5; ‡Corticosteroids in 2, interferon in 5, tocilizumab in 2 (note some patients received more than one agent).

CRemdesivir-treated group were treated with 200mg loading dose on day 1, followed by a maintenance dose administered daily thereafter.