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. 2021 Nov 28:dkab433. doi: 10.1093/jac/dkab433

Table 4.

Subgroup analysis of the primary outcome

Sofosbuvir/daclatasvir (N = 541), n/n (%) Control (N = 542), n/n (%) P
Men 220/291 (76) 224/294 (76) 0.962
Women 185/250 (78) 187/248 (75) 0.716
Patients ≥60 years old 170/248 (69) 184/266 (69) 0.891
Patients <60 years old 245/293 (84) 227/276 (82) 0.783
Any comorbiditya 215/285 (75) 203/279 (73) 0.469
No comorbidity 200/256 (78) 208/263 (79) 0.6474
Days since symptom onset >4 days 320/422 (76) 321/422 (76) 0.936
Days since symptom onset ≤4 days 95/119 (80) 90/120 (75) 0.372
Days since symptom onset >8 days 109/140 (78) 121/148 (82) 0.443
Days since symptom onset ≤8 days 306/401 (76) 290/394 (74) 0.473
Patients with O2 saturation >90% at baseline 214/254 (84) 215/257 (84) 0.984
Patients with O2 saturation ≤90% at baseline 201/287 (70) 196/285 (69) 0.705
PCR positive at baseline 326/430 (76) 315/426 (74) 0.529
PCR negative at baseline 89/111 (80) 96/116 (83) 0.444
Taking dexamethasone 220/298 (74) 184/272 (68) 0.105
Not taking dexamethasone 195/243 (80) 227/270 (84) 0.257

P value calculated using χ2 test.

a

Any comorbidity defined as those with any of hypertension, diabetes, ischaemic heart disease, COPD or asthma.