Skip to main content
. 2021 Jan 27;11(2):e297. doi: 10.1002/ctm2.297

TABLE 3.

Reasons for concomitant medication use for the 44 COVID‐19 patients in the experimental group and the control group

Experimental group (N = 26) Control group (N = 18)
Category Severe (N = 16) Critically ill (N = 10) P a Severe (N = 10) Critically ill (N = 8) P b P c
Symptomatic treatment, n (%) 14 (87.50) 10 (100.00) .508 10 (100.00) 8 (100.00) N/A .505
Antiviral therapy, n (%) 15 (93.75) 8 (80.00) .538 10 (100.00) 8 (100.00) N/A .258
Antibacterial treatment, n (%) 9 (56.25) 6 (60.00) 1.000 8 (80.00) 6 (75.00) 1.000 .167
Hormone, n (%) 7 (43.75) 7 (70.00) .248 7 (70.00) 7 (87.50) .588 .105
Gut microflora modulator, n (%) 1 (6.25) 0 (0.00) 1.000 3 (30.00) 1 (12.50) .588 .142
Extracorporeal blood purification system, n (%) 1 (6.25) 9 (90.00) <.001* 2 (20.00) 7 (87.50) .015* .447
Traditional Chinese medicine treatment, n (%) 9 (56.25) 6 (60.00) 1.000 6 (60.00) 7 (87.50) .314 .325
Basic disease medication, n (%) 2 (12.50) 3 (30.00) .340 2 (20.00) 5 (62.50) .145 .183

Note.

*

Represents significant difference (P < .05); P a value is the experimental group of the difference between severe and critically ill patients in each type of combination medication in the experimental group; P b is the difference test between severe and critically ill patients in each type of combination medication in the control group; P c is the test group in each type of combination medication test the difference with the control group (do not distinguish the severity of the disease); “n” represents number; “N/A” represents not applicable.