Table 1

Demographic, clinical and laboratory characteristics and outcomes of studied groups

Immunomodulatory drugs-naïve patients (n=381)Patients with ADs treated with immunomodulatory drugs (n=30)P value
Age (mean±SD), years62.6±17.155.1±13.60.020
Gender (female/male)0.643.280.001
Clinical and laboratory manifestations
 Fever (%)85 (22.3)8 (26.7)0.519
 Dyspnoea (%)274 (71.9)24 (80.0)0.036
 Cough (%)223 (58.57)16 (53.3)0.129
 Myalgia (%)124 (32.5)17 (56.7)0.006
 Malaise (%)117 (30.7)15 (50.0)0.001
 Nausea/vomiting/diarrhoea (%)63 (16.5)7 (23.3)0.085
 Anorexia (%)57 (14.9)10 (33.3)0.050
 Taste loss (%)38 (10)6 (20.0)0.001
 Anosmia (%)32 (8.4)7 (23.3)0.001
 Sore throat (%)30 (7.9)4 (13.3)0.080
 Lymphopenia (%)278 (72.9)13 (43.3)0.015
 High C-reactive protein (%)328 (86.1)21 (70.0)0.078
Level of care
 Admitted in ward (%)155 (40.7)11 (36.7)0.889
 Admitted in ICU (%)89 (23.4)7 (23.3)
 Intubated and mechanically ventilated (%)137 (36.0)12 (40.0)
The time interval from the onset of symptoms to admission, median (IQR) days7 (3, 10)6 (3.5, 11)0.912
The time interval from the onset of symptoms to mechanical ventilations, median (IQR) days0 (0, 2)2.5 (0, 6.75)0.096
Duration of admission in ICU, median (IQR) days9 (5, 16)12.5 (4, 18)0.711
Duration of intubation, median (IQR) days4 (2, 10)5 (1.5, 13.5)0.889
Death (%)95 (24.9)8 (26.7)0.491
  • AD, autoimmune disease; ICU, intensive care unit.;