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. 2023 Nov 13;12(12):618–626. doi: 10.1093/jpids/piad101

Table 1.

Demographic and Clinical Characteristic of Individuals With SARS-CoV-2 Infection

Total Patients 462
Age (median [range]) in years 11 [0–24]
Sex (%)
 Female 208 (45.02)
 Male 254 (54.98)
Race (%)
 Black 244 (52.81)
 White 187 (40.48)
 Multiracial 20 (4.33)
 Asian 5 (1.08)
 Unknown 1 (0.22)
 Other 5 (1.08)
Ethnicity (%)
 Non-Hispanic/non-Latino 400 (86.58)
 Hispanic/Latino 50 (10.82)
 Not specified 12 (2.60)
Diagnosis (%)
 HIV 26 (5.63)
 Leukemia/Lymphoma 87 (18.83)
 SCD 140 (30.30)
 ST/NO 145 (31.39)
 Othera 64 (13.85)
Cancer diagnosis (%)
 Yes 245 (53.03)
 No 217 (46.97)
 Received chemotherapy (%)
  Yes 100 (40.82)
  No 145 (59.18)
SARS-COV-2 vaccination prior to infection (%)
 No 369 (79.87)
 Yes 93 (20.13)
Number of vaccine doses (median [IQR]) 2.00 [1.00, 2.00]
 Pfizer-BioNTech (%)
  Yes 67 (72.04)
 Moderna (%)
  Yes 10 (10.75)
 Janssen (%)
  Yes 18 (19.35)
Reason for testing (%)
 Symptoms 172 (37.23)
 Asymptomatic screening 290 (62.77)
 Did the patient become symptomatic? (%)
  No 205 (70.69)
  Yes 85 (29.31)
Was episode initial or a reinfection (%)
 Initial infection 454 (98.27)
 Reinfection 8 (1.73)
Days from previous infectious episode (median [IQR]) 91.00 [74.25, 142.50]
SARS-CoV2- Variant (%)
 Omicron 202 (43.72)
 Ancestral 103 (22.29)
 Delta 61 (13.20)
 Alpha 10 (2.16)
 Epsilon 1 (0.22)
 Undetermined 85 (18.40)
Symptoms within 28 days of Day 0? (%)
 Yes 247 (53.46)
 No 215 (46.54)
 Fever (%)
  Yes 155 (62.75)
  No 92 (37.25)
 Headache (%)
  Yes 47 (19.03)
  No 200 (80.97)
 Cough (%)
  Yes 157 (63.56)
  No 90 (36.44)
 Sore throat (%)
  Yes 42 (17.00)
  No 205 (83.00)
 Loss of smell or taste (%)
  Yes 26 (10.53)
  No 221 (89.47)
 Shortness of breath (%)
  Yes 22 (8.91)
  No 225 (91.09)
 Diarrhea (%)
  Yes 20 (8.10)
  No 227 (91.90)
Hospitalization (%)
 Yes 51 (11.04)
 Already hospitalized for reasons other than COVID-19 26 (5.63)
 No 385 (83.33)
ICU (%)
 Yes 8 (1.73)
 No 69 (14.94)
 Not hospitalized 385 (83.33)
Any respiratory symptoms at Day 0? (%)
 No 281 (61.22)
 Yes 178 (38.78)
 Respiratory symptoms at Day 0 (%)
  LRTI 17 (9.55)
  URTI 161 (90.45)
Progression to LRTI (%)
 No 440 (99.55)
 Unknown 1 (0.23)
 Yes 1 (0.23)
Death (%)
 Yes 2 (0.43)
 No 460 (99.57)
MIS-C (%)
 Yes 1 (0.26)
 No 380 (99.74)
Received steroids within 28 days (%)
 Yes 12 (2.65)
 No 440 (97.35)
Received convalescent plasma within 28 days (%)
 Yes 2 (0.43)
 No 460 (99.57)
Received remdesivir within 28 days (%)
 Yes 24 (5.19)
 No 438 (94.81)
 Remdesivir usage (%)
  Prevent progression 15 (62.50)
  Treatment of severe COVID-19 9 (37.50)
  Duration of remdesivir use (median [IQR]) 3.00 [3.00, 5.00]

aFor a complete list of conditions included in Other please refer to Supplementary Table 16.