Skip to main content

Table 2 Patient characteristics

From: Characteristics and outcomes of COVID-19 patients presumed to be treated with sotrovimab in NHS hospitals in England

Characteristic

Patients

(n = 10,096)

Age, years

 

 Mean (SD)

56.40 (16.4)

 Median (IQR)

57 (44–69)

Age group, years, n (%)

 

 12–54

4412 (43.7)

 55–64

2278 (22.6)

 65–74

1961 (19.4)

 ≥ 75

1445 (14.3)

Female sex, n (%)

4238 (42)

Ethnicity, n (%)a

 

 White

6955 (68.9)

 Asian/Asian British

619 (6.1)

 Black/Black British/Caribbean or African

239 (2.4)

 Mixed

114 (1.1)

 Other

329 (3.3)

 Unknown

1840 (18.2)

Previous admission for COVID-19, n (%)

298 (3.0)

High-risk comorbidities, n (%)c

 Active cancer

910 (9.0)

 Down syndrome

107 (1.1)

 HIV

b

 Immune deficienciesd

338 (3.3)

 Patients being treated for immune-mediated inflammatory disorderse

4337 (43.0)

 Patients with hematologic diseases and stem cell transplant recipients

602 (6.0)

 Patients with liver disease

438 (4.3)

 Rare neurologic conditionsf

1053 (10.4)

 Severe renal disease

1422 (14.1)

 Solid organ transplant recipients

280 (2.8)

No comorbidity, n (%)

2633 (26.1)

  1. a Percentages calculated based on removal of “unknown” group from the denominator;
  2. b Small number suppression applied
  3. c As defined by the UK Medicines & Healthcare products Regulatory Agency [13]
  4. d common variable immunodeficiency; undefined primary antibody deficiency on immunoglobulin (or eligible for IgG); hyper-IgM syndromes; Good’s syndrome; severe combined immunodeficiency; autoimmune polyglandular syndromes/autoimmune polyendocrinopathy, ectodermal dystrophy; primary immunodeficiency associated with impaired type I interferon signalling; X-linked agammaglobulinaemia (and other primary agammaglobulinaemias); any patient with a secondary immunodeficiency likely to be eligible for receipt of immunoglobulin replacement therapy
  5. e IMID treated with rituximab or other B cell depleting therapy in the last 12 months; IMID with active/unstable disease on corticosteroids, cyclophosphamide, tacrolimus, cyclosporin or mycophenolate; IMID with stable disease on either corticosteroids, cyclophosphamide, tacrolimus, cyclosporin or mycophenolate; IMID patients with active/unstable disease including those on biological monotherapy and on combination biologicals with thiopurine or methotrexate
  6. f multiple sclerosis; motor neurone disease; myasthenia gravis; Huntington’s disease
  7. COVID-19, coronavirus disease 2019; HIV, human immunodeficiency virus; IMID, immune-mediated inflammatory disorders; IQR, interquartile range; SD, standard deviation