TABLE 2.
Infusion Characteristics (N = 132)
Criteria | Results |
---|---|
Veterans Health Administration COVID-19 Index score, No. (%) | |
Low risk (0%–8.7%) | 88 (66) |
Moderate risk (8.8%–16%) | 22 (17) |
High risk (16.1%–21.2%) | 14 (11) |
Extreme risk (> 21.3%) | 8 (6) |
| |
Referral type, No. (%) | |
Infectious disease monoclonal antibody team | 101 (77) |
Inpatient | 19 (14) |
Not infectious disease | 12 (9) |
| |
Infusion location, No. (%) | |
Outpatient | 108 (82) |
Inpatient | 24 (18) |
| |
Time to infusion, median (range), d | |
From initial symptom | 6 (0–9) |
From positive test result | 2 (0–8) |
| |
Monoclonal antibody infusion, No. (%) | |
Bamlanivimaba | 20 (15) |
Bamlanivimab-etesevimabb | 12 (9) |
Casirivimab-imdevimab | 100 (76) |
| |
COVID-19 immunoglobulin G detectedc | 9 (9) |
Bamlanivimab Mab infusion therapy was halted on April 16, 2021, due to increased resistance by the COVID-19 viral variant.
Bamlanivimab-etesevimab was paused on June 25, 2021, over concerns of reduced susceptibility with the circulating variants of concern.
Available for 104 patients.