Table 3.
Outcome | All SARD patients with COVID-19 (n=704) | Any outpatient treatment (n=426)* | Nirmatrelvir/ritonavir use (n=307) | Monoclonal antibody use (n=105) | No outpatient treatment (n=278) |
---|---|---|---|---|---|
Hospitalization | 58 (8.2%) | 9 (2.1%) | 4 (1.3%) | 5 (4.8%) | 49 (17.6%) |
Death | 3 (0.4%) | 1 (0.2%) | 1 (0.3%) | 0 (0.0%) | 2 (0.7%) |
Severe COVID-19 (hospitalization or death) | 58 (8.2%) | 9 (2.1%) | 4 (1.3%) | 5 (4.8%) | 49 (17.6%) |
Rebound | N/A | N/A | 25/311** (8.0%) | N/A | N/A |
There were no severe COVID-19 outcomes among molnupiravir (n=5), remdesivir (n=3), or combination (n=6; 4 received nirmatrelvir/ritonavir and monoclonal antibodies and 2 received molnupiravir and monoclonal antibodies) users.
The denominator for COVID-19 rebound also includes 4 patients who used nimatrelvir/ritonavir as a combination with monoclonal antibodies. There was also 1 COVID-19 rebound case among 7 molnupiravir users (14.3%).
COVID-19, coronavirus disease 2019; N/A, not applicable; SARD, systemic autoimmune rheumatic disease; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2.