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. 2023 Aug 29;16(11):2048–2058. doi: 10.1093/ckj/sfad184

Table 3:

Comparing risks of outcome events within 28-days after a positive test between sotrovimab/molnupiravir versus untreated patients in the OpenSAFELY-UKRR dataset.

Outcomes HR (95% CI) for sotrovimab (ref = untreated) P-value HR (95% CI) for molnupiravir (ref = untreated) P-value
28-day COVID-19-related hospitalisation/death
 Model 1 0.38 (0.23–0.63) <.001 0.94 (0.51–1.74) .844
 Model 2 0.33 (0.20–0.55) <.001 0.79 (0.43–1.45) .443
 Model 3 0.38 (0.23–0.63) <.001 0.79 (0.43–1.47) .463
 Model 4 0.38 (0.23–0.63) <.001 0.81 (0.44–1.49) .492
28-day all-cause hospitalisation/death
 Model 1 0.74 (0.59–0.92) .008 1.01 (0.70–1.44) .975
 Model 2 0.74 (0.59–0.94) .012 1.00 (0.70–1.44) .995
 Model 3 0.78 (0.61–0.98) .037 1.05 (0.73–1.50) .810
 Model 4 0.78 (0.62–0.98) .039 1.07 (0.75–1.54) .704

In this analysis, 4588 untreated patients, 1624 sotrovimab users and 439 molnupiravir users were included (after excluding those whose positive test date was missing or outside of the study period). Model 1 adjusted for age and sex and stratified by region; Model 2 additionally adjusted for high-risk cohort categories, KRT modality and duration; Model 3 additionally adjusted for ethnicity, IMD quintiles, vaccination status, calendar date; and Model 4 additionally adjusted for BMI category, diabetes, hypertension, chronic cardiac and respiratory diseases.