Table 3.
Subgroup analyses of all-cause mortality.
| Subgroups | Total (N = 4886) |
||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Nirmatrelvir-ritonavir (N = 1462) |
Molnupiravir (N = 3424) |
ARR (95% CI) (%) | Adjusted HR (95% CI)a | p-value for interaction | |||||||
| Events | Rate (%) | Follow-up time (days) | Incidence rate (per 10,000 person days) | Events | Rate (%) | Follow-up time (days) | Incidence rate (per 10,000 person days) | ||||
| All-cause mortality | |||||||||||
| Age, years | 0.127 | ||||||||||
| <70 | 6 | 2.24 | 23,828 | 2.52 (0.92, 5.48) | 14 | 2.03 | 61,289 | 2.28 (1.25, 3.83) | −0.21 (0.09, 3.22) | NAb | |
| ≥70 | 68 | 5.70 | 103,219 | 6.59 (5.12, 8.35) | 259 | 9.48 | 229,767 | 11.27 (9.94, 12.73) | 3.78 (1.62, 6.12) | 0.566 (0.401–0.798) | |
| Sex | 0.227 | ||||||||||
| Male | 41 | 6.02 | 58,868 | 6.96 (5.00, 9.45) | 137 | 8.59 | 135,116 | 10.14 (8.51, 11.99) | 2.57 (0.32, 4.83) | 0.873 (0.468–1.631) | |
| Female | 33 | 4.23 | 68,179 | 4.84 (3.33, 6.80) | 136 | 7.43 | 155,940 | 8.72 (7.32, 10.32) | 3.20 (1.35, 5.06) | 0.571 (0.265–1.229) | |
| CCI | 0.894 | ||||||||||
| ≤5 | 35 | 3.88 | 79,095 | 4.43 (3.08, 6.15) | 115 | 5.86 | 169,545 | 6.78 (5.60, 8.14) | 1.98 (0.35, 3.61) | 0.614 (0.321–1.174) | |
| >5 | 39 | 6.96 | 47,952 | 8.13 (5.78, 11.12) | 158 | 10.81 | 121,511 | 13.00 (11.05, 15.20) | 3.85 (1.21, 6.49) | 0.772 (0.402–1.482) | |
| COVID-19 vaccination status | 0.326 | ||||||||||
| 0–1 dose | 15 | 8.88 | 14,411 | 10.41 (5.83, 17.17) | 62 | 15.20 | 33,051 | 18.76 (14.38, 24.05) | 6.32 (0.80, 11.85) | NAb | |
| ≥2 doses | 59 | 4.56 | 112,636 | 5.24 (3.99, 6.76) | 211 | 7.00 | 258,005 | 8.18 (7.11, 9.36) | 2.44 (0.98, 3.89) | 0.549 (0.372–0.81) | |
HR, Hazard ratio; CI, Confidence interval; CCI, Charlson Comorbidity Index.
Hazard ratios were obtained from stratified Cox proportional hazard regression adjusted by sex, age, Charlson Comorbidity Index, vaccination status, hospitalisation, eGFR, renal replacement therapy, pre-existing comorbidities and medication use within 90 days at baseline.
Not applicable due to insufficient events observed.