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Table 2 Study outcomes in nirmatrelvir-ritonavir group vs. azvudine

From: Real-world effectiveness of nirmatrelvir-ritonavir versus azvudine in hospitalized patients with COVID-19 during the omicron wave in Beijing: a multicenter retrospective cohort study

Outcomes

Crude incidence (%)

Person-days

Crude incidence rate per 1000 person-days (95% CI)

HR (95% CI) a

All-cause death b

    

 Nirmatrelvir-ritonavir

36 (7.4%)

13,030

2.8 (2.1–3.6)

Reference

 Azvudine

43 (8.8%)

12,746

3.4 (2.6–4.3)

1.27 (0.81–2.00)

Composite disease progression c

    

 Nirmatrelvir-ritonavir

42 (8.6%)

12,804

3.3 (2.5–4.2)

Reference

 Azvudine

49 (10.1%)

12,530

3.9 (3.1–4.9)

1.22 (0.80–1.86)

Clinical improvement d

    

 Nirmatrelvir-ritonavir

376 (77.4%)

6818

55.1 (50.8–59.9)

Reference

 Azvudine

389 (80.0%)

6366

61.1 (56.4–66.2)

1.10 (0.95–1.27)

  1. HR hazard ratio, CI confidence interval
  2. aHR was estimated using Cox proportional hazard regression
  3. bDefined as all-cause mortality recorded within 28 days after exposure
  4. cDefined as new incidents of invasive mechanical ventilation or death within 28 days after exposure
  5. dDefined as 2 points or higher improvement in clinical symptoms recorded within 28 days after exposure