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. 2023 Mar 8. Online ahead of print. doi: 10.1016/j.jfma.2023.02.008

Table 1.

Comparisons of clinical and virological characteristics, and outcomes among COVID-19 patients receiving nirmatrelvir/ritonavir and molnupiravir.

Total (n = 85) Nirmatrelvir/ritonavir (n = 58) Molnupiravir (n = 27) P
Demographics
Age, years 58.5 (38.0–78.0) 49.0 (34.0–72.0) 73.3 (55.0–84.0) 0.002
Gender, male 47 (55.3) 32 (55.2) 15 (55.6) >0.99
Vaccine status 0.24
No vaccinations 37 (43.5) 25 (43.1) 12 (44.4)
1 dose 14 (16.5) 7 (12.1) 7 (25.9)
2 doses 8 (9.4) 5 (8.6) 3 (11.1)
3 doses 26 (30.6) 21 (36.2) 5 (18.2)
Comorbidities
Diabetes mellitus 19 (22.4) 7 (12.1) 12 (44.4) 0.002
Cardiovascular disorder 18 (21.2) 6 (10.3) 12 (44.4) 0.001
Chronic lung disease 3 (3.5) 2 (3.5) 1 (3.7) >0.99
Chronic kidney disease 13 (15.3) 1 (1.7) 12 (44.4) <0.001
Chronic liver diseases 6 (7.1) 3 (5.2) 3 (11.1) 0.38
Neurodevelopmental disorder 0 (0) 0 (0) 0 (0) >0.99
Psychiatric disorder 1 (1.2) 0 (0) 1 (3.7) 0.32
Dementia 6 (7.1) 1 (1.7) 5 (18.5) 0.01
Active tuberculosis 1 (1.2) 0 (0) 1 (3.7) 0.32
Obesity, BMI≥25 37 (43.5) 23 (39.7) 14 (51.9) 0.35
Cigarette smoker 10 (11.8) 8 (13.8) 2 (7.4) 0.49
Immunosuppression 17 (20.0) 12 (20.7) 5 (18.5) >0.99
Active cancer 25 (29.4) 17 (29.3) 8 (29.6) >0.99
Numbers of risk factors 2 (1-3) 1.5 (1-3) 4 (1-5) <0.001
Pulmonary ordinal scale at baseline 3 (3-3) 3 (3-3) 3 (3-3) >0.99
Initial laboratory data
White blood cell count ( × 109/L) 6.8 (5.2–9.1) 6.8 (4.9–9.0) 6.7 (5.4–9.6) 0.62
Lymphocyte count ( × 109/L) 1.1 (0.7–1.5) 1.1 (0.7–1.6) 1.1 (0.7–1.3) 0.82
Lymphopenia (<0.8 × 109/L) 24 (31.2) 16 (32.0) 8 (29.6) >0.99
Neutrophil count ( × 109/L) 4.8 (3.3–7.4) 4.9 (3.2–6.9) 4.7 (3.4–8.1) 0.58
Hemoglobin (g/dL) 12.5 (10.4–13.7) 12.8 (11.5–14.3) 12.1 (10.1–13.3) 0.09
Platelet count ( × 109/L) 218 (152–276) 239 (165.5–280) 200 (136–266) 0.15
C-reactive protein (mg/dL) 1.6 (0.7–4.2) 1.1 (0.5–3.4) 2.1 (1.1–5.5) 0.06
Ferritin (ng/mL) 299.9 (161.8–529.1) 256.5 (121.4–421.9) 391.1 (211.8–988.0) 0.02
Procalcitonin (ng/mL) 0.10 (0.06–0.21) 0.08 (0.05–0.15) 0.15 (0.09–0.58) 0.02
D-dimer (mg/L) 0.7 (0.3–1.8) 0.4 (0.2–1.1) 1.8 (0.7–5.2) <0.001
Albumin (g/dL) 4.1 (3.6–4.6) 4.3 (3.9–4.7) 3.7 (3.6–4.0) 0.02
Total bilirubin (mg/dL) 0.6 (0.4–0.8) 0.6 (0.4–0.8) 0.6 (0.4–0.7) 0.87
AST (U/L) 25.5 (18.5–35.5) 22.5 (17.0–35.0) 28.0 (21.0–37.0) 0.33
ALT (U/L) 19.0 (12.0–29.0) 20.0 (14.0–37.0) 14.0 (12.0–23.0) 0.11
Lactate dehydrogenase (U/L) 203.0 (170.0–247.5) 203.0 (168.5–245.5) 206.0 (176.5–247.5) 0.46
Creatine kinase (U/L) 89 (36–164) 86.5 (38.5–162.5) 96 (35–187) 0.61
BUN (mg/dL) 15.9 (11.1–23.8) 13.6 (10.8–18.1) 28.8 (16.6–41.4) <0.001
Creatinine (mg/dL) 0.9 (0.7–1.2) 0.9 (0.7–1.0) 1.6 (0.7–3.1) 0.02
Virological parameter
Ct value of index RT-PCR test 16.6 (14.0–23.6) 17.0 (14.1–23.9) 15.6 (13.6–23.6) 0.36
Ctlowest value within 5 days of index RT-PCR testa 16.2 (14.0–19.1) 16.4 (14.0–19.7) 15.6 (13.6–18.3) 0.32
Numbers of RT-PCR test 3 (3-4) 3 (3-4) 3 (3-4) >0.99
Intervals between index and last RT-PCR test, days 9 (8-12) 8 (7-12) 9 (8-12) 0.44
Time-to-initiation antiviral, days
From index date 1 (0–1) 1 (0–2) 1 (0–1) 0.24
From symptom onset 2 (1-3) 2 (1-3) 1 (1-2) 0.03
Outcomes
Viral rebound 11 (12.9) 10 (17.2) 1 (3.7) 0.16
Time to viral rebound after index RT-PCR test, days 10.0 (8.0–12.0) 9.5 (8.0–11.0) 16.0 0.15
Time to viral rebound after completion of antivirals, days 5.0 (2.0–8.0) 4.5 (2.0–6.0) 11.0 0.11
Clinical improvementb 73 (85.6) 51 (87.9) 22 (81.5) 0.51
Follow-up duration, days 11 (9-16) 10 (9-15) 12 (10-22) 0.04

Continuous variables, median (interquartile); categoric variables, n (%).

Abbreviation: BMI, body mass index; AST, aspartate aminotransferase; ALT, alanine aminotransferase; BUN, blood urea nitrogen; PCR, polymerase chain reaction.

a

Ctlowest, the lowest Ct value within 5 days of index PCR among patients with and without viral rebound.

b

Clinical improvement was defined as substantial decline of an ordinal score ≥2 at end of follow-up.