Real-World Effectiveness of Nirmatrelvir-Ritonavir and Its Acceptability in High-Risk COVID-19 Patients

被引:1
|
作者
Kim, Min-Kyung [1 ]
Lee, Kyung-Shin [2 ]
Ham, Sin Young [3 ]
Choi, Youn Young [4 ]
Lee, Eunyoung [5 ]
Lee, Seungjae [3 ]
Lee, Bora [6 ]
Jeon, Jaehyun [1 ]
Chin, Bumsik [1 ]
Kim, Yeonjae [1 ]
Kim, Gayeon [1 ]
Jang, Hee -Chang [7 ]
Choi, Jae-Phil [8 ,9 ]
Park, Sang -Won [10 ]
机构
[1] Natl Med Ctr, Dept Internal Med, Div Infect Dis, Seoul, South Korea
[2] Natl Med Ctr, Publ Hlth Res Inst, Seoul, South Korea
[3] Seoul Vet Hosp, Med Ctr, Seoul, South Korea
[4] Natl Med Ctr, Dept Pediat, Seoul, South Korea
[5] Seoul Natl Univ, Dept Internal Med, Boramae Med Ctr, Seoul, South Korea
[6] Natl Med Ctr, Dept Internal Med, Div Pulm & Crit Care Med, Seoul, South Korea
[7] Korea Dis Control & Prevent Agcy, Natl Inst Infect Dis, Korea Natl Inst Hlth, Cheongju, South Korea
[8] Seoul Med Ctr, Dept Internal Med, Div Infect Dis, Seoul, South Korea
[9] Seoul Med Ctr, Dept Internal Med, Div Infect Dis, 156 Shinnae Ro, Seoul 02053, South Korea
[10] Seoul Natl Univ, Dept Internal Med, Boramae Med Ctr, 20 Boramae Ro 5 Gil, Seoul 07061, South Korea
关键词
Nirmatrelvir-Ritonavir; COVID-19; Effectiveness; Retrospective Cohort Study; CORONAVIRUS DISEASE 2019; PROPENSITY-SCORE; MORTALITY;
D O I
10.3346/jkms.2023.38.e272
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Nirmatrelvir-ritonavir is highly effective in preventing severe coronavirus disease 2019 (COVID-19) in high-risk patients with mild-to-moderate severity. However, real-world performance data are limited, and the drug is not so acceptable to the COVID-19 patients at high risk who need it in Korea.Methods: To evaluate the effectiveness of nirmatrelvir-ritonavir, we conducted a propensity score-matched retrospective cohort study on patients with mild-to-moderate COVID-19 at high risk for a severe disease who were hospitalized at four hospitals in South Korea from February 2022 to April 2022. A total of 236 patients in the treatment group (administered nirmatrelvir-ritonavir) and 236 in the matched control group (supportive care only) were analyzed for the primary outcome, i.e., the time to oxygen support-free survival. The secondary outcome was a composite result of disease progression. The reason for not prescribing nirmatrelvir-ritonavir to the indicated patients was also investigated.Results: The treatment group showed significantly longer oxygen support-free survival than the matched control group (adjusted hazard ratio [aHR], 0.07; 95% confidence interval [CI], 0.01-0.31; P < 0.001). Multivariate Cox regression analysis showed that age (aHR, 1.03; 95% CI, 1.00-1.07), National Early Warning Score-2 at admission (aHR, 1.36; 95% CI, 1.08-1.71), nirmatrelvir-ritonavir treatment, female sex (aHR, 0.37; 95% CI, 0.15-0.88), and time from symptom onset to admission (aHR, 0.67; 95% CI, 0.48-0.95) were significantly associated with oxygen therapy. However, none of the factors were related to the composite outcome. In the unmatched control group, 19.9% of 376 patients had documented explanations for nirmatrelvir-ritonavir non-prescription, and 44.0% of these were due to contraindication criteria. In the treatment group, 10.9% of patients discontinued the medication primarily because of adverse events (71.4%), with gastrointestinal symptoms being the most common (50.0%).Conclusion: Nirmatrelvir-ritonavir treatment significantly reduced oxygen therapy requirements in high-risk patients with COVID-19 during the omicron variant surge in South Korea. Physicians are encouraged to consider the active use of nirmatrelvir-ritonavir and to be watchful for gastrointestinal symptoms during medication.
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页数:12
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