Division of Infectious Diseases, Department of Internal Medicine, National Medical Center, Seoul, Korea.
Public Health Research Institute, National Medical Center, Seoul, Korea.
J Korean Med Sci. 2023 Sep 4;38(35):e272. doi: 10.3346/jkms.2023.38.e272.
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.
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.
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; < 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%).
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.
尼马瑞韦/利托那韦在轻度至中度严重程度的高危患者中预防严重 2019 冠状病毒病(COVID-19)非常有效。然而,实际性能数据有限,而且该药在韩国需要它的高危 COVID-19 患者中并不那么受欢迎。
为了评估尼马瑞韦/利托那韦的疗效,我们对 2022 年 2 月至 2022 年 4 月期间在韩国四家医院住院的患有轻度至中度 COVID-19 且有发展为重症疾病高风险的 236 名患者进行了倾向评分匹配的回顾性队列研究。治疗组(给予尼马瑞韦/利托那韦)和 236 名匹配的对照组(仅支持性护理)分析了主要结局,即无吸氧支持生存时间。次要结局是疾病进展的综合结果。还调查了未给指示患者开具尼马瑞韦/利托那韦的原因。
治疗组的无吸氧支持生存时间明显长于匹配对照组(调整后的危险比[aHR],0.07;95%置信区间[CI],0.01-0.31;<0.001)。多变量 Cox 回归分析显示,年龄(aHR,1.03;95%CI,1.00-1.07)、入院时国家早期预警评分-2(aHR,1.36;95%CI,1.08-1.71)、尼马瑞韦/利托那韦治疗、女性(aHR,0.37;95%CI,0.15-0.88)和从症状出现到入院的时间(aHR,0.67;95%CI,0.48-0.95)与吸氧治疗显著相关。然而,这些因素均与复合结局无关。在未匹配的对照组中,376 名患者中有 19.9%有记录的尼马瑞韦/利托那韦非处方解释,其中 44.0%是由于禁忌标准。在治疗组中,10.9%的患者因不良事件(71.4%)主要停止用药,胃肠道症状最为常见(50.0%)。
在韩国奥密克戎变体激增期间,尼马瑞韦/利托那韦治疗显著降低了 COVID-19 高危患者对吸氧治疗的需求。鼓励医生积极考虑使用尼马瑞韦/利托那韦,并在用药期间注意胃肠道症状。