College of Pulmonary and Critical Care Medicine, The Eighth Medical Center, Chinese PLA General Hospital, Beijing, China.
Chinese PLA Medical School, Beijing, China.
Ann Med. 2024 Dec;56(1):2313062. doi: 10.1080/07853890.2024.2313062. Epub 2024 Feb 14.
The effectiveness of nirmatrelvir-ritonavir has mainly been shown in non-hospitalized patients with mild-to-moderate coronavirus disease 2019 (COVID-19). The real-world effectiveness of nirmatrelvir-ritonavir urgently needs to be determined using representative in-hospital patients with COVID-19 during the Omicron wave of the pandemic.
We performed a multicentre, retrospective study in five Chinese PLA General Hospital medical centers in Beijing, China. Patients hospitalized with COVID-19 from 10 December 2022 to 20 February 2023 were eligible for inclusion. A 1:1 propensity score matching was performed between the nirmatrelvir-ritonavir group and the control group.
1010 recipients of nirmatrelvir-ritonavir and 1010 matched controls were finally analyzed after matching. Compared with matched controls, the nirmatrelvir-ritonavir group had a lower incidence rate of all-cause death (4.6/1000 vs. 6.3/1000 person-days, = 0.013) and a higher incidence rate of clinical improvement (47.6/1000 vs. 45.8/1000 person-days, = 0.012). Nirmatrelvir-ritonavir was associated with a 22% lower all-cause mortality and a 14% higher incidence of clinical improvement. Initiation of nirmatrelvir-ritonavir within 5 days after symptom onset was associated with a 50% lower mortality and a 26% higher clinical improvement rate. By contrast, no significant associations were identified among patients receiving nirmatrelvir-ritonavir treatment more than 5 days after symptom onset. Nirmatrelvir-ritonavir was also associated with a 50% increase in survival days and a 12% decrease in days to clinical improvement.
Among hospitalized patients with COVID-19 during the Omicron wave in Beijing, China, the early initiation of nirmatrelvir-ritonavir was associated with clinical benefits of lowering mortality and improving clinical recovery.
奈玛特韦/利托那韦主要在轻症至中度 2019 冠状病毒病(COVID-19)的非住院患者中显示出有效性。奥密克戎流行期间,迫切需要使用具有代表性的住院 COVID-19 患者来确定奈玛特韦/利托那韦的真实世界疗效。
我们在中国北京的五家解放军总医院医学中心进行了一项多中心、回顾性研究。符合条件的患者为 2022 年 12 月 10 日至 2023 年 2 月 20 日期间住院的 COVID-19 患者。奈玛特韦/利托那韦组与对照组进行了 1:1 倾向评分匹配。
匹配后最终分析了 1010 例奈玛特韦/利托那韦组和 1010 例匹配对照组患者。与匹配对照组相比,奈玛特韦/利托那韦组全因死亡率(4.6/1000 与 6.3/1000 人天, = 0.013)较低,临床改善发生率(47.6/1000 与 45.8/1000 人天, = 0.012)较高。奈玛特韦/利托那韦与全因死亡率降低 22%和临床改善发生率提高 14%相关。症状出现后 5 天内开始使用奈玛特韦/利托那韦与死亡率降低 50%和临床改善率提高 26%相关。相比之下,在症状出现后 5 天以上开始接受奈玛特韦/利托那韦治疗的患者中未发现显著相关性。奈玛特韦/利托那韦还与生存天数增加 50%和临床改善天数减少 12%相关。
在中国北京奥密克戎流行期间,住院 COVID-19 患者早期使用奈玛特韦/利托那韦与降低死亡率和改善临床康复相关。