Department of Nutrition, Chi Mei Medical Centre, Tainan, Taiwan.
Department of Nutrition, Chi Mei Medical Centre, Tainan, Taiwan; Department of Nutrition and Health Sciences, Chang Jung Christian University, Tainan, Taiwan.
Int J Antimicrob Agents. 2023 Dec;62(6):106984. doi: 10.1016/j.ijantimicag.2023.106984. Epub 2023 Sep 26.
To investigate the association between nirmatrelvir plus ritonavir (NMV-r) and the outcomes of non-hospitalized obese patients with coronavirus disease 2019 (COVID-19).
This retrospective cohort study used the TriNetX research network to identify non-hospitalized obese adult patients with COVID-19 between 1 January 2022 and 30 June 2023. Propensity score matching was used to match patients receiving NMV-r (NMV-r group) with those not receiving NMV-r (control group). The primary outcome was the compositive outcome of all-cause emergency department (ED) visits, hospitalization or death during the 30-day follow-up period.
Using propensity score matching methods, two cohorts of 30,969 patients each with balanced baseline characteristics were identified. During the follow-up period, the NMV-r group had a lower risk of all-cause ED visits, hospitalization or death [4.80% (n=1489) vs 5.50% (n=1705); hazard ratio (HR) 0.900, 95% confidence interval (CI) 0.839-0.965]. Compared with the control group, the NMV-r group had a lower risk of all-cause ED visits (HR 0.812, 95% CI 0.740-0.891) and all-cause mortality (HR 0.089, 95% CI 0.027-0.288). The lower risk in the NMV-r group compared with the control group was observed consistently in most subgroup analyses according to body mass index (30.0-34.9 kg/m: HR 0.68, 95% CI 0.55-0.82; 35.0-39.9 kg/m: HR 0.67, 95% CI 0.52-0.87), age (4-64 years: HR 0.83, 95% CI 0.75-0.92; ≥65 years: HR 0.88, 95% CI 0.79-0.98), sex (men: HR 0.69, 95% CI 0.60-0.79; women: HR 0.69, 95% CI 0.63-0.76) and vaccination status (unvaccinated: HR 0.75, 95% CI 0.70-0.81).
NMV-r is associated with reduced risk of all-cause ED visits, hospitalization and death for non-hospitalized obese patients with COVID-19. Accordingly, these findings support the use of NMV-r in obese patients.
探讨奈玛特韦/利托那韦(NMV-r)与非住院肥胖 2019 冠状病毒病(COVID-19)患者结局的相关性。
本回顾性队列研究使用 TriNetX 研究网络,于 2022 年 1 月 1 日至 2023 年 6 月 30 日期间,确定非住院肥胖成年 COVID-19 患者。采用倾向评分匹配法,将接受 NMV-r 治疗的患者(NMV-r 组)与未接受 NMV-r 治疗的患者(对照组)进行匹配。主要结局为 30 天随访期间全因急诊就诊、住院或死亡的复合结局。
采用倾向评分匹配方法,共确定了两组各 30969 例具有平衡基线特征的患者。在随访期间,NMV-r 组全因急诊就诊、住院或死亡的风险较低[4.80%(n=1489)比 5.50%(n=1705);风险比(HR)0.900,95%置信区间(CI)0.839-0.965]。与对照组相比,NMV-r 组全因急诊就诊(HR 0.812,95% CI 0.740-0.891)和全因死亡率(HR 0.089,95% CI 0.027-0.288)的风险较低。根据体重指数(BMI)(30.0-34.9 kg/m:HR 0.68,95% CI 0.55-0.82;35.0-39.9 kg/m:HR 0.67,95% CI 0.52-0.87)、年龄(4-64 岁:HR 0.83,95% CI 0.75-0.92;≥65 岁:HR 0.88,95% CI 0.79-0.98)、性别(男性:HR 0.69,95% CI 0.60-0.79;女性:HR 0.69,95% CI 0.63-0.76)和疫苗接种状态(未接种疫苗:HR 0.75,95% CI 0.70-0.81),NMV-r 组与对照组相比,全因 ED 就诊、住院和死亡的风险降低趋势一致。
NMV-r 可降低非住院肥胖 COVID-19 患者全因 ED 就诊、住院和死亡的风险。因此,这些发现支持在肥胖患者中使用 NMV-r。