Coronavirus and Other Respiratory Viruses Division, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Influenza Division, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Clin Infect Dis. 2024 May 15;78(5):1175-1184. doi: 10.1093/cid/ciad696.
BACKGROUND: Nirmatrelvir/ritonavir (N/R) reduces severe outcomes from coronavirus disease 2019 (COVID-19); however, rebound after treatment has been reported. We compared symptom and viral dynamics in individuals with COVID-19 who completed N/R treatment and similar untreated individuals. METHODS: We identified symptomatic participants who tested severe acute respiratory syndrome coronavirus 2-positive and were N/R eligible from a COVID-19 household transmission study. Index cases from ambulatory settings and their households contacts were enrolled. We collected daily symptoms, medication use, and respiratory specimens for quantitative polymerase chain reaction for 10 days during March 2022-May 2023. Participants who completed N/R treatment (treated) were propensity score matched to untreated participants. We compared symptom rebound, viral load (VL) rebound, average daily symptoms, and average daily VL by treatment status measured after N/R treatment completion or 7 days after symptom onset if untreated. RESULTS: Treated (n = 130) and untreated participants (n = 241) had similar baseline characteristics. After treatment completion, treated participants had greater occurrence of symptom rebound (32% vs 20%; P = .009) and VL rebound (27% vs 7%; P < .001). Average daily symptoms were lower among treated participants without symptom rebound (1.0 vs 1.6; P < .01) but not statistically lower with symptom rebound (3.0 vs 3.4; P = .5). Treated participants had lower average daily VLs without VL rebound (0.9 vs 2.6; P < .01) but not statistically lower with VL rebound (4.8 vs 5.1; P = .7). CONCLUSIONS: Individuals who completed N/R treatment experienced fewer symptoms and lower VL but rebound occured more often compared with untreated individuals. Providers should prescribe N/R, when indicated, and communicate rebound risk to patients.
背景:尼马曲韦/利托那韦(N/R)可降低 2019 年冠状病毒病(COVID-19)的重症结局;然而,有报道称治疗后会出现反弹。我们比较了完成 N/R 治疗和未接受类似治疗的 COVID-19 患者的症状和病毒动力学。
方法:我们从 COVID-19 家庭传播研究中确定了患有症状性、SARS-CoV-2 检测阳性且符合 N/R 治疗条件的参与者。招募了门诊环境中的索引病例及其家庭接触者。我们在 2022 年 3 月至 2023 年 5 月期间收集了 10 天的每日症状、药物使用情况和定量聚合酶链反应呼吸道标本。完成 N/R 治疗(治疗组)的参与者通过倾向评分与未接受治疗的参与者匹配。我们比较了治疗状态后的症状反弹、病毒载量(VL)反弹、平均每日症状和平均每日 VL,治疗组在 N/R 治疗完成后测量,未治疗组在症状出现后 7 天测量。
结果:治疗组(n=130)和未治疗组(n=241)的基线特征相似。治疗完成后,治疗组的症状反弹发生率更高(32%比 20%;P=0.009)和 VL 反弹发生率更高(27%比 7%;P<0.001)。无症状反弹的治疗组的平均每日症状较低(1.0 比 1.6;P<0.01),但有症状反弹的组无统计学差异(3.0 比 3.4;P=0.5)。无 VL 反弹的治疗组的平均每日 VL 较低(0.9 比 2.6;P<0.01),但有 VL 反弹的组无统计学差异(4.8 比 5.1;P=0.7)。
结论:与未接受治疗的个体相比,完成 N/R 治疗的个体的症状和 VL 更少,但反弹更为常见。医生在必要时应开具 N/R 处方,并向患者传达反弹风险。
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