Yang Huqin, Gao Leyi, Xue Yi, Zhang Zhijin, Guan Lujia, Zhang Haifan, Ma Haomiao, Li Xuyan, Li Jieqiong, Tong Zhaohui
Department of Respiratory and Critical Care Medicine, Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Laboratory for Clinical Medicine, Capital Medical University, Beijing, China.
J Med Virol. 2025 May;97(5):e70377. doi: 10.1002/jmv.70377.
Nirmatrelvir-ritonavir (NMV-r) has been widely used to treat coronavirus disease 2019 (COVID-19) for a standard period of 5-days. However, there are increasing reports of patients with persistent severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) positivity after the standard 5-day course of NMV-r treatment. Moreover, the clinical characteristics of these patients and the efficacy of extending NMV-r treatment duration are not fully understood. We conducted a prospective study involving hospitalized patients with COVID-19. In total, 310 patients were included: 133 with SARS-CoV-2 RNA positivity after completion of the standard course of NMV-r (positive group) and 177 without SARS-CoV-2 positivity (negative group). A subset of patients (n = 37) in the positive group extended the treatment with NMV-r. Patients in the positive group had higher severity scores, neutrophil counts, lactate dehydrogenase levels, and viral loads at admission. Following the standard 5-day NMV-r course, the positive group showed a significantly increased risk of composite disease progression outcomes (hazard ratio [HR] 3.35, 95% confidence interval [CI]: 2.07-5.44; p < 0.0001). This group also demonstrated higher risks of 28-day all-cause mortality, initiation of invasive mechanical ventilation, intensive care unit (ICU) admission and prolonged hospitalization. However, no significant differences in clinical outcomes were observed between the standard and the extended treatment groups in the unadjusted analysis. After adjustment for baseline characteristics, the extended treatment group demonstrated significantly better outcomes compared with the standard treatment group. Specifically, the extended treatment group had lower rates of composite disease progression (HR: 0.39, 95% CI: 0.20-0.79; p = 0.009), invasive mechanical ventilation (HR: 0.24, 95% CI: 0.08-0.73; p = 0.01), and ICU admission (HR: 0.15, 95% CI: 0.02-0.94; p = 0.04), along with a shorter length of hospital stay (HR: -13.54, 95% CI: -26.01 to -1.07; p = 0.033). SARS-CoV-2 positivity after NMV-r treatment is common and associated with worse clinical outcomes. Extending NMV-r therapy may reduce disease progression risk; this finding requires confirmation in future studies.
奈玛特韦-利托那韦(NMV-r)已被广泛用于治疗2019冠状病毒病(COVID-19),标准疗程为5天。然而,越来越多的报告称,在接受标准的5天NMV-r治疗疗程后,仍有严重急性呼吸综合征冠状病毒2(SARS-CoV-2)持续阳性的患者。此外,这些患者的临床特征以及延长NMV-r治疗疗程的疗效尚不完全清楚。我们对住院的COVID-19患者进行了一项前瞻性研究。总共纳入了310例患者:133例在完成NMV-r标准疗程后SARS-CoV-2 RNA呈阳性(阳性组),177例SARS-CoV-2呈阴性(阴性组)。阳性组中的一部分患者(n = 37)延长了NMV-r治疗。阳性组患者入院时的严重程度评分、中性粒细胞计数、乳酸脱氢酶水平和病毒载量更高。在接受标准的5天NMV-r疗程后,阳性组出现复合疾病进展结局的风险显著增加(风险比[HR] 3.35,95%置信区间[CI]:2.07 - 5.44;p < 0.0001)。该组在28天全因死亡率、有创机械通气启动、重症监护病房(ICU)入院和住院时间延长方面也显示出更高的风险。然而,在未调整分析中,标准治疗组和延长治疗组之间未观察到临床结局的显著差异。在对基线特征进行调整后,延长治疗组与标准治疗组相比显示出明显更好的结局。具体而言,延长治疗组的复合疾病进展率较低(HR:0.39,95% CI:0.20 - 0.79;p = 0.009)、有创机械通气率较低(HR:0.24,95% CI:0.08 - 0.73;p = 0.01)以及ICU入院率较低(HR:0.15,95% CI:0.02 - 0.94;p = 0.04),同时住院时间更短(HR:-13.54,95% CI:-26.01至-1.07;p = 0.033)。NMV-r治疗后SARS-CoV-2阳性很常见,且与更差的临床结局相关。延长NMV-r治疗可能会降低疾病进展风险;这一发现需要在未来的研究中得到证实。