Department of Medicine, University of Colorado School of Medicine, Aurora, USA.
Department of Biostatistics and Informatics, Colorado School of Public Health, Aurora, USA.
Int J Infect Dis. 2023 Mar;128:310-317. doi: 10.1016/j.ijid.2022.10.002. Epub 2022 Oct 10.
Sotrovimab effectively prevented progression to severe disease and mortality following infection with pre-Omicron SARS-CoV-2 variants. We sought to determine whether sotrovimab is similarly effective against SARS-CoV-2 Omicron variant infection.
Observational cohort study of non-hospitalized adult patients with SARS-CoV-2 infection from December 26, 2021, to March 10, 2022, using electronic health records from a statewide health system. We propensity-matched patients not receiving authorized treatment for each patient treated with sotrovimab. The primary outcome was 28-day hospitalization; secondary outcomes included mortality. We also propensity-matched sotrovimab-treated patients from the Omicron and Delta phases. Logistic regression was used to determine sotrovimab effectiveness during Omicron and between variant phases.
Of 30,247 SARS-CoV-2 Omicron variant infected outpatients, we matched 1542 receiving sotrovimab to 3663 not receiving treatment. Sotrovimab treatment was not associated with reduced odds of 28-day hospitalization (2.5% vs 3.2%; adjusted odds ratio [OR] 0.82, 95% CI 0.55, 1.19) or mortality (0.1% vs 0.2%; adjusted OR 0.62, 95% CI 0.07, 2.78). Between phases, the observed treatment OR was higher during Omicron than during Delta (OR 0.85 vs 0.39, respectively; interaction P-value = 0.053).
Real-world evidence demonstrated that sotrovimab was not associated with reduced 28-day hospitalization or mortality among COVID-19 outpatients during the Omicron BA.1 phase.
索特罗维单抗可有效预防感染 pre-Omicron SARS-CoV-2 变体后向严重疾病和死亡的进展。我们旨在确定索特罗维单抗对 SARS-CoV-2 奥密克戎变体感染是否同样有效。
对 2021 年 12 月 26 日至 2022 年 3 月 10 日期间,来自全州卫生系统的电子健康记录中,患有 SARS-CoV-2 感染的非住院成年患者进行了观察性队列研究。我们对每位接受索特罗维单抗治疗的患者进行了未接受授权治疗的患者的倾向匹配。主要结局是 28 天住院率;次要结局包括死亡率。我们还对奥密克戎和德尔塔阶段的接受索特罗维单抗治疗的患者进行了倾向匹配。使用逻辑回归确定奥密克戎期间和变体阶段之间的索特罗维单抗有效性。
在 30247 名 SARS-CoV-2 奥密克戎变体感染的门诊患者中,我们匹配了 1542 名接受索特罗维单抗治疗的患者和 3663 名未接受治疗的患者。索特罗维单抗治疗与降低 28 天住院率(2.5%比 3.2%;调整后的优势比 [OR] 0.82,95%置信区间 0.55,1.19)或死亡率(0.1%比 0.2%;调整后的 OR 0.62,95%置信区间 0.07,2.78)无关。在阶段之间,奥密克戎期间观察到的治疗 OR 高于德尔塔期间(分别为 OR 0.85 比 0.39,交互 P 值=0.053)。
真实世界证据表明,在奥密克戎 BA.1 阶段,索特罗维单抗与 COVID-19 门诊患者 28 天住院率或死亡率降低无关。