Comparable Outcomes for Bebtelovimab and Ritonavir-Boosted Nirmatrelvir Treatment in High-Risk Patients With Coronavirus Disease-2019 During Severe Acute Respiratory Syndrome Coronavirus 2 BA.2 Omicron Epoch

被引:32
|
作者
Razonable, Raymund R. [1 ]
O'Horo, John C. [1 ]
Hanson, Sara N. [2 ]
Arndt, Richard F. [3 ]
Speicher, Leigh L. [4 ]
Seville, Teresa A. [5 ]
Hall, Scott T. [6 ]
Pike, Marsha L. [1 ]
Heyliger, Alexander [1 ]
Larsen, Jennifer J. [1 ]
Ganesh, Ravindra [1 ]
Tulledge-Scheitel, Sidna M. [1 ]
机构
[1] Mayo Clin, Rochester, MN 55905 USA
[2] Mayo Clin Hlth Syst Mankato, Mankato, MN USA
[3] Mayo Clin Hlth Syst Eau Claire, Eau Claire, WI USA
[4] Mayo Clin, Jacksonville, FL 32224 USA
[5] Mayo Clin, Phoenix, AZ USA
[6] Mayo Clin Hlth Syst, Franciscan Skemp Healthcare, La Crosse, WI USA
来源
JOURNAL OF INFECTIOUS DISEASES | 2022年 / 226卷 / 10期
关键词
SARS-CoV-2; bebtelovimab; COVID-19; hospitalization; monoclonal antibodies; nirmatrelvir; Paxlovid; ritonavir;
D O I
10.1093/infdis/jiac346
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
This real-world retrospective cohort study of 3607 high-risk patients with mild to moderate coronavirus 2019 disease demonstrates that the rates of severe disease progression by day 30 did not differ significantly between bebtelovimab (1.4%) and oral nirmatrelvir-ritonavir (1.2%) treatment. The effectiveness of bebtelovimab in real-world settings has not been assessed. In this retrospective cohort study of 3607 high-risk patients, bebtelovimab was used more commonly than nirmatrelvir-ritonavir for treatment of coronavirus disease 2019 (COVID-19) among older patients, immunosuppressed patients, and those with multiple comorbid conditions. Despite its use in patients with multiple comorbid conditions, the rate of progression to severe disease after bebtelovimab (1.4% [95% confidence interval, 1.2%-1.7%]) was not significantly different from that for nirmatrelvir-ritonavir treatment (1.2% [.8%-1.5%]). Our findings support the emergency use authorization of bebtelovimab for treatment of COVID-19 during the Omicron epoch dominated by BA.2 and subvariants.
引用
收藏
页码:1683 / 1687
页数:5
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