AZD7442(替沙吉维单/西加维单)在以色列暴露前预防新冠肺炎住院治疗的有效性

IF 4.7 3区 医学 Q1 INFECTIOUS DISEASES
Infectious Diseases and Therapy Pub Date : 2025-02-01 Epub Date: 2025-01-07 DOI:10.1007/s40121-024-01100-3
Samah Hayek, Joseph Levy, Galit Shaham, Noa Dagan, Danielle Serby, Hadar Duskin-Bitan, Sabada Dube, Cátia Ferreira, Idit Livnat, Carla Talarico, Sylvia Taylor, Sudhir Venkatesan, Adva Yarden, Ran D Balicer, Doron Netzer, Alon Peretz
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引用次数: 0

摘要

简介:AZD7442(替沙吉维单抗/西加维单抗)在以色列不同变体循环中免疫功能低下个体3个月和6个月时对COVID-19住院治疗的有效性进行了测定。方法:这是一项回顾性队列研究,使用来自以色列Clalit卫生服务的数据。确定了在2022年2月15日至12月11日期间有资格接受AZD7442 300 mg的免疫功能低下个体。使用“滚动队列”方法,接受AZD7442 300 mg作为暴露前预防(PrEP)的免疫功能低下个体与未暴露个体的倾向评分(PS)匹配为1:1。采用日历时间Cox比例风险回归模型,校正后匹配的非平衡协变量,估计风险比(hr)和95%置信区间(ci)。结果:总体而言,2444名暴露于azd7442的免疫功能低下个体与未暴露个体的ps匹配。在匹配人群中,随访6个月,AZD7442 300 mg对COVID-19住院的未调整HR(未调整不平衡协变量)为0.68 (95% CI 0.43-1.08),协变量调整HR为0.64 (95% CI 0.40-1.03)。协变量校正瞬时危险图显示,AZD7442 300 mg的有效性从第90天开始减弱。随访3个月时,匹配人群中AZD7442 300 mg对COVID-19住院治疗的未调整风险比为0.43 (95% CI 0.21-0.91);没有足够的事件进行协变量调整分析。结论:我们的研究结果表明,AZD7442 300 mg降低了免疫功能低下个体的COVID-19住院率;然而,由于缺乏足够的事件来产生结论性的结果,这些发现受到限制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effectiveness of AZD7442 (Tixagevimab/Cilgavimab) for Pre-Exposure Prophylaxis Against COVID-19 Hospitalization in Israel During the Omicron Sub-Variant Time Period.

Introduction: The effectiveness of AZD7442 (tixagevimab/cilgavimab) against COVID-19 hospitalizations was determined at 3 and 6 months among immunocompromised individuals in Israel during different variant circulations.

Methods: This was a retrospective cohort study using data from Clalit Health Services in Israel. Immunocompromised individuals eligible to receive AZD7442 300 mg between 15 February and 11 December 2022 were identified. Immunocompromised individuals receiving AZD7442 300 mg as pre-exposure prophylaxis (PrEP) were propensity score (PS)-matched 1:1 to unexposed individuals using a "rolling cohort" approach. Calendar time Cox proportional hazards regression models were performed with adjustment for post-matched unbalanced covariates to estimate hazard ratios (HRs) and 95% confidence intervals (CIs).

Results: Overall, 2444 AZD7442-exposed immunocompromised individuals were PS-matched to unexposed individuals. In the matched population, up to 6 months of follow-up, AZD7442 300 mg presented an unadjusted HR (without adjustment for the unbalanced covariates) of 0.68 (95% CI 0.43-1.08) and covariate-adjusted HR of 0.64 (95% CI 0.40-1.03) against COVID-19 hospitalization. Covariate-adjusted instantaneous hazards plots showed that the effectiveness of AZD7442 300 mg waned from Day 90. Up to 3 months of follow-up, the unadjusted HR was 0.43 (95% CI 0.21-0.91) for AZD7442 300 mg against COVID-19 hospitalization in the matched population; there were insufficient events to allow covariate-adjusted analysis.

Conclusion: Our results suggest that AZD7442 300 mg reduced COVID-19 hospitalizations among immunocompromised individuals; however, the findings are limited by a lack of sufficient events to produce conclusive results.

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来源期刊
Infectious Diseases and Therapy
Infectious Diseases and Therapy Medicine-Microbiology (medical)
CiteScore
8.60
自引率
1.90%
发文量
136
审稿时长
6 weeks
期刊介绍: Infectious Diseases and Therapy is an international, open access, peer-reviewed, rapid publication journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of infectious disease therapies and interventions, including vaccines and devices. Studies relating to diagnostic products and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to, bacterial and fungal infections, viral infections (including HIV/AIDS and hepatitis), parasitological diseases, tuberculosis and other mycobacterial diseases, vaccinations and other interventions, and drug-resistance, chronic infections, epidemiology and tropical, emergent, pediatric, dermal and sexually-transmitted diseases.
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