Hayek Samah, Levy Joseph, Shaham Galit, Dagan Noa, Serby Danielle, Duskin-Bitan Hadar, Yarden Adva, Ferreira Cátia, Livnat Idit, Dube Sabada, Taylor Sylvia, Venkatesan Sudhir, Balicer Ran D, Netzer Doron, Peretz Alon
Department of Epidemiology and Preventive Medicine, School of Public Health, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Innovation Division, Clalit Research Institute, Clalit Health Services, Tel Aviv, Israel.
Infect Dis Ther. 2024 Jun;13(6):1379-1389. doi: 10.1007/s40121-024-00981-8. Epub 2024 May 10.
AZD7442 is a combination of two neutralizing antibodies (tixagevimab/cilgavimab) with demonstrated efficacy in reducing the risk of symptomatic coronavirus disease 2019 (COVID-19) among individuals at high risk of severe COVID-19 ≤ 6 months after administration. On February 15, 2022, the Israeli Ministry of Health (IMoH) authorized the administration of 300 mg AZD7442 as pre-exposure prophylaxis (PrEP) against severe acute respiratory syndrome coronavirus 2 infection among immunocompromised individuals aged ≥ 12 years. This study describes the real-world uptake of AZD7442 in Israel.
This descriptive, observational study analyzed data from Israel's largest health maintenance organization, Clalit Health Services (CHS). Individuals were assessed for AZD7442 eligibility between February 13 and December 11, 2022, and were included if they were aged ≥ 12 years, had ≥ 1 year of continuous CHS membership, had ≥ 1 moderate or severe immunocompromising condition, and were eligible for AZD7442 per IMoH recommendations during this time frame.
Overall, 19,161 AZD7442-eligible individuals with immunocompromising conditions were identified during the study period; 2829 (14.8%) received AZD7442. A higher proportion of individuals receiving AZD7442 were older (aged ≥ 65 years), male, not current smokers and residents in large cities; required more physician visits (> 50 visits); and had ≥ 1 COVID-19 hospitalization over 12 months, while uptake was lowest among ultra-orthodox Jewish individuals. AZD7442 uptake was also higher among individuals with multiple comorbidities (Charlson Comorbidity Index ≥ 5), including hypertension, diabetes and chronic kidney disease. In specific immunocompromised types, AZD7442 uptake was highest among individuals with lung transplantation (41%), primary immunodeficiency (32%), bone marrow transplantation (29%) and multiple myeloma (25%) or those receiving anti-CD20 therapy (26%) and was lowest in individuals with lymphoma (8%).
These results show AZD7442 uptake among the eligible population of Israel in 2022 was relatively low, at 14.8%. Uptake was generally higher among immunocompromised individuals who may be perceived to be frail or at highest risk of COVID-19 infection and complications, although at 25-41%, further improvements in uptake would be more impactful. These results also indicate there is opportunity to expand AZD7442 uptake across immunocompromised groups and ensure more equitable uptake among some other sociodemographic groups. Overall, this study will help inform and reassess future implementation strategies for vulnerable populations.
AZD7442是两种中和抗体(替沙格韦单抗/西加韦单抗)的组合,已证明其在给药后≤6个月内可降低2019冠状病毒病(COVID-19)重症高危个体出现症状性COVID-19的风险。2022年2月15日,以色列卫生部(IMoH)批准对年龄≥12岁的免疫功能低下个体使用300mg AZD7442进行严重急性呼吸综合征冠状病毒2感染的暴露前预防(PrEP)。本研究描述了AZD7442在以色列的实际使用情况。
这项描述性观察性研究分析了以色列最大的健康维护组织——克拉利特医疗服务公司(CHS)的数据。在2022年2月13日至12月11日期间对个体进行AZD7442适用性评估,纳入标准为年龄≥12岁、连续加入CHS≥1年、有≥1种中度或重度免疫功能低下状况且在此时间段内根据IMoH建议符合使用AZD7442的条件。
总体而言,在研究期间共识别出19161名符合AZD7442使用条件的免疫功能低下个体;其中2829人(14.8%)接受了AZD7442。接受AZD7442的个体中,年龄较大(≥65岁)、男性、非当前吸烟者以及大城市居民的比例更高;需要更多的门诊就诊次数(>50次);在12个月内有≥1次COVID-19住院经历,而极端正统犹太人群体的使用率最低。在患有多种合并症(查尔森合并症指数≥5)的个体中,包括高血压、糖尿病和慢性肾脏病患者,AZD7442的使用率也更高。在特定的免疫功能低下类型中,肺移植个体(41%)、原发性免疫缺陷个体(32%)、骨髓移植个体(29%)和多发性骨髓瘤患者(25%)或接受抗CD20治疗的个体(26%)中AZD7442的使用率最高,而淋巴瘤患者中使用率最低(8%)。
这些结果表明,2022年以色列符合条件人群中AZD7442的使用率相对较低,为14.8%。在可能被认为身体虚弱或COVID-19感染及并发症风险最高的免疫功能低下个体中,使用率总体较高,尽管为25%-41%,但进一步提高使用率将更有意义。这些结果还表明,有机会在免疫功能低下群体中扩大AZD7442的使用,并确保在其他一些社会人口学群体中更公平地使用。总体而言,本研究将有助于为弱势群体的未来实施策略提供信息并进行重新评估。