COVID-19疫苗增强剂在系统性自身免疫性疾病和风湿病患者中的吸收和有效性

Yonah C Ziemba,Eric P Elkin,Elham Kazemian,Brigid M Wilson,Hinnah Siddiqui,Cheryl B Schleicher,Crystal A Hsiao,David A Zidar,Lawrence H Kushi,Jane C Figueiredo,Jacek Skarbinski,James M Crawford
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摘要

目的评估COVID-19增强疫苗接种和疫苗有效性(VE)在降低系统性自身免疫性和风湿病(SARDs)患者COVID-19住院率方面的作用。方法回顾性分析美国4个卫生系统中接受抗风湿药物治疗的成年SARDs患者。暴露为:1)在2022年1月1日之前额外接种了一剂单价COVID-19疫苗,随访至2022年8月31日;(2)在2022年9月1日至2023年8月31日期间接种了二价COVID-19疫苗。结果截至2022年1月1日,在201,165例SARDs患者中,126,756例(63%)接受了一种单价增强剂。在94,842人-年的随访期间,接受单价增强剂的患者的COVID-19住院率为每1000人-年15.6人,未接受单价增强剂的患者为每1000人-年20.1人,调整后的VE为38%(95%置信区间[CI] 31% - 44%),需要接种疫苗的人数为267人(CI 230-325)。在二价疫苗研究期间随访233,622人年的246,991例SARDs患者中,接种二价疫苗的87,906例(36%)患者的COVID-19住院率为每1000人年7.9例,而未接种二价疫苗的患者为每1000人年10.2例。二价疫苗的调整VE为32% (CI 24% - 39%),需要接种617个(CI 500-838)。结论COVID-19加强疫苗接种对自身免疫性疾病患者重症COVID-19有显著保护作用。因此,在这一免疫功能低下的高危人群中,应优先增加疫苗接种。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
COVID-19 vaccine booster uptake and effectiveness among persons with systemic autoimmune and rheumatic diseases.
OBJECTIVE To assess COVID-19 booster uptake and vaccine effectiveness (VE) in reducing COVID-19 hospitalization in persons with systemic autoimmune and rheumatic diseases (SARDs). METHODS Adult patients with SARDs receiving disease modifying anti-rheumatic drugs at four health systems in the United States were identified retrospectively. Exposures were: 1) receipt of an additional dose of monovalent COVID-19 vaccine prior to January 1, 2022, with follow-up to August 31, 2022; and (2) receipt of bivalent COVID-19 vaccine between September 1, 2022 to August 31, 2023. RESULTS Among 201,165 patients with SARDs, 126,756 (63%) had received one monovalent booster as of January 1, 2022. During 94,842 person-years of follow-up, the COVID-19 hospitalization rate was 15.6 per 1000 person-years among those who had received a monovalent booster versus 20.1 per 1000 person-years among those who had not, with an adjusted VE of 38% (95% confidence interval [CI] 31% - 44%) and a number needed to vaccinate of 267 (CI 230-325). Among 246,991 patients with SARDs with 233,622 person-years of follow-up in the bivalent study period, the COVID-19 hospitalization rate was 7.9 per 1000 person-years for the 87,906 (36%) patients who received the bivalent vaccine, versus 10.2 per 1000 person-years for the patients who did not. The adjusted VE of the bivalent vaccine was 32% (CI 24% - 39%) with a number needed to vaccinate of 617 (CI 500-838). CONCLUSION COVID-19 booster vaccinations provided significant protection against severe COVID-19 in persons with autoimmune disease. Thus, increasing vaccine uptake should be prioritized in this high-risk immunocompromised population.
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