Department of Research & Evaluation, Kaiser Permanente Southern California, Pasadena.
Department of Health Systems Science, Kaiser Permanente Bernard J. Tyson School of Medicine, Pasadena, California.
JAMA Intern Med. 2024 Aug 1;184(8):932-940. doi: 10.1001/jamainternmed.2024.1640.
Data describing the early additional protection afforded by the recently recommended BNT162b2 XBB vaccine (Pfizer-BioNTech; 2023-2024 formulation) are limited.
To estimate the association between receipt of the BNT162b2 XBB vaccine and medically attended COVID-19 outcomes among US adults 18 years and older.
DESIGN, SETTING, AND PARTICIPANTS: This test-negative case-control study was performed to estimate the effectiveness of the BNT162b2 XBB vaccine against COVID-19-associated hospitalization and emergency department (ED) or urgent care (UC) encounters among adults in the Kaiser Permanente Southern California health system between October 10, 2023, and December 10, 2023. Cases were those presenting with an acute respiratory illness and who had a positive SARS-CoV-2 polymerase chain reaction test; controls had an acute respiratory illness but tested negative for SARS-CoV-2.
The primary exposure was receipt of the BNT162b2 XBB vaccine compared with not receiving an XBB vaccine of any kind, regardless of prior COVID-19 vaccination or SARS-CoV-2 infection history. Receipt of prior (non-XBB) versions of COVID-19 vaccines was also compared with being unvaccinated to estimate remaining protection from older vaccines.
Analyses for cases and controls were conducted separately for COVID-19 hospital admissions and ED/UC encounters. Adjusted odds ratios and 95% CIs were estimated from multivariable logistic regression models that were adjusted for patient demographic and clinical characteristics. Estimation of vaccine effectiveness was calculated as 1 - odds ratio × 100%.
Among 2854 cases and 15 345 controls (median [IQR] age, 56 [37-72] years; 10 658 [58.6%] female), adjusted estimation of effectiveness of the BNT162b2 XBB vaccine received a median of 34 days prior vs not having received an XBB vaccine of any kind was 62% (95% CI, 32%-79%) against COVID-19 hospitalization and 58% (95% CI, 48%-67%) for ED/UC visits. Compared with being unvaccinated, those who had received only older versions of COVID-19 vaccines did not show statistically significant reduced risk of COVID-19 outcomes, including hospital admission.
Findings of this case-control study reaffirm current recommendations for broad age-based use of annually updated COVID-19 vaccines given that (1) the BNT162b2 XBB vaccine provided statistically significant additional protection against a range of COVID-19 outcomes and (2) older versions of COVID-19 vaccines offered little, if any, long-term protection, including against hospital admission, regardless of the number or type of prior doses received.
关于最近推荐的 BNT162b2 XBB 疫苗(辉瑞-生物科技;2023-2024 配方)提供的早期额外保护的数据有限。
估计美国 18 岁及以上成年人接种 BNT162b2 XBB 疫苗与有医疗记录的 COVID-19 结局之间的关联。
设计、设置和参与者:这项阴性病例对照研究旨在估计 BNT162b2 XBB 疫苗对 2023 年 10 月 10 日至 2023 年 12 月 10 日期间 Kaiser Permanente 南加州卫生系统中成年人 COVID-19 相关住院和急诊部(ED)或紧急护理(UC)就诊的有效性。病例是指出现急性呼吸道疾病且 SARS-CoV-2 聚合酶链反应检测呈阳性的患者;对照组则是出现急性呼吸道疾病但 SARS-CoV-2 检测呈阴性的患者。
主要暴露是接种 BNT162b2 XBB 疫苗,而不是接种任何类型的 XBB 疫苗,无论先前是否接种过 COVID-19 疫苗或 SARS-CoV-2 感染史如何。与未接种疫苗相比,还比较了先前(非 XBB)版本的 COVID-19 疫苗接种情况,以估计来自旧疫苗的剩余保护作用。
对病例和对照组分别进行 COVID-19 住院和 ED/UC 就诊的分析。多变量逻辑回归模型调整了患者的人口统计学和临床特征,估计了调整后的优势比和 95%置信区间。疫苗有效性的估计值计算为 1-优势比×100%。
在 2854 例病例和 15345 例对照组(中位数[IQR]年龄,56[37-72]岁;10658[58.6%]女性)中,与未接种任何 XBB 疫苗相比,在接种 BNT162b2 XBB 疫苗中位数 34 天前,疫苗对 COVID-19 住院的有效性估计为 62%(95%CI,32%-79%),对 ED/UC 就诊的有效性估计为 58%(95%CI,48%-67%)。与未接种疫苗相比,仅接种过旧版 COVID-19 疫苗的人群 COVID-19 结局的风险并未显著降低,包括住院。
这项病例对照研究的结果再次证实了目前基于年龄广泛使用每年更新的 COVID-19 疫苗的建议,原因是(1)BNT162b2 XBB 疫苗对一系列 COVID-19 结局提供了具有统计学意义的额外保护,(2)旧版 COVID-19 疫苗提供的长期保护作用很小,如果有的话,包括住院治疗,无论之前接种过多少剂或哪种类型的疫苗。