CDC COVID-19 Response Team, Atlanta, Georgia.
Vanderbilt Institute for Clinical and Translational Research, Department of Emergency Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
JAMA. 2021 Nov 23;326(20):2043-2054. doi: 10.1001/jama.2021.19499.
A comprehensive understanding of the benefits of COVID-19 vaccination requires consideration of disease attenuation, determined as whether people who develop COVID-19 despite vaccination have lower disease severity than unvaccinated people.
To evaluate the association between vaccination with mRNA COVID-19 vaccines-mRNA-1273 (Moderna) and BNT162b2 (Pfizer-BioNTech)-and COVID-19 hospitalization, and, among patients hospitalized with COVID-19, the association with progression to critical disease.
DESIGN, SETTING, AND PARTICIPANTS: A US 21-site case-control analysis of 4513 adults hospitalized between March 11 and August 15, 2021, with 28-day outcome data on death and mechanical ventilation available for patients enrolled through July 14, 2021. Date of final follow-up was August 8, 2021.
COVID-19 vaccination.
Associations were evaluated between prior vaccination and (1) hospitalization for COVID-19, in which case patients were those hospitalized for COVID-19 and control patients were those hospitalized for an alternative diagnosis; and (2) disease progression among patients hospitalized for COVID-19, in which cases and controls were COVID-19 patients with and without progression to death or mechanical ventilation, respectively. Associations were measured with multivariable logistic regression.
Among 4513 patients (median age, 59 years [IQR, 45-69]; 2202 [48.8%] women; 23.0% non-Hispanic Black individuals, 15.9% Hispanic individuals, and 20.1% with an immunocompromising condition), 1983 were case patients with COVID-19 and 2530 were controls without COVID-19. Unvaccinated patients accounted for 84.2% (1669/1983) of COVID-19 hospitalizations. Hospitalization for COVID-19 was significantly associated with decreased likelihood of vaccination (cases, 15.8%; controls, 54.8%; adjusted OR, 0.15; 95% CI, 0.13-0.18), including for sequenced SARS-CoV-2 Alpha (8.7% vs 51.7%; aOR, 0.10; 95% CI, 0.06-0.16) and Delta variants (21.9% vs 61.8%; aOR, 0.14; 95% CI, 0.10-0.21). This association was stronger for immunocompetent patients (11.2% vs 53.5%; aOR, 0.10; 95% CI, 0.09-0.13) than immunocompromised patients (40.1% vs 58.8%; aOR, 0.49; 95% CI, 0.35-0.69) (P < .001) and weaker at more than 120 days since vaccination with BNT162b2 (5.8% vs 11.5%; aOR, 0.36; 95% CI, 0.27-0.49) than with mRNA-1273 (1.9% vs 8.3%; aOR, 0.15; 95% CI, 0.09-0.23) (P < .001). Among 1197 patients hospitalized with COVID-19, death or invasive mechanical ventilation by day 28 was associated with decreased likelihood of vaccination (12.0% vs 24.7%; aOR, 0.33; 95% CI, 0.19-0.58).
Vaccination with an mRNA COVID-19 vaccine was significantly less likely among patients with COVID-19 hospitalization and disease progression to death or mechanical ventilation. These findings are consistent with risk reduction among vaccine breakthrough infections compared with absence of vaccination.
全面了解 COVID-19 疫苗接种的益处需要考虑疾病衰减,即尽管接种了 COVID-19 疫苗但病情严重程度低于未接种疫苗的人。
评估 mRNA COVID-19 疫苗-mRNA-1273(Moderna)和 BNT162b2(辉瑞-BioNTech)与 COVID-19 住院之间的关联,以及在 COVID-19 住院患者中,与进展为重症疾病的关联。
设计、地点和参与者:这是一项在美国 21 个地点进行的病例对照分析,纳入了 2021 年 3 月 11 日至 8 月 15 日期间住院的 4513 名成年人,截至 2021 年 7 月 14 日,患者可获得 28 天的死亡和机械通气结局数据。最终随访日期为 2021 年 8 月 8 日。
COVID-19 疫苗接种。
评估了先前接种疫苗与(1)COVID-19 住院之间的关联,在这种情况下,病例患者是因 COVID-19 住院的患者,对照组患者是因其他诊断而住院的患者;以及(2)COVID-19 住院患者疾病进展之间的关联,其中病例和对照组分别为 COVID-19 患者进展为死亡或机械通气的患者。通过多变量逻辑回归来衡量关联。
在 4513 名患者中(中位年龄,59 岁[IQR,45-69];2202 名[48.8%]女性;23.0%非西班牙裔黑人个体,15.9%西班牙裔个体,20.1%有免疫功能受损情况),1983 名是 COVID-19 病例患者,2530 名是没有 COVID-19 的对照组患者。未接种疫苗的患者占 COVID-19 住院患者的 84.2%(1669/1983)。COVID-19 住院与疫苗接种可能性降低显著相关(病例患者,15.8%;对照组患者,54.8%;调整后的 OR,0.15;95%CI,0.13-0.18),包括对 SARS-CoV-2 Alpha(8.7% vs 51.7%;aOR,0.10;95%CI,0.06-0.16)和 Delta 变体(21.9% vs 61.8%;aOR,0.14;95%CI,0.10-0.21)。这种关联在免疫功能正常的患者中更强(11.2% vs 53.5%;aOR,0.10;95%CI,0.09-0.13),而在免疫功能受损的患者中较弱(40.1% vs 58.8%;aOR,0.49;95%CI,0.35-0.69)(P<.001),而且在 BNT162b2 接种超过 120 天后较弱(5.8% vs 11.5%;aOR,0.36;95%CI,0.27-0.49),而不是 mRNA-1273(1.9% vs 8.3%;aOR,0.15;95%CI,0.09-0.23)(P<.001)。在 1197 名因 COVID-19 住院的患者中,28 天内死亡或有创机械通气与疫苗接种可能性降低相关(12.0% vs 24.7%;aOR,0.33;95%CI,0.19-0.58)。
COVID-19 住院和疾病进展为死亡或机械通气的患者中,接种 mRNA COVID-19 疫苗的可能性显著降低。这些发现与疫苗突破性感染的风险降低一致,而不是未接种疫苗。