Department of Biomedical Sciences, Seoul National University Graduate School, Seoul, Republic of Korea.
Department of Biomedical Informatics, Korea University College of Medicine, Seoul, Republic of Korea.
J Infect Public Health. 2024 Apr;17(4):650-656. doi: 10.1016/j.jiph.2024.02.005. Epub 2024 Feb 10.
Although one of the characteristics of COVID-19 is accompanied by acute pneumonia immediately after infection, large-scale cohort studies focused on this issue are lacking. In addition, there is interest in how COVID-19 vaccinations reduce the incidence of acute pneumonia for people infected with different strains of SARS-CoV-2. Thus, we assess the short-term incidence of pneumonia after COVID-19 with the vaccination and SARS-CoV-2 variants.
As data for 2136,751 COVID-19 patients between January 01, 2020 and February 28, 2022 was collected, they were observed for one month from the day of infection. Patients in retrospective cohort study were classified according to doses of the received vaccine and the epidemic phase when SARS-CoV-2 variants prevailed. Multivariable logistic regression analysis calculated adjusted odds ratios (aOR) and 95% confidence intervals (CIs) for the pneumonia risk.
In B.1.1.7-B.1.351, B.1.617.2, and B.1.617.2 variants, the aORs (95% CIs; p-value) for incidence of pneumonia were 0.93 (0.89-0.98; <0.001), 0.74 (0.70-0.78; <0.001), and 0.04 (0.038-0.043; <0.001), respectively, compared to the original strain. More than 80% of patients have received the second and more doses of the vaccine (average age=44.67 years). The aORs (95% CIs; p-value) for pneumonia were 0.61 (0.58-0.64; <0.001), 0.39 (0.38-0.40; <0.001), and 0.18 (0.166-0.184; <0.001) in patients who received the first (N = 68,216), second (N = 898,838), and ≥ third doses (N = 836,173), respectively, compared to unvaccinated patients. According to the received vaccine (second dose of mRNA or viral vector), those who received BNT162b2 and mRNA-1273 (N = 787,980) had lower risk of pneumonia, compared to that in those who received h ChAdOx1 nCov-19 and AD26. COV2-S (N = 89,024).
Our findings suggest that the second and ≥ third doses (61% and 82% of risk aversion effect increased, respectively) of the COVID-19 vaccine can prevent the COVID-19-related pneumonia, regardless of the variants.
虽然 COVID-19 的一个特征是感染后立即伴有急性肺炎,但缺乏针对这一问题的大规模队列研究。此外,人们还关注 COVID-19 疫苗如何降低不同 SARS-CoV-2 株感染人群急性肺炎的发病率。因此,我们评估了 COVID-19 疫苗接种和 SARS-CoV-2 变异对肺炎短期发病率的影响。
收集了 2020 年 1 月 1 日至 2022 年 2 月 28 日期间 2136751 例 COVID-19 患者的数据,从感染之日起观察一个月。回顾性队列研究的患者根据接种疫苗的剂量和 SARS-CoV-2 变异流行时所处的流行阶段进行分类。多变量逻辑回归分析计算了肺炎风险的调整优势比(aOR)和 95%置信区间(CI)。
在 B.1.1.7-B.1.351、B.1.617.2 和 B.1.617.2 变异株中,与原始株相比,肺炎发病率的 aOR(95%CI;p 值)分别为 0.93(0.89-0.98;<0.001)、0.74(0.70-0.78;<0.001)和 0.04(0.038-0.043;<0.001)。超过 80%的患者已接种第二剂及以上疫苗(平均年龄=44.67 岁)。与未接种疫苗的患者相比,接受第一剂(N=68216)、第二剂(N=898838)和≥第三剂(N=836173)的患者的 aOR(95%CI;p 值)分别为 0.61(0.58-0.64;<0.001)、0.39(0.38-0.40;<0.001)和 0.18(0.166-0.184;<0.001)。根据接种疫苗(mRNA 或病毒载体的第二剂),与接种 h ChAdOx1 nCov-19 和 AD26.CO2-S(N=89024)的患者相比,接种 BNT162b2 和 mRNA-1273(N=787980)的患者发生肺炎的风险较低。
我们的研究结果表明,COVID-19 疫苗的第二剂和≥第三剂(风险规避效应分别增加 61%和 82%)可预防 COVID-19 相关肺炎,无论变异株如何。