Sir HN Reliance Foundation Hospital and Research Centre, Mumbai, Maharashtra, India.
PLoS One. 2022 Oct 27;17(10):e0276759. doi: 10.1371/journal.pone.0276759. eCollection 2022.
India started its vaccination programme for Coronavirus-19 infection (COVID-19) on 16 January 2021 with CovishieldTM (Oxford/Astra Zeneca vaccine manufactured by Serum Institute of India) and Covaxin ® (Bharat Biotech, India). We designed the present study to study the effectiveness of vaccines for COVID-19 in prevention of breakthrough infections and severe symptomatic cases among health care workers in a real-life scenario in Mumbai, India. Furthermore, we also wanted to study the factors associated with this effectiveness.
This is cohort analysis of secondary data of 2762 individuals working in a tertiary health care setting in Mumbai, India (16 January 2021 to 16 October 2021). Vaccination records of all groups of health care staff (including the date of vaccination, type of vaccine taken, and date of positivity for COVID-19) were maintained at the hospital. The staff were tested for COVID-19 at least once a week and when symptomatic. The observation time for everyone was divided into unvaccinated, partially vaccinated (14 days after the first dose); and fully vaccinated (14 days after the second dose). If the individual was found to be positive, the day of positivity was considered the 'day of the event' for that individual. We combined unvaccinated/partially vaccinated into one group and completely vaccinated in the other group. We estimated hazard ratios (HR) and their 95% confidence intervals. The vaccine effectiveness (VE) was assessed as (1-HR)*100.
The mean age (SD) of the study participants was 32.3 (8.3) years; majority of these individuals had taken Covishield TM (99.0%) and only 0.9% (n = 27) had taken Covaxin ®. The incidence rate in the overall population was 0.067/100 person-days (PD). The incidence rate was significantly higher in the unvaccinated/partially vaccinated group compared with the fully vaccinated group (0.0989 / 100 PD vs 0.0403/100 PD; p < 0.001). The adjusted HR (aHR) in the fully vaccinated group compared with the unvaccinated/partially vaccinated group in the complete cohort was 0.30 (95% CI: 0.23, 0.39). Thus, the vaccine effectiveness (VE) for full vaccination was 70% (95% CI: 61%, 77%). It remained the same in the Covishield TM only cohort. The VE in completely vaccinated and with a history of previous infection was 88% (95% CI: 80%, 93%). Only 11 health care workers required hospitalization over the entire observation period; the incidence rate in our cohort was 0.0016 / 100 PD. None of the HCWs reported any severe adverse events after vaccination.
In this real-world scenario, we did find that complete vaccination reduced the rate of infection, particularly severe infection in health care personnel even during the severe delta wave in the country. Even among those infected, the hospitalisation rates were very low, and none died. We did not record any major side effects of vaccination in these personnel. Previous infection with COVID-19 and complete vaccination had a significantly higher effectiveness in prevention of infection.
印度于 2021 年 1 月 16 日开始针对冠状病毒 19 感染(COVID-19)开展疫苗接种计划,使用的疫苗为 CovishieldTM(印度血清研究所生产的牛津/阿斯利康疫苗)和 Covaxin ®(印度 Bharat Biotech 公司)。我们设计本研究旨在探讨 COVID-19 疫苗在预防印度孟买医疗保健工作者突破性感染和严重症状病例方面的有效性。此外,我们还研究了与这种有效性相关的因素。
这是对在印度孟买的一家三级医疗机构中工作的 2762 名个体的二次数据分析(2021 年 1 月 16 日至 2021 年 10 月 16 日)。所有医疗保健人员(包括接种日期、接种的疫苗类型和 COVID-19 阳性日期)的疫苗接种记录均在医院保存。工作人员每周至少接受一次 COVID-19 检测,出现症状时也进行检测。每个人的观察时间分为未接种、部分接种(第一剂后 14 天)和完全接种(第二剂后 14 天)。如果个体被发现呈阳性,则将阳性日期视为该个体的“事件日期”。我们将未接种/部分接种的个体合并为一组,完全接种的个体合并为另一组。我们估计了危险比(HR)及其 95%置信区间。疫苗有效性(VE)评估为(1-HR)*100。
研究参与者的平均年龄(SD)为 32.3(8.3)岁;这些个体大多接种了 Covishield TM(99.0%),只有 0.9%(n=27)接种了 Covaxin ®。总体人群的发病率为 0.067/100 人天(PD)。未接种/部分接种组的发病率明显高于完全接种组(0.0989/100 PD 比 0.0403/100 PD;p<0.001)。完全接种组与未接种/部分接种组在整个队列中的调整后 HR(aHR)为 0.30(95%CI:0.23,0.39)。因此,完全接种的疫苗有效性(VE)为 70%(95%CI:61%,77%)。在仅使用 Covishield TM 的队列中也是如此。完全接种且有既往感染史的 VE 为 88%(95%CI:80%,93%)。整个观察期间只有 11 名医护人员需要住院治疗,我们的队列发病率为 0.0016/100 PD。没有医护人员报告接种疫苗后出现任何严重不良事件。
在这种真实情况下,我们确实发现完全接种疫苗可降低感染率,尤其是在该国严重的德尔塔波期间,降低医疗保健人员的严重感染率。即使在感染的个体中,住院率也非常低,没有死亡。我们在这些人员中没有记录到任何疫苗接种的主要副作用。COVID-19 的既往感染和完全接种在预防感染方面具有更高的有效性。