Institute for Clinical Research, National Institutes of Health, Ministry of Health, Malaysia.
Institute for Clinical Research, National Institutes of Health, Ministry of Health, Malaysia.
Vaccine. 2022 Sep 16;40(39):5675-5682. doi: 10.1016/j.vaccine.2022.08.032. Epub 2022 Aug 24.
There is a notable lack of vaccine effectiveness studies using test-negative case-controlled approach in low- and middle-income countries which have different logistic, demographic and socio-economic conditions from high-income countries. We aimed to estimate the effectiveness of BNT162b2 vaccine against COVID-19 infection over time, intensive care unit admission, severe or critical disease and death due to COVID-19. This study was conducted in the resident population of Labuan aged ≥18 years who had been tested for SARS-CoV-2 by Reverse-Transcriptase Polymerase Chain Reaction between 1 March 2021 and 31 October 2021. We used a test-negative case-control design where 2644 pairs of cases and controls were matched by age, sex, testing date, nationality and testing reason. Analysis was stratified by age group to estimate age effect (<60 years and ≥60 years). Of 22217 individuals tested by Reverse-Transcriptase Polymerase Chain Reaction, 5100 were positive for SARS-CoV-2 and aged 18 years and above. Overall vaccine effectiveness ≥ 14 days after the second dose was 65.2% (95% CI: 59.8-69.9%) against COVID-19 infection, 92.5% (95% CI: 72.3-98.8%) against intensive care unit admission, and 96.5% (95% CI: 82.3-99.8%) against COVID-19 deaths. Among infected individuals, vaccine effectiveness was 79.2% (95% CI: 42.3-94.1%) in preventing severe or critical disease due to COVID-19. Vaccine effectiveness for ≥60 years was 72.3% (95% CI: 53.4-83.9%) in fully vaccinated individuals, higher than 64.8% (95% CI: 49.3-59.1%) for those <60 years. Two doses of BNT162b2 were highly effective against COVID-19 infection, severe or critical disease, intensive care unit admission and death due to COVID-19. This study addresses a gap in literature on BNT162b2 vaccine effectiveness in low- and middle-income populations and demonstrates the feasibility of such a study design in a resource limited setting while supporting evidence of waning immunity.
在逻辑、人口统计和社会经济条件与高收入国家不同的低收入和中等收入国家中,使用病例对照测试阴性的方法进行疫苗有效性研究明显不足。我们旨在随着时间的推移,估计 BNT162b2 疫苗对 COVID-19 感染、入住重症监护病房、因 COVID-19 导致的严重或危急疾病和死亡的有效性。这项研究是在年龄在 18 岁及以上的纳闽居民中进行的,他们在 2021 年 3 月 1 日至 2021 年 10 月 31 日期间通过逆转录聚合酶链反应检测 SARS-CoV-2。我们使用了病例对照测试阴性的设计,其中 2644 对病例和对照按年龄、性别、检测日期、国籍和检测原因进行匹配。按年龄组分层分析,以估计年龄效应(<60 岁和≥60 岁)。在接受逆转录聚合酶链反应检测的 22217 个人中,有 5100 人 SARS-CoV-2 检测呈阳性,年龄在 18 岁及以上。第二剂后≥14 天的总体疫苗有效性为 65.2%(95%CI:59.8-69.9%),预防 COVID-19 感染,92.5%(95%CI:72.3-98.8%)预防重症监护病房入院,96.5%(95%CI:82.3-99.8%)预防 COVID-19 死亡。在感染人群中,疫苗对 COVID-19 引起的严重或危急疾病的预防有效性为 79.2%(95%CI:42.3-94.1%)。完全接种疫苗的≥60 岁人群的疫苗有效性为 72.3%(95%CI:53.4-83.9%),而<60 岁人群的疫苗有效性为 64.8%(95%CI:49.3-59.1%)。两剂 BNT162b2 对 COVID-19 感染、严重或危急疾病、重症监护病房入院和 COVID-19 死亡有高度有效性。这项研究解决了关于 BNT162b2 疫苗在低收入和中等收入人群中的有效性的文献中的一个空白,并证明了在资源有限的环境中进行这种研究设计的可行性,同时支持免疫减弱的证据。