Gogoi Gayatri, Gogoi Gourangie, Mahanta Bhupendra N, Borkakoty Biswajyoti, Borpujari Porikhit, Ahmed Tanzil S, Neog Rahul, Roy Sunia, Medhi Mithu
Department of Pathology, Assam Medical College and Hospital, Dibrugarh, Assam, India.
Department of Community Medicine, Assam Medical College and Hospital, Dibrugarh, Assam, India.
J Family Med Prim Care. 2024 Aug;13(8):3362-3367. doi: 10.4103/jfmpc.jfmpc_169_24. Epub 2024 Jul 26.
COVID-19 an infectious disease caused by the SARS-CoV-2 virus, started in late 2019 and became a pandemic within a short period. To respond to the pandemic vaccines like Covishield, Covaxin, Sputnik V, Covovax, etc., were developed rapidly. However, there were raising concerns about the development of immunity as well as adverse events following vaccination.
To compare anti-SARS-CoV-2 IgG antibody titres at different time-points post-vaccination between baseline seropositive and seronegative groups and to assess the adverse events following the 1 dose of Covishield vaccine among adult beneficiaries attending vaccination centre in a tertiary care hospital of Upper Assam.
Prospective Cohort study was conducted from July 2021 to June 2022 among adult beneficiaries receiving the Covishield vaccine. The oral questionnaire was used incorporating socio-demographic variables, and clinical profiles including co-morbidities and adverse events following vaccination. Data analysis was done by Microsoft Excel and SPSS.
Out of a total of 146 study participants, IgG estimation showed 61% as seropositive and the rest as seronegative. A total of 55.40% had minor adverse events, majority of them were females (53.08%) and 88.80% belonged to 18-59 years compared to 11.11% above 60 years of age. The majority (71.60%) did not have any co-morbidities and the major AEFI was NIL among the study participants. The study group had 61% seropositive previously infected.
Covishield vaccination induces an immune response and 90% seroconversion is achieved after 1 dose (booster dose). Antibody titres of the seropositive group by natural infection of SARS-CoV-2 were higher than seronegative cohort seroconverted by vaccination. The AEFI observed were minor and can be commented as safer.
2019年末开始出现由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)病毒引起的传染性疾病COVID-19,并在短时间内成为大流行病。为应对该大流行病,如Covishield、Covaxin、Sputnik V、Covovax等疫苗迅速研发出来。然而,人们对疫苗接种后的免疫发展以及不良事件越来越担忧。
比较基线血清学阳性和血清学阴性组在接种疫苗后不同时间点的抗SARS-CoV-2 IgG抗体滴度,并评估上阿萨姆邦一家三级护理医院接种中心成年受益者接种1剂Covishield疫苗后的不良事件。
2021年7月至2022年6月对接受Covishield疫苗的成年受益者进行前瞻性队列研究。采用口服问卷收集社会人口统计学变量以及包括合并症和疫苗接种后不良事件在内的临床资料。数据分析通过Microsoft Excel和SPSS进行。
在总共146名研究参与者中,IgG检测显示61%为血清学阳性,其余为血清学阴性。共有55.40%的人出现轻微不良事件,其中大多数为女性(53.08%),88.80%属于18 - 59岁,60岁以上者占11.11%。大多数(71.60%)没有任何合并症,研究参与者中主要的疑似预防接种异常反应为无。研究组中61%的血清学阳性者曾被感染。
接种Covishield疫苗可诱导免疫反应,1剂(加强剂量)后血清转化率达90%。通过SARS-CoV-2自然感染的血清学阳性组的抗体滴度高于通过疫苗接种血清转化的血清学阴性队列。观察到的疑似预防接种异常反应为轻微,可认为该疫苗更安全。