Heleena Rayamajhi, Sammodavardhana Kaudinnyayana, A. Khadka, Sudha Sen Malla
{"title":"卫生保健专业人员第一次和第二次接种SARS-CoV 2 (covisshield)疫苗后自我报告的不良反应","authors":"Heleena Rayamajhi, Sammodavardhana Kaudinnyayana, A. Khadka, Sudha Sen Malla","doi":"10.3126/mjsbh.v21i1.40663","DOIUrl":null,"url":null,"abstract":"Introduction: The ChAdOx 1 n Cov-19 vaccine, called Covishield, was rolled out in Nepal targeting health care professionals. The study was conducted to assess the pattern of self-reported adverse events following immunization and to compare AEFI on the basis of previous COVID status.\nMethods: A cross sectional study of four months duration was conducted in Shree Birendra Hospital, a tertiary care hospital, in Kathmandu, Nepal. AEFI associated with first and second dose of Covishield were assessed for a period of seven days from the day of vaccination in health care professionals and comparison was done based on COVID status.\nResults: A total of 100 vaccine recipients were included in the study, out of which 83% showed AEFI. The most commonly reported AEFI after first dose were headache (56%), injection site tenderness (42%), myalgia (29%), fatigue (24%), dizziness (20%), pyrexia (19%), malaise (17%), nausea (10%), chills (8%), vomiting (2%) and arthralgia (1%) while among the AEFI after second dose were injection site tenderness (36%), headache (15%), myalgia (12%), fatigue (11%), nausea (9%), malaise (8%), pyrexia (8%), chills (5%), rashes (3%), drowsiness (3%), arthralgia (1%) and dizziness (1%). Previously infected participants were found to be prone to develop systemic adverse effects. The most of the adverse effects were subsided within four days and commonly used medication was paracetamol to relieve the symptoms. \nConclusions: AEFI following the first and second dose of vaccine were mild. Systemic adverse effects were more frequent in those with the history of COVID-19 infection.","PeriodicalId":33963,"journal":{"name":"Medical Journal of Shree Birendra Hospital","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-07-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Self-reported Adverse Effects in Health Care Professionals Following First and Second Dose Vaccination Against SARS-CoV 2 (Covishield)\",\"authors\":\"Heleena Rayamajhi, Sammodavardhana Kaudinnyayana, A. Khadka, Sudha Sen Malla\",\"doi\":\"10.3126/mjsbh.v21i1.40663\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction: The ChAdOx 1 n Cov-19 vaccine, called Covishield, was rolled out in Nepal targeting health care professionals. The study was conducted to assess the pattern of self-reported adverse events following immunization and to compare AEFI on the basis of previous COVID status.\\nMethods: A cross sectional study of four months duration was conducted in Shree Birendra Hospital, a tertiary care hospital, in Kathmandu, Nepal. AEFI associated with first and second dose of Covishield were assessed for a period of seven days from the day of vaccination in health care professionals and comparison was done based on COVID status.\\nResults: A total of 100 vaccine recipients were included in the study, out of which 83% showed AEFI. The most commonly reported AEFI after first dose were headache (56%), injection site tenderness (42%), myalgia (29%), fatigue (24%), dizziness (20%), pyrexia (19%), malaise (17%), nausea (10%), chills (8%), vomiting (2%) and arthralgia (1%) while among the AEFI after second dose were injection site tenderness (36%), headache (15%), myalgia (12%), fatigue (11%), nausea (9%), malaise (8%), pyrexia (8%), chills (5%), rashes (3%), drowsiness (3%), arthralgia (1%) and dizziness (1%). Previously infected participants were found to be prone to develop systemic adverse effects. The most of the adverse effects were subsided within four days and commonly used medication was paracetamol to relieve the symptoms. \\nConclusions: AEFI following the first and second dose of vaccine were mild. Systemic adverse effects were more frequent in those with the history of COVID-19 infection.\",\"PeriodicalId\":33963,\"journal\":{\"name\":\"Medical Journal of Shree Birendra Hospital\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-07-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Medical Journal of Shree Birendra Hospital\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3126/mjsbh.v21i1.40663\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical Journal of Shree Birendra Hospital","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3126/mjsbh.v21i1.40663","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
简介:ChAdOx 1 n Covid-19疫苗名为Covishield,在尼泊尔推出,针对医疗保健专业人员。该研究旨在评估免疫接种后自我报告的不良事件模式,并根据既往新冠肺炎状况比较AEFI。方法:在尼泊尔加德满都的三级护理医院Shree Birendra医院进行为期四个月的横断面研究。在卫生保健专业人员中,从接种疫苗之日起的七天内,对与第一剂和第二剂Covishield相关的AEFI进行评估,并根据新冠肺炎状况进行比较。结果:共有100名疫苗接种者被纳入研究,其中83%的人出现了AEFI。第一次给药后最常见的AEFI是头痛(56%)、注射部位压痛(42%)、肌痛(29%)、疲劳(24%)、头晕(20%)、发热(19%)、不适(17%)、恶心(10%)、发冷(8%)、呕吐(2%)和关节痛(1%),发热(8%)、发冷(5%)、皮疹(3%)、嗜睡(3%),关节痛(1%)和头晕(1%)。先前被感染的参与者被发现容易产生系统性不良反应。大多数不良反应在四天内消退,常用药物是扑热息痛来缓解症状。结论:接种第一剂和第二剂疫苗后的不良反应轻微。在有新冠肺炎感染史的患者中,系统性不良反应更为常见。
Self-reported Adverse Effects in Health Care Professionals Following First and Second Dose Vaccination Against SARS-CoV 2 (Covishield)
Introduction: The ChAdOx 1 n Cov-19 vaccine, called Covishield, was rolled out in Nepal targeting health care professionals. The study was conducted to assess the pattern of self-reported adverse events following immunization and to compare AEFI on the basis of previous COVID status.
Methods: A cross sectional study of four months duration was conducted in Shree Birendra Hospital, a tertiary care hospital, in Kathmandu, Nepal. AEFI associated with first and second dose of Covishield were assessed for a period of seven days from the day of vaccination in health care professionals and comparison was done based on COVID status.
Results: A total of 100 vaccine recipients were included in the study, out of which 83% showed AEFI. The most commonly reported AEFI after first dose were headache (56%), injection site tenderness (42%), myalgia (29%), fatigue (24%), dizziness (20%), pyrexia (19%), malaise (17%), nausea (10%), chills (8%), vomiting (2%) and arthralgia (1%) while among the AEFI after second dose were injection site tenderness (36%), headache (15%), myalgia (12%), fatigue (11%), nausea (9%), malaise (8%), pyrexia (8%), chills (5%), rashes (3%), drowsiness (3%), arthralgia (1%) and dizziness (1%). Previously infected participants were found to be prone to develop systemic adverse effects. The most of the adverse effects were subsided within four days and commonly used medication was paracetamol to relieve the symptoms.
Conclusions: AEFI following the first and second dose of vaccine were mild. Systemic adverse effects were more frequent in those with the history of COVID-19 infection.