Adu-Fokuo Douglas, C. Feng, Yin Emily, Giwa Elizabeth
{"title":"Study of adverse events following 2018 sub-national yellow fever vaccination in Ghana","authors":"Adu-Fokuo Douglas, C. Feng, Yin Emily, Giwa Elizabeth","doi":"10.17352/jvi.000055","DOIUrl":null,"url":null,"abstract":"Background: According to the Centers for Disease Control and Prevention (CDC), globally there is an estimated 200,000 cases of Yellow Fever Virus yearly, causing 30,000 deaths annually, with 90% of cases occurring in Africa. Where about 20% to 50% of people who get infected and develop severe symptoms from the yellow fever virus die. WHO report showed that Ghana was among 27 African countries with a high risk of yellow fever outbreak at any time. In response, there was a need to amplify the immunization campaign against yellow fever. Ghana in collaboration with WHO, GAVI, the Vaccine Alliance, and UNICEF began a sub-national campaign to vaccinate approximately 5.3 million people against yellow fever targeting people between ages 10 and 60 years from November 28 to December 4, 2018. 459 Adverse Events Following the Immunization (AEFI) in Ghana were reported from 28th November 2018 to 1st January 2019. The yellow fever vaccine is regarded as one of the safest, but with few adverse events. Therefore, there is a need to assess the severity of the reported adverse events following immunization in the 2018 sub-national yellow fever immunization program in Ghana. Objective: To study the Seriousness of adverse events following yellow fever vaccination in Ghana. Methodology: A retrospective review of AEFI data through a surveillance system during a Yellow Fever vaccination campaign in Ghana. The data comprised suspected 459 adverse events following the immunization (AEFI). The reported AEFI from 28th November 2018 to 1st January 2019 was used for this study as secondary data. A total of 5.3 million people were vaccinated. All vaccine recipients were between the ages of 10 years to 60 years. Data were analyzed using frequencies and descriptive statistics in STATA version 15. Findings and discussions: The study showed 459 (0.00086%) per 5.3 million recipients reported adverse events. The AEFI occurred mostly among females and persons aged 30-39 years. Out of the 459 recipients with adverse events, 432 (99.3%) recovered, and 3 (0.7%) died. The most common adverse event per region, sex, and age group is fever. The study also revealed AEFIs may have contributed to the death of 3 (0.000056%) per 5.3 million recipients. However, a causality assessment done by the Vaccine Safety Review Committee of independent experts showed no causality between the reported AEFI (deaths) and the YF vaccination. This indicates that the benefits of the vaccination outweigh the risk of adverse events or fatalities. Conclusion: In conclusion, it was found that the benefits of the Yellow Fever Vaccination (YFV 17D) outweigh the risk of adverse events or fatalities. Reported Adverse Events following the 2018 sub-national yellow fever vaccination per 5.3 million recipients were 459 representing 0.0086%. There was no causality between reported deaths 3 (0.000056%) and the YF immunization. The adverse events that follow yellow fever immunization are not strong and suggest that most of the respondents do not have serious repercussions after the vaccination. Therefore, YF vaccination has saved millions of people from potential vaccine-preventable deaths in Ghana and beyond its borders and did not cause more harm than health benefits.","PeriodicalId":330981,"journal":{"name":"Journal of Vaccines and Immunology","volume":"42 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Vaccines and Immunology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17352/jvi.000055","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: According to the Centers for Disease Control and Prevention (CDC), globally there is an estimated 200,000 cases of Yellow Fever Virus yearly, causing 30,000 deaths annually, with 90% of cases occurring in Africa. Where about 20% to 50% of people who get infected and develop severe symptoms from the yellow fever virus die. WHO report showed that Ghana was among 27 African countries with a high risk of yellow fever outbreak at any time. In response, there was a need to amplify the immunization campaign against yellow fever. Ghana in collaboration with WHO, GAVI, the Vaccine Alliance, and UNICEF began a sub-national campaign to vaccinate approximately 5.3 million people against yellow fever targeting people between ages 10 and 60 years from November 28 to December 4, 2018. 459 Adverse Events Following the Immunization (AEFI) in Ghana were reported from 28th November 2018 to 1st January 2019. The yellow fever vaccine is regarded as one of the safest, but with few adverse events. Therefore, there is a need to assess the severity of the reported adverse events following immunization in the 2018 sub-national yellow fever immunization program in Ghana. Objective: To study the Seriousness of adverse events following yellow fever vaccination in Ghana. Methodology: A retrospective review of AEFI data through a surveillance system during a Yellow Fever vaccination campaign in Ghana. The data comprised suspected 459 adverse events following the immunization (AEFI). The reported AEFI from 28th November 2018 to 1st January 2019 was used for this study as secondary data. A total of 5.3 million people were vaccinated. All vaccine recipients were between the ages of 10 years to 60 years. Data were analyzed using frequencies and descriptive statistics in STATA version 15. Findings and discussions: The study showed 459 (0.00086%) per 5.3 million recipients reported adverse events. The AEFI occurred mostly among females and persons aged 30-39 years. Out of the 459 recipients with adverse events, 432 (99.3%) recovered, and 3 (0.7%) died. The most common adverse event per region, sex, and age group is fever. The study also revealed AEFIs may have contributed to the death of 3 (0.000056%) per 5.3 million recipients. However, a causality assessment done by the Vaccine Safety Review Committee of independent experts showed no causality between the reported AEFI (deaths) and the YF vaccination. This indicates that the benefits of the vaccination outweigh the risk of adverse events or fatalities. Conclusion: In conclusion, it was found that the benefits of the Yellow Fever Vaccination (YFV 17D) outweigh the risk of adverse events or fatalities. Reported Adverse Events following the 2018 sub-national yellow fever vaccination per 5.3 million recipients were 459 representing 0.0086%. There was no causality between reported deaths 3 (0.000056%) and the YF immunization. The adverse events that follow yellow fever immunization are not strong and suggest that most of the respondents do not have serious repercussions after the vaccination. Therefore, YF vaccination has saved millions of people from potential vaccine-preventable deaths in Ghana and beyond its borders and did not cause more harm than health benefits.
背景:根据疾病控制和预防中心(CDC)的数据,全球每年估计有20万例黄热病病毒,每年造成3万人死亡,其中90%的病例发生在非洲。大约20%到50%的人感染并出现严重的黄热病病毒症状后死亡。世卫组织的报告显示,加纳是27个非洲国家中黄热病随时爆发的高风险国家之一。为此,有必要扩大针对黄热病的免疫运动。加纳与世卫组织、全球疫苗免疫联盟、疫苗联盟和联合国儿童基金会合作,于2018年11月28日至12月4日开展了一项次国家级运动,为大约530万人接种黄热病疫苗,目标人群为10至60岁的人群。2018年11月28日至2019年1月1日,加纳报告了459起免疫接种后不良事件。黄热病疫苗被认为是最安全的疫苗之一,但几乎没有不良事件。因此,有必要评估加纳2018年次国家级黄热病免疫规划中免疫接种后报告的不良事件的严重程度。目的:研究加纳黄热病疫苗接种后不良事件的严重程度。方法:在加纳黄热病疫苗接种运动期间通过监测系统对AEFI数据进行回顾性审查。数据包括免疫接种后疑似459起不良事件(AEFI)。本研究使用2018年11月28日至2019年1月1日报告的AEFI作为次要数据。总共有530万人接种了疫苗。所有疫苗接种者的年龄在10岁至60岁之间。使用STATA version 15中的频率和描述性统计分析数据。研究结果和讨论:研究显示,每530万接受者中有459人(0.00086%)报告了不良事件。AEFI主要发生在女性和30-39岁人群中。459例有不良事件的受者中,432例(99.3%)康复,3例(0.7%)死亡。各地区、性别和年龄组最常见的不良事件是发烧。该研究还显示,每530万接受aefi治疗者中有3人(0.000056%)死亡。然而,由独立专家组成的疫苗安全审查委员会进行的因果关系评估显示,报告的急性急性呼吸道感染(死亡)与接种YF疫苗之间没有因果关系。这表明疫苗接种的益处大于不良事件或死亡的风险。结论:总之,发现黄热病疫苗接种(YFV 17D)的益处大于不良事件或死亡的风险。2018年次国家级黄热病疫苗接种后报告的不良事件为每530万接种者459例,占0.0086%。报告的死亡3(0.000056%)与儿童免疫接种之间没有因果关系。黄热病免疫接种后的不良事件并不严重,这表明大多数应答者在接种疫苗后没有产生严重后果。因此,在加纳及其境外,接种YF疫苗使数百万人免于疫苗可预防的潜在死亡,其危害并不大于健康益处。