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Clinical Surveillance and Evaluation of Suspected Ebola Cases in a Vaccine Trial During an Ebola Epidemic: The Sierra Leone Trial to Introduce a Vaccine Against Ebola

机译:埃博拉流行病疫苗试验中涉嫌埃博拉病例的临床监测与评价:塞拉利昂试验引入艾博拉疫苗

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The Sierra Leone Trial to Introduce a Vaccine Against Ebola (STRIVE), an Ebola vaccine trial conducted during the 2014–2016 Ebola epidemic, coordinated with the Sierra Leone national response to identify Ebola cases among trial participants. The early symptoms of Ebola are similar to common vaccine reactions, so it was important to differentiate these to avoid unnecessary referral to an Ebola facility and an increased risk of Ebola exposure. STRIVE developed a modified version of the national case definition and case management algorithm to distinguish between symptoms associated with both Ebola and vaccination with the candidate Ebola vaccine (rVSV?G-ZEBOV-GP) from those typically associated only with Ebola. For participants who presented ≤48 hours after vaccination, we used the more stringent modified case definition to trigger referral for Ebola evaluation. Participants whose symptoms did not meet case definitions could also be referred to an Ebola facility, based on clinical judgment. No Ebola cases were diagnosed among the 8651 STRIVE participants. Fifty participants were evaluated for Ebola, of whom 34 (68%) were tested after vaccination; 22 deceased participants, all of whom underwent postmortem Ebola testing, as required during the Ebola epidemic, and had negative test results, were excluded from analysis. Seven of 34 participants (21%) had symptom onset ≤48 hours after vaccination, of whom 3 met the modified case definition. The most common diagnosis among those evaluated for Ebola was malaria. STRIVE demonstrates the feasibility of conducting Ebola surveillance among persons vaccinated with rVSV-ZEBOV during an Ebola epidemic and introduces a modified case definition and case management algorithm to distinguish vaccine reactions from early symptoms of Ebola that may be useful for reducing unnecessary Ebola evaluations among persons vaccinated during Ebola outbreaks.
机译:塞拉利昂试验将疫苗引入艾博拉(争夺),在2014-2016埃博拉流行病期间进行的埃博拉疫苗试验,与塞拉利昂国家反应协调,以识别审判参与者之间的福音病例。埃博拉的早期症状与常见的疫苗反应类似,因此很重要,以避免不必要的转诊到埃博拉的设施以及埃博拉暴露的风险增加。努力开发了一个改进版的国家案例定义和案例管理算法,区分与埃博拉和候选埃博拉疫苗(RVSV?G-Zebov-GP)的症状与通常仅与埃博拉的症状的疫苗接种。对于疫苗接种后呈现≤48小时的参与者,我们使用更严格的修改案例定义来触发埃博拉评估的推荐。根据临床判断,症状未符合案例定义的症状未符合案例定义的参与者也可以被提及埃博拉机构。在8651名争取参与者中没有诊断埃博拉病例。为埃博拉评估了50名参与者,其中34名(68%)在疫苗接种后进行了测试; 22名已故的参与者,所有这些都是在埃博拉流行病中所要求的止咳后埃博拉病毒检测,并从分析中排除了负面测试结果。 34名参与者中的7名(21%)疫苗后患有症状≤48小时,其中3个符合修改的案例定义。对埃博拉评价的最常见的诊断是疟疾。努力展示在埃博拉疫情中与RVSV-Zebov接种疫苗接种的人中埃博拉病毒的可行性,并引入修改的案例定义和病例管理算法,以区分埃博拉早期症状的疫苗反应,这对于减少疫苗的人之间可能有用可用于减少不必要的埃博拉病毒评估在埃博拉疫情期间。

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