Immunisation and Countermeasures, Public Health England, London, England.
Statistics and Modelling Economics Department, Public Health England, London, England.
PLoS Med. 2020 Sep 14;17(9):e1003225. doi: 10.1371/journal.pmed.1003225. eCollection 2020 Sep.
Early studies of narcolepsy after AS03-adjuvanted pandemic A/H1N12009 vaccine (Pandemrix) could not define the duration of elevated risk post-vaccination nor the risk in children aged under 5 years who may not present until much older.
METHODS/FINDINGS: Clinical information and sleep test results, extracted from hospital notes at 3 large pediatric sleep centers in England between September 2017 and June 2018 for narcolepsy cases aged 4-19 years with symptom onset since January 2009, were reviewed by an expert panel to confirm the diagnosis. Vaccination histories were independently obtained from general practitioners (GPs). The odds of vaccination in narcolepsy cases compared with the age-matched English population was calculated after adjustment for clinical conditions that were indications for vaccination. GP questionnaires were returned for 242 of the 244 children with confirmed narcolepsy. Of these 5 were under 5 years, 118 were 5-11 years, and 119 were 12-19 years old at diagnosis; 39 were vaccinated with Pandemrix before onset. The odds ratio (OR) for onset at any time after vaccination was 1.94 (95% confidence interval [CI] 1.30-2.89), The elevated risk period was restricted to onsets within 12 months of vaccination (OR 6.65 [3.44-12.85]) and was highest within the first 6 months. After one year, ORs were not significantly different from 1 up to 8 years after vaccination. The ORs were similar in under five-year-olds and older ages. The estimated attributable risk was 1 in 34,500 doses. Our study is limited by including cases from only 3 sleep centers, who may differ from cases diagnosed in nonparticipating centers, and by imprecision in defining the centers' catchment population. The potential for biased recall of onset shortly after vaccination in cases aware of the association cannot be excluded.
In this study, we found that vaccine-attributable cases have onset of narcolepsy within 12 months of Pandemrix vaccination. The attributable risk is higher than previously estimated in England because of identification of vaccine-attributable cases with late diagnoses. Absence of a compensatory drop in risk 1-8 years after vaccination suggests that Pandemrix does not trigger onsets in those in whom narcolepsy would have occurred later.
早期关于 AS03 佐剂大流行性 A/H1N12009 疫苗(Pandemrix)接种后发作的嗜睡症的研究无法确定接种后风险升高的持续时间,也无法确定 5 岁以下儿童的风险,这些儿童可能要到更晚才会出现症状。
方法/发现:2017 年 9 月至 2018 年 6 月,在英格兰的 3 个大型儿科睡眠中心,对嗜睡症病例的临床信息和睡眠测试结果进行了审查,这些病例年龄在 4-19 岁之间,症状始于 2009 年 1 月以后,由专家小组确认诊断。通过向全科医生(GP)独立获取疫苗接种史。调整了可能表明接种疫苗的临床条件后,计算了嗜睡症病例与年龄匹配的英国人群相比的接种疫苗几率。对于 244 例确诊的嗜睡症患儿中的 242 例,我们收到了 GP 问卷。其中 5 例年龄小于 5 岁,118 例年龄在 5-11 岁之间,119 例年龄在 12-19 岁之间;39 例在发病前接种了 Pandemrix。任何时间接种后发病的比值比(OR)为 1.94(95%置信区间 [CI] 1.30-2.89)。高危期仅限于接种后 12 个月内的发病(OR 6.65 [3.44-12.85]),且在最初的 6 个月内最高。接种后 1 年,OR 与接种后 1 至 8 年没有显著差异。在 5 岁以下和年龄较大的儿童中,OR 相似。估计归因风险为每 34500 剂疫苗 1 例。我们的研究受到限制,仅包括来自 3 个睡眠中心的病例,这些病例可能与未参与中心诊断的病例不同,并且对中心集水区人群的定义也不精确。无法排除病例在接种疫苗后不久因对嗜睡症的发病存在意识而回忆发病的潜在偏倚。
在这项研究中,我们发现接种疫苗后嗜睡症的发病时间在 Pandemrix 接种后 12 个月内。由于确定了疫苗可归因病例的晚发性诊断,英国的归因风险高于之前的估计。接种后 1-8 年风险没有下降表明,Pandemrix 不会在以后会出现嗜睡症的人群中引发发作。