Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.
Faculty of Medicine, University of Coimbra, Coimbra, Portugal.
JAMA. 2020 Dec 1;324(21):2187-2194. doi: 10.1001/jama.2020.20449.
A 4-component meningococcus group B vaccine (4CMenB) is the only vaccine in use to prevent group B invasive meningococcal disease in young children, but no matched controlled studies have evaluated it.
To determine the association between receipt of 4CMenB and invasive group B meningococcal disease.
DESIGN, SETTING, AND PARTICIPANTS: Matched incidence density case-control study. Patients presenting from October 2014 to March 2019 were ascertained, with follow-up until death or discharge (last follow-up in June 2019) in 31 pediatric services in Portugal. Children and adolescent residents in Portugal with laboratory-confirmed invasive meningococcal disease were included. Controls, usually 2 per case, with unrelated conditions who were at the same hospital at the same time were matched for sex, age, and residence.
Immunization with 4CMenB, ascertained from the national database (2-4 doses are recommended, depending on age).
The primary outcome was group B invasive meningococcal disease in fully vaccinated cases compared with controls. The secondary outcomes were all serogroup invasive meningococcal disease in fully vaccinated cases compared with controls and group B and all serogroup invasive meningococcal disease in cases compared with controls who received at least 1 vaccine dose.
Of 117 patients with invasive meningococcal disease, 98 were eligible for inclusion and 82 had group B invasive meningococcal disease; 69 were old enough to have been fully vaccinated and considered protected. Among these 69 cases, the median (interquartile range) age was 24 (4.5-196) months, 42 were male, and the median (interquartile range) duration of hospitalization was 8 (0-86) days. Five of 69 cases (7.2%) and 33 of 142 controls (23.1%) were fully vaccinated (difference, -16.0% [95% CI, -26.3% to -5.7%]; odds ratio [OR], 0.21 [95% CI, 0.08-0.55]). For all serogroup invasive meningococcal disease, 6 of 85 cases (7.1%) and 39 of 175 controls (22.3%) were fully vaccinated (difference, -15.2% [95% CI, -24.3% to -6.1%]; OR, 0.22 [95% CI, 0.09-0.53]). For group B disease, 8 of 82 cases (9.8%) and 50 of 168 controls (29.8%) received at least 1 vaccine dose (difference, -20.0% [95% CI, -30.3% to -9.7%]; OR, 0.18 [95% CI, 0.08-0.44]) and for all serogroup invasive meningococcal disease, 11 of 98 cases (11.2%) and 61 of 201 controls (30.3%) received at least 1 vaccine dose (difference, -19.1% [95% CI, -28.8% to -9.5%]; OR, 0.23 [95% CI, 0.11-0.49]).
During the first 5 years of vaccine availability in Portugal, vaccination with 4CMenB was less likely among children who developed invasive meningococcal disease compared with matched controls without invasive meningococcal disease. These findings may help inform the use of the 4CMenB vaccine in clinical practice.
ISRCTN Identifier: ISRCTN10901628.
目前唯一用于预防儿童侵袭性 B 群脑膜炎球菌病的疫苗是四价脑膜炎球菌 B 型疫苗(4CMenB),但尚未有匹配对照研究评估其效果。
确定接种 4CMenB 与侵袭性 B 群脑膜炎球菌病之间的关联。
设计、地点和参与者:这是一项匹配发病率密度病例对照研究。在葡萄牙的 31 家儿科服务机构中,确定了 2014 年 10 月至 2019 年 3 月期间出现的患者,并进行随访,直至死亡或出院(最后一次随访时间为 2019 年 6 月)。本研究纳入了葡萄牙居住的实验室确诊为侵袭性脑膜炎球菌病的儿童和青少年患者。对照组通常为每例病例 2 名,与同期在同一医院的非相关疾病患者相匹配,以性别、年龄和居住地为匹配因素。
从国家数据库中确定 4CMenB 免疫接种情况(根据年龄推荐接种 2-4 剂)。
主要结局为完全接种疫苗的病例与对照组相比,发生 B 群侵袭性脑膜炎球菌病的情况。次要结局为完全接种疫苗的病例与对照组相比,所有血清群侵袭性脑膜炎球菌病的情况,以及病例与对照组相比,至少接种 1 剂疫苗的 B 群和所有血清群侵袭性脑膜炎球菌病的情况。
在 117 例侵袭性脑膜炎球菌病患者中,有 98 例符合纳入标准,其中 82 例为 B 群侵袭性脑膜炎球菌病;69 例年龄足够大,已完全接种疫苗并被认为受到保护。在这 69 例病例中,中位(四分位间距)年龄为 24(4.5-196)个月,42 例为男性,中位(四分位间距)住院时间为 8(0-86)天。5 例(7.2%)和 33 例(23.1%)的病例完全接种疫苗(差异为-16.0%[95%CI,-26.3%至-5.7%];比值比[OR]为 0.21[95%CI,0.08-0.55])。对于所有血清群侵袭性脑膜炎球菌病,8 例(7.1%)和 39 例(22.3%)的病例完全接种疫苗(差异为-15.2%[95%CI,-24.3%至-6.1%];OR 为 0.22[95%CI,0.09-0.53])。对于 B 群疾病,8 例(9.8%)和 50 例(29.8%)的对照组至少接种了 1 剂疫苗(差异为-20.0%[95%CI,-30.3%至-9.7%];OR 为 0.18[95%CI,0.08-0.44]),对于所有血清群侵袭性脑膜炎球菌病,11 例(11.2%)和 61 例(30.3%)的对照组至少接种了 1 剂疫苗(差异为-19.1%[95%CI,-28.8%至-9.5%];OR 为 0.23[95%CI,0.11-0.49])。
在葡萄牙疫苗上市的前 5 年期间,与未发生侵袭性脑膜炎球菌病的对照组相比,接种 4CMenB 的儿童发生侵袭性脑膜炎球菌病的可能性较低。这些发现可能有助于为临床实践中使用 4CMenB 疫苗提供信息。
ISRCTN 标识符:ISRCTN85442025。