Winje Brita Askeland, Vestrheim Didrik Frimann, White Richard Aubrey, Steens Anneke
Division of Infection Control and Environmental Health, Norwegian Institute of Public Health, P.O. Box 222, Skøyen, 0213 Oslo, Norway.
Microorganisms. 2021 Aug 20;9(8):1774. doi: 10.3390/microorganisms9081774.
The elderly and adults with medical risk conditions remain at high risk of invasive pneumococcal disease (IPD), highlighting the importance of adequate preventive efforts. In an observational population-based study in Norway (pop ≥ 5 years, 2009-2017) covering six years post-PCV13 implementation, we explored the incidence and risk of IPD associated with age and comorbidities. We obtained the data on 5535 IPD cases from the Norwegian Surveillance System for Communicable Diseases and the population data from Statistics Norway. To define comorbidities, we obtained ICD-10 codes from the Norwegian Patient Registry for the cases and the Norwegian population. The average annual decrease in PCV13 IPD incidence was significant in all risk groups and decreased post-PCV13 introduction by 16-20% per risk group, implying a nondifferential indirect protection from the childhood vaccination. The IPD incidence remained high in the medical risk groups. The relative importance of medical risk conditions was 2.8 to 6 times higher in those aged 5-64 versus ≥65 years for all types of IPD, since age itself is a risk factor for IPD. In groups without medical risk, the risk of IPD was eight times higher in those aged ≥65 compared to those 5-64 years (RR 8.3 (95% CI 7.3-9.5)). Our results underscore the need for age- and risk-group-based prevention strategies.
老年人和有医疗风险状况的成年人仍然面临侵袭性肺炎球菌疾病(IPD)的高风险,这凸显了充分预防措施的重要性。在挪威一项基于人群的观察性研究(对象为年龄≥5岁,时间为2009 - 2017年)中,涵盖了13价肺炎球菌结合疫苗(PCV13)实施后的六年,我们探讨了IPD的发病率以及与年龄和合并症相关的风险。我们从挪威传染病监测系统获得了5535例IPD病例的数据,并从挪威统计局获得了人口数据。为了定义合并症,我们从挪威患者登记处获取了病例和挪威人群的国际疾病分类第十版(ICD - 10)编码。在所有风险组中,PCV13引入后IPD发病率的年均下降均显著,每个风险组在引入PCV13后发病率下降了16% - 20%,这意味着儿童疫苗接种带来了无差异的间接保护。在有医疗风险的组中,IPD发病率仍然很高。对于所有类型的IPD,5 - 64岁人群中医疗风险状况的相对重要性比≥65岁人群高2.8至6倍,因为年龄本身就是IPD的一个风险因素。在没有医疗风险的组中,≥65岁人群的IPD风险比5 - 64岁人群高8倍(相对风险8.3(95%置信区间7.3 - 9.5))。我们的结果强调了基于年龄和风险组的预防策略的必要性。