Nakafero Georgina, Grainge Matthew J, Card Tim, Mallen Christian D, Nguyen Van-Tam Jonathan S, Abhishek Abhishek
Academic Rheumatology, School of Medicine, University of Nottingham, Nottingham, UK.
Nottingham NIHR BRC, Nottingham.
Rheumatology (Oxford). 2025 Mar 1;64(3):962-968. doi: 10.1093/rheumatology/keae160.
The uptake and safety of pneumococcal vaccination in people with immune-mediated inflammatory diseases (IMIDs) is poorly understood. We investigated the UK-wide pneumococcal vaccine uptake in adults with IMIDs and explored the association between vaccination and IMID flare.
Adults with IMIDs diagnosed on or before 1 September 2018, prescribed steroid-sparing drugs within the last 12 months and contributing data to the Clinical Practice Research Datalink Gold, were included. Vaccine uptake was assessed using a cross-sectional study design. Self-controlled case series analysis investigated the association between pneumococcal vaccination and IMID flare. The self-controlled case series observation period was up to 6 months before and after pneumococcal vaccination. This was partitioned into a 14-day pre-vaccination induction, 90 days post-vaccination exposed and the remaining unexposed periods.
We included 32 277 patients, 14 151 with RA, 13 631 with IBD, 3804 with axial SpA and 691 with SLE. Overall, 57% were vaccinated against pneumococcus. Vaccine uptake was lower in those younger than 45 years old (32%), with IBD (42%) and without additional indication(s) for vaccination (46%). In the vaccine safety study, data for 1067, 935 and 451 vaccinated patients with primary-care consultations for joint pain, autoimmune rheumatic disease flare and IBD flare, respectively, were included. Vaccination against pneumococcal pneumonia was not associated with primary-care consultations for joint pain, autoimmune rheumatic disease flare and IBD flare in the exposed period, with incidence rate ratios (95% CI) 0.95 (0.83-1.09), 1.05 (0.92-1.19) and 0.83 (0.65-1.06), respectively.
Uptake of pneumococcal vaccination in UK patients with IMIDs was suboptimal. Vaccination against pneumococcal disease was not associated with IMID flare.
免疫介导的炎症性疾病(IMIDs)患者对肺炎球菌疫苗的接种情况及安全性尚不清楚。我们调查了全英国IMIDs成年患者的肺炎球菌疫苗接种情况,并探讨了疫苗接种与IMID病情复发之间的关联。
纳入2018年9月1日前确诊为IMIDs、在过去12个月内使用过免疫抑制剂且向临床实践研究数据链黄金数据库提供数据的成年患者。采用横断面研究设计评估疫苗接种情况。自我对照病例系列分析调查肺炎球菌疫苗接种与IMID病情复发之间的关联。自我对照病例系列观察期为肺炎球菌疫苗接种前后各6个月。这被分为接种前14天诱导期、接种后90天暴露期和其余非暴露期。
我们纳入了32277例患者,其中14151例为类风湿关节炎(RA)患者,13631例为炎症性肠病(IBD)患者,3804例为中轴型脊柱关节炎(axial SpA)患者,691例为系统性红斑狼疮(SLE)患者。总体而言,57%的患者接种了肺炎球菌疫苗。45岁以下患者(32%)、IBD患者(42%)以及无其他疫苗接种指征的患者(46%)的疫苗接种率较低。在疫苗安全性研究中,分别纳入了1067例、935例和451例因关节疼痛、自身免疫性风湿病病情复发和IBD病情复发而进行初级保健咨询的接种疫苗患者的数据。在暴露期,接种肺炎球菌肺炎疫苗与因关节疼痛、自身免疫性风湿病病情复发和IBD病情复发而进行的初级保健咨询无关,发病率比(95%CI)分别为0.95(0.83 - 1.09)、1.05(0.92 - 1.19)和0.83(0.65 - 1.06)。
英国IMIDs患者的肺炎球菌疫苗接种率不理想。接种肺炎球菌疾病疫苗与IMID病情复发无关。