Division of Gastroenterology, John T. Milliken Department of Medicine, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA.
VA Center for Clinical Management Research, VA Ann Arbor Health Care System, Ann Arbor, MI, USA.
Inflamm Bowel Dis. 2020 May 12;26(6):919-925. doi: 10.1093/ibd/izz189.
Patients with inflammatory bowel disease (IBD) are at increased risk for pneumonia, and corticosteroids are reported to amplify this risk. Less is known about the impact of corticosteroid-sparing IBD therapies on pneumonia risk or the efficacy of pneumococcal vaccination in reducing all-cause pneumonia in real-world IBD cohorts.
We performed a population-based study using an established Veterans Health Administration cohort of 29,957 IBD patients. We identified all patients who developed bacterial pneumonia. Cox survival analysis was used to determine the association of corticosteroids at study entry and as a time-varying covariate, corticosteroid-sparing agents (immunomodulators and antitumor necrosis-alpha [TNF] inhibitors), and pneumococcal vaccination with the development of all-cause pneumonia.
Patients with IBD who received corticosteroids had a greater risk of pneumonia when controlling for age, gender, and comorbidities (hazard ratio [HR] 2.21; 95% confidence interval [CI], 1.90-2.57 for prior use; HR = 3.42; 95% CI, 2.92-4.01 for use during follow-up). Anti-TNF inhibitors (HR 1.52; 95% CI, 1.02-2.26), but not immunomodulators (HR 0.91; 95% CI, 0.77-1.07), were associated with a small increase in pneumonia. A history of pneumonia was strongly associated with subsequent pneumonia (HR = 4.41; 95% CI, 3.70-5.27). Less than 15% of patients were vaccinated against pneumococcus, and this was not associated with a reduced risk of pneumonia (HR = 1.02; 95% CI, 0.80-1.30) in this cohort.
In a large US cohort, corticosteroids were confirmed to increase pneumonia risk. Tumor necrosis-alpha inhibitors were associated with a smaller increase in the risk of pneumonia. Surprisingly, pneumococcal vaccination did not reduce all-cause pneumonia in this population, though few patients were vaccinated.
炎症性肠病(IBD)患者患肺炎的风险增加,皮质类固醇据报道会增加这种风险。皮质类固醇保留 IBD 疗法对肺炎风险的影响或肺炎球菌疫苗接种在降低真实世界 IBD 队列中全因肺炎的疗效知之甚少。
我们使用已建立的退伍军人健康管理局队列对 29957 名 IBD 患者进行了一项基于人群的研究。我们确定了所有发生细菌性肺炎的患者。Cox 生存分析用于确定研究开始时的皮质类固醇以及作为时变协变量的皮质类固醇保留剂(免疫调节剂和抗肿瘤坏死因子-α [TNF] 抑制剂)以及肺炎球菌疫苗接种与全因肺炎的发展之间的关联。
在控制年龄、性别和合并症的情况下,接受皮质类固醇治疗的 IBD 患者发生肺炎的风险更高(先前使用的危险比 [HR] 2.21;95%置信区间 [CI],1.90-2.57;HR = 3.42;95%CI,2.92-4.01)。抗 TNF 抑制剂(HR 1.52;95%CI,1.02-2.26),而不是免疫调节剂(HR 0.91;95%CI,0.77-1.07),与肺炎风险略有增加相关。肺炎史与随后的肺炎密切相关(HR = 4.41;95%CI,3.70-5.27)。该队列中不到 15%的患者接种了肺炎球菌疫苗,这与降低肺炎风险无关(HR = 1.02;95%CI,0.80-1.30)。
在一项大型美国队列研究中,皮质类固醇被证实会增加肺炎风险。肿瘤坏死因子-α 抑制剂与肺炎风险增加较小相关。令人惊讶的是,肺炎球菌疫苗接种并未降低该人群的全因肺炎,尽管很少有患者接种了疫苗。