Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA, USA.
Division of Gastroenterology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA, USA.
Aliment Pharmacol Ther. 2022 Jan;55(1):64-72. doi: 10.1111/apt.16610. Epub 2021 Oct 19.
There are limited data on the incidence of pneumonia and pneumonia-related hospitalisation in the IBD population, and on any association of IBD medications with such outcomes.
To evaluate the impact of IBD medications on the risk of pneumonia, pneumonia-related hospitalisations and death.
We conducted a retrospective cohort study of IBD patients from the nationwide Veteran Affairs (VA) dataset. The exposure of interest was different IBD medication groups. We estimated the incidence rate of pneumonia, pneumonia-related hospitalisation and mortality based on IBD medication subgroups. We used a multivariable Cox regression to estimate the adjusted hazard ratios (AHR) and 95% confidence intervals (CIs) for these outcomes.
Out of 56 410 patients with IBD, 3759 developed pneumonia, 1489 were hospitalised, and 248 died within 30 days of their pneumonia diagnosis. The crude incidence rates of pneumonia, pneumonia-related hospitalisation and pneumonia-related mortality were 6.47, 2.52 and 0.43, respectively, per 1000 person-years. In multivariable Cox regression analysis, compared to 5-ASA alone, anti-TNF medication was associated with an increased risk of pneumonia (AHR 1.39; 95% CI 1.22-1.59) and hospitalisation (AHR 1.61; 95% CI 1.31-1.98). Use of prednisone in the prior 30 days was associated with increased risk of pneumonia (AHR 2.14; 95% CI 1.92-2.38) and hospitalisation (AHR 2.44; 95% CI 2.08-2.88).
Anti-TNF medications and prednisone use may be associated with increased risk of developing pneumonia and pneumonia-related hospitalisation. Physicians should evaluate the risk-benefit ratio of IBD medications, especially in the elderly population.
关于炎症性肠病(IBD)患者中肺炎和与肺炎相关的住院治疗的发生率,以及 IBD 药物与这些结果的任何关联,数据有限。
评估 IBD 药物对肺炎、与肺炎相关的住院治疗和死亡风险的影响。
我们对来自全国退伍军人事务部(VA)数据集的 IBD 患者进行了回顾性队列研究。感兴趣的暴露因素是不同的 IBD 药物治疗组。我们根据 IBD 药物亚组估计肺炎、与肺炎相关的住院治疗和死亡率的发生率。我们使用多变量 Cox 回归来估计这些结果的调整后风险比(AHR)和 95%置信区间(CI)。
在 56410 名 IBD 患者中,有 3759 人发生了肺炎,1489 人住院,248 人在肺炎诊断后 30 天内死亡。肺炎、与肺炎相关的住院治疗和肺炎相关死亡率的粗发生率分别为每 1000 人年 6.47、2.52 和 0.43。在多变量 Cox 回归分析中,与单独使用 5-ASA 相比,抗 TNF 药物与肺炎(AHR 1.39;95%CI 1.22-1.59)和住院治疗(AHR 1.61;95%CI 1.31-1.98)的风险增加相关。在过去 30 天内使用泼尼松与肺炎(AHR 2.14;95%CI 1.92-2.38)和住院治疗(AHR 2.44;95%CI 2.08-2.88)的风险增加相关。
抗 TNF 药物和泼尼松的使用可能与发生肺炎和与肺炎相关的住院治疗的风险增加相关。医生应评估 IBD 药物的风险效益比,特别是在老年人群中。