Department of Gastroenterology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
J Dig Dis. 2017 Jul;18(7):388-394. doi: 10.1111/1751-2980.12499.
The aim of this study was to explore the long-term risk of infection in patients with Crohn's disease (CD) on infliximab (IFX) therapy.
All CD patients treated with IFX were recruited from January 2008 to December 2015. Their characteristics and infectious events during IFX therapy were prospectively collected, and the risk of infection was evaluated using Cox regression.
Seventy CD patients receiving IFX were consecutively recruited. During a median of 15 months, 15 patients experienced 17 infectious events which occurred within a median of 21 weeks after the initiation of IFX therapy. Of 17 infectious events, eight were viral infections, six were bacterial infections, and the others were fungal infections. IFX was discontinued in 6 (40.0%) out of 15 cases due to infections. Compared with those without infections, patients with infectious events were more likely of Montreal B1 (inflammatory) behavior, with concomitant use of systemic corticosteroids when infliximab was started but less mucosal healing when infections occurred (P < 0.05). By Cox hazard ratio (HR) analysis, patients with B1 behavior had a higher risk of developing infections than those with B3 (fistulizing) behavior (HR 4.897, P = 0.010). Successful corticosteroid withdrawal (HR 0.275, P = 0.035) or mucosal healing (HR 0.155, P = 0.002) were associated with a lower risk of infections.
Long-term use of IFX in CD patients has a high risk of infections. Failure in mucosal healing and increased concomitant use of systemic corticosteroids are independent risk factors of infections during IFX therapy.
本研究旨在探讨接受英夫利昔单抗(IFX)治疗的克罗恩病(CD)患者的长期感染风险。
本研究纳入了 2008 年 1 月至 2015 年 12 月期间接受 IFX 治疗的所有 CD 患者。前瞻性收集他们在 IFX 治疗期间的特征和感染事件,并使用 Cox 回归评估感染风险。
本研究连续纳入了 70 例接受 IFX 治疗的 CD 患者。在中位 15 个月的时间内,15 例患者发生了 17 次感染事件,这些事件发生在 IFX 治疗开始后的中位 21 周内。在 17 次感染事件中,8 次为病毒感染,6 次为细菌感染,其余为真菌感染。由于感染,有 6(40.0%)例患者停用了 IFX。与无感染患者相比,发生感染的患者更有可能具有蒙特利尔 B1(炎症性)行为,在开始使用 IFX 时同时使用全身皮质类固醇,但在发生感染时黏膜愈合较差(P<0.05)。通过 Cox 风险比(HR)分析,具有 B1 行为的患者发生感染的风险高于具有 B3(瘘管性)行为的患者(HR 4.897,P=0.010)。成功停用皮质类固醇(HR 0.275,P=0.035)或黏膜愈合(HR 0.155,P=0.002)与感染风险降低相关。
长期使用 IFX 治疗 CD 患者感染风险较高。黏膜愈合不良和同时使用全身皮质类固醇增加是 IFX 治疗期间感染的独立危险因素。