Patrick Desmond, Doecke James, Irwin James, Hanigan Katherine, Simms Lisa, Howlett Mariko, Radford-Smith Graham
Department of Gastroenterology and Hepatology, The Royal Brisbane and Women's Hospital, IBD Unit, Ned Hanlon Building, Level 9, Butterfield Street, Herston, Brisbane, Queensland, 4029, Australia.
CSIRO Health and Biosecurity/Australian E-Health Research Centre, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.
Therap Adv Gastroenterol. 2018 Nov 13;11:1756284818809789. doi: 10.1177/1756284818809789. eCollection 2018.
Patients on immunosuppression at the time of acute severe ulcerative colitis have been suggested to be at a higher risk of colectomy than those who are treatment-naïve. The aim of this study was to examine the effect of immunosuppressive therapy on the risk of colectomy.
We conducted a retrospective observational cohort study using prospective data examining the 30 day and 1 year colectomy rates of 200 consecutive patients with an index episode of acute severe ulcerative colitis as defined by the Truelove and Witts criteria.
Immunosuppression on admission was shown not to increase colectomy rate at 30 days post-admission (immunomodulator: = 0.422, oral steroids: = 0.555). A total of 24 patients underwent colectomy between 30 days and 1 year. A three-fold higher risk of colectomy at 1 year was seen in those requiring an immunomodulator prior to the index admission compared with those started during the index admission [41% 14% odds ratio (OR): 2.93 (1.19-7.24 = 0.016)]. Factors most predictive of colectomy at 30 days were abdominal radiographic colonic dilation ⩾5.5 cm, first presentation of ulcerative colitis, C-reactive protein ⩾ 45 mg/l on day 3 of therapy and bowel frequency ⩾8 on day 3.
The need for an immunomodulator prior to admission with acute severe ulcerative colitis increases the medium-term colectomy rate by three-fold at 1 year. Prospective studies are needed to confirm these findings and develop strategies to reduce the high risk in this subgroup of patients.
有研究表明,急性重症溃疡性结肠炎患者在接受免疫抑制治疗时,与未接受过治疗的患者相比,接受结肠切除术的风险更高。本研究旨在探讨免疫抑制治疗对结肠切除术风险的影响。
我们进行了一项回顾性观察队列研究,使用前瞻性数据,研究200例符合Truelove和Witts标准定义的急性重症溃疡性结肠炎首发患者的30天和1年结肠切除率。
入院时接受免疫抑制治疗并未增加入院后30天的结肠切除率(免疫调节剂: = 0.422,口服类固醇: = 0.555)。共有24例患者在30天至1年期间接受了结肠切除术。与在首次入院期间开始使用免疫调节剂的患者相比,在首次入院前需要免疫调节剂的患者在1年时接受结肠切除术的风险高出三倍[41% 14% 比值比(OR):2.93(1.19 - 7.24 = 0.016)]。30天时最能预测结肠切除术的因素是腹部X线结肠扩张≥5.5 cm、溃疡性结肠炎首次发作、治疗第3天C反应蛋白≥45 mg/l以及治疗第3天排便频率≥8次。
急性重症溃疡性结肠炎入院前需要免疫调节剂会使1年时的中期结肠切除率增加三倍。需要进行前瞻性研究来证实这些发现,并制定策略以降低该亚组患者的高风险。