Division of Gastroenterology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.
Division of Gastroenterology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.
Clin Gastroenterol Hepatol. 2023 Feb;21(2):541-542.e1. doi: 10.1016/j.cgh.2022.01.033. Epub 2022 Feb 2.
Approximately 20% of patients with ulcerative colitis (UC) who undergo total proctocolectomy (TPC) with ileal pouch-anal anastomosis (IPAA) develop chronic pouch inflammation (CPI). Given the involvement of the small bowel in CPI, there is no consensus on whether it should be managed more like UC or Crohn's disease (CD). Despite limited evidence, biologics are often used for CPI with clinical response rates of 20%-60% with adalimumab and infliximab, 50%-80% with ustekinumab, and 30%-70% with vedolizumab. Earlier biologic therapy has been associated with greater rates of response and favorable long-term outcomes in patients with CD, however not UC. The impact of earlier initiation of biologic therapy on CPI clinical outcomes has not been elucidated. The aim of this study was to assess whether timing of biologic initiation relative to CPI diagnosis impacts clinical and endoscopic remission.
约 20%接受全结肠直肠切除术(TPC)和回肠袋肛管吻合术(IPAA)的溃疡性结肠炎(UC)患者会发展为慢性袋炎(CPI)。鉴于 CPI 涉及小肠,目前对于其治疗方法是否更类似于 UC 或克罗恩病(CD)尚无共识。尽管证据有限,但生物制剂通常用于治疗 CPI,阿达木单抗和英夫利昔单抗的临床缓解率为 20%-60%,乌司奴单抗为 50%-80%,维得利珠单抗为 30%-70%。在 CD 患者中,更早开始生物制剂治疗与更高的缓解率和良好的长期结局相关,但在 UC 患者中并非如此。更早开始生物制剂治疗对 CPI 临床结局的影响尚未阐明。本研究旨在评估生物制剂治疗开始的时间相对于 CPI 诊断是否会影响临床和内镜缓解。