Comparative risk of postoperative complications in ulcerative colitis patients following preoperative advanced therapies: a network meta-analysis with meta-regression.

IF 8.7
Mohammad Al Hayek, Maria Manuela Estevinho, Maia Kayal, Osamah Al Hayek, Alessandro Armuzzi, Johan Burisch, Qasi Najah, Vipul Jairath, Steven D Wexner, Edward V Loftus, Laurent Peyrin-Biroulet, Silvio Danese, Muhammed Elhadi, Fernando Magro
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Abstract

Background: The expanding use of biologic and small-molecule therapies for ulcerative colitis (UC) has raised concerns regarding perioperative safety. We conducted a network meta-analysis to compare short-term postoperative complications associated with preoperative exposure to these agents in patients undergoing colorectal surgery.

Methods: We systematically searched PubMed, Web of Science, and the Cochrane Library through September 15, 2025, for cohort studies of adults with UC who were exposed to biologic or small-molecule therapy within 12 weeks prior to surgery. Interventions included biologic therapy, small-molecule therapy, and no biologic or small-molecule therapy (control). The primary outcome was overall postoperative complications at 30 and 90 days. Venous thromboembolism (VTE) was assessed as a key secondary outcome. Random-effects network meta-analysis was performed using risk ratios (RRs) with 95% confidence intervals (CIs).

Results: Sixteen retrospective cohort studies involving 3235 patients were included. At 30 days, ustekinumab and tofacitinib were associated with lower overall postoperative complication rates than control (RR: 0.29; 95% CI: 0.09-0.96; and RR: 0.66; 95% CI: 0.46-0.96, respectively). Anti-tumor necrosis factor (TNF) therapy was associated with higher complication rates compared with vedolizumab, ustekinumab, and tofacitinib at 30 days (RR: 1.27; 95% CI: 1.00-1.63; RR: 3.67; 95% CI: 1.12-12.03; and RR: 1.61; 95% CI: 1.14-2.27, respectively). At 90 days, anti-TNF therapy was associated with higher complication rates than control (RR 1.20, 95% CI 1.03-1.40), although the 90-day analysis was based on limited data. VTE rates were similar across treatments at both time points.

Conclusion: Preoperative ustekinumab and tofacitinib were associated with fewer 30-day postoperative complications than control or anti-TNF therapy, while vedolizumab was associated with fewer complications than anti-TNF therapy. At 90 days, anti-TNF therapy was associated with higher complication rates compared with control. These findings, particularly at 90 days based on limited data, should be interpreted with caution and require confirmation in well-designed prospective studies with rigorous adjustment for confounding factors.

溃疡性结肠炎患者术前高级治疗后术后并发症的比较风险:一项带有meta回归的网络meta分析。
背景:生物和小分子治疗溃疡性结肠炎(UC)的广泛应用引起了人们对围手术期安全性的关注。我们进行了一项网络荟萃分析,比较结肠直肠手术患者术前暴露于这些药物相关的短期术后并发症。方法:我们系统地检索PubMed、Web of Science和Cochrane Library,检索截止到2025年9月15日的成人UC患者在手术前12周内接受生物或小分子治疗的队列研究。干预措施包括生物治疗、小分子治疗和无生物或小分子治疗(对照组)。主要结局是30天和90天的总体术后并发症。静脉血栓栓塞(VTE)被评估为一个关键的次要结局。随机效应网络荟萃分析采用95%置信区间的风险比(rr)。结果:纳入16项回顾性队列研究,涉及3235例患者。在第30天,ustekinumab和tofacitinib与对照组相比,总体术后并发症发生率较低(RR: 0.29; 95% CI: 0.09-0.96; RR: 0.66; 95% CI: 0.46-0.96)。与维多单抗、乌斯特金单抗和托法替尼相比,抗肿瘤坏死因子(TNF)治疗在30天的并发症发生率更高(RR: 1.27; 95% CI: 1.00-1.63; RR: 3.67; 95% CI: 1.12-12.03; RR: 1.61; 95% CI: 1.14-2.27)。尽管90天的分析基于有限的数据,但与对照组相比,抗tnf治疗与更高的并发症发生率相关(RR 1.20, 95% CI 1.03-1.40)。两个时间点的静脉血栓栓塞率相似。结论:术前ustekinumab和tofacitinib与对照或抗tnf治疗相比,术后30天并发症较少,而vedolizumab与抗tnf治疗相比并发症较少。在第90天,与对照组相比,抗tnf治疗与更高的并发症发生率相关。这些发现,特别是基于有限数据的90天的发现,应谨慎解释,并需要在设计良好的前瞻性研究中进行确认,并严格调整混杂因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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