Gaëlle Tyrode, Zaher Lakkis, Dewi Vernerey, Antoine Falcoz, Valentine Clairet, Line Alibert, Stéphane Koch, Lucine Vuitton
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The primary end point was endoscopic POR (Rutgeerts score ≥i2). Factors associated with POR were assessed by univariate and multivariable analyses.</p><p><strong>Results: </strong>A total of 85 patients were included, 30 in the Kono-S group and 55 in the control group. At baseline, there was no significant difference between the 2 groups regarding CD characteristics or known POR risk factors, including previous exposure to biologics. At 6 to 12 months, endoscopic POR rate did not differ significantly between groups (56.7% in the Kono-S group vs 49.1% in the control group; P = .50), nor did endoscopic POR according to the modified Rutgeerts score ≥i2b (46.7% in the Kono-S group vs 40% in the control group; P = .55). Severe endoscopic POR rates were 23.3% and 18.2% in each group, respectively. Clinical recurrence rate was similar in both groups, and no recurrent surgery occurred. By multivariable analysis, the type of anastomosis was not associated with endoscopic POR (OR, 1.229; 95% CI, 0.461-3.274, P = .68); however, postoperative treatment with anti-TNF was (OR, 0.337; 95% CI, 0.131-0.865 P = .02).</p><p><strong>Conclusions: </strong>Kono-S anastomosis was not associated with a reduced rate of endoscopic POR. 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We aimed to compare the endoscopic POR rate after Kono-S vs standard ileocolic anastomosis.</p><p><strong>Methods: </strong>The study included all consecutive CD patients operated on for ileocolic resection with a Kono-S anastomosis between February 2020 and March 2022. These patients were prospectively followed, and colonoscopy was performed 6 to 12 months after surgery. Patients were compared with a historical cohort of patients operated on with a conventional anastomosis in the same center. The primary end point was endoscopic POR (Rutgeerts score ≥i2). Factors associated with POR were assessed by univariate and multivariable analyses.</p><p><strong>Results: </strong>A total of 85 patients were included, 30 in the Kono-S group and 55 in the control group. At baseline, there was no significant difference between the 2 groups regarding CD characteristics or known POR risk factors, including previous exposure to biologics. At 6 to 12 months, endoscopic POR rate did not differ significantly between groups (56.7% in the Kono-S group vs 49.1% in the control group; P = .50), nor did endoscopic POR according to the modified Rutgeerts score ≥i2b (46.7% in the Kono-S group vs 40% in the control group; P = .55). Severe endoscopic POR rates were 23.3% and 18.2% in each group, respectively. Clinical recurrence rate was similar in both groups, and no recurrent surgery occurred. By multivariable analysis, the type of anastomosis was not associated with endoscopic POR (OR, 1.229; 95% CI, 0.461-3.274, P = .68); however, postoperative treatment with anti-TNF was (OR, 0.337; 95% CI, 0.131-0.865 P = .02).</p><p><strong>Conclusions: </strong>Kono-S anastomosis was not associated with a reduced rate of endoscopic POR. 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引用次数: 0
摘要
背景:克罗恩病(CD)的手术切除率仍然很高。减少术后复发(POR)具有挑战性。除了药物治疗外,手术吻合技术还可以降低POR。我们的目的是比较Kono-S与标准回结肠吻合后的内镜POR率。方法:该研究包括2020年2月至2022年3月期间接受回结肠切除术并进行Kono-S吻合的所有连续CD患者。对这些患者进行前瞻性随访,并在手术后6至12个月进行结肠镜检查。将患者与在同一中心进行传统吻合手术的历史患者队列进行比较。主要终点是内镜下POR(Rutgeerts评分≥i2)。通过单变量和多变量分析评估与POR相关的因素。结果:共纳入85例患者,其中Kono-S组30例,对照组55例。在基线时,两组在CD特征或已知POR风险因素(包括之前接触过生物制品)方面没有显著差异。在6-12个月时,各组的内镜POR发生率没有显著差异(Kono-S组为56.7%,对照组为49.1%;P = .50),根据改良Rutgeerts评分≥i2b的内镜POR也没有(Kono-S组为46.7%,对照组为40%;P = .55)。各组的严重内镜POR发生率分别为23.3%和18.2%。两组患者的临床复发率相似,均未发生复发性手术。通过多变量分析,吻合类型与内镜POR无关(OR,1.229;95%CI,0.461-3.274,P = .68);然而,抗TNF的术后治疗是(OR,0.337;95%CI,0.131-0.865 P = .结论:Kono-S吻合与内镜下POR发生率的降低无关。这些结果值得在前瞻性、随机、多中心研究中得到证实。
KONO-S Anastomosis Is Not Superior to Conventional Anastomosis for the Reduction of Postoperative Endoscopic Recurrence in Crohn's Disease.
Background: Surgical resection rates remain high in Crohn's disease (CD). Reducing postoperative recurrence (POR) is challenging. Besides drug therapy, the surgical anastomosis technique may reduce POR. We aimed to compare the endoscopic POR rate after Kono-S vs standard ileocolic anastomosis.
Methods: The study included all consecutive CD patients operated on for ileocolic resection with a Kono-S anastomosis between February 2020 and March 2022. These patients were prospectively followed, and colonoscopy was performed 6 to 12 months after surgery. Patients were compared with a historical cohort of patients operated on with a conventional anastomosis in the same center. The primary end point was endoscopic POR (Rutgeerts score ≥i2). Factors associated with POR were assessed by univariate and multivariable analyses.
Results: A total of 85 patients were included, 30 in the Kono-S group and 55 in the control group. At baseline, there was no significant difference between the 2 groups regarding CD characteristics or known POR risk factors, including previous exposure to biologics. At 6 to 12 months, endoscopic POR rate did not differ significantly between groups (56.7% in the Kono-S group vs 49.1% in the control group; P = .50), nor did endoscopic POR according to the modified Rutgeerts score ≥i2b (46.7% in the Kono-S group vs 40% in the control group; P = .55). Severe endoscopic POR rates were 23.3% and 18.2% in each group, respectively. Clinical recurrence rate was similar in both groups, and no recurrent surgery occurred. By multivariable analysis, the type of anastomosis was not associated with endoscopic POR (OR, 1.229; 95% CI, 0.461-3.274, P = .68); however, postoperative treatment with anti-TNF was (OR, 0.337; 95% CI, 0.131-0.865 P = .02).
Conclusions: Kono-S anastomosis was not associated with a reduced rate of endoscopic POR. These results warrant confirmation in prospective, randomized, multicenter studies.
期刊介绍:
Inflammatory Bowel Diseases® supports the mission of the Crohn''s & Colitis Foundation by bringing the most impactful and cutting edge clinical topics and research findings related to inflammatory bowel diseases to clinicians and researchers working in IBD and related fields. The Journal is committed to publishing on innovative topics that influence the future of clinical care, treatment, and research.