首页> 外文期刊>Colon & Rectum >Laparoscopic Ileocecal Resection versus Infliximab for Terminal Ileitis in Crohn's Disease: a Randomized, Controlled, Open-Label, Multicentre Trial Lancet Gastroenterol Hepatol 2017;2:785-92
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Laparoscopic Ileocecal Resection versus Infliximab for Terminal Ileitis in Crohn's Disease: a Randomized, Controlled, Open-Label, Multicentre Trial Lancet Gastroenterol Hepatol 2017;2:785-92

机译:腹腔镜同性恋切除对克罗恩病的末尾inileitis intiximab术语:随机,受控,开放标签,多长期试验柳叶肠胃肠肝肝肝庚醇2017; 2:785-92

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Background: Patients with ileocaecal Crohn's disease who have not responded to conventional therapy are commonly treated with biological agents, but surgery can also offer excellent short-term and long-term results. We compared laparoscopic ileocaecal resection with inflixi-mab to assess how they affect health-related quality of life. Methods: In this randomised, controlled, open-label trial, adults with non-stricturing, ileocaecal Crohn's disease, in whom conventional therapy has failed were randomly allocated (1:1) from 29 teaching hospitals and tertiary care centres in the Netherlands and the UK, by an internet randomisation module with biased-coin minimisation for participating centres and perianal fistula to receive laparoscopic ileocaecal resection or infliximab. Eligible patients were aged 18-80 years, had active Crohn's disease of the terminal ileum, and had not responded to at least 3 months of conventional therapy with glucocorticosteroids, thiopuri-nes, or methotrexate. Patients with diseased terminal ileum longer than 40 cm or abdominal abscesses were excluded. The primary outcome was quality of life on the Inflammatory Bowel Disease Questionnaire (IBDQ) at 12 months. Secondaiy outcomes were general quality of life, measured by the Short Form-36 (SF-36) health survey and its physical and mental component subscales, days unable to participate in social life, days on sick leave, morbidity (additional procedures and hospital admissions), and body image and cos-mesis. Analyses of the primary outcome were done in the intention-to-treat population, and safety analyses were done in the per-protocol population. This trial is registered at the Dutch Trial Registry (NTR1150). Findings: Between May 2, 2008 and October 14, 2015, 73 patients were allocated to have resection and 70 to receive infliximab. Corrected for baseline differences, the mean IBDQ score at 12 months was 178.1 (95% confidence interval, CI: [171.1-185.0]) in the resection group versus 172.0 (164.3-179.6) in the infliximab group (mean difference: 6.1 points; 95% CI: [-4.2 to 16.4]; P = 0.25). At 12 months, the mean SF-36 total score was 112.1 (95% CI: [108.0-116.2]) in the resection group versus 106.5 (102.1-110.9) in the infliximab group (mean difference: 5.6; 95% CI: [-0.4 to 11.6]), the mean physical component score was 47.7 (45.7-49.7) versus 44.6 (42.5-46.8; mean difference: 3.1, 4.2 to 6.0), and the mean mental component score was 49.5 (47.0-52.1) versus 46.1 (43.3-48.9; mean difference 3.5, -0.3 to 7.3). Mean numbers of days of sick leave were 3.4 days (standard deviation, SD: 7.1) in the resection group versus 1.4 day (4.7) in the infliximab group (P< 0.0001), days not able to take part in social life were 1.8 day (6.3) versus 1.1 day (4.5; P = 0.20), days of scheduled hospital admission were 6.5 days (3.8) versus 6.8 days (3.2; P — 0.84), and the number of patients who had unscheduled hospital admissions were 13 (18%) of 73 versus 15 (21%) of 70 (P = 0.68). Body image scale mean scores in the patients who had resection were 16.0; (95% CI: [15.2-16.8]) at baseline versus 17.8 (17.1-184) at 12 months, and cosmetic scale mean scores were 17.6 (16.6-18.6) versus 18.6 (17.6-19.6). Surgical intervention-related complications classified as Ilia or worse on the Clavien-Dindo scale occurred in four patients in the resection group. Treatment-related serious adverse events occurred in two patients in the infliximab group. During a median follow-up of 4 years (interquartile range, IQR: 2-6), 26 (37%) of 70 patients in the infliximab group had resection and 19 (26%) of 73 patients in the resection group received anti-TNF. Interpretation: Laparoscopic resection in patients with limited (diseased terminal ileum < 40 cm), non-stricturing, ileocaecal Crohn's disease in whom conventional therapy has failed could be considered a reasonable alternative to infliximab therapy.
机译:背景:对患有常规治疗患者的患者患者通常用生物药物治疗,但手术也可以提供出色的短期和长期结果。我们将腹腔镜对象与英夫利·米巴尔进行比较,以评估它们如何影响与健康有关的生活质量。方法:在这种随机,受控,开放式试验中,具有非严格的成年人,常规治疗失败的IleocaeCal Crohn病人(1:1)来自荷兰的29家教学和第三级护理中心英国,通过互联网随机化模块,具有偏置硬币最小化的参与中心和肛周瘘,以接受腹腔镜对象切除或英夫利昔单抗。符合条件的患者年龄18-80岁,患有活跃的克罗恩病,终端肠道疾病,并没有应对至少3个月的常规治疗葡糖皮质激素,Thiopuri-Nes或甲氨蝶呤。患有患病患者患者,患者患者患者长于40厘米或腹部脓肿。主要结果是在12个月内对炎症性肠病疾病调查问卷(IBDQ)的生活质量。替代结果是一般生活质量,通过短的形式-36(SF-36)卫生调查及其身体和精神成分分量来衡量,日子无法参与社会生活,病假日的日子,发病率(额外的程序和医院招生)和身体形象和Cos-mesis。在意图对治疗人口中进行了主要结果的分析,并且在每协定人口中进行了安全分析。此试验在荷兰试验登记处注册(NTR1150)。调查结果:2008年5月2日至2015年10月14日之间,分配了73名患者进行切除,70例接受英夫利昔单抗。纠正基线差异,12个月的平均IBDQ评分为178.1(95%置信区间,CI:[171.1-185.0])在英夫利昔单抗组中的172.0(164.3-179.6)(平均差异:6.1点; 95%CI:[-4.2至16.4]; p = 0.25)。在12个月时,平均SF-36总得分为112.1(95%CI:[108.0-116.2])在FlowixImab组中的106.5(102.1-110.9)中(平均差异:5.6; 95%CI:[ -0.4至11.6]),平均物理分量得分为47.7(45.7-49.7),而44.6(42.5-46.8;平均差异:3.1,4.2至6.0),平均精神成分评分为49.5(47.0-52.1)与46.1(43.3-48.9;平均差异3.5,-0.3至7.3)。切除组的病假日的平均天数为3.4天(标准偏差,SD:7.1),与英夫利昔单抗组(P <0.0001)中的1.4天(4.7),天不能够参加社会生活的日子为1.8天(6.3)与1.1天(4.5; p = 0.20),预定医院入院的天数为6.5天(3.8),而6.8天(3.2; p-0.84),以及未划分的医院入院的患者的数量为13(18) %73与15(21%)为70(p = 0.68)。身体图像规模平均分数在切除切除16.0; (95%CI:[15.2-16.8])在基线而不是17.8(17.1-184),12个月,化妆品尺度平均分数为17.6(16.6-18.6),而不是18.6(17.6-19.6)。外科干预相关的并发症被归类为伊利亚或克拉夫尼亚 - DINDO规模差异发生在切除组中的四名患者中。治疗相关的严重不良事件发生在英夫利昔单抗组中的两名患者中。在4岁的中位后续(IQR:2-6),26例(37%)的70名患者中,英夫利昔单抗组的70名患者患有19例(26%)的分解组患者的抗切除症TNF。解释:腹腔镜切除有限公司(患病末端<40厘米),常规治疗失败的术语患者,无狭窄,常规治疗失败的疾病可能被视为富集昔单抗治疗的合理替代品。

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