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Use of Accelerated Induction Strategy of Infliximab for Ulcerative Colitis in Hospitalized Patients at a Tertiary Care Center

机译:在高等教育中心住院患者溃疡性结肠炎加速诱导策略的使用

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BackgroundInfliximab can prevent colectomy in patients hospitalized with acute severe ulcerative colitis (ASUC). In cases of ASUC, fecal losses of infliximab may lead to low drug levels and reduced efficacy.AimTo determine 90-day colectomy risk and postoperative complications in patients receiving single-dose and accelerated induction of infliximab for ASUC.MethodsWe conducted a retrospective review of patients hospitalized with ASUC requiring infliximab therapy between 2013 and 2017 at the University of Michigan. Patients were excluded if they had an enteric infection, received an anti-TNF previously, or received cyclosporine during the same admission. The primary outcome was colectomy within 90 days of admission. Patients receiving single-dose induction infliximab were compared to those receiving accelerated rescue induction with two doses of infliximab prior to day 14. Administration of accelerated induction was guided by a protocol, suggesting administering a second dose of infliximab to those with only a partial response in CRP 3 days after the initial dose. Postoperative outcomes including 30-day readmission rates and complications were compared using descriptive statistics.ResultsFrom 2013 to 2017, 66 patients with ASUC met our criteria. Thirty-three received accelerated induction (50.0%). The colectomy rate in the accelerated induction group was 30.3% versus 24.2% in the single-dose induction group (p=0.58). There was no detected difference in postoperative outcomes between the accelerated and single-dose rescue induction.ConclusionsIn this retrospective review, 69.7% of those failing to respond to single-dose infliximab were able to avoid colectomy with an accelerated rescue induction strategy without worsening postoperative outcomes. Larger studies of accelerated dosing infliximab are needed.
机译:BackgroundInfliximab可以预防与急性严重溃疡性结肠炎(ASUC)住院的患者的联络术。在ASUC的情况下,英夫利昔单抗的粪便损失可能导致药物水平低,效率降低。确定接受单剂量和加速诱导ASUC的患者的联合术风险和术后并发症。ASUCMethodswe对患者进行了回顾性审查在密歇根大学期间,用ASUC住院治疗2013年至2017年的嗜活增生治疗。如果患者患有肠溶感染,以前接受过抗TNF或在同一录取期间接受环孢菌素的患者被排除在外。在入院的90天内,主要结果是联合肌瘤。将接受单剂量诱导inciximab的患者与第14天之前的两剂英夫利昔单抗的接受加速救援诱导进行比较。通过方案引导加速诱导的施用,表明将第二剂量的英夫利昔单抗施用给那些,只有部分反应初始剂量后3天CRP。使用描述性统计数据比较了包括30天的入院率和并发症的术后结果。从2013年至2017年,ASUC的66名患者达到了我们的标准。三十三个接受加速诱导(50.0%)。加速诱导组的联菌率为30.3%,在单剂量诱导基团中对24.2%(p = 0.58)。在加速和单剂量救援诱导之间没有检测到的术语结果。结论这种回顾性审查,69.7%未能对单剂量嗜活增生的那些人能够避免具有加速救援诱导策略的联系术,而不会恶化术后结果。需要对加速给药的较大研究。

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