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Kidney transplantation in patients with inflammatory bowel diseases ( IBD IBD ): analysis of transplantation outcome and IBD IBD activity

机译:肾移植患者炎症肠疾病(IBD IBD):移植成果和IBD IBD活动分析

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Summary Inflammatory bowel diseases ( IBD ) is a systemic disorder with possible renal involvement, yet data regarding the outcome of kidney transplantation ( KT ) in those patients, and IBD course post KT , are scarce. In this retrospective analysis, we studied the outcome of 12 IBD kidney recipients (seven Crohn's disease, five ulcerative colitis; primary kidney disease was IgA nephropathy in five, polycystic disease in four), compared to two control groups: matched controls and a cohort of recipients with similar kidney disease. During a follow‐up period of 60.1 (11.0–76.6) months (median, interquartile range), estimated 5‐year survival was 80.8 vs. 96.8%, with and without IBD , respectively ( P = 0.001). Risk of death with a functioning graft was higher with IBD ( HR = 1.441, P = 0.048), and with increased age ( HR = 1.109, P = 0.05). Late rehospitalization rate was higher in IBD [incidence rate ratio = 1.168, P = 0.030], as well as rate of hospitalization related to infection [1.42, P = 0.037]. All patients that were in remission before KT , remission was maintained. Patients that were transplanted with mild or moderate disease remained stable or improved with Infliximab or Adalimumab treatment. In conclusion, IBD is associated with an increased risk of mortality, hospitalization because of infection and late rehospitalization after KT . Clinical course of IBD is stable after KT .
机译:发明内容炎症性肠病(IBD)是一种具有可能肾脏受累的全身性疾病,但是关于这些患者的肾移植(KT)结果的数据,以及IBD课程kt,是稀缺的。在这种回顾性分析中,我们研究了12个IBD肾脏受体的结果(七克罗恩疾病,五种溃疡性结肠炎;原发性肾脏疾病是IGA肾病,四种,多囊疾病四分之二),与两种对照组相比:匹配的对照和群组具有相似肾病的接受者。在60.1的后续期间(11​​.0-76.6)个月(中位数,狭隘的范围),估计5年生存率为80.8 vs.96.8%,分别有和没有IBD(P = 0.001)。 IBD(HR = 1.441,P = 0.048)的功能接枝死亡的风险较高,年龄增加(HR = 1.109,P = 0.05)。 IBD的后期再生活力率较高[入射率比= 1.168,P = 0.030],以及与感染相关的住院率[1.42,P = 0.037]。所有在KT之前的缓解患者,保持缓解。用温和或中度疾病移植的患者保持稳定或随英匹昔单抗的治疗稳定或改善。总之,IBD与增加的死亡风险增加,由于感染和KT后的后期重新治疗。 KT后IBD的临床过程是稳定的。

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