Guslandi Mario, Giollo Patrizia, Testoni Pier Alberto
Gastroenterology Unit, S. Raffaele University Hospital, Milan, Italy.
Curr Ther Res Clin Exp. 2004 May;65(3):292-6. doi: 10.1016/S0011-393X(04)80097-3.
The role of enteric flora in the pathogenesis of inflammatory bowel disease constitutes the rationale for the use of antibiotics as adjuvant agents in the treatment of ulcerative colitis (UC) and Crohn's disease.
The aim of this study was to assess, in a preliminary fashion, the efficacy of the nonabsorbable antibiotic rifaximin in the treatment of exacerbation of UC in patients with a history of poor corticosteroid tolerance.
This open label pilot study was conducted in the Gastroenterology Unit, S. Raffaele University Hospital (Milan, Italy). Male and female patients aged 18 to 65 years with an established diagnosis of left-sided UC who were experiencing a clinical relapse during maintenance treatment with mesalamine and with a history of poor tolerance to corticosteroid therapy were included in the study. They received rifaximin 400 mg BID for 4 weeks while continuing to receive mesalamine 2.4 g/d. Disease activity before and after treatment was assessed using Rachmilewitz's Activity Index (RAI). A final RAI score <6 was considered clinical remission.
Ten patients (9 men, 1 woman; mean [sd]age, 48.1 [12.3] years [range, 23-64 years]) participated in the study. The RAI decreased in all patients. Rifaximin treatment induced clinical remission in 7 patients (70%). No adverse effects were reported.
Due to our study design, no definitive Conclusions can be drawn. However, our preliminary data suggest that rifaximin may be beneficial in the treatment of active UC, obviating corticosteroid therapy in most cases.
肠道菌群在炎症性肠病发病机制中的作用构成了将抗生素用作溃疡性结肠炎(UC)和克罗恩病治疗辅助药物的理论依据。
本研究旨在初步评估不可吸收抗生素利福昔明对皮质类固醇耐受性差的UC患者病情加重的治疗效果。
这项开放标签的试点研究在意大利米兰圣拉斐尔大学医院胃肠病科进行。纳入年龄在18至65岁之间、确诊为左侧UC且在美沙拉嗪维持治疗期间出现临床复发、有皮质类固醇治疗耐受性差病史的男性和女性患者。他们在继续接受每日2.4g美沙拉嗪治疗的同时,接受利福昔明400mg每日两次,共4周。使用拉赫米列维茨活动指数(RAI)评估治疗前后的疾病活动度。最终RAI评分<6被视为临床缓解。
10名患者(9名男性,1名女性;平均[标准差]年龄为48.1[12.3]岁[范围23 - 64岁])参与了研究。所有患者的RAI均下降。利福昔明治疗使7名患者(70%)实现临床缓解。未报告不良反应。
由于我们的研究设计,无法得出明确结论。然而,我们的初步数据表明,利福昔明可能对活动性UC的治疗有益,在大多数情况下可避免使用皮质类固醇治疗。