Lashner B A, Hanauer S B, Silverstein M D
Section of Gastroenterology, University of Chicago Medical Center, Illinois 60637.
Dig Dis Sci. 1990 Jul;35(7):827-32. doi: 10.1007/BF01536795.
Epidemiologic studies have documented an association between nonsmoking and ulcerative colitis and case reports have demonstrated that symptoms improve with smoking and worsen with removal of a nicotine source. A double-blind randomized crossover trial for individual ulcerative colitis patients (single-patient trial, or N of 1 clinical trial) was designed to study the safety, patient acceptance, and the effectiveness of nicotine gum in improving patient symptoms and proctoscopic appearance of involved colon. Seven nonsmoking patients chewed up to 10 squares/day (20 mg) of nicotine gum or placebo gum for two weeks. Therapy was crossed-over every two weeks over the eight-week trial. Effectiveness was judged from comparisons between nicotine-gum and placebo-gum periods of patient self-reported symptoms at the conclusion of each two-week period using visual analog scales and proctoscopic appearance using ordered categorical scales. Three of seven patients, all three of whom were former smokers, demonstrated sufficient improvement without adverse effects to warrant institution of nicotine gum into their drug treatment regimens. Three patients demonstrated an uncertain response, despite tolerating the drug, and have not had nicotine gum added to their regimens. One patient could not tolerate the medication and was withdrawn from the study. No serious side effects were noted. We conclude that a randomized trial for an individual patient is a useful method for evaluating treatment regimens for ulcerative colitis and that nicotine gum may be effective therapy for individual patients with ulcerative colitis who demonstrate an objective response with few adverse effects.
流行病学研究已证明非吸烟与溃疡性结肠炎之间存在关联,病例报告表明症状在吸烟时改善,而在去除尼古丁来源时恶化。一项针对个体溃疡性结肠炎患者的双盲随机交叉试验(单患者试验,即N-of-1临床试验)旨在研究尼古丁口香糖在改善患者症状及受累结肠直肠镜检查外观方面的安全性、患者接受度和有效性。7名非吸烟患者每天咀嚼多达10片(20毫克)尼古丁口香糖或安慰剂口香糖,为期两周。在为期八周的试验中,每两周进行一次治疗交叉。有效性通过在每两周结束时使用视觉模拟量表比较尼古丁口香糖期和安慰剂口香糖期患者自我报告的症状,以及使用有序分类量表比较直肠镜检查外观来判断。7名患者中有3名,且这3名均为既往吸烟者,显示出足够的改善且无不良反应,因此有理由将尼古丁口香糖纳入其药物治疗方案。3名患者尽管耐受该药物,但反应不确定,未将尼古丁口香糖添加到其治疗方案中。1名患者无法耐受该药物,退出了研究。未观察到严重副作用。我们得出结论,针对个体患者的随机试验是评估溃疡性结肠炎治疗方案的一种有用方法,且尼古丁口香糖可能是对有客观反应且不良反应少的个体溃疡性结肠炎患者的有效治疗方法。