Cuomo Antonio, Sgambato Dolores, D'Auria Mauro Valeriano, Miranda Agnese, Ferrante Emanuele, Romano Marco
Gastroenterology Unit "Umberto I" Hospital, Nocera Inferiore, Salerno, Italy.
Hepatogastroenterology Unit, Università Degli Studi Della Campania "Luigi Vanvitelli", Naples, Italy.
Dig Dis. 2018;36(2):130-135. doi: 10.1159/000485614. Epub 2018 Jan 16.
Mesalazine 1 g suppository/die is used for mild to moderately active ulcerative proctitis (UP). Whether addiction of Multi Matrix System (MMX) mesalazine increases the remission rate of UP and prevents proximal extension of disease is unknown.
This is a retrospective study on 116 outpatients with UP who had been treated with one of the following regimens: (1) MMX mesalazine 1.2 g/die plus mesalazine suppositories for 8 ± 2 weeks and, subsequently, MMX mesalazine 1.2 g/die plus rectal mesalazine 1 g every other day for at least 6 months; (2) mesalazine 1 g suppositories/die alone for 8 ± 2 weeks and, subsequently, rectal mesalazine 1 g every other day for 6 more months. Patients were evaluated clinically at 2 months (±2 weeks) and endoscopically at 6 months (±2 weeks). For categorical variables, Pearson chi-square test was used.
A total of 46 of 55 patients (84%) on combined therapy and 49 of 61 patients (80%) on rectal mesalazine reached clinical remission (p > 0.05; OR 0.79, 95% CI 0.30-2.07). At 6 months follow-up, proximal extension of disease was observed in 7 of 55 (14%) patients on combined therapy and in 18 of 61 (29%) patients on rectal mesalazine alone (p < 0.05; OR 2.87, 95% CI 1.09-7.53).
Oral MMX mesalazine plus rectal mesalazine combined treatment is associated with prevention of proximal extension of the disease compared with rectal mesalazine alone.
美沙拉嗪1克栓剂/日用于治疗轻至中度活动性溃疡性直肠炎(UP)。多基质系统(MMX)美沙拉嗪是否会增加UP的缓解率并预防疾病近端扩展尚不清楚。
这是一项对116例UP门诊患者的回顾性研究,这些患者接受了以下方案之一的治疗:(1)MMX美沙拉嗪1.2克/日加美沙拉嗪栓剂治疗8±2周,随后,MMX美沙拉嗪1.2克/日加直肠用美沙拉嗪1克隔日治疗至少6个月;(2)单独使用美沙拉嗪1克栓剂/日治疗8±2周,随后,直肠用美沙拉嗪1克隔日再治疗6个月。在2个月(±2周)时对患者进行临床评估,在6个月(±2周)时进行内镜评估。对于分类变量,使用Pearson卡方检验。
联合治疗组的55例患者中有46例(84%)、直肠用美沙拉嗪组的61例患者中有49例(80%)达到临床缓解(p>0.05;OR 0.79,95%CI 0.30 - 2.07)。在6个月的随访中,联合治疗组的55例患者中有7例(14%)出现疾病近端扩展,单独使用直肠用美沙拉嗪组的61例患者中有18例(29%)出现疾病近端扩展(p<0.05;OR 2.87,95%CI 1.09 - 7.53)。
与单独使用直肠用美沙拉嗪相比,口服MMX美沙拉嗪加直肠用美沙拉嗪联合治疗与预防疾病近端扩展相关。