Isomura Yoshihiro, Yamaji Yutaka, Yamada Atsuo, Watanabe Yoshitaka, Suzuki Hirobumi, Kobayashi Yuka, Yoshida Shuntaro, Watabe Hirotsugu, Hirata Yoshihiro, Yoshida Haruhiko, Koike Kazuhiko
Department of Gastroenterology, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.
Gastrointest Endosc. 2014 Jul;80(1):118-25. doi: 10.1016/j.gie.2013.12.030. Epub 2014 Feb 8.
Nonsteroidal anti-inflammatory drugs (NSAIDs) cause a high frequency of mucosal injuries in the small intestine. However, no reliable intervention, other than cessation of NSAIDs, has been established.
To evaluate whether irsogladine maleate reduces these injuries while continuing NSAID therapy.
Prospective, interventional, endoscopist-blinded, randomized, controlled trial (RCT).
University hospital.
Patients regularly taking conventional NSAIDs for more than 4 weeks.
We initially examined small-intestinal mucosal injuries by capsule endoscopy (CE) and screened participants for the RCT. In the RCT, patients with any mucosal injury were randomly assigned to the irsogladine group (4 mg/day) or the control group.
The primary endpoint was the rate of mucosal injury improvement after 4 weeks of treatment monitored with a second CE.
Sixty-one patients were evaluated with the first CE. Small intestine mucosal injuries were found in 41 patients (67.2%) and erosive or ulcerative lesions in 21 patients (34.4%). The injury prevalence was not different with gastroprotective drug treatment. Of 41 patients enrolled, 39 (19 patients in the irsogladine group and 20 in the control group) completed the study. The improvement rate was significantly higher in the irsogladine group (16/19 patients; 84.2%) than in the control group (9/20 patients; 45.0%; P = .02).
Asymptomatic lesions, single-institution data, and single-blind setting.
Irsogladine maleate was effective for reducing NSAID-induced small-intestinal mucosal injury. (University Hospital Medical Information Network Clinical Trials Registry number UMIN000001507.).
非甾体抗炎药(NSAIDs)会导致小肠黏膜损伤的高发生率。然而,除了停用NSAIDs外,尚未确立可靠的干预措施。
评估在继续使用NSAIDs治疗的同时,马来酸伊索前列定是否能减轻这些损伤。
前瞻性、干预性、内镜医师盲法、随机对照试验(RCT)。
大学医院。
规律服用传统NSAIDs超过4周的患者。
我们最初通过胶囊内镜(CE)检查小肠黏膜损伤,并筛选参加RCT的受试者。在RCT中,有任何黏膜损伤的患者被随机分配到伊索前列定组(4毫克/天)或对照组。
主要终点是用第二次CE监测治疗4周后黏膜损伤的改善率。
61例患者接受了首次CE评估。41例患者(67.2%)发现小肠黏膜损伤,21例患者(34.4%)发现糜烂性或溃疡性病变。使用胃保护药物治疗时,损伤发生率无差异。在纳入的41例患者中,39例(伊索前列定组19例,对照组20例)完成了研究。伊索前列定组的改善率(16/19例患者;84.2%)显著高于对照组(9/20例患者;45.0%;P = 0.02)。
无症状病变、单中心数据和单盲设置。
马来酸伊索前列定对减轻NSAIDs引起的小肠黏膜损伤有效。(大学医院医学信息网络临床试验注册号UMIN000001507。)