Talley N J, Lauritsen K, Tunturi-Hihnala H, Lind T, Moum B, Bang C, Schulz T, Omland T M, Delle M, Junghard O
Department of Medicine, University of Sydney, Nepean Hospital, Penrith, NSW, Australia.
Aliment Pharmacol Ther. 2001 Mar;15(3):347-54. doi: 10.1046/j.1365-2036.2001.00943.x.
Most patients with gastro-oesophageal reflux disease (GERD), regardless of endoscopic status, suffer symptomatic relapse within 6 months of stopping acid suppressant therapy.
To assess the efficacy of 'on-demand' treatment of GERD with esomeprazole, the first proton pump inhibitor developed as an optical isomer.
In this multicentre, double-blind study, 342 endoscopy-negative GERD patients demonstrating complete resolution of heartburn during the final week of a 4-week treatment period with esomeprazole 20 mg or omeprazole 20 mg once daily were randomized to receive esomeprazole 20 mg or placebo on demand (maximum of one dose per day) for a further 6 months. Use of rescue antacids was permitted.
All 342 patients (191 males), aged 19-79 (mean 49) years, were evaluable in the intention-to-treat analysis. The proportion of patients who discontinued treatment due to insufficient control of heartburn was significantly higher among placebo compared to esomeprazole recipients (51% vs. 14%; P < 0.0001). Patients randomized to esomeprazole on-demand therapy remained in the study longer than those in the placebo group (mean 165 vs. 119 days). Over 50% took the study medication for periods of 1--3 consecutive days (esomeprazole) or 4--13 consecutive days (placebo). Use of antacids was > 2-fold higher among placebo recipients. The frequency of adverse events was similar in the two groups, when adjusted for time spent in the study, as were the clinical laboratory profiles.
On-demand therapy with esomeprazole 20 mg is effective and well tolerated in maintaining symptom control in endoscopy-negative GERD.
大多数胃食管反流病(GERD)患者,无论内镜检查结果如何,在停止抑酸治疗后的6个月内都会出现症状复发。
评估埃索美拉唑对GERD进行“按需”治疗的疗效,埃索美拉唑是首个作为光学异构体开发的质子泵抑制剂。
在这项多中心、双盲研究中,342例内镜检查阴性的GERD患者在接受为期4周的每日一次20 mg埃索美拉唑或20 mg奥美拉唑治疗的最后一周烧心症状完全缓解,这些患者被随机分配,在接下来的6个月中按需接受20 mg埃索美拉唑或安慰剂治疗(每天最多一剂)。允许使用急救抗酸剂。
在意向性分析中,所有342例患者(191例男性),年龄19 - 79岁(平均49岁)均可评估。与接受埃索美拉唑治疗的患者相比,安慰剂组中因烧心症状控制不佳而停药的患者比例显著更高(51% 对14%;P < 0.0001)。随机接受埃索美拉唑按需治疗的患者在研究中的停留时间比安慰剂组更长(平均165天对119天)。超过50% 的患者连续1 - 3天(埃索美拉唑)或4 - 13天(安慰剂)服用研究药物。安慰剂组患者使用抗酸剂的频率高出两倍多。调整在研究中的时间后,两组不良事件的发生率相似,临床实验室指标也相似。
20 mg埃索美拉唑按需治疗在维持内镜检查阴性的GERD患者症状控制方面有效且耐受性良好。