Morgan D G, O'Mahony M F J, O'Mahony W F, Roy J, Camacho F, Dinniwell J, Horbay G L A, Husein-Bhabha F A
Division of Gastroenterology, St Joseph's Healthcare, Hamilton, Canada.
Can J Gastroenterol. 2007 Dec;21(12):820-6. doi: 10.1155/2007/203201.
OBJECTIVE: To evaluate continuous therapy (COT) and on-demand therapy (ODT) with rabeprazole 20 mg for maintenance in uninvestigated gastroesophageal reflux disease (GERD). METHODS: This randomized, open-label study enrolled 331 GERD (heartburn-predominant) patients with a pre-existing proton pump inhibitor history of one month or longer, to an acute four-week trial with 20 mg rabeprazole daily for heartburn management. Patients who achieved satisfactory heartburn control during the acute phase (three days or less of heartburn, with no more than one episode rated as moderate, and heartburn rated satisfactorily or completely controlled with minimal rescue antacid use in the seven days preceding randomization) were randomly assigned to six months of rabeprazole 20 mg given as either daily COT or daily ODT, which was initiated upon symptom recurrence and stopped upon symptom resolution. Rescue antacid usage was permitted and tracked. Primary efficacy was measured as the proportion of heartburn-free days over six months. RESULTS: For the 268 patients, the mean percentage of heartburn-free days for the COT group and for the ODT group were 90.3%+/-14.8% and 64.8%+/-22.3%, respectively (P<0.0001). COT was associated with an increased number of medication intake days (154+/-40.2) versus ODT (68+/-46.1), with less heartburn episodes observed with COT versus ODT, respectively (n=7, n=26, P<0.0001). Ninety-two per cent of COT patients and 79% of ODT patients were either 'satisfied' or 'very satisfied' with treatment. The mean usage of antacids was low and similar in both groups. COT and ODT regimens were safe and well-tolerated, with a similar incidence of adverse events. CONCLUSION: Results based on symptom assessments favour COT with rabeprazole 20 mg for maintenance therapy in patients with uninvestigated GERD; however, both therapy types are safe and acceptable treatment options for selected patients.
目的:评估20毫克雷贝拉唑持续治疗(COT)和按需治疗(ODT)在未经调查的胃食管反流病(GERD)维持治疗中的效果。 方法:这项随机、开放标签研究纳入了331名以烧心为主的GERD患者,这些患者既往使用质子泵抑制剂的时间为1个月或更长,进行为期四周的急性试验,每天服用20毫克雷贝拉唑以控制烧心症状。在急性期达到满意烧心控制的患者(烧心天数为3天或更少,不超过1次发作被评为中度,且在随机分组前7天使用最少的急救抗酸剂即可使烧心症状得到满意或完全控制)被随机分配接受为期6个月的20毫克雷贝拉唑治疗,分为每日持续治疗(COT)或症状复发时开始、症状缓解时停止的每日按需治疗(ODT)。允许并跟踪急救抗酸剂的使用情况。主要疗效指标为6个月内无烧心天数的比例。 结果:对于268名患者,COT组和ODT组无烧心天数的平均百分比分别为90.3%±14.8%和64.8%±22.3%(P<0.0001)。COT组的用药天数增加(154±40.2天),而ODT组为(68±46.1天),COT组观察到的烧心发作次数少于ODT组(分别为n=7,n=26,P<0.0001)。92%的COT组患者和79%的ODT组患者对治疗“满意”或“非常满意”。两组抗酸剂的平均使用量较低且相似。COT和ODT方案安全且耐受性良好,不良事件发生率相似。 结论:基于症状评估的结果支持在未经调查的GERD患者中使用20毫克雷贝拉唑进行持续治疗以维持疗效;然而,对于选定的患者,这两种治疗类型都是安全且可接受的治疗选择。
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