Mizuki Akira, Tatemichi Masayuki, Sakakibara Terue, Miura Yukihiko, Zeki Shigeyuki, Ohata Mitsuru, Matsuo Kenji, Kawamura Fumio, Nagata Hiroshi
Department of Internal Medicine, Keiyu Hospital, Yokohama, Japan.
Department of Preventive Medicine, Tokai University School of Medicine, Isehara, Japan.
Curr Ther Res Clin Exp. 2016 Nov 25;79:1-7. doi: 10.1016/j.curtheres.2016.11.002. eCollection 2016.
Approximately 20% to 40% of patients with gastroesophageal reflux disease (GERD) are refractory to standard-dose proton-pump inhibitor (PPI) treatment.
We compared the efficacy and quality-of-life effects of 20 mg once daily (QD) versus 10 mg twice daily (BID) rabeprazole (RPZ) in patients with refractory GERD-related symptoms and sleep disturbances.
This multicenter, prospective, randomized, open-label study included patients in whom PPI treatment >4 weeks was ineffective. According to the Global Overall Symptom (GOS) scale, PPI-refractory GERD was defined as ≥1 category with >3 points among 10 specific upper gastrointestinal symptoms. Seventy-eight patients were randomly assigned to 20 mg QD and 10 mg BID RPZ groups for 8 weeks. Efficacy was evaluated using self-reported questionnaires, including the GOS scale and Pittsburg Sleep Quality Index (PSQI), whereas quality of life was assessed using the Short-Form 8 Health Survey (SF-8), at 4 and 8 weeks. Patients showing improvement at 8 weeks received follow-up every 4 to 8 weeks.
GOS scale scores were significantly improved at 8 weeks in both groups, with no significant intergroup differences. Although SF-8 scores showed an increasing trend over 8 weeks in both groups, the physical component summaries in the 10 mg BID group significantly improved. The mental component summaries clearly improved in the 10 mg BID group. Of the 74 cases (4 missing), 51 (68.9%) had PSQI scores ≥5.5. PSQI scores remained unchanged during follow-up in both groups. The recurrence rate was not significantly different (46.1% vs 47.1% in the 20 mg QD and 10 mg BID groups, respectively) during the follow-up period at median (interquartile range) 24.0 (30.5) months.
In patients with refractory GERD, there was no significant difference in GOS scale score, PSQI, or recurrence rate between the groups. With regard to subscores of the SF-8, the 10 mg BID group might be potentially effective.
约20%至40%的胃食管反流病(GERD)患者对标准剂量质子泵抑制剂(PPI)治疗无效。
我们比较了20毫克每日一次(QD)与10毫克每日两次(BID)雷贝拉唑(RPZ)对难治性GERD相关症状和睡眠障碍患者的疗效及生活质量影响。
这项多中心、前瞻性、随机、开放标签研究纳入了PPI治疗超过4周无效的患者。根据全球总体症状(GOS)量表,PPI难治性GERD被定义为在10种特定上消化道症状中,≥1类症状得分>3分。78例患者被随机分为20毫克QD组和10毫克BID RPZ组,治疗8周。在第4周和第8周时,使用自我报告问卷评估疗效,包括GOS量表和匹兹堡睡眠质量指数(PSQI),而生活质量则使用简短健康调查(SF-8)进行评估。在第8周显示改善的患者每4至8周接受一次随访。
两组在第8周时GOS量表评分均显著改善,组间无显著差异。虽然两组的SF-8评分在8周内均呈上升趋势,但10毫克BID组的身体成分总结显著改善。10毫克BID组的心理成分总结明显改善。在74例(4例缺失)病例中,51例(68.9%)的PSQI评分≥5.5。两组在随访期间PSQI评分均保持不变。在中位(四分位间距)24.0(30.5)个月的随访期内,复发率无显著差异(20毫克QD组和10毫克BID组分别为46.