O'Hara Fintan John, Costigan Conor, Mc Namara Deirdre
Gastroenterology, Tallaght University Hospital, Dublin, Ireland.
Gastroenterology, Trinity College Dublin, Dublin, Ireland.
Endosc Int Open. 2025 Mar 14;13:a24656918. doi: 10.1055/a-2465-6918. eCollection 2025.
Small bowel capsule endoscopy (SBCE) is crucial in diagnosing small bowel diseases, yet incomplete examinations often result from prolonged gastric transit time. This study aimed to assess the efficacy of orally administered peppermint oil solution as a prokinetic agent to improve SBCE completion rates in patients with delayed gastric transit risk factors.
Conducted as a single-center, prospective, open-label, non-inferiority trial, the study involved 132 patients identified as at risk for delayed gastric transit. Participants were divided into three groups: peppermint oil solution group (n = 57), real-time monitoring and intravenous prokinetics group (n = 75), and control group without risk factors (n = 193). Primary outcomes included SBCE completion rates, gastric transit time (GTT), small bowel transit time (SBTT), diagnostic yield, and bowel preparation quality.
Completion rates were high and comparable among groups, with 94.7% in the peppermint group, 90.7% in the real-time monitoring group, and 95.3% in the control group. The peppermint group exhibited a significantly shorter mean GTT of 42.3 minutes compared with 57.0 minutes in the real-time monitoring group ( = 0.0423). However, SBTT was longer in the peppermint group at 246 minutes versus 193 minutes in the real-time monitoring group ( = 0.0081), although similar to the control group at 228.3 minutes ( = 0.2612). Diagnostic yield and bowel preparation quality were consistent across all groups.
Oral peppermint oil solution is a safe and effective alternative to traditional prokinetics, enhancing SBCE completion rates while reducing time and resource use in the endoscopy unit.
小肠胶囊内镜检查(SBCE)对于诊断小肠疾病至关重要,但胃排空时间延长常导致检查不完整。本研究旨在评估口服薄荷油溶液作为促动力剂对提高有胃排空延迟风险因素患者的SBCE完成率的疗效。
本研究为单中心、前瞻性、开放标签、非劣效性试验,纳入132例被确定有胃排空延迟风险的患者。参与者分为三组:薄荷油溶液组(n = 57)、实时监测与静脉使用促动力剂组(n = 75)和无风险因素对照组(n = 193)。主要结局包括SBCE完成率、胃排空时间(GTT)、小肠排空时间(SBTT)、诊断率和肠道准备质量。
各组完成率均较高且相当,薄荷组为94.7%,实时监测组为90.7%,对照组为95.3%。薄荷组的平均GTT显著缩短,为42.3分钟,而实时监测组为57.0分钟(P = 0.0423)。然而,薄荷组的SBTT较长,为246分钟,而实时监测组为193分钟(P = 0.0081),尽管与对照组的228.3分钟相似(P = 0.2612)。所有组的诊断率和肠道准备质量一致。
口服薄荷油溶液是传统促动力剂的一种安全有效的替代方法,可提高SBCE完成率,同时减少内镜检查科室的时间和资源消耗。