Department of Surgery, Iatriko Medical Center, Palaio Faliro, Greece; Weight Management Program, Holyoke Medical Center, Holyoke, Massachusetts.
Department of Surgery, Iatriko Medical Center, Palaio Faliro, Greece.
Surg Obes Relat Dis. 2017 Jul;13(7):1174-1182. doi: 10.1016/j.soard.2017.02.016. Epub 2017 Feb 21.
The Elipse Balloon is a swallowable gastric balloon for weight loss that can be deployed without the use of endoscopy or anesthesia. This study aims to report on 12-month safety and efficacy outcomes.
Private hospital, Athens, Greece.
This was a prospective, nonrandomized open trial. Twelve patients between 18 and 64 years of age with a body mass index (BMI) of 27.0 to 40.0 kg/m were enrolled. The Elipse capsule is swallowed with water and its location in the stomach is confirmed by x-ray. All patients received diet and exercise counseling only during the therapy period (0-4 mo). Eight months later they were seen in clinic to assess 12-month outcomes.
There were 7 (58.3%) females and 5 (41.7%) males. The mean age was 41 years, mean BMI was 35.9 kg/m, mean weight was 103.5±15.8 kg, and mean waist circumference was 117.6±14.9 cm. All patients swallowed the balloon. Eleven (91.7%) balloons were filled and were included in subsequent analysis. All balloons were excreted safely, and no serious adverse events were reported. Accommodative symptoms were not severe and of very short duration. Mean excess weight loss percentage and total weight loss percentage were 50.2% and 14.6% at balloon excretion and 17.6% and 5.9% at 12 months, respectively. There was a statistically significant improvement in patients' weight, BMI, body fat, waist circumference, diastolic blood pressure, HbA1C, cholesterol, thyroid stimulating hormone, aspartate transaminase, and alanine transaminase at balloon excretion. Quality of life was significantly improved at excretion and 12 months.
This study is the first to demonstrate 12-month efficacy and performance outcomes of the Elipse Balloon.
Elipse 球囊是一种可吞咽的减肥胃球囊,无需使用内窥镜或麻醉即可部署。本研究旨在报告 12 个月的安全性和疗效结果。
希腊雅典的一家私立医院。
这是一项前瞻性、非随机开放试验。共纳入 12 名年龄在 18 至 64 岁之间、BMI 为 27.0 至 40.0kg/m 的患者。Elipse 胶囊用水吞咽,通过 X 射线确认其在胃中的位置。所有患者在治疗期间(0-4 个月)仅接受饮食和运动咨询。8 个月后,他们在诊所就诊,以评估 12 个月的结果。
有 7 名(58.3%)女性和 5 名(41.7%)男性。平均年龄为 41 岁,平均 BMI 为 35.9kg/m,平均体重为 103.5±15.8kg,平均腰围为 117.6±14.9cm。所有患者均吞咽了球囊。11 个(91.7%)球囊充盈并纳入后续分析。所有球囊均安全排出,无严重不良事件报告。适应性症状不严重且持续时间很短。球囊排出时,平均超重减轻百分比和总体重减轻百分比分别为 50.2%和 14.6%,12 个月时分别为 17.6%和 5.9%。患者的体重、BMI、体脂、腰围、舒张压、HbA1C、胆固醇、甲状腺刺激激素、天门冬氨酸转氨酶和丙氨酸转氨酶在球囊排出时均有统计学显著改善。排出时和 12 个月时的生活质量均显著改善。
本研究首次证明了 Elipse 球囊的 12 个月疗效和性能结果。