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Magnetic Compression Anastomosis (Magnamosis): First-In-Human Trial

机译:磁性压缩吻合术(MASMAMIS):首先人体试验

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Background Magnetic compression anastomosis (magnamosis) uses a pair of self-centering magnetic Harrison Rings to create an intestinal anastomosis without sutures or staples. We report the first-in-human case series using this unique device. Study Design We conducted a prospective, single-center, first-in-human pilot trial to evaluate the feasibility and safety of creating an intestinal anastomosis using the Magnamosis device. Adult patients requiring any intestinal anastomosis to restore bowel continuity were eligible for inclusion. For each procedure, 1 Harrison Ring was placed in the lumen of each intestinal segment. The rings were brought together and mated, and left to form a side to side, functional end to end anastomosis. Device movement was monitored with serial x-rays until it was passed in the stool. Patients were monitored for adverse effects with routine clinic appointments, as well as questionnaires. Results Five patients have undergone small bowel anastomosis with the Magnamosis device. All 5 patients had severe systemic disease and underwent complex open urinary reconstruction procedures, with the device used to restore small bowel continuity after isolation of an ileal segment. All devices passed without obstruction or pain. No patients have had any complications related to their anastomosis, including anastomotic leaks, bleeding, or stricture at median follow-up of 13 months. Conclusions In this initial case series from the first-in-human trial of the Magnamosis device, the device was successfully placed and effectively formed a side to side, functional end to end small bowel anastomosis in all 5 patients. No patients have had any anastomotic complications at intermediate follow-up.
机译:背景技术磁性压缩吻合术(MASMAMIS)使用一对自定心磁哈里逊环,以产生没有缝合或钉的肠吻合术。我们使用这个独特的设备报告一体式案例系列。研究设计我们进行了一项前瞻性单中心,先进的先导试验试验,以评估使用大米病装置产生肠吻合术的可行性和安全性。需要任何肠吻合恢复肠连续性的成年患者有资格包含。对于每种程序,将1个哈里森环放入每个肠道段的内腔中。将环置于搭配和交配,左侧形成一侧,功能末端至末端吻合。用串行X射线监测设备移动,直到它通过粪便。监测患者对常规诊所任命以及调查问卷进行不良反应。结果5名患者随着肉体吻合的肠吻合术。所有5名患者患有严重的全身性病和经过复杂的开放式泌尿重建程序,该装置用于在分离髂骨段后恢复小肠连续性。所有设备都通过而不妨碍或疼痛。没有患者与其吻合有关的任何并发症,包括吻合泄漏,出血或在13个月的中间随访时狭窄。结论在这一初始案例系列中,从一体式试验的大米病装置,该器件成功地放置并有效地形成了一侧到侧,功能末端以终端小肠吻合术在所有5名患者中。没有患者在中间随访中患有任何吻合组件。

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