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Prospective trial evaluating new circular and linear stapler devices for gastrointestinal anastomosis: preliminary data

机译:评估新型圆形和线性吻合器用于胃肠道吻合术的前瞻性试验:初步数据

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摘要

Several commercial models of stapler devices are available. This study evaluated the ease of use, effectiveness and safety of new commercial stapling devices for gastrointestinal anastomosis. A total of 11 patients (5 men) requiring surgical therapy for benign or malignant disease of the digestive tract were recruited between July and October 2006. Eleven patients were treated with KYGW circular stapler or KYFB linear stapler (Changzhou Kangdi Medical Stapler). In these patients, 14 staplers were used and 21 stapled sutures (16 linear, 5 circular) were performed. Number of anastomoses successfully completed, postoperative anastomotic fistula or dehiscence, days to take fluid and normal diet, length of hospital stay and anastomotic stenosis were recorded. A 10-point questionnaire enquiring about the instrument and anastomotic features was administered to surgeons immediately after the operation in the study group and in 10 control patients treated with standard CDH circular and SDH linear staples (Ethicon Endo-Surgery). Mean scores on the questionnaire for the experimental and control groups were good (>7.5) and did not significantly differ for handling, closing ease, bleeding, and overall satisfaction. No case of intra-abdominal sepsis, leakage or intestinal obstruction was recorded in the study group. In the 5 patients with colorectal anastomosis, the anastomotic lumen at 15 days was wide open and at 3 months there were no strictures. These new instruments are valuable for performing gastrointestinal anastomosis and are in conformity with clinical requirements; their use is simple and seems to be safe.
机译:有几种钉书机设备的商业型号。这项研究评估了用于胃肠道吻合的新型商用吻合器的易用性,有效性和安全性。 2006年7月至2006年10月,共招募11例需要手术治疗消化道良性或恶性疾病的患者(5名男性)。11例患者接受了KYGW圆形吻合器或KYFB线性吻合器(常州康迪医用吻合器)治疗。在这些患者中,使用了14根订书机,并进行了21根缝合线(16根线性,5根圆形)。记录成功完成吻合术的次数,术后吻合瘘或裂开,采取液体和正常饮食的天数,住院时间和吻合口狭窄。在研究组和10名接受标准CDH圆形和SDH线性吻合钉治疗的对照患者(Ethicon Endo-Surgery)手术后,立即向外科医师进行了10点问卷调查,询问了器械和吻合口的特征。实验组和对照组的问卷平均得分均良好(> 7.5),并且在处理,闭合舒适度,出血和总体满意度方面无显着差异。在研究组中没有记录到腹内脓毒症,渗漏或肠梗阻的病例。在5例大肠吻合患者中,吻合腔在15天时是敞开的,在3个月时没有狭窄。这些新仪器对于进行胃肠道吻合非常有价值,并且符合临床要求。它们的使用很简单,而且似乎很安全。

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