首页> 外文期刊>BMC research notes >Effect of a proprietary intraluminal stiffening wire device on cecal intubation time and rate with used colonoscopes; a randomized, controlled trial
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Effect of a proprietary intraluminal stiffening wire device on cecal intubation time and rate with used colonoscopes; a randomized, controlled trial

机译:使用专用结肠镜在专用腔内加强线装置对盲肠插管时间和速率的影响;随机对照试验

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Background Colonoscopes are designed with balance between flexibility, required to negotiate angulations, and stiffness, required to counteract the propensity for looping in unfixed sections of the colon, which retards advancement of the instrument. Colonoscopy can be challenging with old instruments that have lost native stiffness and become less responsive to torquing. A new intraluminal stiffening device has become available in two grades of stiffness. However, there is no published evidence of its effectiveness. This randomized, controlled trial was designed to determine the effectiveness of the stiffening wires in improving cecal intubation rate and time following routine application. A secondary analysis determines effectiveness of application only after intractable failure with the unaided colonoscope. Methods The colonoscope tested was an Olympus CF-100TL, approximately fifteen years old. Patients were randomly assigned to the unaided colonoscope or the standard or firm wire introduced routinely on entry into transverse colon. Each phase of colonoscopy was timed. Failure to advance the colonoscope for 5?minutes (despite usual manipulations to minimize looping) required switching to another intervention according to a prescribed methodology and the originally assigned intervention was recorded as failed. Results The study was terminated after accrual of 112 participants (target sample size 480) because the colonoscope required repairs (no damage attributable to stiffening wires) which would have been uneconomical. There were no statistically significant differences between per-protocol cecal intubation rates (81.1, 71.1 and 70.3 percent respectively), a finding which persisted after multiple imputation for a virtual sample size of 480. Similarly, there were no statistically significant differences between per-protocol cecal intubation times (15, 16.2 and 13.9?minutes). However, a statistically significant improvement in cecal intubation rate (from 81.1% to 97.3%, P?=?0.0313) was achieved when the wires were applied after intractable failure of the unaided colonoscope in the first intervention group. Conclusions Routine application of either stiffening wire does not improve caecal intubation rate nor time compared to the unaided colonoscope. However, application of the stiffening wires after intractable failure of the unaided colonoscope enabled a statistically significant improvement in cecal intubation rate. Trial Registration clinicaltrials.gov Identifier: NCT01115010
机译:背景技术结肠镜的设计要在平衡弯曲所需的灵活性和抵抗结肠的未固定部分成环的倾向所需的刚度之间取得平衡,这阻碍了器械的发展。结肠镜检查对于已经失去天然刚度并且对扭矩的响应变得较不灵敏的旧器械可能具有挑战性。一种新的腔内加固装置已经可以提供两种等级的刚度。但是,没有公开的证据证明其有效性。该随机对照试验旨在确定加强线在常规应用后改善盲肠插管率和时间的有效性。辅助分析仅在使用独立结肠镜进行顽固性治疗后才能确定应用的有效性。方法测试的结肠镜是一台大约15岁的Olympus CF-100TL。患者被随机分配到无助结肠镜或进入横结肠时常规引入的标准或牢固的金属丝。结肠镜检查的每个阶段都是定时的。未能将结肠镜推进5分钟(尽管通常进行了操作以最大程度地减少循环),需要根据规定的方法切换至另一种干预措施,并且最初分配的干预措施被记录为失败。结果招募了112名参与者(目标样本量480)后终止了该研究,因为结肠镜需要进行修理(没有因金属丝变硬造成的损坏),这是不经济的。每种方案的盲肠插管率之间没有统计学上的显着差异(分别为81.1%,71.1%和70.3%),这一发现在多次插补后仍然存在,虚拟样本量为480。类似地,每种方案之间也没有统计学上的显着差异盲肠插管时间(15、16.2和13.9分钟)。然而,在第一个干预组中,在无辅助结肠镜的顽固性衰竭后应用导线,盲肠插管率有统计学上的显着提高(从81.1%增至97.3%,P1 =?0.0313)。结论与单独的结肠镜相比,常规应用两种加固线都不会提高盲肠插管率或时间。然而,在无辅助结肠镜顽固性衰竭后应用加强线,能够实现盲肠插管率的统计学显着改善。试验注册临床试验.gov标识符:NCT01115010

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