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A randomized trial of a fully covered self-expandable metallic stent versus plastic stents in anastomotic biliary strictures after liver transplantation

机译:完全覆盖自膨胀金属支架与塑料支架在肝移植术后吻合胆道狭窄中的随机试验

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Background: Post-liver-transplant biliary anastomotic strictures (ASs) are currently managed with repeated endoscopic retrograde cholangiopancreatographies (ERCPs) inserting multiple plastic stents. Fully covered self-expanding metal stents (FCSEMSs) are being increasingly reported in the management of this condition, however no prospective randomized trials have been performed to date. Aim: The aim of this study was to determine whether FCSEMSs decrease overall numbers of ERCPs needed to achieve stricture resolution and to establish the safety, efficacy and costeffectiveness in this setting. Methods: Two tertiary referral centres performed this open-label prospective randomized trial. A total of 32 patients consented and subsequently 20 were randomized with 10 in the FCSEMS arm and 10 in the plastic arm. The FCSEMS arm had the stent in situ for 12 weeks with the plastic stent arm undergoing 3-monthly multiple plastic stenting with or without dilatation over a year. Results: The median number of ERCPs performed per patient in the FCSEMS was 2 versus 4.5 (p = 0.0001) in the plastic stenting arm. Stricture resolution was achieved in all 10 patients with FCSEMSs compared with 8/10 in the plastic arm [p = not significant (NS)]. Complications occurred in 1/10 patients in the FCSEMS arm versus 5/10 in the plastic arm (p = 0.051). Days in hospital for complications was 6 in the FCSEMS versus 56 in the plastic arm (p = 0.11). Cost analysis shows that the FCSEMS arm was more cost effective. No cases of FCSEMS migration were seen. Conclusions: FCSEMSs reduced the number of ERCPs needed to achieve stricture resolution with similar recurrence rates between arms. The FCSEMSs may do so with fewer complications making it cost effective.
机译:背景:肝移植术后胆管吻合口狭窄(ASs)目前通过插入多个塑料支架的内窥镜逆行胰胆管造影术(ERCP)进行治疗。在这种情况的治疗中,越来越多地报道了完全覆盖的自膨胀金属支架(FCSEMS),但是迄今为止尚未进行任何前瞻性随机试验。目的:本研究的目的是确定FCSEMS是否减少了达到严格解决方案所需的ERCP总数,并确定了在这种情况下的安全性,有效性和成本效益。方法:两个三级转诊中心进行了这项开放标签的前瞻性随机试验。共有32位患者同意,随后将20位患者随机分组,其中FCSEMS组为10位,塑料组为10位。 FCSEMS臂在原位放置了12周的支架,塑料支架臂接受了为期3个月的多次塑料支架植入(有或没有扩张),历时一年。结果:FCSEMS中每个患者执行的ERCP的中位数为2个,而塑料支架置入术中为4.5个(p = 0.0001)。在所有10例FCSEMS患者中,均达到了严格的分辨率,而在塑料臂中则为8/10 [p =不显着(NS)]。 FCSEMS组的并发症发生率为1/10,而塑料组的并发症发生率为5/10(p = 0.051)。 FCSEMS中因并发症而住院的天数为6天,而整形臂则为56天(p = 0.11)。成本分析表明,FCSEMS部门更具成本效益。没有观察到FCSEMS迁移的案例。结论:FCSEMS减少了达到狭窄解决方案所需的ERCP数量,并且两臂之间的复发率相似。 FCSEMS可以减少并发症,从而使其具有成本效益。

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