Bazerbachi Fateh, Heffley Jason D, Abu Dayyeh Barham K, Nieto Jose, Vargas Eric J, Sawas Tarek, Zaghlol Raja, Buttar Navtej S, Topazian Mark D, Wong Kee Song Louis M, Levy Michael, Keilin Steve, Cai Qiang, Willingham Field F
Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, United States.
Division of Digestive Diseases, Department of Medicine, Emory University, Atlanta, Georgia, United States.
Endosc Int Open. 2017 Sep;5(9):E861-E867. doi: 10.1055/s-0043-114665. Epub 2017 Sep 12.
Benign gastrointestinal (GI) strictures are often refractory to standard endoscopic interventions. Fully covered coaxial lumen-apposing metal stents (LAMS) have emerged as a novel therapy for these strictures. The aim of this study was to evaluate the safety and efficacy of LAMS for refractory GI strictures.
A retrospective analysis was performed for patients who underwent LAMS placement for benign luminal strictures in three US centers between January 2014 and December 2016. The primary outcomes were technical success and initial clinical success of LAMS placement. Secondary outcomes were stent migration, rate of re-intervention, and adverse events.
A total of 49 patients underwent 56 LAMS placement procedures. Previous treatment had failed in 39 patients (79.6 %), and anastomotic strictures were the indication in 77.6 % (38/49), with the most common site being gastrojejunal (34.7 % [17/49]). Technical success was achieved in all procedures and initial clinical success was achieved in 96.4 % of all procedures (54/56). Patient initial clinical success was 95.9 % (47/49). Stent migration occurred in 17.9 % of procedures, and was more likely to occur at sites in the lower GI tract ( = 0.02). The mean stent dwell time was 100.6 days, and the mean follow-up was 169.8 days. Minor adverse events, not requiring hospitalization, occurred in 33.9 % of procedures, including subsequent stricture progression (10.7 %). In cases where LAMS were removed, mean follow-up time was 102.2 days. The re-intervention rate was 75 % at 300 days follow-up after stent removal. Of the LAMS placed at anastomotic strictures, 36.4 % required re-intervention, with approximately two-thirds of these re-interventions requiring placement of a new stent or surgery.
LAMS placement was successful for the management of refractory GI strictures, with good technical and initial clinical success rates. However, re-intervention rates after LAMS removal were high, and many strictures were not resolved by an extended period of stenting with these coaxial stents. LAMS placement offers additional therapeutic options and in selected cases might be considered a destination therapy for patients with recalcitrant benign strictures.
良性胃肠道(GI)狭窄通常对标准内镜干预治疗效果不佳。全覆膜同轴管腔贴附金属支架(LAMS)已成为治疗这些狭窄的一种新方法。本研究旨在评估LAMS治疗难治性GI狭窄的安全性和有效性。
对2014年1月至2016年12月期间在美国三个中心接受LAMS置入治疗良性管腔狭窄的患者进行回顾性分析。主要结局指标为LAMS置入的技术成功率和初始临床成功率。次要结局指标为支架移位、再次干预率和不良事件。
共有49例患者接受了56次LAMS置入手术。39例患者(79.6%)先前治疗失败,吻合口狭窄占77.6%(38/49),最常见部位为胃空肠(34.7%[17/49])。所有手术均取得技术成功,96.4%的手术(54/56)取得初始临床成功。患者初始临床成功率为95.9%(47/49)。17.9%的手术发生支架移位,在下消化道部位更易发生(P = 0.02)。支架平均留置时间为100.6天,平均随访时间为169.8天。33.9%的手术发生轻微不良事件,无需住院治疗,包括随后的狭窄进展(10.7%)。在取出LAMS的病例中,平均随访时间为102.2天。支架取出后300天随访时再次干预率为75%。在吻合口狭窄处置入的LAMS中,36.4%需要再次干预,其中约三分之二的再次干预需要置入新支架或进行手术。
LAMS置入术治疗难治性GI狭窄取得成功,技术成功率和初始临床成功率良好。然而,LAMS取出后的再次干预率较高,且许多狭窄通过使用这些同轴支架延长支架置入时间并未得到解决。LAMS置入术提供了额外的治疗选择,在某些情况下,对于顽固性良性狭窄患者可考虑作为一种终极治疗方法。