Endoscopy Unit, Sant'Andrea University Hospital, "Sapienza" University of Rome, Italy; Gastro Unit, Division of Endoscopy, Copenhagen University Hospital Herlev, Denmark; Endoscopy Unit, Nuovo Regina Margherita Hospital, Rome, Italy.
Gastro Unit, Division of Endoscopy, Copenhagen University Hospital Herlev, Denmark.
Dig Liver Dis. 2020 Nov;52(11):1294-1301. doi: 10.1016/j.dld.2020.04.021. Epub 2020 Jun 3.
Endoscopic ultrasound-guided gastro-enteric anastomosis (EUS-GEA) using lumen-apposing metal stents (LAMS) is emerging as a minimally invasive alternative to surgery across several indications. Literature on this subject is heterogeneous, with variable reporting of techniques and outcomes. Our aim was to perform a meta-analysis of published data on EUS-GEA, providing a pooled estimate of technical and clinical outcomes.
The protocol was registered in PROSPERO (Reg. no. CRD42018111110). PubMed, Embase, Scopus, and Web of Science databases were searched until February 2019 for studies describing patients undergoing EUS guided enteric anastomosis. PRISMA methodology was used. Pooled technical and clinical success rates as well as pooled adverse events rates were calculated. Study quality, publication bias, and heterogeneity were explored.
Twelve studies including 290 patients were included, published between 2016 and 2019. All studies but one were retrospective. Main procedure indication was gastric outlet obstruction (62.4%), followed by ERCP access (27.9%) in patients with gastric bypass surgery. Direct puncture technique was the most frequently adopted (68.2%). Pooled technical success rate (12 studies, 290 patients) was 93.5% [95% confidence interval (CI) 89.7-6.0%; I:0%], while clinical success rate (11 studies, 260 patients) was 90.1% [95%CI 85.5-93.4%; I:0%]. Pooled total adverse events rate (11 cohorts, 261 patients) was 11.7% [95%CI 8.2-16.6%; I:0%], mainly mild/moderate: 10.6% [95%CI 7 - 15.6%]. No publication bias or significant heterogeneity was found.
EUS-GEA has a high rate of technical and clinical success when performed in expert centers. The procedure appears to be relatively safe, and might represent a non-inferior minimally invasive alternative to surgery. The paucity of long-term clinical outcomes suggests prudency and need for further research, especially regarding non-malignant indications.
内镜超声引导下胃肠吻合术(EUS-GEA)使用 lumen-apposing 金属支架(LAMS),正在成为多种适应证下替代手术的微创选择。关于这个主题的文献是异质的,技术和结果的报告各不相同。我们的目的是对发表的关于 EUS-GEA 的数据进行荟萃分析,提供技术和临床结果的汇总估计。
该方案已在 PROSPERO(注册号:CRD42018111110)中注册。直到 2019 年 2 月,我们在 PubMed、Embase、Scopus 和 Web of Science 数据库中搜索了描述接受 EUS 引导肠吻合术的患者的研究。使用 PRISMA 方法。计算了汇总技术和临床成功率以及汇总不良事件发生率。研究质量、发表偏倚和异质性进行了探讨。
共纳入 12 项研究,包括 290 例患者,发表时间为 2016 年至 2019 年。除一项研究外,所有研究均为回顾性研究。主要手术适应证为胃出口梗阻(62.4%),其次为胃旁路手术后 ERCP 入路(27.9%)。最常采用的是直接穿刺技术(68.2%)。汇总技术成功率(12 项研究,290 例患者)为 93.5%[95%置信区间(CI)89.7-6.0%;I:0%],而临床成功率(11 项研究,260 例患者)为 90.1%[95%CI 85.5-93.4%;I:0%]。汇总总不良事件发生率(11 个队列,261 例患者)为 11.7%[95%CI 8.2-16.6%;I:0%],主要为轻度/中度:10.6%[95%CI 7-15.6%]。未发现发表偏倚或显著异质性。
在专家中心进行 EUS-GEA 具有较高的技术和临床成功率。该手术相对安全,可能是手术的非劣效微创替代方法。缺乏长期临床结果表明需要谨慎和进一步研究,特别是针对非恶性适应证。