Abstract
Endoscopic ultrasound (EUS)-guided interventions have evolved rapidly in recent years, with dedicated metal stents playing a crucial role in this process. Specifically, the invention of biflanged short metal-covered stents, including lumen-apposing metal stents (LAMS), and modifications in a variety of tubular self-expandable metal stents (SEMS), have led to innovations in EUS-guided interventions. LAMS or non-LAMS stents are commonly used in the EUS-guided drainage of pancreatic fluid collections, especially in cases of walled-off necrosis. Additionally, LAMS is commonly considered for drainage of the EUS-guided gallbladder or dilated common bile duct and EUS-guided gastroenterostomy. Fully or partially covered tubular SEMS with several new designs are being considered for EUS-guided biliary drainage. This review focuses on advances in SEMS for EUS-guided interventions and discusses related research results.
Endoscopic ultrasound (EUS)-guided interventions have rapidly evolved in recent years for the management of various pancreatobiliary diseases, with dedicated stents playing a crucial role in this process. In particular, lumen-apposing metal stents (LAMS) have revolutionized EUS-guided interventions. More recently, with the development of electrocautery-enhanced (EC)-LAMS, the procedure has become safer and more efficient with a shorter procedure time. Novel dedicated tubular self-expandable metal stents (SEMS), either fully or partially covered with innovative antimigratory designs, are being considered for EUS-guided biliary drainage (EUS-BD) procedures. This review focuses on advances in SEMS for EUS-guided interventions and discusses related research results.
LAMS is a short, fully covered dumbbell-shaped metal stent with a large diameter and antimigratory properties and was first reported by Binmoeller and Shah1 in 2011 for transluminal drainage. LAMS offers several advantages over traditionally used double-pigtail plastic stents for EUS-guided transmural drainage (EUS-TD) of pancreatic fluid collections, including a large diameter that provides improved drainage of thick or viscous contents, a wide lumen as a conduit for subsequent endoscopic interventions in the target structure, and reduced risk of migration or leakage due to their apposing property.2 Conventionally delivered LAMS also have these advantages; however, they require multiple steps for avoiding adverse events and failure of accurate deployment.3 To overcome these limitations, the novel EC-LAMS has been developed for EUS-TD that allows the endoscopist alone to deploy the SEMS in quick sequential steps. Currently, there are two popularly used types of EC-LAMS in EUS-TD: the Hot AXIOS (Boston Scientific Corporation) and the Niti-S Hot SPAXUS (Taewoong Medical), both of which were modified from an earlier version of the non-cautery-based LAMS (Fig. 1).1,4-7 The EC system eliminates the need for additional accessories such as EUS puncture needles, guidewires, or dilator devices, thereby reducing procedural complexity and the risk of adverse events.5,7 LAMS are commonly used for draining intra-abdominal fluid collections (especially peri-pancreatic fluid collections [PFC]), decompressing obstructed common bile duct (CBD), establishing gastrointestinal luminal anastomosis, and creating fistulous tracts between organs for potential future endoscopic interventions.2 In contrast to the two aforementioned LAMS, the biflanged SEMS with reduced lumen apposing capability including–NAGI stent (Taewoong Medical), Aixstent (Leufen Medical), and Hanarostent Plumber (M.I Tech.) are being used mainly for the drainage of PFC (Table 1). Therefore, the choice of LAMS type can be determined based on the clinical situation and local availability.
PFC can develop as a local complication of severe acute pancreatitis, progressing to pseudocyst or walled-off necrosis (WON) after a variable period. The PFC is the most common indication for EUS-guided transmural drainage.8 Traditionally, double double-pigtail plastic stents have been mainly used for the transmural drainage of pancreatic pseudocysts or WON. However, currently available dedicated short biflanged SEMS, with or without lumen-apposing capability, which effectively drain owing to their wider diameter and reduce the risk of stent occlusion, are increasingly being used (Fig. 2). Wide flares at both ends prevent stent migration.
In a recent randomized controlled trial, the duration of the drainage procedure was the only notable difference between LAMS and plastic stents in the treatment of WON, as treatment outcomes showed no significant difference.9 The authors suggested that patients should undergo follow-up imaging and have the stent removed after 3 weeks if the WON has resolved. This approach helps reduce the adverse events associated with LAMS.9 In contrast, a recent meta-analysis suggests that SEMS are more effective in resolving WON, with fewer instances of bleeding, a slight tendency towards lower occlusion and perforation rates, but a higher migration rate compared to plastic stents.10 However, in a more recent randomized trial, LAMS were not found to be superior to double-pigtail plastic stents for the treatment of a large WON (>15 cm).11 The result of this study may have been influenced by the protocol applied to the plastic stents group, which involved weekly dilatation to 20 mm. The insertion of coaxial short double-pigtail plastic stents through LAMS can reduce the rate of adverse events and stent occlusion in EUS-guided drainage of WON.12 The European Society of Gastrointestinal Endoscopy recommends that LAMS should be retrieved within 4 weeks to prevent stent-related adverse effects.13
A recent multicenter study demonstrated that a 15-mm-long EC-LAMS was feasible and safe for the drainage of the PFC located 10 to 14 mm from the luminal wall. In the present study, the technical and clinical success rates were high (97%). Only one patient experienced recurrence during a median follow-up of 123 days, with minimal complications.14
EUS-BD is performed frequently when endoscopic retrograde cholangiopancreatography (ERCP) fails or is infeasible. Depending on the access routes and clinical practice methods, EUS-BD procedures include EUS-guided antegrade stenting (EUS-AGS), choledochoduodenostomy (EUS-CDS), and hepaticogastrostomy (EUS-HGS).
EUS-AGS involves the placement of a stent through the stricture or papilla to the duodenum using an intrahepatic duct access. The benefit of EUS-AGS is the re-establishment of the physiological drainage of bile into the duodenum; however, there is a risk of pancreatitis due to antegrade guidewire and stent manipulation outside the papilla.15 Stent dysfunction can occur due to the reflux of duodenal contents (similar to SEMS placed using a duodenoscope) such as food material, leading to sludge formation or ascending infection.16 A recently available covered SEMS with a long duodenal extension has been used in EUS-AGS to prevent reflux cholangitis and tumor in-growth.17 This approach has demonstrated favorable clinical outcomes, with technical and clinical success rates reaching 96% and 84%, respectively. The reintervention rate was low at 8.3%; however, but there was an increased incidence of post-procedural pancreatitis (24%) in patients with non-pancreatic cancers.17
In EUS-CDS, an anastomosis is established between the duodenum and CBD using either a tubular-covered biliary SEMS or LAMS. According to a recent literature review spanning from 2015 to 2020, the overall technical success rate was 95.0%, and the overall clinical success rate was 97.0%.18 Sufficient sealing of the anastomosis can be challenging when using a plastic stent or an uncovered SEMS, that can increase the risk of bile leakage. As a result, either a fully covered SEMS or LAMS is preferred for EUS-CDS. According to a recent meta-analysis comparing the efficacy of LAMS and SEMS for EUS-CDS, the rates of clinical and technical success, post-procedure adverse events, and reintervention were similar between the two types of stents.19
In a recent guideline, it is recommended to utilize partially or fully covered SEMS for EUS-HGS because of the increased risk of bile leakage with uncovered SEMS and challenges associated with placing pure double-pigtail stents.15 However, there is a risk of migration of fully covered SEMS, which can lead to bile leak, persistent biliary obstruction, and subsequent cholangitis. To address these limitations, the use of hybrid SEMS has been proposed.20,21 Hybrid SEMS are partially covered SEMS equipped with anchoring flaps specifically designed to prevent stent migration (Fig. 3). In a long-term follow-up study evaluating the effectiveness of newly developed hybrid SEMS, no instances of stent migration were observed during the median follow-up period of 148.5 days, and the mean duration of stent patency was recorded as 166.3 days.20 Based on a recent study, it was found that covered SEMS could be a more suitable choice for patients with malignant biliary obstruction undergoing EUS-HGS. This preference is justified by the longer time until recurrent biliary obstruction.22
For patients with cholecystitis and high-risk surgical candidates, EUS-guided gallbladder drainage (EUS-GBD) has demonstrated technical and clinical success rates comparable to those of percutaneous techniques.23,24 In the transmural approach to EUS-GBD, a stent is inserted under EUS guidance from the duodenum or stomach into the gallbladder. The use of pigtail plastic stents and biliary SEMS is not suitable due to their risk of leakage, potential for contralateral wall injury or occlusions caused by their longer length, and the risk of migration due to the absence of flanges.25 LAMS have successfully addressed these limitations by featuring a short length with large flanges and offering a wide range of diameters (6–20 mm, Fig. 4). This allows for the passage of gallstones or the endoscope as required during therapeutic cholecystoscopy.26,27 The commonly employed LAMS sizes for EUS-GBD encompass saddle lengths of 10 and 15 mm, along with inner diameters of 10, 15, and 20 mm.25 It is customary to routinely place a double-pigtail plastic biliary stent across the LAMS as a potential measure to mitigate complications such as bleeding, stent obstruction, and contralateral wall injury resulting from the LAMS. However, this practice has not been universally adopted.28
Advancements in EUS have facilitated the emergence of EUS-guided gastroenterostomy (EUS-GE) as a potentially minimally invasive approach that utilizes LAMS. It has emerged as a safe and effective palliative procedure for gastric outlet obstruction (GOO) in patients unfit for surgery.29-31 A recent large multicenter study including 310 patients with GOO showed that EUS-GE can be performed in patients with nutritional deficiencies without compromising the technical (97.9% vs. 100%) and clinical success rates (94.1% vs. 94.3%) when compared to surgical gastrojejunostomy. Additionally, EUS-GE showed a lower occurrence of adverse events (13.4% vs. 33.3%, p<0.001) while enabling earlier resumption of diet and chemotherapy. A 15 mm or 20 mm diameter, 10 mm long EC-LAMS was used in this study.32 Another comparative study demonstrated that the technical success rate of EUS-GE was comparable to that of surgical gastrojejunostomy, while exhibiting significantly fewer adverse events (8% vs. 41%, p=0.01).33
Endoscopic ultrasound-directed transgastric ERCP (EDGE) provides a nonsurgical biliary intervention in patients with Roux-en-Y gastric bypass for bariatric treatment. EUS-guided gastrogastrostomy is first performed using LAMS to establish a conduit between the gastric pouch and the excluded remnant stomach. Once the LAMS stent is sufficiently dilated, a duodenoscope is passed to perform ERCP. EDGE appears to have successfully addressed the technical difficulties associated with enteroscopy-assisted ERCP.34 While there is growing guidance on the technical execution of EDGE, with limited data regarding the removal of LAMS and the long-term closure of fistulas. While immediate removal of the LAMS during the index procedure might provide practical and economic benefits, it could also result in free perforation. Therefore, it is recommended to remove the stent gradually over time as long as no further interventions are deemed necessary after tract maturation.15
Recently, several new types of stents have been developed. Tornado stent (S&G Biotech Inc.) is a fully covered, braided, twisted SEMS with spirally coiled ends. It was constructed using a nitinol wire coated with silicone (Fig. 5A). An animal study showed that EUS-GBD using the Tornado stent was technically feasible without any adverse events.35 The authors highlighted that the Tornado stent’s relatively flexible spiral coiled ends may help to reduce the occurrence of serious adverse events such as bleeding or stent burying. The risk of mechanical complications may be lower because the spiral-coiled ends on both sides have a fixation effect without a flange. Furthermore, the presence of spiral-coiled ends is expected to decrease the risk of stent migration and ascending infection compared with tubular SEMS. Spring Stopper Stent (Taewoong Medical) is a recently developed, partially covered SEMS designed for EUS-HGS. It features a spring-line anchoring function on the gastric side (Fig. 5B). This pilot retrospective study demonstrated the feasibility and safety of a Spring Stopper Stent for EUS-HGS. Spring-like anchoring on the gastric side appears to be an effective mechanism for preventing migration.36
With the remarkable advancements in SEMS, the scope of EUS-guided interventions is expanding and becoming more efficient. Recent developments in dedicated stents have made this procedure simpler and safer. However, the development of LAMS requires further technical refinements to enhance its safety profile and broaden its applications to other indications. In clinical practice, LAMS is recommended for EUS-guided WON/pseudocyst drainage, EUS-GBD, and EUS-GE, with different diameters based on the distance between the lumens. Covered or hybrid SEMS are useful in EUS-CDS and EUS-HGS. Additionally, it is crucial to conduct well-designed randomized trials and prospective studies to critically evaluate the impact of this technology on EUS-guided interventions.
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