|Year : 2019 | Volume
| Issue : 1 | Page : 36-42
Placement of lumen-apposing metal stents to drain pseudocysts and walled-off pancreatic necrosis can be safely performed on an outpatient basis: A multicenter study
Douglas G Adler1, Janak Shah2, Jose Nieto3, Kenneth Binmoeller2, Yasser Bhat2, Linda Jo Taylor1, Ali A Siddiqui4
1 Division of Gastroenterology and Hepatology, University of Utah Hospital, Salt Lake City, UT, USA
2 Division of Gastroenterology, California Pacific Medical Center, San Francisco, CA, USA
3 Department of Gastroenterology, Borland-Groover Clinic, Jacksonville, FL, USA
4 Division of Gastroenterology and Hepatology, Thomas Jefferson University Hospital, Philadelphia, PA, USA
|Date of Submission||20-Dec-2016|
|Date of Acceptance||22-Apr-2017|
|Date of Web Publication||17-May-2018|
Dr. Ali A Siddiqui
Thomas Jefferson University, 132 S. 10th Street, Main Building, Philadelphia, PA 19107
Source of Support: None, Conflict of Interest: None
Backgrounds and Objectives: No study on the use of lumen-apposing fully covered self-expanding metal stent (LAMS) to drain pancreatic fluid collections (PFCs) has evaluated outcomes of patients in the outpatient setting. The objective of this multicenter study was to evaluate the clinical outcomes, success rate, and adverse events of the LAMS for endoscopic ultrasound (EUS)-guided transmural drainage of patients with symptomatic PFCs on an inpatient versus an outpatient basis. Methods: This was a multicenter, retrospective study conducted at 4 tertiary care centers. Results: We identified eighty patients with PFCs in whom EUS-guided transmural drainage using the LAMS was performed. The mean age of the patients was 53.1 years old. Mean size of the PFC was 11.8 ± 5.1 cm. A total of 33 patients had PFCs drained in an outpatient setting while 47 patients underwent PFC drainage as inpatients. The overall technical success (ability to access and drain a PFC by placement of transmural stents) was 98.7% (79 patients). There was no statistically significant difference in the technical success rate between the inpatient and outpatient groups (100% vs. 98%, respectively, P = 1). There was no significant difference in resolution of PFCs in the inpatient and outpatient groups (91% vs. 87% respectively; P = 1). The number of procedures required for PFC resolution was significantly lower in the inpatient group as compared to the outpatients (2.3 vs. 3.1 respectively, P = 0.025). Procedure-related adverse events were significantly lower in the inpatient group compared to the outpatient group (P < 0.01). There was no significant difference in the 2 groups in terms of development of adverse events requiring endoscopic reintervention within 30 days of initial stent placement (P = 0.69). Conclusion: This study shows that LAMS placement for PFCs can be performed safely on an outpatient basis with overall technical and clinical outcomes that are comparable to those seen in inpatients.
Keywords: Acute pancreatitis, endosonography, pancreatic fluid collections
|How to cite this article:|
Adler DG, Shah J, Nieto J, Binmoeller K, Bhat Y, Taylor LJ, Siddiqui AA. Placement of lumen-apposing metal stents to drain pseudocysts and walled-off pancreatic necrosis can be safely performed on an outpatient basis: A multicenter study. Endosc Ultrasound 2019;8:36-42
|How to cite this URL:|
Adler DG, Shah J, Nieto J, Binmoeller K, Bhat Y, Taylor LJ, Siddiqui AA. Placement of lumen-apposing metal stents to drain pseudocysts and walled-off pancreatic necrosis can be safely performed on an outpatient basis: A multicenter study. Endosc Ultrasound [serial online] 2019 [cited 2019 May 24];8:36-42. Available from: http://www.eusjournal.com/text.asp?2019/8/1/36/232608
| Introduction|| |
Pancreatic fluid collections (PFCs) are commonly encountered clinical entities and are thought to arise due to pancreatic duct damage in patients with acute or chronic pancreatitis, pancreatic trauma, iatrogenic injuries (i.e., surgery), and in patients with a disrupted pancreatic duct., PFCs are generally divided into two groups: pancreatic pseudocysts (PPs) and walled-off necrosis (WON). PPs are defined as of fluid collections in the peripancreatic tissues that are surrounded by a well-defined wall and contain no solid material. WONs are defined as consisting of necrotic tissue contained within a wall of reactive tissue. Most PFCs are small and asymptomatic and many resolve spontaneously. Nonetheless, some PFCs become symptomatic usually due to a large size that produces when they increase in size or become infected, leading to symptoms including abdominal pain, early satiety, gastric outlet obstruction, biliary obstruction with concomitant jaundice, and sepsis.
The current management options for symptomatic PFCs include endoscopic, surgical, and percutaneous drainage.,, The surgical approach is most invasive and carries a high mortality and morbidity. PFCs drained through the percutaneous approach are at risk of fistula formation, cyst recurrence, and infections.
In the last decade, endosonography-guided drainage of PFCs through the placement of transmural stents has become the procedure of choice in many tertiary care centers, often viewed as the first-line therapy instead of surgical or interventional radiology approaches. Recently, a novel “saddle-shaped” lumen-apposing fully covered self-expanding metal stent (LAMS) with both proximal and distal anchor flanges has been demonstrated to be both safe and effective for endoscopic transmural drainage of PPs and WONs and is often used in place of a covered biliary metal stent or double-pigtail stents.,,,
To date, no study on the use of LAMS to drain PFCs has evaluated the role and outcomes of patients in the outpatient setting. It is unknown if LAMS placement warrants inpatient admission at the time of placement or is safe to be performed in outpatients. Other high-risk endoscopic procedures, including ERCP, percutaneous endoscopic gastrostomy, and interventional endoscopic ultrasound (EUS) procedures, are routinely performed in the outpatient setting. The objective of this large multicenter study was to evaluate the overall clinical outcomes, success rate, and adverse events of the LAMS for EUS-guided transmural drainage of patients with symptomatic PFCs in the United States, in those undergoing the procedure on an inpatient versus an outpatient basis.
| Methods|| |
This was a multicenter, retrospective study conducted at 4 tertiary care centers. The study was approved by the Institutional Review Boards in all centers. The study concept, hypothesis, and design were investigator initiated and no financial support was received.
The endoscopy database at Thomas Jefferson University Hospital, University of Utah Hospitals and Clinics, Borland-Groover Clinic and California Pacific Medical Center was queried for all patients who had undergone EUS-guided drainage of PFCs (i.e., PP and WON) using the LAMS between February 2012 and June 2016. Only patients with a 3-month or greater follow-up were included in the study. WON consisted of a mature, encapsulated collection of pancreatic, and/or peripancreatic necrotic tissue contained within an enhancing wall of reactive tissue. PP was defined as an encapsulated collection of fluid with a well-defined inflammatory wall usually outside the pancreas with minimal or no necrosis (as per the Revised Atlanta Classification).
Inpatients were already admitted at the time of the procedure. Outpatients were patients who came in as outpatients to the endoscopy suite and in whom there were no plans to admit unless a complication occurred. Patients were hospitalized preprocedure if they had intractable pain, evidence of fevers, or inability to take oral intake or other symptoms of concern. Patients were admitted if they developed a complication from their endoscopy. PFCs were characterized by a variety of techniques including magnetic resonance imaging or computed tomography (CT) as well as EUS on the day of their initial drainage procedure. Indications for drainage of PFCs were as follows: (1) signs or symptoms of infection in the PFC, (2) abdominal pain felt to be attributable to the PFC, (3) gastric outlet or biliary obstruction due to extrinsic compression through the PFC, (4) ongoing systemic illness, anorexia, nausea, vomiting, and weight loss, or (5) rapidly enlarging PFCs. Patients with interposed vessels or significant varices, cystic neoplasms, coagulopathy (international normalized ratio >1.6), and significant thrombocytopenia (platelets <50,000/mm3), or cyst imaging showing that the PFC wall was not in proximity (>1 cm) to the gastric or duodenal lumen were excluded from the study. Data were obtained from inpatient and outpatient hospital records to collect procedural details and overall clinical course of the patient. In addition, records from hospitals in our region are available through our electronic medical record to facilitate data capture from events occurring beyond the site of endoscopic intervention.
Description of the lumen-apposing fully covered self-expanding metal stent
The LAMS (AXIOS™; Boston Scientific, Natick MA) utilized in this study is a saddle-shaped, braided flexible stent made of nitinol that is fully covered with a silicon membrane. The stent is manufactured with bilateral double-walled anchoring flanges designed to hold the stomach or duodenal wall in close apposition to PFC wall. The stent is 10 mm in length and is available in 10 or 15 mm diameter sizes.
All patients underwent procedures by endoscopists with >5 years of active EUS practice (D.G.A., A.A.S., J.N., J.N.S., K.F.B., Y.M.B.). All endoscopists have prior experience with PFC drainage through traditional techniques. PFC drainage was performed in all cases through a therapeutic linear array echoendoscope (GF-UCT180; Olympus, USA). All procedures were performed under general anesthesia and all patients were administered broad-spectrum antibiotics during and after the procedure to decrease the risk of infection. A careful EUS examination before LAMS placement was used to determine the optimal puncture site of the cyst in all patients. Color Doppler was used to exclude interposed vessels at the puncture site 19-gauge EUS fine-needle aspiration needles were used to perform the initial puncture into the cyst under real-time imaging. The cyst contents were then aspirated for visual inspection (e.g., viscosity, debris, pus) and sent for fluid analysis (e.g., tumor markers, cytology, culture) if felt to be warranted the discretion of the endoscopist. A 0.035” guidewire was then inserted through the needle and allowed to coil several times into the cyst cavity under EUS and fluoroscopic guidance. The needle was then withdrawn over the wire. Cystgastrostomy tract dilation was performed with either an 8F–10F Soehendra dilator (Cook Medical, Winston-Salem NC, USA) or a 6 mm or 8 mm wire-guided balloon (Hurricane, Boston Scientific, Natick MA, USA) based on the preference of the endoscopist. After the cystgastrostomy was dilated, the LAMS delivery catheter was advanced over the wire and into the cyst cavity. Of note, the LAMS device used in this study was the so-called “Cold-Axios” that did not have a diathermic tip on the catheter. Once the LAMS catheter was in good position in the PFC, the distal half of the stent was deployed under EUS guidance with or without fluoroscopic guidance at the discretion of the endoscopist. Deployment of the proximal flange of the stent was then performed under endoscopic guidance. The selection of stent diameter was at the discretion of the endoscopist; although, in general, if the PFC was felt to contain significant debris, a 15 mm LAMS was placed to facilitate the future necrosectomy procedures. The deployed stent lumen was then dilated up to 10 or 15 mm with a controlled radial expansion balloon (Boston Scientific) to allow for optimal stent luminal expansion if felt to be indicated by the endoscopist.
In patients with WON, subsequent endoscopic necrosectomy procedures were performed using a standard upper endoscope advanced through the LAMS at times dictated by the preference of the endoscopist, usually every 3–7 days until complete resolution of the necrotic cavity as confirmed endoscopically and/or by results obtained through cross-sectional imaging.
Any complication occurring or after during the procedure including perforation, bleeding, infection, development of pancreatitis or worsening of existing pancreatitis, hypotension, or respiratory distress was carefully documented. The electronic medical records of hospital admissions, emergency room visits, and/or clinic visits were also compiled in an effort to identify any delayed complication (up to 30 days after procedure).
All patients underwent contrast-enhanced CT of the abdomen at 4–8 weeks after LAMS placement followed in an outpatient clinic visit. LAMS removal was performed when complete cyst decompression was achieved, i.e., the PFC had completed resolved without any residual intracystic solid or fluid component remaining.
Technical success was defined as the ability to place and deploy a LAMS stent transmurally without difficulty. Successful drainage of the PFC based on endoscopy or cross-sectional imaging results 1 month after the therapy with at least a 50% reduction in PFC size and resolution of clinical symptoms as documented in clinic follow-up notes, respectively.
Immediate procedure-related adverse events were defined as those that occurred within 1 week after the procedure. Reinterventions included the need to replace or remove migrated LAMS, repeat PFC drainage due to LAMS stent occlusion, cyst cavity infection with inadequate drainage through the LAMS, enlarging cyst size despite LAMS placement, or worsening of clinical symptoms due to the PFC.
The primary outcome of this study was to evaluate the overall long-term success and adverse event rate of LAMS usage in inpatients versus outpatients. Patients were considered inpatients if they were either inpatients at the time of PFC placement or admitted to the hospital after LAMS placement. Patients were considered outpatients if they came from home for their LAMS placement and returned home the same day without being admitted to the hospital at all. Outpatients were carefully monitored for any adverse event that would require inpatient admission after being discharged to home.
Long-term success was defined as complete resolution of the pseudocyst and resolution of the patient's symptoms without need for reintervention at 3 months following initial treatment as demonstrated by ambulatory clinic follow-up and cross-sectional imaging. Secondary outcomes evaluate included adverse events, number of endoscopic reinterventions, and PFC recurrence rates after the stent removal.
This was a retrospective cohort study. We divided the subjects into 2 groups according to the setting of the PFC drainage 1) outpatient and 2) inpatient. Outcomes between the groups were compared using the Student's t test for continuous variables and the Chi-square test for categorical variables. Generalized linear modeling (GLM) were performed on categorical and continuous variables, respectively, in order to assess any difference in outcomes in the outpatient versus inpatient setting. Statistical significance was determined a priori at P ≤ 0.05.
| Results|| |
Patient demographics and pancreatic fluid collection characteristics
From February 2012 to June 2016, we identified 80 patients with PFCs in whom EUS-guided transmural drainage using the LAMS was performed. All PFCs developed after the episodes of acute pancreatitis. The mean age of the patients was 53.1 ± 15 years and 40% were female. The etiology of pancreatitis was gallstone (49%), alcohol (30%), idiopathic (8%), drug-induced (2%), autoimmune (1%), and hypertriglyceridemia (10%). The clinical presentation in patients that required drainage included abdominal pain, nausea and vomiting, anorexia and early satiety, and biliary obstruction [Table 1].
|Table 1: Patient demographics and pancreatic fluid collection characteristics|
Click here to view
PFCs were located in the pancreatic head (5%), pancreatic body and tail (84%), and involved the pancreatic head/body/tail (11%). Mean size of the PFC was 11.8 ± 5.1 cm in the long axis (range, 4.8–25 cm).
Of the eighty patients, 12 presented with PP and 68 patients had WONs. There was no significant difference in sex, etiology, or cyst size between patients with PP and WON. Patients with WON were younger (51.7 vs. 61 years respectively, P = 0.04) and were predominantly white (82.3% vs. 50% respectively, P = 0.02) when compared to those with PP. Twenty percent of patients had failed prior endoscopic or interventional radiology intervention before our endoscopist intervention.
Inpatients and outpatients that underwent pancreatic fluid collection drainage
There were 33 patients whose PFC cavity was drained in an outpatient setting while 47 patients underwent PFC drainage using the LAMS as inpatients. Transgastric drainage was performed in 74 patients (92.5%), 5 patients (6.25%) had transduodenal drainage, and 1 (1.25%) patients had multiport stent drainage/debridement. Seventy-two patients had a 15 mm wide x10 mm long LAMS placed and 8 had a 10 mm × 10 mm diameter LAMS placed. The median duration that the stents remained implanted was 1 month (range, 1–6 months). Nine patients had a concomitant ERP with transpapillary pancreatic stent placement for a concomitant pancreatic duct leak contributing to WONs as seen on MRCP. Twenty-two patients had placement of an 8Fr nasocystic catheter due to the presence of large amount of solid debris inside the WON cavity and nasocystic lavage was performed with bolus perfusions of saline for 1–2 days after initial LAMS placement [Table 2].
The overall technical success (ability to access and drain a PFC by the placement of transmural stents) was 98.7% (79 patients). There was no statistically significant difference in the technical success rate between the inpatient and outpatient groups (100% vs. 98% respectively, P = 1). Unsuccessful placement of the LAMS in 1 patient in the outpatient group was as a result of stent maldeployement.
Long-term follow-up (6 months)
On 6-month follow-up, overall clinical success with successful eradication of the PFC was achieved in 72/80 (90%) patients. There was no difference in the percentage of inpatients (84.8%) and outpatients (85.1%) who were found to have WON. Similarly, there was no difference in the number of patients with WON in whom elective direct endoscopic necrosectomy (DEN) was performed when comparing the inpatient and outpatient groups (78.8% vs. 78.7%, respectively; P = 1). There was no significant difference in complete resolution of PFCs in the inpatient and outpatient groups (91% vs. 87%, respectively; P = 1). The mean number of procedures required for PFC resolution after initial stent placement was significantly lower in the inpatient group as compared to the outpatients (2.3 vs. 3.1, respectively, P = 0.025).
There was no significant difference in resolution of WON between patients with or without nasocystic tube irrigation placed at the time of initial procedure (93.2% vs. 87.4%, respectively; P = 0.26). Similarly, there was no significant difference in resolution of the WON between patient with or without transpapillary pancreatic stent placement at the time of initial procedure (90% vs. 88.7%; P = 1). No recurrence of WON or a pseudocyst was seen after the removal of the stents in any of the groups. These findings are summarized in [Table 3].
|Table 3: Results of endoscopic ultrasound-guided drainage/debridement of pancreatic fluid collections|
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Procedure-related adverse events
There was one procedure-related adverse event in the inpatient group; this was significant hemorrhage due to inadvertent puncture of an artery, which was successfully treated with coil embolization by interventional radiology [Table 2].
There were eight procedure-related adverse events in the outpatient group: 3 perforations, 6 episodes of clinically significant bleeding at the cystenterostomy/stent site, 1 suprainfection, and 3 episodes of self-limited bleeding at the stent site after the procedure that resolved with local injection of epinephrine. One 63 year old male patient who developed a perforation after stent maldeployement had the perforation closed using an over-the-scope clip; he then had placement of a fully covered biliary metal stent through a new puncture site to drain the WON; this patient did well and had complete resolution of his WON. Two patients developed pneumoperitoneum after failed transmural drainage/debridement due to LAMS maldeployement. The LAMS were removed. The operators then could not successfully advance the guidewire into the WON cavity. The guidewire was repeatedly advanced into the abdominal cavity despite multiple attempts; therefore, another stent could not be placed safely to drain the pseudocyst. These patients were sent to surgery and had primary repair of the gastric perforation and underwent cystgastrostomy.
Procedure-related adverse events were significantly lower in the inpatient group compared to the outpatient group (P < 0.01). There was no procedure-related mortality in either group.
Late adverse events after initial stent placement
In the inpatient group, 3/33 (9%) patients required reintervention due to the following reasons: 1 patient had occlusion of the LAMS as a result of necrotic debris and 2 patients had infection of the PFC cavity requiring endoscopic debridement and irrigation.
The need for endoscopic reintervention in the outpatient group was seen in 3/47 (6%) of cases due to the following reasons: one patient had occlusion of the LAMS as a result of necrotic debris and 2 patients had infection of the PFC cavity requiring endoscopic debridement and irrigation. There was no significant difference in the 2 groups in terms of development of adverse events requiring endoscopic reintervention within 30 days of initial stent placement (P = 0.69). Patients who had secondary infection of the PFC as a result of occluded stents were all successfully managed by endoscopic replacement of stents and placement of a nasocystic drain.
| Discussion|| |
The use of LAMS to endoscopically drain and debride PFCs including PP and WON is undergoing a period of exponential growth with this technology rapidly disseminating into widespread clinical practice. Historically, PFC drainage and LAMS placement have often perceived as a procedure that frequently warrants inpatient hospitalization. This study demonstrates that the placement of LAMS in patients with PFCs can be safely performed on an outpatient basis and does not automatically warrant inpatient hospitalization.
This study included 80 patients, the vast majority of whom had WON. As such, this represents a cohort of, overall, significantly ill patients. The overall technical success in our study was very high (98.7%) and was similar to, or better than, that seen in other studies of the use of LAMS to drain PFCs.,, There was no statistically significant difference in the technical success rate between the inpatient and outpatient groups. The proportion of patients with WON was the same in our inpatient and outpatient subgroups as was the percentage of patients in both groups who required DEN, further demonstrating that outpatient LAMS placement and debridement can be performed in patients with sequelae of severe acute pancreatitis.
Our study showed no significant difference in the rate of complete resolution of PFCs in the inpatient and outpatient groups (91% vs. 87%). The number of procedures required for PFC resolution after the initial stent placement was statistically significantly lower in the inpatient group as compared to the outpatient although this essentially amounted to only one more procedure in the outpatient group (approximately 2 vs. 3, respectively). The reason for this difference in total number of procedure required is unclear at this time.
There were more adverse events related to the LAMS placement itself in the outpatient group, but there was no significant difference in the 2 groups in terms of development of adverse events requiring endoscopic reintervention within 30 days of initial stent placement. It is unclear why there were more adverse events during the LAMS placement in the outpatient group although patients who are referred for planned outpatient LAMS procedures can always be admitted afterward for subsequent observation and/or care as needed. The fact that the rate of delayed adverse events was the same between the two groups argues that in patients who undergo an uneventful LAMS procedure further demonstrates that these patients can be safely discharged without inordinate fear of poor outcomes.
Our study shows that as experience grows with interventional EUS procedures in general, and PFC drainage specifically, our comfort level with performing these procedures in outpatients can grow as well. A similar evolution occurred in the world of ERCP approximately 2 decades ago. Previously, ERCP-based maneuvers such as sphincterotomy, stone extraction, and stent placement were felt to warrant subsequent inpatient admission and observation. Studies from the 1990s showed that these and other maneuvers could be safely performed on outpatients.,,, Similar findings were seen when laparoscopic cholecystectomy transitioned from a purely inpatient procedure to a predominately outpatient procedure.,,
Overall, this study shows that LAMS placement for PFCs including both PP and WON can be performed safely on an outpatient basis with overall technical and clinical outcomes that are comparable to those seen in inpatients. Patients with a planned outpatient LAMS procedure who develop an adverse event during the procedure can always be admitted for inpatient care afterward. Stable outpatients who tolerate LAMS placement without difficulty can be safely discharged home on the same day as their procedure.
| Conclusion|| |
This study shows that LAMS placement for PFCs can be performed safely on an outpatient basis with overall technical and clinical outcomes that are comparable to those seen in inpatients.
Financial support and sponsorship
This study was funded entirely through existing intramural funds and salary support.
Conflicts of interest
Douglas G. Adler is a speaker and consultant for Boston Scientific Janak Shah is a consultant for Boston Scientific Jose Nieto is a speaker and consultant for Boston Scientific Kenneth Binmoeller is a consultant for Boston Scientific and inventor of the LAMS Yasser Bhat has no conflicts of interest Linda Jo Taylor has no conflicts of interest Ali A. Siddiqui is a consultant for Boston Scientific.
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[Table 1], [Table 2], [Table 3]