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DOI: 10.1055/a-2165-7436
Cold snare polypectomy for duodenal adenomas in familial adenomatous polyposis: a prospective international cohort study
TRIAL REGISTRATION: Registration number (trial ID): NCT04677998, Trial registry: ClinicalTrials.gov (http://www.clinicaltrials.gov/), Type of Study: Prospective
Abstract
Background and study aims In patients with familial adenomatous polyposis (FAP), endoscopic resection of duodenal adenomas is commonly performed to prevent cancer and prevent or defer duodenal surgery. However, based on studies using different resection techniques, adverse events (AEs) of polypectomy in the duodenum can be significant. We hypothesized that cold snare polypectomy (CSP) is a safe technique for duodenal adenomas in FAP and evaluated its outcomes in our centers.
Patients and methods We performed a prospective international cohort study including FAP patients who underwent CSP for one or more superficial non-ampullary duodenal adenomas of any size between 2020 and 2022. At that time, this technique was common practice in our centers for superficial duodenal adenomas. The primary outcome was the occurrence of intraprocedural and post-procedural AEs.
ResultsIn total, 133 CSPs were performed in 39 patients with FAP (1–18 per session). Median adenoma size was 10 mm (interquartile range 8–15 mm), ranging from 5 to 40 mm; 27 adenomas were ≥20 mm (20%). Of the 133 polypectomies, 109 (82%) were performed after submucosal injection. Sixty-one adenomas (46%) were resected en bloc and 72 (54%) piecemeal. Macroscopic radical resection was achieved for 129 polypectomies (97%). Deep mural injury type II occurred in three polyps (2%) with no delayed perforation after prophylactic clipping. There were no clinically significant bleeds, perforations or other post-procedural AEs. Histopathology showed low-grade dysplasia in all 133 adenomas.
Conclusions CSP for (multiple) superficial non-ampullary duodenal adenomas in FAP seems feasible and safe. Long-term prospective research is needed to evaluate whether protocolized duodenal polypectomies prevent cancer and surgery.
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Introduction
Familial adenomatous polyposis (FAP) is an inherited disorder resulting in the development of numerous colorectal adenomas, requiring colectomy at a young age to prevent colorectal cancer [1]. Nearly all patients with FAP also develop adenomas in the duodenum. The life-time risk for duodenal cancer is 4% to 10% [2] [3] [4] [5], and this cancer accounts for one of the most common FAP-related causes of death [6].
Conventionally, extensive duodenal polyposis is considered a criterion for prophylactic duodenectomy to prevent malignant transformation; however, treatment burden for duodenectomy is high with significant morbidity (Clavien-Dindo III/IV 16%-53%) and mortality (0%-2%) risks [7] [8]. With the technical advance in endoscopic resection made over the last two decades, many centers with expertise in FAP have started to perform endoscopic polypectomy in the duodenum. In an attempt to either prevent duodenal cancer and prevent or defer the need for surgical duodenectomy, many centers with expertise in FAP have started to perform endoscopic polypectomies in the duodenum.
Several studies shown that endoscopic treatment of duodenal adenomas resulted in downstaging of duodenal polyposis graded by Spigelman stage [9] [10] [11]. And because the Spigelman stage is associated with duodenal cancer risk, performing polypectomies might indeed reduce this risk. In one study, 74% of patients were free from duodenal surgery at 89 months after polypectomy [9]. This potential advantage, however, should be weighed against the risk of complications of endoscopic treatment.
In the large bowel, current guidelines advice cold snare polypectomy (CSP) for non-pedunculated colorectal polyps < 10 mm and accumulating evidence suggests that CSP might also be effective and safe in 10- to 19-mm and even larger colorectal polyps [12]. Compared to cautery-based techniques, CSP is associated with a lower risk of delayed bleeding, perforation, and post-polypectomy syndrome and a shorter procedure time [13] [14] [15] [16], which is favorable in a condition such as FAP in which multiple polyps often are removed in one session.
Compared to the colon, the complication risk of polypectomy in the duodenum is higher, presumably due to the thinner wall and increased vascularity. In two retrospective studies in FAP that included different resection techniques, the risk of perforation after endoscopic polypectomy in the duodenum was 2% to 3% and the risk of delayed bleeding 13% to 20% [9] [10]. All delayed bleedings in Roos et al. occurred after polypectomy of large adenomas, all >20 mm. This considerable risk of adverse events (AEs) indicates a need for careful selection of lesions that can be safely resected, as well as a discussion about the preferred resection technique for duodenal adenomas in FAP. A few studies assessed the safety of CSP for duodenal adenomas. In a study including 10 patients with FAP, 332 CSPs were performed, mainly on polyps <10 mm (97%), and no (serious) AEs occurred, except for one intra-procedural bleed managed with hemoclips [17]. The same authors confirmed the safety of CSP in a recent update including 2413 CSPs [11]. In the sporadic setting, studies have shown that complications after duodenal CSP are rare (delayed bleeding 0%–4%, perforation 0%–4%), including comparative studies showing that these risks are higher after hot snare polypectomy (HSP) (delayed bleeding 8.7%–16.8%, perforation 1.4%–5.9%) [18] [19] [20] [21] [22]. A recently published European guideline, however, still recommends HSP for duodenal adenomas >5 mm [23].
We aimed to evaluate the safety of CSP for superficial non-ampullary duodenal adenomas in a consecutive series of patients with FAP in our expert centers.
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Patients and methods
Study design and subjects
From 2020 on, centers that participate in the European FAP Consortium have collected findings of endoscopic surveillance of patients with FAP in a prospectively maintained database. One of the aims of this prospective database is to study the safety and efficacy of endoscopic resection techniques for duodenal adenomas. For this study, we evaluated all CSPs for non-ampullary duodenal adenomas performed between 2020 and 2022 during one or more sessions in patients with FAP. A diagnosis of FAP was defined as having a constitutional pathogenic variant of the APC gene and/or having more than 100 colorectal adenomas and a family history of FAP.
The study was approved by the institutional review boards of all participating hospitals. All included patients gave informed consent prior to data collection. The study was registered at ClinicalTrials.gov (NCT04677998).
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CSP procedure
In the centers of the European FAP Consortium, the aim of duodenal polypectomy, apart from cancer prevention, is to prevent endoscopically unmanageable disease in the future, thereby obviating the need for duodenal surgery. The indications for performing polypectomy of non-ampullary duodenal adenomas are: adenomas ≥10 mm and adenomas ≥5 mm when in total more than 20 duodenal adenomas are present. All superficial adenomas are resected using CSP, while more protruding lesions are resected using HSP. Duodenal polypectomies were performed under sedation (propofol or midazolam plus fentanyl) by endoscopists with expertise in FAP on dedicated endoscopy lists in tertiary referral centers. Patients on vitamin K antagonists or direct-acting anticoagulants temporarily discontinued these drugs. Single-agent antiplatelet use was continued or discontinued depending on local protocols. Gastroscopes, duodenoscopes or pediatric colonoscopes were used for the included procedures. CO2 insufflation was used.
The procedure included assessment of the duodenum and stomach after which the adenomas with an indication for polypectomy were removed during one or multiple procedures, depending on the number and complexity of the lesions. The location, morphology, and size of the adenoma was assessed by the endoscopist prior to polypectomy, with or without narrow band imaging at the discretion of the endoscopists. Whether the submucosa was injected to lift the lesion, with or without adrenaline, was also left to the discretion of the endoscopist. Submucosal lifting and CSP was referred to as cold endoscopic mucosal resection (EMR) in some previous studies [20] [22]. Most lesions of 5 to 9 mm were resected en bloc with CSP and lesions ≥10 mm with piecemeal CSP. The post-polypectomy site was carefully inspected to rule out residual adenomatous tissue and to check for hemostasis and deep mural injury. Hemoclips were placed at the endoscopist’s discretion. Post-procedural clinical admission for observation was not routinely planned for all patients, but left to the discretion of the treating endoscopist and local protocols. Standard prescription of prophylactic proton pump inhibitors was not advised, but left to the discretion of the treating endoscopist. No standard post-procedural dietary restrictions were advised. [Video 1] shows an en bloc CSP followed by a piecemeal CSP during the same session in a patient with extensive duodenal polyposis.
Quality:
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Follow-up
Patients were evaluated 2 to 4 weeks after the procedure at the outpatient clinic or via a telephone consultation, to ensure that possible AEs were identified, discussed, and evaluated. Follow-up endoscopy was scheduled after 3 to 6 months when macroscopic resection was incomplete, high-grade dysplasia was present in the resected adenoma and/or when there were other lesions in the duodenum and/or stomach that required intervention. Otherwise, follow-up endoscopy was scheduled after 1 year. During follow-up endoscopy, the polypectomy scar(s) were assessed to detect recurrences.
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Outcome
The primary outcome was the occurrence of procedure-related AEs occurring within 30 days after CSP. AEs were evaluated using the validated Adverse Events in GI Endoscopy classification [24]. Deep mural injury was scored according to the Sydney classification system [25].
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Statistical analysis
Descriptive statistics were used for this study. Continuous variables are presented as means with standard deviation for normally-distributed variables and as medians with interquartile ranges (IQRs) for skewed-distributed variables. Categorical variables are presented as numbers and percentages. All analyses were performed using SPSS 26 (IBM Corp. Released 2019. IBM SPSS Statistics for Windows, Version 26.0. Armonk, New York, United States: IBM Corp).
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Results
Patient characteristics and included procedures
Thirty-nine consecutive FAP patients from three centers underwent CSP for a total of 133 superficial non-ampullary duodenal adenomas. During the same time period, 25 duodenal adenomas were resected with HSP. One patient underwent combined CSP and HSP of a large duodenal adenoma which, on histopathology, appeared to be an adenocarcinoma.
Patient characteristics are presented in [Table 1]. The median age at (first) CSP was 47. Of the 39 patients, 22 (56%) had undergone an endoscopic duodenal polypectomy before entering the study. The total number of CSPs per patient in the study period varied from one to 22 with a maximum of 18 CSPs per session. No patients were on anticoagulants at time of CSP.
[Table 2] summarizes the characteristics of the lesions and procedure outcomes. The median adenoma size was 10 mm (IQR 8–15). Fifty percent of the lesions were between 10 and 19 mm and 20% were ≥20 mm. Nearly all adenomas were located in D2 (69%) or D3 (26%) and had a flat elevated (IIa) (63%) or sessile (Is) (37%) appearance. Prior to CSP, most adenomas (82%) were submucosally lifted. Sixty-one lesions (46%) were resected en bloc and 72 (54%) piecemeal, resulting in a macroscopic radical resection rate of 97%. Most common difficulties during CSP were an unstable view (13%) and difficult location (5%). In 8% of lesions, hemoclips were prophylactically placed to prevent delayed bleeding or perforation.
In terms of intraprocedural AEs, no bleeding or perforation occurred. Three CSPs (2%) in three different patients resulted in full exposure of the muscularis propria, classified as deep mural injury type II (n=3). All three cases of muscularis propria exposure occurred after submucosal lifting and piecemeal resection for adenomas measuring 25, 20, and 45 mm, with the use of a dedicated cold snare. In two lesions there was a suspicion of submucosal scarring, which might have been caused by previous biopsies. All three resection sites were prophylactically closed with hemoclips to prevent delayed perforation, which did not occur ([Fig. 1]). All three patients were admitted for observation.


After eight of 42 polypectomy sessions (19%), the patients were admitted for one or two nights due to either the resection of large adenomas (n=3) or a high number of resected adenomas (n=5). These admissions were planned and, therefore, not counted as AEs. Also, in the three cases of deep mural injury, the admission was had been planned prior to the procedure because of the number or size of the lesion(s). No delayed complications were observed either during the admission period nor the 4-week follow-up. Histology showed a tubular adenoma in 90% of lesions and tubulovillous adenoma in 10%. All lesions contained low-grade dysplasia; no high-grade dysplasia or cancer was detected.
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Discussion
In this multicenter study, we investigated the safety of CSP for the removal of superficial non-ampullary duodenal adenomas in FAP. We demonstrated that, in experienced hands, CSP is a safe technique, regardless of the size or number of adenomas resected during the same procedure.
Our series confirms the safety of CSP for duodenal adenomas because no bleeding or perforation was observed. [Table 3] summarizes the available series on duodenal CSP in the sporadic and FAP setting showing the occurrence of intraprocedural bleeding (0%-90%), delayed bleeding (0%), and perforation (0%). These studies included CSPs with (cold EMR) and without submucosal lifting. Because the AE rate was low in all studies, we cannot state whether lifting results in fewer AEs. In the present study, most adenomas were lifted before CSP, and adenomas that were resected without lifting had a maximum size of 15 mm. We cannot draw any conclusions about larger lesions, but it might be hypothesized that performing CSP without lifting for larger adenomas might result in an increased risk of AEs. The only AE that occurred was deep mural injury type II during three procedures. In two of these lesions, there was a suggestion of submucosal scarring, which might have been caused by previous biopsies and might increase the risk of AEs and non-radical resection. Numbers are too small to further study this in the present series. In our current endoscopic surveillance protocol, we do not advise taking routine biopsies to prevent submucosal scarring [26]. Another factor that might increase the AE risk is the morphology of the adenoma. Resecting more bulky adenomas might result in a higher risk of bleeding, which is the reason to perform HSP for these adenomas in our current practice.
Author, year |
Setting |
Design |
N of CSPs |
Adenoma size* |
Intraprocedural bleeding |
Delayed bleeding |
Perforation |
*Mean or median |
|||||||
Choksi 2015 [27] |
Sporadic |
Retrospective |
15 |
24 mm |
0 |
1 (7%) |
0 |
Maruoka 2017 [21] |
Sporadic |
Prospective |
30 |
4 mm |
27 (90%)† |
0 |
0 |
Hamada 2018 [17] |
FAP |
Prospective |
332 |
NR |
1 (3%) |
0 |
0 |
Dang 2021 [18] |
Sporadic |
Retrospective |
43 |
26.5 mm |
0 |
0 |
0 |
Trivedi 2022 [19] |
Sporadic |
Retrospective |
41 |
12 mm |
4 (10%) |
0 |
0 |
Repici 2022 [20] |
Sporadic |
Retrospective |
33 |
31.5 mm |
0 |
0 |
0 |
Wang 2023 [22] |
Sporadic |
Prospective |
50 |
30 mm |
1 (2%) |
2 (4%) |
2 (4%) |
Present series |
FAP |
Prospective |
133 |
10 mm |
0 |
0 |
0 |
Two studies retrospectively compared CSP to HSP, showing that AEs occurred less frequently after CSP [19] [20], with intraprocedural bleeding occurring in 10% to 13% after HSP, delayed bleeding in 9% to 17%, and perforation in 1% to 10%. However, because these studies were both retrospective and might suffer from selection bias, one should be careful about drawing conclusions. No detailed information on lesion morphology was provided, and superficial lesions may have been resected using CSP and the bulkier lesions with HSP. Moreover, CSP has recently been introduced as a resection technique in the duodenum. Trivedi et al. showed that HSP was used for all but one lesion in polypectomies between 2006 and 2012, whereas most lesions were resected using CSP between 2018 and 2021. This timing is relevant due to the evolution of hemostatic techniques, which were not available or widely used in the early years of duodenal polypectomy for FAP. Therefore, it is difficult to compare bleeding rates between the two techniques. Besides, the resection technique will be based on polyp morphology, introducing another bias. A randomized trial would eliminate most of these biases, but it is questionable whether a randomized trial is necessary or ethically justifiable, with such positive current data on CSP.
In terms of efficacy, evaluating adenoma recurrences after duodenal polypectomy might be of importance. In this study, we did not report on recurrences after CSP. FAP patients undergoing duodenal polypectomy usually have numerous adenomas and sometimes multiple adenomas are removed during the same procedure. We believe that this clinical setting does not lend itself to studying adenoma recurrence, because this is clinically less relevant, given that patients usually have multiple duodenal adenomas and should undergo regular surveillance endoscopies anyway. This is in contrast to the sporadic setting, in which usually one polyp is removed in an otherwise normal duodenum and surveillance might be terminated after complete removal. Two studies in the sporadic setting comparing CSP to HSP did not find a difference in recurrence rate [19] [20]. Polyp size was found to be a predictor of recurrence in univariate analysis [19]. Removing adenomas ≥5 mm rather than ≥10 mm as recommended by current guidelines might result in fewer recurrences and more en bloc resections. It could also prevent unmanageable duodenal disease with multiple large adenomas, which may require more complex polypectomies in the future. Takeuchi et al. [11] introduced a different endoscopic approach, called intensive downstaging polypectomy for duodenal polyposis in FAP, in which all large and small duodenal adenomas are resected, mostly using CSP. It resulted in downstaging of duodenal polyposis in most patients (71%). However, whether removing adenomas <5 mm results in a lower risk of developing duodenal cancer is debatable. This intensive strategy with frequent endoscopies including a high number of polypectomies results in a burden for the patients and potentially also an increased complication risk. Although future studies will have to guide the trade-off between safety and efficacy of CSP in terms of recurrence and feasibility, taking into account lesion size and morphology, we believe CSP is the preferred method for resecting (multiple) superficial duodenal adenomas in FAP. Whereas in the past data from retrospective studies were used for counseling, reporting on different resection techniques combined, we are now able to more accurately inform patients about risks before they undergo CSP.
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Conclusions
We demonstrated the safety of CSP in FAP patients, but not its efficacy in preventing cancer and surgery. Long-term prospective data from a large FAP cohort are needed to evaluate whether protocolized removal of duodenal adenomas is an effective strategy and, more specifically, which adenomas should be removed. As a European consortium, we hope to provide such data in future years.
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Conflict of Interest
Arthur S. Aelvoet: none to declare. John G. Karstensen: JGK consultancy for SNIPR BIOME, Boston Scientific, and AMBU and speaker's fee from Norgine. Barbara A.J. Bastiaansen: speaker's fee from Olympus, Tillotts Pharma AG and Ovesco Endoscopy AG. Monique van Leerdam: review and editorial fee from Elsevier Francesc Balaguer: FB has received an honorarium for consultancy from Sysmex, CPP Pharmaceuticals, and One-Two Therapeutics, speaker's fees from Norgine, and editorial fee from Elsevier. Michal Kaminski: speaker’s fee from Olympus, Fujifilm, Boston Scientific, Medtronic, AlfaSigma, IPSEN, consultancy fee from Olympus, ERBE, AlfaSigma. Roel Hompes: none to declare. Patrick M.M. Bossuyt: none to declare. Luigi Ricciardiello: consultancy and unrestricted research grant from SLA Pharma AG. Andrew Latchford: none to declare. Rodrigo Jover: consultancy for CPP Pharmaceuticals Maria Daca-Alvarez: none to declare. Maria Pellise: endoscopic equipment on loan of FujiFilm, research grant from FujiFilm, ZiuZ and Casen Recordati, consultancy for FujiFilm, Olympus and speaker's fee from Olympus, Medtronic and FujiFilm. Evelien Dekker: endoscopic equipment on loan of FujiFilm and Olympus, research grant from FujiFilm, consultancy for FujiFilm, Olympus, Ambu and InterVenn, and speaker's fee from Olympus, GI Supply, Norgine, IPSEN, PAION and FujiFilm.
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References
- 1 Bussey HJR. Familial polyposis coli: family studies, histopathology, differential diagnosis and results of treatment. Baltimore: John Hopkins University Press; 1975
- 2 Lepistö A, Kiviluoto T, Halttunen J. et al. Surveillance and treatment of duodenal adenomatosis in familial adenomatous polyposis. Endoscopy 2009; 41: 504-509
- 3 Björk J, Akerbrant H, Iselius L. et al. Periampullary adenomas and adenocarcinomas in familial adenomatous polyposis: cumulative risks and APC gene mutations. Gastroenterology 2001; 121: 1127-1135
- 4 Bülow S, Christensen IJ, Højen H. et al. Duodenal surveillance improves the prognosis after duodenal cancer in familial adenomatous polyposis. Colorectal Dis 2012; 14: 947-952
- 5 Groves CJ, Saunders BP, Spigelman AD. et al. Duodenal cancer in patients with familial adenomatous polyposis (FAP): results of a 10 year prospective study. Gut 2002; 50: 636-641
- 6 Ghorbanoghli Z, Bastiaansen BA, Langers AM. et al. Extracolonic cancer risk in Dutch patients with APC (adenomatous polyposis coli)-associated polyposis. J Med Genet 2018; 55: 11-14
- 7 Walsh RM, Augustin T, Aleassa EM. et al. Comparison of pancreas-sparing duodenectomy (PSD) and pancreatoduodenectomy (PD) for the management of duodenal polyposis syndromes. Surgery 2019; 166: 496-502
- 8 Aelvoet AS, Bastiaansen BAJ, Fockens P. et al. Pancreas-preserving total duodenectomy for advanced duodenal polyposis in patients with familial adenomatous polyposis: short and long-term outcomes. HPB (Oxford) 2022; 24: 1642-1650
- 9 Roos VH, Bastiaansen BA, Kallenberg FGJ. et al. Endoscopic management of duodenal adenomas in patients with familial adenomatous polyposis. Gastrointest Endosc 2021; 93: 457-466
- 10 Moussata D, Napoleon B, Lepilliez V. et al. Endoscopic treatment of severe duodenal polyposis as an alternative to surgery for patients with familial adenomatous polyposis. Gastrointest Endosc 2014; 80: 817-825
- 11 Takeuchi Y, Hamada K, Nakahira H. et al. Efficacy and safety of intensive endoscopic intervention for multiple duodenal adenomas in patients with familial adenomatous polyposis: A prospective cohort study. Endoscopy 2023; 55: 515-523
- 12 Ferlitsch M, Moss A, Hassan C. et al. Colorectal polypectomy and endoscopic mucosal resection (EMR): European Society of Gastrointestinal Endoscopy (ESGE) Clinical Guideline. Endoscopy 2017; 49: 270-297
- 13 Horiuchi A, Nakayama Y, Kajiyama M. et al. Removal of small colorectal polyps in anticoagulated patients: a prospective randomized comparison of cold snare and conventional polypectomy. Gastrointest Endosc 2014; 79: 417-423
- 14 Paspatis GA, Tribonias G, Konstantinidis K. et al. A prospective randomized comparison of cold vs hot snare polypectomy in the occurrence of postpolypectomy bleeding in small colonic polyps. Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland 2011; 13: E345-E348
- 15 Ichise Y, Horiuchi A, Nakayama Y. et al. Prospective randomized comparison of cold snare polypectomy and conventional polypectomy for small colorectal polyps. Digestion 2011; 84: 78-81
- 16 Rex DK, Anderson JC, Pohl H. et al. Cold versus hot snare resection with or without submucosal injection of 6- to 15-mm colorectal polyps: a randomized controlled trial. Gastrointest Endosc 2022; 96: 330-338
- 17 Hamada K, Takeuchi Y, Ishikawa H. et al. Safety of cold snare polypectomy for duodenal adenomas in familial adenomatous polyposis: a prospective exploratory study. Endoscopy 2018; 50: 511-517
- 18 Dang DT, Suresh S, Vance RB. et al. Outcomes of cold snare piecemeal EMR for nonampullary small-bowel adenomas larger than 1 cm: a retrospective study. Gastrointest Endosc 2022; 95: 1176-1182
- 19 Trivedi M, Klapheke R, Youssef F. et al. Comparison of cold snare and hot snare polypectomy for the resection of sporadic nonampullary duodenal adenomas. Gastrointest Endosc 2022; 96: 657-664
- 20 Repici A, Capogreco A, Spadaccini M. et al. Cold versus hot EMR for large duodenal adenomas. Gut 2022; 71: 1763-1765
- 21 Maruoka D, Matsumura T, Kasamatsu S. et al. Cold polypectomy for duodenal adenomas: a prospective clinical trial. Endoscopy 2017; 49: 776-783
- 22 Wang H, Sidhu M, Gupta S. et al. Cold snare EMR for the removal of large duodenal adenomas. Gastrointest Endosc 2023; 97: 1100-1108
- 23 Vanbiervliet G, Moss A, Arvanitakis M. et al. Endoscopic management of superficial nonampullary duodenal tumors: European Society of Gastrointestinal Endoscopy (ESGE) Guideline. Endoscopy 2021; 53: 522-534
- 24 Nass KJ, Zwager LW, van der Vlugt M. et al. Novel classification for adverse events in GI endoscopy: the AGREE classification. Gastrointest Endosc 2022; 95: 1078-1085
- 25 Burgess NG, Bassan MS, McLeod D. et al. Deep mural injury and perforation after colonic endoscopic mucosal resection: a new classification and analysis of risk factors. Gut 2017; 66: 1779-1789
- 26 Aelvoet AS, Pellisé M, Bastiaansen BAJ. et al. Personalized endoscopic surveillance and intervention protocols for patients with familial adenomatous polyposis: the European FAP Consortium strategy. Endosc Int Open 2023; 11: E386-E393
- 27 Choksi N, Elmunzer BJ, Stidham RW RW. et al. Cold snare piecemeal resection of colonic and duodenal polyps ≥1 cm. Endosc Int Open 2015; 3: E508-E513
Correspondence
Publication History
Received: 12 June 2023
Accepted after revision: 28 August 2023
Accepted Manuscript online:
04 September 2023
Article published online:
10 November 2023
© 2023. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/).
Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany
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References
- 1 Bussey HJR. Familial polyposis coli: family studies, histopathology, differential diagnosis and results of treatment. Baltimore: John Hopkins University Press; 1975
- 2 Lepistö A, Kiviluoto T, Halttunen J. et al. Surveillance and treatment of duodenal adenomatosis in familial adenomatous polyposis. Endoscopy 2009; 41: 504-509
- 3 Björk J, Akerbrant H, Iselius L. et al. Periampullary adenomas and adenocarcinomas in familial adenomatous polyposis: cumulative risks and APC gene mutations. Gastroenterology 2001; 121: 1127-1135
- 4 Bülow S, Christensen IJ, Højen H. et al. Duodenal surveillance improves the prognosis after duodenal cancer in familial adenomatous polyposis. Colorectal Dis 2012; 14: 947-952
- 5 Groves CJ, Saunders BP, Spigelman AD. et al. Duodenal cancer in patients with familial adenomatous polyposis (FAP): results of a 10 year prospective study. Gut 2002; 50: 636-641
- 6 Ghorbanoghli Z, Bastiaansen BA, Langers AM. et al. Extracolonic cancer risk in Dutch patients with APC (adenomatous polyposis coli)-associated polyposis. J Med Genet 2018; 55: 11-14
- 7 Walsh RM, Augustin T, Aleassa EM. et al. Comparison of pancreas-sparing duodenectomy (PSD) and pancreatoduodenectomy (PD) for the management of duodenal polyposis syndromes. Surgery 2019; 166: 496-502
- 8 Aelvoet AS, Bastiaansen BAJ, Fockens P. et al. Pancreas-preserving total duodenectomy for advanced duodenal polyposis in patients with familial adenomatous polyposis: short and long-term outcomes. HPB (Oxford) 2022; 24: 1642-1650
- 9 Roos VH, Bastiaansen BA, Kallenberg FGJ. et al. Endoscopic management of duodenal adenomas in patients with familial adenomatous polyposis. Gastrointest Endosc 2021; 93: 457-466
- 10 Moussata D, Napoleon B, Lepilliez V. et al. Endoscopic treatment of severe duodenal polyposis as an alternative to surgery for patients with familial adenomatous polyposis. Gastrointest Endosc 2014; 80: 817-825
- 11 Takeuchi Y, Hamada K, Nakahira H. et al. Efficacy and safety of intensive endoscopic intervention for multiple duodenal adenomas in patients with familial adenomatous polyposis: A prospective cohort study. Endoscopy 2023; 55: 515-523
- 12 Ferlitsch M, Moss A, Hassan C. et al. Colorectal polypectomy and endoscopic mucosal resection (EMR): European Society of Gastrointestinal Endoscopy (ESGE) Clinical Guideline. Endoscopy 2017; 49: 270-297
- 13 Horiuchi A, Nakayama Y, Kajiyama M. et al. Removal of small colorectal polyps in anticoagulated patients: a prospective randomized comparison of cold snare and conventional polypectomy. Gastrointest Endosc 2014; 79: 417-423
- 14 Paspatis GA, Tribonias G, Konstantinidis K. et al. A prospective randomized comparison of cold vs hot snare polypectomy in the occurrence of postpolypectomy bleeding in small colonic polyps. Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland 2011; 13: E345-E348
- 15 Ichise Y, Horiuchi A, Nakayama Y. et al. Prospective randomized comparison of cold snare polypectomy and conventional polypectomy for small colorectal polyps. Digestion 2011; 84: 78-81
- 16 Rex DK, Anderson JC, Pohl H. et al. Cold versus hot snare resection with or without submucosal injection of 6- to 15-mm colorectal polyps: a randomized controlled trial. Gastrointest Endosc 2022; 96: 330-338
- 17 Hamada K, Takeuchi Y, Ishikawa H. et al. Safety of cold snare polypectomy for duodenal adenomas in familial adenomatous polyposis: a prospective exploratory study. Endoscopy 2018; 50: 511-517
- 18 Dang DT, Suresh S, Vance RB. et al. Outcomes of cold snare piecemeal EMR for nonampullary small-bowel adenomas larger than 1 cm: a retrospective study. Gastrointest Endosc 2022; 95: 1176-1182
- 19 Trivedi M, Klapheke R, Youssef F. et al. Comparison of cold snare and hot snare polypectomy for the resection of sporadic nonampullary duodenal adenomas. Gastrointest Endosc 2022; 96: 657-664
- 20 Repici A, Capogreco A, Spadaccini M. et al. Cold versus hot EMR for large duodenal adenomas. Gut 2022; 71: 1763-1765
- 21 Maruoka D, Matsumura T, Kasamatsu S. et al. Cold polypectomy for duodenal adenomas: a prospective clinical trial. Endoscopy 2017; 49: 776-783
- 22 Wang H, Sidhu M, Gupta S. et al. Cold snare EMR for the removal of large duodenal adenomas. Gastrointest Endosc 2023; 97: 1100-1108
- 23 Vanbiervliet G, Moss A, Arvanitakis M. et al. Endoscopic management of superficial nonampullary duodenal tumors: European Society of Gastrointestinal Endoscopy (ESGE) Guideline. Endoscopy 2021; 53: 522-534
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