Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:
Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_538_Библиотеки_им_академика_М_И_Перельмана.pdf
Скачиваний:
0
Добавлен:
29.08.2026
Размер:
86 Мб
Скачать
4 Endoscopy
75
40. Saltzman JR, et al. Bowel preparation before colonoscopy. Gastrointest Endosc. 2015;81(4):781–94.
41. Clark BT, Rustagi T, Laine L.What level of bowel prep quality requires early repeat colonoscopy: systematic review and meta­analysis of the impact of preparation quality on adenoma detec­tion rate. Am J Gastroenterol. 2014;109(11):1714–23; quiz 1724.
42. Tariq H, et al. Evaluation of the combined effect of factors inuencing bowel preparation and adenoma detection rates in patients undergoing colonoscopy. BMJ Open Gastroenterol. 2019;6(1):e000254.
43. Khashab MA, et al. Antibiotic prophylaxis for GI endoscopy. Gastrointest Endosc. 2015;81(1):81–9.
44. Yip T, etal. Risks and outcomes of peritonitis after exible colo­noscopy in CAPD patients. Perit Dial Int. 2007;27(5):560–4.
45. Piraino B, et al. ISPD position statement on reducing the risks of peritoneal dialysis-related infections. Perit Dial Int. 2011;31(6):614–30.
46. Zuckerman MJ, etal. ASGE guideline: the management of low­molecular- weight heparin and nonaspirin antiplatelet agents for endoscopic procedures. Gastrointest Endosc. 2005;61(2):189–94.
47. Feagins LA. Management of anticoagulants and antiplatelet agents during colonoscopy. Am J Med. 2017;130(7):786–95.
48. Douketis JD, et al. Perioperative bridging anticoagulation in patients with atrial brillation. N Engl J Med. 2015;373(9):823–33.
49. Cataldo PA.Colonoscopy without sedation. Dis Colon Rectum. 1996;39(3):257–61.
50. Takahashi Y, etal. Sedation-free colonoscopy. Dis Colon Rectum. 2005;48(4):855–9.
51. Yörük G, etal. Colonoscopy without sedation. Turk J Gastroenterol. 2003;14(1):59–63.
52. Trummel JM, Chandrasekhara V, Kochman ML. Anesthesia for colonoscopy and lower endoscopic procedures. Anesthesiol Clin. 2017;35(4):679–86.
53. Predmore Z, etal. Anesthesia service use during outpatient gas­troenterology procedures continued to increase from 2010 to 2013 and potentially discretionary spending remained high. Am J Gastroenterol. 2017;112(2):297–302.
54. Patel S, et al. Deep sedation occurs frequently during elective endoscopy with meperidine and midazolam. Am J Gastroenterol. 2005;100(12):2689–95.
55. Singh H, etal. Propofol for sedation during colonoscopy. Cochrane Database Syst Rev. 2008;(4):CD006268.
56. Goudra BG, etal. Safety of non-anesthesia provider-administered propofol (NAAP) sedation in advanced gastrointestinal endo­scopic procedures: comparative meta-analysis of pooled results. Dig Dis Sci. 2015;60(9):2612–27.
57. Chen SC, Rex DK.Review article: registered nurse- administered propofol sedation for endoscopy. Aliment Pharmacol Ther. 2004;19(2):147–55.
58. Rex DK.Endoscopist-directed propofol. Gastrointest Endosc Clin N Am. 2016;26(3):485–92.
59. Meral M, etal. Is ileocecal valve intubation essential for rou­tine colonoscopic examination? Eur J Gastroenterol Hepatol. 2018;30(4):432–7.
60. Kennedy G, et al. Routine ileal intubation during screen­ing colonoscopy: a useful maneuver? Surg Endosc. 2008;22(12):2606–8.
61. Ten Cate EM, etal. Post-surgical surveillance of locally advanced ileal carcinoids found by routine ileal intubation during screening colonoscopy: a case series. J Med Case Rep. 2014;8:444.
62. Saad A, Rex DK. Routine rectal retroexion during colonos­copy has a low yield for neoplasia. World J Gastroenterol. 2008;14(42):6503–5.
63. Kim SY, etal. Comparison of carbon dioxide and air insufation during consecutive EGD and colonoscopy in moderate-sedation patients: a prospective, double-blind, randomized controlled trial. Gastrointest Endosc. 2017;85(6):1255–62.
64. Memon MA, etal. Carbon dioxide versus air insufation for elec­tive colonoscopy: a meta-analysis and systematic review of ran­domized controlled trials. Surg Laparosc Endosc Percutan Tech. 2016;26(2):102–16.
65. Sajid MS, et al. Carbon dioxide insufation vs conventional air insufation for colonoscopy: a systematic review and meta­analysis of published randomized controlled trials. Color Dis. 2015;17(2):111–23.
66. Wu J, Hu B. The role of carbon dioxide insufation in colo­noscopy: a systematic review and meta-analysis. Endoscopy. 2012;44(2):128–36.
67. Rabenstein T, Radaelli F, Zolk O. Warm water infu­sion colonoscopy: a review and meta-analysis. Endoscopy. 2012;44(10):940–51.
68. Anderson JC, etal. Comparing adenoma and polyp miss rates for total underwater colonoscopy versus standard CO2: a ran­domized controlled trial using a tandem colonoscopy approach. Gastrointest Endosc. 2019;89(3):591–8.
69. Ribeiro MD, Soares J. Chromoendoscopy. Endoscopy. 2009;41(1):93.
70. Har-Noy O, et al. Chromoendoscopy, narrow-band imaging or white light endoscopy for neoplasia detection in inammatory bowel diseases. Dig Dis Sci. 2017;62(11):2982–90.
71. Iannone A, etal. Chromoendoscopy for surveillance in ulcerative colitis and Crohn’s disease: a systematic review of randomized trials. Clin Gastroenterol Hepatol. 2017;15(11):1684–1697.e11.
72. Kahi CJ, et al. High-denition chromocolonoscopy vs. high­denition white light colonoscopy for average-risk colorectal can­cer screening. Am J Gastroenterol. 2010;105(6):1301–7.
73. Atkinson NSS, et al. Narrow-band imaging for detection of neoplasia at colonoscopy: a meta-analysis of data from individ­ual patients in randomized controlled trials. Gastroenterology. 2019;157(2):462–71.
74. Rastogi A, etal. High accuracy of narrow band imaging with­out magnication for the real-time characterization of polyp histology and its comparison with high-denition white light colonoscopy: a prospective study. Am J Gastroenterol. 2009;104(10):2422–30.
75. Bisschops R, et al. Chromoendoscopy versus narrow band imaging in UC: a prospective randomised controlled trial. Gut. 2018;67(6):1087–94.
76. Gralnek IM, et al. Standard forward-viewing colonoscopy versus full-spectrum endoscopy: an international, multicen­tre, randomised, tandem colonoscopy trial. Lancet Oncol. 2014;15(3):353–60.
77. Hassan C, etal. Full-spectrum (FUSE) versus standard forward-
programme. Gut. 2017;66(11):1949–55.
78. Ridol TJ, Valente MA, Church JM.Achieving a complete colonic evaluation in patients with incomplete colonoscopy is worth the effort. Dis Colon Rectum. 2014;57(3):383–7.
79. Chen Y, et al. Magnetic endoscopic imaging vs standard colo­noscopy: meta-analysis of randomized controlled trials. World J Gastroenterol. 2013;19(41):7197–204.
80. Teshima CW, et al. Single-balloon-assisted colonoscopy in patients with previously failed colonoscopy. Gastrointest Endosc. 2010;71(7):1319–23.
81. Johnson CD, et al. Accuracy of CT colonography for detection of large adenomas and cancers. N Engl J Med. 2008;359(12):1207–17.
82. Pickhardt PJ.Imaging and screening for colorectal cancer with CT colonography. Radiol Clin N Am. 2017;55(6):1183–96.
83. Parsa N, Vemulapalli KC, Rex DK.Performance of radiographic imaging after incomplete colonoscopy for nonmalignant causes in clinical practice. Gastrointest Endosc. 2020;91(6):1371–7.
84. Shin LK, Poullos P, Jeffrey RB.MR colonography and MR enterog­raphy. Gastrointest Endosc Clin N Am. 2010;20(2):323–46.
76
M. D. Zelhart and B. R. Kann
85. Joseph DA, etal. Colorectal cancer screening: estimated future colonoscopy need and current volume and capacity. Cancer. 2016;122(16):2479–86.
86. Markowitz GS, etal. Renal failure due to acute nephrocalcinosis following oral sodium phosphate bowel cleansing. Hum Pathol. 2004;35(6):675–84.
87. Church JM. Pre-colonoscopy bowel preparation intolerance: a sign of upper gastrointestinal pathology. Aust N Z J Surg. 1991;61(10):796–7.
88. Wernli KJ, etal. Risks associated with anesthesia services during colonoscopy. Gastroenterology. 2016;150(4):888–94; quiz e18.
89. Bilotta F, et al. Cardiovascular effects of intravenous propofol administered at two infusion rates: a transthoracic echocardio­graphic study. Anaesthesia. 2001;56(3):266–71.
90. Herman LL, etal. Risk factors associated with vasovagal reactions during colonoscopy. Gastrointest Endosc. 1993;39(3):388–91.
91. Eckardt VF, et al. Complications and adverse effects of colonoscopy with selective sedation. Gastrointest Endosc. 1999;49(5):560–5.
92. Wang D, etal. The use of propofol as a sedative agent in gastroin­testinal endoscopy: a meta-analysis. PLoS One. 2013;8(1):e53311.
93. Bielawska B, et al. Anesthesia assistance in outpatient colonos­copy and risk of aspiration pneumonia, bowel perforation, and splenic injury. Gastroenterology. 2018;154(1):77–85 e3.
94. Church J. Complications of colonoscopy. Gastroenterol Clin N Am. 2013;42(3):639–57.
95. Shi X, et al. Lower rate of colonoscopic perforation: 110,785 patients of colonoscopy performed by colorectal surgeons in a large teaching hospital in China. Surg Endosc. 2014;28(8):2309–16.
96. Reumkens A, etal. Post-colonoscopy complications: a systematic review, time trends, and meta-analysis of population-based stud­ies. Am J Gastroenterol. 2016;111(8):1092–101.
97. Luning TH, etal. Colonoscopic perforations: a review of 30,366 patients. Surg Endosc. 2007;21(6):994–7.
98. Alsowaina KN, et al. Management of colonoscopic perfora­tion: a systematic review and treatment algorithm. Surg Endosc. 2019;33(12):3889–98.
99. Loffeld RJ, Engel A, Dekkers PE.Incidence and causes of colo­noscopic perforations: a single-center case series. Endoscopy. 2011;43(3):240–2.
100. Iqbal CW, et al. Surgical management and outcomes of 165 colonoscopic perforations from a single institution. Arch Surg. 2008;143(7):701–6; discussion 706–7.
101. Levy I, Gralnek IM. Complications of diagnostic colonos­copy, upper endoscopy, and enteroscopy. Best Pract Res Clin Gastroenterol. 2016;30(5):705–18.
102. Park JY, etal. The outcomes of management for colonoscopic perforation: a 12-year experience at a single institute. Ann Coloproctol. 2016;32(5):175–83.
103. Martinez-Perez A, etal. Laparoscopic vs. open surgery for the treatment of iatrogenic colonoscopic perforations: a systematic review and meta-analysis. World J Emerg Surg. 2017;12:8.
104. Di Saverio S, etal. Minimally invasive laparoscopic management of colonoscopic perforation avoiding laparotomy and colostomy: when and how to perform primary repair- a video vignette. Color Dis. 2016;18(8):817–8.
105. Lohsiriwat V. Colonoscopic perforation: incidence, risk fac­tors, management and outcome. World J Gastroenterol. 2010;16(4):425–30.
106. Paspatis GA, et al. Diagnosis and management of iatrogenic endoscopic perforations: European Society of Gastrointestinal Endoscopy (ESGE) Position Statement. Endoscopy. 2014;46(8):693–711.
107. Magdeburg R, etal. Endoclipping of iatrogenic colonic perfora­tion to avoid surgery. Surg Endosc. 2008;22(6):1500–4.
108. Kim JS, et al. Endoscopic clip closure versus surgery for the treatment of iatrogenic colon perforations developed during diag­nostic colonoscopy: a review of 115,285 patients. Surg Endosc. 2013;27(2):501–4.
109. Cho SB, et al. Therapeutic options for iatrogenic colon perfora­tion: feasibility of endoscopic clip closure and predictors of the need for early surgery. Surg Endosc. 2012;26(2):473–9.
110. Taku K, et al. Iatrogenic perforation associated with therapeu­tic colonoscopy: a multicenter study in Japan. J Gastroenterol Hepatol. 2007;22(9):1409–14.
111. An SB, et al. Decision-making in the management of colono­scopic perforation: a multicentre retrospective study. Surg Endosc. 2016;30(7):2914–21.
112. Committee, A.S.o.P., et al. Complications of colonoscopy. Gastrointest Endosc. 2011;74(4):745–52.
113. Sorbi D, et al. Postpolypectomy lower GI bleeding: descriptive analysis. Gastrointest Endosc. 2000;51(6):690–6.
114. Kavic SM, Basson MD.Complications of endoscopy. Am J Surg. 2001;181(4):319–32.
115. Guo SB, et al. Application of endoscopic hemoclips for non­variceal bleeding in the upper gastrointestinal tract. World J Gastroenterol. 2009;15(34):4322–6.
116. Strate LL, Gralnek IM. ACG clinical guideline: management of patients with acute lower gastrointestinal bleeding. Am J Gastroenterol. 2016;111(5):755.
117. Jaruvongvanich V, et al. Risk factors for delayed colonic post­polypectomy bleeding: a systematic review and meta-analysis. Int J Color Dis. 2017;32(10):1399–406.
118. Watabe H, etal. Risk assessment for delayed hemorrhagic compli­cation of colonic polypectomy: polyp-related factors and patient­related factors. Gastrointest Endosc. 2006;64(1):73–8.
119. Hui AJ, etal. Risk of colonoscopic polypectomy bleeding with anticoagulants and antiplatelet agents: analysis of 1657 cases. Gastrointest Endosc. 2004;59(1):44–8.
120. Sawhney MS, etal. Risk factors for severe delayed postpolypec­tomy bleeding. Endoscopy. 2008;40(2):115–9.
121. Shalman D, Gerson LB. Systematic review with meta-analysis: the risk of gastrointestinal haemorrhage post-polypectomy in patients receiving anti-platelet, anti-coagulant and/or thienopyri­dine medications. Aliment Pharmacol Ther. 2015;42(8):949–56.
122. Rossetti A, et al. Transarterial embolization in acute colonic bleeding: review of 11 years of experience and long-term results. Int J Color Dis. 2013;28(6):777–82.
123. Ko CW, Dominitz JA. Complications of colonoscopy: mag­nitude and management. Gastrointest Endosc Clin N Am. 2010;20(4):659–71.
124. Hirasawa K, et al. Coagulation syndrome: delayed perforation after colorectal endoscopic treatments. World J Gastrointest Endosc. 2015;7(12):1055–61.
125. Kim HW. What is different between postpolypectomy fever and postpolypectomy coagulation syndrome? Clin Endosc. 2014;47(3):205–6.
126. Shin YJ, etal. CT ndings of post-polypectomy coagulation syn­drome and colonic perforation in patients who underwent colono­scopic polypectomy. Clin Radiol. 2016;71(10):1030–6.
127. Piccolo G, et al. Presentation and management of splenic injury after colonoscopy: a systematic review. Surg Laparosc Endosc Percutan Tech. 2014;24(2):95–102.
128. Jehangir A, etal. A systematic review of splenic injuries during colonoscopies: Evolving trends in presentation and management. Int J Surg. 2016;33 Pt A:55–9.
129. Michetti CP, Smeltzer E, Fakhry SM. Splenic injury due to colonoscopy: analysis of the world literature, a new case report, and recommendations for management. Am Surg. 2010;76(11):1198–204.
4 Endoscopy
77
130. Stein DF, Myaing M, Guillaume C.Splenic rupture after colonos­copy treated by splenic artery embolization. Gastrointest Endosc. 2002;55(7):946–8.
131. Holubar S, etal. Splenic rupture: an unusual complication of colo­noscopy. Am Surg. 2007;73(4):393–6.
132. Low DE, et al. Prospective assessment of risk of bacte­remia with colonoscopy and polypectomy. Dig Dis Sci. 1987;32(11):1239–43.
133. Wilson W, et al. Prevention of infective endocarditis: guide­lines from the American Heart Association: a guideline from the American Heart Association Rheumatic Fever, Endocarditis, and Kawasaki Disease Committee, Council on Cardiovascular Disease in the Young, and the Council on Clinical Cardiology, Council on Cardiovascular Surgery and Anesthesia, and the Quality of Care and Outcomes Research Interdisciplinary Working Group. Circulation. 2007;116(15):1736–54.
134. Spach DH, Silverstein FE, Stamm WE.Transmission of infection by gastrointestinal endoscopy and bronchoscopy. Ann Intern Med. 1993;118(2):117–28.
135. Kovaleva J, et al. Transmission of infection by exible gastro­intestinal endoscopy and bronchoscopy. Clin Microbiol Rev. 2013;26(2):231–54.
136. Nelson DB, et al. Technology status evaluation report. Transmission of infection by gastrointestinal endoscopy. May
2001. Gastrointest Endosc. 2001;54(6):824–8.
137. Epstein L, et al. New Delhi metallo-beta-lactamase-producing carbapenem-resistant Escherichia coli associated with exposure to duodenoscopes. JAMA. 2014;312(14):1447–55.
138. Ofstead CL, et al. Re-evaluating endoscopy-associated infec­tion risk estimates and their implications. Am J Infect Control. 2013;41(8):734–6.
139. Shin SP, Kim WH.Recent update on microbiological monitoring of gastrointestinal endoscopes after high-level disinfection. Clin Endosc. 2015;48(5):369–73.
140. Larsen S, Kalloo A, Hutess S.The hidden cost of colonoscopy including cost of reprocessing and infection rate: the implications for disposable colonoscopes. Gut. 2020;69(2):197–200.
141. Yong E, etal. Efciency of an endoscopy suite in a teaching hos­pital: delays, prolonged procedures, and hospital waiting times. Gastrointest Endosc. 2006;64(5):760–4.
142. Sauer BG, et al. Efciency of endoscopy units can be improved with use of discrete event simulation modeling. Endosc Int Open. 2016;4(11):E1140–5.
143. Berg BP, et al. Estimating the cost of no-shows and evalu­ating the effects of mitigation strategies. Med Decis Mak. 2013;33(8):976–85.
144. Childers RE, etal. The role of a nurse telephone call to prevent no­shows in endoscopy. Gastrointest Endosc. 2016;84(6):1010–1017 e1.
145. Tsai MH, et al. Changing anesthesia block allocations improves endoscopy suite efciency. J Med Syst. 2019;44(1):1.
146. Rex DK. Detection measures for colonoscopy: considerations on the adenoma detection rate, recommended detection thresh­olds, withdrawal times, and potential updates to measures. J Clin Gastroenterol. 2020;54(2):130–5.
147. Barclay RL, et al. Colonoscopic withdrawal times and ade­noma detection during screening colonoscopy. N Engl J Med. 2006;355(24):2533–41.
148. Shaukat A, et al. Longer withdrawal time is associated with a reduced incidence of interval cancer after screening colonoscopy. Gastroenterology. 2015;149(4):952–7.
149. Rex DK, et al. Quality indicators for colonoscopy. Gastrointest Endosc. 2015;81(1):31–53.
150. Wang HS, etal. Adenoma detection rate is necessary but insuf­cient for distinguishing high versus low endoscopist performance. Gastrointest Endosc. 2013;77(1):71–8.
151. Zhao S, et al. Magnitude, risk factors, and factors associated with adenoma miss rate of tandem colonoscopy: a systematic review and meta-analysis. Gastroenterology. 2019;156(6):1661–1674 e11.
152. Spier BJ, et al. Colonoscopy training in gastroenterology fel­lowships: determining competence. Gastrointest Endosc. 2010;71(2):319–24.
153. Weis JJ, etal. FES exam outcomes in year two of a prociency- based endoscopic skills curriculum. Surg Endosc. 2020;34(2):961–6.
154. Mizota T, et al. Development of a fundamentals of endoscopic surgery prociency-based skills curriculum for general surgery residents. Surg Endosc. 2020;34(2):771–8.
155. Vassiliou MC, et al. Global Assessment of Gastrointestinal Endoscopic Skills (GAGES): a valid measurement tool for techni­cal skills in exible endoscopy. Surg Endosc. 2010;24(8):1834–41.
Endoscopic Management ofPolyps andEndolumenal Surgery
WilliamForrestJohnston andEmreGorgun
5
Abbreviations
ESGE European Society of GI Endoscopy EMR Endoscopic mucosal resection ESD Endoscopic submucosal dissection CELS Combined endoscopic-laparoscopic surgery ELS Endolumenal surgery
Key Concepts
• Endolumenal surgery is the forefront of minimally inva­sive surgery and is rapidly developing.
• Colon and rectal surgeons should be involved in the pro­gression of endolumenal surgery as it will offer benet to patients.
• New endolumenal techniques can be used to address large polyps that once required resection and treat malignant large bowel obstructions.

Introduction

Colonoscopy was initially described as a way to screen patients for mucosal abnormalities in the colon and has been adopted as the standard for colorectal cancer screening and prevention. However, when retrograde colonoscopy was rst described in 1969, “there were some who said it couldn’t be done, shortly followed by those who said it couldn’t be done safely, followed by those who declared that it required a tricky
W. F. Johnston Ochsner Clinic, Department of Colon and Rectal Surgery, New Orleans, LA, USA
E. Gorgun ( Cleveland Clinic, Department of Colorectal Surgery, Cleveland, OH, USA e-mail: gorgune@ccf.org
*)
skill which few would be able to acquire” [1]. Time has proved otherwise. Colonoscopic polypectomy has been demonstrated to decrease the incidence of colorectal cancer and has been widely adopted by the medical community [2]. With advances in technology, colonoscopy has progressed dramatically, and exible colonoscopy is now used with various platforms that enable advanced endoscopic surgical procedures to be effec­tively completed. Endolumenal surgery is a rapidly progres­sive eld in gastrointestinal surgery performed by both surgeons and gastroenterologists that offers the benets of non-invasive surgery done in an outpatient setting. However, endolumenal surgeons are confronted with the challenge of operating through a exible scope in a conned space that is frequently moving. Similar to opponents of early colonos­copy, there are many physicians in various stages of opposi­tion. Due to the benets to the patient, endoscopic surgery has the potential to be the next leap forward in minimally invasive surgery. This chapter will discuss the technical aspects of endolumenal surgery, ranging from forceps polypectomy to endoscopic submucosal dissection and colonic stenting.

Forceps

There are three commonly available options for forceps polyp­ectomy: cold biopsy forceps, jumbo cold biopsy forceps, and hot biopsy forceps. For cold biopsy, the standard forceps open to 6 mm, and jumbo cold forceps open to 8.6 mm. Jumbo biopsy forceps have been shown to be superior to standard cold forceps for complete resection [3]. Historically, hot biopsy for­ceps were commonly used for polyp resection with the theo­retical benet of fulgurating any remaining dysplastic tissue around the polyp. However, this theoretical advantage has been refuted. A retrospective review of 62 hot biopsy polypectomies demonstrated a 17% rate of persistent polypoid tissue on repeat endoscopy 1–2weeks after the original treatment [4].
Additionally, hot biopsy is associated with an increased
risk of delayed hemorrhage compared to cold biopsy [5].
© Springer Nature Switzerland AG 2022 S. R. Steele et al. (eds.), The ASCRS Textbook of Colon and Rectal Surgery, https://doi.org/10.1007/978-3-030-66049-9_5
79
80
W. F. Johnston and E. Gorgun
Furthermore, hot biopsy alters the polyp morphology and creates more histological architectural distortion and frag­mentation than cold biopsy [6]. For the aforementioned rea­sons, the European Society of GI Endoscopy (ESGE) has recommended against the use of hot biopsy forceps [7].
Cold biopsy forceps have also been described as an
adjunct to difcult to remove large spreading polyps. While these polyps are typically removed with snare (described below), some polyps will not allow snare resection as the snare will slide over the polyp. In these situations, cold for­ceps are used to methodically avulse all visible polypoid tis­sue. Following avulsion of the mucosa, the submucosa and margins can be treated with soft coagulation from the tip of a hot snare. This technique, deemed CAST for Cold-forceps Avulsion with adjuvant Snare-Tip soft coagulation, has been reported as an effective and safe strategy for the management of non-lifting large laterally spreading (LST) colonic lesions [8]. CAST is easy to use, does not require additional equip­ment, and is useful adjunctive technique for organ sparing.

Snare

Endoscopic snare allows resection of larger lesions and more tissue compared to forceps. Incomplete resection of polyps by any method is associated with interval development of colorectal cancer in patients undergoing colonoscopy [9]. In removal of polyps <6mm, snare excision has a higher rate of complete resection compared to forceps removal (93% for cold snare vs. 76% for cold biopsy forceps, p<0.001) [10].
Snares vary in size, shape, and ability for coagulation.
Hot snares are the traditional method for endoscopic snaring but have waned in popularity over recent years due to com­plications including increased risk of delayed bleeding and thermal injury. Use of a cold snare without electrocautery is associated with lower rate of post-polypectomy hemorrhage and shorter time for polypectomy and colonoscopy [11, 12]. Complete resection rates with cold snare are equivalent to hot snare [13]. Dedicated cold snares have been further improved with use of a thinner wire that more easily cuts tis­sue. Compared to traditional snares used without cautery, dedicated thin-wire cold snares have a higher rate of com­plete resection, especially with polyps 8–10mm in size or sessile polyps [14]. The 2017 guidelines from ESGE recom­mend cold snare polypectomy as the preferred method for polyps <5mm in size and strongly favor cold snare polypec­tomy for polyps 6–9mm in size [7]. Hot snare polypectomy has been reserved for sessile polyps 10–19mm in size after submucosal injection has been used to decrease the risk of thermal injury. Hot snare is also recommended for peduncu­lated polyps to decrease the rate of bleeding.
Bleeding after polypectomy is infrequent but may result
in hospitalization, repeat colonoscopy, and poor patient
experience. The rate of bleeding after polypectomy is approximately 1–2 per 1000 patients and is 10 times the rate of bleeding compared to colonoscopy without polypectomy [15]. Bleeding after cold snare polypectomy tends to be immediate and can be addressed at the time of initial colo­noscopy, while bleeding after hot snare is often delayed and not apparent at the initial colonoscopy. Bleeding after hot snare occurs 0.1–0.7% of polypectomies and can occur up to 30days after the procedure [16]. Prophylactic clip placement after routine polypectomy does not decrease the risk of delayed bleeding [17], and this practice should be avoided as it drastically increases the cost of the procedure without sub­stantial benet. Selective use of endoscopic clips is discussed later in the chapter.
Tips forOptimal Snaring
Polypectomy is required in 30–40% of all colonoscopies. To make polypectomy easier, the polyp should be positioned at the bottom half of the screen because the instrument channel on the colonoscope exits the scope at the 5 o’clock position. Occasionally, the lesion cannot be placed in the inferior aspect of the screen due to tortuosity of the colon or location behind a prominent fold. In those situations, working with the scope tip further away from the lesion may facilitate pol­ypectomy by producing a favorable angle of attack to the polyp. Additionally, jumbo forceps removal may be techni­cally easier for polyps in a challenging location if the size is small. If a snare is applicable, lesions are more easily grasped with dedicated cold snares, since they have a thinner wire that can grip the tissue better than an electrocautery compat­ible snare. If a hot snare is used after a lift for a larger lesion, consideration should be given for use of a non-oval-shaped snare. Snares with some angulation, like a hexagonal snare, tend to grasp tissue better as well as have a greater proximal opening compared to standard oval or round snares. Figure5.1 shows different type of snares.
Care should be taken during polypectomy to ensure that complete resection of the polyp has been performed. In a prospective study of over 1400 patients, there was a 10% rate of incomplete resection for polyps 5–20mm. Risk factors for incomplete resection included larger size and sessile serrated polyps vs. adenoma [18]. Any remaining polyp tissue after snare polypectomy can be removed with repeat snare exci­sion or cold forceps avulsion.

Lifting

Flat lesions may require submucosal lift to separate the desired tissue for resection from the underlying colonic mus­cular wall and decrease the risk of full-thickness mechanical
Exacto (cold)
Snare
(Lasso)
Snare
Cleveland
(snare with injection needle)
5 Endoscopic Management ofPolyps andEndolumenal Surgery
Fig. 5.1 Different types of snares (Reprinted with permission, Cleveland Clinic Center for Medical Art & Photography ©2020. All Rights Reserved)
81
Small
Standard
Oval
Lariat Snare
disruption or thermal injury from a hot snare. Common sub­mucosal lifting agents include saline, hyaluronic acid, glyc­erol, dilute albumin, and proprietary gels. For most polyps, submucosal saline injection sufces and provides a lift that lasts approximately 3minutes [19]. Normal saline has proven equivalent to other lifting solutions in terms of complete resection rate, post-procedural bleeding, and post­polypectomy syndrome or perforation [20]. For more com­plex lesions requiring a longer resection time, a more durable solution is desirable. Viscous solutions are often more dura­ble and provide a more localized lift with less lateral diffu­sion. Multiple solutions exist, ranging from hydroxyethyl starch (hetastarch) to more expensive proprietary solutions like Eleview® (Medtronic, Dublin, Ireland) and ORISE® (Boston Scientic, Marlborough, MA) that can last for over 40minutes [21].
Adequate lift is critical to allow for advanced endoscopic techniques. Ideal injections are submucosal, but endoscopic injections can be easily misplaced in deeper layers (subsero­sal or intramuscular). Addition of colored dye to the injected solution can help delineate the submucosal layer as the over­lying mucosa is thin and the color of the solution will be readily appreciated. Correctly placed submucosal injections
Jumbo Hexagonal Needle Tip Anchor
Braided Ridge
Snare
Clinic
©2019
iSnare
tend to create more focal and taller lifts, while subserosal or intramuscular injections will create a less prominent and broader lift [22]. Submucosal injection can be facilitated by starting to inject solution prior to putting the needle into the mucosa so that the injectant will push away submucosal lay­ers once penetrating the overlying mucosa. Alternatively, the needle can be placed into the colon wall and then gently withdrawn back into the submucosal layer. It is easier to cre­ate a lift when injecting in a tangential direction to the bowel wall and avoiding injecting perpendicular to the bowel wall. Techniques for submucosal injection are also applicable to endoscopic tattoo placement to avoid tattoo dispersing throughout the abdomen. If a larger area is needed to lift, injections should be directed at the border of the prior sub­mucosal cushion to stay in the submucosal plane (Fig. 5.2).
Submucosal lift injections can be performed in a dynamic technique to make a taller lift. The needle placement in the submucosa is conrmed with a small amount of injection to demonstrate an adequate lift plane followed by a large­volume rapid injection. During the large-volume injection, the needle and scope can be re-directed within the submu­cosa to generate a tall and long-lasting lift [23]. For lesions that are on a fold, submucosal injection should start on the
82
Fig. 5.2 To perform a submucosal injection, the injection needle should be tangential (parallel) to the mucosa. Fluid is injected as the needle is advanced to push away the muscularis and create and submu­cosal expansion to lift the overlying tissue (Reprinted with permission, Cleveland Clinic Center for Medical Art & Photography ©2020. All Rights Reserved)
proximal/oral part of the bowel to lift the lesion toward the scope. Lesions that do not lift may be due to entry into the incorrect plane, scarring from past attempts at injection or polypectomy, or related to more advanced lesions that have invaded into the submucosa.

Endoscopic Mucosal Resection

Lesions that are too large for simple polypectomy can be treated with endoscopic mucosal resection (EMR). EMR is regularly used for polyps ranging from 20mm to 50mm in size. EMR is a technique designed for sessile or at lesions that are conned to the supercial layer of the colon wall. The most common EMR method is the lift and cut technique, in which the lesion is lifted with a submucosal injection fol­lowed by snare polypectomy. With expansion of the submu­cosal space, the polyp can be removed without injury to the muscular layer of the bowel. The goal is to completely remove the polyp with as few snare excisions as possible [7]. EMR is started with a submucosal injection to lift the lesion to create space for resection. Since lesions with EMR are often larger than simple polypectomy, a solution with a lon­ger durability than saline is desired. The ESGE recommends the addition of a staining dye (e.g., methylene blue or indigo carmine) to the submucosal injection to help identify lesion margins and deep tissue injury. The submucosal lift protects the underlying muscularis propria while decreasing resis­tance in the desired resection plane. The lesion is then resected with snare in as few pieces as possible with care to make sure that the entire lesion is removed. A normal margin of 2–3mm of healthy-appearing tissue should be included to ensure complete removal. To decrease the risk of leaving
W. F. Johnston and E. Gorgun
islands of polyp tissue, piecemeal snaring should be done sequentially with the snare aligned along the margin of the prior resection. If there are any small remaining amounts of polypoid tissue, these can be ablated with electrocautery or removed with forceps. Following resection, clips can be selectively placed for tissue approximation (Fig.5.3). Hot snare is commonly used during EMR.However, cold snare has also been shown to be effective for piecemeal resection after submucosal lift for polyps up to 55mm with a low rate of recurrent disease or complication [24].
The major drawback of EMR is that larger lesions cannot be excised in en bloc fashion. EMR has been shown to be safe and effective for lesions smaller than 20 mm [25]. Lesions greater than 2 cm are often excised in piecemeal fashion, which limits the pathologic assessment of the polyp. Piecemeal resection can theoretically allow small amounts of polypoid tissue to remain that would result in recurrent polyp growth. While early experience with EMR indicated recur­rent polyp formation on follow-up colonoscopy in 30% of patients [26], a recent prospective multicenter trial of 1000 EMR procedures demonstrated a lower recurrence rate (17% overall). For smaller polyps (20mm in size), recurrence rate was 5% [27]. Risk factors for recurrence were increased size (OR = 8.2 for polyp >40 mm vs. 20 mm), APC usage (OR = 2.4), and bleeding (OR = 1.6). APC usage likely results in supercial ablation of the polyp, but does not eradi­cate the polyp tissue. The lack of efcacy of APC has been conrmed with other studies evaluating APC versus avulsion for the treatment of small amounts of residual polyp tissue after EMR.Avulsion with hot biopsy forceps was associated with a signicantly lower adenoma recurrence rate compared to ablation with APC (10% recurrence with avulsion vs. 59% recurrence with APC on follow-up colonoscopy in 1 study of 278 patients with EMR of colon lesion >2cm) [28].
Clip
While routine use of prophylactic clips after polypectomy is discouraged due to cost, endoscopic clips can be used selec­tively to re-approximate mucosa after EMR or be placed on bleeding vessels in an effort to increase hemostasis. Risk fac­tors for post-polypectomy bleeding include large polyp size, proximal location, use of anticoagulant or antiplatelet agents, and the presence of multiple comorbidities [29]. In a recent multicenter randomized control trial, endoscopic clip appli­cation to close the mucosal defects of polypectomies for non-pedunculated polyps larger than 20mm was associated with a decreased rate of post-polypectomy bleeding [30]. The benet of clip application was most pronounced in the proximal colon with an absolute risk reduction of 6.3% (9.6% bleed without clips vs. 3.3% bleed with clips, p < 0.001). Clip application for large polyps in the distal
5 Endoscopic Management ofPolyps andEndolumenal Surgery
83
Fig. 5.3 EMR technique. (a) Large at lesion in the right colon. (b) Lift with submucosal injection. (c) Piecemeal EMR resection with snare. (d) Endoscopic clip placement for closure
colon did not affect the rate of post-polypectomy bleeding. Application of clips has also been shown to decrease the rate of delayed bleeding even if complete mucosal re­approximation could not be accomplished [31]. Therefore, consideration should be given for selective use of clips fol­lowing endoscopic resection of large polyps (>2cm), par­ticularly in the proximal colon.
underwater EMR, the air is evacuated and the lumen is lled with 500mL to 1L sterile water. The edges of the polyp are marked with APC.The polyp is removed in piecemeal fash­ion with a snare on cutting current to include all of the prior APC marks. Any small remnant tissue is treated hot biopsy coagulation. It is hypothesized that the water distends and attens the colon to prevent the muscularis from being brought into the snare excision. When compared to tradi­tional EMR, selective groups have demonstrated that under-
Underwater EMR
water EMR allows increased complete macroscopic resection and decreased recurrence rates [33]. Additionally, underwa-
Underwater EMR was described in 2012 as a method to avoid submucosal injection during resection of large polyps with EMR [32]. As described above, submucosal injection may be in the wrong layer leading to intramuscular injection. Furthermore, submucosal injection may make snare applica­tion more challenging as the snare may slip over the dis­tended mucosa and not grasp the polyp. To perform
ter EMR has been used to increase rates of salvage endo­scopic resection for recurrent polyps after past attempts at endoscopic resection [34].
Underwater techniques have also been applied to endo­scopic submucosal dissection (ESD) [35]. Polyp resection while submerged in water can allow the edge of mucosa to oat away from the submucosa and therefore improve the
84
W. F. Johnston and E. Gorgun
endoscopic view of the dissection plane. Additionally, sub­merging the process of ESD in uid allows greater heat dis­sipation, which theoretically decreases thermal injury. Potential benets of underwater endoscopic resection must be balanced against the increased time requirement for water instillation.

Endoscopic Submucosal Dissection

Whereas EMR is limited in terms of size of en bloc excision, ESD is useful for larger lesions where complete histological evaluation is desired. ESD was rst popularized in Japan in the 1990s for treatment of early gastric cancer. The gastric wall is thick and therefore allows for safe submucosal dissec­tion with a margin for error. Colonic ESD was rst described in the early 2000s [36]. The thin wall of the colon makes colonic ESD more challenging due to increased risk of full­thickness injury. However, the benet of ESD is a more com­plete resection with lower recurrence rate. In a retrospective study of over 350 patients comparing colonic ESD and EMR, colonic ESD has a sevenfold lower recurrence rate. However, the complete resection of ESD comes at the cost of a nearly vefold increased rate of perforation (6.2% ESD perforation vs. 1.3% EMR perforation) [37].
Colonic ESD allows resection of large benign lesions that traditionally required surgical resection. Dissection is per­formed in the submucosal layer under the lesion using a dedicated electrosurgical knife. Recent studies have shown that only 20% of polyps that were deemed endoscopically unresectable and referred to a surgeon for resection have invasive malignancy on nal pathology [38, 39]. The rate of malignancy is even lower when carefully evaluating polyp morphology (see patient selection for ESD below). Large polyps that appeared benign to the endoscopist have less than 10% cancer rate [40]. This data suggests that the vast majority of patients with large benign-appearing colonic pol­yps can be treated adequately with endoscopic resection, saving these patients the morbidity of a larger colon resec­tion. Comparing ESD to laparoscopic formal resection, patients treated with ESD had a signicantly shorter hospital stay and decreased hospital nancial cost [41]. Complication rates were similar, but the severity of complications was less in the patients treated with ESD compared to surgical resection.
ESD Complications
Prior to considering any intervention, one must be aware of the potential complications. Similar to most endoscopic pol­ypectomy techniques, the most common complications after ESD are abdominal pain, bleeding, perforation, and tumor recurrence. Post-ESD electrocoagulation syndrome is
similar to post- polypectomy syndrome and can be seen in up to 40% of patients [42]. Post-ESD bleeding occurs in approx­imately 2–7% of patients [43, 44]. ESD is also associated with a 5–20% perforation rate [45]. Risk of perforation is associated with increased tumor size and the presence of brosis. Perforation during ESD of lesions that are malig­nant can result in potential tumor seeding of the abdomen, as evidenced from the more robust gastric cancer literature. In a review of 22 perforations during gastric ESD, 2 patients (9%) had peritoneal seeding [46]. Lastly, endoscopic meth­ods at resection carry the potential for recurrence. Local recurrence after ESD is remarkably low (approximately 1%) [43]. Furthermore, none of the recurrences contained inva­sive cancer and all were adequately managed with repeat endoscopic resection in this series.
Patient Selection forESD
Careful selection of patients for attempted EMR and ESD is key. Procedural selection is based on the size of the tumor and the risk of underlying carcinoma. If the lesion is <2cm, EMR is often favored. ESD is typically reserved for lesions >2 cm without features of malignancy. For patients where the diagnosis is unclear, ESD is an acceptable technique for excisional biopsy of lesions that have an increased risk of carcinoma but should be used with caution as the risk of full­thickness injury may be increased due to distortion of the submucosa from malignant invasion or brosis.
When doing a colonoscopy or preparing for ESD, the potential for underlying malignancy can be assessed by endoscopic characterization of the polyp appearance. Appearance of the lesion is critical and can be evaluated with one of several available classication systems, including Paris, Kudo pit pattern, or Narrow-band Imaging International Colorectal Endoscopic (NICE) classication. The gross morphology of the lesion is described by the Paris pattern, which divides lesions into polypoid vs. non-polypoid appear­ance. The non-polypoid supercial lesions are then divided based on their level of protrusion into the lumen (slightly elevated, at, slightly depressed, and excavated). There is a clear inverse relationship between supercial lesion protru­sion and the risk of submucosal invasion [47]. However, there is signicant inter-observer variability in the classica­tion of polyps according to the Paris system, suggesting that a simpler three-category classication of pedunculated, ele­vated, or depressed may be more widely applicable [48]. Depressed lesions have an increased rate of malignancy.
Pit patterns are based on the specic arrangement of glands in different lesions and can help determine hyper­plastic vs. adenomatous vs. malignant lesions [49]. Narrow­band imaging (NBI) is commonly available technology that lters light into specic blue and green waveforms that will highlight vessels and mucosal tissue. NBI can be used to
be suggested by an irregular vessel or surface pattern, and is often associated with atypical morphology (e.g., depressed area).
5 Endoscopic Management ofPolyps andEndolumenal Surgery
85
Type 1
Color Same or lighter than background
Vessels
Surface
Pattern
Most likely
pathology
Examples
None, or isolated lacy vessels
coursing across the lesion
Dark or white spots of uniform size,
or homogeneous absence of
pattern
Hyperplastic
Type 2 Type 3
Browner relative to background
(verify color arises from vessels)
Brown vessels surrounding white
structurs**
Ova, tubular or branched
white structure
surrounded by brown vessels**
Adenoma***
Brown to dark brown relative to background; sometimes patchy
whiter areas
Has area(s) of disrupted or missing
vessels
Amorphous or absent surface
pattern
Deep submucosal
invasive cancer
* Can be applied using colonoscopes with or without optical (zoom) magnification
** These structures (regular or irregular) may represent the pits and the epithelium of the crypt opening.
*** Type 2 consists of Vienna classification types 3,4 and superficial 5 (all adenomas with either low or high grade dysplasia,
or with superficial submucosal carcinoma). The presence of high grade dyslasia or superficial submucosal carcinoma may
Fig. 5.4 NICE classication. NICE, NBI International Colorectal Endoscopic; NBI narrow-band imaging (Reused with permission from Hayashi etal. [50]. Copyright © Elsevier 2013)
classify the polyp as hyperplastic, adenomatous, or malig­nant based on lesion color, vascular pattern, and surface pat­tern according to the NICE classication (Fig. 5.4) [50]. Accurate endoscopic assessment allows appropriate selec­tion of polyps for EMR/ESD and avoidance of polyps that are better treated with resection due to concern for underly­ing malignancy.
The ability of the polyp to lift after submucosal injection has also been used to assess the potential for invasive malig­nancy. If tumor extends into the submucosa, the submucosa will not expand with injection. In a study of over 270 lesions, non-lifting sign had an overall accuracy of 95% for detecting
of 98%, positive predictive value of 80%, and negative pre­dictive value of 95% [51]. Furthermore, inadequate lift dra­matically increases the likelihood of full-thickness injury as the submucosal layer is not expanded and there is conse­quently no buffer. Lesions may not lift well if there is brosis from prior attempts at resection or if the injection is too deep in the colon wall. The multiple reasons why a polyp will not adequately lift may explain why endoscopic assessment is more sensitive than the non-lifting sign for detecting inva­sion in at or depressed lesions. Thus, in patients where the polyp does not lift well, there remains a role for ESD as long as the polyp has a benign morphologic appearance.
an invasive malignancy, with a sensitivity of 62%, specicity