Abstract
Colonoscopy is an important and frequently performed procedure. It is effective in the prevention of colorectal cancer and is an important test in the investigation of many gastrointestinal symptoms. This review focuses on developments over the last 5 years that have led to changes in aspects of colonoscopy, including patient preparation, technical factors, therapeutic procedures, safety, and quality.
Keywords: Colonoscopy, colorectal cancer
Introduction
Colonoscopy remains the gold-standard investigation for inspecting the mucosa of the colon for pathology such as cancer, adenomas, or inflammation. It remains preferable, in many situations, to other imaging modalities such as computed tomography (CT) colonography or barium enema due to the capacity to intervene and sample or remove pathology encountered.
Emerging evidence over the last 5 years has led to important changes in the practice of colonoscopy throughout the patient journey. This review will focus on important practical developments and areas of interest. We will look at all aspects of colonoscopy, from the preparation, through the procedure and endoscopic therapy, to safety and quality assurance.
Indications for colonoscopy
Colorectal cancer screening
Colorectal cancer is the second most common cancer worldwide 1. There is variation in screening practices globally 2. Most screening programs employ a non-invasive test such as fecal occult blood testing to identify higher risk patients needing to undergo colonoscopy. Many screening programs are now using or moving towards using newer non-invasive tests, such as fecal immunochemical testing (FIT) or fecal DNA tests, which are associated with greater uptake and detection rates for adenomas and colorectal cancer 3, 4. In higher income settings, colonoscopy may be offered as the screening test. In the USA, a national survey estimated 65% of adults to be engaged with colorectal cancer screening, with colonoscopy being the most commonly used test 5. Such widespread colonoscopy screening appears to be reducing colorectal cancer incidence in the USA 6.
Preparation for colonoscopy
An adequate level of bowel cleansing is critical for the efficacy of colonoscopy. Key quality indicators including cecal intubation rate and adenoma detection rate (ADR) are higher in patients with adequate bowel preparation 7. Furthermore, there is an improved rate of detection of flat lesions within the proximal colon in patients with adequate bowel preparation compared to those with inadequate preparation 8. Up to 1 in 5 colonoscopies are considered to have imperfect bowel preparation quality 9. Inadequate bowel preparation leads to lower ADRs and more missed lesions, and results in increased costs associated with rescheduling of the colonoscopy or organization of alternative investigations 10.
Recent years have seen the development of bowel cleansers that are more acceptable to patients. Preparations have evolved from large-volume (7–12 L) solutions with hypertonic saline to osmotically balanced solutions containing polyethylene glycol (PEG) and electrolytes. Introduction of split-dose bowel preparation regimens, where half the dose is given the day before the test and half on the day of the test, has significantly enhanced the ability to achieve high-quality cleansing with adequate preparation achieved in 85% compared with 63% in single-dose preparations 11. Split-dose regimens have resulted in improved ADRs and detection of flat lesions 5. The timing between the last dose of bowel preparation and colonoscopy has been shown to correlate with the quality of bowel preparation, and ideally should be less than 4 hours 12. Safety concerns have been raised regarding the use of sodium phosphate preparations and the associated risk of major fluid shift and electrolytes as well as chronic kidney disease from acute phosphate nephropathy 13. These risks make it an unsuitable first-line bowel preparation agent, and careful patient selection and appropriate cautions need to be taken before its use. In patients with renal failure, PEG is now the main recommended bowel preparation.
Patient education and willingness to participate in bowel preparation improves the outcome of cleansing. The delivery of both oral and written instructions for bowel preparation, as opposed to written alone, has been shown to be an independent predictor of adequate level of cleansing 14.
The above evolutionary changes in bowel preparation have increased its efficacy, safety, and patient tolerability, resulting in higher quality colonoscopy.
Sedation
Current UK practice in colonoscopy is to use light conscious sedation or an unsedated approach. Maximum recommended doses of commonly used agents include midazolam (up to 5 mg) and fentanyl (up to 100 mcg) or pethidine (up to 50 mg). Unsedated colonoscopy, often using Entonox, is increasingly prevalent owing to improvements in technique. In the English Bowel Cancer Screening Program in 2014, 29.4% of colonoscopies were performed unsedated (personal correspondence, Professor M.D. Rutter). No difference in adenoma detection was observed in the unsedated group 15.
In some areas of the world, deeper sedation with propofol or general anesthesia is the preferred approach, although this may not be associated with improved adenoma detection, patient experience, or cost effectiveness, and has been shown to be associated with increased risk of complications 16, 17.
Procedural developments
Improving adenoma detection
An important objective of screening and surveillance colonoscopy is adenoma detection. Decreased incidence of post-colonoscopy colorectal cancer has been observed among colonoscopists with higher ADRs 18. An important paper by Corley et al. has also demonstrated an inverse relationship between ADR and interval cancer incidence and mortality from colorectal cancer. Based on 314,872 colonoscopies performed by 136 gastroenterologists, each 1.0% increase in ADR was associated with a 3.0% decrease in the risk of colorectal cancer (hazard ratio, 0.97; 95% confidence interval, 0.96–0.98) 19. The progress in understanding the importance and relevance of ADR has led to its recognition as the key performance indicator of colonoscopy and a useful tool for quality improvement, as discussed later in this paper.
A number of recent advances have sought to overcome some of the barriers to adenoma detection. Regular feedback of performance indicators to colonoscopists, ideally with peer comparators, has been shown to positively affect adenoma detection 20. The introduction of a simple training package and a bundle of simple maneuvers (withdrawal time >6 minutes, rectal retroversion, Buscopan use, and right lateral positioning on withdrawal) led to an increase in adenoma detection among a group of colonoscopists in the Quality Improvement in Colonoscopy (QIC) study 21.
New technologies to facilitate examination of difficult-to-access mucosa are currently being evaluated, although not all studies of quality improvement have been successful. These aim to increase the exposure of mucosa behind haustral folds, rectal valves, the ileocecal valve, and at flexures. Innovations included cap-assisted colonoscopy 22, the Third Eye® Retroscope® 23, wider-angle colonoscopes 24, and the Endocuff® device 25. Improving the definition of the colonoscopy image has been shown to increase adenoma detection, particularly small and flat lesions 26.
Chromoendoscopy is the technique of enhancing mucosal inspection using a dye applied to the mucosa. Commonly used dyes include indigo carmine and methylene blue. Dye spray chromoendoscopy has become the standard technique for colonoscopic surveillance for dysplasia in inflammatory bowel disease, increasing pathology detection and reducing unnecessary biopsies when compared to random biopsy protocols 27.
Dye spray colonoscopy may also increase adenoma detection in routine colonoscopy, but the incremental gain in detection of diminutive lesions is offset by increased procedure time 28.
Electronic image processing allows “virtual chromoendoscopy” with mucosal enhancement without physical dye application. Systems such as Narrow Band Imaging (Olympus), FICE (Fujinon), and i-scan (Pentax) have made such technology widely available. These techniques are particularly useful for lesion classification but have not consistently been shown to improve adenoma detection. The NICE system and Kudo’s pit pattern can help differentiate hyperplastic lesions from neoplastic lesions and identify higher grades of dysplasia that may be associated with submucosal invasion. This has become an important tool in planning management of lesions and deciding whether a lesion is resectable endoscopically or may require a surgical approach.
Improved lesion interrogation using electronic image enhancement has been proposed as an alternative to conventional polypectomy and histology. The American Society of Gastrointestinal Endoscopy (ASGE) has proposed a Preservation and Integration of Valuable endoscopic Innovations (PIVI) statement identifying criteria that a resect and discard strategy would have to meet to be acceptable for widespread use. An important driver for this strategy is the cost associated with pathological examination of small polyps which have an extremely low risk of containing advanced dysplasia. The DISCARD study demonstrated that in a single center with expert endoscopists, a resect and discard strategy accurately recognized adenomas with a sensitivity of 94% and accurately predicted appropriate surveillance strategy in 98% 29.
Water-assisted colonoscopy
The first report of a water-based colonoscopy technique was from Falchuk and colleagues in 1984, which showed that water infusion facilitates scope insertion in patients with diverticulosis 30. Water-assisted colonoscopy (WAC) involves water infusion during scope insertion, instead of traditional air or CO 2 insufflation. Main variations include water immersion (WI), during which water is infused to inflate the lumen during scope insertion and then aspirated during withdrawal, and water exchange (WE), where removal of infused water occurs predominantly during insertion 31.
Recent reports have shown that WAC, especially the WE technique, may lead to improved patient comfort with less sedation, aid in completion of difficult or previously incomplete procedures (due to angulations or redundant colons), as well as increase ADRs, the latter being a well-acknowledged predictor of interval cancer risk between colonoscopies 14, 32, 33. Therapeutic indications of WAC have also been described, such as endoscopic resolution of sigmoid volvulus in patients with high surgical risks, as well as polypectomy 34. Underwater endoscopic mucosal resection (EMR) has recently been proposed as an option in the excision of challenging lesions, such as in cases of failed conventional EMR and recurrent polyps, with promising outcomes in terms of recurrence and complication rates 17, 35.
Prolongation of cecal intubation time (CIT) is the main limitation of WAC. Some studies point to a significant prolongation, while others describe similar CIT 36, 37. With regard to safety, data so far show that the procedure is safe and does not interfere with patients’ fluid and electrolyte status 36.
Management of colonic pathology
Management of large colonic polyps
Endoscopic removal of large pre-malignant or suspected early malignant gastrointestinal (GI) lesions poses a challenge in that a complete resection that allows for staging and appropriate further management is warranted in these cases.
Traditionally, EMR, a technique that comprises submucosal injection of lifting solution followed by snare excision, has been used for such lesions. However, EMR is considered suboptimal for large lesions where there is an increased risk of submucosal invasion and therefore a need for a more oncologically sound, en-bloc resection that allows adequate staging. With piecemeal EMR, recurrence rates are significant (16% in a large Australian series), but recurrence is manageable endoscopically in the majority of cases 38 for colorectal lesions larger than 10 mm 39. The obvious need for a technique that allows for en-bloc removal of large, advanced esophagogastric and colorectal lesions recently led Japanese endoscopists to develop endoscopic submucosal dissection (ESD) as a more efficient alternative. This technique is based on the use of endoscopic knives to achieve a deep submucosal, en-bloc excision that allows for accurate histopathologic staging 40. Excellent pre-excision lesion assessment is warranted based on size, morphology, and surface pattern. To justify an attempt of endoscopic resection, advanced imaging modalities, mainly high-definition and chromoendoscopy, are utilized to achieve a meticulous lesion assessment.
Therapeutic indications of ESD in the colorectum include polyps that are suspicious of early neoplastic submucosal involvement as defined by endoscopic appearance (lesions with focal depression, irregular surface patterns, or poor submucosal lift), polyps larger than 2 cm, and polyps that pose difficulties to conventional EMR, such as areas of recurrence after previous polypectomy 23, 34.
Accurate recognition of colonic lesions with submucosal invasion can be challenging, and considerable variation in proficiency has been demonstrated among western endoscopists 41.
It should be stressed that ESD is a highly demanding modality in terms of endoscopist skill and requires specialized training and a certain volume of procedures to ensure competency 42. Perforation is a potentially severe complication of the technique, with a risk of 6–20% in colorectal lesions 43, 44. Surgery is still considered the gold standard for the treatment of most lesions that also fulfill criteria for ESD, although the latter appears to be superior in terms of periprocedural morbidity and mortality when performed by experienced endoscopists 23, 34.
Discussion of the management options for large colonic polyps by a multidisciplinary team is recommended, as regional variation in surgical management rates has been observed in England 45. Recent consensus guidelines on the management of large non-pedunculated colonic polyps have suggested a range of key performance indicators that aim to measure and improve standards of management of large polyps 46. There is likely to be a variation in performance of advanced polypectomy techniques and a subsequent variation in recurrence rates (which may be associated with risk of interval cancer) 47.
Serrated lesions
Previously, the majority of colorectal cancers were thought to arise from the “adenoma-carcinoma” sequence as a result of an accumulation of genetic mutations 48. This process is slow, taking 10–15 years for normal mucosa to progress to malignancy, thus offering the opportunity of a long latent phase in which to detect and remove the malignant precursor (adenoma).
Recent years have seen the increasing recognition and understanding of an alternative pathway for the development of colorectal cancer. This arose from the appreciation of the hyperplastic polyposis syndrome, in which multiple hyperplastic polyps are present in the colon and associated with an increased lifetime risk of colorectal cancer of 20–50% 49.
Serrated lesions are now thought to represent an alternative pathway to colorectal cancer through mutations in BRAF, CpG island methylation, and subsequently methylation of MLH1 50. Hyperplastic polyps, which are very common and occur in up to 95% of individuals, progress to sessile serrated adenomas (SSAs), of which a proportion may have cytological dysplasia. A separate, morphologically and histologically different polyp called a traditional serrated adenoma (TSA) is recognized. SSAs or TSAs can be challenging to detect at colonoscopy due to their flat appearance and relative lack of differentiation from the background mucosa. They tend to occur in the proximal colon where lesion detection is impaired by prominent haustral folds 51.
Serrated lesions are thought to be clinically important due to their association with the presence of synchronous advanced neoplasia 52. They may also be a significant cause of advanced neoplasia or cancer detected following colonoscopy, presumably due to the increased likelihood of not being detected and subsequent rapid progression 53.
Increased awareness of serrated lesions and appreciation of their subtle appearance may aid detection 54. They commonly have an adherent mucosal cap, which obscures detection. Recently, an open shape pit pattern (type II-O) has been described to aid differentiation of dysplastic SSA from hyperplastic polyps; however, the clinical applicability of this is limited 55.
Post procedure management
Complications
Recognized important or commonly occurring complications of colonoscopy include bleeding, colonic perforation, and those related to sedation or anesthetic use. Current estimates of the frequency of such events depend on the indication for the colonoscopy, relevant patient factors, such as comorbidity, and whether endoscopic therapy is delivered during the procedure.
In the English NHS Bowel Cancer Screening Program, the overall rate of bleeding following colonoscopy is 0.65%, bleeding requiring transfusion 0.04%, and colonic perforation 0.06%. Risk of adverse events increases if polypectomy is performed. Factors relating to the polyp, including cecal location and increasing size, are associated with increasing risk of bleeding or perforation 56.
Endoscopic management of bleeding and perforation, including clip placement, over-the-scope closure devices, and endoscopic suturing techniques, may reduce the need for surgical intervention following such complications 57, 58.
Quality assessment
Measurement and monitoring of colonoscopy quality is central to ensuring consistently high levels of performance, patient experience and safety. A variety of key performance indicators are used to measure colonoscopic performance, the most widely used being ADR. This requires histological confirmation of polyp type and is therefore potentially time consuming. Polyp detection rate is simpler to measure and can be used as a surrogate marker 59. The importance of ADR as a measure of colonoscopic performance is discussed earlier in this review.
Limitations of ADR include its restriction to counting only one or more adenomas. Detection of multiple adenomas is not reflected. In patient populations with a high prevalence of adenomas, such as higher risk screening populations, measures of the total number of adenomas detected, such as mean number of adenomas per procedure, may be more appropriate 13.
Other technical measures of colonoscopic performance, including cecal intubation rate, complication rates, and sedation rates, are widely used. Patient-reported measures are under-represented, and a validated patient-reported experience measure for colonoscopy could improve our ability to measure and enhance patient experience.
The ability to benchmark individual or unit measures of colonoscopic performance against regional or national measures is crucial to continuous improvement in quality. The National Endoscopy Database (NED) Project in the United Kingdom and the GI Quality Improvement Consortium (GIQUiC) initiative in the USA aim to provide high-quality, large-volume data to generate individual, regional, and national metrics to aid benchmarking, drive quality improvement, and identify gaps in quality or understanding that could be improved through further research.
Conclusion
Colonoscopy is a commonly performed investigation. In the era of mass population screening for colorectal cancer, it is being performed more frequently than ever before. Advances in patient preparation, technical components of the procedure, and management of pathology will contribute to improvements in performance quality, safety, and ultimately patient experience.
Editorial Note on the Review Process
F1000 Faculty Reviews are commissioned from members of the prestigious F1000 Faculty and are edited as a service to readers. In order to make these reviews as comprehensive and accessible as possible, the referees provide input before publication and only the final, revised version is published. The referees who approved the final version are listed with their names and affiliations but without their reports on earlier versions (any comments will already have been addressed in the published version).
The referees who approved this article are:
Paul C Schroy III, Department of Medicine, Boston Medical Center, Boston University School of Medicine, Boston, MA, USA
Rajesh N Keswani, Division of Gastroenterology and Hepatology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA
Funding Statement
The author(s) declared that no grants were involved in supporting this work.
[version 1; referees: 2 approved]
References
- 1. GLOBOCAN: Estimated cancer incidence, mortality and prevalence worldwide in 2012.2012. Reference Source [Google Scholar]
- 2. Schreuders EH, Ruco A, Rabeneck L, et al. : Colorectal cancer screening: a global overview of existing programmes. Gut. 2015;64(10):1637–49. 10.1136/gutjnl-2014-309086 [DOI] [PubMed] [Google Scholar]
- 3. Zorzi M, Fedeli U, Schievano E, et al. : Impact on colorectal cancer mortality of screening programmes based on the faecal immunochemical test. Gut. 2015;64(5):784–90. 10.1136/gutjnl-2014-307508 [DOI] [PubMed] [Google Scholar]; F1000 Recommendation
- 4. Imperiale TF, Ransohoff DF, Itzkowitz SH, et al. : Multitarget stool DNA testing for colorectal-cancer screening. N Engl J Med. 2014;370(14):1287–97. 10.1056/NEJMoa1311194 [DOI] [PubMed] [Google Scholar]; F1000 Recommendation
- 5. Centers for Disease Control and Prevention (CDC): Vital signs: colorectal cancer screening test use--United States, 2012. MMWR Morb Mortal Wkly Rep. 2013;62(44):881–8. [PMC free article] [PubMed] [Google Scholar]; F1000 Recommendation
- 6. Edwards BK, Ward E, Kohler BA, et al. : Annual report to the nation on the status of cancer, 1975–2006, featuring colorectal cancer trends and impact of interventions (risk factors, screening, and treatment) to reduce future rates. Cancer. 2010;116(3):544–73. 10.1002/cncr.24760 [DOI] [PMC free article] [PubMed] [Google Scholar]; F1000 Recommendation
- 7. Froehlich F, Wietlisbach V, Gonvers JJ, et al. : Impact of colonic cleansing on quality and diagnostic yield of colonoscopy: the European Panel of Appropriateness of Gastrointestinal Endoscopy European multicenter study. Gastrointest Endosc. 2005;61(3):378–84. 10.1016/S0016-5107(04)02776-2 [DOI] [PubMed] [Google Scholar]; F1000 Recommendation
- 8. Parra-Blanco A, Nicolas-Perez D, Gimeno-Garcia A, et al. : The timing of bowel preparation before colonoscopy determines the quality of cleansing, and is a significant factor contributing to the detection of flat lesions: a randomized study. World J Gastroenterol. 2006;12(38):6161–6. [DOI] [PMC free article] [PubMed] [Google Scholar]; F1000 Recommendation
- 9. Rex DK, Imperiale TF, Latinovich DR, et al. : Impact of bowel preparation on efficiency and cost of colonoscopy. Am J Gastroenterol. 2002;97(7):1696–700. 10.1111/j.1572-0241.2002.05827.x [DOI] [PubMed] [Google Scholar]
- 10. Bucci C, Rotondano G, Hassan C, et al. : Optimal bowel cleansing for colonoscopy: split the dose! A series of meta-analyses of controlled studies. Gastrointest Endosc. 2014;80(4):566–576.e2. 10.1016/j.gie.2014.05.320 [DOI] [PubMed] [Google Scholar]; F1000 Recommendation
- 11. Cohen LB: Split dosing of bowel preparations for colonoscopy: an analysis of its efficacy, safety, and tolerability. Gastrointest Endosc. 2010;72(2):406–12. 10.1016/j.gie.2010.04.001 [DOI] [PubMed] [Google Scholar]; F1000 Recommendation
- 12. Siddiqui AA, Yang K, Spechler SJ, et al. : Duration of the interval between the completion of bowel preparation and the start of colonoscopy predicts bowel-preparation quality. Gastrointest Endosc. 2009;69(3 Pt 2):700–6. 10.1016/j.gie.2008.09.047 [DOI] [PubMed] [Google Scholar]; F1000 Recommendation
- 13. Markowitz GS, Perazella MA: Acute phosphate nephropathy. Kidney Int. 2009;76(10):1027–34. 10.1038/ki.2009.308 [DOI] [PubMed] [Google Scholar]
- 14. Hassan C, Fuccio L, Bruno M, et al. : A predictive model identifies patients most likely to have inadequate bowel preparation for colonoscopy. Clin Gastroenterol Hepatol. 2012;10(5):501–6. 10.1016/j.cgh.2011.12.037 [DOI] [PubMed] [Google Scholar]; F1000 Recommendation
- 15. Lee TJ, Rees CJ, Blanks RG, et al. : Colonoscopic factors associated with adenoma detection in a national colorectal cancer screening program. Endoscopy. 2014;46(3):203–11. 10.1055/s-0033-1358831 [DOI] [PubMed] [Google Scholar]
- 16. Dominitz JA, Baldwin LM, Green P, et al. : Regional variation in anesthesia assistance during outpatient colonoscopy is not associated with differences in polyp detection or complication rates. Gastroenterology. 2013;144(2):298–306. 10.1053/j.gastro.2012.10.038 [DOI] [PMC free article] [PubMed] [Google Scholar]; F1000 Recommendation
- 17. Wernli KJ, Brenner AT, Rutter CM, et al. : Risks Associated With Anesthesia Services During Colonoscopy. Gastroenterology. 2015; pii: S0016-5085(15)01813-2. 10.1053/j.gastro.2015.12.018 [DOI] [PMC free article] [PubMed] [Google Scholar]; F1000 Recommendation
- 18. Kaminski MF, Regula J, Kraszewska E, et al. : Quality indicators for colonoscopy and the risk of interval cancer. N Engl J Med. 2010;362(19):1795–803. 10.1056/NEJMoa0907667 [DOI] [PubMed] [Google Scholar]; F1000 Recommendation
- 19. Corley DA, Jensen CD, Marks AR, et al. : Adenoma detection rate and risk of colorectal cancer and death. N Engl J Med. 2014;370(14):1298–306. 10.1056/NEJMoa1309086 [DOI] [PMC free article] [PubMed] [Google Scholar]; F1000 Recommendation
- 20. Abdul-Baki H, Schoen RE, Dean K, et al. : Public reporting of colonoscopy quality is associated with an increase in endoscopist adenoma detection rate. Gastrointest Endosc. 2015;82(4):676–82. 10.1016/j.gie.2014.12.058 [DOI] [PMC free article] [PubMed] [Google Scholar]; F1000 Recommendation
- 21. Rajasekhar PT, Rees CJ, Bramble MG, et al. : A multicenter pragmatic study of an evidence-based intervention to improve adenoma detection: the Quality Improvement in Colonoscopy (QIC) study. Endoscopy. 2015;47(3):217–24. 10.1055/s-0034-1391563 [DOI] [PubMed] [Google Scholar]
- 22. Pohl H, Bensen SP, Toor A, et al. : Cap-assisted colonoscopy and detection of Adenomatous Polyps (CAP) study: a randomized trial. Endoscopy. 2015;47(10):891–7. 10.1055/s-0034-1392261 [DOI] [PubMed] [Google Scholar]; F1000 Recommendation
- 23. Siersema PD, Rastogi A, Leufkens AM, et al. : Retrograde-viewing device improves adenoma detection rate in colonoscopies for surveillance and diagnostic workup. World J Gastroenterol. 2012;18(26):3400–8. 10.3748/wjg.v18.i26.3400 [DOI] [PMC free article] [PubMed] [Google Scholar]; F1000 Recommendation
- 24. Adler A, Aminalai A, Aschenbeck J, et al. : Latest generation, wide-angle, high-definition colonoscopes increase adenoma detection rate. Clin Gastroenterol Hepatol. 2012;10(2):155–9. 10.1016/j.cgh.2011.10.026 [DOI] [PubMed] [Google Scholar]; F1000 Recommendation
- 25. Floer M, Biecker E, Fitzlaff R, et al. : Higher adenoma detection rates with endocuff-assisted colonoscopy - a randomized controlled multicenter trial. PLoS One. 2014;9(12):e114267. 10.1371/journal.pone.0114267 [DOI] [PMC free article] [PubMed] [Google Scholar]; F1000 Recommendation
- 26. Rex DK, Helbig CC: High yields of small and flat adenomas with high-definition colonoscopes using either white light or narrow band imaging. Gastroenterology. 2007;133(1):42–7. 10.1053/j.gastro.2007.04.029 [DOI] [PubMed] [Google Scholar]; F1000 Recommendation
- 27. Rutter MD, Saunders BP, Schofield G, et al. : Pancolonic indigo carmine dye spraying for the detection of dysplasia in ulcerative colitis. Gut. 2004;53(2):256–60. 10.1136/gut.2003.016386 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28. Brooker JC, Saunders BP, Shah SG, et al. : Total colonic dye-spray increases the detection of diminutive adenomas during routine colonoscopy: a randomized controlled trial. Gastrointest Endosc. 2002;56(3):333–8. 10.1016/S0016-5107(02)70034-5 [DOI] [PubMed] [Google Scholar]
- 29. Ignjatovic A, East JE, Suzuki N, et al. : Optical diagnosis of small colorectal polyps at routine colonoscopy (Detect InSpect ChAracterise Resect and Discard; DISCARD trial): a prospective cohort study. Lancet Oncol. 2009;10(12):1171–8. 10.1016/S1470-2045(09)70329-8 [DOI] [PubMed] [Google Scholar]; F1000 Recommendation
- 30. Falchuk ZM, Griffin PH: A technique to facilitate colonoscopy in areas of severe diverticular disease. N Engl J Med. 1984;310(9):598. 10.1056/NEJM198403013100919 [DOI] [PubMed] [Google Scholar]
- 31. Leung FW: Water-aided colonoscopy. Gastroenterol Clin North Am. 2013;42(3):507–19. 10.1016/j.gtc.2013.05.006 [DOI] [PubMed] [Google Scholar]
- 32. Lee TJ, Rutter MD, Blanks RG, et al. : Colonoscopy quality measures: experience from the NHS Bowel Cancer Screening Programme. Gut. 2012;61(7):1050–7. 10.1136/gutjnl-2011-300651 [DOI] [PubMed] [Google Scholar]
- 33. Anderson JC: Water-aided colonoscopy. Gastrointest Endosc Clin N Am. 2015;25(2):211–26. 10.1016/j.giec.2014.11.002 [DOI] [PubMed] [Google Scholar]
- 34. Sugimoto S, Mizukami T: Diagnostic and therapeutic applications of water-immersion colonoscopy. World J Gastroenterol. 2015;21(21):6451–9. 10.3748/wjg.v21.i21.6451 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35. Binmoeller KF, Weilert F, Shah J, et al. : "Underwater" EMR without submucosal injection for large sessile colorectal polyps (with video). Gastrointest Endosc. 2012;75(5):1086–91. 10.1016/j.gie.2011.12.022 [DOI] [PubMed] [Google Scholar]; F1000 Recommendation
- 36. Rex DK: Water exchange vs. water immersion during colonoscope insertion. Am J Gastroenterol. 2014;109(9):1401–3. 10.1038/ajg.2014.235 [DOI] [PubMed] [Google Scholar]
- 37. Cadoni S, Falt P, Gallittu P, et al. : Water Exchange Is the Least Painful Colonoscope Insertion Technique and Increases Completion of Unsedated Colonoscopy. Clin Gastroenterol Hepatol. 2015;13(11):1972–80.e1–3. 10.1016/j.cgh.2015.04.178 [DOI] [PubMed] [Google Scholar]
- 38. Moss A, Williams SJ, Hourigan LF, et al. : Long-term adenoma recurrence following wide-field endoscopic mucosal resection (WF-EMR) for advanced colonic mucosal neoplasia is infrequent: results and risk factors in 1000 cases from the Australian Colonic EMR (ACE) study. Gut. 2015;64(1):57–65. 10.1136/gutjnl-2013-305516 [DOI] [PubMed] [Google Scholar]; F1000 Recommendation
- 39. Hotta K, Fujii T, Saito Y, et al. : Local recurrence after endoscopic resection of colorectal tumors. Int J Colorectal Dis. 2009;24(2):225–30. 10.1007/s00384-008-0596-8 [DOI] [PubMed] [Google Scholar]
- 40. Yamamoto K, Michida T, Nishida T, et al. : Colorectal endoscopic submucosal dissection: Recent technical advances for safe and successful procedures. World J Gastrointest Endosc. 2015;7(14):1114–28. [DOI] [PMC free article] [PubMed] [Google Scholar]; F1000 Recommendation
- 41. Aziz Aadam A, Wani S, Kahi C, et al. : Physician assessment and management of complex colon polyps: a multicenter video-based survey study. Am J Gastroenterol. 2014;109(9):1312–24. 10.1038/ajg.2014.95 [DOI] [PubMed] [Google Scholar]
- 42. Oyama T, Yahagi N, Ponchon T, et al. : How to establish endoscopic submucosal dissection in Western countries. World J Gastroenterol. 2015;21(40):11209–20. 10.3748/wjg.v21.i40.11209 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43. Saito Y, Fukuzawa M, Matsuda T, et al. : Clinical outcome of endoscopic submucosal dissection versus endoscopic mucosal resection of large colorectal tumors as determined by curative resection. Surg Endosc. 2010;24(2):343–52. 10.1007/s00464-009-0562-8 [DOI] [PubMed] [Google Scholar]
- 44. Kim ES, Cho KB, Park KS, et al. : Factors predictive of perforation during endoscopic submucosal dissection for the treatment of colorectal tumors. Endoscopy. 2011;43(7):573–8. 10.1055/s-0030-1256339 [DOI] [PubMed] [Google Scholar]
- 45. Lee TJ, Rees CJ, Nickerson C, et al. : Management of complex colonic polyps in the English Bowel Cancer Screening Programme. Br J Surg. 2013;100(12):1633–9. 10.1002/bjs.9282 [DOI] [PubMed] [Google Scholar]
- 46. Rutter MD, Chattree A, Barbour JA, et al. : British Society of Gastroenterology/Association of Coloproctologists of Great Britain and Ireland guidelines for the management of large non-pedunculated colorectal polyps. Gut. 2015;64(12):1847–73. 10.1136/gutjnl-2015-309576 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47. Pohl H, Srivastava A, Bensen SP, et al. : Incomplete polyp resection during colonoscopy-results of the complete adenoma resection (CARE) study. Gastroenterology. 2013;144(1):74–80.e1. 10.1053/j.gastro.2012.09.043 [DOI] [PubMed] [Google Scholar]; F1000 Recommendation
- 48. Vogelstein B, Fearon ER, Hamilton SR, et al. : Genetic alterations during colorectal-tumor development. N Engl J Med. 1988;319(9):525–32. 10.1056/NEJM198809013190901 [DOI] [PubMed] [Google Scholar]
- 49. Jass JR, Burt RW: Hyperplastic polyposis. In: Hamilton SR: Aaltonen LA. editors. WHO International classification of tumors: pathology and genetics of tumors of the digestive system.Lyon: Springer; Verlin.2000;133–4. Reference Source [Google Scholar]
- 50. Leggett B, Whitehall V: Role of the serrated pathway in colorectal cancer pathogenesis. Gastroenterology. 2010;138(6):2088–100. 10.1053/j.gastro.2009.12.066 [DOI] [PubMed] [Google Scholar]; F1000 Recommendation
- 51. Snover DC, Jass JR, Fenoglio-Preiser C, et al. : Serrated polyps of the large intestine: a morphologic and molecular review of an evolving concept. Am J Clin Pathol. 2005;124(3):380–91. 10.1309/V2EP-TPLJ-RB3F-GHJL [DOI] [PubMed] [Google Scholar]
- 52. Li D, Jin C, McCulloch C, et al. : Association of large serrated polyps with synchronous advanced colorectal neoplasia. Am J Gastroenterol. 2009;104(3):695–702. 10.1038/ajg.2008.166 [DOI] [PubMed] [Google Scholar]
- 53. Schreiner MA, Weiss DG, Lieberman DA: Proximal and large hyperplastic and nondysplastic serrated polyps detected by colonoscopy are associated with neoplasia. Gastroenterology. 2010;139(5):1497–502. 10.1053/j.gastro.2010.06.074 [DOI] [PubMed] [Google Scholar]
- 54. Hazewinkel Y, López-Cerón M, East JE, et al. : Endoscopic features of sessile serrated adenomas: validation by international experts using high-resolution white-light endoscopy and narrow-band imaging. Gastrointest Endosc. 2013;77(6):916–24. 10.1016/j.gie.2012.12.018 [DOI] [PubMed] [Google Scholar]
- 55. Kimura T, Yamamoto E, Yamano HO, et al. : A novel pit pattern identifies the precursor of colorectal cancer derived from sessile serrated adenoma. Am J Gastroenterol. 2012;107(3):460–9. 10.1038/ajg.2011.457 [DOI] [PubMed] [Google Scholar]
- 56. Rutter MD, Nickerson C, Rees CJ, et al. : Risk factors for adverse events related to polypectomy in the English Bowel Cancer Screening Programme. Endoscopy. 2014;46(2):90–7. 10.1055/s-0033-1344987 [DOI] [PubMed] [Google Scholar]
- 57. Raju GS, Saito Y, Matsuda T, et al. : Endoscopic management of colonoscopic perforations (with videos). Gastrointest Endosc. 2011;74(6):1380–8. 10.1016/j.gie.2011.08.007 [DOI] [PubMed] [Google Scholar]
- 58. Kantsevoy SV, Bitner M, Mitrakov AA, et al. : Endoscopic suturing closure of large mucosal defects after endoscopic submucosal dissection is technically feasible, fast, and eliminates the need for hospitalization (with videos). Gastrointest Endosc. 2014;79(3):503–7. 10.1016/j.gie.2013.10.051 [DOI] [PubMed] [Google Scholar]; F1000 Recommendation
- 59. Rajasekhar PT, Lee TJ, Rutter MD, et al. : PWE-188 Using a "conversion factor" to estimate adenoma detection rate. Gut. 2012;61:A372–A373. 10.1136/gutjnl-2012-302514d.188 [DOI] [Google Scholar]