Substantial and sustained improvement of serrated polyp detection after a simple educational intervention: results from a prospective controlled trial

Arne G C Bleijenberg, Monique E van Leerdam, Marloes Bargeman, Jan Jacob Koornstra, Yasmijn J van Herwaarden, Manon Cw Spaander, Silvia Sanduleanu, Barbara A J Bastiaansen, Erik J Schoon, Niels van Lelyveld, Evelien Dekker, Joep E G IJspeert, Arne G C Bleijenberg, Monique E van Leerdam, Marloes Bargeman, Jan Jacob Koornstra, Yasmijn J van Herwaarden, Manon Cw Spaander, Silvia Sanduleanu, Barbara A J Bastiaansen, Erik J Schoon, Niels van Lelyveld, Evelien Dekker, Joep E G IJspeert

Abstract

Objective: Serrated polyps (SPs) are an important cause of postcolonoscopy colorectal cancers (PCCRCs), which is likely the result of suboptimal SP detection during colonoscopy. We assessed the long-term effect of a simple educational intervention focusing on optimising SP detection.

Design: An educational intervention, consisting of two 45 min training sessions (held 3 years apart) on serrated polyp detection, was given to endoscopists from 9 Dutch hospitals. Hundred randomly selected and untrained endoscopists from other hospitals were selected as control group. Our primary outcome measure was the proximal SP detection rate (PSPDR) in trained versus untrained endoscopists who participated in our faecal immunochemical test (FIT)-based population screening programme.

Results: Seventeen trained and 100 untrained endoscopists were included, who performed 11 305 and 51 039 colonoscopies, respectively. At baseline, PSPDR was equal between the groups (9.3% vs 9.3%). After training, the PSPDR of trained endoscopists gradually increased to 15.6% in 2018. This was significantly higher than the PSPDR of untrained endoscopists, which remained stable around 10% (p=0.018). All below-average (ie, PSPDR ≤6%) endoscopists at baseline improved their PSPDR after training session 1, as did 57% of endoscopists with average PSPDR (6%-12%) at baseline. The second training session further improved the PSPDR in 44% of endoscopists with average PSPDR after the first training.

Conclusion: A simple educational intervention was associated with substantial long-term improvement of PSPDR in a prospective controlled trial within FIT-based population screening. Widespread implementation of such interventions might be an easy way to improve SP detection, which may ultimately result in fewer PCCRCs.

Trial registration number: NCT03902899.

Keywords: colonic polyps; colonoscopy; colorectal cancer.

Conflict of interest statement

Competing interests: ED: took endoscopic equipment on loan of Olympus and FujiFilm, received a research grant from FujiFilm, received a honorarium for consultancy from FujiFilm, Tillots, Olympus, JEGI Supply and Cancer Prevention Pharmaceuticals and a speakers' fee from Olympus, Roche and JEGI Supply. EJS: received consultancy and speakers honorarium for FujiFilm.

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ.

Figures

Figure 1
Figure 1
(A) PSPDR before and after training; (B) ADR before and after training. ADR, adenoma detection rate; PSPDR, proximal serrated polyp detection rate.
Figure 2
Figure 2
Effect of training sessions 1 and 2 per endoscopist, stratified according to their PSPDR at baseline, after the first training and after the second training. For example, of the seven endoscopists with average PSPDR at baseline, four (57%) moved up to ‘above-average PSPDR’ after training session 1, while three remained in the ‘average PSPDR’ group. PSPDR, proximal serrated polyp detection rate.
Figure 3
Figure 3
PSPDR before and after training. PSPDR, proximal serrated polyp detection rate.

References

    1. Siegel R, Naishadham D, Jemal A. Cancer statistics, 2012. CA Cancer J Clin 2012;62:10–29. 10.3322/caac.20138
    1. Ferlay J, Soerjamotaram I, Ervik M, et al. . Cancer incidence and mortality worldwide: IARC CancerBase No. 11. Lyon, France: International Agency for Research on Cancer, 2013.
    1. Fearon ER, Vogelstein B. A genetic model for colorectal tumorigenesis. Cell 1990;61:759–67. 10.1016/0092-8674(90)90186-I
    1. Zauber AG, Winawer SJ, O'Brien MJ, et al. . Colonoscopic polypectomy and long-term prevention of colorectal-cancer deaths. N Engl J Med Overseas Ed 2012;366:687–96. 10.1056/NEJMoa1100370
    1. Jass JR. Classification of colorectal cancer based on correlation of clinical, morphological and molecular features. Histopathology 2007;50:113–30. 10.1111/j.1365-2559.2006.02549.x
    1. Bettington M, Brown I, Rosty C, et al. . Sessile serrated adenomas in young patients may have limited risk of malignant progression. J Clin Gastroenterol 2019;53:e113–6. 10.1097/MCG.0000000000001014
    1. Snover DC. Update on the serrated pathway to colorectal carcinoma. Hum Pathol 2011;42:1–10. 10.1016/j.humpath.2010.06.002
    1. East JE, Atkin WS, Bateman AC, et al. . British Society of gastroenterology position statement on serrated polyps in the colon and rectum. Gut 2017;66:1181–96. 10.1136/gutjnl-2017-314005
    1. Rex DK, Ahnen DJ, Baron JA, et al. . Serrated lesions of the colorectum: review and recommendations from an expert panel. Am J Gastroenterol 2012;107:1315–29. 10.1038/ajg.2012.161
    1. 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;77:916–24. 10.1016/j.gie.2012.12.018
    1. Kahi CJ, Hewett DG, Norton DL, et al. . Prevalence and variable detection of proximal colon serrated polyps during screening colonoscopy. Clin Gastroenterol Hepatol 2011;9:42–6. 10.1016/j.cgh.2010.09.013
    1. IJspeert JEG, van Doorn SC, van der Brug YM, et al. . The proximal serrated polyp detection rate is an easy-to-measure proxy for the detection rate of clinically relevant serrated polyps. Gastrointest Endosc 2015;82:870–7. 10.1016/j.gie.2015.02.044
    1. Brenner H, Hoffmeister M, Arndt V, et al. . Protection from right- and left-sided colorectal neoplasms after colonoscopy: population-based study. J Natl Cancer Inst 2010;102:89–95. 10.1093/jnci/djp436
    1. Mulder SA, van Soest EM, Dieleman JP, et al. . Exposure to colorectal examinations before a colorectal cancer diagnosis: a case-control study. Eur J Gastroenterol Hepatol 2010;22:437–43. 10.1097/MEG.0b013e328333fc6a
    1. Brenner H, Chang-Claude J, Seiler CM, et al. . Protection from colorectal cancer after colonoscopy: a population-based, case-control study. Ann Intern Med 2011;154:22–30. 10.7326/0003-4819-154-1-201101040-00004
    1. Arain MA, Sawhney M, Sheikh S, et al. . Cimp status of interval colon cancers: another piece to the puzzle. Am J Gastroenterol 2010;105:1189–95. 10.1038/ajg.2009.699
    1. Kaminski MF, Regula J, Kraszewska E, et al. . Quality indicators for colonoscopy and the risk of interval cancer. N Engl J Med 2010;362:1795–803. 10.1056/NEJMoa0907667
    1. Corley DA, Jensen CD, Marks AR, et al. . Adenoma detection rate and risk of colorectal cancer and death. N Engl J Med 2014;370:1298–306. 10.1056/NEJMoa1309086
    1. Coe SG, Crook JE, Diehl NN, et al. . An endoscopic quality improvement program improves detection of colorectal adenomas. Am J Gastroenterol 2013;108:219–26. 10.1038/ajg.2012.417
    1. Ussui V, Coe S, Rizk C, et al. . Stability of increased adenoma detection at colonoscopy. follow-up of an endoscopic quality improvement program-EQUIP-II. Am J Gastroenterol 2015;110:489–96. 10.1038/ajg.2014.314
    1. Wallace MB, Crook JE, Thomas CS, et al. . Effect of an endoscopic quality improvement program on adenoma detection rates: a multicenter cluster-randomized controlled trial in a clinical practice setting (EQUIP-3). Gastrointest Endosc 2017;85:538–45. 10.1016/j.gie.2016.07.042
    1. Racho RG, Krishna M, Coe SG, et al. . Impact of an endoscopic quality improvement program focused on adenoma detection on sessile serrated adenoma/polyp detection. Dig Dis Sci 2017;62:1464–71. 10.1007/s10620-017-4582-2
    1. World Medical Association World Medical association Declaration of Helsinki: ethical principles for medical research involving human subjects. JAMA 2013;310:2191–4. 10.1001/jama.2013.281053
    1. European Parliament and the Council of the European Union, General Data ProtectionRegulation (GDPR) OJ L 119, 04.05.2016; cor. OJ L 127, 23.5.2018; 2016.
    1. Bronzwaer MES, Depla ACTM, van Lelyveld N, et al. . Quality assurance of colonoscopy within the Dutch national colorectal cancer screening program. Gastrointest Endosc 2019;89:1–13. 10.1016/j.gie.2018.09.011
    1. IJspeert JEG, Bastiaansen BAJ, van Leerdam ME, et al. . Development and validation of the wasp classification system for optical diagnosis of adenomas, hyperplastic polyps and sessile serrated adenomas/polyps. Gut 2016;65:963–70. 10.1136/gutjnl-2014-308411
    1. Casparie M, Tiebosch ATMG, Burger G, et al. . Pathology databanking and biobanking in the Netherlands, a central role for PALGA, the nationwide histopathology and cytopathology data network and archive. Cell Oncol 2007;29:19–24. 10.1155/2007/971816
    1. core team R. R: a language and environment for statistical computing. Vienna, Austria, 2018.
    1. Bates D, Mächler M, Bolker B, et al. . Fitting Linear Mixed-Effects Models Using lme4. J Stat Softw 2015;67:48 10.18637/jss.v067.i01
    1. Leggett B, Whitehall V. Role of the serrated pathway in colorectal cancer pathogenesis. Gastroenterology 2010;138:2088–100. 10.1053/j.gastro.2009.12.066
    1. Sawhney MS, Farrar WD, Gudiseva S, et al. . Microsatellite instability in interval colon cancers. Gastroenterology 2006;131:1700–5. 10.1053/j.gastro.2006.10.022
    1. Torlakovic E, Skovlund E, Snover DC, et al. . Morphologic reappraisal of serrated colorectal polyps. Am J Surg Pathol 2003;27:65–81. 10.1097/00000478-200301000-00008
    1. 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;124:380–91. 10.1309/V2EP-TPLJ-RB3F-GHJL
    1. Goldstein NS, Bhanot P, Odish E, et al. . Hyperplastic-like colon polyps that preceded microsatellite-unstable adenocarcinomas. Am J Clin Pathol 2003;119:778–96. 10.1309/DRFQ0WFUF1G13CTK
    1. Kambara T, Simms LA, Whitehall VLJ, et al. . Braf mutation is associated with DNA methylation in serrated polyps and cancers of the colorectum. Gut 2004;53:1137–44. 10.1136/gut.2003.037671
    1. Crockett SD, Gourevitch RA, Morris M, et al. . Endoscopist factors that influence serrated polyp detection: a multicenter study. Endoscopy 2018;50:984–92. 10.1055/a-0597-1740
    1. Rijksinstituut voor Volksgezondheid en Milieu (RIVM) Landelijke monitoring en Evaluatie Bevolkingsonderzoek Darmkanker; 2014.
    1. Rijksinstituut voor Volksgezondheid en Milieu (RIVM) Landelijke monitoring Bevolkingsonderzoek Darmkanker; 2015.
    1. Rijksinstituut voor Volksgezondheid en Milieu (RIVM) Landelijke monitoring Bevolkingsonderzoek Darmkanker; 2016.
    1. Rijksinstituut voor Volksgezondheid en Milieu (RIVM) Landelijke monitoring Bevolkingsonderzoek Darmkanker; 2017.
    1. Stegeman I, van Doorn SC, Mundt MW, et al. . Participation, yield, and interval carcinomas in three rounds of biennial FIT-based colorectal cancer screening. Cancer Epidemiol 2015;39:388–93. 10.1016/j.canep.2015.03.012
    1. Kapidzic A, Grobbee EJ, Hol L, et al. . Attendance and yield over three rounds of population-based fecal immunochemical test screening. Am J Gastroenterol 2014;109:1257–64. 10.1038/ajg.2014.168
    1. Zorzi M, Hassan C, Capodaglio G, et al. . Long-Term performance of colorectal cancerscreening programmes based on the faecal immunochemical test. Gut 2018;67:2124–30. 10.1136/gutjnl-2017-314753
    1. Jensen CD, Corley DA, Quinn VP, et al. . Fecal immunochemical test program performance over 4 rounds of annual screening: a retrospective cohort study. Ann Intern Med 2016;164:456–63. 10.7326/M15-0983
    1. IJspeert JEG, Madani A, Overbeek LIH, et al. . Implementation of an e-learning module improves consistency in the histopathological diagnosis of sessile serrated lesions within a nationwide population screening programme. Histopathology 2017;70:929–37. 10.1111/his.13155
    1. Fry DE. The Hawthorne effect revisited. Dis Colon Rectum 2018;61:6–7. 10.1097/DCR.0000000000000928
    1. Barclay RL, Vicari JJ, Doughty AS, et al. . Colonoscopic withdrawal times and adenoma detection during screening colonoscopy. N Engl J Med 2006;355:2533–41. 10.1056/NEJMoa055498
    1. Overholt BF, Brooks-Belli L, Grace M, et al. . Withdrawal times and associated factors in colonoscopy: a quality assurance multicenter assessment. J Clin Gastroenterol 2010;44:e80–6. 10.1097/MCG.0b013e3181bf9b02
    1. Jover R, Zapater P, Polanía E, et al. . Modifiable endoscopic factors that influence the adenoma detection rate in colorectal cancer screening colonoscopies. Gastrointest Endosc 2013;77:381–9. 10.1016/j.gie.2012.09.027
    1. Butterly L, Robinson CM, Anderson JC, et al. . Serrated and adenomatous polyp detection increases with longer withdrawal time: results from the new Hampshire colonoscopy registry. Am J Gastroenterol 2014;109:417–26. 10.1038/ajg.2013.442
    1. Lee TJW, Blanks RG, Rees CJ, et al. . Longer mean colonoscopy withdrawal time is associated with increased adenoma detection: evidence from the bowel cancer screening programme in England. Endoscopy 2013;45:20–6. 10.1055/s-0032-1325803
    1. Shaukat A, Arain M, Thaygarajan B, et al. . Is BRAF mutation associated with interval colorectal cancers? Dig Dis Sci 2010;55:2352–6. 10.1007/s10620-010-1182-9

Source: PubMed

3
Abonneren