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Original article Clinical endoscopy| Volume 84, ISSUE 6, P959-968.e7, December 2016

Endoscopic mucosal resection: learning curve for large nonpolypoid colorectal neoplasia

Published:April 21, 2016DOI:https://doi.org/10.1016/j.gie.2016.04.020

      Background and Aims

      Colorectal EMR for nonpolypoid neoplasia achieves better outcomes when performed by expert endoscopists. The time point at which the endoscopist achieves expert level remains to be defined. The objective of this study was to establish a learning curve of colorectal EMR for nonpolypoid neoplasia based on residual tissue on surveillance colonoscopy and adverse event rate.

      Methods

      Five hundred seventy-eight consecutive patients underwent EMR of colorectal neoplasia by 1 of 3 primary endoscopists between December 2004 and September 2013 in a tertiary academic center. Primary analyses focused on the largest lesion for patients with more than 1 lesion (median age, 69 years; median polyp size, 30 mm; 51% en bloc resection). Data on surveillance colonoscopy were available for 74%. Learning curves were calculated for each of the 3 main outcome measurements: the presence of residual neoplasia on surveillance colonoscopy, endoscopic assessment of incomplete EMR, and the occurrence of an immediate bleeding adverse event.

      Results

      Residual neoplasia on surveillance colonoscopy was present for 23.2% of patients, the rate of endoscopist-assessed incomplete EMR was 27.6%, and immediate bleeding adverse events occurred in 6.9% of patients. Although there was between-endoscopist variability, the overall rates of residual neoplasia and incomplete EMR decreased to below 20% to 25% after 100 EMRs; initial decreases in both rates were observed for earlier EMRs. Immediate bleeding adverse events occurred at a low frequency for each endoscopist across all EMRs. Perforation requiring surgical intervention occurred in 1 patient (0.2%).

      Conclusions

      This study demonstrated that an unexpectedly high number of 100 colorectal EMR procedures for large nonpolypoid colorectal neoplasia are required to achieve a plateau phase for crucial outcomes.

      Abbreviations:

      APC (argon plasma coagulation), ASA (American Society of Anesthesiologists), ESD (endoscopic submucosal dissection), NBI (narrow-band imaging), OR (odds ratio)
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      References

        • Kaltenbach T.
        • Friedland S.
        • Maheshwari A.
        • et al.
        Short- and long-term outcomes of standardized EMR of nonpolypoid (flat and depressed) colorectal lesions ≥1 cm (with video).
        Gastrointest Endosc. 2007; 65: 857-865
        • Belle S.
        • Haase L.
        • Pilz L.R.
        • et al.
        Recurrence after endoscopic mucosal resection-therapy failure?.
        Int J Colorectal Dis. 2014; 29: 209-215
        • Su M.Y.
        • Hsu C.M.
        • Ho Y.P.
        • et al.
        Endoscopic mucosal resection for colonic non-polypoid neoplasms.
        Am J Gastroenterol. 2005; 100: 2174-2179
        • Wang A.Y.
        • Ahmad N.A.
        • Zaidman J.S.
        • et al.
        Endoluminal resection for sessile neoplasia in the GI tract is associated with a low recurrence rate and a high 5-year survival rate.
        Gastrointest Endosc. 2008; 68: 160-169
        • Heresbach D.
        • Kornhauser R.
        • Seyrig J.A.
        • et al.
        A national survey of endoscopic mucosal resection for superficial gastrointestinal neoplasia.
        Endoscopy. 2010; 42: 806-813
        • Brooker J.C.
        • Saunders B.P.
        • Shah S.G.
        • et al.
        Endoscopic resection of large sessile colonic polyps by specialist and non-specialist endoscopists.
        Br J Surg. 2002; 89: 1020-1024
        • Uraoka T.
        • Parra-Blanco A.
        • Yahagi N.
        Colorectal endoscopic submucosal dissection in Japan and Western countries.
        Dig Endosc. 2012; 24: 80-83
        • Yamamoto S.
        • Uedo N.
        • Ishihara R.
        • et al.
        Endoscopic submucosal dissection for early gastric cancer performed by supervised residents: assessment of feasibility and learning curve.
        Endoscopy. 2009; 41: 923-928
        • Sakamoto T.
        • Saito Y.
        • Fukunaga S.
        • et al.
        Learning curve associated with colorectal endoscopic submucosal dissection for endoscopists experienced in gastric endoscopic submucosal dissection.
        Dis Colon Rectum. 2011; 54: 1307-1312
        • Iacopini F.
        • Bella A.
        • Costamagna G.
        • et al.
        Stepwise training in rectal and colonic endoscopic submucosal dissection with differentiated learning curves.
        Gastrointest Endosc. 2012; 76: 1188-1196
        • Probst A.
        • Golger D.
        • Anthuber M.
        • et al.
        Endoscopic submucosal dissection in large sessile lesions of the rectosigmoid: learning curve in a European center.
        Endoscopy. 2012; 44: 660-667
        • Buchner A.M.
        • Guarner-Argente C.
        • Ginsberg G.G.
        Outcomes of EMR of defiant colorectal lesions directed to an endoscopy referral center.
        Gastrointest Endosc. 2012; 76: 255-263
        • Khashab M.
        • Eid E.
        • Rusche M.
        • et al.
        Incidence and predictors of “late” recurrences after endoscopic piecemeal resection of large sessile adenomas.
        Gastrointest Endosc. 2009; 70: 344-349
        • Moss A.
        • Bourke M.J.
        • Williams S.J.
        • et al.
        Endoscopic mucosal resection outcomes and prediction of submucosal cancer from advanced colonic mucosal neoplasia.
        Gastroenterology. 2011; 140: 1909-1918
        • Ahlenstiel G.
        • Hourigan L.F.
        • Brown G.
        • et al.
        Actual endoscopic versus predicted surgical mortality for treatment of advanced mucosal neoplasia of the colon.
        Gastrointest Endosc. 2014; 80: 668-676
        • Ah Soune P.
        • Menard C.
        • Salah E.
        • et al.
        Large endoscopic mucosal resection for colorectal tumors exceeding 4 cm.
        World J Gastroenterol. 2010; 16: 588-595
        • Woodward T.A.
        • Heckman M.G.
        • Cleveland P.
        • et al.
        Predictors of complete endoscopic mucosal resection of flat and depressed gastrointestinal neoplasia of the colon.
        Am J Gastroenterol. 2012; 107: 650-654
        • Kim H.H.
        • Kim J.H.
        • Park S.J.
        • et al.
        Risk factors for incomplete resection and complications in endoscopic mucosal resection for lateral spreading tumors.
        Dig Endosc. 2012; 24: 259-266
        • Swan M.P.
        • Bourke M.J.
        • Alexander S.
        • et al.
        Large refractory colonic polyps: is it time to change our practice? A prospective study of the clinical and economic impact of a tertiary referral colonic mucosal resection and polypectomy service (with videos).
        Gastrointest Endosc. 2009; 70: 1128-1136
        • Baxter N.N.
        • Sutradhar R.
        • Forbes S.S.
        • et al.
        Analysis of administrative data finds endoscopist quality measures associated with postcolonoscopy colorectal cancer.
        Gastroenterology. 2011; 140: 65-72
        • Gupta S.
        • Bassett P.
        • Man R.
        • et al.
        Validation of a novel method for assessing competency in polypectomy.
        Gastrointest Endosc. 2012; 75: 568-575
        • Kaminski M.F.
        • Regula J.
        • Kraszewska E.
        • et al.
        Quality indicators for colonoscopy and the risk of interval cancer.
        N Engl J Med. 2010; 362: 1795-1803
        • Hotta K.
        • Oyama T.
        • Shinohara T.
        • et al.
        Learning curve for endoscopic submucosal dissection of large colorectal tumors.
        Dig Endosc. 2010; 22: 302-306
        • Choi I.J.
        • Kim C.G.
        • Chang H.J.
        • et al.
        The learning curve for EMR with circumferential mucosal incision in treating intramucosal gastric neoplasm.
        Gastrointest Endosc. 2005; 62: 860-865
        • Parra-Blanco A.
        • Arnau M.R.
        • Nicolas-Perez D.
        • et al.
        Endoscopic submucosal dissection training with pig models in a Western country.
        World J Gastroenterol. 2010; 16: 2895-2900
        • Herreros de Tejada A.
        ESD training: a challenging path to excellence.
        World J Gastrointest Endosc. 2014; 6: 112-120

      Linked Article

      • Learning curve for EMR of large nonpolypoid colorectal neoplasia: an alternative analysis method using longitudinal models
        Gastrointestinal EndoscopyVol. 85Issue 6
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          We read with interest the article by Bhurwal et al1 describing the EMR learning curve. The study followed 3 endoscopists and recorded repeated outcome measures with increasing EMR procedure numbers. The authors used graphical evaluation and the test of linear trend to report their findings. We believe that conducting logistic regression and examining the test of trend in this setting is not optimal, given that the observations in the analyzed dataset were not independent but rather were interrelated because they were performed by the same 3 endoscopists over a period of time.
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