Endosc Int Open 2014; 02(04): E235-E240
DOI: 10.1055/s-0034-1377613
Original article
© Georg Thieme Verlag KG Stuttgart · New York

Factors predicting clinical outcomes of endoscopic submucosal dissection in the rectum and sigmoid colon during the learning curve

Mikhail Agapov
Vladivostok Clinical Railway Hospital – Endoscopy, Vladivostok, Russian Federation
,
Ekaterina Dvoinikova
Vladivostok Clinical Railway Hospital – Endoscopy, Vladivostok, Russian Federation
› Author Affiliations
Further Information

Publication History

submitted 24 March 2014

accepted after revision 23 June 2014

Publication Date:
25 September 2014 (online)

Background and study aims: Colorectal endoscopic submucosal dissection (ESD) is associated with significant technical difficulty, long procedure time, and increased risk of complications, especially perforation. This study aimed to determine the factors associated with clinical results of ESD during the learning curve.

Patients and methods: In total, 44 patients with sessile and flat rectal and sigmoid colon lesions underwent ESD from November 2009 to September 2013. The procedure time, resection method, tumor size, location, gross morphology, presence of fibrosis, histologic findings, rates of en bloc and piecemeal resections and perforation were analyzed. The ESD procedure was classified as technically difficult in the case of procedure time > 120 minutes and/or piecemeal resection. The whole study time was divided into two periods: first period: resections 1 – 22, second period: resections 23 – 44.

Results: En bloc and R0 resection have been achieved in 84.1 % of lesions. The mean procedure time was 119.95 ± 11.22 minutes (range 25 – 360 minutes). Perforation was seen in five cases (11.4 %). A larger tumor size was a risk factor for difficult ESD (P = 0.0001). A finding of fibrosis was a risk factor for piecemeal ESD (P = 0.0074), and perforation (P = 0.0012). There was a high direct positive correlation between tumor size and operation time (r = 0.83, P < 0.0001, 0.95 and 0.99 confidence interval for rho 0.71 – 0.904). There was no significant difference between the first and second period in terms of mean procedure time, en bloc resection or complication rate.

Conclusion: A larger tumor size was associated with technically difficult ESD. Severe submucosal fibrosis was a risk factor for both piecemeal resection and perforation.

 
  • References

  • 1 Haggar FA, Boushey RP. Colorectal cancer epidemiology: incidence, mortality, survival, and risk factors. Clin Colon Rectal Surg 2009; 22: 191-197
  • 2 Hotta K, Fujii T, Saito Y et al. Local recurrence after endoscopic resection of colorectal tumors. Int J Colorectal Dis 2009; 24: 225-230
  • 3 Tanaka S, Haruma K, Oka S et al. Clinicopathologic features and endoscopic treatment of superficially spreading colorectal neoplasms larger than 20 mm. Gastrointest Endosc 2001; 54: 62-66
  • 4 Santos CE, Malaman D, Pereira-Lima JC. Endoscopic mucosal resection in colorectal lesion: A safe and effective procedure even in lesions larger than 2 cm and in carcinomas. Arq Gastroenterol 2011; 48: 242-247
  • 5 Kobayashi N, Yoshitake N, Hirahara Y et al. Matched case-control study comparing endoscopic submucosal dissection and endoscopic mucosal resection for colorectal tumors. J Gastroenterol Hepatol 2012; 27: 728-733
  • 6 Yoshida N, Yagi N, Naito Y et al. Safe procedure in endoscopic submucosal dissection for colorectal tumors focused on preventing complications. World J Gastroenterol 2010; 16: 1688-1695
  • 7 Uraoka T, Parra-Blanco A, Yahagi N. Colorectal endoscopic submucosal dissection: is it suitable in western countries?. J Gastroenterol Hepatol 2013; 28 : 406-414
  • 8 Coman RM, Gotoda T, Draganov PV. Training in endoscopic submucosal dissection. World J Gastrointest Endosc 2013; 5: 369-378
  • 9 Inada Y, Yoshida N, Kugai M et al. Prediction and treatment of difficult cases in colorectal endoscopic submucosal dissection. Gastroenterol Res Pract 2013; Article ID 523084
  • 10 Matsumoto A, Tanaka S, Oba S et al. Outcome of endoscopic submucosal dissection for colorectal tumors accompanied by fibrosis. Scand J Gastroenterol 2010; 45: 1329-1337
  • 11 Yoshida N, Naito Y, Yagi N et al. Importance of histological evaluation in endoscopic resection of early colorectal cancer. World J Gastrointest Pathophysiol 2012; 3: 51-59
  • 12 Dixon MF. Gastrointestinal epithelial neoplasia: Vienna revisited. Gut 2002; 51: 130-131
  • 13 Tanaka S, Terasaki M, Kanao H et al. Review current status and future perspectives of endoscopic submucosal dissection for colorectal tumors. Dig Endosc 2012; 24: 73-79
  • 14 Toyonaga T, Man-i M, Chinzei R et al. Endoscopic treatment for early stage colorectal tumors: The comparison between EMR with small incision, simplified ESD, and ESD using the standard flush knife and the ball tipped flush knife. Acta Chir Iugosl 2010; 57: 41-46
  • 15 Tanaka S, Terasaki M, Hayashi N et al. Warning for unprincipled colorectal endoscopic submucosal dissection: accurate diagnosis and reasonable treatment strategy. Dig Endosc 2013; 25: 107-116
  • 16 Ohata K, Ito T, Chiba H et al. Effective training system in colorectal endoscopic submucosal dissection. Dig Endosc 2012; 24: 84-89
  • 17 Niimi K, Fujishiro M, Kodashima S et al. Long-term outcomes of endoscopic submucosal dissection for colorectal epithelial neoplasms. Endoscopy 2010; 42: 723-729
  • 18 Kaltenbach T, Soetikno R, Kusano C et al. Development of expertise in endoscopic mucosal resection and endoscopic submucosal dissection. Tech Gastrointest Endosc 2011; 13: 100-104
  • 19 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
  • 20 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
  • 21 Białek A, Pertkiewicz J, Karpińska K et al. Treatment of large colorectal neoplasms by endoscopic submucosal dissection: a European single-center study. Eur J Gastroenterol Hepatol 2014; 26: 607-615
  • 22 Yoshida N, Naito Y, Kugai M et al. Efficient hemostatic method for endoscopic submucosal dissection of colorectal tumors. World J Gastroenterol 2010; 16: 4180-4186
  • 23 Lee EJ, Lee JB, Lee SH et al. Endoscopic submucosal dissection for colorectal tumors – 1,000 colorectal ESD cases: one specialized institute’s experiences. Surg Endosc 2013; 27: 31-39
  • 24 Thorlacius H, Uedo N, Toth E. Implementation of endoscopic submucosal dissection for early colorectal neoplasms in Sweden. Gastroenterol Res Pract 2013; Article ID 758202
  • 25 Goto O, Fujishiro M, Kodashima S et al. Is it possible to predict the procedural time of endoscopic submucosal dissection for early gastric cancer?. J Gastroenterol Hepatol 2009; 24: 379-383
  • 26 Ahn JY, Choi KD, Choi JY et al. Procedure time of endoscopic submucosal dissection according to the size and location of early gastric cancers: analysis of 916 dissections performed by 4 experts. Gastrointest Endosc 2011; 73: 911-916
  • 27 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: 573-578
  • 28 Hotta K, Oyama T, Shinohara T et al. Learning curve for endoscopic submucosal dissection of large colorectal tumors. Dig Endosc 2010; 22: 302-306
  • 29 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
  • 30 Saito Y, Uraoka T, Yamaguchi Y et al. A prospective, multicenter study of 1111 colorectal endoscopic submucosal dissections (with video). Gastrointest Endosc 2010; 72: 1217-1225