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Rupert WL Leong Director of Endoscopy Senior Staff Specialist Gastroenterologist Concord & Bankstown Hospitals Conjoint Associate Professor UNSW  AIBDA Symposium Colorectal Cancer Surveillance What should we be doing?     New endoscopy techniques and targeted biopsies are now the standard of care
[object Object],[object Object],[object Object],[object Object]
Definitions ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object]
Why newer endoscopic techniques are required?  ,[object Object],[object Object],[object Object],[object Object],[object Object],Eaden  et al .  GI Endosc  2000 Connell  et al .  Gastroenterol  1994 Rubin  et al .  Gastroenterol   1992 Kandiel  et al .  Visible Human J Endosc.  2008
What is being done? Australia ,[object Object],[object Object],[object Object],[object Object],[object Object],Fok I,  et al .  J Gastroenterol Hepatol  2010 (Abst)  Majority of GE  already use   newer endoscopic techniques Efthymiou, Taylor, Kamm, et al.  Inflamm Bowel Dis . 2011
What is Being Done? Overseas ,[object Object],[object Object],[object Object],Centres of excellence use  newer techniques
Why newer endoscopic techniques are required?  Sporadic Cancer Normal Colon Aberrant crypt foci  Adenoma Carcinoma Normal Colon Inflammation Flat Dysplasia Carcinoma IBD Cancer
How newer techniques identify flat dysplasia?  ,[object Object],[object Object],[object Object],[object Object],Tada  et al .  Endosc . 1977;8:70–74.
Chromoendoscopy
Is chromoendoscopy difficult? No ,[object Object],[object Object],[object Object],[object Object],[object Object]
Is it difficult? No ,[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object]
Does it work? Yes
Which technique has a higher yield of dysplasia?  ,[object Object]
CE in UC Surveillance ,[object Object],[object Object],[object Object],Kiesslich  et al .  Gastroenterol  2003 Conventional  (n = 81) Chromoendoscopy (n = 84)  P Intra-epithelial neoplasias   - low grade - high grade 8 2 24 8 <0.005 Cancer 1 3  (2 A’s, 1 B) ns Flat mucosa IN 4  (on random Bx) 24 <0.001
CE in UC Surveillance ,[object Object],[object Object],Rutter  et al .  Gut  2004 Conventional  (n = 100) CE (n = 100)  P Dysplasia: - non-targeted - pre-dye target - dye targeted - 0/ 2,904 biopsies - 2/ 43  (15-20mm) - *+7/ 114  (2-6mm) 0.02 0.06 * Duration (median) 11min 10min ns
CE in UC Surveillance ,[object Object],[object Object],Hurlstone  et al .  Endoscopy  2005  Conventional  (n = 350) High Mag-CE (n = 350)  P Intra-epith neoplasia - non-targeted - targeted 24 - 38/12,482  (0.14%) - 3/369   (1.6%) 69 - 20/12,850  (0.16%) - 49/644   (8%) <0.0001 Cancer 1 3 ns Duration (median) 13min 24min <0.02
CE in Colitis Surveillance ,[object Object],[object Object],Marion  et al .  Am J Gastroienterol  2008 0.09% 20.7% Conventional  (n = 102) CE (n = 102)  P ,[object Object],[object Object],[object Object],3/3264 Bx LGD 12/50 LGD 1/50 HGD 16/82 LGD 1/82 HGD   0.001 Duration (median) 15min 22min ns
Dysplasia Yield Conventional Chromoendoscopy P Kiesslich Gastro.  2003 (n = 163) 3X <0.005 35min 44min ns Rutter  Gut  2004 (n = 100) 3.5X 0.02 11min 10min ns Hurlstone  Endos.  2005  (n = 350) 10X <0.0001 13min 24min Marion AJG  2008 (n = 102) 230X <0.0002 15min 22min
NBI vs CE UC Surveillance ,[object Object],[object Object],[object Object],Pellise M,  et al . Gastrointest  Endosc  2011 NBI (n = 33/27) CE (n = 27/33)  P Per-Pt true pos 11/16 12/16 0.727 Withdrawal time 15.7 26.9 <0.01
[object Object],[object Object],van den Broek  Am J Gastroenterol  2011  ,[object Object]
Is it recommended?  ,[object Object],Itzkowitz, Present.  Inflamm Bowel Dis  2005  BSG 2011 ,[object Object]
Does it matter?  ,[object Object],[object Object],Selinger  et al .  J Gastroenterol Hepatol.  2011(abst)
New Endoscopic Techniques ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object]
Rupert WL Leong Director of Endoscopy Senior Staff Specialist Gastroenterologist Concord & Bankstown Hospitals Conjoint Associate Professor UNSW  AIBDA Symposium Colorectal Cancer Surveillance What should we be doing?     New endoscopy techniques and targeted biopsies are now the standard of care
[object Object],[object Object],[object Object]
Is it messy? ,[object Object],[object Object]
Costs ,[object Object],[object Object],[object Object]
Is it difficult? No ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Kiesslich  et al .  Gastroenterol  2003
Procedure/ Withdrawal Times Conventional Chromoendoscopy P Kiesslich Gastro.  2003 (n = 163) 3X <0.005 35min 44min ns Rutter  Gut  2004 (n = 100) 3.5X 0.02 11min 10min ns Hurlstone  Endos.  2005  (n = 350) 10X <0.0001 13min 24min Marion AJG  2008 (n = 102) 230X <0.0002 15min 22min
Time Saving ,[object Object],[object Object],[object Object]
What about training & safety? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
New Endoscopic Techniques ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]

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2011 Debate on Chromoendoscopy for IBD colitis surveillance

  • 1. Rupert WL Leong Director of Endoscopy Senior Staff Specialist Gastroenterologist Concord & Bankstown Hospitals Conjoint Associate Professor UNSW AIBDA Symposium Colorectal Cancer Surveillance What should we be doing?  New endoscopy techniques and targeted biopsies are now the standard of care
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  • 8. Why newer endoscopic techniques are required? Sporadic Cancer Normal Colon Aberrant crypt foci Adenoma Carcinoma Normal Colon Inflammation Flat Dysplasia Carcinoma IBD Cancer
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  • 21. Dysplasia Yield Conventional Chromoendoscopy P Kiesslich Gastro. 2003 (n = 163) 3X <0.005 35min 44min ns Rutter Gut 2004 (n = 100) 3.5X 0.02 11min 10min ns Hurlstone Endos. 2005 (n = 350) 10X <0.0001 13min 24min Marion AJG 2008 (n = 102) 230X <0.0002 15min 22min
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  • 28. Rupert WL Leong Director of Endoscopy Senior Staff Specialist Gastroenterologist Concord & Bankstown Hospitals Conjoint Associate Professor UNSW AIBDA Symposium Colorectal Cancer Surveillance What should we be doing?  New endoscopy techniques and targeted biopsies are now the standard of care
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  • 33. Procedure/ Withdrawal Times Conventional Chromoendoscopy P Kiesslich Gastro. 2003 (n = 163) 3X <0.005 35min 44min ns Rutter Gut 2004 (n = 100) 3.5X 0.02 11min 10min ns Hurlstone Endos. 2005 (n = 350) 10X <0.0001 13min 24min Marion AJG 2008 (n = 102) 230X <0.0002 15min 22min
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Notes de l'éditeur

  1. Therefore, random biopsies need to be taken throughout the bowel previously exposed to inflammation. It’s been calculated that taking at least 33 quadrantic random biopsies at 10cm intervals are required to yield a 90% confidence of picking up a dysplastic lesion if present. However, only 2% of gastroenterologists take &gt;20 biopsies, let alone 33 biopsies; 50% only take 6 – 10 biopsies. Even when surveillance colonoscopies occur, a significant number of patients still present with symptomatic bowel cancer. Routine colonoscopy and random biopsies may not be adequate to pick up cancers and this review was from St Mark’s hospital, one of the leaders in IBD.
  2. However, finding dysplasia in IBD poses a major challenges to endoscopists. Because dysplasia in IBD develops in flat mucosa which is difficult to see in comparison to sporadic polyps.
  3. What new endoscopic technologies offer include: - improved resolution of tissue imaging plus magnification to increase the sensitivity of finding lesions - the use of special light properties that interact with tissue to differentiate lesions, - and technologies that allow for immediate in situ histology.
  4. CE is low in cost, requires no special equipment apart from a spray catheter and a wide variety of contrast agents can be used. In IBD surveillance they tend to be methylene blue or indigo carmine.
  5. Prospective randomised study
  6. Take home points: - despite protocol 4 quadrant random biopsies, on average only 29 biopsies per person - random biopsies are rarely positive - pre-dye targeted biopsies are good; 4.6% yield (15 – 20mm lesions) - yield in dye targeted = an additional 7 cases or a 3.5 fold increase in detection, smaller dysplastic lesions
  7. In another prospective study from the UK recruiting 350 patients into a conventional colonoscopy arm and another 350
  8. In another prospective study from the UK recruiting 350 patients into a conventional colonoscopy arm and another 350
  9. Although you may be in the minority of gastroenterologists in Australia that do not use advanced imaging techniques, this debate emphasises on what you SHOULD be doing. Based on that, ladies and gentleman, I hope that you would all agree that
  10. Although you may be in the minority of gastroenterologists in Australia that do not use advanced imaging techniques, this debate emphasises on what you SHOULD be doing. Based on that, ladies and gentleman, I hope that you would all agree that
  11. So how is CE performed? 1. Strict patient selection: symptoms in remission and or optimised medical therapy to induce remission whenever possible. 2. Unmasking the mucosa with an excellent bowel prep, removing mucus and using washes. 3. IV buscopan or glucagon can be used to reduce peristalsis. Air insufflation is required. 4. Full length staining refers to pan-chromoendoscopy of the whole colon, starting at the caecum. 5. Add dye in a segmental fashion every 20 – 30cm. On average 60 – 100ml of solution is required. 6. Crypt pattern is detected using magnifying colonoscopy 7. Endoscopic targeting of lesions is required