Endoscopic activity in inflammatory bowel disease: clinical significance and application in practice

Kyeong Ok Kim

doi:10.5946/ce.2022.108

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Review Endoscopic activity in inflammatory bowel disease: clinical significance and application in practice: Kyeong Ok Kim^,; Clinical Endoscopy 2022;55(4):480-488.
DOI: https://doi.org/10.5946/ce.2022.108
Published online: July 28, 2022

Division of Gastroenterology and Hepatology, Department of Internal Medicine, Yeungnam University College of Medicine, Daegu, Korea

Correspondence: Kyeong Ok Kim Division of Gastroenterology and Hepatology, Department of Internal Medicine, Yeungnam University College of Medicine, 170 Hyeonchung-ro, Nam-gu, Daegu 42415, Korea E-mail: kokim@yu.ac.kr

• Received: March 27, 2022 • Revised: April 22, 2022 • Accepted: April 26, 2022

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Abstract
INTRODUCTION
ENDOSCOPIC DISEASE ACTIVITY INDICES IN ULCERATIVE COLITIS
ENDOSCOPIC ACTIVITY INDEX FOR CROHN'S DISEASE
WHY DOES ENDOSCOPIC ACTIVITY MATTER IN INFLAMMATORY BOWEL DISEASE?
HOW TO APPLY ENDOSCOPIC ACTVITY IN PRACTICE
CONCLUSIONS
NOTES
REFERENCES

Abstract

Endoscopy is vital for diagnosis, assessing treatment response, monitoring and surveillance in patients with inflammatory bowel disease (IBD). With the growing importance of mucosal healing as a treatment target, the assessment of disease activity by endoscopy has been accepted as the standard of care for IBD. There are many endoscopic activity indices for facilitating standardized reporting of the gastrointestinal mucosal appearance in IBD, and each index has its strengths and weaknesses. Although most endoscopic indices do not have a clear-cut validated definition, endoscopic remission or mucosal healing is associated with favorable outcomes, such as a decreased risk of relapse. Therefore, experts suggest utilizing endoscopic indices for monitoring disease activity and optimizing treatment to achieve remission. However, the regular monitoring of endoscopic activity is limited in practice owing to several factors, such as the complexity of the procedure, time consumption, inter-observer variability, and lack of a clear-cut, validated definition of endoscopic response or remission. Although experts have recently suggested consensus-based definitions, further studies are needed to define the values that can predict long-term outcomes.
Keywords: Endoscopy; Disease activity; Inflammatory bowel diseases; Mucosal healing

INTRODUCTION

The role of endoscopy is central to the evaluation and management of inflammatory bowel disease (IBD), especially in the diagnosis, tissue acquisition, treatment-response evaluation, surveillance of colorectal dysplasia, and monitoring of mucosal healing (MH).¹^-³ In addition, endoscopy is also used for therapeutic purposes.⁴ Although achieving clinical remission is considered the goal of IBD treatment, endoscopic disease activity might last even in the clinical remission state.⁵^-⁹ Hence, there remains a risk of under-or over-treatment when management strategies are determined solely based on symptoms. As endoscopic remission or MH is significantly associated with favorable clinical outcomes, more emphasis has been placed on achieving it, as a treatment target for IBD.¹⁰^,¹¹ Recent advancements in biologics have made MH realizable, resulting in a paradigm shift in IBD management goals away from clinical remission and toward MH.¹² MH, being relatively more objective and quantifiable than clinical remission, is a superior treatment endpoint.

However, for accurate assessment of MH, standardized systems are needed to report the different gastrointestinal mucosal appearances in IBD. Various endoscopic activity indices have been developed to enable physicians to interpret endoscopic findings and translate them into validated scores that grade disease activity. Such indices have been introduced for ulcerative colitis (UC) and Crohn's disease (CD). Each index has its individual strengths and weaknesses; however, most remain to be fully validated due to differences in the parameters employed and the inter-observer agreements.¹ Herein, we aimed to review the features, strengths, and weaknesses of the most common endoscopic activity indices for IBD, their clinical significance, and the factors to be considered for their practical application.

ENDOSCOPIC DISEASE ACTIVITY INDICES IN ULCERATIVE COLITIS

Ever since Truelove and Witts introduced the first UC severity scoring system in 1955, various other endoscopic scoring systems for UC have been developed.¹³ Although each scoring system differs slightly, they all score the mucosal activity in UC in terms of erythema, edema, loss of fine vascular pattern, and granularity.¹⁴ In addition, mucosal friability, spontaneous bleeding, and ulceration have also been evaluated and are considered to indicate severe disease.¹⁴ Truelove and Witts classified the gastrointestinal lesions as normal or near-normal, improved, or no change/worse based on these endoscopic findings.¹³ Among the various scoring systems, this review focuses on ones that are currently the most commonly used in trials or practice: the Mayo endoscopic sub-score (MES) and the Ulcerative Colitis Endoscopic Index of Severity (UCEIS), which is a more recently validated system.

The MES was first introduced by Schroeder et al.¹⁵ as a component of the Mayo Clinical Activity Index. The MES provides a score ranging from 0 to 3 based on four mucosal descriptors, including erythema, friability, vascular pattern, and erosions or ulceration by definition (Table 1). Although it has not yet been validated, MES has been widely used in clinical trials and routine practice owing to its ease of use.¹⁶ However, it only describes the most severely involved segment and does not reflect disease extension or focal healing. Moreover, in MES, friability has been listed as a component of both mild and moderate disease activity, leading to the overlapping of patients between the two levels of disease severity and is thus a limitation of the scoring system. Inter-observer variability is another limitation of MES.¹⁷ For overcoming these limitations, a modified Mayo Clinic Endoscopic Score has been developed and applied in several studies.¹⁸^-²⁰ In this updated system, the total sum of the scores of the five segments of the colon is calculated and then multiplied by the number of intestinal segments involved.²¹ Yet, this system remains to be validated.¹

In 2012, another scoring system was prospectively developed by Travis et al.,²²^,²³ known as the UCEIS, which employed the sum of the scores of three mucosal descriptors, including vascular pattern (scored 0-2), bleeding (score 0 to 3), and erosion/ulcers (score 0 to 3) (Fig. 1). Each score reflects the most severe lesion; hence, microscopic involvement cannot be determined.¹ This system can be easily applied in routine clinical trials and practice, although a moderate inter-observer agreement has been reported.²³ In comparison to MES, the UCEIS scoring system is more objective, has more specificity, and has better sensitivity for UC disease activity.²⁴ Although each study uses its own definitions, there is no validated definition of endoscopic remission or criteria for categorizing mild, moderate, and severe UC in the UCEIS system.¹⁶

ENDOSCOPIC ACTIVITY INDEX FOR CROHN'S DISEASE

It is more challenging to develop an endoscopic index for CD that can accurately assess mucosal lesions in CD because, unlike UC, CD involves multiple locations and phenotypes.²⁵^,²⁶ To date, two validated endoscopic scoring systems exist for CD. The first system is the Crohn's Disease Endoscopic Index of Severity (CDEIS), reported in 1989 by the Groupe d’Etudes Therapeutiques des affections Inflammatoires du tube Digestif²⁷ which was validated prospectively and reproducible with a good inter-observer agreement.²⁴^,²⁸^,²⁹ The CDEIS includes parameters such as the presence of superficial or deep ulcers and the percentage of ulcerated or affected surfaces. These parameters were individually scored for the five colon segments (ileum, right colon, transverse colon, left and sigmoid colon, and rectum), summed, and then divided by the number of segments involved. An additional score was provided for cases with stenosis (ulcerated or non-ulcerated in each segment).²⁷ The total score ranged from 0 to 44 and has been accepted as the gold standard for assessing endoscopic disease activity in CD with high sensitivity. CDEIS correlates well with disease activity.²⁷ Although not formally validated, CDEIS scores ≤7 are considered to denote endoscopic resolution, while CDEIS scores ≤3 as complete resolution.¹ Nevertheless, CDEIS is considered weak because it is too complex to assess and calculate, and training is needed to evaluate the extent, affected surface, and depth of the ulcer.

To overcome the complexity of CDEIS, the Simple Endoscopic Score for CD (SES-CD) was developed in 2004.³⁰ The SES-CD evaluates ulcers based on size and affected ulcerated surfaces. The affected intestinal surfaces and the presence of stenosis were scored from 0 to 3 in all five segments and summed.³⁰ These two endoscopic scores in CD correlated well with each other.³⁰

The Rutgeerts et al.³¹ postoperative endoscopic index is the only endoscopic activity index available for postoperative CD and was developed in 1984.³² The scores were used to evaluate endoscopic recurrence in the neoterminal ileum after ileocolic resection based on the extent of the aphthous ulcer, large ulcer, or luminal narrowing in the ileum from i0 to i4 (Fig. 2). Although not fully validated, a Rutgeerts score of 3 or 4 within one year of ileocolic resection indicated a higher risk of clinical recurrence after three years than in those with 0 or 1 (> 90.1% vs. 10% to 15%).³² Meanwhile, i2, defined as more than five aphthous ulcers in the neoterminal ileum or lesions confined to the ileocolonic anastomosis, showed conflicting clinical outcomes, and the risk of recurrence in anastomotic lesions was uncertain.³³ Therefore, a modified Rutgeerts score, which subdivides i2 lesions into i2a (isolated anastomosis lesion) and i2b (>5 aphthous ulcers in the neoterminal ileum), has been suggested (Fig. 2).³⁴ A recent retrospective study showed that i2a did not increase the risk of disease progression compared with i2b.³⁵ Table 1 summarizes the included endoscopic descriptors, inter-observer agreement, strength, and weakness of common endoscopic indices used to evaluate UC and CD severity.

WHY DOES ENDOSCOPIC ACTIVITY MATTER IN INFLAMMATORY BOWEL DISEASE?

Although clinical symptoms do not always correlate with endoscopic activity, the clinical outcomes of IBD can be predicted based on endoscopic severity. In patients with acute, severe UC, the incidence of colectomy was significantly higher in patients with UCEIS scores >5 than in those with lower UCEIS scores (p=0.012).³⁶ The presence of severe lesions as determined by endoscopy increased the risk of colectomy in patients with CD from 6% to 31% after 12 months of examination.³⁷

Recently, many studies have demonstrated that MH is associated with prolonged remission, reduced risk of hospitalization, and surgical procedures.³⁸^-⁴⁴ MH reduces features of bowel damage in CD, such as fistula development, the requirement of immunosuppressive agents, and the risk for colorectal cancer.⁴⁵^-⁴⁸ In particular, patients with UC in endoscopic remission had a similar risk of colorectal cancer as that of the general population.⁴⁹ In addition, MH can improve the quality of life.¹¹ In this context, a patient with Rutgeerts score i0 or i1 showed a significantly lower risk of clinical recurrence postoperatively.³² Based on this evidence, the International Organization for the Study of Inflammatory Bowel Disease (IOIBD) has recommended closely monitoring the disease activity to achieve endoscopic remission as a long-term treatment target.¹²

HOW TO APPLY ENDOSCOPIC ACTVITY IN PRACTICE

When to assess?

The timing of endoscopy is essential for predicting long-term prognosis through mucosal evaluation. Endoscopic assessment should be considered when aggravated clinical symptoms and elevated inflammatory markers, such as C-reactive protein or calprotectin, are constantly observed as well as at the time of initial diagnosis.¹⁶ In these cases, endoscopy provides critical information for appropriate clinical decision-making. With a particular emphasis on achieving MH, follow-up endoscopy at 3 to 6 months after starting the therapy is suggested for assessing the treatment response.¹⁶ As ileocolonoscopy within 6 to 12 months after ileocolectomy is known to be a significant predictor of long-term outcomes; follow-up endoscopy at this time is recommended in CD patients who underwent ileocolonic resection.³²

Which index is better to use?

Although the assessment of endoscopic activity is essential for predicting clinical outcomes, its routine application in practice is limited for several reasons. First, in the case of CD, both CDEIS and SES-CD are complex and time-consuming. Second, a consensus regarding the best index for assessing endoscopic activity in both CD and UC is currently unavailable. There are many studies regarding endoscopic activity and clinical outcomes; however, the index used may vary, and there is no clarity regarding which system is more accurate. Recently, one study compared the MES and UCEIS in patients with acute severe UC in whom tacrolimus was used. Both UCEIS and MES significantly decreased after tacrolimus induction. However, when they considered the score change in remission, responder and non-responder only the UCEIS score decreased in responders, whereas there was no significant change in the MES. Based on these results, the UCEIS was concluded to reflect the clinical outcomes more accurately than the MES.⁵⁰ There are no comparative studies between these two indices with respect to CD; however, considering that the SES-CD requires fewer calculations, it could be easier to use than CDEIS. Therefore, the updated Selecting Therapeutic Targets in Inflammatory Bowel Disease (STRIDE) II guidelines recommend using SES-CD for CD patients and MES or UCEIS for assessing disease activity using endoscopy.¹²

How much healing do we need to improve clinical outcomes?

A validated standard definition of endoscopic response or remission has not yet been reported. Recently, members of the IOIBD have developed a consensus definition in clinical trials using the Delphi process among IBD experts. In UC, a decrease in MES ≥1 or UCEIS ≥2 was suggested as an endoscopic response, and a UCEIS score of 0 was considered to indicate endoscopic remission.⁵¹ However, these definitions were used in clinical trials and could differ from those appropriate in routine practice. Therefore, more studies are needed to define predictive values for improved long-term outcomes. In the case of CD, a decrease in the CDEIS or SES-CD by >50% was considered an endoscopic response,⁵² based on the results of a post-hoc analysis of the Study of Biologic and Immunomodulator Naive Patients in Crohn's Disease trials, which reported that a >50% decrease in both SES-CD and CDEIS scores at 26 weeks was a significant predictor of corticosteroid-free clinical remission at 50 weeks.⁵³ They also suggested that achieving an SES-CD score of 0-2 indicates endoscopic remission. In postoperative CD, a Rutgeerts score of i0-i1 was suggested to predict endoscopic remission after ileocolectomy.⁵²

Although many studies support that MH can improve clinical outcomes, the degree of healing required for predicting better outcomes remains controversial. According to the ACT 1 trial, the corticosteroid-free remission rates at weeks 30 and 54 were significantly different from those with the cut-off MES score of 1 at week eight after treatment with infliximab. In addition, colectomy-free survival was substantially higher in patients with MES of 0 to 1 than in those with an MES score >1.5 Another meta-analysis also reported that the risk of colectomy was not significantly different between complete and partial MH in UC and CD.⁵⁴ Meanwhile, Barreiro-de Acosta et al.⁵⁵ recently evaluated whether the risk of relapse increases as the MES increases from 0 to 1. The results showed that relapse within five months occurred more frequently in patients with MES of 1 (36.6%) than in those with MES of 0 (9.4%, p<0.001), and MES of 1 was the only independent factor associated with UC relapse (odds ratio, 6.27; 95% confidence interval, 2.73–14.4; p<0.001).

Although more evidence is needed to confirm, experts in STRIDE II reached a consensus regarding the target definition of endoscopic healing as a score in SES-CD <3 or absence of ulceration in CD and MES=0 or UCEIS ≤1 in UC.¹² Based on studies that show the benefits of optimizing treatment to target MH,⁵⁴^,⁵⁶^,⁵⁷ they also recommend escalating treatment if the previous treatment could not achieve the target.¹² The application of endoscopic assessment in clinical practice is summarized in Figure 3.

CONCLUSIONS

Evaluation of endoscopic activity has become crucial in IBD management because MH has been associated with favorable long-term clinical outcomes. Although numerous endoscopic scoring systems are currently available, for clinical research and routine practice, the MES and UCEIS are used in UC, the CDEIS and SES-CD are employed in CD, and the Rutgeerts score is used in post-ileocolonic resection. The application of these scoring systems in clinical settings is limited because of their complexity, inter-observer variability, lack of validation, and lack of consensus regarding the definition of disease severity. Moreover, the degree of MH necessary to improve long-term outcomes remains unclear. However, endoscopic assessment has become an important standard of care, and we need to fully understand each endoscopic activity index and apply it in practice after accurate interpretation. We also need to optimize the treatment to achieve MH for better patient outcomes.

Conflicts of Interest

The author has no conflicts of interest.

Funding

None.

Fig. 1.

Endoscopic features of each descriptor in ulcerative colitis endoscopic index of severity.

Fig. 2.

Rutgeerts score for postoperative Crohn's disease (i2a and i2b by modified Rutgeerts score)

Fig. 3.

Suggested algorithm for endoscopic assessment and application in practice. CRP, C-reactive protein; CD, Crohn's disease; UC, ulcerative colitis; SES-CD, Simple Endoscopic Score for Crohn's Disease; CDEIS, Crohn's Disease Endoscopic Index of Severity; UCEIS, Ulcerative Colitis Endoscopic Index of Severity.

Table 1.

Endoscopic scoring systems commonly used in ulcerative colitis and Crohn's disease

Scoring system		Descriptors	Score range	Segment consideration	Inter-observer agreement (κ score)	Interpretation	Strength	Weakness
UC	MES	Erythema, vascularity, friability, bleeding, erosions ulceration	0. Normal or inactive disease	Most severe finding	0.53 Inexperienced	0. Normal	1. Widely used in clinical trials	1. No consideration of distribution and extend
			1. Decreased vascularity, mild friability, erythema		0.71 Experienced	1. Mild	2. Easy to use	2. Overlap between scores in some descriptors
			2. Marked erythema, absence vascularity, friability, erosion			2. Moderate
			3. Ulcers and spontaneous bleeding			3. Severe
	UCEIS	Vascularity	1. Vascular pattern: 0–2, bleeding and ulceration: 0–3	Most severe area	0.5 Experienced	Not validated, But usually	1. Only validated index in UC	1. No validated severity definition
		Bleeding	2. Total score: 0–8			Remission ≤1	2. Easy to assess
		Erosions/ulcerations				Mild 2–4	3. Better score range than MES	2. No consideration regarding change and healing
						Moderate 5–6
						Severe 7–8
CD	CDEIS	1. Superficial ulcer	Total score: 0–44	5, Terminal ileum, ascending, ransverse, descending and sigmoid colon, rectum	0.67 Inexperienced	Not validated: but usually	1. Consider segments that are not visualized	1. Difficult to assess size of surface, ulcer and ulcer depth
		2. Deep ulcer			0.83 Experienced	Healed: ≤3	2. Good correlation with disease surface	2. Difficult to calculate
		3. Surface affected				Mild: <5	3. Prognostic relevance
		4. Ulcerated surface				Moderate:5–15
						Severe: >15
	SES-CD	1. Ulcer size (aphthous <0.5 cm, large 0.5–2 cm, very large >2 cm)	1. Total: 0-56 (total of all segments)	5, Terminal ileum, ascending, transverse, descending, and sigmoid colon, rectum	0.68 Inexperienced	Not validated but usually	1. Simpler than CDEIS	1. Underestimation in case only 1 segment is involved
		2. Surface ulcerated	2. Value of each descriptors: 0–3		0.93 Experienced	Healed: 0–2,	2. Clear definition of score	2. No consideration of uninvolved segments
		3. Surface affected				Mild: 3–6, Moderate: 7–15	3. Prognostic relevance
		4. Stricture				Severe: ≥16
Post-op CD	Rutgeerts score	1. Aphthous ulcers (≤5 and >5)	Score of each descriptor, i0 to i4 (in modified RS, i2 subdivided into i2a, i2b)	Neoterminal ileum examined	0.57 Inexperienced	Validated	1. Gold standard in post-op setting	1. Not fully validate
		2. Large ulcers			0.71 Experienced	Low risk : i0–i1	2. Validated cut off	2. Only available in prediction of post-op recurrence
		3. Inflamed intervening mucosa				Medium risk: i2	3. Easy to use
		4. Diffuse inflammation				High risk: i3–i4

UC, ulcerative colitis; CD, Crohn's disease; MES, Mayo endoscopic sub-score; UCEIS, Ulcerative Colitis Endoscopic Index of Severity; CDEIS, Crohn's Disease Endoscopic Index of Severity; SES-CD, Simple Endoscopic Score for Crohn's Disease; RS, Rutgeerts score.

REFERENCES

1. Lee JS, Kim ES, Moon W. Chronological review of endoscopic indices in inflammatory bowel disease. Clin Endosc 2019;52:129–136.Article PubMed PMC PDF
2. Kim KO, Chiorean MV. Advanced neoplasia detection using chromoendoscopy and white light colonoscopy for surveillance in patients with inflammatory bowel disease. Intest Res 2020;18:438–446.Article PubMed PMC PDF
3. Ham NS, Myung SJ. Endoscopic molecular imaging in inflammatory bowel disease. Intest Res 2021;19:33–44.Article PubMed PMC PDF
4. Pokala A, Shen B. Update of endoscopic management of Crohn's disease strictures. Intest Res 2020;18:1–10.Article PubMed PMC PDF
5. Colombel JF, Rutgeerts P, Reinisch W, et al. Early mucosal healing with infliximab is associated with improved long-term clinical outcomes in ulcerative colitis. Gastroenterology 2011;141:1194–1201.Article PubMed
6. Modigliani R, Mary JY, Simon JF, et al. Clinical, biological, and endoscopic picture of attacks of Crohn's disease. Evolution on prednisolone. Groupe d'Etude Thérapeutique des Affections Inflammatoires Digestives. Gastroenterology 1990;98:811–818.Article PubMed
7. Rutgeerts P, Sandborn WJ, Feagan BG, et al. Infliximab for induction and maintenance therapy for ulcerative colitis. N Engl J Med 2005;353:2462–2476.Article PubMed
8. Baars JE, Nuij VJ, Oldenburg B, et al. Majority of patients with inflammatory bowel disease in clinical remission have mucosal inflammation. Inflamm Bowel Dis 2012;18:1634–1640.Article PubMed
9. Gomes P, du Boulay C, Smith CL, et al. Relationship between disease activity indices and colonoscopic findings in patients with colonic inflammatory bowel disease. Gut 1986;27:92–95.Article PubMed PMC
10. Peyrin-Biroulet L, Ferrante M, Magro F, et al. Results from the 2nd Scientific Workshop of the ECCO. I: Impact of mucosal healing on the course of inflammatory bowel disease. J Crohns Colitis 2011;5:477–483.Article PubMed
11. Neurath MF, Travis SP. Mucosal healing in inflammatory bowel diseases: a systematic review. Gut 2012;61:1619–1635.Article PubMed
12. Turner D, Ricciuto A, Lewis A, et al. STRIDE-II: an update on the Selecting Therapeutic Targets in Inflammatory Bowel Disease (STRIDE) initiative of the International Organization for the Study of IBD (IOIBD). Determining therapeutic goals for treat-to-target strategies in IBD. Gastroenterology 2021;160:1570–1583.Article PubMed
13. Truelove SC, Witts LJ. Cortisone in ulcerative colitis; final report on a therapeutic trial. Br Med J 1955;2:1041–1048.Article PubMed PMC
14. Fefferman DS, Farrell RJ. Endoscopy in inflammatory bowel disease: indications, surveillance, and use in clinical practice. Clin Gastroenterol Hepatol 2005;3:11–24.Article PubMed
15. Schroeder KW, Tremaine WJ, Ilstrup DM. Coated oral 5-aminosalicylic acid therapy for mildly to moderately active ulcerative colitis. A randomized study. N Engl J Med 1987;317:1625–1629.Article PubMed
16. Christensen B, Rubin DT. Understanding endoscopic disease activity in IBD: how to incorporate it into practice. Curr Gastroenterol Rep 2016;18:5.Article PubMed PDF
17. Walsh A, Palmer R, Travis S. Mucosal healing as a target of therapy for colonic inflammatory bowel disease and methods to score disease activity. Gastrointest Endosc Clin N Am 2014;24:367–378.Article PubMed
18. D'Haens G, Feagan B, Colombel JF, et al. Challenges to the design, execution, and analysis of randomized controlled trials for inflammatory bowel disease. Gastroenterology 2012;143:1461–1469.Article PubMed
19. Kamm MA, Sandborn WJ, Gassull M, et al. Once-daily, high-concentration MMX mesalamine in active ulcerative colitis. Gastroenterology 2007;132:66–75.Article PubMed
20. Feagan BG, Sandborn WJ, D'Haens G, et al. The role of centralized reading of endoscopy in a randomized controlled trial of mesalamine for ulcerative colitis. Gastroenterology 2013;145:149–157.Article PubMed
21. Lobatón T, Bessissow T, De Hertogh G, et al. The modified Mayo endoscopic score (MMES): a new index for the assessment of extension and severity of endoscopic activity in ulcerative colitis patients. J Crohns Colitis 2015;9:846–852.Article PubMed
22. Travis SP, Schnell D, Krzeski P, et al. Developing an instrument to assess the endoscopic severity of ulcerative colitis: the Ulcerative Colitis Endoscopic Index of Severity (UCEIS). Gut 2012;61:535–542.Article PubMed PMC
23. Travis SP, Schnell D, Krzeski P, et al. Reliability and initial validation of the ulcerative colitis endoscopic index of severity. Gastroenterology 2013;145:987–995.Article PubMed
24. Tontini GE, Bisschops R, Neumann H. Endoscopic scoring systems for inflammatory bowel disease: pros and cons. Expert Rev Gastroenterol Hepatol 2014;8:543–554.Article PubMed
25. Cicero G, Mazziotti S. Crohn's disease at radiological imaging: focus on techniques and intestinal tract. Intest Res 2021;19:365–378.Article PubMed PMC PDF
26. Hart L, Bessissow T. Endoscopic scoring systems for the evaluation and monitoring of disease activity in Crohn's disease. Best Pract Res Clin Gastroenterol 2019;38-39:101616.Article PubMed
27. Mary JY, Modigliani R. Development and validation of an endoscopic index of the severity for Crohn's disease: a prospective multicentre study. Groupe d'Etudes Thérapeutiques des Affections Inflammatoires du Tube Digestif (GETAID). Gut 1989;30:983–989.Article PubMed PMC
28. Annese V, Daperno M, Rutter MD, et al. European evidence based consensus for endoscopy in inflammatory bowel disease. J Crohns Colitis 2013;7:982–1018.Article PubMed
29. Daperno M, Castiglione F, de Ridder L, et al. Results of the 2nd part Scientific Workshop of the ECCO. II: Measures and markers of prediction to achieve, detect, and monitor intestinal healing in inflammatory bowel disease. J Crohns Colitis 2011;5:484–498.Article PubMed
30. Daperno M, D'Haens G, Van Assche G, et al. Development and validation of a new, simplified endoscopic activity score for Crohn's disease: the SES-CD. Gastrointest Endosc 2004;60:505–512.Article PubMed
31. Rutgeerts P, Geboes K, Vantrappen G, et al. Natural history of recurrent Crohn's disease at the ileocolonic anastomosis after curative surgery. Gut 1984;25:665–672.Article PubMed PMC
32. Rutgeerts P, Geboes K, Vantrappen G, et al. Predictability of the postoperative course of Crohn's disease. Gastroenterology 1990;99:956–963.Article PubMed
33. Sandborn WJ, Feagan BG, Hanauer SB, et al. A review of activity indices and efficacy endpoints for clinical trials of medical therapy in adults with Crohn's disease. Gastroenterology 2002;122:512–530.Article PubMed
34. Domènech E, Mañosa M, Bernal I, et al. Impact of azathioprine on the prevention of postoperative Crohn's disease recurrence: results of a prospective, observational, long-term follow-up study. Inflamm Bowel Dis 2008;14:508–513.Article PubMed
35. Ollech JE, Aharoni-Golan M, Weisshof R, et al. Differential risk of disease progression between isolated anastomotic ulcers and mild ileal recurrence after ileocolonic resection in patients with Crohn's disease. Gastrointest Endosc 2019;90:269–275.Article PubMed PMC
36. Corte C, Fernandopulle N, Catuneanu AM, et al. Association between the ulcerative colitis endoscopic index of severity (UCEIS) and outcomes in acute severe ulcerative colitis. J Crohns Colitis 2015;9:376–381.Article PubMed
37. Allez M, Lemann M, Bonnet J, et al. Long term outcome of patients with active Crohn's disease exhibiting extensive and deep ulcerations at colonoscopy. Am J Gastroenterol 2002;97:947–953.Article PubMed
38. Shah SC, Colombel JF, Sands BE, et al. Mucosal healing is associated with improved long-term outcomes of patients with ulcerative colitis: a systematic review and meta-analysis. Clin Gastroenterol Hepatol 2016;14:1245–1255.Article PubMed
39. Frøslie KF, Jahnsen J, Moum BA, et al. Mucosal healing in inflammatory bowel disease: results from a Norwegian population-based cohort. Gastroenterology 2007;133:412–422.Article PubMed
40. Feagan BG, Reinisch W, Rutgeerts P, et al. The effects of infliximab therapy on health-related quality of life in ulcerative colitis patients. Am J Gastroenterol 2007;102:794–802.Article PubMed
41. Meucci G, Fasoli R, Saibeni S, et al. Prognostic significance of endoscopic remission in patients with active ulcerative colitis treated with oral and topical mesalazine: a prospective, multicenter study. Inflamm Bowel Dis 2012;18:1006–1010.Article PubMed
42. Ardizzone S, Cassinotti A, Duca P, et al. Mucosal healing predicts late outcomes after the first course of corticosteroids for newly diagnosed ulcerative colitis. Clin Gastroenterol Hepatol 2011;9:483–489.Article PubMed
43. Shah SC, Colombel JF, Sands BE, et al. Systematic review with meta-analysis: mucosal healing is associated with improved long-term outcomes in Crohn's disease. Aliment Pharmacol Ther 2016;43:317–333.Article PubMed
44. Baert F, Moortgat L, Van Assche G, et al. Mucosal healing predicts sustained clinical remission in patients with early-stage Crohn's disease. Gastroenterology 2010;138:463–468.Article PubMed
45. Rutgeerts P, Diamond RH, Bala M, et al. Scheduled maintenance treatment with infliximab is superior to episodic treatment for the healing of mucosal ulceration associated with Crohn's disease. Gastrointest Endosc 2006;63:433–442.Article PubMed
46. Rutgeerts P, Feagan BG, Lichtenstein GR, et al. Comparison of scheduled and episodic treatment strategies of infliximab in Crohn's disease. Gastroenterology 2004;126:402–413.Article PubMed
47. Solberg IC, Lygren I, Jahnsen J, et al. Clinical course during the first 10 years of ulcerative colitis: results from a population-based inception cohort (IBSEN Study). Scand J Gastroenterol 2009;44:431–440.Article PubMed
48. Rutter M, Saunders B, Wilkinson K, et al. Severity of inflammation is a risk factor for colorectal neoplasia in ulcerative colitis. Gastroenterology 2004;126:451–459.Article PubMed
49. Rutter MD, Saunders BP, Wilkinson KH, et al. Thirty-year analysis of a colonoscopic surveillance program for neoplasia in ulcerative colitis. Gastroenterology 2006;130:1030–1038.Article PubMed
50. Ikeya K, Hanai H, Sugimoto K, et al. The ulcerative colitis endoscopic index of severity more accurately reflects clinical outcomes and long-term prognosis than the Mayo endoscopic score. J Crohns Colitis 2016;10:286–295.Article PubMed PMC
51. Vuitton L, Peyrin-Biroulet L, Colombel JF, et al. Defining endoscopic response and remission in ulcerative colitis clinical trials: an international consensus. Aliment Pharmacol Ther 2017;45:801–813.Article PubMed PDF
52. Vuitton L, Marteau P, Sandborn WJ, et al. IOIBD technical review on endoscopic indices for Crohn's disease clinical trials. Gut 2016;65:1447–1455.Article PubMed
53. Ferrante M, Colombel JF, Sandborn WJ, et al. Validation of endoscopic activity scores in patients with Crohn's disease based on a post hoc analysis of data from SONIC. Gastroenterology 2013;145:978–986.Article PubMed
54. Bouguen G, Levesque BG, Pola S, et al. Feasibility of endoscopic assessment and treating to target to achieve mucosal healing in ulcerative colitis. Inflamm Bowel Dis 2014;20:231–239.Article PubMed
55. Barreiro-de Acosta M, Vallejo N, de la Iglesia D, et al. Evaluation of the risk of relapse in ulcerative colitis according to the degree of mucosal healing (Mayo 0 vs 1): a longitudinal cohort study. J Crohns Colitis 2016;10:13–19.Article PubMed
56. Bouguen G, Levesque BG, Pola S, et al. Endoscopic assessment and treating to target increase the likelihood of mucosal healing in patients with Crohn's disease. Clin Gastroenterol Hepatol 2014;12:978–985.Article PubMed
57. Fukuda T, Naganuma M, Sugimoto S, et al. Efficacy of therapeutic intervention for patients with an ulcerative colitis Mayo endoscopic score of 1. Inflamm Bowel Dis 2019;25:782–788.Article PubMed

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Endoscopic activity in inflammatory bowel disease: clinical significance and application in practice

Clin Endosc. 2022;55(4):480-488. Published online July 28, 2022

DOI: https://doi.org/10.5946/ce.2022.108

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Figure

Endoscopic activity in inflammatory bowel disease: clinical significance and application in practice

Fig. 1. Endoscopic features of each descriptor in ulcerative colitis endoscopic index of severity.

Fig. 2. Rutgeerts score for postoperative Crohn's disease (i2a and i2b by modified Rutgeerts score)

Fig. 3. Suggested algorithm for endoscopic assessment and application in practice. CRP, C-reactive protein; CD, Crohn's disease; UC, ulcerative colitis; SES-CD, Simple Endoscopic Score for Crohn's Disease; CDEIS, Crohn's Disease Endoscopic Index of Severity; UCEIS, Ulcerative Colitis Endoscopic Index of Severity.

Fig. 1.

Fig. 2.

Fig. 3.

Endoscopic activity in inflammatory bowel disease: clinical significance and application in practice

Scoring system		Descriptors	Score range	Segment consideration	Inter-observer agreement (κ score)	Interpretation	Strength	Weakness
UC	MES	Erythema, vascularity, friability, bleeding, erosions ulceration	0. Normal or inactive disease	Most severe finding	0.53 Inexperienced	0. Normal	1. Widely used in clinical trials	1. No consideration of distribution and extend
			1. Decreased vascularity, mild friability, erythema		0.71 Experienced	1. Mild	2. Easy to use	2. Overlap between scores in some descriptors
			2. Marked erythema, absence vascularity, friability, erosion			2. Moderate
			3. Ulcers and spontaneous bleeding			3. Severe
	UCEIS	Vascularity	1. Vascular pattern: 0–2, bleeding and ulceration: 0–3	Most severe area	0.5 Experienced	Not validated, But usually	1. Only validated index in UC	1. No validated severity definition
		Bleeding	2. Total score: 0–8			Remission ≤1	2. Easy to assess
		Erosions/ulcerations				Mild 2–4	3. Better score range than MES	2. No consideration regarding change and healing
						Moderate 5–6
						Severe 7–8
CD	CDEIS	1. Superficial ulcer	Total score: 0–44	5, Terminal ileum, ascending, ransverse, descending and sigmoid colon, rectum	0.67 Inexperienced	Not validated: but usually	1. Consider segments that are not visualized	1. Difficult to assess size of surface, ulcer and ulcer depth
		2. Deep ulcer			0.83 Experienced	Healed: ≤3	2. Good correlation with disease surface	2. Difficult to calculate
		3. Surface affected				Mild: <5	3. Prognostic relevance
		4. Ulcerated surface				Moderate:5–15
						Severe: >15
	SES-CD	1. Ulcer size (aphthous <0.5 cm, large 0.5–2 cm, very large >2 cm)	1. Total: 0-56 (total of all segments)	5, Terminal ileum, ascending, transverse, descending, and sigmoid colon, rectum	0.68 Inexperienced	Not validated but usually	1. Simpler than CDEIS	1. Underestimation in case only 1 segment is involved
		2. Surface ulcerated	2. Value of each descriptors: 0–3		0.93 Experienced	Healed: 0–2,	2. Clear definition of score	2. No consideration of uninvolved segments
		3. Surface affected				Mild: 3–6, Moderate: 7–15	3. Prognostic relevance
		4. Stricture				Severe: ≥16
Post-op CD	Rutgeerts score	1. Aphthous ulcers (≤5 and >5)	Score of each descriptor, i0 to i4 (in modified RS, i2 subdivided into i2a, i2b)	Neoterminal ileum examined	0.57 Inexperienced	Validated	1. Gold standard in post-op setting	1. Not fully validate
		2. Large ulcers			0.71 Experienced	Low risk : i0–i1	2. Validated cut off	2. Only available in prediction of post-op recurrence
		3. Inflamed intervening mucosa				Medium risk: i2	3. Easy to use
		4. Diffuse inflammation				High risk: i3–i4

Table 1. Endoscopic scoring systems commonly used in ulcerative colitis and Crohn's disease