Copyright
©The Author(s) 2017.
World J Meta-Anal. Aug 26, 2017; 5(4): 85-102
Published online Aug 26, 2017. doi: 10.13105/wjma.v5.i4.85
Published online Aug 26, 2017. doi: 10.13105/wjma.v5.i4.85
Descriptor | Likert scale anchor points | Intra-observer variation(a weighted k) | Inter-observer variation (a weighted k) |
Vascular pattern | Normal (1) Patchy loss (3) Obliterated (5) | 0.61 | 0.42 |
Mucosal erythema | None (1) | 0.43 | 0.35 |
Light red (3) | |||
Dark red (5) | |||
Mucosal surface (Granularity) | Normal (1) | 0.45 | 0.34 |
Granular (3) | |||
Nodular (5) | |||
Mucosal oedema | None (1) | 0.43 | 0.31 |
Probable (3) | |||
Definite (5) | |||
Mucopus | None (1) | 0.47 | 0.4 |
Some (3) | |||
Lots (5) | |||
Bleeding | None (1) | 0.57 | 0.37 |
Mucosal (2) | |||
Luminal mild (3) | |||
Luminal moderate (4) | |||
Luminal severe (5) | |||
Incidental friability | None (1) | 0.49 | 0.4 |
Mild (2) | |||
Moderate (3) | |||
Severe (4) | |||
Very severe (5) | |||
Contact friability | None (1) | 0.34 | 0.3 |
Probable (3) | |||
Definite (5) | |||
Erosions and ulcers | None (1) | ||
Erosions (2) | 0.65 | 0.45 | |
Superficial ulcer (3) | |||
Deep ulcer (4) | |||
Extent of erosions or ulcers | None (1) | 0.6 | 0.42 |
Limited (2) | |||
Substantial (3) | |||
Extensive (4) |
Descriptors | Likert Scale anchor point | Definition |
Vascular pattern | 0: Normal 1: Patchy obliteration 2: Complete obliteration | Normal vascular pattern with arborisation of capillaries clearly defined, or with blurring or patchy loss of capillary margins Complete obliteration |
Bleeding | 0: None 1: Mucosa 2: Luminal mild 3: Luminal moderate or severe | Some spots or streaks of coagulated blood on the surface of the mucosa Some free liquid blood in the lumen Frank blood in the lumen ahead of endoscope or visible oozing from a haemorrhagic mucosa |
Erosions and Ulcers | 0: None 1: Erosions | None Tiny < 5 mm defects in the mucosa, of white or yellow colour with a flat edge |
2: Superficial ulcer | Larger > 5 mm defect in the mucosa, which are discrete fibrin-covered ulcers in comparison with erosions, but remain superficial | |
3: Deep ulcer | Deeper excavated defects in the mucosa, with a slightly raised edge |
Variables | Score | Items |
Stool frequency | 0 | Normal |
1 | 1-2 stools/d more than normal | |
2 | 3-4 stools/d more than normal | |
3 | > 4 stools/d more than normal | |
Rectal bleeding | 0 | None |
1 | Streaks of blood | |
2 | Obvious blood | |
3 | Mostly blood | |
Endoscopic appearance | 0 | Normal |
1 | Mild friability | |
2 | Moderate friability | |
3 | Exudation, spontaneous bleeding | |
Physician global assessment | 0 | Normal |
1 | Mild | |
2 | Moderate | |
3 | Severe |
Ref. | Patient number | Outcomes | |
UCEIS | |||
Validity | Corte et al[18] | 89 | Correlation between UCEIS and outcomes The UCEIS score was directly proportional to requirement of rescue therapy UCEIS ≥ 5 was significantly linked to requiring colectomy 18/54 (33%) patients with UCEIS ≥ 5 compared to 3/33 (9%) with UCEIS ≤ 4 No definition of remission |
Fernandes et al[19] | 108 | Prediction of outcomes in acute severe colitis UCEIS was applied to score of the rectum and sigmoid, seg-UCEIS Seg-UCEIS predicted to develop steroid-refractory disease and the likelihood of colectomy (seg-UCEIS = 14 had a 17 times higher risk of steroid-refractory disease and a 25 times higher risk of requiring colectomy) Every 1 point increase in the UCEIS or Seg-UCEIS increased the need of colectomy by 2.78 and 1.79 respectively Mayo score did not predict these No definition of remission | |
Arai et al[20] | 285 | Reflection of true UC activity and remission The recurrence rate was directly proportional to the UCEIS score (5.0% for UCEIS = 0, 22.4% for UCEIS = 1, 27.0% for UCEIS = 2, 35.7% for UCEIS = 3, 75% for UCEIS = 4-5) The absence of bleeding and mucosal damage were independent factors for continued clinical remission UCEIS ranged from 0 to 5 when clinical remission, Mayo ≤ 1 UCEIS ≤ 1 for clinical remission, which showed sensitivity of 68% and specificity 57% The expected duration of recurrence is also prolonged when UCEIS ≤ 1 | |
Kucharski et al[21] | 49 | Assessment of 9 endoscopic indices correlate well with (1) clinical indices; and (2) histological Geboes Index[22] The UCEIS showed the strongest correlation with the Geboes Index (the coefficient: 0.434 to 0.629) Recommends the UCEIS for the best overall correlations with both clinical and histological indices | |
Responsiveness | Ikeya et al[23] | 41 | The ability to detect to change after Tacrolimus remission induction treatment for moderate to severe UC Although Mayo endoscopic score is easy to use, it does not distinguish depth of ulcers unlike UCEIS Despite UCEIS score improved from 7 to 4, Mayo endoscopic score remained at 3 (severe) An improvement of UCEIS ≥ 3 showed close correlation with clinical remission, colectomy-free and relapse free rates Proposed remission (score 0-1), mild (2-4), moderate (5-6), severe (7-8) UCEIS 1 in remission is only from vascular pattern |
Menasci et al[24] | 80 | Comparison of the global UCEIS score from 5 segments and a traditional method of UCEIS score The regular method of the UCEIS is to score the most inflamed segment of the bowel This was compared with the sum of the score of five colonic segments A very good correlation (Spearman’s r = 0.86, P < 0.0001) for disease with UCEIS score ≤ 5 Less correlation (r = 0.48, P < 0.01) for disease with UCEIS > 5 | |
Reliability | Travis et al[15] | Investigation of intra- and inter-observer consistency assessment 25 readers evaluated 28 videos including 4 duplicates to assess intra-reader reliability The intra and inter-reader reliability ratios for the UCEIS were 0.96 and 0.88 respectively The USCEI revealed a strong correlation with overall assessment of severity without being influenced by knowledge of clinical information No definition of remission | |
Feagan et al[25] | 281 | The effect of centralized review of images on inter-observer variations Patients with UCDAI ≥ 2 were randomised to evaluate the efficacy of delayed mesalamine treatment (4.8 g/d for 10 wk) UCEIS was used as a part of inter-observer agreement study and showed interclass correlation coefficient of 0.83 amongst 7 central readers, which is superior to UCDAI | |
Travis et al[26] | Clinical information influences UCEIS score 40 readers evaluated 28 of 44 videos No discrepancy between blinded and unblended readers Intra- and inter-reader variability demonstrated moderate to substantial agreement (κ = 0.47 to 0.74 and κ = 0.40 to 0.50 respectively) UCEIS correlated well with patient-reported symptoms - rectal bleeding, stool frequency and patient functional assessment (rank correlation = 0.76 to 0.82) | ||
UCDAI | |||
Validity | Higgins et al[27] | 66 | Finding endpoints in disease activity indices for remission and improvement in UC UCDAI < 2.5 for remission, which had a sensitivity and specificity of 0.82 and 0.89 Remission in this study was defined by patients |
Poole et al[28] | 126 | Establish the relationship between the UCDAI and patient reported EQ-5D The UCDAI with or without endoscopy assessment demonstrated a good correlation with EQ-5D Endoscopy assessment may not link with the disease activity | |
Kucharski et al[21] | 49 | Assessment of 9 endoscopic indices correlate well with (1) clinical indices; and (2) histological Geboes Index (22) The UCDAI showed strong correlations with all 9 endoscopic indices (the coefficient in a range of 0.712 to 0.790) The UCDAI showed the highest correlation amongst clinical activity indices with the Geoboes Index (the Spearman’s coefficient 0.478) Compared to UCEIS, the UCDAI is less correlated with the Geboes Index | |
Reliability | Feagan et al[25] | 281 | The effect of centralized review of images on inter-observer variations Patients with UCDAI ≥ 2 were randomised to evaluate the efficacy of delayed mesalamine treatment (4.8 g/d for 10 wk) 31% of patients with UCDAI ≥ 2 enrolled in the RCT initially were considered ineligible by the central readers Inter-observer agreement amongst 7 central readers was good (interclass correlation coefficient: 0.78) |
Guidelines | Definition |
FDA[5] | Clinical remission Mayo score of ≤ 2 with no individual subscore > 1 Rectal Bleeding subscore = 0 Stool Frequency subscore = 0 (at least one point decrease in Stool Frequency subscore from baseline and achieved 1 is considered) Endoscopy subscore = (Mayo score: 0 or 1, UCDAI = 0) Clinical response Reduction in Mayo score ≥ 3 and ≥ 30% from baseline with Rectal Bleeding subscore ≤ 1 Corticosteroid-free remission Clinical remission in patients using oral corticosteroids at baseline who have discontinued them and are in clinical remission at the end of the study |
World Gastroenterology Organisation | Clinical remission UCDAI ≤ 2 (2010 World Gastroenterology Organisation Practice Guideline)[50] Corticosteroid-free remission Decreasing the frequency and severity of recurrence and reliance on corticosteroids |
International Organisation for the Study of IBD | End points = induction of remission = mucosal healing[12] The absence of friability, blood, erosions and ulcers in all visible segments No mention of clinical symptoms |
American College of Gastroenterology | No clear definition[51] |
British Society of Gastroenterology | No clear definition[52] |
European Crohn’s and Colitis Organisation | Remission[53] A complete resolution of symptoms and endoscopic mucosal healing Not been a fully validated definition of remission Suggest the best way forward is a combination of Stool Frequency ≤ 3 No rectal bleeding Normal or quiescence mucosa at endoscopy Clinical response Clinical and endoscopic response depending on the activity index Generally, a decrease in the activity index > 30% plus a decrease in the rectal bleeding and endoscopic subscores |
Ref. | Year | Type of study | Drug/subject of study | Entry criteria | Primary endpoint | Secondary endpoint | Remission/clinical improvement | Length of study |
Hartman et al[54] | 2016 | Randomised, double-blind, placebo-controlled study | AVX-470, oral | 36 patients with Mayo score 5-12 and Mayo ES ≥ 2 | Not set, but implies clinical response at week 4 | Not set | Remission was not defined. Clinical response Mayo reduction ≥ 3 | 4 wk |
Lin et al[55] | 2015 | Prospective, multi-centre study | Faecal calprotectin | 52 patients with UC | N/A | N/A | Endoscopic remission: UCEIS < 3 | N/A |
Magro et al[56] ACERTIVE study | 2016 | Cross-sectional multi-centre study | Faecal calprotectin/ lipocalin | 371 patients Mayo partial score < 2, montreal classification < 2 | Remission: UCEIS ≤ 1 Mucosal healing: Mayo ES = 0 |
Ref. | Year | Drug | Entry criteria | Primary endpoint | Secondary endpoint | Remission/clinical improvement | Length of study |
Randomised clinical trials - to induce remission | |||||||
Mesalazine (5-ASA) | |||||||
Marteau etal[58] | 2005 | Pentasa (PR + PO vs PO alone) | UCDAI: 3-8 | Remission at week 4 | Remission rate at week 8 Improvement at week 4 and 8 | Remission: UCDAI ≤ 1 Clinical improvement: A decrease of UCDAI ≥ 2 | 8 wk |
D’Haens etal[59] | 2006 | SPD476 - MMX mesalazine | UCDAI: 4-10 + endoscopic score ≥1 PGA score ≤ 2 | Remission | Change in UCDAI, FS, histology at week 8 Change in symptoms | Remission: UCDAI ≤ 1 (with RB 0, SF ≤ 1 ) at week 8 | 8 wk |
Sandborn etal[60] | 2007 | MMX Multi Matrix System mesalazine | UCDAI: 4-10 + endoscopic score ≥1 PGA score ≤ 2 | Clinical/endoscopic remission at 8 wk | Proportion of clinical improvement Proportion of patients as treatment failure Change in: RB, SF, FS | Clinical remission: UCDAI ≤ 1 Endoscopic remission: UCDAI endoscopic subscore ≤ 1 Clinical improvement: A decrease of UCDAI ≥ 3 Treatment failure: Unchanged or worsened UCDAI | 8 wk |
Lichtenstein et al[61] | 2007 | SPD476 - MMX mesalazine OD vs BD | UCDAI: 4-10 | Clinical and endoscopic remission at week 8 | Comparison of remission rate at week 8 | Clinical remission: UCDAI ≤ 1 with RB/SF/EI = 0 | 8 wk |
Kamm et al[62,63] MEZAVANT study | 2007 2009 | MEZAVANT MMX Mesalamine | Mild - mod UC: UCDAI 4-10 + endoscopic subscore ≥ 1, PGA ≤ 2 | Clinical + Endoscopic remission at week 8 | Clinical remission Clinical improvement Change in UCDAI | Clinical + endoscopic remission: UCDAI ≤ 1 + subscore RB/SF = 0, No mucosal friability + a ≥ 1 reduction in EI Clinical improvement: Decrease in UCDAI ≥ 3 | 8 wk |
Ito et al[64] | 2010 | Asacol vs PentasaTime-dependent vs pH dependent Mesalamine | UCDAI: 3-8 and blood stool score ≥ 1 | To demonstrate Asacol over Pentasa AND the decrease in UCDAI | Macroscopic changes | Remission: UCDAI ≤ 2 and no blood diarrhoea Clinical improvement: UCDAI decreased by ≥ 2 | 8 wk |
Hiwatashi etal[65] | 2010 | Mesalazine - dose study | UCDAI: 6-8 | Change in UCDAI at week 8 | Remission, improvement, efficacy | Remission: UCDAI ≤ 1 Efficacy: Decrease of UCDAI ≥ 2 | 8 wk |
Flourié et al[66] MOTUS study | 2013 | Mesalazine, Pentasa OD or BD in total of 4 g/d | UCDAI: 3-8 | UCDAI ≤ 1 after 8 wk | Complete remission (UCDAI = 0) at 8 wk UCDAI decreased by ≥ 2 at 8 wk Clinical remission at week 4, 8, 12 Mucosal healing at 8 wk | Complete remission: UCDAI = 0 Endoscopic remission: UCDAI endoscopic subscore: 0 or 1 Clinical remission: UCDAI ≤ 1 | 12 wk |
Probert et al[42] PINCE study | 2013 | Mesalazine (pentasa) enema | UCDAI: 3-8 | Remission rate (UCDAI < 2) at 4 wk | Remission rate at 8 wk, improvement at week 2, 4 and 8 Time to cessation of RB QoL (EQ-5D) | Remission: UCDAI ≤ 1 Clinical improvement: UCDAI decreased by ≥ 2 | 8 wk |
Sun et al[67] | 2016 | Mesalazine (modified-release vs enteric-coated tablets) | UCDAI: 3-8 + bloody stool score > 1 | The decrease in UCDAI | Remission rate Efficacy rate | Remission: UCDAI ≤ 2 + bloody stool 0 Clinical improvement: A decrease of UCDAI ≥ 2 | 8 wk |
Suzuki etal[68] | 2016 | pH dependent release mesalamine, asacol dose | UCDAI: 6 - 10 Rectal bleeding score ≥ 1 | Decrease in UCDAI | Remission: UCDAI ≤ 2 Rectal bleeding score: 0 Improvement UCDAI decreased by ≥ 2 | 8 wk | |
Thiazole compounds | |||||||
Mantzaris etal[69] | 2004 | Azathioprine alone (2.2 mg/kg) vs combination with olsalazine (0.5 g TID) | Steroid-dependent remission | Relapse rate | Time to relapse Time to discontinuation Severity of relapse | Remission: UCDAI ≤ 1 Relapse: New symptoms + UCDAI > 3 | 2 yr |
Schreiber etal[70] | 2007 | Tetomilast - Thiazole compound | UCDAI: 4-11 | Clinical improvement: UCDAI decreased by ≥ 3 at 8 wk | Remission Clinical improvement at week 4 IBDQ-32 score Proportion of pts with improved Flexible Sigmoidscopy score Time to clinical improvement Time to remission | Clinical improvement: UCDAI decreased by ≥ 3 Remission: UCDAI ≤ 1 | 8 wk |
Steroids | |||||||
Travis et al[71] CORE II study | 2012 | Budesonide MMX | UCDAI: 4-10 | Clinical/endoscopic remission at week 8 | Clinical improvement Endoscopic improvement at week 8 | Clinical/endoscopic Remission: UCDAI ≤ 1 + RB/SF/EI = 0 Clinical improvement: A decrease of UCDAI ≥ 3 Endoscopic improvement: A decrease of EI ≥ 1 | 8 wk |
Probiotics | |||||||
Vernia etal[72] | 2000 | Sodium Butyrate | Mild-moderate UC | Remission or marked improvement | Remission: UCDAI ≤ 2 Positive response: Decrease of UCDAI ≥ 2 | 6 wk | |
Mahmood etal[73] | 2005 | Human recombinant trefoil factor 3 enema | UCDAI: >3 | Remission at week 2 | Clinical significant improvement in clinical and histological scores at 2 and 4 wk | Remission: UCDAI ≤ 1 without RB Clinical improvement: A decrease of UCDAI >3 | 4 wk |
Lichtenstein et al[74] | 2007 | Bowman-Birk inhibitor concentrate - soy extract with high protease inhibitor activity | UCDAI: 4-10 | Remission at week 8 | Remission: UCDAI ≤ 1 + no RB or SF Clinical improvement: UCDAI decrease ≥ 1 | ||
Tursi et al[75] | 2009 | VSL #3 (probiotic) | UCDAI 3-8, endoscopic subscore ≥ 3 | Decrease in UCDAI of ≥ 50% | Activity of relapsing UC Remission Improvement Change in objective and subjective symptoms | Remission: UCDAI ≤ 2 | 8 wk |
Sood et al[76] | 2009 | VSL #3 probiotic | UCDAI 3-9 with endoscopic subscore ≥ 2 | Clinical improvement at week 6 | Clinical remission | Clinical remission: UCDAI ≤ 2 Clinical improvement: A decrease UCDAI by 50% | 12 wk |
Tamaki etal[77] | 2016 | Bifidobacterium longum 536 (probiotic) | UCDAI 3-9 | Change in UCDAI | Remission Improvement of Objective and subjective symptoms Endoscopic improvement in Mayo subscore | Remission: UCDAI ≤ 2 | 8 wk |
Helminth therapy Garg etal[78] | 2014 | Helminth Trichuris suis ova | UCDAI of ≥ 4 | Clinical improvement | Clinical remission | Clinical improvement: Decrease in the UCDAI of ≥ 4 Clinical remission: UCDAI of ≤ 2 | 12 wk |
Nicotine therapy | |||||||
Ingram etal[79] | 2005 | Nicotine enema 6 mg/d | Confirmed UC with inflamed mucosa grade > 2 | Clinical remission | Improvement in the UCDAI | Clinical remission: UCDAI EI ≤ 1 and No RB for 1 wk | 6 wk |
Randomised clinical trials - to maintain remission | |||||||
Lichtenstein et al[80-82] and Zakko etal[83] | 2010 2012 2015 2016 | Mesalamine granules 1.5 g/d, OD | Previously achieved remission with steroids for > 1 mo and < 12 mo | Percentage of patients relapse-free at 6 mo | Mean changes from baseline at month 6 | Relapse: UCDAI RB ≥ 1 and EI ≥ 2 Remission: UCDAI RB = 0, EI < 2 | 6 mo |
Bokemeyer et al[43] and Dignass etal[84] | 2009 2011 | Mesalazine, Pentasa OD or BD in total of 2 g/d | Clinical remission: UCDAI < 2 | To demonstrate OD is not inferior to BD | Time to relapse between 2 groups UC-DAI total and subscores between 2 groups | Remain in remission UCDAI ≤ 2 | 12 mo |
- Citation: Jitsumura M, Kokelaar RF, Harris DA. Remission endpoints in ulcerative colitis: A systematic review. World J Meta-Anal 2017; 5(4): 85-102
- URL: https://www.wjgnet.com/2308-3840/full/v5/i4/85.htm
- DOI: https://dx.doi.org/10.13105/wjma.v5.i4.85