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12 Utility and Limitations of Endoanal Ultrasound in the Diagnosis of Crohns... 199
Table 1 Ultrasound classication (de la Portilla Int J Colorectal Dis)
Type of stula Description
Type I Supercial stula (subcutaneous) Type II Only affects the smooth muscle (inter-sphincteric) Type III Affects the striated and smooth muscle (transsphincteric, suprasphincteric) Type IV The pathway does not reach the complex sphincter because it ascends parallel to
Nomenclature Anal stula (AF), number of pathways (nT),type of pathways (I, II, III, IV)
the anal canal to enter the rectum (blind, extrasphincteric)
accompanied by an (a) if it has an abscess, (s) if it has a probe, and (h) if it is a horse-shoe path
Each description of a pathway should be separated by a semicolon (;)
Example:
AF3T:IIIas;IIh;I (anal stula with three pathways)
1. Pathway with a probe that affects both sphincters and has an abscess
(IIIas)
2. Pathway in the form of a horse-shoe with no associated collection
(IIh)
3. Supercial pathway with no associations (I)
Fig. 7 Large ischiorectal abscess in a patient presenting with pain and purulent discharge

4 Conclusion

Endoanal ultrasound is a simple, valuable, and inexpensive imaging modality for the evaluation of stulas related to Crohns disease, providing excellent imaging of the anorectal region, including the anal sphincters and the intersphincteric planes. In addition, with the 3D high-resolution transducers and oxygen peroxide enhanced
200 L. C. C. Oliveira
technique, it can demonstrate adequate position of the internal opening, essential for planning surgical approach, minimizing the risks of sphincter damage and anal incontinence.

5 Cross-References

Anorectal Anatomy Related to Anal Fistula and AbscessAnorectal Physio logy Related to Anal Fistula and AbscessEndoanal Ultrasound in the Diagnosis of Cryptoglandular Anal Fistulas and
Abscesses
Future Perspect ives in the Diagnosis of Anal Fistula and AbscessMagnetic Resonance and Traditional Radiology in the Diagnosis of
Cryptoglandular Anal Fistula and Abscess
Magnetic Resonance Imaging in the Diagnosis, Characterization, and Manage-
ment of Crohns Fistula

References

Alabiso ME, Iasiello F, Pellino G et al (2016) #D-EAUS and MRI in the activity of anal stulas in
Crohns disease. Gastroenterol Res Pract 2016:1895694 Botti F, Losco A, Vigano C, Oreggia B, Prati M, Cointessini AE (2013) Imaging techniques and
combined medical and surgical treatment of perianal Crohns disease. J Ultrasound 18(1):19–35 de la Portilla F, Durán V, Maestre MV et al (2015) Effectiveness of a three-dimensional anorectal
ultrasound in perianal Crohns disease: incompatibility with clinical and surgical examinations.
Int J Colorectal Dis 30(4):529–534 Fleshman J, Tay R (2014) Crohns disease. In: Abcarian H (ed) Anal stula. Springer, New York,
pp 139–157 Losco A, Viganò C, Conte D, Cesana BM, Basilisco G (2009) Assessing the activity of perianal
Crohns disease: comparison of clinical indices and computer-assisted anal ultrasound. In amm
Bowel Dis 15:742–749 Orsoni P, Barthet M, Portier F et al (1999) Prospective comparison of endosonographic, magnetic
resonance imaging and surgical ndings in anorectal stula and abscess complicating Crohns
disease. Br J Surg 86:360–364 Parks AG, Gordon PH, Hardcastle JD (1976) A classication of stula-in-ano. Br J Surg 63:1–12 Santoro GA, Fortling B (2007) The advantages of volume rendering in three-dimensional endo-
sonographic of the anorectum. Dis Colon Rectum 50(3):359–368 Santoro GA, Murad-Regadas SM (2017) Endoanal ultrasonographic imaging of the anorectal
region. In: Practical pelvic oor ultrasonography. Springer, pp 253–276 Siddiqui MRS, Ashraan H, Tozer P et al (2012) A diagnostic accuracy meta-analysis of endoanal
ultrasound and MRI for perianal stula assessment. Dis Colon Rectum 55:576–585 Toyonaga T, Tanaka Y, Song JF et al (2008) Comparison of accuracy of physical examination and
endoanal ultrasonography for preoperative assessment in patients with acute and chronic anal
stula. Tech Coloproctol 12(3):217–223 Viganò C, Losco A, Caprioli F, Basilisco G (2011) Incidence and clinical outcomes of
intersphincteric abscesses diagnosed by anal ultrasonography in patients with Crohns disease.
Inamm Bowel Dis 17(10):2102–2108 Zawadzki A, Starck M, Bohe M, Thorlacius H (2012) A unique 3D endoanal ultrasound feature of
perianal Crohns stula: the Crohn ultrasound stula sign. Colorectal Dis 14:e608– e611
Magnetic Resonance Imaging in the Diagnosis, Characterization,
13
and Management of Crohn’s Fistula
Matthew Vincent, Phillip F. C. Lung, and Kapil Sahnan
Contents
1 Introduction . ............... .................................................................. 202
2 Imaging ...... . ................. ........................................................ ...... 203
3 Diagnosis ....................... ......................................... .................... 203
4 MRI Technique .......................................... .................................... 204
5 Disease Monitoring .......................................................................... 205
6 Future Directions ... . . . ...... . . . . ...... . . . . ...... . . . ..... . . . . . ...... . . . ....... . . . ...... . . . . .. 208
7 Conclusion ................................................................................... 209
8 Cross-References .......................... ............................................. ..... 209
References ............................ ............................................... ............ 209
Abstract
Complex stulizing perianal Crohn’s disease (pCD) is a challenging afiction to
manage. Imaging alongside clinical examination helps the clinician elucidate the
morphology of the stula which is one of the rst steps of forming a management
strategy. MRI is and remains the gold standard investigation and can be used to
plan interventions and even further along the management pathway to assess the
effect of the healing intervention.
M. Vincent Department of Metabolism, Digestion, and Reproduction, Imperial College London, Hammersmith Hospital, London, UK e-mail: matthew.vincent@nhs.net
P. F. C. Lung Fistula Research Unit, St Marks Hospital and Academic Institute, Harrow, UK e-mail: philliplung@nhs.net
K. Sahnan ( Fistula Research Unit, St Marks Hospital and Academic Institute, Harrow, UK
Department of Surgery and Cancer, Imperial College London, St Marys Hospital, London, UK e-mail: ks303@doctors.org.uk
© Springer Nature Switzerland AG 2022 C. Ratto et al. (eds.), Anal Fistula and Abscess, Coloproctology,
https://doi.org/10.1007/978-3-030-76670-2_15
*)
201
202 M. Vincent et al.
Keywords
MRI · Fistula · Crohns disease

1 Introduction

Crohn’s disease (CD) is a type of inammatory bowel disease (IBD) that globally affects between 4 and 250 people per 100,000 population with a varied presentation (Tarrant et al. 2008 ). Between a third and a half of all patients have perianal manifestations (Keighley and Allan 1986). These are broadly classed as stulizing (encompassing abscesses and Crohn’s perianal stulas) and non-stulizing (ssures/ ulcers, strictures/stenosis, skin tags) (Adegbola et al. 2018). A recent epidemiolog­ical study found the prevalence of Crohn’s disease in the United Kingdom to be 400 in 100,000, with the incidence at 14.3 per 100,000 person-years, peaking at 18– 30 years and 60–70 years (King et al. 2020).
CD is characterized by full-thickness microscopic inammation with cobblestoning and abscess formation seen as hallmarks on endoscopic examination. Fistulizing perianal Crohns disease (pCD) repres ents an especially aggressive phenotype that is notoriously difcult to treat, is associated with signicant morbid­ity, and carries a greater chance of the patient suffering a severe and disabling disease course, stulas being known to cause pain and discharge, resulting in reduced quality of life (Mahadev et al. 2011). Schwartz and colleagues demonstrated that the cumulative risk of at least 1 perianal stula 1 year after CD diagnosis was 12%, after 10 years was 21%, and after 20 years was 26% in a population study (Schwartz et al. 2002).
Optimal management of pCD relies on multidisciplinary discussion with input from a gastroenterologist, IBD nurse, radiologist, and colorectal surgeon. Initial assessment includes a history, examination including proctosigmoidoscopy followed by imaging, and ideally with magnetic resonance imaging (MRI). The aim is to assess the patient in terms of their general health (comorbidities), their CD (con­comitant luminal disease, previous/current therapies, etc.), and then specically their perianal manifestations (previous surgeries, current symptoms, etc.). Morphological assessment of the tract can be performed through imaging and examination under anesthesia (EUA), whereby one aim s to delineate the anatomy of the tracts them­selves and their relation to the sphincter and levator plate (Tozer et al. 2011). Established treatment principles involve drain ing the sepsis and aggressively man­aging proctitis while treating the stula medically, usually with a combination of antibiotics, thiopurines, and anti-TNF therapies (Adegbola et al. 2020).
This book chapter will provide an overview of the role of MRI in the diagnosis and characterization of pCD, its role in the management and tracking of disease course in patients, and nally its capacity to be used for operative planning of complex stulizing disease.
13 Magnetic Resonance Imaging in the Diagnosis, Characterization, and.. . 203

2 Imaging

The European Crohns and Colitis Organisation’s (ECCO) guidelines (Gionchetti et al. 2017) state that contrast-enhanced pelvic MRI is considered the ideal initial procedure for the assessment of perianal stulizing CD. MRI has been shown to be more effective in the assessment of treatment response in pCD, while also being crucial for preoperative planning, and more recently, to enable conversion into 3D models that facilitate surgical understanding of this condition.
While MRI has been shown to be the gold standard imaging method of diagnos­ing and characterizing pCD, other imaging modalities have been trialed and have their place in the evaluation of the condition. Endoanal ultrasound (EUS) and transperineal ultrasound (TPUS) represent low-cost, quick imaging methods that, in the hands of skilled operators, have high sensitivity and specicity for identifying stulizing disease (Schwartz et al. 2001). The main drawbacks of ultrasonography include a relatively low sensitivity to detect secondary or deep tracts (Buchanan et al.
2004) and their inability to differentiate brosing stula tracts from acutely inamed
disease.

3 Diagnosis

The perianal stulizing disease is typically categorized according to the Parks classication as intersphincteric, transsphincteric, suprasphincteric, and extra­sphincteric relative to its anatomical relationship to the anal sphincter complex (Parks et al. 1976). A stula can then be further described as simpleif it consists of one tract connecting two epithelialized surfaces and complex if it contains any extensions or branches off this primary tract (Parks et al. 1976). Another method of classifying perianal stulas is the St. James University Hospital categorization system, which gives grades of 1 to 5 based on the anatomical features of the tract as well as the presence of secondary extensions or abscesses (Morris et al. 2000). Accurate understanding of the anatomical relations of the stula tract is essential to ensure effective clearance of any sepsis in the initial operation, thereby decreasing the likelihood of recurrence (Choen and Phillips 1991). Studi es have shown that inaccurate evaluation of stula anatomy by surgeons, which can occur in scarred and complex disease, leads to increased recurrence and therefore worse outcomes (Beckingham et al. 1996; Spencer et al. 1998). Moreover, injudicious operations will lead to scarring and derangement of pelvic anatomy, making further operations more difcult. As such, precise and reliable assessment of stula anatomy and its anatomical relations is essential in the management of pCD.
MRI in pCD has a sensitivity of 97% and a specicity of 96% (Sahni et al. 2008). MRI is especially useful in detecting abscesses (sensitivity 96%, specicity 97%) and horseshoe stulas (sensitivity 100%, specicity 100%) (Beets-Tan et al. 2001).
204 M. Vincent et al.
This is especially valuable when these are not associated with any induration or clinical signs of their presence (Garros et al. 2014).
Beets-Tan et al. (2001) assessed the clinical value of preoperative MRI in the early 2000s by having patients due for EUA undergo MRI prior to their operation. The MRI ndings were shared with the surgeons during the operation, with the option of then continuing to operate based on their novel ndings. The study showed that in 21% of patients, MRI revealed more anatomical information than EUA alone. This effect was more signicant in patients with Crohns disease, as 40% had additional anatomical information on MRI compared to EUA.
Buchanan et al. (2002) further looked into the effect of preoperative MRI on EUA and long-term clinical outcome in 40 patients. At the end of the operation, MRI ndings were revealed, and the surgeons could decide whether to perform a further exploration under anesthesia or leave the operation as is. In operations where the MRI and EUA ndings disagreed and surgeons did not perform further exploration, the authors found that 50% of these patients developed disease recurrence, all of which were at the site predicted by MRI. The authors found that the use of MRI to inform surgery led to a 75% decrease in disease recurrence.

4 MRI Technique

To enable accurate assessment of the anal canal and perianal stulas, sagittal views are performed, which allow correct orientation along the plane of the anal canal (Fig. 1), resulting in true axial and coronal sequences through the anal canal. The eld of view should include all of the anal canal and stulating disease and extend above the levator plate to allow assessment of the rectum and supralevator disea se.
Fig. 1 Orientating the MRI in the correct plane
13 Magnetic Resonance Imaging in the Diagnosis, Characterization, and.. . 205
Fat-suppressed T2 weighted sequences are used to make the T2 high signa l stula more visible, while nonfat-suppressed sequences provide more detail on anal canal and pelvic oor anatomy.
Coronal and sagittal images can guide the clinician to the level of the internal opening and its relation to the anorectal anatomy, such as the levators. Axial sequences show the stula in relation to the internal and external sphincters. Pre­and post- gadolinium T1 sequences have also been used to problem solve and identify enhancing stulas, although it remains unclear how this relates to stula activity.
There are a few limitations to the use of MRI in evaluating pCD. One is the relative expense of the imaging modality, making it prohibitive in certain environ­ments. Another drawback is that, while MRI is effective in identifying abscesses and stula tracts, it is not as good at identifying ulcerations or strictures (Garros et al.
2014; Scholeeld et al. 1997). Schwartz and colleagues found that, in their study of
32 patients with perianal Crohns stula, diagnostic accuracy could be improved if any two modalities (MRI, endoanal ultrasound, EUA) were used in combination (Schwartz et al. 2001).

5 Disease Monitoring

One of the drawbacks of clinical trials on interventions in pCD has been the inability to produce a rigorous, objective outcome measure of disease improvement. The ACCENT-II trial evaluating the role of Iniximab in treatment for pCD used clinical remission (dened as a decrease of >50% in the drainage of stulizing disease) as their primary outcome measure (Sands et al. 2004). However, it has been well­reported that the decrease in stula drainage is only a marker of external stula closure, and does not reect the internal stula environment (Ng et al. 2009;Van Assche et al. 2003; Jones and Tremaine 2005).
The perianal disease activity index (PDAI) represents a validated score to assess disease burden in patients with perianal Crohns disease (Pikarsky et al. 2002). The scale consists of point scores relating to a number of disease aspects including the presence of abscesses, stula, incontinence, and ulcers. While the PDAI has been shown to associate with disease severity, a number of the scoring parameters represent binary factors (i.e., presence of stula, presence of multiple abscesses) that do not measure how the individual factor changes over time in response to treatment (i.e., shrinkage of stula, decrease in size of the abscess, etc.). The stula disease assessment (FDA) dened clinical remission as the cessation of drainage from all external openings and clinical improvement as a decrease in >50% in the drainage of stulizing disease (Present et al. 1999). This index has the limitation of only looking at stula drainage, which purely focuses on the patency of the external opening and may not reect the internal stula environment (Ng et al. 2009; Jones and Tremaine 2005).
Further studies (Tozer et al. 2012) reveal that, despite clinical remission, stula tracts in asymptomatic patients remained T2 hyperintense for a median of 13 months.
206 M. Vincent et al.
This deep healing,i.e., the resolution of T2 hyperintensity of stula tracts, has been seen as a more effective and prognostically relevant method of evaluating disease progression than clinical remission (Chambaz et al. 2019) and currently can only be demonstrated through MR imaging.
Recently, in response to the lack of a standardized measurement of disease activity in perianal Crohns disease, a core outcome set was developed in order to better standardize clinical trials and allow for meta-analyses of trial data (Sahnan et al. 2019a). This consisted of patient-reported outcomes (including incontinence, general quality-of-life assessment) and clinically derived outcomes including a validated disease activity score. MR imaging was incl uded as an optional outcome, with stula response on MRI and an activity-based MRI score responsive to change being the aspects recommended. A numbe r of groups have attempted to develop such a score, with varying degrees of success.
Van Assche et al. (2003) developed a stula scoring system to assess perianal stula activity through imaging. The components of the Van Assche score reect characteristics that may increase stula complexity or activity such as the complexity of the stulizing disease, number of stulas, and presence of proctitis. While it has been used to determine disease response to treatments including iniximab, it has been shown to lack sensitivity to change over time (Ng et al. 2009; Samaan et al.
2017) and has a weak correlation with PDAI (r ¼ 0.371, p ¼ 0.036) (Horsthuis et al.
2011), limiting its utility in assessing treatment progression (Fig. 2).
Samaan et al. (2017) reviewed the characteristics of the Van Assche index and through expert consensus agreement modied the score by removing areas of disagreement and adding some further elements. On attempted validation, the modied Van Assche score was found to have similar problems with the original, namely, its insensitivity to clinical response over time, and had no benet over the original score (van Rijn et al. 2020).
Recently, the MAGNIFI-CD score was developed f ollowing further modica­tion to the van Assche and modied van Assche scores through further expert consensus and internal validation using a cohort of patients gleaned from a trial for stem cell treatment for pCD (Hindryckx et al. 2019). The authors found that the MAGNIFI-CD score provided better inter- and intra-rater variability with increased sensitivity to changes in disease status compared with the original and modied Van Assche indices. The major limitation with this score is its novelty, as it has only undergone internal validation and is still awaiting external assessment through a clinical trial. Notably, the MAGNIFI-CD score was found to correlate poorly with clinical determinants of perianal Crohns disease severity including the PDAI and FDA, further showing the heterogeneity of assessment measures for disease activity.
Along with the variations on the Van Assche score, a number of other groups have looked into radiological methods of quantifying disease. Ng et al. (2009) developed a more holistic scoring system, preferring to re
ect an overall gestalt of the MRI image over time (improving, worsening, no improvement, remission) to reect disease progression following treatment. Villa and colleagues (2012) have looked into a method of quantifying the degree of inammation in stula tracts by taking the
13 Magnetic Resonance Imaging in the Diagnosis, Characterization, and.. . 207
Fig. 2 Van Assche score. (Adapted form Van Assche et al. (2003))
Number of fistula tracks
None 0 Single, unbranched 1 Single, branched 2 Multiple 3
Locaon
Extra- or intersphincteric 1 Transsphincteric 2 Suprasphincteric 3
Extension
Infralevator 1 Supralevator 2
Hyperintensity on T2-weighed images
Absent 0 Mild 4 Pronounced 8
Collecons (cavies > 3mm diameter)
Absent 0 Present 4
Rectal wall involvement
Normal 0 Thickened 2
degree of T1 hyperintensity following gadolinium injection compared with sur­rounding fat. This technique was shown to correlate well with objective clinical indices including PDAI and FDA. Fistula diameter (Barnhoorn et al. 2020) has also been used as a measure for radiological disease burden. These measures have been used occasionally but have not gained widespread traction overall in monitoring pCD radiologically.
The use of MRI to assess the overall volume of stulating disease as an objective measure of disease activity has been recently evaluated as a possible index for treatment response in Crohns disease (Lung et al. 2018). The authors measured stula volumes manually, taking on average roughly 4 min per case, which may be prohibitively time-consuming depending on reporting burden. Fistula volume did not correlate signicantly with clinical activity, which is likely due to the studys small size as a proof-of-concept paper. Further research is needed to validate stula volume and other scoring systems, as an objective and reliable outcome measure, if found to be related to clinical outcomes, would be attractive for use in clinical trials.
At present, there is no consensus on radiological outcome measures to accurately characterize the response of stulating pCD to treatment with studies using a variety of measures, limiting valid comparisons between studies.
208 M. Vincent et al.

6 Future Directions

Previous MRI innovations include reducing scan times by utilizing higher eld strengths and greater signal-to-noise ratio (Dagia et al. 2010), breath-hold image capture (Magnano et al. 2003), fat suppression (Essary et al. 2007), and the use of oral/intravenous contrast agents, such as gadolinium (Darbari et al. 2004; Laghi et al.
2003).
While MRI is known to be effective in accurately characterizing stula anatomy, the images are still a two-dimensional representation of a complex three-dimensional (3D) structure. The surgeonsability to understand the ndings of the study relies on their ability to read the MRI images or understand the radiologistsreport. Moreover, the surgeon still has to mentally reconstruct the 2D image into a 3D picture in order for the study to be useful in preoperative planning. One method to improve under­standing of two-dimensional images is 3D reconstruction.
Wake and colleagues evaluated surgeonsabilities to correctly reconstruct in a three-dimensional model the location of a renal tumor using CT and MRI images with and without 3D reconstructions (Wake et al. 2019). Surgeons reviewed CT and MRI imaging of renal tumors and then were asked to reproduce the location of the tumor on a 3D model of a kidney. The authors found that surgeons found difculty in reproducing imaging ndings and in 25% there was no overlap between the imaging and the surgeonsguesses. The ability of surgeons to reproduce these ndings was signicantly improved by 3D reconstructions of the images, with all of the recon­structions having some overlap with the true anatomical ndings and an increase in a subjective overlap score noted, showing that even experienced surgeons may benet from 3D representations of cross-sectional imaging.
3D reconstructions of MRI images have previously been shown to be effective in aiding in modeling the complex anatomy involved in pelvic operations (Sands et al.
2004; Ng et al. 2009; Zeng et al. 2016; Li et al. 2018; Tang et al. 2009). Sahnan and
colleagues evaluated the effectiveness of segmentation of 2D MRI images in creat­ing three-dimensional models of perianal Crohns stula (Sahnan et al. 2018a). MRI images were performed with manual segmentation of the levator ani, anal sphincters, and stula tract done. These structures were then reconstructed in three dimensions, allowing for easy characterization of the anatomy of the stula tract. This recon­struction is especially helpful for visualizing complex stula with multiple exten­sions above the levator ani in order to help with operative planning. Along with 3D modeling, MRI images have also been manipulated using an immersive reality platform to allow trainee surgeons to simulate complex stula operations (Sahnan et al. 2019b).
Along with virtual 3D reconstructions of images, a physical three-dimensional model of anatomical structures is an effective way to communicate operative anatomy and easily facilitate the simulation of operations prior to the real thing. 3D printing has been used in a number of surgical situations in order to facilitate effective rehearsal for the actual operation (Bianchi et al. 2019). MRI images of perianal stulas were manipulated in order to produce three-dimensional models consisting of the stula tract, external sphincter/levator ani, and internal sphincter