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Research Article | Volume 17 Issue 8 (August, 2025) | Pages 52 - 55
Assessment of Bowel Ultrasound among Inflammatory Bowel Disease Patients
 ,
 ,
1
Assistant Professor, Department of Radio-diagnosis, MIMER Medical College, Talegaon, Pune, Maharashtra, India
2
Assistant Professor Department of Radio-diagnosis, MIMER Medical College, Talegaon, Pune, Maharashtra, India
3
Associate Professor Department of Community Medicine, MIMER Medical College, Talegaon, Pune, Maharashtra, India
Under a Creative Commons license
Open Access
Received
July 20, 2025
Revised
Aug. 2, 2025
Accepted
Aug. 11, 2025
Published
Aug. 18, 2025
Abstract

Background: Inflammatory Bowel Disease (IBD), comprising Crohn’s disease (CD) and ulcerative colitis (UC), requires timely diagnosis and frequent monitoring. While colonoscopy remains the gold standard, bowel ultrasound (BUS) is emerging as a non-invasive and cost-effective alternative. Objective: This study aimed to evaluate the diagnostic accuracy and clinical utility of bowel ultrasound in assessing disease activity and complications in IBD patients, compared with colonoscopy and clinical indices. Methods: A prospective observational study was conducted on 120 patients with confirmed IBD (68 with CD and 52 with UC). Each underwent bowel ultrasound and colonoscopy within 72 hours. BUS parameters—bowel wall thickness (BWT), vascularity (Limberg score), presence of complications (strictures, fistulas), and bowel wall stratification—were recorded and compared with colonoscopic findings and the Harvey-Bradshaw Index (HBI) or Mayo score. Data were analyzed using SPSS v26.0. Correlation and agreement were assessed using Pearson’s r and Cohen’s kappa (κ). Results: BUS detected increased BWT (>3 mm) in 83.3% of patients with active disease. A significant correlation was observed between BWT and disease activity scores (r = 0.74, p < 0.001). Limberg score ≥2 was observed in 71.2% of active CD cases. BUS showed 89.4% sensitivity and 84.1% specificity in detecting active disease compared to colonoscopy. For CD patients, BUS detected strictures in 21 cases and fistulas in 7 cases. The agreement between BUS and colonoscopy for disease activity was substantial (κ = 0.76). Conclusion: Bowel ultrasound is a reliable, non-invasive, and repeatable tool for assessing disease activity and complications in IBD patients. It demonstrates high concordance with colonoscopy, supporting its integration into routine IBD management, especially for monitoring and follow-up.

Keywords
INTRODUCTION

Inflammatory Bowel Disease (IBD), which includes Crohn’s disease (CD) and ulcerative colitis (UC), is a chronic, relapsing inflammatory condition of the gastrointestinal tract with a significant global burden [1]. The pathogenesis involves genetic susceptibility, environmental factors, immune dysregulation, and gut microbiota alterations [2]. Accurate and timely assessment of disease activity is vital for guiding treatment decisions and improving outcomes [3].

 

While colonoscopy is considered the gold standard for evaluating mucosal inflammation and disease extent, it is invasive, costly, and carries risks such as perforation and sedation-related complications [4]. Therefore, there is growing interest in non-invasive, point-of-care imaging tools like bowel ultrasound (BUS) that offer real-time assessment of intestinal inflammation [5].

 

Recent studies have shown that BUS can detect bowel wall thickening, hypervascularity, loss of wall stratification, and complications like strictures and fistulas, particularly in CD [6]. For UC, although confined to the mucosa, increased bowel wall thickness and hyperemia have also been visualized using ultrasound [7]. Moreover, BUS offers advantages such as repeatability, lack of ionizing radiation, and immediate results, making it ideal for disease monitoring.

 

Despite these benefits, BUS remains underutilized in clinical practice, partly due to variability in operator expertise and limited data comparing it with colonoscopy or clinical indices. There is a need for more real-world data to validate its diagnostic performance and clinical utility.

MATERIALS AND METHODS

A total of 120 adult patients (aged 18–65 years) with a confirmed diagnosis of IBD (either CD or UC) based on clinical, endoscopic, histological, and radiological criteria were included.

 

Inclusion Criteria:

  • Confirmed diagnosis of CD or UC
  • Willingness to undergo colonoscopy and BUS within 72 hours
  • Informed consent

 

Exclusion Criteria:

  • Previous bowel surgery
  • Pregnancy
  • Uncooperative patients
  • Incomplete colonoscopy due to poor bowel preparation

 

Ultrasound Examination:

All BUS examinations were performed by a single experienced radiologist using a high-frequency linear probe (7–12 MHz) in a fasting state. Parameters recorded included:

  • Bowel Wall Thickness (BWT): >3 mm considered abnormal
  • Limberg Score (vascularity grading via Doppler)
  • Bowel wall stratification (normal, blurred, or absent)
  • Detection of complications: strictures, fistulas, abscesses

 

Colonoscopy and Disease Activity Scores:
Colonoscopy was performed by a blinded endoscopist. Disease activity was scored using:

  • Harvey-Bradshaw Index (HBI) for CD
  • Mayo Score for UC

 

Statistical Analysis:

Data were analyzed using SPSS v26. Continuous variables were expressed as mean ± standard deviation (SD) and compared using t-tests or ANOVA. Categorical variables were compared using chi-square tests. Correlation was assessed using Pearson’s correlation coefficient (r), and agreement was measured using Cohen’s kappa (κ). A p-value <0.05 was considered statistically significant.

RESULTS

Demographic and Clinical Data:

Of 120 IBD patients, 68 had CD and 52 had UC. The mean age was 37.4 ± 11.6 years, with 56.7% males. Table 1 presents the baseline characteristics.

 

Bowel Wall Thickness and Disease Activity:

In CD patients, increased BWT (>3 mm) was found in 83.8% of those with moderate-to-severe disease (HBI >8). The mean BWT in active CD was 5.8 ± 1.4 mm vs. 2.9 ± 0.6 mm in remission (p < 0.001). For UC patients, mean BWT in active disease was 4.2 ± 0.9 mm compared to 2.5 ± 0.5 mm in remission (p = 0.003).

 

Vascularity and Wall Stratification:

A Limberg score ≥2 was seen in 71.2% of active CD patients. Loss of wall stratification correlated with higher disease activity (p < 0.01).

 

Correlation with Disease Activity Indices:

Strong positive correlation was observed between BWT and HBI for CD (r = 0.74, p < 0.001), and between BWT and Mayo score for UC (r = 0.61, p = 0.002).

 

Complications Detected by BUS:

BUS detected 21 strictures, 7 fistulas, and 3 abscesses in CD patients. All findings were later confirmed on colonoscopy or MRI. In UC, no transmural complications were identified.

 

Diagnostic Accuracy:

Compared with colonoscopy, BUS showed:

  • Sensitivity: 89.4%
  • Specificity: 84.1%
  • Positive Predictive Value: 91.8%
  • Negative Predictive Value: 80.0%
  • Kappa (κ) agreement: 0.76 (substantial agreement) (Table 1-5)

 

Table 1: Baseline Characteristics of Study Population

Variable

Value

Total patients

120

Crohn’s Disease (CD)

68

Ulcerative Colitis (UC)

52

Mean Age (years)

37.4 ± 11.6

Male (%)

56.7%

Female (%)

43.3%

 

Table 2: Bowel Wall Thickness (BWT) and Disease Activity

Group

Mean BWT (mm)

p-value

CD - Active

5.8 ± 1.4

< 0.001

CD - Remission

2.9 ± 0.6

< 0.001

UC - Active

4.2 ± 0.9

0.003

UC - Remission

2.5 ± 0.5

0.003

 

Table 3: Correlation of BUS Parameters with Disease Activity Scores

Parameter

Correlation Coefficient (r)

p-value

BWT vs HBI (CD)

0.74

< 0.001

BWT vs Mayo Score (UC)

0.61

0.002

 

Table 4: Complications Detected by BUS in CD Patients

Complication

Detected by BUS (n)

Confirmed by Colonoscopy/MRI (n)

Strictures

21

21

Fistulas

7

7

Abscesses

3

3

 

Table 5: Diagnostic Accuracy of BUS Compared to Colonoscopy

Metric

Value

Sensitivity

89.4%

Specificity

84.1%

Positive Predictive Value

91.8%

Negative Predictive Value

80.0%

Cohen’s Kappa (κ)

0.76

DISCUSSION

This study supports the growing body of evidence that bowel ultrasound is a valuable diagnostic and monitoring tool for IBD. The strong correlation between BWT and disease activity in both CD and UC aligns with findings from Calabrese et al., who reported similar diagnostic performance of BUS in monitoring mucosal inflammation [8].

 

In CD patients, ultrasound's ability to detect complications such as strictures and fistulas is particularly beneficial. According to Novak et al., BUS demonstrated 85–90% sensitivity for detecting strictures and 70–75% for fistulas [9], comparable to our findings.

 

For UC, although the disease is limited to the mucosa, increased BWT and hypervascularity were reliably detected in active disease, echoing the observations of Ripollés et al. [10]. The correlation between BUS parameters and clinical indices (HBI, Mayo score) further validates its utility.

 

However, the performance of BUS can be influenced by operator experience, patient body habitus, and bowel gas interference [11]. Despite these limitations, BUS remains a non-invasive, rapid, and radiation-free imaging modality.

Comparatively, while colonoscopy allows direct mucosal visualization and biopsy, its invasiveness limits frequent usage. The integration of BUS for routine follow-up can reduce the dependency on endoscopy and improve patient comfort.

 

Our study is limited by its single-center design and the operator dependency of ultrasound. Future multicentric studies with larger cohorts and standardized BUS protocols are warranted.

CONCLUSION

Bowel ultrasound is a reliable, non-invasive imaging tool for assessing disease activity and detecting complications in IBD. It shows high correlation and agreement with colonoscopy and clinical indices. Incorporating BUS into routine IBD care may enhance disease monitoring, reduce reliance on invasive procedures, and improve patient compliance.

REFERENCES
  1. Abraham C, Cho JH. Inflammatory bowel disease. N Engl J Med. 2009;361(21):2066–78. doi:10.1056/NEJMra0804647
  2. Khor B, Gardet A, Xavier RJ. Genetics and pathogenesis of inflammatory bowel disease. Nature. 2011;474(7351):307–17. doi:10.1038/nature10209
  3. Peyrin-Biroulet L, Sandborn W, Sands BE, et al. Selecting therapeutic targets in inflammatory bowel disease (STRIDE): determining therapeutic goals for treat-to-target. Am J Gastroenterol. 2015;110(9):1324–38. doi:10.1038/ajg.2015.233
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  6. Maaser C, Maconi G, Kucharzik T, et al. ECCO-ESGAR guideline for diagnostic assessment in IBD part 1: initial diagnosis, monitoring of known IBD, detection of complications. J Crohns Colitis. 2019;13(2):144–64. doi:10.1093/ecco-jcc/jjy113
  7. Novak KL, Wilson SR. The role of ultrasound in evaluating disease activity in ulcerative colitis. Curr Opin Gastroenterol. 2011;27(4):320–5. doi:10.1097/MOG.0b013e328348474c
  8. Calabrese E, Zorzi F, Pallone F. Transabdominal bowel ultrasound in Crohn's disease: an underused resource. Dig Liver Dis. 2010;42(11):791–8. doi: 10.1016/j.dld.2010.03.019
  9. Novak KL, Kaplan GG, Panaccione R, et al. Ultrasound for evaluation of Crohn's disease: comparative accuracy with MR enterography and endoscopy. Clin Gastroenterol Hepatol. 2013;11(8):894–902. doi: 10.1016/j.cgh.2013.01.030
  10. Ripollés T, Martínez-Pérez MJ, Paredes JM, et al. Crohn's disease: correlation of findings at contrast-enhanced US with severity at endoscopy. Radiology. 2009;253(1):241–8. doi:10.1148/radiol.2531081984
  11. Maconi G, Nylund K, Ripolles T, et al. EFSUMB recommendations and clinical guidelines for intestinal ultrasound (GIUS) in inflammatory bowel diseases. Ultraschall Med. 2018;39(3):304–17. doi:10.1055/s-0043-124667
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