Corresponding author.
Contributed equally.
This study aimed to investigate whether a real-time artificial intelligence (AI)-assisted polyp detection system can improve adenoma detection rates (ADRs) in real-world colonoscopy practice.
This single-center, retrospective, propensity score-matched study collected data from consecutive patients who underwent colonoscopy—either AI-assisted or standard colonoscopy— between March 2023 and February 2024. Propensity score matching was conducted to adjust for baseline characteristics across the groups.
During the study period, 1,085 patients who underwent colonoscopy were eligible for inclusion. After propensity score matching, 474 patients who underwent AI-assisted colonoscopy and 474 who underwent standard colonoscopy were included in the primary analysis. The ADR was significantly higher in the AI-assisted colonoscopy group than in the standard colonoscopy group (35.9% vs. 26.4%;
AI-assisted colonoscopy significantly improves ADRs in real-world colonoscopy practice.
Received 2025 Feb 19; Accepted 2025 May 20; Collection date 2025.
Colorectal cancer (CRC) ranks as the third most common cancer and is the second leading cause of cancer-related mortality worldwide [
Recent advances in artificial intelligence (AI) have led to the introduction of computer-aided detection (CADe) in colonoscopy practice to enhance quality and address operator-dependent limitations. Multiple randomized controlled trials (RCTs) have demonstrated that AI-assisted colonoscopy significantly increases ADRs compared with standard colonoscopy [
This single-center, retrospective, propensity score-matched study was conducted at Hallym University Dongtan Sacred Heart Hospital. The study protocol was approved by the Institutional Review Board of Hallym University Dongtan Sacred Heart Hospital (approval no. HDT 2023-04-001) and adhered to the ethical guidelines of the Declaration of Helsinki.
All patients who underwent colonoscopy for routine indications between March 2023 and February 2024 were included. Indications for colonoscopy included CRC screening, post-polypectomy surveillance, and diagnostic colonoscopy for symptomatic patients. Exclusion criteria included colonoscopy for resection of known colorectal polyps, poor bowel preparation (Boston Bowel Preparation Scale [BBPS] total score < 6 or any segment < 2; the BBPS is a validated scoring system developed at Boston University School of Medicine to assess bowel cleanliness during colonoscopy [
Of the four active endoscopy units, two were equipped with AI-assisted endoscopy systems. Patients were randomly assigned to each endoscopy unit by the nurse in charge according to the routine workflow of the endoscopy department. Therefore, patients assigned to AI-assisted endoscopy units underwent colonoscopy with a real-time AI-based polyp detection system, while those assigned to conventional endoscopy units underwent standard colonoscopy. Four experienced endoscopists (each having performed at least 3000 colonoscopies) and five endoscopy trainees (first-year gastroenterology fellows) performed the colonoscopies. All participants were aware that their colonoscopy performance was being monitored for the study.
All colonoscopies were performed using a video endoscopy system and a high-definition endoscope (Fujifilm ELUXEO 7000 system and 600 series colonoscopes; FUJIFILM, Tokyo, Japan) with standard white-light imaging. Chromoendoscopy and image-enhanced endoscopy were not used in standard inspection for polyp detection but were occasionally used for lesion characterization after polyp detection at the discretion of each endoscopist. Distal attachments, such as transparent caps, were used according to the endoscopist’s preference. All patients who underwent colonoscopy received standard bowel preparation with polyethylene glycol-based or oral sulfate-based preparation regimens. Most patients received standard sedation during endoscopy using available sedative agents (e.g., midazolam and/or propofol); however, some patients opted not to be sedated based on personal preferences or underlying medical conditions. All detected polyps were removed endoscopically unless invasive cancer was suspected, in which case they were histologically evaluated.
Data from all consecutive patients who underwent colonoscopy between March 2023 and February 2024 were collected retrospectively: age, sex, body mass index (BMI), indications for colonoscopy, grade of bowel preparation, inspection time, and characteristics of detected polyps (location, size, morphology, and histologic findings) were recorded on a standardized data collection sheet. Bowel preparation was assessed using the BBPS [
The SmartEndo system (INFINITT Healthcare, Seoul, Korea) was used for the study. SmartEndo is a real-time, computer-aided polyp detection system based on a deep-learning algorithm that can be integrated with any endoscopic system. The system automatically detects colorectal polyps during colonoscopy and displays a green box on the screen for identified lesions, accompanied by alarm sounds. The details of the proposed network for automatic polyp detection are shown in Fig.
Illustration of proposed SmartEndo-Net architecture for colorectal polyp detection. It consists of a top-down pathway with ResNet-50 and a Feature pyramid network (FPN) with lateral connections from the backbone. For each scale, two subnets are utilized to classify and regress the predicted bounding box. As a result, when the predicted probability of the bounding box exceeds the threshold value of 0.5, both a green bounding box and an alarm sound are activated
The primary outcome was the ADR, defined as the percentage of colonoscopies with at least one adenoma among all colonoscopies. Secondary outcomes included lesion detection rates (for advanced adenomas, sessile serrated lesions [SSLs], polyps, and non-neoplastic lesions) and the number of lesions per colonoscopy (including adenomas, advanced adenomas, SSLs, polyps, and non-neoplastic lesions). The detection rates and number of lesions were calculated by the endoscopists. The characteristics of detected polyps in each group were presented through a per-polyp analysis. Advanced adenomas were defined as the presence of any of the following: any adenomas ≥ 10 mm, high-grade dysplasia (or intramucosal carcinoma), and adenomas with a villous component. Non-neoplastic lesions were defined as polyps that are neither adenomas nor SSLs. The predictors of ADR were analyzed using regression analysis.
Propensity score matching analysis was performed using the nearest neighbor method based on age, sex, BMI, indications for colonoscopy, bowel preparation scale, and inspection time. Continuous variables were presented as means ± standard deviations (SD) and compared using the t-test. Categorical variables were presented as numbers (%) and compared using the chi-square test (or Fisher’s exact test, if appropriate). Multivariate logistic regression analysis was performed to identify predictive factors for adenoma detection, with results presented as odds ratios (ORs) and 95% confidence intervals (CIs). A
A total of 1,992 patients underwent colonoscopy between March 2023 and February 2024. Among these, 820 underwent AI-assisted colonoscopy, while 1,172 underwent standard colonoscopy. After excluding 907 patients based on predefined exclusion criteria, 1,085 patients remained eligible. Propensity score matching was conducted based on age, sex, BMI, indications for colonoscopy, bowel preparation scale score, and inspection time. Consequently, 948 patients (474 in each group) were included in the final analysis. The study flowchart is shown in Fig.
Study flowchart
AI, artificial intelligence; CRC, colorectal cancer; BMI, body mass index
Table
Baseline characteristics of the patients
| Original cohort | Matched cohort | |||||
|---|---|---|---|---|---|---|
AI group ( | SC group ( | AI group ( | SC group ( | |||
| Age | 55.4 ± 12.9 | 55.4 ± 13.5 | 0.977 | 55.4 ± 12.9 | 54.9 ± 13.1 | 0.543 |
| Female sex | 222 (46.8) | 283 (46.3) | 0.914 | 222 (46.8) | 231 (48.7) | 0.603 |
| BMI (kg/m2) | 24.01 ± 3.65 | 24.08 ± 3.64 | 0.744 | 24.01 ± 3.65 | 24.07 ± 3.70 | 0.807 |
| Indication | < 0.001 | < 0.001 | ||||
Screening Surveillance Symptomatic | 48 (10.1) 317 (66.9) 109 (23.0) | 95 (15.5) 335 (54.8) 181 (29.6) | 48 (10.1) 317 (66.9) 109 (23.0) | 46 ( 9.7) 316 (66.7) 112 (23.6) | ||
| BBPS | 8.61 ± 0.75 | 8.75 ± 0.63 | 0.001 | 8.61 ± 0.75 | 8.70 ± 0.69 | 0.059 |
| Inspection time (s) | 452.8 ± 162.2 | 440.3 ± 173.2 | 0.222 | 452.8 ± 162.2 | 445.5 ± 176.6 | 0.505 |
Values are presented as mean ± standard deviation or numbers (%)
BMI, body mass index; BBPS, Boston Bowel Preparation Scale; AI, AI-assisted colonoscopy; SC, standard colonoscopy
Table
Lesion detection outcomes according to colonoscopy groups
| AI group | SC group | |||
|---|---|---|---|---|
| Lesion detection rates (%) | ||||
| Adenomas | 35.9 | 26.4 | 0.002 | |
| Advanced adenomas* | 3.2 | 2.1 | 0.418 | |
| Sessile serrated lesions | 5.5 | 3.0 | 0.076 | |
| Any polyps | 53.2 | 46.2 | 0.038 | |
| Non-neoplastic lesions† | 17.3 | 18.4 | 0.734 | |
| Number of lesions per colonoscopy (mean ± SD) | ||||
| Adenomas | 0.69 ± 1.22 | 0.43 ± 0.91 | < 0.001 | |
| Advanced adenomas | 0.04 ± 0.21 | 0.02 ± 0.16 | 0.298 | |
| Sessile serrated lesions | 0.07 ± 0.32 | 0.05 ± 0.33 | 0.276 | |
| Any polyps | 1.23 ± 1.65 | 0.93 ± 1.39 | 0.002 | |
| Non-neoplastic lesions | 0.22 ± 0.56 | 0.23 ± 0.54 | 0.858 | |
SD, standard deviation; AI, AI-assisted colonoscopy; SC, standard colonoscopy
*Advanced adenomas were defined as adenomas ≥ 10 mm, and/or with villous histology, and/or with high-grade dysplasia
†Non-neoplastic lesions were defined as lesions other than adenomas or sessile serrated lesions
A total of 1,175 polyps were detected in the full cohort (
Characteristics of the detected lesions
| AI group | SC group | |||
|---|---|---|---|---|
| Location | 0.151 | |||
| Proximal* | 353 (60.5) | 333 (56.2) | ||
| Distal† | 230 (39.5) | 259 (43.8) | ||
| Size | 0.239 | |||
| ≤ 5 mm | 390 (66.9) | 422 (71.3) | ||
| 6–9 mm | 166 (28.5) | 149 (25.2) | ||
| ≥ 10 mm | 27 ( 4.6) | 21 ( 3.5) | ||
| Morphology | 0.062 | |||
| Flat | 205 (35.2) | 177 (29.9) | ||
| Protruded | 378 (64.8) | 415 (70.1) | ||
| Histologic findings | 0.059 | |||
| Adenoma with LGD | 326 (55.9) | 298 (50.3) | ||
| Adenoma with HGD or villous adenoma | 3 ( 0.5) | 12 ( 2.0) | ||
| Invasive carcinoma | 0 ( 0.0) | 0 ( 0.0) | ||
| SSL without dysplasia | 24 ( 4.1) | 21 ( 3.5) | ||
| SSL with dysplasia | 10 ( 1.7) | 8 ( 1.4) | ||
| Hyperplastic polyp | 106 (18.2) | 132 (22.3) | ||
| Traditional serrated adenoma | 0 ( 0.0) | 2 ( 0.3) | ||
| Others‡ | 114 (19.6) | 119 (20.1) | ||
Values are presented with numbers (%)
AI, AI-assisted colonoscopy; SC, standard colonoscopy; LGD, low-grade dysplasia; HGD, high-grade dysplasia; SSL, sessile serrated lesion
* Proximal colon was defined as the segment extending from the cecum to the splenic flexure
†Distal colon was defined as the segment extending from the descending colon to the rectum
‡Others included inflammatory polyps, lymphoid aggregates, and nonspecific findings
The ADRs of the four experienced endoscopists were 19.0%, 40.7%, 21.4%, and 45.7%, respectively. Based on their ADRs, endoscopists were categorized as high detectors if their ADR was ≥ 25% and low detectors if it was < 25%. Additionally, five endoscopy trainees performed 114 colonoscopies (33 AI-assisted and 81 standard), achieving an overall ADR of 34.2%.
Table
Lesion detection rates categorized by endoscopists
| Lesion detection rates of endoscopy trainees (%) | ||||
|---|---|---|---|---|
| Adenomas | AAs* | SSLs | Any polyps | |
| AI group ( | 51.5 | 0 | 6.1 | 72.7 |
| SC group ( | 27.2 | 3.7 | 2.5 | 50.6 |
| 0.023 | 0.555 | 0.578 | 0.051 | |
| Lesion detection rates of high-detectors† (%) | ||||
| Adenomas | AAs | SSLs | Any polyps | |
| AI group ( | 45.8 | 4.4 | 8.0 | 64.9 |
| SC group ( | 39.2 | 3.3 | 3.3 | 61.3 |
| 0.162 | 0.713 | 0.043 | 0.451 | |
| Lesion detection rates of low-detectors‡ (%) | ||||
| Adenomas | AAs | SSLs | Any polyps | |
| AI group ( | 20.0 | 2.1 | 2.1 | 34.2 |
| SC group ( | 19.3 | 1.4 | 3.4 | 32.8 |
| 0.945 | 0.718 | 0.563 | 0.817 | |
AI, AI-assisted colonoscopy; SC, standard colonoscopy; AA, advanced adenoma; SSL, sessile serrated lesion
*Advanced adenomas were defined as adenomas ≥ 10 mm, and/or with villous histology, and/or with high-grade dysplasia
†High-detector was defined as an endoscopist with an adenoma detection rate of ≥ 25%
‡Low-detector was defined as an endoscopist with an adenoma detection rate of < 25%
A logistic regression analysis was performed to identify factors associated with adenoma detection (Table
Predicting factors associated with adenoma detection
| Univariate analysis | Multivariate analysis | |||
|---|---|---|---|---|
| OR (95% CI) | OR (95% CI) | |||
| Age | 1.044 (1.033–1.056) | < 0.001 | 1.043 (1.031–1.056) | < 0.001 |
| Sex | ||||
| Male | 1.000 | 1.000 | ||
| Female | 0.540 (0.415–0.703) | < 0.001 | 0.584 (0.436–0.782) | < 0.001 |
| BMI | 1.051 (1.015–1.089) | 0.005 | 1.021 (0.982–1.063) | 0.294 |
| Indication | ||||
| Screening | 1.000 | 1.000 | ||
Surveillance Symptomatic | 0.802 (0.555–1.161) 0.282 (0.179–0.445) | 0.243 < 0.001 | 0.616 (0.414–0.918) 0.303 (0.186–0.492) | 0.017 < 0.001 |
| Bowel preparation (BBPS) | 0.894 (0.747–1.072) | 0.226 | 1.010 (0.828–1.231) | 0.923 |
| Inspection time | < 0.001 | |||
| < 6 min | 1.000 | 1.000 | ||
| ≥ 6 min | 6.602 (4.389–9.931) | < 0.001 | 5.689 (3.460–9.353) | |
| Colonoscopy | ||||
| Standard | 1.000 | 1.000 | ||
| AI-assisted | 1.427 (1.103–1.847) | 0.007 | 1.448 (1.090–1.924) | 0.011 |
OR, odds ratio; CI, confidence interval; BMI, body mass index; BBPS, Boston Bowel Preparation Scale
This study aimed to evaluate the effectiveness of AI-assisted colonoscopy in a real-world setting. AI-assisted colonoscopy resulted in significantly higher ADRs and APCs compared to standard colonoscopy (ADR, 35.9% vs. 26.4%; APC, 0.69 vs. 0.43). However, the detection rates of advanced adenomas and SSLs did not significantly differ between the two groups.
Multiple RCTs have evaluated the effectiveness of AI-assisted colonoscopy, and a recent meta-analysis of 21 RCTs confirmed that AI-assisted colonoscopy increases the ADR [
In contrast, other studies have reported that AI-assisted colonoscopy does not significantly improve ADR in real-world settings [
Although CADe is a valuable tool in colonoscopy, the role of endoscopists remains crucial, as polyp detection depends on their ability to ensure adequate mucosal exposure and identify abnormalities [
A limitation of AI-assisted colonoscopy is its inability to detect lesions in areas that are not fully exposed. Various mucosal exposure devices, such as transparent caps and Endocuff Vision, have been extensively studied for their efficacy. The Endocuff, a device designed to flatten colon folds and improve mucosal visibility, has demonstrated efficacy in several RCTs, significantly improving ADR compared to standard colonoscopy [
This study’s non-randomized observational design enhances the applicability of its findings to real-world clinical practice. Additionally, propensity score matching reduced group bias, improving the reliability of our findings. Baseline characteristics such as age, sex, and BMI showed no significant differences, and these were further minimized in the matched cohort, indicating an effective bias control. Using a concurrent control group was another strength of this study. While historical controls are susceptible to various biases, concurrent control groups minimize differences caused by time-related changes and external factors, thereby providing greater validity.
This study had some limitations. First, it was conducted at a single center, limiting the generalizability of the results and emphasizing the need for multicenter studies to improve external validity. In addition, since this was a non-blinded study, there is a possibility of selection bias in patient allocation. However, we minimized this potential bias by applying propensity score matching to adjust for baseline characteristics between the two groups. Second, the relatively small number of endoscopists, with two of the four endoscopists having an ADR < 25%, may have influenced the findings. Including endoscopists with low baseline ADRs may have contributed to the overall increase in the ADR observed in this study. Future studies adjusting for endoscopists’ baseline ADRs will provide a clearer assessment of the true impact of AI. Third, the endoscopists’ awareness of AI usage may have prompted more careful evaluations, potentially influencing the results. Implementing a blinded design may yield more relevant findings in future studies. Furthermore, the study excluded patients with complicated colonic conditions, such as inflammatory bowel disease or polyposis syndrome, limiting the applicability of the findings to these populations. Therefore, future studies should include a broader range of patients. Moreover, the study did not establish a connection between improved ADRs and long-term patient benefits, such as reduced CRC incidence, highlighting the need for further research to evaluate these long-term outcomes. Finally, we did not perform a separate analysis of detection rates for laterally spreading tumors (LST), particularly the non-granular (LST-NG) subtype. These lesions are known to be easily missed and more difficult to achieve complete resection, making them clinically significant [
In conclusion, AI-assisted colonoscopy significantly improved ADR in real-world settings, demonstrating its potential to enhance screening quality and facilitate early polyp detection. The synergy between CADe and the endoscopist’s careful observation offers promising advancements in CRC prevention.
Not applicable.
Adenoma Detection Rate
Artificial Intelligence
Adenomas per Colonoscopy
Boston Bowel Preparation Scale
Body Mass Index
Computer-Aided Detection
Confidence Interval
Colorectal Cancer
Feature Pyramid Network
High-Grade Dysplasia
Low-Grade Dysplasia
Laterally Spreading Tumors
Odds Ratio
Polyp Detection Rate
Randomized Controlled Trial
Standard Colonoscopy
Standard Deviation
Sessile Serrated Lesion
Sessile Serrated Lesion Detection Rate
Da Yeon Ham and Jae Gon Lee: data curation, formal analysis, and original draft writing; Chung Il Ahn and Sea Hyub Kae: methodology and validation; Hyun Joo Jang: conceptualization, methodology, review writing and editing; all authors approved the final manuscript.
This work was supported by Medical Artificial Intelligence Clinic Program through the National Information Technology Industry Promotion Agency (NIPA), funded by the Korea government (MSIT) (No. ITAS1313220110010001000200200). The funding source had no role in the design and conduct of the study; in the collection, analysis, and interpretation of the data; or in the preparation, review, or approval of the manuscript.
The data support the findings of this study and are available within the article.
The study protocol was approved by the Institutional Review Board (IRB) of Hallym University Dongtan Sacred Heart Hospital (approval no. HDT 2023-04-001). Due to the retrospective nature of this study, which analyzes data obtained from completed medical procedures, and the strict confidentiality measures outlined in the study protocol to protect participants’ personal information, the IRB judged that the possibility of violating participants’ rights was minimal. Accordingly, the need for consent to participate was also waived by the ethics committee that approved this study. This study adhered to the ethical guidelines of the Declaration of Helsinki.
Not applicable.
The authors declare no competing interests.
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Da Yeon Ham and Jae Gon Lee contributed equally to this work.
The data support the findings of this study and are available within the article.