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AI-guided bowel preparation reduces laxative volume from 1586.2 mL to 1245.5 mL in colonoscopy patientsAI guidance helps patients drink less liquid before colonoscopy

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Key Takeaway
Consider AI-guided bowel preparation to potentially reduce laxative volume while maintaining adequate cleansing scores.

This randomized controlled trial enrolled 513 patients undergoing colonoscopy for bowel cleansing using sodium phosphate solution. Patients were assigned to either an AI-guided preparation group (n=255) or a standard practice control group (n=258). The primary outcomes were the volume of laxatives used and the rate of adequate bowel cleansing based on the Boston Bowel Preparation Scale (BBPS).

The AI-guided group consumed significantly less bowel-cleansing solution, with 1245.5 (SD 377.2) mL compared to 1586.2 (SD 50.4) mL in the control group (P<.001). The rate of adequate preparation was noninferior in the AI group (93.3% vs 88.8%; 1-sided P<.001). Additionally, medication adherence was higher in the AI-guided group (96.9% vs 91.5%, P=.009).

Safety data indicated a lower incidence of adverse reactions in the AI-guided group (2%) compared to the control group (5.8%, P=.02). Secondary outcomes, including segmental BBPS scores, adenoma detection rate, polyp detection rate, and advanced ADR, showed no significant differences between groups. While the study suggests AI can reduce unnecessary laxative volume while maintaining cleansing quality, specific limitations were not reported.

Preparing for a colonoscopy often involves drinking large amounts of laxative solution. This process can be uncomfortable and difficult to manage, but a new study suggests technology might make it easier on patients. Researchers tested an AI-guided system that used a computer model to help determine exactly how much liquid was needed to clean the bowel effectively.

The trial included over 500 patients. Those guided by the AI were able to drink significantly less of the cleansing solution compared to those following standard practices. Despite drinking less, the AI group achieved similar cleaning quality scores and had higher rates of staying on track with their medication.

Safety was also a factor in the findings. The group using the AI-guided method reported fewer adverse reactions than the group using standard methods. While the AI did not change how many polyps were found during the procedure, it did make the preparation process more efficient and potentially easier for patients to complete.

What this means for you:
AI guidance can reduce the amount of laxative liquid patients drink before a colonoscopy without lowering cleaning quality.

Common questions

Does using AI to guide my prep make it safer?

The study found that the group using AI guidance had a lower rate of adverse reactions, with only 2% of patients experiencing issues compared to 5.8% in the standard practice group.

Will I still get a high-quality cleaning if I drink less liquid?

Yes. The study showed that the rate of adequate bowel preparation was not inferior in the AI-guided group, meaning it achieved similar cleansing quality to standard practices.

Does the AI change how many polyps are found during the procedure?

No, the study did not find any significant differences in polyp detection rates or advanced adenoma detection rates between the AI-guided group and the standard practice group.

Study Details

Study typeRct
Sample sizen = 255
EvidenceLevel 2
PublishedJul 2026
View Original Abstract ↓
BACKGROUND: Sufficient bowel preparation is critical for increasing the quality of colonoscopy. However, current bowel preparation guidelines have limitations. We used a constructed and validated convolutional neural network model to assist patients in assessing the adequacy of bowel preparation and guide the use of laxatives based on individual variations. OBJECTIVE: This research intended to explore the influence of AI-guided bowel preparation on patients' use of laxatives and bowel cleansing quality. METHODS: We conducted a prospective randomized controlled trial that included patients who had a colonoscopy at the First Affiliated Hospital of Zhengzhou University and used sodium phosphate solution for bowel cleansing. Included individuals were randomly categorized into 2 groups: the AI-guided group, which used an AI program to assess the adequacy of bowel cleansing and stopped the use of laxatives once the assessment was passed, and the control group, which evaluated bowel preparation adequacy based on standard practices and used the recommended doses of laxatives. The primary outcomes were the amount of laxatives used and the rate of adequate bowel cleansing based on the Boston Bowel Preparation Scale (BBPS). Other outcomes included overall BBPS scores, BBPS scores by colon region, adenoma detection rate (ADR), polyp detection rate, and advanced ADR, as well as adverse reactions and compliance. RESULTS: This study included 513 patients (AI-guided group: n=255, 49.7%; control group: n=258, 50.3%). The volume of bowel-cleansing solution consumed by patients in the AI-guided group was 1245.5 (SD 377.2) mL, significantly lower than the 1586.2 (SD 50.4) mL in the control group (P<.001). Reduced use of laxatives was independently predicted by younger age, lower BMI, and higher defecation frequency. The rate of adequate bowel preparation in the AI group was not inferior to that in the control group (238/255, 93.3% vs 229/258, 88.8%, respectively; 1-sided P<.001 for noninferiority). No significant differences were observed in segmental or total BBPS scores, ADR, polyp detection rate, and advanced ADR between the 2 groups. Additionally, the medication adherence rate in the AI-guided group was significantly higher than in the control group (247/255, 96.9% vs 236/258, 91.5%, respectively; P=.009), whereas the incidence of adverse reactions was notably lower (5/255, 2% vs 15/258, 5.8%, respectively; P=.02). CONCLUSIONS: Using the AI-driven bowel preparation program to assist patients in personalized bowel preparation can reduce unnecessary use of laxatives while achieving results comparable to those of standard practices. TRIAL REGISTRATION: ClinicalTrials.gov NCT06610630; https://clinicaltrials.gov/study/NCT06610630.
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