ABSTRACT
The US Multi-Society Task Force on Colorectal Cancer updated the 2014 consensus recommendations on colonoscopy preparation in 2025. For patients at low risk of inadequate preparation, key updates include simplifying dietary restrictions and using 2-L over 4-L regimens for improved tolerability while maintaining efficacy. Split-dose administration of bowel preparation is universally recommended. The guidelines emphasize same-day dosing as acceptable only for afternoon procedures, recommend oral simethicone as an adjunct for improved visualization, and establish preparation adequacy tracking as a quality metric.
Two-liter regimens are preferred over 4-L regimens as they improve patient tolerability while maintaining equivalent bowel cleansing efficacy (low risk for poor preparation).
Dietary restrictions can be limited to 1 day before colonoscopy using low-residue or low-fiber foods; clear-liquid–only diets are unnecessary for most outpatients at low risk for inadequate preparation.
Split-dose administration is recommended for all regimens; same-day dosing is acceptable only for afternoon procedures, with the second dose completed at least 2 hours before the procedure.
A preparation adequacy rate of 90% or greater is now recommended for both endoscopists and endoscopy units.
Colorectal cancer remains the second leading cause of cancer death in the United States.1 Colonoscopy is considered the gold standard for detecting and removing precancerous lesions, but its effectiveness depends critically on adequate bowel preparation.2 Inadequate preparation leads to missed lesions, incomplete examinations, and the need for earlier repeat procedures. This article highlights the key changes and recommendations from the 2025 US Multi-Society Task Force on Colorectal Cancer consensus recommendations3 on optimizing bowel preparation for colonoscopy.
WHO WROTE THE GUIDELINES?
The US Multi-Society Task Force on Colorectal Cancer updated the 2014 consensus recommendations4 and published their work in 2025.3 The Task Force represents each of the 3 gastroenterological societies: the American College of Gastroenterology, American Gastroenterological Association, and American Society for Gastrointestinal Endoscopy. The 2025 consensus provides updated evidence-based recommendations for outpatients undergoing colonoscopies at low risk for inadequate bowel preparation.3 A literature review was led by the primary author, who developed statements with evidence tables to be reviewed by the entire committee. The strength of the statement was assessed based on the quality of evidence.
WHAT ARE THE MAIN RECOMMENDATIONS?
Patient education and navigation
Dietary modifications
Limit dietary restrictions to the day before the colonoscopy only.
Use low-residue or low-fiber foods or full liquids for early and midday meals when using split-dose regimens (examples are provided in the consensus). This recommendation is based on randomized trials, meta-analyses, and prospective dietary studies.7,8 There was no benefit in bowel preparation adequacy with longer and more restrictive diets, and patients found the 1-day diet restriction easier to tolerate and adhere to.7,8 However, if a patient is at risk for inadequate preparation (eg, inpatient, constipation, history of inadequate preparation, cirrhosis, certain medications, diabetes), these recommendations do not apply. Table 1 details which foods are low residue and which should be avoided.3
Low- and high-residue diets for colonoscopy preparation
Purgative selection
No single bowel preparation agent is recommended.
Two-liter regimens are suggested over 4-L preparations. In a recent meta-analysis of 17 studies (N = 7,528 patients),9 low-volume bowel preparations demonstrated similar efficacy to high-volume preparations in terms of achieving an adequate bowel cleanse (86.1% vs 87.4%, relative risk 1.00, 95% confidence interval 0.98–1.02, with low heterogeneity: I2 = 17%). However, a smaller volume preparation was significantly superior in terms of compliance or completion (relative risk 1.06, 95% confidence interval 1.02–1.10), tolerability (relative risk 1.39, 95% confidence interval 1.12–1.74), and willingness to repeat bowel preparation (relative risk 1.41, 95% confidence interval 1.20–1.66).
Selection of a bowel preparation should consider patient comorbidities, previous preparation adequacy, cost, allergies, and other individual factors. Hyperosmolar preparations should be avoided in patients at risk of clinical consequences from fluid shifts (eg, renal insufficiency, congestive heart failure). These include sodium picosulfate plus magnesium oxide (CLENPIQ) and magnesium citrate.
Details on different types of preparations are given in Table 2.3
Commonly used bowel preparation regimens
Dosing strategy
Split-dose administration is recommended for all patients regardless of whether a high- or low-volume preparation is being used. This involves drinking half of the preparation the evening before the procedure to clear out solid stool and drinking the second half the morning of the procedure (4–6 hours before) to clear chyme that entered the colon overnight. A split-dose preparation is associated with an increased adenoma detection rate.10 Some barriers to adherence include procedures scheduled before 10 AM and travel time of over 1 hour.
Same-day dosing is an acceptable alternative to split-dose administration for patients with an afternoon colonoscopy (not morning).11
Adjunctive agents
Oral simethicone (≥ 320 mg) is suggested to improve visualization. A meta-analysis of 38 randomized controlled trials showed that oral simethicone significantly increased the rate of adequate bowel preparation (relative risk 1.13, P < .0001), reduced foam and bubbles (relative risk 1.28, P < .00001), and improved patient acceptability (relative risk 1.15, P = .01). The benefit was most pronounced when doses greater than or equal to 320 mg were used. Notably, while simethicone improved visualization quality, it did not significantly impact overall adenoma detection rates in the general analysis.12
Inadequate preparation management
Modify bowel preparation instructions for patients with a history of inadequate preparation or at risk for it as follows: split-dose 4 L polyethylene glycol (PEG) and electrolyte lavage solution, bisacodyl 15 mg the afternoon before the colonoscopy, and a more restrictive diet (low-residue diet days 3 and 2 before colonoscopy and clear liquids day 1 before; Figure 13).13 In a randomized trial of 256 patients with previous inadequate cleansing, all participants received a 3-day low-residue diet and bisacodyl 10 mg the day before colonoscopy, combined with either split-dose 4 L PEG or split-dose 2 L PEG plus ascorbic acid. The 4-L PEG regimen achieved significantly higher adequate preparation rates than the 2-L regimen (81.1% vs 67.4%, odds ratio 2.07, 95% confidence interval 1.16–3.69).4,13
Repeat colonoscopy within 12 months.14
WHAT IS DIFFERENT FROM PREVIOUS GUIDELINES?
Simplified dietary approach
A simplified dietary approach was recommended in 2014, but it was a weak recommendation. Since that time, more studies have been published and now it is a strong recommendation to limit restrictions to a single day before colonoscopy, allowing low-residue solid foods for most meals. This change reflects robust evidence that prolonged dietary restrictions provide no meaningful benefit while significantly increasing patient burden and reducing compliance.
Volume preference shift
The 2014 recommendations said that either 2-L or 4-L volumes could be used. The 2025 recommendations now explicitly prefer 2-L over 4-L regimens, representing a significant departure from traditional high-volume approaches. This preference acknowledges that equivalent preparation quality can be achieved with lower volumes while substantially improving patient tolerance and willingness to repeat procedures. However, comorbid conditions, medications, and cost must be taken into consideration.
Simethicone integration
The 2014 consensus did not recommend oral simethicone, but the 2025 consensus does recommend at least 320 mg of oral simethicone. The shift in recommendation reflects accumulating evidence for improved visualization and adenoma detection. However, this is still a weak recommendation.
DO OTHER SOCIETIES AGREE OR DISAGREE?
The European Society of Gastrointestinal Endoscopy guideline15 generally aligns with US Multi-Society Task Force recommendations3 on split dosing and dietary simplification.
International consensus on the fundamentals—split dosing, minimizing dietary burden, and individualized preparation—is strong, though implementation details and quality monitoring standards differ across healthcare systems.
HOW WILL THIS CHANGE DAILY PRACTICE?
The 2025 US Multi-Society Task Force recommendations are poised to reshape how endoscopy practices approach bowel preparation, with implications far beyond simple protocol adjustments. The shift toward patient-centered regimens—particularly the allowance of solid low-residue foods the day before—will enhance patient experience by reducing hunger, nausea, and anxiety, thereby improving willingness to undergo repeat procedures. At the same time, dietary simplification requires comprehensive revision of patient education materials and staff training. Many practices have long relied on complex, multi-day restriction sheets; transitioning to streamlined low-residue instructions will require retraining of nursing staff and confidence-building among clinicians accustomed to clear-liquid protocols.
Operationally, several changes present significant challenges. Universal adoption of split-dose regimens means offices must deliver clear guidance on morning dosing, even if this requires patients to wake at 3 AM to 4 AM for early morning procedures. This practical hurdle underscores the need for enhanced patient education and may prompt some centers to reconsider scheduling patterns. Likewise, the Task Force’s preference for 2-L preparations is likely to accelerate adoption of lower-volume regimens, improving tolerability but necessitating adjustments in procurement, prescribing habits, and insurance coverage.
Perhaps the most transformative change is the mandate to track preparation adequacy at both the unit and individual endoscopist level, with a benchmark of 90%. Most practices currently lack systems for such granular monitoring, so implementation will require new data collection processes, regular reporting, and targeted quality improvement initiatives. The strong endorsement of patient navigation—via apps, automated reminders, or dedicated staff—offers a proven strategy to raise adequacy rates, yet requires meaningful investment of time and resources. For smaller practices, collaboration or shared technology solutions may be necessary to meet these expectations cost-effectively.
An important practical consideration in open-access systems is clarifying responsibility for bowel preparation instructions. In many healthcare systems, primary care clinicians order colonoscopies while endoscopy units provide preparation instructions. Some gastroenterology practices and institutions allow for a low-residue diet, while others do not. To avoid confusing patients, it is important to clarify the instructions patients will receive, including instructions provided on the institution’s or practice’s website and through a patient portal or mail.
WHEN WOULD THE GUIDELINES NOT APPLY?
The US Multi-Society Task Force acknowledges important limitations in applying these recommendations, particularly for complex patient populations, patients at risk for an inadequate preparation, and challenging clinical scenarios. Risk factors for inadequate bowel preparation quality include cirrhosis, Parkinson disease, tricyclic antidepressant use, diabetes, opiate use, gastroparesis, previous colorectal surgery, constipation, tobacco use, and age over 65; while not true of all risk factors, many impact intestinal motility.16,17 Understanding these exceptions is crucial for safe and effective implementation.
Hospitalized patients represent a significant population where standard outpatient protocols may not apply. Inpatients often have multiple comorbidities, delayed procedure scheduling, medication interactions, and limited mobility that complicate preparation regimens. The timing requirements for split dosing become particularly challenging when procedures are scheduled urgently or when patients cannot reliably self-administer preparations. These patients may require individualized approaches with nursing supervision and modified timing protocols.
Patients with severe renal insufficiency or heart failure cannot safely use hyperosmotic preparations.18 Similarly, patients with significant gastrointestinal disorders such as severe gastroparesis, inflammatory bowel disease with strictures, or previous extensive colorectal surgery may need specialized approaches based on their altered anatomy and physiology.
Neurologically impaired patients, including those with dementia, Parkinson disease, or developmental disabilities, may be unable to comply with standard preparation instructions. These patients often require caregiver assistance, modified regimens, and sometimes inpatient preparation protocols that fall outside the scope of these outpatient-focused recommendations.19
Pregnancy presents unique challenges where both preparation agents and procedure timing must be carefully considered. The guidelines do not address obstetric considerations, and these patients require individualized management in consultation with obstetric clinicians.20
Cultural and language barriers may limit the applicability of standard education and navigation approaches. Patients with limited English proficiency, cultural dietary restrictions, or health literacy challenges may need enhanced support beyond what these guidelines specifically address. Practices serving diverse populations must develop culturally appropriate adaptations while maintaining preparation effectiveness.21
Emergency or urgent procedures often cannot accommodate the ideal timing recommendations, particularly for split-dose regimens. In these situations, clinicians must balance preparation quality against clinical urgency, often accepting suboptimal preparation in favor of timely diagnosis or treatment.
Resource-limited settings may lack access to patient navigation systems or low-volume preparations. Rural practices or those in underserved areas may need to adapt recommendations based on available resources while striving to achieve optimal preparation quality within existing constraints.
DISCLOSURES
Dr. Beveridge has disclosed teaching and speaking for Asofarma, GastroGirl, and Vindico, and consulting for Sanofi, Takeda Pharmaceuticals, and Christopher Place Healthcare. Dr. Kawas reported no relevant financial relationships which, in the context of their contributions, could be perceived as a potential conflict of interest.
- Copyright © 2026 The Cleveland Clinic Foundation. All Rights Reserved.

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