Colonoscopic examinations are performed routinely in hospitalized patients for a variety of indications. However, numerous limitations exist in hospitalized patients preventing an endoscopist from performing high quality examinations; possibly necessitating repeated procedures leading to increased cost and re-exposure to their inherent risks. One such prominent challenge lays in the adequacy of bowel cleansing. Inpatient status has been shown to be a predictor of poor bowel preparation as these patients are older, less mobile and have more co morbidities than the outpatient population. Currently, no standardized (or optimized) bowel preparation type or regimen for administration exists for the hospital inpatient population undergoing colonoscopy. Studies in the outpatient population have demonstrated that timing and choice of cathartic medication effects the cleanliness of the bowel preparation but there is no such clinical evidence for in-patients who receive whatever cathartic agent is on hospital formulary. The purpose of the study is compare efficacy, patient satisfaction, and adverse effects associated with low volume cathartic (Pico-Salax) to the current standard volume 4 liter (PEG-Lyte) and the effect of alternate timing of dosages.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
126
Given at the start of the bowel preparation the day before colonoscopy
280g reconstituted in 4 liters of water
Two sachets, Each sachet has 10mg dose
St Joseph Hospital
Hamilton, Ontario, Canada
RECRUITINGOttawa Bowel Prep Score
Using a standardized, validated score for measuring quality of bowel preparation
Time frame: 30 minutes after procedure
Procedures Cancelled or repeated due to inadequate bowel preparation
If bowel preparation is deemed inadequate to the point the procedure must be cancelled or rescheduled
Time frame: During admission (average of 2 weeks)
Individual Components of Ottawa Bowel Prep Score
Each section of prep score evaluating the right, mid, and left colon, as well as the fluid score will be analyzed individually
Time frame: 30 minutes after procedure
Adverse Effects
Any adverse effects that may be attributed to the intervention
Time frame: Up to 48 hours after procedure
Tolerability of the preparation
A questionnaire to assess the overall tolerability of the preparation.
Time frame: Within 1 day of intervention
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