Patient Satisfaction
Conditions
Brief summary
This study aim to examine the safety and feasibility of unsedated colonoscopy in patients with high risk for sedation (ASA score≥3).
Detailed description
This was a two-part study: Part 1 was a retrospective study of patients with ASA score≥3 that underwent unsedated colonoscopy from May 2021 to August 2022 at Sheba medical center, who were contacted up to one year after the procedure and were asked to assess their satisfaction and pain level on a standard Likert score from 1-5. Part 2 was a prospective study which included high risk patients who were scheduled for an anesthesiologist-assisted sedated-colonoscopy and who consented to undergo an unsedated procedure. The primary outcome was patients' satisfaction during and up to one week after the procedure. Pain level, adverse events and hemodynamic parameters during the procedure were secondary outcomes. Baseline State-Trait Anxiety Inventory (STAI) questionnaire were also administered and results examined vis-à-vis satisfaction scores
Interventions
PROCEDUREun-sedated colonoscopies
un-sedated colonoscopies in high risk patients with ASA\>=3
Sponsors
Sheba Medical Center
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
Yes
Inclusion criteria
* Only adults (\>18 years of age) that will be assessed as high risk and require an anesthesiologist clinic assessment prior to the procedure and anesthesiologist presence during the procedure.
Exclusion criteria
1. Patients that are planned to go through both gastroscopy and colonoscopy procedures. 2. Patients with known adhesions and/or prior small bowel obstructions. 3. Patients that are planned to have a complicated procedure (complicated polypectomy etc). 4. Patients that are not able to give their consent with a full understanding of the procedure. 5. Patients that are pregnant. 6. Patients with a heart rate above 120 bpm or less than 40 bpm at the baseline as measured before starting the procedure. 7. Patients with a systolic blood pressure above 180mmHg or bellow 90mmHg as measured at the baseline before starting the procedure.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| satisfaction rate | up to 1 week after the date of the procedure | Overall satisfaction score as assessed by Likert scale post-procedure |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Recovery time after the procedure | up to 24 hours after the procedure | the time lapse between extraction of colonoscope from the rectum and discharge of the patient from the Endoscopy recovery unit. |
| Complications or adverse effects rates during the procedure | from the beginning of the procedure until the end of the procedure | perforations, post-polypectomy bleeding, bradycardia (defined as pulse rate under 40 bpm), low oxygen saturation (defined as saturation below 90% under nasal oxygen cannula) or hemodynamically instability (defined as systolic blood pressure below 90mmHg and diastolic blood pressure below 60mmHg) |
| Complete examination rates | from the beginning of the procedure until the end of the procedure | how many examination were completed up to cecum intubation without need for sedation |
Countries
Israel
Outcome results
None listed