A multicenter, prospective trial of total colonoscopy using a short double-balloon endoscope in patients with previous incomplete colonoscopy

Gastrointest Endosc. 2012 Apr;75(4):813-8. doi: 10.1016/j.gie.2011.11.020. Epub 2012 Jan 26.

Abstract

Background: There is no specific insertion method for patients who previously underwent an incomplete colonoscopy. No multicenter prospective study using a double-balloon endoscope (DBE) for total colonoscopy was previously performed.

Objective: To demonstrate the effectiveness and safety of using short DBEs in patients who previously underwent incomplete colonoscopies.

Design: A multicenter, prospective trial.

Setting: Four tertiary care academic centers and 6 community hospitals.

Patients: Patients with a history of incomplete colonoscopy, ages 20 to 79 years, were included. Exclusion criteria were colonoscopy performed by endoscopists with experience in fewer than 1000 cases, history of colectomy, poor bowel preparation, inflammatory bowel disease, active bowel obstruction, and active bleeding.

Intervention: Total colonoscopies using short DBEs were attempted in all patients.

Main outcome measurements: Primary endpoint was the cecal intubation rate. Secondary endpoints were time to cecal intubation, complications, and tolerability.

Results: A total of 110 patients (62 males, median age 66.5 years) were included. Fifty-four patients had a history of abdominal surgery. The cecal intubation rate was 100% (110/110). Median intubation time was 12 minutes (range 4-47 minutes). Mild mucosal tears without symptoms occurred in 1 patient. For 64.5% of patients, intravenous sedatives and/or analgesics were used during examinations. Based on questionnaires, 50.9% had no pain, 31.8% slight pain, and 17.3% tolerable pain. Moreover, 96.4% of patients answered that their examination was more comfortable than their previous colonoscopy.

Limitation: Uncontrolled trial.

Conclusion: The use of a short DBE is an effective and safe method for total colonoscopy in patients who previously underwent incomplete colonoscopies. (

Clinical trial registration number: UMIN3464.).

Publication types

  • Clinical Trial
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Cecum*
  • Chi-Square Distribution
  • Clinical Competence
  • Colonoscopy / adverse effects
  • Colonoscopy / instrumentation*
  • Deep Sedation*
  • Double-Balloon Enteroscopy* / adverse effects
  • Female
  • Humans
  • Intubation* / adverse effects
  • Male
  • Middle Aged
  • Pain / etiology
  • Patient Satisfaction
  • Time Factors
  • Young Adult