Background and study aims: Colonoscopy with inhaled methoxyflurane (Penthrox) is well tolerated in unselected
subjects and is not associated with respiratory depression. The aim of this prospective
study was to compare the feasibility, safety, and post-procedural outcomes of portable
methoxyflurane used as an analgesic agent during colonoscopy with those of anesthesia-assisted
deep sedation (AADS) in subjects with morbid obesity and/or obstructive sleep apnea
(OSA).
Patients and methods: The outcomes of 140 patients with morbid obesity/OSA who underwent colonoscopy with
either Penthrox inhalation (n = 85; 46 men, 39 women; mean age 57.2 ± 1.1 years) or
AADS (n = 55; 27 men, 28 women; mean age, 54.9 ± 1.1 years) were prospectively assessed.
Results: All Penthrox-assisted colonoscopies were successful, without any requirement for
additional intravenous sedation. Compared with AADS, Penthrox was associated with
a shorter total procedural time (24 ± 1 vs. 52 ± 1 minutes, P < 0.001), a lower incidence of hypotension (3 /85 vs. 23 /55, P < 0.001), and a lower incidence of respiratory desaturation (0 /85 vs. 14 /55, P < 0.001). The patients in the Penthrox group recovered more rapidly and were discharged
much earlier than those in the AADS group (27 ± 2 vs. 97 ± 5 minutes, P < 0.0001). Of those who underwent colonoscopy with Penthrox, 90 % were willing to
receive Penthrox again for colonoscopy. More importantly, of the patients who underwent
colonoscopy with Penthrox and had had AADS for previous colonoscopy, 82 % (28 /34)
preferred to receive Penthrox for future colonoscopies. Penthrox-assisted colonoscopy
cost significantly less than colonoscopy with AADS ($ 332 vs. $ 725, P < 0.001), with a cost saving of approximately $ 400 for each additional complication
avoided.
Conclusions: Compared with AADS, Penthrox is highly feasible and safe in patients with morbid
obesity/OSA undergoing colonoscopy and is associated with fewer cardiorespiratory
complications. Because of the advantages of this approach in regard to procedural
time, recovery time, and cost benefit in comparison with AADS, further evaluation
in a randomized trial is warranted.