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Medline ® Abstract for Reference 38

of 'Management of chronic constipation in adults'

Lubiprostone, a locally acting chloride channel activator, in adult patients with chronic constipation: a double-blind, placebo-controlled, dose-ranging study to evaluate efficacy and safety.
Johanson JF, Ueno R
Aliment Pharmacol Ther. 2007;25(11):1351.
BACKGROUND: Lubiprostone, a locally acting type-2 chloride channel activator, induces intestinal fluid secretion.
AIM: To assess efficacy and safety of oral lubiprostone at multiple doses for the treatment of chronic constipation.
METHODS: A total of 129 patients with chronic constipation were randomized to receive lubiprostone (24, 48 or 72 mcg/day) or placebo for 3 weeks. Spontaneous bowel movement (SBM) frequency, rescue medication use, symptom assessments and adverse events (AEs) were tracked.
RESULTS: Over the double-blinded period, mean SBM frequencies were higher for lubiprostone groups (5.1-6.1) vs. placebo (3.8) and the overall difference was statistically significant (P = 0.046). SBM frequencies at week 1 were significantly higher in patients taking lubiprostone 48 or 72 mcg/day (P<or = 0.003) and, at week 2, all three lubiprostone doses yielded significantly higher SBM rates vs. placebo (P<or = 0.020). Significantlylarger proportions of patients taking lubiprostone 48 and 72 mcg/day also experienced a SBM on the first treatment day (P<or = 0.009). The most common AEs were nausea, headache and diarrhoea.
CONCLUSIONS: Lubiprostone improved SBM rates in a dose-dependent manner. AEs were tolerable for most patients. Increased AE severity at 72 mcg/day did not provide a clear risk-to-benefit advantage compared with lubiprostone 48 mcg/day, the dose chosen for subsequent Phase 3 studies.
Rockford Gastroenterology Associates, Rockford, IL, USA. johnfj@uic.edu