Literature DB >> 21658093

Pharmacokinetics of two formulations of omeprazole administered through a gastrostomy tube in patients with severe neurodevelopmental problems.

Koen Boussery1, Julie De Smet, Pieter De Cock, Saskia Vande Velde, Els Mehuys, Peter De Paepe, Jean Paul Remon, Jan F P Van Bocxlaer, Myriam Van Winckel.   

Abstract

AIMS: Omeprazole is often administered through a gastrostomy tube as either (i) a Multiple Unit Pellet System (MUPS®) tablet disintegrated in water (MUPS® formulation), or (ii) a suspension in 8.4% sodium bicarbonate (suspension formulation). This bioavailability study evaluates this practice in tube-fed patients with severe neurodevelopmental problems.
METHODS: Nonblinded, two-phase cross-over trial.
RESULTS: In seven of 10 patients, bioavailability was higher for the suspension formulation than for the MUPS® formulation. Median (90% confidence interval) area under the plasma concentration-time curve ratio (MUPS® over suspension) was 0.5 (0.06-2.37).
CONCLUSIONS: In this population, omeprazole MUPS® formulation has no apparent advantage over the more easily administered suspension formulation. British Journal of Clinical Pharmacology
© 2011 The British Pharmacological Society. No claim to original US government works.

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Year:  2011        PMID: 21658093      PMCID: PMC3244649          DOI: 10.1111/j.1365-2125.2011.04038.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  18 in total

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  1 in total

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