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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/34236
Title: A randomised, double-blind study of polyethylene glycol 4000 and lactulose in the treatment of constipation in children
Authors: Suporn Treepongkaruna
Nipat Simakachorn
Paneeya Pienvichit
Wandee Varavithya
Yothi Tongpenyai
Philippe Garnier
Hélène Mathiex-Fortunet
Mahidol University
Maharaj Nakhon Ratchasima Hospital
Ipsen
Keywords: Medicine
Issue Date: 19-Jun-2014
Citation: BMC Pediatrics. Vol.14, No.1 (2014)
Abstract: Background: Chronic constipation is frequent in children. The objective of this study is to compare the efficacy and safety of PEG 4000 and lactulose for the treatment of chronic constipation in young children.Methods: This randomised, double-blind study enrolled 88 young children aged 12 to 36 months, who were randomly assigned to receive lactulose (3.3 g per day) or PEG 4000 (8 g per day) for four weeks. The primary efficacy variable was stool frequency during the fourth week of treatment. Secondary outcomes were the number and frequency of subjective symptoms associated with defecation at each visit.Results: Stool frequency was comparable in the two groups at baseline (lactulose: 0.7 ± 0.5; PEG 4000: 0.5 ± 0.55). Mean stool frequency increased from 0.70 ± 0.50 stools/day at baseline to 0.80 ± 0.41 at Week 4 in the lactulose group and from 0.50 ± 0.55 to 1.10 ± 0.55 stools/day in the PEG 4000 group. A significant difference was observed in the adjusted mean change from baseline, which was 0.15 stools/day in the lactulose group and 0.51 stools/day in the PEG 4000 group, with a least-squares mean difference of 0.36 stools/day [95% CI: 0.16 to 0.56]. With respect to secondary outcome variables, stool consistency and ease of stool passage improved more in the PEG 4000 group (p = 0.001). The incidence of adverse events was similar in both groups, the majority of which were mild.Conclusions: PEG 4000 has superior efficacy to lactulose for the treatment of chronic constipation in young children and is well tolerated.Trial registration: US National Institute of Health Clinical Trials database; study NCT00255372 first registered 17th November 2005. © 2014 Treepongkaruna et al.; licensee BioMed Central Ltd.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84902707161&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/34236
ISSN: 14712431
Appears in Collections:Scopus 2011-2015

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