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Effect of Polydextrose/Fructooligosaccharide Mixture on Constipation Symptoms in Children Aged 4 to 8 Years
Mauro Sérgio Toporovski1, Mauro Batista de Morais2, Abrão Abuhab3
1Faculdade de Ciências Médicas da Santa Casa de São Paulo, Responsável pela Disciplina de Gastroenterologia Pediátrica, São Paulo 01234-001, Brazil.
Insights
A daily food supplement mixture of polydextrose (PDX) and fructooligosaccharide (FOS) significantly reduced constipation symptoms in children. This intervention improved bowel movement frequency, stool consistency, and decreased abdominal pain.
Area of Science:
- Pediatric Gastroenterology
- Nutritional Science
Background:
- Childhood constipation is a prevalent gastrointestinal issue.
- Dietary interventions are explored to manage pediatric constipation effectively.
Purpose of the Study:
- To evaluate the efficacy of a polydextrose (PDX) and fructooligosaccharide (FOS) mixture in alleviating constipation symptoms in children.
Main Methods:
- A 45-day prospective interventional study involving 105 children with constipation.
- Daily administration of a food supplement containing PDX (4.17 g) and FOS (0.45 g).
- Symptom assessment at 15, 30, and 45 days.
Main Results:
- A statistically significant reduction in constipation symptoms was observed.
- Bowel movements per week increased, with fewer children experiencing <3/week (59.7% to 11.7%).
- Significant decreases in dry stools (Bristol type 1 & 2 from 68.8% to 7.8%), defecation pain (79.2% to 10.4%), defecation fear (68.8% to 3.9%), and abdominal pain (84.2% to 2.6%).
Conclusions:
- The PDX/FOS mixture effectively reduced constipation symptoms in children.
- The intervention demonstrated good tolerability with a low rate of adverse effects.
- Further research with a placebo control group is recommended.
Abstract:
Constipation is a frequent problem in children. We evaluated the effect of a mixture (polydextrose [PDX] and fructooligosaccharide [FOS]) in children with constipation. We performed a prospective interventional study with a mixture (PDX 4.17 g and FOS 0.45 g) in a daily dose of food supplement. The intervention lasted 45 days, with visits at 15, 30, and 45 days after administration. The sample comprised 105 patients, of whom 77 completed the intervention. A statistically significant reduction in the frequency of symptoms was observed at the end of the study. The frequency of children with fewer than three bowel movements per week dropped from 59.7% to 11.7%, and there was a decrease in the frequency of Bristol type 1 and 2 dry stools (68.8% to 7.8%), pain on defecation (79.2% to 10.4%), and fear of defecation (68.8% to 3.9%). The proportion of children with abdominal pain symptoms decreased from 84.2% to 2.6% at the end of the study. A relevant limitation of the present study was the lack of a control group treated with placebo. The administration of the PDX/FOS mixture was accompanied by a significant reduction in the frequency of constipation symptoms of the children evaluated. The tolerability was very good, and the rate of adverse effects was low.
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