Nosocomial Infection Clinical Trial
Official title:
Lactulose for the Prevention of Nosocomial Infections in Children
The purpose of this study is to assess the ability of lactulose, a prebiotic agent, to prevent hospital acquired infection in children
Despite the adoption of norms regarding enteric isolation, nosocomial infectious diarrhea is
common in children(1;2). Viral pathogens, especially rotavirus are responsible for most of
the cases. Depending on population, type of hospital, and standard of care, the reported
incidence rate ranges from 8 to 33 episodes per 100 admissions(1). Infants and toddlers are
at the highest risk of acquiring nosocomial viral gastroenteritis(1;2).
Probiotic bacteria have been shown to be beneficial in the prevention and treatment of
gastrointestinal infections as well as reduction of viral shedding(3;4). A recent study by
Szajewska et al. (2) showed a significant reduction of nosocomial infections from 33% to 7%
by prophylactic treatment with LGG during the hospital stay. Another study however, did not
show any difference(1).
Another approach is to use prebiotic treatment. Prebiotics are defined as non-digestible
substances that, when ingested, selectively promote the growth and establishment of
beneficial probiotic-like bacteria normally present in the gut(5).
Lactulose is a semi-synthetic disaccharide made from lactose by a chemical reaction which
was first described in 1930(6).
In contrast to other prebiotics, lactulose has up to now been mainly used as a medicinal
drug for constipation and hepatic encephalopathy(6). In 1957 Petuely published the basic
work about lactulose as "the bifidus factor" which was confirmed by MacGillivray et
al(6).They found that the composition of the colonic microflora of bottle-fed babies is very
much like that of adults while if lactulose is added to the formula milk such babies have
the same composition as breast-fed babies.
Lactulose has been used for 40 years in the treatment of constipation [10] and for more than
30 years for encephalopathy.The dosages used in PSE are up to four times higher than those
usually applied in constipation. No putative or definite evidence of mutagenic, genotoxic or
teratogenic effects of lactulose has been obtained in human use. Animal studies in rats and
rabbits also did not reveal any teratogenic or reproduction-toxicologic effects, and even
high dosages have had no deleterious effects(6)
Our hypothesis is that lactulose, with its proven prebiotic properties, given to children
during their hospital stay, would be beneficial in reducing nosocomial infections.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double-Blind, Primary Purpose: Prevention
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