LACTOBACILLUS GG ADMINISTERED IN ORAL REHYDRATION SOLUTION TO CHILDREN WITH ACUTE DIARRHEA: A MULTICENTER EUROPEAN TRIAL

Author(s):  
S Guandalini
2000 ◽  
Vol 30 (1) ◽  
pp. 54-60 ◽  
Author(s):  
Stefano Guandalini ◽  
Licia Pensabene ◽  
Mona Abu Zikri ◽  
Jorge Amil Dias ◽  
Luigi Gobio Casali ◽  
...  

PEDIATRICS ◽  
1995 ◽  
Vol 95 (2) ◽  
pp. 191-197
Author(s):  
Susana Molina ◽  
Carolina Vettorazzi ◽  
Janet M. Peerson ◽  
Noel W. Solomons ◽  
Kenneth H. Brown

Objective. To assess the effects of glucose (G)-oral rehydration solution (ORS), rice dextrin (RD)-ORS, and rice flour (RF)-ORS on fluid intake, rapidity of rehydration, and stool output of children with acute diarrhea and mild or moderate dehydration. Methods. The study was a randomized, double-masked clinical trial. One hundred forty-six male infants, ages 3 to 36 months, were randomly assigned to one of three treatment groups. Clinical evaluations and fluid balances were conducted every 2 to 4 hours for 48 hours. Principal outcome variables were ORS consumption, recovery of hydration status, and fecal output. Results. The groups were similar at admission with regard to age, nutritional status, history of the current episode, and clinical status. There were no differences in ORS consumption by treatment group during any period of study. During the first 6-hour period, patients in group RF had less stool output (16 ± 14 g/kg/body weight) than those in group G (22 ± 20 g/kg) or RD (21 ± 19 g/kg; P < .05). After 12 hours of hospitalization, there were no differences by treatment group. Recovery of hydration status, changes in serum sodium and potassium, and duration of diarrhea in the hospital were similar in all three groups. Conclusion. There was a 24% to 27% reduction in stool output during the first 6 hours of treatment among children who received RF-ORS compared with those who received G-ORS or RD-ORS, but this effect did not persist after the first 12 hours of therapy. Because this difference was of small magnitude and limited duration, it has minor clinical importance. Thus, we conclude that the three solutions had similar efficacy for children with acute, watery diarrhea and mild or moderate dehydration.


1990 ◽  
Vol 116 (6) ◽  
pp. 868-875 ◽  
Author(s):  
Mathuram Santosham ◽  
Ibrahim M. Fayad ◽  
Mohamed Hashem ◽  
Julius G. Goepp ◽  
Mamdouh Refaf ◽  
...  

1995 ◽  
Vol 20 (4) ◽  
pp. 408-416 ◽  
Author(s):  
Denis V. Barclay ◽  
Joaquina Gil-Ramos ◽  
José O. Mora ◽  
Henri Dirren

PEDIATRICS ◽  
1999 ◽  
Vol 104 (3) ◽  
pp. e29-e29 ◽  
Author(s):  
Christopher Duggan ◽  
Jack Lasche ◽  
Martha McCarty ◽  
Kathleen Mitchell ◽  
Robert Dershewitz ◽  
...  

2002 ◽  
Vol 141 (5) ◽  
pp. 677-682 ◽  
Author(s):  
Rajiv Bahl ◽  
Nita Bhandari ◽  
Manju Saksena ◽  
Tor Strand ◽  
Geeta T. Kumar ◽  
...  

PEDIATRICS ◽  
1991 ◽  
Vol 87 (5) ◽  
pp. 619-622
Author(s):  
Mathuram Santosham ◽  
Julius Goepp ◽  
Barbara Burns ◽  
Raymond Reid ◽  
R. Bradley Sack ◽  
...  

The introduction of a soy-based, lactose-free formula during the acute phase of diarrheal illness in infants has been shown to reduce stool output and duration of diarrhea in hospitalized patients. In the United States, most infants with acute diarrhea are treated as outpatients. In the present study, infants with diarrhea who were treated as outpatients were randomly assigned to receive either a soy-based, lactose-free formula alternating with oral rehydration solution from the beginning of therapy ("early feeding") or oral rehydration solution alone for the first 24 hours of therapy, followed by a soy-based, lactose-free formula alternating with oral rehydration solution (control group). Twenty-nine infants were randomly assigned to the early-feeding group and 27 to the control group. Twenty-one (72%) of 29 in the early-feeding group resolved their diarrhea at the end of 48 hours of therapy compared with 12 (44%) of 27 in the group fed oral rehydration solution only (P = .02). It is concluded that the introduction of a soy-based, lactose-free formula from the beginning of therapy for acute diarrhea in children treated as outpatients is safe and may shorten duration of diarrhea while maintaining adequate caloric intake.


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