TY - JOUR
T1 - Reduced osmolarity oral rehydration solution for treating dehydration due to diarrhoea in children: Systematic review: Systematic review
AU - Hahn, Seokyung
AU - Kim, Yaejean
AU - Garner, Paul
PY - 2001/7/14
Y1 - 2001/7/14
N2 - Objectives: To compare reduced osmolarity oral rehydration solution with standard World Health Organization oral rehydration solution in children with acute diarrhoea. Design: Systematic review of randomised controlled trials. Studies: 15 randomised controlled trials including 2397 randomised patients. Outcomes: The primary outcome was unscheduled intravenous infusion; secondary outcomes were stool output, vomiting, and hyponatraemia. Results: In a meta-analysis of nine trials for the primary outcome, reduced osmolarity rehydration solution was associated with fewer unscheduled intravenous infusions compared with standard WHO rehydration solution (odds ratio 0.61, 95% confidence interval 0.47 to 0.81). Three trials reported that no patients required unscheduled intravenous infusion. Trials reporting secondary outcomes suggested that in the reduced osmolarity rehydration solution group, stool output was lower (standardised mean difference in the log scale −0.214 (95% confidence interval −0.305 to −0.123; 13 trials) and vomiting was less frequent (odds ratio 0.71, 0.55 to 0.92; six trials). Six trials sought presence of hyponatraemia, with events in three studies, but no significant difference between the two arms. Conclusion: In children admitted to hospital with dehydration associated with diarrhoea, reduced osmolarity rehydration solution is associated with reduced need for unscheduled intravenous infusions, lower stool volume, and less vomiting compared with standard WHO rehydration solution. Oral rehydration solution prevents death from diarrhoea in many developing countries Children receiving a reduced osmolarity rehydration solution were less likely to need intravenous infusion than those receiving WHO rehydration solution Reduced osmolarity rehydration solution also reduced stool output and vomiting No difference was found in rates of hyponatraemia.
AB - Objectives: To compare reduced osmolarity oral rehydration solution with standard World Health Organization oral rehydration solution in children with acute diarrhoea. Design: Systematic review of randomised controlled trials. Studies: 15 randomised controlled trials including 2397 randomised patients. Outcomes: The primary outcome was unscheduled intravenous infusion; secondary outcomes were stool output, vomiting, and hyponatraemia. Results: In a meta-analysis of nine trials for the primary outcome, reduced osmolarity rehydration solution was associated with fewer unscheduled intravenous infusions compared with standard WHO rehydration solution (odds ratio 0.61, 95% confidence interval 0.47 to 0.81). Three trials reported that no patients required unscheduled intravenous infusion. Trials reporting secondary outcomes suggested that in the reduced osmolarity rehydration solution group, stool output was lower (standardised mean difference in the log scale −0.214 (95% confidence interval −0.305 to −0.123; 13 trials) and vomiting was less frequent (odds ratio 0.71, 0.55 to 0.92; six trials). Six trials sought presence of hyponatraemia, with events in three studies, but no significant difference between the two arms. Conclusion: In children admitted to hospital with dehydration associated with diarrhoea, reduced osmolarity rehydration solution is associated with reduced need for unscheduled intravenous infusions, lower stool volume, and less vomiting compared with standard WHO rehydration solution. Oral rehydration solution prevents death from diarrhoea in many developing countries Children receiving a reduced osmolarity rehydration solution were less likely to need intravenous infusion than those receiving WHO rehydration solution Reduced osmolarity rehydration solution also reduced stool output and vomiting No difference was found in rates of hyponatraemia.
U2 - 10.1136/bmj.323.7304.81
DO - 10.1136/bmj.323.7304.81
M3 - Article
SN - 0959-8146
VL - 323
SP - 81
EP - 85
JO - BMJ
JF - BMJ
IS - 7304
ER -