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Diarrhoea and vomiting caused by gastroenteritis in children under 5 years




            8.2.1       Adsorbent agents

            8.2.1.1     Kaolin

                        Evidence overview
                        A  trial 166   conducted  in  the  Gambia  included  children  with  diarrhoea  aged  between  3  and
                        18 months (n = 97). Those requiring antibiotic therapy or with positive diagnosis for malaria were
                        excluded. Participants were allocated to treatment with kaolin and ORS solution (n = 45) or to
                        administration of ORS solution alone (n = 52). The method of randomisation was inadequate (birth
                        order allocation) and allocation concealment and follow-up were not reported. Compliance with
                        the doses of kaolin was poor in 33% of the participants. The outcomes considered were duration
                        of diarrhoea and the number of stools per day in both groups. [EL = 1−]
                        No  statistically  significant  differences  were  found  between  the  kaolin  and  the  ORS  solution
                        groups in the mean duration of diarrhoeal episodes or in the mean number of stools per day.

                        Evidence summary
                        There was a lack of high-quality evidence for the effectiveness of kaolin in the treatment of acute
                        diarrhoea in children. A quasi-randomised controlled trial [EL = 1−] showed no differences in the
                        duration of acute diarrhoea or in the number of stools per day between children receiving kaolin
                        with rehydration therapy and children receiving rehydration therapy alone.

            8.2.1.2     Activated charcoal

                        Evidence overview
                        One  RCT  was  identified  that  included  39  children  aged  between  1½  months  and  10  years
                        with  acute  gastroenteritis  and  severe  dehydration  (n  =  39). 167   [EL  =  1−]  Children  with  acute
                        gastroenteritis  due  to  Entamoeba  histolytica  were  excluded.  Participants  were  allocated  to
                        treatment with activated charcoal with oral and IV rehydration solution (n = 16) or oral and IV
                        rehydration alone (n = 23). The method of randomisation, allocation concealment, follow-up and
                        baseline comparability of the two groups were poorly reported. The outcomes considered were
                        duration of diarrhoea and fluid therapy administered.
                        The study found that the group receiving the activated charcoal had a statistically significantly
                        shorter mean duration of diarrhoea (mean 2.12 days) than the control group (mean 3.00 days)
                        (WMD  −0.88  days;  95%  CI  −1.50  to  −0.26  days).  Children  in  the  activated  charcoal  group
                        required statistically significantly less ORS solution (mean 3.25 packs) than the control group
                        (mean 5.43 packs), (WMD −2.18 packs; 95% CI −3.84 to −0.52 packs). There was no statistically
                        significant difference in the mean IVT (Ringer’s lactate solution) required between groups.

                        Evidence summary

                        There  was  some  evidence  from  a  poorly  reported  RCT  suggesting  that  the  additional  use  of
                        activated  charcoal  in  the  treatment  of  children  with  gastroenteritis  shortened  the  duration  of
                        the  diarrhoea  and  reduced  the  amount  of  ORT  required  when  compared  with  the  standard
                        rehydration therapy alone. On the other hand, the same trial showed no difference in the amount
                        of IV rehydration therapy required between the children receiving activated charcoal and the
                        children who did not received the adsorbent agent.

            8.2.1.3     Smectite

                        Evidence overview
                        One relevant systematic review of trials comparing smectite with placebo or no treatment for
                        diarrhoea in children was identified. 168  This well-conducted systematic review included nine
                        RCTs published between 1986 and 2002. Two trials were conducted in France, one in Italy,
                        one in Lithuania, two in Thailand, one in Egypt and one in China. The nine studies included
                        data from 1238 participants: 622 received smectite and 616 received placebo or no additional
                        treatment. Even though it was reported that the doses of smectite were similar across the studies,


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