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Fluid management




                           GDG translation from evidence to recommendation

                           There  was  no  definitive  evidence  on  the  optimum  IV  fluid  regimen  for  the  management  of
                           hypovolaemic shock in the dehydrated child with gastroenteritis. However, there was widespread
                           consensus that whatever the cause of shock, a bolus of IV fluid should immediately be given. 97,106
                           Currently, the main focus of discussion regarding fluid administration in patients with shock is on
                           the optimal choice of fluid. This includes discussion of crystalloid versus colloid fluids, especially
                           in relation to septicaemic or critically ill patients. The use of albumin solutions in particular is
                           controversial. 107–109  The GDG considered that for children with shock due to dehydration from
                           gastroenteritis, 0.9% sodium chloride solution is an appropriate and readily available fluid for
                           bolus administration.
                           In hypovolaemic shock associated with gastroenteritis, rapid recovery would be expected in most
                           children following the administration of a 20 ml/kg bolus of 0.9% sodium chloride solution. 97,106
                           If an immediate response does not occur, a further 20 ml/kg bolus should be given. In the absence
                           of prompt response to bolus fluid administration, it is important to consider whether factors other
                           than hypovolaemia, for example septicaemia, might be responsible. In this case, expert advice
                           should be sought from a paediatric intensive care specialist.

                           With regard to the treatment of dehydration (as opposed to shock) with IVT, the GDG recognised
                           that there was a lack of evidence from clinical trials to inform practice in this area. For example,
                           the WHO recommends the use of Ringer’s lactate solution for IV rehydration. There has been
                           much discussion on the optimal choice of IV maintenance fluids for children, particularly since
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                           the National Patient Safety Agency (NPSA) issued a specific alert on this matter in 2007.  The
                           NPSA alert reinforced an existing trend away from the use of hypotonic solutions such as 0.18%
                           sodium chloride. This reflected concerns about the risk of hyponatraemia. 111
                           The  NPSA  has  recommended  the  use  of  isotonic  solutions  such  as  0.9%  sodium  chloride
                           with or without 5% glucose for children with a range of conditions associated with a risk of
                           hyponatraemia, including those with diarrhoea. There has been some controversy regarding the
                           NPSA recommendations. The use of 0.9% sodium chloride solution provides more salt to the
                           child than is to be found in an average diet. It appears that most children do not experience
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                           adverse effects with this increased salt load, but some may do.  Concern has been expressed at a
                           possible risk of hypernatraemia and hyperchloraemic acidosis. However, because gastroenteritis
                           is associated with increased salt losses, the use of 0.9% sodium chloride solution in these children
                           has not been challenged. Furthermore, the NPSA recommendations emphasise the importance of
                           careful monitoring of plasma electrolytes during IVT.
                           The GDG agreed with the NPSA recommendations on this matter. The GDG also considered that
                           it was important for clinicians to be aware that metabolic acidosis might not be due to persisting
                           shock. Such misinterpretation could lead to the administration of excessive fluid. 113
                           As discussed earlier in relation to ORT, there is usually no precise way of determining the exact
                           fluid deficit and hence the required replacement volume. If a child is considered to be in a
                           state of hypovolaemic shock, their intravascular volume has been significantly depleted owing to
                           fluid loss. To reach this stage, it is generally accepted that they are at least 10% dehydrated, i.e.
                           they will have lost at least 100 ml/kg of total body fluid. The GDG agreed that once shock was
                           corrected with fluid bolus administration, it was safest to assume that the child might be 10%
                           dehydrated and they should therefore receive 100 ml/kg as deficit replacement.
                           For those who are dehydrated but without shock, in keeping with the recommendation for ORT, a
                           volume of 50 ml/kg IV was considered by the GDG to be an appropriate initial deficit replacement
                           volume. Regular reassessment would be necessary to determine whether this was sufficient to
                           reverse the signs of clinical dehydration. Further replacement would be given subsequently if this
                           was necessary.
                           The GDG was conscious of a lack of high-quality evidence regarding the optimal time period
                           over which IV fluids should be administered to children with dehydration. With ORT it is widely
                           accepted that rehydration can and should be completed quickly – typically over a 4 hour period.
                           Traditionally, IV rehydration has been performed over a 24 hour time period, and this approach is
                           still in common use. This practice probably evolved from experience with the use of subcutaneous
                           fluid replacement in children in the 1940s.  The NPSA patient safety alert on IV infusions for
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