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Diarrhoea and vomiting caused by gastroenteritis in children under 5 years




                        could be taken if the urine output was said to be normal. The GDG also agreed that carers were
                        acutely aware of any change in the child’s behaviour (irritability, lethargy) and appearance (for
                        example ‘sunken eyes’), and so it seemed appropriate to specifically enquire about these.

                        With regard to the role of physical signs in the detection of dehydration, the GDG examined
                        the evidence from the systematic review and identified two limitations to the included studies.
                        First, the review appeared to report on children with 5% dehydration or worse and, given the
                        symptoms and signs identified, the GDG strongly suspected that many of the patients might have
                        been considerably more than 5% dehydrated. Therefore, the stronger associations reported for
                        CRT, abnormal skin turgor and abnormal breathing pattern did not mean that these signs would
                        be useful for the detection of less severe dehydration. On the contrary, the GDG considered
                        that those signs suggested the presence of relatively severe dehydration. Second, neither the
                        prevalence of dehydration nor the post-test probabilities of dehydration were presented. One or
                        other of these parameters was needed to interpret the likelihood ratios presented.
                        Therefore, this study did not provide reliable evidence on the value of symptoms and signs for the
                        detection of lesser degrees of dehydration. However, the GDG agreed that the presence of one or
                        more symptoms or signs evaluated in those studies and conventionally employed in assessment
                        for dehydration would suggest clinically significant dehydration.
                        The study of CRT using a digital technique (DCRT) showed a relationship between abnormal DCRT
                        and dehydration. However, this remains an experimental technique that is not yet established as
                        a method for routine clinical use.

                        Clinical assessment of dehydration severity
                        The GDG recognised that there was a lack of compelling evidence to support efforts to accurately
                        distinguish varying degrees of dehydration on the basis of symptoms and signs. In the absence of
                        such evidence, any system of classification was inevitably arbitrary and subjective and based on
                        the clinician’s judgement and a ‘global assessment’ of the child’s condition.
                        In the past, it was common to describe three levels of dehydration, referred to as mild (3–5%),
                        moderate  (6–9%)  and  severe  (≥10%),  with  an  implication  that  it  was  possible  to  make  such
                        distinctions  based  on  the  clinical  assessment  (see Table  4.5). A  number  of  recent  guidelines
                        (Tables 4.3 and 4.4) had adopted simpler schemes in which just two degrees of dehydration
                        were  to  be  distinguished  –  ‘some  dehydration’  (or  ‘mild  to  moderate  dehydration’),  variably
                        defined as 3–8% or 5–10% dehydration, and ‘severe dehydration’, variably defined as ≥9% or
                        >10% dehydration. Even these simpler classifications could be difficult to implement in clinical
                        practice. The GDG considered that it was not possible to accurately distinguish ‘sunken’ and ‘very
                        sunken’ or ‘deeply sunken’ eyes, or between skin pinch retracting ‘slowly’ and ‘very slowly’, or
                        between ‘dry’ and ‘very dry’ mucous membranes. There was also no evidence on the reliability
                        of these various signs either individually or in combination in distinguishing varying degrees of
                        dehydration. In addition, there was no evidence to justify arbitrary categorisation on the basis of
                        specific numbers of clinical symptoms or signs as had been suggested (Table 4.3).
                        The GDG decided to adopt a new and even simpler clinical assessment scheme (Table 4.6)
                        Patients would merely be classified as follows: ‘no clinically detectable dehydration’, ‘clinical
                        dehydration’  and  ‘clinical  shock’. With  this  assessment  scheme  the  clinician  would  have  to
                        recognise the presence of clinical dehydration. This simplified scheme does not imply that the
                        degree of dehydration is uniform, but rather acknowledges the difficulties in accurately assessing
                        dehydration  severity.  The  GDG  recognised  that  experienced  clinicians  could  distinguish
                        marked differences in the severity of dehydration. They also considered that clinical signs were
                        likely to be more pronounced and numerous in those with severe dehydration. However, firm
                        recommendations linking clinical symptoms and signs with specific varying levels of dehydration
                        were impossible. The crucial point however, is that the scheme is all that is required to guide
                        fluid management (Chapter 5). In this guideline a standard fluid regimen is recommended for all
                        (non-shocked) children with dehydration, with adjustments being made to the fluid regimen over
                        time based on regular reassessment during the rehydration process.
                        The GDG was aware of the crucial importance of identifying those children with hypovolaemic
                        shock. They  would  require  specific  emergency  management  with  administration  of  IV  fluid
                        boluses (Section 5.4) and so it was essential that signs of shock should be recognised without
                        delay. Many patients with hypovolaemic shock were likely to have obvious and pronounced


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