Diarrhoea and vomiting

Published on 23/06/2015 by admin

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Last modified 22/04/2025

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7.8 Diarrhoea and vomiting

Clinical evaluation

History

Examination

General observation

In the absence of a life-threatening emergency it is always worthwhile to make a careful observation of the child, either whilst talking with the carer or to the child. This general observation phase is invaluable in the paediatric assessment, particularly in young children. During this observation look and listen for the following:

Note that the ABCD approach (airway, breathing, circulation, disability) is utilised.

Assessment of the state of hydration is critical. It is well recognised that clinicians tend to overestimate the degree of dehydration, consequently excessive amounts of intravenous fluid may be administered. Accurate premorbid and current weight may aid this assessment. The following is a revised guide for the assessment of dehydration:

Always check carefully for a rash, as petechiae and purpura may be inconspicuous or subtle. Examination of the ears, nose and throat, is frequently left until the end of the examination, to avoid potential distress impairing the remainder of the examination.

Cardiovascular and respiratory status

It is important to evaluate the cardiovascular and respiratory systems in the infant with vomiting for the following reasons:

The pulse rate and pulse volume may identify a rapid thready pulse indicating poor perfusion. Capillary refill is often thought to be a poor indicator of circulatory status, as the peripheral perfusion (hands and feet) may be affected by environmental temperature. The comparison of central (anterior chest) and peripheral capillary refill, with other data like heart rate, pulse volume and consciousness state, allows an assessment of the adequacy of the circulation. The presence of shock indicates inadequate tissue perfusion. It is present when there is a rapid, thready pulse, delayed capillary refill, especially if central (>2 seconds), and abnormal neurological status including agitation, lethargy, or coma. The diagnosis of shock is not reliant on the presence of hypotension, particularly in children. Delay in identifying shock until the child is hypotensive risks severe compromise and potential progress to cardiac arrest.

Septicaemia, with or without meningitis, may cause fever, vomiting and diarrhoea. Some bacterial pathogens that cause gastroenteritis may also cause septicaemia, such as Salmonella and Shigella.

Respiratory examination of the infant with fever, cough and vomiting may identify tachypnoea and grunt that alert the clinician to the possibility of pneumonia. Grunting is an expiratory noise, usually intermittent, and generates PEEP (positive end expiratory pressure) by partially closing the glottis during expiration. Percussion note for dullness may be more valuable than auscultation for crackles or bronchial breathing. Be aware of the child with abdominal pain and grunt as they may have a lower lobe pneumonia.

Investigations

Remember, only order tests that aid the decision making and management of the patient. Reference ranges are frequently based on the standard deviation in a population, so a result outside the range may not necessarily indicate abnormality or pathology. This may inadvertently lead the clinician to order more unnecessary tests.

Not every child who is medically assessed requires investigations. The tests required depend on the possible differential diagnoses and the severity of illness (Table 7.8.1). Don’t forget simple bedside tests like urine analysis (UA) and blood glucose. This information can be invaluable in assessing the child with diarrhoea and vomiting. In this context, check the specific gravity and for ketones. Glycosuria may indicate diabetic ketoacidosis. If the UA is positive for nitrites or leucocytes, then an appropriately collected urine specimen should be cultured. The specimen to be cultured should be collected attempting to minimise contamination, even if re-collection is required.

Table 7.8.1 Tests that may be useful in the child with vomiting or diarrhoea

Common tests:

Less common tests:

AXR, abdominal X-ray; CXR, chest X-ray; RIA, radioimmunoassay.

Generally urine culture is unnecessary where acute gastroenteritis is likely (i.e. when there is diarrhoea) but is mandatory in the infant or baby with acute vomiting and fever. Urinary symptoms like dysuria and frequency can be expected in children from about 4 or 5 years of age, allowing a more selective approach to those who require urine culture. ‘Bag urines’ (collected in an adhesive, sterile plastic bag) have a high contamination rate and are best avoided when performing a urine culture, but are satisfactory for a simple UA. Although more difficult to collect, a ‘clean catch urine’ provides a sample less likely to be contaminated. This is collected with an open nappy, a poised parent, with an open sterile container, waiting patiently to ‘catch’ the spontaneously voided urine. Those babies and infants deemed to be at higher risk of a UTI or who are more seriously unwell may require more rapid testing by either a suprapubic aspirate (‘bladder tap’) or an in–out catheter urine collection. Any child who is toilet trained and requires a urine culture should have mid-stream urine collected.

The child who is previously well and thriving who presents with vomiting and hypoglycaemia, if ketotic, is likely to be hypoglycaemic from starvation. In the absence of ketonuria, metabolic and endocrine abnormalities need to be considered. It may be necessary to assay growth hormone, insulin and cortisol, as well as performing a urine metabolic screen. Collecting appropriate specimens when hypoglycaemic is important. Blood samples collected in a lithium heparin tube (plasma) and plain tube (serum) should allow blood glucose to be measured concurrently with hormone levels. Other samples may also be needed. Consultation with a paediatrician or paediatric endocrinologist may be prudent.

In a young, breastfed infant with blood in vomitus or stool it is important to distinguish swallowed maternal blood from infant’s blood. An Apt test distinguishes between the two due to presence of HbF. To perform the test, add the bloody stool/vomitus to a test tube with about 5 mL of tap water. This lyses the red blood cells. After allowing to settle, the “supernatant” should be pink to continue. If so, add 1 mL of 1% sodium hydroxide. Remaining pink indicates infant’s blood (HbF) whereas changing to a yellow-brown colour over 2 minutes indicates maternal (adult) blood.

The microscopy of the diarrhoeal stool may be important. The presence of stool white cells, without a viral or bacterial pathogen, in the young infant, may indicate cows’ milk protein intolerance.

Management

Intravenous fluids

The management will depend on the need for immediate resuscitation and subsequently, the provisional diagnosis. A fluid bolus is used to restore circulating volume and is therefore warranted when signs of shock are present. This must not be confused with strategies of ‘rapid rehydration’ in dehydrated children. Intravenous fluids containing dextrose must not be used as volume expanders. The choice of crystalloid fluid for a bolus is either normal saline (0.9%) or Hartmann’s solution. If these crystalloids are not available, and a bolus is required, then a colloid should be used (e.g. 4% NSA or Gelofusine).

In dehydrated, but not cardiovascular compromised children, it is safer to commence initial intravenous rehydration with fluids that contain at least 75 mmol L–1 sodium, i.e. 0.45–0.9% NaCl solution. Commonly available fluids include 0.45% NaCl + 5% glucose, 0.9% NaCl (normal saline) and Hartmann’s solution. Normal saline (0.9% NaCl) with 5% glucose is also currently available. Hypoglycaemia is not infrequent, both at presentation or subsequently, thus dextrose-containing fluids are appropriate in all children, particularly in the young infant or those who have had insufficient caloric intake and are ketotic. Intravenous fluids are commonly manufactured as ‘isotonic’ with plasma, by varying the glucose concentration to balance the sodium chloride (e.g. 0.45% NaCl + 5% glucose). The addition of dextrose to many commercially available solutions (such as normal saline) makes them ‘hypertonic’ compared to plasma. However, due to rapid equilibration of the dextrose with extravascular space this is not clinically significant. In this context, 0.9% NaCl + 2.5% glucose is an appropriate intravenous fluid to use (may be made by adding 50 mL of 50% glucose to 450 mL of 0.9% NaCl).

Be aware of the potential of SIADH in unwell children. The rate of fluid administration may need to be altered depending upon the initial biochemistry, the diagnosis and the clinical progress of the child. Monitoring fluid balance is essential in the unwell infant or child.

Nasogastric rehydration is commonly used in dehydrated infants with gastroenteritis. See Chapter 7.12.