Chapter 28. Caring for children with gastrointestinal problems
Julia M. Winter
LEARNING OUTCOMES
• Identify the causes and management of vomiting in infants and children.
• Identify the causes of acute and chronic diarrhoea in infants and children.
• Recognise and distinguish between presentation of acute and chronic disorders.
• Identify the causes of sudden acute gastrointestinal problems requiring surgery.
• Consider the management of both acute and chronic gastrointestinal disorders, adopting a family-centred approach to care.
• Review the changes in incidence in chronic gastrointestinal disorders, considering causes and implications for healthcare practice.
Glossary
Anal stenosis
Narrowing or stricture of the anal canal and sphincter.
Atresia
Absence or closure or a natural passage or channel, imperforation.
Bulimia
An eating disorder, which is characterised by self-induced vomiting after eating.
Cell hyperplasia
The abnormal multiplication or increase in the number of cells in normal arrangement in a tissue.
Cirrhosis
Liver disease characterised pathologically by loss of the normal microscopic structure.
Fundoplication
Mobilisation of the lower end of the oesophagus and wrapping (plication) of the fundus of the stomach around it. Done as a treatment for reflux.
Haemolytic uraemic syndrome
A pathological condition with involves the rupture (haemolysis) of red blood cells, subsequent anaemia, low platelet count and kidney failure.
Hirschsprung’s disease
Congenital aganglionosis of colon leading to loss of gut motility.
Imperforate anus
A congenital obstruction of the anal opening.
Intussusception
Telescoping of one portion of the intestine into another.
Jejunal biopsy
Tissue sampling of the jejunum.
Malrotation
Failure during normal embryonic development of normal rotation of all or part of an organ.
Meconium ileus
Obstructed bowel due to impacted, tenacious meconium.
Myopathies
Disease of muscles.
Neurofibromatosis
Growth of neurofibromas (smooth soft or firm tumours) anywhere in the myelinated nervous system (autosomal inheritance).
Organic causes
A disease that occurs as a result of anatomical or physiological abnormality.
Pyloric stenosis
A congenital disorder in which the pylorus is thickened causing obstruction of the gastric outlet.
Scleroderma
Hardening of skin.
Steatosis
Fatty degeneration.
Systemic lupus erythematosus
A chronic autoimmune disease.
Villous atrophy
Wasting or flattening of the villi.
Vomiting
Vomiting in infants and children is a common problem and therefore likely to be experienced by the majority of families and all children’s nurses. Causes of vomiting are diverse and are summarised in Table 28.1. This table shows that causes of vomiting differ between infants and older children. Some are associated with anatomical dysfunction requiring surgery. Other causes of vomiting can be medically managed. One common problem, which lends itself in most cases to medical management, is gastro-oesophageal reflux.
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Activity
Choose one of the problems requiring surgery:
• Using a systematic approach, plan the care the child would require before and after surgery.
• How could you make sure you adopted a family-centred approach?
You can check principles of pre- and postoperative care on the companion PowerPoint presentation.
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Go to:
and using the search facility identify:
• incidence
• pathophysiology
• diagnosis
• management
of pyloric stenosis, intussusception and Hirschsprung’s disease.
You can find images of most of the conditions mentioned at:
Infant | Older child/adolescent |
---|---|
Overfeeding (> 200 mL/kg/day) | Gastroenteritis |
Gastrointestinal obstruction | |
Pyloric stenosis | |
Duodenal or ileal atresia | |
Congenital malrotation | |
Hirschsprung’s disease | |
Meconium ileus (in cystic fibrosis) | |
Intussusception | |
Gastro-oesophageal reflux | Systemic infection |
Whooping cough | Raised intracranial pressure |
Systemic infection (e.g. urinary tract) | Migraine Bulimia Poisoning Pregnancy |
Gastro-oesophageal reflux
Gastro-oesophageal reflux (refluxing of stomach contents into the oesophagus) is frequently seen, to varying degrees, in infants.
Aetiology
The most common cause is functional immaturity of the gastro-oesophageal sphincter. It is more frequently seen in children with a neurological condition, such as cerebral palsy, and also in children with Down syndrome. Whereas mild reflux (possetting) is generally harmless (although it increases the amount of laundry!) it becomes problematic when associated with failure to thrive or complications develop. These include oesophageal scarring, due to refluxing of gastric acid, which can lead to strictures. There is also the risk of aspiration and potentially apnoea. Diagnostic investigations aim to assess any aspiration risk, degree of severity and structural abnormality such as hiatus hernia.
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Look at the diagram showing relevant anatomy and position of affected sphincter at:
Diagnosis
Diagnostic investigations include:
• contrast studies: show degree of reflux, strictures, altered anatomy of oesophageal junction
• 24-hour pH probe studies: detect presence of gastric acid in oesophagus
• ultrasound of gastro-oesophageal junction: can demonstrate reflux but no other anatomical defects
• radionuclide scan: aspiration.
Management
Management centres mainly on thickening feeds with products such as Carobel® and nursing the infant in a more upright position. In more severe cases, drugs to increase gut motility and speed stomach emptying have been used. However, the condition is viewed by some as a normal physiological variant (Bourke & Drumm 2002) and only those infants whose condition is complicated, for example, by aspiration, need further medical of surgical intervention.
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Look at the information for parents offered online by Great Ormond Street Hospital:
It is important that an accurate medical and nursing assessment is made of infants and children presenting with vomiting to identify and treat quickly any significant underlying medical problems. Key points to consider are (Miall et al 2003):
• the overall state of the child, including level of consciousness, circulatory and respiratory function. Does the child need urgent resuscitation?
• feeding history: the child who is being overfed and vomiting the excess will seem happy and thriving, as will a child with some minor regurgitation. However, other more serious causes of vomiting will lead to weight loss, failure to thrive and, in more severe cases, potentially dehydration and death
• pattern of vomiting, e.g. projectile vomiting presenting from 3 to 6 weeks may indicate pyloric stenosis. Bile-stained vomiting is suggestive of obstruction and needs further investigation as a matter of urgency
• vomiting following paroxysms of coughing is suggestive of whooping cough: check immunisation status
• access to poisons such as medication, alcohol and other chemicals
• febrile: infection both within and outside of the gastrointestinal systems can cause vomiting. If diarrhoea is present, gastroenteritis is likely. If not it is useful to consider urinary tract infection, meningitis and middle ear infection.
Key investigations are summarised in Table 28.2.
Investigation | Significance |
---|---|
Urea and electrolytes | Imbalance in gastroenteritis and pyloric stenosis |
Chloride | Depleted in pyloric stenosis |
pH and bicarbonate | Metabolic alkalosis common in pyloric stenosis |
Toxicology | If poisoning suspected or to exclude |
pH monitoring and barium swallow | To show gastro-oesophageal reflux |
Presence of gastric peristalsis during feeding and presence of pyloric tumour on palpation | Indicate pyloric stenosis |
Bile-stained vomit | Intestinal obstruction |
Urine for culture | Presence of infection |
Diarrhoea: acute and chronic
As with vomiting, diarrhoea is also a common childhood problem and may be experienced in conjunction with vomiting or on its own. Causes of diarrhoea can be broadly categorised as infectious, inflammatory/allergy mediated or due to malabsorption.
Acute infectious diarrhoea
Acute infectious diarrhoea is a common medical problem of childhood accounting for significant numbers of hospital admissions. Although most cases are an unpleasant and debilitating experience, poor management – particularly in the vulnerable young child or in severe cases – can lead to life-threatening dehydration. It is a major cause of morbidity and mortality in developing countries.
Causative organisms
These can be both viral and bacterial, with trends in seasonal causes seen and a correlation between age group and vulnerability to type of organisms. A summary is shown in Table 28.3.
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Other less common bacterial causes of diarrhoea include Yersinia enterocolitica, Vibrio cholerae, staphylococci and Clostridium spp:
• What can you find out about these organisms?
Organism | Epidemiology/pathology | Symptoms |
---|---|---|
Rotavirus | Most common causative organism in UK, Particularly affecting the under 2s More common in cooler times of year Damages mucosa with severe inflammatory changes Incubation 1–3 days Transmission: faecal/oral | Fever >38°C for approx. 48 hours Vomiting, profuse watery diarrhoea, may last up to a week |
Adenovirus | Second most common viral cause, most common in younger age groups More common in cooler months Mucosal damage (check if Norwalk group) Incubation within 24 hours Transmission: faecal/oral, person to person or droplet | May have associated respiratory infection Diarrhoea not usually vomiting |
Giardia (protozoan) | Most common cause of non-bacterial diarrhoea in North America Favours cool moist conditions More common in children May be asymptomatic carriers Pathophysiology not proven – suspect either produces toxin or causes mechanical obstruction of the absorptive surface of intestine Incubation up to 1 week Transmission: contaminated food, water sources, person to person | Diarrhoea average 1 week May be longer and may be transient or persistent disaccharide intolerance |
Escherichia coli | Common in newborns More common in summer Produces toxins, which bind to mucosal villi and cause profuse secretion of water and electrolytes. Can also invade and destroy epithelium Incubation variable Transmission: contaminated and undercooked food, person to person | Fever, green watery and explosive diarrhoea, abdominal distension Usually settles 3–10 days Note: E. coli 157 also causes abdominal cramps, haemorrhagic colitis and haemolytic uraemic syndrome |
Salmonella spp | More common in toddler age groups More common in summer Invades connective tissue of small bowel and colon – local inflammation and secretion of fluids. Local oedema Incubation period 6–72 hours Transmission: carried in poultry, eggs and other food sources; also by pets | Variable degrees of symptoms, including fever and chills, vomiting cramps and diarrhoea (may be bloody) Can have infection at other sites causing local symptoms or septicaemia Note: S. typhi causes fever, fatigue, cough, diarrhoea and weight loss |
Shigella | More common in toddler age groups More common in late summer Causes enterotoxin production – see above Incubation 1–7 days Transmission: person to person or fomites | Sudden high fever Abdominal cramps Watery diarrhoea with mucus and blood May also have headache, neck stiffness and potential for convulsions with fever |
Campylobacter jejuni | More common in toddler age groups and young adults More common in late summer Enterotoxin production and loss of absorptive surface from villi Incubation 1–7 days Transmission: birds are most common host. Carried on foods and milk | Fever, watery or sticky diarrhoea may be blood and leucocytes Vomiting Usually self-limiting rarely leads to complications such as haemolytic uraemic syndrome, septicaemia Infectivity can be limited with erythromycin |
As most acute episodes of gastroenteritis are self-limiting, management focuses primarily on assessment of the degree of dehydration and replacing fluid loss. This is successfully achieved in most cases with the use of oral rehydration solution (ORS). Other factors to consider from a nursing perspective include enabling family management of the child with an acute attack at home and education to minimise the risk of further episodes that might be caused, for example, by poor food handling and preparation techniques. If the child is admitted, minimising the risk of infection to other patients is also of considerable importance.
Although acute gastroenteritis is the most common cause of diarrhoea, particularly in the preschool child, other causes of diarrhoea could be considered.
Reflect on your practice
Reflect on your practice
• What nursing interventions can you implement to reduce the risk of infection to others in the ward environment?
• How can you ensure that resident family is not posing an infection threat?
• Using Paediatric Early Warning Scoring Systems (Haines et al 2005), what signs would alert you to a deteriorating child?
You will find additional guidance in the Royal College of Nursing (RCN) publication ‘Good practice in infection control’ (RCN 2004).
Malabsorption and food allergies
Cystic fibrosis
Aetiology
Cystic fibrosis (CF) is an autosomal recessive inherited disorder. It is more common in the Caucasian population, and currently affects 1:2500 live births in the UK. The gene responsible is located on the long arm of chromosome 7, with <F508 being the most common mutation, although 900 other variations were found between 1989 and 2001 (Cystic Fibrosis Trust 2001); 1 in 20 individuals is likely to be a carrier.
The disease primarily affects the exocrine glands. Sufferers do not have normal life expectancy, although this is improving with treatment advances.
Activity
Activity
Check your understanding of autosomal recessive inheritance. Draw a diagram to illustrate this and check if you are correct by checking on the companion PowerPoint presentation.
Exocrine glands regulate production of sweat and mucous. Affected individuals may present with varying symptoms, dependent on the degree of severity. Symptoms commonly include digestive and respiratory problems but overall can include:
• shortness of breath
• persistent cough
• hyperhydrosis (excessive sweating)
• limited lung capacity
• ‘salty’ skin
• wheezing
• abdominal pain
• pneumonia
• excessive appetite but little weight gain
• large, foul-smelling stools
• diarrhoea
• impaired fertility
• reduced bone mass.
Children affected by cystic fibrosis, regardless of symptom severity, have increased sodium and chloride levels in saliva and sweat. Children with cystic fibrosis are unable to effectively reabsorb sodium and chloride leading to increased losses, particularly in warmer conditions. This creates an increased risk of dehydration, hypochloraemia and hyponatraemia.
Symptoms are caused by production of viscous mucous, which accumulates, obstructing the mucous-secreting glands in affected organs. There is also obstruction of small passages, namely the bronchioles of the lungs, pancreatic and biliary ducts.