Paediatric GI Disorders Flashcards

1
Q

What other symptoms can be associated with chronic constipation in children?

A
Poor appetite
Irritable
Lack of energy
Abdominal pain or distension
Withholding or straining
Diarrhoea
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2
Q

What are some common causes of chronic constipation in children?

A

Social- poor diet, potty training/school toilet anxieties
Physical- intercurrent illness/medication
Family history
Psychological- including abuse
Organic

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3
Q

Describe the pathophysiology of worsening chronic constipation

A

Cycle in constipation; holding stools causes larger/harder stool, which leads to a more painful bowel movement, which leads to fecal holding. Chronic fecal holding can cause excessive stretching of the colon and a megarectum.

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4
Q

How is chronic constipation treated?

A

Explanation
Make sure stools don’t get hard again
Re-train bowel
Remove impaction- movicol impaction (first few days really unpleasant),
Social factors- diet
Psychological- reduce aversive factors, make going to the toilet a pleasant experience, reward good behaviour and retrain bowel
Soften stool and stimulate defecation- osmotic laxative (lactulose or movicol/laxido to soften stool) or stimulant laxatives (senna, picosulphate to aggravate bowel and make it start to notice presence of stools again) Keep treatment going for how long constipation has been present (ie 3 month history = 3 month treatment)

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5
Q

Why are incidences of colectomies higher in paediatric IBD than adult?

A

Crohn’s and ulcerative colitis are generally both much worse than adult presentations. Pancolitis is very common in paediatric IBD

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6
Q

What is the commonest presentation of Crohn’s disease in children?

A

Pan-enteric disease

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7
Q

What are the symptoms of ulcerative colitis in children?

A
Diarrhoea
Rectal bleeding 
Abdominal pain
Fever
Weight loss
Growth failure
Arthritis
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8
Q

How do symptoms of crohn’s and ulcerative colitis vary from each other in children?

A

Crohns has similar symptoms to ulcerative colitis but vary depending on where the disease is. Systemic symptoms are more common in Crohns than UC and diarrhoea/rectal bleeding are less common in Crohns. Abdominal masses can be present in crohns but generally not so in UC

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9
Q

How is IBD diagnosed in children?

A

History and examination- exclude infection, extra-intestinal manifestations, growth and sexual development
Laboratory investigations- FBC, inflammatory markers, fecal calprotectin (normal FC rules out IBD), ESR
Definitive investigations- colonoscopy + endoscopy, MRI, mucosal biopsy, capsule endoscopy, enteroscopy

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10
Q

What are the aims of treatment of paediatric IBD?

A

Induce and maintain remission
Correct nutritional deficiencies (iron, Vit D)
Maintain normal growth and development
Promote quality of life and normal psycho-social development

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11
Q

How is paediatric Crohn’s treated?

A

Induce remission- Nutritional therapy first line, steroids second line
Maintain remission- Thiopurines
Step-up therapy- Anti-TNF
Surgery- For complications, not curative

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12
Q

How is ulcerative colitis treated?

A

Induce remission- 5-ASA first line, steroids second line
Maintain remission- 5-ASA first line, thiopurines second line
Step-up therapy- anti-TNF
Surgery- for failure to respond to medical therapy. Is curative

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13
Q

What are the types of vomiting in children?

A

Vomiting with retching
Projectile vomiting
Bilious vomiting
Effortless vomiting

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14
Q

What are the phases of vomiting with retching and what is each characterised by?

A

Pre-ejection: pallor, nausea + tachycardia
Ejection: retching and vomiting
Post-ejection: weakness, lethargy + shivering

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15
Q

What are the possible stimulants of the vomiting centre in children?

A
Enteric pathogens
Intestinal inflammation
Metabolic disorder
Infection
Head injury
Visual stimuli
Middle ear stimuli
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16
Q

Who is pyloric stenosis most common in?

A

Babies 4-12 weeks

Boys > girls

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17
Q

What are the symptoms of pyloric stenosis?

A

Projectile, non-bilious vomiting (important to clarify that vomit is white/clear- NOT green as this indicates presence of bile)
Weight loss
Dehydration +/- shock

18
Q

What is the characteristic electrolyte disturbance associated with pyloric stenosis?

A

Metabolic alkalosis
Hypochloraemia
Hypokalaemia

19
Q

What are the causes of bilious vomiting in children?

A
Usually intestinal obstruction, which can be caused by:
•Intestinal atresia (in newborns only)
•Malrotation +/- volvulus
•Intussusception 
•Ileus
•Crohn’s disease with strictures
20
Q

What investigations can be useful in bilious vomiting?

A

Abdominal x-ray
Consider contrast meal
Surgical opinion re exploratory laparotomy

21
Q

What is the most common cause of effortless vomiting?

A

Almost always oesophageal reflux

22
Q

In what paediatric cases will gastro-oesophageal reflux not be self-limiting?

A

Cerebral palsy
Progressive neurological problems
Oesophageal atresia +/- TOF operated
Generalised GI motility problem

23
Q

What are the presenting symptoms of reflux?

A
Vomiting 
Haematemesis
Feeding problems
Failure to thrive
Apnoea
Cough
Wheeze
Chest infection
Sandifer’s syndrome (GORD + spastic torticollis (involuntary movements of neck) + dystonia)
24
Q

How is paediatric reflux assessed medically?

A

History and examination often sufficient
Radiology- video fluoroscopy, barium swallows
pH study
Oesophageal impedance monitoring
Endoscopy (always done under GA in paediatrics)

25
Q

How is reflux treated?

A
Feeding advice (thickeners for liquids, behavioural programmes, feeding positions)
Nutritional support (calorie supplements, exclusion diets (ie milk), NG tubes, gastrostomy)
Medical treatment (prokinetic drugs, acid suppressant drugs)
Surgery (if persistent GORD or failure of medical therapy, Nissen fundoplication)
26
Q

How is acute, persistent chronic diarrhoea defined?

A

4 or more loose stools per day
Persists for one week- acute
Persists for two to four weeks- persistent
Persists for more than 4 weeks- chronic

27
Q

What are the causes of diarrhoea in children?

A

Motility disturbance- Toddler diarrhoea, irritable bowel syndrome
Active secretion/osmotic- Acute infective diarrhoea, irritable bowel disease
Malabsorption of nutrients/secretory- Food allergy, coeliac disease, cystic fibrosis

28
Q

What are the main types of diarrhoea in paediatrics?

A

Osmotic
Secretory
Motility
Inflammatory

29
Q

What is osmotic diarrhoea?

A

Movement of water into bowel to equilibrate osmotic gradient
Usually a feature of malabsorption
Clinical remission with removal of causative agent

30
Q

What is secretory diarrhoea?

A

Classically associated with toxin production from bacteria

31
Q

What is motility diarrhoea?

A

Classical toddler’s diarrhoea

Other causes include IBS, congenital hyperthyroidism and chronic intestinal pseudo-obstruction

32
Q

What is inflammatory diarrhoea?

A

Mixed bag
Malabsorption due to intestinal damage
Secretory effect of cytokines
Protein exudate across inflamed epithelium

33
Q

What are the features of osmotic diarrhoea?

A
Stool volume- Small (<200ml/24hrs)
Response to fasting- Diarrhoea stops
Stool sodium <70 mmol/L
Stool potassium <30 mmol/L
Stool chloride	<35 mmol/L
Stool pH	<5.5 mmol/L
34
Q

What are the features of secretory diarrhoea?

A
Stool volume- Large (>200ml/24hrs)
Response to fasting- Diarrhoea continues
Stool sodium >70 mmol/L
Stool potassium >40 mmol/L
Stool chloride	>40 mmol/L
Stool pH	>6 mmol/L
35
Q

What are the causes of fat malabsorption?

A

Pancreatic disease- typically CF

Hepatobiliary disease- chronic liver disease, cholestasis

36
Q

What is the incidence of coeliac disease?

A

~1% of the western population

37
Q

What are the symptoms of coeliac disease?

A
Abdominal bloating
Diarrhoea
Failure to thrive
Short stature
Constipation
Tiredness 
Dermatitis herpatiformis
38
Q

How is coeliac disease investigated?

A
Serological screens (anti-tissue transglutaminase, anti-endomysial, anti-gliadin)
Duodenal biopsy (gold standard- should rarely diagnose without)
Genetic testing (HLA DQ2, DQ8)
39
Q

What are the histological features of coeliac disease?

A

Lymphocytic infiltration of surface epithelium
Partial/total villous atrophy
Crypt hyperplasia

40
Q

When can coeliac disease be diagnosed without a biopsy?

A
If ALL of the following are present:
•Symptomatic child
•Anti TTG >10 times upper limit of normal
•Positive anti-endomysial antibodies
•HLA DQ2, DQ8 +ve
41
Q

How is coeliac disease managed?

A

Gluten free diet for life

42
Q

What is a possible complication of untreated coeliac disease?

A

Small bowel lymphoma