23 - Gastroenterology Flashcards

1
Q

Coeliac’s disease has a prevalence of 1% in children (1:100). What is the pathophysiology of coeliac’s disease?

A

Autoimmune condition where exposure to gluten causes an immune reaction that creates inflammation in the small intestine

Autoantibodies (Anti-TTG and anti-EMA) are created in response to gluten that target the epithelial cells of the intestine and lead to inflammation

Usually in jejunum, causes atrophy of the intestinal villi so malabsorption

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2
Q

What are some associations with coeliac disease?

A
  • Down’s syndrome
  • Type 1 diabetes
  • Thyroid disease
  • Other autoimmune conditions e.g RA, Addison’s
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3
Q

How may coeliac disease present in a child?

A

Younger children tend to have GI symptoms but older children have extra GI symptoms. Can present at any age

  • Asymptomatic
  • Failure to thrive
  • Diarrhoea/Steatorrhea
  • Weight loss
  • Abdominal pain
  • Fatigue
  • Mouth ulcers
  • Anaemia secondary to iron, B12 or folate deficiency (in older children)
  • Dermatitis herpetiformis
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4
Q

What are some differentials for coeliac’s?

A

Think of other malabsorption conditions

  • Cystic fibrosis
  • Inflammatory bowel disease
  • Post – gastroenteritis
  • Autoimmune enteropathy
  • Eosinophilic enteritis
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5
Q

What genetic associations are found in coeliac’s and what auto-antibodies are found?

(image important)

A

Genetic

  • HLA-DQ2 gene (90%)
  • HLA-DQ8 gene

Auto-antibodies (ALWAYS TEST FOR TOTAL IGA TOO)

  • Tissue transglutaminase antibodies (anti-TTG)
  • Endomysial antibodies (EMAs)
  • Deaminated gliadin peptides antibodies (anti-DGPs)
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6
Q

What investigations are done to diagnose coeliac’s disease?

A

Patient must remain on gluten diet during investigations for at least 6 weeks before as otherwise may not detect antibodies

  • Total immunoglobulin A levels: to exclude IgA deficiency
  • Anti-TTG antibodies (first choice)
  • Anti-endomysial antibodies
  • Endoscopy and intestinal biopsy: If positive serology. Crypt hypertrophy and villous atrophy
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7
Q

What are the indications for coeliac serology in children?

A
  • Persistent unexplained abdominal or gastrointestinal symptoms
  • Faltering growth
  • Prolonged fatigue
  • Unexpected weight loss
  • Severe or persistent mouth ulcers
  • Unexplained iron, vitamin B12 or folate deficiency
  • Type 1 diabetes, at diagnosis
  • Autoimmune thyroid disease, at diagnosis
  • First‑degree relatives of people with coeliac disease
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8
Q

How is coeliac disease managed in children?

A
  • Life-long gluten free diet
  • Annual follow up to check for symptoms, diet compliance, development, growth and long term complications
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9
Q

What are some complications of coeliac’s disease if left unmanaged?

A
  • Anaemia
  • Osteoporosis
  • Malignancy (Non Hodgkin Lymphoma, EATL, Small bowel adenocarcinoma)
  • Infertility
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10
Q

What is the epidemiology and pathophysiology of GORD in children?

A

Only GORD if symptomatic, can be asymptomatic which is physiological called GOR

Epidemiology

  • Occurs in 40% of infants in first 2 weeks as LOS still developing until 6 months
  • 1% of children under 13 have it

Pathophysiology

  • Low tone of lower oesophageal sphincter so reflux out of stomach to oesophagus
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11
Q

What are some risk factors for GORD in children?

A
  • Prematurity
  • Parental history of heartburn
  • Obesity
  • Hiatus hernia
  • History of congenital diaphragmatic hernia
  • History of congenial oesophageal atresia
  • Neurodisability (eg. cerebral palsy)
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12
Q

How may GORD present in children?

A

Frequent effortless regurgitation of feeds is normal

  • Chronic cough
  • Hoarse cry
  • Back arching
  • Drawing knees to chest
  • Excess crying or unsettled after feeding
  • Reluctance to feed
  • Pneumonia
  • Poor weight gain
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13
Q

What are some differentials for GORD in infants?

A

If onset is >6 months of age or symptoms persist beyond 1 year then reflux is unlikely

  • Pyloric stenosis: Frequent, forceful (projectile) vomiting in <2 month olds
  • Intestinal obstruction: bile-stained vomit,
  • Upper GI bleed: haematemesis
  • Sepsis
  • Raised ICP: rapidly increasing head circumference (>1cm per week), persistent headache and vomiting following periods of recumbence
  • UTI
  • CMPA
  • Possetting
  • Overfeeding
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14
Q

How is GORD investigated and managed?

A

Ix

  • No investigation if feeding and gaining weight
  • Rule out other causes e.g urine dipstick

Mx

  • Conservative (advice on keeping baby upright, burping after feeds, thickened formula)
  • Medical (Infant gaviscon, omeprazole)
  • Surgical in severe cases (fundoplication)
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15
Q

What is the medical management for GORD in infants?

A
  • Alginate mixed with water and feed (Gaviscon)
  • If not resolved with this in 2 weeks then trial PPI (Omeprazole) or H2 antagonist (Ranitidine)
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16
Q

If GORD is severe, what investigation is done before fundoplication?

A
  • Barium Meal
  • Endoscopy

Only do fundoplication if failure to thrive or apneas

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17
Q

What are some complications with GORD?

A

90% of infants will spontaneously resolve within the first year of life as they change diet and start to sit upright

  • Reflux oesophagitis
  • Recurrent aspiration pneumonia
  • Recurrent acute otitis media (>3 episodes in 6 months)
  • Dental erosion (especially in children with neurodisability)
  • Apnoea
  • Apparent life-threatening events (ALTE): apnoea, colour change, change in muscle tone, choking and gagging
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18
Q

What is Sandifer’s syndrome?

A

Brief episodes of abnormal movements associated with GORD in infants. The infants are usually neurologically normal

  • Torticollis: forceful contraction of the neck muscles causing twisting of the neck
  • Dystonia: abnormal muscle contractions causing twisting movements, arching of the back or unusual postures

Tends to resolve as reflux resolves but refer to rule out infantile spasms and seizures

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19
Q

What are some red flags that point away from GORD to another diagnosis?

A
  • Frequent, forceful (projectile) vomiting
  • Bile-stained (green or yellow-green) vomit
  • Abdominal distension, tenderness, or palpable mass
  • Blood in vomit
  • Bulging fontanelle or altered responsiveness (for example lethargy or irritability)
  • Rapidly increasing head circumference (more than 1 cm each week); persistent morning headache and vomiting worse in the morning
  • Blood in the stool
  • Chronic diarrhoea
  • Dysuria
  • Appearing unwell or fever
  • Onset of regurgitation and/or vomiting after 6 months of age or persisting after 1 year of age
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20
Q

What is important to ask in the history if you suspect GORD?

A

Feeding history

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21
Q

When should a baby with GORD be admitted?

A
  • Haematemesis
  • Malena
  • Dysphagia
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22
Q

What are the differences between UC and Crohn’s, both being forms of IBD with periods of exacerbation and remission?

A

NESTS

UC-CLOSE UP

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23
Q

How does IBD tend to present in children?

A
  • Poor growth
  • Diarrhoea
  • Abdominal pain
  • Bleeding
  • Weight loss
  • Anaemia
  • Fever
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24
Q

What are some extra-intestinal manifestations of IBD in children?

A
  • Finger clubbing
  • Erythema nodosum
  • Pyoderma gangrenosum
  • Episcleritis and iritis
  • Inflammatory arthritis
  • Primary sclerosing cholangitis (UC)
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25
Q

What investigations are done for IBD in children?

A
  • Blood tests for anaemia, infection, thyroid, kidney and liver function. A raised CRP indicates active inflammation
  • Faecal calprotectin
  • Endoscopy (OGD and colonoscopy) with biopsy: gold standard
  • Imaging with ultrasound, CT and MRI can be used to look for complications such as fistulas, abscesses and strictures
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26
Q

How is IBD generally managed in children?

A
  • Any child presenting with symptoms of IBD should be referred to secondary care for specialist assessment and management with MDT
  • Monitor growth and pubertal development especially when treated with steroids. Get dietician input
  • Inducing remission during flares and maintaining remission
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27
Q

What is the medical management for Crohn’s?

A

Inducing Remission

  • Steroids: First line e.g. oral prednisolone or IV hydrocortisone).
  • Immunosupressants: if above doesn’t work

Maintaining Remission

  • First line: Azathioprine or Mercaptopurine
  • Second Line: Methotrexate, Infliximab, Adalimumab
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28
Q

When should children with Crohn’s be referred for surgery?

A
  • If just affects distal ileum then resect
  • Surgery can also be used to treat strictures and fistulas secondary to Crohn’s
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29
Q

What is the medical management for UC?

A

Inducing Remission

Mild to moderate disease

  • First line: aminosalicylate (e.g. mesalazine oral or rectal)
  • Second line: corticosteroids (e.g. prednisolone)

Severe disease

  • First line: IV corticosteroids (e.g. hydrocortisone)
  • Second line: IV ciclosporin

Maintaining Remission

  • Aminosalicylate (e.g. mesalazine oral or rectal)
  • Azathioprine
  • Mercaptopurine
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30
Q

What surgery can be done for UC?

A
  • Panproctocolectomy: left with either a permanent ileostomy or something called an ileo-anal anastomosis (J-pouch)
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31
Q

What monitoring needs to be done for children with UC?

A
  • Bone health
  • Height and body weight plotted on growth chart
  • Pubertal development
32
Q

What is the definition of constipation in children and some of the causes for this?

A

Less than 3 stools per week or significant difficulty passing stool

  • Idiopathic (most common, lifestyle issues e.g lack of fibre, dehydrated)
  • Hirschprung’s
  • CF
  • Hypothyroidism
  • Cow’s milk intolerance
  • Anal stenosis
  • Sexual abuse
33
Q

What are some typical features in the history for constipation in children?

A
  • Hard stools that are difficult to pass
  • Rabbit dropping stools
  • Straining and painful passages of stools
  • Abdominal pain
  • Holding an abnormal posture, referred to as retentive posturing
  • Rectal bleeding associated with hard stools
  • Overflow soiling
  • Hard stools may be palpable in abdomen
34
Q

What is encopresis?

A

Faecal incontinence, usually a sign of chronic constipation where the rectum becomes stretched and loses sensation. Not pathological until 4 years

Other rarer causes of encopresis include:

  • Spina bifida
  • Hirschprung’s disease
  • Cerebral palsy
  • Learning disability
  • Psychosocial stress
  • Abuse
35
Q

What are some lifestyle factors in children that lead them to become constipated?

A
  • Habitually not opening the bowels so lose sensation
  • Low fibre diet
  • Poor fluid intake and dehydration
  • Sedentary lifestyle
  • Psychosocial problems such as a difficult home or school environment
  • Pain or anal fissure
36
Q

What are some red flags in children when they have constipation that point away from a diagnosis of idiopathic constipation?

A
  • Not passing meconium within 48 hours of birth: CF or Hirschsprung’s
  • Neurological signs or symptoms: cerebral palsy or spinal cord lesion
  • Vomiting: intestinal obstruction or Hirschsprung’s
  • Ribbon stool: anal stenosis
  • Abnormal anus: anal stenosis, IBD or sexual abuse
  • Abnormal lower back or buttocks: spina bifida
  • Failure to thrive: coeliac disease, hypothyroidism or safeguarding
  • Acute abdominal pain and bloating: obstruction or intussusception
37
Q

What might you find on examination of a child with constipation?

A
  • Distended abdomen
  • Hard mass in abdomen (faeces)
  • Anal fissure
  • Haemorrhoids
38
Q

Before treating a child with constipation what needs to be done?

A

Assessed for faecal impaction:

  • Symptoms of severe constipation
  • Overflow soiling
  • Faecal mass palpable in the abdomen (only specialist can do DRE)
39
Q

What are the general points of management in idiopathic constipation?

A
  • Correct any reversible factors, e.g high fibre diet and good hydration
  • Start maintenance laxatives
  • Disimpaction regime if faecal impaction
  • Good toilet habits e.g praise, toilet scheduling, star charts
40
Q

What lifestyle changes can parents make for children with idiopathic constipation?

A

ERIC PROGRAMME

  • High fibre diet
  • High fluid intake
  • Regular toileting e.g after meals, before bed
  • Toilet positioning
  • Exercise
  • Praise for going to toilet
41
Q

What is the disimpaction regime?

A
  • Escalating doses of polyethene glycol 3350+electrolytes (Movicol)
  • If no disimpaction after 2 weeks add a stimulant laxative
  • Warn parents will make it worse before better and may have soiling
42
Q

What is the maintenance regime for constipation?

A
  • Movicol first line
  • Stimulant added if above not working
  • Stay on laxative for a few weeks after regular bowel habit established then slowly reduce
43
Q

What are some examples of functional GI disorders in children?

A

Always be careful not to miss diagnoses like IBD, always recheck for them every few months, especially if growth issues

44
Q

What is the pathophysiology of functional GI disorders in children and how can this guide our treatment?

A

Psychological intervention is important

45
Q

What is the criteria for abdominal migraine in children?

A

May occur in young children before they develop traditional migraines as they get older

Episodes of central abdominal pain lasting more than 1 hour. Examination will be normal.

There may be:

  • Nausea and vomiting
  • Anorexia
  • Pallor
  • Headache
  • Photophobia
  • Aura
46
Q

How does mesenteric adenines present?

A

Diffuse central abdominal pain in the context of a previous URTI

US abdo will show enlarged mesenteric lymph nodes with a normal appendix.

Will improve spontaneously, appendicitis will not

47
Q

What is oesophageal atresia?

A
  • Blind-ending oesophagus
  • Associated with tracheooesophageal fistula
  • More common in trisomies – Downs/Pataus/Edwards
  • VACTERL
48
Q

How may oesophageal atresia present?

A
  • Polyhydramnios
  • Difficulty feeding
  • Overflow saliva and blowing bubbles
  • Choking and cyanotic spells
49
Q

How is oesophageal atresia diagnosed and managed?

A
  • Inability to pass a catheter into the stomach, X-rays show it coiled in the oesophagus
  • Stop feeding and suck out any oesophageal pouch
  • Primary surgical repair and look for other anomalies (50% have VACTERL)
50
Q

What is gastroschisis and how is it managed?

A

Anterior abdominal wall defect to the side of the umbilicus with evisceration of the bowel and no covering of the bowel

Management

  • Vaginal delivery may be attempted
  • At delivery, cover exposed bowel in clingfilm, keep the baby warm and hydrated and aim to close the defect surgically as soon as possible, may be staged procedure
  • Need TPN for few weeks
51
Q

What is exomphalos and how is it managed?

A

Abdominal contents protrude through the anterior abdominal wall but are covered in an amniotic sac formed by amniotic membrane and peritoneum

Associations

  • Beckwith-Wiedemann syndrome
  • Down’s syndrome
  • Cardiac and kidney malformations

Management

  • C-section to reduce the risk of sac rupture
  • Staged repair with loose elastic bandage at 6-12 months, harder than gastroschisis
52
Q

How may an infant with hepatitis present?

A
  • Asymptomatic
  • Jaundice
  • Poor growth
  • Splenomegaly
  • Enlarged liver
53
Q

How do you distinguish hepatitis from biliary atresia in children?

A

In biliary atresia baby is growing normally and does not have enlarged spleen but this is opposite in hepatitis

Also blood tests and liver biopsy can help tell the difference

54
Q

What are some causes and how is hepatitis treated in children?

(image important)

A
  • Vitamin supplements
  • Phenobarbital to control seizures but also stimulates liver to excrete additional bile
  • Hepatitis A virus usually resolves itself within six months
  • If cirrhotic then liver transplant
55
Q

Can a mother with Hep B or C breastfeed?

A

Yes - vaccinate baby for Hep B at 2, 3, 4 months but no vaccine for Hep C

56
Q

What is the criteria for acute liver failure in children?

A

Rapid decline of hepatic function, jaundice, coagulopathy (INR >1.5) and hepatic encephalopathy in patients with no evidence of previous liver disease.

57
Q

What are some causes of acute liver failure in children?

A

Viral and bacterial infections: CMV, EBV, Herpes, Parvovirus, Hep B/C

Metabolic disorders: mitochondrial disorder, galactosemia and tyrosinemia

Toxic hepatitis: mushrooms, acetaminophen, valproate or fluconazole

58
Q

What investigations are done for acute liver failure in children?

A
  • FBC
  • G+S
  • U+Es and CRP
  • LFTs, GT and conjugated bilirubin
  • Blood glucose
  • Arterial blood gas
  • Blood for toxicology (including paracetamol level)
  • Urine metabolic screen (less than 5 years)
  • Autoantibodies ANA/SMA/LKM
  • Coeliac (EMA and TTGA)
  • Serology (Hep A,B,C, E)
  • Opthalmology (Kayser-Fleischer rings, chorioretinitis, cataracts, specific signs of metabolic disorders)
59
Q

What is the management for acute liver failure in children?

A

General

  • Daily IV Vit K
  • Ranitidine IV or orally/NG
  • Lactulose TDS to achieve BO 3-4x per day
  • If signs of encephalopathy nurse with head elevated at 10-20 degrees
  • If encephalopathy grade 3 or above requires ventilation and sedation
  • Maintain circulating volume and avoid fluid overload
  • Make sure fluids have glucose in to keep blood glucose >4.5
60
Q

What are the criteria for liver transplant in children?

A

Always be thinking about encephalopathy

61
Q

What are causes of diarrhoea in children?

(image important)

A

Diarrhoea usually lasts for 5-7 days and stops within 2 weeks. If >2 weeks it is chronic

  • Sepsis
  • Infections: Viral (Rotavirus), Parasitic, HUS
  • IBS
  • IBD
  • Coeliac’s
  • NEC
  • Food intolerance (Cow’s milk)
  • Toddler’s Diarrhoea (contains undigested food)
  • Thyrotoxicosis
  • Post gastroenteritis lactose intolerance
62
Q

It is rare to do tests for acute diarrhoea in children but a stool culture may be done. When do you need to do a stool culture for diarrhoea in children?

A
  • Suspect sepsis
  • Blood or mucus in stool
  • Child is immunocompromised

You should consider doing a stool culture if:

  • Recent travel abroad
  • Not stopped by day 7
63
Q

What is the most important thing to assess when a child has diarrhoea?

A

DEHYDRATION

Assess hydration status as normal, dehydrated or shocked

64
Q

What children with diarrhoea are at risk of being dehydrated?

A
65
Q

How is acute diarrhoea in children managed?

A
  • Increased fluid intake: admit for IV fluids if clinically dehydrated
  • Avoid antidiarrhoeals
  • Avoid fruit juice and carbonated drinks
  • Hygiene advice: hand washing, avoid nursery for 48 hours after last episode, do not go swimming
66
Q

If a child has chronic diarrhoea what do you need to be considering?

A
  • Coeliac’s
  • Lactose intolerance
  • Toddler’s diarrhoea (limit fruit juice)
  • IBD
  • IBS
  • Parasitic infection
67
Q

What are some causes of vomiting in children?

A
  • Posseting: effortless and normal after feeds
  • GORD
  • Over-feeding (150mL/kg/day is normal)
  • Pyloric stenosis (projectile, at ~8 weeks old)
  • Any infection, eg UTI
  • Adverse food reaction
  • Infective gastroenteritis
  • Pharyngeal pouch
  • Raised intracranial pressure
  • Intestinal obstruction
68
Q

What are some general and specific red flags for vomiting in infants?

A

General: signs of dehydration e.g drowsy or floppy, dry mucous membranes and sunken eyes

Specific

  • Projectile vomiting around 6-8 weeks of age
  • Bile-stained vomit and abdominal distention:
  • Bloody stool with vomiting
  • Paroxysmal coughing to the point of vomiting
  • Seizures/bulging fontanelle with vomiting: raised intracranial pressure
69
Q

What is very important to assess in vomiting children?

A

Are they dehydrated? Do they need IV fluids?

70
Q

What are some medical causes of abdominal pain in children?

A
71
Q

What are some surgical causes of abdominal pain in children?

A
  • Appendicitis
  • Intususseption
  • Bowel obstruction
  • Testicular torsion
72
Q

What are some red flags for serious pathology behind abdominal pain in children?

A
  • Persistent or bilious vomiting
  • Severe chronic diarrhoea
  • Fever
  • Rectal bleeding
  • Weight loss or faltering growth
  • Dysphagia
  • Nighttime pain
  • Abdominal tenderness
73
Q

Recurrent abdominal pain with no underlying cause is common in children, especially during stressful life events e.g loss of a relative or bullying. The leading theory for the cause is increased sensitivity and inappropriate pain signals from the visceral nerves in response to normal stimuli.

How can this be managed?

A
  • Distract child from pain with other activities
  • Encourage parents not to ask about or focus on the pain
  • Advice about sleep, regular meals, healthy balanced diet, staying hydrated, exercise and reducing stress
  • Probiotic supplements
  • Avoid NSAIDs such as ibuprofen
  • Address psychosocial triggers and exacerbating factors
  • Support from a school counsellor or child psychologist
74
Q

How is abdominal migraine managed?

A

Similar to adult migraines, managing acute attacks and prevention

Treating the acute attack:

  • Low stimulus environment (quiet, dark room)
  • Paracetamol
  • Ibuprofen
  • Sumatriptan

Preventative medications:

  • Pizotifen, a serotonin agonist.
  • Propranolol,
  • Cyproheptadine
  • Flunarazine
75
Q

What is the issue with taking Pizotifen for abdominal migraines?

A

Withdrawal symptoms

e.g depression, anxiety, poor sleep, tremor

Need to withdraw slowly