23 - Gastroenterology Flashcards
Coeliac’s disease has a prevalence of 1% in children (1:100). What is the pathophysiology of coeliac’s disease?
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
What are some associations with coeliac disease?
- Down’s syndrome
- Type 1 diabetes
- Thyroid disease
- Other autoimmune conditions e.g RA, Addison’s
How may coeliac disease present in a child?
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
What are some differentials for coeliac’s?
Think of other malabsorption conditions
- Cystic fibrosis
- Inflammatory bowel disease
- Post – gastroenteritis
- Autoimmune enteropathy
- Eosinophilic enteritis
What genetic associations are found in coeliac’s and what auto-antibodies are found?
(image important)
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)
What investigations are done to diagnose coeliac’s disease?
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
What are the indications for coeliac serology in children?
- 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
How is coeliac disease managed in children?
- Life-long gluten free diet
- Annual follow up to check for symptoms, diet compliance, development, growth and long term complications
What are some complications of coeliac’s disease if left unmanaged?
- Anaemia
- Osteoporosis
- Malignancy (Non Hodgkin Lymphoma, EATL, Small bowel adenocarcinoma)
- Infertility
What is the epidemiology and pathophysiology of GORD in children?
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
What are some risk factors for GORD in children?
- Prematurity
- Parental history of heartburn
- Obesity
- Hiatus hernia
- History of congenital diaphragmatic hernia
- History of congenial oesophageal atresia
- Neurodisability (eg. cerebral palsy)
How may GORD present in children?
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
What are some differentials for GORD in infants?
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
How is GORD investigated and managed?
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)
What is the medical management for GORD in infants?
- Alginate mixed with water and feed (Gaviscon)
- If not resolved with this in 2 weeks then trial PPI (Omeprazole) or H2 antagonist (Ranitidine)
If GORD is severe, what investigation is done before fundoplication?
- Barium Meal
- Endoscopy
Only do fundoplication if failure to thrive or apneas
What are some complications with GORD?
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
What is Sandifer’s syndrome?
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
What are some red flags that point away from GORD to another diagnosis?
- 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
What is important to ask in the history if you suspect GORD?
Feeding history
When should a baby with GORD be admitted?
- Haematemesis
- Malena
- Dysphagia
What are the differences between UC and Crohn’s, both being forms of IBD with periods of exacerbation and remission?
NESTS
UC-CLOSE UP
How does IBD tend to present in children?
- Poor growth
- Diarrhoea
- Abdominal pain
- Bleeding
- Weight loss
- Anaemia
- Fever
What are some extra-intestinal manifestations of IBD in children?
- Finger clubbing
- Erythema nodosum
- Pyoderma gangrenosum
- Episcleritis and iritis
- Inflammatory arthritis
- Primary sclerosing cholangitis (UC)
What investigations are done for IBD in children?
- 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
How is IBD generally managed in children?
- 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
What is the medical management for Crohn’s?
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
When should children with Crohn’s be referred for surgery?
- If just affects distal ileum then resect
- Surgery can also be used to treat strictures and fistulas secondary to Crohn’s
What is the medical management for UC?
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
What surgery can be done for UC?
- Panproctocolectomy: left with either a permanent ileostomy or something called an ileo-anal anastomosis (J-pouch)