Gastroenterology Flashcards

1
Q

What are the typical features suggesting constipation?

A
Less than 3 stools a week
Hard stools difficult to pass
Rabbit dropping stools
Straining and painful
Abdominal pain
Holding abnormal posture - retentive posturing
Rectal bleeding with hard stools
Overflow soiling with faecal impaction
Hard stools palpable in abdomen
Loss of sensation of need to open bowels
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2
Q

What is encopresis?

A

Faecal incontinence
Not considered pathological until 4 years of age
Sign of chronic constipation because rectum is stretched and loses sensation
Loose stools leak out

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3
Q

What are rarer causes of encopresis?

A
Spina bifida
Hirschsprung's disease
Cerebral palsy
Learning disability
Psychosocial stress
Abuse
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4
Q

What lifestyle factors can cause constipation?

A
Habitually not opening bowels
Low fibre diet
Poor fluid intake and dehydration
Sedentary lifestyle
Psychosocial problems
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5
Q

What are secondary causes of constipation?

A
Hirschsprung's
Cystic fibrosis - meconium ileus
Hypothyroidism
Spinal cord lesions
Sexual abuse
Intestinal obstruction
Anal stenosis
Cows milk intolerance
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6
Q

What are the red flags indicating a serious condition causing constipation?

A

Not passing meconium within 48 hours of birth - CF or Hirschsprung’s
Neurological signs or symptoms - lower limbs
Vomiting - obstruction
Ribbon stool - anal stenosis
Abnormal anus
Abnormal lower back or buttocks
Failure to thrive - coeliac, hypothyroid, safeguarding
Acute severe abdominal pain and bloating

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7
Q

What are the complications of constipation?

A
Pain
Reduced sensation
Anal fissures
Haemorrhoids
Overflow and soiling
Psychosocial morbidity
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8
Q

What is the NICE guidelines on management of constipation if faecal impact is present?

A

Polyethylene glycol and electrolytes - Movicol Paediatric Plan
Add stimulant if does not lead to disimpaction after 2 weeks
Substitute with osmotic laxative e.g. lactulose if not tolerated

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9
Q

What is the maintenance therapy for constipation?

A

Movicol
Add stimulant laxative if no response
Substitute stimulant if not tolerated
Continue at maintenance dose for several weeks after regular bowel habit established

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10
Q

What are the red flag clinical features in the vomiting child?

A

Bile stained - obstruction
Haematemesis - oesophagi’s, ulceration, oral/nasal bleeding
Projectile - pyloric stenosis
Vomiting at end of coughing - whooping cough
Abdo distention - obstruction
Hepatosplenomegaly - chronic liver disease
Bulging fontanelle or seizures - raised ICP
Failure to thrive - GORD, coeliac

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11
Q

What is GORD?

A

Where contents of stomach reflux through lower oesophageal sphincter
In babies is normal due to immaturity of LOS; provided otherwise well and growing

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12
Q

What is the presentation of GORD?

A
Signs of problematic reflux:
Chronic cough
Hoarse cry
Distress, crying, unsettled
Reluctance to feed
Pneumonia
Poor weight gain
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13
Q

What advise is given to relieve GORD?

A

Small frequent meals
Burping regularly to help milk settle
Not overfeeding
Keeping baby upright after feeding

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14
Q

Who is more severe GORD a problem in?

A

Children with cerebral palsy or other neurodevelopment disorders
Preterm infants, especially if have bronchopulmonary dysplasia
Following surgery for oesophageal atresia or diaphragmatic hernia

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15
Q

What are complications of GORD?

A
Failure to thrive
Oesophagitis
Iron deficiency anaemia
Recurrent pulmonary aspiration
Cough or wheeze, apnoea
Dystonic neck posturing
Apparent life threatening events
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16
Q

What investigations are required for GORD?

A

Usually clinical diagnosis
May be indicated if history atypical, complications or failure to respond to tx

24 hour oesophageal pH monitoring
24 hour impedance monitoring
Endoscopy with biopsies for oesophagitis

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17
Q

What is the management of problematic cases of GORD?

A

Gaviscon mixed with feeds
Thickened milk or formula
Ranitidine
Omeprazole

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18
Q

What is Sandifer’s syndrome?

A

Rare condition
Causes brief episodes of abnormal movements associated with GORD

Torticollis - forceful contraction of neck muscles causing twisting of neck

Dystonia - abnormal muscle contractions causing twisting movements, arching of the back, unusual postures

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19
Q

What is colic?

A

Paroxysmal inconsolable crying or screaming
Accompanied with drawing up of the knees
Passage of excessive flatus

Typically occurs in first few weeks and resolves by 4 months

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20
Q

What are surgical causes of acute abdominal pain?

A
Acute appendicitis
Intestinal obstruction
Intussusception
Inguinal hernia
Peritonitis
Inflamed Meckel's
Pancreatitis
Trauma
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21
Q

What are medical causes of acute abdominal pain?

A
Gastroenteritis
UTI, pyelonephritis
Hydronephritis
Renal calculus
HSP
DKA
Sickle cell anaemia
Hepatitis
IBD
Constipation
Psychological
Lead poisoning
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22
Q

What are extra-abdominal causes of acute abdominal pain?

A

Upper respiratory tract infection
Lower lobe pneumonia
Torsion of testes
Hip and spine

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23
Q

What is mesenteric adenitis?

A

Swollen inflamed lymph nodes in the abdomen

Diagnosis can only be made definitively if large mesenteric nodes and normal appendix in laparotomy/laparoscopy

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24
Q

What is recurrent abdominal pain?

A

Pain sufficient to interrupt normal activities

Lasts for at least 3 months

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25
What are causes of recurrent abdominal pain?
``` >90% no cause IBS, constipation, dyspepsia Abdominal migraine, ulcers Dysmenorrhoea, cysts, PID Psychosocial Hepatitis, gallstones UTI, PUJ obstruction ```
26
What are signs and symptoms which suggest an organic disease as cause for recurrent abdominal pain?
``` Epigastric pain at night Haematemesis - ulcer Diarrhoea, weight loss Growth failure Blood in stools Vomiting Jaundice - liver disease Dysuria, secondary enuresis Bilious vomiting, abdo distension ```
27
What are the symptoms of IBS?
``` Abdominal pain, often worse before or relieved by defecation Explosive, loose or mucous stools Bloating Feeling of incomplete defecation Constipation ```
28
What is functional dyspepsia?
Symptoms of peptic ulceration, abdo pain, nausea More non specific symptoms Early satiety Bloating Post prandial vomiting Delayed gastric emptying due to gastric dysmotility Treatment with hypoallergenic diet
29
What are the symptoms of duodenal ulcers?
Less common in kids H pylori causes nodular antral gastritis Epigastric pain waking them at night FH of peptic ulceration
30
What conditions can mimic gastroenteritis?
``` Sepsis, meningitis RTI, otitis media, Hep A Pyloric stenosis Intussusception Acute appendicitis NEC DKA Haemolytic uraemic syndrome Coeliac disease Cow's milk protein intolerance ```
31
What is the most frequent cause of gastroenteritis in developed world?
Rotavirus Also adenovirus, norovirus Bacteria less common, blood in stools if so Campylobacter jejuni Shigella - high fever E coli - dehydrating diarrhoea
32
What children are at an increased risk of dehydration?
Infants under 6 months or low birth weight Passed >6 diarrhoeal stools in past 24 hours Vomited three or more times in previous 24 hours Unable to tolerate fluids Malnourished
33
What occurs in hypernatraemic dehydration?
Water loss exceeds relative sodium loss Due to high insensible water losses e.g. high fever, hot/dry environment Depression of fontanelle Reduced tissue elasticity Sunken eyes are all less obvious Water drawn out of brain and cerebral shrinkage Leads to jittery movement, increased muscle tone Hyperreflexia, seizures
34
What are the red flag signs of dehydration suggestive the child is at risk of shock?
``` Appears unwell or deteriorating Altered responsiveness Sunken eyes Tachycardia Tachypnoea Reduced skin turgor ```
35
How can disorders causing malabsorption manifest in children?
Abnormal stools Failure to thrive or poor growth Specific nutrient deficiencies
36
What is the cause of coeliac disease?
Antibodies: anti-tissue transglutaminase anti-endomysial anti-EMA Inflammation in small intestine, atrophy of intestinal villi
37
What is the presentation of coeliac disease?
``` Failure to thrive Diarrhoea Fatigue Weight loss Mouth ulcers Anaemia secondary to iron, B12 or folate deficiency Dermatitis herpetiformis ``` Rarely can present with neurological symptoms e.g. neuropathy, cerebellar ataxia, epilepsy
38
What condition is coeliac often tested alongside at diagnosis?
Type 1 diabetes
39
What are the genetic associated with coeliac?
HLA-DQ2 | HLA-DQ8
40
What are the auto antibodies in coeliac?
anti TTG anti EMA Deaminated gliadin peptides antibodies Important to test total immunoglobulin A levels, if total IgA is low coeliac test will be negative even when they have the condition Can then test for IgG version
41
How is coeliac diagnosed?
Remain on gluten diet Check total immunoglobulin A to exclude IgA deficiency Raised anti-TTG antibodies Raised anti-endomysial Crypt hypertrophy and villous atrophy on biopsy
42
What conditions is coeliac disease associated with?
``` Type 1 diabetes Thyroid disease Autoimmune hepatitis Primary biliary cirrhosis Primary sclerosing cholangitis Down's ```
43
What are the complications of untreated coeliac disease?
``` Vitamin deficiency Anaemia Osteoporosis Ulcerative jejunitis Enteropathy associated T cell lymphoma of intestine Non-Hodgkin lymphoma Small bowel adenocarcinoma ```
44
What are the features of Crohn's?
``` No blood or mucus Entire GI tract Skip lesions Terminal ileum most affected Transmural - full thickness inflammation Smoking is a risk factor ``` Also associated with weight loss, strictures, fistulas
45
What are the features of ulcerative colitis?
``` Continuous inflammation Limited to colon, rectum Only superficial mucosa Smoking is protective Excrete blood and mucus Use aminosalicylates Primary sclerosis cholangitis ```
46
What is the presentation of Crohn's in children?
Growth failure Puberty delayed Abdominal pain, diarrhoea, weight loss General ill health - fever, lethargy, weight loss
47
What are the extra-intestinal manifestations of Crohn's in children?
``` Oral lesions Perianal skin tags Uveitis Arthralgia Erythema nodosum ```
48
What investigations are helpful in confirming Crohn's or diagnosing a relapse?
Raised inflammatory markers - platelet count, ESR, CRP Iron deficiency anaemia Low serum albumin
49
What is seen on endoscopy in Crohn's?
Hallmark is presence of non-caseating epithelioid cell granulomata Small bowel imaging may reveal narrowing, fissuring, mucosal irregularitis Bowel wall thickening
50
How is remission in Crohn's induced?
Steroids - oral prednisolone or IV hydrocortisone Second line - azathioprine, mercaptopurine, methotrexate, infliximab
51
How is remission maintained in Crohn's?
First line - azathioprine, mercaptopurine Or methotrexate, infliximab, adalimumab
52
When is surgery required in Crohn's?
If affecting distal ileum, can surgically resect to prevent further flares Treat strictures and fistulas
53
What is used to induce remission in ulcerative colitis?
Mild/mod disease - aminosalicylate e.g. mesalazine, or corticosteroids If severe - IV corticosteroids first line or IV ciclosporin
54
What is used to maintain remission in ulcerative colitis?
Aminosalicylate e.g. mesalazine oral or rectal Azathioprine Mercaptopurine
55
When can surgery be offered in ulcerative colitis?
Panproctocolectomy will remove the disease | Left with ileostomy or oleo-anal anastomosis U pouch
56
What is the presentation of ulcerative colitis in children?
Children often have pancolitis Rectal bleeding, diarrhoea, colicky pain Weight loss and growth failure less common
57
What is seen on histology in ulcerative colitis?
Confluent colitis Mucosal inflammation Crypt damage - cryptitis, abscesses, crypt loss Ulceration
58
What are the clinical features of liver disease in children?
``` Encephalopathy Jaundice Epistaxis Cholestasis - pruritus, pale stools, dark urine Ascites, hypotonia, neuropathy Rickets Varices, portal HTN Spider naevi Muscle wasting - malnourished Splenomegaly Liver palms, clubbing ```
59
What are the causes of conjugated prolonged neonatal jaundice?
Bile duct obstruction - biliary atresia or choledochal cyst Neonatal hepatitis syndrome Intrahepatic biliary hypoplasia
60
What are the causes of neonatal hepatitis syndrome?
``` Congenital infection Inborn errors of metabolism A1 antitrypsin deficiency Galactosaemia Tyrosinaemia Errors of bile acid synthesis Progressive familial intrahepatic cholestasis CF Intestinal failure associated liver disease ```
61
What are the clinical features of viral hepatitis?
``` Nausea Vomiting Abdominal pain Lethargy Most children don't develop jaundice Large tender liver 30% have splenomegaly Liver transaminases elevated ```
62
What are the types of viral hepatitis and their transmission?
Hep A - faecal oral, vaccination for travellers Bed rest, change of diet ``` Hep B - Perinatal transmission Infected blood Needlestick injuries Renal dialysis Horizontal spread in families (Sexual transmission) ``` Chronic infection by vertical transmission, can cause risk of cirrhosis or hepatocellular carcinoma Interferon therapy Hep C - High in drug users, vertical transmission more common if also have HIV D - co infection or super infection, E - water
63
What are the causes of acute liver failure in children?
Fulminant hepatitis Massive hepatic necrosis, loss of liver function with or without encephalopathy ``` Infection - viral hepatitis Poisons/drugs - Paracetamol, isoniazid, phalloides mushrooms Metabolic - Wilson's Autoimmune hepatitis Reye's syndrome ```
64
What are the signs of acute liver failure?
``` Jaundice Encephalopathy Coagulopathy Hypoglycaemia Electrolyte disturbances ``` Early signs of encephalopathy - alternate periods of irritability, confusion, drowsiness, aggression
65
What are some of the complications of acute liver failure?
Cerebral oedema Haemorrhage from gastritis or coagulopathy Sepsis Pancreatitis
66
How can fulminant hepatitis be diagnosed?
``` Transaminases very raised Alkaline phosphatase increased Coagulation very abnormal EEG shows encephalopathy CT may show cerebral oedema ```
67
What is the management of acute liver failure?
Maintain blood glucose >4 with IV dextrose Prevent sepsis; broad spectrum antibiotics and antifungals Prevent haemorrhage, IV Vit K, FFP, cryoprecipitate, PPIs Treat cerebral oedema by fluid restriction, mannitol Urgent transfer to liver unit
68
What features of acute liver failure suggest poor prognosis?
Shrinking liver Rising bilirubin and falling transaminases Worsening coagulopathy Progression to coma Without transplantation, 70% likely to die
69
What is Reye syndrome?
Acute non inflammatory encephalopathy | Microvesicular fatty infiltration of liver
70
What are the causes of chronic liver disease in children?
``` Post viral Hep B, C Autoimmune hepatitis Drugs - nitrofurantoin, NSAIDs IBD PSC - +- ulcerative colitis Wilson's Alpha 1 antitrypsin def CF Neonatal liver disease Bile duct lesions ```
71
What is autoimmune hepatitis?
More common in girls May present as acute hep, fulminant hep or CLD Autoimmune features - rash, SLE, arthritis, haemolytic anaemia, nephritis Respond to prednisolone, azathioprine
72
What is Wilson's disease?
Autosomal recessive Reduced synthesis of caeruloplasmin and defective excretion of copper in bile Leads to copper in liver, brain, kidney, cornea Liver disease, neuropsychiatric features, extrapyramidal signs Kayser Fleischer rings from age 7 Tx with penacillamine, promotes copper excretion, zinc to reduce absorption
73
What occurs in cirrhosis?
End result of any liver disease, extensive fibrosis May be asymptomatic if compensated, then: palmar and plantar erythema Spider naevi Malnutrition, hypotonia
74
What are the investigations for cirrhosis?
Screen for known cause of chronic liver disease Upper GI endoscopy to detect varices, gastritis Abdominal ultrasound Liver biopsy
75
What are some of the consequences of cirrhosis?
``` Portal hypertension Splenomegaly Oesophageal varices Ascites - umbilical hernias Spontaneous bacterial peritonitis - undiagnosed fever, pain, tenderness Encephalopathy Renal failure ```
76
What are the indications for transplantation in chronic liver failure?
Sever malnutrition unresponsive to intensive nutritional therapy Recurrent complications Failure of growth and development Poor quality of life
77
What are some of the complications post liver transplantation?
``` Primary non function of liver Hepatic artery thrombosis Biliary leaks, strictures Rejection Sepsis ```
78
What is important in the management of children with liver disease?
Nutrition - high protein high carbohydrate, NG or TPN Vit K, A, E, D Pruritus - loose clothing, emollients, phenobarbital to stimulate bile flow, ursodeoxycholic acid
79
What occurs in Vitamin A deficiency?
Night blindness in adults Retinal changes in infants Give oral supplements
80
What occurs in Vitamin E deficiency?
Peripheral neuropathy Haemolysis Ataxia High oral doses needed
81
What occurs in Vitamin D deficiency?
Rickets Pathological fractures Vit D resistant rickets indicates renal tubular acidosis