Gastrointestinal Presentations Flashcards

1
Q
PYLORIC STENOSIS
✔️ epidemiology
✔️ risk factors
✔️ clinical features
✔️ assessment / examination
✔️ appropriate investigations
✔️ management
A

EPIDEMIOLOGY
Most commonly occurs in infants aged 2 to 6 weeks.

RISK FACTORS
✔️ first born
✔️ male gender
✔️ Caucasian
✔️ maternal history of pyloric stenosis
✔️ recent macrolide antibiotic use

CLINICAL FEATURES
✔️ projectile vomiting immediately after meals (non-bilious)
✔️ infant irritable and hungry after vomit
✔️ initially normal bowel motions –> progressively reduced due to poor oral intake
✔️ poor growth and FTT

ASSESSMENT / EXAMINATION
✔️ weight reveals FTT on growth chart
✔️ assess hydration status
✔️ palpable pyloric mass (“olive-like”) located in the RUQ
✔️ visible “golf ball” peristalsis within the RUQ

APPROPRIATE INVESTIGATIONS
✔️ urine dipstick
✔️ blood glucose levels
✔️ FBC + WCC
✔️ UECs –> hypochloremia, hypokalaemia
✔️ VBG –> hypochloremic, hypokalaemic metabolic alkalosis
✔️ abdominal USS –> only indicated in clinical diagnosis cannot be made

MANAGEMENT

  1. Keep NBM
  2. Insert NGT
  3. Correct electrolyte and metabolic derangement within 24 to 48 hours
  4. Referral to paediatric surgery
  5. Ramstedt’s Pyloromyomectomy –> involves making an incision into the muscular layer of the pylorus whilst maintaining the mucosal layer

N.B. Surgery teams will not operate until metabolic alkalosis and electrolyte disturbances have been fixed, due to high risk of apnoeas.

COMPLICATIONS
✔️ apnoea (due to metabolic alkalosis)
✔️ poor growth
✔️ micronutrient deficiencies

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2
Q

What are the key electrolyte abnormalities associated with PYLORIC STENOSIS?

A

✔️ hypochloremia
✔️ hypokalaemia
✔️ hypochloremic hypokalaemic metabolic alkalosis

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3
Q
GASTRO OESOPHAGEAL REFLUX (DISEASE)
✔️ epidemiology
✔️ risk factors
✔️ clinical features
✔️ assessment / examination
✔️ appropriate investigations
✔️ management
A

EPIDEMIOLOGY
GOR begins at 8 weeks of age, peaks between 6 to 8 weeks and tends to subside by ~12 months.

RISK FACTORS
Nil. Around 40% of healthy babies experience physiological GOR many times per day.

Cow’s Milk Protein Allergy (CMPA) is a risk factor for GORD; 40% of infants with GORD have IgE CMPA.

CLINICAL FEATURES
✔️non-projectile, effortless vomiting after meals
✔️ minimal irritability

GORD may be suspected in the case of:
✔️ refusal to feed
✔️ highly irritable
✔️ aspiration
✔️ night-time cough or wheeze
✔️ poor weight gain 
✔️ haematemesis

ASSESSMENT / EXAMINATION
Infants with GOR(D) will typically examine normal.

INVESTIGATIONS
Nil.

MANAGEMENT

  1. Encourage mother to hold baby upright for 20 to 30 minutes after feeding.
  2. “Burp” the baby after every meal.
  3. Trial smaller, more regular feeds.
  4. Thickened fluids (?)
  5. Trial elimination of cows milk from maternal diet for 2 weeks.
  6. Four week trial of PPI (e.g. omeprazole) if options have not alleviated symptoms.

Note that side effects of PPIs can include:
✔️ increased risk of community acquired pneumonia
✔️ osteoporosis / increased future fracture risk
✔️ gastroenteritis
✔️ micronutrient deficiencies

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4
Q
INTUSSUSCEPTION
✔️ epidemiology
✔️ risk factors
✔️ clinical features
✔️ assessment / examination
✔️ appropriate investigations
✔️ management
A

EPIDEMIOLOGY
Broad age demographic is 2 months to 2 years; most commonly involved age is 5 to 9 months.

RISK FACTORS
✔️ 90% of cases are idiopathic
✔️ 10% of cases have a “lead point” (e.g. Meckels’ Diverticulum, HSP, lymphoma)

Other risk factors include:
✔️ recent surgery
✔️ recent intussusception
✔️ recent rotavirus vaccination

CLINICAL FEATURES
✔️ intermittent, recurrent abdominal pain (increased frequency over 12 to 24 hours)
✔️ extreme irritability, crying and pallor during these episodes
✔️ child may be completely well in between
✔️ vomiting, non-bilious to begin with; bilious is a late sign
✔️ diarrhoea, “red current” jelly stained
✔️ dehydration and poor oral intake

ASSESSMENT / EXAMINATION
✔️ large palpable “sausage shaped” mass in the right quadrant which crosses the midline
✔️ abdominal distension –> bowel obstruction
✔️ guarding and rigidity –> peritonitis, perforation
✔️ red current jelly seen in stools –> bowel ischaemia

APPROPRIATE INVESTIGATIONS

  1. urine dipstick + MCS
  2. FBC + WCC
  3. UECs
  4. VBG
  5. Coags
  6. Group + Hold
  7. Abdo USS –> telescoping sign

MANAGEMENT

  1. Adequate pain relief
  2. Gain IV access
  3. Appropriate IV fluids (resuscitation, bolus, maintenance)
  4. Early referral to paediatric surgery
  5. Keep NBM
  6. Insert NGT if bowel obstruction suspected
  7. Air enema –> contraindicated if peritonitis, perforation or shock; must perform where there is a paediatric surgery team nearby for emergency / urgent laparotomy
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5
Q

Define CHRONIC ABDOMINAL PAIN.

A

Chronic abdominal pain is defined as abdominal pain that lasts > 3 months duration in a child > 3 years of age with at least 3 episodes in this period of time.

Chronic abdominal pain may be:
✔️ functional (~90% of cases)
✔️ organic (~10% of cases)

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6
Q

Identify organic causes of CHRONIC ABDOMINAL PAIN.

A
✔️ Coeliac Disease
✔️ IBD 
✔️ IBS
✔️ Lactose intolerance
✔️ Chronic / severe constipation
✔️ Hepatitis
✔️ Pancreatic 
✔️ Gynaecological issues (females)

N.B. Organic causes of chronic abdominal pain rarely present with abdominal pain alone. Other features of underlying disease are also present (e.g. vomiting and diarrhea, weight loss, fever).

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7
Q

What features distinguish organic versus functional chronic abdominal pain.

A

Functional abdominal pain tends to be:
✔️ non-specific / vague in characteristic and location
✔️ does not wake child at night
✔️ not associated with any food or activity
✔️ nil vomiting or diarrhoea
✔️ nil fever
✔️ psychosocial stressors may be present

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8
Q

What are some RED FLAG features of chronic abdominal pain?

A
✔️ child < 5 years of age
✔️ pain away from midline
✔️ anaemia
✔️ fever
✔️ GI blood loss
✔️ rash
✔️ pain that wakes child at night
✔️ persistent vomiting and / or diarrhoea 
✔️ weight loss and / or failure to thrive
✔️ joint pain
✔️ family history of IBD
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9
Q

Outline differential diagnoses for ACUTE ABDOMINAL PAIN.

A
SURGICAL CAUSES
✔️ small bowel obstruction
✔️ intussusception 
✔️ volvulus
✔️ acute appendicitis 
✔️ incarnated hernia
✔️ testicular torsion
✔️ ovarian torsion / cyst
✔️ ruptured ovarian cyst 
NON-SURGICAL CAUSES
✔️ gastroenteritis 
✔️ mesenteric adenitis
✔️ constipation
✔️ UTI
✔️ DKA
✔️ IBD / IBS
✔️ HSP
✔️ gynaecological problems (females)
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10
Q

Define CONSTIPATION.

A

Constipation is the irregular passage of hard stools.

N.B. a child who passes one soft bowel motion every week is less likely to be constipated than a child who passes a hard, painful bowel motion every three days.

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11
Q

When is constipation most likely to be seen in children?

A

✔️ introduction of solids foods (between 6 to 9 months)
✔️ toilet training (2 to 4 years)
✔️ beginning day care / school (around 4 to 6 years)
✔️ may be precipitated by acute dehydration secondary to a viral illness

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12
Q

What is the diagnosis of FUNCTIONAL CONSTIPATION according to the Rome IV Criteria?

A

Functional constipation requires at least TWO of the following criteria to have been met in the last one month in a child > 2 years of age:

✔️ less than two bowel motions per week
✔️ passage of hard, painful stools
✔️ passage of large-diameter stools
✔️ abnormal posturing
✔️ presence of large fecal mass in the rectum
✔️ at least one incontinence episode per week (school-aged children)

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13
Q

Identify some organic causes of constipation (medical and surgical).

A
MEDICAL CAUSES
✔️ hypokalaemia
✔️ hypothyroidism
✔️ hypercalcaemia
✔️ cow's milk protein allergy
✔️ lactose intolerance
✔️ coeliac disease
✔️ IBD / IBS
✔️ neurological disorders
SURGICAL CAUSES
✔️ small bowel obstruction
✔️ volvulus
✔️ Hirchsprung's Disease
✔️ anatomical malformations of the anus
✔️ spinal cord abnormalities
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14
Q

Identify RED FLAGS for constipation.

A

✔️ child age < 6 months
✔️ delayed passage of meconium (Hirschsprung’s Disease)
✔️ ribbon-like stools (anus malformation)
✔️ weight loss / poor growth
✔️ persistent vomiting
✔️ anal mass

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15
Q
Outline the appropriate management of constipation including: 
✔️ behavioural modification
✔️ dietary modification
✔️ oral medications
✔️ rectal medications
A

BEHAVIOURAL MODIFICATIONS
✔️ encourage toilet time –> sitting on the toilet for 5 to 10 minutes three times per day, 30 minutes after a meal (reward the act of sitting on the toilet, rather than the passage of a stool)
✔️ modification of position –> use a stool to make sure the child’s knees are higher than their hips; encourage leaning forward
✔️ keep a diary
✔️ reward / sticker system
✔️ delay toilet training until the child is passing relatively pain-free stools

DIETARY MODIFICATIONS
✔️ encourage a well-balanced diet, high in fruit, vegetables and whole-grains
✔️ encourage high fibre intake
✔️ avoid excessive cows’ milk consumption (<500mL per day)
✔️ encourage appropriate fluid intake

ORAL MEDICATIONS
✔️ stool softeners (e.g. Coloxyl)
✔️ osmotic laxatives (e.g. Lactulose)
✔️ iso-osmotic laxatives (e.g. Movicol)
✔️ motility agents (e.g. Senna)
✔️ lubricant (e.g. Parrafin oil)

RECTAL MEDICATIONS
✔️ rarely indicated in children

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16
Q

Define ENURESIS.

A

Enuresis is defined as the spontaneous passage of urine after bladder control has been obtained, commonly known as “bedwetting…”

N.B. mono spontaneous enuresis (MSE) is defined as enuresis without any other symptoms of lower urinary tract infection / abnormality or bladder dysfunction.

17
Q

Compare PRIMARY versus SECONDARY ENURESIS.

A

Secondary enuresis occurs when a child has been “dry” for six months previously and is suggestive of an underlying cause for the bedwetting.

Common causes of secondary enuresis include: 
✔️ diabetes mellitus / insipidus
✔️ psychosocial / emotional distress
✔️ UTI / cystitis 
✔️ neurogenic bladder
✔️ cerebral palsy
✔️ seizures
✔️ constipation
✔️ thread worm / pin worm infection
18
Q

At what age is day time and night time bladder control acquired?

A

Day time bladder control is usually acquired by 4 years of age.

Night time bladder control should not be expected until a child is between 4 to 7 years of age.

19
Q

What symptoms should be enquired about in regards to ENURESIS?

A

✔️ onset of symptoms (acute versus chronic)
✔️ has the child been “dry” for > 6 months
✔️ daytime urinary symptoms (e.g. burning, stinging, foul-smell, polyuria, polydipsia, polyphagia)
✔️ bedwetting pattern (number of nights per week, number of episodes per night, time of night etc)
✔️ fluid intake throughout day
✔️ fluid intake at night
✔️ bowel habits (constipation, diarrhoea, soiling)
✔️ sleeping arrangements and bedtime routine
✔️ medical conditions
✔️ family history (including enuresis)
✔️ family history of renal pathologies

20
Q

Outline general management of ENURESIS.

A

GENERAL STRATEGIES
✔️ reassure parents that enuresis is quite common in children; prevalence decreases as the child gets older
✔️ constipation should be treated, if present
✔️ do NOT restrict fluids throughout the day
✔️ DO restrict caffeinated drinks throughout the day

BEDWETTING ALARM
✔️ requires referral to GP to paediatrician
✔️ may take 6 to 8 weeks to work
✔️ depends on a cooperative family that is very supportive of the child
✔️ “overtraining” the bladder should occur once night time continence has been obtained

MEDICATIONS
✔️ tricyclic antidepressants are no longer indicated
✔️ desmopressin may be indicated in children that cannot achieve continence through bed-wetting alarm

21
Q

Define JAUNDICE in infants and identify the classification system.

A

Jaundice is defined as the yellowing of skin and mucus membranes. In adults this tends to occur > 17 mmol / L, however, can occur at varying levels in infants.

Jaundice in infants is classified based on the timing of onset, as:

  1. early jaundice (<24 hours)
  2. mid jaundice (24 hours to 10 days)
  3. late jaundice (>10 days)
22
Q

Outline common causes for jaundice in each of the different categories.

A
EARLY JAUNDICE (<24 hours) --> always pathological!!
✔️ haemolytic disease of the newborn
✔️ sepsis
✔️ maternal infection (EBV, CMV)
✔️ inborn errors of metabolism 
MID JAUNDICE
✔️ physiological
✔️ dehydration
✔️ sepsis
✔️ bruising
✔️ polycythemia
✔️ inborn error of metabolism
LATE JAUNDICE
✔️ breast milk jaundice
✔️ sepsis
✔️ hypothyroidism
✔️ haemolytic anaemia
✔️ hereditary spherocytosis
✔️ biliary atresia (14 to 21 days)
23
Q

Outline appropriate investigations for JAUNDICE.

A
✔️ urine dipstick + MCS
✔️ FBC + WCC
✔️ total serum bilirubin
✔️ LFTs
✔️ UECs
✔️ TFTs
✔️ abdominal USS (?)

Consider metabolic screen and haemolytic screen if jaundice is severe / unknown cause despite first-line investigations.

24
Q

Define KERNICTERUS.

A

Kernicterus is a complication of severe / prolonged jaundice. It tends to occur when plasma bilirubin levels exceed 500 mmol / L.

Clinical presentation includes: 
✔️ lethargy
✔️ hypo or hypertonia
✔️ high-pitched cry
✔️ spasmodic torticollis 
✔️ setting sun sign
✔️ back arching
✔️ seizures
✔️ death
✔️ permanent vision / hearing abnormalities; severe neurodisability
25
Q

Define BILIARY ATRESIA.

A

Biliary atresia is a congenital condition in which abnormal narrowing of the hepatic bile ducts (left or right hepatic duct OR common hepatic duct) prevents appropriate outflow of bile. This leads to back flow of bile into the liver, which can cause liver cirrhosis.

26
Q

Outline the clinical presentation of BILIARY ATRESIA.

A

✔️ prolonged jaundice (>10 days; typically 14 to 21 days)
✔️ dark urine
✔️ pale, foul-smelling stools
✔️ irritability, particularly when feeding
✔️ failure to thrive
✔️ enlarged spleen

27
Q

What is the management of BILIARY ATRESIA?

A

Kasai procedure –> involves stenting of the obstructed ducts. Should be performed within 8 months of life to reduce the likelihood of requiring a liver transplant.

28
Q
INDIRECT INGUINAL HERNIA
✔️ description
✔️ clinical presentation
✔️ examination
✔️ investigations and management
A

DESCRIPTION
A hernia is protrusion of bowel contents though a weakening in the abdominal wall.

Inguinal hernias may be direct (through a weakening within the abdominal wall; acquired) or indirect (through open processes vaginalis / deep inguinal ring; congenital).

Indirect inguinal hernias are located superior and lateral to the inferior epigastric vessels.

CLINICAL PRESENTATION AND EXAMINATION
✔️ unilateral 
✔️ non-tender scrotal mass
✔️ cannot get above
✔️ opaque (non transilluminate)
✔️ testes are palpable; completely seperate from the hernia
✔️ reducible 

MANAGEMENT
Surgery is required for management.

If reducible, book for elective surgery.

If incarcerated or strangulated, book for emergency surgery.

29
Q
HYDROCELE
✔️ description
✔️ clinical presentation
✔️ examination
✔️ investigations and management
A

DESCRIPTION
Hydrocele is collection of fluid between the visceral and parietal layers of the tunica vaginalis.

CLINICAL PRESENTATION
✔️ unilateral or bilateral scrotal mass
✔️ non-tender
✔️ enlarges throughout the day (due to effects of gravity)

EXAMINATION
✔️ cannot get above
✔️ testes palpable beneath
✔️ transilluminate

MANAGEMENT
Most congenital hydroceles resolve by 2 years of age.

Refer to surgery if not resolved within 18 to 24 months.

30
Q
VARICOCELE
✔️ description
✔️ clinical presentation
✔️ examination
✔️ investigations and management
A

DESCRIPTION
Varicocele is abnormal dilation of the pampiniform plexus within the spermatic cord.

CLINICAL PRESENTATION
✔️ asymptomatic / not painful
✔️ unilateral scrotal swelling (usually left sided)
✔️ palpated above the testes
✔️ feels like a "bag of worms"

EXAMINATION
✔️ can get above testes
✔️ seperate from testes
✔️ does NOT transilluminate

MANAGEMENT
Requires no surgery.

31
Q
UNDESCENDED TESTES
✔️ description
✔️ clinical presentation
✔️ examination
✔️ investigations and management
A

DESCRIPTION
1 in 60 male infants have undescended testes. 99% of these descend by 12 months of age.
The testes may be located within the external inguinal ring, inguinal canal or abdominal cavity.

CLINICAL PRESENTATION
✔️ asymptomatic for the child
✔️ detected at newborn baby check

EXAMINATION
Testes (bilateral or unilateral) not located within the scrotum.

INVESTIGATIONS AND MANAGEMENT
If testes is detected as undescended at birth, the child should be reviewed by paediatrician or GP at 12 weeks.

If testes still have not descended, the child should be booked for surgery.

MANAGEMENT
Orchidopexy between 6 to 12 months of age is indicated if the testes have not descended by 12 weeks.

32
Q
TESTICULAR TORSION
✔️ description
✔️ clinical presentation
✔️ examination
✔️ investigations and management
A

DESCRIPTION
Testicular torsion is a surgical emergency. It occurs when the contents of the spermatic cord “twist” around itself.

This leads to obstructed venous draining, swelling, oedema, impaired vascular supply and necrosis.

Risk factors include:
✔️ pre-pubescent male
✔️ family history 
✔️ previous testicular torsion
✔️ "Bell Clapper" deformity

CLINICAL PRESENTATION
✔️ severe and acute unilateral testicular pain
✔️ nausea and vomiting
✔️ +/- abdominal pain
✔️ loss of cremesteric reflex
✔️ Phrehn’s reflex -ve (i.e. pain does not resolve with elevation of the testes)

INVESTIGATIONS
Diagnosis should be clinical.

Doppler USS may aid diagnosis.

MANAGEMENT
Immediate surgical intervention is required with 6 hours of symptom onset to prevent permenant ischemia to testes.