Paediatric Surgery Flashcards

1
Q

what does bilious vomiting suggest until proven otherwise?

A

bowel obstruction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

outline the pain ladder management in children

A
  • paracetamol
    • 20mg/ kg 4-6hourly
  • ibuprofen
    • 10mg/kg 8 hourly
  • weak opioids- codeine NOT to be used in <12y/o
  • strong opioids
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what are the sentinel signs of pathology in children? ie markers of disease

A
  • abdominal pain
  • bilious vomiting
  • temperature
  • tone
  • colour
  • reduced feeding
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

main investigations?

A

urine - always

FBC- only if diagnostic uncertainty

electrolytes- only if child dehydrated / very sick

X-Ray- rarely

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

features of classical appendicitis in children?

A
  • murphy’s triad
    • fever
    • pain
    • vomiting
  • tenderness over McBurney’s point
  • unusual >4years old
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Features of Non-Specific Abdo Pain?

A
  • central and constant
  • short duration
  • no temperature
  • not worse on movement
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

main diagnoses linked to NSAP?

A
  • mesenteric adenitis
    • inflammation/swelling of lymph nodes in abdomen
  • pneumonia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

pathophysiology of Pyloric Stenosis?

A

hypertrophy of gastric pylorus causing upper GI obstruction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

when does pyloric stenosis typically present?

A

3-6 weeks

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

in who is PS more likely?

A

boys > girls

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

presenting features of PS, including O/E?

A
  • projectile milky non-bilious vomiting after every feed
  • weight loss
  • palpable olive mass in RUQ
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

investigations and findings of PS?

A
  • Capillary Blood Gas
    • hypochloraemic, hypokalaemic metabolic alkalosis
  • Test feed first
  • USS to confirm (thickened pylorus)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

management of PS?

A
  • NBM
  • IV fluids
  • surgical pyloromyotomy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

at what age is malrotation more common?

what is the pathology?

A
  • first few months of life
  • failure of midgut to rotate during embryogenesis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

presentation of malrotation?

A

bilious vomiting (green)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Ix of malrotation?

A

upper GI contrast study

17
Q

Management of malrotation?

A

surgery

18
Q

complication of malrotation?

A

volvulus

19
Q

when does intussusception present?

A

6-12months

  • often preceded by viral infection
20
Q

how does intussusception present?

A
  • bilious vomiting
  • recurrent episodes of screaming & drawing up of the legs
  • redcurrant jelly stools
21
Q

examination findings in intussusception

A
  • sausage shaped mass
  • prolonged capillary refill
22
Q

why do you get a prolonged capillary refill?

A

because of third space fluid loss, child is very dehydrated

23
Q

investigation + management of intussusception

A

investigation: USS abdo
management: air enema, surgery only if failed reduction / suspected strangulation

24
Q

what is gastroschisis + management

A

gastroschisis is a defect in the abdominal wall which leads to the herniation & expsoure of the gut contents

management: early / delayed closure & TPN

25
Q

what is exomphalos? what is it associated with?

A

umbilical defect which leads to the expsure of abdominal organs, covered by viscera

-associated with trisomies, cardiac neuro and renal abnormalities

26
Q

pathology of biliary atresia?

A

congenital condition where section of extrahepatic bile duct is narrowed or absent –> disrupted excretion of billirubin

27
Q

presentation of biliary atresia?

A
  • jaundice beyond 2 weeks
  • pale stools
  • dark urine
28
Q

signs of biliary atresia O/E?

A
  • jaundice
  • hepatomegaly
  • splenomegaly
29
Q

Ix of biliary atresia?

A
  • raised ALP
  • raised liver enzymes
  • raised conjugated billirubin
30
Q

Mx of biliary atresia?

A

kasai procedure