Pediatric Surgery review Flashcards

1
Q

What drug can you give to keep ductus arteriosus patent in neonates?

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

What drug can you give in an attempt to pharmacologically close a patent ductus arteriosus?

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

What procedure do you perform to close a patent ductus arteriosus in a neonate?

A
  • left anterolateral thoracotomy, can be performed at bedside
  • clip PDA
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

describe a Duhamel proceudre

A

aganglionic rectal stump is left in place, ganglionic colon is brought posterior to stump and a common channel is made between the two

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

what surgical options are available for Hirschsprung’s disease?

A
  • Soave
  • Duhamel
  • Swenson
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Describe the Soave procedure

A

submucosal endorectal dissection, resection of aganalionic rectum with pull through of ganglionic colon and end to end anastomosis…a muscular layer from the aganglionic rectum is left surrounding the colon pulled through

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Describe the Swenson procedure

A

full thickness resection of aganglionic rectum and pull through of sigmoid colon to create end to end anastomosis with rectal stump

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Air filled stomach and air filled duodenum on plain film in a neonate…what is this called and what is it associated with?

A
  • double bubble sign

- duodenal atresia or a duodenal web

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

neonate with bilious emesis, plain film with double bubble sign and no distal air noted…next step?

A
  • upper GI contrast study, will confirm Duodenal atresia but more importantly need to rule in or out midgut volvulus (lack of air distally)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

3 month old with inguinal hernia presents to ED, bowel noted to be in hernia…next step?

A
  • attempt reduction, if successful admit for 1-2 days of observation then repair the hernia (allows for edema to subside)
  • if reduction fails take to OR for open reduction and repair
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

unable to pass an NGT in a neonate…what is first on the differential?

A

Esophageal atresia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

most common form of esophageal atresia?

A

atresia with a distal tracheoesophageal fistula (you’ll see gas in GI tract distally from inspired air

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

VACTERRL syndrome

A
Vertebral
Anal
Cardiac
Trachea
Esophagus
Renal
Radial Bone
Limb
  • defects that are associated with each other
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is unicameral bone cyst?

A
  • cyst in the bone filled with cytokines that cause bone resorption
  • typically asx but can present with pathologic fracture
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

how do you treat a fracture from a simple bone cyst?

A
  • cast and see if it heals

- if this fails can do methylprednisolone injection

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

Characteristics of a mesenteric Cyst?

A
  • no solid component

- freely mobile and perpendicular to mesentery

17
Q

8 year old with 1 cm mass on lateral neck, mom said it comes and goes with some fluid drainage…next step?

A
  • total surgical excision likely a brachial cleft anomaly
18
Q

Surgical treatment for thyroglossal duct cyst?

A

Sistrunk procedure

removal of cyst and its track as well as central portion of the hyoid bone

19
Q

Fetal structural abnormalities that are associated with increased amniotic fluid?

A

esophageal atresia
intestinal atresia
craniofacial abnormalities

20
Q

Cardiac abnormalities seen in Tertralogy of Fallot?

A
  • pulmonary artery stenosis
  • ventricular septal defect
  • overriding aorta with deviation of origin to the right
  • concentric right ventricular hypertrophy
21
Q

Type III choledochal cyst

A

intraduodenal or intrapancreatic dilations, distal to CBD

22
Q

treatment for Type III choledochal cyst

A

if < 3cm can get an ERCP and marsupialize the cyst

if > 3cm will need formal resection and reconstruction

23
Q

Type I choledochal cyst

A

extra hepatic biliary dilation(s)

  • some argue Type I and IV are a spectrum of the same entity
24
Q

treatment for type I choledochal cyst

A

resection with roux-en-y hepaticpjejunostomy

25
Q

Type IV choledochal cyst

A

extra-hepatic and or intra-hepatic cyst

26
Q

treatment for type IVa and V choledochal cyst

A

orthotropic liver transplantation if diffuse, segmental resection if isolated

27
Q

Caroli Disease

A

multi-focal intrahepatic biliary dilation, can be segmental or diffuse

AKA type V choledochal cyst disease

28
Q

Type II choledochal cyst

A

singular diverticulum protruding from CBD

29
Q

treatment for Type II choledochal cyst

A

resection of diverticulum, reconstruction is normally not needed

30
Q

how much blood do you give in pediatric trauma

A

10 mL/kg

31
Q

how much fluid do you give in pediatric trauma, what is your bolus dose?

A

20 mL/kg

32
Q

child with multiple liver masses and elevated alpha-fetoprotein…what do they have?

A

hepatoblastoma

33
Q

how do you test adequacy of pyloromyotomy

A
  • edges should be freely mobile, independent of each other
34
Q

most common intestinal atresia

A

jejunal atresia

35
Q

most common cause of jejunal atresia

A

intrauterine vascular accident

36
Q

new born male has an undescended testicle, with no other symptoms, when does this become a problem?

A

if it has not spontaneously descended in the first 4 months of life surgery will likely be needed

37
Q

when do kids present with pyloric stenosis typically

A

2-8 weeks of age