GI Flashcards

(52 cards)

1
Q

Most common type of tracheo esophageal fistula

A

Esophageal atresia with fistula between trachea and distal esophagus( Type 1a and 3 depending on classifn system)

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2
Q

Reason for enlarged gastric bubble in TEF

A

Fistula between trachea and distal esophagus leading to air entering stomach (not usually seen in types 1b and 1e)

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3
Q

Syndrome associated with TEF

A

VACTERL

Verterbal
Ano-rectal malformations
Cardiac abnormalities
Tracheo
Esophageal fistula
Renal, Radial aplasia
Limb

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4
Q

Investigation of choice for TEF

A

Flexible bronchoscopy looking
- presence of fistula to proximal segment
- presence of fistula to distal segment

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5
Q

Incision for TEF

A

4th of 5th intercostal space

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6
Q

Steps for TEF ligation and repair

A

Isolate azygos vein

Interrupted sutures
1. Posterior first
2. Then anterior

Check whether NGT is able to pass thru patent repair
- on POD5 inject dye to check for leak and whether feeds can be started

Place chest tube to drain saliva leak

Monitor in NICU

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7
Q

What does double bubble sign with absent distal colonic and rectal suggest

A

Duodenal atresia or annular pancreas

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8
Q

Part of pregnancy duodenal atresia usually occurs

A

1st trimester: Failure of recanalization

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9
Q

Windsock appearance suggests?

A

Duodenal webs/intraluminal duodenal diverticulum

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10
Q

syndrome associated with duodenal atresia

A

T21

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11
Q

Suspicion in newborn with NBNB projectile vomiting

A

Hypertrophic pyloric stenosis

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12
Q

First steps for newly diagnosed duodenal atresia

A
  1. Order TTE tro cardiac abnormalities
  2. Drip and suck the neonate
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13
Q

Direction umbilical vein catheter usually goes in

A

Superiorly

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14
Q

Why duodenal atresia usually p/w bilious vomiting

A

Usually distal to ampulla of vater

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15
Q

How duodeno-duodenostomy is usually performed for duodenal atresia

A

side to side anastomosis b/w D1 and D3, D2 often too atretic

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16
Q

Radiological invx to confirm small bowel atresia

A

Barium enema

Barium follow through would be too dilated

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17
Q

Most common types of duodenal atresia and the etiology

A

Type 1 and 3a, usually due to vascular accident/ischemia

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18
Q

Part of pregnancy where jejunal and ileal atresia tend to occur

A

2nd and 3rd trimester due to ischemia

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19
Q

Risk factor for short gut syndrome

A

DJ flexure to ileocecal valve <60cm

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20
Q

Options for jejunal and ileal atresia mx

A
  1. Stoma
  2. Bowel resection
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21
Q

How suction rectal biopsy is done

A

3 biopsys starting 3cm from rectum, 3cm apart

22
Q

Mx of hirschsprung

A

Non surgical: rectal washout 2-3x a day

Surgical

1) Transverse colon colostomy as temporizing

2) Definitive is pull through eg Duhamel, Swensen

23
Q

Invx for hirschsprungs disease

A
  1. Suction rectal biopsy to confirm diagnosis
  2. Barium enema to delineate anatomical segment
  3. XR to look for dilated bowel segments
23
Q

What to check for intraop in Pull through

A

intraop frozen section to check for ganglion cells present at dentate line via pull through

24
Common cx of anorectal malformations in boys
Fistula to genito urinary system - check intra op if present, needs to be ligated
25
Reason for double barrel stoma with division in ARM for boys
Reduce entry of fecal output into distal segment that may cause UTIs/ fecaluria
26
Mx of Ano rectal malformations
LAARP/PSARP Laparoscopic/ Posterior sagittal AnoRecto Plasty
27
Side of umbilical cord that gastroschisis usually comes out of
Almost always on the right side of the umbilical cord
28
Syndromes predisposing to omphalocele/exomphalos
T13,18,21 edwards patau downs Beckwith Wiedemann syndrome
29
Temporizing measure for closing large omphalocele
A silo sutured to the skin to help reduce heat and fluid loss
30
Common organs involved in omphalocele
Stomach, small intestine, liver and spleen
31
How to monitor for excessive intra abdominal pressure when replacing an omphalocele
1. Intra vesical pressure management 2. Looking for desaturation
32
Types of congenital diaphragmatic hernia
1. 80% bochdalek foramen left posterolateral 2. 10% right sided 3. 5% morgagni foramen anterior
33
Cx of Congenital diaphragmatic hernia
1. Pulmonary hypotension 2. Pulmonary hypoplasia 3.
34
Acute medical Mx of CDH
Intubation and ventilatory support 1.High frequency oxygen ventilation 2. Nitric oxide to help with pulmonary vasodilation 3. extra corporeal membrane oxygenation for severe cases
35
Signs and Sx of Hypertrophic Pyloric stenosis
Sx 1. NBNB projectile vomiting Signs 1. Olive shaped mass at the LUQ
36
Invx for Hypertrophic Pyloric Stenosis
Biochemical 1. RP for electrolytes hypokalemia hypochloremia, low bicarb, BE less than -2 2. ABG for metabolic acidosis 3. Urine for paradoxical aciduria Imaging 1. Transabdominal US
37
US finding for Hypertrophic Pyloric Stenosis
Hypertrophied muscles around pylorus Can include Dynamic study
38
Mx of hypertrophic pyloric stenosis
Pyloromyotomy( open vs lap vs transumbilical) - Split pyloric muscles without entering the lumen trial of feeds 4hrs after
39
Barium enema findings for Hirschsprungs disease
1. Transition zone with funneling 2. Reversal of rectosigmoid ratio
40
Sign of HAEC
Hirschsprung associated enterocolitis Sawtooth appearance from mucosal edema
41
Age group where intussusception is common
6 months to 6 years
42
Most common cause of intussuception
Infection causing hypertrophy of Peyer Patches or lymphadenitis
43
First line management of intussusception
Air enema
44
What to consent for in open reduction of intussusception
Appendicectomy so RUQ pain won't lead to diagnostic dilemma
45
Possible pathological lead points to expect in patients outside of 6m to 6y
1. Meckel 2. Polyps 3. Hamartoma 4. Masses eg lymphoma, GIST 5. IgA Vasculitis/HSP
46
Number of air enema reductions before converting to open reduction
3-4 attempts with high pressures not >120mmHg
47
Mx of intuss with suspected pathological lead point
Open reduction with exploration
48
Mx of indirect inguinal hernia in neonate/infant
Surgical herniotomy due to high risk of cx( incarceration, obstruction, strangulation and perforation)
49
Age where hydrocele is
50
51
Radiological signs of Hirschsprungs
1. Transition point 2. Mosaic colonic pattern