Miscellaneous Topics Flashcards

(51 cards)

1
Q

What is Intussusception?

A

An acquired invagination of the proximal bowel into the distal bowel

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2
Q

What is the most frequent cause of bowel obstruction and infants and toddlers?

A

Intussusception

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3
Q

The Intussusception telescopes into the distal bowel by:

A

Peristaltic activity

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4
Q

In Intussusception, the mesentery of the proximal bowel is compressed, resulting in:

A

Venous obstruction + Bowel wall edema -> Arterial insufficiency -> Necrosis

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5
Q

What are the types of Intussusception?

A

1) Primary (idiopathic)
2) Secondary

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6
Q

Is there a lead point in primary Intussusception?

A

No

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7
Q

What is the cause of primary Intussusception?

A

Hypertrophy Peyer patches within the bowel wall

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8
Q

Primary Intussusception occurs frequently after recent:

A

1) URTI
2) Gastroenteritis

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9
Q

Which viruses could lead to a primary Intussusception?

A

1)Adenovirus
2) Rotavirus

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10
Q

Is there a lead point in secondary Intussusception?

A

Yes

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11
Q

Secondary Intussusception increases in proportion with:

A

Age

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12
Q
A
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13
Q

What is the most common cause of secondary Intussusception?

A

Meckel’s Diverticulum

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14
Q

Most patients who develop Intussusception are:

A

Well-nourished, healthy infant boys
(4-9 months old)

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15
Q

The classic presentation of Intussusception is an infant or a young child with:

A

1) Intermittent crampy abdominal pain
2) “Currant Jelly” stools
3) Palpable mass

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16
Q

Why do we see “Currant Jelly” stools in Intussusception?

A

Due to bowel ischemia and mucosal sloughing

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17
Q

What imaging should you order if you suspect intussusception?

A

1) X-Ray
2) Ultrasound

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18
Q

What do you see on Ultrasound for intussusception in the transverse plane?

A

Target or ‘donut’ lesion

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19
Q

What do you see on Ultrasound for intussusception in the longitudinal plane?

A

Pseudokidney sign

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20
Q

What is the Initial management for intussusception?

A

1) Immediate decompression (NG Tube)
2) NPO
3) IV fluid resuscitation and maintenance IVF
4) Correct electrolyte disturbances

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21
Q

What is the non-operative management for intussusception?

A

Hydrostatic/Pneumatic Reduction (Under fluoroscopy or ultrasound guidance)

22
Q

What are the contraindications for Hydrostatic/Pneumatic Reduction in Intussusception?

A

1) Perforation/Peritonitis
2) Persistent hypotension/tachycardia
3) Sepsis

23
Q

What are the indications for operative management for intussusception?

A

1) Nonoperative reduction is unsuccessful or incomplete
2) Signs of peritonitis/ pneumoperitoneum
3) Presence of a lead point (secondary intussusception)

24
Q

What are the risk factors for Hypertrophic Pyloric Stenosis (HPS)?

A

1) Family history
2) Male gender
3) Younger maternal age
4) Being a first-born infant
5) Maternal feeding patterns

25
What are some genetic factors that may play a role in HPS?
1) Race 2) Sex (Increased frequency in males) 3) First-born infants with a positive family history
26
What are some environmental factors that may play a role in HPS?
1) Method of feeding (breast vs formula) 2) Seasonal variability 3) Exposure to erythromycin 4) Transpyloric feeding in premature infants
27
What are some other factors that may play a role in HPS?
1) Excessive substance P 2) Decreased neurotrophins 3) Deficient nitric oxide synthase 4) Gastrin hypersecretion
28
The main etiology for HPS is:
Unknown
29
What is the main symptom that HPS presents with?
Nonbilious, progressive projectile vomiting (of recent feedings)
30
When does HPS present?
In a full-term neonate (about 2-8 weeks old)
31
How does HPS present on clinical exam?
1) If: a) Early: Appears well b) Late: Signs of dehydration 2) Visible gastric peristaltic waves 3) Palpable pylorus "olive sign"
32
What electrolyte abnormality do you look for in HPS?
Hypochloremic hypokalemic metabolic alkalosis
33
What imaging do you do for HPS?
Ultrasound
34
How do you diagnose HPS on Ultrasound?
1) Muscle thickness of ≥4 mm 2) Pyloric length of ≥16 mm
35
If the US findings for HPS are vague, then we should do:
Upper gastrointestinal series
36
What are the pre-op supportive measures for HPS?
1) NPO +/- gastric decompression 2) IV fluid resuscitation 3) Correction of electrolytes
37
What are the surgical options for HPS?
1) Laparotomy 2) Laparoscopic Pyloromyotomy
38
Is HPS a surgical emergency?
No, but it's urgent
39
What are the complications of surgery for HPS?
1) Mucosal perforation 2) Postoperative emesis 3) Prolonged postoperative emesis
40
41
What are the two main congenital abdominal wall defect seen in infants?
1) Gastroschisis 2) Omphalocele
42
Which congenital abdominal wall defect is covered by a peritoneal sac: Gastroschisis or Omphalocele?
Omphalocele
43
Which congenital abdominal wall defect is NOT covered by a peritoneal sac: Gastroschisis or Omphalocele?
Gastroschisis
44
Where is the defect location in an Omphalocele?
Midline through the umbilical ring
45
Where is the defect location in Gastroschisis?
Usually to the right of the umbilicus
46
Which congenital abdominal wall defect contains herniation of ONLY the bowel?
Gastroschisis
47
Which congenital abdominal wall defect contains herniation of bowel AND organs?
Omphalocele
48
How can we detect Gastroschisis in utero?
Via Ultrasound at 20 weeks gestation
49
To check for Gastroschisis in utero, we need to perform an ultrasound at __ weeks gestation.
20
50
What do you see on ultrasound in Gastroschisis?
1) Bowel loops floating freely in amniotic fluid 2) IUGR
51
Abnormal maternal __ is universally elevated in Gastroschisis
Alpha-Fetoprotein