Pediatric GI 2: Abdominal Pain In Children Flashcards

1
Q

How does the blood flow of umbilical cord work?

A

Muscular umbilical arteries
- carries deoxygenated blood from the fetus to the placenta

Umbilical vein
- carries oxygenated blood from placenta back to the fetus

  • contains 20mL/kg
  • should delay clamping of the course at delivery for 30-60sec

Remain anatomically patent for 10-20 days

  • umblilical arteries -> lateral umbilical ligaments
  • Umbilical vein -> ligementum teres
  • ductus venosus -> ligamentum venosum
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2
Q

What kind of defects can occur from delayed separation of the umblilcal cord (>1 month)

A

Neutrophil chemotactic defects and overwhelming bacterial infections

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3
Q

Single umbilical artery defect

A

Present in approximately 5-10/1,000 with it being 35-70/1,000 in twin births

Very common in trisomies and 30% of infants with this defect result in congenital structural abnormalities
- it does NOT work the other way around (just because you have a single umbilical artery doesn’t mean you have a trisomy)

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4
Q

Other umbilical cord abnormalities

A

Abnormally short cords:
- fetal hypotonia, oligohydramnios, uterine constraint

Long cord (>70cm): 
- increase the risk for true knots wrapping around the fetus and causing prolapses 

Straight uncoiled cords:
- associated with anomalies, fetal distress, intrauterine fetal demise

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5
Q

Omphalocele

A

A herniation or protrusion of the abdominal contents into the base of the umbilical cord

  • the sac is covered with peritoneum without overlying skin and includes the distal umbilical cord into the sac
  • can see herniation of the intestines into the cord in 1/5,000 births
  • can see herniation of liver and intestines into the cord in 1/10,000 births

50-70% have associated malformations and 30% have trisomies
- (the 30% is even higher if the liver is not within the sac)

Treatment = cover sac with moist sterile dressings and prompt surgical repair

  • usually normal survival rates is >90%
  • if cant get to surgery = moist/sterile dressings can encourage epithelialization of the sac
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6
Q

What is the most common genetic condition that is seen with omphalocele’s?

A

Beckwith-Wiedemann syndrome
- 11p15 mutation in IGF-2 gene

Causes:

  • fasting hypoglycemia
  • omphaloceles
  • macrosomia
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7
Q

GERD in children

A

Is the most common esophageal disorder in children
- is ONLY pathological GERD if symptoms are seen due to frequent/persistent GER

nearly all infants have some reflux symptoms that dont require therapy

Symptoms:

  • heartburn
  • poor weight gain
  • upper respiratory symptoms
  • wheezing
  • irritability
  • apnea And bradycardia (more common in preterm infants)
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8
Q

Happy spitters

A

Physiological GER that is evident in first few months of life
- peaks at 4 months and resolves spontaneously in up to 88% by 1 yr of age with almost all gone by 2 years

will show recurrent regurgitation without exhibiting discomfort or refusal to eat and failure to gain weight (differs from GERD)

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9
Q

Sandifer syndrome

A

Is a combination of GERD and opisthotonos (abnormal posturing and back arching)
- uncommon manifestation

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10
Q

What are red flag warning signs for GERD / happy spitters?

A

Billous emesis

Frequent projectile emesis

GI bleeding

Lethargy

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11
Q

Diagnosis of GERD and other reflex diseases

A

Upper GI studies and I-GERQ)

Use endoscopy if needed to diagnosis for erosive esophagitis and complications of GERD
- also can be used to therapeutically dilate reflux-induced strictures

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12
Q

Treatment of GERD

A

1) Thickening feeding
- either prethickened formulas or tablespoon of rice/oat cereal per 1oz of formula

2) short trial of hypoallergenic diets in infants
3) lifestyle changes: avoid smoke exposure/proper feeding positioning/hydrolysis infant formulas/ avoid acidic foods/ weight reduction if obese

4) Histamine-2 antagonists for kids
- 1st line in younger children and mild GERD

5) PPIs and antiacids
- 1st line in severe/erosive GERD
- infants under 10 kg = 5mg PO daily
- infants 10-20 kg = 10mg PO daily
- infants 20 kg = 20mg PO daily

be careful with rice though since it increases risk of arsenic exposure

cant give meds until later in life

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13
Q

What kind of positioning worsens GERD?

A

Seated positions worsens infant reflux
- supine positioning also worsens reflux however this is the position recommended for sleeping to reduce risk of SUDS!!

Prone positioning and upright carried position helps minimize reflux symptoms
- should promote this position during awake time

Sleep in older children should be on their left side with only the head elevated (dont get abdominal flexion or compression working)

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14
Q

Foreign bodies

A

Usually under 5 years old

Coins are by far the most commonly ingested foreign body

Most common lodge point = cricophayngeus (upper esophageal sphincter)

children with development delays and psychiatric disorders are at high risk

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15
Q

Symptoms of foreign bodies

A
  • 30% may show asymptomatic*
  • need to follow up on any history of foreign body ingestion even if no symptoms are present

Symptoms:

  • acute bouts of choking/gagging and coughing
  • excessive salivation
  • dysphagia
  • emesis
  • pain in the neck/throat/sternal notch pain
  • stridor
  • wheezing
  • cyanosis
  • dyspnea
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16
Q

How to diagnosis foreign body

A

Plan A-P xray of neck/chest/abdomen

Plan lateral xray of neck/chest

also assess for risk for airway compromise and consult surgery if you feel risk for airway perforation

17
Q

What is the most dangerous non sharp foreign body

A

Button batteries
- need removal within 2 hrs or will induce mucosal injuries in 1 hr and complete erosion of esophageal layers in 4 hrs

sharp objects, magnets or anything that’s producing respiratory symptoms needs remove within 12 hrs of presentation

18
Q

How to tell if a coin is in the esophagus or the trachea on films?

A

Esophagus = coin is flat in AP-view and lateral edge in lateral films

Trachea = coin lateral edge is in AP-view and flat surface in lateral films

note Button-batteries have “double halo” sign vs a coin which doesnt

19
Q

What is pentaology of Cantrell?

A

A genetic condition that can occur in infants which produces all or some of the follow 5 abnormalities

1) abnormal pericardium morphology
- sclerotic pericardium
- ectopic cordis (heart is outside of thorax)
2) ventricular septal defect
3) congenital diaphragmatic hernia
4) Omphalocele
5) abnormalities of the sternum
- sternal cleft