Pedi GI Flashcards

(52 cards)

1
Q

When is pyloric stenosis typically noticed in infants

A

withing the first 3-5 weeks of life, rare after 12

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2
Q

Clinical presentation of pyloric stenosis

A
  • 3 to 6 week old with post prandial non bilious projectile vomiting
  • weight loss
  • hungry after vomiting
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3
Q

PE for a baby with pyloric stenosis

A
  • appears think
  • palpable olive at lateral edge of rectus
  • peristaltic waves may be visualized pre emesis
  • may be jaundice
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4
Q

Diagnostics of pyloric stenosis

A

-ultrasound

-

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5
Q

Treatment of pyloric stenosis

A
  • correct hydration status first

- pyloromyotomy

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6
Q

When is intussesception most commonly seen

A

3 months to 5 years old

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7
Q

Where is the typical site of intussusception

A

near the iliocecal junction

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8
Q

Etiology of intussusception

A

proximal bowel telescopes into distal segment–> associated mesentary dragged along–> venous and lymphatic congestion–> intestinal edema–> possible ischemia

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9
Q

What causes intusscusception

A

most cases idiopathic

  • virus
  • post infectious bacterial enteritis
  • lead point from underlying pathology
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10
Q

Clinical manifestations of intusscusception

A
  • sudden, severe, crampy, progressive pain
  • child will be incosolable with legs drawn up
  • non bilious vomiting post pain
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11
Q

Presentation of intusscusception between episodes

A
  • normal and pain free
  • stool main contain gross or occult blood
  • currant jelly stool
  • may feel sausage shaped mass of right side of abdomen
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12
Q

Test to look for intusscusception

A

ultrasound!

“bull’s eye” or “coiled spring”

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13
Q

Intusscusception on xray

A

shows crescent sign

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14
Q

Non operative treatment for intusseception

A
  • enema with hydrostatic or pneumatic pressure

* treatment of choice in stable pt w/o signs of perforation

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15
Q

When is surgical treatment indicated

A

if non operative approach failed

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16
Q

What always gets referred to surgery whether acute or intermittent and presently asymptomatic

A

intusseception

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17
Q

What is phenylketonuria

A

deficiency of pkenylalanine hydroxylase

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18
Q

What does a deficiency of PAH cause

A

increase in serum and urine phennylalanine—> intellectual disability

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19
Q

Increased phenylalanine interfers with what

A
  • brain growth
  • mylenination
  • neurotransmitter sunthesis
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20
Q

Clinical findings in untreated PKU patients

A
  • mental disability and impaired IQ-epilepsy
  • abnormal gait
  • pigmentation issues
  • eczema
  • blood and urine may smell mousy
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21
Q

When should treatment of PKU be started

A

by one weeks of life

22
Q

When do levels of phenylalanine need to be monitored

A
  • weekly for the first year
  • twice a month years 1 to 12
  • monthly after 12 for life
23
Q

How does a child less than 5 present with appendicitis

A

listless, feverish kid with diffuse pain, womitting, rebound, gaurding–> perforated

24
Q

Treatment of non perforated appendicitis in kids

A
  • fluids
  • pain control, anti pyretics, anti emetics
  • NPO
  • pre op abx (cefoxitin)
25
Treatment for perforated appendicitis in kids
- fluids - pain control, anti pyretics, anti emetics - NPO - amp/gent/flagyl
26
When is surgery typically done in a kid with non perforated appendicitis
within 6-8 hours may be 24-48 of IV abx first
27
Normal stooling pattern in newborn. 0-3 months. Less than 2 years. By 4 year
Newborn: NL stool withing 36 hours 0-3 months: 3 to 4 stools a day Less than 2: 1 to 2 per day By 4 years old: once a day
28
Organic causes of constipation
- anatomic - metabolic - neuropathic - interstinal nerve or muscle disorders - abdominal musculature disorder - food intolerance
29
Functional causes of constipation
- painful defecation - toilet training issues - dietary issues
30
Treatment of constipation
- treat the cause - ensure enough fluids, dietary fiber - no cows milk until 1 - dont force toilet training
31
interventional treatment for infants with constipation
- glycerine suppository | - ubricated thermometer
32
Interventional treatment for older children with constipation
- glycerine suppository - miralax - ? enema - laxative?
33
What is encopresis
involuntary leakage of stool unto the underpants with or without constipation
34
What is the most common cause of encopresis
constipation
35
When does encopresis
-most often around tiems of toilet training, teasing about stooling and school onset
36
Diagnosis of encopresis
psychiatric diagnosis, must have 1. voluntary /involuntary passage fo stool outside of bathroom or diaper 2. one event a month for at 3 months 3. age older than 4 years 4. stooling not a result of laxatives or illness involving colon such at colitis
37
Treatment of encopresis
- clean out--> miralax - stool softeners - scheduled stooling - parental and patient educations
38
What is hirschprung's disease
incomplete migration of neural cells in the mysenteric and submucosal plexus--> part of the colon lack ganglion cells--> results in the affected segment constricting and the proximal segment becoming distended with feces
39
What part of the colon does hirchprung's disease often affect
rectosigmoid
40
Signs and symptoms of hirschprung's disease in newborns? children?
newborn: failure to have complete stooling or stool Child: swollen belly, vomiting, constipation, diarrhea -failure to thrive, fatigue
41
Gold standard of diagnosis of hirschprung's disease
biopsy
42
Other diagnostic tools for hirschprung's disease
- manometry of anorectum - barium enema - xray
43
Treatment of hirschprung's disease
surgical excision of the affected area with anastomosis of the healthy ends
44
Meckel's diverticulum?
congential diverticulum of the small intestine
45
Who gets Meckel's? Where is it
``` 2% of population 2:1 male to female 2 years old 2 feet from iliocecal valve 2 inches in length ```
46
How is Meckel's diagnosed
typically an incidental finding because it is asx
47
If Meckel's shows symptoms, what are they?
- GI bleeding - intestinal obstruction - peritonitis - diverticulitis - appendicitis - fistulae
48
How is Meckel;s treated
excision then treat accompanied pathology
49
What is malrotation
congenital anomaly of the mid gut leading to - small intestine found on R side - cecum displaced into epigastric region - ligament of Treitz displaced - fibrous band form leading to obstruction - narrow base of small intestine-->volvulus
50
How does malrotation present
infant with - bilious vomiting - abd pain - abd distention - melena and or mucousy stool
51
What things can you used to support your clinical suspicion of malrotation
- abd xray - UGI series - contrast enema
52
How do you treat malrotation
surgery