Neonates GI Flashcards

1
Q

What is necrotising enterocolitis?
what age is it common in?

A

2-4 week premature baby

Necrosis (tissue death)
+/- infection (KEEPS) of the intestine due to ischemia + infection, inflammation

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2
Q

RF for necrotising enterocolitis?

A

Indomethacin use (NSAID)
Low breast fed
premature
low birth weight

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3
Q

Sx of necrotising enterocolitis?

A

Abdo distension (with absent bowel sounds)
Erythematous shiny taught skin
Bile streaked vomiting
Bloody stools
Resp distress + feed intolerance

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4
Q

Dx of necrotising enterocolitis?

A

Bloods - FBC, U+E, Clotting screen, sepsis culture, MC+S

Abdo xray

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5
Q

What is seen on abdominal xray in necrotising enterocolitis?

A

Pneumatosis intestinalis (gas within bowel)
Pneumoperitoneum (air in abdo cavity)
Dilated bowel loops

-Rigler sign (‘double walled’ sign - gas outlining both sides of bowel wall)
-Football sign
(both indicate pneumoperitoneum)

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6
Q

Tx of necrotising enterocolitis?

A

Total parenteral feed (through vein)
IV ceftriaxone + vancomycin
Last line = laparotomy (remove necrotic bowel)

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7
Q

Complications of necrotising enterocolitis?

A

perforation
sepsis
shock
DIC

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8
Q

What is oesophageal atresia?

A

Congenital defect where the oesophagus terminates into a blind pouch rather than connecting normally to stomach - separates upper and lower oes
blind ending oesophagus

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9
Q

What is the MC oesophageal atresia, what is it called when it is distally?

A

MC = Proximal blind ending 85%

Distally = tracheo-oesophageal fistula (abnormal connection between trachea + oesophagus)

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10
Q

Rf for oesophageal atresia?

A

Trisomies
VACTERL (Vertebral defects, anorectal anomalies, cardiac defects, trachea-oesophageal fistula/oesoph atresia)
IVF baby

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11
Q

Sx antenatally and postnatally of oesophageal atresia?

A

Antenatal = Polyhydramnios (baby’s inability to swallow and absorb amniotic fluid)

Postnatally =
feed regurgitation,
frothy saliva,
3C (cough, choke, cyanotic),
Difficulty passing NG tube

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12
Q

Dx of oesophageal atresia?

A

NG tube radiologically guided = blind end

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13
Q

Tx of oesophageal atresia?

A

Anastamosis surgery ASAP after birth

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14
Q

What is duodenal atresia?

A

Congenital defect = blind ending duodenum, duodenal stenosis at Ampulla of vater (just distal) - intestinal obstruction

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15
Q

RF for duodenal atresia?

A

Downs!!!
Maternal GDM
VACTERL
CHD
IVF baby
Annular pancreas (ring of pancreas surrounding 2nd part of duodenum)

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16
Q

1/3 of all duodenal atresia are Px who have?

A

Downs

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17
Q

Sx of duodenal atresia?

A

post feed bilous vomiting

18
Q

Dx of duodenal atresia?

A

Abdo X ray

19
Q

What would be seen on an abdo xray in a Px with duodenal atresia?

A

Double bubble sign (bubble in stomach + patent part of duodenum)

20
Q

Tx of duodenal atresia?

A

duodenoduodenostomy
IV fluids
NG decomp ASAP

21
Q

Neonatal Jaundice:
<24hr causes?

A

Pathological
TORCH,
haemolytic anemia,
Rh/ABO incompatability,
Sepsis

22
Q

Neonatal Jaundice:
1 day to 2 weeks causes?

A

Physiological (low RBC lifespan initially)
Breastfeeding

23
Q

Neonatal Jaundice:
>2 weeks causes?

A

Pathological:
Biliary atresia
choledochal cyst (biliary cyst)
Hypothyroid (congenital)
Criggler Najjar
CF

24
Q

what are the days for physiological jaundice for term and preterm babies?

A

<14d term
<21d pre term

25
Dx of neonatal jaundice?
Bloods: FBC, U+E, LFT, TFT (if High bilirubin = 24hr transcutaneous bilirubinometer)
26
Tx of neonatal jaundice?
>359 = phototherapy (bili = lumirubin = renally excreted) >428 = exchange transfusion
27
Complication of neonatal jaundice?
if unconjugated = Kernicterus (unconj bilirubin accumulation in basal ganglia therefore neurological Sx) - risk of dyskinetic CP
28
What is biliary atresia?
1 or more extrahepatic duct stenosed - obstructive jaundice F>M 1/12000
29
RF for biliary atresia?
CFC5 Downs maternal DM
30
Sx of biliary atresia?
Prolonged jaundice with biliary obstruction Sx (dark urine, pale/chalky white stool)
31
Dx of biliary atresia?
High conjugated bilirubin Abdo USS = triangle cord sign + Gall bladder abnormality Cholangiography
32
Ddx of biliary atresia?
choledochal cyst
33
Tx of biliary atresia?
'Kasai' procedure = hepatoportoentero-ostomy (creates new pathway from liver to gut to bypass fibroses bile ducts)
34
When is the best time to Treat biliary atresia?
the earlier the better <10 weeks = 'golden period'
35
What is gastroschisis and omphalocele?
congenital defects of abdo wall resulting in intestinal herniation
36
Gastroschisis: adjacent to? peritoneum? systemically? AFP? RF? Mode of delivery?
Adjacent to abdo wall No peritoneum systemically well High AFP (Abdo wall defect) - immediate repair Prematurity Can try vaginal delivery
37
Omphalocele: through? peritoneum? % have CHD/NTD? AFP? RF? Mode of delivery?
Through umbilicus Layer of peritoneum 40-80% have CHD/NTD - staged repair over 12 months High AFP Trisomies should do C - section
38
What is neonatal hepatitis syndrome?
Neonatal hepatitis is inflammation of the liver that occurs only in early infancy, usually between one and two months after birth
39
Causes of neonatal hepatitis syndrome?
Galactosemia - can't metabolise milk properly (cow, formula, breast) - jaundice + hepatomegaly = gram -ve sepsis A1AT Viral Idiopathic
40
Dx of neonatal hepatitis syndrome?
High conjugated bilirubin + liver biopsy - multinucleate rolettes
41
Tx of neonatal hepatitis syndrome?
Dietician initiates special, non milk feed soy milk formula