Mehl. pulmo: TEF, choanal, diaph hernia, NRDS 11-01 (2) Flashcards

1
Q

TEF = Tracheoesophageal fistula.
HY peds condition

A

.

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2
Q

TEF. definition?

A

proximal esophagus ends in a blind pouch + the distal esophagus connects to the trachea.

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3
Q

proximal esophagus ends in a blind pouch + the distal esophagus connects to the trachea.?

A

TEF = Tracheoesophageal fistula.

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4
Q

TEF. CP?

A

Will present as a neonate who coughs up milk with initial feeding

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5
Q

Will present as a neonate who coughs up milk with initial feeding?

A

TEF.

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6
Q

TEF. what is highest yield point regarding diagnostic?

A

Highest yield point about TEF is that diagnosis is made via insertion of
nasogastric tube (which cannot be inserted fully because it hits the blind
pouch of the esophagus).

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7
Q

TEF. embriology abnormality?

A

An NBME Q wants “endoderm” as the abnormal embryology for TEF (makes sense, since esophagus is epithelial lining of the gut -> endoderm)

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8
Q

Weird condition in which the nasal passages don’t develop patency, so
the neonate is an obligate mouth-breather?

A

Choanal atresia.

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9
Q

Choanal atresia. definition?

A

Weird condition in which the nasal passages don’t develop patency, so the neonate is an obligate mouth-breather

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10
Q

Choanal atresia.
CP?

A

Will present as a child who becomes blue/hypoxic while breast feeding (because he can’t breathe through the nose), then cries/becomes pink once detaching from the breast

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11
Q

Will present as a child who becomes blue/hypoxic while breast feeding
(because he can’t breathe through the nose), then cries/becomes pink
once detaching from the breast?

A

Choanal atresia.

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12
Q

Choanal atresia. how made diagnosis?

A

Similar to TEF, diagnosis is made via insertion of nasogastric tube.

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13
Q

Choanal atresia. part of what syndrome?

A

Part of CHARGE syndrome

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14
Q

CHARGE syndrome?

A

Part of CHARGE syndrome -> Coloboma of the eye (hole in the eye), Heart defects, Atresia of the choanae, Renal defects, Genitourinary
anomalies, Ear anomalies

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15
Q

Congenital diaphragmatic
hernia. one of the highest yield ped condition.

Cause?

A

Caused by failure of formation of pleuroperitoneal membranes.

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16
Q

Caused by failure of formation of pleuroperitoneal membranes?

A

Congenital diaphragmatic
hernia.

17
Q

Congenital diaphragmatic
hernia. occur on what side?

A

Always occurs on the left, where bowel from the abdomen can herniate
up into the left-chest.

18
Q

Always occurs on the left, where bowel from the abdomen can herniate
up into the left-chest?

A

Congenital diaphragmatic
hernia.

19
Q

Congenital diaphragmatic
hernia. CP? regarding bowel sounds

A

Can present as decr. bowel sounds in the abdomen + incr. bowel sounds in the
left hemithorax

20
Q

Congenital diaphragmatic
hernia. what vignette might say?

A

Vignette might say there are cystic-appearing areas in the left hemithorax seen on CXR (loops of bowel).

21
Q

Neonatal respiratory distress syndrome (NRDS).
definition? what case, what weeks born?

A

Aka hyaline membrane disease.

The answer on USMLE for respiratory distress in kid who is born <34 weeks’ gestation.

22
Q

NRDS. cause pathophysiology?

A

Due to insufficient surfactant production by type II pneumocytes due to
decr. lamellar bodies (the specialized organelles that produce surfactant).

23
Q

NRDS. lecithin/sphingomyelin?

A

These kids have decr. lecithin/sphingomyelin ratio (i.e., <2.0). Normally it is >2-2.4.

24
Q

NRDS. another name for lecithin?

A

dipalmitoyl phosphatidylcholine

25
Q

NRDS.

USMLE can give simple vignette of NRDS and then ask for various manipulation of the ratio – i.e., “­ incr. sphingomyelin” might be an answer (makes sense, since this would decr. the ratio)

A

.

26
Q

NRDS. decr. surfactant –> ? –> elastics?

A

Decr. surfactant production means decr. alveolar compliance and ­INCR. elastic recoil.

Surfactant is hydrophobic and normally prevents the alveoli from collapsing, so if it’s deficient, the hydrophobic interactions of the alveolar walls enable incr. collapsing/elastic recoil.

27
Q

NRDS. CXR? buzzy

A

CXR shows a “reticulogranular” appearance.
Very buzzy and HY.

28
Q

NRDS. what is done in order to prevent it?

A

In order to prevent NRDS, a pregnant woman giving birth <34 weeks’ gestation must be TWO boluses of corticosteroids within 24 hours of parturition, which accelerate fetal lung maturity.

29
Q

NRDS.

For example, there is a
2CK Q where they tell you a woman giving birth at 33 weeks’ gestation was
given a bolus of corticosteroids 12 hours ago. They ask for next best step –>?

A

answer = “bolus of corticosteroids.”
Sounds weird because they said it was just done, but she needs TWO boluses

30
Q

NRDS. management sequence? 3/4

A

Tactile stimulation –> place under warming lights –> exogenous surfactant and oxygen

31
Q

NRDS. what is tactile stimulation?

A

warming, drying, and rubbing the back or the soles of the feet —–> stimulates spontaneous breathing

32
Q

Tactile stimulation –> place under warming lights –> exogenous surfactant and oxygen. in what pathology?

A

NRDS.