Common ped surgeries lecture Flashcards

1
Q

gastroschisis vs omphacele

A

gastro- gastric contents out
omphacele- central defect in a sac

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2
Q

gastroschisis vs omphacele associated ocnditions

A

gastro- none
omphacele- 50-70% (survival rate drops with ocngenitl heart defect, prematurity)

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3
Q

beckwith weidman syndrom

A

overgrowth syndrome
macroglossia, microsmia

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4
Q

potential complicaitons of surgery for admoninal

A

can impede venous return/hotn
can impair diaphragm- inadequate ventilation
aortocaval compressions- bowel ischemia, decreased co, renal and hepatic functino

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5
Q

When is surgical management unsafe

A

intragastric pressure >20
change in cvp >4
etco2 >50
pip >35

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6
Q

maintenance and replacement fluid for abdominal surg

A

maintenance d5 or d10 .2NS
replacement- isotonic 2-4x maintenance (usually 8-15ml/kg)

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7
Q

when do u need 2 pulse ox

A

abdominal surgery
pre ductal RA
post ductal LF

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8
Q

abdominal anesthetic management

A

AVOID n2o distends bowel

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9
Q

CDH

A

allows herniation of abdominals into the thoracic cavoty

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10
Q

CDH classification

A

posterolateral 80-90%
anteromedial 2%
para esophageal 20%

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11
Q

CDH complications

A

bilat lung hypoplasia
pulmonary htn
lv dysfunction

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12
Q

classic presentation of CDH

A

dyspnea, cyanosis, dextrocardia (heart sounds on wrong side)
bulging chest, decreased breathe sounds, bowel sounds in chest

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13
Q

key to survival for cdh

A

prenatal diagnosis- birth can occur in high level center w experienced surgeons

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14
Q

goals of cdh management

A

maximize arterial oxygenation (mech vent, low pressures >30)
correct acidosis
prevent hypothermia
prevent pain

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15
Q

when can surgery occur for cdh

A

bp normal for 24 hours
preductal sat >85 on fio2 50
lactate <3
uo 1-2ml/kg/hr

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16
Q

after the honeymoon phase of cdh, what might be required ?

A

ecmo, no

17
Q

ecmo criteria

A

wieght >2kg
gestation >35 weeks

18
Q

what meds to avoid with cdh

A

hypothermia
n2o

19
Q

when does pyloric stenosis present

A

2-8 weeks of life

20
Q

pyloric stenosis symptoms

A

hyponatremic, hypokalemic, hypochloremic metabolic alkalosis
vomit out all the salt, chloride, potassium

21
Q
A
22
Q

primary concern of pyloric stenosis management

A

aspiration of gastric fluid

23
Q

TEF classic presentation

A

inability to manage oral secretions
gastric distention
choking on first feed

24
Q

goal TEF ETT

A

below fistula above carina
advance into R mainstem, withdraw until ett breathe sounds are confirmed in L axilla

25
Q

hallmark sign condgenital dislocation of the hip

A

ortalani clock as femoral head moves in and out of acetabulum

26
Q

greatest concern for ocngenital hip dislocation

A

loss of airway
pt must be kept in stage 3 to prevent laryngospasm

27
Q

when will clubfoot be fixed

A

3-6 months

28
Q

what is osteogenesis imperfecta

A

fibroblasts dont work well- they normally heal wounds and form collagen

29
Q

most severe type of OI

A

2- 90% pass by 1 week

30
Q

OI clinical presentation

A

bowing of long bones
deafness
bleeding is rare
HYPERMETABOLIC- NOT MH
airway is usally normal, but be careful w c spine when intubating

31
Q

when would fracture need urgent repair

A

vascular compromise
hotn
large hematoma

32
Q

myelodysplasia

A

Congenital failure in the middle or end of nueral tube
spina bifida- safe, meningocele- bulge in spinal fluid, myelomeningocele- bulge with CSF and nerves- most severe

33
Q

symptoms with scoliosis

A

decreased lung volumes
decreased chest wall compliance
vq MM, chronic hypoxemia
increased PVR, pulmonary htn causing RV failure
get echo if curvature >35, if over 65, restrictive lung disease

34
Q

when to use MEPs

A

scoliosis surgery
propofol, remifent, versed, ketamine

35
Q

PPAP

A

periop precision analgesia platform- improve analgesia and reduce serious immediate long term adverse outcomes

36
Q

scoliosis aneshtetic management

A

low bp map 70
txa 10mg/kg load, then 10mg/kg/hr
aggresive temp management

37
Q

scoliosis problems

A

siadh, hypvolemia, pain