peds deck 12 Flashcards

(50 cards)

1
Q

induction of anesthesia for TEF w/o G-tube

A
  1. inhalational induction 2. followed by topical lidocaine intubation keeping spontaneous vent
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2
Q

induction of anesthesia for TEF with G-tube

A
  1. INH or IV induction with paralysis 2. then place ETT
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3
Q

your doing a TEF repair surgery and the SpO2 is low , and the EtCO2 is low, and you are having a difficult time ventilating, what should you suspect

A

ETT migration into fistula

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4
Q

__________________ is due to failure of the gut to migrate from the yolk sac to the abdomen during gestation

A

omphalocele

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5
Q

_________________ herniated viscera outside of the infant and is covered by a membrane. typically bowel is morphologically and fx’al normal

A

omphalocele

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6
Q

in an omphalocele the umbilical cord is found ________________, and with gastroschisis the umbilical cord is found __________________

A

at the apex of the sac; periumbilical usually to the right

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7
Q

which herniated bowel syndrome is associated with congenital anomalies, like Beckwith-wiedemann, congenital heart disease, and/or exstrophy of the bladder

A

omphalocele

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8
Q

pt presents for omphalocele repair, before taking the pt to the OR, what should you do?

A

have cardiac consult with echocardiogram due to increased risk of congenital anomalies

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9
Q

_________________ develops due to occlusion of the omphalomesenteric artery during gestation –> herniated bowel through the defect without a covering

A

gastroschisis

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10
Q

with bowel herniation, repair of ______________ can wait for several days; however, ______________ needs to be repaired within 12-24 hours

A

omphalocele; gastroschisis

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11
Q

T/F: gastroschisis frequently has other congenital anomalies associated with it

A

false; typically does not have other congenital anomalies associated with it; however omphalocele does

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12
Q

primary goal of neonate with gastroschisis post delivery

A
  1. protection of exposed bowel 2. minimization of fluid/temperature loss
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13
Q

anesthesia implications for gastroschisis

A
  1. pt will have considerable evaporative and 3rd space fluid losses 2. possibly need large amounts of full strength balanced salt solutions 3. cosnider albumin 4. infection risk (d/t exposed bowel) 5. RSI or awake intubation 6. need adequate NMBA 7. remain intubated postoperatively 8. avoid N2O
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14
Q

described the “staged procedure” that can be done for gastroschisis/omphalocele

A
  1. use a silo to contain/cover viscera 2. every 2-3 days size of silo is reduced into the abdomen 3. usually not intubated d/t allowing assessment of appropriate silo reduction without impairing ventilation/circulation
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15
Q

post-op considerations for gastroschisis & omphalocele

A
  1. may need ETT 3-7 days 2. risk of postop HTN and edema 3. monitor intrabdominal pressures (bladder pressure) due to risk of compartment syndrome
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16
Q

imperforate anus is typically seen with what other congenital anomalies

A
  1. VACTERL 2. CHD 3. GU anomalies 4. Trisomy 18 5. Down syndrome
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17
Q

anesthetic considerations for imperforate anus

A
  1. dependent on intervention needed (do they need diverting colostomy first?) 2. typically no NMBA –> stimulate muscle around anus before creating opening
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18
Q

s/sx of pyloric stenosis

A

infants present btwn 2-8 weeks with… 1. nonbilious projectile vomiting 2. hypokalemia 3. hypochloremic metabolic alkalosis 4. if present in newborn = hypoglycemia

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19
Q

T/F: pyloric stenosis is a surgical emergency

A

false - correct fluid and electrolytes first

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20
Q

anesthetic implications for pyloric stenosis

A
  1. F/E imbalances: hypochloremic metabolic alkalosis, hypokalemia, hyponatremia, possible hypocalcemia 2. RSI or awake intubation 3. very short procedure: desflurane, propofol 4. mininimal postop pain - no opioids 5. extubate when fully awake
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21
Q

________________ = THE most common cause of acute abdominal surgery in children

22
Q

anesthetic considerations for appendicitis

A
  1. dehydration due to fever and vomiting 2. 12% increase in fluids for every 1 degree C temp increase 3. if ruptured - pt will be septic 4. RSI with cricoid pressure
23
Q

risk factors for necrotizing enterocolitis

A
  1. prematurity with small birth weight (<1500 g) 2. hypoxemia (birth asphyxia, RDS) 3. CHD
24
Q

theorized pathophysiology of necrotizing enterocolitis

A

mucosal injury –> bacterial infection –> gas formation –> necrosis

25
s/sx of necrotizing enterocolitis
1. hemodynamic/temperature instability 2. poor feeding with residual volume/vomiting 3. abdominal distension 4. bloody stools 5. sepsis/lethargy
26
anesthesia considerations for necrotizing enterocolitis
1. preoperative fluid resuscitation 2. electrolyte imbalances: hyperglycemia, metabolic acidosis, prerenal azotemia 3. avoid N2O 4. careful with myocardial depressants/VD (esp if look septic) 5. RSI or awake intubation 6. broad spectrum antibiotics (zosyn) 7. ensure blood products are readily available
27
________________ is one or more of the cranial sutures close prematurely
craniosynostosis
28
place in order from the most common to least common craniosynostosis
sagittal > coronal > metopic
29
______________ craniosynostosis is the one most commonly associated with syndromes
1. coronal 2. also complex (incl more than one)
30
craniosynostosis is more common in what gender
males
31
two types of craniofacial reconstruction approaches
1. total cranial vault reconstruction 2. strip craniectomy
32
uncorrected cranial vault deformities may lead to
1. increase ICP 2. hydrocephalus 3. psychosocial issues 4. vision loss 5. developmental delay
33
anesthesia implications for craniofacial reconstruction surgery
1. risk of extensive blood loss - have blood in the room 2. fluid management 3. keep the baby warm
34
development of a myelodysplasia has been found to be correlated with insufficient _______________ during pregnancy
folate
35
what are the different presentations of a myelodysplasia
1. spina bifida 2. meningocele 3. meningomyocele 4. arnold chiari malformation
36
______________ myelodysplasia where bones do not close,but CSF and neural tissue are not involved
spina bifida
37
________________ myelodysplasia where there are lesions in the CSF but not the tissues
meningocele
38
________________ myelodysplasia where there are lesions in both CSF and neural tissues typically have loss of bowel and bladder fx and can have anywhere from sensory loss to complete paralysis
meningomyelocele
39
_______________ myelodysplasia that has a caudal displacement of the brain stem
arnold chiari malformation
40
anesthetic considerations for meningomyelocele
1. infection risk 2. fluid and electrolyte considerations (leak of CSF, long surgery) 3. positioning for intubation 4. blood loss - ensure blood in the room 5. increased risk for latex allergy
41
positioning for intubation for myelomeningocele
1. if smaller - can do supine with lesion in a foam donut 2. if larger - lateral decubitus
42
______________ almost alway exists with myelodysplasia
arnold chiaria malformation
43
______________ is an abnormality in the posterior fossa and is associated with obliteration of normal exit of CSF from the fourth ventricle --> hydrocephalus
arnold chiari
44
s/sx associated with arnold chiaria malformation
1. almost always myelodysplasia will have arnold chiari malf. 2. vocal cord paralysis --> stridor, respiratory distress, apnea 3. abnormal swallowing/pulmonary aspiration 4. cranial nerve defects --> abnormal response to hypoxia and hypercarbia 5. unusual breathing or BP patterns
45
________________ is a neural tube defect that is failure of the neural tube to close and can occur anywhere on the head
encephalocele
46
location of encephalocele most common in the US
occiput
47
encephalocele are thought to be due to what?
prenatal exposure to teratogens
48
sx of encephalocele
1. hydrocephalus 2. spastic quadriplegia 3. microcephaly 4. ataxia 5. developmental delay 6. mental and growth retardation 7. seizures 8. vision problems
49
anesthesia concerns with encephalocele
1. potentiall difficult airway 2. difficult to position for surgery and DL 3. difficulty with fluid management
50
eventual s/sx in pt with hydrocephalus
1. increase in head size 2. increase in ICP 3. lethargy 4. vomiting 5. cardio-respiratory problems