Anesthetics for Common Pediatric Procedures Flashcards

1
Q

explanation of tonsillectomy and adenoidectomy procedure (T&A)

A

chronic inflammation and hypertrophy of lymphoid tissue in the pharynx may necessitate surgery to relieve obstruction or to remove the focus of infection

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2
Q

explanation of bilateral myringotomy and tympanoplasty procedure

A

myringotomy creates an opening in tympanic membrane through which fluid can drain
placement of ventilation tube (tympanoplasty) with lumen is frequently also performed.
alleviates pressure from middle ear and serves as a stent allowing continued drainage until tubes are naturally extruded in 6 months to a year

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3
Q

indications for tonsillectomy: most common

A

OSA (80%), infection (20%)

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4
Q

considerations for admission post tonsillectomy

A
<3 years old
abnormal bleeding tendencies
significant OSA
airway abnormalities
other systemic diseases
those living in excessive distance
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5
Q

tonsillectomy 2011 evidence based clinical practice guideline for optimization of perioperative management includes

A

strong recommendation for single intraoperative IV dexamethasone .5mg/kg
strong recommendation against routine administration of perioperative antibiotics
recommendation to advocate for pain management however avoid codeine and ketorlac.

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6
Q

why avoid codeine in pedes?

A

substantial genetic variation in metabolism (CYP450 and CYP2D6) of codeine into morphine, causing cases of breathing problems

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7
Q

T&A induction considerations

A

standard with oral RAE or reinforced ETT. cuffed with 20cmH2O aw pressure. LMA possible. secure midline
muscle relaxants ok but often a relatively quick operation

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8
Q

T&A table turned

A

45-90 degrees

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9
Q

T&A mouth gag

A

requires adequate depth of anesthesia
reevaluate airway after placement to ensure no dislodgment of ETT or LMA
throat pack
(metal thing that holds mouth open)

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10
Q

T&A analgesic management can include

A
fentanyl 1-2mcg/kg IV
tylenol 10-15mg/kg IV
dexamethasone .5-1mg.kg 
zofran .1mg/kg
dexmedetomidine .1-.5mcg/kg IV
consider ketorlac/ibuprufen administration post resection?
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11
Q

cold steel tonsillectomy method

A

stainless steel scissors and scalpels, toothed forceps and herds dissector/retractor are used to dissect the whole tonsil tissue from its capsule. exposes underlying constrictor muscle and hence more pain and more chance of hemorrhage!!! old school method not used much anymore.

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12
Q

electro dissection tonsillectomy method

A

mono polar or bipolar dissection of whole tonsil. head of cautery can reach 300-400 degrees to induce hemostasis, causes more lateral thermal damage and hence more pain and discomfort in the postoperative period.
kinetic energy heats intracellular and extracellular fluids and ruptures localized tissue

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13
Q

microdebrider tonsillectomy method

A

soft tissue shaver. 90-95% of tonsilar tissue is removed. natural, biological dressing is left in place over the pharyngeal muscles, preventing injury, inflammation, and infection. associated with less M&M than the other techniques. less blood loss, less pain.

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14
Q

coblation-cold ablation tonsillectomy method

A

introduced in 1998, energy is used in plasma field to break molecular bonds to excise or dissolve soft tissue at at a temperature of 40-70 degrees celsius and hence maintain integrity of the surrounding tissue. provides dissection, cautery, suction, and hemostasis in the same machine. it is quick, precise, and a smooth procedure.

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15
Q

radio frequency tonsillectomy method

A

cost effective, easy to use, time saving alternative to laser tonsillectomy. mono polar radio frequency energy is transferred by inserting probe into tonsil tissue in three or four sittings. ultimately produce scarring of tonsil tissue and thus reduce the size

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16
Q

laser tonsillectomy method

A

CO2 laser and KTP lasers can be used. less bleeding, less pain, discomfort, and is a day procedure. but more secondary hemorrhage and post operative pain have been noted with laser.

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17
Q

T&A emergence considerations

A

high risk fo laryngospasm, aspiration, and airway reactivity.
OG to empty stomach reduces incidence of emesis.
consideration for deep v awake extubation
coughing can increase bleeding, use of careful soft suction.
recovery position (on one side with head slightly down) allows blood to drain away from vocal cords
be cautious to administer opioids for a restless child as it may indicate airway compromise or hypoxia

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18
Q

T&A and EBL

A

may be difficult to assess due to occult pooling in stomach

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19
Q

bleeding tonsils: emergency

A

ensure adequate IV access (PIVx2, IO)
hypovolemia requiring vigorous resuscitation
potential for hemodynamic instability on induction
H&H, T&C, coagulation studies
RSI based on full stomach, try to adequately preoxygenate. propofol or ketamine followed by 2mg/kg succinylcholine IV
potentially difficult AW securing
OG to empty stomach

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20
Q

BMT indications

A

chronic otitis media, can lead to hearing loss and formation of cholesteatoma

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21
Q

BMT procedure considerations

A

kids often have URI
short OR time, PO midazolam may outlast procedure
consider PR acute
often mask only anesthetic
IV placed if another procedure is being done like a cleft palate repair
d/c sevoflurane during 2nd side

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22
Q

myelodisplasia aka spina bifida definition

A

failure of neural tube to close resulting in herniation of the spinal cord and meninges through a defect

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23
Q

meningocele definition

A

only contains meninges

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24
Q

myelominingocele definition

A

contains meninges and neural elements

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25
Q

hydrocephalus definition

A

condition in which excess CSF builds up within the fluid containing cavities or ventricles of the brain.

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26
Q

myelodisplasia neurosurgery: commonality, what else is present, timeline for repair

A

most common CNS defect that occurs during the first month of gestation.
hydrocephalus is also present and paralysis may occur below lesion
urgent repair required within 24-48 hours due to risk of infection or worsening cord function

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27
Q

myelodisplasia defect risk factors and where its most commonly located

A

risk factors: folate deficiency, chromosomal abnormalities

most common in lumbosacral region

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28
Q

if hydrocephalus is also present with myelodisplasia, what may need to happen?

A

VP shunt will be necessary if arnold chiari malformation is present (hindbrain displaced downward into the foramen magnum, resulting in hydrocephalus)

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29
Q

anesthesia for myelodisplasia repair: preoperatively

A

assess level of lesion and degree of deficit
review systems and rule out additional congenital anomalies
CBC, T&S

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30
Q

anesthesia for myelodisplasia repair: induction and intraoperative considerations
(what are they prone to? OR environmental consideration?)

A

routine monitors, may use intraoperative nerve monitoring (avoid muscle relaxation if motor evoked potential monitoring is utilized)
positioning: supine with sterile donut, lateral if large defect, prone for procedure
induce with inhalation or IV
potential for blood loss if it is large deficit
prone to hypothermia
latex free environment

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31
Q

anesthesia for myelodisplasia repair: postoperative

A

goal is to extubatne

assess need for postop apnea monitoring

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32
Q

what may be the cause of hydrocephalus

A

congenital defect like arnold chiari aqueduct stenosis) or by acquired disease (trauma, infection, tumor)

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33
Q

ventriculoscopy for hydrocephalus neurosurgery

A

use of fiber optic scope through cranial burrr holes to visualize lateral, third, and occasional fourth ventricle. alternatively, shunts may be positioned under ultrasound guidance

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34
Q

ventriculo-peritoneal (VP) shunt for hydrocephalus neurosurgery placement

A

lateral ventricle to peritoneum is most common placement and allows room for growth

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35
Q

ventriculo-atrial (VA) shunt for hydrocephalus neurosurgery placement

A

lateral ventricle to right atrium

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36
Q

endoscopic third ventriculostomy (ETV) for hydrocephalus neurosurgery placement

A

burr hole created in floor of the 3rd ventricle allowing CSF to flow directly into the basal cisterns

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37
Q

incision and positioning for hydrocephalus neurosurgery

A

incision is small, frontal or partietal to occipital.

position is supine with head turned and table 90-180 degrees.

38
Q

anesthesia for creation of CSF shunts: preoperatively

A

assess baseline neurological status and ICP
avoid premeds if ICP is increased
assess for vomiting history and dehydration
routine H&P
if the child has had repeated shunt revisions, review previous anesthesia records for any problems with airway or IV access
IVx1-2

39
Q

anesthesia for creation of CSF shunts: induction

A
standard monitors
propofol, fentanyl, rocuronium
isoflurane or sevoflurrane
GETA
protect and pad eyes
abx: cefazolin 30mg/kg IV
40
Q

anesthesia for creation of CSF shunts: maintenance

A

hyperventilation is undesirable because it may make cannulation fo the ventricle more difficult
maintain paralysis or propofol bolus when tunneling

41
Q

what to be cautious of for specifically VA shunts:

A

caution of air embolism/PPV while vein is open

42
Q

anesthesia for creation of CSF shunts: emergence

A

reversal of paralytic
antiemetics
extubate
fully awake to permit for rapid neurological assessment

43
Q

anesthesia for creation of CSF shunts: postoperative disposition

A

floor, step down, or ICU

44
Q

humerus fracture and 3 types

A

long bone of upper arm
proximal: break in upper part of humerus near shoulder
mid shaft: break in middle
distal: occurs near elbow. usually a part of a more complex elbow injury and sometimes involves loose bone fragments

45
Q

scoliosis etiology can be either (2)

A

idiopathic (most common, mainly affects adolescent girls)
neuromuscular (conditions of muscle weakness or spasticity is cause such as CP, MD, SCI. associated with greater blood loss)

46
Q

which elbow fracture in children is most common

A

supracondylar fractures of the humerus. results from falling with outstretched hand and extended elbow

47
Q

complications of supracondylar fractures of the humerus include

A

compartment syndrome
nerve palsies
late deformities

48
Q

anesthesia for humerus fracture: positioning, type of anesthetic, assessment considerations, emergence considerations

A

supine with table turned 90 degrees
GETA
assess NPO status and full stomach precautious requiring IV and RSI
timing of emergence if cast or splint is placed after closing

49
Q

anesthesia for humerus fracture: estimated length of surgery

A

30-60 minutes for pinning

30-90 minutes for open reduction

50
Q

posterior spinal instrumentation: when is surgical treatment recommended?

A

when curves are greater than 45 degrees while still growing or are continuing to progress greater than 45 degrees when growth stopped

51
Q

posterior spinal fusion for scoliosis goal of surgical treatment is two fold

A
  1. prevent curve progression

2. obtain curve correction

52
Q

describe posterior spinal fusion procedure for scoliosis

A

utilizes metal implants that are attached to the spine, and then connected to a single rod or two rods. posterior versus anterior approach (may require one lung ventilation). no external braces or casts are utilized

53
Q

LOS for postop posterior spinal fusion patients for scoliosis treatment and floor disposition type

A

3-6 days, step down or ICU postop.

54
Q

posterior spinal fusion positioning, duration, monitoring

A

positioning: prone. extra care in positioning ett. tongue and eye protection.
6+ hour surgery
intraoperative neuro monitoring may be utilized with possible wake up test

55
Q

posterior spinal fusion for scoliosis and blood loss

A

potential for significant blood loss. can utilize hypotensive technique on dissection (while still maintaining within 2-% of baseline). can use TXA, cell saver, autologous blood and hemp dilution techniques.

56
Q

posterior spinal fusion for scoliosis: preoperative

A

standard pediatric preoperative evaluation
starting CBC, coagulation, BMP, HCG in female patients
comorrbidities
T&C, set up 2 PRBC’s and cell saver
discuss with the team the nerve monitoring goals and use of paralytics
prepare patient and family for puffy face after prone position

57
Q

restrictive vital capacity % and implications

A

<70% predicted respiratory reserve is adequate

<40% predicted postop ventilation may be required

58
Q

neuromuscular scoliosis and respiratory function/succinylcholine

A

with neuromuscular etiology, may be more sensitive to requiring postoperative ventilation related to muscle weakness
succinylcholine may cause severe rhabdomyolysis with hyperkalemia

59
Q

posterior spinal fusion for scoliosis: case set up

A

cell saver, fluid warmer, blood tubing
aline, PIVx2, consider CVC if difficult access
prepare for prone position with superman arms
spinal underbody bair hugger
eye lubricant with tape, soft bite blocks
standard AW, induction meds, BIS, cerebral oximeter, emergency meds and OG
ensure room temperature is increased prior to bringing patient into OR

60
Q

evoked potential monitoring and dexmedetomidine/opioids

A

compatible with MEP, SSEP, EMG monitoring. low dose dex does not effect MEP’s/SSEP’s but may in high doses. keep

61
Q

evoked potential monitoring and N2O/inhalationals

A

avoid for MEP, SSEP, EMG

62
Q

evoked potential monitoring and ketamine

A

enhances SSEP and MEP amplitude, if ketamine is given as a bolus our discontinued as an infusion IOM team should be informed

63
Q

evoked potential monitoring and propofol

A

in high doses (>130-150mcg/kg/min) will increase latency and decrease amplitude of EP’s

64
Q

complications of posterior spinal fusion for scoliosis

A
spinal cord ischemia
massive blood loss
embolism
accidental extubation
corneal abrasion
visual loss
neurological sequela with loss of SSEP/MEP
65
Q

posterior spinal fusion for scoliosis postoperative considerations

A

plan for extubation if possible
CXR may be obtained at end of procedure with patient supine on inpatient bed. ensure that surgeon has reviewed CXR prior to extubation
pain score 7-9: hydromorphone PCA

66
Q

explanation of nissan laparoscopic fundoplication

A

minimally invasive procedure which is done to restore the function of the lower esophageal sphincter (valve between esophagus and stomach) by wrapping stomach around esophagus
-involves mobilizing muscles around esophagus at the level of LES

67
Q

explanation of infantile hypertrophic pyloric stenosis

A

thickening or swelling of pylorus-muscle between stomach and intestines-that causes severe and forceful vomiting in the first few months of life. enlargement of the pylorus causes a narrowing (stenosis) of the opening from the stomach to the intestines which blocks stomach contents from moving into the intestine
-palpable obstructive lesion, olive shaped enlargement of pylorus

68
Q

when is a nissan fundoplication indicated for children

A

gastric reflux that failed medical management

69
Q

nissen fundoplication anesthetic and surgical technique

A

GETT, often laparoscopic

70
Q

nissen fundoplication and blood loss, fluid shifts, pain

A

not associated with large blood loss, fluid shifts, or pain

71
Q

nissen fundoplication intraoperative consideration to ensure no leaks in anastomosis

A

positioning of bougie within esophagus and insufflation via gastric tube to ensure no leaks

72
Q

when is hypertrophic pyloric stenosis usually diagnosed

A

2-12 weeks of life

73
Q

what is the clinical presentation of hypertrophic pyloric stenosis

A

postprandial projectile emesis, palpable pylorus, visible peristaltic waves

74
Q

what is the surgical correction for hypertrophic pyloric stenosis

A

pylorotomy

75
Q

how quickly does this hypertrophic pyloric stenosis surgery need to occur

A

semi elective to urgent, must be medically managed first due to their dehydration, electrolyte, and acid base derangements.

76
Q

symptoms of pyloric stenosis and subsequent metabolic derangement

A

persistent vomiting depletes Na/K/Cl- and H+ ions causing hypochloremic metabolic alkalosis

77
Q

how do the kidneys attempt to compensate for hyperchloremic metabolic alkalosis related to symptoms of pyloric stenosis

A

kidneys attempt to compensate by excreting sodium bicarbonate
hyponatremia/dehydration worsen, and kidneys attempt to conserve sodium at the expense of hydrogen
because lactate is metabolized to bicarbonate, LR should be avoided

78
Q

anesthesia for pyloric stenosis

A

prior to induction, must suction stomach with OG. (tilt baby in various directions to remove all contents)
RSI with cricoid pressure, propofol, succ/roc
cuffed ETT
quick procedure
extubate awake

79
Q

definition of circumcision procedure

A

most common procedure. foreskin is opened, adhesions are removed, forerskin is separated from glans

80
Q

explanation of hypospadias procedure

A

condition in which the opening of the urethra is on the underside of the penis instead of the tip
location of the opening can vary and can be anywhere from underneath the tip of the penis (more common) to the base of the penis (less common)

81
Q

circumcision population age, type of anesthesia, length of curgery

A

neonates to adults
local, regional, or GA (grown man cant watch this ish)
approx 1 hour to cutting foreskin cauterizing, suturing edges

82
Q

circumcision indications

A

phimosis, recurrent balantis, parental preference

83
Q

most common complication of circumision

A

bleeding

84
Q

hypospadias length of surgery and anesthetic technique

A

1-4hours or +

GA-LMA or ETT. regional is controversial (concern for venous pooling and poor outcomes)

85
Q

how a cleft palate occurs and where it can be located

A

can occur at one of more different places on face such as lips, palate, or gum ridge (alveolus)
right and left sides of face fuse near midline. cleft results when fusion does not properly occur

86
Q

cleft palate and lip stages of repair

A

cleft lip usually 10-12 weeks
cleft palate 12-18 months
alveolar bone graft
pharyngoplasty 5-15 years

87
Q

cleft palate is associated with

A

difficulty feeding, malnutrition, speech development and congenital heart defects.

88
Q

cleft palate induction

A

routine

89
Q

cleft palate airway considerations

A

oral RAE with flexible connector
AW can be difficult with or without syndrome
mouth gag-reassess breath sounds once positioned
no air bubbles
possible AW and tongue edema
extubate once return of protective aw reflexes
protect eyes
secretions and blood-clear airway on emergence

90
Q

cleft palate anesthetic considerations: coagulopathy and how to reduce blood loss

A

may cause significant bleeding. blood loss usually insignificant but occasionally may require transfusion
LA with epinephrine reduces blood loss and provides some analgesia