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
hydrocephalus definition
condition in which excess CSF builds up within the fluid containing cavities or ventricles of the brain.
26
myelodisplasia neurosurgery: commonality, what else is present, timeline for repair
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
27
myelodisplasia defect risk factors and where its most commonly located
risk factors: folate deficiency, chromosomal abnormalities | most common in lumbosacral region
28
if hydrocephalus is also present with myelodisplasia, what may need to happen?
VP shunt will be necessary if arnold chiari malformation is present (hindbrain displaced downward into the foramen magnum, resulting in hydrocephalus)
29
anesthesia for myelodisplasia repair: preoperatively
assess level of lesion and degree of deficit review systems and rule out additional congenital anomalies CBC, T&S
30
anesthesia for myelodisplasia repair: induction and intraoperative considerations (what are they prone to? OR environmental consideration?)
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
31
anesthesia for myelodisplasia repair: postoperative
goal is to extubatne | assess need for postop apnea monitoring
32
what may be the cause of hydrocephalus
congenital defect like arnold chiari aqueduct stenosis) or by acquired disease (trauma, infection, tumor)
33
ventriculoscopy for hydrocephalus neurosurgery
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
34
ventriculo-peritoneal (VP) shunt for hydrocephalus neurosurgery placement
lateral ventricle to peritoneum is most common placement and allows room for growth
35
ventriculo-atrial (VA) shunt for hydrocephalus neurosurgery placement
lateral ventricle to right atrium
36
endoscopic third ventriculostomy (ETV) for hydrocephalus neurosurgery placement
burr hole created in floor of the 3rd ventricle allowing CSF to flow directly into the basal cisterns
37
incision and positioning for hydrocephalus neurosurgery
incision is small, frontal or partietal to occipital. | position is supine with head turned and table 90-180 degrees.
38
anesthesia for creation of CSF shunts: preoperatively
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
anesthesia for creation of CSF shunts: induction
``` standard monitors propofol, fentanyl, rocuronium isoflurane or sevoflurrane GETA protect and pad eyes abx: cefazolin 30mg/kg IV ```
40
anesthesia for creation of CSF shunts: maintenance
hyperventilation is undesirable because it may make cannulation fo the ventricle more difficult maintain paralysis or propofol bolus when tunneling
41
what to be cautious of for specifically VA shunts:
caution of air embolism/PPV while vein is open
42
anesthesia for creation of CSF shunts: emergence
reversal of paralytic antiemetics extubate fully awake to permit for rapid neurological assessment
43
anesthesia for creation of CSF shunts: postoperative disposition
floor, step down, or ICU
44
humerus fracture and 3 types
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
scoliosis etiology can be either (2)
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
which elbow fracture in children is most common
supracondylar fractures of the humerus. results from falling with outstretched hand and extended elbow
47
complications of supracondylar fractures of the humerus include
compartment syndrome nerve palsies late deformities
48
anesthesia for humerus fracture: positioning, type of anesthetic, assessment considerations, emergence considerations
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
anesthesia for humerus fracture: estimated length of surgery
30-60 minutes for pinning | 30-90 minutes for open reduction
50
posterior spinal instrumentation: when is surgical treatment recommended?
when curves are greater than 45 degrees while still growing or are continuing to progress greater than 45 degrees when growth stopped
51
posterior spinal fusion for scoliosis goal of surgical treatment is two fold
1. prevent curve progression | 2. obtain curve correction
52
describe posterior spinal fusion procedure for scoliosis
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
LOS for postop posterior spinal fusion patients for scoliosis treatment and floor disposition type
3-6 days, step down or ICU postop.
54
posterior spinal fusion positioning, duration, monitoring
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
posterior spinal fusion for scoliosis and blood loss
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
posterior spinal fusion for scoliosis: preoperative
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
restrictive vital capacity % and implications
<70% predicted respiratory reserve is adequate | <40% predicted postop ventilation may be required
58
neuromuscular scoliosis and respiratory function/succinylcholine
with neuromuscular etiology, may be more sensitive to requiring postoperative ventilation related to muscle weakness succinylcholine may cause severe rhabdomyolysis with hyperkalemia
59
posterior spinal fusion for scoliosis: case set up
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
evoked potential monitoring and dexmedetomidine/opioids
compatible with MEP, SSEP, EMG monitoring. low dose dex does not effect MEP's/SSEP's but may in high doses. keep
61
evoked potential monitoring and N2O/inhalationals
avoid for MEP, SSEP, EMG
62
evoked potential monitoring and ketamine
enhances SSEP and MEP amplitude, if ketamine is given as a bolus our discontinued as an infusion IOM team should be informed
63
evoked potential monitoring and propofol
in high doses (>130-150mcg/kg/min) will increase latency and decrease amplitude of EP's
64
complications of posterior spinal fusion for scoliosis
``` spinal cord ischemia massive blood loss embolism accidental extubation corneal abrasion visual loss neurological sequela with loss of SSEP/MEP ```
65
posterior spinal fusion for scoliosis postoperative considerations
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
explanation of nissan laparoscopic fundoplication
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
explanation of infantile hypertrophic pyloric stenosis
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
when is a nissan fundoplication indicated for children
gastric reflux that failed medical management
69
nissen fundoplication anesthetic and surgical technique
GETT, often laparoscopic
70
nissen fundoplication and blood loss, fluid shifts, pain
not associated with large blood loss, fluid shifts, or pain
71
nissen fundoplication intraoperative consideration to ensure no leaks in anastomosis
positioning of bougie within esophagus and insufflation via gastric tube to ensure no leaks
72
when is hypertrophic pyloric stenosis usually diagnosed
2-12 weeks of life
73
what is the clinical presentation of hypertrophic pyloric stenosis
postprandial projectile emesis, palpable pylorus, visible peristaltic waves
74
what is the surgical correction for hypertrophic pyloric stenosis
pylorotomy
75
how quickly does this hypertrophic pyloric stenosis surgery need to occur
semi elective to urgent, must be medically managed first due to their dehydration, electrolyte, and acid base derangements.
76
symptoms of pyloric stenosis and subsequent metabolic derangement
persistent vomiting depletes Na/K/Cl- and H+ ions causing hypochloremic metabolic alkalosis
77
how do the kidneys attempt to compensate for hyperchloremic metabolic alkalosis related to symptoms of pyloric stenosis
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
anesthesia for pyloric stenosis
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
definition of circumcision procedure
most common procedure. foreskin is opened, adhesions are removed, forerskin is separated from glans
80
explanation of hypospadias procedure
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
circumcision population age, type of anesthesia, length of curgery
neonates to adults local, regional, or GA (grown man cant watch this ish) approx 1 hour to cutting foreskin cauterizing, suturing edges
82
circumcision indications
phimosis, recurrent balantis, parental preference
83
most common complication of circumision
bleeding
84
hypospadias length of surgery and anesthetic technique
1-4hours or + | GA-LMA or ETT. regional is controversial (concern for venous pooling and poor outcomes)
85
how a cleft palate occurs and where it can be located
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
cleft palate and lip stages of repair
cleft lip usually 10-12 weeks cleft palate 12-18 months alveolar bone graft pharyngoplasty 5-15 years
87
cleft palate is associated with
difficulty feeding, malnutrition, speech development and congenital heart defects.
88
cleft palate induction
routine
89
cleft palate airway considerations
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
cleft palate anesthetic considerations: coagulopathy and how to reduce blood loss
may cause significant bleeding. blood loss usually insignificant but occasionally may require transfusion LA with epinephrine reduces blood loss and provides some analgesia