Common Pediatric Procedures Flashcards

1
Q

Tonsillectomy and Adenoidectomy

A
  • chronic inflammation and hypertrophy of lymphoid tissue in the pharynx may necessitate surgery to relieve obstruction or to remove the focus of infection
  • 3rd most common surgical procedure
  • can be inpatient or outpatient
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2
Q

tonsillitis

A
  • caused by strep or viral agents

- symptoms = inflammation and swelling of the tonsils, sometimes severe enough to cause respiratory obstruction

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3
Q

indications for tonsillectomy

A
  • OSA is most common indication
  • chronic recurrent tonsillitis
  • hypertrophic tonsillitis with OSA
  • unilateral hypertrophic tonsil
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4
Q

considerations for admission post T&A

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

tonsillectomy periop management

A
  • IV dexamethasone 0.5 mg/kg
  • no abx admin
  • good pain management but no codeine and maybe no ketorolac (talk to surgeon)
  • standard induction with oral RAE tape in middle; can also use LMA
  • table turned 45-90 degrees
  • mouth gag -require adequate depth of anesthesia, ensure tube patentcy/placement after gag placed
  • throat pack
  • muscle relaxants OK, but often quick operation
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6
Q

why no codeine in kids?

A

genetic variation in activity of CYP450 enzyme CUP2D6 which metabolizes codeine into morphine (active metabolite)

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7
Q

analgesic management for T&A

A
  • fentanyl 1-2 mcg/kg; 10-15 mg/kg IV
  • dexmethasone 0.5-1 mg/kg; zofran 0.1 mg/kg
  • precedex 0.1-0.5 mcg/kg IV
  • consider toradol/ibuprofen admin post-resection
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8
Q

cold steel tonsillectomy method

A
  • stainless steel scissors and scalpels, toothed forceps and herd’s dissector/retractor used to dissect whole tonsil tissue from its capsule
  • exposes underlying constrictor muscles and hence more PAIN and more chances of hemorrhage
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9
Q

electro dissection tonsillectomy method

A
  • monopolar or bipolar dissection of whole tonsil
  • heat of cautery induces hemostasis
  • lateral thermal damage = PAIN
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10
Q

microdebrider tonsillectomy method

A
  • soft tissue shaver
  • 90-95% tonsillar tissue removed (so it can grow back)
  • associated with less M&M (less blood loss, less pain)
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11
Q

coblation tonsillectomy method

A
  • cold ablation
  • energy used in a plasma field to break the molecular bonds to excise or dissolve the soft tissue at a temperature of 40-70 degrees
  • provides dissection, cautery, suction and hemostasis in the same machine
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12
Q

radiofrequency tonsillectomy method

A
  • mono polar radio frequency used to remove tonsil

- cost-effective, easy to use, and time saving

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13
Q

laser tonsillectomy method

A
  • CO2 laser and KTP lasers can be used
  • less bleeding, less pain, discomfort and is a day procedure
  • more secondary hemorrhage and post op pain noted with this method
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14
Q

T&A emergence

A
  • high risk of laryngospasm, aspiration, airway reactivity (need OGT to empty stomach and reduce risk of emesis)
  • considerations for deep vs awake extubation
  • coughing can increase bleeding, use of careful soft-suction
  • recovery position
  • be cautious to admin opioids for a restless child as it may indicate airway compromise or hypoxia
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15
Q

recovery position for T&A

A

-on one side with head slightly down, allows blood to drain away from vocal cords

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16
Q

highest incidence of bleeding for T&A methods

A

cold steel

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17
Q

the bleeding tonsil… what to do!?

A
  • bleeding may be occult (swallowed) and is emergency
  • post-tonsillectomy bleeding may require surgery
  • ensure adequate IV access
  • hypovolemia requiring vigorous resuscitation
  • potential for hemodynamic instability on induction
  • H&H, T&C, coags
  • considered full stomach –> RSI
  • potential for difficulty obtaining secure airway (swelling)
  • OGT to empty stomach
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18
Q

primary hemorrhage

A

occurs within 24 hours

0.2-2.2%

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19
Q

secondary hemorrhage

A

occurs > 24 hours (up to 5-10 days after)

0.1-3%

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20
Q

myringotomy and tympanostomy (BMT)

A
  • myringotomy = creates opening in tympanic membrane through which fluid can drain
  • tympanostomy = placement of ventilation tube with lumen; alleviates pressure from middle ear and serves as stent allowing continued drainage until tubes naturally extruded in 6 months to a year
  • indicated in chronic otitis media
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21
Q

BMT anesthetic considerations

A
  • often have URI
  • short operative time
  • oral midaz may outlast procedure (consider not giving)
  • often mask-only anesthetic
  • IV placed if another procedure is also being done
  • D/c sevo during second side
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22
Q

myelodysplasia (spina bifida)

A

-failure of neural tube to close resulting in herniation of the spinal cord and meninges through a defect
-most common CNS defect that occurs during first month of gestation
most common in lumbosacral region
-hydrocephalus often present and may need VP shunt
-URGENT repair required within 24-48 hrs due to risk of infection or worsening cord function

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23
Q

meningocele

A

only contains meninges

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24
Q

myelomeningocele

A

contains meninges and neural elements

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25
Q

hydrocephalus

A
  • excess CSF builds up in ventricles
  • “water on the brain” from Greek words
  • may be caused by congenital defect (Chiari or aqueduct stenosis) OR by acquired disease (trauma, infection, tumor)
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26
Q

preop anesthesia considerations for myelodysplasia repair

A
  • assess level of lesion and degree of deficit
  • review of systems and rule out additional congenital anomalies
  • CBC, T&S
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27
Q

intraop anesthesia considerations for myelodysplasia repair

A
  • routine monitors, may use IONM (avoid muscle relaxation if MEPs)
  • positioning - supine, lateral, prone for procedure
  • induce with inhaled or IV
  • potential for blood loss if large defect
  • prone to hypothermia
  • latex free environment
28
Q

postop anesthesia considerations for myelodysplasia repair

A
  • goal = extubate

- assess the need for postop apnea monitoring

29
Q

ventriculoscopy

A

use of fiber optic scope through cranial burr holes to visualize lateral, third, and occasional fourth ventricle; alternative may be placed under US guidance

30
Q

VP shunt

A
  • ventriculo-peritoneal shunt
  • lateral ventricle to peritoneum
  • most common type of shunt and allows room for growth
31
Q

VA shunt

A
  • ventriculo-atrial shunt
  • lateral ventricle to right atrium
  • abdominal pathology use this
32
Q

ETV

A
  • endoscopic third ventriculostomy

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

33
Q

neurosurgery for hydrocephalus anesthesia implications

A
  • incision is small frontal or parietal-occipital
  • position is supine with head turned
  • table 90-180 degrees
34
Q

CSF shunt preop anesthesia considerations

A
  • assess baseline neuro stats and ICP
  • avoid premeds if ICP increased
  • assess for vomiting history and dehydration
  • routine H&P
  • if child has had previous shunt revisions, review old records
  • IV x1-2
35
Q

CSF shunt induction considerations

A
  • standard monitors
  • prop, fent, roc
  • iso or sevo
  • GETA
  • protect and pad eyes
  • abx = ancef 30 mg/kg IV
36
Q

CSF shunt maintenance considerations

A
  • hyperventilation is undesirable because it may make cannulation of the ventricle more difficult
  • maintain paralysis or propofol bolus when tunneling
  • VA shunts - be caution of air embolism/PPV while the vein is open
37
Q

CSF shunt emergence considerations

A
  • reversal of paralytic
  • antiemetics
  • extubate
  • fully awake to permit for rapid neuro assessment
38
Q

humerus fracture

A
  • long bone of upper arm
  • 3 types of fractures depending on the location
  • proximal = break in upper part of humerus near shoulder
  • mid-shaft = break in middle par to humerus
  • distal = break near elbow; usually part of a more complex elbow injury and sometimes involves loose bone fragments
39
Q

scoliosis

A

-sideways curvature of spine

40
Q

idiopathic scoliosis

A

no definite cause and most common form of the condition; mainly affects adolescent girls

41
Q

neuromuscular scoliosis

A

caused by conditions of muscle weakness or spasticity (such as CP, muscular dystrophy, and SCI) and associated with greater bladder loss

42
Q

supracondylar fracture of humerus

A
  • most common elbow fracture in children
  • results from falling with an outstretched hand and extended elbow
  • complications include - compartment syndrome, nerve palsies and late deformities
43
Q

anesthesia for humerus fracture

A
  • supine with table turned 90
  • GETA
  • assess NPO status and full stomach precautions requiring IV and RSI
  • 30-60 min for pinning
  • 30-90 min for open reduction
  • timing of emergence if cast or splint is placed after closing
44
Q

posterior spinal instrumentation

A
  • surgical treatment is recommended for patients whose curves are greater than 45 degrees while still growing or are continuing to progress greater than 45 degrees when growth stopped
  • the goal is to prevent curve progression and obtain some curve correction
  • surgical team utilizes metal implants that are attached to spine and then connected to a single or two rods
  • posterior or anterior approach
  • following surgical treatment, no external bracing or casts are used
  • hospital stay between 3-6 days
  • prone
  • surgical time = 6+ hours
  • significant blood loss potential
  • intraop neuro monitoring used
  • stepdown or ICU post op
45
Q

posterior spinal instrumentation preop anesthesia considerations

A
  • standard peds preop eval
  • starting CBC, coags, BMP, and HCG in females
  • comorbidities
  • T&C/set-up 2 PRBCs, cell saver
  • discuss with the team the nerve monitoring goals and use of paralytics
  • prepare the patient and family for puffy face from prone position
46
Q

respiratory anesthesia implications with posterior spinal instrumentation

A
  • cobb angle - degree will determine amount of impairment of respiratory function
  • restrictive lung disease = decreased TLC + decreased VC
  • VC <40% may mean post op ventilation
  • patients with neuromuscular scoliosis may be more sensitive and require postop ventilation secondary to muscle weakness
47
Q

posterior spinal instrumentation case set up

A
  • cell saver, fluid warmer, and blood tubing
  • a line and PIVx2
  • prepare for prone position with superman arms on spine table
  • consider EKG placement, prone pillow, and underbody bair hugger
  • eye lube, eye tape, bilateral soft bite blocks
  • standard airway, induction meds, BIS, cerebral oximetry, emergency meds, OGT
  • increase room temp
48
Q

evoked potential monitoring

A
  • dex opioids are ok
  • N2O and inhalation agents avoided
  • ketamine enhances SSEPs and MEPs amplitude; if given inform IOM team
  • propofol in high doses increases latency and decreases amplitude of EPs
49
Q

complications of posterior spinal instrumentation

A
  • spinal cord ischemia
  • massive blood loss
  • embolism
  • accidental extubation
  • corneal abrasion
  • visual loss
  • neurological sequele with loss of SSEPs and/or MEPs
50
Q

postop anesthetic implications of posterior spinal instrumentation

A
  • plan for extubation if possible
  • CXR may be obtained at end of procedure prior to exubation
  • pain score 7-9 = hydromorphone PCA
  • ICU or step down
  • LOS 3-6 days
51
Q

Nissen

A

laparoscopic nissen fundoplication is minimally invasive procedure which is done to restore the function of the LES by wrapping the stomach around the esophagus

52
Q

infantile hypertrophic pyloric stenosis

A
  • thickening or swelling of pylorus 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
  • diagnosed between 2-12 weeks of life
  • clinical presentation = postprandial projectile emesis, palpable pylorus, visible parastaltic waves
  • surgical correction = pyloromyotomy
53
Q

Nissen anesthetic implications

A
  • gastric reflux and failed medical management
  • involves mobilizing muscles around esophagus at level of LES
  • GA-ETT
  • often laparoscopic
  • not associated with large blood loss, fluid shifts, or pain
  • positioning of bougie within the eophagus and insufflation via gastric tube to ensure no leaks at the anastomosis
54
Q

pyloric stenosis results in what acid/base disturbance?

A

hypochloremic metabolic alkaosis

55
Q

anesthesia for pyloric stenosis

A
  • prior to induction suction stomach with OGT and tilt baby in various directions to remove all contents
  • HIGH risk for aspiration
  • RSI, cricoid, prop, succ/roc
  • cuffed ETT
  • quick procedure (20 min)
  • extubate AWAKE
56
Q

circumcision

A
  • removal of foreskin from human penis

- most common procedure

57
Q

hypospadias

A
  • condition in which the opening of the urethra is on the underside of the penis instead of at 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)
58
Q

circumcision anesthesia considerations

A
  • neonates to adults
  • local, regional, GA
  • indications = phimosis, recurrent balanitis, parental preference
  • approximately 1 hour, involves cutting foreskin and cauterizing/suturing skin edges
  • most common complication is bleeding
59
Q

hypospadias anesthesia considerations

A
  • 1:250 live male births
  • 1-4 hours
  • GA LMA or ETT
  • regional controversial (concern for venous pooling and poor outcomes)
60
Q

caudal anesthesia benefits

A
  • intra and postop analgesia
  • reduction in systemic opioid requirements and side effects
  • reduction in anesthesia requirements
61
Q

procedures that could utilize caudal

A
  • circ
  • inguinal herniorrhaphy
  • hypospadias
  • anal surgery
  • clubfoot repair
  • other subumbilical procedures
62
Q

contraindications for caudal

A
  • infection around site
  • coagulopathy
  • anatomic abnormalities
  • parental refusal
63
Q

cleft palate

A
  • cleft = opening or space
  • all different and can occur at different places
  • human development –> L and R sides of face fuse near midline; cleft occurs when this fusion doesnt occur properly
  • some genetic but also environmental factors
  • cause not entirely clear but may have associated syndrome with anesthesia implications
64
Q

cleft lip and palate surgery

A
  • may be repaired in stages
  • lip usually at 10-12 weeks
  • palate at 12-18 months
  • alveolar bone graft
  • pharyngoplasty at 5-15 years
  • associated symptoms = difficulty feeding, malnutrition, speech development and congenital heart defects
  • routine induction
  • oral RAE with flexible connector
65
Q

cleft lip and palate anesthesia implications

A
  • airway may be difficult (w or without syndrome)
  • mouth gag (so reassess breath sounds)
  • no air bubbles
  • coagulopathy may cause significant bleeding
  • LA with EPI reduces blood loss and provides some analgesia
  • protect eyes
  • secretions and blood, clear airway on emergence
  • possibility of airway and tongue edema
  • extubate once return of protective airway reflexes
  • no-nos after surgery to protect surgical site from child’s manipulation