Test 4: Pediatric Anesthesia Pt. 3 Flashcards

(92 cards)

1
Q

Most common pediatric airway problems

A
  • Laryngospasm: noxious stimuli of superior laryngeal nerve causes hyperresponsive glottic closure
  • Bronchospasm: increased airways resistance, disorder of smooth muscle
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2
Q

How common is laryngospasm in peds?

A

1.7% which is 2x that of an adult

up to 25% with T&A and other ENT procedures

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3
Q

Risk factors for laryngospasm in peds

A
  • second-hand smoke
  • recent or current URI
  • GERD
  • mechanical irritants (secretions)
  • excitement phase of inhalation induction (stage 2)
  • tracheal intubation during light anesthesia
  • upper airway surgical procedures
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4
Q

What are the early signs of laryngospasm?

A
  • Stridulous or “crowing” noise
  • Tracheal tugging (retraction)
  • Increase breathing efforts
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5
Q

What are the latent signs of laryngospasm?

A
  • Suprasternal, subcostal, and intercostal chest retraction
  • Paradoxical movement of chest and abdomen
  • Minimal or no movement of ventilation
  • Minimal or no anesthesia bag movement
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6
Q

Complication of laryngospasm

A
  • Hypoxemia
  • Cardiac arrest
  • Neg Pressure Pulmonary Edema (more often seen in adults than peds)
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7
Q

How to prevent laryngospasm in peds

A
  • avoid messing with them in stage 2 (IV start, EKG leads, suction, intubation/extubation) etc
  • admin 100% O2 prior to extubation
  • topical lidocaine to suppress laryngeal sensory nerve activity

make sure they are deep enough or fully awake before extubation

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8
Q

Incomplete larygnospasm treatment

A
  • Gentle postivie pressure with 100% O2
  • remove noxious stimuli
  • may need to deepen anesthesia if not resolved (gas or prop)
  • Still spasm? give sux with atropine

call for help

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9
Q

Complete laryngospasm treatment

A
  • 100% O2, positive pressure, deepen anesthesia
  • Larsons point (laryngeal knotch): rocks jaw forward to open cords
  • no air movement? skip prop and go right to sux+atropine

call for help

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10
Q

Bronchospasm fast facts:
- increased risk with in children with ____ and/or current ____
- what will you hear?
- What will you see on your ETCO2?

A
  • Increased risk with children with asthma or current URI
  • you can hear audible wheezes
  • you will see a prominant slope on expiratory portion of ETCO2 (increased alpha angle)
  • you will also have increased ETCO2 and decreased SPO2
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11
Q

First line treatment for Bronchospasm

A
  • remove stimulus and deepen anesthetic
  • inhaled beta agonist

you can also decrease PEEP and increase expiratory time to minimize air trapping

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12
Q

Bronchospasm treatments (not first line)

A
  • corticosteroids
  • IV magnesium
  • epi 5-10 mcg/kg
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13
Q

Pediatric IV and IM dose of Atropine

A
  • IV: 0.01 mg/kg
  • IM: 0.02 mg/kg
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14
Q

Pediatric IV dose of Lidocaine

A
  • 1mg/kg
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15
Q

Pediatric IV dose of Glycopyrrolate.

A
  • 0.01 mg/kg
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16
Q

Pediatric IV dose of Propofol
Pediatric infusion dose of Propofol

A
  • 2-3 mg/kg
  • 50-200 mcg/kg/min
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17
Q

Pediatric IV and IM dose of Succinylcholine

A
  • IV: 2 mg/kg
  • IM: 4 mg/kg
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18
Q

What are the five main causes of pediatric airway management difficulties?

A
  • Inflammatory
  • Congenital
  • Iatrogenic (caused by us)
  • Neoplastic
  • Trauma
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19
Q

What is Croup?

A

A cause of airway obstruction that occurs d/t a viral etiology with swelling and inflammation of the subglottic area of the trachea.

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20
Q

What can cause croup?

A
  • too large ETT
  • multiple DL attempts
  • surgical positioning
  • surgical time
  • age
  • URI
  • coughing on ETT
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21
Q

Croup most commonly occurs in children between what ages?

A

6 months to 3 years

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22
Q

What are the symptoms of Croup?

A
  • URI symptoms that progress from stridor to hoarseness
  • “Barky Cough”, they sound like a seal
  • Low-grade fever (100 - 100.4 F)
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23
Q

Medical treatment for Croup

A
  • Comfort position, sitting upright and slightly bending forward
  • Humidified O2 (cooled)
  • Racemic epinephrine nebulized aerosol (0.05ml/kg) rebound swelling can occur, likely will be admitted to monitor
  • Steroids 0.5 mg/kg)
  • Intubation is rare
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24
Q

Syndromes associated with difficult airway

A
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25
Anesthesia considerations for Downs Syndrome patients
* Large tongue * a small mouth * Atlantoaxial instability * Inhalation induction bradyarrhythmias
26
Things to remember if your pt has a potentially difficult airway
- no NMBDs - prepare difficult airway equipment - 100% FiO2 - IV access - use external manipulation of the trachea if possible *low threshold for progressing down the difficult airway algorithm quickly* ## Footnote Thrown in an LMA to ventilate if you need
27
What are examples of extrathoracic upper airway obstruction?
* Foreign body * Epiglotottitis * Laryngospasm
28
What are examples of intrathoracic lower airway obstruction?
* Asthma * Bronchiolitis
29
At what age is foreign body aspiration common?
6 months - 3 years old
30
Treatment of foreign body aspiration
* Usually removed with a rigid bronchoscopy * May require post-op steroids * Consider TIVA b/c you may not get much gas when they are maipulating the airway
31
Anesthesia considerations for foreign body aspiration
- Probably wont intubate with a rigid bronch - TIVA (can mask when rigid scope is in) - topical lidocaine to decrease bronchospasm/laryngospasm when the scope goes in - Want pt spontaneously breathing b/c PPV could push the FB farther down the bronchus
32
Epiglottitis Vs. Croup
Epiglottitis is more emergent, while croup is urgent
33
Things to remember about autism
- developmental delay in social and communication - changes in routine are difficult - sensative to sensory stimuli (light, sound etc) - preop is important (triggers and soothing things) - premedication is important +/- parental presence - reunite with parents in PACU asap
34
Things to remember about trisomy 21
- most frequent chromosomal anomaly - risk for difficult **ventilation**/intubation - everything about this airway will scream obstruction (large tongue, OSA, subglottic stenosis, palate narrow etc) *air on the side of smaller ETT b/c of subglottic stenosis*
35
Why do we not worry about cardiac issues with trisomy 21?
Trick question! - 40-50% have congenital heart disease - most common is AV septal defect - 2nd most common is VSD - additional: PDA, TOF (tet.) - brady is very common in inhalation induction (independent of a heart condition) *go very slow with inhalation induction* - they have low levels of circulating catecholemines ## Footnote have glyco (0.01mg/kg) and atropine (0.02mg/kg) ready!
36
Additional considerations for trisomy 21 care
- Likely have developmental delays (propbabily need to premedicate) - strabismus - hypotonia - hyperflexible joints - GERD common - epilepsy - thyroid disease - increased incidence of leukemia
37
What is VATER syndrome? (i.e. VACTERL association)
**V**ertebral anomalies *most common* **a**nal atresia **c**ardiovascular anomalies **t**racheoesophageal fistula *most common* **e**sophageal atresia **r**enal and/or radial anomalies **l**imb defects exact cause is unknown (not hereditary)
38
What is Charge syndrome?
**C**oloboma (hole in the eye structures) **h**eart defects **a** choanal atresia (back of nasal passage obstructed) **r**estruction of growth/development **g**enitourinary problems **e**ar anomalies
39
What is DiGeorge syndrome? (Catch22)
**C**ardiac **a**bnormal face **t**hymic hypoplasia (blood needs to be irriadiated b/c thymus isn't working) **c**left palate **h**ypocalcemia (d/t hypoparathyroid) **22**q11.2 gene deletion
40
Dental restoration procedures
- many pts need dental work under GA (they cant tolerate going to the dentist) - we share the airway - nasal intubation
41
Strabismus repair procedures
- corrects extraocular muscles and re-establishes the visual axis - GA with LMA or ETT and inhalational induction - Anesthetic concerns: careful preop exam (underlying conditions?), **anticipate oculocardiac reflex**, PONV common
42
Describe the oculocardiac reflex
- happens b/c of Extraoccular muscles - causing pressure on the globe - Afferent pathway to ophthalmic branch CNV (trigeminal ganglion) stimulates Efferent pathway of vagus (cardiac depressor) - bradycardia, AV block, ventricular ectopy, asystole - **response decreases with repeated stimulation** *first treatment is ask the surgeon to stop*
43
What is retinopathy of prematurity
- Higher PaO2 that can cause abnormal vascular growth - retinal maturation is complete at ~44 weeks - **if caring for preemies, maintain SpO2 at 89-94%** - risk factors: <30 weeks gestation, or <1000g birthweight - goal of surgery is to preserve the retina (uses laser or cryotherapy)
44
Anesthesia techniques for Tonsils and Adenoids
* Inhalation induction, deep intubation * Use a drying agent (robinul) * Opioids * Zofran and Decadron (0.5mg/kg for airway swelling) * Deep extubation (usually)
45
Complications for a T&A
Bleeding - primary: within 6-24 hours postop - secondary: 5-10 days postop Airway fire - maintain low FiO2 <30% - avoid N2O
46
Post-tonsillar bleed, what should we know/do?
- emergency, considered full stomach - pre-oxygenate - RSI with cric pressure (difficult to do awake intubation with peds) - ETT 1/2 size smaller - lost lots of blood (IV, fluids and potentially blood) - antiemetics - OGT - extubate awake
47
Cleft lip/palate surgeries
- defect in palatal growth in the first trimester - primary lip repaired ~3-6 months - primary palate repaired ~6-12 months - syndromes commonly associated with cleft lip & palate
48
Anesthesia technique for cleft lip/palate
- GETA (oral rae) - awake extubation - acetaminophen and opioids - potential for postop obstruction
49
What is pyloric stenosis (Infantile Hypertrophic Pyloric Stenosis/ Gastric Outlet Obstruction)?
* Narrowing of the pylorus, the lower part of the stomach, through which food and other stomach contents pass to enter the duodenum. * When an infant has pyloric stenosis, the muscles in the pylorus have become enlarged to the point where gastric emptying is prevented * **olive shaped mass just below xiphoid process**
50
What are the causes of Pyloric Stenosis?
* Multifactorial. Some researchers believe that maternal hormones could be a contributing cause. * May be that the thickening of the muscle is the stomach's response to some type of allergic reaction in the body. * Infants may lack receptors in the pyloric muscle that detect nitric oxide, a chemical in the body that tells the pylorus muscle to relax → leading to hypertrophy
51
Pyloric stenosis is about ___ times more likely to occur in firstborn male infants.
4x
52
Most infants who develop pyloric stenosis are usually between ____ weeks and ____ months of age
2 weeks and 12 weeks
53
The first symptom of pyloric stenosis.
* Projectile vomiting * The breast milk or formula is ejected forcefully from the mouth in an arc, sometimes over a distance of several feet * The vomitus will not contain bile
54
Pyloric stenosis anesthesia management
- assess acid/base balance (lots of vomiting) - correct hypovolemia and e-lyte abnormalities - neonate is considered a full stomach - before inducing anesthesia, suction stomach until clear - RSI - extubate awake - concern for postop apnea (these babies are very weak d/t lack of nutrition **avoid narcotics, just do rectal tylenol**
55
Inguinal hernia repair considerations
- prevalent in preterm neonates - concerns for small bowel incarceration and ipsilateral testicular injury - open or laparoscopic
56
Inguinal hernia repair considerations for anesthesia
- anesthesia technique (provider preferance) - spinal or caudal - inhalational or IV induction - LMA or ETT - concern for postop apnea
57
Omphalocele and Gastroschisis: what is it?
- defects in the abd wall that occur during gestation when the visceral organs fail to move from the yolk sack in the the abd cavity (outside of body) - usually have other issues too (cardiac, GU, metabolic, malrotation, Meckel diverticulum or intenstinal atresia) - Omphalocele outcomes are poor (covered by membrane) - Gastroschisis (not covered by memebrane) ## Footnote Beckwith-Wiedemann syndrome associated with these GI abnormaliites too
58
Anesthetic concerns for Omphalocele/ Gastroschisis
- **severe dehydration (more with gastro) and temp loss** - high risk for sepsis - other associated abnormalities - avoid increased IAB - postop vent requirements - lungs will be more squished when the GI is back in the body - less freedom of movement needs support
59
OR anesthesia considerations, and what % N2O should you use for Omphalocele/gastro?
**NO N2O!** - air expands with N2O remember? - adequate IV access (x2) - prepare for colloid administration - yes NMBD (open abdomen) - a-line (guide fluid mangement) - pulse ox on UE and LE (monitor perfesion in both)
60
What is Necrotizing Enterocolitis (NEC)?
- intestinal inflammatory condition **emergency** - secondary to bowel ischemia and immaturity - probable bacterial invasion - delayed oral feeding - occurs usually in preterm babies with gestational age <32 weeks, weight <1500g *common to see in premies with PDA*
61
Common lab findings in a pt with NEC
- hyperkalemia - hyponatremia - metabolic acidosis - hyper or hypo glycemia - DIC in severe cases
62
How is NEC diagnosed?
Imaging studies
63
Common S/S of NEC
- increased gastric residuals with feedings - ABD distension - bilious vomiting - lethargy - rectal bleeding - fever - hypothermia - oliguria - jaundice - apnea/bradycardia
64
Initial medical interventions for NEC:
- ensure adequate oxygenation - manage hypovolemia and acidosis - withhold enteral feeding - NG decompression - ABx Surgical intervention - ex-lap with dead bowel resection, colostomy or peritoneal lavage
65
What is Malrotation and Midgut Volvulus?
- The intestine becomes twisted and ischemic = volvulus **emergent** - presentation 1st week of life - **bilious vomiting** Sugery = Ladd procedure
66
Anesthetic concerns for volvulus
- fluid replacement - e-lyte management - full stomach - increased IAP = less FRC!! plus all the other GI considerations we have been talking about
67
Congenital diaphragmatic hernia (CDH)
Abdominal content protrude into thoracic cavity and act as a space occupying lesion - prevents normal lung growth (lung can be small) - 80% of these are on the L side
68
Congenital diaphragmitic hernia s/s at birth, how to diagnose
- dyspnea - tachycardia - cyanosis - absence of breath sounds on affected side - severe retractions - scaphoid abdomen - barrel chest Dx: with US prenatally
69
How do we treat congenital diaphragmatic hernia
possibility for prenatal intrauterine surgical intervention (goal to revers pulmonary hypoplasia) - if born, median age of operation is ~4 days (may be done at bedside) - possibility for 1 lung ventilation - *no double lumen tube, R mainstam the tube*
70
Anesthesia management for congenital diaphragmatic hernia
- likely intubated already - consider atropine IV prior to induction - VAA and meds and guided by how unstable they are (likely need TIVA) - likely only need opioids and NMBD - vent strategies - premissive hypercarbia with high-frequency oscillatory ventilation - avoid inflating stomach with air - control PVR factors! - PIP should be maintained <25-30 cmH2O - postop goal to keep PaO2>150mmhg and slowly wean to lower O2 over 72 hours
71
Tracheoesophageal fistula and esophageal atresia
Fistual to esophagus through trachea - cannot pass OGT into stomach immediately after birth - coughing/choking after first feeding *assume they have another congenital issue too*
72
TEF and EA procedure
- Preformed via R side thoracotomy - fistula ligated then anastomosis of the 2 ends are put together
73
Anesthesia for TEF and EA
- ECHO preop - minimize oral feedings - place balloon-tipped catheter to suctions nasopharyngeal secretions that accumulate in the esophageal pouch - gastrostomy tube - **maintain spont. breathing** - PPV will go into stomach - may need bronch after induction (ENT may place for you)
74
Imperforated Anus
Diagnosed with neonate does not pass meconium within the first few days after birth - ranges from mild stenosis to complete anal atrasia **may be associated with VACTERL**
75
Difference b/w male and female pts with imperforated anus
- in males: surgery is urgent to allow passage of meconium via colostomy - in females: common presence of rectovaginal fistula (so the procedure can be delayed a few weeks)
76
Neonate hydrocephalus
d/t obstruction of CSF flow leading to increased ICP - bluging anterior fontanelle, irritability, somnolence, vomiting, LOC and/or CV collapse - may need VP shunt *risk of delying surgery includes brain herniation*
77
Anesthesia manegement for hydrocephalus
- control ICP - RSI - goal to extubate at the end of procedure - VAAs cause cerebral vascular dilation at >1 MAC and can increase ICP
78
Myelomeningocele
- form of spina bifida: most common CNS defect that occurs during the first month of gestation **decreased FA intake is the cause** - **failure of neural tube to close leads to herniation of the spinal cord and meninges through a defect in the spinal column and back** - most often in lubosacral - can be repaired in utero or in first 24 hours of life arnold-chiari malformation will require a VP shunt
79
Pediatric cardiac output is derived from what factors?
* Volume * Heart Rate ## Footnote Starling's Law is not a factor in cardiac output in pediatrics until they are 5-6 years old
80
How many mls of crystalloid should be administered for every 1ml of blood loss?
The 3:1 rule is a fluid resuscitation guideline that states that for every 1 mL of blood loss, 3 mL of crystalloid fluid should be used.
81
Why do neonates (less than 3 or 4 months) need fluids with dextrose?
Neonates have low glycogen stores and cannot break down triglycerides and convert them to usable energy. Therefore, fluids with dextrose (D5, D10) are needed for these patients.
82
How will you make D10 from D50?
Mix 10 mL of D50 with 40 mL of LR.
83
Total blood volume for a preemie
100 mL/kg
84
Total blood volume for a neonate
90 mL/kg
85
Total blood volume for an infant
80 mL/kg
86
Total blood volume for a child
70 mL/kg
87
The formula for calculating the max allowable blood loss
[EBV x (pt Hct - allowed Hct)] / pt Hct
88
What is the max allowable blood loss for an 8 kg infant if Hct is 36?
EBV = 8 kg x 80 mL/kg = 640 Blood Loss = [EBV x (pt Hct - 25)] / pt Hct [640 x (36-25)]/36 = 195 Max allowable blood loss is 195 mL
89
24 kg child, NPO for 6 hours. What will be the fluid deficit?
Use 4-2-1 rule. 4 mL/kg x 10 kg = 40 mL 2 mL/kg x 10 kg = 20 mL 1 mL/ kg x 4 kg = 4 mL 64 mL/hour x 6 hours = 384 mL
90
How do you make 5% albumin if you only have a 25% albumin bottle?
* Get 100 mL NS bag * Take 20 mL NS out of the bag * Replace with 20 mL of 25% albumin.
91
Estimate of RR in Children
20-60 breaths per minute (Note WOB, effort, mechanics, assess sounds, skin tone, pulse ox)
92
What is the number one cause of bradycardia in a child?
Hypoxemia