Week 6 - Neonatal Anesthesia Flashcards

1
Q

What are the classifications of Premature Infants?

A

Premature Infant = born before 37 weeks gestation

Moderate-Late Prematurity = 32-37 weeks
Very Premature = 28-<32 weeks
Extremely Premature = <28 weeks

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2
Q

Define:

  • Gestational Age
  • Chronological Age
  • Postmenstrual Age
  • Corrected Age
  • Post Conceptual Age
A

-Gestational Age: weeks between 1st day of LMP, and
day of delivery
-Chronological Age: Time since birth
-Postmenstrual Age: Gestational Age + Chronological Age
-Corrected Age: Chronological Age reduced by the number of weeks born before 40 weeks gestation
-Post Conceptual Age: Time between conception and delivery (incorrect, should not be used)

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3
Q

Describe Fetal Circulation

A

– Relies on placenta for O2 and CO2 transport
– High pulmonary vascular resistance (deflated atelectatic lungs, hypoxic vasoconstriction)
– Low systemic circulatory resistance (high flow, low impedance of placental vessels)
– Extracardiac Shunts: Ductus Arteriosus (DA), Ductus Venosus (DV)
– Intracardiac Shunt: Foramen Ovale (FO)

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4
Q

Explain the transitional circulation of blood from from fetal to adult

A
  • End of placental blood flow = Increase in aortic pressure
  • Clamping umbilical vein = Doubles SVR
  • Lungs Expand = Decrease PVR
  • Increase in partial pressure of arterial O2 = Decrease in PVR
  • Decrease in RA pressure + Increase in LA pressure = functional closure of the FO
  • DA closes due to increase in SVR & decrease in PVR (kept open by prostaglandins)
  • DV closure mechanism unknown
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5
Q

What factors maintain fetal circulation?

A

Anything that increases PVR: hypoxia, hypercarbia, acidosis, hypothermia

  • May cause circulation to revert back to deoxygenated blood being shunted from right to left via PFO or PDA
  • This explains why some babies are hypoxic despite adequate ventilation with 100% FiO2
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6
Q

How does the neonatal CV system differ from an adult?

A
  • Fewer muscle cells, more connective tissue, fewer and unorganized myofibrils
  • Immature contractile components (sarcoplasmic reticulum and T-tubule network)
  • Neonate myocardium relies on free calcium for contractility — decreasing extracellular ionized calcium (citrate in PRBC, and albumin) decreases contractility!! (replace calcium frequently)
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7
Q

What is persistent pulmonary hypertension in neonates? What is its causes and treatment?

A

Failure of PVR to decrease at birth
-results in maintained right to left flow via PFO or PDA

Possible Causes: meconium aspiration, sepsis, asphyxia, increased muscularization of PA vessels, impaired endothelial nitric oxide release

Treatment: PEEP, exogenous serfactant, iNO, phosphodiesterase-5 inhibitor, inhaled prostaglandin-I2, endothelium receptor antagonists

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8
Q

What is the airway anatomy of a neonate?

A

Cephalad larynx at C3-4 (adults are C4-5)

Hyoid bone at C2-3

Base of tongue more superior to larynx = more acute angle between tongue and glottic opening

Epiglottis is narrow, omega shaped

**makes airway visualization more difficult

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9
Q

Immature lungs predispose neonates to what?

A

Alveolar Collapse and Hypoxia

  • type II pneumocytes produce surfactant at 22-26 weeks and peaks at 35-36 weeks
  • high risk of mechanical lung injury – nasal CPAP, high flow, ETT all common in NICU setting
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10
Q

What can apnea in the neonate lead to?

A

Bradycardia – heart rate 80 bpm or below

*usually at beginning of apnea spell –> then SpO2 falls (can be big trouble)

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11
Q

What is Bronchopulmonary Dysplasia?

A

Need for oxygen 28 postnatal days

  • alveolarization begins at 36 weeks – prematurity interrupts this process = few, but large alveoli
  • low surface area for gas exchange
  • can lead to pulmonary hypertension, RV hypertrophy
  • anesthetic goals: low FiO2, small TV, SpO2 90-94%
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12
Q

How can you help prevent intraventricular hemorrhage in neonates?

A

Avoid hypercarbia, hypoglycemia, hypothermia, rapid increases in BP

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13
Q

What is the renal function and considerations in neonates?

A

Full-term infants on have 30% of normal GFR

  • renal excretion of antibiotics and NMBD is prolonged = increased duration of action, high blood concentrations
  • interval between doses of antibiotics should be increased
  • hyponatremia: neonates are obligate sodium excreters, very prone to hyponatremia
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14
Q

What are some liver function considerations in the neonate?

A

-Fetal liver can synthesize glycogen (98% of it is
used during first 48 hours) — Neonates at high risk of hypoglycemia
-Albumin levels are low = less ability to bind drugs to plasma proteins = increase in free drug
-Liver enzyme production low = low metabolism
-Hyperbilirubinemia common in term infants (Physiologic vs. Pathologic)
-7 days for clotting factors to reach adult levels (Vitamin K commonly given at birth)

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15
Q

What are GI considerations with the neonate?

A
  • Fetal GI function develops late in gestation (intestinal motility increases 29-32 weeks)
  • Prolonged gastric emptying, lower esophageal sphincters are incompetent
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16
Q

What is Necrotizing Enterocolitis?

A

Bowel necrosis due to harmful bacteria in a slow moving intestine that has little GI immune defenses

Early Signs are non-specific (temp instability, poor feeding, lethargy, apnea, bradycardia)
Late Signs = tachycardia, hypotension, metabolic acidosis, thrombocytopenia, peritonitis

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17
Q

What does anemia in a neonate increase the risk of?

A

Apnea

Intraparenchymal Brain Hemorrhage

Periventricular Leukomalacia

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18
Q

How are pharmacokinetics different in the neonate?

A

Cardiac output = 4x faster in neonate –> rapid IV drug onset, rapid metabolism (if liver/kidney function has matured)

Increased total body water and ECF –> water soluble drug dose is higher but can stay in CNS longer due to reduced redistribution

Decreased protein –> less binding sites = greater free drug

Decreased renal excretion due to decreased GFR and tubular function

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19
Q

Why is a neonates response to NDMRs unpredictable?

A

Neonates can be resistant to muscle relaxants: nAchR remains open longer after binding Ach

Neonates can also be sensitive to NDMRs due to
reduction in Ach release at NMJ

*Sugammadex use is controversial in neonates/small children

20
Q

What inhalation anesthetics are use in neonates?

A

Sevoflurane and Isoflurane are most common

-Sevo = rapid induction and emergence

  • Des is contraindicated due to being an airway irritant – not recommended for infants with BPD
  • N2O not routinely used in neonates – reduces FiO2
21
Q

Why are neonates very sensitive to the myocardial depression caused by inhalation anesthetics?

A

Because inhalational anesthetics block calcium channels and neonatal hearts depend on ionized calcium for contractility

**Induce Neonates SLOWLY

22
Q

How does the MAC level change in the neonate?

A

Decreases in neonates <32 weeks gestation — Peaks at 30 days age — Then decreases again

23
Q

What are the neonatal dosages for Fentanyl, Morphine, Remifentanil, Hydromorphone?

A

Fentanyl: 2-10 mcg/kg (half life prolonged, creates hemodynamic stability during surgery but increases risk of postop apnea)

Morphine (most popular): 0.05-0.2 mg/kg (prolonged half life – decreased renal function = risk of active metabolite)

Remifentanil: 0.05-0.1 mcg/kg/min (used in infants for its rapid clearance - NOT common choice)

Hydromorphone = not common to give to neonate population

24
Q

What is the neonatal dose of ketamine?

A

0.25-3 mg/kg — VERY popular in pediatrics

  • provides analgesia, amnesia, and unconsciousness
  • causes increased secretions (use glycopyrrolate)
  • minimal cardiac depressant

*can still depress ventilation and airway reflexes (apnea)

25
Q

What are considerations of benzodiazepine use in neonates?

A

Increased duration due to liver immaturity

Respiratory depression and severe hypotension can occur after bolus administration

26
Q

What are considerations of Propofol use in neonates?

A
  • Used with caution in neonates, may cause significant hypotension, low cardiac output
  • Delayed clearance and recovery in neonate
  • Many providers avoid its use in very preterm infants (29-32 weeks due to hypotension)
  • Reports exist of cardio respiratory collapse in neonates after single induction dose
  • Not routinely used for prolonged infusions such as ICU setting (propofol infusion syndrome)

*Common to use in sedation of full-term infants for
diagnostic scans/procedures — 1-3 mg/kg

27
Q

What are the neonatal dosages of Acetaminophen?

A

PO: 10-15 mg/kg (given preop – not common to give in neonate prior to anesthesia)

PR: 35-40 mg/kg for 1st dose 20mg/kg Q6H for 24 hours (give after induction)

IV (Ofirmev): dosing is based on child’s size

Max Dose = 75 mg/kg per day

28
Q

What is Choanal Atresia?

A

Nasobuccal membrane blocks communication between nasal cavity and nasopharynx

Oral airway usually needed after induction

*associated with CHARGE syndrome

29
Q

What conditions (diseases) cause laryngeal and upper tracheal obstruction in neonates?

A

Webs: membranes that partially or completely cover larynx or trachea

Subglottic Stenosis: most common need for neonatal tracheostomy

30
Q

What is Subglottic Hemangioma?

A

most common vascular tumor in infants

  • related to PHACES syndrome
  • medical therapy attempted first (propranolol - bradycardia/hypotension)
  • surgical therapy
31
Q

What are anesthetic considerations in neonatal airway surgery?

A
  • Patients may be slowly induced with Sevofluane if no IV present, but always kept spontaneously breathing (IV placed prior to induction if airway compromise expected)
  • Prior to surgical intervention – anesthetic transitioned to TIVA with possible agents: propofol, dexmedetomidine, ketamine, remifentanil
  • Glycopyrrolate usually given early in anesthetic
  • Specific combination of anesthetic very provider dependent – NARROW margin of error in keeping patient spontaneously breathing, adequately anesthetized, yet NOT apneic
32
Q

What are preoperative anesthetic considerations for Tracheoesophageal Fistula/Esophageal Atresia surgery in neonates?

A

-Usually babies can be optimized: IV access, labs
(including type and screen), correct anemia and electrolyte imbalances, evaluate for congenital anomalies, echo (?!)
-Know what type of defect exists!! – Preop imaging, rigid bronchoscopy while spontaneous breathing immediately prior to surgical correction to view fistula
-Special Equipment: Fiberoptic scope at appropriate size, CMAC with appropriate blade
-In-depth discussion of anesthetic plan with all members of care team may be necessary

33
Q

What are intraoperative anesthetic considerations for Tracheoesophageal Fistula/Esophageal Atresia surgery in neonates?

A
  • Mostly done via thoracoscopy, with lung isolation not necessary – tip of ETT placed above carina, but distal to the fistula. (Purposely right-main stem, then withdraw ETT until bilateral breath sounds heard) - Verify with fiber optic
  • Usually baby kept spontaneously breathing until fistula is isolated & ligated – if stomach becomes inflated, surgeon may have to needle decompress
  • Gastrostomy may be performed – allow for Fogarty catheter to be placed through stomach to occlude fistula from below
34
Q

What are anesthetic considerations for congenital diaphragmatic hernia repair in a neonate?

A

Neonates are stabilized prior to surgical intervention: including jet ventilation, measures to reduce PVR, iNO, and ECMO

NG should always be in place

Small TV (high RR), limited peak inspiration pressures, NO, N2O, may need 1 lung ventilation

35
Q

What are anesthetic considerations for congenital bronchogenic and pulmonary cysts in neonates?

A
  • Anesthetic planned around location of cyst
  • May require spontaneous respiration during intubation or bronchial blocker in case of cyst rupture (so contents don’t fall into lung tissue)

*rupture may cause hemorrhage or bronchopulmonary fistula formation

36
Q

What are anesthetic considerations for congenital lobar emphysema in neonates?

A
  • No N2O
  • If positive pressure is needed, low peak airway pressures/IVs
  • Single lung ventilation may be needed
  • Epidural catheter threaded up from caudal space may be useful for pain control
37
Q

What are anesthetic considerations for hypertrophic pyloric stenosis in neonates?

A

Considered FULL STOMACH – empty the stomach with OG placed in various positions prior while awake, then modified RSI

No opioid used - only LA and acetaminophen

38
Q

What are anesthetic considerations for omphalocele and gastroschisis?

A

Continue volume resuscitation

Prevent hypothermia

39
Q

What are anesthetic considerations for NEC?

A

Huge volume losses: need large IV access – hopefully time for CVC
-albumin 5%, massive transfusion

Hyperkalemia and renal failure common

Inotropic support usually needed (epi, dopamine, milrinone)

40
Q

What are anesthetic considerations for myelomeningocele in neonates?

A
  • Usually patient can be induced supine with donut padding around defect – (may have to be lateral if very large defect)
  • Prepare for transfusion, may not be needed
  • Large IV access critical (anticipate possibility of large blood loss)
  • Usually extubate to ICU afterward
  • Treat as latex allergy as increased sensitivity has been reported with this diagnosis
  • +/- muscle relaxants: discuss with surgical team prior to administration
41
Q

What do you need to set up airway supplies for neonates?

A
  • ETT sizes 2.0 to 3.5 (size 2.0 and 2.5 are uncuffed, micropremie)
  • Miller 0 (nice to have CMAC)
  • Neonatal circuit with neonatal HME
  • Size 1 or 2 mask
  • Shoulder roll
  • Percordial or Esophageal stethoscope
42
Q

How do you calculate minimal allowable blood loss (MABL) in neonates?

A

EBV x (Child’s Hct - Minimum acceptable Hct) / Child’s Hct

43
Q

How do you calculate the volume of PRBCs in a neonate?

A

(Desired Hct - Present Hct) x EBV (70mL/kg x 10kg) / Hct of PRBCs

44
Q

What is the blood volume of a preterm infant, term infant, and 3 months to 1 year old?

A

Preterm = 90-100 mL/kg

Term = 80-90 mL/kg

3 months - 1 year = 70-80 mL/kg

*preterm neonates can be up to 90% water – term neonate 75%

45
Q

What questions should you ask during preop exam for a neonate?

A
  • Gestational Age
  • Any known prenatal concerns (including no prenatal care)
  • Any maternal factors that would influence baby (gestational diabetes, hypertension, drug abuse)
  • Any suspected syndromes or anomalies
  • Is patient being fed (NPO guidelines still apply) – If not, how are they receiving glucose (and other nutrients)
  • Any apnea/brady (sometimes documented as “spells” by NICU)
  • Airway and Oxygen use
  • Any existing IV access – Labs!
  • Consent can be tricky and time consuming