NICU Flashcards

1
Q

List 5 examples of infants at risk of hypoglycemia

A
  1. Infant of a diabetic mother
  2. Weight <10th percentile (SGA)
  3. Weight >90th percentile (LGA)
  4. Intrauterine growth restriction (IUGR)
  5. Perinatal asphyxia
  6. Preterm infants (<37 weeks GA)
  7. Maternal labetalol use
  8. Late preterm exposure to antenatal steroids
  9. Metabolic conditions (CPT-1 deficiency [Inuit infants in particular])
  10. Syndromes associated with hypoglycemia (e.g. Beckwith-Wiedemann)
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2
Q

List 5 clinical signs of neonatal hypoglycemia

A
  • Jitteriness
  • Irritability
  • Cyanosis
  • Respiratory distress (apnea or tachypnea)
  • Tachycardia
  • Temperature instability
  • Feeding difficulties
  • Neuro symptoms: hypotonia, poor suck, and seizures or coma
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3
Q

Describe the expected physiological response to hypoglycemia for ketones, growth hormone, insulin, cortisol and catecholamines

A

Ketones: ↑

Growth hormone: ↑

Catecholamines:`↑

Cortisol: ↑

Insulin: ↓

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4
Q

What is considered a low blood glucose measurement in the following populations?

<72 HOURS OF LIFE

DOCUMENTED HYPERINSULINISM

>72 HOURS OF LIFE

A

<72h = <2.8

Documented hyperinsulinism, >72h = <3.3

  • If <2.8, do critical sample (if not already done)
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5
Q

How long do you have to screen the following populations for hypoglycemia?:

IDM/LGA

SGA/preterm infants (<36wk GA)

A

IDM/LGA = 12 hours if levels remain ≥2.6

SGA/preterm infants (<36wks GA) = 24 hours if no feeding concerns and infant is well

  • If there has been ≥1 reading <2.6, it is reasonable to screen 1-2 times on Day 2 to ensure levels remain above 2.6

Once 2 consecutive BG ≥2.6, continue monitoring pre-feed or every 3-6h.

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6
Q

You plan on sending an infant home from the hospital who has been experiencing persistent hypoglycemia. What should you do prior to discharge?

A
  1. A 5-6 hour fast prior to discharge
    • Maintenance of glucose level ≥3.3 at 4 and 5 hours postfeed should be documented before discharge is considered.
  2. Underlying diagnosis for neonatal hypoglycemia should be ascertained and specific medical management initiated (e.g. diazoxide in hyperinsulinism)
  3. Counsel parents regarding frequency of feeding, home blood glucose monitoring, medication delivery (if needed) or other treatment measures for hypoglycemia
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7
Q

Describe the essential approaches to treating hypoglycemia in the newborn and their corresponding treatment options.

What are conjunctive treatments for hyperinsulinism and GH deficiency?

A
  1. Increasing energy intake
    • Orally
      • Increase frequency of breasfeeding
      • Supplementing feeds (order of preference): EBM, donor milk, formula
        • 5mL/kg with 1st BG <2.6 (asymptomatic)
          • can be used for 2nd BG <2.6 WITH gel
        • 8mL/kg with 2nd BG <2.6 (asymptomatic)
      • Intrabuccal 40% dextrose gel (0.5mL/kg)
    • Intravenously
      • IV glucose
        • Wean once glucose levels stable for 12h
  2. Mobilizing energy stores
    • Glucagon
    • Corticosteroids

Conjunctive treatments

  • Hyperinsulinism
    • Diazoxide
    • Octreotide
  • GH deficiency
    • recombinant GH
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8
Q

What is one non-pharmacological measure that has been associated with reducing the incidence of hypoglycemia and may be considered in at-risk infants

A

Delaying the first bath

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9
Q

List 3 indications for initiation of IV dextrose in a hypoglycemic infant.

What orders would you provide to initiate IV intervention? How would you change your management for persistent hypoglycemia?

A
  1. Symptomatic or unwell
    • Give bolus 2mL/kg over 15 minutes, as well
  2. If BG <1.8
  3. Not tolerating feeds
  4. BG <2.6 x 3 (failed 2 interventions PO)

Initial IV: 80mL/kg/day of D10W, repeat glucose check in 30 minutes (if delay in IV insertion, give 40% dextrose gel 0.5mL/kg)

  • Increase D10W infusion q30min by 1mL/kg/h until within target range
  • Then, calculate the lowest GIR the BG is within target range
    • GIR = infusion rate (ml/kg/h) x [dextrose] (%)/6
  • Then, calculate the [D%W] needed to stay within maximum daily TFI
    • Can give up to D20W in peripheral line
  • Check electrolytes in 8-12h
  • Introduce enteral feeds as tolerated
    • Can breastfeed above TFI during transitional period (risk of over-hydration is low)
    • If supplemented: do not exceed 100mL/kg/day total
  • Once glucose ≥2.6 x 12h, can start to wean IV
    • Repeat BG q3h until full enteral feeds and 2 normal BGs

HIGH GIR

  • 8-10 → consider level 3 care + CVL
  • >10 →
    • Medication
      • Initial: Glucagon 0.1-0.3mg/kg bolus or 10-30µg/kg/h)
      • Others: hydrocortisone, diazoxide, octreotide
    • if >72h need further investigation
      • Critical sample
        • plasma glucose, beta-hydroxybutyrate, insulin, GH, cortisol, acylcarnitine + carnitine profiles, bicarbonate, FFA, lactate
      • Endocrinology referral
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10
Q

List 5 risk factors for Intraventricular or Intraparenchymal Hemorrhage

A
  1. ROM > 72h
  2. Breech delivery via SVD
  3. Increased urgency of delivery
  4. Hypothermia
  5. Use of vasopressors and inotropes
  6. HD-PDA
  7. Hypocapnia
    • PCO2 <35mmHg = risk of PVL
    • PCO2 >60mmHg = risk of IVH
  8. Pressure-limited ventilation
  9. Early use of HFO
  10. Transportation of preterm infant (noise, vibration, acceleration)
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11
Q

What is the highest risk period for acute preterm brain injury?

A

First 72 hours = critical window

95% IVH/intraparenchymal lesions are detected by Day 5

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12
Q

List 5 ways to prevent acute brain injury in preterm infants

A
  1. Maintain PCO2 between 45-55mmHg (minimize lung injury/ BPD)
  2. Normothermia
  3. Antenatal corticosteroids (if ≥48h prior to birth)
  4. Umbilical cord milking
  5. Delayed cord clamping up to 180s
  6. Neutral, midline head position with ↑HOB 30˚
  7. Volume-targeted ventilation (for first 72h)
  8. Nurturing environment (skin-to-skin contact, maternal voice exposure and interaction, light cycling, low noise level)
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13
Q

What strategies can be used to prevent acute brain injury for all premature neonates < 35 weeks?

A
  • Transfer at-risk mothers to tertiary care centre to deliver (if able)
  • C-section for very preterm + malpresenting infant
  • Delayed cord clamping (30-120s) if not in need of immediate resuscitation (consider cord milking in this case)
  • Avoid inotropes with hypotension unless a combination of other signs are present (↑lactate, ↑CRT, ↓u/o, ↓cardiac output)
  • Avoid lung hyperinflation (use volume-targeted ventilation)
  • Treat hypotension with slowly infused bolus before inotropes + CXR
  • Target PCO2 45-55mmHg to minimize lung injury + BPD
  • Maintain head in neutral, midline position with ↑HOB 30˚

<35 weeks

  • If risk of delivery in ≤7 days offer antenatal corticosteroids

<34 weeks

  • If delivery imminent (≤24h) consider intrapartum MgSO4 (↓ risk of cerebral palsy)

<33 weeks

  • Maternal antibiotic prophylaxis if PPROM and expecting to deliver
    • Penicillin + macrolide (if allergic to PCN → macrolide only)
  • If PPROM, preterm labour, unexplained NRFHR or chorio:
    • BCx + Abx prophylaxis x 36-48h (until BCx negative)

<32 weeks

  • Prevent hypothermia
    • Polyethylene bag or wrapping
    • Hat
    • Maintain room temperature between 25-26˚C
    • preheated radiant warmer with servo-control
    • Thermal mattress
  • Consider prophylactic indomethacin or ibuprofen for high-risk extremely preterm infants
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14
Q

List 3 goals of postnatal period care

A
  1. Foster development of parenting skills
  2. Promote physical well-being of mother and infant
  3. Support relationship among mother, infant and family members
  4. Strengthen the mother’s knowledge and confidence
  5. Facilitate development of feeding skills

All parents should receive counselling on:

  • Infant care
  • Signs of illness and how to respond
  • Infant safety - including safe sleep practices
  • Importance of smoke-free environment
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15
Q

What is the role of the health-care provider during the postnatal course?

A
  1. Evaluate the infant’s physical health
  2. Identify early problems
  3. Assist with establishment of feeding
  4. Observe parent-infant interaction
  5. Identify psychosocial stressors
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16
Q

Identify 2 populations that are at increased risk for readmission after postpartum discharge.

A
  1. First-time parent
  2. Low household income
  3. Younger GA
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17
Q

Identify 5 criteria that must be met prior to discharge of a healthy term infant.

A
  1. CCHD performed and normal
  2. Physical exam (with measurements) complete and documented with no additional in-hospital or ongoing observations or treatments needed
  3. Temperature is stable (open cot, appropriately dressed)
  4. Urine and at least 1 stool have been passed
  5. ≥2 successful feeds documented
  6. Maternal serologies reviewed and mother received all immunizations and/or medications
  7. NBS complete at ≥24h (or arrangements to screen within first 7d confirmed)
  8. Successful cardiorespiratory adaptation with normal, stable HR and RR
  9. Hearing screen completed or scheduled
  10. Bilirubin screening complete with appropriate follow-up PRN
  11. Vitamin K and ophthalmia neonatorum prophylaxis given
  12. Approved car seat in place + parents have demonstrated they can position the seat and secure infant properly

Must have an appropriate follow-up plan with scheduled visit 24-72h postdischarge

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18
Q

List 2 PROS and 2 CONS of early discharge of dyad following delivery

A

PROS

  • Facilitates family integration
  • Enhances parent-infant bonding
  • Allows mother to recover in quieter home environment with family support
  • Decreases exposure to nosocomial infection

CONS

  • Decreased parental education time
  • Untimely identification of postnatal problems
  • Increased readmissions for jaundice and dehydration
  • Shorter duration of breastfeeding
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19
Q

List 5 maternal and 5 infant risk factors for safe discharge after delivery

A

MATERNAL

  • Young age
  • Language barrier
  • Inadequate housing
  • Lack of family support
  • Inadequate prenatal care
  • Unstable parental relationships
  • Medications/substance use - ETOH, drugs
  • Depression
  • Low educational level

INFANT

  • Abnormal prenatal screen/ultrasound findings
  • Birth weight
  • Serologies not protective
  • Risk factors for infection/sepsis
  • Abnormal glucose homeostasis
  • DDH
  • Birth injury
  • Apgar score, need for stabilization at birth +/- low umbilical pH
  • Risk factors for early-onset neonatal jaundice
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20
Q

Describe the types of hemorrhagic disease of the newborn, their expected time course and etiology

A
  1. Early onset (<24h)
    • Maternal medications that inhibit vitamin K activity (antiepileptics)
  2. Classic (2-7 days)
    • Low intake of vitamin K
  3. Late onset (2-12 weeks up to 6mo) - typically ICH (50%)
    • Almost exclusively breastfed infants
      • low vitamin K intake
      • chronic malabsorption
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21
Q

Describe the recommended management options to prevent hemorrhagic disease of the newborn including dosing.

A
  • Parenteral Vitamin K
    • IM injection x 1 within 6h of delivery + after initial stabilization and maternal/newborn interaction
      • use pain minimizing strategies
    • Dosing
      • ≤1500g = 0.5mg
      • >1500g = 1mg
  • Oral Vitamin K (less effective, ↑failure rate, takes 5 days to achieve same effect as IM)
    • 2mg with first feed, 2-4 weeks and 6-8 weeks
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22
Q

List 4 indications for imaging the neonatal brain

A
  1. Infection
  2. Unexplained apneas
  3. Neonatal encephalopathy (NE)
  4. Suspected structural brain abnormalities
  5. Metabolic disorders
  6. Birth injuries
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23
Q

List the imaging modalities available for imaging the neonatal brain, indications for their use and disadvantages

A
  • Head Ultrasound
    • Indication: assessment for intraventricular hemorrhage
    • Advantages: safe, portable, readily available
    • Disadvantages: posterior fossa may not be well visualized, operator dependent, not useful for encephalopathy
  • CT Head
    • Indication: Urgent situations (unstable infant), suspicion of trauma or skull fracture
    • Advantages: offers imaging when patient too unstable
    • Disadvantages: ionizing radiation, grey/white contrast is poor, underestimates severity of injuries to white matter
  • MRI Brain (modality of choice for TERM brain)
    • Indications: Neonatal encephalopathy, metabolic disorders, structural concerns
    • Advantages: no radiation, improved diagnostic accuracy, no need for sedation
    • Disadvantages: higher costs
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24
Q

Describe the recommended timing for imaging of the neonatal brain following hypoxic ischemic encephalopathy

What are the 2 patterns of injury that can be seen with HIE, their location and the type of impairment associated with it?

A

Timing: DOL 3-5 (if cooled → DOL 4-5) to confirm diagnosis + extent (if exam not consistent with MRI findings or diagnostic ambiguity exists, repeat MRI in 10-14 days [maximal injury visible at this time for watershed injuries])

Patterns of Injury

  1. Watershed (50%) → cognitive impairment/language
    • Location: between major arterial supplies and deep in the sulci → cortical necrosis
    • Seen with prolonged partial hypoxia-ischemia
    • Impairment: cognitive impairment, predicts language outcomes
  2. Basal ganglia/thalamic (25%) → CP
    • Location: deep grey matter → sensorimotor cortex
    • Seen with acute, profound hypoxia-ischemia
    • Impairment: If loss of normal signal intensity in PLIC (posterior limb of internal capsule) → associated with severe motor and cogntivie disability → CP
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25
Q

What is the best imaging for neonatal stroke?

What type of stroke is most common and where is its common location?

A

MRI

Arterial infarction → LEFT MCA

1-2mo: injury evolves into tissue loss & cysts

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26
Q

Where would you expect to find the injury caused from a bilirubin encephalopathy on MRI?

A

Globus pallidus + subthalamic nuclei

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27
Q

What is the inclusion criteria for therapeutic cooling for HIE?

What are exclusions for therapeutic cooling? List 2.

A

Must be:

  • ≥36 weeks GA (possibly 35)
  • ≤6h of life
  • Meet Criteria A+C or B+C

If meets criteria, but then returns to normal within 30-45min after birth, cooling may be deferred with careful ongoing observation for signs of returning encephalopathy.

CRITERIA

  • A:​ pH ≤7.0 or BE ≥-16
  • B: pH 7.01-7.15 or BE -10 to -15.9 AND Apgar ≤5 at 10min or ≥10min PPV AND History of acute perinatal event (e.g. uterine rupture, placental abruption, cord prolapse)
  • C: Evidence of mod-severe encephalopathy - seizures or ≥3/6 categories with ≥1 sign present

If criteria met, offer therapeutic cooling. If difficult to categorize, consult tertiary care neonatologist

EXCLUSIONS

  • <35 weeks GA
  • Clinically significant coagulopathy
  • Evidence of severe head trauma or intracranial bleeding
  • Moribund (in terminal decline)
  • Major congenital or genetic abnormalities for whom no further aggressive treatment is planned
  • Severe IUGR
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28
Q

You are working in a community hospital and are caring for an infant with HIE who you have just determined meets criteria for therapeutic cooling. Describe strategies for initiation of cooling while awaiting transportation.

A
  • Initiate passive cooling
    • Turn off warmer
    • Take off hat/blanket
    • Check rectal temperature q15min to prevent ≤33˚C (target is 33.5˚C ± 0.5˚C)
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29
Q

Describe the possible complications with HIE/therapeutic cooling

When would you consider discontinuing therapeutic cooling prematurely?

A
  • Seizures
  • Discomfort (treat w/low dose morphine ≤10mcg/kg/h)
  1. Hypotension despite inotropic support
  2. PPHN with hypoxiemia despite adequate treatment
  3. Clinically significant coagulopathy, despite treatment
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30
Q

List 4 goals of therapeutic cooling for HIE

How quickly should the baby be rewarmed?

A
  1. Minimize fluctuations in CO2
  2. Avoid hyperoxia
  3. Ensure adequate tissue perfusion with appropriate use of vasopressors/intropes
  4. Maintain normal blood glucose
  5. Treat hyperbilirubinemia
  6. Minimize unnecessary stimulation or handling

Rewarming

  • After 72h of cooling, rewarm 0.5˚C q1-2h
    • if seizures/worsening encephalopathy - recool x 24h then resume warming
      • treat with antiepileptics - obtain serum levels in first 72h if redosing is needed
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31
Q

How should follow-up be arranged for an infant with HIE who has received therapeutic cooling?

What consequences/morbidity are you screening for with follow-up appointments?

A
  • NNFU for minimum of 2y (ideally until school age)
  • Care by community pediatrician

Consequences/morbidity

  1. Cerebral palsy (30%)
  2. Severe visual impairment/blindness (25%)
  3. Hearing loss (~18%)
  4. Learning disability (30-50%)
  5. Behavioural difficulties
  6. Epilepsy (13%, 7% require antiepileptics at school age)
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32
Q

What is the most common type of neonatal sepsis?

When does it typically present?

What is the most common mechanism?

What bacteria is most commonly responsible?

What is the most common presenting symptom?

What percentage of infants born to mothers colonized with GBS develop this type of sepsis without intrapartum antibiotic prophylaxis?

A

Early-onset neonatal bacterial sepsis

Symptomatic within 24h of birth

Cause: vertical transmission of organisms colonizing birth canal

GBS,Escherichia coli, GAS, S. pneumoniae, Enterococcus, Enterobacter, Staph aureux, H. influenzae

Respiratory distress

1-2%

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33
Q

List 4 risk factors for early-onset sepsis in the neonate

A
  • Prolonged ROM >18h
  • History of previous infant with invasive GBS disease
  • Maternal fever ≥38˚C
  • GBS bacteriuria at any time during the current pregnancy
  • Intrapartum GBS colonization during current pregnancy
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34
Q

When should screening for GBS colonization be performed?

If screening positive or history of GBS bacteriuria during the pregnancy, what is considered adequate prophylaxis?

Does IAP decrease the incidence of late-onset GBS disease?

A

Between 35-37 weeks GA.

Adequate prophylaxis = ≥4h prior to delivery for SVD or ROM (not needed for cold section)

  • IV Pen G 5 million units OR Ampicillin 2g (If allergy: Cefazolin IV 2g [low risk], or IV erythromycin/clindamycin or IV vancomycin)
  • Should be considered inadequate if IV clindamycin or IV vancomycin used (due to lack of clinical trials)

No - does not decrease incidence of late-onset GBS disease

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35
Q

What tests should be performed when concerned for early-onset bacterial sepsis in the neonate?

A

Tests

  • Blood culture
    • WBC <5 x 10^9/L or ANC <1.5 x 10^9/L
  • CBC/diff
  • If blood culture positive:
    • LP (should be done if BCx positive)
      • Considered positive if: WBC >20-25cells/mm3
      • pleocytosis, low glucose, high protein
    • CSF culture
  • If respiratory distress:
    • CXR
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36
Q

List 5 signs of sepsis in a neonate.

A
  1. Respiratory distress
  2. Temperature instability
  3. Tachycardia
  4. Seizures
  5. Hypotonia
  6. Lethargy
  7. Poor peripheral perfusion
  8. Hypotension
  9. Acidosis
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37
Q

What is the management for early-onset neonatal sepsis?

A

Preterm (35-36wks)

  • if stable enough to remain with their mother, manage similar to term, but observe for 48h rather than 24h

Term (≥37wks)

  • See photo

Before discharge

  • Parents to understand signs of sepsis and are able to seek medical care if signs develop
  • Ready access to health care
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38
Q

List 5 risk factors for acute encephalopathy in the presence of severe hyperbilirubinemia

A
  1. Acidosis
  2. Prematurity
  3. Dehydration
  4. Hyperosmolarity
  5. Respiratory distress
  6. Hydrops
  7. Hypoalbuminemia
  8. Hypoxia
  9. Seizures
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39
Q

List 5 risk factors for the development of severe hyperbilirubinemia in the newborn

A
  • <38wks gestational age
  • Previous sibling with severe hyperbilirubinemia
  • visible jaundice <24h or before discharge
  • visible bruising
  • Male sex
  • Cephalohematoma
  • Maternal age ≥25yo
  • Asian or European background
  • Dehydration
  • Exclusive and partial breastfeeding
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40
Q

When should a direct antiglobulin test be performed?

When should a G6PD deficiency test be performed?

A
  1. Clinically jaundiced infants of mothers with group O blood
  2. Infants with elevated risk of needing therapy (high-intermediate risk zone)
  3. Antenatal maternal antibodies

G6PD

  • all infants with severe hyperbilirubinemia
  • screen at-risk infants (Mediterranean, Middle Eastern, African or Southeast Asian origin)
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41
Q

At what level should a total conjugated bilirubin concentration prompt further investigation?

A

>18 µmol/L or >20% TSB concentration

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42
Q

List 4 side effects of phototherapy.

A
  1. Temperature instability
  2. Intestinal hypermotility
  3. Diarrhea
  4. Interference with maternal-infant interaction
  5. Bronze discolouration of the skin (rare)
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43
Q

How should you manage an infant who presents with severe hyperbilirubinemia?

Once ready for discharge, what follow-up should you arrange?

A
  • Place under intensive phototherapy
  • Continue breastfeeding
  • Repeat bilirubin concentration within 2-6h of initiating treatment to confirm treatment response
  • Consider supplemental fluids administered orally or by IV infusion
  • If isoimmunization present, provide IVIG
  • If unsuccessful in controlling the rising bilirubin concentration, initiate exchange transfusion (consider in healthy term infant between 375-425 µmol/L)
    • Before starting: Collect blood for red cell fragility, enzyme deficiency and metabolic disorders, hemoglobin electrophoresis and chromosome analysis

Follow-up

  • Breastfeeding support in community
  • Infants with isoimmunization: order repeat hemoglobin
    • If low at discharge: at 2 weeks
    • If normal at discharge: at 4 weeks
  • If exchange transfusion:
    • Refer for NNFU
    • Ensure hearing screen with brainstem auditory evoked potentials is completed
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44
Q

Describe the recommended management for neonatal ocular prophylaxis during a shortage of erythromycin ointment

What is the contraindication to administering Ceftriaxone in a neonate?

What is the best means of preventing ophthalmia neonatorum?

A
  • Gonorrhea
    • No test done → test mother at delivery**
    • Positive test
      • Treated but not followed up → test mother at delivery**
      • No treatment
        • Baby asymptomatic → assume baby is infected: test with conjunctival swab for gonococcus + IM/IV Ceftriaxone x 1 dose
        • Baby unwell →
          • Conjunctival swab + BCx + CSF Cx
          • Paediatric ID consult
    • Negative test
      • Low risk → no treatment
      • High-risk → test mother at delivery**

**Discharge infant if close follow-up can be assured while awaiting results (counsel to contact immediately if develops eye irritation/discharge)

If close follow-up CANNOT BE ASSURED AND it is NOT POSSIBLE for the infant to remain in hospital while awaiting results → treat with IM Ceftriaxone (50mg/kg [max 125mg]) x 1 before discharge

  • Chlamydia
    • Positive, no treatment → closely monitor for symptoms (conjunctivitis, pneumonitis) + treat if infection occurs

Contraindication - if neonate is receiving IV calcium (administer cefotaxime 100mg/kg IM or IV)

Best prevention: Screen pregnant mothers for gonorrhea and chlamydia infection (treat and follow-up those infected)

  • if positive, test after treatment to ensure therapeutic success
    • test again in 3rd trimester or at delivery
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45
Q

What is the appropriate management of an infant exposed to Chlamydia trachomatis?

A

Close clinical follow-up

Test conjunctival and nasopharygeal secretions of symptomatic infants → treat if positive

Erythromycin PO 50mg/kg divided QID x 14 days

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46
Q

What level of hematocrit is required for neonatal polycythemia?

List 4 causes of neonatal polycythemia.

A

≥65%

Causes

  1. Passive fetal RBC transfusion
    • Twin-twin transfusion
    • Delayed cord clamping
    • Maternal-fetal transfusion
  2. Increased fetal erythropoiesis
    • postdates
    • SGA
    • LGA
    • Infant of diabetic mother
    • Chromosomal abnormalities (trisomies 13, 18, 21)
    • Androgenital syndrome
    • Neonatal Graves disease
    • Hypothyroidism
    • Infants of hypertensive mothers (or taking propranolol)
    • Beckwith-Wiedemann Syndrome
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47
Q

What is the most common cause of perinatal brachial plexus palsy (PBPP)?

List 3 risk factors for PBPP.

What is the prognosis?

A

Birth trauma

Risk factors for PBPP

  • Shoulder dystocia
  • Large for gestational age
  • Maternal diabetes
  • Instrumental delivery

Prognosis:

  • 75% recover completely within the first month of life
  • 25% will have residual deficits (if incomplete recovery by 3-4 weeks, full recovery is unlikely)
    • refer to multidisciplinary team
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48
Q

What are the most frequent indications for blood transfusions in the newborn?

Describe strategies to decrease risk of transfusion.

What is a major risk of rapid and massive transfusion?

A
  1. Acute treatment of perinatal or surgical hemorrhagic shock
  2. ‘top-ups’ for recurrent correction of anemia of prematurity (used to maintain levels >75)

Strategies to decrease risk of transfusion

  1. Leukoreduction (decreases CMV risk)
  2. Irradiated (decreases GVHD risk)
  3. Screening donors
  4. Cross-matching (starting at 4mo)

Implementing iron supplementation between 4-6wks of age (physiological 2-3mg/kg/day; if deficient: 4-6mg/kg/day) at onset of reticulocytosis, results in higher Hgb and iron stores after 6mo.

Risk of rapid/massive transfusion = hyperkalemia

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49
Q

What are the transfusion thresholds for anemia of prematurity?

A

Week 1

  • Resp support = 115
  • No support = 100

Week 2

  • Resp support = 100
  • No support = 85

Week ≥3

  • Resp support = 85
  • No support = 75
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50
Q

What are strategies to minimize iatrogenic blood loss in premature infants?

A
  • Noninvasive CO2 monitoring for ventilated preterm infants
  • Noninvasive bilirubin monitoring devices before phototherapy is recommended
  • Point-of-care testing
  • Limit blood sampling to the minimum required for safe clinical care
    • Use marked tubes to indicate minimum volume to collect
    • Cluster blood samples to reduce skin breaks and painful procedures
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51
Q

In what time period can Neonatal HSV infections present?

List 2 prevention strategies for neonatal HSV.

Describe 2 clinical presentations of neonates where you should consider neonatal HSV.

A

In the first 6 weeks of life (typically initial sx in first 4wks)

Prevention strategies

  • C-section delivery
  • Maternal antiviral therapy
  • Anticipatory guidance for prospective mothers/partners
  • Identification of high-risk pregnancies

Clinical Presentations

  • <6wks
  • Suspected sepsis (esp. if presenting w/seizure, AbN CSF, not improving rapidly, -ve CSF at 24h, unexplained hepatitis)
  • Unexplained coagulopathy or bleeding from venipuncture sites
  • Pneumonia NYD, not improving after 24h Abx
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52
Q

List the 3 classifications of maternal HSV and their risk of transmission.

A
  1. Newly acquired
    • First-episode primary infection (no hx of antibodies)
      • 60% transmission
    • First-episode non-primary infection
      • ≤30% transmission
  2. Recurrent
    • < 2% transmission
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53
Q

List the 3 classifications of neonatal HSV infections and the duration of treatment

Which is most common in newly acquired maternal HSV?

What indicates a poor prognosis?

A
  • Disseminated HSV (involves multiple organs) - 21 days
    • **More common in newly acquired maternal HSV**
    • Highest mortality rate (29%)
    • If nasopharyngeal PCR+ and pneumonia = presume disseminated
  • Localized CNS HSV - 21 days
    • If fever, irritability and abnormal CSF findings (**seizures)
    • Mortality rate (14%)
  • Skin, eye and mucous membrane (SEM) infection - 14 days

Poor prognosis

  • Higher viral loads in CSF
  • Persistence of HSV in CSF in patients on acyclovir
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54
Q

What is the recommended investigations/managements for:

  • Asymptomatic term infant potential exposed to HSV
    • Suspected 1st-episode genital HSV at delivery
    • Recurrent genital HSV
  • Symptomatic HSV
A
  • Asymptomatic term infant potential exposed to HSV
    • Suspected 1st-episode genital HSV at delivery
      • Initial management
        • Mucous membrane swabs (conjunctivae, mouth, nasopharynx) at 24-hours of life regardless of delivery type +/- blood PCR (if available)
        • Treatment with IV Acyclovir x 10 days for:
          • Vaginal delivery
          • C-Section delivery with ROM
        • C-section delivery NO ROM or Recurrent genital HSV:
          • Discharge to reliable caregiver aware of NHSV symptoms
      • Ongoing management
        • If HSV testing negative → continue observation
        • If HSV testing positive → admit to hospital
          • Do CSF + blood PCR + transaminases
          • Start Acyclovir IV
            • If CSF/blood positive → 21 days (min)
              • Repeat CSF near end of 21-day course, if remains positive, continue with weekly sampling until negative
            • If CSF/blood negative → 14 days
  • Symptomatic HSV (or positive test in asymptomatic)
    • Testing:
      • PCR testing:
        • CSF, mucous membrane swabs, vesicular lesions blood
          • Nasopharyngeal PCR if pneumonia present
        • Transaminases (evidence for disseminated)
    • Start Acyclovir IV 60mg/kg/day divided q8h
    • If ocular involvement:
      • Treat with topical ophthalmic agent→ trifluridine
      • Ophthalmology consult
    • Suppressive therapy for CNS disease (consider for disseminated)
      • PO Acyclovir (300mg/m^2/dose TID) x 6 months
        • adjust for growth
      • CBC, urea/Cr monthly
    • Neonatal follow-up clinic
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55
Q

Provide 1 infection control recommendation for each specific target group:

Neonates with HSV infection and exposed neonates

Mothers with active HSV

Staff with orofacial or skin lesions

A
  • Neonates with HSV infection and exposed neonates
    • ​Use contact precautions with:
      • Mucocutaneous lesions until crusted
      • Asymptomatic neonates whose mothers have active HSV lesions (until end of incubation period - 14 days) or until samples are negative
  • Mothers with active HSV
    • Use contact precautions until lesions crusted
    • If herpes labialis, wear disposable mask when caring for infant <6wks or until lesions healed (crusted and dried)
      • No kissing infant
    • Keep skin lesions covered whenever newborn present
  • Staff with orofacial or skin lesions
    • Meticulous hand hygiene + keep lesions covered (if not possible, avoid direct care)
    • Wear surgical mask for orolabial lesions
    • Avoid contact if active herpetic whitlow
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56
Q

Describe adverse effects associated with retinopathy of prematurity screening.

List 2 methods to decrease these risks.

A
  1. Distress
  2. Pain
  3. Apnea

Decrease risks

  • Topical anesthetics
  • Pacifiers
  • Swaddling
  • Sucrose
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57
Q

What are the screening recommendations for ROP?

A
  • Screening:
    • <31 weeks BGA
      • Start at 31wks CGA or 4 weeks of life (whichever is LATER)
    • BW≤1250g
    • BW 1251-2000g with unstable clinical course (respiratory disease, hypotension w/inotropes, prolonged ventilatory or oxygen therapy)

Use of specialized digital retinal photography (RetCam)

  • should have ≥1 indirect ophthalmoscopic examination by an ophthalmologist before treatment or cessation of screening

Discharged infants with ROP should be followed by an ophthalmologist (often have strabismus, cataracts, amblyopia and refractive errors)

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58
Q

List 4 risks of surfactant replacement therapy

A

Short-term risks

  • During instillation
    • Bradycardia
    • Hypoxemia
    • Blockage of endotracheal tube
  • Pulmonary hemorrhage
  • Overdistension
  • Hyperventilation
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59
Q

List 2 indications for surfactant replacement therapy

A
  1. Intubated infants with RDS
    • should be administered before transport
    • <29 weeks: consider immediate intubation followed by surfactant
  2. Intubated infants with MAS requiring >50% FiO2
  3. Sick newborn infants with pneumonia and Oi >15
  4. Intubated infants with pulmonary hemorrhage which leads to clinical deterioration
  5. Infants with RDS with persistent or recurrent oxygen (≥30%) and ventilatory requirements within the first 72h of life should have repeated doses of surfactant (maximum 3)
    • Can be considered as early as 2h after initial dose (more commonly 4-6h after)
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60
Q

List 3 complications of maternal depression in the neonate

Which SSRI may have an associated risk of increased cardiac malformations (septal, RVOT, conotruncal and LVOT defects)?

How long should babies with late-trimester SSRI exposure be observed in hospital for neurobehavioural or respiratory symptoms?

A
  1. Low birth weight
  2. Preterm birth
  3. Slightly higher risk of miscarriage
  4. Respiratory distress
  5. Increased length of hospital stay
  6. Poor maternal-child bonding
  7. Cognitive, behavioural and emotional consequences
  8. With SSRI use:
    • PPHN (risk is negligible)
    • Admission to NICU

Paroxetine

Minimum of 48 hours

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61
Q

List 4 signs or symptoms associated with SSRI exposure in the neonate (SSRI neonatal behavioural syndrome [SNBS]).

When are these symptoms typically present and how long do they last?

A
  1. Tachypnea
  2. Cyanosis
  3. Jitteriness/tremors
  4. Increased muscle tone
  5. Feeding disturbance

Present within hours

Resolve within 2 weeks

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62
Q

Regarding twin-twin transfusion syndrome which vessel from the placenta is supplying the donor and recipient?

List 4 complications associated with the donor

List 4 complications associated with the recipient

A
  • Donor→ arterial
  • Recipient → venous

Complications

  • Donor
    • Oligohydramnios
    • Small for gestational age
    • Malnourished
    • Pale
    • Anemic
    • Hypovolemia
    • Hypoglycemia
    • Microcardia
    • Small glomeruli
    • Thin walled arterioles
  • Recipient
    • Polyhydramnios
    • Hydrops
    • Large for gestational age
    • Plethoric
    • Polycythemia
    • Hypervolemia
    • Cardiac hypertrophy
    • Myocardial dysfunction
    • Tricuspid regurgitation
    • Right ventricular outflow obstruction
    • Thick-walled arterioles
    • Large glomeruli
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63
Q

Which 2 populations of infants are at highest risk for BPD?

When are postnatal corticosteroids used to prevent BPD?

What complication is associated with use of dexamethasone in the first 7 days of life?

A

Highest risk for BPD

  1. Exposed to chorioamnionitis
  2. <28 weeks GA

When postnatal CS are used:

  1. Infants at highest risk for BPD: Hydrocortisone in the first 24-48h after birth x 10 days (risk of late-onset sepsis; do not combine with indomethacin)
    • Physiologic replacement: 1mg/kg/d x 7d→ 0.5mg/kg/d x 3d
    • associated with increased survival without BPD
  2. Infants who remain ventilated after 7d post birth with INCREASING O2 requirements + WORSENING lung disease
    • Low-dose Dexamethasone: 0.15-0.2mg/kg/d tapered over a short course (7-10d)

Dex <7d of life: increased risk of cerebral palsy

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64
Q

List 4 contributing factors to BPD.

A
  1. Early gestational age
  2. Low birth weight
  3. Lung barotrauma
  4. Exposure to hyperoxia
  5. Lung inflammation
  6. Pre- and post-natal infections
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65
Q

What is the criteria of an apnea in apnea of prematurity?

Below what gestational age is at risk for apnea of prematurity?

When should it resolve?

How long should an infant have no apneas before considered safe for discharge

A

Cessation of breathing for ≥20s OR 10-20s if accompanied by bradycardia (<80 bpm) or SpO2 <37wks BGA

<35 weeks GA

Typically by 40wks CGA (most by 36wks)

(if BGA <28wks, can continue until 44wks CGA)

At least 5-7 days is suggested

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66
Q

In infants born <34 wks GA, what 4 factors indicate readiness for discharge? Parental factors?

What is the recommended target SpO2 for infants with BPD?

A
  1. Thermoregulation - maintain body temperature (~37˚C) fully clothed in an open cot
  2. Respiratory stability - maintenance of SpO2 >90-95% RA
  3. Feeding skills and sustained weight gain - successful feeding by breast and/or bottle without major cardiorespiratory compromise
  4. Control of breathing - apnea free for 5-7 days

Parental (are able to:)

  1. Independently and confidentaly care for their infant
  2. Provide medications, nutritional supplements and any special medical care
  3. Recognize signs and symptoms of illness and respond appropriately, especially in emergency situations
  4. Understand the importance of infection control measures and a smoke-free environment

SpO2 90-95%

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67
Q

List 3 physiological changes associated with intubation

List 2 ways these physiological responses can be reduced or eliminated.

A
  1. Systemic and pulmonary hypertension
    • Systemic HTN → adequate analgesia
  2. Bradycardia
    • Can be avoided with atropine
  3. Intracranial hypertension
    • Avoided with muscle relaxants
  4. Hypoxia
    • Can be avoided with:
      • Preoxygenation
      • Use of blade that allows continuous oxygen insufflation into pharynx during procedure

Reduced/Eliminated

  1. Vagolytics
  2. Muscle relaxants
  3. Analgesic
  4. Preoxygenation
  5. Gentle technique
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68
Q

What are the complications of premedicating an infant for intubation?

When is it acceptable to intubate an infant without premedication?

A
  1. Chest wall rigidity (chest freeze) → potent short-acting opiates (avoided if given slowly, treated by giving a muscle relaxant or opioid antagonist)
  2. Respiratory depression
  3. Malignant hyperthermia, hyperkalemia, rhabdomyolysis → succinylcholine
  • Emergency intubations during resuscitation
  • Infants in whom instrumentation of the airway is likely to be extremely difficult (e.g. with severely abnormal airways + need to breathe on their own)
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69
Q

List 2 indications for treatment with inhaled nitric oxide (iNO)

What is the starting dose recommended?

When should you consider weaning?

A
  1. ≥35wks GA + hypoxemic respiratory failure failing to respond to respiratory management
  2. OI (oxygenation index) >20 to 25
  3. PaO2 <100mmHg despite 100% FiO2
  4. May consider in premature infants with respiratory failure 2˚ oligohydramnios

Not effective for most infants with CDH.

Starting dose: 20ppm (should expect ↑PaO2 ≥20mmHg in ≤30min)

  • If no response, increase to 40ppm ( >40ppm → potential for ↑toxicity without additional benefit)

Weaning: Improvement in oxygenation AND 4-6h period of stability of ↓FiO2 to 60-80% or OI falls to ≤10.

  • ↓50% q4-6h (as long as OI ≤10)
  • Once 5ppm, ↓1ppm q4h and d/c at 1ppm if <60% FiO2 w/PaO2 >50mmHg constantly

If cannot be weaned after 7 days, consider other lung/cardiac disease

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70
Q

Name 2 risk factors associated with inhaled nitric oxide (iNO)

A
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71
Q

List 2 populations where kangaroo care should be delayed

A
  1. <27wks GA who require high humidification
  2. Abdominal wall defect (pre-op)
  3. Neural tube defect (pre-op)
  4. Newly postoperative patients (stability NYD)
  5. Significant HD instability (wide BP swings, significant bradycardia, apnea or oxygen desaturation with handling, associated with prolonged recovery)
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72
Q

List 4 benefits of kangaroo care in preterm infants

Identify 2 barriers to implementation of kangaroo care.

A
  1. Promotes maternal-infant bonding and breastfeeding
    • Breastfeeding: longer duration, higher volumes of milk expression, higher exclusive breastfeeding rates
  2. Promotes stability of cardiorespiratory function and temperature
  3. ↑ mature sleep organization (↑sleep time [quiet sleep], ↓active sleep)
  4. ↓nosocomial infections
  5. ↓pain with bedside procedures

Barriers to implementation

  1. Poor staff knowledge
  2. Inadequate training
  3. Discomfort with the process
  4. Lack of time and/or resources
  5. Lack of privacy
  6. Parental reluctance
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73
Q

List 2 reasons preterm infants are at lower risk for opioid withdrawal

A
  1. Shorter in utero exposure time
  2. Decreased placental transmission
  3. Inability to fully excrete drugs by immature kidneys/liver
  4. Minimal fat stores leading to lower deposition/activity of opioids
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74
Q

What are 3 adverse effects of opioid use in pregnancy?

How long should opioid-exposed babies be screened after delivery for withdrawal symptoms?

A
  1. Prematurity
  2. Low birth weight
  3. Spontaneous abortion
  4. SIDS
  5. Infant neurobehavioural abnormalities

3-5 days

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75
Q

List 4 non-pharmacological strategies to decrease symptoms from neonatal abstinence syndrome (NAS).

What are 3 benefits of having the dyad room-in together during monitoring of NAS?

A
  1. Skin-to-skin contact
  2. Safe Swaddling
  3. Quiet environment (lower lighting, minimal stimulation)
  4. Music or Massage therapy
  5. Gentle waking
  6. Developmental positioning
  7. Parent rooming in with baby (near term/term, medically stable, adequate support in place, ongoing assessment needed)

Benefits of Rooming-in

  1. Increased breastfeeding initiation rates
  2. Lower NICU admissions
  3. Less need for pharmacotherapy
  4. Shorter hospital stays
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76
Q

When should pharmacotherapy be initiated in Neonatal Abstinence Syndrome (NAS)?

What is the recommended first line management? Describe available adjuncts for management.

When can discharge be considered?

A

Using Finnegan scoring: 3 scores ≥8 OR 2 scores ≥12

  • 1st line: morphine or methadone
    • morphine: 0.32mg/kg/day q4-6h PO (↓10% daily dose q48-72h)
  • 2nd line: Buprenorphine
  • Adjuncts:
    • Phenobarbital - polysubstance abuse cases
    • Clonidine - autonomic symptoms present

Discharge

  • 72h if asymptomatic and no medication started
  • If phamacotherapy started:
    • Tolerating morphine wean
    • Consistent withdrawal scores < 8
    • Clear, documented weaning plan
    • When adequate medical and social follow-up available
      • Referral to PCP
      • Nutritional and family supportive resources
      • Infant neurodevelopmental assessment
      • Ensure safe, supportive home for discharge
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77
Q

What is the most accurate assessment for determining gestational age?

Describe the situations where palliative care, shared-care and intensive care would be recommended for extremely preterm infants.

What are additional risk factors that would increase the likelihood of mortality in an extremely preterm infant.

A

First trimester crown-rump length with ultrasound (accurate within 3-8d)

Palliative Care

  • 24wk GA w/ELBW (350g)
  • ≤22wks

Shared-care

  • 23-24wks
  • 25wk w/fetal anemia and abnormal placental blood flow

Intensive Care (antenatal CS should be given if this is an option + risk of delivery is high)

  • ≥25 wks
  • Late 24th wk, well growth with antenatal corticosteroids, born in a tertiary centre

Risk Factor

  • SGA
  • No antenatal corticosteroids
  • Multiple gestations
  • GA early within week of gestation
  • Birth outside of a tertiary centre
  • Acute chorioamnionitis
  • Major congenital anomalies present on ultrasound
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78
Q

List 2 benefits of human breast milk in the preterm infant.

List 2 risks associated with donor breast milk.

List 3 indications for donor breast milk.

A
  1. Lower incidence of necrotizing enterocolitis
  2. Lower incidence of severe infections
  3. Reduced colonization by pathogenic organisms
  4. Decreased length of hospital stay
  5. Improved neurodevelopmental outcomes

Risks with PHDM

  1. Infection - screened for HBV, HCV, HIV, Human T cell leukemia virus
  2. Contamination - “food poisoining”
  3. Allergy

13% of protein content is denatured in PHDM. Carbohydrates, fats and solids are unchanged.

All beneficial immune cells are inactivated (IgM antibodies completely removed)

Indications

  • Prematurity
  • GI surgery
  • Malabsorption or Feeding intolerance
  • Immunodeficiency
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79
Q

In standard-risk women of child-bearing age, what is recommended to prevent neural tube defects (NTD)?

List 4 factors associated with increased risk for neural tube defect.

What is recommended to prevent NTD in high-risk women?

A
  • Encourage eating folate-rich foods (leafy vegetables, legumes, red meat, offal), fortified grain products
  • Daily multivitamin → Folate 0.4-1.0mg + Vitamin B12
    • SOGC: 2-3mo before conception, throughout pregnancy + ≥6wks postpartum (or until breastfeeding stops)

Risk Factors

  1. Birth of previous child with NTD (highest risk factor)
  2. Family history of NTD
  3. Maternal obesity
  4. Maternal Hispanic origin (or eat flour alternatives)
  5. Use of some anticonvulsants
  6. Low socioeconomic status (greatest burden of NTD)

As above, except with Folate 5.0mg

  • SOGC: ≥3mo before conception → 10-12wks postpartum
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80
Q

List 5 conditions that have been associated with Vitamin D deficiency

List 2 conditions in the neonate that are associated with maternal Vitamin D deficiency

A
  1. Osteoporosis
  2. Asthma
  3. Autoimmune diseases (RA, MS, IBD)
  4. Diabetes
  5. Disturbed muscle function
  6. Resistance to Tuberculosis
  7. Pathogenesis of certain types of cancer
  8. Weak dental enamel

Neonatal conditions 2˚ Maternal Vit D Deficiency

  1. Rickets
  2. Hypocalemia
  3. Dental malformations
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81
Q

What populations should receive 800IU/day of Vitamin D between October and April?

What is the recommended dosing of Vitamin D for premature infants and infants during first year?

What are the recommendations regarding maternal Vitamin D supplementation (pregnant/lactating women) to maintain sufficiency?

A
  1. North of 55th parallel
  2. Between 40th-55th parallel + RFs for Vit D deficiency (dark skin, breastfed, maternal deficiency)

Premature: 200 IU/kg/day (max 400 IU/d)

Infants: 400IU daily

Maternal: Consider 2000 IU/day with monitoring of 25-OH Vit D and calcium for side effects.

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82
Q

List 5 benefits of breastfeeding.

A
  1. ↓ incidence of bacterial infections
  2. ↓ hospital admissions 2˚ infection
  3. ↓ severe respiratory illnesses
  4. ↓ SIDS
  5. ↑ performance on neurocognitive testing
  6. Economical

Maternal benefits

  1. ↓ breast + ovarian cancers
  2. ↑ postpartum weight loss
  3. Delay in return of ovulation
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83
Q

List 4 contraindications to breastfeeding excluding medications.

List 4 medications or drugs contraindicated in breastfeeding.

A

Mothers:

  1. HIV-positive
  2. Human T-cell lymphotropic virus type 1 and 2
  3. Active tuberculosis (until treated ≥2 weeks + not contagious)
  4. Active HSV lesions on both breasts
  5. Receiving cytotoxic chemotherapy (for duration of treatment)
  6. Receiving radioactive isotopes or radiation therapy (during treatment course)

Infants

  1. Galactosemia

Medications

  1. Amphetamines
  2. Cocaine
  3. Cyclophosphamide
  4. Clozapine
  5. Doxorubicin
  6. Ecstasy (MDMA)
  7. Immunosuppressants
  8. Heroin
  9. Gold salts
  10. Thiouracil
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84
Q

At what age have children developed the advanced oral motor coordination required to properly handle chunky food pieces such as nuts, whole grapes and hot dog wheels?

A

3 years

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85
Q

Identify the 2 types of approaches to cessation of breastfeeding.

A
  1. Gradual weaning (infant-led)
    • occurs as the infant begins to accept increasing amounts of foods while still breastfeeding on demand.
    • Wean usually completes between 2-4yo
  2. Planned weaning (mother-led)
    • Reasons: inadequate supply, concerns regarding infant growth, painful feedings or mastitis, returning to work, new pregnancy, wishing an alternate caregiver to give feedings, eruption of baby’s teeth
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86
Q

What guidance would you provide a mother whose infant has suddenly refused to breastfeed

A

“Nursing Strike”

  • Minimize Distractions: Make feeding time quiet and special
  • Increase cuddling and soothing of baby
  • Offer breast when infant is very sleepy or just waking up
  • Offer breast using different nursing positions, alternating sides or nursing in different rooms

If this is not effective, a physician should evaluate the infant for presence of possible illness.

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87
Q

In regards to hearing screening, what is the ideal timing for screening, confirmation of diagnosis and intervention?

What is the average age at diagnosis in areas of Canada without screening programs?

What is the most common type and cause of hearing loss in children?

A
  • Screening: ≤1mo
  • Confirmation of diagnosis: ≤3mo
  • Intervention: ≤6mo

Average age at diagnosis = ~24 months (2yo)

Most common type: Sensorineural hearing loss

Most common cause: 50% genetics (most common → error in production of gap junction protein connexin 26)

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88
Q

List 4 risk factors for neonatal sensorineural hearing loss

A
  • ABCDs
    • Affected family member
    • Bilirubin
    • Congenital intrauterine infection (CMV, rubella, toxo, HSV)
    • Defects of ear, nose and throat - Branchial Oto Renal syndrome + CHARGE syndrome (most common)
    • Small at birth (<1500g), low apgar, NICU
      • NICU stay >2 days OR involving any of the following (regardless of duration):
        • ECMO
        • Assisted ventilation
        • Ototoxic drug use
        • Hyperbilirubinemia requiring exchange transfusion
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89
Q

List 4 infections associated with congenital sensorineural hearing loss

A
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90
Q

List 3 functional outcomes of delayed diagnosis/intervention of neonatal sensorineural hearing loss

A
  1. Impaired socioemotional development
    • Low academic achievement
    • Underemployment
    • Increased social maladaption
    • Psychological distress
  2. Decreased literacy
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91
Q

What are the 2 types of hearing screening tests performed?

Which is performed first in an newborn with no risk factors?

Describe intervention strategies if hearing loss is detected.

A
  1. OAE - otoacoustic emission (1st if no RFs)
  2. AABR - automated auditory brainstem response (if RFs)
    • ​​tests for auditory neuropathy (vestibular nerve function)

Hearing loss intervention

  • Audiological
  • Medical/surgical
    • Hearing aid
    • Cochlear implant
      • eligible children for bilateral implants should receive them between 8-12mo + auditory oral therapy
    • Bone-anchored hearing aid
    • Brainstem-implanted auditory device
  • Educational/(re)habilitation
  • Child and family support
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92
Q

What is the recommended compression to ventilation ratio for neonatal resuscitation

What is the preferred method of heart rate assessment when administering chest compressions?

What initial FiO2 should you use for infants <35 weeks

What is the recommended dosing for epinephrine in neonatal resucitation?

At what gestational age should you use strategies to optimize thermoregulation?

What ETT tube size is recommended for a 3.75kg infant?

A

3 compressions: 1 ventilation

Cardiac monitor

21-30%

Epinephrine (1:10 000) ETT 1mL/kg (0.1mg/kg) [max 3mL]; IV 0.1mL/kg (0.01mg/kg)

<32 weeks GA

ETT 3.5

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93
Q

Describe the treatment for polycythemia

A

Treatment

  • Confirm hematocrit with venous sample
  • Treat dehydration
  • Closely monitor ins/outs, blood glucose and bilirubin levels
  • Hct 60-70%
    • Monitor closely
    • Hydrate with enteral intake/administration of IV fluids
  • Hct 70-75% + symptoms worsen despite aggressive IV hydration
    • Partial exchange transfusion (with NS)
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94
Q

List 4 signs or symptoms of neonatal polycythemia.

What are 2 complications associated with neonatal polycythemia?

A

Signs/Symptoms

  • Irritability
  • Lerthargy
  • Tachypnea
  • Respiratory distress
  • Cyanosis
  • Feeding disturbances
  • Hyperbilirubinemia
  • Hypoglycemia
  • Thrombocytopenia

Complications

  • Stroke
  • Seizures
  • Pulmonary hypertension
  • Necrotizing enterocolitis
  • Renal vein thrombosis
  • Renal failure
95
Q

What 4 things can you do while waiting for the neonatal transport team to transfer your baby with PPHN (pH 7.32, pCO2 48, HCO3 18, FiO2 80%, SpO2 91% preductal, 82% postductal)?

A
  1. Intubate and secure airway
  2. Target normocarbia and correct acidosis
  3. Obtain secure vascular access - insert UVC, possible UAC
  4. Minimize handling
  5. Provide sedation

Transportation

  1. Obtain copies of pertinent records and medical images
  2. Obtain a maternal blood sample and colostrum for early feeding, if able
  3. Retain the placenta, double-bagged in a sealed container without formaldehyde, for pathology examination
96
Q

What characteristic findings are seen on this CXR?

A
  • Air bronchograms
  • Diffuse, fine reticular granularity of the parenchyma (ground-glass appearance)
  • Low lung volumes

= Respiratory Distress Syndrome

97
Q

What characteristic findings are seen on this CXR?

A
  • Prominent perihilar pulmonary vascular markings
  • Fluid in intralobar fissures
  • Rarely, small pleural effusions

= Transient tachypnea of the newborn

98
Q

What characteristic findings are seen on this CXR?

A
  • Patchy infiltrates
  • coarse streaking of both lung fields
  • increased AP diameter
  • Flattening of the hemidiaphram

= Meconium aspiration syndrome

99
Q

List 4 clinical signs associated with neonatal thyrotoxicosis.

How will you manage this infant?

A
  1. Irritability
  2. Tachycardia (including SVT +/- cardiac failure simulating cardiomyopathy)
  3. Polycythemia
  4. Craniosynostosis
  5. Bone age advancement
  6. Poor feeding
  7. Failure to thrive

Management:

  • Self-limited disease (can take up to 6mo)
  • May need methimazole and beta-blockers to control hyperthyroidism and cardiovascular symptoms
  • If minimally affected, observe without treatment
100
Q

What features are associated with / at risk in Infant of a Diabetic Mother?

A
  • Preterm labour
  • LGA (or IUGR if vascular disease associated)
  • Hypoglycemia (25-50%)
    • Presents as jittery, tremulous, hyperexcitable
  • Hypocalcaemia
  • Hypomagnesemia
  • Tachypnea
    • Can be due to RDS (higher incidence)
    • Can be due to hypoglycemia, hypothermia, polycythemia, cardiac failure, TTN or cerebral edema from asphyxia/HIE
  • Cardiomegaly
    • 30% with 5-10% in heart failure
    • Asymmetric septal hypertrophy or transient hypertrophic subaortic stenosis
  • Hyperbilirubinemia from polycythemia
  • Renal vein thrombosis
    • Suspect if flank mass, hematuria and thrombocytopenia
  • Congenital anomalies
    • Congenital heart
      • VSD, ASD, TGA, truncus, DORV, tricuspid atresia, coarct
    • Lumbosacral agenesis
    • Neural tube defects
    • Hydronephrosis
    • Renal agenesis and dysplasia
    • Duodenal or anorectal atresia
    • Situs inversus
    • Double ureter
    • Holoprosencephaly
    • Small left colon syndrome (delayed development of left colon, transient, can have abdo distension)
101
Q

What are the differences in presentation of TORCH infections? (ie. Toxo, Rubella, CMV, HSV, Syphilis)

A
102
Q

Child with brachial plexus injury. How long before if no change in exam is prognosis poor? a. 1 month b. 3 month c. 9 month d. 1 year

A

b. 3 month - surgery indicated if function not improving by 3 months - more likely to be total nerve disruption or nerve root avulsion

103
Q

A term newborn is born to a heroin addicted mom. On initial assessment the baby is apneic but HR is greater than 100. After 30 seconds, the baby continues to be apneic despite adequate bag and mask ventilation. What is the next step in your management? a. IM Narcan b. Intubate and give Narcan down the ETT c. Continues to support ventilation until baby breathes on his own d. Epinephrine 1:10000

A

c. Continues to support ventilation until baby breathes on his own

104
Q

Full term baby delivered after traumatic forceps delivery. Now 1 month old with vomiting, lethargy and red plaque on back of hand. What lab test would you check. 1. Glucose 2. calcium 3. potassium 4. alp 5. creatinine

A
  1. calcium - subcutaneous fat necrosis - rubbery/firm red/violaceous plaques or nodules on cheek, butt, back, thigh, arm A rare but potentially life-threatening complication is hypercalcemia. It manifests at 1-6 mo of age as lethargy, poor feeding, vomiting, failure to thrive, irritability, seizures, shortening of the QT interval on electrocardiography, or renal failure
105
Q

In counseling a woman who has had a child with a meningomyelocele, what would you tell her as regards her next pregnancy: a. take folic acid prior to conception and then for 10 weeks afterwards b. ultrasound at 16 weeks c. amniocentesis at 16 weeks d. alpha-fetoprotein at 16 weeks

A

ANSWER: a. take folic acid prior to conception and then for 10 weeks afterwards (PROBABLY THE MOST CORRECT BUT TECHNICALLY SOGC SAYS FOR FULL T1 and NELSON SAY TILL WEEK 12) *b. ultrasound at 16 weeks (typically week 18-22) c. amniocentesis at 16 weeks (no only if US (+) then discuss) d. alpha-fetoprotein at 16 weeks (PIR routine in past; SOGC not routine now)

106
Q

IUGR neonate with bony changes, cataracts and hepatosplenomegaly. What’s the most likely diagnosis? a. congenital syphilis b. congenital rubella c. congenital CMV d. congenital toxoplasmosis

A

b. congenital rubella - neonatal findings: - IUGR, interstitial pneumonitis, radiolucent bone disease, HSM, TCP, dermal erythropoiesis (blueberry muffin lesions)

107
Q

Mom ivdu. Early latent syphilis. Titer from 6 months ago and now. They have dropped by 8 times. Baby is born. What do you do to for the baby: a) Observe b) Tryomonial screen and RPR c) CSF RPR d) Swab baby

A

b) Treponemal screen and RPR - mom with primary, secondary or early latent syphilis treated at least 4 weeks prior to delivery with at least 4 fold drop in titres - RPR and TT at 0, 3, 6, 18 months as well as clinical assessment monthly x3 months and with each additional serum screen

108
Q

Mom is IVDU. Her blood work: HEB B + HepC +. Baby’s blood work at 6 mo, hep B and hep C ab negative. What to do: a) Rest Hepc in 6 months b) No further investigations c) PCR

A

b) No further investigations - for a child at any age born to a mother with hep C who has absent Hep C antibodies, there is no need to test PCR and the interpretation is that either vertical transmission did not occur or the child cleared the infection

109
Q

Mom hep B positive. What do you do for baby ?

A
  • Hep B vaccine at birth, 1-2m, 6m and HBIG as soon after delivery as possible (<12h)
110
Q

Klehauer betke test - question about what it is

A

Used to determine if there is fetal blood in maternal circulation such as fetal maternal haemorrhage (test done on maternal blood sample)

111
Q

EcG: baby is thrombocytopenic, mild elevated liver enzymes, ecg shows complete heart block. What does mom have?

A

SLE (or other autoimmune condition like RA or Sjogren) - baby has congenital lupus

112
Q

You are examining a newborn infant, born at full term, 2600g. He has a flat nasal bridge, a thin upper lip and a smooth philtrum. He is mildly hyptonic. Which of the following ingestions is it important to inquire about in your history of the mother’s pregnancy: a. Cocaine b. Alcohol c. Marijuana d. Heroin

A

b. Alcohol

113
Q

Mother of 2 hour newborn who has a mass on the scalp that crosses suture lines. The mother took phenytoin during pregnancy and the child was delivered via vacuum delivery. Give two reasons why the child has this lesion.

A

in utero use of phenytoin (can predispose to bleeding) and caput succedaneum from vacuum

114
Q

Picture of a CT scan of the head with intracranial calcifications. What is the diagnosis?

A

Congenital CMV (periventricular calcifications, ventriculomegaly, microcephaly, HSM, TCP, SNHL, chorioretinitis), congenital toxoplasmosis (chorioretinitis, hydrocephalus and CNS lesions), HIV

115
Q

A 24 hr old newborn is seen with a report of scant U/O, the creat is 85. What is this most consistent with: a. Maternal creat b. Creat cannot be interpreted without a urea c. Creat is elevated for this newborn d. Creat cannot be interpreted without a urine creat

A

a. Maternal creat

116
Q

Which of the following are true? (a) fetal p02 is 25-30 (b) the incidence of asymptomatic PFO in the adult population is 10% c) Umbilical veins close before umbilical arteries

A

ANSWER: (a) fetal p02 is 25-30 (umbilical venous pO2 is 30-35 (highest pO2 in fetus), but it mixes with systemic blood so pO2 entering the RA is 26-28mmHg) (b) the incidence of asymptomatic PFO in the adult population is 10% - also true, it’s 10-25%

117
Q

2-week old child with a 1 week history of stool mixed with blood in an infant? Bottlefeeding well, passed stool in first 24 hours. Most likely dx? a. anal fissure b. cow milk protein allergy enterocolitis c. Meckel’s diverticulum

A

b. cow milk protein allergy enterocolitis

118
Q

A 1 week old breastfed baby comes in to your office for newborn care. There is bright red blood mixed in with the stool. The baby did not have any bleeding or bruising with the Vitamin K injection at birth or with the newborn screen. The anus appears normal and there is no evidence of a fissure. List the most likely cause of the blood in the stool.

A

Cow’s milk protein intolerance

119
Q

All of the following are normal in term newborns except: a) Hypotonia post feed b) Irregular respiratory pattern in REM sleep c) Sigh following a brief period of apnea d) Mild cyanosis with feeding

A

d) Mild cyanosis with feeding

120
Q

1 mo 2 day old with a vesicle noted on the upper lip? a. Sucking blister b. HSV c. Varicella d. Epidermolysis bullosa

A

a. Sucking blister - Sucking Pads o Calluses/vesicles found on lips in first few months o Confirmed by observing neonate sucking the affected area

121
Q

2 month old baby with poor feeding, hepatomegaly, crackles, soft systolic murmur. What is the most likely diagnosis? 1. congenital infection 2. CHF 3. Sepsis

A
  1. CHF
122
Q

Newborn was recently extubated after a course of systemic corticosteroids. What is the likely side effect? 1. hypotension 2. hypoglycemia 3. leucopenia 4. hypertrophic cardiomyopathy

A
  1. hypertrophic cardiomyopathy - SE of steroids include HTN, hyperglycaemia, GI bleed and perforation
123
Q

A 12 hour old infant born at term had mild polyhydramnios on 20 week U/S. Now the baby is grunting intermittently with lots of secretions. He improves with intermittent suctioning. What diagnosis is this most consistent with: a. TEF/esophageal atresia b. Duodenal atresia

A

a. TEF/esophageal atresia

124
Q

Child with bubbling oral secretions, difficulties passing an NG tube. Also noted to have a hemivertebrae. What to do? a. echocardiography b. spine MRI c. MRI head

A

a. echocardiography VACTERL association - cardiac abnormalities in 50% of patients with TEF

125
Q

2-day old baby with antenatal hydro, confirmed on post-natal U/S to have moderate-severe hydronephrosis. BW shows normal renal function, baby seems to be peeing well. a. consult urology prior to discharge b. DMSA c. arrange for an outpatient VCUG d. follow up in 2 months

A

a. consult urology prior to discharge

126
Q

Newborn with persistent bradycardia. ECG given. Looks like heart block… identify the problem. What 2 things is this child at risk for?

A
  1. Cardiac arrest/Death 2. Syncope 3. Dizziness 4. For infants and toddlers → night terrors, tiredness with frequent naps & irritability
127
Q

Which of the following is associated with polyhydramnios a. IUGR b. Hirschsprung’s disease c. esophageal atresia d. renal agenesis

A

c. esophageal atresia (can’t swallow fluid) *renal issues - get oligohydramnios (can’t pee fluid out) *IUGR + polyhydramnios - think trisomy 18

128
Q

What to do with a mom who is about to deliver at 23-weeks? a. resuscitation is not indicated b. all babies born >22 completed weeks should be resuscitated c. parents ideas about resuscitation and palliation should be taken into account

A

c. parents ideas about resuscitation and palliation should be taken into account

129
Q

You are counseling a pregnant teenage girl and her boyfriend at 23 weeks gestation. She is in labour. You discuss the high morbidity at this gestational age, if the baby survives at all. What is true about the resuscitation of this newborn: a. Since they are teenagers, the physician decides. b. There is legislation in Canada that says all babies 22 weeks and older require resuscitation. c. The parents’ wishes should be supported whether they want to resuscitate or not. d. Given the high mortality at this gestation, the baby should not be resuscitated.

A

c. The parents’ wishes should be supported whether they want to resuscitate or not. 22 weeks - palliative care recommended 23-24 weeks - could go either way (parent preference) 25+ weeks - recommend early intensive care as default Above is in context of no additional risk factors (SGA, multiple gestation, no antenatal corticosteroids, delivering outside tertiary care centre)

130
Q

Expected survival rate for an infant born at 25 weeks gestation: a) >90% b) 75% c) 50% d) 25% e) <10%

A

b) 75%

131
Q

The outcome in neonates since the introduction of surfactant is best described as: a. decreased mortality b. decreased BPD c. increased air leaks d. increased IVH e. decreased PDA

A

a. decreased mortality *and decreased air leaks

132
Q

Newborn baby born at 27 weeks, no spontaneous resps. What to do? a. put in polyethylene plastic bag and stimulate b. warm, dry and stimulate c. positive-pressure ventilation

A

a. put in polyethylene plastic bag and stimulate - plastic bag for all babies <32 weeks, stimulate, if apneic then start PPV

133
Q

Newborn, a 30-week premie. Not breathing after stimulation. What do you do? a. self-inflating bag, room air b. self-inflating bag, oxygen reservoir c. self-inflating bag, oxygen reservoir with O2 being blown through d. anesthesia bag, connected to oxygen source

A

d. anesthesia bag, connected to oxygen source

134
Q

Newborn baby has copious oral secretions and respiratory distress. What is the most appropriate next test? a) Insertion of orogastric catheter b) CXR c) Abdominal U/S d) Barium swallow

A

a) Insertion of orogastric catheter - concern with lots of secretions and resp distress is TEF

135
Q

Which of the following newborns requires surfactant administration according to recent guidelines: a. Any newborn being transferred between centres b. A 29 week infant with no symptoms being transferred between centres c. A critically ill infant who has required 3 doses of surfactant in the first 18 hours d. An infant with RDS who is intubated and requiring more than 50% O2 after 72 hours

A

b. A 29 week infant with no symptoms being transferred between centres - ?best answer, none are really right - CPS: - infants delivered at <29 weeks gestation outside tertiary care centre should be considered for immediate intubation and surfactant after stabilization NRP- prior studies suggested babies born at <30 weeks should get prophylactic surfactant even if they weren’t intubated… now immediate use of CPAP is considered an alternative to surfactant administration

136
Q

Term male, delivered by emergency C-section for fetal distress. Meconium present, suctioned below cords. Now needing 100% O2. Radial Gas PaO2 80. Umbilical gas PaO2 40. What is the diagnosis? a) PPHN b) Meconium aspiration c) TGA

A

a) PPHN - PPHN should be suspected in all infants with cyanosis - hypoxemia is present in all cases - intermittently unresponsive to 100% O2 - oxygen saturation or PAO2 gradient between preductal (right radial artery) and post ductal (umbilical artery) sites of sampling imply shunting across PDA

137
Q

Unstable premature neonate on Ventilator with ++02 needs. Desating frequently with handling and recovering with bagging. What do you do? d) Increase sedation e) Steroids f) surfactant a) Minimize handling, increase sedation

A

a) Minimize handling, increase sedation - suspect PPHN - labile sats that recover well with bagging

138
Q

Newborn has significant respiratory distress and CXR that is consistent with pneumonia. She is ventilated with PIP 36, PEEP 5 rate 60 bpm, FiO2 1.0, she is not saturating very well. What is the likely diagnosis? What intervention should you start now?

A
  1. Hypoxic Respiratory failure or PPHN 2. iNO - effective in term infants with hypoxemic resp failure
139
Q

You are taking care of a newborn ventilated baby born at 26 weeks who is now 29 weeks CGA with pulmonary interstitial emphysema on CXR. He is currently ventilated with the following settings: rate 40, PIP 18, PEEP 4, 60% O2. You receive the following blood gas: pH 7.20, pCO2 58, pO2 56, HCO3 19, base deficit -6. a. What change in ventilator settings do you make? b. 48 hours later the baby is suddenly mottled, and has the following bloodwork: Na 139, K6.8, pH 7.18, pCO2 38, pO2 68, HCO3 12, base deficit -12. The baby’s urine output is 2.5 cc/kg/hr. What complication has most likely occurred?

A

a. increase rate (best strategy for ventilation in PIE is permissive hypercapnia since escalating support can worsen PIE - increase rate over pressures to control ventilation) b. Metabolic acidosis from poor cardiac output from bad PIE or pneumothorax

140
Q

You are treating a 38 week old newborn who was flat at birth but improved with 2 minutes of PPV. Now at 12 hours of age the baby is tachypneic at 70, BP is 38/20 (mean 32). You take the following CXR. (CXR with left-sided pneumothorax, RUL collapse but no mediastinal shift) c. What is your management?

A

Needle decompression

141
Q

A newborn term infant had thin meconium at delivery but had good APGAR scores and required only 2 minutes of free flow O2. Now at 12 hours of age he has increasing work of breathing. On CXR there is hyperinflation of the RUL with mediastinal shift. What is the most likely diagnosis: a. Meconium aspiration syndrome b. Neonatal pneumonia c. CCAM d. Congenital lobar emphysema

A

d. Congenital lobar emphysema ● Congenital lobar emphysema (CLE), also known as congenital alveolar overdistension, is a developmental anomaly of the lower respiratory tract that is characterized by hyperinflation of one or more of the pulmonary lobes - intrinsic obstruction creates ball-valve mechanism

142
Q

What are 4 ways in which meconium aspiration causes respiratory problems?

A
  1. inactivation of surfactant 2. airway obstruction - can lead to distal atelectasis/ball valve mechanism can lead to pneumothorax 3. reactive pneumonitis 4. pneumonia (meconium is sterile but an excellent growth medium for bacteria like e. coli, and inhibits phagocytosis by PMNs)
143
Q

16 week male born at 28 weeks GA. Hospitalized with RSV bronchiolitis. pCO2=60; pO2=94 in 50% oxygen. Chest X-ray shows RML infiltrate. Tachypneic. Best management: a. intubate and ventilate b. humidified oxygen and monitor closely c. ribavirin d. steroids e. antibiotics

A

a. intubate and ventilate - best option, IRL would probably try CPAP first

144
Q

Description of a newborn with respiratory distress. What are your 4 management options.

A
  1. suction mouth and nose and ensure nares patent 2. supplemental O2 by nasal prongs 3. CPAP 4. intubate and ventilate
145
Q

Newborn term, AGA baby , cried at birth, Apgars 9 and 9. Few hours later found to be in respiratory distress. RR 80, HR high. Cap refill 4-5 seconds, BP 48/32. Hyperinflated chest with minimal indrawing. Cannot hear breath sounds on left, cannot hear heart sounds. Baby is turning cyanotic. What investigation do you do (1)? What is your possible diagnosis (1) Baby’s heart rate is now 80 and is more cyanotic. What one investigation do you want to do

A
  1. transillumination 2. pneumothorax 3. needle decompression
146
Q

12h old Newborn has a sat of 80%. Increases to 85% with 100% 02. Mild tachypnea rr65. CXR has no abnormalities. What next initial management should be done? a. Intubate and ventilate b. Prostaglandins c. Antibiotics

A

b. Prostaglandins

147
Q

(CXR of a newborn with ?narrow mediastinum and ?normal pulmonary vasculature) You are asked to see a term newborn in the delivery room after an uneventful delivery and resuscitation. The baby has a RR of 70 and is cyanotic. a. What is the most likely diagnosis? b. What one treatment will you start immediately?

A

a. Cyanotic congenital heart disease (?TGA given narrow mediastinum) b. PGE

148
Q

A 3 day old is tachypneic, cyanosed despite 100% O2. Bilateral crackles on exam with weak peripheral pulses and no heart murmur. What is the diagnosis: 1. HLHS 2. Sepsis 3. AV fistula

A
  1. HLHS
149
Q

Child with cyanosis, O2 sat 80% doesn’t improve with oxygen. Pan systolic murmur grade III/IV. CXR normal and ECG shows right axis deviation. What is the diagnosis?

A

?TOF

150
Q

A 3-day-old infant develops poor perfusion, diminished peripheral pulses, and decreased urine output. What medication would you administer: a) atropine b) morphine c) bicarbonate d) furosemide e) prostaglandins

A

e) prostaglandins - if antibiotics were an option that could also be a good consideration

151
Q

3 day infant cyanosis with crying, investigation a ECG b CXR c ABG d bld cx e echo

A

e echo - crying increases right sided pressure which increases right to left shunting (and therefore increases cyanosis)

152
Q

Bili question. 37 weeker. Mild lethargy. Total bili 280 @ 30 weeks (?meant hours). No ABO. Give 3 bili charts. Mgt? a. Follow-up in 24 hours b. Phototherapy and repeat bili in 6 hours c. Exchange d. IVIG

A

b. Phototherapy and repeat bili in 6 hours - medium risk line (only significant lethargy counts as a risk factor) - at/above exchange line; no use for IVIG if no ABO

153
Q

3 week old infant has jaundice. His birth weight was 3250g and he now weighs 3490g. He is breastfeeding well. Hemoglobin is 127 and total bilirubin is 270, conjugated bilirubin is 8. Coombs test is negative. What should be done? a) Admit for phototherapy b) Referral to gastroenterology c) Reassess in 1 week d) Recommend switching from breastfeeding to formula

A

c) Reassess in 1 week Breast milk jaundice

154
Q

What are risk factors for unconjugated hyperbilirubinemia in a neonate? a) Prematurity b) LGA c) male

A

a) Prematurity

155
Q

Which of the following is the best predictor of risk of Rh autoimmune hemolytic disease at the time of delivery? a. Bili in the cord b. Hb in the cord c. Mom’s Anti-Rh titres d. Gestational age

A

c. Mom’s Anti-Rh titres o Any infant of Rh-negative mom should be tested for DAT, type, Hg ▪ If DAT positive, baseline bili should be measured

156
Q

A baby has a direct hyperbilirubinemia. He was treated for an E. coli sepsis. He has hepatomegaly on exam. Which test will likely yield the diagnosis a. RBC GALT function b. G6PD level c. Osmotic Fragility d. RBC glucose-phosphate-1 deficiency

A

a. RBC GALT function Galatosemia

157
Q

You are seeing a 1 wk old Chinese boy with 1 day of jaundice. His bili is 270 (mostly indirect), Hg 95 retics 9%, Mom is AB+ and he is B+. He otherwise looks well. What is the diagnosis? a. Sepsis b. Thalassemia c. G6PD def d. ABO incompatibility

A

c. G6PD def

158
Q

Baby with bili of 280 and conjugated 200? What is the most likely cause based on incidence? a. Breastfeeding jaundice b. Hemolysis ABO c. Neonatal hepatitis d. Galactosemia

A

c. Neonatal hepatitis

159
Q

4 risk factors for increased chance of kernicterus in a baby with hyperbilirubinemia.

A
  1. prematurity 2. sepsis/acidosis 3. Rh/ABO incompatibility 4. jaundice within first 24 hours of life 5. very high bilirubin level 6. asphyxia 7. G6PD deficiency
160
Q

You are called from a family doctor about a 5 day old jaundiced baby. Well looking. Total bili is 355, direct is normal. He is breastfed. What do you recommend? 1. septic work up 2. investigate for a metabolic disease 3. coombs test and hg 4. start phototherapy 5. observe

A
  1. start phototherapy
161
Q

Baby with jaundice, low platelet count, looks septic. What is the cause? (Lab values given). (a) TORCH infection (b) galactosemia (c) bacterial sepsis

A

could be TORCH infection or sepsis - might lean toward sepsis since that would be worse to miss

162
Q

A 32 week gestation infant with Rh incompatibility has received 5 exchange transfusions. He now has vomiting, diarrhea, and abdominal distension. Most likely diagnosis: a) sepsis b) acute gastroenteritis c) portal vein thrombosis d) necrotizing enterocolitis

A

d) necrotizing enterocolitis - exchange transfusion or any blood transfusion is a risk factor for NEC

163
Q

3 week old who is brought to the office because mother thinks he is too yellow. Breastfed. Otherwise well. Total bili is 180. Direct is 8. What do you do? A) septic workup B) investigate for blood group incompatibility C) reassure mother that condition may last for 4-12 weeks D) investigate for metabolic disease

A

C) reassure mother that condition may last for 4-12 weeks - breastfeeding jaundice

164
Q

36 wk baby 2.1 kg (5lbs) at birth, day 7 jittery, irritable, on exam HR 218, T 37.5, RR 70 bp 90/60. Face is flushed, eyes wide open, alert but irritable, normal tone and normal cry, jaundiced, DTR’s 2/4 and symmetric. There is hepatosplenomegaly. What is the likely diagnosis (1), List 2 tests to confirm your diagnosis

A
  1. Likely diagnosis is congenital hyperthyroidism 2. Two tests to confirm= T4 and TSH - mom with Graves - antibodies that bind to TSH receptor in thyroid (stimulating release of T3 and T4 even though there is no TSH) cross placenta - Ix: low TSH, high T3 and T4
165
Q

33 week premature infant is born to a mother with hypertension. Baby is SGA. What other associated findings do you expect? a) polycythemia b) hyperglycemia c) hypomagnesimia d) hypercalcemia

A

a) polycythemia

166
Q

Baby with symmetric IUGR. Cause? a) smoking b) preeclampsia c) congenital infection d) placental insufficiency

A

c) congenital infection

167
Q

Baby with low apgars at birth. Picture of hypoxia. What complications would you expect over the next few days

A

Neurological - Seizures, HIE, ischemic brain injury Pulmonary - RDS, PPHN Cardiac - cardiac ischemia leading to dysfunction → muscle and conduction Renal - AKI GI - feeding intolerance, increased risk of NEC Metabolic - mitochondrial dysfunction leading to a catabolic state, decreased energy reserve Heme - thrombocytopenia, polycythemia, coagulopathies

168
Q

GBS positive mom with antibiotics given 4hrs before delivery. Would like to go home. What would be your plan? (no risk factors were given!) a. can be discharged at 48 hrs b. normal newborn care

A

b. normal newborn care

169
Q

Mom with unknown GBS. First baby. List 3 criteria for offering intrapartum abx therapy.

A
  • preterm labour with imminent risk of delivery - preterm, prelabour rupture of membranes - rupture of membranes >18 hours - intrapartum fever 38 or higher
170
Q

Mom with fever, PROM but inadequate abx therapy. Unknow GBS. Babe is born and perfectly well. Obstetrician tells you mom has chorio. What do you do: a) Cultures and abx b) CBC and observe 24 hrs c) Observe 24 hrs d) Full septic work up

A

c) Observe 24 hrs - observe for 24-48 hours - could consider CBC at 4 hours

171
Q

A newborn with 37.3 axillary temperature. What should be done next? a) Repeat after 20 minutes of unbundling b) Do a tympanic temperature c) Do CBC d) Full Septic W/U

A

a) Repeat after 20 minutes of unbundling

172
Q

Newborn with axillary temperature of 37.8 degrees, well normal exam. What do you do? a) Full septic work up and antibiotics b) Rectal temperature c) Take off all clothes for 20 minutes and recheck temperature d) CBC and diff

A

b) Rectal temperature - axillary temp recommended for screening given very small risk of perforation with rectal temp

173
Q

Mother with +ve GBS never got treated intrapartum abx. Baby born 32 wk now 9 days. Has been having increasing apneas in the past 24 h. Blood culture done shows GP cocci in clusters after 18 h of culture. What most diagnosis a. GBS b. Strep viridans c. S aureus d. Coag neg staph

A

d. Coag neg staph (clusters) - staph in cluster, strep in chains - CONS is most common cause of late onset sepsis, especially in very low BW infants

174
Q

3 week old with previous e coli sepsis and persistent jaundice. What is the likely problem. 1. Increased osmotic fragility 2. RBC galactose phosphate uradyl transferase deficiency 3. RBC glu – 1 – phosphate dehydrogenase deficiency

A
  1. RBC galactose phosphate uradyl transferase deficiency - galactosemia - dx: positive reducing substances in urine (galactosuria) tx: soy formula (NO lactose)
175
Q

Pregnant mom who has a previous child. She is GBS positive, comes in at 6:00pm and gets IV penicillin. At 8:00pm, she delivers a healthy baby boy at 39 weeks. Babe is well and has a normal CBC. She is wondering when she can go home (she lives close to the hospital) a. start amp/gent b. observe until 24 hours c. observe until 48 hours d. full septic work-up

A

b. observe until 24 hours → for at least 24 h and then reassess prior to discharge.

176
Q

You are working in the NICU, and are called to see a 4 day old female born at 28 weeks. She has vomited with her last 2 NG feeds and now is noted to be distended with discoloration of the abdominal skin. You are concerned about necrotizing enterocolitis. You place the baby NPO, start antibiotic treatment and order an abdominal XR. a. Name 3 XR signs of NEC.

A

a. pneumatosis intestinalis - portal venous air - pneumoperitoneum - loss of normal bowel gas pattern (distended bowel, loss of hexagonal pattern, stacking of bowel loops) - bowel wall edema

177
Q

2 day old infant presents with fever of 39.5 ax. He is breastfed and his weight has fallen from 3.8 to 3.5 kg. He is lethargic but rouses during the examination. His fontanelle is normal. Na 150, K 7.3, Cl 110, BUN 8, Cr 110, uncong bili 190, normal CBC. What is the likely diagnosis? a) hypernatremic dehydration due to decreased fluid intake b) hypertonic breast milk c) diabetes insipidus d) sepsis e) meningitis

A

d) sepsis

178
Q

SGA prem, now 2 weeks old in NICU, baby presents with septic picture. a.) List 3 bacteria that could be responsible. b.) Initial choice of antibiotic treatment

A

a. GBS, E. coli, staph aureus, coag negative staph b. cloxacillin and tobramycin (CONS most likely), or vanco and tobra if have resistance

179
Q

Premature baby with apneas, temp instability, abdo distention with bowel loops palpable, not tolerating feeds. a.) Management/treatment x4 lines

A

a. NPO - NG to LIS - ampicillin, tobramycin, metronidazole - IV fluids/TPN - blood culture - refer to tertiary care centre with pediatric surgery

180
Q

Newborn with a TSH of 25. What do you do? a. start thyroxine b. repeat neonatal screen c. bring them into the office as soon as possible d. thyroid ultrasound

A

c. bring them into the office as soon as possible

181
Q

Term BB, mom with gestational diabetes. DOL 1. Glucose 1.4. What is your next step in management? a. Bolus glucose by NG b. Bolus 1 cc/kg of D50W c. Run IV D10 @ 80 cc/kg/day d. Frequent breastfeeding

A

c. Run IV D10 @ 80 cc/kg/day

182
Q

Male 3 weeks old. Presents with shock, hyperpigmented scrotum, low NA 115, K 6.8. What is your most important investigation? What is your immediate management?

A

Concern for CAH - ABCs - in shock therefore needs IV access and fluid bolus - hydrocortisone - Ix: 17-OHP

183
Q

3 week old has hypocalcemia. Most likely diagnosis?

A

transient hypoparathyroidism

184
Q

A 6 day old infant presents in shock with a glucose of 1.8 and cardiomegaly on CXR. Which of the following is the most likely etiology of the shock: a. Cardiac b. Sepsis c. Endocrine d. Metabolic

A

d. Metabolic - big heart? either muscle cell hypertrophy or deposition of lipids or glycogen IEMs: - amino acid: maple syrup urine disease - glycogen: hepatic glycogen storage disease - glucose: hereditary fructose intolerance - fatty acid: galactosemia, MCAD/SCAD/LCAD/VLCAD deficiency, carnitine palmitoyl transferase deficiency

185
Q

You are called to see a 2.5 kg term newborn with jitteriness. You do a bedside glucose, which is 1.7. You decided to insert an IV and give the baby a bolus of 2cc/kg of D10. a. Please write an ongoing fluid order for this baby, to be started after the bolus is complete (1 line).

A

D10W IV at TFI 80ml/kg/day

186
Q

A 2.2 kg term newborn breast feeds well at birth and then is seen at 2 hours of age with a BS of 1.9. He is asymptomatic. What is the best initial management: a. feed and recheck BS in 1 hour b. IV dextrose at 4-6 mg/kg/hr c. IV D10 2cc/kg then dextrose at 4-6 mg/kg/hr d. Supplement BF with bottle and recheck BS

A

a. feed and recheck BS in 1 hour

187
Q

Infantile cystinosis. What do you get? a. cataracts b. end stage renal failure c. nephrocalcinosis

A

c. nephrocalcinosis (the first clinical signs of infantile cystinosis appear between three and six months of age; they are largely due to impaired proximal tubular reabsorptive capacity - hypercalciuria part of this) - renal failure is later presentation if not treated - cataracts by 12-16 months

188
Q

Picture of rocker bottom feet (aka congenital vertical talus)– what condition do you need to think about?

A

T18 T13 18q deletion syndrome spina bifida, arthrogryposis

189
Q

TPN – list four metabolic complications

A
  1. hypernatremia 2. TPN cholestasis 3. hypertriglyceridemia 4. hypoalbuminemia
190
Q

3 week male infant with vomiting, lethargy, decr. po intake Na 118, K 8. Most important lab test? A) vasopression B) 17OHP C) cortisol D) calcium E) renin

A

B) 17OHP

191
Q

Newborn weighs 1.8 kg. Jittery and found to have glucose 1.3. Repeat glucose is 0.8 What is this baby’s glucose requirement in mg/kg/min (1)?. Write your IV order (1)

A
  1. GIR = 5.5mg/kg/min 2. bolus 2cc/kg of D10W IV over 5 minutes, then run D10W at TFI of 80ml/kg/day
192
Q

10 day old baby with failure to thrive, jaundice, hepatomegaly, blood culture positive for E.Coli. What underlying disorder may the child have? What test can you do to confirm this diagnosis (1)?

A
  1. galactosemia 2. RBC GALT (galactose-1-phosphate uridyl transferase) activity
193
Q

You are discussing with a mother the prognosis of her child born at 31 weeks gestation. There was thin meconium at birth. APGARs were 8 and 9. Head ultrasound showed a small intraventricular hemorrhage at one week of age. She is concerned because he is not yet walking and has stiff legs. a) the child likely has spastic diplegia which is often associated with prematurity and intraventricular hemorrhage b) the history is unusual in that children with CP usually have a history suggestive of birth asphyxia c) IVH would cause PVL which would result in hemiplegia d) there will be progressive decline in his development

A

a) the child likely has spastic diplegia which is often associated with prematurity and intraventricular hemorrhage

194
Q

Ex-29 week prem with hyperreflexia and gross motor delay. Had history of Grade II IVH and PVL. Advise the mother about the likely cause of CP in this child. What would you see on a CT that is specific to this?

A
  • IVH leading to PVL is the cause of this child’s CP (PVL in prems is the most common cause of spastic diplegia) - CT would show focal areas of necrosis in the periventricular white matter
195
Q

What is the number one cause of central apnea in a 34 week prem who is now at 8 week of age? a) Seizure b) RSV c) Apnea of prematurity d) IEM

A

c) Apnea of prematurity

196
Q

Ex-30 week prem, now at 39 weeks corrected has had an uneventful course. He had apnea of prematurity treated with caffeine. He is still having apneas with occasional bradycardia 5-6 times a day. What is the likely cause? a) Apnea of prematurity b) Seizures c) GERD

A

a) Apnea of prematurity

197
Q

An ex-1500g premature infant presents with a prolonged apnea spell at 5 weeks of age. Extensive laboratory workup is unremarkable. On sending the parents home, you suggest: a. infant should always sleep on side b. infant should sleep in parents’ room c. infant should sleep in own room, but parents should check on infant hourly d. an audio monitor should be placed on infant’s room e. parents should not use heavy blankets in the crib

A

b. infant should sleep in parents’ room

198
Q

A 4-hour-old term infant has developed tachypnea, RR 60, and has had several episodes of apnea. After initial investigations, what would you do: a) observe for further deterioration b) intubate c) antibiotics d) prostaglandins

A

c) antibiotics

199
Q

2 month old ex 32 weeker who was ventilated with Ua/Uv lines. Now has HSM but has an otherwise normal physical exam. What is the likely cause? 1. hepatic hemangioma 2. portal vein thrombosis 3. hereditary spherocytosis 4. congenital CMV 5. fungal infection

A
  1. portal vein thrombosis - leading to portal hypertension
200
Q

Baby prem 33 weeks with RDS. Heart rate is 50 apneic and limp? What are your next 2 management steps?

A
  1. give positive pressure ventilation with flow-inflatig bag and prepare for intubation 2. start chest compressions
201
Q

Neonate with BPD being treated with furosemide. List 4 side effects.

A
  1. hyponatremia 2. hypokalemia 3. hypochloremia 4. hypercalciuria 5. nephrocalcinosis 6. dehydration
202
Q

An infant born at 26 weeks gestation is now 28 weeks (2 weeks old). He is doing well and is going to be transferred to a level II nursery. When should he be screened for ROP. a) if normal now, no need to do further follow-up b) do eye exam now c) do eye exam at 32 weeks d) do eye exam at 38 weeks e) do eye exam at 52 weeks

A

c) do eye exam at 32 weeks (technically should be 31 weeks) - if born at less than 28 weeks, screen at 31 weeks CGA, if born at 28+ weeks, screen at 4 weeks of life

203
Q

Which is an indication of seizure activity in a neonate? A. tachycardia B. abnormal eye movements C. irregular breathing D. irritability E. vomiting

A

B. abnormal eye movements

204
Q

Newborn with trisomy 21, non-bilious vomiting after feeds. What’s the test? a. Abdominal ultrasound b. Barium swallow with follow through c. Abdominal Xray d. observe for now

A

c. Abdominal Xray Usually duodenal atresia would present with bilious emesis, but initially may be non bilious and then progress to bilious - AXR shows double bubble

205
Q

Newborn diagnosed with interrupted aortic arch, what to start? a. dopamine b. prostaglandin c. nitric oxide d. indomethacin

A

b. prostaglandin

206
Q

You are called to the newborn nursery to see a 4 hour old newborn female in respiratory distress. The RR is 70 and you note increased working of breathing. The nurses have also noted that the baby has a significant amount of oral secretions. a. What one test is required to make the diagnosis?

A

a. attempt to insert NG with CXR showing NG coiled in esophagus

207
Q

What advice should you give to parents to prevent positional plagiocephaly: a. Children should be put to sleep in car seats b. Children should be put to sleep on their sides c. Children should be put on their stomachs as much as possible when awake

A

c. Children should be put on their stomachs as much as possible when awake

208
Q

Child with distress, can’t pass NG through nare. List 3 other findings on physical exam you’d look for?

A

50% associated with other anomalies; 10-20% have full CHARGE - coloboma - heart murmur - GU abnormalities - ear abnormalities - square face, arched eyebrows, prominent forehead

209
Q

Baby with constipation. Barium enema shows rectal ampulla narrow with dilated proximal bowel. a.) 2 investigations to confirm the diagnosis. b.) What would you expect as the result of each investigation.

A
  • rectal biopsy: aganglionic cells - rectal manometry: failure of internal anal sphincter to relax with rectal distension
210
Q

Question where neonate has thrombocytopenia and mom’s plts are normal. Mgt?

A

Neonatal alloimmune thrombocytopenia - mgmt: platelet transfusion with maternal washed platelets or HPA1a (PLA1) negative platelets

211
Q

Description of newborn with petechiae. WBC normal, Hgb normal, plt 9. Rest of exam is normal. List 3 most likely causes aside from sepsis.

A
  1. neonatal alloimmune thrombocytopenia 2. autoimmune thrombocytopenia (maternal ITP) 3. TORCH infection - congenital rubella or CMV
212
Q

Fullterm baby delivered to an O+ mom. Looks well but pale. Hb is 70, he is hemodynamically stable. What is the most likely diagnosis? 1. ABO incompatability 2. Chronic fetal maternal hemorrhage 3. Rh incompatability

A
  1. ABO incompatability
213
Q

Which of the following predisposes to late hemorrhagic disease of the newborn: 1. breastfeeding 2. prematurity 3. cystic fibrosis 4. maternal phenytoin 5. oral antibiotics

A
  1. breastfeeding - maternal phenytoin is a risk factor for early HDN
214
Q

Newborn with platelets of 12, transfused and post-transfusion platelets were 16. Mom’s CBC was normal. What do you do? a. transfuse single donor platelets b. transfuse PLA-1 negative platelets c. give IVIG d. give steroids

A

b. transfuse PLA-1 negative platelets (same thing as HPA-1: for alloimmune)

215
Q

Most likely cause of late hemorrhagic disease of the newborn? a. phenytoin use in mom b. baby did not get Vit K prophylaxis c. oral antibiotics d. cystic fibrosis

A

b. baby did not get Vit K prophylaxis

216
Q

Newborn with plethora and lethargy. HCR 0.72, Hb 240, Glu 3.2 on venous blood. What to do? a) Exchange transfusion b) IV D10W c) Septic workup

A

a) Exchange transfusion

217
Q

Polycythemic newborn. Hb 240, Hct 0.75. Wt 2000g. Child requires a partial exchange transfusion. What fluid do you use as the diluent? How much blood do you replace to decrease the Hct to 0.5?

A
  1. NS 2. Volume = blood volume x (observed-desired hct)/observed hct = (2kg x 80ml/kg) x (0.75-0.5)/0.75 = 160ml x 0.25 / 0.75 = 40/0.75 = 53.3ml
218
Q

Baby born at home at 38 wks by midwife. Now presents at 7 days with melena. Hb 70, MCV 112, plts normal. What is the most likely diagnosis?

A

Vitamin K deficient bleeding (previously hemorrhagic disease of the newborn)

219
Q

You are called to see a 2 day old newborn male with jitteriness. At birth he was found to have a cleft palate, but has been bottle feeding well since. On physical examination, you note that the baby has a harsh systolic murmur. a. What is the most likely diagnosis? b. What is the reason for the baby’s jitteriness?

A

a. Di George b. Hypocalcemia

220
Q

Newborn is sneezing, what medication in mom could this be associated with? a. methadone b. IDM on insulin c. clindamycin

A

a. methadone

221
Q

3 day old baby with tachypnea, jitteriness, myoclonus and normal glucose. Treatment? a. Amp/gent b. Vit B c. Morphine

A

c. Morphine (NAS)

222
Q

Abstinence from methadone? Neonatal symptoms? a. Hyporeflexia b. Constipation c. Sneezing d. Lethargy

A

c. Sneezing

223
Q

Baby born to heroin addicted mom. Apneic despite bag and mask ventilation. Best management? a. Narcan b. Intubate until baby breathes on his own c. Bag and mask ventilation until baby breathes on his own

A

c. Bag and mask ventilation until baby breathes on his own

224
Q

A mother is given Demerol 90 minutes prior to delivery. The baby is suctioned and stimulated but remains apneic with a pulse of 80. Next step in management: a. bag and mask b. more stimulation c. Narcan d. Antibiotics

A

a. bag and mask

225
Q

In utero exposure to cocaine results in which of the following in the newborn: a) hearing deficits b) microcephaly c) hypotension d) spinal dysraphism

A

b) microcephaly

226
Q

What is true about neonatal chest compressions: 1. ? Required after 30 seconds of PPV with HR less than 60 2. Chest compressions to be done at a ratio of 5:1 with every breath 3. 2 finger technique is preferred 4. Required after no response to stimulation

A
  1. Required after 30 seconds of PPV with HR less than 60 → there should effective ventilation PPV and an advanced airway before chest compressions
227
Q

Baby born at 41 wks. Meconium staining. Flat babe requiring resuc. Apgars 2 at 1 min 3 at 5 min and 6 at 7 min. what 5 things may you expect with this baby in the near future. What 2 tests at discharge, if normal would suggets a good neurological outcome for this child

A
  1. seizures, hypotonia, hypertonia, hypotension, respiratory distress, acute tubular necrosis/AKI, GI perforation, SIADH or electrolyte abnormalities (low Na, Ca, hypoglycemia), DIC 2. Good neuro outcome: normal EEG and MRI
228
Q

Newborn with an Erb’s palsy. Which is true? a. extension at the wrist b. preserved grasp c. symmetric moro

A

b. preserved grasp

229
Q

Baby with renal mass and hematuria. Most likely associated with? a. IDM b. polycythemia c. dehydration d. UVC

A

a. IDM Presentation of RVT: Sudden onset gross hematuria (can also be microscopic), Unilateral or bilateral flank masses, Hypertension, Oliguria - perinatal risk factors including asphyxia present in 31% of cases - maternal diabetes in 8% - dehydration in 1.5% - polycythemia not mentioned

230
Q

Antenatal U/S shows moderate hydro. U/S at 24 hrs normal. What to do next and why.

A

repeat U/S after first 3 days of life, as can have false negative results prior to this while baby still digressing

231
Q

Description of child with prune belly. Weak abdominal musculature. Cryptocidism. Baby in intubated in NICU. Bilateral abdominal masses on exam. What is this associated with. a) Bilateral wilms b) Polycystic kidneys c) Multicystic kidneys d) Hydronephrosis

A

d) Hydronephrosis

232
Q

List 4 non-infectious risk factors of hearing loss in the newborn period.

A
  1. hyperbilirubinemia 2. anatomic ear abnormalities (atresia or stenosis of ear canal) 3. ototoxic medications (aminoglycosides, loop diuretics) 4. family history of childhood SNHL 5. mechanical ventilation >5 days 6. BW <1500g 7. apgars <5 at 1 minute, <7 at 5 minutes
233
Q

4 biologic determinants of child development.

A
  1. genetics 2. in utero exposure to teratogens 3. low birth weight 4. post natal illness 5. prematurity 6. exposure to toxic/hazardous substances