NICU Flashcards
(233 cards)
List 5 examples of infants at risk of hypoglycemia
- Infant of a diabetic mother
- Weight <10th percentile (SGA)
- Weight >90th percentile (LGA)
- Intrauterine growth restriction (IUGR)
- Perinatal asphyxia
- Preterm infants (<37 weeks GA)
- Maternal labetalol use
- Late preterm exposure to antenatal steroids
- Metabolic conditions (CPT-1 deficiency [Inuit infants in particular])
- Syndromes associated with hypoglycemia (e.g. Beckwith-Wiedemann)
List 5 clinical signs of neonatal hypoglycemia
- Jitteriness
- Irritability
- Cyanosis
- Respiratory distress (apnea or tachypnea)
- Tachycardia
- Temperature instability
- Feeding difficulties
- Neuro symptoms: hypotonia, poor suck, and seizures or coma
Describe the expected physiological response to hypoglycemia for ketones, growth hormone, insulin, cortisol and catecholamines
Ketones: ↑
Growth hormone: ↑
Catecholamines:`↑
Cortisol: ↑
Insulin: ↓
What is considered a low blood glucose measurement in the following populations?
<72 HOURS OF LIFE
DOCUMENTED HYPERINSULINISM
>72 HOURS OF LIFE
<72h = <2.8
Documented hyperinsulinism, >72h = <3.3
- If <2.8, do critical sample (if not already done)
How long do you have to screen the following populations for hypoglycemia?:
IDM/LGA
SGA/preterm infants (<36wk GA)
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.
You plan on sending an infant home from the hospital who has been experiencing persistent hypoglycemia. What should you do prior to discharge?
- 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.
- Underlying diagnosis for neonatal hypoglycemia should be ascertained and specific medical management initiated (e.g. diazoxide in hyperinsulinism)
- Counsel parents regarding frequency of feeding, home blood glucose monitoring, medication delivery (if needed) or other treatment measures for hypoglycemia
Describe the essential approaches to treating hypoglycemia in the newborn and their corresponding treatment options.
What are conjunctive treatments for hyperinsulinism and GH deficiency?
-
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)
- 5mL/kg with 1st BG <2.6 (asymptomatic)
- Intrabuccal 40% dextrose gel (0.5mL/kg)
- Intravenously
- IV glucose
- Wean once glucose levels stable for 12h
- IV glucose
- Orally
-
Mobilizing energy stores
- Glucagon
- Corticosteroids
Conjunctive treatments
- Hyperinsulinism
- Diazoxide
- Octreotide
- GH deficiency
- recombinant GH
What is one non-pharmacological measure that has been associated with reducing the incidence of hypoglycemia and may be considered in at-risk infants
Delaying the first bath
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?
- Symptomatic or unwell
- Give bolus 2mL/kg over 15 minutes, as well
- If BG <1.8
- Not tolerating feeds
- 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
- Critical sample
- Medication
List 5 risk factors for Intraventricular or Intraparenchymal Hemorrhage
- ROM > 72h
- Breech delivery via SVD
- Increased urgency of delivery
- Hypothermia
- Use of vasopressors and inotropes
- HD-PDA
- Hypocapnia
- PCO2 <35mmHg = risk of PVL
- PCO2 >60mmHg = risk of IVH
- Pressure-limited ventilation
- Early use of HFO
- Transportation of preterm infant (noise, vibration, acceleration)
What is the highest risk period for acute preterm brain injury?
First 72 hours = critical window
95% IVH/intraparenchymal lesions are detected by Day 5
List 5 ways to prevent acute brain injury in preterm infants
- Maintain PCO2 between 45-55mmHg (minimize lung injury/ BPD)
- Normothermia
- Antenatal corticosteroids (if ≥48h prior to birth)
- Umbilical cord milking
- Delayed cord clamping up to 180s
- Neutral, midline head position with ↑HOB 30˚
- Volume-targeted ventilation (for first 72h)
- Nurturing environment (skin-to-skin contact, maternal voice exposure and interaction, light cycling, low noise level)
What strategies can be used to prevent acute brain injury for all premature neonates < 35 weeks?
- 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
List 3 goals of postnatal period care
- Foster development of parenting skills
- Promote physical well-being of mother and infant
- Support relationship among mother, infant and family members
- Strengthen the mother’s knowledge and confidence
- 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
What is the role of the health-care provider during the postnatal course?
- Evaluate the infant’s physical health
- Identify early problems
- Assist with establishment of feeding
- Observe parent-infant interaction
- Identify psychosocial stressors
Identify 2 populations that are at increased risk for readmission after postpartum discharge.
- First-time parent
- Low household income
- Younger GA
Identify 5 criteria that must be met prior to discharge of a healthy term infant.
- CCHD performed and normal
- Physical exam (with measurements) complete and documented with no additional in-hospital or ongoing observations or treatments needed
- Temperature is stable (open cot, appropriately dressed)
- Urine and at least 1 stool have been passed
- ≥2 successful feeds documented
- Maternal serologies reviewed and mother received all immunizations and/or medications
- NBS complete at ≥24h (or arrangements to screen within first 7d confirmed)
- Successful cardiorespiratory adaptation with normal, stable HR and RR
- Hearing screen completed or scheduled
- Bilirubin screening complete with appropriate follow-up PRN
- Vitamin K and ophthalmia neonatorum prophylaxis given
- 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
List 2 PROS and 2 CONS of early discharge of dyad following delivery
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
List 5 maternal and 5 infant risk factors for safe discharge after delivery
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
Describe the types of hemorrhagic disease of the newborn, their expected time course and etiology
- Early onset (<24h)
- Maternal medications that inhibit vitamin K activity (antiepileptics)
- Classic (2-7 days)
- Low intake of vitamin K
- Late onset (2-12 weeks up to 6mo) - typically ICH (50%)
- Almost exclusively breastfed infants
- low vitamin K intake
- chronic malabsorption
- Almost exclusively breastfed infants
Describe the recommended management options to prevent hemorrhagic disease of the newborn including dosing.
-
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
- IM injection x 1 within 6h of delivery + after initial stabilization and maternal/newborn interaction
-
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
List 4 indications for imaging the neonatal brain
- Infection
- Unexplained apneas
- Neonatal encephalopathy (NE)
- Suspected structural brain abnormalities
- Metabolic disorders
- Birth injuries
List the imaging modalities available for imaging the neonatal brain, indications for their use and disadvantages
- 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
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?
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
- 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
- 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






