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NICU Basics Kirsti Martin, MD PGY5 NICU Basics Kirsti Martin, MD PGY5

NICU Basics Kirsti Martin, MD PGY5 - PowerPoint Presentation

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NICU Basics Kirsti Martin, MD PGY5 - PPT Presentation

NICU Learning Objectives Learn about transitional physiology and how this relates to neonatal resuscitation Learn the differences between sick and well infants and when an infant needs a higher level of care in a NICU ID: 933591

infant day blood feeds day infant feeds blood tpn weeks infants respiratory risk premature care preterm hours prematurity due

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Slide1

NICU Basics

Kirsti Martin, MD PGY5

Slide2

NICU Learning Objectives

Learn about transitional physiology and how this relates to neonatal resuscitation

Learn the differences between sick and well infants, and when an infant needs a higher level of care in a NICU

Learn about the care of and diseases affecting premature infants, to gain perspective when you care for them in a primary care setting

Learn and build upon basic ICU concepts in your first exposure to ICU care

Do as much cool stuff as possible!

Slide3

Today’s Learning Objectives

Learn some basics about prematurity, including

Definition

Potential Complications

Delivery Room Management

Systems-Based Approach to Preterm Admission

Milestones of the Hospital Course

Discharge Criteria

Highlight important information to know on your first day in the NICU

Slide4

Prematurity

Preterm labor

Maternal infection

Neonatal infection

Premature rupture of membranes

Advanced cervical dilation

….. ?

Preterm induction of labor or preterm c-section delivery

Most commonly seen for pre-eclampsia

Delivery for fetal decelerations in HR while mother admitted for other reasons (non-reassuring fetal heart tracing)

Slide5

Prematurity

Periviability

– 23-24 weeks gestation

Lungs still in canalicular phase of embryonic development

Canaliculi form from terminal bronchioles

 respiratory

bronchioli

and alveolar ducts (not sacs yet)

Type 1 pneumocytes (primary structural cell of alveoli) just differentiating from type II

Capillary network surrounding terminal bronchioles from mesenchyme just forming

Surfactant begins to be produced by type II pneumocytes by 24 weeks

Parents counseled about active ICU care vs comfort care without resuscitation

Extremely preterm – less than 28 weeks gestation

Very preterm – less than 32 weeks gestation

Thought process behind the care of these infants is similar, with lower gestational ages more complicated due to higher risk for hemodynamic instability, poor respiratory status, feeding intolerance,

etc

Slide6

Prematurity

Infants born less than 32 weeks or 1500g (3

lbs

4.9 oz) at risk for

Respiratory Distress Syndrome – difficulty with oxygenation and/or ventilation due to lack of surfactant production

Bronchopulmonary dysplasia – the lasting respiratory effects of being born prematurely with underdeveloped lungs; can involve chronic changes to lungs as a result of mechanical ventilation – defined as the need for oxygen or respiratory support at 36 weeks corrected gestational age

Intraventricular hemorrhage – bleeding of the vessels in the germinal matrix, found in the lateral ventricles of the brain

Necrotizing enterocolitis – disease of the intestines with multifactorial causes; can cause bowel inflammation/necrosis, abdominal perforation requiring abdominal surgery for resection of affected areas

Retinopathy of prematurity – abnormal development of retinal blood vessels secondary to exposure to supplemental oxygen; can cause blindness

Apnea of prematurity – prolonged pauses in breathing secondary to immature neural regulation of breathing

Hypothermia

Hypo/hyperglycemia

Infection

……

Slide7

How we care for preterm infants

The OB team calls you to say that they will be going to the OR shortly for the delivery of a 27+4 week infant

Mother is a 29 year old G1P0; came to triage for rupture of membranes earlier today, and now the fetal heart rate keeps decreasing into the 80s before recovering; lasting ~3 minutes

Prenatal labs –

A+, ab negative, Hep

BsAg

neg, HIV negative, RPR non-reactive

, rubella immune, varicella immune, G/C negative, GBS unknown

Mother received one dose of

betamethasone

this morning, as well as

IV magnesium

and

antibiotics

Estimated fetal weight from this morning’s ultrasound is 800g

Slide8

Important Highlights

Blood type and antibody status

Risk of hyperbilirubinemia due to hemolysis from Rh disease, ABO incompatibility, other Ab mediated process

HIV

If positive would need to initiate treatment urgently (IV zidovudine)

HepBsAg

If positive or unknown, would need Hep B vaccine and HBIG within 12

hrs

RPR

If positive would need to initiate treatment urgently (IV penicillin)

Betamethasone

Antenatal steroids work to rapidly mature the fetal lung to prepare for birth

Complete course (two doses 24

hrs

apart; complete 48

hrs

from first dose) decreases risk of BPD, IVH, NEC,

etc

Magnesium

A tocolytic but has also been shown to decrease the risk of cerebral palsy in premature infants

Antibiotics

Treat an infection that may have been caused by or be a result of premature rupture of membranes

May partially treat fetal infection

Slide9

Delivery Room

All infants less than 32 weeks

Thermal mattress

Thermal hat

Plastic wrap

Infant mask

RAM cannula

NeoPuff

Appropriate laryngoscope and ET tube

Surfactant

Slide10

NeoPuff

Demonstration

https://www.youtube.com/watch?v=G9-KezhaXJM

Slide11

Infant is born

Infant with good tone and spontaneous respirations, so delayed cord clamping x30 seconds

By transfer to the warmer, infant no longer breathing

Simultaneously

Infant placed in

NeoWrap

, on the thermal mattress, and thermal hat placed

RAM cannula placed into nose and pulse oximeter placed on right hand

Nurse listens to heart rate

HR is 70, and infant is still not breathing

Breaths given via RAM cannula – NIPPV (non-invasive positive pressure ventilation) with peak inspiratory pressure (PIP) 25 and positive end-expiratory pressure (PEEP) 7

HR increases to 140, breath sounds are heard bilaterally, and infant begins to have spontaneous respiratory effort

FiO2 is titrated to maintain saturations appropriate for time of life

At 10 minutes of life, on NIPPV 25/7 x30, FIO2 30%, infant placed in transporter and brought to NICU for admission

Slide12

Systems

Respiratory – consider the need for early surfactant based on FIO2 requirement, work of breathing, or blood gas

Access- place UVC with goal to be finished with placement and

xray

by 1 hour of life

Cardiovascular – make sure blood pressure/perfusion is appropriate

FEN/GI – write TPN/IV fluids and feeds for the infant

Hematology – assess the infant’s hematology status

ID – assess the infant’s risk for infectious disease

Neuro – is the infant at risk for IVH?

Slide13

Respiratory

During transport, infant with desaturations requiring increase in NIPPV to 28/8 x30, FiO2 40%

Due to high FiO2 requirement suggestive of respiratory distress syndrome, infant will likely benefit from administration of exogenous surfactant to decrease surface tension in the alveoli and prevent atelectasis, promote gas exchange

Infant is intubated, surfactant is administered by injection through a feeding tube into the ET tube in two equal aliquots, and infant is extubated back to NIPPV (INSURE method)

After surfactant, FiO2 decreases to 21% (nice job!)

Sometimes, the need for surfactant is not this obvious early on

FiO2 requirement doesn’t happen until later (if at all)

May have good oxygenation but poor ventilation (need blood gas to tell)

Apnea of prematurity may start with resultant worsening respiratory status

Slide14

Access

Central access required to provide concentrated IV nutrition (total parenteral nutrition, TPN)

Also used to draw labs

Umbilical venous catheter

Inserted through umbilical vein, passes through ductus venosus, into the inferior vena cava

Goal location above diaphragm, at ~T7-8

All infants less than 31 weeks or 1500g; 31-32 weeks depends on clinical preference

Umbilical arterial catheter

Inserted into one of two umbilical arteries, passes into internal iliac artery, common iliac artery, and into aorta

Carrier fluid is run through the line, and outputs a blood pressure waveform

Goal location is T6-9

Less commonly used in our unit unless infant requires significant respiratory support or is hemodynamically unstable

Slide15

You place the UVC

You’ve placed the UVC in to your estimated depth, draw back on your syringe, and see blood (good job!)

Draw your initial labs now – 2.5 to 3 ml

Venous blood gas – assess respiratory and metabolic status

Blood glucose

Complete blood count with differential

Blood culture

Type and Screen (if cannot be obtained from cord blood)

Extra for repository study

Call for x-ray to confirm placement

Slide16

Respiratory

VBG - pH 7.25/pCO2 55/pO2 75/HCO3 19/ base excess -4

At the time the VBG was drawn, the transcutaneous CO2 monitor (TCOM) was reading 58

As you settle the infant after securing the UVC and putting the top of the “giraffe” (humidified

isolette

) down, the TCOM continues to downtrend and settles at 45

Infant receives first dose of caffeine at 4 hours of life (20 mg/kg), then daily after this (10 mg/kg) for prevention of apnea of prematurity

Slide17

Cardiovascular

Blood pressure typically obtained by cuff pressure, less commonly via UAC

Desired mean arterial pressure (MAP) = infant’s gestational age in weeks

Premature infants can have slight dip in MAP a few hours after birth (just below expected range), but if perfusion is good, urine output is stable, and infant otherwise stable, will typically recover without extra intervention

Slide18

Hematology

CBC

WBC count 10.5 with ANC 3000, 2 bands, 50 neutrophils

Hb/

Hct

15.3/45.7

Platelets 200

Normal premature

Hct

is 45, normal term

Hct

is 55

Transfuse PRBCs on first day for less than 35

Normal platelets 150-450k

Transfusion thresholds vary with illness severity; typically between 30-50k

Assess white blood cell count to see if it suggests infection

Normal WBC count roughly 5,000-30,000

Make sure ANC >1500

Calculate the I:T ratio (

bands+other immature forms divided by neutrophils plus all immature forms)

 if >0.2, more suggestive of infection

Slide19

Hematology

Order daily serum total bilirubin levels to start the second day of life

Premature infants at higher risk for hyperbilirubinemia due to

Increased RBC turnover due to decreased life span of premature RBC

 increased bilirubin production

Decreased bilirubin clearance and conjugation due to immature liver

Increased enterohepatic circulation of bilirubin

At higher risk for bilirubin induced neurologic dysfunction

Due lower albumin

 more free, unbound bilirubin that can cross the blood-brain barrier

See survival guide for premature bilirubin curve for when to start phototherapy

Slide20

Infectious Disease

All infants under 32 weeks get 48 hour “sepsis rule out”

While blood culture pending, ampicillin and gentamicin given x48 hours

Dosage and intervals in Epic!

Optimal coverage for most common neonatal infections - Group B strep, E. coli

Remember to obtain mother’s HIV,

HepB

, RPR, and GBS status

GBS frequently unknown with preterm delivery, that’s ok

Slide21

Fluids/Feeds

Enteral feeds must be advanced slowly due to small stomach and risk of NEC

Breast milk or donor breast milk (need consent)

Preterm formula has significantly increased risk of NEC vs breast milk

Fed via small orange feeding tube either through nose or mouth into stomach

Refer to feeding protocol for recommendations for fluid amounts by GA

On your survival guide!

For 27

weekers

, we start at 90 ml/kg/day

Start feeds at 10 ml/kg/day within 6-8 hours of birth, advance by 10 ml/kg BID

Start TPN/Intralipids and carrier fluid through the second port of UVC at 80 ml/kg/day

Slide22

Feeds

Starting at 10 ml/kg/day

10 ml

x 0.8 kg = 8 ml/day

kg/day

8 ml/day divided by 8 feeds in 24 hours (feeds are q3hrs) =

1 ml q3hrs

To increase by 10 ml/kg BID

10 ml/kg = 1 ml q3hrs as above

Write to increase feeds by 1 ml every 12 hours

Slide23

Maximum Feeds

Max feeds are typically 160 ml/kg/day

Use birthweight to calculate this until infant surpasses birth weight

160 ml

x 0.8 kg = 128 ml/day , divided by 8 feeds/day =

16 ml/feed

kg/day

Initial feed order –

Start feeds at 1 ml q3hrs. Advance by 1 ml q12hrs to a max of 16 ml q3hrs.

Slide24

TPN/Carrier fluid

Stock TPN started on first day typically – protein and glucose (D10 base)

Carrier fluids (heparinized ½ sodium acetate at 0.5 ml/

hr

or 12 ml/day) plus TPN to equal 80 ml/kg/day

Carrier fluid –---

12 ml

divided by 0.8 kg = 15 ml/kg/day

day

80 ml/kg/day – 15 ml/kg/day = 65 ml/kg/day

TPN ----

65 ml

x 0.8 kg = 52 ml/day, divided by 24

hr

/day = 2.16 ml/

hr

(2.2 ml/

hr

)

kg/day

Slide25

Intralipids

The source of fat in TPN; stock TPN does not include this

When you write custom TPN the next day, you must account for the intralipid as part of your total fluids

1g IL = 5 ml/kg/day, 2g IL = 10 ml/kg/day, 3g IL = 15 ml/kg/day

Total fluids of 80 ml/kg/day = 15 ml/kg/day carrier + 65 ml/kg/day TPN/IL

So if we start 2g IL, our TPN amount will decrease from 65 to 55 ml/kg/day

55 ml

x 0.8 kg = 44 ml/day, divided by 24

hrs

/day = 1.8 ml/

hr

kg/day

Slide26

Decreasing IV fluids

(TPN/IL) 80 ml/kg/day + (feeds) 80 ml/kg/day = Total fluid 160 ml/kg/day

Feeds will continue to increase, but your TPN will need to decrease as feeds increase to keep total fluids at 160 ml/kg/day

Feeds increase by 1 ml every 12 hours

The IV fluid equivalent of 1 ml feed every 3 hours is

1 ml

= 0.33 ml/

hr

3 hours

With each feed increase of 1 ml every 12

hrs

, decrease IV fluids by 0.3 ml/

hr

to maintain TF 160 ml/kg/day

Slide27

Other things to order on admission

AM daily BMP while on TPN, to adjust TPN electrolytes or fluid status as needed

AM daily triglycerides as needed when intralipid introduced or increased

Head ultrasound to assess for IVH one week from birth; would rather have it 7-10 days out than earlier than 7 days from birth

Caffeine!

Vitamin K and erythromycin!

Slide28

General Progression of Hospital Course

Infant weans slowly from NIPPV to CPAP over the course of weeks; FiO2 remains in the low 20s, increasing mostly with apnea of prematurity spells; at 32-33 weeks CGA, infant trialed off of CPAP in room air, and is hopefully successful!

Sometimes need positive pressure for longer, sometimes need low flow nasal cannula; some infants go home with nasal cannula

Caffeine discontinued when apnea spells decrease (around 33+5 weeks)

UVC comes out between DOL 5 and 6 when feeds reach 120 ml/kg/day, reaches full feeds by 1 week

Feed and grow!

At 34 weeks, neurologically mature enough to suck, swallow, and breathe; can start to learn to orally feed at breast or with bottle

Slide29

Discharge Criteria

No apnea, bradycardia, or desaturation spells at rest requiring intervention for at least 5 days

Must be 10 days off of caffeine

Must be 1800 grams (4 pounds –

carseats

do not fit infants smaller than this)

Must be able to keep themselves warm in an open crib while dressed and swaddled

Must be able to take enough feeds by mouth (without NG tube) to stay hydrated and gain weight; typically between 120 and 160 ml/kg/day

Must pass

carseat

test without A/B/D episodes

Typically between 37-44 weeks CGA

Slide30

Note

This is how an uncomplicated, ideal NICU course may go, and there are plenty of infants who have uncomplicated, ideal courses!

However, there are many things that can go wrong, or be more severe, that make things more complicated – you will learn about all of these things along the way!

Keep this system by system thought process in your head with each premature admission, and you will be able to write the admission orders and understand the care super well!

Never be afraid to ask for help!