Module 7: Magdalena Flashcards

1
Q

What are common complications of multiple pregnancies (3)?

A
  • premature birth: about 60% twins born premature. length of pregnancy decrease with each additional baby (for twins, 35 weeks)
  • low birth weight (LBW): more than half of twins born with LBW
  • twin-to-twin transfusion syndrome (TTTS): occurs when a connection between the two babies’ blood vessels in the placenta causes one baby to get too much blood flow and the other too little
  • gestational hypertension or preeclampsia: characterized by high blood pressure, protein in the urine, and generalized edema. baby must be delivered early to prevent serious complication
  • gestational diabetes: This condition can cause the baby to grow especially large, increasing the risk of injuries to mother and baby during vaginal birth. Babies born to women with gestational diabetes also may have breathing and other problems during the newborn period.
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2
Q

What is Twin-to-Twin Transfusion Syndrome (TTTS)? treatment?

A
  • TTTS occurs when a connection between the two babies’ blood vessels in the placenta causes one baby to get too much blood flow and the other too little.
  • TTTS can be treated with laser surgery to seal off the connection between the babies’ blood vessels.
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3
Q

What are the two types of twins?

A
  • identical (monozygotic): One egg is fertilized and splits to form two embryos. twins share placenta
  • fraternal (dizygotic): Two separate eggs are fertilized by two separate sperm to form two separate embryos. separate placenta
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4
Q

What is the difference between monozygotic and dizgyotic twins?

A

monozygotic (identical)
- One egg is fertilized and splits to form two embryos.
- The fetuses share the same genetic material.
- When the split occurs will determines if the twins will share a placenta, with either one or two amnions, or if they each develop their own placenta.
- In general, the later the split occurs, the more likely that the twins will share one placenta

Dizygotic (fraternal):
- Two separate eggs are fertilized by two separate sperm to form two separate embryos.
- Fraternal twins are more common because each baby develops from a separate egg and sperm.
- Since each has a different egg and a different sperm, it is like siblings being born at the same time.

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5
Q

What is monochorionic diamniotic twins?

A

For monochorionic diamniotic twins:
- Fetuses share a single placenta.
- They are always identical twins.
- They have a higher risk for complications because two fetuses have to grow on a single placenta.
- The placenta is not always equally divided between the fetuses.
- Each fetus’s blood circulation is connected through blood vessels in the common placenta, and blood may pass disproportionately from one baby to the other, leading to the twin-to-twin transfusion syndrome. (TTTS).

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6
Q

What is dichorionic diamniotic twins?

A

For dichorionic diamniotic twins:
- Fetuses each have their own placenta with its own chorion and amnion.
- Most of these twins are fraternal; only a minority of these twins will be identical.

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7
Q

What is patent ductus ateriosus (PDA)?

A
  • The ductus arteriosus is a normal pathway in the fetal circulatory system that allows blood to bypass the lungs and flow into the descending aorta to ultimately return to the placenta for oxygenation.
  • After birth, as a result of decreasing pressure in the lungs and increased pressure in the aorta, the blood flow changes direction and flows from the aorta to the pulmonary artery (left-to-right shunt).
  • Functional closure of the ductus normally occurs within the first few hours to several days after birth.
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8
Q

What is echocardiogram?

A
  • a non-invasive procedure that uses high-frequency sound waves to generate a visual picture of the heart
  • The examination allows for evaluation of anatomic structures, including valves, chambers, and vessels, and gives information about the structure and function of the heart, as well as the direction of blood flow through the heart.
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9
Q

What is the direction of blood flow through infants PDA?

A
  • direction of blood flow through infants PDA is LEFT to RIGHT (aorta to pulmonary artery)
  • After birth, as a result of decreasing pressure in the lungs and increased pressure in the aorta, the blood flow changes direction and flows from the aorta to the pulmonary artery (left-to-right shunt).
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10
Q

Why is blood being shunted from Left to Right in infant PDA?

A
  • Blood is being shunted in this way because of the pressure gradient between the pulmonary artery and the aorta.
  • This pressure gradient is such that the pressure in the aorta is higher than the pressure in the pulmonary artery.
  • Blood flows along the path of least resistance: away from areas of higher pressure towards areas of lower pressure.
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11
Q

Why does PDA cause pulmonary hyperperfusion?

A
  • A PDA allows blood to re-enter the pulmonary circuit, thereby increasing pulmonary blood flow.
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12
Q

What are 5 signs and symptoms of PDA that you would expect to see in preterm infant?

A
  • Systolic murmur: due to blood shunting through the ductus arteriosus
  • Wide pulse pressures: caused by the run-off of blood flow from the aorta to the pulmonary artery during diastole, therefore lowering diastolic BP and creating a widening pulse pressure
  • Hypotension: due to a drop in diastolic pressure
  • Bounding peripheral pulses: high stroke volume/wide pulse pressure
  • Active precordium: due to increased volume of blood in left heart

**Congestive heart failure is often listed as a sign of PDA. This is certainly true; however, it is a later sign than the five signs listed above.

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13
Q

What is meant by the term “conservative management” for a patent ductus arteriosus?

A

Conservative management involves strategies:
- to decrease preload (fluid restriction),
- optimize gas exchange (respiratory support), and
- mitigate excessive pulmonary blood flow:
= permissive hypercapnia,
= avoiding metabolic alkalosis,
= avoiding excessive 02 supplementation

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14
Q

What are 3 potential medications that can be used for pharmacological treatment of a PDA?

A
  • Indomethacin,
  • ibuprofen, and
  • acetaminophen
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15
Q

What are the potential side effects and contraindications of using acetaminophen to treat PDA?

A

side effects—unpredictable absorption when given enterally, potential for liver toxicity

Contraindications—none

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16
Q

What are the potential side effects and contraindications of using ibuprofen to treat PDA?

A

Side effects—oliguria, thrombocytopenia (can inhibit platelet aggregation), hyperbilirubinemia (can displace bilirubin from albumin), pulmonary hypertension

Contraindications—infection, active bleeding, thrombocytopenia, NEC, significant renal impairment

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17
Q

What are the potential side effects and contraindications of using indomethacin to treat PDA?

A

Side effects—renal impairment, oliguria, hyperkalemia, white matter damage, NEC, intestinal perforation, platelet dysfunction

Contraindications—thrombocytopenia, intracerebral hemorrhage, active bleeding, sepsis, liver damage with hyperbilirubinemia, intestinal perforation

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18
Q

What is head ultrasound (HUS)?

A
  • uses sound waves positioned over the fontanelles to show the internal structures of the brain, including the ventricles and the blood vessels
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19
Q

When is head ultrasound routinely done in NICU?

A
  • on preterm infants (less than 32 weeks) is on day 3–5 of life,
  • at 32 weeks corrected, and
  • at term to monitor for brain injury.
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20
Q

What is the most common type of intracranial hemorrhage seen in neonatal period?

A

Intraventricular hemorrhage (IVH)
- IVH mainly occurs in infants less than 32 weeks gestation, with the incidence increasing with decreasing gestational age
- Approximately half of all IVHs occur within the first 24 hours of life, and 95% within the first five days.
- This really highlights the importance of developmentally supportive care in those first few hours and days!

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21
Q

What are the 2 major risk factors for IVH in neonate?

A

prematurity:
- The periventricular area of the brain is growing rapidly and is richly supplied by blood vessels.
- These blood vessels are very thin.
- Pressure autoregulation is immature:
= Pressure autoregulation is a physiologic mechanism that functions to prevent increases in systemic blood pressure from creating increases in cerebral blood pressure.
= Pressure autoregulation is immature in preterm infants, meaning that any increase in systemic blood pressure creates an increase in cerebral blood pressure.

hypoxia:
- hypoxia leads to redistribution of blood flow such that more blood is delivered to vital organs—the heart and brain.
- In this way, hypoxia can lead to IVH by increasing cerebral blood flow through fragile blood vessels in the periventricular region of the brain.
- Any perinatal or neonatal event that results in hypoxia or alters cerebral blood flow increases the risk of IVH.

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22
Q

Why are preterm infants at risk for developing IVH (3)?

A
  • They have limited abilities to autoregulate cerebral blood pressure: increases in systemic blood pressure result in higher cerebral blood pressures.
  • They are at risk for respiratory distress and hypoxia: causes increased blood flow to the brain (and heart).
  • Their blood vessels are thin-walled and fragile: rupture easily if either pressure and/or volume increase.
  • The periventricular (subependymal) region of the brain is growing and developing at a rapid pace and is well supplied with blood vessels: therefore, the most vulnerable area for hemorrhage.
  • They are frequently stressed by painful, invasive, or uncomfortable procedures: Stress can lead to both hypoxia and elevated blood pressure.
  • They frequently need hypertonic IV solutions, volume expansion, and medications: can rapidly expand the intravascular space, leading to increased intracranial blood volume and pressure.
  • Hypotension – the fragile germinal matrix of preterm infants is vulnerable at both ends of normal blood pressure boundaries and is especially unable to handle large fluctuations in blood pressure.
  • Infection – preterm infants who experience infection either prenatally or postnatally are at an increased risk for IVH.
  • Acidosis – severe acidosis is associated with higher odds of IVH in preterm infants.
  • Coagulopathy – severe derangement of coagulation is associated with increased risk for IVH in preterm infants.
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23
Q

What are potential cues infant might display would alert to consider the possibility of IVH (3)?

A
  • decreased muscle tone (flaccidity)
  • tonic posturing
  • hypotension
  • level of alertness and state
  • apnea
  • sudden drop in hematocrit
  • pallor, mottling
  • temperature instability
  • full or tense fontanelle
  • seizures
  • oculomotor disturbances (abnormal eye movements)
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24
Q

What are nursing strategies we can use to prevent IVH in infants (3)?

A
  • Keep head in a midline position for the first 24h of life (*few initial studies showed positive outcomes).
  • Administer prenatal glucocorticoids
  • Maintain oxygenation.
  • Regulate acid-base balance.
  • Ensure IV fluids and medications are administered at the appropriate rates.
  • Minimize stress with pain management and comfort measures (DSC).
  • Reduce and pace handling.
  • Maintain normal body temperature.
  • Provide adequate calories, nutrients, and fluids.
  • Protect newborn from infection.
  • Monitor and maintain blood pressure.
  • Suction only as needed.
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25
Q

What is Hypoxic-Ischemic Encephalopathy (HIE)?

A
  • combination of hypoxia and ischemia is a common cause of brain injury in both term and preterm infant
  • Hypoxia: low levels of oxygen
  • ischemia: low levels of perfusion

**HIE may be due to any condition leading to decreased oxygen supply (hypoxia) and decreased blood supply (ischemia).

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26
Q

What is the first initial insult of HIE?

A

Hypoxemia and/or ischemia cause:
- a deprivation of glucose and oxygen supply to the brain, which causes a primary energy failure and initiates a cascade of biochemical events that lead to cell dysfunction and ultimately to cell death.

The Sympathetic Nervous System is stimulated:
- resulting in shunting of blood to vital organs (brain, heart, and adrenals) to maintain adequate cardiac output and cerebral perfusion.
- As the hypoxic-ischemic event progresses, there is a decrease in cardiac output and cerebral perfusion, which leads to anaerobic metabolism.
- As the brain reverts to anaerobic metabolism, it causes a rapid depletion of high-energy phosphate reserves (ATP).
- Cellular function is compromised, resulting in an increase of intracellular sodium, calcium and water, tissue acidosis, and electrical failure of neural tissue.

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27
Q

What is the reperfusion injury of HIE?

A
  • This phase is where irreversible cell death begins (6–18 hours after oxygenation and perfusion has been restored).
    -The phase begins with a brief period of restored cellular function (normal vital signs, pH, absence of seizures).
  • Clinical deterioration quickly follows because of mitochondrial dysfunction as a result of the initial insult, and continued cell injury and cell death can occur.
  • The period between the primary phase of injury and the secondary phase is the therapeutic window for potential neuro-protective interventions
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28
Q

What is Periventricular Leukomalacia (PVL)?

A
  • white matter brain injury seen mainly in preterm infants, especially those born before 32 weeks.
  • PVL occurs as a result of hypoxic-ischemic injury
  • it is death or damage to areas of white matter surrounding the ventricles
29
Q

What is cystic PVL?

A
  • Diagnostic imaging (ultrasound/MRI) shows areas of brain tissue loss that look like holes in the brain, and there can also be development of cysts known as cystic PVL
30
Q

What are infants at risk for as they get older with PVL (2)? treatment (3)?

A
  • delayed mental development,
  • motor disorders (cerebral palsy), and
  • vision and hearing impairment.

Treatment is supportive care and symptom management:
- physiotherapy,
- occupational therapy, and
- speech therapy.

31
Q

Summary Neurological System

A

In all newborns, cerebral blood flow is immature, meaning that as systemic blood pressure fluctuates, so does cerebral blood pressure and flow. If systemic blood pressure increases (due to fluid overload, early hypoxia, pain, suctioning, stress), cerebral blood flow will increase and in a preterm infant, this can lead to an IVH.

If systemic blood pressure drops (due to shock or prolonged hypoxia), cerebral blood flow drops and this can lead to PVL in a preterm infant (vulnerable periventricular region) and HIE in a term/post-term newborn (vulnerable cerebral cortex). When an infant is experiencing hypoxia, the cardiac output increases and redistribution of blood flow sends more blood to the heart and brain to compensate for the lack of O2. This increases the risk for IVH in the vulnerable preterm infant. Over time, prolonged hypoxia will lead to a drop in cardiac output, a drop in systemic blood pressure, and decreased cerebral blood flow, increasing the risk for PVL in a preterm infant and HIE in a term/post-term newborn. As well, hypoxia further reduces autoregulation of cerebral blood flow.

32
Q

What are your priorities when planning care of infant this shift?

A
  • Do bedside safety checks.
  • Check the IV site.
  • While the IV site is being checked, do a visual head-to-toe assessment of Magdalena.
  • If it’s time for handling, do a thorough head-to-toe assessment; if it is not time to handle yet, keep Magdalena as undisturbed as possible as the IV is checked and do a thorough assessment later.
  • Calculate her total fluids to make sure that they are correct.
  • Check to make sure that the TPN is running at the correct rate.
  • Check to see if she is on any medications and what time they are due.
  • Check to see if there is enough EBM for the shift.
  • Check what the last blood work results were and when she is due again.
33
Q

What are some pain assessment tools (2)?

A
  • Premature Infant Pain Profile (PIPP),
  • Neonatal Infant Pain Score (NIPS), and
  • Neonatal Pain and Sedation Scale (N-PASS).
  • These tools rely on signs such as facial expression, vital signs, tone, crying/irritability, and oxygen requirements as an overall assessment of pain
34
Q

What are 3 non-pharmacologic interventions for management of pain in neonates?

A
  • oral sucrose/glucose: use of sucrose as a method of reducing pain in infants undergoing single-event procedures such as heel lances, venipuncture, and IM injections in both term and preterm infants without any significant side effects
  • breastfeeding or breastmilk: Infants who are breastfed during painful procedures show significantly less physiologic responses
  • skin to skin contact: infants are supported with skin-to-skin contact during painful procedures, they show less motor disorganization and extension movements, improved autonomic stability, less crying, and lower cortisol levels, and lower pain score

other interventions:
- non-nutritive sucking (pacifier),
- swaddling,
- holding,
- facilitated tucking (manually flexing and
- supporting the infants arms and legs), and
- gentle pressure to the head and abdomen.

35
Q

What are 3 pharmacological management of pain in neonates?

A
  • Opioids
  • morphine and
  • fentanyl
36
Q

What are non-pharmacologic interventions we can use to support infant during painful or stressful procedures (4)?

A
  • sucrose/glucose/breast milk
  • breastfeeding
  • swaddling
  • facilitated tucking
  • skin-to-skin contact
  • holding
  • non-nutritive sucking
  • gentle sensory stimulation (gentle massage, quiet singing)
    **ideally a combination of some of the above interventions
37
Q

Infant PCO2 high and pH low while bicarb and BE are high.

A
  • HIGH PCO2 and LOW pH: respiratory acidosis
  • BE and the HC03 are increasing in an attempt to compensate and neutralize pH.
  • This is partially compensated respiratory acidosis.
  • Persistently elevated CO2 values and acidotic pH values, if uncorrected, stimulate the kidneys to retain HCO3 and other bases.
  • When excess HCO3 and other bases are added to excess CO2, the pH is neutralized.
38
Q

What is one factor that increases risk of tissue injury?

A
  • the nature of the IV solution; hypertonic solutions with high concentrations of calcium, potassium, glucose, or amino acids have been identified as high risk for causing injury.
39
Q

What is family centred care?

A
  • Patient- and family-centred care is an approach to the planning, delivery, and evaluation of health care that is grounded in mutually beneficial partnerships among health care providers, patients, and families. It redefines the relationships in health care.
  • Patient- and family-centred practitioners recognize the vital role that families play in ensuring the health and well-being of infants, children, adolescents, and family members of all ages. They acknowledge that emotional, social, and developmental supports are integral components of health care. They promote the health and well-being of individuals and families and restore dignity and control to them.
  • Trauma-informed family-centred care in the NICU is a commitment to protecting and preserving the integrity of a family in crisis, ensuring optimal infant-parent attachment and parental role development to promote short-term and long-term family integrity
40
Q

What are 4 core concepts of family centred care?

A
  • Respect and dignity: Health care practitioners listen to and honour patient and family perspectives and choices. Patient and family knowledge, values, beliefs, and cultural backgrounds are incorporated into the planning and delivery of care.
  • Information-sharing: Health care practitioners communicate and share complete and unbiased information with patients and families in ways that are affirming and useful. Patients and families receive timely, complete, and accurate information in order to effectively participate in care and decision-making.
  • Participation: Patients and families are encouraged and supported in participating in care and decision-making at the level they choose.
  • Collaboration: Patients, families, health care practitioners, and health care leaders collaborate in policy and program development, implementation, and evaluation; in facility design; in professional education; and in research; as well as in the delivery of care.
41
Q

What is developmentally supportive care?

A
  • Within the developmental care approach, infants are viewed to be active participants in their own care, and the approach is focused on interventions that protect the immature central nervous system.
  • It supports the behavioural organization of each individual infant, enhancing physiological stability, protecting sleep rhythms, and promoting growth and maturation.
  • These interventions include handling and positioning measures, reduction of noxious environmental stimuli, and cue-based care.
42
Q

What are the aims of DSC (4)?

A
  • reduction of the infant’s stress and agitation
  • energy conservation and enhanced recovery
  • caregiver understanding of infant’s behavioural cues (signs of stability or stress)
  • encouragement and support of parents in the primary caregiver role
  • minimization of potential harm due to the extrauterine environment
  • promotion of normal growth and development
  • prevention of abnormal postures
  • stabilization at each stage of infant’s neuro-developmental maturation and support of emerging behaviours and organization
  • enhanced family emotional and social well-being
43
Q

What is the link between family centred care and developmentally supportive nursing inteventions?

A
  • For example, providing containment for a preterm infant during procedures is developmentally supportive and is a skill that parents can easily acquire with support from nurses.
  • This manual skill provides comfort and motoric containment, and promotes flexion.
  • If parents are able to provide containment for their infants during nursing care or painful procedures, then their participation in caregiving is validated and they may begin to feel as though they are contributing to their baby’s comfort: central principles of family-centred-care.
  • Another example is skin-to-skin contact, which allows for family participation that is mutually beneficial for the infant and the family member.
44
Q

What positive physiologic responses of premature infants who experience skin-to-skin contact (3)?

A
  • Infants who participate in skin-to-skin contact often show signs of neurobehavioural stability (stable HR, RR, sats, and sleep wake states).
  • They also have improved thermoregulation, and
  • lower risk of sepsis and hypoglycemia, as well as lower overall mortality rates.
  • Breast feeding rates are improved, and attachment is also supported through skin-to-skin contact.
  • Skin-to-skin contact supports long-term neurodevelopment, improving cognitive development and
  • reducing the risk for future mental health issues such as anxiety and bipolar disorder.
  • Infant’s pain and stress is also decreased during periods of skin-to-skin contact.
45
Q

Whats the difference between fraternal twins vs identical twins?

A

fraternal twins:
- Fraternal twins are the result when two different eggs (ova) are fertilized by two different sperm (dizygotic)
- leads to the development of two separate placentas, each with its own chorion and amnion

identical twins:
- Identical twins develop when a fertilized egg splits.
- Monochorionic (one placenta) twins are at higher risk for complications since they share a common placenta due to entangled umbilical cords

46
Q

Whats the difference between right to left shunting and left to right shunting?

A

Right to left shunting (Cyanotic):
- Deoxygenated blood to systemic circulation = bad. Eg: ToF

Left to right shunting (Acyanotic):
- Systemic blood travels to pulmonary circulation = not as dangerous but associated with complications. Eg: PDA

47
Q

What is patent ductus arteriosus (PDA)?

A
  • In utero it allows oxygenated blood from the placenta to bypass the lungs and enter the circulation
  • The blood flow through the PDA is Right to Left in utero (Pulmonary artery to Aorta)
  • Most term infants PDA closes within 8-40 hours after birth
48
Q

What are 3 causes the closure of PDA?

A
  • (1) increase oxygen and (2) decrease prostaglandin and (3) rubella (unknown)
  • In response to increased arterial oxygen concentrations due to an increase in pulmonary function
  • Decrease in Prostaglandin E (PGE)
  • Remember the premature has immature musculature which is less responsive to increasing oxygen levels.
49
Q

What are the PDA signs and symptoms (4)?

A
  • Bounding pulses
  • Widened pulse pressure
  • Active precordium
  • Murmur
  • Hypotension
  • Labile saturations
  • Over time may show signs of CHF and pulmonary edema due to volume overload of left ventricle
50
Q

What are PDA treatment?

A

Conservative
- fluid restriction
- respiratory support
- oxygenation
- Ventilation

Pharmacological
- NSAIDs (inhibit prostaglandin): Indomethacin, Ibuprofen
- Acetaminophen

Surgical
- ligation
- coil occlusion

51
Q

What is the difference between PDA in prematurity vs PDA in PPHN?

A

PDA in prematurity:
- shunting: left to right
- PVR: low

PDA in PPHN: maintain fetal circulation
- shunting: right to left
- PVR: high

52
Q

Whats intraventricular hemorrhage?

A
  • Bleeding into the ventricles of the brain
  • One characteristic of the immature brain is a weakness of the blood vessels next to the ventricles
  • These blood vessels are thin and vulnerable to fluctuations in blood flow, which can cause them to rupture and bleed
  • The younger and smaller the baby, the higher the risk these blood vessels may be ruptured
  • A rupture causes blood to flow into the ventricle or ventricles of the brain
  • Half occur in the first 24 hours
  • 95% occur in the first 5 days
  • head ultrasound done at day 3-5, 32 weeks, term
53
Q

What are the risk factors for IVH (4)?

A

Prematurity
- Fragile blood vessels in the brain

Asphyxia
- increased blood flow to brain, leading to rupture of vessels

Hypoxia
- Diving reflex initially causes increased blood flow to the brain during hypoxia. Hypoxia also causes lactic acid production, accumulation of lactic acid produces edema and cell necrosis

Auto regulation
- A term infant is able to constrict arteries during episodes of decreased blood pressure to maintain constant cerebral blood flow.
- This cannot be sustained long term.
- Premature infants have decreased or no ability to auto-regulate

-Chorioamnionitis
- Sepsis
- Hypotension
- Acidosis
- Treatment with bicarbonate
- Coagulopathy
- PDA

54
Q

What are the grades of IVH?

A

Grade I
- periventricular bleeding only – germinal matrix hemorrhage

Grade II
- blood in ventricles (10-50% of ventricles)

Grade III
- Over 50% of ventricular area – usually includes ventricular dilation

*Grade IV (sometimes used)
- diffuse cerebral bleeding (other than just germinal matrix)

55
Q

What are the signs and symptoms of IVH (4)?

A
  • Full fontanel
  • Decreased hematocrit or hemoglobin
  • Poor perfusion
  • Apnea
  • Pallor
  • Posturing
  • Altered pupils
  • Temperature instability
  • Areflexia
56
Q

What are some prenatal prevention to IVH? postnatal prevention?

A

prenatal prevention:
- Preventing preterm delivery
- Maternal transport to a level 3 neonatal center
- Antenatal steroid administration
- Other potential options being studied:
Vitamin K, Phenobarbital, magnesium sulphate

postnatal prevention: DSC
- Keep Hob at 30 degrees
- Avoid rapid infusions for volume expansion
- Administer bicarbonate slowly – (rarely used)
- Monitor BP – watch for fluctuations
- Maintain temperature
- Suction and handle only as needed
- Monitor blood gases
- Keep head in midline position for first 24h of life (extreme prems) – few initial studies*
- Developmentally supportive care – if we can prevent IVH for the first 72 hours, we can prevent most IVH’s!
- Provide pain and stress management

57
Q

What are some complications of mild bleed IVH? Massive bleed?

A

Mild bleed
- Asymptomatic
- Changes in muscle tone
- Apneas
- Seizure

Massive bleed with dilation of ventricles
- Acute change in brain function
- Brainstem abnormalities
- Seizures
- Post-hemorrhagic hydrocephalus (PHH)
- Periventricular Leukomalacia (PVL)

58
Q

What is the etiology of HIE? outcomes of HIE?

A
  • Antepartum events (20%): maternal hypertension, maternal diabetes, (IUGR)
  • Intrapartum events (35%) : placental abruption, cord prolapse, traumatic delivery
  • Postnatal cardiopulmonary failure (10%)

outcomes:
- death occurs in first week of life due to multiple organ failure
- severe neurologic disabilities die in their infancy from aspiration pneumonia
- long term complications: epilepsy, CP, dystonia, ataxia, hearing loss

59
Q

What are the stages and signs/symptoms of HIE?

A
  • Stage 1: hyperalertness, jitters, increased reflexes
  • Stage 2: hypotonia, seizures, strong grasp, weak suck, pupils constricting and reacting, respirations varying
  • Stage 3: seizures within first 12 hours of life, apnea, bradycardia, ventilator dependency, severe hypotonia, coma, absent or depressed reflexes, multiorgan failure
60
Q

What are the phases of HIE?

A
  • Initial Insult: tissue is first injured by the initial lack of 02 and blood flow
  • Therapeutic window: The period between the primary phase and the secondary phase – potential for neuroprotective interventions
  • Reperfusion Injury: This phase is where irreversible cell death begins (8-16 hours after initial insult)
  • Clinical deterioration quickly follows because the absence of oxygen and nutrients from blood during the ischemic period creates a condition in which the restoration of circulation results in inflammation and oxidative damage
61
Q

What are the treatment for HIE (3)?

A
  • Ventilation support
  • Maintenance of normal blood pressure
  • Temperature regulation – avoid hyperthermia
  • Maintain normal glucose & electrolytes
  • Prevent fluid overload
  • Control Seizures
62
Q

What are the hypothermia treatment for HIE? neurological stabilization for HIE?

A
  • Mild hypothermia (3-4°C below the baseline temperature) applied within a few hours (no later than 6 h) of hypoxicischemic injury is neuroprotective
  • Control of cerebral edema
  • Allows metabolic rate to slow – reducing reperfusion injury
  • Lowers rates of neurodevelopmental disability

Neurological stabilziation
- Therapeutic hypothermia (33°C to 34 °C for 72 hrs) is ordered within the first 6 hrs of life
- Therapeutic normothermia (36°C to 36.5 °C for 72 hrs) is ordered as a substitute neuroprotective strategy in order to prevent hyperthermia after 8 hrs of age

63
Q

What is the cooling criteria for HIE?

A
  • Equal to or greater than 36 weeks GA and started within 6 hours of birth
  • No contraindications (severe PPHN, major congenital abnormalities, evidence of head trauma or intracranial hemorrhage, withdrawal of support recommendation, severe uncorrected coagulopathy)

Prenatal event:
- Abruptio placenta
- Cord prolapse
- Non- reassuring FHR
- Severe variable decelerations
- Late decelerations

And ONE of the follwoing:
- Apgar score of < 5 at 10 min or
- Continued resuscitation at 10 min or
- Cord/bld gas within 1 hr of life with pH <7.00 or
- Base Deficit > 12 or Lactate > 5 mmol/L

64
Q

How does infant cooling work for HIE?

A
  • not well understood
  • reduced metabolic rate and energy depletion
  • reduced cerebral metabolism and ATP consumption, decreasing cell membrane damage from free radical production
  • reduced cell death
  • reduced vascular permeability, edema, and disruptions of blood-brain barrier functions
  • Puts the infant into “hibernation
65
Q

What is periventricular leukomalacia (PVL)?

A
  • White-matter injury is a form of brain injury characterized by the death of white matter near the cerebral ventricles due to damage and softening of the brain tissue
  • Is the most common ischemic brain injury in premature infants because the periventricular region is developing and richly vascularized
  • major cause is thought to be changes in blood flow to area around the ventricles of brain
  • This area is fragile and prone to injury, especially before 32 weeks of gestation
  • condition involves the death of small area of brain tissue around ventricles
  • The damage creates “holes” in the brain
66
Q

What are the causes of PVL (3)? how can it be identified?

A
  • Infection around the time of delivery may also play a role in causing PVL
  • The more premature or ill the infant is the higher the risk for PVL
  • Hypoxia
  • Infants who have had an IVH are also at increased risk for developing PVL
  • Any condition before, during, or after birth that interferes with the blood flow to the periventricular tissue in the brain can increase the risk

Identified:
- only be identified by a head ultrasound, MRI scan or CT scan of the brain

67
Q

What are the outcomes of PVL?

A
  • Unfortunately, lost nerve fibers do not regenerate: may learn how to compensate for the lost nerve fibers to some extent, but replacement does not appear to occur
  • The prognosis for individuals with PVL depends upon the severity of the brain damage
  • some children exhibit fairly mild symptoms, while others have significant deficits and disabilities
  • PVL is one of the most important causes of cerebral palsy and other long-term handicaps
68
Q

What is the treatment for PVL?

A
  • no specific treatment
  • treatment is symptomatic and supportive
69
Q

What is TIAAC?

A
  • Trauma-informed age-appropriate care is a developmental concept that recognizes the physiological, neurobiological and psychoemotional sequelae of trauma in early life and
  • aims to mitigate the deleterious effects associated with the trauma experience through the provision of evidence-based, age-appropriate caring strategies