Alterations in ICR
Early
Decline
Late
Early Alterations in ICR
Altered LOC
Behavioral changes
Respiratory changes
Decline Alterations in ICR
Disorientated
Continuous stimulation to arouse
Reflexive positioning to painful stimulus
Late Alterations in ICR
No response to stilmulus (coma)
Levels of Level of Consciousness (LOC)
Full Consciousness
Lethargy
Obtundation
Stupor
Coma
Full Consciousness
The patient is alert, attentive, and follows commands. If asleep, she responds promptly to external stimulation and, once awake, remains attentive.
Lethargy
The patient is drowsy but awakens—although not fully—to stimulation. She will answer questions and follow commands, but will do so slowly and inattentively.
Obtundation
The patient is difficult to arouse and needs constant stimulation in order to follow a simple command. She may respond verbally with one or two words, but will drift back to sleep between stimulation.
Stupor
The patient arouses to vigorous and continuous stimulation; typically, a painful stimulus is required. She may moan briefly but does not follow commands. Her only response may be an attempt to withdraw from or remove the painful stimulus.
Coma
The patient does not respond to continuous or painful stimulation. She does not move—except, possibly, reflexively—and does not make any verbal sounds.
The Glasgow Coma Scale (GCS)
used to give a standardized numeric score of the neurologic patient assessment. This is a widely used measurement tool that consists of three components: eye opening, verbal response, and motor response
GCS Scale Range: Minor (mild) Head injury
GCS score = 13-15
GCS Scale Range: Moderate Head Injury
GCS score = 9-12
GCS Scale Range: Severe head injury
GCS score = 3-8
GCS Scale Range: Brain Death
Less than 3
True
True or False: A child with a GCS score of 9-12 should be hospitalized
What is the best score to get in the GCS?
15
Head injury Diagnostic Tests
Neuroimaging: CT/MRI
Skull X-Rays
EEG
Brain biopsy:Â
Lumbar Puncture: CSF assessment
Pharmacology Sedative
Lorazepam (Ativan)
Interventions and Therapies for ICP
May require mechanical ventilation
IV Fluids: possible fluid restrictions
Control seizures: seizure precautions: Seizure drugs
Medications to reduce ICP: Osmotic Diuretics Steroids
ICP Monitors: Hyperventilate to reduce paCO2:
Bolt placement
Surgical Procedures to reduce IICP:
Burr holes
Craniotomy
Internal/external shunts
Nursing Interventions: Assessment Priorites
Monitoring ICP
Vital Signs
LOC and pupillary response to light
Full respiratory assessment (w/ ABGs)
Monitoring fluid intake and output
Sunset Eyes
Rim of the sclera above the irises
Early Signs of increased ICP in Infants
•irritability/lethargy
•High Pitched cry
•Bulging, tense fontanel
•Wide cranial sutures
•↑ Head circumference
•Dilated scalp veins
•Poor feeding or vomiting
Early Signs of increased ICP in Children
•Headache
•Vomiting (projectile)
•Dizziness
•↓ pulse and RR
•Blurred vision, Diplopia
•Sluggish, unequal pupils
•↓ LOC, irritability
•Slurred speech
Late Signs of increased ICP
Severely ↓ LOC
↓ motor & sensory response (PGCS)
↑ B/P, widened pulse pressure
Bradycardia
Irregular Respirations
Cheyne-Stokes respirations
Decerebrate & decorticate posturing
Fixed & dilated pupils
Cushing's Triad
Brain herniation
(refers to a set of signs that are indicative of increased intracranial pressure (ICP), or increased pressure in the brain.
consists of bradycardia,, irregular respirations, and a widened pulse pressure)
True
True or False: Cushing’s triad is indicative of a medical emergency and medical attention is required.
Crushing’s Triad Clinical Manifestations
Increased BP with widened pulse pressure
Bradycardia
Irregular respirations (also known as Cheyne–Stokes respirations)
Cheyne-Stokes respirations consist of periods of slow, deep breaths followed by periods of apnea, when breathing comes to a complete stop.
Early Sign
Sunset eyes is a(n) [Fill in the blank] of increased ICP in infants and toddlers with hydrocephalus
Hydrocephalus
A brain condition that happens when Cerebrospinal fluid can’t drain from the brain. It pools, causing a buildup of fluid in the skull.Â
Treatment for Hydrocephalus
Ventriculo-Peritoneal Shunt (VP Shunt)
Post-op VP Shunt
 Lie flat for 24 hours (on unaffected side)
 Vital signs and neurological status
 Pain management
 IV fluids
 Antibiotics
 The shunt will be checked to make sure it is working properly
 Measure head circumference
Complications of VP Shunt
 Blood clot or bleeding in the brain
 Brain swelling (monitor of s/s of increased ICP)
 The shunt may stop working and fluid will begin to build up in the brain again
 Infection
 Damage to brain tissue
 Seizures
Parental Teaching (S/S)
Headache
vomiting
drowsiness
fever
need immediate evaluation!
Neural Tube Defects
Malformation of the spinal cord and spinal canal
Defect in vertebrae through which the spinal cord contents can protrude
Neural Tube Defects Types
Occulta
Meningocele
Myelomeningocele
Occulta
Mildest form
Small separation of the spinal bones
Usually lower spine
Abnormal tuft of hair
Collection of fat
Small dimple or a birthmark
Spinal nerves aren’t involved
No neurologic problems
Neural Tube Defects Causes
Cause unknown
Folic acid deficiency plays a part
Genetic component
Viral trigger
Neural Tube Defects Risk Factors
Neural tube defect in a previous child
Lack of folic acid
Medications: valproic acid, carbamazepine
Maternal diabetes
95% no known family history
Neural Tube Defects Screening & Dx
 Blood tests
Maternal serum alpha-fetoprotein test (MSAFP)
Human chorionic gonadotropin (HCG),
Estriol
 Ultrasound
 Amniocentesis
X-rays, CT scans or MRI
performed after delivery to determine the  degree of the impairment
Neural Tube Defects Prevention
 Folic acid (vitamin B-9) 400 micrograms:
start at least 1 month prior to conception and during the first trimester of pregnancy
Neural Tube Defects Nutrition
fortified breakfast cereals
dark green vegetables
egg yolks
some fruits
Spina bifida
Type of Neural Tube Defect
Occurs when the neural tube fails to close (osseous spine)
Meningocele
Rarest form of spina bifida
Protective covering around the spinal cord (meninges) pushes out through the opening in the vertebrae
 Spinal cord develops normally
 Sac can be repaired with very little damage to nearby nerves
Myelomeningocele
 Most severe form
 Spinal canal remains open along several vertebrae in the lower or middle back
 Spinal cord and membranes protrude at birth, forming a sac on the baby’s back
 Tissues and nerves are directly exposed
 Neurologic impairment - partial or complete paralysis, is common
Meningocele Treatment
Involves surgery to put the meninges back in place and close the opening over the meningocele. This surgery usually occurs soon after birth.
Myelomeningocele Treatment
Surgery within hours to several days after birth
↓ risk of infection
Helps protect the spinal cord from additional trauma
Tx hydrocephalus w/ ventriculo-peritoneal shunt
Irreparable nerve damage has already occurred!