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NeurologyNeurologyNeurologyNeurology
Elisa A. Mancuso, RNC-NIC, MS, Elisa A. Mancuso, RNC-NIC, MS, FNSFNS
Professor of NursingProfessor of Nursing
Peripheral nerves– Not completely myelinated @ birth.
• ↑ Myelinization = ↑ Coordination
1st Gross motor function then fine motor
Primitive reflexes disappear by 5 months. – Moro, Fencing, Step
• Primitive reflexes evolve to meaningful movements
• Reappearance/persistent reflexes – Neurological disease
Assessment
• Cognitive –– √ Appropriateness, speech
• Gross and fine motor- – √ Strength, coordination, gait
• Sensory- – √ Reflexes, pain, temperature
• Cranial nerves I-XII-– √ Motor & sensory
• Developmental milestones-– √ Delay or deviation from expected
milestones. • Obtain accurate history!
– √ family/genetic – √ any past head injuries or trauma at birth
Glasgow Coma Scale• Eye Opening
• Spontaneous 4• To Verbal Stimuli 3• To Pain Only 2• No response 1
• Verbal Response• Coos & babbles/Oriented 5• Irritable cries/Confused 4• Cries to pain/Inappropriate words 3• Moans to pain/Non specific words 2• No response 1
• Motor Response• Moves Purposely/Obeys commands 6• Withdraws to touch/localizes painful stimuli 5• Withdraws to pain 4• Decorticate posturing/Flexion 3• Decerebrate posturing/Extension 2• No response 1
Intracranial Pressure (ICP)
Etiology ↑ ICP1. Mass
•Brain tumor, head trauma2. Generalized brain edema
•Hypoxia, encephalopathy3. ↑ Blood Volume
•IVH, obstruction of jugular veins
4. ↑ CSF production-•Meningitis
Signs and Symptoms • Differ according to developmental
level
Infant1. Poor feeding or vomiting2. Irritability3. Lethargy4. Bulging Anterior Fontanel5. ↑ HC6. High pitched cry7. Sun setting sign-
√ Eyes deviated downward
Signs and Symptoms
Child1. HA2. Diplopia3. Mood swings4. Slurred speech5. Papilledema (48 hours of ↑ICP)6. Altered LOC7. N/V especially in AM
1. ↑ pressure from lying flat
Therapy• Maintain Patent Airway • Supine & ↑ HOB @ 30 • Avoid Prone & head turned to side
– ↓ venous drainage and ICP• Avoid CO2 retention
– CO2 = Cerebral vasodilatation – blood flow and ICP
• Hyperventilation = ↓ CO2 – Cerebral vasoconstriction – ↓ blood flow & ↓ICP– √ for cerebral hypoxia & ischemia
• If Pt mechanically ventilated • only suction PRN!
Therapy
• ICP monitoring – Catheter in ventricle– √ pressure in brain. – Glasgow Coma scale <7
• Manitol– Osmotic diuretic
Unconscious Child• Head trauma, infection, ICP, tumor• √ LOC
– ∆ = earliest indicator of ∆ in neuro status!
– Lethargy• √ Pupillary response
– Fixed and dilated pupils•MEDICAL EMERGENCY!!!•↑ pressure on oculomotor nerve
• √ VS =↓ HR ↓ RR ↑ BP ↑ Temp
Nursing Interventions• ↓ ICP & Maintain ABCs• Turn and position q2H• Passive ROM• Don’t leave on affected side > 30
min • Seizure precautions• Assess skin• Thermoregulation (↑ temp can ↑ICP)
Nursing Interventions
• Eye care– Artificial tears– Cover to prevent corneal abrasions
• Mouth care– Tooth brushing– Dental Care
• Incontinence – Foley care– May need suppositories to
stimulate BM
Nursing Interventions
Nutrition • Tube feedings
•NGT- Short term•PEG- Gastrostomy- Long term
• TPN– Broviac – √ Labs, Glucose, LFTs,
Neoplasms
• High incidence in 5-10 years old
• Prognosis is best – when tumor is completely
removed
• >60% found in– cerebellum and brain stem
Signs and Symptoms
• First cardinal sign = ↑ ICP• HA• Irritability• Projectile vomiting • Personality changes• Location/size of tumor
– Focal Affects (Behavior, Speech) – Cerebellar tumor = Ataxia
Glioblastoma (Astrocytoma)
• Tumor of brain or spinal cord (astrocytes)
• Most common brain tumor in children
• 75% survival rate
Signs and symptoms
• Depends on location of tumor• Headache • Ataxia• Eyes deviating (cover/uncover
test)• Hemiparesis• + Babinski• Staring spells• ↑ ICP
Diagnosis• Complete Neuro exam & cranial
nerves• CT scan, MRI, Pet Scan
Treatment • Chemotherapy• Radiation• Surgery
– Retain as much viable tissue as possible!
Nursing Interventions
• Pre-op: Prepare child and family– Assess developmental milestones– Shave all/part of head – Extensive dsg with multiple drains
• Post-Op– √ LOC & Glasgow Coma Scale – √ VS– √ Infection– Restrict fluids post-op– √ I & O– External shunts/drains/monitors (√ for
ICP)– Increase HOB slowly- No
trendelenburg!– No Narcotics = ↓ cerebral functioning
Seizure Disorder• Epilepsy is recurrent seizure activity
– Does not occur with a known cause i.e. infection, tumor
• Seizure is excessive discharge of neurons.
• Status Epilepticus – Prolonged or recurrent seizures – Not regaining consciousness >30
minutes
Etiology • Primary
– Linked to genetic predisposition – Include febrile, absence and benign seizures– Early infancy from birth trauma or
congenital defects
• Secondary or symptomatic seizure – A temporary or permanent structural or
metabolic abnormality. – Cerebral lesions, malformations, metabolic
disorders and hypoxia. – Late infancy and early childhood from acute
infections – meningitis.• Idiopathic
– Most common = >3 years 50% of seizures.
Diagnosis• Family Hx & Hx of symptoms
– Behavior before, during and after seizure
• Any predisposing illnesses/fever• LP
– √ Infection or metabolic causes• CT scan, MRI
– √ trauma, tumor, malformation• √ Labs
– Serum Calcium, Glucose, & Magnesium • Electroencephalogram (EEG)
– Measures voltage in brain – Sharp waves on EEG = Epilepsy– ↓sensory stimulation during exam
Classification of Seizures
Generalized • Both cerebral hemispheres and ∆ in
LOC •Tonic-Clonic•Absence•Myoclonic•Atonic
Partial • One hemisphere affected & ∆ in LOC• Symptoms occur on one side of body
• Partial• Simple partial• Complex partial
Generalized Seizures
1. Tonic clonic• Aura• LOC• Tonic phase (10-20 secs)• Clonic phase (>30 sec)• Post-ictal State
Generalized Seizure2. Absence seizure “petit-mal”• ↑ Incidence btwn 4-12 years• RT brain immaturity• Usually cease at puberty • Brief LOC may be mistaken for
daydreaming• Minimal or no alteration in muscle
tone• Sudden arrest of activity with no
memory of event• Lasts 5-20 seconds up to 20 times/day
Partial Seizures1. Simple partial• Localized motor symptoms• Somatosensory and autonomic
symptoms• Unilateral hand or 1 side of body• No LOC!• Eyes deviate toward opposite side• Jacksonian• Sylvian/Rolandic
Partial Seizures2. Complex• Psychomotor seizures-most
common• Age 3-adolescence• Period of altered behavior &
repeated purposeless activities• Last 5-10 minutes• Aura• Lip, smacking, chewing, drooling• May yell out, inappropriate
behavior
Status Epilepticus• Medical emergency • Prolonged or recurrent seizures • Not regaining consciousness >30
minutes• Most common cause
– Sudden withdrawal of anticonvulsant meds
• LOC can last hours or days• Maintain airway • Will most likely be intubated• Ativan (lorazipam)
– Quicker onset & longer acting – Less respiratory depression than
valium
Medication Therapy• Controls symptoms• Prevent seizures or decrease # & activity• Raise the seizure threshold• Decrease responsiveness to neurons• Loading & maintenance doses• Phenobarbital (luminal)
– Therapeutic level 10-40 mcg/ml √ respirations can cause respiratory
arrest!
• Dilantin (phenytoin) – Therapeutic level 10-20mcg/ml. – SE hyperplasia of gums!
Medication Therapy
• Tegretol (carbamazepine)– Therapeutic level 4-12 mcg/ml-– Monitor LFT’s! Hepatotoxic. – SE neutropenia √ WBC’s!
• Valproic Acid (depakene)– Therapeutic level 50-110
mcg/ml-– Monitor LFT’s!
Nursing Interventions• Monitor serum drug levels• Seizure precautions
– Padded bed rails– O2 & Suction
• Teaching plan– Parents, Pt, School, Sports, Community
etc.– Type of seizure– Medications & SEs
• Med alert bracelet• Protocol for discontinuing seizure meds:
1. Pt should be seizure free for 2 years2. Normal EEG3. Slowly taper doses 4. EEG’s Q 6 months
Meningitis • Bacterial meningitis 10-15% mortality
rate• Acute inflammation of the meninges
– Infection: URI, OM or sinusitis– Bacteria enters CNS/brain via nasal cavity,
sinuses.– HIB, Group B strep, S.pneumoniae and
Neisseria meningitides
• N. Meningitides is most invasive disease. – 13 serogroups– Vaccine only covers A,B,C,Y and W-135
Incidence • ↑ Risk <1 year of age and >15
yrs• Deficiencies in terminal
complement• URI• HIV• Asplenia• Crowding• Smoking or passive exposure
Clinical Signs • Depend on age and organism• Nucchal Rigidity “stiff neck”• Brudzinski’s sign• Kernig’s sign• Abrupt onset fever and chills• Vomiting & No Nausea• HA• Seizures• Irritability• Anorexia• Petechiae and pupura = Sepsis
– disseminated disease
Diagnosis• CBC with Diff• BC• NP/Pharyngeal cultures• Lumbar Puncture LP
– √ CSF color, consistency, pressure of fluid.
– Sterile procedure– √ Complications;
•Infection, bleeding, spinal fluid leak,
•Hematoma, Spinal HA
CSF Fluid Analysis• Clear, cloudy or bloody• Bacterial or viral meningitis
– ↑ Protein– ↓ Glucose– WBC (PMN cells)
• Gram stain- +/- • Culture-identifies organism • √ pressure >15 = ↑ ICP• ↑ Blood = ↓ skill or traumatic tap
Contraindications to LP
• ↑ ICP- – Need CT scan. – If LP done fatal herniation can occur
• Bleeding disorders• Overlying skin infection
(Staph/MRSA)• Unstable patient
Therapy• Respiratory isolation right away!• Antibiotics 2-3 immediately!!!!
– Meningitic dose (2x usual dose)– Cephalosporins and Ampicillin
• Dexamethasone– ↓ inflammation
• Phenobarbital– ↓ seizure activity
• Mannitol – ↓ brain edema
Nursing Interventions
• Keep HOB >30%• Quiet environment • Frequent neurochecks & VS• Maintain Isolation• Prophylaxis medication =
Rifampin – Persons in close contact – Urine turns orange and stains
contact lenses
Reyes SyndromeAcute Toxic Encephalopathy• ↑ Incidence with 6-11 years & virus infection • (flu/varicella)
• + Relationship when treating fever with ASA
• NH4 accumulates and builds up urea →– Brain edema, necrosis of neurons and cell
death– Fatty infiltration of liver cells, kidney and
myocardium– Impaired hepatic, renal and cardiac function
Signs and symptoms• A history of preceding URI or chickenpox • Nausea and vomiting x 24
hours/intractable• Mental status changes • Lethargy • Confusion • Combative behavior • Loss of consciousness or coma may
develop • Seizures • Hepatomegaly
Diagnosis
• ↑↑ LFT’s 2x normal• Prolonged pt/ptt• ↑↑ NH4 4x normal• Palliative Support• ↑↑ Mortality if pt is in coma =
40%
Cerebral Palsy• Impaired neuromuscular control
– Abnormality in cortex, basal ganglia and cerebellum
• Brain injured area determines type of neuromuscular disability
• Non-progressive
Etiology
• Developmental anomalies• Infections• Toxins• Cerebral trauma• Hypoxia • Vascular occlusion RT IVH
Clinical signs
• Abnormal muscle tone: hyper or hypotonicity
• Impaired coordination and motor function
• Delayed gross motor development• Abnormal postures • Persistent primitive reflexes• Spasticity or uncontrolled movements • Seizures• Sensory impairments
ClassificationsSpastic• Most common with cortex
involvement. • Muscles very tense with any
stimulus• Sudden jerking movements
Dyskinetic• Injury at basal ganglia. • Slow, writhing, uncontrolled,
involuntary movements involving all extremities
ClassificationsAtaxic• Cerebellum affected. • “Clumsy” characterized by loss of
coordination, equilibrium and kinesthetic sense
Rigid• Rare form with poor prognosis. • Rigidity of flexor and extensor
muscles. • Tremors at rest and with
movement Mixed
Therapy• Early recognition and intervention is
goal• Maximize child physical abilities
– (Child intellectually intact)• Multidisciplinary team approach-
– PT, OT, Neurologist, Orthopedic surgeon, RN, social worker
• Family support & community via UCP• Treat symptoms
– Baclofen pump- skeletal muscle relaxant• Increase locomotion, communication
and self-help• Correct defects
– Contractures or spastic deformities– Braces
Retinoblastoma
• Most common congenital intraocular tumor
• 60% non-hereditary and unilateral• 25% genetic & bilateral• 15% genetic & unilateral• Red inflamed eye. • Persistent redness, irritation & itchy• Leukokoria • Loss of red reflex• Strabismus-25% present • Glaucoma
Therapy • Genetic counseling • Early stage
– Radiation or cyrosurgery• Late stage
– Radiation, Chemo– Enucleation– Fit with prosthesis in 3 weeks
• 90% survival rate• Unaffected eye is fine!