The Child with Cerebral Dysfunction
Developmental Characteristics of the Pediatric Nervous System
- Immaturity at Birth: The nervous system is not fully mature when a child is born.
- Brain Growth Indicators: Brain volume and growth are directly reflected in measurements of head circumference.
- Physiological Performance: Cerebral blood flow and oxygen consumption in children up to the age of 6 are twice that of adults.
- Trimester Development:
* The brain and spinal cord develop during the FIRST trimester of pregnancy.
* Malformations during this period can be attributed to maternal infection, substance abuse, or dietary deficiencies.
- Growth Patterns:
* Rapid growth occurs during infancy and early childhood.
* Growth becomes more gradual during later childhood and through adolescence.
* Growth follows a cephalocaudal (head-to-toe) and proximodistal (center-outward) direction.
- Cranial Anatomy:
* The fontanels are not closed at birth, which allows the head to expand to accommodate swelling or other causes of increased intracranial pressure (ICP).
* The infant's brain is highly vascular, making it more prone to hemorrhage when subjected to force or shaking.
* Critical anatomical layers include the dura layer, the subdural space, and the blood-brain barrier (BBB).
- Spinal Development: The vertebrae are not completely ossified in children, leading to a greater risk for compression fractures and spinal injury.
Clinical Evaluation of Neurological Status
- Comprehensive Assessment Components:
* Medical History: Identifying baseline and onset of symptoms.
* Physical Examination: Evaluating core physical indicators.
- Physical Findings:
* Vital Signs: Monitoring for fluctuations related to neurological distress.
* High-Pitched Cry: A specific "cat-like" cry is often indicative of neurological trauma or dysfunction.
* Ocular Signs (Pupils): Assessment for unequal, "blown" (dilated/unresponsive), or pinpoint pupils (referencing Figure 30.3, p. 1118).
* Cranial Signs: Increased head circumference and bulging fontanels.
* Motor Activity: Changes in activity levels, strength, symmetry, and coordination of movement.
* Reflex Activity: Assessment of primitive and deep tendon reflexes.
* Sensory Responses: Reaction to stimuli.
* Alertness/Behavior: Evaluation of the child's behavioral baseline.
* Posturing: Identification of abnormal neurological positioning.
Pediatric Glasgow Coma Scale (P−GCS)
- Level of Consciousness (LOC): Altered LOC is the earliest indicator of a change in neurological status.
- Three-Part Assessment Structure (Figure 30.2):
1. Eyes: Maximum score of 4.
2. Verbal Response: Maximum score of 5.
3. Motor Response: Maximum score of 6.
- Scoring Thresholds:
* Score of 15: Indicates an unaltered or normal LOC.
* Score of 8 or Below: Defines a state of coma.
* Score of 3: Represents the worst possible score, indicating an extremely decreased LOC, deep coma, or death.
Diagnostic Procedures for Neurological Evaluation
- Imaging:
* Computed Tomography (CT) scans.
* Magnetic Resonance Imaging (MRI).
* Nuclear brain scans.
- Laboratory Testing:
* Comprehensive blood testing, inclusive of drug testing.
- Specialized Tests:
* Lumbar puncture (LP) or spinal tap.
* Electroencephalogram (EEG).
* Auditory and visual evoked potential tests to assess sensory pathways.
Traumatic Brain Injury (TBI) and Head Trauma
- Definition: Unintentional head injury or TBI ranges from mild bruises or cuts to serious internal conditions.
- Etiologies: Commonly caused by sports injuries, road traffic accidents, and child abuse.
- Pathology: Dependent on the specific force of impact.
- Concussion:
* The most common head injury observed in pediatric patients.
* Manifestations: Headache (HA) is most common. Also includes sleep-related issues, cognitive difficulties, dizziness, visual disruptions, balance issues, nausea/vomiting (N/V), light sensitivity, and tinnitus (ringing in ears).
* Management: Limit physical and cognitive activity for the first 24−48 hours; rest and Over-the-Counter (OTC) Non-Steroidal Anti-Inflammatory Drugs (NSAIDs).
- Contusion and Laceration:
* Refers to the actual bruising or tearing of cerebral tissue.
* Causes slowing of blood flow and localized swelling.
* Manifestations: Loss of consciousness, N/V, seizures, and impairments in speech, vision, or hearing.
* Timeline: May occur within 12 hours of the initial TBI.
* Intervention Threshold: Medical intervention is required if intracranial pressure (ICP) exceeds 20mmHg.
* Example: Shaken Baby Syndrome (SBS).
Complications of Head Injury
- Epidural Hematoma:
* Occurs more frequently in children older than 2 years of age.
* Common examples include Motor Vehicle Accidents (MVAs) and child abuse.
- Subdural Hematoma:
* Occurs primarily in infancy (ages 0−4 months).
* More common than epidural hematomas.
* Causes: Birth trauma, violent shaking, or falls.
- Subarachnoid Hematoma:
* Characterized by a sudden onset of a severe headache (HA).
* Associated with vascular malformations or brain tumors.
- Cerebral Edema:
* Typically peaks within 24−72 hours post-injury.
* Results in changes to neurological status and elevated ICP.
- Postconcussion Syndrome: Diagnosis made when concussion symptoms persist for more than 4 weeks after the initial injury.
- Posttraumatic Headache: Occurs days to months following the head injury.
- Posttraumatic Seizures: Typically occur between 24 hours to 1 week following a head injury.
Medical Referral Criteria for Head Injuries
- Seek immediate medical attention if the child:
* Vomits 3 or more times or continues vomiting for 4−6 hours after injury.
* Shows swelling in front of or above the earlobe.
* Exhibits fluid leakage from the ears or nose.
* Presents with blackened eyes.
* Displays confusion or abnormal behavior.
* Has difficulty speaking or arousing from sleep.
* Reports blurred vision or diplopia (double vision).
* Demonstrates an unsteady gait.
* Has dilated, fixed, or unequal pupils.
* Experiences seizures.
* Sustained injury at high speeds, with great force, or under suspicious circumstances.
* Experienced a fall from a height greater than the height of the child.
* Experienced loss of consciousness or amnesia.
* Reports discomfort lasting more than 10 minutes after injury.
* Reports a headache that is severe, worsening, interfering with sleep, or lasting more than 24 hours.
Submersion Injury
- Pathophysiology: Death results from the aspiration of water while the child is submerged. This can occur in even small quantities of water, such as a pail, toilet, or bathtub.
- Clinical Presentation: Depends heavily on the duration of loss of consciousness and the neurological status following resuscitation.
- Treatment and Nursing Care:
* Requires rapid assessment to determine specific needs.
* Interventions: CPR, Oxygen (O2), or mechanical ventilation; continuous monitoring of vital signs (VS).
* Laboratory Monitoring: Blood gases and pH levels.
* Metabolic/Therapeutic Care: Rewarming for hypothermia; treatment for seizures; management of hypo/hyperglycemia.
* Hospitalization: All children should be hospitalized for 48−72 hours.
* Complication Surveillance: Monitor for aspiration pneumonia, respiratory compromise, and cerebral edema.
* Supportive Care: Provide chest physiotherapy; assist parents with coping mechanisms.
* Prevention: Crucial focus for nursing education.
Encephalitis
- Definition: Inflammation of the brain tissue leading to neurological dysfunction.
- Etiology: Usually caused by a virus or an autoimmune condition.
- Prognosis: High rate of mortality; can cause permanent neurological damage.
- Epidemiology: Most cases occur between ages 2−10 years.
- Clinical Manifestations:
* Neurological: Headache, confusion, hallucinations, seizures, behavioral changes, and light sensitivity.
* Systemic: Fever, rash, weakness, respiratory distress, and Gastrointestinal (GI) distress.
* Infants: May present with a bulging fontanel.
- Medical Treatment:
* Acyclovir (Zovirax): Administered for 14−21 days.
* Corticosteroids: Used to reduce inflammation.
Reye Syndrome
- Definition: Acute encephalopathy characterized by cerebral edema and fatty changes in the liver, usually following a viral illness.
- Etiology: Exact cause is unknown. There is a strong association with the use of aspirin during viral infections (e.g., varicella/chickenpox or influenza).
- Manifestations: Fever, profound impairment of consciousness, disordered hepatic function, N/V, malaise, and progressive neurological deterioration.
- Diagnosis:
* History of a viral illness 4−7 days prior to symptom onset.
* Liver biopsy is the definitive diagnostic tool.
- Treatment and Management:
* Requires early diagnosis and aggressive treatment.
* Maintain effective cerebral perfusion and control rising ICP.
* Conduct frequent neurological assessments and monitor Intake and Output (I&O).
* Provide a restful, non-stimulating environment.
* Monitor for signs of bleeding and impaired coagulation due to liver involvement.
Epilepsy and Seizure Types
- Definition: Characterized by 2 or more unprovoked seizures occurring at least 24 hours apart.
- Statistics: Approximately 1 in 10 children will experience one or more seizures in their first 16 years. Onset is highest in the first few months of life.
- Etiological Factors:
* Infants: Malformations or genetics (e.g., Dravet Syndrome).
* Childhood: Acute infections or idiopathic (unknown) causes.
* General: Trauma or alcohol exposure.
- Classification of Seizures:
* Motor or Non-Motor Nature.
* Tonic-Clonic: Tonic phase (stiffening) and Clonic phase (jerking).
* Myoclonic: Brief jerking lasting less than 1 second.
* Atonic: Sudden loss of muscle tone and limpness.
* Epileptic Spasms: Sudden bending or extension of limbs and trunk.
* Absence Seizures: Staring and unresponsiveness.
- Categorization by Awareness and Scope:
1. Generalized: Involves jerking, limb weakness, rigidity, twitching, spasms, sudden loss of movement, eyelid movements, or staring.
2. Focal: Starts with an "aura." Can include impaired or complete awareness. Motor/non-motor signs: repeated mouth/hand movements, muscle spasms, heat/cold sensations, inability to move, altered consciousness, and increased heart rate (HR).
3. Unknown: Involves both motor and non-motor movements. May include stiffness, convulsions, bladder/bowel incontinence, and bluish pallor of the face due to lack of oxygen.
Management and Education for Epilepsy
- Pharmacological Treatment: Antiepileptic Drugs (AEDs) decrease seizure incidence and severity. Examples include Phenytoin (Dilantin), Carbamazepine (Tegretol), and Valproic Acid (Depakote).
- Alternative Therapies:
* Diet: High fat, low carbohydrate, and moderate protein (Ketogenic diet).
* Vagus Nerve Stimulation (VNS).
* Brain Surgery.
- Patient and Family Education:
* School: Inform the school of medication use.
* Documentation: Maintain a trigger journal to track time, severity, and potential causes.
* Safety: Adolescents must be educated on alcohol use. Children should never be unsupervised around water or in areas where falls are possible. Address driving regulations for adolescents.
* Identification: Wear a medication ID bracelet or necklace.
* Medication Withdrawal: A child may be considered for coming off medication after remaining seizure-free for 2 years.
- Emergency Care During Seizure:
* Remain calm.
* Place the child on their side.
* Keep the child away from hazards.
* NEVER put anything in the mouth and do NOT restrain the child.
Febrile Seizures
- Epidemiology: Typically occur in children younger than 5 years with a fever over 100.4∘F. Often accompanies viral fever-inducing illnesses.
- Subtypes:
1. Simple: Most common; affects the whole body; lasts less than 15 minutes; does not recur within 24 hours. Recovery takes about one hour.
2. Complex: Focal (affects one part of the body); lasts longer than 15 minutes; occurs more than once in a 24-hour period. Recovery takes longer than one hour.
- Clinical Presentation: Presentation matches other seizures (jerking, stiffening, rolling eyes, loss of consciousness) but is uniquely tied to a fever present at the time or developing within hours.
- Management: Usually no specific treatment required. Focus on parent education.
- Hospitalization Criteria: Recommended only if the seizure lasts over 15 minutes, a serious infection is present, the child remains unresponsive, or the child is under 6 months old.
Headache Disorders in Children
- Primary Headaches: Not caused by an underlying condition; prevalent in children.
- Tension Headaches:
* Described as bilateral pressure or tightness around the head, neck, or shoulder muscles.
* Often triggered by stress.
* Treatment: OTC medications (Motrin/Ibuprofen or Tylenol/Acetaminophen), hydration, or Oral Rehydration Solution (ORS). Medication should not be used more than 2−3 days per week.
- Migraines:
* Can affect all ages, including infants.
* Episodic: Occurs fewer than 15 days per month.
* Chronic: Occurs 15 or more days per month for at least 3 months.
* Phases:
1. Prodrome: Up to 72 hours prior; includes aura, restlessness, fatigue, mood changes, and light/sound sensitivity.
2. Headache Phase: Pulsing/throbbing pain (moderate to severe, 1 or both sides), N/V, light/sound sensitivity, vision changes. Duration: 4−72 hours (younger children may only last 2 hours).
3. Postdrome: Fatigue, mood changes, or concentration difficulty after pain subsides.
* Notes: Facial pallor is common in younger children.
Hydrocephalus
- Classification:
* Acquired vs. Congenital.
* Communicating: No obstruction; caused by inadequate absorption or over-production of cerebrospinal fluid (CSF).
* Non-communicating: Flow of CSF is blocked by an obstruction.
* Expected Pressure or Ex-vacuo.
- Infant Manifestations: Increased head circumference, bulging/non-pulsating anterior fontanels, dilated scalp veins, "sun-setting" eyes (eyes deviated downward), irritability, lethargy, seizures, vomiting, and low muscle tone.
- Child Manifestations: Irritability, HA, N/V, vision problems/crossed eyes, difficulty walking or staying awake, poor appetite, gait/balance issues, urinary incontinence, and poor school performance.
- Diagnosis:
* Fetal ultrasound as early as 14−15 weeks.
* Infants: Head circumference crossing 1 or more percentile lines.
* Older children: CT and MRI.
- Surgical Treatment:
* Ventriculoperitoneal (VP) Shunt: Drains into the peritoneal cavity (used for neonates and young infants).
* Ventriculoatrial (VA) Shunt: Drains into the right atrium (used for older children).
* Endoscopic Third Ventriculostomy (ETV): A hole is made in the bottom of the ventricle allowing drainage (used for children younger than 2).
- Nursing Care: Educate on signs of shunt failure (malfunction) or infection. Meningitis vaccination is a key prevention method.
Pediatric Brain Tumors
- Gliomas: Tumors originating from Central Nervous System (CNS) cells. Classified as low-grade (benign) or high-grade (malignant).
* Astrocytoma: Most common; can occur anywhere in the brain/spinal cord; typically does not spread.
* Ependymoma: Third most common; usually found in the back of the brain.
* Brainstem Glioma: Affects brainstem functions; can be diffuse or focal.
* Optic Nerve Glioma: Affects vision.
- Medulloblastoma: Embryonal brain tumor located in the lower back of the brain (midline of the 4th ventricle).
* Traits: Highly aggressive, malignant, and spreads easily.
- Clinical Presentation: Morning headaches that resolve after vomiting; loss of balance, changed handwriting, fatigue, personality changes, and sensory problems.
- Diagnosis & Treatment: MRI and biopsy. Treatment includes surgery to remove the tumor and surrounding tissue. Infants under 6 months with low-grade tumors may simply be monitored.
Neuroblastoma
- Definition: A tumor that starts in the adrenal glands, originating from "neuroblasts" (immature embryonic nerve cells).
- Epidemiology: Primarily seen in children under 5 years old.
- Detection: Can be congenital and seen on prenatal ultrasound, but usually diagnosed after symptoms appear from metastasis.
- Manifestations: Lump or pain in the abdomen, chest, or pelvis; blue/purple skin lesions; changes in eye appearance; difficulty breathing; limb weakness; and sudden muscle movements.
- Diagnosis: Bone marrow aspiration and testing for catecholamines in the urine (UA).
- Treatment: Radiation, chemotherapy, bone marrow transplant, and/or immunotherapy.
Test Yourself: Discussion and Questions
- Question 1 (Chronic Migraines): A nurse is reviewing the health history of a pediatric client who reports chronic migraines. Which of the following would the nurse expect to find?
* Options: A. The headaches occur once a week; B. The client is more than 12 years old; C. The headaches have been occurring for at least 3 months; D. The client experiences painful headaches occasionally.
* Correct Answer: C (Definition of chronic migraines involves at least 3 months of symptoms).
- Question 2 (TBI Match):
* 1. Concussion = C (A bump from a fall causes the brain to bounce against the skull)
* 2. Contusion/laceration = D (A blow to the head from a hockey stick causes a cut)
* 3. Epidural hematoma = A (Car accident trauma causes blood to pool between the skull and the membrane covering the brain)
* 4. Subdural hematoma = B (A fall from a horse causes blood to pool on the surface of the brain and press against tissue)
- Question 3 (Encephalitis Assessment Questions):
* Correct Inquiries: "Was the child bitten by an insect lately?" (A); "Have you noticed a change in behavior in your child?" (B); "Have you traveled outside the country lately?" (D); and "Does the child have any immunodeficiency disorders?" (E). Smoking during pregnancy (C) is not a standard assessment question for acute encephalitis.