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 66 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 (BBBBBB).
  • 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 30.330.3, p. 11181118).     * 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 (PGCSP-GCS)

  • Level of Consciousness (LOCLOC): Altered LOCLOC is the earliest indicator of a change in neurological status.
  • Three-Part Assessment Structure (Figure 30.230.2):     1. Eyes: Maximum score of 44.     2. Verbal Response: Maximum score of 55.     3. Motor Response: Maximum score of 66.
  • Scoring Thresholds:     * Score of 15: Indicates an unaltered or normal LOCLOC.     * Score of 8 or Below: Defines a state of coma.     * Score of 3: Represents the worst possible score, indicating an extremely decreased LOCLOC, deep coma, or death.

Diagnostic Procedures for Neurological Evaluation

  • Imaging:     * Computed Tomography (CTCT) scans.     * Magnetic Resonance Imaging (MRIMRI).     * Nuclear brain scans.
  • Laboratory Testing:     * Comprehensive blood testing, inclusive of drug testing.
  • Specialized Tests:     * Lumbar puncture (LPLP) or spinal tap.     * Electroencephalogram (EEGEEG).     * Auditory and visual evoked potential tests to assess sensory pathways.

Traumatic Brain Injury (TBITBI) and Head Trauma

  • Definition: Unintentional head injury or TBITBI 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 (HAHA) is most common. Also includes sleep-related issues, cognitive difficulties, dizziness, visual disruptions, balance issues, nausea/vomiting (N/VN/V), light sensitivity, and tinnitus (ringing in ears).     * Management: Limit physical and cognitive activity for the first 244824-48 hours; rest and Over-the-Counter (OTCOTC) Non-Steroidal Anti-Inflammatory Drugs (NSAIDsNSAIDs).
  • 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/VN/V, seizures, and impairments in speech, vision, or hearing.     * Timeline: May occur within 1212 hours of the initial TBITBI.     * Intervention Threshold: Medical intervention is required if intracranial pressure (ICPICP) exceeds 20mmHg20\,mmHg.     * Example: Shaken Baby Syndrome (SBSSBS).

Complications of Head Injury

  • Epidural Hematoma:     * Occurs more frequently in children older than 22 years of age.     * Common examples include Motor Vehicle Accidents (MVAsMVAs) and child abuse.
  • Subdural Hematoma:     * Occurs primarily in infancy (ages 040-4 months).     * More common than epidural hematomas.     * Causes: Birth trauma, violent shaking, or falls.
  • Subarachnoid Hematoma:     * Characterized by a sudden onset of a severe headache (HAHA).     * Associated with vascular malformations or brain tumors.
  • Cerebral Edema:     * Typically peaks within 247224-72 hours post-injury.     * Results in changes to neurological status and elevated ICPICP.
  • Postconcussion Syndrome: Diagnosis made when concussion symptoms persist for more than 44 weeks after the initial injury.
  • Posttraumatic Headache: Occurs days to months following the head injury.
  • Posttraumatic Seizures: Typically occur between 2424 hours to 11 week following a head injury.

Medical Referral Criteria for Head Injuries

  • Seek immediate medical attention if the child:     * Vomits 33 or more times or continues vomiting for 464-6 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 1010 minutes after injury.     * Reports a headache that is severe, worsening, interfering with sleep, or lasting more than 2424 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: CPRCPR, Oxygen (O2O_2), or mechanical ventilation; continuous monitoring of vital signs (VSVS).     * Laboratory Monitoring: Blood gases and pHpH levels.     * Metabolic/Therapeutic Care: Rewarming for hypothermia; treatment for seizures; management of hypo/hyperglycemia.     * Hospitalization: All children should be hospitalized for 487248-72 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 2102-10 years.
  • Clinical Manifestations:     * Neurological: Headache, confusion, hallucinations, seizures, behavioral changes, and light sensitivity.     * Systemic: Fever, rash, weakness, respiratory distress, and Gastrointestinal (GIGI) distress.     * Infants: May present with a bulging fontanel.
  • Medical Treatment:     * Acyclovir (Zovirax): Administered for 142114-21 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/VN/V, malaise, and progressive neurological deterioration.
  • Diagnosis:     * History of a viral illness 474-7 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 ICPICP.     * 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 22 or more unprovoked seizures occurring at least 2424 hours apart.
  • Statistics: Approximately 11 in 1010 children will experience one or more seizures in their first 1616 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 11 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 (HRHR).     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 (AEDsAEDs) 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 22 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 55 years with a fever over 100.4F100.4^\circ F. Often accompanies viral fever-inducing illnesses.
  • Subtypes:     1. Simple: Most common; affects the whole body; lasts less than 1515 minutes; does not recur within 2424 hours. Recovery takes about one hour.     2. Complex: Focal (affects one part of the body); lasts longer than 1515 minutes; occurs more than once in a 2424-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 1515 minutes, a serious infection is present, the child remains unresponsive, or the child is under 66 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 (ORSORS). Medication should not be used more than 232-3 days per week.
  • Migraines:     * Can affect all ages, including infants.     * Episodic: Occurs fewer than 1515 days per month.     * Chronic: Occurs 1515 or more days per month for at least 33 months.     * Phases:         1. Prodrome: Up to 7272 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/VN/V, light/sound sensitivity, vision changes. Duration: 4724-72 hours (younger children may only last 22 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 (CSFCSF).     * Non-communicating: Flow of CSFCSF 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, HAHA, N/VN/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 141514-15 weeks.     * Infants: Head circumference crossing 11 or more percentile lines.     * Older children: CTCT and MRIMRI.
  • Surgical Treatment:     * Ventriculoperitoneal (VPVP) Shunt: Drains into the peritoneal cavity (used for neonates and young infants).     * Ventriculoatrial (VAVA) Shunt: Drains into the right atrium (used for older children).     * Endoscopic Third Ventriculostomy (ETVETV): A hole is made in the bottom of the ventricle allowing drainage (used for children younger than 22).
  • 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 (CNSCNS) 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 4th4^{th} 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: MRIMRI and biopsy. Treatment includes surgery to remove the tumor and surrounding tissue. Infants under 66 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 55 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 (UAUA).
  • 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 1212 years old; C. The headaches have been occurring for at least 33 months; D. The client experiences painful headaches occasionally.     * Correct Answer: C (Definition of chronic migraines involves at least 33 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.