Neuro
Prevention = highest priority, as neural tissue does not regenerate, leading to likely permanent nervous system degeneration.
Nursing interventions focus on:
Preventive measures
Supporting families and children in coping with mental or physical function loss
Providing comfort
Crafting an environment that promotes the child's development and self-esteem.
Assessing Neurologic Disorders
History Taking
Chief Concerns:
Seizures
Loss of consciousness
Delayed developmental tasks
Headaches
Clumsiness in motor tasks
Past Medical History:
Infection during pregnancy
Difficult birth process
Head injury history
Family Medical History:
Seizures or headaches in family members.
Physical Examination Findings
Signs indicating neurologic issues:
Increased head circumference
Bulging fontanelles and forehead
Unequal pupil sizes and responses
Projectile vomiting
Widening blood pressure measurements
Decreased pulse rate
Headache
Elevated body temperature
Pain upon neck flexion
Ineffective sucking
Decreased respiratory rate
Spasticity of muscles
Neurologic Examination
Key Components
Cerebral Function: Assessment of overall cognitive and emotional state.
Cranial Nerve Function: Detailing the functions of each cranial nerve and how to assess them (see TABLE 49.2).
Cerebellar Function: Evaluating balance and coordination.
Motor Function: Testing muscle strength and mobility.
Sensory Function: Assessing sensation across various modalities.
TABLE 49.2 - Cranial Nerve Function
Cranial Nerve | Function | Assessment |
|---|---|---|
I (Olfactory) | Sense of smell | Ability to recognize common odors while eyes are closed. |
II (Optic) | Vision | Assess vision fields and acuity; examine retinas. |
III (Oculomotor) | Motor control of upper eyelid and eye muscles | Pupillary reaction and eye movement abilities. |
IV (Trochlear) | Movement of major eye muscles | Similar to III assessment. |
V (Trigeminal) | Facial sensation, mastication | Assess sensory touch and strength of bite. |
VI (Abducens) | Eye movement | Similar to III assessment. |
VII (Facial) | Facial muscles, salivation | Observe facial symmetry and identify taste sensations. |
VIII (Acoustic) | Hearing and equilibrium | Respond to whispered words and perform balance tests. |
IX (Glossopharyngeal) | Swallowing | Assess gag reflex and swallowing ability. |
X (Vagus) | Sensation from internal organs | Similar to IX assessment. |
XI (Accessory) | Neck and shoulder movement | Assess shoulder elevation and neck rotation. |
XII (Hypoglossal) | Tongue movement | Assess symmetry and strength of tongue. |
Diagnostic Testing
Common Procedures:
Lumbar puncture
Ventricular tap
Imaging studies such as X-rays, CT scans, and MRIs
Electroencephalography (EEG)
Nuclear medicine studies (brain scans)
Normal Properties of Cerebrospinal Fluid (CSF)
Parameters Include:
Opening pressure: Newborns (8-10 cm H₂O), Children (10-18 cm H₂O)
Appearance: Clear and colorless
Cell count: 0-8/mm³
Protein content: 15-45 mg/100 ml
Glucose level: 60%-80% of serum glucose.
Albumin/globulin (A/G) ratio: 8:1
Abnormal Findings and Implications
High/Low Pressures:
Lowered pressure may indicate obstruction, while elevated pressure can suggest infection or hemorrhage.
CSF Appearance:
Cloudy fluid may indicate infection; red discoloration may indicate bleeding.
Cell Count:
Elevated WBC counts could suggest viral, bacterial, or fungal infections.
Increased Intracranial Pressure (ICP)
Causes:
Increased CSF volume
Blood entering CSF
Cerebral edema
Head trauma
Hydrocephalus
Space-occupying lesions
Signs and Symptoms of Increased ICP
Increased head circumference, bulging fontanelles, vomiting, eye changes, vital sign changes (elevated temperature, BP changes), and altered mentation such as irritability or confusion.
Neurocutaneous Syndromes
Sturge-Weber Syndrome
Characteristics:
Port-wine birthmark
Associated hemiparesis
Cognitive challenges
Possible seizures and glaucoma.
Neurofibromatosis (Von Recklinghausen Disease)
Characteristics:
Irregular skin pigmentation with café-au-lait spots
Possible hearing impairment and vision loss.
Cerebral Palsy
Types of Cerebral Palsy
Pyramidal (spastic)
Extrapyramidal (dyskinetic)
Ataxic
Mixed type
Assessment Considerations for Cerebral Palsy
History of potential anoxia at birth or prenatal issues.
Physical assessments can include strabismus, visual perception problems, and possibly cognitive delays.
Infection of the Nervous System
Types of infections include bacterial meningitis, viral meningitis, encephalitis, Reye syndrome, Guillain-Barré syndrome, and botulism.
Assessment and Symptoms of Infections
Bacterial Meningitis:
Symptoms can include high fever, severe headache, vomiting, altered consciousness, and signs of nuchal rigidity. CSF typically cloudy with elevated WBC and decreased glucose.
Viral Meningitis:
Symptoms include mild headache and fever; CSF is clear and shows normal glucose levels.
Encephalitis:
Symptoms such as high fever, headache, confusion, and potential lethargy.
Guillain-Barré Syndrome:
Symptoms include muscle weakness that typically starts in the legs and can progress upwards.
Therapeutic Techniques for Neurologic Disorders
Bacterial Meningitis
Treatment typically involves antibiotics, potential corticosteroids, and supportive care.
Encephalitis
Supportive treatments may include antipyretics and possibly antivirals like acyclovir.
Guillain-Barré Syndrome
Supportive care focused on monitoring respiratory function and may involve immune therapies.
Inflammatory Disorders
Carpal Tunnel Syndrome
Symptoms include numbness and pain in the thumb and fingers.
Bell's Palsy
Abrupt onset typically associated with viral infections like herpes.
Assessing Paroxysmal Disorders
Recurrent Seizures
Requires a history of the events preceding the seizure and thorough neurological evaluation.
Breath Holding Episodes
Often tied to stress or anger, characterized by temporary loss of consciousness.
Headaches
Requires careful history taking and assessment of associated symptoms.
Spinal Cord Injury
Assessment Considerations
Critical to maintain spinal precautions if an injury is suspected following trauma. Various assessment protocols must be followed to ensure the safety of the child during evaluation.
Ataxic Disorders
Ataxia-Telangiectasia & Friedreich Ataxia
Assessment focuses on developmental delays, gait disturbances, and signs of progressive neurological decline.
Nursing Diagnoses
Risk for Disuse Syndrome and Interrupted Family Processes can be prominent diagnoses within the context of care for children with neurologic disorders.
Questions and Answers Section
Question: What may frighten a child with bacterial meningitis the most? Answer: Masks worn by staff due to the need for respiratory isolation precautions.
Question: What is a common finding in Reye syndrome? Answer: Recent influenza illness and the possible use of aspirin following viral illness.
Question: What is a typical manifestation of absence seizures? Answer: Rapid blinking for 10 seconds.
Question: Which drug might be prescribed for a child with migraines? Answer: Ergotamine tartrate (Cafergot) to relieve headache.