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Neurological Disorders in the Pediatric Patient Presented by Marlene Meador RN, MSN Neurological System of Children Top Heavy Cranial bones- thin, not well developed Brain highly vascular with small subarachnoid space Excessive spinal mobility Wedge-shaped cartilaginous vertebral bodies Etiology and Pathophysiology Altered Mental Status Mnemonic = Mitten Metabolic Infections Toxins Trauma Endocrine Neurological/Neoplasm Neurological Assessment Vital Signs Eyes Behavior Respiratory Status Motor Function Skin Children’s Coma Scale Assessment: Infant Irritability and restlessness Full to bulging fontanelles Increase in FOC Poor feeding, poor sucking, projectile vomiting Distension of superficial scalp veins Nuchal rigidity and seizures (late signs) Assessment: Child early signs Irritability, lethargy Sudden change in mood Headache Vomiting Ataxia Nuchal rigidity Deterioration of cognitive ability Assessment Child: Late signs Changes in Vital signs Seizures Photophobia Positive Kernig’s sign Positive Brudzinski’s sign Opisthostonos Therapeutic Intervention Nursing care Medications Corticosteroid (decadron) Osmotic diuretic (Manitol) Nursing Care Minimize activity Monitor IV rate Place in semi-fowlers Monitor VS, Neuro VS, and behavior Treat for pain Organize care Educate parents Critical Thinking What would you expect as a first sign of IICP in an infant? What would you expect as an initial sign of IICP in a 10 year old child? Meningitis Bacterial Meningitis Vs. Viral Meningitis Bacterial Meningitis Potentially Fatal Viral Meningitis Same signs and symptoms, may be milder and self-limiting. Usually lasts a few days Assessment Infants & Young Children Fever not always present Lethargy Alterations in sleep and feeding habits Nuchal rigidity (late sign) Assessment: Childhood & Adolescence Hyperthermia S&S of IICP Complications of Meningitis IADH Intravascular coagulation with thrombocytopenia CSF obstruction Nerve Damage Diagnostic Tests: Lumbar Puncture Serum Glucose Level Blood Cultures Therapeutic Interventions Mediation Therapy Antibiotics Ampicillin Claforan Rocephin Nursing Care Assess Antibiotic therapy Monitor lab values Strict I&O Isolation Monitor FOC Nursing Care cont... CSF culture Temperature control Seizure activity Environment Planning Education Hydrocephalus Hydro= Water Cephaly= of the head/brain Etiology and Pathophysiology: Congenital anomalies Trauma Unknown causes Types of Hydrocephalus Non-communicating or Obstructive Communicating Clinical Manifestations 1. 2. 3. 4. 5. Infants- prior to fusion of cranial sutures FOC Changes in assessment of skull Forehead Eyes Behavior changes Clinical Manifestations After closure of cranial sutures: 1. Eyes S & S of IICP 2. Diagnostic Tests LP MRI/ CT scan Skull X-ray FOC Transillumination Interventions: Surgical Shunting to bypass the point of obstruction by shunting the fluid to another point of absorption Complications of Shunts Infections Blocked shunts Seizures Nursing Interventions Monitor VS and neurological status Assess functioning of the shunt Assess operative site Assess for infection Positioning of the patient Activity of patient Promote nutrition Education Critical Thinking What is the most important assessment data on a child who has just had a shunt placement for hydrocephalus? What is the most important teaching for the parents or caregivers? Spina Bifida Most common defect of the CNS Occurs when there is a failure of the osseous spine to close around the spinal column. Clinical Manifestations: Visualization of the defect Motor sensory, reflex and sphincter abnormalities Flaccid paralysis of legs- absent sensation and reflexes, or spasticity Malformation Abnormalities in bladder and bowel function Diagnostic Tests: Prenatal detection Ultrasound Alpha-fetoprotein Following Birth: NB assessment X-ray of spine X-ray of skull Surgical Intervention Immediate surgical closure Prior to closure keep sac moist & sterile Maintain NB in prone position with legs in abduction Nursing Interventions: Pre-OP: Place in prone position Sterile moist dressing with normal saline or antibiotic solution Maintain proper abduction of legs and alignment of hips Meticulous skin care Protect from feces or urine Keep in isolette Post-Op Nursing Interventions Assess surgical site Monitor VS and neuro VS Institute latex precautions Encourage contact with parents/care givers Positioning Skin Care Nursing Interventions cont... Antibiotic therapy Prevent UTI Education Emphasize the normal, positive abilities of the child Critical Thinking Would you expect a 5-year-old with meningomyelocele to have bladder/bowel sphincter control? Which type of neural tube defect is most likely to have no outward signs or symptoms? Cerebral Palsy (CP) Static Encephalopathy- spastic CP most common type (80%) – Nonspecific term give to disorders characterized by impaired movement and posture – Non-progressive – Abnormal muscle tone and coordination Assessment Jittery (easily startled) Weak cry (difficult to comfort) Experience difficulty with eating (muscle control of tongue and swallow reflex) Uncoordinated or involuntary movements (twitching and spasticity) Assessment cont... Alterations in muscle tone – Abnormal resistance – Keeps legs extended or crossed – Rigid and unbending Abnormal posture – Scissoring and extension (legs feet in plantar flexion) – Persistent fetal position (>5 months) Diagnostic Tests: EEG, CT, or MRI Electrolyte levels and metabolic workup Neurologic examination Developmental assessment Complications Increased incidence of respiratory infection Muscle contractures Skin breakdown Injury Goals & Interventions: Early detection Mental Retardation “Significant sub average, general intellectual functioning existing concurrently with deficits in adaptive behavior and manifested during the developmental period”. American Association of Mental Deficiency Down Syndrome Trisomy 21- the most common chromosomal abnormality resulting in mild to profound mental retardation Assessment See syllabus Primary concern with cardiac and GI anomalies What are the most obvious indications of Down’s Syndrome in a newborn? Goals and Interventions Primary focus on the parents and care givers to provide support and achieve a realistic view of the child’s capabilities Support siblings Refer to family counseling services Support parents in feelings of guilt and chronic sorrow Hyperfunction/Hypofunction Pediatric Seizures – Febrile seizures- occur as a result of rapidly increasing core temperature (101.8 F– 38.8C) – General seizures- occur as a result of insult of the nervous system Clinical Manifestations Tonic-clonic- absence seizures, minor motor-atonic Partial seizures- partial simple or partial complex Diagnostic Tests: EEG CT, MRI Lumbar puncture CBC Metabolic screen for glucose, phosphorus and lead levels Jitteriness –vs- Seizure Jittery – Responsive Seizure – Not responsive to stimuli – Gaze Okay – Abnormal gaze Goals: Primary focus to identify the cause and eliminate the seizure with minimum side effects using the least amount of medication while maintaining a normal lifestyle for the child. Interventions Febrile seizures Seizure precautions During seizure activity Education Autism Most severe pervasive developmental disorder of childhood. Moderate to severely incapacitating with lifelong developmental disabilities Etiology/Pathophysiology – Cause unknown – Possible genetic or prenatal hypoxic event Clinical Manifestations of Autism Developmental disturbances of verbal and social language skills Abnormal response to sensation/stimuli (difficulty distinguishing self from environment) Repetition of self-stimuli May have savant capabilities Does not show pain with injuries Dependent on severity of condition Diagnosis Extensive and thorough interview of family regarding behaviors Behaviors classically begin before age 3 Direct observation of child Nursing Care of Hospitalized Child with Autism Attempt to maintain child’s daily routines from home- very ritualistic Work closely with family to decrease anxiety Provide for the child’s safety-particularly if ritual self stimulation is potentially harmful (head banging, biting) Shaken Baby Syndrome Intracranial & retinal bleeding Physical abuse causing a whip-lash induced trauma to the child’s brain Nursing Interventions Assessment- observe for S&S of: – Hemorrhage to sclera – Apnea – Seizures – Respiratory irregularities – Increased intracranial pressure (ICP) – Drowsiness or lethargy Long Term Prognosis Complete recovery is rare Mental retardation Cerebral Palsy Death Legal Implications Nurses must report suspected child abuse to Child Protective Services (CPS). It is not your obligation to prove the abuse you must report any suspicion. CPS will document and follow through on the case *remember…the abuser may not be the person you suspect, and disclosure to the wrong individual may endanger the child. Please contact me with any further questions. Marlene >^,,^< [email protected]