R3
Introduction
Age related differences and procedure related issues different from adult neuroanesthesia
Neuroanatomy Neurophysiology Neuropathophysiology Review anesthesia considerations for selected neurosurgical procedures
Neuroanatomy
Size : Doubles in the first year Weight : 80% of adult weight by the age of two, larger
percent of TBW(10% vs 2%)
Open fontanelle
Noninvasive assessment of ICP US imaging of intracranial structures Untreated progressive hydrocephalus Fusion of the skull sutures is not complete until adolescence
Spinal Cord
Anatomical position
Tethered cord
Spinal cord migration hindered (progressive neurologic deficits)
Middline dimple over spine above the gluteal fold (asymptomatic tethered cord) -Increased risk of neurologic injury with regional anesthesia or diagnositic lumbar puncture
Neuropathology
Brain tumor
Second m/c malignancy of childhood after leukemia Children supra and infratentorial tumors
Involve midline structures
Neuropharmacology
Effects of Inhalation anesthetics and IV anesthetics on CBF and CBV
Similar in children and adults Sevoflurane less inc. in CBV than halothane Isoflurane, sevoflurane, desflurane Quantitatively similar effect on CBF Propofol Dec. CBF velocity in excess of change in MAP consistent CO2 reactivity plateaus at 30mmHg Epileptiform EEG changes Described in children during sevoflurane anesthesia.(>1.5MAC)
Fluid Management
Preop dehydration is common
Isotonic crystalloid
Choice for intraop. maintenance and hydration Exacerbate brain edema Increase the risk of neurologic injury Beneficial in resuscitation after traumatic head injury in children
Hypotonic fluid (Ringers lactate 273mOsm/L) Glucose containing fluid Hypertonic saline
Diuretics
Mannitol
Furosemide (0.3~0.4mg/kg)
Sitting position
Complication of procedure
Procedure
Encephalocele Repair
Herniation of cranial contents
M/C located in the occipital region Undertaken in the early neonatal period High incidence of anomalies of other organ system Avoiding trauma to the lesion during airway management may be challenging. Substantial blood loss from vascular structures within occipital encephaloceles.
Anesthetic consideration
Myelomeningocele Repair
Protrusion of meninges and dysplastic neural tissue through midline bony defects of the spine
Repair Features
Congenital heart defect(ASD) 1/3 Short trachea 1/3 Arnold Chiari malformation present in most pt. with myelomeningocele
Intraop. N. stimulation
Necessary to reverse neuromuscular blockade. Repair of large lesions
Anesthetic consideration
Significant fluid requirements and transfusion
Repair
In the first six months (Improves skull geometry and allows for normal brain growth ) Strip craniectomy, calvarial reconstruction and endoscopic craniectomy
Feature of craniosynostosis
Intracranial hypertension 23% Elevated ICP more common in multiple suture
synostosis
Endoscopic precedure
Encephalodurosynangiosis
Moya Moya
Progressive occlusive cerebrovascular Transient or permanent neurologic deficits d/t inadequate cerebral blood flow Transposing the temporal artery to the surface of the brain via a small craniotomy
Stimulate formation of collateral vessels.
Surgical procedure
Goal of anesthesia
Minimize neurologic morbidity
By avoiding agitation, hyperventilation,increase in cerebral metabolism assoc. with painful stimuli, By maintaining normacarbia, maintaing systemic blood pr.
Encephalodurosynangiosis
Postop period
Risk for cerebral ischemia and stroke (As collateral circulation develops) Avoiding dehydration, fever, hyperventilation and agitation d/t pain
Excellent in most children after cranial revascularization
Anesthetic consideration
Guideline
Tx of cerebral perfusion pr. And Hypotension Tx of ICP > 20mmHg, correction of hypoxia Avoidance of prophylactic hyperventilation
Option
Recommended therapy