Neurosurgery Flashcards

1
Q

What is Functional Neurosurgery?

A

-Surgical management of disorders with no gross anatomical target
-Treatment of movement disorders: Parkinson’s, dystonia, essential tremor, epilepsy, OCD
-Ongoing research and treatment of pain, depression, Tourette, headaches, chronic pain, MS
-Goal: provide symptomatic relief, improve quality of life

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2
Q

What is Deep Brain Stimulator Therapy?

A

-One of the most common Functional Neurosurgeries.
-Placement of electrodes into deep brain structures, connected to pulse generator
-Exact mechanism of action is not fully understood
-Advantages over surgical ablation: nondestructive, reversible, and adjustable.
-Well documented safety and long term benefits.
-Inhibition and/or activation of GABAnergic cells and decrease in production of glutamate
-Parkinsons (need dose of Levodopa on DOS), essential tremor, seizures, dystonias

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3
Q

Describe the Anesthetic Management of Deep Brain Stimulator therapy?

A

DBS insertion often a 2-part procedure:
1st – awake craniotomy for lead placement
2nd – GETA for electrode and generator placement

Anesthetic goals: suitable surgical conditions, patient safety and comfort

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4
Q

What are Contraindications/Cautions for DBS therapy?

A

Contraindications: coagulopathy, recent use of antiplatelets, and uncontrolled HTN

Caution with: confusion, extreme anxiety, communication difficulties

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5
Q

Describe the Initial Insertion of a Vagal Nerve Stimulator.

A

-Indicated for seizures unresponsive to meds
-Electrical stimulation to vagus nerve in neck, electrode tunneled to chest wall generator
-GETA
-Can cause bradycardia when testing device

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6
Q

Describe a Generator Change of a Vagal Nerve Stimulator?

A

-Can be done under local/sedation
-Similar to pacemaker battery
-Chest wall pocket

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7
Q

Describe anesthetic management of a Spinal Cord Stimulator

A

Anesthetic technique is surgeon and pt dependent:
-Sedation (heavy MAC)
-GETA

-+/- IONM
-Prone positioning
-May require “wake-up” test to determine proper lead placement
-Often a very challenging anesthetic due to chronic pain and opioid use
-Can be very painful procedure if laminectomy and during tunneling

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8
Q

What is Spinal Cord Stimulation used for?

A

-Spinal cord stimulation is a pain-relief technique that delivers a low-voltage electrical current to the spinal cord to block the sensation of pain.
-It is widely used and efficient alternative for the management of refractory chronic pain that is unresponsive to conservative therapies
-Mechanism of action originally based on Gate-Control Theory, but as more research is done, it also seems to activate GABA and adenosine receptors

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9
Q

What is a Baclofen Pump used for?

A

-Baclofen indicated for relief of spasticity r/t to paralysis, CP)
-Lateral position, exposed abdomen and spine
-Allows for access to abdomen and laminectomy site
-Abdominal wall pocket with pump, contains baclofen, tunneled tubing to spine, insertion site in spine at above level of spasticity
-GETA
-Positioning challenge r/t contractures

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10
Q

What are indications for Craniotomy?

A

-Gliomas - most common, large areas of edema, respond to corticosteroids
-Meningioma – slow glowing, very vascular
-Pituitary adenoma – arise from sella turcica, associated endocrine dysfunction
-35% are secondary neoplasms (breast, lung)
-Slow growing, can be very large before symptoms appear

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11
Q

Describe setup and maintenance of Craniotomy

A

-Euvolemic, arterial line, 2 large bore IV’s, monitor fluids, ICP if available, avoid fluids with dextrose, Lactated Ringers, T&C,
-Blood sugar monitoring, ABG’s
-2 large bore IV’s with extensions if arms tucked (careful of kinking) one IV with blood tubing
-Adequate relaxation and anesthesia
-Intra operative neuro monitoring?
-Arterial line
-Decadron (none for TBI)
-Antibiotics
-Anti-convulsant, mannitol available
-Extension for circuit, IV’s, BIS monitor, Precordial stethoscope, Esophageal
-Bair hugger, fluid warmer
-Drips available if needed, propofol, neo, +/- esmolol, have lebatolol
-Propofol ready for PINS, or if tunnel procedure, have in line ready to go
-Full Reversal, smooth wake up, prevent bucking (lidocaine)
-Intubated to ICU? Monitors, Report

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12
Q

Describe Management of Pituitary Surgery?

A

-Evaluate pt for hormone hypersecretion
-Steroids (hydrocortisone) typically given intra-op
-Transphenoidal or endoscopic nasal approach more commonly used than intracranial approach, bed may be 90 degrees or 180
-GETA , sitting or semi-fowlers position (caution with VAE)
-Tumor may grow around optic nerve, internal carotid artery, or cavernous sinus – be prepared for blood loss
-Monitor for post-op DI, SIADH
-Tx for DI – DDAVP, vasopressin gtt, fluid restriction
-Pt may suffer from acromegaly or cushing’s syndrome. Airway, cardiac concerns
-Visual Disturbances

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13
Q

Describe Transsphenoidal Tumor Resection.

A

-Endoscopic approach decreases trauma, minimizes blood loss, allows for direct assessment to pituitary, decreased incidence of DI and hypopituitarism.
-Less invasive and pt often go home POD 3

Anesthetic goals: optimize cerebral oxygenation, maintain hemodynamic stability, provide ideal surgical field (minimal EBL), and smooth emergence

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14
Q

Describe Posterior Fossa Surgery

A

Posterior Fossa holds vital structures.
-Cerebellum, mid pons, medulla
-GETA
-TIVA v ½ MAC, PIV x 2 or central line, Aline, IONM
-Positioning challenges – prone, lateral, sitting

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15
Q

What are risks associated with the Sitting Position?

A

VAE, pneumocephalus, quadriplegia from severe neck flexion, spinal cord compression, increase cerebral venous congestion

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16
Q

Describe monitoring and treatment of Venous Air Embolism?

A

Prevention – decrease gradient between heart and surgical field, normo- to slight hypervolemia,

Monitoring – Precordial doppler (standard) – Right side, 4th intercostal space, TEE – most sensitive monitor, abrupt decrease in EtCo2, HOTN

Treatment – Notify surgeon to flood field, 100% FiO2, lower HOB, CVC aspiration, cardiopulmonary support if needed

17
Q

What are complications associated with Posterior Fossa Surgery?

A

-Arrhythmias are common with brainstem manipulation
-Bradycardia most frequent - usually subsides with cessation of stimulus
-Tell surgeon you have bradycardia
-Severe HTN
-Hemodynamic control is essential
-May have extreme PONV – consider postop intubation
-Delayed emergence – consider brainstem, cranial nerve injuries
-May elect to delay emergence 2o airway edema, airway protection, brainstem manipulation, N/V
-Pre-Extubation Criteria – LOC, airway and/or gag reflexes, airway swelling, respiratory pattern

Consider deep extubation for hemodynamic stability, cerebral pressures

18
Q

What is Craniosynostosis?

A

Premature closure of cranial sutures
-Can be associated with other syndromes
-May present with airway challenge
-If severe deformity – manage ICP, protect airway
-Based on severity, can be done open or endoscopic
-Elective surgical management (done 6 mo – 2 yrs old): correct the skull deformity, prevent progression, reduce risk of raised ICP
-Have blood in Room, large IV’s

19
Q

Describe anesthetic management of Craniosynostosis.

A

Traditional open procedures are VERY bloody, child can exsanguinate rapidly.
-Have blood in Room, large IV’s or central line, art line
-Standard GETA
-Start PRBC transfusion once incision made, be prepared with FFP, plts, cryo on hand if needed
-Careful with fluid overload
-Consider TXA bolus and infusion
-Monitor for VAE

20
Q

List the normal timeline of Fontanelle closure.

A

Anterior Fontanelle- 18 months

Posterior Fontanelle- 2 months

Anterior Lateral- 2 months

Posterior Lateral- 2 years

21
Q

Describe anesthetic management of Traumatic Brain Injury

A

-Check for other injuries: Facial fractures, C-spine instability
-Art line, large bore IV’s
-Hemodynamic control: keep CPP
-T&C with blood available
-Pressors set up and ready to go
-ICP management
-HOB, mannitol, Lasix in room
-Shearing injury (When you hit head, brain goes back and rubs on cranial bones, and then comes forward again)
-NO STEROIDS WITH TBI!!!
-Tight glucose control: vulnerable to hypoglycemia

22
Q

What is pre-anesthetic evaluation of a TBI?

A

Important for baseline neuro exam:
-Nausea, vomiting
-Altered mental status
-Pupillary size and reactivity
-Seizures
-Visual disturbances, photophobia
-Headaches
-Extremity numbness, tingling, weakness
-Airway
-Glasgow

Labs:
-CBC
-BMP
-Coags

Diagnostics:
-EKG
-Echo
-CT
-MRI

Blood available ?

23
Q

Describe different positioning concerns with neurosurgery?

A

Mayfield or Garner-Wells tongs (Pins):
-Can be very stimulating
-Ensure adequate anesthetic depth (caution with agent bolus – IONM changes)

Sitting:
-Air embolism
-Oral RAE ETT (away from surgical field)

Prone:
-Pressure points
-Post-op visual disturbances, airway swelling

Lateral:
-Pressure points

24
Q

Describe Anesthesia Maintenance for Neurosurgery?

A

-TIVA or volatile at ½ MAC+ TIVA (Propofol, dexmedetomidine, narcotics, inhalation agent)
-Ensure all IVs working, bed may be turned and arms tucked
-A-line transducing
-Close monitoring of potential position injuries
-Maintain acceptable BP, CO2 levels (consider hyperventilation)
-Control of ICP is critical (ICP control – head up, ETT tape not too tight, BP acceptable, CSF drain functioning, enough anesthetic agent?)
-Anticonvulsants- If seizure— 20mg propofol, tell surgeon immediately-cold saline on brain
-Normothermia
-Monitor labs (Na, glucose, osmolarity) especially for signs of DI (alterations in ADH, need for vasopressin, stress response ↑cortisol
-Fluid management (IVF – LR, plamalyte, NS; avoid glucose containing solutions. May need mannitol or hypertonic saline to control edema)
-Vasoactive agents

25
Q

What is Central Neurogenic DI?

A

-Diuresis (16% 5-10 days after injury)
-Hypernatremia, hypovolemia, Polyuria- decrease in ADH

Causes: damage to post pituitary

Treatment- DDAVP (synthetic hormone similar to ADH)

26
Q

What is Syndrome of Inappropriate Anti-diuretic hormone (SIADH)?

A

(33% after TBI)
-Renal absorption of water, concentrated urine, hyponatremia, hypervolemia*
-Disruption of pituitary/hypothalamus
-SIADH- Volume expansion

27
Q

What is Cerebral Salt Wasting Syndrome?

A

-Lose Na and ECF, increased levels of ADH
-Dehydration, hypotension, hyponatremia
-CSWS-Volume depletion

28
Q

Describe initial management of Acute Spinal Injury Stabilization?

A

-May have undiagnosed secondary injury: Facial, brain, thoracic, abdominal, pelvic

Respiratory status:
-Intubation → awake FOI, video scope, in-line stabilization
-Succinylcholine OK 1st 24 hrs-3days then avoid due to Upregulation of Ach receptor sites and can cause hyperkalemia

Hemodynamic support

29
Q

What is Spinal Shock?

A

Impaired spinal autoregulation.
-Skin is pink, vasodilated, cool and clammy
-Sensory-motor deficits and flaccid paralysis below level of injury usually lasting up to 6 weeks followed by spasticity
-Autonomic impairment, hypovolemia
-Ensure proper fluid balance (crystalloid, colloid, product)
-Respiratory status-C3,C4,C5-keep the diaphragm alive. VC may have dropped. In line stabilization for intubation
-Cardiac accelerators T1-4. If these are effected, will have unopposed vagal tone (bradycardia)

30
Q

What is Autonomic Hyperreflexia?

A

Pain below the level of injury is attenuated by descending inhibitory tracts. However, after spinal cord injury, these inhibitory tracts are not able to get through.
-Profound sympathetic responses to stimulus below level of injury are unopposed.

31
Q

Lesions at what level are likely to develop Autonomic Hyperreflexia?

A

85% are Lesions above T6 (the higher the lesion the higher the probability) Can be at T7 and above. Even high thoracic transections are vulnerable.

32
Q

What are symptoms of Autonomic Hyperreflexia above the level of injury?

A

Compensatory above-Nasal stuffiness, headache, pulmonary edema, bradycardia, vasodilation

33
Q

What are symptoms of Autonomic Hyperreflexia below the level of injury?

A

Vasoconstriction.
-HTN, vasoconstriction, bradycardia, arrhythmias

34
Q

What is the Anesthetic Management of Autonomic Hyperreflexia?

A

-Minimize triggers-cutaneous, visceral pain, full bladder, kinked catheter etc
-GETA or spinal anesthesia for procedures
-Use of vasodilators- Have Nipride on hand

35
Q

Describe anesthetic management of ACDF?

A

-Anterior stabilization of cervical spine with removal of disc
-Retractor can compress airway = edema, high PIPs, coughing
-Need for cervical stability during DL – FOI or glidescope
-NIMS ETT to monitor nerves – no paralytics or LTA
-Surgeon may position in extreme extension – monitor ETT placement
-PIV x 2, ± Aline (not typically)
-Maintain MAPs > 85 mmHg for cord perfusion
-Arms tucked
-Intra-operative nerve monitoring
-Posterior approach the patient will be in PINS

36
Q

Describe Anesthetic Management of Anterior Posterior Cervical Fusion (APCF)

A

-Same anesthetic management as PCF
-Consider post-op intubation due to potential for airway swelling and difficult re-intubation
-Typically surgeon does anterior portion then posterior
-Surgeon will position head
-Head pins typically used

37
Q

Describe anesthetic management of Scoliosis Surgery?

A

-Very long, bloody case.
-GETA with IONM. TIVA (?)
-2 large PIV or central line
-Aline
-Prone position for long surgery (careful with pressure points, eyes)
-Blood products available
-Pain control methods
-Busy surgery for both surgeon and anesthesia
-Commonly seen during early summer months in pre-teen – teenagers

38
Q

Describe Anesthetic Management of
Spinal Stabilization

A

Positioning concerns:
-Prone, lateral, extreme lateral

Post-op vision loss (prone):
-Decrease Blood pressure, pressure to eye, fluid overload

-Techniques to accommodate IONM
-Potential for excessive EBL and need for transfusion
-Post-op extubation +/ (Facial, airway swelling, deflate cuff and check for leak)
-Pain control: Multi-modal, opioid sparing