EEG And ICP Monitoring Flashcards

1
Q

How much energy does the cerebrum require?

A

3-5 ml O2/min/100g tissue

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2
Q

Normal Cerebral Blood Flow is ___.

A

50 ml/min/100 g tissue 750 ml/min for brain Delivers 150 ml O2/min

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3
Q

O2 extraction from cerebral blood flow is:

A

35-50%

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4
Q

What is the equation for Cerebral Perfusion Pressure (CPP)?

A

CPP = MAP - ICP

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5
Q

Cerebral blood flow is:

A
  • Tightly regulated except post-trauma
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6
Q

Cerebral blood flow stays around ____, as long as MAP is between _____ mm Hg.

A

50 ml/100g/min , 50-100

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7
Q

CBF is reduced by

A
  1. Head injury 2. Intracranial hypertension 3. Hypotension 4. Hyperventilation 5. Vasospasm
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8
Q

Ways of directly monitoring ICP:

A
  1. Ventricular catheters 2. Subdural/subarachnoid bolts 3. Epidural transducers 4. Intraparenchymal fiber optic devices
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9
Q

What is the Monroe-Kellie hypothesis:

A

The skull is a fixed volume. If one or more of these components increases, ICP rises: - Blood - CSF - Brain

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10
Q

ICP determined by:

A
  • Brain mass (80%) - Blood flow (10%) - CSF volume (10%)
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11
Q

ICP monitoring physical set up

A
  1. Connection of device to transducer 2. Watertight fluid interface 3. Deformation of transducer membrane converted to electrical pulsations and amplified and displayed as a waverform
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12
Q

Zeroing of ICP Monitors requires:

A
  • Zeroing to room air - Catheter tip transducers only zeroed prior to insertion - External transducers can be zeroed anytime
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13
Q

Indication for ICP monitoring:

A

-GCS < 8 (or higher if CT of concern {Hematoma, Edema, Contussion, etc}) -Normal CT with GCS 40 2. Posturing 3. SBP < 90 mm Hg -Sedation precluding clinical assessment

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14
Q

ICP monitoring is useful in:

A
  1. Head injury 2. Poor grade SAH 3. Intracerebral hematoma 4. Meningitis 5. Stroke 6. Allows calculation of CPP 7. Info on intracerebral compliance
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15
Q

ICP Values:

A

Normal: 7-15 mm Hg Abnormal: > 20 mm Hg If > 25 mm Hg, aggressive management indicated

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16
Q

High ICP:

A

will cause internal or external herniation of the brain, distortion and pressure on cranial nerves and vital neurological centers

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17
Q

When ICP is elevated cerebral perfusion will be:

A

Impeded and operating conditions difficult or impossible

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18
Q

When brain volume increases

A

loss of CSF and reduction of venous blood volume act to compensate

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19
Q

Subdural hematoma can lead to:

A

Tentorial herniation

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20
Q

Hemorrhage can lead to:

A

Subfalcine herniation

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21
Q

Devices to measure ICP:

A
22
Q

What is the Gold Standard of ICP measuring?

A

Intraventricular drain and transducer b/c you can control ICP by CSF drainage and zero externally

23
Q

What are the contraindications of intraventricular drain and transducer?

A
  • Bleeding
  • Blockage
  • Infection risk
  • Insertion difficulties
24
Q

Which ventricle is the intraventricular catheter placed?

A

Lateral ventricle (frontal horn)

25
Q

What are the positive points of the intraparenchymal pressure monitor?

A
  • Lower infection risk
  • Less risk of hermorrage
  • Excellent metrological properties (less drift)
26
Q

What are the negatives to a intraparenchymal pressure monitor?

A
  • Underestimate very high ICP
  • Drift a problem after several days
27
Q

What are the contraindications of intraparenchymal pressure monitors?

A
  • Intracranial infection
  • Coagulopathies
  • Severe skull fractures
  • Conditions where CFS drainage is necessary
28
Q

Phase 1 of the ICP Waveform:

A

P1: Percussion wave (arterial pulsation)

29
Q

Phase 2 of ICP waveform:

A

P2: Rebound wave (Intracranial compliance)

30
Q

Phase 3 of ICP waveform:

A

P3: Dichrotic wave (venous pulsations)

31
Q

ICP Management: Decrease brain water w/

A
  • hyperosmolar diuretics (Mannitol w/ intact BBB 0.25 - 1 g/kg)
  • Loop diuretics (Lasix)
  • Corticosteroids
32
Q

ICP Management: Reduce CSF Volume by:

A
  • Drainage (Ventricular, lumbar subarachnoid, head elevation)
33
Q

Auto regulation is impaired by:

A
  • Inhalational anesthetics
  • Direct acting vasodilators (Adenosine, Prostacyclin, Ca++ Channel blockers, NTG, Nitroprusside)
34
Q

Transcranial Doppler (TCD) Ultrasonography:

A
  • Allows CBF velocity measurement (continuous or intermittent)
  • Most usefule for vasospasm post subarachnoid hemorrhage
    • Vasospasm: increased flow velocity
    • Ratio of ICA:MCA flow allows monitoring independent of rising ICP
35
Q

Continuous Electroencephalogram (EEG) Monitoring:

A

The summation and recording of postsynaptic potentials from the pyramidal cells of the cerebral cortex; reflects metabolic activity of the brain

36
Q

EEG is a tracing:

A

Of voltage fluctuations versus time recorded from electrodes placed over scalp in specific array; represent fluctuating dendritic potentials from superficial cortical layers;

37
Q

Disadvantages of EEG:

A
  • Required Amplification
  • Deep parts of the brain are not well sampled
  • Detects cortical dysfunction but rarely discloses its etiology
  • Relatively low sensitivty and specificty
  • Subject to electrical and physiological artifacts
  • Influenced by state of alertness, hypoglycemia, drugs
  • Small or deep lesions might not produce an EEG abnormality
  • Limited time sampling and spatial sampling
38
Q

Placement of EEG Electrodes:

A
  • Usually 21 or more
  • Spaced at 10 or 20% of distances btwn specified anatomic landmarks
  • Odd # of electrodes over left, even over right
39
Q

Indication for EEG:

A
  • Craniotomy for cerebral aneurysm clipping when a temporary clip is used
  • Carotid Endarterectomy (under GA)
  • Cardiopulmonary bypass
  • Extra cranial-intracranial bypass procedures
  • Pharmacologic depression of brain for “cerebral protection”
40
Q

EEG Waveforms: Beta

A

13 - 30 Hz; Awake and alert (short and frequent)

41
Q

EEG Waveforms: Alpha

A

8-13 Hz; closed eyes, relaxed (Tall and frequent)

42
Q

EEG Waveforms: Theta

A

4-7 Hz Tall and infrequent (GA)

43
Q

EEG Waveforms: Delta

A

0-4 Hz, Deep sleep, deep sedation (Very tall and very infrequent)

44
Q

EEG Artifacts

A
  • Eye-induced artifacts (includes eye blinks and eye mvmt)
  • Gloss kinetic artifacts
  • Poor grounding
  • IV drips
  • Body mvmt
  • EKG artifact
45
Q

EEG Monitors: Continuous Electroencephalography

A
  • BIS algorithm
  • Snap
  • State entropy/Respone entropy (Datex-Ohmeda algorithm)
  • SEDLine monitor (Patient state analyzer)
  • A-Line AEP Monitor/2 (EEG plus AEP) and Cerebral State Monitor (EEG Only)
    • EEG and Auditory Evoked Potentials
  • Narcotrend (EEG Monitor)
46
Q

The EEG is NOT

A

A predictor of mvmt under GA

47
Q

EEG Monitoring: Activation

A

High frequency, Low voltage; Light Anesthesia, Surgical stimulation

48
Q

EEG Monitoring: Depression

A

Low frequency, high voltage; Deep anesthesia, cerebral compromise

49
Q

Agents That Activate

A
  • Subanesthetic inhalationals
  • Low dose barbiturates/benzodiazepines
  • Small doses of etomidate
  • N2O
  • Ketamine
  • Mild hypercapnia
  • Stimulation (surgical)
  • Early hypoxia
50
Q

Agents That Depress

A
  • 1-2 MAC gases
  • Barbiturates/propofol/etomidate
  • Narcotics- dose dependent
  • Hypocapnia
  • Hypothermia
  • Late hypoxia