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Pertemuan Ilmiah Berkala PERDATIN 2014 
Grand Clarion Hotel and Convention-Makassar 
Syafruddin Gaus 
Dept. of Anesthesiology, Intensive Care, and Pain Management 
Faculty of Medicine, Hasanuddin University
Introduction 
 Patients with neurologic disease undergoing 
surgical procedures have increased risk of 
ischemic / hypoxic damage to the CNS 
 Risk may be related to hemodynamic / 
embolic events associated with: 
* non-neurosurgical operation (CPB) 
* neurosurgical procedure (temporary 
clipping during cerebral aneurysm surgery
Introduction 
 Intraoperative neurophysiologic monitoring 
may improve patient outcome by: 
 allowing early diagnosis of ischemia/hypoxia 
before irreversible damage occurs 
 enabling surgeons to provide optimal operative 
treatment as indicated by the monitoring 
parameter.
Introduction 
 The brain can be monitored in terms of: 
 function 
 cerebral blood flow (CBF) & intracranial 
pressure (ICP) 
 brain oxygenation and metabolism
Monitoring of Function 
 Electroencephalograms (EEG) 
 Raw EEG 
 Computerized Processed EEG: Compressed 
spectral array, Density spectral array, Aperiodic 
analysis, Bispectral analysis (BIS) 
 Evoked Potential 
 Sensory EP: 
○ Somatosensory EP 
○ Visual EP 
○ Brain stem auditory EP 
 Motor EP: 
- Transcranial magnetic MEP 
- Transcranial electric MEP 
- Direct spinal cord stimulation 
 EMG 
- Cranial nerve function (V, VII, IX, X, XI, XII)
EEG 
 Result of excitatory postsynaptic potential 
 EEG Waves : 
 Beta: high freq, low amp (awake state) 
 Alpha: med freq, high amp (eyes closed while 
awake) 
 Theta: Low freq (not predominant) 
 Delta: very low freq hugh amp (depressed 
functions/deep coma) 
 EEG waves reflects state of arousal and 
metabolism depends on energy 
substrates supply  blood flow
EEG 
 Sudden development of delta waves 
coincident with surgical manuver  
injury warning 
 In penumbra region, EEG poorly predict 
brain damage 
 Anesthetics & hypothermia causes EEG 
changes  multifactorial interpretation
EEG 
 Indication: 
 Surgery that place the brain at risk 
(difficulties: restricted access) 
 Anesthesia induced metabolic suppresion 
 Seizure monitoring in ICU
Indication for EEG 
Monitoring  Carotid endarterectomy 
 Cerebral aneurysm surgery when 
temporary clipping is used. 
 Cardiopulmonary bypass 
procedure 
 Extracranial-intracranial bypass 
procedure 
 Deliberate metabolic supression 
for cerebral protection. 
Newfield P, Cottrell JE. Handbook of 
Neuroanesthesia;2012
Bispectral Index 
 Bispectral analysis (BIS) 
 Monitor degree of hypnosis (40-60  
adequate hypnosis) 
 Doesn’t detect ischemia
Evoked Potential Monitoring 
 Sensory Evoked Potential (SEP) 
 Time-locked, event related, pathway specific 
EEG in respones of peripheral stimulus 
 Resistant to IV anesthetics, recordable in 
inhalation anesthetics (dose related) 
 Monitor integrity of the pathway from 
periphery to the cortex
Evoked Potential Monitoring 
• Somatosensory Evoked Potential (SSEP) 
○ Electrical stimulator placed at median, ulnar, or 
posterior tibial nerves. 
○ Used in spinal column surgery to asses potential 
risk to the spinal cord 
• Visual Evoked Potential (VEP) 
○ Using LED goggles to create stimulus 
○ Difficult to perform 
• Brainstem Auditory Evoked Potential (BAEP) 
○ Repetitive clicks delivered to the ear 
○ Reflects the VIII nerve & brainstem “well-being”
Indication for SEP Monitoring 
SSEP Monitoring: 
 Spinal column surgery 
 Carotid endarterectomy 
 Cerebral aneurysm 
surgery 
BAEP Monitoring: 
 Acoustic neurinoma 
 Vertebral-basilar 
aneurysm 
 Other posterior fossa 
procedure. 
SSEP: somatosensory evoked potential 
BAEP: brain stem auditory evoked potential
Evoked Potential Monitoring 
 Motor Evoked Potential (MEP) 
 Monitors motoric pathway  as a 
complement of SSEP 
 Basically an electromyographic using train 
of four stimuli 
 Instant feedback 
 Can’t be recorded if muscle relaxant used
Monitoring of CBF and ICP 
 Absolute CBF. 
 Nitrous oxide wash in (jugular bulb 
cannulation) invasive 
 Xenon clearance non invasive 
 Relative CBF 
 Laser Doppler Flowmeter (LDF) measure 
flow quantitatively (1 mm brain tissue). 
 Requires a burr hole.
Monitoring of CBF and ICP 
 Transcranial Doppler (TCD) –overview- 
 Measure CBF velocity in the Circle of Willis 
noninvasively and continuously 
 Intraoperative middle cerebral artery 
measured by placing probe over zygomatic 
arch 
 Qualitative assesment tools for ICP 
 Detects air / particulate emboli
Monitoring of CBF and ICP 
 Transcranial Doppler (TCD) –principles- 
 Flow can be measured if the vessel diameter 
remain constant Basal Cerebral Arteries 
 The diameter remain constant as the vascular 
resistance changes or during administration of 
IV or inhaled anesthetics 
 The diameter only constricts during vasospasm 
in subarachnoid hemorhage 
 Once confirmed by angiography, TCD can track 
patient’s response to therapy of the vasospasm 
 Changes in flow velocity correlates with CBF
Monitoring of CBF and ICP 
 Transcranial Doppler (TCD) –clinical app- 
 Carotid endarterectomy: 
○ Detection of ischemia if 60% Vmca decrease from 
baseline 
○ Detection of microemboli 
○ Diagnosis of postoperative hyperperfusion syndrome 
○ Diagnosis of postoperative intimal flap or thrombosis 
 Cardiac Surgery (cognitive dysfunction 30-70%): 
○ Cerebral emboli during cardiopulmonary bypass 
○ Cerebrl perfusion during cardiopulmonary bypass 
 Closed Head Injury: 
○ Assess autoregulation, diagnose hyperemia, 
vasospasm, and intracranial circulatory arrest 
Diagnosis of brain death
Monitoring of CBF and ICP 
 ICP monitoring: 
 Optimizes Cerebral Perfusion Pressure 
(CPP) 
 Prevents possible herniation 
 Methods: ventriculostomy, subarachnoid 
bolt, epidural sensor, fiberoptic 
intraparenchymal monitor (commonly used) 
 Can be incorporated with LDF, brain 
temperature, PaO2, PaCO2, and pH 
monitoring
Monitoring of Cerebral 
Oxygenation and Metabolism 
 Invasive monitoring: 
 Brain tissue oxygenation 
 Jugular bulb venous oximetry monitoring 
 Microdialysis catheter 
 Non-Invasive monitoring: 
 Near Infrared Spectroscopy (NIRS)
Monitoring of Cerebral 
Oxygenation and Metabolism 
 Brain tissue oxygenation (Po2) 
 Po2 monitor is useful to assess O2 demand and 
supply 
 The tissue Po2 monitor is placed intraparenchymal-ly 
in conjunction with ICP monitor. 
 Reveals regional or local O2 levels 
 O2 tension 10 mmHg: threshold for brain hypoxia
Monitoring of Cerebral 
Oxygenation and Metabolism 
 Brain tissue oxygenation (Po2) 
 Po2 : increasing supply O2 (supplemental O2, 
raising CPP, treating anemia) 
 Po2 : decreasing demand (propofol or barbiturate 
therapy) 
 Loss of cerebral autoregulation: may demonstrate 
hyperoxia that could occur with cerebral hyperemia 
 Monitor placement ? Normal brain parenchyma or 
adjacent to the injured brain
Monitoring of Cerebral 
Oxygenation and Metabolism 
 Jugular bulb venous oximetry monitoring 
 Provide GLOBAL cerebral oxygen 
demand and supply 
 Relative CBF estimated by calculation of 
arteriovenous oxygen content 
difference reflects oxygen balance 
 Intraoperative cerebral ischemia can be 
diagnosed readily 
 Limitation: unable to detect focal 
ischemia
Monitoring of Cerebral 
Oxygenation and Metabolism 
 Interpretation of jugular venous oxygen 
saturation (SjvO2) 
 Increased values: >90% indicates absolute/relative 
hyperemia 
○ Reduced metabolic need  comatose/brain death 
○ Excessive flove  sever hypercapnia 
○ AVM 
 Normal Values: 60-70%  focal ischemia? 
 Decreased Values: <50%  increased O2 extraction, 
indicates a potential risk of ischemia injury 
○ Increased demand: seizure / fever 
○ Decreased supply: decreased flow, decreased hematocrit 
 As ischemiaprogress to infarction: O2 
consumption decreases
Monitoring of Cerebral 
Oxygenation and Metabolism 
 Microdialysis catheters 
 Small catheter inserted with ICP/tissue PO2 
monitor 
 Artificial cerebrospinal fluidequilibrates with 
extracellular fluid chemical composition 
analysis 
 Markers: 
○ Lactate/pyruvate ratio  onset of ischemia 
○ High level glycerol inadequate energy to 
maintain cellular integrity membrane 
breakdown 
○ Glutamate neuronal injury and a factor in its 
exacerbation 
 Catheter placement is important small 
coverage
Monitoring of Cerebral 
Oxygenation and Metabolism 
 Near-infrared Spectroscopy (NIRS) 
 Transcranial oximetry 
 Measure cerebral regional O2 reflected 
by the chromophobes in the brain 
 Limits: 
○ Intersubject variability 
○ Potential contamination from 
extracranial blood 
○ Lack definable threshold 
 Might be promising in neonate & infant 
due to thin skull & scalp
Summary 
 Neurophysiologic monitoring not universally 
adopted but in many centers has become 
routine monitor for some surgical procedures 
 Ideal neurophysiologic monitoring in the 
neurosurgical procedure should be: non-invasive 
(v.s invasive), high sensitivity & 
specificity, cost effective, easy to use, simple 
instrumentation, and real time or continous 
monitoring.
neurophysiologic monitoring final

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neurophysiologic monitoring final

  • 1. Pertemuan Ilmiah Berkala PERDATIN 2014 Grand Clarion Hotel and Convention-Makassar Syafruddin Gaus Dept. of Anesthesiology, Intensive Care, and Pain Management Faculty of Medicine, Hasanuddin University
  • 2. Introduction  Patients with neurologic disease undergoing surgical procedures have increased risk of ischemic / hypoxic damage to the CNS  Risk may be related to hemodynamic / embolic events associated with: * non-neurosurgical operation (CPB) * neurosurgical procedure (temporary clipping during cerebral aneurysm surgery
  • 3. Introduction  Intraoperative neurophysiologic monitoring may improve patient outcome by:  allowing early diagnosis of ischemia/hypoxia before irreversible damage occurs  enabling surgeons to provide optimal operative treatment as indicated by the monitoring parameter.
  • 4. Introduction  The brain can be monitored in terms of:  function  cerebral blood flow (CBF) & intracranial pressure (ICP)  brain oxygenation and metabolism
  • 5. Monitoring of Function  Electroencephalograms (EEG)  Raw EEG  Computerized Processed EEG: Compressed spectral array, Density spectral array, Aperiodic analysis, Bispectral analysis (BIS)  Evoked Potential  Sensory EP: ○ Somatosensory EP ○ Visual EP ○ Brain stem auditory EP  Motor EP: - Transcranial magnetic MEP - Transcranial electric MEP - Direct spinal cord stimulation  EMG - Cranial nerve function (V, VII, IX, X, XI, XII)
  • 6. EEG  Result of excitatory postsynaptic potential  EEG Waves :  Beta: high freq, low amp (awake state)  Alpha: med freq, high amp (eyes closed while awake)  Theta: Low freq (not predominant)  Delta: very low freq hugh amp (depressed functions/deep coma)  EEG waves reflects state of arousal and metabolism depends on energy substrates supply  blood flow
  • 7. EEG  Sudden development of delta waves coincident with surgical manuver  injury warning  In penumbra region, EEG poorly predict brain damage  Anesthetics & hypothermia causes EEG changes  multifactorial interpretation
  • 8. EEG  Indication:  Surgery that place the brain at risk (difficulties: restricted access)  Anesthesia induced metabolic suppresion  Seizure monitoring in ICU
  • 9. Indication for EEG Monitoring  Carotid endarterectomy  Cerebral aneurysm surgery when temporary clipping is used.  Cardiopulmonary bypass procedure  Extracranial-intracranial bypass procedure  Deliberate metabolic supression for cerebral protection. Newfield P, Cottrell JE. Handbook of Neuroanesthesia;2012
  • 10. Bispectral Index  Bispectral analysis (BIS)  Monitor degree of hypnosis (40-60  adequate hypnosis)  Doesn’t detect ischemia
  • 11. Evoked Potential Monitoring  Sensory Evoked Potential (SEP)  Time-locked, event related, pathway specific EEG in respones of peripheral stimulus  Resistant to IV anesthetics, recordable in inhalation anesthetics (dose related)  Monitor integrity of the pathway from periphery to the cortex
  • 12. Evoked Potential Monitoring • Somatosensory Evoked Potential (SSEP) ○ Electrical stimulator placed at median, ulnar, or posterior tibial nerves. ○ Used in spinal column surgery to asses potential risk to the spinal cord • Visual Evoked Potential (VEP) ○ Using LED goggles to create stimulus ○ Difficult to perform • Brainstem Auditory Evoked Potential (BAEP) ○ Repetitive clicks delivered to the ear ○ Reflects the VIII nerve & brainstem “well-being”
  • 13. Indication for SEP Monitoring SSEP Monitoring:  Spinal column surgery  Carotid endarterectomy  Cerebral aneurysm surgery BAEP Monitoring:  Acoustic neurinoma  Vertebral-basilar aneurysm  Other posterior fossa procedure. SSEP: somatosensory evoked potential BAEP: brain stem auditory evoked potential
  • 14. Evoked Potential Monitoring  Motor Evoked Potential (MEP)  Monitors motoric pathway  as a complement of SSEP  Basically an electromyographic using train of four stimuli  Instant feedback  Can’t be recorded if muscle relaxant used
  • 15. Monitoring of CBF and ICP  Absolute CBF.  Nitrous oxide wash in (jugular bulb cannulation) invasive  Xenon clearance non invasive  Relative CBF  Laser Doppler Flowmeter (LDF) measure flow quantitatively (1 mm brain tissue).  Requires a burr hole.
  • 16. Monitoring of CBF and ICP  Transcranial Doppler (TCD) –overview-  Measure CBF velocity in the Circle of Willis noninvasively and continuously  Intraoperative middle cerebral artery measured by placing probe over zygomatic arch  Qualitative assesment tools for ICP  Detects air / particulate emboli
  • 17. Monitoring of CBF and ICP  Transcranial Doppler (TCD) –principles-  Flow can be measured if the vessel diameter remain constant Basal Cerebral Arteries  The diameter remain constant as the vascular resistance changes or during administration of IV or inhaled anesthetics  The diameter only constricts during vasospasm in subarachnoid hemorhage  Once confirmed by angiography, TCD can track patient’s response to therapy of the vasospasm  Changes in flow velocity correlates with CBF
  • 18. Monitoring of CBF and ICP  Transcranial Doppler (TCD) –clinical app-  Carotid endarterectomy: ○ Detection of ischemia if 60% Vmca decrease from baseline ○ Detection of microemboli ○ Diagnosis of postoperative hyperperfusion syndrome ○ Diagnosis of postoperative intimal flap or thrombosis  Cardiac Surgery (cognitive dysfunction 30-70%): ○ Cerebral emboli during cardiopulmonary bypass ○ Cerebrl perfusion during cardiopulmonary bypass  Closed Head Injury: ○ Assess autoregulation, diagnose hyperemia, vasospasm, and intracranial circulatory arrest Diagnosis of brain death
  • 19. Monitoring of CBF and ICP  ICP monitoring:  Optimizes Cerebral Perfusion Pressure (CPP)  Prevents possible herniation  Methods: ventriculostomy, subarachnoid bolt, epidural sensor, fiberoptic intraparenchymal monitor (commonly used)  Can be incorporated with LDF, brain temperature, PaO2, PaCO2, and pH monitoring
  • 20. Monitoring of Cerebral Oxygenation and Metabolism  Invasive monitoring:  Brain tissue oxygenation  Jugular bulb venous oximetry monitoring  Microdialysis catheter  Non-Invasive monitoring:  Near Infrared Spectroscopy (NIRS)
  • 21. Monitoring of Cerebral Oxygenation and Metabolism  Brain tissue oxygenation (Po2)  Po2 monitor is useful to assess O2 demand and supply  The tissue Po2 monitor is placed intraparenchymal-ly in conjunction with ICP monitor.  Reveals regional or local O2 levels  O2 tension 10 mmHg: threshold for brain hypoxia
  • 22. Monitoring of Cerebral Oxygenation and Metabolism  Brain tissue oxygenation (Po2)  Po2 : increasing supply O2 (supplemental O2, raising CPP, treating anemia)  Po2 : decreasing demand (propofol or barbiturate therapy)  Loss of cerebral autoregulation: may demonstrate hyperoxia that could occur with cerebral hyperemia  Monitor placement ? Normal brain parenchyma or adjacent to the injured brain
  • 23. Monitoring of Cerebral Oxygenation and Metabolism  Jugular bulb venous oximetry monitoring  Provide GLOBAL cerebral oxygen demand and supply  Relative CBF estimated by calculation of arteriovenous oxygen content difference reflects oxygen balance  Intraoperative cerebral ischemia can be diagnosed readily  Limitation: unable to detect focal ischemia
  • 24. Monitoring of Cerebral Oxygenation and Metabolism  Interpretation of jugular venous oxygen saturation (SjvO2)  Increased values: >90% indicates absolute/relative hyperemia ○ Reduced metabolic need  comatose/brain death ○ Excessive flove  sever hypercapnia ○ AVM  Normal Values: 60-70%  focal ischemia?  Decreased Values: <50%  increased O2 extraction, indicates a potential risk of ischemia injury ○ Increased demand: seizure / fever ○ Decreased supply: decreased flow, decreased hematocrit  As ischemiaprogress to infarction: O2 consumption decreases
  • 25. Monitoring of Cerebral Oxygenation and Metabolism  Microdialysis catheters  Small catheter inserted with ICP/tissue PO2 monitor  Artificial cerebrospinal fluidequilibrates with extracellular fluid chemical composition analysis  Markers: ○ Lactate/pyruvate ratio  onset of ischemia ○ High level glycerol inadequate energy to maintain cellular integrity membrane breakdown ○ Glutamate neuronal injury and a factor in its exacerbation  Catheter placement is important small coverage
  • 26. Monitoring of Cerebral Oxygenation and Metabolism  Near-infrared Spectroscopy (NIRS)  Transcranial oximetry  Measure cerebral regional O2 reflected by the chromophobes in the brain  Limits: ○ Intersubject variability ○ Potential contamination from extracranial blood ○ Lack definable threshold  Might be promising in neonate & infant due to thin skull & scalp
  • 27. Summary  Neurophysiologic monitoring not universally adopted but in many centers has become routine monitor for some surgical procedures  Ideal neurophysiologic monitoring in the neurosurgical procedure should be: non-invasive (v.s invasive), high sensitivity & specificity, cost effective, easy to use, simple instrumentation, and real time or continous monitoring.