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Introduction to the methodology of EEG recording

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Title: Introduction to the methodology of EEG recording


1
Introduction to the methodology of EEG recording
  • Friday October 20th
  • 2006

2
Summary
  • A. Generators and modulators of EEG signal
  • B. Understanding instrumentation
  • C. Main ethical issues
  • D. Physiological and electronical sources of
    noise
  • E. Constraints for experimental protocols in EEG
  • F. Configuration of EEG recording system and
    selection of montage
  • G. Management of connectics
  • H. Paste-up and problem solving during the
    recording session
  • I. Digitization
  • J. Cleaning/decontamination  of sensitive
    equipment / equipment maintenance

3
A. Generators and modulators of EEG signal
4
Generators of EEG signal
  • When reached by an input, the presynaptic neuron
  • Releases some neurotransmitter in the synaptic
    cleft
  • The dendritic process of the post-synaptic
    neuron
  • shows a local change in its membranes
    permeability
  • generates a primary (intracellular) current from
    the locus of the synapse to the soma
  • Generates a secondary/return extracellular
    current to close the loop

5
Generators of EEG signal
  • Cortical pyramidal neurons, arranged in layers
  • The movement of the ions is creating an open
    field (no cancellation)
  • When a local community of tens of thousands of
    neurons are activated simultaneously by some
    input, a signal can be detected as far as at the
    surface of the scalp
  • This signal is EXTREMELY tiny, and requires many
    precautions when measured

6
Generators of EEG signal
  • And the miracle occurs

7
Modulators
  • Age
  • Children
  • Changes in frequency content due to the size of
    the loops in the anatomical networks
  • Changes in the conduction time due to
    myelinization
  • Change in the amplitude of the signal due to
    myelinization
  • Adult
  • Increased variability over 40
  • Vigilance
  • Chronopsychology (more details next)
  • Drugs
  • Caffeine
  • Body temperature
  • Hormonal cycles (women)
  • Laterality

8
Modulators
  • Circadian rhythms
  • Global power is maximal during the afternoon
  • Theta power has two peaks at 4pm and midnight
  • Induced alpha is maximal in the afternoon
  • Beta is maximal between 5pm and 7pm
  • The modulation is dependent on the location of
    the electrodes

9
B. Understanding instrumentation
10
Overview
  • Junction skin-electrode
  • Analog conduction
  • Differential amplifiers
  • ADC
  • Integration of triggers
  • Transfer to the CPU / storage

11
Transduction
  • The living tissues contain free ions
  • The wire is conveying electrons
  • The transfer of the signal from one material to
    the other requires a chemical transformation
  • Oxidation or reduction (AC)

12
Transduction
  • Eg. Ag / AgCl electrode
  • OXIDATION
  • If an electron moves from the wire to the
    electrode toward the conductive gel
  • It reacts with AgCl
  • e- AgCl -gt Ag Cl-
  • Cl- becomes hydrated and enters the conductive
    paste
  • REDUCTION
  • If ion moves from the conductive gel to the
    electrode
  • It reacts with solid Ag
  • Ag Cl- -gt e- AgCl
  • AgCl becomes insoluble
  • one electron is liberated to the wire
  • REVERSIBLE

13
Transduction
  • Eg. Ag / AgCl electrode
  • The Ag/AgCl electrode is non-polarizable (or
    minimally polarizable)
  • POLARIZATION
  • The anion (Cation) is unable to move freely
    across the gel/electrode border
  • The concentration of ions at the border is
    altered.
  • Ions concentrate over the border with the
    electrode and create a steady potential
    (bi-layer, capacitance)
  • This steady potential hampers the movement of the
    charges
  • This is important since the biopotential we
    intend to measure is in the range of 1/1000 of
    the half-cell potential (local potential at the
    junction between the conductive paste and the
    electrode)

14
Analog conduction
  • As soon as the potentials are digital, they are
    immune to noise (not to deletion)
  • Between the cap and the ADC, the minuscule
    currents are traveling through the cables and in
    the amplifier.
  • Contamination through movements of the cables
  • Contamination by cross-talk inside the amplifier
    and at the multiplexer of the ADC

15
Differential amplification
  • We amplified to push the deflection of the pens
    (mechanical)
  • We amplify to bring the signal in the range of
    the ADC (usually 0-1 to 0-5 V)
  • But more importantly, the purpose is differential
    amplification

16
Differential amplification
  • Principle of differential amplification the CMR
  • (Signal noise) (noise)
  • Take a scalp electrode (say C3) and a fixed point
    (GND)
  • Measure one potential difference
  • Take a reference electrode (say MA1) and a fixed
    point
  • Measure a second potential difference
  • (Signal noise) (noise) a very clean signal

17
Differential amplification
  • The ability of the amplifier to reject the common
    mode noise is called the CMRR

18
Differential amplification
  • Amplifier Input impedance
  • Separate the differential input with a high
    resistance

19
Analog-to-Digital Conversion
  • Sampling frequency Nyquist and aliasing

20
Analog-to-Digital Conversion
  • Sampling frequency
  • ADC range
  • Quantization

21
Acquisition and storage
  • Data acquisition and storage
  • Reasonable sampling rate
  • Backup

22
Understanding instrumentation
  • Quikcap
  • Headbox
  • Power unit
  • System unit

23
C. Main ethical issues
24
Electrical safety
  • Security for the subject and security for the
    equipment
  • Faulty connections
  • Additional devices (response pads, sensors)
  • Ground loops
  • Static discharges
  • Chassis leakage
  • EMI in crossing wires
  • Isolation amplifiers (Neuroscan system) are
    regulated by IEC 601-1 specifications.
  • Additional devices connected to Neuroscan have to
    be detailed in the application to the EEG
    committee
  • Order to plug or unplug the components

25
Infection risk
  • Most of the supplies, especially those in contact
    with the subject (eg. needles), are disposable
  • Any supply in contact with the subject does not
    return to the main.
  • eg. the gel is sampled in a cup. Do NEVER refill
    a syringe in the main container.
  • Moderate skin preparation a subject should never
    be bleeding as a result of skin preparation.
  • Inspection for the presence of blood after
    experiment (to choose the decontamination
    procedure)
  • Decontamination of non-disposable equipment
  • Is regulated by American Electroencephalographic
    Society. Report of the Committee on Infectious
    Diseases. J Clin Neurophysiol 199411128-132..

26
Infection risk
Object Classification Use of Item Decontamination required after cleaning
Critical Enters vascular system or sterile body tissues Sterilization and holding in sterilized state. High level disinfection is not sufficient
Semi-Critical Comes in contact with non-intact skin or intact mucous membranes High level disinfection (by heat or chemicals)
Non-Critical Comes in contact with intact skin Intermediate or low level disinfection
Spaulding's classification of devices/medical
instruments
27
D. Physiological and electronical sources of noise
28
Interferences
  • Physiological artifact
  • Ocular domain
  • Muscular domain
  • EKG
  • Respiratory
  • Movement
  • EDR/sweating
  • Subjects instruction and online monitoring
  • Instrumental noise
  • EMI wireless or line noise (60 Hz)
  • Sway of the cable
  • Electrodes poorly attached (pop)
  • Electrode noise
  • Amplifier noise
  • Flicker noise (DC recordings!)
  • Amplifier blocking
  • Shielding and guarding

29
Interferences
  • Artifacts from the ocular domain

30
Interferences
  • With proper alignment of EOG electrodes,
    horizontal EOG do not pick up the signal from
    vertical eye movements

GOOD
BAD
31
Interferences
  • Saccade / eye movements

32
Interferences
  • Muscles

33
Interferences
  • How life could be easy without muscles

34
Interferences
  • (and with enough time to average thousands)

35
Interferences
  • EKG

36
Interferences
  • Respiratory

37
Interferences
  • Movement

38
Interferences
  • EDR/sweating

39
Interferences
  • Physiological artifact
  • Ocular domain
  • Muscular domain
  • EKG
  • Respiratory
  • Movement
  • EDR/sweating
  • Subjects instruction and online monitoring
  • Instrumental noise
  • Flicker noise (DC recordings!)
  • EMI wireless or line noise
  • electrode noise
  • amplifier noise
  • Sway of the cable
  • Electrodes poorly attached (pop)
  • Amplifier blocking
  • Shielding and guarding

40
Interferences
  • A cell phone

41
Interferences
  • Poor contact / Electrode pop

42
Interferences
  • 60 Hz

43
E. Constraints for experimental protocols in EEG
44
Protocols
  • Paradigms
  • Evoked response
  • Steady-state paradigms
  • A single source of variation between conditions
    All other things being equal
  • A good Stimulation/recording coupling time
    accuracy in analog and digital stimuli/triggers
  • Subject screening
  • Day-before instruction
  • Accepting or rejecting a volunteer
  • artifacts instruction, task instructions,
  • Online monitoring of data quality and management
    of breaks

45
F. Configuration of EEG recording system and
selection of montage
46
Configuration
  • Configuration of data recorder (scan-acquire
    mode)
  • Sampling frequency
  • DC/AC recording (DC and EDR resident on the skin
    DC and choice of electrodes)
  • Triggers
  • Selection of montage
  • Only referential recording
  • Reference electrodes
  • Ground electrode
  • Ancillary recording (EOG, surface EMG, EKG)

47
Montage 10 percent
48
Montage equidistant (eg. EGI)
49
Montage 128 NSL
50
Montage reference
  • Choice of the reference electrode
  • Cephalic/non cephalic
  • Well-attached
  • Single electrode or pair of electrode
  • Pair physically or digitally linked
  • Position of the ground
  • In midline for ERL
  • Remontage

51
Next sessionpractical sessionG. Management of
connectics H. Paste-up and problem solving
during the recording session I. Digitization
J. Cleaning/decontamination  of sensitive
equipment / equipment maintenance
52
G. Management of connectics
53
Cables everywhere
  • Main cables are present in continuous
  • Cables being specific to an experiment are
    removed after each experiment

54
H. Paste-up and problem solving during the
recording session
55
Transduction
  • Practical recommendation
  • Do not mix electrodes metal
  • Do not mix gels
  • homogenous contact skin-gel-electrode

56
  • Electrodes impedance
  • Poor impedance
  • Is the electrodes surface clean (eg did I
    perforate a crust into the electrodes hole while
    injecting conductive gel?). Did I rub enough the
    scalp? Did the subject come with inadequate hair
    condition? Is the electrode filled enough?
  • Infinite impedance
  • Am I sure that theres no damage to the wires?
  • Amplifiers gain error
  • Poor signal on some electrodes

57
I. Digitization
58
J. Cleaning/decontamination  of sensitive
equipment / equipment maintenance
59
Cleaning
60
  • Cleaning
  • Equipment maintenance
  • Troubleshooting / identification of noise source
    /
  • Problem report
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