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Biomedical Instrumentation B18/BME2
Biomedical
Instrumentation
A. Intro & ECG
B18/BME2
Dr Gari Clifford
(Based on slides from
Prof. Lionel Tarassenko)
Biomedical Instrumentation B18/BME2
Who am I?
 UL in Biomed Eng
 Dir CDT in Healthcare Innovation @ IBME
 Signal Processing & Machine Learning for
Clinical Diagnostics
 mHealth for Developing Countries
 Low Cost Electronics
 EWH / OxCAHT
Biomedical Instrumentation B18/BME2
Vital signs monitoring
Clinical need
 Every day, people die unnecessarily in hospitals
 20,000 unscheduled admissions to Intensive Care p.a.
 23,000 avoidable in-hospital cardiac arrests per annum
 Between 5% and 24% of patients with an unexpected
cardiac arrest survive to discharge
 Vital sign abnormalities observed up to 8 hours
beforehand in >50% of cases
Biomedical Instrumentation B18/BME2
Identifying at-risk patients
 Acutely ill patients in hospital (e.g. in the Emergency Dept)
have their vital signs (heart rate, breathing rate, oxygen
levels, temperature, blood pressure) continuously monitored
but…
 Patient monitors generate very high numbers of false alerts
(e.g. 86-95% of alarms - MIT studies in ‘97 & ‘06)
 Nursing staff mostly ignore alarms from monitors (“alarm
noise”), apart from the apnoea alarm, and tend to focus
instead on checking the vital signs at the time of the 4-hourly
observations
Biomedical Instrumentation B18/BME2
Continuous bedside monitoring in
Emergency Department
Biomedical Instrumentation B18/BME2
Course Overview
1. The Electrocardiogram (ECG)
2. The Electroencephalogram (EEG)
3. Respiration measurement using Electrical Impedance
Plethysmography/Pneumography
4. Oxygen Saturation using Pulse Oximetry
5. Non-invasive Blood Pressure
Biomedical Instrumentation B18/BME2
Course text books
 Biomedical Engineering Handbook, Volume I,
2nd Edition, by Joseph D. Bronzino (Editor),
December 1999, ISBN: 0-849-30461-X
 Medical Instrumentation: Application and
Design, 3rd Edition, by John G. Webster
(Editor), December 1997, ISBN: 0-471-15368-0
Biomedical Instrumentation B18/BME2
Relevant lecture notes
 OP-AMP CIRCUITS – Year 1, pages 1 to 42
 FILTER CIRCUITS – Year 1, pages 1 to 15
 INSTRUMENTATION – Year 2, pages 1 to 4, 17-18, 22
to 28 and 38 to 52.
 Please e-mail val.mitchell@eng.ox.ac.uk if you would
like copies of the above.
 Course website:
http://www.robots.ox.ac.uk/~gari/teaching/b18/
Biomedical Instrumentation B18/BME2
Quick Vote
 Do you want all these lectures printed out
each day?
(You can use
laptops etc to
take notes,
just don’t
check your
email.)
Biomedical Instrumentation B18/BME2
ToDo (for you)
 Sign up on weblearn for revision sessions
(15 max per session)
 B18 (Undergrad)
 Question sheet 1: three sessions, 9 a.m. - noon on Friday of
Week 7, in LR4
 Question sheet 2: three sessions 9 a.m. - noon on Friday of
Week 8, in LR4
 MSc:
 Question sheet 1: a single session for all students, 3 - 5 p.m.
on Friday of Week 7, in LR3
 Question sheet 2: a single session for all students, 3 - 5 p.m.
on Friday of Week 8, in LR3
Hand in sheets before hand!
Biomedical Instrumentation B18/BME2
Biomedical
Instrumentation
1. The Electrocardiogram
(ECG)
Biomedical Instrumentation B18/BME2
The Electrocardiogram
 If two surface electrodes are attached to
the upper body (thorax), the following
electrical signal will be observed:
 This is the electrocardiogram or ECG
Biomedical Instrumentation B18/BME2
The origin of the ECG
 Atrial and ventricular contractions are the result
of carefully timed depolarisations of the cardiac
muscle cells
• The timing of the heart cycle depends on:
 Stimulus from the pacemaker cells
 Propagation between muscle cells
 Non-excitable cells
 Specialised conducting cells (Atrio-Ventricular Node)
Biomedical Instrumentation B18/BME2
Important specific structures
 Sino-atrial node = pacemaker (usually)
 Atria
 After electrical excitation: contraction
 Atrioventricular node (a tactical pause)
 Ventricular conducting fibers (freeways)
 Ventricular myocardium (surface roads)
 After electrical excitation: contraction
Biomedical Instrumentation B18/BME2
Excitation of the Heart
Biomedical Instrumentation B18/BME2
Excitation of the Heart
Biomedical Instrumentation B18/BME2
Cardiac Electrical Activity
 Putting it al together:
Biomedical Instrumentation B18/BME2
Approximate model of ECG
 To a first approximation, the
heart can be considered to
be an electrical generator.
 This generator drives (ionic)
currents into the upper body
(the thorax) which can be
considered to be a passive,
resistive medium
 Different potentials will be
measured at different points
on the surface of the body
Biomedical Instrumentation B18/BME2
Recording the ECG
Points P1 and P2 are arbitrary observation points on the torso;
RP is the resistance between them, and RT1 , RT2 are lumped
thoracic medium resistances.
.
P1
P2RA
LLRL
LA
P1
P2
RT1
RT2
RP
Biomedical Instrumentation B18/BME2
Typical ECG signal
Biomedical Instrumentation B18/BME2
Components of the ECG waveform
• P-wave: a small low-voltage deflection caused by the
depolarisation of the atria prior to atrial contraction.
• QRS complex: the largest-amplitude portion of the ECG,
caused by currents generated when the ventricles depolarise
prior to their contraction.
Biomedical Instrumentation B18/BME2
Components of the ECG waveform
• T-wave: ventricular repolarisation.
• P-Q interval: the time interval between the beginning of the P
wave and the beginning of the QRS complex.
• Q-T interval: characterises ventricular repolarisation.
Biomedical Instrumentation B18/BME2
Recording the ECG
 To record the ECG we need a transducer capable of
converting the ionic potentials generated within the
body into electronic potentials
 Such a transducer is a pair of electrodes and are:
 Polarisable (which behave as capacitors)
 Non-polarisable (which behave as resistors)
 Both; common electrodes lie between these two extremes
 The electrode most commonly used for ECG signals,
the silver-silver chloride electrode, is closer to a non-
polarisable electrode.
Biomedical Instrumentation B18/BME2
Silver-silver chloride electrode
 Electrodes are usually metal discs and a salt of that
metal.
 A paste is applied between the electrode and the skin.
 This results in a local solution of the metal in the paste at
the electrode-skin interface. Some of the silver dissolves
into solution producing Ag+ ions:
 Ag → Ag+ + e-
 Ionic equilibrium takes place when the electrical field is
balanced by the concentration gradient and a layer of
Ag+ ions is adjacent to a layer of Cl- ions.
Biomedical Instrumentation B18/BME2
Electrode-electrolyte interface
Illustrative diagram of electrode-electrolyte interface in case of Ag-AgCl electrode
Electrode
Gel
Ag
e-
Ag Ag
e-
Ag
Ag+
Cl-
Ag+
Ag+
Cl-
Cl-
e-
Cl-
Ag+
Current I
Biomedical Instrumentation B18/BME2
Silver-silver chloride electrode
 Electrodes are usually metal discs and a salt of that metal.
 A paste is applied between the electrode and the skin.
 This results in a local solution of the metal in the paste at
the electrode-skin interface.
 Ionic equilibrium takes place when the electrical field is
balanced by the concentration gradient and a layer of Ag+
ions is adjacent to a layer of Cl- ions.
 This gives a potential drop E called the half-cell potential
(normally 0.8 V for an Ag-AgCl electrode)
Biomedical Instrumentation B18/BME2
Silver-silver chloride electrode
 The double layer of charges also has
a capacitive effect.
 Since the Ag-AgCl electrode is
primarily non-polarisable, there is a
large resistive effect.
 This gives a simple model for the
electrode.
 However, the impedance is not infinite
at d.c. and so a resistor must be
added in parallel with the capacitor.
Electrode
Gel
Skin
Ag → Ag+ + e-
Ag+ Ag+ Ag+ Ag+ Ag+ Ag+ Ag+
Cl- Cl- Cl- Cl- Cl- Cl- Cl-
Biomedical Instrumentation B18/BME2
Silver-silver chloride electrode
 The double layer of charges also has
a capacitive effect.
 Since the Ag-AgCl electrode is
primarily non-polarisable, there is a
large resistive effect.
 This gives a simple model for the
electrode.
 However, the impedance is not infinite
at d.c. and so a resistor must be
added in parallel with the capacitor.
Biomedical Instrumentation B18/BME2
The Overall Model
 The resistors and capacitors may not be exactly equal.
 Half cell potentials E and E' should be very similar.
 Hence V should represent the actual difference of ionic
potential between the two points on the body where the
electrodes have been placed.
Biomedical Instrumentation B18/BME2
Electrode placement
VI = (potential at LA) – (potential at RA)
VII = (potential at LL) – (potential at RA)
VIII = (potential at LL) – (potential at LA)
The right leg is usually grounded (but see later)
Biomedical Instrumentation B18/BME2
ECG Amplification
 Problems in ECG amplification
 The signal is small (typical ECG peak
value ~1mV) so amplification is needed
 Interference is usually larger amplitude
than the signal itself
Biomedical Instrumentation B18/BME2
1st Problem: Electric Field Interference
 Capacitance between power lines and
system couples current into the patient
 This capacitance varies but it is of the order
of 50pF (this corresponds to 64MΩ at 50Hz
... recall Xc=1/C )
 If the right leg is connected to the common
ground of the amplifier with a contact
impedance of 5kΩ, the mains potential will
appear as a ~20mV noise input.
RA
LLRL
LA
Electrical power system
50 pF
5kΩ
the 50 Hz interference is common to
both measuring electrodes !
(common mode signals)
Biomedical Instrumentation B18/BME2
The solution
 The ECG is measured as a differential signal.
 The 50Hz noise, however, is common to all the
electrodes.
 It appears equally at the Right Arm and Left Arm
terminals.
 Rejection therefore depends on the use of a
differential amplifier in the input stage of the
ECG machine.
 The amount of rejection depends on the ability
of the amplifier to reject common-mode voltages.
Biomedical Instrumentation B18/BME2
Common Mode Rejection Ratio
(CMRR)
CMRR = Ad / Acm
(ratio of differential gain to
common mode gain)
vin= vcm+ vd vout= Acmvcm + AdvdAd & Acm
Biomedical Instrumentation B18/BME2
Three Op-Amp Differential Amplifier
Biomedical Instrumentation B18/BME2
Three Op-Amp Differential Amplifier
Ad1 =
)
2
1)((
)1(
)1(
1
2
12
'
1
'
2
1
1
2
2
1
2'
2
2
1
2
1
1
2'
1
2
'
22
1
21
2
1
'
1
R
R
vvvv
v
R
R
v
R
R
v
v
R
R
v
R
R
v
R
vv
R
vv
R
vv
i









1
22
1
R
R

.
Ad1 =
Biomedical Instrumentation B18/BME2
Ad1 =
)
2
1)((
)1(
)1(
1
2
12
'
1
'
2
1
1
2
2
1
2'
2
2
1
2
1
1
2'
1
2
'
22
1
21
2
1
'
1
R
R
vvvv
v
R
R
v
R
R
v
v
R
R
v
R
R
v
R
vv
R
vv
R
vv
i









When v1 = v2 = vcm, Acm = 1
Three Op-Amp Differential Amplifier
Biomedical Instrumentation B18/BME2
Ad1 =
)
2
1)((
)1(
)1(
1
2
12
'
1
'
2
1
1
2
2
1
2'
2
2
1
2
1
1
2'
1
2
'
22
1
21
2
1
'
1
R
R
vvvv
v
R
R
v
R
R
v
v
R
R
v
R
R
v
R
vv
R
vv
R
vv
i









21
21
cmcm
dd
A.A
A.A
CMRR =
Three Op-Amp Differential Amplifier
CMRR is product of CMRR
for each input amplifier
Biomedical Instrumentation B18/BME2
2nd problem: Magnetic Induction
 Current in magnetic fields
induces voltage in the loop
formed by patient leads
RA
LLRL
LA
 The solution is to minimise
the coil area (e.g. by twisting
the lead wires together)
Biomedical Instrumentation B18/BME2
3rd problem:
Source impedance unbalance
 If the contact impedances are not balanced (i.e. the
same), then the body’s common-mode voltage will be
higher at one input to the amplifier than the other.
Biomedical Instrumentation B18/BME2
3rd problem:
Source impedance unbalance
 If the contact impedances are not balanced (i.e. the
same), then the body’s common-mode voltage will be
higher at one input to the amplifier than the other.
 Hence, a fraction of the common-mode voltage will be
seen as a differential signal.
 see problem on example sheet
Biomedical Instrumentation B18/BME2
Summary
 Output from the differential amplifier consists of
three components:
 The desired output (ECG)
 Unwanted common-mode signal because the
common-mode rejection is not infinite
 Unwanted component of common-mode signal
(appearing as pseudo-differential signal at the input)
due to contact impedance imbalance
Biomedical Instrumentation B18/BME2
 The common-mode voltage can be
controlled using a Driven right-leg circuit.
 A small current (<1µA) is injected into the
patient to equal the displacement currents
flowing in the body.
Driven right-leg circuitry
Biomedical Instrumentation B18/BME2
Driven right-leg circuitry
RA
LLRL
LA
RA
RL
+
-
-
+
A1
A2
LA
R2
R2
R1
-
+
A4
Ra
Ra
R0
Biomedical Instrumentation B18/BME2
Driven right-leg circuitry
Biomedical Instrumentation B18/BME2
 The common-mode voltage can be controlled using
a Driven right-leg circuit.
 A small current (<1µA) is injected into the patient to
equal the displacement currents flowing in the body.
 The body acts as a summing junction in a feedback
loop and the common-mode voltage is driven to a
low value.
 This also improves patient safety (R0 is v. large –
see notes).
Driven right-leg circuitry
Biomedical Instrumentation B18/BME2
Other patient protection
 (Defib Protection)
 Isolation
 Filtering
 Amplification
 Anti-alias filtering
 Digitization
Biomedical Instrumentation B18/BME2
Static defibrillation protection
 For use in medical situations, the ECG
must be able to recover from a 5kV, 100A
impulse (defibrillation)
 Use large inductors and diodes
Biomedical Instrumentation B18/BME2
Patient Isolation
 Opto-isolators
 DC-DC
Converters
Biomedical Instrumentation B18/BME2
RF Shielding & Emissions
 Electromagnetic compatibility (EMC)
 the ability of a device to function (a) properly in its intended electromagnetic environment,
and (b) without introducing excessive EM energy that may interfere with other devices
 Electromagnetic disturbance (EMD)
 any EM phenomenon that may degrade the performance of equipment, such as medical
devices or any electronic equipment. Examples include power line voltage dips and
interruptions, electrical fast transients (EFTs), electromagnetic fields (radiated emissions),
electrostatic discharges, and conducted emissions
 Electromagnetic interference (EMI)
 degradation of the performance of a piece of equipment, transmission channel, or system
(such as medical devices) caused by an electromagnetic disturbance
 Electrostatic discharge (ESD)
 the rapid transfer of electrostatic charge between bodies of different electrostatic potential,
either in proximity in air (air discharge) or through direct contact (contact discharge)
 Emissions
 electromagnetic energy emanating from a device generally falling into two categories:
conducted and radiated. Both categories of emission may occur simultaneously, depending
on the configuration of the device
Biomedical Instrumentation B18/BME2
Testing
Biomedical Instrumentation B18/BME2
Physiological effects of electricity:
 Electrolysis
 Neural stimulation
 Tissue heating
Electrical safety
(from Lecture B)
Biomedical Instrumentation B18/BME2
Electrolysis
 Electrolysis takes place when direct current
passes through tissue.
 Ulcers can be developed, for example if a
d.c. current of 0.1 mA is applied to the skin
for a few minutes.
 IEC601 limits the direct current (< 0.1 Hz)
that is allowed to flow between a pair of
electrodes to 10 μA.
Biomedical Instrumentation B18/BME2
 An action potential occurs if the normal
potential difference across a nerve
membrane is reversed for a certain
period of time.
 This results in a sensation of pain (if
sensory nerve has been stimulated) or
muscle contraction (if motor nerve has
been simulated).
Neural stimulation
Biomedical Instrumentation B18/BME2
Hazards of neural stimulation
• The effects of neural stimulation depend on the amplitude
and frequency of the current, as well as the location of the
current injection.
 If the current is injected through the skin, 75 mA – 400 mA
at 50 Hz can cause ventricular fibrillation.
Beware: under normal (dry) conditions, the impedance of the skin
at 50 Hz is usually between 10 kΩ and 100 kΩ; if the skin is wet,
the impedance can be 1 kΩ or less.
 If the current is directly applied to the heart wall (e.g. failure
of circuitry in a cardiac catheter), 100μA can cause
ventricular fibrillation.
Biomedical Instrumentation B18/BME2
Tissue heating
 The major effect of high-frequency
(> 10 kHz) electrical currents is heating.
 The local effect depends on the current
amplitude and frequency as well as the
length of exposure.
 Think about your mobile phone usage…
Biomedical Instrumentation B18/BME2
Electricity can also be good for you…
 Electrical shock is also applied to patients in
clinical practice for therapeutic purposes.
 These applications make use of the neural
stimulation effect:
 Pacemakers (to stimulate the heart)
 Defibrillators (to stop ventricular fibrillation)
 Implantable Stimulators for Neuromuscular Control
(to help paralysed patients regain some neuromuscular
control).
Biomedical Instrumentation B18/BME2
Electricity can also be good for you…

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Bio Medical Lecture

  • 1. Biomedical Instrumentation B18/BME2 Biomedical Instrumentation A. Intro & ECG B18/BME2 Dr Gari Clifford (Based on slides from Prof. Lionel Tarassenko)
  • 2. Biomedical Instrumentation B18/BME2 Who am I?  UL in Biomed Eng  Dir CDT in Healthcare Innovation @ IBME  Signal Processing & Machine Learning for Clinical Diagnostics  mHealth for Developing Countries  Low Cost Electronics  EWH / OxCAHT
  • 3. Biomedical Instrumentation B18/BME2 Vital signs monitoring Clinical need  Every day, people die unnecessarily in hospitals  20,000 unscheduled admissions to Intensive Care p.a.  23,000 avoidable in-hospital cardiac arrests per annum  Between 5% and 24% of patients with an unexpected cardiac arrest survive to discharge  Vital sign abnormalities observed up to 8 hours beforehand in >50% of cases
  • 4. Biomedical Instrumentation B18/BME2 Identifying at-risk patients  Acutely ill patients in hospital (e.g. in the Emergency Dept) have their vital signs (heart rate, breathing rate, oxygen levels, temperature, blood pressure) continuously monitored but…  Patient monitors generate very high numbers of false alerts (e.g. 86-95% of alarms - MIT studies in ‘97 & ‘06)  Nursing staff mostly ignore alarms from monitors (“alarm noise”), apart from the apnoea alarm, and tend to focus instead on checking the vital signs at the time of the 4-hourly observations
  • 5. Biomedical Instrumentation B18/BME2 Continuous bedside monitoring in Emergency Department
  • 6. Biomedical Instrumentation B18/BME2 Course Overview 1. The Electrocardiogram (ECG) 2. The Electroencephalogram (EEG) 3. Respiration measurement using Electrical Impedance Plethysmography/Pneumography 4. Oxygen Saturation using Pulse Oximetry 5. Non-invasive Blood Pressure
  • 7. Biomedical Instrumentation B18/BME2 Course text books  Biomedical Engineering Handbook, Volume I, 2nd Edition, by Joseph D. Bronzino (Editor), December 1999, ISBN: 0-849-30461-X  Medical Instrumentation: Application and Design, 3rd Edition, by John G. Webster (Editor), December 1997, ISBN: 0-471-15368-0
  • 8. Biomedical Instrumentation B18/BME2 Relevant lecture notes  OP-AMP CIRCUITS – Year 1, pages 1 to 42  FILTER CIRCUITS – Year 1, pages 1 to 15  INSTRUMENTATION – Year 2, pages 1 to 4, 17-18, 22 to 28 and 38 to 52.  Please e-mail val.mitchell@eng.ox.ac.uk if you would like copies of the above.  Course website: http://www.robots.ox.ac.uk/~gari/teaching/b18/
  • 9. Biomedical Instrumentation B18/BME2 Quick Vote  Do you want all these lectures printed out each day? (You can use laptops etc to take notes, just don’t check your email.)
  • 10. Biomedical Instrumentation B18/BME2 ToDo (for you)  Sign up on weblearn for revision sessions (15 max per session)  B18 (Undergrad)  Question sheet 1: three sessions, 9 a.m. - noon on Friday of Week 7, in LR4  Question sheet 2: three sessions 9 a.m. - noon on Friday of Week 8, in LR4  MSc:  Question sheet 1: a single session for all students, 3 - 5 p.m. on Friday of Week 7, in LR3  Question sheet 2: a single session for all students, 3 - 5 p.m. on Friday of Week 8, in LR3 Hand in sheets before hand!
  • 12. Biomedical Instrumentation B18/BME2 The Electrocardiogram  If two surface electrodes are attached to the upper body (thorax), the following electrical signal will be observed:  This is the electrocardiogram or ECG
  • 13. Biomedical Instrumentation B18/BME2 The origin of the ECG  Atrial and ventricular contractions are the result of carefully timed depolarisations of the cardiac muscle cells • The timing of the heart cycle depends on:  Stimulus from the pacemaker cells  Propagation between muscle cells  Non-excitable cells  Specialised conducting cells (Atrio-Ventricular Node)
  • 14. Biomedical Instrumentation B18/BME2 Important specific structures  Sino-atrial node = pacemaker (usually)  Atria  After electrical excitation: contraction  Atrioventricular node (a tactical pause)  Ventricular conducting fibers (freeways)  Ventricular myocardium (surface roads)  After electrical excitation: contraction
  • 17. Biomedical Instrumentation B18/BME2 Cardiac Electrical Activity  Putting it al together:
  • 18. Biomedical Instrumentation B18/BME2 Approximate model of ECG  To a first approximation, the heart can be considered to be an electrical generator.  This generator drives (ionic) currents into the upper body (the thorax) which can be considered to be a passive, resistive medium  Different potentials will be measured at different points on the surface of the body
  • 19. Biomedical Instrumentation B18/BME2 Recording the ECG Points P1 and P2 are arbitrary observation points on the torso; RP is the resistance between them, and RT1 , RT2 are lumped thoracic medium resistances. . P1 P2RA LLRL LA P1 P2 RT1 RT2 RP
  • 21. Biomedical Instrumentation B18/BME2 Components of the ECG waveform • P-wave: a small low-voltage deflection caused by the depolarisation of the atria prior to atrial contraction. • QRS complex: the largest-amplitude portion of the ECG, caused by currents generated when the ventricles depolarise prior to their contraction.
  • 22. Biomedical Instrumentation B18/BME2 Components of the ECG waveform • T-wave: ventricular repolarisation. • P-Q interval: the time interval between the beginning of the P wave and the beginning of the QRS complex. • Q-T interval: characterises ventricular repolarisation.
  • 23. Biomedical Instrumentation B18/BME2 Recording the ECG  To record the ECG we need a transducer capable of converting the ionic potentials generated within the body into electronic potentials  Such a transducer is a pair of electrodes and are:  Polarisable (which behave as capacitors)  Non-polarisable (which behave as resistors)  Both; common electrodes lie between these two extremes  The electrode most commonly used for ECG signals, the silver-silver chloride electrode, is closer to a non- polarisable electrode.
  • 24. Biomedical Instrumentation B18/BME2 Silver-silver chloride electrode  Electrodes are usually metal discs and a salt of that metal.  A paste is applied between the electrode and the skin.  This results in a local solution of the metal in the paste at the electrode-skin interface. Some of the silver dissolves into solution producing Ag+ ions:  Ag → Ag+ + e-  Ionic equilibrium takes place when the electrical field is balanced by the concentration gradient and a layer of Ag+ ions is adjacent to a layer of Cl- ions.
  • 25. Biomedical Instrumentation B18/BME2 Electrode-electrolyte interface Illustrative diagram of electrode-electrolyte interface in case of Ag-AgCl electrode Electrode Gel Ag e- Ag Ag e- Ag Ag+ Cl- Ag+ Ag+ Cl- Cl- e- Cl- Ag+ Current I
  • 26. Biomedical Instrumentation B18/BME2 Silver-silver chloride electrode  Electrodes are usually metal discs and a salt of that metal.  A paste is applied between the electrode and the skin.  This results in a local solution of the metal in the paste at the electrode-skin interface.  Ionic equilibrium takes place when the electrical field is balanced by the concentration gradient and a layer of Ag+ ions is adjacent to a layer of Cl- ions.  This gives a potential drop E called the half-cell potential (normally 0.8 V for an Ag-AgCl electrode)
  • 27. Biomedical Instrumentation B18/BME2 Silver-silver chloride electrode  The double layer of charges also has a capacitive effect.  Since the Ag-AgCl electrode is primarily non-polarisable, there is a large resistive effect.  This gives a simple model for the electrode.  However, the impedance is not infinite at d.c. and so a resistor must be added in parallel with the capacitor. Electrode Gel Skin Ag → Ag+ + e- Ag+ Ag+ Ag+ Ag+ Ag+ Ag+ Ag+ Cl- Cl- Cl- Cl- Cl- Cl- Cl-
  • 28. Biomedical Instrumentation B18/BME2 Silver-silver chloride electrode  The double layer of charges also has a capacitive effect.  Since the Ag-AgCl electrode is primarily non-polarisable, there is a large resistive effect.  This gives a simple model for the electrode.  However, the impedance is not infinite at d.c. and so a resistor must be added in parallel with the capacitor.
  • 29. Biomedical Instrumentation B18/BME2 The Overall Model  The resistors and capacitors may not be exactly equal.  Half cell potentials E and E' should be very similar.  Hence V should represent the actual difference of ionic potential between the two points on the body where the electrodes have been placed.
  • 30. Biomedical Instrumentation B18/BME2 Electrode placement VI = (potential at LA) – (potential at RA) VII = (potential at LL) – (potential at RA) VIII = (potential at LL) – (potential at LA) The right leg is usually grounded (but see later)
  • 31. Biomedical Instrumentation B18/BME2 ECG Amplification  Problems in ECG amplification  The signal is small (typical ECG peak value ~1mV) so amplification is needed  Interference is usually larger amplitude than the signal itself
  • 32. Biomedical Instrumentation B18/BME2 1st Problem: Electric Field Interference  Capacitance between power lines and system couples current into the patient  This capacitance varies but it is of the order of 50pF (this corresponds to 64MΩ at 50Hz ... recall Xc=1/C )  If the right leg is connected to the common ground of the amplifier with a contact impedance of 5kΩ, the mains potential will appear as a ~20mV noise input. RA LLRL LA Electrical power system 50 pF 5kΩ the 50 Hz interference is common to both measuring electrodes ! (common mode signals)
  • 33. Biomedical Instrumentation B18/BME2 The solution  The ECG is measured as a differential signal.  The 50Hz noise, however, is common to all the electrodes.  It appears equally at the Right Arm and Left Arm terminals.  Rejection therefore depends on the use of a differential amplifier in the input stage of the ECG machine.  The amount of rejection depends on the ability of the amplifier to reject common-mode voltages.
  • 34. Biomedical Instrumentation B18/BME2 Common Mode Rejection Ratio (CMRR) CMRR = Ad / Acm (ratio of differential gain to common mode gain) vin= vcm+ vd vout= Acmvcm + AdvdAd & Acm
  • 35. Biomedical Instrumentation B18/BME2 Three Op-Amp Differential Amplifier
  • 36. Biomedical Instrumentation B18/BME2 Three Op-Amp Differential Amplifier Ad1 = ) 2 1)(( )1( )1( 1 2 12 ' 1 ' 2 1 1 2 2 1 2' 2 2 1 2 1 1 2' 1 2 ' 22 1 21 2 1 ' 1 R R vvvv v R R v R R v v R R v R R v R vv R vv R vv i          1 22 1 R R  . Ad1 =
  • 37. Biomedical Instrumentation B18/BME2 Ad1 = ) 2 1)(( )1( )1( 1 2 12 ' 1 ' 2 1 1 2 2 1 2' 2 2 1 2 1 1 2' 1 2 ' 22 1 21 2 1 ' 1 R R vvvv v R R v R R v v R R v R R v R vv R vv R vv i          When v1 = v2 = vcm, Acm = 1 Three Op-Amp Differential Amplifier
  • 38. Biomedical Instrumentation B18/BME2 Ad1 = ) 2 1)(( )1( )1( 1 2 12 ' 1 ' 2 1 1 2 2 1 2' 2 2 1 2 1 1 2' 1 2 ' 22 1 21 2 1 ' 1 R R vvvv v R R v R R v v R R v R R v R vv R vv R vv i          21 21 cmcm dd A.A A.A CMRR = Three Op-Amp Differential Amplifier CMRR is product of CMRR for each input amplifier
  • 39. Biomedical Instrumentation B18/BME2 2nd problem: Magnetic Induction  Current in magnetic fields induces voltage in the loop formed by patient leads RA LLRL LA  The solution is to minimise the coil area (e.g. by twisting the lead wires together)
  • 40. Biomedical Instrumentation B18/BME2 3rd problem: Source impedance unbalance  If the contact impedances are not balanced (i.e. the same), then the body’s common-mode voltage will be higher at one input to the amplifier than the other.
  • 41. Biomedical Instrumentation B18/BME2 3rd problem: Source impedance unbalance  If the contact impedances are not balanced (i.e. the same), then the body’s common-mode voltage will be higher at one input to the amplifier than the other.  Hence, a fraction of the common-mode voltage will be seen as a differential signal.  see problem on example sheet
  • 42. Biomedical Instrumentation B18/BME2 Summary  Output from the differential amplifier consists of three components:  The desired output (ECG)  Unwanted common-mode signal because the common-mode rejection is not infinite  Unwanted component of common-mode signal (appearing as pseudo-differential signal at the input) due to contact impedance imbalance
  • 43. Biomedical Instrumentation B18/BME2  The common-mode voltage can be controlled using a Driven right-leg circuit.  A small current (<1µA) is injected into the patient to equal the displacement currents flowing in the body. Driven right-leg circuitry
  • 44. Biomedical Instrumentation B18/BME2 Driven right-leg circuitry RA LLRL LA RA RL + - - + A1 A2 LA R2 R2 R1 - + A4 Ra Ra R0
  • 46. Biomedical Instrumentation B18/BME2  The common-mode voltage can be controlled using a Driven right-leg circuit.  A small current (<1µA) is injected into the patient to equal the displacement currents flowing in the body.  The body acts as a summing junction in a feedback loop and the common-mode voltage is driven to a low value.  This also improves patient safety (R0 is v. large – see notes). Driven right-leg circuitry
  • 47. Biomedical Instrumentation B18/BME2 Other patient protection  (Defib Protection)  Isolation  Filtering  Amplification  Anti-alias filtering  Digitization
  • 48. Biomedical Instrumentation B18/BME2 Static defibrillation protection  For use in medical situations, the ECG must be able to recover from a 5kV, 100A impulse (defibrillation)  Use large inductors and diodes
  • 49. Biomedical Instrumentation B18/BME2 Patient Isolation  Opto-isolators  DC-DC Converters
  • 50. Biomedical Instrumentation B18/BME2 RF Shielding & Emissions  Electromagnetic compatibility (EMC)  the ability of a device to function (a) properly in its intended electromagnetic environment, and (b) without introducing excessive EM energy that may interfere with other devices  Electromagnetic disturbance (EMD)  any EM phenomenon that may degrade the performance of equipment, such as medical devices or any electronic equipment. Examples include power line voltage dips and interruptions, electrical fast transients (EFTs), electromagnetic fields (radiated emissions), electrostatic discharges, and conducted emissions  Electromagnetic interference (EMI)  degradation of the performance of a piece of equipment, transmission channel, or system (such as medical devices) caused by an electromagnetic disturbance  Electrostatic discharge (ESD)  the rapid transfer of electrostatic charge between bodies of different electrostatic potential, either in proximity in air (air discharge) or through direct contact (contact discharge)  Emissions  electromagnetic energy emanating from a device generally falling into two categories: conducted and radiated. Both categories of emission may occur simultaneously, depending on the configuration of the device
  • 52. Biomedical Instrumentation B18/BME2 Physiological effects of electricity:  Electrolysis  Neural stimulation  Tissue heating Electrical safety (from Lecture B)
  • 53. Biomedical Instrumentation B18/BME2 Electrolysis  Electrolysis takes place when direct current passes through tissue.  Ulcers can be developed, for example if a d.c. current of 0.1 mA is applied to the skin for a few minutes.  IEC601 limits the direct current (< 0.1 Hz) that is allowed to flow between a pair of electrodes to 10 μA.
  • 54. Biomedical Instrumentation B18/BME2  An action potential occurs if the normal potential difference across a nerve membrane is reversed for a certain period of time.  This results in a sensation of pain (if sensory nerve has been stimulated) or muscle contraction (if motor nerve has been simulated). Neural stimulation
  • 55. Biomedical Instrumentation B18/BME2 Hazards of neural stimulation • The effects of neural stimulation depend on the amplitude and frequency of the current, as well as the location of the current injection.  If the current is injected through the skin, 75 mA – 400 mA at 50 Hz can cause ventricular fibrillation. Beware: under normal (dry) conditions, the impedance of the skin at 50 Hz is usually between 10 kΩ and 100 kΩ; if the skin is wet, the impedance can be 1 kΩ or less.  If the current is directly applied to the heart wall (e.g. failure of circuitry in a cardiac catheter), 100μA can cause ventricular fibrillation.
  • 56. Biomedical Instrumentation B18/BME2 Tissue heating  The major effect of high-frequency (> 10 kHz) electrical currents is heating.  The local effect depends on the current amplitude and frequency as well as the length of exposure.  Think about your mobile phone usage…
  • 57. Biomedical Instrumentation B18/BME2 Electricity can also be good for you…  Electrical shock is also applied to patients in clinical practice for therapeutic purposes.  These applications make use of the neural stimulation effect:  Pacemakers (to stimulate the heart)  Defibrillators (to stop ventricular fibrillation)  Implantable Stimulators for Neuromuscular Control (to help paralysed patients regain some neuromuscular control).
  • 58. Biomedical Instrumentation B18/BME2 Electricity can also be good for you…