a. intro & ecg · biomedical instrumentation b18/bme2 vital signs monitoring clinical need...
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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 [email protected] 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
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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
P2 RA
LL RL
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
LL RL
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 + Advd Ad & 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
212
'
1
'
2
1
1
22
1
2'
2
2
1
21
1
2'
1
2
'
22
1
21
2
1
'
1
R
Rvvvv
vR
Rv
R
Rv
vR
Rv
R
Rv
R
vv
R
vv
R
vvi
1
221
R
R
.
Ad1 =
Biomedical Instrumentation B18/BME2
Ad1 =
)2
1)((
)1(
)1(
1
212
'
1
'
2
1
1
22
1
2'
2
2
1
21
1
2'
1
2
'
22
1
21
2
1
'
1
R
Rvvvv
vR
Rv
R
Rv
vR
Rv
R
Rv
R
vv
R
vv
R
vvi
When v1 = v2 = vcm, Acm = 1
Three Op-Amp Differential Amplifier
Biomedical Instrumentation B18/BME2
Ad1 =
)2
1)((
)1(
)1(
1
212
'
1
'
2
1
1
22
1
2'
2
2
1
21
1
2'
1
2
'
22
1
21
2
1
'
1
R
Rvvvv
vR
Rv
R
Rv
vR
Rv
R
Rv
R
vv
R
vv
R
vvi
21
21
cmcm
dd
A.A
A.ACMRR =
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
LL RL
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
LL RL
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…