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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)

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Page 1: A. Intro & ECGgari/teaching/b18/lecture_slides/B18... · Biomedical Instrumentation B18/BME2 Vital signs monitoring Clinical need Every day, people die unnecessarily in hospitals

Biomedical Instrumentation B18/BME2

Biomedical

Instrumentation A. Intro & ECG

B18/BME2

Dr Gari Clifford

(Based on slides from

Prof. Lionel Tarassenko)

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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

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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

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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

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Biomedical Instrumentation B18/BME2

Continuous bedside monitoring in

Emergency Department

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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

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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

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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/

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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.)

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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!

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Biomedical Instrumentation B18/BME2

Biomedical

Instrumentation

1. The Electrocardiogram

(ECG)

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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

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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)

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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

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Biomedical Instrumentation B18/BME2

Excitation of the Heart

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Biomedical Instrumentation B18/BME2

Excitation of the Heart

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Biomedical Instrumentation B18/BME2

Cardiac Electrical Activity Putting it al together:

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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

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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

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Biomedical Instrumentation B18/BME2

Typical ECG signal

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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.

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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.

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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.

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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.

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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

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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)

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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-

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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.

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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.

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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)

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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

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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)

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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.

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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

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Biomedical Instrumentation B18/BME2

Three Op-Amp Differential Amplifier

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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 =

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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

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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

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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)

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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.

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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

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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

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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

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Biomedical Instrumentation B18/BME2

Driven right-leg circuitry

RA

LL RL

LA

RA

RL

+

-

-

+

A1

A2

LA

R2

R2

R1

-

+

A4

Ra

Ra

R0

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Biomedical Instrumentation B18/BME2

Driven right-leg circuitry

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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

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Biomedical Instrumentation B18/BME2

Other patient protection

(Defib Protection)

Isolation

Filtering

Amplification

Anti-alias filtering

Digitization

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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

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Biomedical Instrumentation B18/BME2

Patient Isolation

Opto-isolators

DC-DC

Converters

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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

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Biomedical Instrumentation B18/BME2

Testing

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Biomedical Instrumentation B18/BME2

Physiological effects of electricity:

Electrolysis

Neural stimulation

Tissue heating

Electrical safety (from Lecture B)

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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.

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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

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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.

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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…

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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).

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Biomedical Instrumentation B18/BME2

Electricity can also be good for you…