Transcript document

ECE 501 Introduction to BME
ECE 501
Dr. Hang
Part IV Bioinstrumentation
Electrocardiogram
ECE 501
Dr. Hang
Introduction
Number of deaths for leading causes of death in US (2004)*
•
•
•
•
•
•
•
•
•
•
Heart disease: 654,092
Cancer: 550,270
Stroke (cerebrovascular diseases): 150,147
Chronic lower respiratory diseases: 123,884
Accidents (unintentional injuries): 108,694
Diabetes: 72,815
Alzheimer's disease: 65,829
Influenza/Pneumonia: 61,472
Nephritis, nephrotic syndrome, and nephrosis: 42,762
Septicemia: 33,464
* http://www.cdc.gov/nchs/fastats/lcod.htm
ECE 501
Dr. Hang
Introduction
• Physiology
•Instrumentation
• Medicine
ECE 501
Dr. Hang
Physiology
What is the Heart?
•
The heart is a very specialized muscle that pumps
blood through the body, transporting oxygen, carbon
dioxide, nutrients and waste.
• The heart is located in the middle of the chest, between
the lungs. Its bottom is tipped to the left.
ECE 501
Dr. Hang
Physiology
The Heart as a Pump
• The heart is like two pumps: one pumping blood into the
body and one pumping blood out of the body.
• The heart is about as big as two clenched fists put
together.
• The heart pumps blood in beats.
ECE 501
Dr. Hang
Physiology
The Hard Work of the Heart
ECE 501
Dr. Hang
Physiology
Anatomy of the Heart
ECE 501
Dr. Hang
Physiology
Heart Chambers
• Atrium is a chamber that pumps blood into the heart.
• Ventricle is a chamber that pumps blood out of the
heart.
• The atria and the ventricles regulate blood flow by
pumping blood in and out of the heart.
ECE 501
Dr. Hang
Physiology
Heart Chambers
ECE 501
Dr. Hang
Physiology
Heart Valves
• There are four valves in the heart.
• These are unidirectional valves that allow blood flow in
only one direction.
• They prevent blood from flowing back to the chamber
that it has just left.
ECE 501
Dr. Hang
Physiology
Heart Valves
ECE 501
Dr. Hang
Physiology
Heart Valves
• The tricuspid valve and the mitral valve are also called
A-V valves, because they separate an atrium from a
ventricle.
• The pulmonary valve and the aortic valve are also called
arterial valves, because they separate a ventricle from
an artery.
ECE 501
Dr. Hang
Physiology
Arteries and Veins
• Artery is a blood vessel that delivers blood out of the
heart. The two arteries of the heart are connected to
ventricles.
• Vein is a blood vessel that delivers blood into the heart.
The two veins of the heart are connected to atria.
ECE 501
Dr. Hang
Physiology
Arteries and Veins
ECE 501
Dr. Hang
Physiology
Pulmonary Circulation
ECE 501
Dr. Hang
Physiology
Pulmonary Circulation
ECE 501
Dr. Hang
Physiology
Pulmonary Circulation
ECE 501
Dr. Hang
Physiology
Systemic Circulation
ECE 501
Dr. Hang
Physiology
Systemic Circulation
ECE 501
Dr. Hang
Physiology
Systemic Circulation
ECE 501
Dr. Hang
Physiology
Blood Vessels
ECE 501
Dr. Hang
Physiology
Diffusion
• The exchange of molecules between cells and blood
occurs at the capillary level.
• Capillaries are very small blood vessels with very
thin walls.
• Oxygen and nutrients diffuse from the blood into the
cell and carbon dioxide and waste diffuse from the
cell into the blood.
ECE 501
Dr. Hang
Physiology
The Cardiac Cycle: Phase I
ECE 501
Dr. Hang
Physiology
The Cardiac Cycle: Phase II
ECE 501
Dr. Hang
Physiology
The Cardiac Cycle: Phase III
ECE 501
Dr. Hang
Physiology
The Cardiac Cycle: Phase IV
ECE 501
Dr. Hang
Physiology
The Cardiac Cycle: Phase V
ECE 501
Dr. Hang
Physiology
The Cardiac Cycle: Phase VI
ECE 501
Dr. Hang
Physiology
The Cardiac Cycle: Phase VII
ECE 501
Dr. Hang
Physiology
Muscle Types: Skeletal Muscle
– Fast-twitching
– Voluntary control
– Gets tired
– Arms, legs etc.
ECE 501
Dr. Hang
Physiology
Muscle Types: Smooth Muscle
– Slow-twitching
– Involuntary control
– Does not get tired
– Stomach, bladder, blood vessels etc.
ECE 501
Dr. Hang
Physiology
Resting Membrane Potential
ECE 501
Dr. Hang
Physiology
Resting Membrane Potential
Goldman Equation
RT  PK [ K ]o  PNa [ Na]o  PCl [Cl ]i 
ln 

F  PK [ K ]i  PNa [ Na]i  PCl [Cl ]o 
PK : Permeabili ty coefficien t of K 
E
PNa : Permeabili ty coefficien t of Na 
PCl : Permeabili ty coefficien t of Cl 
[ K ]o : Extracellu lar concentrat ion of K 
[ Na]o : Extracellu lar concentrat ion of Na 
[Cl ]o : Extracellu lar concentrat ion of Cl 
[ K ]i : Intracellu lar concentrat ion of K 
[ Na]i : Intracellu lar concentrat ion of Na 
[Cl ]i : Intracellu lar concentrat ion of Cl 
ECE 501
Dr. Hang
Physiology
Action Potential
Once the cell is electrically stimulated (typically by an
electric current from an adjacent cell), it begins a
sequence of actions involving the influx and efflux of
multiple cations and anions that together produce the
action potential of the cell, propagating the electrical
stimulation to the cells that lie adjacent to it
ECE 501
Dr. Hang
Physiology
Action Potential: Phase 4
Phase 4 is the resting membrane potential. This is the
period that the cell remains in until it is stimulated by
an external electrical stimulus (typically an adjacent
cell).
ECE 501
Dr. Hang
Physiology
Action Potential: Phase 0
Phase 0 is the rapid depolarization phase. The slope
of phase 0 is determined by the maximum rate of
depolarization of the cell and is known. This phase is
due to opening of the fast Na+ channels and the
subsequent rapid increase in the membrane
conductance to Na+ and a rapid influx of ionic current
in the form of Na+ ions into the cell.
ECE 501
Dr. Hang
Physiology
Action Potential: Phase 1
Phase 1 of the action potential occurs with the closure
of the fast Na+ channels. The transient net outward
current causing the small downward deflection of the
action potential is due to the movement of K+ and Clions.
ECE 501
Dr. Hang
Physiology
Action Potential: Phase 2
This "plateau" phase of the cardiac action potential is
sustained by a balance between inward movement of
Ca2+ through calcium channels and outward
movement of K+ through the potassium channels
ECE 501
Dr. Hang
Physiology
Action Potential: Phase 3
During phase 3 of the action potential, the Ca2+
channels close, while the K+ channels are still open.
This ensures a net outward current, corresponding to
negative change in membrane potential, This net
outward, positive current (equal to loss of positive
charge from the cell) causes the cell to repolarize.
ECE 501
Dr. Hang
Physiology
“Electrical Circuit” of the Heart
ECE 501
Dr. Hang
Physiology
The S-A node
• The S-A Node is the most important element in the
electrical circuit of the heart.
• It starts the cardiac cycle by periodically generating
action potentials without any external stimulation.
(Therefore, it is said to be autorhythmic.)
• It is also known as the pacemaker of the heart.
ECE 501
Dr. Hang
Physiology
The A-V node
• The atrioventricular node periodically receives action
potentials via the junctional fibers.
• The most important function of the A-V node is to
regulate the timing of the ventricular contraction by
delaying the action potentials.
• The delayed action potentials are spread over the
ventricles to cause a contraction
ECE 501
Dr. Hang
Physiology
The Electrical Cycle
ECE 501
Dr. Hang
Physiology
The Electrical Cycle
ECE 501
Dr. Hang
Physiology
The Electrocardiogram
• The electrocardiogram (ECG) is a standardized
way to measure and display the electrical
activity of the heart.
• Physicians can diagnose problems with the
heart by analyzing its ECG and comparing it to
the ECG of a healthy heart.
ECE 501
Dr. Hang
Physiology
ECG Waves
ECE 501
Dr. Hang
Physiology
ECG Intervals
ECE 501
Dr. Hang