Instu Final Part 1
Instu Final Part 1
1. The electrical activity of the heart can be described by the movement of an electrical dipole which
consists of a positive charge and a negative charge separated by a variable distance
2. The cardiac vector is the line joining the two charges. To fully describe the cardiac vector, its
magnitude and direction must be known.
3. The electrical activity of the heart does not consist of two moving charges, but the electric field
which is the result of the depolarization and repolarization of the cardiac muscle can be
represented by the simple model of a charged dipole
v Lead I — This axis goes from shoulder to shoulder, with the negative electrode placed on the right
shoulder and the positive electrode placed on the left shoulder. This results in a 0 degree angle of
orientation. I = LA – RA
v Lead II — This axis goes from the right arm to the left leg, with the negative electrode on the shoulder and
the positive one on the leg. This results in a +60 degree angle of orientation. II = LL – RA
v Lead III — This axis goes from the left shoulder (negative electrode) to the right or left leg (positive
electrode). This results in a +120 degree angle of orientation. III = LL - LA
There are three augmented unipolar limb leads. These are termed unipolar leads because there is a single
positive electrode that is referenced against a combination of the other limb electrodes.
v The positive electrodes for these augmented leads are located on the left arm (aVL), the right arm (aVR),
and the left leg (aVF).
v In practice, these are the same electrodes used for leads I, II and III. (The ECG recorder does the actual
switching and rearranging of the electrode designations).
v The three augmented leads are depicted as shown to the figure using the axial reference system. v The
aVL lead is at -30° relative to the lead I axis; aVR is at -150° and aVF is at +90°
Figure : Driven-right-leg circuit for minimizing common-mode interference. The circuit derives common-mode
voltage from a pair of averaging resistors connected to v3 and v4 in Figure. The right leg is not grounded but is
connected to output of the auxiliary op amp.
P Wave: the depolarization being generated in and spreading through the Sinoatrial node. The SA node is too small for its depolarization
to be detected on most ECGs. The depolarization travels through the atria, towards the Atrioventricular node. The depolarization travels
through the largest amount of tissue in the atria, which creates the highest point in the P wave.
PR Segment: Depolarization travels through the AV node. Like the SA node, the AV node is too small for the depolarization of its tissue to
Q Wave: The action potential starts traveling down the left bundle branch about 5 milliseconds before it starts traveling down the right
bundle branch. This causes the depolarization of the interventricular septum tissue to spread from left to right. This gives rise to a
R Wave: Following depolarization of the interventricular septum, the depolarization travels towards the apex of the heart, which creates
the R wave.
S Wave: Then the depolarization travels throughout both ventricles from the apex of the heart, following the action potential in
the Purkinje fibers. This phenomenon creates a negative deflection in all three limb leads, forming the S wave on the ECG.
ST segment: Ventricular contraction occurs between ventricular depolarization and repolarization. During this time, there is no movement
of charge, so no deflection is created on the ECG. This results in the flat ST segment after the S wave.
T Wave: The epicardium is the first layer of the ventricles to repolarize, followed by the myocardium. The endocardium is the last layer to
repolarize. This causes repolarization to start from the apex of the heart and move upwards. This creates the T wave.
U wave: The U wave is hypothesized to be caused by the repolarization of the interventricular septum. It normally has a low amplitude,
1. **Pericardium:** The outermost layer of the heart is the pericardium, a double-walled sac that contains the heart and the roots of the great
vessels. It consists of two layers: the outer fibrous pericardium and the inner serous pericardium.
2. **Epicardium:** This is the thin, outermost layer of the heart wall. It is also known as the visceral layer of the serous pericardium. The epicardium
is composed of connective tissue and fat and serves to protect the heart.
3. **Myocardium:** The middle and thickest layer of the heart is the myocardium. It is composed of cardiac muscle cells and is responsible for the
4. **Endocardium:** The innermost layer is the endocardium, which lines the chambers of the heart and covers the heart valves. It consists of
1. **Aortic Valve:** Located between the left ventricle and the aorta, the aortic valve allows blood to flow from the left ventricle to the aorta, which
2. **Pulmonary Valve:** Situated between the right ventricle and the pulmonary artery, the pulmonary valve allows blood to be pumped from the
3. **Tricuspid Valve:** Found between the right atrium and the right ventricle, the tricuspid valve prevents the backflow of blood from the ventricle
4. **Mitral Valve:** Positioned between the left atrium and the left ventricle, the mitral valve (also known as the bicuspid valve) prevents the
13. What is action potential?? Describe cardiac and muscle Action potential
Action potential graph of heart
the cardiac action potential:
1. **Resting Membrane Potential:** Around -90 mV, maintained by potassium efflux, sodium, and calcium influx.
2. **Depolarization (Phase 0):** Rapid increase in membrane potential due to sodium influx through voltage-gated channels.
3. **Early Repolarization (Phase 1):** Brief repolarization with some potassium efflux.
4. **Plateau (Phase 2):** Sustained membrane potential near 0 mV, balanced by calcium influx and potassium efflux.
5. **Late Repolarization (Phase 3):** Potassium efflux continues, calcium channels begin to close.
6. **Restoration of Resting Membrane Potential (Phase 4):** Sodium-potassium pumps restore resting state, preparing for the next action potential.
1. **Duration and Phases:** The action potential in cardiac muscle cells is longer and more prolonged than in
skeletal muscle cells. It consists of five phases: 0, 1, 2, 3, and 4.
2. **Phase 0 (Depolarization):** Rapid depolarization occurs due to the influx of sodium ions (Na+) through
voltage-gated sodium channels. This phase is triggered by the opening of these channels when the membrane
potential reaches a certain threshold.
3. **Phase 1 (Initial Repolarization):** Brief repolarization happens due to the transient opening of potassium
channels, leading to a small outward flow of potassium ions (K+).
4. **Phase 2 (Plateau Phase):** This phase is characterized by a prolonged period of relatively stable membrane
potential. Calcium ions (Ca2+) slowly enter the cell while potassium ions continue to flow out. The balance
between these ions maintains the plateau.
5. **Phase 3 (Rapid Repolarization):** Repolarization resumes due to increased potassium ion efflux, primarily
through delayed rectifier potassium channels, leading to the restoration of the resting membrane potential.
6. **Phase 4 (Resting Potential):** The cell remains at rest until the next depolarization event. During this phase,
the membrane potential slowly drifts back to the resting state, maintained by the activity of sodium-potassium
pumps and leak channels.
1. **Duration and Phases:** Skeletal muscle action potentials are briefer and consist of only three phases:
depolarization, repolarization, and the refractory period.
2. **Depolarization:** Similar to cardiac muscle, depolarization occurs in response to the opening of voltage-
gated sodium channels, leading to a rapid influx of sodium ions into the cell.
3. **Repolarization:** Repolarization follows rapidly, initiated by the closure of sodium channels and the opening
of voltage-gated potassium channels. Potassium ions exit the cell, restoring the resting membrane potential.
4. **Refractory Period:** After repolarization, there is a refractory period during which the muscle cell cannot be
restimulated. This period ensures that the muscle cell completes its contraction before receiving another signal.
"Volume conduction" in the context of the heart refers to the transmission of electrical signals through the
fluid (blood) and conductive tissues of the heart.
If you put a cell into the center of a container filled with salt solution, the solution will be charged and
become a volume conductor. The nearer a point away from the positive pole, the higher the potential is. The
potential at a given point can be calculated by the equation:
V = E (cos a/r2)
The body acts as a conductor of the electrical currents generated by the heart, it is possible to place
electrodes on the body surface and measure cardiac potentials.
By convention, a wave of depolarization heading toward the positive electrode is recorded as a positive
voltage (upward deflection in the recording).
18.
Types
Precordial Leads
The transverse plane ECG is recorded unipolarly with respect to an indifferent electrode formed by summing
the signals from the left and right arms and the left leg (LA + RA + LL). Six electrodes are usually used,
labelled V1 to V6. The electrodes are placed close to the heart and their position is more critical than the
position of the frontal plane electrodes. They are placed on a line running round the chest from right of the
midline to beneath the left axilla.
EMG
2. Types of EMG
qIntramuscular: -Invasive recording of EMG directly from the Motor Unit
-Needle electrode & Fine wire electrode
-Used in Nerve Conduction study
qExtramuscular: -Noninvasive recording of EMG from the surface of the muscle
-Surface electrode
-Used in muscle study
There are two types of EMG signals:
1. **Surface EMG (sEMG):** This type of signal is obtained by placing electrodes on the skin above the muscle of
interest. sEMG captures the summation of electrical activity from multiple muscle fibers underneath the
electrode area.
2. **Intramuscular EMG (iEMG):** This involves inserting a needle electrode directly into the muscle tissue to
record electrical activity within a specific muscle or muscle group. iEMG provides more detailed information
about individual motor units and their firing patterns.
Electromyography (EMG) signals originate from the electrical activity produced by muscles during contraction or
relaxation. These signals are generated by the depolarization of muscle fibers, creating electrical impulses that
can be detected and recorded. The primary source of EMG signals is the neuromuscular junction, where motor
neurons transmit electrical signals to muscle fibers, causing them to contract.
Both types of EMG signals provide valuable information about muscle function, neuromuscular control, and can
aid in diagnosing neuromuscular disorders, evaluating muscle activity during movement, or assessing muscle
rehabilitation progress.
4. How EMG signal is generated
qElectromyogram signal is the summation of individual Motor Unit Action Potential generated by the Motor
Units at the activation zone of the muscle.
qAfter the motor units are stimulated , their pulses are recorded (as a sum) by the electrode and displays as
Electromyogram signal within the pickup range of the recording electrode.
Bipolar Configuration:
❑ Bipolar configuration is used to acquire EMG signal using two EMG detecting
surfaces with the help of a reference electrode.
❑ The two detecting surfaces are placed only 1-2 cm from each other.
❑ The signals from the two EMG surfaces are connected to a differential
amplifier.
❑ The limitations of the monopolar configuration are removed by this
configuration. This is the most commonly used electrode configuration
8. Applications of EMG
❑ EMG is used as a diagnostic tool for identifying:
▪ Neuromuscular diseases, assessing low back pain
▪ Disorders of motor control
❑ EMG signals are also used as :
▪ A control signal for prosthetic devices such as prosthetic hands , arms
and lower limbs
Electromyography (EMG) finds a wide range of applications across various fields
due to its ability to measure and analyze muscle activity and electrical signals
generated by muscles. Here are several notable applications:
Electrodes