SlideShare a Scribd company logo
CARDIOVASCULAR SYSTEM
(CVS)
Outline
• Overview of the CVS
• Circulation
• Cardiac Muscle
• Conduction system in the heart
• Cardiac Cycle
• ECG
• ECG leads and their placement
CARDIOVASCULAR SYSTEM
• Cardiovascular system includes heart
and blood vessels.
• Heart pumps blood into the blood
vessels.
• Blood vessels circulate the blood
throughout the body.
• Blood transports nutrients and oxygen
to the tissues and removes carbon
dioxide and waste products from the
tissues.
HEART
• Heart is a muscular organ that pumps blood
throughout the circulatory system.
• It is situated in between two lungs in the
mediastinum.
• It is made up of four chambers ie,
• two atria and two ventricles.
• The musculature of ventricles is thicker
than that of atria.
• Force of contraction of heart depends
upon the muscles.
Heart Chambers
CIRCULATION
DIVISIONS OF CIRCULATION
• Blood flows through two divisions of
circulatory system:
1. Systemic circulation
2. Pulmonary circulation.
„SYSTEMIC CIRCULATION
• Systemic circulation is otherwise known as
greater circulation.
• Blood pumped from left ventricle passes
through a series of blood vessels, arterial
system and reaches the tissues.
Systemic circu.. Cont’d
• Exchange of various substances between
blood and the tissues occurs at the
capillaries.
• After exchange of materials, blood enters
the venous system and returns to right
atrium of the heart.
• From right atrium, blood enters the right
ventricle.
• Thus, through systemic circulation,
oxygenated blood is supplied from heart to
the tissues and venous blood returns to the
heart from tissues.
PULMONARY CIRCULATION
• Blood is pumped from right ventricle to
lungs through pulmonary artery.
• Exchange of gases occurs between
blood and alveoli of the lungs at
pulmonary capillaries.
• Oxygenated blood returns to left atrium
through the pulmonary veins.
• Thus, left side of the heart contains
oxygenated or arterial blood and the
right side of the heart contains
deoxygenated or venous blood.
The
Circulatory
System
CARDIAC MUSCLE CONTRACTION
Generation and transmission of impulses in cardiac muscle
Cardiac muscle
Recap properties;
• Has one nucleus
• Intercalated discs
• Have large mitochondria
• Myogenic
• Straited
Funny channels
• Poorly selective cation channels
• Conduct more current as the membrane
potential becomes more negative close to -40
(hyperpolarization)
• Conduct both potassium and sodium ions
• Found in the SAN cells and activity causes the
membrane potential to slowly become more
positive (depolarize) to create a pacemaker
potential
The fast Na+ channel
• Voltage-dependent channels
• Functions:
– Permit Na+ to go in
– Keep K+ from going out
– Prevent Ca2+ from getting stuck in the channel and
interfering with Na+ permeability
Potassium channels
• Two main types of K+ channels
• Create a transmembrane "leak" of potassium
ions which causes hyperpolarization
• Activated by a specific depolarizing voltage
change
• located mainly inside the cellular membrane
Calcium channels
• L-type Ca++ channels (Long-lasting)
• T-type Ca++ channels (Transient)
• Respond to voltage changes across the
membrane differently
• L-type channels
– Respond to higher membrane potentials
– Open more slowly, and remain open longer than
T-type channels.
• Important in sustaining an action potential,
thus the plateau seen in the cardiac muscles
Calcium channels
• T-type channels initiate action potentials
• Because of their rapid kinetics, T-type
channels are commonly found in cells
undergoing rhythmic electrical behavior
– Neuron cell bodies involved in rhythmic activity
such as walking and breathing
– Pacemaker cells (SAN and AVN)
Cardiac muscle contraction
• Voltage regulated fast Na+ channels open initiating
an action potential
• Wave of depolarization travels down the T-tubules
resulting in the release of Ca++
– 20-30% of Ca++ needed for contraction comes from the
outside of the cells
• Acts as a stimulus for the release of the Ca++ from the sacoplasmic
reticulum
– For calcium to enter the cell, depolarization wave caused
by opening of the Na+ channels, opens the slow Ca++
channels
Cardiac Electrophysiology
Action Effect
Depolarization The electrical charge of a cell is altered by a
shift of electrolytes on either side of the cell
membrane.
This change stimulates the muscle cells to
contract
Repolarization Chemical pumps re-establish an internal
negative charge as the cells return to their
resting state.
Cardiac muscle contraction
Myocardial contraction:
• Heart muscle:
– Is stimulated by nerves and is self-excitable
(automaticity)
– Contracts as a unit
– Has a long (250 ms) absolute refractory period
• Cardiac muscle contraction is similar to skeletal
muscle contraction
• Autorhythmic cells:
– Initiate action potentials
– Have unstable resting potentials (pacemaker
potentials)
Sequence of excitation
Sequence of excitation
• Sinoatrial (SA) node generates impulses about
75 times/minute
• Atrioventricular (AV) node delays the impulse
by approximately 0.1 second
• Impulse passes from atria to ventricles via the
atrioventricular bundle (bundle of His)
Sequence of excitation
Sequence Excitation of Cardiac Muscle
THE CARDIAC CYCLE
Cardiac Cycle
Cardiac Cycle: the electrical, pressure and
volume changes that occur in a functional
heart between successive heart beats.
• Phase of the cardiac cycle when
myocardium is relaxed is termed diastole.
• Phase of the cardiac cycle when the
myocardium contracts is termed systole.
– Atrial systole: when atria contract.
– Ventricular systole: when ventricles contract.
Definitions
• Cardiac cycle
– Sequence of events in one heartbeat
• Systole
– Contraction phase (ventricular contraction)
• Diastole
– Relaxation phase (atrial and ventricular relaxation)
• Stroke volume
– Amount of blood ejected from either ventricle in a
single contraction
• Cardiac output
– Amount of blood pumped through the cardiovascular
system per minute (SV x HR)
Mechanical Events of the Cardiac Cycle
1. Ventricular Filling Period [ventricular diastole,
atrial systole]
2. Isovolumetric Contraction Period [ventricular
systole]
3. Ventricular Ejection Period [ventricular systole]
4. Isovolumetric Relaxation Period [ventricular
diastole]
Cardiac Cycle
• Electrical changes in heart tissue cause
mechanical, i.e. muscle contraction, changes
• Thus, changes in electrical membrane
potential of specific parts of the heart tissue
represent mechanical events in specific areas
of the heart tissue.
Electrical Events of the Cardiac Cycle
• Each wave or interval represents
depolarization or repolarization of
myocardial tissue.
• P wave represents depolarization of atria
which causes atrial contraction.
• QRS complex reflects depolarization of
ventricles which causes contraction.
• T wave reflects repolarization of muscle
fibers in ventricles.
Cardiac cycle
Has 2major phases: Systole and Diastole
Systole: (contraction-pumping phase of the cycle)
• Atrial systole
• Ventricular systole
• (depolarization-contraction phase)
Diastole: (relaxing-filling phase of the cycle)
• Atrial relaxation & filling
• Ventricular relaxation & filling
• (constitutes cardiac repolarization phase)
CARDIAC CYCLE
Stroke volume
• The volume of blood ejected in one ventricular
contraction is the stroke volume.
• SV is the difference between the volume of blood
in the ventricle before ejection (end-diastolic
volume) and the volume remaining in the
ventricle after ejection (end-systolic volume).
• Stroke volume is about 70 mL.
• Thus S.V=EDV-ESV
Cardiac output
• The total volume of blood ejected per unit
time
• Depends on the volume ejected on a single
beat (stroke volume) and the number of beats
per minute (heart rate).
• approximately 5000 mL/min in a 70-kg man
(based on a stroke volume of 70 mL and a
heart rate of 72 beats/min).
• Thus C.O= S.V x H.R
Frank-Starling relationship
• “The volume of blood ejected by the ventricle depends
on the volume present in the ventricle at the end of
diastole”
• The volume present at the end of diastole, depends on
the volume returned to the heart (venous return).
• Therefore, S.V and C.O correlate directly with E.D.V,
which correlates with V.R.
• The Frank-Starling relationship governs normal
ventricular function and ensures that the volume the
heart ejects in systole equals the volume it receives in
venous return
Cardiac Cycle
Coordination of :
• Electrical Changes
• Pressure Changes in Left Atria, Left Ventricle
and Aorta
• Ventricular Volume Changes
• Cardiac Valves
Cardiac Output
Cardiac Output is the volume of blood pumped each
minute, and is expressed by the following equation:
• CO = SV x HR
• Where:
– CO is cardiac output expressed in L/min (normal ~5 L/min)
– SV is stroke volume per beat
– HR is the number of beats per minute
Heart Rate (HR)
Heart rate is directly proportional to cardiac output
• Adult HR is normally 80-100 beats per minute (bpm.)
Heart rate is modified by autonomic, immune, and local factors.
• Example:
1. An increase in parasympathetic activity via M2 cholinergic receptors in
the heart will decrease the heart rate.
2. An increase in sympathetic activity via B1 and B2 adrenergic receptors
throughout the heart will increase the heart rate.
Stroke Volume (SV)
• SV = EDV – ESV
• Is determined by three factors: preload, afterload, and
contractility.
• Preload gives the volume of blood that the ventricle has
available to pump
• Contractility is the force that the muscle can create at the
given length
• Afterload is the arterial pressure against which the muscle will
contract.
– These factors establish the volume of blood pumped with each heart
beat.
Cardiac Volumes
• SV = end diastolic volume (EDV) - end systolic
volume (ESV)
• EDV = amount of blood collected in a ventricle
during diastole
• ESV = amount of blood remaining in a
ventricle after contraction
The ECG
Electrical changes in the heart muscle as recorded
on the body surface
Electro-cardiogram
• Is a series of waves and deflections recording the
heart’s electrical activity from a certain “view.”
• Many views, each called a lead, monitor voltage
changes between electrodes placed in different
positions on the body.
• Leads I, II, and III are bipolar leads, which consist
of two electrodes of opposite polarity (positive
and negative). The third (ground) electrode
minimizes electrical activity from other sources.
What is an ECG?
Limb leads
• Electrodes are placed on
the right arm (RA), left
arm (LA), right leg (RL),
and left leg (LL).
• With only four electrodes,
six leads are viewed.
• Standard leads: I, II, III
• Augmented leads: aVR,
aVL, aVF
• Einthoven’s Triangle
Limb leads and augmented leads
Standard leads
• Lead I is the voltage between the (positive) left
arm (LA) electrode and right arm (RA) electrode:
– I=LA-RA
• Lead II is the voltage between the (positive) left
leg (LL) electrode and the right arm (RA)
electrode:
– II=LL-RA
• Lead III is the voltage between the (positive) left
leg (LL) electrode and the left arm (LA) electrode:
– III=LL-LA
Augmented limb leads
• Leads aVR, aVL, and aVF are the augmented
limb leads.
• Derived from the same three electrodes as
leads I, II, and III
• These use the Goldberger's central terminal as
their negative pole which is a combination of
inputs from other two limb electrodes
Precordial leads
• The precordial leads lie in the transverse
(horizontal) plane, perpendicular to the other
six leads. The six precordial electrodes act as
the positive poles for the six corresponding
precordial leads: (V1, V2, V3, V4, V5 and V6).
• Wilson's central terminal is used as the
negative pole
ECG leads
• Leads aVR, aVL, and aVF are unipolar leads and
consist of a single positive electrode and a
reference point (with zero electrical potential)
that lies in the center of the heart’s electrical
field.
• Leads V1–V6 are unipolar leads and consist of a
single positive electrode with a negative
reference point found at the electrical center of
the heart.
• Voltage changes are amplified and visually
displayed on an oscilloscope and graph paper.
• An ECG tracing looks different in each lead because the
recorded angle of electrical activity changes with each
lead.
• Several different angles allow a more accurate
perspective than a single one would.
• The ECG machine can be adjusted to make any skin
electrode positive or negative. The polarity depends on
which lead the machine is recording.
• A cable attached to the patient is divided into several
different-colored wires: three, four, or five for
monitoring purposes, or ten for a 12-lead ECG.
Lead interpretation
• LEADS I,II and VL look at the left lateral surface of the
heart.
• III and VF at the inferior surface.
• And VR looks at the atria.
• AVR and II look at the heart from opposite directions.
• Leads VI and V2 look at the right ventricle.
• V3 and V4 look at the septum between the
ventricles and the anterior wall of the left ventricle.
• V5 and V6 look at the anterior and lateral walls of
the left ventricle.
ECG leads
Electrical components
Methods of counting heart rate
• Heart rate is calculated as the number of
times the heart beats per minute. It usually
measures ventricular rate (the number of QRS
complexes) but can refer to atrial rate (the
number of P waves).
• Method chosen to calculate HR varies
according to rate and regularity on the ECG
tracing
Practical sessions
Procedure
1. Position patient supine. Ensure a comfortable positioning.
2. Explain procedure to dispel fears or myths. Instruct patient to lie as still
as possible.
3. Attach electrodes
1. Limb leads
1. Right/left arm, right/left leg
2. Precordial leads
1. V1 = 4th intercostal space to right of sternal border
2. V2 = 4th intercostal space to left of sternal border
3. V3 = midway between leads V2 and V4
4. V4 = midclavicular line, above the 5th interspace
5. V5 = anterior axillary line at the same level as V4
6. V6 = midaxillary line at the same level as leads V4 and V5
Procedure
How to Read an ECG
• Basics
– Always approach ECG reading in a systematic,
stepwise fashion
1. Rate
• To determine the rate you must first know the paper speed
(usually 25mm/sec)
– 5 large blocks = 1 second
– 1 large block = 0.2 second (200 msec)
– 1 small block = 0.04 second (40 msec)
– Rate = (# of QRS) x 60 seconds
# of seconds 1 min
1. Rate (continued)
• If speed is 25mm/sec, it is much easier to estimate the rate
using the rule
“300-150-100 -- 75-60-50”
• Also…depending on the ECG machine, sometimes the HR will
be provided!
2. Rhythm
• Is there a P-wave before every Q and a Q-wave after every P?
– No P-waves
• Narrow complex QRS: Atrial fibrillation
• Wide complex: ventricular rhythm (Idioventricular, Ventricular tachycardia, Ventricular fibrillation)
– P-wave present
• Fixed PR interval
– Normal PR interval
» If P wave is positive in II → Sinus rhythm
» If P wave is negative in II → Junctional rhythm
– Prolonged PR interval
» QRS always present = First degree AV block
» Regularly “dropped” QRS = Second deg. AV block (Mobitz Type II)
– Sawtooth” p-wave pattern = Atrial flutter
• Variable PR interval
– Second degree AV block (Mobitz Type I/Wenckebach)
– Different P-wave morphologies
» Wandering pacemaker
» Multifocal atrial tachycardia
• P-wave and Q-wave independent
– Third degree (Complete) AV block
2. Rhythm
4. P-Wave and PR interval
• P Wave
– P wave represents atrial depolarization
• PR Interval
– PR interval is beginning of P wave to beginning of QRS
– Normal interval is 120-200 milliseconds (3-5 small boxes)
– Why would PR interval be lengthened?...blocks
• 1st degree - consistently lengthened PR
• 2nd degree (Type 1) - Wenckebach
• 2nd degree (Type 2) - will regularly drop beat, PR interval less important
• 3rd degree - no relation between P and QRS, P waves regular, QRS regular and wide
– Why would PR interval be shortened?
• ectopic atrial foci (e.g. wandering pacemaker, multifocal atrial tachycardia)
• accessory tracts, Wolf-Parkinson-White syndrome (WPW)
5. QRS
• QRS Complex
– Normal width is <120 ms (3 small squares)
– What causes widened QRS?
• RBBB (RSR’ in V1; wide S wave in I, V5-6)
• LBBB (wide R in I, V5-6; no Q in I, V5-6; displaced ST and T waves opposite
to major deflection of QRS)
• Ventricular beat
• Accessory tracts
– Detect ventricular hypertrophy by height of QRS
• S in V1 + R in V5 or V6 ≥ 35 mm → LVH
• R in AVL ≥11mm → LVH
• If R wave (any +ve defl’n ) in V1 → Likely RVH
6. ST Segment
• ST Segment
– Elevation = active infarction (vessel occluded),
pericarditis, aneurysm of ventricle
– Look at lead where elevation occurs to determine
vessel occluded
– Depression = ischemia, digoxin toxicity,
hypokalemia, elevated intracranial pressure
– An old MI will be seen as Q wave (1/3 of QRS
complex)
7. T Waves
• T Waves
– Usually will be in same direction as QRS
– T wave inversion caused by ischemia or old
infarction
8. QT Interval
• QT Interval
– From end of QRS complex to end of T wave
– Long QT is >500 ms (QTc >440ms) → can predispose
to Torsades des pointes
– What causes long QT?
• Ischemia
• Electrolyte abnormalities (↓ K, Mg, Ca)
• Congenital
• Drugs (many including antiarrhythmics, quinolones, TCA)

More Related Content

Similar to Cardiovascular system- ECG.pdf

Cardio physio
Cardio physioCardio physio
Cardio physio
drjopogs
 
Conduction system and ecg
Conduction system and ecgConduction system and ecg
Conduction system and ecg
Asha damodar
 
CVS 2 IMPULSE GENERATION.ppt
CVS 2 IMPULSE GENERATION.pptCVS 2 IMPULSE GENERATION.ppt
CVS 2 IMPULSE GENERATION.ppt
kimkosh279
 
HAP I CLASS.pptx
HAP I CLASS.pptxHAP I CLASS.pptx
HAP I CLASS.pptx
Santhi Dasari
 
First cardiovascular physiology
First cardiovascular physiologyFirst cardiovascular physiology
First cardiovascular physiology
arun kumar
 
Heart
HeartHeart
cardiovascular anatomy and physiology
cardiovascular anatomy and physiologycardiovascular anatomy and physiology
cardiovascular anatomy and physiology
TariqQazi7
 
Unit 3 cardiovascular system nrs237
Unit 3 cardiovascular system nrs237Unit 3 cardiovascular system nrs237
Unit 3 cardiovascular system nrs237
menwar
 
Cardiovascular System (1).pptx
Cardiovascular System (1).pptxCardiovascular System (1).pptx
Cardiovascular System (1).pptx
JHCONAS
 
Cardiovascular system
Cardiovascular systemCardiovascular system
Cardiovascular system
Nisha Mhaske
 
Cardio vascular system ..PHYSIOLOGY - .pptx
Cardio vascular system ..PHYSIOLOGY - .pptxCardio vascular system ..PHYSIOLOGY - .pptx
Cardio vascular system ..PHYSIOLOGY - .pptx
gul1213916
 
cardiovascular physiology-for anesthesia
cardiovascular physiology-for anesthesiacardiovascular physiology-for anesthesia
cardiovascular physiology-for anesthesia
Abdullah Saad
 
Electrophysiology of heart.pptx
Electrophysiology of heart.pptxElectrophysiology of heart.pptx
Electrophysiology of heart.pptx
Jhansi Uppu
 
Cardiovascular physiology
Cardiovascular physiologyCardiovascular physiology
Cardiovascular physiology
Jesse Spurr
 
Cardiovascular Physiology - Structure of Heart.ppt
Cardiovascular Physiology - Structure of Heart.pptCardiovascular Physiology - Structure of Heart.ppt
Cardiovascular Physiology - Structure of Heart.ppt
Jamakala Obaiah
 
Fisiologi Jantung pada manusia normal untuk mahasiswa
Fisiologi Jantung pada manusia normal untuk mahasiswaFisiologi Jantung pada manusia normal untuk mahasiswa
Fisiologi Jantung pada manusia normal untuk mahasiswa
AldoFerly
 
CARDIOVASCULAR SYSTEM - ANATOMY & PHYSIOLOGY
CARDIOVASCULAR SYSTEM - ANATOMY & PHYSIOLOGYCARDIOVASCULAR SYSTEM - ANATOMY & PHYSIOLOGY
CARDIOVASCULAR SYSTEM - ANATOMY & PHYSIOLOGY
Kameshwaran Sugavanam
 
ECG complete lecture notes along with interpretation
ECG complete lecture notes along with interpretationECG complete lecture notes along with interpretation
ECG complete lecture notes along with interpretation
DrSUVANATH
 
Basic ECG
Basic ECGBasic ECG
Basic ECG
MEEQAT HOSPITAL
 
ECG complete lecture presentation, ECG waveform and leads placement
ECG complete lecture presentation, ECG waveform and leads placementECG complete lecture presentation, ECG waveform and leads placement
ECG complete lecture presentation, ECG waveform and leads placement
DrSUVANATH
 

Similar to Cardiovascular system- ECG.pdf (20)

Cardio physio
Cardio physioCardio physio
Cardio physio
 
Conduction system and ecg
Conduction system and ecgConduction system and ecg
Conduction system and ecg
 
CVS 2 IMPULSE GENERATION.ppt
CVS 2 IMPULSE GENERATION.pptCVS 2 IMPULSE GENERATION.ppt
CVS 2 IMPULSE GENERATION.ppt
 
HAP I CLASS.pptx
HAP I CLASS.pptxHAP I CLASS.pptx
HAP I CLASS.pptx
 
First cardiovascular physiology
First cardiovascular physiologyFirst cardiovascular physiology
First cardiovascular physiology
 
Heart
HeartHeart
Heart
 
cardiovascular anatomy and physiology
cardiovascular anatomy and physiologycardiovascular anatomy and physiology
cardiovascular anatomy and physiology
 
Unit 3 cardiovascular system nrs237
Unit 3 cardiovascular system nrs237Unit 3 cardiovascular system nrs237
Unit 3 cardiovascular system nrs237
 
Cardiovascular System (1).pptx
Cardiovascular System (1).pptxCardiovascular System (1).pptx
Cardiovascular System (1).pptx
 
Cardiovascular system
Cardiovascular systemCardiovascular system
Cardiovascular system
 
Cardio vascular system ..PHYSIOLOGY - .pptx
Cardio vascular system ..PHYSIOLOGY - .pptxCardio vascular system ..PHYSIOLOGY - .pptx
Cardio vascular system ..PHYSIOLOGY - .pptx
 
cardiovascular physiology-for anesthesia
cardiovascular physiology-for anesthesiacardiovascular physiology-for anesthesia
cardiovascular physiology-for anesthesia
 
Electrophysiology of heart.pptx
Electrophysiology of heart.pptxElectrophysiology of heart.pptx
Electrophysiology of heart.pptx
 
Cardiovascular physiology
Cardiovascular physiologyCardiovascular physiology
Cardiovascular physiology
 
Cardiovascular Physiology - Structure of Heart.ppt
Cardiovascular Physiology - Structure of Heart.pptCardiovascular Physiology - Structure of Heart.ppt
Cardiovascular Physiology - Structure of Heart.ppt
 
Fisiologi Jantung pada manusia normal untuk mahasiswa
Fisiologi Jantung pada manusia normal untuk mahasiswaFisiologi Jantung pada manusia normal untuk mahasiswa
Fisiologi Jantung pada manusia normal untuk mahasiswa
 
CARDIOVASCULAR SYSTEM - ANATOMY & PHYSIOLOGY
CARDIOVASCULAR SYSTEM - ANATOMY & PHYSIOLOGYCARDIOVASCULAR SYSTEM - ANATOMY & PHYSIOLOGY
CARDIOVASCULAR SYSTEM - ANATOMY & PHYSIOLOGY
 
ECG complete lecture notes along with interpretation
ECG complete lecture notes along with interpretationECG complete lecture notes along with interpretation
ECG complete lecture notes along with interpretation
 
Basic ECG
Basic ECGBasic ECG
Basic ECG
 
ECG complete lecture presentation, ECG waveform and leads placement
ECG complete lecture presentation, ECG waveform and leads placementECG complete lecture presentation, ECG waveform and leads placement
ECG complete lecture presentation, ECG waveform and leads placement
 

Recently uploaded

Skin Diseases That Happen During Summer.
 Skin Diseases That Happen During Summer. Skin Diseases That Happen During Summer.
Skin Diseases That Happen During Summer.
Gokuldas Hospital
 
Demystifying Fallopian Tube Blockage- Grading the Differences and Implication...
Demystifying Fallopian Tube Blockage- Grading the Differences and Implication...Demystifying Fallopian Tube Blockage- Grading the Differences and Implication...
Demystifying Fallopian Tube Blockage- Grading the Differences and Implication...
FFragrant
 
Physical demands in sports - WCSPT Oslo 2024
Physical demands in sports - WCSPT Oslo 2024Physical demands in sports - WCSPT Oslo 2024
Physical demands in sports - WCSPT Oslo 2024
Torstein Dalen-Lorentsen
 
Test bank for karp s cell and molecular biology 9th edition by gerald karp.pdf
Test bank for karp s cell and molecular biology 9th edition by gerald karp.pdfTest bank for karp s cell and molecular biology 9th edition by gerald karp.pdf
Test bank for karp s cell and molecular biology 9th edition by gerald karp.pdf
rightmanforbloodline
 
CHEMOTHERAPY_RDP_CHAPTER 3_ANTIFUNGAL AGENT.pdf
CHEMOTHERAPY_RDP_CHAPTER 3_ANTIFUNGAL AGENT.pdfCHEMOTHERAPY_RDP_CHAPTER 3_ANTIFUNGAL AGENT.pdf
CHEMOTHERAPY_RDP_CHAPTER 3_ANTIFUNGAL AGENT.pdf
rishi2789
 
CHEMOTHERAPY_RDP_CHAPTER 6_Anti Malarial Drugs.pdf
CHEMOTHERAPY_RDP_CHAPTER 6_Anti Malarial Drugs.pdfCHEMOTHERAPY_RDP_CHAPTER 6_Anti Malarial Drugs.pdf
CHEMOTHERAPY_RDP_CHAPTER 6_Anti Malarial Drugs.pdf
rishi2789
 
Histololgy of Female Reproductive System.pptx
Histololgy of Female Reproductive System.pptxHistololgy of Female Reproductive System.pptx
Histololgy of Female Reproductive System.pptx
AyeshaZaid1
 
pharmacology for dummies free pdf download.pdf
pharmacology for dummies free pdf download.pdfpharmacology for dummies free pdf download.pdf
pharmacology for dummies free pdf download.pdf
KerlynIgnacio
 
NAVIGATING THE HORIZONS OF TIME LAPSE EMBRYO MONITORING.pdf
NAVIGATING THE HORIZONS OF TIME LAPSE EMBRYO MONITORING.pdfNAVIGATING THE HORIZONS OF TIME LAPSE EMBRYO MONITORING.pdf
NAVIGATING THE HORIZONS OF TIME LAPSE EMBRYO MONITORING.pdf
Rahul Sen
 
LOW BIRTH WEIGHT. PRETERM BABIES OR SMALL FOR DATES BABIES
LOW BIRTH WEIGHT. PRETERM BABIES OR SMALL FOR DATES BABIESLOW BIRTH WEIGHT. PRETERM BABIES OR SMALL FOR DATES BABIES
LOW BIRTH WEIGHT. PRETERM BABIES OR SMALL FOR DATES BABIES
ShraddhaTamshettiwar
 
Osteoporosis - Definition , Evaluation and Management .pdf
Osteoporosis - Definition , Evaluation and Management .pdfOsteoporosis - Definition , Evaluation and Management .pdf
Osteoporosis - Definition , Evaluation and Management .pdf
Jim Jacob Roy
 
Cervical Disc Arthroplasty ORSI 2024.pptx
Cervical Disc Arthroplasty ORSI 2024.pptxCervical Disc Arthroplasty ORSI 2024.pptx
Cervical Disc Arthroplasty ORSI 2024.pptx
LEFLOT Jean-Louis
 
Medical Quiz ( Online Quiz for API Meet 2024 ).pdf
Medical Quiz ( Online Quiz for API Meet 2024 ).pdfMedical Quiz ( Online Quiz for API Meet 2024 ).pdf
Medical Quiz ( Online Quiz for API Meet 2024 ).pdf
Jim Jacob Roy
 
10 Benefits an EPCR Software should Bring to EMS Organizations
10 Benefits an EPCR Software should Bring to EMS Organizations   10 Benefits an EPCR Software should Bring to EMS Organizations
10 Benefits an EPCR Software should Bring to EMS Organizations
Traumasoft LLC
 
Travel Clinic Cardiff: Health Advice for International Travelers
Travel Clinic Cardiff: Health Advice for International TravelersTravel Clinic Cardiff: Health Advice for International Travelers
Travel Clinic Cardiff: Health Advice for International Travelers
NX Healthcare
 
DECLARATION OF HELSINKI - History and principles
DECLARATION OF HELSINKI - History and principlesDECLARATION OF HELSINKI - History and principles
DECLARATION OF HELSINKI - History and principles
anaghabharat01
 
Nano-gold for Cancer Therapy chemistry investigatory project
Nano-gold for Cancer Therapy chemistry investigatory projectNano-gold for Cancer Therapy chemistry investigatory project
Nano-gold for Cancer Therapy chemistry investigatory project
SIVAVINAYAKPK
 
CLEAR ALIGNER THERAPY IN ORTHODONTICS .pptx
CLEAR ALIGNER THERAPY IN ORTHODONTICS .pptxCLEAR ALIGNER THERAPY IN ORTHODONTICS .pptx
CLEAR ALIGNER THERAPY IN ORTHODONTICS .pptx
Government Dental College & Hospital Srinagar
 
CHEMOTHERAPY_RDP_CHAPTER 2 _LEPROSY.pdf1
CHEMOTHERAPY_RDP_CHAPTER 2 _LEPROSY.pdf1CHEMOTHERAPY_RDP_CHAPTER 2 _LEPROSY.pdf1
CHEMOTHERAPY_RDP_CHAPTER 2 _LEPROSY.pdf1
rishi2789
 
Hemodialysis: Chapter 5, Dialyzers Overview - Dr.Gawad
Hemodialysis: Chapter 5, Dialyzers Overview - Dr.GawadHemodialysis: Chapter 5, Dialyzers Overview - Dr.Gawad
Hemodialysis: Chapter 5, Dialyzers Overview - Dr.Gawad
NephroTube - Dr.Gawad
 

Recently uploaded (20)

Skin Diseases That Happen During Summer.
 Skin Diseases That Happen During Summer. Skin Diseases That Happen During Summer.
Skin Diseases That Happen During Summer.
 
Demystifying Fallopian Tube Blockage- Grading the Differences and Implication...
Demystifying Fallopian Tube Blockage- Grading the Differences and Implication...Demystifying Fallopian Tube Blockage- Grading the Differences and Implication...
Demystifying Fallopian Tube Blockage- Grading the Differences and Implication...
 
Physical demands in sports - WCSPT Oslo 2024
Physical demands in sports - WCSPT Oslo 2024Physical demands in sports - WCSPT Oslo 2024
Physical demands in sports - WCSPT Oslo 2024
 
Test bank for karp s cell and molecular biology 9th edition by gerald karp.pdf
Test bank for karp s cell and molecular biology 9th edition by gerald karp.pdfTest bank for karp s cell and molecular biology 9th edition by gerald karp.pdf
Test bank for karp s cell and molecular biology 9th edition by gerald karp.pdf
 
CHEMOTHERAPY_RDP_CHAPTER 3_ANTIFUNGAL AGENT.pdf
CHEMOTHERAPY_RDP_CHAPTER 3_ANTIFUNGAL AGENT.pdfCHEMOTHERAPY_RDP_CHAPTER 3_ANTIFUNGAL AGENT.pdf
CHEMOTHERAPY_RDP_CHAPTER 3_ANTIFUNGAL AGENT.pdf
 
CHEMOTHERAPY_RDP_CHAPTER 6_Anti Malarial Drugs.pdf
CHEMOTHERAPY_RDP_CHAPTER 6_Anti Malarial Drugs.pdfCHEMOTHERAPY_RDP_CHAPTER 6_Anti Malarial Drugs.pdf
CHEMOTHERAPY_RDP_CHAPTER 6_Anti Malarial Drugs.pdf
 
Histololgy of Female Reproductive System.pptx
Histololgy of Female Reproductive System.pptxHistololgy of Female Reproductive System.pptx
Histololgy of Female Reproductive System.pptx
 
pharmacology for dummies free pdf download.pdf
pharmacology for dummies free pdf download.pdfpharmacology for dummies free pdf download.pdf
pharmacology for dummies free pdf download.pdf
 
NAVIGATING THE HORIZONS OF TIME LAPSE EMBRYO MONITORING.pdf
NAVIGATING THE HORIZONS OF TIME LAPSE EMBRYO MONITORING.pdfNAVIGATING THE HORIZONS OF TIME LAPSE EMBRYO MONITORING.pdf
NAVIGATING THE HORIZONS OF TIME LAPSE EMBRYO MONITORING.pdf
 
LOW BIRTH WEIGHT. PRETERM BABIES OR SMALL FOR DATES BABIES
LOW BIRTH WEIGHT. PRETERM BABIES OR SMALL FOR DATES BABIESLOW BIRTH WEIGHT. PRETERM BABIES OR SMALL FOR DATES BABIES
LOW BIRTH WEIGHT. PRETERM BABIES OR SMALL FOR DATES BABIES
 
Osteoporosis - Definition , Evaluation and Management .pdf
Osteoporosis - Definition , Evaluation and Management .pdfOsteoporosis - Definition , Evaluation and Management .pdf
Osteoporosis - Definition , Evaluation and Management .pdf
 
Cervical Disc Arthroplasty ORSI 2024.pptx
Cervical Disc Arthroplasty ORSI 2024.pptxCervical Disc Arthroplasty ORSI 2024.pptx
Cervical Disc Arthroplasty ORSI 2024.pptx
 
Medical Quiz ( Online Quiz for API Meet 2024 ).pdf
Medical Quiz ( Online Quiz for API Meet 2024 ).pdfMedical Quiz ( Online Quiz for API Meet 2024 ).pdf
Medical Quiz ( Online Quiz for API Meet 2024 ).pdf
 
10 Benefits an EPCR Software should Bring to EMS Organizations
10 Benefits an EPCR Software should Bring to EMS Organizations   10 Benefits an EPCR Software should Bring to EMS Organizations
10 Benefits an EPCR Software should Bring to EMS Organizations
 
Travel Clinic Cardiff: Health Advice for International Travelers
Travel Clinic Cardiff: Health Advice for International TravelersTravel Clinic Cardiff: Health Advice for International Travelers
Travel Clinic Cardiff: Health Advice for International Travelers
 
DECLARATION OF HELSINKI - History and principles
DECLARATION OF HELSINKI - History and principlesDECLARATION OF HELSINKI - History and principles
DECLARATION OF HELSINKI - History and principles
 
Nano-gold for Cancer Therapy chemistry investigatory project
Nano-gold for Cancer Therapy chemistry investigatory projectNano-gold for Cancer Therapy chemistry investigatory project
Nano-gold for Cancer Therapy chemistry investigatory project
 
CLEAR ALIGNER THERAPY IN ORTHODONTICS .pptx
CLEAR ALIGNER THERAPY IN ORTHODONTICS .pptxCLEAR ALIGNER THERAPY IN ORTHODONTICS .pptx
CLEAR ALIGNER THERAPY IN ORTHODONTICS .pptx
 
CHEMOTHERAPY_RDP_CHAPTER 2 _LEPROSY.pdf1
CHEMOTHERAPY_RDP_CHAPTER 2 _LEPROSY.pdf1CHEMOTHERAPY_RDP_CHAPTER 2 _LEPROSY.pdf1
CHEMOTHERAPY_RDP_CHAPTER 2 _LEPROSY.pdf1
 
Hemodialysis: Chapter 5, Dialyzers Overview - Dr.Gawad
Hemodialysis: Chapter 5, Dialyzers Overview - Dr.GawadHemodialysis: Chapter 5, Dialyzers Overview - Dr.Gawad
Hemodialysis: Chapter 5, Dialyzers Overview - Dr.Gawad
 

Cardiovascular system- ECG.pdf

  • 2. Outline • Overview of the CVS • Circulation • Cardiac Muscle • Conduction system in the heart • Cardiac Cycle • ECG • ECG leads and their placement
  • 3. CARDIOVASCULAR SYSTEM • Cardiovascular system includes heart and blood vessels. • Heart pumps blood into the blood vessels. • Blood vessels circulate the blood throughout the body. • Blood transports nutrients and oxygen to the tissues and removes carbon dioxide and waste products from the tissues.
  • 4. HEART • Heart is a muscular organ that pumps blood throughout the circulatory system. • It is situated in between two lungs in the mediastinum. • It is made up of four chambers ie, • two atria and two ventricles. • The musculature of ventricles is thicker than that of atria. • Force of contraction of heart depends upon the muscles.
  • 6. CIRCULATION DIVISIONS OF CIRCULATION • Blood flows through two divisions of circulatory system: 1. Systemic circulation 2. Pulmonary circulation. „SYSTEMIC CIRCULATION • Systemic circulation is otherwise known as greater circulation. • Blood pumped from left ventricle passes through a series of blood vessels, arterial system and reaches the tissues.
  • 7. Systemic circu.. Cont’d • Exchange of various substances between blood and the tissues occurs at the capillaries. • After exchange of materials, blood enters the venous system and returns to right atrium of the heart. • From right atrium, blood enters the right ventricle. • Thus, through systemic circulation, oxygenated blood is supplied from heart to the tissues and venous blood returns to the heart from tissues.
  • 8. PULMONARY CIRCULATION • Blood is pumped from right ventricle to lungs through pulmonary artery. • Exchange of gases occurs between blood and alveoli of the lungs at pulmonary capillaries. • Oxygenated blood returns to left atrium through the pulmonary veins. • Thus, left side of the heart contains oxygenated or arterial blood and the right side of the heart contains deoxygenated or venous blood.
  • 10. CARDIAC MUSCLE CONTRACTION Generation and transmission of impulses in cardiac muscle
  • 11. Cardiac muscle Recap properties; • Has one nucleus • Intercalated discs • Have large mitochondria • Myogenic • Straited
  • 12. Funny channels • Poorly selective cation channels • Conduct more current as the membrane potential becomes more negative close to -40 (hyperpolarization) • Conduct both potassium and sodium ions • Found in the SAN cells and activity causes the membrane potential to slowly become more positive (depolarize) to create a pacemaker potential
  • 13. The fast Na+ channel • Voltage-dependent channels • Functions: – Permit Na+ to go in – Keep K+ from going out – Prevent Ca2+ from getting stuck in the channel and interfering with Na+ permeability
  • 14. Potassium channels • Two main types of K+ channels • Create a transmembrane "leak" of potassium ions which causes hyperpolarization • Activated by a specific depolarizing voltage change • located mainly inside the cellular membrane
  • 15. Calcium channels • L-type Ca++ channels (Long-lasting) • T-type Ca++ channels (Transient) • Respond to voltage changes across the membrane differently • L-type channels – Respond to higher membrane potentials – Open more slowly, and remain open longer than T-type channels. • Important in sustaining an action potential, thus the plateau seen in the cardiac muscles
  • 16. Calcium channels • T-type channels initiate action potentials • Because of their rapid kinetics, T-type channels are commonly found in cells undergoing rhythmic electrical behavior – Neuron cell bodies involved in rhythmic activity such as walking and breathing – Pacemaker cells (SAN and AVN)
  • 17. Cardiac muscle contraction • Voltage regulated fast Na+ channels open initiating an action potential • Wave of depolarization travels down the T-tubules resulting in the release of Ca++ – 20-30% of Ca++ needed for contraction comes from the outside of the cells • Acts as a stimulus for the release of the Ca++ from the sacoplasmic reticulum – For calcium to enter the cell, depolarization wave caused by opening of the Na+ channels, opens the slow Ca++ channels
  • 18. Cardiac Electrophysiology Action Effect Depolarization The electrical charge of a cell is altered by a shift of electrolytes on either side of the cell membrane. This change stimulates the muscle cells to contract Repolarization Chemical pumps re-establish an internal negative charge as the cells return to their resting state.
  • 20. Myocardial contraction: • Heart muscle: – Is stimulated by nerves and is self-excitable (automaticity) – Contracts as a unit – Has a long (250 ms) absolute refractory period • Cardiac muscle contraction is similar to skeletal muscle contraction • Autorhythmic cells: – Initiate action potentials – Have unstable resting potentials (pacemaker potentials)
  • 22. Sequence of excitation • Sinoatrial (SA) node generates impulses about 75 times/minute • Atrioventricular (AV) node delays the impulse by approximately 0.1 second • Impulse passes from atria to ventricles via the atrioventricular bundle (bundle of His)
  • 24. Sequence Excitation of Cardiac Muscle
  • 26. Cardiac Cycle Cardiac Cycle: the electrical, pressure and volume changes that occur in a functional heart between successive heart beats. • Phase of the cardiac cycle when myocardium is relaxed is termed diastole. • Phase of the cardiac cycle when the myocardium contracts is termed systole. – Atrial systole: when atria contract. – Ventricular systole: when ventricles contract.
  • 27. Definitions • Cardiac cycle – Sequence of events in one heartbeat • Systole – Contraction phase (ventricular contraction) • Diastole – Relaxation phase (atrial and ventricular relaxation) • Stroke volume – Amount of blood ejected from either ventricle in a single contraction • Cardiac output – Amount of blood pumped through the cardiovascular system per minute (SV x HR)
  • 28. Mechanical Events of the Cardiac Cycle 1. Ventricular Filling Period [ventricular diastole, atrial systole] 2. Isovolumetric Contraction Period [ventricular systole] 3. Ventricular Ejection Period [ventricular systole] 4. Isovolumetric Relaxation Period [ventricular diastole]
  • 29. Cardiac Cycle • Electrical changes in heart tissue cause mechanical, i.e. muscle contraction, changes • Thus, changes in electrical membrane potential of specific parts of the heart tissue represent mechanical events in specific areas of the heart tissue.
  • 30. Electrical Events of the Cardiac Cycle • Each wave or interval represents depolarization or repolarization of myocardial tissue. • P wave represents depolarization of atria which causes atrial contraction. • QRS complex reflects depolarization of ventricles which causes contraction. • T wave reflects repolarization of muscle fibers in ventricles.
  • 31. Cardiac cycle Has 2major phases: Systole and Diastole Systole: (contraction-pumping phase of the cycle) • Atrial systole • Ventricular systole • (depolarization-contraction phase) Diastole: (relaxing-filling phase of the cycle) • Atrial relaxation & filling • Ventricular relaxation & filling • (constitutes cardiac repolarization phase)
  • 33. Stroke volume • The volume of blood ejected in one ventricular contraction is the stroke volume. • SV is the difference between the volume of blood in the ventricle before ejection (end-diastolic volume) and the volume remaining in the ventricle after ejection (end-systolic volume). • Stroke volume is about 70 mL. • Thus S.V=EDV-ESV
  • 34. Cardiac output • The total volume of blood ejected per unit time • Depends on the volume ejected on a single beat (stroke volume) and the number of beats per minute (heart rate). • approximately 5000 mL/min in a 70-kg man (based on a stroke volume of 70 mL and a heart rate of 72 beats/min). • Thus C.O= S.V x H.R
  • 35. Frank-Starling relationship • “The volume of blood ejected by the ventricle depends on the volume present in the ventricle at the end of diastole” • The volume present at the end of diastole, depends on the volume returned to the heart (venous return). • Therefore, S.V and C.O correlate directly with E.D.V, which correlates with V.R. • The Frank-Starling relationship governs normal ventricular function and ensures that the volume the heart ejects in systole equals the volume it receives in venous return
  • 36. Cardiac Cycle Coordination of : • Electrical Changes • Pressure Changes in Left Atria, Left Ventricle and Aorta • Ventricular Volume Changes • Cardiac Valves
  • 37. Cardiac Output Cardiac Output is the volume of blood pumped each minute, and is expressed by the following equation: • CO = SV x HR • Where: – CO is cardiac output expressed in L/min (normal ~5 L/min) – SV is stroke volume per beat – HR is the number of beats per minute
  • 38. Heart Rate (HR) Heart rate is directly proportional to cardiac output • Adult HR is normally 80-100 beats per minute (bpm.) Heart rate is modified by autonomic, immune, and local factors. • Example: 1. An increase in parasympathetic activity via M2 cholinergic receptors in the heart will decrease the heart rate. 2. An increase in sympathetic activity via B1 and B2 adrenergic receptors throughout the heart will increase the heart rate.
  • 39. Stroke Volume (SV) • SV = EDV – ESV • Is determined by three factors: preload, afterload, and contractility. • Preload gives the volume of blood that the ventricle has available to pump • Contractility is the force that the muscle can create at the given length • Afterload is the arterial pressure against which the muscle will contract. – These factors establish the volume of blood pumped with each heart beat.
  • 40. Cardiac Volumes • SV = end diastolic volume (EDV) - end systolic volume (ESV) • EDV = amount of blood collected in a ventricle during diastole • ESV = amount of blood remaining in a ventricle after contraction
  • 41.
  • 42. The ECG Electrical changes in the heart muscle as recorded on the body surface
  • 43. Electro-cardiogram • Is a series of waves and deflections recording the heart’s electrical activity from a certain “view.” • Many views, each called a lead, monitor voltage changes between electrodes placed in different positions on the body. • Leads I, II, and III are bipolar leads, which consist of two electrodes of opposite polarity (positive and negative). The third (ground) electrode minimizes electrical activity from other sources.
  • 44.
  • 45. What is an ECG?
  • 46.
  • 47. Limb leads • Electrodes are placed on the right arm (RA), left arm (LA), right leg (RL), and left leg (LL). • With only four electrodes, six leads are viewed. • Standard leads: I, II, III • Augmented leads: aVR, aVL, aVF • Einthoven’s Triangle
  • 48. Limb leads and augmented leads
  • 49. Standard leads • Lead I is the voltage between the (positive) left arm (LA) electrode and right arm (RA) electrode: – I=LA-RA • Lead II is the voltage between the (positive) left leg (LL) electrode and the right arm (RA) electrode: – II=LL-RA • Lead III is the voltage between the (positive) left leg (LL) electrode and the left arm (LA) electrode: – III=LL-LA
  • 50.
  • 51. Augmented limb leads • Leads aVR, aVL, and aVF are the augmented limb leads. • Derived from the same three electrodes as leads I, II, and III • These use the Goldberger's central terminal as their negative pole which is a combination of inputs from other two limb electrodes
  • 52.
  • 53. Precordial leads • The precordial leads lie in the transverse (horizontal) plane, perpendicular to the other six leads. The six precordial electrodes act as the positive poles for the six corresponding precordial leads: (V1, V2, V3, V4, V5 and V6). • Wilson's central terminal is used as the negative pole
  • 54.
  • 55.
  • 56. ECG leads • Leads aVR, aVL, and aVF are unipolar leads and consist of a single positive electrode and a reference point (with zero electrical potential) that lies in the center of the heart’s electrical field. • Leads V1–V6 are unipolar leads and consist of a single positive electrode with a negative reference point found at the electrical center of the heart. • Voltage changes are amplified and visually displayed on an oscilloscope and graph paper.
  • 57. • An ECG tracing looks different in each lead because the recorded angle of electrical activity changes with each lead. • Several different angles allow a more accurate perspective than a single one would. • The ECG machine can be adjusted to make any skin electrode positive or negative. The polarity depends on which lead the machine is recording. • A cable attached to the patient is divided into several different-colored wires: three, four, or five for monitoring purposes, or ten for a 12-lead ECG.
  • 58. Lead interpretation • LEADS I,II and VL look at the left lateral surface of the heart. • III and VF at the inferior surface. • And VR looks at the atria. • AVR and II look at the heart from opposite directions. • Leads VI and V2 look at the right ventricle. • V3 and V4 look at the septum between the ventricles and the anterior wall of the left ventricle. • V5 and V6 look at the anterior and lateral walls of the left ventricle.
  • 60.
  • 61.
  • 62.
  • 64. Methods of counting heart rate • Heart rate is calculated as the number of times the heart beats per minute. It usually measures ventricular rate (the number of QRS complexes) but can refer to atrial rate (the number of P waves). • Method chosen to calculate HR varies according to rate and regularity on the ECG tracing
  • 66. Procedure 1. Position patient supine. Ensure a comfortable positioning. 2. Explain procedure to dispel fears or myths. Instruct patient to lie as still as possible. 3. Attach electrodes 1. Limb leads 1. Right/left arm, right/left leg 2. Precordial leads 1. V1 = 4th intercostal space to right of sternal border 2. V2 = 4th intercostal space to left of sternal border 3. V3 = midway between leads V2 and V4 4. V4 = midclavicular line, above the 5th interspace 5. V5 = anterior axillary line at the same level as V4 6. V6 = midaxillary line at the same level as leads V4 and V5
  • 68.
  • 69. How to Read an ECG • Basics – Always approach ECG reading in a systematic, stepwise fashion
  • 70. 1. Rate • To determine the rate you must first know the paper speed (usually 25mm/sec) – 5 large blocks = 1 second – 1 large block = 0.2 second (200 msec) – 1 small block = 0.04 second (40 msec) – Rate = (# of QRS) x 60 seconds # of seconds 1 min
  • 71. 1. Rate (continued) • If speed is 25mm/sec, it is much easier to estimate the rate using the rule “300-150-100 -- 75-60-50” • Also…depending on the ECG machine, sometimes the HR will be provided!
  • 72. 2. Rhythm • Is there a P-wave before every Q and a Q-wave after every P? – No P-waves • Narrow complex QRS: Atrial fibrillation • Wide complex: ventricular rhythm (Idioventricular, Ventricular tachycardia, Ventricular fibrillation) – P-wave present • Fixed PR interval – Normal PR interval » If P wave is positive in II → Sinus rhythm » If P wave is negative in II → Junctional rhythm – Prolonged PR interval » QRS always present = First degree AV block » Regularly “dropped” QRS = Second deg. AV block (Mobitz Type II) – Sawtooth” p-wave pattern = Atrial flutter • Variable PR interval – Second degree AV block (Mobitz Type I/Wenckebach) – Different P-wave morphologies » Wandering pacemaker » Multifocal atrial tachycardia • P-wave and Q-wave independent – Third degree (Complete) AV block
  • 74. 4. P-Wave and PR interval • P Wave – P wave represents atrial depolarization • PR Interval – PR interval is beginning of P wave to beginning of QRS – Normal interval is 120-200 milliseconds (3-5 small boxes) – Why would PR interval be lengthened?...blocks • 1st degree - consistently lengthened PR • 2nd degree (Type 1) - Wenckebach • 2nd degree (Type 2) - will regularly drop beat, PR interval less important • 3rd degree - no relation between P and QRS, P waves regular, QRS regular and wide – Why would PR interval be shortened? • ectopic atrial foci (e.g. wandering pacemaker, multifocal atrial tachycardia) • accessory tracts, Wolf-Parkinson-White syndrome (WPW)
  • 75. 5. QRS • QRS Complex – Normal width is <120 ms (3 small squares) – What causes widened QRS? • RBBB (RSR’ in V1; wide S wave in I, V5-6) • LBBB (wide R in I, V5-6; no Q in I, V5-6; displaced ST and T waves opposite to major deflection of QRS) • Ventricular beat • Accessory tracts – Detect ventricular hypertrophy by height of QRS • S in V1 + R in V5 or V6 ≥ 35 mm → LVH • R in AVL ≥11mm → LVH • If R wave (any +ve defl’n ) in V1 → Likely RVH
  • 76. 6. ST Segment • ST Segment – Elevation = active infarction (vessel occluded), pericarditis, aneurysm of ventricle – Look at lead where elevation occurs to determine vessel occluded – Depression = ischemia, digoxin toxicity, hypokalemia, elevated intracranial pressure – An old MI will be seen as Q wave (1/3 of QRS complex)
  • 77. 7. T Waves • T Waves – Usually will be in same direction as QRS – T wave inversion caused by ischemia or old infarction
  • 78. 8. QT Interval • QT Interval – From end of QRS complex to end of T wave – Long QT is >500 ms (QTc >440ms) → can predispose to Torsades des pointes – What causes long QT? • Ischemia • Electrolyte abnormalities (↓ K, Mg, Ca) • Congenital • Drugs (many including antiarrhythmics, quinolones, TCA)