This document provides an overview of several cardiac arrhythmias and conditions including:
1. Accelerated idioventricular rhythm (AIVR), which results when an ectopic ventricular pacemaker exceeds the sinus node rate. AIVR is seen post-myocardial infarction and features a regular rhythm between 50-110 bpm with three or more QRS complexes.
2. Atrial flutter, a supraventricular tachycardia caused by a reentry circuit in the right atrium with a rate of around 300 bpm. The ventricular rate is determined by AV conduction.
3. Atrial fibrillation, the most common sustained arrhythmia characterized by irregularly irregular rhythm without
Electrolyte and metabolic ECG abnormalitiesAby Thankachan
Electrolyte and metabolic ECG abnormalities
Precise guide for Allied Health Science Students especially cardiac specialty students, DGNM, B.Sc Nursing & M.Sc Nursing Students .
Electrolyte and metabolic ECG abnormalitiesAby Thankachan
Electrolyte and metabolic ECG abnormalities
Precise guide for Allied Health Science Students especially cardiac specialty students, DGNM, B.Sc Nursing & M.Sc Nursing Students .
The anatomy of heart, ECG, sensors, transducers, heart sound, blood pressure, blood volume, blood flow, circulatory systems are discussed related to engineering concepts.
Repolarization ST wave Abnormalities
Precise guide for Allied Health Science Students especially cardiac specialty students, DGNM, B.Sc Nursing & M.Sc Nursing Students regarding Repolarization ST wave Abnormalities.
The right and left atria are the two smaller chambers of the heart that are responsible for filling the ventricles with blood before it is circulated throughout the body. When multiple electrical stimuli originate outside of the sinoatrial node, they have the potential for causing rapid and irregular contractions in the atria. It is believe that these stimuli originate in tissue located near the pulmonary veins and are perpetuated by a series of re-entry circuits. Although an EKG technician is not responsible for diagnosing and treating patients, they should recognize common signs of atrial fibrillation on the electrocardiogram including absent P waves, loss of the isoelectric baseline, rhythm abnormalities, QRS changes, and fibrillatory waves. Symptoms of the condition may include things like shortness of breath, confusion, fatigue, chest pain, lightheadedness, and more. Physicians may order additional studies such as echocardiograms and Holter monitoring for more informed evaluation.
Blood Pressure (BP) is one of the vital hemodynamic parameters that we often aim to optimize for critically ill patients. Our decisions regarding BP targets, and ensuing use (or avoidance) of vasopressor agents, may directly impact on outcomes for these patients. Despite being a fundamental tenet of critical care, there is a lack of quality evidence to suggest optimal BP targets or to guide the use of vasopressors for individual patients with shock. A mean arterial BP (MAP) of 65-70 mmHg is an often-cited initial BP target for patients during vasopressor therapy. Use of vasopressors to maintain MAP of 65 mmHg or greater remains one of the core clinical criteria in the new definition of septic shock. However, such standard targets are unlikely to be applicable to all patients, many of whom would have a basal MAP higher than 65-70 mmHg, often to a varying degree, during their usual pre-illness state. Therefore, a vasopressor therapy guided by standard BP thresholds may result in a variable degree of untreated relative hypotension, which is associated with new-onset acute kidney injury (AKI). From a physiological standpoint, any relative reduction in net perfusion pressure across an organ’s vasculature can overwhelm its autoregulatory mechanisms, which are already under stress during a shock state. In a recent major RCT, among patients with chronic hypertension, targeting a higher MAP of 80-85 mmHg, versus 65-70 mmHg, showed a lower incidence of subsequent AKI, but with no difference in mortality. However, this RCT did not take patients’ pre-illness basal BP into account, making it difficult to extrapolate these results to those patients with chronic hypertension, who usually have a well-controlled basal BP, or to those patients, who although have a higher-than-normal basal BP but are not formally diagnosed with hypertension. Accounting for a patient’s pre-illness basal BP can minimize variation in the degree of untreated relative hypotension that is often inadvertently accepted in conventional care. It is a simple, but untested, strategy. Further, new tools that can monitor cerebral autoregulation in real-time are on the horizon and have shown some promise in suggesting an optimal BP for individual patients with shock. This technology can further help adjust the initial BP target as a patient deteriorates or recovers from the shock state.
The anatomy of heart, ECG, sensors, transducers, heart sound, blood pressure, blood volume, blood flow, circulatory systems are discussed related to engineering concepts.
Repolarization ST wave Abnormalities
Precise guide for Allied Health Science Students especially cardiac specialty students, DGNM, B.Sc Nursing & M.Sc Nursing Students regarding Repolarization ST wave Abnormalities.
The right and left atria are the two smaller chambers of the heart that are responsible for filling the ventricles with blood before it is circulated throughout the body. When multiple electrical stimuli originate outside of the sinoatrial node, they have the potential for causing rapid and irregular contractions in the atria. It is believe that these stimuli originate in tissue located near the pulmonary veins and are perpetuated by a series of re-entry circuits. Although an EKG technician is not responsible for diagnosing and treating patients, they should recognize common signs of atrial fibrillation on the electrocardiogram including absent P waves, loss of the isoelectric baseline, rhythm abnormalities, QRS changes, and fibrillatory waves. Symptoms of the condition may include things like shortness of breath, confusion, fatigue, chest pain, lightheadedness, and more. Physicians may order additional studies such as echocardiograms and Holter monitoring for more informed evaluation.
Blood Pressure (BP) is one of the vital hemodynamic parameters that we often aim to optimize for critically ill patients. Our decisions regarding BP targets, and ensuing use (or avoidance) of vasopressor agents, may directly impact on outcomes for these patients. Despite being a fundamental tenet of critical care, there is a lack of quality evidence to suggest optimal BP targets or to guide the use of vasopressors for individual patients with shock. A mean arterial BP (MAP) of 65-70 mmHg is an often-cited initial BP target for patients during vasopressor therapy. Use of vasopressors to maintain MAP of 65 mmHg or greater remains one of the core clinical criteria in the new definition of septic shock. However, such standard targets are unlikely to be applicable to all patients, many of whom would have a basal MAP higher than 65-70 mmHg, often to a varying degree, during their usual pre-illness state. Therefore, a vasopressor therapy guided by standard BP thresholds may result in a variable degree of untreated relative hypotension, which is associated with new-onset acute kidney injury (AKI). From a physiological standpoint, any relative reduction in net perfusion pressure across an organ’s vasculature can overwhelm its autoregulatory mechanisms, which are already under stress during a shock state. In a recent major RCT, among patients with chronic hypertension, targeting a higher MAP of 80-85 mmHg, versus 65-70 mmHg, showed a lower incidence of subsequent AKI, but with no difference in mortality. However, this RCT did not take patients’ pre-illness basal BP into account, making it difficult to extrapolate these results to those patients with chronic hypertension, who usually have a well-controlled basal BP, or to those patients, who although have a higher-than-normal basal BP but are not formally diagnosed with hypertension. Accounting for a patient’s pre-illness basal BP can minimize variation in the degree of untreated relative hypotension that is often inadvertently accepted in conventional care. It is a simple, but untested, strategy. Further, new tools that can monitor cerebral autoregulation in real-time are on the horizon and have shown some promise in suggesting an optimal BP for individual patients with shock. This technology can further help adjust the initial BP target as a patient deteriorates or recovers from the shock state.
The rhythm is best analyzed by looking at a rhythm strip.
On a 12 lead ECG this is usually a 10 second recording from Lead II.
Confirm or corroborate any findings in this lead by checking the other leads.
A longer rhythm strip, recorded perhaps recorded at a slower speed, may be helpful.
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
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MANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdfJim Jacob Roy
Cardiac conduction defects can occur due to various causes.
Atrioventricular conduction blocks ( AV blocks ) are classified into 3 types.
This document describes the acute management of AV block.
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Anti ulcer drugs and their Advance pharmacology ||
Anti-ulcer drugs are medications used to prevent and treat ulcers in the stomach and upper part of the small intestine (duodenal ulcers). These ulcers are often caused by an imbalance between stomach acid and the mucosal lining, which protects the stomach lining.
||Scope: Overview of various classes of anti-ulcer drugs, their mechanisms of action, indications, side effects, and clinical considerations.
2. Accelerated Idioventricular
Rhythm (AIVR)
Burns E. Accelerated Idioventricular Rhythm (April 10, 2017). Retrieved
from https://lifeinthefastlane.com/ecg-library/aivr/
PowerPlugs Templates for PowerPoint Preview 2
3. • Results when the rate of an ectopic ventricular
pacemaker exceeds that of the sinus node.
• It is often associated with increased vagal tone
and decreased sympathetic tone.
AIVR
Quora.com
AIVR is classically seen in the
reperfusion phase of an
acute STEMI (post
thrombolysis).
5. Fusion beat
A fusion beat occurs when electrical
impulses from different sources act upon
the same region of the heart at the same
time.
If it acts upon the ventricular chambers it is
called a ventricular fusion beat.
Colliding currents in the atrial
chambers produce atrial fusion beats.
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Understanding Electrocardiography 8 Ed. Elsevier Health Sciences. 2003. p. 245
6. Capture beat
Capture beat is the return of
atrial control over
ventricular contraction,
following a period of
atrioventricular dissociation.
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7. Fusion vs. capture beat
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Capture beat
Fusion beat
9. Causes of AIVR
• Reperfusion phase of an acute myocardial infarction is
the most common cause!
• Beta-sympathomimetics: isoprenaline, adrenaline!
• Drug toxicity: digoxin, cocaine and volatile
anaesthetics (desflurane)!
• Electrolyte abnormalities!
• Cardiomyopathy, congenital heart disease,
myocarditis!
• Return of spontaneous circulation (ROSC) following
cardiac arrest!
• Athletic heart!
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10. Treatment
It is important to treat the
underlying cause.
It is self limiting and resolves
when sinus rate exceeds that
of the ventricular foci.
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11. Accelerated Junctional Rhythm
(AJR)
Burns E. Accelerated Junctional Rhythm (April 10, 2017).
Retrieved from https://lifeinthefastlane.com/ecg-
library/accelerated-junctional-rhythm/
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12. AJR
Accelerated junctional rhythm (AJR) occurs
when the rate of an AV junctional pacemaker
exceeds that of the sinus node:
• increased automaticity in the AV node
• decreased automaticity in the sinus node
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AV node
16. ECG features
• Narrow complex rhythm: QRS duration <120 ms.
• Ventricular rate usually 60-100 bpm.
• Retrograde P waves may be present and can appear
before, during or after the QRS complex.
• Retrograde P waves are usually inverted in the inferior
leads (DII, DIII, aVF), but upright in aVR + V1.
• AV dissociation may be present with the ventricular
rate usually greater than the atrial rate.
• There may be associated ECG features of digoxin effect
and toxicity.
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17. Retrograde P wave occuring after the
QRS complex.
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19. Example
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Negative P waves in DII, DIII and aVF!
Positive P waves in aVR and V1!
Rate 115 bmp
20. Anterior STEMI
Burns E. Accelerated Junctional Rhythm (April 10, 2017).
Retrieved from https://lifeinthefastlane.com/ecg-
library/anterior-stemi/
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21. Anterior STEMI
• Anterior STEMI results from the occlusion of the
left anterior descending artery (LAD).
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HeartUpdate.com
22. Anterior STEMI
STEMI nomenclature based on the location of
the maximal ST elevation:
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Septal STEMI V1-V2
Anterior STEMI V2-V5
Anteroseptal STEMI V1-V4
Anterolateral STEMI V3-V6, DI, aVL
Extensive anterior/anterolateral V1-V6, DI, aVL
23. Anterior-inferior STEMI
• It is due to occlusion of a “wraparound” LAD.
ECG pattern:
• simultaneous ST elevation in the precordial
and inferior leads due to occlusion of a variant
(type III) LAD
Type III LAD wraps around the cardiac apex to
supply both the anterior and inferior walls of the
left ventricle.
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25. Left main coronary artery occlusion
• Widespread ST depression with ST elevation in
aVR that is bigger than in V1.
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Healio.com
26. Wellen´s syndrome
• Deep precordial T wave inversions or biphasic T waves in
V2-V3, indicating critical proximal LAD stenosis.
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Type A with biphasic
T waves (25%).
Type B with deeply
and symmetrically
inverted (75%).
27. De Winter´s T waves
• Upsloping ST depression with symmetrically
peaked T waves in the precordial leads: indicates
acute LAD occlusion.
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28. Arrhythmogenic Right Ventricular
Cardiomyopathy (ARVC)
Burns E. Arrhythmogenic Right Ventricular Cardiomyopathy
(August 29, 2017). Retrieved from
https://lifeinthefastlane.com/ecg-library/basics/arrhythmogenic-
right-ventricular-cardiomyopathy/
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29. ARVC
• An inherited myocardial disease associated
with paroxysmal ventricular
arrhythmias and sudden cardiac death.
• Naxos disease: ARVC, woolly hair and skin
changes.
• The second most common cause of sudden
cardiac death in young people, after
hyperthrophic obstructive cardiomyopathy.
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31. Atrial flutter
Burns E. Atrial flutter (April 10, 2017). Retrieved from
https://lifeinthefastlane.com/ecg-library/atrial-flutter/
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32. Atrial flutter
Atrial flutter is a type of supraventricular tachycardia caused
by a re-entry circuit within the right atrium.
The length of the re-entry circuit corresponds to the size of
the right atrium.
Atrial rate is around 300 bpm (range 200-400).
Ventricular rate is determined by the AV conduction ratio
(degree of AV block).
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33. Atrial flutter
Atrial flutter with 1:1
conduction is associated
with severe haemodynamic
instability and progression
to ventricular fibrillation.
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35. Ventricular rate
Ventricular rate is a fraction of the atrial rate.
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Ventricular rate Block
150 bmp 2:1
100 bmp 3:1
75 bmp 4:1
36. Anticlockwise reentry atrial flutter
• This is the commonest form of atrial
flutter (90% of cases).
Retrograde atrial conduction produces:
• inverted flutter waves in leads DII, DIII
and aVF
• positive flutter waves in V1
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37. Clockwise reentry atrial flutter
Anterograde atrial conduction
produces:
•positive flutter waves in leads DII,
DIII and aVF
•broad, inverted flutter waves in V1
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39. Atrial fibrillation
Burns E. Atrial fibrillation (August 29, 2017). Retrieved from
https://lifeinthefastlane.com/ecg-library/atrial-fibrillation/
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40. Atrial fibrillation
• It is the most common sustained
arrhythmia.
Complications of AF include:
• haemodynamic instability
• cardiomyopathy
• cardiac failure
• embolic events
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42. ECG changes
• Irregularly irregular rhythm.
• No P waves.
• Absence of an isoelectric baseline.
• Variable ventricular rate.
• QRS complexes usually <120 ms.
• Fibrillatory waves can be fine (amplitude <0.5mm)
or coarse (amplitude >0.5mm).
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43. Atrial fibrillation classification
AF with rapid ventricular response is when the
ventricular rate is >100 bpm.
Slow AF is when the ventricular rate is <60 bpm.
Causes of slow AF are hypothermia, digoxin toxicity
and sinus node dysfunction.
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44. Atrial fibrillation classification
• First episode is the initial detection of AF regardless of
symptoms or duration.
• Recurrent AF is when more than 2 episodes of AF
occure.
• Paroxysmal AF is self terminating episode that lasts
less than 7 days.
• Persistent AF is not self terminating episode with
duration more than 7 days.
• Long-standing persistent AF lasts up to 1 year.
• Permanent AF lasts more than 1 year in which rhythm
control interventions are not pursued or are
unsuccessful.
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