Various coronary physiological measurements can be made in the cardiac catheterization laboratory using sensor-tipped guidewires; they include the measurement of poststenotic absolute coronary flow reserve, the relative coronary flow reserve, and the pressure-derived fractional flow reserve of the myocardium. Ambiguity regarding abnormal microcirculation has been reduced or eliminated with measurements of relative coronary flow reserve and fractional flow reserve. The role of microvascular flow impairment can be separately determined with coronary flow velocity reserve measurements. In addition to lesion assessment before and after intervention, emerging applications of coronary physiology include the determination of physiological responses to new pharmacological agents, such as glycoprotein IIb/IIIa blockers, in patients with acute myocardial infarction. Measurements of coronary physiology in the catheterization laboratory provide objective data that complement angiography for clinical decision-making
Various coronary physiological measurements can be made in the cardiac catheterization laboratory using sensor-tipped guidewires; they include the measurement of poststenotic absolute coronary flow reserve, the relative coronary flow reserve, and the pressure-derived fractional flow reserve of the myocardium. Ambiguity regarding abnormal microcirculation has been reduced or eliminated with measurements of relative coronary flow reserve and fractional flow reserve. The role of microvascular flow impairment can be separately determined with coronary flow velocity reserve measurements. In addition to lesion assessment before and after intervention, emerging applications of coronary physiology include the determination of physiological responses to new pharmacological agents, such as glycoprotein IIb/IIIa blockers, in patients with acute myocardial infarction. Measurements of coronary physiology in the catheterization laboratory provide objective data that complement angiography for clinical decision-making
Coronary artery calcification (CAC) results in reduced vascular compliance, abnormal vasomotor responses, and impaired myocardial perfusion.
The presence of CAC is associated with worse outcomes in the general population and in patients undergoing revascularization
Two recognized types of CAC are
Atherosclerotic (Intimal)
Medial artery calcification
Coronary artery calcification (CAC) results in reduced vascular compliance, abnormal vasomotor responses, and impaired myocardial perfusion.
The presence of CAC is associated with worse outcomes in the general population and in patients undergoing revascularization
Two recognized types of CAC are
Atherosclerotic (Intimal)
Medial artery calcification
The cardiac conduction system is a network of specialized cardiac muscle cells that initiate and transmit the electrical impulses responsible for the coordinated contractions of each cardiac cycle. These special cells are able to generate an action potential on their own (self-excitation) and pass it on to other nearby cells (conduction), including cardiomyocytes.
CONDUCTIVE SYSTEM OF HEART .pptx BY MRS. WINCY THIRUMURUGAN .PROFESSOR.NURSIN...WINCY THIRUMURUGAN
MEANING.
The conducting system of the heart consists of cardiac muscle cells and conducting fibers (not nervous tissue) that are specialized for initiating impulses and conducting them rapidly through the heart.
It provides the heart its automatic rhythmic beat.
The purpose is to
Generating rhythmical electrical impulses to cause rhythmical contraction of the heart muscle. Conducting these impulses rapidly throughout the heart.
This pathway is made up of 5 elements:
The sino-atrial (SA) node.
The atrio-ventricular (AV) node.
The bundle of His.
The left and right bundle branches.
The Purkinje fibers.
SINOATRIAL NODE
The sinoatrial (SA) node is a collection of specialized cells (pacemaker cells), and is located in the upper wall of the right atrium, at the junction where the superior vena cava enters.
These pacemaker cells can spontaneously generate electrical impulses. The wave of excitation created by the SA node spreads via gap junctions across both atria, resulting in atrial contraction (atrial systole) – with blood moving from the atria into the ventricles.
The SA node is supraventricular and is sensitive to parasympathetic and sympathetic influence.
The SA node generates impulses and influenced by the Autonomic Nervous System:
Sympathetic nervous system – increases firing rate of the SA node, and thus increases heart rate.
Parasympathetic nervous system – decreases firing rate of the SA node, and thus decreases heart rate
THE INTER NODAL PATHWAYS consist of three bands (anterior, middle, and posterior) that lead directly from the SA node to the next node in the conduction system, the atrioventricular node. The impulse takes approximately 50 m s (milliseconds) to travel between these two nodes.
Bachmann's bundle (BB), also known as the interatrial bundle, myocardial strands connecting the right and left atrial walls and is considered to be the main pathway of interatrial conduction.
THE AV NODEThe AV node is located in the posterior wall of the right atrium immediately behind the tricuspid valve.
Cause of Slow Conduction in the A-V Node
What is the significance of AV nodal delay?
The cardiac impulse does not travel from the atria to the ventricles too rapidly.
It is primarily the AV node and it’s adjacent fibers that delay this transmission into the ventricles
AV BUNDLE OR BUNDLE OF HIS
From the AV node arises a special conducting pathway .
RIGHT AND LEFT BUNDLE BRANCHES
FASCICLE
The right bundle branch contains one fascicle.
The left bundle branch into three fascicles:
The left anterior,
The left posterior, and
The left septal fascicle.
PURKINJE FIBRES
The LT and RT bundle branches divides in turn course sidewise around each ventricular chamber and back toward the base of heart.
The ends of Purkinje fibers penetrate about one third of the way into muscle mass and finally become continuous with cardiac muscle fibers
,abundant with glycogen and extensive gap junctions, rapidly transmit cardiac action potentials in 0.03sec
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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.
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
These lecture slides, by Dr Sidra Arshad, offer a quick overview of physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
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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
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
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
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TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
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Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
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- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
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3. 1. The sinoatrial (SA) node is a spindle-shaped structure composed
of a fibrous tissue matrix with closely packed cells. It is 10-20 mm
long, 2-3 mm wide, and thick, tending to narrow caudally toward
the inferior vena cava (IVC). The SA node is located less than 1
mm from the epicardial surface, laterally in the right atrial sulcus
terminalis at the junction of the anteromedial aspect of the
superior vena cava (SVC) and the right atrium (RA).
2. The artery supplying the sinus node branches from the right
coronary artery in 55-60% of hearts or the left circumflex artery in
40-45% of hearts. The artery approaches the node from a
clockwise or counterclockwise direction around the SVC–RA
junction.[3]
3. The SA node is densely innervated with postganglionic
adrenergic and cholinergic nerve terminals. Neurotransmitters
modulate the SA node discharge rate by stimulation of beta-
adrenergic and muscarinic receptors. Both beta1 and beta2
adrenoceptors subtypes are present in the SA node. The human
SA node contains a more than 3-fold greater density of beta-
adrenergic and muscarinic cholinergic receptors than the adjacent
atrial tissue.[4]
4. Anatomic evidence suggests the presence of 3
intra-atrial pathways: (1) anterior internodal
pathway, (2) middle internodal tract, and (3)
posterior internodal tract.
The anterior internodal pathway begins at the
anterior margin of the SA node and curves
anteriorly around the SVC to enter the anterior
interatrial band, called the Bachmann. This band
continues to the left atrium (LA), with the anterior
internodal pathway entering the superior margin
of the AV node. The Bachmann bundle is a large
muscle bundle that appears to conduct the cardiac
impulse preferentially from the RA to the LA.
5. The middle internodal tract begins at the superior
and posterior margins of the sinus node, travels
behind the SVC to the crest of the interatrial
septum, and descends in the interatrial septum to
the superior margin of the AV node.
The posterior internodal tract starts at the posterior
margin of the sinus node and travels posteriorly
around the SVC and along the crista terminalis to
the eustachian ridge and then into the interatrial
septum above the coronary sinus, where it joins
the posterior portion of the AV node. These groups
of internodal tissue are best referred to as
internodal atrial myocardium, not tracts, as they
do not appear to be histologically discrete
specialized tracts
6.
7. The compact portion of the atrioventricular
(AV) node is a superficial structure located just
beneath the RA endocardium, anterior to the
ostium of the coronary sinus, and directly
above the insertion of the septal leaflet of the
tricuspid valve. It is at the apex of a triangle
formed by the tricuspid annulus and the
tendon of Todaro, which originates in the
central fibrous body and passes posteriorly
through the atrial septum to continue with the
eustachian valve
8.
9. In 85-90% of human hearts, the arterial supply
to the AV node is a branch from the right
coronary artery that originates at the posterior
intersection of the AV and interventricular
grooves (crux). In the remaining 10-15% of the
hearts, a branch of the left circumflex coronary
artery provides the AV nodal artery.
Fibers in the lower part of the AV node may
exhibit automatic impulse formation.
The main function of the AV node is
modulation of the atrial impulse transmission
to the ventricles to coordinate atrial and
ventricular contractions.
10. The bundle of His is a structure that connects with the distal
part of the compact AV node, perforates the central fibrous
body, and continues through the annulus fibrosus, where it
is called the nonbranching portion as it penetrates the
membranous septum.
Connective tissue of the central fibrous body and
membranous septum encloses the penetrating portion of the
AV bundle, which may send out extensions into the central
fibrous body. Proximal cells of the penetrating portion are
heterogeneous and resemble those of the compact AV node;
distal cells are similar to cells in the proximal bundle
branches.
Branches from the anterior and posterior descending
coronary arteries supply the upper muscular
interventricular septum with blood, which makes the
conduction system at this site more impervious to the
ischemic damage, unless the ischemia is extensive
11.
12. The bundle branches originate at the superior margin
of the muscular interventricular septum, immediately
below the membranous septum, with the cells of the
left bundle branch cascading downward as a
continuous sheet onto the septum beneath the
noncoronary aortic cusp. The right bundle branch
continues intramyocardially as an unbranched
extension of the AV bundle down the right side of the
interventricular septum to the apex of the right
ventricle and base of the anterior papillary muscle. The
anatomy of the left bundle branch system may be
variable and may not conform to a constant bifascicular
division. However, for clinical purposes and
electrocardiography (ECG), the concept of a
trifascicular system remains useful
13.
14. The terminal Purkinje fibers connect with the
ends of the bundle branches to form
interweaving networks on the endocardial
surface of both ventricles, which transmit the
cardiac impulse almost simultaneously to the
entire right and left ventricular endocardium.
Purkinje fibers tend to be less concentrated at
the base of the ventricle and the papillary
muscle tips. They penetrate only the inner third
of the endocardium. Purkinje fibers appear to
be more resistant to ischemia than ordinary
myocardial fibers.
15.
16.
17. Myocardial cells have several different electrophysiologic
properties:
1. Automaticity - refers to the ability to spontaneously
generate an electrical impulse.
2. Excitability - means that the cardiac cells have the
ability to respond to an electrical impulse.
3. Conductivity - allows for transmission of the electrical
impulse to another cardiac cell.
4. Contractility - refers to the ability to contract after an
electrical impulse is received.
5. Rhythmicity - is the cell's ability to send electrical
impulses in a regularly and evenly paced manner.,
and
Refractoriness - refers to the cell's inability to respond
to another electrical impulse
18. Myocardial cells contain actin and myosin
filaments and contracts by means of the sliding
filament mechanism. Myocardial cells are
joined by gap junctions, due to which electrical
impulses can spread to all cells in the mass.
19.
20.
21.
22. SA node Represented on the ECG as P wave
AV node conduction is represented on the ECG as the PR
Interval
The Bundle Branch and purkinje fibre depolarisation constitutes
ventricular depolarisation Represented on the ECG as the QRS
Atrial repolarisation occurs within the QRS & therefore is masked
Ventricular repolarisation is represented on the ECG as a T wave
23.
24. 1. RBBB( rt vent vol overload)
2. Prolonged PR interval (atrial enlargement
leading to increassed internodal conduction
distance)
3. Crochetage (M shaped) in inferior ECG leads
4. ostium primum a - left axis deviation.
ostium secundum - right axis deviation.
25.
26. The relationship of the defect to the ostium of
the coronary sinus, membranous portion of the
AV septum, and commissural area between the
septal and anterior tricuspid leaflets is studied
because these features serve as guides to the
location of the AV node and penetrating
portion of the bundle of His
To avoid damaging the AV node,the sutures
must not be placed too far from the edge
anteriorly.
27.
28. Because coronary sinus ASDs are close to the
AV node, stitches must be placed near the edge
of the defect superiorly in tissue that may not
be strong. For these reasons, patch closure is
generally advisable.
29. 1. When the right superior pulmonary veins
enter more cephalad in the SVC (more than
about 2 cm above the cavoatrial junction)
2. when the SVC is small (as in the presence
of bilateral SVCs)
To avoid sinus node dysfunction with incisions
across the cavoatrial junction
30. sinus venosus malformation with right upper and middle lobe pulmonary veins
entering superior vena cava (SVC). A, Right upper and middle pulmonary veins entering
SVC. Right atrial appendage is amputated. B, High SVC or innominate vein is
cannulated. Dashed line indicates the transecting incision in SVC
31. C, Cephalad end of transected SVC is anastomosed to amputated right atrial appendage. For
mobilization, azygos vein is divided. D, Small incision is made in right atrial wall. Lateral edge of
SVC orifice is sutured to lower rim of subcaval atrial septal defect (ASD), or the pathway is
completed with a pericardial or polytetrafluoroethylene patch. Cardiac end of transected SVC is
closed. E, Right pulmonary vein blood now flows (arrows) across the roofed ASD into left atrium
32. 1. Closure of ASDs in children has been shown to
improve AV conduction, decrease AV nodal
refractory periods, and improve sinus node
function in most patients early
postoperatively
2. Presumably this improvement results from
reduction in RV and right atrial volume after
ablation of the left-to-right shunt at the atrial
level.
33. In patients over about age 40, almost half of
those not in atrial fibrillation preoperatively
develop it late postoperatively. This tendency
to atrial fibrillation or flutter late
postoperatively may be less when venous
cannulation is directly into the venae
cavae rather than through the right
atrial appendage
34. prevalence of changed heart rhythms
after repair is similar in patients with
fossa ovalis ASDs and those with sinus
venosus malformation
sick sinus syndrome or junctional
rhythm late postoperatively are seen in
patients where incision is made across the
cavoatrial junction for SV type ASD
35.
36. 1. Truex described the location of the specialized
conduction tissue in hearts with VSD.
2. In a more detailed study, Lev expanded on
this topic
3. Kirklin and DuShane developed a surgical
technique that avoided producing heart block
during VSD repair
37.
38. the AV node and penetrating portion of the bundle
of His are in their normal position in hearts with
perimembranous VSDs.
As the bundle penetrates the fibrous right trigone
of the central fibrous body at the base of the
noncoronary cusp of the aortic valve, it lies along
the posteroinferior border of perimembranous and
inlet-type VSDs. As the bundle continues along the
inferior border of the VSD (at times slightly to the
left or right of the free edge),the left bundle branch
fascicles emerge from the branching portion. Only
the right bundle branch remains when the bundle
reaches the level of the muscle of Lancisi.
39. The perimembranous VSD is intimately
associated with the bundle of His which in a d-
loop heart passes through the tricuspid
annulus at the posterior and inferior corner of
the VSD.
The bundle soon branches into the right
and left bundle branch
40. Repair of perimembranous ventricular septal defect (VSD) from right atrium,
continuous suture technique.
Right atriotomy is parallel to atrioventricular groove from right atrial appendage toward
inferior vena cava. Stay sutures are placed to expose tricuspid orifice. Superior edge of
VSD is not visible because of overlying anterior leaflet of tricuspid valve.
Atrioventricular node lies within triangle of Koch,with bundle of His penetrating to
ventricular septum at posterior angle of VSD, where it is particularly vulnerable to injury
41. Bundle of His crosses beneath septal leaflet of tricuspid valve. Stitches must not penetrate
tricuspid anulus or into atrial myocardium, to preserve integrity of conduction system
42. Via rt ventriclotomy At a point 5 to 7 mm below inferior margin of VSD, suture line is tran
septal leaflet onto ventricular septum. Stitching continues along inferior rim of VSD,
with stitches placed 5 to 7 mm below rim until reaching muscle of Lancisi. An alternative
technique uses interrupted pledgeted mattress sutures for very thin portions of the
septal leaflet and posteroinferior edge of defect (conduction system) to facilitate secure
suture placement while avoiding conduction system. Remainder of suture line employs
a continuous suture technique.
43. for Perimembranous Ventricular Septal Defect the RV approach
may be used for repair of perimembranous VSDs and results in
low hospital mortality even in patients with high Rp.
The RV approach has the advantage that the nadir of the
noncoronary cusp of the aortic valve, which is the area of the right
trigone and bundle of His, can be accurately visualized, which
may be helpful in choosing the suture technique that will
minimize prevalence of heart block
The RV approach has the disadvantages of
(1) leaving a scar in the RV,
(2) being associated with a higher prevalence of complete RBBB
than with an atrial approach,
and (3) possibly resulting in more ventricular arrhythmias late
postoperatively.
.
44. The right atrial approach may be used almost
exclusively, a practice begun in about 1960 at
the Mayo Clinic. An accurate repair can be
obtained through a right atrial approach in
nearly all cases. Associated infundibular
pulmonary stenosis can be excised. An RV scar
is avoided, and occurrence of RBBB is lower
than with the transventricular approach.H11
With the right atrial approach, however,
techniques must be accurate to avoid damaging
the tricuspid valve , leaflets or chordae
45. Since the right atrium must connect with the left ventricle
(i.e. atrioventricular discordance), it is not surprising that
the conduction system is abnormal. Pioneering work in this
area was undertaken by Anderson and colleagues.
In corrected transposition (C-TGA), the functional
atrioventricular node arises anteriorly and superiorly and is
usually lodged between the annulus of the mitral valve .
This functional AV node is therefore superior to the usual
location of the AV node which may be present as an
accessory node.
46. Often there is a posterior atrioventricular node in its usual
position within the triangle of Koch, but it is usually
disconnected from the remainder of the conduction tissue.
The conduction system in C-TGA is more tenuous than that
of normal hearts. Fibrosis of the junction between the
atrioventricular node and the atrioventricular bundle has
been seen in older patients
Artrial switch operation- Post operative arrhythmia less
compared to Mustard and Senning operation.
47.
48. Categorised – Left or right – based on morphological
operative single ventricle
Single right ventricle- no conduction disturbances.
Single left ventricle- AV node is hypoplastic
- Prolonged PR interval culminating
in complete heart block
49. Complete absence
of communication
between the right
atrium and right
ventricle
About 3 % of
congenital heart
disease
50. SA node is normal.
Posterior small AV node originates in close relation
to Tendon of Todaro.
Occasionally, the branching bundle may
be in close proximity to the posteroinferior rim of the
foramen and the right bundle-branch may lie
subendocardially in the rim of the defect.
51. It is important, therefore, to appreciate
that the atrioventricular node is in close relation to the
tendon of Todaro, which is a readily identifiable
landmark during surgical exposure.
Closure of the foramen should usually be
accomplished safely provided that
deep sutures are not placed in the posteroinferior
quadrant.
52. Usual type of arrythmias with Atrial surgery are SVT
of which AF, Atrial flutter and junctional rhythms
are most common.
In large ostium primum type defect because of
posteriorly displaced AV node , it is frequently
associated with prolonged AV conduction.
Small osteum secundum defect causes no problem
during repair.
53. Hypothermia, ischemic arrest , direct injury to
conduction system, haematoma, injury to SA nodal
artery , oedema , forign body reaction to suture
material all are responsible for arrhythmias
The most common conduction disturbance that
occurs after ventricular surgery is RBB block .
RBBB can be due to direct injury to main RBB or
right ventriculotomy ( in fallots tetrology surgery )
by disrupting the right ventricular subendocardial
purkinje network
54. Clockwise from anterolateral commissure are the aortic cusps, conduction system,
Atrioventricular septum, coronary sinus, and circumflex coronary artery,
which are at risk when bites are taken too deeply
Mitral valve
56. Care must be taken while removing
calcium from the region of the
membranous septum and right trigone,
Beneath the noncoronary cusp–
right coronary cusp commissuret and
rigorous avoidance of suture penetration
of the membranous septum near
its junction with the muscular septum