This document discusses central venous pressure (CVP) monitoring and pulmonary artery catheterization. It begins by defining CVP and its normal values. It then lists indications for central venous cannulation and complications. Next, it discusses pulmonary artery pressure monitoring, normal values, waveforms, and complications of pulmonary artery catheterization. It also briefly discusses invasive arterial pressure monitoring.
Comprehensive presentation on intra arterial blood pressure with a good insight into the the basic physics and brief look into the risks and complications.
Hemodynamic monitoring- Hemodynamic monitoring refers to the measurement of pressure, flow and oxygenation within the cardiovascular system. Hemodynamic monitoring is amandatory process in all the critical care units to assess the patients progress. This presentation is aimed to create an insight on Hemodynamic monitoring.
Comprehensive presentation on intra arterial blood pressure with a good insight into the the basic physics and brief look into the risks and complications.
Hemodynamic monitoring- Hemodynamic monitoring refers to the measurement of pressure, flow and oxygenation within the cardiovascular system. Hemodynamic monitoring is amandatory process in all the critical care units to assess the patients progress. This presentation is aimed to create an insight on Hemodynamic monitoring.
Assessment of haemodynamics a critically ill patient and its management has always been a matter if debate. Over time a lot of studies and therapeutic interventions have been carried out. This presentation is a review of such interventions and their impact on the outcome.
Assessment of haemodynamics a critically ill patient and its management has always been a matter if debate. Over time a lot of studies and therapeutic interventions have been carried out. This presentation is a review of such interventions and their impact on the outcome.
central venous pressure and intra-arterial blood pressure monitoring. invasiv...prateek gupta
central venous pressure and intra-arterial blood pressure monitoring. various sites for cvp and Ibp insertion. working principle for cvp and ibp. indication and complication. various waveform of cvp and ibp
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
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
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 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
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.
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
3. • CVP ~ Right Atrial Pressure ~Right ventricular end diastolic
volume (preload)
• Reflects a patient’s
• Cardiac function →venous return to the heart
• Right ventricular function
• Intravascular fluid volume status
• Normal CVP values range 2- 6mmHg or 4-12cmH20
INTRODUCTION
DR KRISHNA KUMAR 312/5/2018
4. INDICATIONS FOR CENTRAL VENOUS
CANNULATION
• Central venous pressure monitoring
• Pulmonary artery catheterization and monitoring
• Temporary hemodialysis
• Drug administration
• Concentrated vasoactive drugs
• Hyperalimentation
• Chemotherapy
• Agents irritating to peripheral veins
• Prolonged antibiotic therapy
DR KRISHNA KUMAR 412/5/2018
5. • Rapid infusion of fluids (via large cannulas)
• Trauma
• Major surgery
• Aspiration of air emboli
• Inadequate peripheral intravenous access
• Sampling site for repeated blood testing
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10. CVP VALUES
• Increased in
Fluid overload
Right heart failure
Cardiac tamponade
Pleural effusion
Tension pneumothorax
Mechanical ventilation
• Decreased in
Hypovolemia
Shock
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11. Tricuspid regurgitation
increases mean CVP, and
the waveform displays a tall
systolic c-v wave that obliterates
the x
descent.
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12. Tricuspid stenosis increases
mean CVP, the diastolic y
descent is attenuated, and
the end-diastolic a wave is
prominent.
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13. Atrial fibrillation
Note absence of the a
wave,
a prominent c wave,
and a preserved v
wave and y descent
DR KRISHNA KUMAR 1312/5/2018
14. COMPLICATIONS OF CENTRAL VENOUS
PRESSURE MONITORING
• Mechanical
• Vascular injury
• Arterial
• Venous
• Cardiac tamponade
• Respiratory compromise
• Airway compression from
hematoma
• Pneumothorax
• Nerve injury
• Arrhythmias
• Thromboembolic
• Venous thrombosis
• Pulmonary embolism
• Arterial thrombosis and
embolism
• Catheter or guidewire embolism
• Infectious
• Insertion site infection
• Catheter infection
• Bloodstream infection
• Endocarditis
DR KRISHNA KUMAR 1412/5/2018
16. • Lewis Daxter (1945): first pulmonary artery catherization
• In 1970, Swan, Ganz, and colleagues introduced pulmonary
artery catheterization into clinical practice for the hemodynamic
assessment of patients with acute myocardial infarction
DR KRISHNA KUMAR 1612/5/2018
17. INDICATIONS
• Surgical patients associated with high risk of complications from
hemodynamic changes
• Advance cardiopulmonary diseases
• Goal directed fluid therapy
DR KRISHNA KUMAR 1712/5/2018
18. PULMONARY ARTERY CATHETERIZATION
• The standard PAC
7.0- to 9.0-fr circumference,
110 cm in length marked at 10-cm intervals,
Four internal lumina.
Distal port at the catheter tip - pulmonary artery pressure monitoring,
Second port more proximal - for CVP monitoring.
Third lumen leads to a balloon near the tip, and
Fourth lumen houses wires for a temperature thermistor, the end of which
lies just proximal to the balloon.
DR KRISHNA KUMAR 1812/5/2018
21. ADDITIONAL GUIDELINES FOR PULMONARY
ARTERY CATHETER INSERTION
• From a right IJV puncture site, the right atrium should be
reached when the PAC is inserted 20 to 25 cm, the right
ventricle at 30 to 35 cm, the pulmonary artery at 40 to 45 cm,
and the wedge position at 45 to 55 cm.
• For other sites extra distance required
• Lt IJV/ Rt & Lt EJV : 5-10 cm
• Femoral veins : 15cm
• Antecubital veins : 30-35 cms
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22. a wave follows “P” wave on ECG
v wave follows the QRS complex on ECG
RAP = mean (average) of a wave
• Right atrial pressure (RAP) is measured by the distal tip of the PAC
on insertion or by the proximal port post insertion.
a = atrial systole
v = ventricular systole
Right Atrium
Tricuspid valve
Pulmonic valve
P
QRS
DR KRISHNA KUMAR 2212/5/2018
23. MEASUREMENT OF RIGHT ATRIAL PRESSURE (RA)
FROM PULMONARY ARTERY CATHETER
a wave follows “P”
wave on ECG
v wave follows the
QRS complex on ECG
• Right atrial pressure (RAP) is measured by the distal tip of the PAC
on insertion or by the proximal port post insertion.
a = atrial systole
v = ventricular systole
Right Atrium
Tricuspid valve
Pulmonic valveP
DR KRISHNA KUMAR 2312/5/2018
24. RA WAVEFORM
“c” wave = closure of the tricuspid valve
“x” decent = follows closure of the tricuspid valve,
“y” decent = follows closure of the pulmonic valve
DR KRISHNA KUMAR 2412/5/2018
25. ALTERATIONS IN RA PRESSURE
• Reflects filling volume of the right atrium
• Low pressure consistent with hypovolemia:
• Trauma-> blood loss
• Dehydration
• Loss of fluid from drains
• Vomiting, diarrhea
• Burns
• 3rd spacing of fluid
• Consistent with tachycardia, ↓ urine output, dry skin & mucous
membranes
DR KRISHNA KUMAR 2512/5/2018
26. CLINICAL SITUATIONS CONSISTENT WITH
ELEVATIONS IN RA PRESSURES
• Tricuspid stenosis, regurgitation
• RV ischemia or failure
• Pulmonary hypertension
• Pulmonic stenosis
• Pulmonary embolism
• Atrial ventricular dissociation with loss of synchrony
• Atrial arrythmias, A-V conduction blocks)
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28. Onset of systole follows QRS complex on ECG
End diastole occurs at the onset of systole.
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29. ALTERATIONS IN RVP
Reflects filling volume of right ventricle
• Low pressure consistent with low volume
• Usually accompanies low RAP
• Elevation associated with:
• Hypervolemia
• Pulmonary embolism
• Outflow obstruction
• RV infarct/failure
• Pericarditis/tamponade
• LV failure
• Primary and secondary pulmonary
hypertension (PHTN)
• Pulmonic stenosis
• COPD
DR KRISHNA KUMAR 2912/5/2018
30. PA
systolic
PA
diastolic
Dicrotic notch
Represents closure of the pulmonic valve
• Pulmonary artery pressure (PAP) is measured from the distal tip of PAC on insertion and
distal tip post insertion.
• It has a systolic and diastolic component.
• Systolic pressure follows QRS on ECG.
• Diastole begins at the closure of the pulmonic valve and continues to next onset of systole.
Pulmonic valve
QRS
DR KRISHNA KUMAR 3012/5/2018
31. ALTERATIONS IN PAP
Represents filling volume in the pulmonary artery and resistance to
flow within the pulmonary circuit
• Low pressure consistent with hypovolemia
• Consistent with ↓ RAP and ↓ RVP
• High pressure consistent with
• PHTN
• COPD
• ARDS
• Pulmonary embolism (PE)
• Mitral stenosis
• Left ventricular heart failure
DR KRISHNA KUMAR 3112/5/2018
33. PULMONARY ARTERY WEDGE PRESSURE
• PAOP or PAWP is pressure within the pulmonary arterial
system when catheter tip ‘wedged’ in the tapering branch of one
of the pulmonary arteries in most patients this estimates LVEDP
thus is an indicator of LVEDV (preload of the left ventricle)
• Normally 6-12mmhg (1-5mmhg less than the pulmonary artery
diastolic pressure)
• PCWP >18 mmhg in the context of normal oncotic pressure
suggests left heart failure
DR KRISHNA KUMAR 3312/5/2018
34. • Pulmonary capillary wedge pressure (PCWP) or pulmonary artery wedge
pressure (PAWP) is measured from the distal port of PAC with balloon
inflated.
a = atrial systole
v = ventricular systole
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35. Catheter tip looks “through” the pulmonary circulation to “see” the left atrial
pressure.
PCWP indirectly measures left atrial pressure
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36. ALTERATIONS OF PCWP
• Low pressure consistent with hypovolemia
• Elevations consistent with:
• Mitral stenosis/regurgitation
• Aortic stenosis/regurgitation
• Acute LV ischemia/infarct
• LV failure
• Atrial ventricular dissociation with loss of synchrony
• Both RA and PCWP elevated in cardiac tamponade, constrictive
pericarditis, and hypervolemia
DR KRISHNA KUMAR 3612/5/2018
41. INTRODUCTION
• Intra-arterial blood pressure (IBP) measurement is often
considered to be the gold standard of blood pressure
measurement.
• Despite its increased risk, cost, and need for technical expertise
for placement and management, its utility in providing crucial
and timely information outweighs its risks in many cases
DR KRISHNA KUMAR 4112/5/2018
42. INDICATIONS FOR ARTERIAL CANNULATION
Continuous, real-time blood pressure monitoring
Planned pharmacologic or mechanical cardiovascular manipulation
Repeated blood sampling
Failure of indirect arterial blood pressure measurement, e.g. burns
or obesity
Supplementary diagnostic information from the arterial waveform
DR KRISHNA KUMAR 4212/5/2018
43. BASIC PRICIPLES
• The pressure waveform of the arterial pulse is transmitted via
the column of fluid, to a pressure transducer where it is
converted into an electrical signal.
• This electrical signal is then processed, amplified and converted
into a visual display by a microprocessor.
DR KRISHNA KUMAR 4312/5/2018
44. PERCUTANEOUS RADIAL ARTERY
CANNULATION
• The radial artery is the most common site for invasive blood
pressure monitoring because it is technically easy to cannulate
and complications are uncommon
• Modified Allen’s test
DR KRISHNA KUMAR 4412/5/2018
49. COMPLICATIONS OF DIRECT ARTERIAL PRESSURE
MONITORING
• Hemorrhage
• Misinterpretation of data
• Distal ischemia
• Pseudoaneurysm
• Arteriovenous fistula
• Arterial embolization
• Infection
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50. PHYSICAL PRINCIPLES
• A wave is a disturbance that travels through a medium,
transferring energy but not matter.
• One of the simplest waveforms is the sine wave
DR KRISHNA KUMAR 5012/5/2018
51. • Fourier Analysis
The arterial waveform is clearly not a simple sine wave, but
it can be broken down into a series of many component sine
waves
The process of analysing a complex waveform in terms of its
constituent sine waves is called Fourier Analysis.
DR KRISHNA KUMAR 5112/5/2018
53. • The natural frequency of a system determines how rapidly the
system oscillates after a stimulus
• The damping coefficient reflects frictional forces acting on the
system and determines how rapidly it returns to rest after a
stimulus
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54. NATURAL FREQUENCY
• It is important that the IBP system has a very high natural
frequency – at least eight times the fundamental frequency of
the arterial waveform (the pulse rate).
DR KRISHNA KUMAR 5412/5/2018
55. NATURAL FREQUENCY
• The natural frequency of a system may be increased by:
Reducing the length of the cannula or tubing
Reducing the compliance of the cannula
Reducing the density of the fluid used in the tubing
Increasing the diameter of the cannula or tubing
DR KRISHNA KUMAR 5512/5/2018
56. DAMPING
• Anything that reduces energy in an oscillating system will reduce the
amplitude of the oscillations. This is termed damping.
• Some degree of damping is required in all systems (critical damping),
but if excessive (overdamping) or insufficient (underdamping) the
output will be adversely effected.
DR KRISHNA KUMAR 5612/5/2018
58. Factors that cause overdamping include:
Friction in the fluid pathway
Three way taps
Bubbles and clots
Vasospasm
Narrow, long or compliant tubing
Kinks in the cannula or tubing
DR KRISHNA KUMAR 5812/5/2018
59. FAST-FLUSH TEST / SQUARE WAVE TEST
• Provides a convenient bedside method for determining dynamic
response of the system
• Natural frequency is inversely proportional to the time between
adjacent oscillation peaks
• The damping coefficient can be calculated mathematically, but
it is usually determined graphically from the amplitude ratio
DR KRISHNA KUMAR 5912/5/2018
63. COMPONENTS OF AN IBP MEASURING SYSTEM
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64. COMPONENTS OF AN IABP MEASURING
SYSTEM
• Intra-arterial cannula
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65. COMPONENTS OF AN IABP MEASURING
SYSTEM
• Intra-arterial cannula
• Fluid filled tubing
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66. COMPONENTS OF AN IABP MEASURING
SYSTEM
• Intra-arterial cannula
• Fluid filled tubing
• Transducer
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67. WHEATSTONE BRIDGE
• The Wheatstone bridge is a network of four resistors connected, with
a battery or DC voltage source (electromotive force) connected
between A and C and a voltmeter (V) connected between B and D.
• The bridge is said to be “balanced” when the voltmeter reads zero
potential difference between points B and D.
• From Ohm’s law (V = IR), it is easy to show that balance occurs when
Rx = Rs × (R2/R1)
• If Rs is an adjustable standard resistor and R1 and R2 are fixed
known resistors, then the balanced bridge provides a very precise
means of determining Rx, the unknown resistance.
• In this case, the transducer, itself, is the unknown resistance Rx.
DR KRISHNA KUMAR 6712/5/2018
68. • The transducer is usually a soft silicone diaphragm attached to
a Wheatstone bridge.
• It converts the pressure change into a change in electrical
resistance of the circuit. This can be viewed as waveform.
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69. COMPONENTS OF AN IBP MEASURING
SYSTEM
• Intra-arterial cannula
• Fluid filled tubing
• Transducer
• Infusion/flushing system
• Signal processor, amplifier and display
DR KRISHNA KUMAR 6912/5/2018
71. LEVELLING AND ZEROING
• Zeroing :
For a pressure transducer to read accurately, atmospheric
pressure must be discounted from the pressure
measurement.
This is done by exposing the transducer to atmospheric
pressure and calibrating the pressure reading to zero.
DR KRISHNA KUMAR 7112/5/2018
72. • Levelling :
The pressure transducer must be set at the appropriate level in
relation to the patient in order to measure blood pressure
correctly.
Defined as "the selection of a position of interest at which the
reference standard (zero ) is set".
This is usually taken to be level with the patient’s heart, at the
4th intercostal space, in the mid-axillary line.
DR KRISHNA KUMAR 7212/5/2018
73. A transducer too low over reads, a transducer too high under
reads.
The phlebostatic axis corresponds roughly with the position
of the RA, and this level has generally been accepted as the
ideal reference level.
It was therefore adopted as the reference level for CVP
measurement.
For arterial pressure measurements, at least since 2001 or
so we have been also leveling the arterial lines at the
phlebostatic axis.
For every 10cm below the phlebostatic axis, the art line will
add 7.4mmHg of pressure.
DR KRISHNA KUMAR 7312/5/2018
74. NORMAL ARTERIAL PRESSURE WAVEFORMS
• The systolic waveform components consist of a steep pressure
upstroke, peak, and ensuing decline, and immediately follow the
ECG R wave.
• The downslope of the arterial pressure waveform is interrupted
by the dicrotic notch, continues its decline during diastole after
the ECG T wave, and reaches its nadir at end-diastole
DR KRISHNA KUMAR 7412/5/2018
76. • Systolic upstroke:
This is the ventricular ejection.
The slope of this segment has some vague relationship with
the rate of flow through the aortic valve (probably more so
when measured in the actual aorta). When its slope is
slurred, there may be aortic stenosis.
DR KRISHNA KUMAR 7612/5/2018
77. • Peak systolic pressure:
This is the maximum pressure generated during the
systolic ejection.
• Systolic decline
This is the rapid decline in arterial pressure as the
ventricular contraction comes to an end.
This decline is even more rapid when there is a left
ventricular outflow tract obstruction (and systole comes to an
abrupt halt before the left ventricle is finished with the
ejection).
DR KRISHNA KUMAR 7712/5/2018
78. • Dicrotic notch:
In perfect circumstances, when measured in the aorta, this
notch is very sharp and it actually does represent the closing
of the aortic valve. As you move further out
As mentioned below, the dicrotic notch position varies with
the position of the arterial line.
A suspiciously low dicrotic notch could mean very poor
vascular resistance, eg. in a situation like severe septic
shock.
• Diastolic runoff:
This is the rapid decline in arterial pressure as the
ventricular contraction comes to an end.
DR KRISHNA KUMAR 7812/5/2018
79. • As the pressure wave travels from the central aorta to the
periphery, the arterial upstroke becomes steeper, the systolic
peak increases, the dicrotic notch appears later, the diastolic
wave becomes more prominent, and end-diastolic pressure
decreases.
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81. AIR BUBBLES IN LINE
• Air bubbles can result in a lower frequency response and
greater resonance response.
• Small amount may augment systolic pressure reading; while
large amount cause an over-damped system.
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82. ABNORMAL ARTERIAL PRESSURE WAVEFORMS
• Morphologic features of individual arterial pressure waveforms
can provide important diagnostic information
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84. SYSTOLIC PRESSURE VARIATION - SPV
• The difference between the maximal and minimal value of
systolic blood pressure during one mechanical breath
• This cyclic variation in systemic arterial pressure is known as
the systolic pressure variation
• In a mechanically ventilated patient, normal SPV is 7 to 10 mm
Hg, with Δ Up being 2 to 4 mm Hg and Δ Down being 5 to 6 mm
Hg.
DR KRISHNA KUMAR 8412/5/2018
85. SYSTOLIC PRESSURE VARIATION - SPV
SPV can be divided into two components by interposing a brief
(5sec) apnea, and using the systolic blood pressure during apnea
as a reference value:
▼down
▲ up
The difference between the maximal systolic
value and the systolic blood pressure during
apnea.
The difference between the apneic systolic blood
pressure and the minimal systolic value.
DR KRISHNA KUMAR 8512/5/2018
88. • Pulse pressure is the difference between systolic and diastolic
arterial pressure
• In mechanically ventilated patients:
• PP is maximum at the end of inspiratory period
• PP is minimum during the expiratory period
DR KRISHNA KUMAR 8812/5/2018
91. THERMODILUTION CARDIAC OUTPUT
MONITORING
• The thermodilution technique has become the de facto clinical
standard for measuring cardiac output because of its ease of
implementation
• For thermodilution, a known volume of iced or room-temperature
fluid is injected as a bolus into the proximal (right atrium) lumen
of the PAC, and the resulting change in the pulmonary artery
blood temperature is recorded by the thermistor at the catheter
tip.
• In adults, an injectate volume of 10 mL should be used, whereas
in children, an injectate volume of 0.15 mL/kg is recommended.
DR KRISHNA KUMAR 9112/5/2018
92. • The thermodilution technique measures right ventricularoutput.
• Usually, three cardiac output measurements performed in rapid
succession are averaged to provide a more reliable result.
• When only a single injection was used to determine cardiac
output, a difference between sequential cardiac output
measurements of 22% was required to suggest a clinically
significant change.
• In contrast, when three injections are averaged to determine the
thermodilution measurement, a change greater than 13%
indicates a clinically significant change in cardiac output
DR KRISHNA KUMAR 9212/5/2018
93. Sources of error in thermodilution
cardiac output monitoring
• Intracardiac shunts
• Tricuspid or pulmonic valve regurgitation
• Inadequate delivery of thermal indicator
Central venous injection site within catheter introducer sheath
Warming of iced injectate
• Thermistor malfunction from fibrin or clot
• Pulmonary artery blood temperature fluctuations
Following cardiopulmonary bypass
Rapid intravenous fluid administration
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94. CONTINUOUS THERMODILUTION CARDIAC
OUTPUT MONITORING
• In brief, small quantities of heat are released from a 10-cm
thermal filament incorporated into the right ventricular portion of
a PAC, approximately 15 to 25 cm from the catheter tip, and the
resulting thermal signal is measured by the thermistor at the tip
of the catheter in the pulmonary artery.
• Reproducibility and precision appear to be better with the CCO
method compared with the standard bolus thermodilution
technique.
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95. • Although these catheters are more expensive than standard
PACs, obviating the need for bolus injections reduces nursing
workload and the potential risk of fluid overload or infection.
• As a result, a cardiac output measured by the CCO method may
provide a more accurate measurement of global cardiac output
for patients
DR KRISHNA KUMAR 9512/5/2018
96. TRANSPULMONARY THERMODILUTION
CARDIAC OUTPUT
• Icecold saline is injected into a central venous line while the change
in temperature is measured in a large peripheral artery (femoral,
axillary, or brachial artery) via a special arterial catheter equipped
with a thermistor.
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97. • Mathematic derivation from the transpulmonary thermodilution
curve
• Extravascular lung water
• Measure of pulmonary edema
• Guide fluid therapy in patients with acute lung injury or
sepsis.
• Other derived indices
• Global end-diastolic volume and
• Intrathoracic blood volume.
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98. • These indices are a better measure of cardiac preload than
traditional measurements such as CVP or pulmonary artery
wedge pressure.
• The last parameter derived from the transpulmonary
thermodilution curve is called the cardiac function index,
calculated using cardiac output and the intrathoracic blood
volume.
• It correlates closely with echocardiography-derived left
ventricular ejection fraction.
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100. THE STEWART-HAMILTON EQUATION FOR
MEASURING CARDIAC OUTPUT
• The basic physics
If you inject a known amount of a substance upstream, the
change in its concentration downstream is related to the rate
of the flow.
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103. FICK'S PRINCIPLE OF CARDIAC OUTPUT
MEASUREMENT
• The principle:
" the total uptake of (or release of) a substance by the peripheral
tissues is equal to the product of the blood flow to the peripheral
tissues and the arterial-venous concentration difference (gradient)
of the substance."
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105. • VO2 ( oxygen consumption)
Can also be estimated. Conventionally, resting metabolic
consumption of oxygen is
3.5 ml of O2 per kg per minute, or
125ml O2 per square meter of body surface area per minute.
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106. • So, in a normal person, with a body surface area of 2m2 and
thus with a VO2 of 250ml per minute,
CO = 250ml / (200ml – 150ml)
= 250 / 50
= 5 L/min
DR KRISHNA KUMAR 10612/5/2018
107. PULSE CONTOUR CARDIAC OUTPUT (PICCO)
• PiCCO uses a combination of two techniques for advanced
haemodynamic and volumetric monitoring
• Transpulmonary thermodilution
• Pulse contour analysis
• The thermodilution technique calculates volumetric measurements
of preload and cardiac output.
• Pulse contour analysis provides continuous cardiac output and
stroke volume variation.
• PiCCO requires the insertion of a CVP catheter and a
thermodilution arterial line.
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108. • Indications for PiCCO
Shock: cardiogenic, hypovolaemic, septic
Sepsis
Trauma
Pulmonary oedema
Acute lung injury
Burns
Any condition that requires assessment of haemodynamic
and/ or volumetric function
DR KRISHNA KUMAR 10812/5/2018
109. • PULSE CONTOUR ANALYSIS: Continuous analysis
The PiCCO system continually estimates the stroke volume from
the arterial waveform, using an arterial catheter.
Cardiac output is then estimated from the stroke volume and heart
rate.
Provides continuous beat by beat parameters which are obtained
from the shape of the arterial pressure wave
The area under the arterial curve during systole, minus the
background diastolic area, is assumed to be proportional to the
stroke volume. This means that the stroke volume and thus the
cardiac output can be measured beat to beat.
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110. The initial transpulmonary thermodilution calibrates the
parameters & the algorithm is then capable of computing each
single stroke volume
Continuous CO readings are achieved using the area under the
systolic part of the curve, a calibration factor (cal) derived from
the thermodilution run, the heart rate (HR) and the individual’s
aortic compliance (which is termed C (p) and characterised by
the thermodilution CO and the measured BP).
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111. PARAMETERS MEASURED & NORMAL VALUES
• Thermodilution Parameters
CO – Cardiac Output: 4 - 8litres/min
CI – Cardiac Index : 3- 5litres/min/m₂
Preload
GEDI – Global end diastolic index: 680- 800ml/m₂
ITBVI – Intra thoracic blood volume index: 850-1000ml/m₂
Pulmonary oedema
ELWI –Extravascular lung water index: 3-7mls/kg
PVPI - Pulmonary vascular permeability index: 1.0- 3.0
Contractility
CFI - Cardiac function index: 4.5- 6.5%
GEF - Global ejection fraction: 25- 35%
DR KRISHNA KUMAR 11112/5/2018
113. LITHIUM DILUTION CARDIAC
OUTPUT MONITORING
• Derives its fundamental basis from indicator dilution principles
• In brief, following an intravenous bolus injection of a small dose
of lithium chloride, an ion-selective electrode attached to a
peripheral arterial catheter measures the lithium dilution curve,
from which the cardiac output is derived.
• The lithium indicator can be injected through a peripheral
intravenous catheter with similar measurement accuracy, thus
eliminating the need for a central venous line.
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115. • Advantages over Thermodilution PiCCO
The concentration stays the same throughout the arterial circulation, and
thus
You don’t need a big central artery to sample the lithium.
You don’t need to inject the lithium through a central vein
The technique shows good agreement with PA catheter thermodilution
measurement.
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116. • Limitations
Same as all dilution methods, you get inaccurate results if there are
shunts in the heart.
If you are already on lithium, this background lithium concentration will
cause the machine to overestimate your cardiac output.
“electrode drift” can occur if there are high doses of muscle relaxants
present
You do end up disposing of some blood each time you sample.
DR KRISHNA KUMAR 11612/5/2018
117. OTHER METHODS FOR MONITORING
CARDIAC OUTPUT AND PERFUSION
• PARTIAL CO2 REBREATHING CARDIAC OUTPUT
MONITORING
based on a restatement of the Fick equation for carbon
dioxide elimination rather than oxygen uptake.
Q˙ =V˙ CO2/(CvCO2 −CaCO2)
where Q˙ = cardiac output
V˙ co2 = rate of carbon dioxide elimination
Cvco2 = carbon dioxide content of mixed venous blood
Caco2 = carbon dioxide content of arterial blood
DR KRISHNA KUMAR 11712/5/2018
118. • GASTRIC TONOMETRY
Gastric tonometry aims at monitoring gastric circulation as
an early indication of splanchnic hypoperfusion
• ESOPHAGEAL DOPPLER CARDIAC OUTPUT MONITORING
• BIOIMPEDANCE CARDIAC OUTPUT MONITORING
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