This document discusses various intravenous induction agents used in anesthesia. It begins by providing an overview of the ideal properties of IV induction drugs and then discusses the mechanisms of action, pharmacokinetics, effects on organ systems, uses, doses and complications of specific drugs - barbiturates, propofol, ketamine and etomidate. It also presents several case scenarios and asks which IV induction drug would be most appropriate in each case. The document aims to educate attendees on the properties and appropriate uses of common IV induction agents.
A powerpoint explaining in detail about all the intravenous induction agents and their clinical uses, pharmacokinetics & pharmacodynamics, adverse effects and complications.
A basic overview on the management of intra-operative bronchospasm: the risk factors, triggers, diagnosis, prevention and management. Includes a case scenario – discussion.
properties, classification and principle of action of intravenous induction agent.
pharmacokinetics
comparison between properties of various agent
summary of ketamine, propofol, thiopenton etomidate , bzd and opioids.
Neuromuscular monitoring, also known as train of four monitoring, is a technique used during recovery from the application of general anesthesia to objectively determine how well a patient's muscles are able to function. It involves the application of electrical stimulation to nerves and recording of muscle response using, for example, an acceleromyograph. Neuromuscular monitoring is typically used when neuromuscular-blocking drugs have been part of the general anesthesia and the doctor wishes to avoid postoperative residual curarization (PORC) in the patient, that is, the residual paralysis of muscles stemming from these drugs.
A powerpoint explaining in detail about all the intravenous induction agents and their clinical uses, pharmacokinetics & pharmacodynamics, adverse effects and complications.
A basic overview on the management of intra-operative bronchospasm: the risk factors, triggers, diagnosis, prevention and management. Includes a case scenario – discussion.
properties, classification and principle of action of intravenous induction agent.
pharmacokinetics
comparison between properties of various agent
summary of ketamine, propofol, thiopenton etomidate , bzd and opioids.
Neuromuscular monitoring, also known as train of four monitoring, is a technique used during recovery from the application of general anesthesia to objectively determine how well a patient's muscles are able to function. It involves the application of electrical stimulation to nerves and recording of muscle response using, for example, an acceleromyograph. Neuromuscular monitoring is typically used when neuromuscular-blocking drugs have been part of the general anesthesia and the doctor wishes to avoid postoperative residual curarization (PORC) in the patient, that is, the residual paralysis of muscles stemming from these drugs.
Newer opioids remifentanil safety issues are discussed in this slide shows.
If any query please contact with me @ my email account
dr.omarfarukraihan@gmail.com
complete and detail study on the topic of general anesthetics by the collaboration of teacher and students for the student , teachers and other health care professionals to learn more on the topics
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
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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.
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
Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
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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.
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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
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.
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
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.
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.
1. Dr. ASHISH NAIR
MBBS, MD ANAESTHESIA
FELLOW IN REGIONAL ANESTHESIA
IDCCM
JDept of Anesthesiology
BVUMC & Hospital – Pune
2. By the end of presentation;we should know
What are IV induction agents.
Properties
Metabolism
Pharmacokinetics
MOA
Systemic Action
CNS
CVS
RS
Doses
Uses
Side effects.
6/23/2017 2
4. Case scenario-1
A patient with intestinal
obstruction having wheezing
requires an emergency laparotomy.
Which induction drug would you
use?
6/23/2017 4
5. Case scenario-2
A patient a history of golttic cancer;
has signs of respiratory distress
and marked stridor; requires a
tracheostomy.
Which IV induction drug would
you use?
6/23/2017 5
6. Case scenario-3
A patient requires a burns
dressing change.
Which induction drug would you
use?
6/23/2017 6
7. Case scenario-4
A patient with a history of heart
failure and MI requires a general
anaesthetic for cholecytectomy .
Which induction drug would you
choose?
6/23/2017 7
8. Case Scenario-5
Which IV induction drug would
be most appropriate to use in a
hypovolaemic patient.
(Blunt Trauma abdomen)
6/23/2017 8
9. Case Scenario-6
A patient with porphyria comes for
an inguinal hernia repair and is
requesting a general anaesthetic.
Which induction drug would you
use?
6/23/2017 9
10. Case Scenario-7
An adult patient requires sedation
on the intensive care unit.
Which of the induction drugs
would be appropriate to run as an
infusion?
6/23/2017 10
11. Case Scenario-8
Patient coming for Fibroadenoma
excision under GA (Day care
surgery).
Drug of choice for induction ??
6/23/2017 11
12. HISTORY
1872
• PIERRE-CYPRIEN ORE’ (French Surgeon) used chloral hydrate
1864
• ADOLF VON BAYER – On Saint Barbara’s Day discovered barbituric
acid. Coined the term Barbitute as acombination of Barbara and urea.
(no sedative properties)
• 1n 1903 – Emil fischer discovered hexobarbital. Helmut Weese studied
it
1934
• JOHN LUNDY of clinic of mayo studied sod .thiopental – balanced
anesthesia
• In 1941 – pearl harbour – many deaths with use of STP due to
cardiovascular depressant effects.
13. HISTORY
1956 - Replacements like
• HYDROXYDIONE (thrombophlebitis)
• ALTHESIN (mixture of alphaxolone and alphadolone; has rapid onset
and recovery; rejected because of hypersensitivty reactions)
• PROPANIDID (rejected because of hypersensitivity reactions)
In 1973 – Etomidate – minimal hemodynamic
depression .
1962 – 1978
• Ketamine –
• Benzodiazepines were studied for anxiolysis without same degree of
sedation as thiopentone ;1963 – diazepam 1978 - midazolam
1977
• Propofol was discovered
14. What are IV induction
drugs
These are drugs that, when given intravenously in an
appropriate dose, cause a rapid loss of
consciousness.
They are used:
To induce anaesthesia prior to other drugs being given
to maintain anaesthesia.
As the sole drug for short procedures.
To maintain anaesthesia for longer procedures by
intravenous infusion.
To provide sedation
15. IDEAL IV INDUCTION DRUG
Physical properties
• Water soluble & stable in solution
• Stable on exposure to light
• Long shelf life
• No pain on intravenous injection
• Non-irritant when injected subcutaneously
• Low incidence of thrombophlebitis
• Cheap
16. Pharmacokinetic properties
Rapid onset in one arm-brain circulation time
Rapid redistribution to vessel rich tissue
Rapid clearance and metabolism
No active metabolites
Pharmacodynamics properties
High therapeutic ratio
Minimal cardiovascular and respiratory effects
No histamine release/hypersensitivity reactions
No emetic effects
No involuntary movements
No emergence nightmares
No hang over effect
No adrenocortical suppression
Safe to use in porphyria
18. e.g.
Thiopental
Thiamylal
Pentobarbital
Secobarbital
Methohexital
Mechanisms of Action
Depress the reticular activating
Suppress transmission of excitatory
neurotransmitters (acetylcholine)
Enhance transmission of inhibitory
neurotransmitters (GABA)
BARBITURATES
19. Structure
Barbiturates are barbituric acid derivatives
Pale yellow colored powder
Kept in environment of nitrogen
The sodium salts of the barbiturates are water
soluble
pH of 2.5% thiopental: 10.5 (highly alkaline)
Shelf life : 2 wk 2.5% thiopental solution
BARBITURATES
20. Pharmacokinetics
Highly protein bound (80%)
The duration of action of is determined by redistribution,
not metabolism or elimination
Maximal brain uptake within 30 s
Subsequent redistribution to the peripheral lowers plasma and brain
concentration to 10% of peak levels within 20–30 min
This pharmacokinetic profile correlates with clinical
experience—patients typically lose consciousness
within 30 s and awaken within 20 min.
BARBITURATES
21. BARBITURATES
BIOTRANSFORMATION
Hepatic oxidation to inactive water-soluble metabolites.
EXCRETION
Renal excretion
Important for less protein-bound and less lipid-soluble agents such as
phenobarbital,
Water-soluble end products of hepatic biotransformation.
23. Effects on Organ Systems
CARDIOVASCULAR
First effect dose dependent peripheral vasodilatation
Negative inotropic effect - ↓ Ca to myocardial fiber
↓BP
↓ CO (↓venous return , vasodilatation, -veinotropic effect , ↓CNS symp outflow
)
Tachycardia ( 10-36 %) Via baroreceptor mediated symp reflex in response to ↓
CO & BP
CAD patient on induction ↑HR - ↑myocardial demand of O2
ECG changes :-prolonged QT , flattened T wave ,vent arrhythmia
BARBITURATES
24. RESPIRATORY
Ventilatory response to hypercapnia and hypoxia ---
Decreases
Tidal volume --- decreased
Respiratory rate --- decreased
Bronchospasm in asthmatic patients or laryngospasm
in lightly anesthetized patients
Barbiturates do not completely depress noxious
airway reflexes Airway reflexes preserved;not
suitable for LMA insertion ,may cause coughing and
laryngospasm
Release of histamine
6/23/2017 24
25. RESPIRATORY SYSTEM
Dose related resp depression,peak resp depression
after (1-1.5 min) after adm of bolus dose .
More susceptible patient ch lung disease,Airway obst
Apnea :- transient apnea for 25 sec only in 20 % cases.
Double apnea :- 1 st during adm of drug > transient
>after 4-5 breath 2 nd apnea last for longer period .
during this period ventilation must be assessed –
controlled ventilation .
26. CNS EFFECT
Sedation and loss of consciousness
Retrograde amnesia and depression of vasomotor centre.
Induction and maintenance of anesthesia
Rate of adm α onset
Termination of effect take 5-10 min to awake ( after bolus )
Awakening depend on :-
Volume of distribution
Plasma concentration
Redistribution and Clearance
Alteration in metabolism
CNS sensitivity ↑ with age
27. CNS
Pupil and eye :- initially pupil contract but then dilate .
Pupillary response is lost with surgical anaesthesia .
loss of eyelash reflex is commonly used as endpoint for
adequate induction dose .
Following traumatic brain injury, infusion of thiopental to
produce a “barbiturate coma” lowers intracranial pressure
and may improve neurological outcome.
Anticonvulsant property
Burst suppression of EEG can be induced with high doses
when used in treatment of status epilepticus or intractable
rise in ICP following head injury .
28. BARBITURATES
Cerebral blood flow --- Decrease
Intracranial pressure---Decrease
Cerebral perfusion pressure--- Increased
(CPP equals cerebral artery pressure minus cerebral venous pressure or
intracranial pressure.)
Cerebral oxygen consumption --- Decrease
(This effect of barbiturates may protect the brain from transient
episodes of focal ischemia (eg, cerebral embolism) but probably not
from global ischemia (eg, cardiac arrest).
have an antianalgesic effect by lowering the pain threshold
29. BARBITURATES
RENAL
Reduce renal blood flow and glomerular filtration rate in
proportion to the fall in blood pressure.
HEPATIC
Hepatic blood flow is decreased.
Induction of hepatic enzymes increases the rate of metabolism of
some drugs
The induction of aminolevulinic acid synthetase stimulates the formation of
porphyrin (an intermediary in heme synthesis), which may precipitate
acute intermittent porphyria or variegate porphyria in susceptible
individuals.
IMMUNOLOGICAL
Sulfur-containing thiobarbiturates evoke mast cell histamine
release in vitro, whereas oxybarbiturates do not.
30. SODIUM THIOPENTONE
Indications
Induction of anaesthesia
Control convulsions
Decreases ICP
Neuroprotection
Contraindications
COPD
Severe asthama
Porphyria
Previous hypersensitivity
Allergy to sulphur
PRECAUTIONS :
Stenoticvalvular disease
Severe hepatic disease
Renal impairment
31. BARBITURATES
Intra-arterial Injection
Immediate, intense vasoconstriction and excruciating
pain that radiates along the distribution of the artery.
Severe Vasoconstriction may obscure distal arterial
pulses.
Gangrene and permanent nerve damage may occur.
SPECIFIC COMPLICATION :
32. Mechanism of Damage
Due to be the precipitation of thiopental crystals
inflammatory response and arteritis
microembolization that follows, eventually results in
occlusion of the distal circulation.
Treatment
Immediate attempts to dilute the drug --- injection of saline
Prevention of arterial spasm & sustain adequate blood flow—
lidocaine, papaverine, or phenoxybenzamine
stellate ganglion block or brachial plexus block
BARBITURATES
34. Structure
Alkylphenol
Propofol (2,6-diisopropylphenol)
Propofol is not water soluble
1% solution (10 mg/mL) --- an oil-in-water emulsion
Containing
soybean oil
glycerol
egg lecithin
Mechanisms of Action
Facilitation of inhibitory neurotransmission mediated by
GABA.
Propofol
35. Pharmacokinetics
DISTRIBUTION
High lipid solubility
onset of action that is almost as rapid as that of thiopental
(one-arm-to-brain circulation time).
Awakening from a single bolus dose is also rapid due to a
very short initial distribution half-life (2–8 min).
Recovery --- rapid
Hangover --- less
This makes it a good agent for outpatient anesthesia.
BIOTRANSFORMATION
Hepatic and extra hepatic metabolism
EXCRETION
Primarily excreted in the urine
chronic renal failure does not affect clearance of the parent drug.
Propofol
36. Effects on organ
CARDIOVASCULAR
Blood pressure
Propofol causes the most marked fall in blood
pressure of all the induction drugs & is d/t fall in
systemic vascular resistance accompanied with slight
increase in heart rate
The fall in blood pressure is dose dependent and is
most marked in the elderly and in shocked patients.
This can be minimized by slow injection – avoiding
inadvertent overdose.
HEART RATE
No change /Bradycardia
Propofol
37. RESPIRATORY
Profound respiratory depressant following an induction
dose---apnea
Inhibits hypoxic ventilatory drive and depresses the
normal response to hypercarbia.
Depression of upper airway reflexes
Helpful during intubation or laryngeal mask placement in the
absence of paralysis.
Lower incidence of wheezing
Safe in asthmatic patients
6/23/2017 37
38. Propofol
CEREBRAL
Cerebral blood flow---- decreases
Intracranial pressure---- decreases.
Antiemetic effects
preferred drug for outpatient anesthesia.
Anticonvulsant properties (ie burst suppression)
used to terminate status epilepticus.
Safely administered to epileptic patients.
Intraocular pressure----Decreases
39. Use :
Induction of Anesthesia 1.5 to 2.5 mg/kg
Intravenous Sedation 25 to 100 µg/kg per minute IV
Maintenance of Anesthesia 100 to 300 µg/kg per minute
IV
Nonhypnotic Therapeutic Applications
Antiemetic Effects
Mech –unknown
10 to 15 mg IV
Anticonvulsant Activity
Attenuation of Bronchoconstriction
Propofol
40. Propofol
Specific complication
Lactic Acidosis or propofol infusion syndrome
Prolonged high-dose infusions of propofol (>75 µg/kg per minute)
for longer than 24 hours.
Mechanism –
Unclear
Cytopathic hypoxia of the electron transport chain and impaired
oxidation of long-chain fatty acids
C/F
Unexpected tachycardia
Diagnosis
Arterial blood gases and serum lactate concentrations
Treatment
Metabolic acidosis in its early stages is reversible with
discontinuation of propofol administration.
41. Pain on Injection
Most common
Reduced by
1% lidocaine
Potent short-acting opioid eg Fentanyl
Bacterial Growth
Supports the growth of Escherichia coli and Pseudomonas aeruginosa.
Recommendation:
An aseptic technique be used in handling propofol.
The contents of the ampule containing propofol should be withdrawn into a
sterile syringe immediately after opening and administered promptly.
The contents of an opened ampule must be discarded if they are not used within
6 hours.
Propofol
42. PROPOFOL
Advantages
Rapid induction
Anti emetic effect
TIVA
Agent of choice for day care
surgery
Disadvantages
Induction apnoea
Hypotension
Dose dependant bradycardia
Dose dependant resp
depression
Pain during injection
It is also euphorigenic but
does not have residual
psychotic effects like
Ketamine
44. Ketamine Mechanisms of Action
NMDA(N-methyl-D-
aspartate) receptor
antagonist.
Produce dissociative
Anaesthesia
Structure :
structural analogue of
phencyclidine
6/23/2017 44
45. PHARMACOKINETICS
ABSORPTION
Intravenously or intramuscularly
Peak plasma levels are usually achieved within 10–15 min
after intramuscular injection.
DISTRIBUTION
Ketamine is more lipid soluble and less protein bound than
thiopental
Half-life is 10–15 min
Awakening is due to redistribution to peripheral
compartments.
BIOTRANSFORMATION
Liver to several metabolites (eg, norketamine)
EXCRETION
End products of biotransformation are excreted renally
KETAMINE
46. Ketamine
uses
Induction of general anesthesia 0.5-2 mg/kg IV;
4-6 mg/kg IM
Maintenance of general anesthesia 0.5-1 mg/kg IV with N2O 50% in
O2
15-45 µg/kg/min IV with N2O 50-
70% in O2
30-90 µg/kg/min IV without N2O
Sedation and analgesia 0.2-0.8 mg/kg IV over 2-3 min 2-
4 mg/kg IM
Preemptive/preventive analgesia 0.15-0.25 mg/kg IV
Intra thecal ketamine 0.5-0.75 mg/kg
47. Effects on organ system
Central Nervous System
cerebral blood flow --- Increase
CMRO2---Increase
Intracranial Pressure--- Increase
Cardiovascular System
Sympathetic nervous system stimulation
Systemic and pulmonary arterial blood pressure---- increased
Heart rate ---- increased
Cardiac output---- increased
Myocardial oxygen requirements ---- increased
KETAMINE
48. But in Critically ill patients
Unexpected decreases in systemic blood pressure and cardiac output,
which may reflect a depletion of endogenous catecholamine stores and
exhaustion of sympathetic nervous system compensatory mechanisms.
Unmasking of ketamine's direct myocardial depressant effects.
Ventilation and Airway
Depression of ventilation: not significant
Upper airway skeletal muscle tone:maintained,
Upper airway reflexes : intact
Salivary and tracheobronchial mucous gland: Increased secretions are
increased
Use antisialagogue before ketamine
Bronchodilatory effects
Drug of choice for induction patients with asthma
KETAMINE
49. Specific Complications
Emergence Delirium (Psychedelic Effects)
• In postoperative period visual, auditory, proprioceptive,
and confusional illusions, which may progress to delirium.
• Dreams and hallucinations can occur up to 24 hours after
the administration of ketamine.
• Mechanisms
• Emergence delirium probably occurs secondary to
ketamine-induced depression of the inferior colliculus
and medial geniculate nucleus, thus leading to the
misinterpretation of auditory and visual stimuli.
KETAMINE
50. The loss of skin and musculoskeletal sensations results in a decreased ability to
perceive gravity producing a sensation of bodily detachment or floating in space
FACTORS ASSOCIATED WITH AN INCREASED
INCIDENCE
Age greater than 15 years
Female gender
Dose greater than 2 mg/kg IV
History of frequent dreaming
PREVENTION OF KETAMINE-INDUCED EMERGENCE
DELIRIUM
Midazolam (administer IV about 5 minutes before induction
of anesthesia with ketamine)
Prospective discussion with patient about side effects of
ketamine
KETAMINE
51. KETAMINE
ADVANTAGE
increase HR,BP,CO
In asthmatic
For short procedure
Combination with BZD
can use in cardiac
catheterization and
angiography .
In OPD surgical procedure
Good analgesic property
DISADVANTAGE
limb movement and
Nystagmus
Emergence phenomenon
in 50 %
Hypertensive
Increased ICP , IOT
Uterine stimulation
Schizophrenia , psychosis
Poor muscle relaxation
52. KETAMINE
INDICATION
CVS except IHD
Resp. disorder
Hemodynamica compromised
states ( pericarditis , cardiac
tamponade , CM , shock )
Traumatic and septic shock
As component in TIVA with
midaz and propofol provide
better hemodynamic stability
In cancer patient , neuropathy
Phantom or ischaemic limb pain
Fibromyalgia , visceral pain
Migraine
CONTRAINDICATION
↑ ICP , SOL brain
Large size Infarct
Ophthalmic injury
IHD
Vascular aneurysm
Schizophrenia
54. Structure
Carboxylated imidazole-containing compound
Commercial Preparation
Etomidate is prepared as a fat emulsion, and pain on
injection and venous irritation is unlikely.
Mechanism of Action
GABA receptors
ETOMIDATE
55. Uses
Etomidate (0.2 to 0.4 mg/kg IV)
As an alternative to propofol or barbiturates for the
induction of anesthesia, especially in the presence of
an unstable cardiovascular system.
ETOMIDATE
56. Effects on organ system
Central Nervous System
Potent direct cerebral vasoconstrictor that decreases cerebral blood
flow and CMRO2
Activate seizure foci
Caution in patients with focal epilepsy
Facilitate the localization of seizure foci in patients undergoing
the cortical resection of epileptogenic tissue.
ETOMIDATE
57. Cardiovascular System
Cardiovascular stability (minimal changes in heart rate, stroke
volume, cardiac output)
Preferred for Induction of anesthesia in patients with little or no
cardiac reserve.
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ETOMIDATE
58. Ventilation
Depressant effects on ventilation
Pain on Injection
Pain on injection and venous irritation has been virtually
eliminated with use of etomidate preparations utilizing a lipid
emulsion vehicle rather than propylene glycol
Myoclonus (spontaneous movements)
Caution in the use of this drug for the induction of anesthesia in patients
with a history of seizure activity.
Adrenocortical Suppression
lasts 4 to 8 hours after an intravenous induction dose of
etomidate.
Be considered desirable from the standpoint of “stress-free”
anesthesia.
ETOMIDATE
59. ETOMIDATE
Clinical use Dose
Induction of general anaesthesia 0.2-0.6mg/kg I.V
Maintainance of general
anaesthesia
10mcg/kg/min I.V. with N2o & an
opiate
Sedation & Analgesia Limited to periods of brief sedation
because of inhibition of steriod
synthesis
61. E.g.
Midazolam
Diazepam
MECHANISM OF ACTION
Facilitating the actions of γ-aminobutyric acid (GABA),
the principal inhibitory neurotransmitter in the CNS
Benzodiazepines do not activate GABAA receptors but
rather enhance the affinity of the receptors for GABA.
BENZODIAZEPINE
63. EFFECTS ON ORGAN SYSTEMS
CARDIOVASCULAR
Minimal cardiovascular depressant effects even at induction
doses.
Arterial blood pressure
Cardiac output decline slightly
Peripheral vascular resistance
Heart rate ---- slight rise
Midazolam tends to reduce blood pressure and peripheral
vascular resistance more than diazepam.
BENZODIAZEPINE
64. RESPIRATORY
Depress the ventilatory response to CO2
Apnea may be less common after benzodiazepine
induction than after barbiturate induction.
Ventilation must be monitored in all patients receiving
intravenous benzodiazepines, and resuscitation
equipment must be immediately available.
BENZODIAZEPINE
65. CEREBRAL
Cerebral oxygen consumption, cerebral blood flow, and
intracranial pressure----Reduce
Anti seizures properties
Antegrade amnesia------premedication
Mild muscle-relaxant property --- mediated at the
spinal cord level, not at the neuromuscular junction.
Slower loss of consciousness and a longer recovery
BENZODIAZEPINE
67. E.g.
Morphine
Fentanyl
Sufentanyl
Meperidine
Mechanisms of Action
Opioids bind to specific receptors located throughout the central
nervous system and other tissues.
Four major types of opioid receptor
µ
Κ
σ
δ
Opiate–receptor activation inhibits the presynaptic release and postsynaptic response to
excitatory neurotransmitters (eg, acetylcholine, substance P) from nociceptive neurons.
OPIOIDS
69. EFFECTS ON ORGAN SYSTEMS
CARDIOVASCULAR
Do not seriously impair cardiovascular function.
Cardiac contractility--- do not depress (except meperidine)
Heart rate
Increase ----Meperidine
Decrease ---High doses of morphine, fentanyl, sufentanil.
Blood pressure --- Decreased
As a result of bradycardia, venodilation, and decreased sympathetic reflexes
Meperidine and morphine --- can lead to profound drops in systemic
vascular resistance and arterial blood pressure due to histamine release
The effects of histamine release can be minimized in susceptible patients by
slow opioid infusion, adequate intravascular volume, or pretreatment with
H1 and H2 histamine antagonists.
OPIOIDS
70. RESPIRATORY
Respiratory rate– decrease
Apneic threshold( the highest PaCO2 at which a patient remains
apneic) --- elevated
Hypoxic drive -- decreased.
Histamine-induced bronchospasm --- Morphine and meperidine
Chest wall rigidity ( fentanyl, sufentanil, and alfentanil)
Enough to prevent adequate ventilation.
Centrally mediated muscle contraction
After large drug boluses
Effectively treated with neuromuscular blocking agents.
Blunt airway reflex
OPIOIDS
71. CEREBRAL
Effects on cerebral perfusion and intracranial pressure -
--variable
Cerebral oxygen consumption, cerebral blood flow, and
intracranial pressure--- slight reduction.
Stimulation of the medullary chemoreceptor trigger
zone is ----high incidence of nausea and vomiting.
Physical dependence
Use of opioids in epidural and subdural spaces has
revolutionized pain management.
Management of perioperative shivering ---Intravenous
meperidine
OPIOIDS
72. GASTROINTESTINAL
slow gastric emptying time by reducing peristalsis.
Biliary colic may result from opioid-induced
contraction of the sphincter of Oddi.
ENDOCRINE
Stress response to surgical stimulation ---decresed
Ischemic heart disease patients may benefit from
attenuation of the stress response .
OPIOIDS
73. Case Scenario 1
A patient with intestinal obstruction having
wheezing requires an emergency laparotomy. Which
induction drug would you use?
75. Case Scenario 2
A patient a history of golttis cancer has signs of
respiratory distress and marked stridor requires a
tracheostomy. Which IV induction drug would you
use?
76. Any difficult airway
Avoid ----IV induction drugs and muscle relaxants
(respiratory depressant properties)
It may not be possible to perform facemask ventilation
should this patient become apnoeic.
Inhalational induction with halothane or sevoflurane
should be employed.
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77. Case Scenario 3
A patient requires a burns dressing change. Which
induction drug would you use?
78. Ketamine is an ideal drug to be used for minor
procedures. For burns dressing changes, a sub-
anaesthetic dose can be used.
It will provide sedation and analgesia, preserving the
protective airway reflexes.
Propofol + ketamine
Propofol + fentanyl
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79. A patient with a history of heart failure and MI requires
a general anaesthetic for cholecytectomy . Which
induction drug would you choose?
Case Scenario 4
80. Etomidate due to its limited effect on the
cardiovascular system.
High dose Fentanyl
Be cautious while using Propofol and thiopental
Avoid Ketamine
The lowest possible dose is given, it is given slowly
and it is titrated to effect with Intra-arterial blood
pressure monitoring.
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81. Case Scenario 5
Which IV induction drug would be most appropriate to use
in a hypovolaemic patient. (Blunt Trauma abdomen)
83. Case Scenario 6
A patient with porphyria comes for an inguinal hernia repair
and is requesting a general anaesthetic. Which induction
drug would you use?
85. Case Scenario 7
An adult patient requires sedation on the
intensive care unit. Which of the induction
drugs would be appropriate to run as an
infusion?
86. Preferred -- Midazolam , Propofol
Avoid
Thiopental
due to accumulation
etomidate
effect on adrenal steroid hormone synthesis
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87. Case Scenario 8
Patient coming for Fibroadenoma excision under GA
( Day care surgery). Drug of choice for induction ??