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HISTORY OF
ANAESTHESIA
Presenter-
Dr Chimi Handique
PGT
Dept of Pharmacology
HISTORY OF
ANAESTHESIA
Presenter-
Dr Chimi Handique
PGT
Dept of Pharmacology
Anaesthesia : A clinical and philosophical concept
It is in the Hippocratic Corpus, that the word ‘anaesthesia’
was used for the first time in a medical context as reversible
loss of sensation and unconsciousness, when Hippocrates
writes:
“For when they [breaths] pass through the flesh and puff it
up, the parts of body affected lose the power of feeling
[‘anaestheta’]”.
Anaesthesia : Aclinical and philosophical concept
It is in the Hippooatic Corpus, that the word 'anaesthesia'
was usedfor theftrst time in a medical context as reversible
loss of sensation and unconsciousness, when Hippocrates
writes:
"For when they[breaths]pass through theflesh andpuffit
up, the parts ofbody gfected lose the power of
feeling
['anaestheta']'.'
What was done to a patient before an operation ?
It was the custom then, as for centuries afterward, to bind the patient to
the table with ropes or straps. His screams were disregarded, but if he
struggled too Violently, assistants grasped his arms and legs.
Whatwas done to a patient b+re an operation ?
Wellcorne Irnages
It was the custom then, as for centuries afterward, to bind the patient to
the table with ropes or straps. His screams were disregarded, but if he
struggled oo Violently, assistants grasped his arms and legs.
• Pain had not prevented surgery in the past, but it had made it
almost an unbearable, excruciating agony.
• In January 1843, George Wilson, a medical student who
underwent surgery to amputate an infected leg, described his
experience of surgery without anaesthesia and analgesia.
• “Of the agony it occasioned, I will say nothing. Suffering so great
as I underwent cannot be expressed in words. ... The particular
pangs are now forgotten;but the black whirlwind of emotion, the
horror of great darkness, and the sense of desertion by God and
man, bordering close upondespair, which swept throughmy
mind and overwhelmed my heart, I can never forget ...”
Pain had not prevented surgery in the past, but it had made it
almost an unbearable, excruciating agony.
' n January 1843, George Wilson, a medical student who
nderwent surgery to amputate an infected leg, described his
xperience of surgery without anaesthesia and analgesia.
"Ofthe agony it occasioned, I will say nothing. Suffering so great
as I underwent cannot be expressed in words. The particular
pangs are nowforgotten;but the blackwhirlwind ofemotion, the
horror ofgreat darkness, and the sense ofdesertion by God and
man, bordering close upon despair, which swept through my
ind and overwhelmed my heart, I can neverforget
By the early1840s successive cultural and medical changes
basedon newerhumanistic standards had resultedin the view
that physical painis purposeless.
This new concept regardingpain prevention and its relief is the
social scenery for the discovery of modern ‘anaesthesia’ during
the middle of the 19thcentury.
By the early 1840s successive cultural and medical changes
based on newer humanistic standards had resulted in the view
that physical pain is purposeless,
This new concept regarding pain prevention and its reli# the
soul sceneryfor the discovoy ofmodern 'anaesthesia 'during
the middle ofthe 19th centuy,
• The word “Anaesthesia“ was
coined by Oliver Wendell
Holmes in 1846.
• It originates from the Greek an
- "without” and “aisthēsis”
refers to the inhibition
of sensation.
Oliver Wendell Holmes
(1809–1894)
The word "Anaesthesia" was
coined by Oliver Wendell
Holmes in 1846.
It originates from the Greek an
'without" and "aisthésis
refe s the inhibition
to
Ofs nsation.
Oliver Wendell Holmes
(1809-1894)
In a letter to William T. G. Morton, the first practitioner
to publicly demonstrate the use of ether during surgery,
he wrote:
"Everybody wants to have a hand in a great
discovery. All I will do is to give a hint or two as to
names—or the name—to be applied to the state
produced and the agent. The state should, I think, be
called 'Anaesthesia.' This signifies insensibility—more
particularly ... to objects of touch.“
In a letter to William T. G. Morton, the first practitioner
to publicly demonstrate the use of ether during surgery,
he wrote:
"Everybody wants to have a hand in a great
discovery. All I will do is to give a hint or two as to
names or the name to be applied to the state
produced and the agent. The state should, I think, be
called 'Anaesthesia.' This signifies insensibility more
particularly ... to objects of touch."
A Brief Overview
ABriefOven'iew
• Attempts at producing a state of general anaesthesia can be
traced throughout recorded history.
• The Renaissance saw significant advances
in anatomy and surgical technique. However, despite all this
progress, surgery remained a treatment of last resort.
• An appreciation of the germ theory of disease led rapidly to the
development of antiseptic techniques in surgery reducing the
overall morbidity and mortality of surgery to a far more
acceptable rate.
Attempts at producing a state of general anaesthesia can be
raced throughout recorded history.
he Renaissance saw significant advances
in anatomy and surgical technique. However, despite all this
prog ess, surgery remained a treatment of last resort.
' An a preciation of the germ theory of disease led rapidly to the
devel pment of antiseptic techniques in surgery reducing the
overa I morbidity and mortality of surgery to a far more
acceptable rate.
• Concurrent with these developments were the significant
advances in pharmacology and physiology which led to the
development of general anesthesia and the control of pain.
• In the 20th century, the safety and efficacy of general anesthesia
was improved by the routine use of tracheal intubation and other
advanced airway management techniques.
• Significant advances in monitoring and new anesthetic
agents with improved pharmacokinetic and pharmacodynamic
characteristics also contributed to this trend.
Concurrent with these developments were the significant
dvances in which led to the
pharmacology and physiology
development of general anesthesia and the control of pain.
, In the 20th century the safety and efficacy of general anesthesia
was improved by the routine use of tracheal intubation and other
adva ced airway management techniques.
Signi Icant advances in monitoring and new anesthetic
agent with improved pharmacokinetic and pharmacodynamic
charac eristics also contributed to this trend.
TIMELINE OF
ANESTHESIA
• Antiquity
• Middle ages and Renaissance
• 18th Century
• 19th Century
• 20th Century
• 21st Century
TIMELINE OF
ANESTHESIA
' Antiquity
' Middle ages and Renaissance
' 18th Century
' 19th Century
' 20th Century
' 21st Century
Antiquity
Antiquity saw the dawn of anesthesia.
This era saw the uses of poppy,
mandrake, Indian hemp, cocaine and
carotid compression.
Antiquity
Antiquity saw the dawn of anesthesia.
This era saw the uses of poppy,
mandrake, Indian hemp, cocaine and
carotid compression.
Origin of Opium
iunt
Opium, is a very popular ancient pain relieving and euphoria
inducing remedy.
It is first said to have been cultivated in lower mesopotamia
(Southwest Asia) in 3400 BC.
Sumerians referred it as “hul-gil” which means “joy plant”
Sumerians passed this “miracle drug” to the Assyrians who in
turn passed opium to the Babylonians and then to the
Egyptians.
3400 BC
3400 BC
is a very popular ancient pain relieving and euphoria
Opium
inducing remedy.
is first said to have been cultivated in lower mesopotamia
(Southwest Asia) in 3400 BC.
Sunlerians referred it as which means
hul-gil joy plant
Sumerians passed this "miracle drug" to the Assyrians who in
turn passed opium to the Babylonians and then to the
Egy tians.
• The knowledge and use of opium
passed on from Egypt across
Mediterranean Sea trade routes to
various civilizations including the
Phoenicians and the Greeks.
• Later, around 330 BC, Alexander the
Great and his armies introduced
opium to the people of India, Persia
and other eastern and Middle Eastern
kingdoms.
The knowledge and use of opium
passed on from Egypt across
Mediterranean Sea trade routes to
various civilizations including the
Phoenicians and the Greeks.
La er, around 330 BC, Alexander the
Gre t and his armies introduced
opi m to the people of India, Persia
and other eastern and Middle Eastern
king oms.
2
Prior to the introduction of opium to ancient India and China,
these civilizations pioneered the use of cannabis incense and
aconitum. By the 8th century AD, Arab traders had brought
opiumto India and China.
Prior to the introduction ofopium to ancient India and China,
these civilizations pioneered the use of cannabis incense and
aconituwu By the 8th centuty AD, Arab traders had brought
opium to India and China
• Pictographs showing practice of
Acupuncture in China on bone
and Tortoise shells with
inscriptions dating from the time
of Shang dynasty have been
found, and it is thought that
these were used for divination in
the art of healing.
1600 BC
1600 BC
ictographs showing practice of
puncture in China on bone
and Tortoise shells with
inscr•ptions dating from the time
of Shang dynasty have been
foun , and it is thought that
these were used for divination in
thea of healing.
• Sushruta in Sushruta
Samhita advocated the use of
wine with incense
of cannabis for anaesthesia.
• The use of henbane and
of Sammohini and Sanjivani
are reported at a later period
600 BC
600 BC
in
Sushruta
Susruta
(600 BC)
Sushruta
Samhita advocated the use of
wme with incense
o, cannabis for anaesthesia.
The use of henbane and
of ammohini and Sanjivani
are r ported at a later period
• Assyrians and Egyptians used
carotid compression to produce
brief unconsciousness before
circumcision or cataract surgery.
• In a passage in
History of Animals, Aristotle says of the jugular veins: “If these
veins are pressed externally, men, though not actually choked,
become insensible, shut their eyes, and fall flat on the ground."
400 BC
400 BC
Assyrians and Egyptians used
carotid compression to produce
rief unconsciousness before
circumcision or cataract surgery.
Ina assage in
roti
artery
Hist ry ofAnimals, Aristotle says of the jugular veins: "If these
veins are pressed externally, men, though not actually choked,
become insensible, shut their eyes, and fall flat on the ground. "
• Pedanius Dioscorides, a Greek
surgeon in the Roman army of
Emperor Nero, recommended
mandrake boiled in wine to
"cause the insensibility of those
who are to be cut or cauterized.”
in his writings in De Materia
Medica
C. 64 BC
C. 64 BC
a Greek
Pedanius Dioscorides
surgeon in the Roman army of
Emperor Nero, recommended
I iandrake boiled in wine to
"cause the insensibility of those
who are to be cut or cauterized."
in his writings in De Materia
Me ica
• Hua Tuo of China used to perform surgery
under anesthesia using a formula he had
developed and called mafeisan.
• The word mafeisan probably means
something like "cannabis boil powder".
• The exact composition of mafeisan, similar to all of Hua Tuo's clinical
knowledge, was lost when he burned his manuscripts, just before his
death.
CA 160
cA 160
' H a Tuo of China used to perform surgery
u der anesthesia using a formula he had
developed and called mafeisan.
The word mafeisan probably means
something like ' cannabis boil powder O Wood Library:Musau
The exact composition of mafeisan, similar to all of Hua Tuo's clinical
knowled e, was lost when he burned his manuscripts, just before his
death.
&
Ages
History of Ether
History of Ether
CTH CR
Origin
• The compound may have been created by Jābir ibn Hayyān in
the 8th century .
• Alchemist Ramon Llull has also been credited with
discovering diethyl ether in 1275, althoughthere is no
contemporary evidence of this.
Origin
' The compoundmay have been created byJäbir ibnHayyän in
the 8th century.
' Alchemist Ramon Llull has also been creditedwith
discovering diethyl ether in 1275, although there is no
contemporat•y evidence ofthis,
• Paracelsus (1493–1541) isolated
substances that resulted from interaction of
alcohol and vitriol and demonstrated its
action in chickens.
• He noted chickens enjoy sweet vitriol
[ether] - after which they "undergo
prolonged sleep, awake unharmed".
• However, he did not extend this discovery
from farm animals to people.
1525
1525
Paracelsus (1493-1541) isolated
s bstances that resulted from interaction of
Icohol and vitriol and demonstrated its
action in chickens.
He noted chickens enjoy sweet vitriol
[ether after which they "undergo
prolonged sleep, awake unharmed".
Howe r, he did not extend this discovery
from fa animals to people.
• German physician Valerius Cordus
(1515–1544), is widely credited
with developing a method for
synthesizing ether.
• He synthesized diethyl ether by
distilling ethanol and sulphuric acid
into what he called by the poetic
Latin name oleum dulci vitrioli, or
"sweet oil of vitriol”
1540
1540
erman physician Valerius Cordus
( 515—1544), is widely credited
ith developing a method for
synthesizing ether.
He ynthesized diethyl ether by
distill ng ethanol and sulphuric acid
into hat he called by the poetic
Latin name oleum dulci vitrioli or
"swee of vitriol"
• The name ether was given to the substance in 1729 by August
Sigmund Frobenius.
• WilliamT. G. Morton was First in the worldto publicly and
successfully demonstrate the use of ether anesthesia for
surgery.
' Thename ether was givento the substance in 1729 byAugust
Sigmund Frobenius,
' William T, G, Mortonwas First intheworldto publiclyand
successfully demonstrate the use ofether anesthesiafor
surgoy,
Developments in 18th century
pmentsin18thcenboy
Develo
OF GAS.
Tcu: Nitrous Oxide. or Gas.
It is of equivalent
it by au'tracti"',.• pret of tLe Oxygen ft-ota thet Nitrie Oxide.
Oxygen angi Nitr€:gen. of Sir i)avy. it was
History of Nitrous oxide
• Joseph Priestley (1733–1804) was an
English chemist who discovered nitrous
oxide (1772), nitric oxide, ammonia,
hydrogen chloride and oxygen(1774).
• He originally named nitrous oxide as "nitrous air, diminished”,
on account of his preparative method of allowing NO to
standing in contact with moist iron filing
.
1771-1786
1771-1786
' Joseph Priestley (1733—1804) was an
English chemist who discovered nitrous
oxide (1772), nitric oxide, ammonia,
hydrogen chloride and oxygen(1774).
11774
Discovny OF
He riginally named nitrous oxide as nitrous air, diminished
on ccount of his preparative method of allowing NO to
stan ing in contact with moist iron filing
Priestley’s apparatus
Priestley’s Experiment
Priestley's apparatus
(c)
(d)
Priestley's Experiment
• Priestley was clearly perplexed as to the nature of his diminished
nitrous air.
• A candle burnt with an increased brightness in the gas. When
mice were placed in a bell-jar of N2O their liveliness was
reduced and they soon died.
• In contrast they seemed livelier if they respired oxygen, which
Priestley subsequently discovered.(1774).
• But general anaesthesia by the inhalation of nitrous oxide wasn't
demonstrated for over 40 years till December 1844 by US
dentist Horace Wells.
Priestley was clearly perplexed as to the nature of his diminished
nitrous air.
A candle burnt with an increased brightness in the gas. When
mice were placed in a bell-jar of N20 their liveliness was
reduced and they soon died.
' Inhcontrast they seemed livelier if they respired oxygen, which
Prie tley subsequently discovered.(1774).
But eneral anaesthesia by the inhalation of nitrous oxide wasn't
dem nstrated for over 40 years till December 1844 by US
dentist Horace wells
Developments in 19th Century
Developments in 19th Century
JULY, 1800
Even though N2O was discovered by
Joseph Priestley it Humphry Davy who
spotted its medical potential
In 1798, Humphry Davy was appointed
laboratory superintendent of the Pneumatic
Institute in Bristol, UK. This was an
establishment founded on the belief that
the recently discovered gases might have
curative applications
JULY, 1800
Eve though N20 was discovered by
Jos ph Priestley it who
Humphry Davy
spo ted its medical potential
In 1798, Humphry Davy was appointed
laboratoyy superintendent of the Pneumatic
Institute in Bristol, UK. This was an
establishment founded on the belief that
the rece tly discovered gases might have
curative ap lications
• Curiously, the use of this gas in therapy is barely mentioned: a
couple of accounts of its use on paralysed patients, and that's about
the extent.
• It is at the end of this book “the history, chemistry, physiology and
recreational use of nitrous oxide” that he makes his off-repeated
statement about the possible use of nitrous oxide in surgery:
"As nitrous oxide in its extensive operation appears capable of
destroying physical pain, it may probably be used with advantage
during surgical operations in which no great effusion of blood takes
place."
Curiously, the use of this gas in therapy is barely mentioned: a
ouple of accounts of its use on paralysed patients, and that's about
he extent.
It is at the end of this book "the history, chemistry, physiology and
recreational use of nitrous oxide" that he makes his off-repeated
state ent about the possible use of nitrous oxide in surgery:
"As nitrous oxide in its extensive operation appears capable of
destroying physical pain, it may probably be used with advantage
during surgical operations in which no great effusion of blood takes
place,"
• Henry Hill Hickman (1800–1830)
experimented with the use of carbon
dioxide as an anesthetic in the 1820s.
• He would make the animal insensible,
effectively via almost suffocating it
with carbon dioxide, then determine
the effects of the gas by amputating
one of its limbs.
.
1824
1824
(1800-1830)
Henry Hill Hickman
experimented with the use of carbon
dioxide as an anesthetic in the 1820s.
He ould make the animal insensible,
effectively via almost suffocating it
wit
the
one
carbon dioxide, then determine
ffects of the gas by amputating
f its limbs.
• In 1824, Hickman submitted the results of his research to
the Royal Society in a short treatise entitled Letter on
suspended animation: with the view of ascertaining its
probable utility in surgical operations on human subjects.
• The response was an 1826 article in The Lancet titled
'Surgical Humbug' that ruthlessly criticized his work.
• Hickman died four years later at age 30. Though he was
unappreciated at the time of his death, his work has since been
positively reappraised and he is now recognized as one of the
fathers of anesthesia
' In 1824, Hickman submitted the results of his research
the Royal Society in a short treatise entitled Letter
suspended animation: with the view of ascertaining
probable utility in surgical operations on human subjects.
to
on
its
The response was an 1826 article in The Lancet titled
'Surgical Humbug' that ruthlessly criticized his work.
Hic man died four years later at age 30. Though he was
unappreciated at the time of his death, his work has since been
posit•vely reappraised and he is now recognized as one of the
fathe of anesthesia
• Crawford W. Long had observed in the
ether frolics gatherings, that some
participants experienced bumps and
bruises, but afterward had no recall of
what had happened.
• He postulated that that diethyl ether
produced pharmacologic effects similar to
those of nitrous oxide.
• On 30 March 1842, he administered
diethyl ether by inhalation to a man named
James Venable, in order to remove a cysts
from the man's neck.
1842
1842
had observed in the
rawford W. Long
ether frolics gatherings, that some
articipants experienced bumps and
ruises, but afterward had no recall of
what had happened.
He postulated that that diethyl ether
prodåced pharmacologic effects similar to
those of nitrous oxide.
On 0 March 1842, he administered
dieth ether by inhalation to a man named
James Venable, in order to remove a cysts
from t e man's neck.
CRAWCOROW LONG
• Dr. Horace Wells (1815-1848) volunteered to inhale nitrous
oxide for his own dental extraction back in December of 1844.
• Wells then began to administer nitrous oxide to his patients,
successfully performing several dental extractions over the next
couple of weeks.
1845
1845
, Dr. orace wells (1815-1848) volunteered to inhale nitrous
oxide for his own dental extraction back in December of 1844.
Wells then began to administer nitrous oxide to his patients,
succe sfully performing several dental extractions over the next
couple of weeks.
• In spite of these convincing results being reported by Wells to the
medical society in Boston already in December 1844, this new
method was not immediately adopted by other dentists.
• The reason for this was most likely that Wells, in January 1845 at
his first public demonstration to the medical faculty in Boston, had
been partly unsuccessful, leaving his colleagues doubtful
regarding its efficacy and safety the partial anesthetic was judged
as a "humbug."
spite of these convincing results being reported by Wells to the
edical society in Boston already in December 1844, this new
ethod was not immediately adopted by other dentists.
The reason for this was most likely that Wells, in January 1845 at
his first public demonstration to the medical faculty in Boston, had
been partly unsuccessful, leaving his colleagues doubtful
regar ing its efficacy and safety the partial anesthetic was judged
as a "humbug."
HISTORY OF ETHER DOME
HISTORY OF ETHER DOME
• On October 16,1846 William T. G. Morton (1819-1868)
became first in the world to publicly and successfully
demonstrate the use of ether anesthesia for surgery. This occurred
at what came to be called "The Ether Dome," at Massachusetts
General Hospital.
1846
1846
On ctober 16,1846 (1819-1868)
William T. G, Morton
beca e first in the world to publicly and successfully
demo strate the use of ether anesthesia for surgery. This occurred
at whåt came to be called at Massachusetts
The Ether Dome
Genera Hospital.
The Ether Dome is a surgical operating amphitheater in
the Bulfinch Building at Massachusetts General
Hospital in Boston.
It was the site of the first public demonstration of the use of
inhaled ether as a surgical anesthetic on 16 October 1846.
The ether Dome is a surgical operating amphitheater in
the Bu finch Building at Massachusetts General
Hospital in Boston.
It was t e site of the first public demonstration of the use of
inhaled ether as a surgical anesthetic on 16 October 1846.
• Crawford Long, had previously administered ether in 1842,
but this went unpublished until 1849.
• The Ether Dome event occurred when William T. G. Morton,
used ether to anesthetize Edward Gilbert Abbott.
• John Collins Warren, the first dean of Harvard Medical
School, then painlessly removed part of a tumor from Abbott's
neck.
• After Warren had finished, and Abbott regained consciousness,
Warren asked the patient how he felt.
had previously administered ether in 1842,
' Crawford Long
but this went unpublished until 1849.
The Ether Dome event occurred when William T. G, Morton,
used ether to anesthetize Edward Gilbert Abbott.
the first dean of Harvard Medical
' Joi n Collins Warren
School, then painlessly removed part of a tumor from Abbott's
neck.
Afte Warren had finished, and Abbott regained consciousness,
Warren asked the patient how he felt.
• Reportedly, Abbott said, "Feels as if my neck's been
scratched". Warren then turned to his medical audience and
uttered "Gentlemen, this is no Humbug".
• This was presumably a reference to the unsuccessful
demonstration of nitrous oxide anesthesia by Horace Wells in
the same theater the previous year, which was ended by cries
of "Humbug!" after the patient groaned with pain..
Reportedly, Abbott said, "Feels as if my neck's been
scratched". Warren then turned to his medical audience and
uttered "Gentlemen, this is no Humbug",
This was presumably a reference to the unsuccessful
de onstration of nitrous oxide anesthesia by Horace Wells in
the ame theater the previous year, which was ended by cries
of" umbug!" after the patient groaned with pain..
History of Chloroform
Catde•
Wii/
Hist0TY ofChloroform
• Chloroform was discovered independently
in 1831 by the USA's Samuel Guthrie,
France's Eugène Soubeiran, and
Germany's Justus von Liebig.
• Prof. James Y. Simpson (1811-1870)-
Scottish obstetrician begins administering
chloroform to women for pain during
childbirth.
• Chloroform quickly became a popular
anesthetic for surgery and dental
procedures as well.
1847
1847
Chloroform was discovered independently
in 1831 by the USA's Samuel Guthrie,
Soubeiran, and
France's Eugene
Germany's Justus von Liebig.
James Y. Simpson (1811-1870)-
Scottish obstetrician begins administering
chloroform to women for pain during
chilåbirth.
Ch oroform quickly became a popular
anesthetic for surgery and dental
proc dures as well.
• Dr. John Snow (1813-1858) who was a
fulltime anesthetist since 1847,
popularized obstetric anesthesia by
chloroforming Queen Victoria for the
birth of Prince Leopold (1853) and
Princess Beatrice (1857).
1853 & 1857
1853 & 1857
Dr. John Snow (1813-1858) who was a
fulltime anesthetist since 1847,
popularized obstetric anesthesia
chloroforming Queen Victoria for
bi h of Prince Leopold (1853)
Princess Beatrice (1857).
by
the
and
John Snow
The First Anaesthetist
• Knowledge of the narcotic effect of chloroform spread rapidly,
but very soon reports of sudden deaths mounted.
• The first fatality was a 15-year-old girl called Hannah Greener,
who died on January 28, 1848.
• Between 1864 and 1910 numerous commissions in UK studied
chloroform, but failed to come to any clear conclusions.
• The reservations about chloroform could not halt its soaring
popularity. Between about 1865 and 1920, chloroform was
used in 80 to 95% of all narcoses performed in UK and
German-speaking countries.
Knowledge of the narcotic effect of chloroform spread rapidly,
but very soon reports of sudden deaths mounted.
The first fatality was a 15-year-old girl called Hannah Greener,
who died on January 28, 1848.
Between 1864 and 1910 numerous commissions in UK studied
chloroform, but failed to come to any clear conclusions.
The reservations about chloroform could not halt its soaring
pop larity. Between about 1865 and 1920, chloroform was
use in 80 to 9500 of all narcoses performed in UK and
German-speaking countries.
History of Cocaine
History ofCocaine
cocam
TOOTHACHE DROPS
Instantaneous Cure !
15
Prepared by the
LLOYD MANUFACTURING CO.
219 HUDSON AVE., ALBANY, N. Y.
For sale by all Druggists.
ntlhm•
• Dr. Karl Koller (1857-1944)-Viennese
ophthalmologist and colleague of
Sigmund Freud, introduced cocaine as
an anesthetic for eye surgery.
• Koller recognized its tissue-numbing capabilities, and in 1884
demonstrated its potential as a local anaesthetic to the medical
community.
1884
1884
(1857-1944)-Viennese
Dr. Karl Koller
ophthalmologist and colleague of
Sigmund Freud, introduced cocaine as
an anesthetic for eye surgery.
Koll r recognized its tissue-numbing capabilities, and in 1884
dem nstrated its potential as a local anaesthetic to the medical
community.
• Koller's findings were a medical
breakthrough. Prior to his discovery,
performing eye surgery was difficult
because the involuntary reflex
motions of the eye to respond to the
slightest stimuli.
• Later, cocaine was also used as a
local anaesthetic in other medical
fields such as dentistry
Koller's findings were a medical
breakthrough. Prior to his discovery,
performing eye surgery was difficult
because the involuntary reflex
motions of the eye to respond to the
slightest stimuli.
Lat r, cocaine was also used as a
loca anaesthetic in other medical
field such as dentistry
aCOCAINE(
'OCHLORIDE Topical
t Coeæt-e
• Dr. August Bier (1861-1949) was a
German surgeon.
• On 16 August 1898, Bier performed
the first operation under spinal anesthesia at the Royal Surgical
Hospital of the University of Kiel.
• The subject was scheduled to undergo segmental resection of
his left ankle, which was severely infected with tuberculosis.
1898
1898
Dr. August Bier (1861-1949) was a
German surgeon.
' On 16 August 1898, Bier performed
the Irst operation under spinal anesthesia at the Royal Surgical
Ho ital of the University of Kiel.
The subject was scheduled to undergo segmental resection of
his I t ankle, which was severely infected with tuberculosis.
• But Bier dreaded the prospect of general anesthesia because he had
suffered severe adverse side effects during multiple previous
operations. Therefore, Bier suggested "cocainization" of the spinal
cord as an alternative to general anesthesia.
• Bier injected 15 mg of cocaine intrathecally, which was sufficient
to allow him to perform the operation. The subject was fully
conscious during the operation, but felt no pain.
B t Bier dreaded the prospect of general anesthesia because he had
su ered severe adverse side effects during multiple previous
op rations. Therefore, Bier suggested "cocainization" of the spinal
co d as an alternative to general anesthesia.
Bier injected 15 mg of cocaine intrathecally, which was sufficient
to allo him to perform the operation. The subject was fully
conscious during the operation, but felt no pain.
• Two hours after the operation, the subject complained
of nausea, vomiting, severe headache, and pain in his back and
ankle.
• The vomiting, back and leg pain improved by the following day,
but the headache was still present.
• Bier performed spinal anesthetics on five more subjects for
lower extremity surgery, using a similar technique and achieving
similar results
wo hours after the operation, the subject complained
f nausea, vomiting, severe headache, and pain in his back and
nkle.
The vomiting, back and leg pain improved by the following day,
butthe headache was still present.
Bier
lowe
simil
performed spinal anesthetics on five more subjects for
extremity surgery, using a similar technique and achieving
r results
20th
C
E
N
T
U
R
y
20th
The 20thcentury saw the transformation of the practices of
tracheotomy, endoscopy and non-surgical tracheal intubation
fromrarelyemployed procedures to essential componentsof the
practices of anesthesia, critical care medicine, emergency
medicine, gastroenterology, pulmonology and surgery.
The 20th centuyy saw the transformation ofthe practices of
tracheotomy, endoscopy and non-surgical tracheal intubation
fromrarely employdprocedures to essential components ofthe
practices ofanesthesia, critical care medicine, emergency
medicine, gastroenterolou, pulmonolog and surgety.
Barbiturates
In 1902, Hermann
Emil Fischer (1852–
1919) and Joseph von
Mering (1849–1908)
discovered that
diethylbarbituric
acid was an
effective hypnotic
agent.
In 1902, Hermann
Emil Fischer (1852—
1919) andJosephvon
Mering (1849—1908)
discovered that
diethylbarbituric
acid was an
effective hypnotic
agent.
• Also called barbital or Veronal, the trade name assigned to it
by Bayer Pharmaceuticals, this new drug became the first
commercially marketed barbiturate.
• It was used as a treatment for insomnia from 1903 until the
mid-1950s.
Also called barbital or Veronal, the trade name assigned to it
by Bayer Pharmaceuticals, this new drug became the first
commercially marketed barbiturate.
It as used as a treatment for insomnia from 1903 until the
mid 1950s.
• Barbitone was prepared by
condensing diethylmalonic ester
with urea in the presence of sodium
ethoxide, and then by adding at least
two molar equivalents of ethyl iodide
to the silver salt of malonylurea or
possibly to a basic solution of the
acid. The result was an odorless,
slightly bitter, white crystalline
powder.
Barbitone
condensing
prepared by
was
diethylmalonic ester
with urea in the presence of sodium
ethoxide, and then by adding at least
wo molar equivalents of ethyl iodide
to the silver salt of malonylurea or
pos ibly to a basic solution of the
acid. The result was an odorless,
slig tly bitter, white crystalline
POW er.
hlemal'
• Alfred Einhorn (1857-1917)-
German chemist develops
procaine and names the substance
"Novocain.“ from the Latin nov-
(meaning new) and -caine, a
common ending for alkaloids used
as anesthetics.
• It was introduced into medical use
by surgeon Heinrich Braun.
1905
Alfred
German
1905
(1857-1917)-
Einhorn
chemist develops
procaine and names the substance
"Novocain." from the Latin nov-
eaning new) and -caine, a
common ending for alkaloids used
as anesthetics.
s introduced into medical use
by surgeon Heinrich Braun
At
• Arthur Guedel publishes his eye signs of
Ether anesthesia in the American Journal of
Surgery.
• He also described 4 stages of ether anaesthesia dividing the
stage III into 4 planes
• His Guedel (oral) airway is still used today.
• He has been memorialized by the Arthur E. Guedel Memorial
Anesthesia Center, San Francisco.
1920
1920
Arthur Guedel publishes his eye signs of
Ether anesthesia in the American Journal of
Surgery.
He also described 4 stages of ether anaesthesia dividing the
stage Ill into 4 planes
His Guedel (oral) airway is still used today.
He as been memorialized by the Arthur E. Guedel Memorial
Ane hesia Center, San Francisco.
HISTORY OF SODIUM THIOPENTAL
Who cares about
your consent or
Supreme Court's
verdict on
Narco Tests
HISTORY OF SODIUMTHIOPENTAL
• Sodium thiopental, the 1st IV
anesthetic, was synthesized in
1934 by Ernest H. Volwiler &
Donalee L. Tabern , working
for Abbott Laboratories.
• In the mid 1930s, Volwiler and Tabern spent three years
screening over 200 candidate compounds in search of a
substance which could be injected directly into the blood
stream to produce unconsciousness
the 1st IV
Sodium thiopental
anesthetic, was synthesized in
1934 by Ernest H, Volwiler &
, working
Donalee L. Tabern
for Abbott Laboratories.
' In he mid 1930s, Volwiler and Tabern spent three years
screening over 200 candidate compounds in search of a
sub tance which could be injected directly into the blood
strea to produce unconsciousness
•It was first used in humans on
8 March 1934 by Ralph M. Waters in
an investigation of its properties,
which were short-term anesthesia and
surprisingly little analgesia.
•Three months later, John Silas Lundy started a clinical trial of
thiopental at the Mayo Clinic at the request of Abbott
Laboratories.
' t was first used in humans on
8 arch 1934 by Ralph M. Waters in
a investigation of its properties,
w ich were short-term anesthesia and
suprisingly little analgesia.
•Three months later, John Silas Lundy started a clinical trial of
thiopental at the Mayo Clinic at the request of Abbott
Labora ories.
• Volwiler and Tabern were awarded U.S. Patent No. 2,153,729 in
1939 for the discovery of thiopental, and they were inducted into
the National Inventors Hall of Fame in 1986.
• The popularity of thiopental-as a swift-onset intravenous agent
for inducing general anesthesia- paved the way for other totally
unrelated intravenous induction agents, such as ketamine,
etomidate, and propofol.
Volwiler and Tabern were awarded U.S. Patent No. 2,153,729 in
939 for the discovery of thiopental, and they were inducted into
he National Inventors Hall of Fame in 1986.
The popularity of thiopental-as a swift-onset intravenous agent
for 1 ducing general anesthesia- paved the way for other totally
unrelated intravenous induction agents, such as ketamine,
etom date, and propofol.
• On 23 January 1942 Griffith and his resident Enid Johnson
administered curare to a young man undergoing
appendicectomy..
Dr. Harold Griffith (1894-1985) & Enid Johnson (1909-2001)
1942
1942
Dr Harold Griffith (1894-1985) & Enid Johnson (1909-2001)
' On 23 January 1942 Griffith and his resident Enid Johnson
administered curare to a young man undergoing
app ndicectomy..
The credit for introducing curare to anaesthetics belongs to Griffith.
Griffith and Johnson reported their use of curare in July 1942, and
the introduction to their report is memorable: ‘Every anaesthetist
has wished at times that he might be able to produce rapid and
complete muscular relaxation in resistant patients under general
anaesthesia”
The credit for introducing curare to anaesthetics belongs to Griffith.
GrTfith and Johnson reported their use of curare in July 1942, and
th introduction to their report is memorable: 'Every anaesthetist
has wished at times that he might be able to produce rapid and
complete muscular relaxation in resistant patients under general
anaesthesia "
• Many new intravenous and inhalational
anesthetics were developed and brought
into clinical use during the second half of
the 20th century.
• Paul Janssen (1926–2003), the founder of Janssen Pharmaceutica, is
credited with the development of over 80 pharmaceutical
compounds.
• Janssen synthesized nearly all of the butyrophenone class
of antipsychotic agents, beginning with haloperidol (1958)
and droperidol (1961).
Many new intravenous and inhalational
anesthetics were developed and brought
into clinical use during the second half of
the 20th century.
Paul Janssen (1926—2003), the founder of Janssen Pharmaceutica, is
credited with the development of over 80 pharmaceutical
com ounds.
Jans en synthesized nearly all of the butyrophenone class
of ntipsychotic agents, beginning with haloperidol (1958)
and d operidol (1961).
• These agents were rapidly integrated into the practice of
anesthesia.
• In 1960, Janssen's team synthesized fentanyl, the first of
the piperidinone-derived opioids.
• Fentanyl was followed by sufentanil (1974), alfentanil
(1976), carfentanil (1976), and lofentanil (1980). Janssen and
his team also developed etomidate (1964),a potent intravenous
anesthetic induction agent.
These agents were rapidly integrated into the practice of
anesthesia.
' In 1960, Janssen's team synthesized fentanyl, the first of
the piperidinone-derived opioids.
' Fen anyl was followed by sufentanil (1974), alfentanil
(19 6), carfentanil (1976), and lofentanil (1980). Janssen and
his eam also developed etomidate (1964),a potent intravenous
anes hetic induction agent.
1956 - UK's Dr. Michael Johnstone clinically introduces
halothane, the first modern-day brominated general
anesthetic.
1963 - Dr. Edmond I. Eger, II described minimum alveolar
concentration (MAC), later characterized as "the
concentration of inhaled anesthetic producing immobility in
50% of patients subjected to a noxious stimulus."
1 56 - UK's Dr.
the
halothane,
anesthetic.
Michael Johnstone
first modern-day
clinically introduces
brominated general
1963 - Dr. Edmond 1. Eger, 11 described minimum alveolar
later characterized as "the
entration (MAC)
entration of inhaled anesthetic producing immobility in
con
of patients subjected to a noxious stimulus."
500
1964- Dr. Günter Corssen et al. begin human trials of the
dissociative intravenous anesthetic ketamine.
1966- Dr. Robert Virtue et al. begin human trials of the inhalational
anesthetic enflurane.
1972- Isoflurane is clinically introduced as an inhalational
anesthetic.
1992- Desflurane is clinically introduced as an inhalational
anesthetic.
1994- Sevoflurane is clinically introduced as an inhalational
anesthetic.
1 64- Dr. Günter Corssen et al. begin human trials of the
dissociative intravenous anesthetic ketamine.
19 6- Dr. Robert Virtue et al. begin human trials of the inhalational
nesthetic enflurane,
is clinically introduced as an inhalational
1972- Isoflurane
anesthetic.
is clinically introduced as an inhalational
1992- esflurane
anest etic.
is clinically introduced as an inhalational
1994- roflurane
anesthetic.
21ST CENTURY
21st Century: Age of Digital Revolution
21st Century: Age ofDigital Revolution
revolution
• Among the most widely used drugs are Propofol, Etomidate,
Barbiturates such as methohexital and thiopentone,
Benzodiazepines such as midazolam and Ketamine.
• The "digital revolution“ of the 21st century has brought newer
technology to the art and science of tracheal intubation.
• Several manufacturers have developed video laryngoscopes
' Among the most widely used drugs are Propofol, Etomidate,
Barbiturates such as methohexital and thiopentone,
Benzodiazepines such as midazolam and Ketamine.
The "digital revolution" of the 21st century has brought newer
tec nology to the art and science of tracheal intubation.
Sev ral manufacturers have developed video laryngoscopes
• Xenon has been used as a general anesthetic. Although it is
expensive, anesthesia machines that can deliver xenon are
about to appear on the European market, because advances in
recovery and recycling of xenon have made it economically
viable.
• New agents based on benzodiazepine, etomidate, and propofol
structures are being developed.
Xenon has been used as a general anesthetic. Although it is
expensive, anesthesia machines that can deliver xenon are
about to appear on the European market, because advances in
recovery and recycling of xenon have made it economically
viable.
' Ne
stru
agents based on benzodiazepine, etomidate, and propofol
tures are being developed.
Conclusion
• Surgery learned many lessons through the ages, but never was
it able to banish Pain.
• More than a century ago, a vapor in the operating-room of the
Massachusetts General Hospital blotted out sufferrings from
surgery.
• It was the most beneficent change in the history of surgery,
and has since been one of the greatest gift to mankind.
• However, the history of anaesthetics will remain an unfinished
work, until some one is able to synthesize a drug that will have
all of the desirable properties of the ideal anaesthetic.
Conclusion
Surgery learned many lessons through the ages, but never was
it able to banish Pain.
More than a century ago, a vapor in the operating-room of the
Massachusetts General Hospital blotted out sufferrings from
surgery.
It as the most beneficent change in the history of surgery,
and has since been one of the greatest gift to mankind.
Ho ever, the history of anaesthetics will remain an unfinished
wor , until some one is able to synthesize a drug that will have
all o the desirable properties of the ideal anaesthetic.
Oräger Julian
07
40 so
os os
56
77
THANK YOU
INTRODUCTION TO
ANAESTHESIA
Fatiş Altındaş
Department of Anesthesiology
INTRODUCTIONTO
ANAESTHESIA
FatisAltlndas
Department ofAnesthesiology
† Dioscorides first used the term
anesthesia in first century AD
„ To describe the narcotic-like effects
† As “a defect of sensation” in Bailey’s
An Universal Etymological English
Dictionary (1721)
Dioscoridesfirstusedtheterm
o
anesthesiainfirstcenturyAD
Todescribethe narcotic-likeeffects
As"adefectofsensation"inBailey's
o
An Universal Etymological English
(1721)
Dictionary
† Oliver Wendell Holmes used its
present meaning (1846)
„ means the sleeplike state
„ makes possible painless surgery
OliverWendellHolmes usedits
o
(1846)
presentmeaning
annakes possible painless surgery
History of Anesthesia
† In ancient time, people used
„ Opium poppy, coca leaves, mandrake
root, alcohol, phlebotomy
† Ancient Egyptians used the
combination of opium poppy and
hyoscyamus morphine and
scopolamine
Historyof Anesthesia
Inancienttime,people used
o
Opium poppy,cocaleaves, mandrake
o
root,alcohol,phlebotomy
AncientEgyptians usedthe
o
combinationofopium poppyand
hyoscyamus
scopolamine
morphineand
Ether
† Prepared in 1540 by Valerius
Cordus
† Used as sedative in
„ tuberculosis
„ asthma and whooping cough
„ remedy for toothache
† Crawford W. Long and William
Clark used it on patients in 1842
Ether
Prepared in1540 byValerius
o
Cordus
Usedassedative in
o
tuberculosis
o
asthmaand whoopingcough
o
remedyfortoothache
o
Crawford W.LongandWilliam
o
Clarkusediton patients in1842
William Morton
(1819-1868)
† The first succesful
surgical
anesthesia, 1846,
Boston
William Morton
(1819-1868)
Thefirstsuccesful
surgical
anesthesia,1846,
Boston
3
7
1. Newspaper repotlet
2. John call Dalton
3. William Williamson
Wellington
4. Abel Lawrence Peitson
5. Char es Hosea Hildreth
6. William Tt'aoma•s
Green Mctlon
7. Jonathan Mason
Warren
B. Gilbert Abbott
g. John Collins Warren
10. H.
11 Charles
Frederick Heywood
12. HeneryJacob Bigelow
13. Augustus Addison
Gould
14. Salomon Davis
Professor James Young
Simpson (1811-
1870)
† found chloroform to
be efficacious and
reasonably safe
† used for Prince
Leopold’s and
Princess Beatrice’s
birhts
Chloroform
Chloroform
ProfessorJamesYoung
Simpson(1811-
1870)
foundchloroformto
o
be efficaciousand
reasonablysafe
usedforPrince
o
Leopold'sand
Princess Beatrice's
birhts
Nitrous oxide (N2O)
† Produced by Joseph Priestly
1772,
† Humphrey Davy first noted
its analgesic properties in
1800.
† Horace Wells first used it in
humans for anesthesia in
1844
† Less popular in tree agents
„ Low potency
„ Tendency to cause asphyxia H. Davy
(N20)
Nitrousoxide
Produced byJoseph Priestly
1772,
HumphreyDavyfirstnoted
itsanalgesic properties in
1800.
I-Horace Wells firstused itin
humansforanesthesiain
1844
Less popularintreeagents
Low potency
Tendencytocause asphyxia H.Davy
Intravenous Anesthesia (IVA)
† Pierre Cyprien Ore
„ Pioneer of IVA
„ Chloral hydrate in
1872
† Barbiturates were
synthesized 1903
„ For induction of
anesthesia
IntravenousAnesthesia(lVA)
Pierre Cyprien Ore
o
Pioneerof1VA
Chloralhydratein
1872
Barbiturates were
o
synthesized1903
Forinductionof
anesthesia
ANGIOCATHS
Regional Anesthesia
† In 1860, Albert Niemann isolated
crystalized alcoloids of coca.
† Karl Koller used cocain for eye block in
1884
† In 1885, first epidural block
† In 1898, first spinal anesthesia by
August Bier
† Second local anesthetic agent (prilocain)
was founded in 1904
† Lidocain was founded in 1946
RegionalAnesthesia
o
o
o
o
In1860,AlbertNiemannisolated
crystalizedalcoloids ofcoca.
Karl Kollerusedcocainforeyeblockin
1884
In1885,firstepidural block
I n 1898,firstspinalanesthesiaby
AugustBier
Secondlocalanestheticagent(prilocain)
wasfounded in1904
Lidocainwasfoundedin1946
Evolution of the specialty
†The development of the
indepented medical specialty
of anesthesiology would not
occur until the early 20th
century.
Evolutionofthe specialty
Thedevelopmentofthe
indepented medicalspecialty
ofanesthesiologywouldnot
occuruntiltheearly20th
century.
† In England, in 1893, the first
organization of physician specialists in
anesthesia, “The Society of
Anesthetists”
† In the United States, the first
organization of physician anesthetists
was formed in 1911.
In England,in1893,thefirst
o
organizationofphysicianspecialistsin
anesthesia,"TheSocietyof
Anesthetists"
Inthe UnitedStates,thefirst
o
organizationofphysiciananesthetists
was formed in1911.
† invented an inhaler
for ether
† published the first
book on general
anaesthesia:On the
Inhalation of Ether
John Snow
the father of anaesthesia
aninhaler
forether
publishedthefirst
o
bookongeneral
anaesthesia : Onthe
InhalationofEther
John Snow
the fatherofanaesthesia
History of Anesthesia in Turkey-1
† The first publications belong to surgeons
† They made great contributions to
anesthesia in Turkey
† Publication of Miralay Ahmet Bey
„ includes the information about the use of
ether
† Ether anesthesia was first used in
Gülhane Askeri Hospital in 1898 by
Rieder Paşa
Historyof AnesthesiainTurkey-1
Thefirst publications belongtosurgeons
Theymadegreatcontributionsto
anesthesia inTurkey
Publication ofMiralayAhmetBey
o
the use of
ether
Etheranesthesia wasfirstusedin
o
GülhaneAskeriHospitalin1898 by
Ri ed e r Pasa
History of Anesthesia in Turkey-2
† Dr. Sadi Sun is the
first anesthesiologist
in Turkey
† The first endotracheal
entubation was
performed by Dr Sun
† In 1955, anesthesia
was accepted as a
medical specialty by
Ministry of Health
Historyof AnesthesiainTurkey-2
Dr.SadiSunisthe
firstanesthesiologist
inTurkey
Thefirstendotracheal
entubationwas
performed by DrSun
In1955,anesthesia
wasacceptedasa
medicalspecialtyby
MinistryofHealth
What is Anesthesiology?
†Practice of medicine
dedicated to the relief of
pain and total care of the
surgical patient before,
during and after surgery.
What isAnesthesiology?
Practiceofmedicine
o
dedicatedtothereliefof
painandtotalcareofthe
duri ngandaftersurgery.
†Anesthesiologists are a
physician who complete a six
years of medical school and
four more year anesthesiology
residency training program.
Anesthesiologistsarea
o
physician whocompleteasix
yearsofmedicalschooland
fourmore yearanesthesiology
residencytrainingprogram.
† Anesthesiologist is the perioperative
physician
† Provides medical care to each patient
„ Evaluating the patient before surgery
(preoperative)
„ Consulting with the surgical team
„ Providing pain control
„ Supporting of life functions during
surgery (intraoperative)
„ Supervising care after surgery
(postoperative)
Anesthesiologististhe perioperative
o
physician
Provides medicalcaretoeachpatient
o
Evaluatingthe patientbefore surgery
(preoperative)
Consultingwiththe surgicalteam
Providing paincontrol
Supporting oflifefunctionsduring
surgery(intraoperative)
Supervisingcareaftersurgery
(postoperative)
In the operating room
† The role of anesthesiologist is to provide
continual medical assessment of the
patient
„ Monitor and control the patient’s vital
functions
† Heart rate, rhythm, breathing, blood pressure,
body temperature, fluid balance
† Immediately diagnose and treat any medical
problems during surgery or recovery period
„ Control pain and level of unconsciousness
Intheoperatingroom
The roleofanesthesiologististo provide
continualmedicalassessmentofthe
patient
patient'svital
functions
IHeartrate,rhythm,breathing,blood pressure,
bodytemperature,fluid balance
Immediately diagnose andtreatany medical
o
problemsduringsurgery orrecovery period
Controlpainand levelofunconsciousness
In the postanesthesia care unit
† Patients are
transferred to recovery
room after surgery
„ Allowing them to emerge
fully from the anesthetics’
effects
† They are observed by
skilled nursing
personnel
„ After stabilization
sufficiently, transferred to
regular room or home
Inthe postanesthesiacareunit
Patientsare
transferredtorecovery
roomaftersurgery
Allowingthem to emerge
fully fromtheanesthetics'
effects
Theyare observed by
skillednursing
personnel
Afterstabilization
sufficiently,transferredto
regularroomorhome
What is Scope of Anesthesiologist?
† Anesthesiologists work in ICU
What isScopeof Anesthesiologist?
Anesthesiologists work inlCU
† Sedation and providing anesthesia outside
the operating room
„ Magnetic resonance imaging, cardiac
catheterization etc.
† Pioneers in cardiopulmonary resuscitation
† In childbirth, anesthesiologists manage the
care of two persons
† Anesthesiologists are also involved in pain
management,
„ to diagnose and treatment of acute and chronic
problems.
Sedationandprovidinganesthesiaoutside
o
theoperatingroom
Magnetic resonanceimaging,cardiac
catheterizationetc.
Pioneersincardiopulmonaryresuscitation
o
Inchildbirth,anesthesiologists managethe
o
careoftwo persons
Anesthesiologistsare alsoinvolvedin pain
o
management,
to diagnoseandtreatmentofacute andchronic
problems.
Happy New Year!
HappyNewYear!
Types of
Anaesthesia
PPT PREPARED BY
DR RAJESH T EAPEN
ATLAS HOSPITAL
RUWI
Types of
Anaesthesia
PPTPREPARED BY
DR RAJESH TEAPEN
ATLAS HOSPITAL
RUWI
Sushruta 800B.C.
wrote first Surgery textbook
Sushruta 800B.C.
wrote first Surgery textbook
Anesthesiology
Making
Surgery
Painless
Anesthesi ogy
Making
Surgery
Painless
Anesthesia
 From Greek anaisthesis means
not sensation
 Listed in Bailey´s English
Dictionary 1721.
 When the effect of ether was
discovered anesthesia” used as a
name for the new phenomenon.
Anesthesia
From Greek anaisthesis means
not sensation
Listed in Bailey's English
Dictionary 1721.
the effect Of ether was
discovered anesthesia" used as a
name for the new phenomenon.
Oxford dictionary
definition
 insensitivity to pain, especially
as artificially induced by the
administration of gases or the
injection of drugs before
surgical operations
Oxford dictionary
definition
insensitivity to pain, especially
as artificially induced by the
administration of gases or the
injection of drugs before
surgical operations
World Anesthesia Day 16th Oct
HISTORY OF ANESTHESIA
• General anesthesia was absent until the mid-
1800s.
• Ether synthesized in 1540 by Cordus
• Ether used as anesthetic in 1842 by Dr. Crawford
W.Long
• Ether publicized as anesthetic in 1846 by Dr.
William Morton.
• Ether is no longer used in modern practice, yet
considered to be the first ‘ideal’ anesthetic
• Chloroform used as anesthetic in 1853 by Dr. John
Snow
• Endotracheal tube discovered in 1878
• Thiopental first used in 1934
HISTORY OF ANESTHESIA
General anesthesia was absent until the mid-
800s.
Ether synthesized in 1540 by Cordus
Ether used as anesthetic in 1842 by Dr. Crawford
W.Long
Ether publicized as anesthetic in 1846 by Dr.
William Morton.
Ether is no longer used in modern practice, yet
onsidered to be the first 'ideal' anesthetic
Chloroform used as anesthetic in 1853 by Dr. John
Snow
Endotracheal tube discovered in 1878
Thiopental first used in 1934
Pre 1846 - The Foundations of
Anaesthesia
……..so the Lord God caused him to fall
into a deep sleep. While the man
was sleeping, the Lord God took out
one of his ribs. He closed up the
opening that was in his side……...
Genesis 2:21 NIrV
Pre 1846 - The Foundations of
—Anaesthesia
so the Lord God caused him to fa//
into a deep sleep, While the man
was s/eeping, the Lord God took out
one ofhis ribs. He closed up the
opening that was in his side
Genesis 2:21 /V1rV
Primitive Anesthesia
 Ancient civilizations- opium poppy,
coca leaves, mandrake root,
alcohol
 Regional anesthesia in ancient
times- compression of nerve
trunks or the application of cold
(cryoanalgesia)
Primitive Anesthesia
Ancient civilizations- opium poppy,
coca leaves, mandrake root,
alcohol
Regional anesthesia in ancient
times- compression of nerve
trunks or the application of cold
(cryoanalgesia)
World Anaesthesia Day
 On 16 October 1846,
John Collins Warren
removed a tumor from
the neck of a local
printer,Edward Gilbert
Abbott. Warren
reportedly quipped,
"Gentlemen, this is no
humbug.
 MGH Boston
World Anaesthesia Day
• On 16 October 1846,
John Collins Warren
removed a tumor from
the neck of a local
printer,Edward Gilbert
Abbott. Warren
reportedly quipped,
"Gentlemen, this is no
humbug.
NIGH Boston
Regional
Anaesthesia
 1884 Sigmund Freud
physiology actions
cocaine
 Carl Koller cocaine
ophthalmological
surgery
Regional
Anaesthesia
1884 Sigmund Freud
physiology actions
cocaine
Carl Koller cocaine
ophthalmological
surgery
Birth of modern Anaesthesia
 1913,Chevalier Jackson-use of direct
laryngoscopy as a means to intubate
the trachea
 Sodium Pentathal - first used in humans
on 8 March 1934 by Ralph M. Waters
Birth of modern Anaesthesia
Chevalier Jackson-use of direct
-1 13,
laryngoscopy as a means to intubate
the trachea
Sodium Pentathal - first used in humans
on 8 March 1934 by Ralph M. Waters
Slide master
Your Text here
"Ether Day, 1846" Pictured are Gilbert Abbott (the patient), John Collins Warren,
MD (the surgeon), William T. G. Morton (the anesthetist) and Henry J. Bigelow. MD (the junior
surgeon).
History
 1845- Horace Wells- N2O
 1846- William Morton- Ether
 1847- Simpson- Chloroform
 1853-John Snow
 1878- ETT
 1884- Cocaine
 1895-98- Spinal
analgesia/anaesthesia
History
1845- Horace wells- N20
1846- William Morton- Ether
1847- Simpson-
1853-John Snow
1878- ETT
1884- Cocaine
1895-98- Spinal
analgesia/anaesthesia
Types Of Anesthesia
Types Of Anesthesia
and
what
kind of
anesthesia
can you
afford?
cæ.VJ
Types
.
Types
Local anesthesia
Topo Infiltraton
Regional anesthesia
Poriphotal
nerve blcH
Epidural
Spinal
Intravenous
regional
Anesthesia
Total tnmgation
General anesthesia
anesthesia
inhalant
anesthesia
Injectable
anesthesia
Anesthetic
adjuncts
intravenous
anesthesia
Triad of General
anaesthesia
Hypnosis
Analgesia Muscle relaxation
ofGeneral
anaesthesia
Hypnosis
Analgesia Muscle relaxation
CLASSIFICATION:
18
General
anaesthetics
Inhalational Intravenous
CLASSIFICATION:
General
anaesthetics
Inhalational Intravenous
INTRODUCTION
• General anaesthetics (GAs) are drugs which produce
reversible loss of all sensations and consciousness. It usually
involves a loss of memory and awareness with insensitivity to
painful stimuli, during a surgical procedure
General anesthesia
need for
unconsciousness
‘Amnesia-hypnosis’
need for analgesia
‘Loss of sensory and
autonomic reflexes’
need for muscle
relaxation
INTRODUCTION
General anaesthetics (GAS) are drugs which produce
reversible loss of all sensations and consciousness. It usually
involves a loss of memory and awareness with insensitivity to
painful stimuli, during a surgical procedure
need for
unconsciousness
'Amnesia-hypnosis'
General anesthesia
need for analgesia
'Loss of sensory and
autonomic reflexes'
need for muscle
relaxation
General anesthetics
Oyveen
Cylinders
General anesthetics
The anesthetist
Vho•s that guy?
Nitrous
Amnesia
sedation
Hypnosis
Coma
Death
Awake
Hypnosis
Hypnosis
Coma
Hypnosis
sedation
Amnesia
Death
Awake
Hypnotic drugs-
intravenous
 Gold standard- thiopentone
 Propofol
others
 Etomidate
 Benzodiazepines
 Ketamine
Hypnotic drugs-
intravenous
Gold standard-
others
Etomidate
Benzodiazepines
Ketamine
Inhalational
anaesthetics
 Nitrous oxide-weak
 Isoflurane
 Sevoflurane
 Desflurane
 Halothane
Inhalational
anaesthetics
Nitrous oxide-weak
Isoflurane
Desflurane
Halothane
Analgesia
 Good analgesia= good
anaesthesia
 Hypnotic sparing effect
 Opiates
 Local anaesthetics
 NSAIDS
 Paracetamol
Analgesia
Good analgesia= good
anaesthesia
Hypnotic sparing effect
Opiates
Local anaesthetics
NSAIDS
Paracetamol
Analgesia-Opiates
 Gold standard – morphine
 Derivatives- diamorphine,
codeine
 Synthetic agents
- Pethidine
- Fentanyl/Alfentanil-short
acting
- Remifentanil-ultra short
acting
Analgesia-Opiates
Gold standard — morphine
Derivatives- diamorphine,
codeine
Synthetic agents
Pethidine
/Alfentanil-short
acting
Remifentanil-ultra short
actina
Analgesia-NSAIDS
 Gold standard- aspirin
 Ibuprofen
 Diclofenac
 Cox-2 inhibitors
Analgesia-NSAIDS
Gold standard- aspirin
• Ibuprofen
• Diclofenac
Cox-2 inhibitors
Muscle relaxation
 Aids intubation
 Helps surgeon/surgery
 Surgery of long duration
 Reduces maintenance dose of
anaesthetics agents
Muscle relaxation
Aids intubation
Helps surgeon/surgery
Surgery oflong duration
Reduces maintenance dose of
anaesthetics agents
Muscle relaxants
 Two types
 Depolarising-short acting
e.g.; suxmethonium
 Non-depolarising-
medium/long acting
- Tracurium
- Vecuronium
- Rocuronium
- Cisatracurium (NIMBEX)
Muscle relaxants
Two types
Depolarising-short acting
e.g.; suxmethonium
Non-depolarising-
medium/long acting
Vecuronium
Rocuronium
Cisatracurium (NIMBEX)
Prerequisites
 Oxygen
 Suction
 Tilting trolley
 Resuscitation drugs
 Monitoring
 Anaesthetist
 Skilled assistance
 Drugs and machine
Prerequisites
Oxygen
Suction
Tilting trolley
Resuscitation drugs
Monitoring
• Anaesthetist
Skilled assistance
Drugs and machine
The 21 st century-digital
revolution
The21 st céntury•
revolution
Phases of
general anaesthesia
 Induction
 Maintenance
 Recovery
Phases of
general anaesthesia
Induction
Maintenance
Recovery
Induction
 Intravenous- majority
 Inhalational- children, needle
phobics
 Monitoring
 Preoxygenation
 Hypnotic/analgesic and or
relaxant
 Mask/LMA/ET tube
Induction
Intravenous- majority
Inhalational- children, needle
phobics
Monitoring
0
Preoxygenation
Hypnotic/analgesic and or
relaxant
Mask/LMA/ET tube
Maintenance
 Intravenous or inhalational
 Oxygen –40%-100%
 Nitrous oxide
 Muscle relaxant
 Analgesia
Maintenance
Intravenous or inhalational
Oxygen —4000-100%
Nitrous oxide
Muscle relaxant
Analgesia
Recovery
 Turn off agent
 Reverse relaxation
 Cough reflex
 Extubate when awake
 Recovery position
 Monitor until discharge
Recovery
Turn offagent
Reverse relaxation
Cough reflex
Extubate when awake
Recovery position
Monitor until discharge
SAMPLE USE ONLY
@ 2009 Nucleus Medical Art All Rights Reserved.
nucleus
MEDICAL
Advantages
 No absolute contraindications
 Quick to establish
 Never fails to work
Advantages
No absolute contraindications
Quick to establish
Neverfails to work
Disadvantages
 Poly-pharmacy
 Effects on various systems
 Allergic reactions
 Recovery profile
 Post operative Nausea &Vomiting
 Awareness
Disadvantages
Poly-pharmacy
Effects on various systems
Allergic reactions
Recovery profile
Post operative Nausea &Vomiting
Awareness
Providing operative conditions
Providing operative conditions
Regional anaesthesia
 Spinal/epidural
- surgery below umbilicus
- Provides analgesia/muscle
relaxation
 Plexus blocks eg brachial plexus
 Intravenous- Bier’s block
Regional anaesthesia
Spinal/epidural
surgery below umbilicus
Provides analgesia/muscle
relaxation
Plexus blocks eg brachial plexus
Intravenous- Bier's block
40
Spinal Block - Position
Spinal Block - Position
Ll
End of cord
Spinal block—lateral position.
End of cord
Spinal block—sitting position.
40
Regional anaesthesia
Analgesia Muscle relaxation
Regional anaesthesia
Analgesia Muscle relaxation
Local anaesthetics
 Lignocaine- quick/short acting
 Bupivacaine/levobupicvacaine
- slow and long action
 Ropivacaine- as above
 Amethocaine- topical
 Prilocaine- intravenous
Local anaesthetics
- quick/short acting
/levobupicvacaine
- slow and long action
Ropivacaine- as above
Amethocaine- topical
j'
Prilocaine- intravenous
Advantages
 Effective alternative to GA
 Avoids polypharmacy
 Allergic reactions
 Extended analgesia
 Patient can remain awake
 Early drink/feed
Advantages
Effective alternative to GA
Avoids polypharmacy
Allergic reactions
Extended analgesia
Patient can remain awake
Early drink/feed
Disadvantages
 Limited scope
 Higher failure rate
 Time constraints
 Anticoagulants/Bleeding
diathesis
 Risk of neural injury
Disadvantages
Limited scope
Higherfailure rate
Time constraints
Anticoagulants/Bleeding
diathesis
j'
Risk ofneural injury
Patient is more important
than our ego; call for help,
whenever patient is in
danger
Your Text here
Patient is more important
than our ego; call for help,
whenever patient is in
000
"Nurse, get on the internet, go to SURGERY.COM,
scroll down and click on the 'Are you totally lost?'
icon.
Slide master
Your Text here
THE IDEAL ANESTHETIST
Reader
Seoee &
*neszhesia Eye
estim
cardiae
Free
foot fast
Counter
Loss Ester.atoc
FieJd Eye
Gas Eye
.anaeoev.y
4
4
block
anesthetics
Srnag
Storn•ch
Met* Bats
droppiro beetles
AB Blood
Table
*4uster
Pacifier
& chest
Shovel
Ernergerwy
Choice of anesthesia
 The patient´s understanding and wishes regarding the type of
anesthesia that could be used
 The type and duration of the surgical procedure
 The patients´s physiologic status and stability
 The presence and severity of coexisting disease
 The patient´s mental and psychologic status
 The postoperative recovery from various kinds of anesthesia
 Options for management of postoperative pain
 Any particular requiremets of the surgeon
 There is major and minor surgery but only major
anesthesia
hoice of anesthesia
The patient's understanding and wishes regarding the type of
anesthesia that could be used
The type and duration of the surgical procedure
The patients's physiologic status and stability
The presence and severity of coexisting disease
The patient's mental and psychologic status
The postoperative recovery from various kinds of anesthesia
Options for management of postoperative pain
• Any particular requiremets of the surgeon
There is major and minorsurgery but only major
anesthesia
Types of anesthesia care
General Anesthesia
 Reversible, unconscious state is
characterised by amnesia (sleep,
hypnosis or basal narcosis),
analgesia (freedom from pain)
depression of reflexes, muscle
relaxation
 Put to sleep
Types of anesthesia care
General Anesthesia
Reversible, unconscious state is
characterised by amnesia (sleep,
hypnosis or basal narcosis),
analgesia (freedom from pain)
depression of reflexes, muscle
relaxation
Put to sleep
Types of anesthesia care
Regional Anesthesia
 A local anethetic is injected to
block or ansthetize a nerve or
nerve fibers
 Implies a major nerve block
administered by an
anesthesiologist (such as spinal,
epidural, caudal, or major
peripheral block)
Types Of anesthesia care
Regional Anesthesia
A local anethetic is injected to
block or ansthetize a nerve or
nerve fi
Implies a major nerve block
administered by an
anesthesiologist (such as spinal,
epidural, caudal, or major
peripheral block)
Types of anesthesia care
Monitored anesthesia care
 Infiltration of the surgical site with a local
anesthesia is performed by the surgeon
 The anasthesiologist may supplement the
local anesthesia with intravenous drugs
that provide systemic analgesia and
sedation and depress the response of the
patient´s autonomic nervous system
Types of anesthesia care
Monitored anesthesia care
Infiltration of the surgical site with a local
anesthesia is performed by the surgeon
The anasthesiologist may supplement the
local anesthesia with intravenous drugs
that provide systemic analgesia and
sedation and depress the response of the
patient's autonomic nervous system
Types of anesthesia care
local anesthesia
 Employed for minor procedures in which the
surgical site is infiltrated with a local anesthetic
vital signs
 May injsuch as lidocaine or bupivacaine
 A perioperative nurse usually monitors the
patient´s ect intravenous sedatives or analgesic
drugs
Types of anesthesia care
local anesthesia
Employed for minor procedures in which the
surgical site is infiltrated with a local anesthetic
vital signs
May injsuch as lidocaine or bupivacaine
A perioperative nurse usually monitors the
patient's ect intravenous sedatives or analgesic
drugs
Thank
you
Macintosh noted: “for the
surgeon the spinal ends
with the injection of the
agent; for the anesthetist it
begins with the injection of
the agent.”
Macintosh noted: "for the
surgeon the spinal ends
with the injection of the
agent; for the anesthetist it
begins with the injection of
the agent."
Thank
you
Types of Anaesthesia
Prof. med. Nabil H. Mohyeddin
Anesthesiologist & Intensivist
Board certified
University Rostock, Germany
nhm1955@hotmail.com
Types ofAnaesthesia
Prof. med, Nabil H, Mohyeddin
Anesthesiologist &Intensivist
Board certified
University Rostock, Germany
nhm1955@hotmail.com
Objectives
 Short History
 Definition/types of anaesthesia
 General anaesthesia/drugs
 Phases of GA
 Regional anaesthesia
Objectives
Short History
Definition/types ofanaesthesia
General anaesthesia/drugs
Phases ofGA
Regional anaesthesia
Early history
 Ancient/Medieval period
- Opium
- Alcohol
- Cannabis
Early history
Ancient/Medieval period
Opium
Alcohol
Cannabis
History
 1845- Horace Wells- N2O
 1846- William Morton- Ether
 1847- Simpson- Chloroform
 1853-John Snow
 1878- ETT
 1884- Cocaine
 1895-98- Spinal analgesia/anaesthesia
History
1845- Horace Wells- N20
1846- William Morton- Ether
1847- Simpson-
1853-John Snow
1878- ETT
1884- Cocaine
1895-98- Spinal analgesia/anaesthesia
History
 1921- Epidurals
 1934- Thiopentone, cyclopropane
 1942- Curare
 1946- Lignocaine
 1951- Suxamethonium
 1952- IPPV
 1956-Halothane
History
1921- Epidurals
1934- Thiopentone, cyclopropane
1942- Curare
1946- Lignocaine
- Suxamethonium
1951
- IPPV
1952
1956-Halothane
Definition
‘Loss of sensation’
 General
 Regional
 Local
Definition
'Loss ofsensation'
General
Regional
Local
Triad of General
anaesthesia
Hypnosis
Analgesia Muscle relaxation
Triad ofGeneral
anaesthesia
Hypnosis
Analgesia Muscle relaxation
Amnesia
sedation
Hypnosis
Coma
Death
Awake
Hypnosis
Hypnosis
Coma
Hypnosis
sedation
Amnesia
Awake
Death
Hypnotic drugs-intravenous
 Gold standard- thiopentone
 Propofol
others
 Etomidate
 Benzodiazepines
 Ketamine
Hypnotic drugs-intravenous
Gold standard-
others
Etomidate
Benzodiazepines
Ketamine
Inhalational anaesthetics
 Nitrous oxide-weak
 Isoflurane
 Sevoflurane
 Desflurane
 Halothane
Inhalational anaesthetics
Nitrous oxide-weak
Isoflurane
Desflurane
Halothane
Analgesia
 Good analgesia= good anaesthesia
 Hypnotic sparing effect
 Opiates
 Local anaesthetics
 NSAIDS
 Paracetamol
Analgesia
Good analgesia= good anaesthesia
Hypnotic sparing effect
Opiates
Local anaesthetics
NSAIDS
Paracetamol
Analgesia-Opiates
 Gold standard – morphine
 Derivatives- diamorphine, codeine
 Synthetic agents
- Pethidine
- Fentanyl/Alfentanil-short acting
- Remifentanil-ultra short acting
Analgesia-Opiates
Gold standard — morphine
Derivatives- diamorphine, codeine
Synthetic agents
Pethidine
/Alfentanil-short acting
Remifentanil-ultra short acting
Analgesia-NSAIDS
 Gold standard- aspirin
 Ibuprofen
 Diclofenac
 Cox-2 inhibitors
Analgesia-NSAIDS
Gold standard- aspirin
Ibuprofen
Diclofenac
Cox-2 inhibitors
Muscle relaxation
 Aids intubation
 Helps surgeon/surgery
 Surgery of long duration
 Reduces maintenance dose of
anaesthetics agents
Muscle relaxation
Aids intubation
Helps surgeon/surgery
Surgery oflong duration
Reduces maintenance dose of
anaesthetics agents
Muscle relaxants
 Two types
 Depolarising-short acting
eg;suxmethonium
 Non-depolarising- medium/long acting
- Tracurium
- Vecuronium
- Rocuronium
Muscle relaxants
Two types
Depolarising-short acting
eg;suxmethonium
Non-depolarising- medium/long acting
Vecuronium
Rocuronium
Prerequisites
 Oxygen
 Suction
 Tilting trolley
 Resuscitation drugs
 Monitoring
 Anaesthetist
 Skilled assistance
 Drugs and machine
Prerequisites
Oxygen
• Suction
Tilting trolley
Resuscitation drugs
Monitoring
Anaesthetist
Skilled assistance
Drugs and machine
Phases of
general anaesthesia
 Induction
 Maintenance
 Recovery
Phases of
general anaesthesia
Induction
Maintenance
Recovery
Induction
 Intravenous- majority
 Inhalational- children, needle phobics
 Monitoring
 Preoxygenation
 Hypnotic/analgesic and or relaxant
 Mask/LMA/ET tube
Induction
Intravenous- majority
Inhalational- children, needle phobics
Monitoring
Preoxygenation
Hypnotic/analgesic and or relaxant
Mask/LMA/ET tube
Stages of anaesthesia
 Alcohol
1.Dizzy, delightful
2.Drunk, disorderly
3.Dead drunk
4.Dangerously deep
 General Anaesthesia
1.Amnesia, analgesia
2.Uninhibited
response to stimuli
3.Surgical anaesthesia
4.Vital centre
depression
Stages ofanaesthesia
Alcohol
1 Dizzy, delightful
2Drunk, disorderly
3.Dead drunk
4.Dangerously deep
General Anaesthesia
1.Amnesia, analgesia
2, Uninhibited
response to stimuli
3.Surgical anaesthesia
4. Vital centre
depression
Maintenance
 Intravenous or inhalational
 Oxygen –40%-100%
 Nitrous oxide
 Muscle relaxant
 Analgesia
Maintenance
Intravenous or inhalational
Oxygen —4000-100%
Nitrous oxide
Muscle relaxant
Analgesia
Recovery
 Turn off agent
 Reverse relaxation
 Cough reflex
 Extubate when awake
 Recovery position
 Monitor until discharge
Recovery
Turn offagent
Reverse relaxation
Cough reflex
Extubate when awake
Recovery position
Monitor until discharge
Advantages
 No absolute contraindications
 Quick to establish
 Never fails to work
Advantages
No absolute contraindications
Quick to establish
Neverfails to work
Disadvantages
 Polypharmacy
 Effects on various systems
 Allergic reactions
 Recovery profile
 Post operative Nausia &Vomiting
 Awareness
Disadvantages
Polypharmacy
Effects on various systems
Allergic reactions
Recovery profile
Post operative Nausia &Vomiting
Awareness
Regional anaesthesia
 Spinal/epidural
- surgery below umbilicus
- Provides analgesia/muscle relaxation
 Plexus blocks eg brachial plexus
 Intravenous- Bier’s block
Regional anaesthesia
Spinal/epidural
surgery below umbilicus
Provides analgesia/muscle relaxation
Plexus blocks eg brachial plexus
Intravenous- Bier's block
iigarnentum
llavum
cauda equino
anterior
epidural space
supraspinous
tigan• ent
interspinous
ligament
posterior
pidura• space
basivertebral vein
Regional anaesthesia
Analgesia Muscle relaxation
Regional anaesthesia
Analgesia Muscle relaxation
Local anaesthetics
 Lignocaine- quick/short acting
 Bupivacaine/levobupicvacaine- slow
and long action
 Ropivacaine- as above
 Amethocaine- topical
 Prilocaine- intravenous
Local anaesthetics
- quick/short acting
/levobupicvacaine- slow
and long action
Ropivacaine- as above
Amethocaine- topical
Prilocaine- intravenous
Advantages
 Effective alternative to GA
 Avoids polypharmacy
 Allergic reactions
 Extended analgesia
 Patient can remain awake
 Early drink/feed
Advantages
Effective alternative to GA
Avoids polypharmacy
Allergic reactions
Extended analgesia
Patient can remain awake
Early drink/feed
Disadvantages
 Limited scope
 Higher failure rate
 Time constraints
 Anticoagulants/Bleeding diathesis
 Risk of neural injury
Disadvantages
Limited scope
Higherfailure rate
Time constraints
Anticoagulants/Bleeding diathesis
Risk ofneural injury
Autonomic
Nervous
system
S. Parasuraman, M.Pharm., Ph.D.,
Associate Professor,
Faculty of Pharmacy, AIMST University
The Autonomic Nervous System
Sympathetic
NorEpi
mydriasis
reduced saliva flow
increased SV & HR
vasoconstriction
reduced peristalsis & secretion
glycogen* glucose
inhibition of bladder contraction
Parasympathetic
ACh
Ganglia (N)
miosis
Sympathetic
ganglia (N)
epinephrine
release
132 bronchodilation
(not innervated)
stimulated saliva flow
decreased HR
Vagal
bronchoconstriction
nerve
stimulates peristalsis
& secretion
stimulates bile release
bladder contraction
Autonomic
Nervous
system
S. Parasuraman, M.Pharm., Ph D
Associate Professor,
Faculty of Pharmacy, AIMST University
Learning Outcomes
• At the end of this session, the student would be able to:
– Briefly describe Sympathetic and parasympathetic
outflow and its functions.
– List the differences between Sympathetic and
Parasympathetic division.
– Explain the adrenergic and cholinergic receptors
Learning Outcomes
' At the end of this session, the student would be able to:
— Briefly describe Sympathetic and parasympathetic
outflow and its functions.
— List the differences between Sympathetic and
Parasympathetic division.
— Explain the adrenergic and cholinergic receptors
Nervous System
Central nervous
system
Peripheral
nervous system
Afferent division
(Sensory)
Efferent division
(Motor)
Somatic system
(voluntary)
Autonomic nervous
(involuntary)
Sympathetic system
(thorcolumbar outflow)
Come from the thoracic
and lumbar regions (T1
to L2/3) of the spinal
cord
Parasympathetic system
(craniosacral outflow)
Come from brainstem
(Cranial Nerves III, VII, IX, X)
or the sacral spinal cord (S2,
S3, S4)
Enteric nervous
system
Nervous System
Central nervous
system
Peripheral
nervous system
Afferent division
(Sensory)
Efferent division
(Motor)
Somatic system
(voluntary)
Sympathetic system
(thorcolumbar outflow)
Come from the thoracic
and lumbar regions (Tl
to L2/3) of the spinal
cord
Autonomic nervous
(involuntary)
Parasympathetic system
(craniosacral outflow)
Enteric nervous
system
Come from brainstem
(Cranial Nerves Ill, VII, X)
or the sacral spinal cord (S2,
Spinal nerves
• There are 31 pairs of
spinal nerves
– 8 cervical
– 12 thoracic
– 5 lumbar
– 5 sacral
– 1 coccygeal
The human spinal column is made
up of 33 bones.
• 7 - cervical region
• 12 - thoracic region
• 5 - lumbar region
• 5 - sacral region
• 4 - coccygeal region
Ci (Atlas)
Os sacrum
Coccyx
Spinal nerves
The human spinal column is made
up of 33 bones.
7 - cervical region
12 - thoracic region
5 - lumbar region
5 - sacral region
4 - coccygeal region
' There are 31 pairs
spinal nerves
Cervical nerves
Thoracic nerves
Lumbar nerves
— 8 cervical
— 12 thoracic
— 5 lumbar
— 5 sacral
— 1 coccygeal
1
2
3
4
5
6
7
8
1
2
3
4
5
6
7
8
9
10
11
12
1
2
3
Spinal cord
End of spinal cord
—Cauda equina
Sacral and coccygeal nerves
4
5
1
2
3
4
5
Filum terminale
Peripheral Nervous System
• Most of the nerves of the peripheral nervous system
are composed of sensory nerve fibres conveying
afferent impulses from sensory end organs to the
brain and motor nerve fibres conveying efferent
impulses from the brain through the spinal cord to
the effector organs.
Peripheral nervous system
Efferent division
(Motor)
Afferent division
(Sensory)
Somatic system
(voluntary)
Autonomic nervous
(involuntary)
Peripheral Nervous System
' Most of the nerves of the peripheral nervous system
are composed of sensory nerve fibres conveying
afferent impulses from sensory end organs to the
brain and motor nerve fibres conveying efferent
impulses from the brain through the spinal cord to
the effector organs.
Peripheral nervous system
Afferent division
Sensor
Efferent division
(Motor)
Somatic system
(voluntary)
Autonomic nervous
(involuntary)
Somatic Nervous System
• The somatic nervous system (SNS or voluntary nervous
system) is the part of the peripheral nervous system.
• The somatic nervous system includes both sensory
(afferent nerves) and motor (efferent nerves) neurons.
• Sensory neurons convey input
from receptors for somatic
senses (tactile, thermal, pain,
and proprioceptive sensations)
and from receptors for the
special senses (sight, hearing,
taste, smell, and equilibrium)
Somatic Nervous System
' The somatic nervous system (SNS or voluntary nervous
system) is the part of the peripheral nervous system.
' The somatic nervous system includes both sensory
afferent nerves) and motor (efferent nerves) neurons.
' Sensory neurons convey input
from receptors for somatic
(tactile, thermal, pain,
senses
and proprioceptive sensations)
and from receptors for the
(sight, hearing,
special senses
taste, smell, and equilibrium)
SKIN
AFFERENT NERVE
SPINAL CORD
MUSCLE
EFFERENT NERVE
Autonomic Nervous System
• The autonomic nervous system is involved in a
complex of reflex activities, which depend on
sensory input to the brain or spinal cord, and
on motor output.
• The majority of the organs of the body are
supplied by both sympathetic and
parasympathetic nerves which have opposite
effects that are finely balanced to ensure the
optimum functioning of the organ.
Autonomic Nervous System
' The autonomic nervous system is involved in a
complex of reflex activities, which depend on
sensory input to the brain or spinal cord, and
on motor output.
' The majority of the organs of the body are
supplied by both sympathetic and
parasympathetic nerves which have opposite
effects that are finely balanced to ensure the
optimum functioning of the organ.
Autonomic Nervous System
• The autonomic nervous system (ANS) is a complex set
of neurons that mediate internal homeostasis
without conscious intervention or voluntary control.
• The ANS maintains blood pressure, regulates the rate
of breathing, influences digestion, urination, and
modulates sexual arousal.
• There are two main branches to the ANS – the
sympathetic nervous system and the
parasympathetic nervous system.
The effects of autonomic control are rapid and essential for homeostasis
Autonomic Nervous System
' The autonomic nervous system (ANS) is a complex set
of neurons that mediate internal homeostasis
without conscious intervention or voluntary control.
' The ANS maintains blood pressure, regulates the rate
of breathing, influences digestion, urination, and
modulates sexual arousal.
' There are two main branches to the ANS — the
sympathetic and the
system
nervous
parasympathetic nervous system
The effects of autonomic control are rapid and essential for homeostasis
Sympathetic nervous system
• Sympathetic nervous system otherwise called as
thoracolumbar system.
• Sympathetic stimulation prepares the body to deal
with exciting and stressful situations, e.g.
strengthening its defences in danger. sympathetic
stimulation mobilises the body for 'fight or flight'.
• Neurones convey impulses from their origin in the
hypothalamus, reticular formation and medulla
oblongata to effector organs and tissues. The first
neurone has its cell body in the brain and its fibre
extends into the spinal cord.
Sympathetic nervous system
' Sympathetic nervous system otherwise called as
thoracolumbar system.
prepares the body to deal
' Sympathetic stimulation
with exciting and stressful situations
strengthening its defences in danger sympathetic
stimulation mobilises the body for 'fight or flight
Neurones convey impulses from their origin in the
hypothalamus, reticular formation and medulla
oblongata to effector organs and tissues. The first
neurone has its cell body in the brain and its fibre
extends into the spinal cord.
Sympathetic nervous system
• Structure of the Sympathetic Division
– Pathway from Spinal Cord to Sympathetic Trunk Ganglia
– Organization of Sympathetic Trunk Ganglia
– Pathways from Sympathetic Trunk Ganglia to Visceral
Effectors
Sympathetic nervous system
• Structure of the Sympathetic Division
— Pathway from Spinal Cord to Sympathetic Trunk Ganglia
Organization of Sympathetic Trunk Ganglia
— Pathways from Sympathetic Trunk Ganglia to Visceral
Effectors
Structure of the sympathetic division of the autonomic nervous system
Trachea and bronchi: Bronchodilation
Liver: Glycogen glucose conversion increased
Iris muscle: Pupil dilated
Blood vessels in heart : Vasoconstriction
Heart: Rate and force of contraction
increased
Salivary glands: Secretion inhibited
Stomach: Peristalsis reduced
Sphincters closed
Intestines: Peristalsis and tone decreased
Vasoconstriction
Kidney: Urine secretion decreased
Bladder: Smooth muscle wall relaxed
Sphincter closed
Sex organs: Generally Vasoconstriction
SYUPAtHEOC DIVISION
(thoracolumbar) pretar*i to rtuscle
of blood a' ttueo organs
Preganglionic new-ons
PostP"91ionÉ nouroru
SINEtg1Äi
Iris muscle: Pupil dilated
Lactrr•l
Salivary glands: Secretion inhibited
Wjcous rnernbrar,o
oc and palate
gland
Blood vessels in heart : Vasoconstriction
Atrial muscle titers
Sweat
Hair
smooth
(each
trurü
tho
Sympathetic
trunk gan#
cte
TtO
712
cervical
gan•ion
Uiddle
interior
cervical
Selan&
Crdiac plexus
Greater
speanehnie /
-z Celiae
ganglion
Aorticore
splanchnié
Odon
Heart
SA'AV
enuscle
Spleen
Heart: Rate and force of contraction
increased
Trachea and bronchi: Bronchodilation
Liver: Glycogen glucose conversion increased
Stomach: Peristalsis reduced
Sphincters closed
Intestines: Peristalsis and tone decreased
solanchnic
meent«ic
ganglion
Renal
ganglions
Lumbar
splanchnic Interior
mesenterie
ganglion
Preverte&al
Rectum
Uret•e
(hsad
gangUa
Urnary 'External
Hypogastric
p&xus
Vasoconstriction
Kidney: Urine secretion decreased
Bladder: Smooth muscle wall relaxed
Sphincter closed
Uton.n /
Sex organs: Generally Vasoconstriction
Structure of the sympathetic division of the autonomic nervous system
Parasympathetic nervous system
• Parasympathetic nervous system otherwise called as
craniosacral outflow.
• Parasympathetic stimulation has a tendency to slow
down body processes except digestion and
absorption of food and the functions of the
genitourinary systems. Its general effect is that of a
'peace maker' allowing restoration processes to occur
quietly and peacefully.
• Cell bodies of parasympathetic preganglionic neurons
are found in nuclei in the brain stem.
Parasympathetic nervous system
' Parasympathetic nervous system otherwise called as
craniosacral outflow.
' Parasympathetic stimulation has a tendency to slow
down body except digestion and
processes
absorption of food the functions of the
and
Its general effect is that of a
genitourinary systems
peace maker allowing restoration processes to occur
quietly and peacefully.
' Cell bodies of parasympathetic preganglionic neurons
are found in nuclei in the brain stem.
Parasympathetic nervous system
• Structure of the Parasympathetic Division
– The cranial parasympathetic outflow consists of
preganglionic axons that extend from the brain stem in four
cranial nerves. The cranial outflow has four pairs of ganglia
and the ganglia associated with the vagus (X) nerve.
– The sacral parasympathetic outflow consists of
preganglionic axons in anterior roots of the second through
fourth sacral spinal nerves.
Parasympathetic nervous system
• Structure of the Parasympathetic Division
— The cranial parasympathetic outflow consists of
preganglionic axons that extend from the brain stem in four
cranial nerves. The cranial outflow has four pairs of ganglia
and the ganglia associated with the vagus (X) nerve.
parasympathetic outflow consists of
— The sacral
preganglionic axons in anterior roots of the second through
fourth sacral spinal nerves.
Structure of the parasympathetic division of the autonomic nervous system
Trachea and bronchi: Bronchoconstriction
Liver: Blood vessels dilated
Secretion of bile increased
Iris muscle: Pupil constricted
Heart: Rate and force of contraction
decreased
Salivary glands: Secretion increased
Stomach: Secretion of gastric juice and
peristalsis increased
Intestines: Digestion and absorption
increased
Kidney: Urine secretion increased
Bladder: Muscle of wall contracted
Sphincters relaxed
Sex organs: Male: erection;
Female: variable
PARASYMPATHETIC DIVES'ON Koy-,
Preganglionic t'ieurms
neurons
OcüotnDtOt (Ill)
ganglia
Facsai (VIV, Ciliary
to
and giards 01 otgat%:
Iris muscle: Pupil constricted
Eye
and
Trans•ars.o
Ascending
Lacnmal q
Salivary glands: Secretion increased
Mcnous
an
Parotxi .
ganglion
Pterygopalatine
ganglion
Submandibular
ganglion
Glossopharynpaj (tX)
Otic
ganglion
Vagus (X
tto
T12
Pelvic
nerves
Coccygeal
Atnai
rmscle ibers
SAiAVnodes
Trac*E0
Bronchi
aro bie du
Stomact
Unnary Extern* Ute
Structure of the parasympathetic division o
Heart: Rate and force of contraction
decreased
Trachea and bronchi: Bronchoconstriction
Liver: Blood vessels dilated
Secretion of bile increased
Stomach: Secretion of gastric juice and
peristalsis increased
Intestines: Digestion and absorption
increased
Kidney: Urine secretion increased
Bladder: Muscle of wall contracted
Sphincters relaxed
Sex organs: Male: erection;
Female: variable
t e autonomic nervous system
Ref: https://backyardbrains.com/experiments/img/AutonomicNervousSystem_web.jpg
AUTONOMIC NERVOUS SYSTEM
( INVOLUNTARY )
PARASYMPATHETIC
CONSTRICTS
PUPIL
STIMULATES
SALIVA ANP TEAR
PRODUCTION
CONSTRICTS
BRONCHI
SCOWS HEART
STIMULATES
STOMACH,
INTESTINES
STIMULATES
URINATION
PROMOTES
ERECTION OF
GENITALS
SYMPATHETIC
PILATES PUPIL
INHIBITS SALIVA
PRODUCTION
PILATES
BRONCH
ACCELERATES
HEART
STIMULATES
EPINEPHRINE
ANP
NOREPINEPHRINE
RELEASE
STIMULATES
GLUCOSE
RELEASE
INHIBITS
STOMACH,
PANCREAS ANP
INTESTINES
INHIBITS
URINATION
PROMOTES
EJACULATION
ANP VAGINA
CONTRACTIONS
Ref: https://backyardbrains.com/experiments/img/AutonomicNervousSystem_web.jpg
Autonomic Motor Pathways
Autonomic Motor Pathways
Autonomic Motor Pathways
• Each division of the ANS has two motor neurons
(preganglionic and postganglionic neuron).
• Preganglionic Neurons
– In the sympathetic division (thoracolumbar division/
thoracolumbar outflow), the preganglionic neurons have
their cell bodies in the lateral horns of the gray matter in
the 12 thoracic segments and the first two (and sometimes
three) lumbar segments of the spinal cord.
– In the parasympathetic division (craniosacral division/
craniosacral outflow), the preganglionic neurons have their
cell bodies in in the nuclei of four cranial nerves in the brain
stem (III, VII, IX, and X) and in the lateral gray matter of the
second through fourth sacral segments of the spinal cord.
Autonomic Motor Pathways
' Each division of the ANS has two motor neurons
(preganglionic and postganglionic neuron).
' Preganglionic Neurons
sympathetic division (thoracolumbar division/
— In the
thoracolumbar outflow) the preganglionic neurons have
their cell bodies in the lateral horns of the gray matter in
the 12 thoracic segments and the first two (and sometimes
three) lumbar segments of the spinal cord.
parasympathetic division (craniosacral division/
— In the
craniosacral outflow) the preganglionic neurons have their
cell bodies in in the nuclei of four cranial nerves in the brain
stem (Ill, VII, IX, and X) and in the lateral gray matter of the
second through fourth sacral segments of the spinal cord.
Autonomic Motor Pathways
Preganglionic Neurons
• Autonomic Ganglia
– There are two major groups of autonomic ganglia
• sympathetic ganglia
• parasympathetic ganglia
• Sympathetic Ganglia:
– The sympathetic ganglia are the sites of synapses between
sympathetic preganglionic and postganglionic neurons.
– There are two major types of sympathetic ganglia:
• sympathetic trunk ganglia (also called vertebral chain
ganglia or paravertebral ganglia)
• prevertebral ganglia (collateral)- Five types of
prevertebral ganglia are celiac ganglion, superior
mesenteric ganglion, inferior mesenteric ganglion,
aorticorenal ganglion and renal ganglion.
Autonomic Motor Pathways
Preqanqlionic Neurons
' Autonomic Ganglia
— There are two major groups of autonomic ganglia
' sympathetic ganglia
' parasympathetic ganglia
' Sympathetic Ganglia
— The sympathetic ganglia are the sites of synapses between
sympathetic preganglionic and postganglionic neurons.
— There are two major types of sympathetic ganglia:
(also called vertebral chain
' sympathetic trunk ganglia
ganglia or paravertebral ganglia)
(collateral)- Five types of
' prevertebral ganglia
prevertebral ganglia are celiac ganglion, superior
mesenteric ganglion, inferior mesenteric ganglion,
aorticorenal ganglion and renal ganglion.
Autonomic Motor Pathways
Preganglionic Neurons
• Autonomic Ganglia
– There are two major groups of autonomic ganglia
• sympathetic ganglia
• parasympathetic ganglia
• parasympathetic ganglia:
– Preganglionic axons of the parasympathetic division
synapse with postganglionic neurons in terminal
(intramural) ganglia. They are the ciliary ganglion,
pterygopalatine ganglion, submandibular ganglion, and otic
ganglion
Autonomic Motor Pathways
Preqanqlionic Neurons
Autonomic Ganglia
— There are two major groups of autonomic ganglia
' sympathetic ganglia
' parasympathetic ganglia
' parasympathetic ganglia
— Preganglionic axons of the parasympathetic division
synapse with postganglionic neurons in terminal
(intramural) ganglia. They are the ciliary ganglion,
pterygopalatine ganglion, submandibular ganglion, and otic
ganglion
Autonomic Motor Pathways
Postganglionic Neurons
• Once axons of sympathetic preganglionic
neurons pass to sympathetic trunk ganglia,
they may connect with postganglionic
neurons.
• A single sympathetic preganglionic fiber has
many axon collaterals (branches) and may
synapse with 20 or more postganglionic
neurons.
Autonomic Motor Pathways
Postqanqlionic Neurons
' Once axons of sympathetic preganglionic
neurons pass to sympathetic trunk ganglia,
they may connect with postganglionic
neurons.
single sympathetic preganglionic fiber has
many axon collaterals (branches) and may
synapse with 20 or more postganglionic
neurons Dendrites covered
with dendritic spines
Cytoplasm of
Schwann cell
Synaptic terminals
Axon
Cell body collateral
Nucleus
Axon Nodes of
Ranvier
Axon
Nucleus
Myelin
sheath
Schwann Terminal
cell branches
Autonomic Motor Pathways
Postganglionic Neurons
• Axons of preganglionic neurons of the
parasympathetic division pass to terminal
ganglia near or within a visceral effector. In the
ganglion, the presynaptic neuron usually
synapses with only four or five postsynaptic
neurons, all of which supply a single visceral
effector, allowing parasympathetic responses
to be localized to a single effector.
Autonomic Motor Pathways
Postqanqlionic Neurons
' Axons of preganglionic neurons of the
parasympathetic division pass to terminal
ganglia near or within a visceral effector. In the
ganglion, the presynaptic neuron usually
synapses with only four or five postsynaptic
all of which supply a single visceral
neurons
effector, allowing parasympathetic responses
to be localized to a single effector.
Autonomic Receptors
Autonomic Receptors
ANS Neurotransmitters and Receptors
ANS Receptor Receptor Sub-type
Parasympathetic
nervous system
Nicotinic cholinergic
receptors
Nn, Nm
Muscarinic cholinergic
receptors
M1, M2, M3, M4,
M5
Sympathetic
nervous system
α adrenergic receptor α1, α2
β adrenergic receptor β1, β2, β3
Sympathetic nervous system Parasympathetic nervous system
ANS Neurotransmitters and Receptors
ANS
Parasympathetic
nervous system
Sympathetic
nervous system
NICOTINIC
RECEPTOR
Preganglionic neuron
Ganglion
Receptor
Nicotinic cholinergic
Muscarinic cholinergic
receptors
a adrenergic receptor
ß adrenergic receptor
Effector cell
ADRENERGIC
RECEPTOR
NE
Postganglionic neuron
Receptor Sub-type
Nn, Nm
MI, M2, M3, M4,
al, a2
ßl, ß2, ß3
MUSCARINIC
NICOTINIC RECEPTOR
Effector cell
RECEPTOR
ACh
Sympathetic nervous system Parasympathetic nervous system
Comparison of Somatic and
Autonomic Motor Neurons
Comparison of Somatic and
Autonomic Motor Neurons
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anesthesiology.pdf

  • 1. HISTORY OF ANAESTHESIA Presenter- Dr Chimi Handique PGT Dept of Pharmacology HISTORY OF ANAESTHESIA Presenter- Dr Chimi Handique PGT Dept of Pharmacology
  • 2. Anaesthesia : A clinical and philosophical concept It is in the Hippocratic Corpus, that the word ‘anaesthesia’ was used for the first time in a medical context as reversible loss of sensation and unconsciousness, when Hippocrates writes: “For when they [breaths] pass through the flesh and puff it up, the parts of body affected lose the power of feeling [‘anaestheta’]”. Anaesthesia : Aclinical and philosophical concept It is in the Hippooatic Corpus, that the word 'anaesthesia' was usedfor theftrst time in a medical context as reversible loss of sensation and unconsciousness, when Hippocrates writes: "For when they[breaths]pass through theflesh andpuffit up, the parts ofbody gfected lose the power of feeling ['anaestheta']'.'
  • 3. What was done to a patient before an operation ? It was the custom then, as for centuries afterward, to bind the patient to the table with ropes or straps. His screams were disregarded, but if he struggled too Violently, assistants grasped his arms and legs. Whatwas done to a patient b+re an operation ? Wellcorne Irnages It was the custom then, as for centuries afterward, to bind the patient to the table with ropes or straps. His screams were disregarded, but if he struggled oo Violently, assistants grasped his arms and legs.
  • 4. • Pain had not prevented surgery in the past, but it had made it almost an unbearable, excruciating agony. • In January 1843, George Wilson, a medical student who underwent surgery to amputate an infected leg, described his experience of surgery without anaesthesia and analgesia. • “Of the agony it occasioned, I will say nothing. Suffering so great as I underwent cannot be expressed in words. ... The particular pangs are now forgotten;but the black whirlwind of emotion, the horror of great darkness, and the sense of desertion by God and man, bordering close upondespair, which swept throughmy mind and overwhelmed my heart, I can never forget ...” Pain had not prevented surgery in the past, but it had made it almost an unbearable, excruciating agony. ' n January 1843, George Wilson, a medical student who nderwent surgery to amputate an infected leg, described his xperience of surgery without anaesthesia and analgesia. "Ofthe agony it occasioned, I will say nothing. Suffering so great as I underwent cannot be expressed in words. The particular pangs are nowforgotten;but the blackwhirlwind ofemotion, the horror ofgreat darkness, and the sense ofdesertion by God and man, bordering close upon despair, which swept through my ind and overwhelmed my heart, I can neverforget
  • 5. By the early1840s successive cultural and medical changes basedon newerhumanistic standards had resultedin the view that physical painis purposeless. This new concept regardingpain prevention and its relief is the social scenery for the discovery of modern ‘anaesthesia’ during the middle of the 19thcentury. By the early 1840s successive cultural and medical changes based on newer humanistic standards had resulted in the view that physical pain is purposeless, This new concept regarding pain prevention and its reli# the soul sceneryfor the discovoy ofmodern 'anaesthesia 'during the middle ofthe 19th centuy,
  • 6. • The word “Anaesthesia“ was coined by Oliver Wendell Holmes in 1846. • It originates from the Greek an - "without” and “aisthēsis” refers to the inhibition of sensation. Oliver Wendell Holmes (1809–1894) The word "Anaesthesia" was coined by Oliver Wendell Holmes in 1846. It originates from the Greek an 'without" and "aisthésis refe s the inhibition to Ofs nsation. Oliver Wendell Holmes (1809-1894)
  • 7. In a letter to William T. G. Morton, the first practitioner to publicly demonstrate the use of ether during surgery, he wrote: "Everybody wants to have a hand in a great discovery. All I will do is to give a hint or two as to names—or the name—to be applied to the state produced and the agent. The state should, I think, be called 'Anaesthesia.' This signifies insensibility—more particularly ... to objects of touch.“ In a letter to William T. G. Morton, the first practitioner to publicly demonstrate the use of ether during surgery, he wrote: "Everybody wants to have a hand in a great discovery. All I will do is to give a hint or two as to names or the name to be applied to the state produced and the agent. The state should, I think, be called 'Anaesthesia.' This signifies insensibility more particularly ... to objects of touch."
  • 9. • Attempts at producing a state of general anaesthesia can be traced throughout recorded history. • The Renaissance saw significant advances in anatomy and surgical technique. However, despite all this progress, surgery remained a treatment of last resort. • An appreciation of the germ theory of disease led rapidly to the development of antiseptic techniques in surgery reducing the overall morbidity and mortality of surgery to a far more acceptable rate. Attempts at producing a state of general anaesthesia can be raced throughout recorded history. he Renaissance saw significant advances in anatomy and surgical technique. However, despite all this prog ess, surgery remained a treatment of last resort. ' An a preciation of the germ theory of disease led rapidly to the devel pment of antiseptic techniques in surgery reducing the overa I morbidity and mortality of surgery to a far more acceptable rate.
  • 10. • Concurrent with these developments were the significant advances in pharmacology and physiology which led to the development of general anesthesia and the control of pain. • In the 20th century, the safety and efficacy of general anesthesia was improved by the routine use of tracheal intubation and other advanced airway management techniques. • Significant advances in monitoring and new anesthetic agents with improved pharmacokinetic and pharmacodynamic characteristics also contributed to this trend. Concurrent with these developments were the significant dvances in which led to the pharmacology and physiology development of general anesthesia and the control of pain. , In the 20th century the safety and efficacy of general anesthesia was improved by the routine use of tracheal intubation and other adva ced airway management techniques. Signi Icant advances in monitoring and new anesthetic agent with improved pharmacokinetic and pharmacodynamic charac eristics also contributed to this trend.
  • 11. TIMELINE OF ANESTHESIA • Antiquity • Middle ages and Renaissance • 18th Century • 19th Century • 20th Century • 21st Century TIMELINE OF ANESTHESIA ' Antiquity ' Middle ages and Renaissance ' 18th Century ' 19th Century ' 20th Century ' 21st Century
  • 12. Antiquity Antiquity saw the dawn of anesthesia. This era saw the uses of poppy, mandrake, Indian hemp, cocaine and carotid compression. Antiquity Antiquity saw the dawn of anesthesia. This era saw the uses of poppy, mandrake, Indian hemp, cocaine and carotid compression.
  • 14. Opium, is a very popular ancient pain relieving and euphoria inducing remedy. It is first said to have been cultivated in lower mesopotamia (Southwest Asia) in 3400 BC. Sumerians referred it as “hul-gil” which means “joy plant” Sumerians passed this “miracle drug” to the Assyrians who in turn passed opium to the Babylonians and then to the Egyptians. 3400 BC 3400 BC is a very popular ancient pain relieving and euphoria Opium inducing remedy. is first said to have been cultivated in lower mesopotamia (Southwest Asia) in 3400 BC. Sunlerians referred it as which means hul-gil joy plant Sumerians passed this "miracle drug" to the Assyrians who in turn passed opium to the Babylonians and then to the Egy tians.
  • 15. • The knowledge and use of opium passed on from Egypt across Mediterranean Sea trade routes to various civilizations including the Phoenicians and the Greeks. • Later, around 330 BC, Alexander the Great and his armies introduced opium to the people of India, Persia and other eastern and Middle Eastern kingdoms. The knowledge and use of opium passed on from Egypt across Mediterranean Sea trade routes to various civilizations including the Phoenicians and the Greeks. La er, around 330 BC, Alexander the Gre t and his armies introduced opi m to the people of India, Persia and other eastern and Middle Eastern king oms. 2
  • 16. Prior to the introduction of opium to ancient India and China, these civilizations pioneered the use of cannabis incense and aconitum. By the 8th century AD, Arab traders had brought opiumto India and China. Prior to the introduction ofopium to ancient India and China, these civilizations pioneered the use of cannabis incense and aconituwu By the 8th centuty AD, Arab traders had brought opium to India and China
  • 17. • Pictographs showing practice of Acupuncture in China on bone and Tortoise shells with inscriptions dating from the time of Shang dynasty have been found, and it is thought that these were used for divination in the art of healing. 1600 BC 1600 BC ictographs showing practice of puncture in China on bone and Tortoise shells with inscr•ptions dating from the time of Shang dynasty have been foun , and it is thought that these were used for divination in thea of healing.
  • 18. • Sushruta in Sushruta Samhita advocated the use of wine with incense of cannabis for anaesthesia. • The use of henbane and of Sammohini and Sanjivani are reported at a later period 600 BC 600 BC in Sushruta Susruta (600 BC) Sushruta Samhita advocated the use of wme with incense o, cannabis for anaesthesia. The use of henbane and of ammohini and Sanjivani are r ported at a later period
  • 19. • Assyrians and Egyptians used carotid compression to produce brief unconsciousness before circumcision or cataract surgery. • In a passage in History of Animals, Aristotle says of the jugular veins: “If these veins are pressed externally, men, though not actually choked, become insensible, shut their eyes, and fall flat on the ground." 400 BC 400 BC Assyrians and Egyptians used carotid compression to produce rief unconsciousness before circumcision or cataract surgery. Ina assage in roti artery Hist ry ofAnimals, Aristotle says of the jugular veins: "If these veins are pressed externally, men, though not actually choked, become insensible, shut their eyes, and fall flat on the ground. "
  • 20. • Pedanius Dioscorides, a Greek surgeon in the Roman army of Emperor Nero, recommended mandrake boiled in wine to "cause the insensibility of those who are to be cut or cauterized.” in his writings in De Materia Medica C. 64 BC C. 64 BC a Greek Pedanius Dioscorides surgeon in the Roman army of Emperor Nero, recommended I iandrake boiled in wine to "cause the insensibility of those who are to be cut or cauterized." in his writings in De Materia Me ica
  • 21. • Hua Tuo of China used to perform surgery under anesthesia using a formula he had developed and called mafeisan. • The word mafeisan probably means something like "cannabis boil powder". • The exact composition of mafeisan, similar to all of Hua Tuo's clinical knowledge, was lost when he burned his manuscripts, just before his death. CA 160 cA 160 ' H a Tuo of China used to perform surgery u der anesthesia using a formula he had developed and called mafeisan. The word mafeisan probably means something like ' cannabis boil powder O Wood Library:Musau The exact composition of mafeisan, similar to all of Hua Tuo's clinical knowled e, was lost when he burned his manuscripts, just before his death.
  • 23. History of Ether History of Ether CTH CR
  • 24. Origin • The compound may have been created by Jābir ibn Hayyān in the 8th century . • Alchemist Ramon Llull has also been credited with discovering diethyl ether in 1275, althoughthere is no contemporary evidence of this. Origin ' The compoundmay have been created byJäbir ibnHayyän in the 8th century. ' Alchemist Ramon Llull has also been creditedwith discovering diethyl ether in 1275, although there is no contemporat•y evidence ofthis,
  • 25. • Paracelsus (1493–1541) isolated substances that resulted from interaction of alcohol and vitriol and demonstrated its action in chickens. • He noted chickens enjoy sweet vitriol [ether] - after which they "undergo prolonged sleep, awake unharmed". • However, he did not extend this discovery from farm animals to people. 1525 1525 Paracelsus (1493-1541) isolated s bstances that resulted from interaction of Icohol and vitriol and demonstrated its action in chickens. He noted chickens enjoy sweet vitriol [ether after which they "undergo prolonged sleep, awake unharmed". Howe r, he did not extend this discovery from fa animals to people.
  • 26. • German physician Valerius Cordus (1515–1544), is widely credited with developing a method for synthesizing ether. • He synthesized diethyl ether by distilling ethanol and sulphuric acid into what he called by the poetic Latin name oleum dulci vitrioli, or "sweet oil of vitriol” 1540 1540 erman physician Valerius Cordus ( 515—1544), is widely credited ith developing a method for synthesizing ether. He ynthesized diethyl ether by distill ng ethanol and sulphuric acid into hat he called by the poetic Latin name oleum dulci vitrioli or "swee of vitriol"
  • 27. • The name ether was given to the substance in 1729 by August Sigmund Frobenius. • WilliamT. G. Morton was First in the worldto publicly and successfully demonstrate the use of ether anesthesia for surgery. ' Thename ether was givento the substance in 1729 byAugust Sigmund Frobenius, ' William T, G, Mortonwas First intheworldto publiclyand successfully demonstrate the use ofether anesthesiafor surgoy,
  • 28. Developments in 18th century pmentsin18thcenboy Develo OF GAS. Tcu: Nitrous Oxide. or Gas. It is of equivalent it by au'tracti"',.• pret of tLe Oxygen ft-ota thet Nitrie Oxide. Oxygen angi Nitr€:gen. of Sir i)avy. it was
  • 30. • Joseph Priestley (1733–1804) was an English chemist who discovered nitrous oxide (1772), nitric oxide, ammonia, hydrogen chloride and oxygen(1774). • He originally named nitrous oxide as "nitrous air, diminished”, on account of his preparative method of allowing NO to standing in contact with moist iron filing . 1771-1786 1771-1786 ' Joseph Priestley (1733—1804) was an English chemist who discovered nitrous oxide (1772), nitric oxide, ammonia, hydrogen chloride and oxygen(1774). 11774 Discovny OF He riginally named nitrous oxide as nitrous air, diminished on ccount of his preparative method of allowing NO to stan ing in contact with moist iron filing
  • 31. Priestley’s apparatus Priestley’s Experiment Priestley's apparatus (c) (d) Priestley's Experiment
  • 32. • Priestley was clearly perplexed as to the nature of his diminished nitrous air. • A candle burnt with an increased brightness in the gas. When mice were placed in a bell-jar of N2O their liveliness was reduced and they soon died. • In contrast they seemed livelier if they respired oxygen, which Priestley subsequently discovered.(1774). • But general anaesthesia by the inhalation of nitrous oxide wasn't demonstrated for over 40 years till December 1844 by US dentist Horace Wells. Priestley was clearly perplexed as to the nature of his diminished nitrous air. A candle burnt with an increased brightness in the gas. When mice were placed in a bell-jar of N20 their liveliness was reduced and they soon died. ' Inhcontrast they seemed livelier if they respired oxygen, which Prie tley subsequently discovered.(1774). But eneral anaesthesia by the inhalation of nitrous oxide wasn't dem nstrated for over 40 years till December 1844 by US dentist Horace wells
  • 33. Developments in 19th Century Developments in 19th Century
  • 34. JULY, 1800 Even though N2O was discovered by Joseph Priestley it Humphry Davy who spotted its medical potential In 1798, Humphry Davy was appointed laboratory superintendent of the Pneumatic Institute in Bristol, UK. This was an establishment founded on the belief that the recently discovered gases might have curative applications JULY, 1800 Eve though N20 was discovered by Jos ph Priestley it who Humphry Davy spo ted its medical potential In 1798, Humphry Davy was appointed laboratoyy superintendent of the Pneumatic Institute in Bristol, UK. This was an establishment founded on the belief that the rece tly discovered gases might have curative ap lications
  • 35. • Curiously, the use of this gas in therapy is barely mentioned: a couple of accounts of its use on paralysed patients, and that's about the extent. • It is at the end of this book “the history, chemistry, physiology and recreational use of nitrous oxide” that he makes his off-repeated statement about the possible use of nitrous oxide in surgery: "As nitrous oxide in its extensive operation appears capable of destroying physical pain, it may probably be used with advantage during surgical operations in which no great effusion of blood takes place." Curiously, the use of this gas in therapy is barely mentioned: a ouple of accounts of its use on paralysed patients, and that's about he extent. It is at the end of this book "the history, chemistry, physiology and recreational use of nitrous oxide" that he makes his off-repeated state ent about the possible use of nitrous oxide in surgery: "As nitrous oxide in its extensive operation appears capable of destroying physical pain, it may probably be used with advantage during surgical operations in which no great effusion of blood takes place,"
  • 36. • Henry Hill Hickman (1800–1830) experimented with the use of carbon dioxide as an anesthetic in the 1820s. • He would make the animal insensible, effectively via almost suffocating it with carbon dioxide, then determine the effects of the gas by amputating one of its limbs. . 1824 1824 (1800-1830) Henry Hill Hickman experimented with the use of carbon dioxide as an anesthetic in the 1820s. He ould make the animal insensible, effectively via almost suffocating it wit the one carbon dioxide, then determine ffects of the gas by amputating f its limbs.
  • 37. • In 1824, Hickman submitted the results of his research to the Royal Society in a short treatise entitled Letter on suspended animation: with the view of ascertaining its probable utility in surgical operations on human subjects. • The response was an 1826 article in The Lancet titled 'Surgical Humbug' that ruthlessly criticized his work. • Hickman died four years later at age 30. Though he was unappreciated at the time of his death, his work has since been positively reappraised and he is now recognized as one of the fathers of anesthesia ' In 1824, Hickman submitted the results of his research the Royal Society in a short treatise entitled Letter suspended animation: with the view of ascertaining probable utility in surgical operations on human subjects. to on its The response was an 1826 article in The Lancet titled 'Surgical Humbug' that ruthlessly criticized his work. Hic man died four years later at age 30. Though he was unappreciated at the time of his death, his work has since been posit•vely reappraised and he is now recognized as one of the fathe of anesthesia
  • 38. • Crawford W. Long had observed in the ether frolics gatherings, that some participants experienced bumps and bruises, but afterward had no recall of what had happened. • He postulated that that diethyl ether produced pharmacologic effects similar to those of nitrous oxide. • On 30 March 1842, he administered diethyl ether by inhalation to a man named James Venable, in order to remove a cysts from the man's neck. 1842 1842 had observed in the rawford W. Long ether frolics gatherings, that some articipants experienced bumps and ruises, but afterward had no recall of what had happened. He postulated that that diethyl ether prodåced pharmacologic effects similar to those of nitrous oxide. On 0 March 1842, he administered dieth ether by inhalation to a man named James Venable, in order to remove a cysts from t e man's neck. CRAWCOROW LONG
  • 39. • Dr. Horace Wells (1815-1848) volunteered to inhale nitrous oxide for his own dental extraction back in December of 1844. • Wells then began to administer nitrous oxide to his patients, successfully performing several dental extractions over the next couple of weeks. 1845 1845 , Dr. orace wells (1815-1848) volunteered to inhale nitrous oxide for his own dental extraction back in December of 1844. Wells then began to administer nitrous oxide to his patients, succe sfully performing several dental extractions over the next couple of weeks.
  • 40. • In spite of these convincing results being reported by Wells to the medical society in Boston already in December 1844, this new method was not immediately adopted by other dentists. • The reason for this was most likely that Wells, in January 1845 at his first public demonstration to the medical faculty in Boston, had been partly unsuccessful, leaving his colleagues doubtful regarding its efficacy and safety the partial anesthetic was judged as a "humbug." spite of these convincing results being reported by Wells to the edical society in Boston already in December 1844, this new ethod was not immediately adopted by other dentists. The reason for this was most likely that Wells, in January 1845 at his first public demonstration to the medical faculty in Boston, had been partly unsuccessful, leaving his colleagues doubtful regar ing its efficacy and safety the partial anesthetic was judged as a "humbug."
  • 41. HISTORY OF ETHER DOME HISTORY OF ETHER DOME
  • 42. • On October 16,1846 William T. G. Morton (1819-1868) became first in the world to publicly and successfully demonstrate the use of ether anesthesia for surgery. This occurred at what came to be called "The Ether Dome," at Massachusetts General Hospital. 1846 1846 On ctober 16,1846 (1819-1868) William T. G, Morton beca e first in the world to publicly and successfully demo strate the use of ether anesthesia for surgery. This occurred at whåt came to be called at Massachusetts The Ether Dome Genera Hospital.
  • 43. The Ether Dome is a surgical operating amphitheater in the Bulfinch Building at Massachusetts General Hospital in Boston. It was the site of the first public demonstration of the use of inhaled ether as a surgical anesthetic on 16 October 1846. The ether Dome is a surgical operating amphitheater in the Bu finch Building at Massachusetts General Hospital in Boston. It was t e site of the first public demonstration of the use of inhaled ether as a surgical anesthetic on 16 October 1846.
  • 44. • Crawford Long, had previously administered ether in 1842, but this went unpublished until 1849. • The Ether Dome event occurred when William T. G. Morton, used ether to anesthetize Edward Gilbert Abbott. • John Collins Warren, the first dean of Harvard Medical School, then painlessly removed part of a tumor from Abbott's neck. • After Warren had finished, and Abbott regained consciousness, Warren asked the patient how he felt. had previously administered ether in 1842, ' Crawford Long but this went unpublished until 1849. The Ether Dome event occurred when William T. G, Morton, used ether to anesthetize Edward Gilbert Abbott. the first dean of Harvard Medical ' Joi n Collins Warren School, then painlessly removed part of a tumor from Abbott's neck. Afte Warren had finished, and Abbott regained consciousness, Warren asked the patient how he felt.
  • 45. • Reportedly, Abbott said, "Feels as if my neck's been scratched". Warren then turned to his medical audience and uttered "Gentlemen, this is no Humbug". • This was presumably a reference to the unsuccessful demonstration of nitrous oxide anesthesia by Horace Wells in the same theater the previous year, which was ended by cries of "Humbug!" after the patient groaned with pain.. Reportedly, Abbott said, "Feels as if my neck's been scratched". Warren then turned to his medical audience and uttered "Gentlemen, this is no Humbug", This was presumably a reference to the unsuccessful de onstration of nitrous oxide anesthesia by Horace Wells in the ame theater the previous year, which was ended by cries of" umbug!" after the patient groaned with pain..
  • 47. • Chloroform was discovered independently in 1831 by the USA's Samuel Guthrie, France's Eugène Soubeiran, and Germany's Justus von Liebig. • Prof. James Y. Simpson (1811-1870)- Scottish obstetrician begins administering chloroform to women for pain during childbirth. • Chloroform quickly became a popular anesthetic for surgery and dental procedures as well. 1847 1847 Chloroform was discovered independently in 1831 by the USA's Samuel Guthrie, Soubeiran, and France's Eugene Germany's Justus von Liebig. James Y. Simpson (1811-1870)- Scottish obstetrician begins administering chloroform to women for pain during chilåbirth. Ch oroform quickly became a popular anesthetic for surgery and dental proc dures as well.
  • 48. • Dr. John Snow (1813-1858) who was a fulltime anesthetist since 1847, popularized obstetric anesthesia by chloroforming Queen Victoria for the birth of Prince Leopold (1853) and Princess Beatrice (1857). 1853 & 1857 1853 & 1857 Dr. John Snow (1813-1858) who was a fulltime anesthetist since 1847, popularized obstetric anesthesia chloroforming Queen Victoria for bi h of Prince Leopold (1853) Princess Beatrice (1857). by the and John Snow The First Anaesthetist
  • 49. • Knowledge of the narcotic effect of chloroform spread rapidly, but very soon reports of sudden deaths mounted. • The first fatality was a 15-year-old girl called Hannah Greener, who died on January 28, 1848. • Between 1864 and 1910 numerous commissions in UK studied chloroform, but failed to come to any clear conclusions. • The reservations about chloroform could not halt its soaring popularity. Between about 1865 and 1920, chloroform was used in 80 to 95% of all narcoses performed in UK and German-speaking countries. Knowledge of the narcotic effect of chloroform spread rapidly, but very soon reports of sudden deaths mounted. The first fatality was a 15-year-old girl called Hannah Greener, who died on January 28, 1848. Between 1864 and 1910 numerous commissions in UK studied chloroform, but failed to come to any clear conclusions. The reservations about chloroform could not halt its soaring pop larity. Between about 1865 and 1920, chloroform was use in 80 to 9500 of all narcoses performed in UK and German-speaking countries.
  • 50. History of Cocaine History ofCocaine cocam TOOTHACHE DROPS Instantaneous Cure ! 15 Prepared by the LLOYD MANUFACTURING CO. 219 HUDSON AVE., ALBANY, N. Y. For sale by all Druggists. ntlhm•
  • 51. • Dr. Karl Koller (1857-1944)-Viennese ophthalmologist and colleague of Sigmund Freud, introduced cocaine as an anesthetic for eye surgery. • Koller recognized its tissue-numbing capabilities, and in 1884 demonstrated its potential as a local anaesthetic to the medical community. 1884 1884 (1857-1944)-Viennese Dr. Karl Koller ophthalmologist and colleague of Sigmund Freud, introduced cocaine as an anesthetic for eye surgery. Koll r recognized its tissue-numbing capabilities, and in 1884 dem nstrated its potential as a local anaesthetic to the medical community.
  • 52. • Koller's findings were a medical breakthrough. Prior to his discovery, performing eye surgery was difficult because the involuntary reflex motions of the eye to respond to the slightest stimuli. • Later, cocaine was also used as a local anaesthetic in other medical fields such as dentistry Koller's findings were a medical breakthrough. Prior to his discovery, performing eye surgery was difficult because the involuntary reflex motions of the eye to respond to the slightest stimuli. Lat r, cocaine was also used as a loca anaesthetic in other medical field such as dentistry aCOCAINE( 'OCHLORIDE Topical t Coeæt-e
  • 53. • Dr. August Bier (1861-1949) was a German surgeon. • On 16 August 1898, Bier performed the first operation under spinal anesthesia at the Royal Surgical Hospital of the University of Kiel. • The subject was scheduled to undergo segmental resection of his left ankle, which was severely infected with tuberculosis. 1898 1898 Dr. August Bier (1861-1949) was a German surgeon. ' On 16 August 1898, Bier performed the Irst operation under spinal anesthesia at the Royal Surgical Ho ital of the University of Kiel. The subject was scheduled to undergo segmental resection of his I t ankle, which was severely infected with tuberculosis.
  • 54. • But Bier dreaded the prospect of general anesthesia because he had suffered severe adverse side effects during multiple previous operations. Therefore, Bier suggested "cocainization" of the spinal cord as an alternative to general anesthesia. • Bier injected 15 mg of cocaine intrathecally, which was sufficient to allow him to perform the operation. The subject was fully conscious during the operation, but felt no pain. B t Bier dreaded the prospect of general anesthesia because he had su ered severe adverse side effects during multiple previous op rations. Therefore, Bier suggested "cocainization" of the spinal co d as an alternative to general anesthesia. Bier injected 15 mg of cocaine intrathecally, which was sufficient to allo him to perform the operation. The subject was fully conscious during the operation, but felt no pain.
  • 55. • Two hours after the operation, the subject complained of nausea, vomiting, severe headache, and pain in his back and ankle. • The vomiting, back and leg pain improved by the following day, but the headache was still present. • Bier performed spinal anesthetics on five more subjects for lower extremity surgery, using a similar technique and achieving similar results wo hours after the operation, the subject complained f nausea, vomiting, severe headache, and pain in his back and nkle. The vomiting, back and leg pain improved by the following day, butthe headache was still present. Bier lowe simil performed spinal anesthetics on five more subjects for extremity surgery, using a similar technique and achieving r results
  • 57. The 20thcentury saw the transformation of the practices of tracheotomy, endoscopy and non-surgical tracheal intubation fromrarelyemployed procedures to essential componentsof the practices of anesthesia, critical care medicine, emergency medicine, gastroenterology, pulmonology and surgery. The 20th centuyy saw the transformation ofthe practices of tracheotomy, endoscopy and non-surgical tracheal intubation fromrarely employdprocedures to essential components ofthe practices ofanesthesia, critical care medicine, emergency medicine, gastroenterolou, pulmonolog and surgety.
  • 59. In 1902, Hermann Emil Fischer (1852– 1919) and Joseph von Mering (1849–1908) discovered that diethylbarbituric acid was an effective hypnotic agent. In 1902, Hermann Emil Fischer (1852— 1919) andJosephvon Mering (1849—1908) discovered that diethylbarbituric acid was an effective hypnotic agent.
  • 60. • Also called barbital or Veronal, the trade name assigned to it by Bayer Pharmaceuticals, this new drug became the first commercially marketed barbiturate. • It was used as a treatment for insomnia from 1903 until the mid-1950s. Also called barbital or Veronal, the trade name assigned to it by Bayer Pharmaceuticals, this new drug became the first commercially marketed barbiturate. It as used as a treatment for insomnia from 1903 until the mid 1950s.
  • 61. • Barbitone was prepared by condensing diethylmalonic ester with urea in the presence of sodium ethoxide, and then by adding at least two molar equivalents of ethyl iodide to the silver salt of malonylurea or possibly to a basic solution of the acid. The result was an odorless, slightly bitter, white crystalline powder. Barbitone condensing prepared by was diethylmalonic ester with urea in the presence of sodium ethoxide, and then by adding at least wo molar equivalents of ethyl iodide to the silver salt of malonylurea or pos ibly to a basic solution of the acid. The result was an odorless, slig tly bitter, white crystalline POW er. hlemal'
  • 62. • Alfred Einhorn (1857-1917)- German chemist develops procaine and names the substance "Novocain.“ from the Latin nov- (meaning new) and -caine, a common ending for alkaloids used as anesthetics. • It was introduced into medical use by surgeon Heinrich Braun. 1905 Alfred German 1905 (1857-1917)- Einhorn chemist develops procaine and names the substance "Novocain." from the Latin nov- eaning new) and -caine, a common ending for alkaloids used as anesthetics. s introduced into medical use by surgeon Heinrich Braun At
  • 63. • Arthur Guedel publishes his eye signs of Ether anesthesia in the American Journal of Surgery. • He also described 4 stages of ether anaesthesia dividing the stage III into 4 planes • His Guedel (oral) airway is still used today. • He has been memorialized by the Arthur E. Guedel Memorial Anesthesia Center, San Francisco. 1920 1920 Arthur Guedel publishes his eye signs of Ether anesthesia in the American Journal of Surgery. He also described 4 stages of ether anaesthesia dividing the stage Ill into 4 planes His Guedel (oral) airway is still used today. He as been memorialized by the Arthur E. Guedel Memorial Ane hesia Center, San Francisco.
  • 64. HISTORY OF SODIUM THIOPENTAL Who cares about your consent or Supreme Court's verdict on Narco Tests HISTORY OF SODIUMTHIOPENTAL
  • 65. • Sodium thiopental, the 1st IV anesthetic, was synthesized in 1934 by Ernest H. Volwiler & Donalee L. Tabern , working for Abbott Laboratories. • In the mid 1930s, Volwiler and Tabern spent three years screening over 200 candidate compounds in search of a substance which could be injected directly into the blood stream to produce unconsciousness the 1st IV Sodium thiopental anesthetic, was synthesized in 1934 by Ernest H, Volwiler & , working Donalee L. Tabern for Abbott Laboratories. ' In he mid 1930s, Volwiler and Tabern spent three years screening over 200 candidate compounds in search of a sub tance which could be injected directly into the blood strea to produce unconsciousness
  • 66. •It was first used in humans on 8 March 1934 by Ralph M. Waters in an investigation of its properties, which were short-term anesthesia and surprisingly little analgesia. •Three months later, John Silas Lundy started a clinical trial of thiopental at the Mayo Clinic at the request of Abbott Laboratories. ' t was first used in humans on 8 arch 1934 by Ralph M. Waters in a investigation of its properties, w ich were short-term anesthesia and suprisingly little analgesia. •Three months later, John Silas Lundy started a clinical trial of thiopental at the Mayo Clinic at the request of Abbott Labora ories.
  • 67. • Volwiler and Tabern were awarded U.S. Patent No. 2,153,729 in 1939 for the discovery of thiopental, and they were inducted into the National Inventors Hall of Fame in 1986. • The popularity of thiopental-as a swift-onset intravenous agent for inducing general anesthesia- paved the way for other totally unrelated intravenous induction agents, such as ketamine, etomidate, and propofol. Volwiler and Tabern were awarded U.S. Patent No. 2,153,729 in 939 for the discovery of thiopental, and they were inducted into he National Inventors Hall of Fame in 1986. The popularity of thiopental-as a swift-onset intravenous agent for 1 ducing general anesthesia- paved the way for other totally unrelated intravenous induction agents, such as ketamine, etom date, and propofol.
  • 68. • On 23 January 1942 Griffith and his resident Enid Johnson administered curare to a young man undergoing appendicectomy.. Dr. Harold Griffith (1894-1985) & Enid Johnson (1909-2001) 1942 1942 Dr Harold Griffith (1894-1985) & Enid Johnson (1909-2001) ' On 23 January 1942 Griffith and his resident Enid Johnson administered curare to a young man undergoing app ndicectomy..
  • 69. The credit for introducing curare to anaesthetics belongs to Griffith. Griffith and Johnson reported their use of curare in July 1942, and the introduction to their report is memorable: ‘Every anaesthetist has wished at times that he might be able to produce rapid and complete muscular relaxation in resistant patients under general anaesthesia” The credit for introducing curare to anaesthetics belongs to Griffith. GrTfith and Johnson reported their use of curare in July 1942, and th introduction to their report is memorable: 'Every anaesthetist has wished at times that he might be able to produce rapid and complete muscular relaxation in resistant patients under general anaesthesia "
  • 70. • Many new intravenous and inhalational anesthetics were developed and brought into clinical use during the second half of the 20th century. • Paul Janssen (1926–2003), the founder of Janssen Pharmaceutica, is credited with the development of over 80 pharmaceutical compounds. • Janssen synthesized nearly all of the butyrophenone class of antipsychotic agents, beginning with haloperidol (1958) and droperidol (1961). Many new intravenous and inhalational anesthetics were developed and brought into clinical use during the second half of the 20th century. Paul Janssen (1926—2003), the founder of Janssen Pharmaceutica, is credited with the development of over 80 pharmaceutical com ounds. Jans en synthesized nearly all of the butyrophenone class of ntipsychotic agents, beginning with haloperidol (1958) and d operidol (1961).
  • 71. • These agents were rapidly integrated into the practice of anesthesia. • In 1960, Janssen's team synthesized fentanyl, the first of the piperidinone-derived opioids. • Fentanyl was followed by sufentanil (1974), alfentanil (1976), carfentanil (1976), and lofentanil (1980). Janssen and his team also developed etomidate (1964),a potent intravenous anesthetic induction agent. These agents were rapidly integrated into the practice of anesthesia. ' In 1960, Janssen's team synthesized fentanyl, the first of the piperidinone-derived opioids. ' Fen anyl was followed by sufentanil (1974), alfentanil (19 6), carfentanil (1976), and lofentanil (1980). Janssen and his eam also developed etomidate (1964),a potent intravenous anes hetic induction agent.
  • 72. 1956 - UK's Dr. Michael Johnstone clinically introduces halothane, the first modern-day brominated general anesthetic. 1963 - Dr. Edmond I. Eger, II described minimum alveolar concentration (MAC), later characterized as "the concentration of inhaled anesthetic producing immobility in 50% of patients subjected to a noxious stimulus." 1 56 - UK's Dr. the halothane, anesthetic. Michael Johnstone first modern-day clinically introduces brominated general 1963 - Dr. Edmond 1. Eger, 11 described minimum alveolar later characterized as "the entration (MAC) entration of inhaled anesthetic producing immobility in con of patients subjected to a noxious stimulus." 500
  • 73. 1964- Dr. Günter Corssen et al. begin human trials of the dissociative intravenous anesthetic ketamine. 1966- Dr. Robert Virtue et al. begin human trials of the inhalational anesthetic enflurane. 1972- Isoflurane is clinically introduced as an inhalational anesthetic. 1992- Desflurane is clinically introduced as an inhalational anesthetic. 1994- Sevoflurane is clinically introduced as an inhalational anesthetic. 1 64- Dr. Günter Corssen et al. begin human trials of the dissociative intravenous anesthetic ketamine. 19 6- Dr. Robert Virtue et al. begin human trials of the inhalational nesthetic enflurane, is clinically introduced as an inhalational 1972- Isoflurane anesthetic. is clinically introduced as an inhalational 1992- esflurane anest etic. is clinically introduced as an inhalational 1994- roflurane anesthetic.
  • 74. 21ST CENTURY 21st Century: Age of Digital Revolution 21st Century: Age ofDigital Revolution revolution
  • 75. • Among the most widely used drugs are Propofol, Etomidate, Barbiturates such as methohexital and thiopentone, Benzodiazepines such as midazolam and Ketamine. • The "digital revolution“ of the 21st century has brought newer technology to the art and science of tracheal intubation. • Several manufacturers have developed video laryngoscopes ' Among the most widely used drugs are Propofol, Etomidate, Barbiturates such as methohexital and thiopentone, Benzodiazepines such as midazolam and Ketamine. The "digital revolution" of the 21st century has brought newer tec nology to the art and science of tracheal intubation. Sev ral manufacturers have developed video laryngoscopes
  • 76. • Xenon has been used as a general anesthetic. Although it is expensive, anesthesia machines that can deliver xenon are about to appear on the European market, because advances in recovery and recycling of xenon have made it economically viable. • New agents based on benzodiazepine, etomidate, and propofol structures are being developed. Xenon has been used as a general anesthetic. Although it is expensive, anesthesia machines that can deliver xenon are about to appear on the European market, because advances in recovery and recycling of xenon have made it economically viable. ' Ne stru agents based on benzodiazepine, etomidate, and propofol tures are being developed.
  • 77. Conclusion • Surgery learned many lessons through the ages, but never was it able to banish Pain. • More than a century ago, a vapor in the operating-room of the Massachusetts General Hospital blotted out sufferrings from surgery. • It was the most beneficent change in the history of surgery, and has since been one of the greatest gift to mankind. • However, the history of anaesthetics will remain an unfinished work, until some one is able to synthesize a drug that will have all of the desirable properties of the ideal anaesthetic. Conclusion Surgery learned many lessons through the ages, but never was it able to banish Pain. More than a century ago, a vapor in the operating-room of the Massachusetts General Hospital blotted out sufferrings from surgery. It as the most beneficent change in the history of surgery, and has since been one of the greatest gift to mankind. Ho ever, the history of anaesthetics will remain an unfinished wor , until some one is able to synthesize a drug that will have all o the desirable properties of the ideal anaesthetic.
  • 80. INTRODUCTION TO ANAESTHESIA Fatiş Altındaş Department of Anesthesiology INTRODUCTIONTO ANAESTHESIA FatisAltlndas Department ofAnesthesiology
  • 81. † Dioscorides first used the term anesthesia in first century AD „ To describe the narcotic-like effects † As “a defect of sensation” in Bailey’s An Universal Etymological English Dictionary (1721) Dioscoridesfirstusedtheterm o anesthesiainfirstcenturyAD Todescribethe narcotic-likeeffects As"adefectofsensation"inBailey's o An Universal Etymological English (1721) Dictionary
  • 82. † Oliver Wendell Holmes used its present meaning (1846) „ means the sleeplike state „ makes possible painless surgery OliverWendellHolmes usedits o (1846) presentmeaning annakes possible painless surgery
  • 83. History of Anesthesia † In ancient time, people used „ Opium poppy, coca leaves, mandrake root, alcohol, phlebotomy † Ancient Egyptians used the combination of opium poppy and hyoscyamus morphine and scopolamine Historyof Anesthesia Inancienttime,people used o Opium poppy,cocaleaves, mandrake o root,alcohol,phlebotomy AncientEgyptians usedthe o combinationofopium poppyand hyoscyamus scopolamine morphineand
  • 84. Ether † Prepared in 1540 by Valerius Cordus † Used as sedative in „ tuberculosis „ asthma and whooping cough „ remedy for toothache † Crawford W. Long and William Clark used it on patients in 1842 Ether Prepared in1540 byValerius o Cordus Usedassedative in o tuberculosis o asthmaand whoopingcough o remedyfortoothache o Crawford W.LongandWilliam o Clarkusediton patients in1842
  • 85. William Morton (1819-1868) † The first succesful surgical anesthesia, 1846, Boston William Morton (1819-1868) Thefirstsuccesful surgical anesthesia,1846, Boston
  • 86.
  • 87. 3 7 1. Newspaper repotlet 2. John call Dalton 3. William Williamson Wellington 4. Abel Lawrence Peitson 5. Char es Hosea Hildreth 6. William Tt'aoma•s Green Mctlon 7. Jonathan Mason Warren B. Gilbert Abbott g. John Collins Warren 10. H. 11 Charles Frederick Heywood 12. HeneryJacob Bigelow 13. Augustus Addison Gould 14. Salomon Davis
  • 88.
  • 89. Professor James Young Simpson (1811- 1870) † found chloroform to be efficacious and reasonably safe † used for Prince Leopold’s and Princess Beatrice’s birhts Chloroform Chloroform ProfessorJamesYoung Simpson(1811- 1870) foundchloroformto o be efficaciousand reasonablysafe usedforPrince o Leopold'sand Princess Beatrice's birhts
  • 90. Nitrous oxide (N2O) † Produced by Joseph Priestly 1772, † Humphrey Davy first noted its analgesic properties in 1800. † Horace Wells first used it in humans for anesthesia in 1844 † Less popular in tree agents „ Low potency „ Tendency to cause asphyxia H. Davy (N20) Nitrousoxide Produced byJoseph Priestly 1772, HumphreyDavyfirstnoted itsanalgesic properties in 1800. I-Horace Wells firstused itin humansforanesthesiain 1844 Less popularintreeagents Low potency Tendencytocause asphyxia H.Davy
  • 91. Intravenous Anesthesia (IVA) † Pierre Cyprien Ore „ Pioneer of IVA „ Chloral hydrate in 1872 † Barbiturates were synthesized 1903 „ For induction of anesthesia IntravenousAnesthesia(lVA) Pierre Cyprien Ore o Pioneerof1VA Chloralhydratein 1872 Barbiturates were o synthesized1903 Forinductionof anesthesia ANGIOCATHS
  • 92. Regional Anesthesia † In 1860, Albert Niemann isolated crystalized alcoloids of coca. † Karl Koller used cocain for eye block in 1884 † In 1885, first epidural block † In 1898, first spinal anesthesia by August Bier † Second local anesthetic agent (prilocain) was founded in 1904 † Lidocain was founded in 1946 RegionalAnesthesia o o o o In1860,AlbertNiemannisolated crystalizedalcoloids ofcoca. Karl Kollerusedcocainforeyeblockin 1884 In1885,firstepidural block I n 1898,firstspinalanesthesiaby AugustBier Secondlocalanestheticagent(prilocain) wasfounded in1904 Lidocainwasfoundedin1946
  • 93. Evolution of the specialty †The development of the indepented medical specialty of anesthesiology would not occur until the early 20th century. Evolutionofthe specialty Thedevelopmentofthe indepented medicalspecialty ofanesthesiologywouldnot occuruntiltheearly20th century.
  • 94. † In England, in 1893, the first organization of physician specialists in anesthesia, “The Society of Anesthetists” † In the United States, the first organization of physician anesthetists was formed in 1911. In England,in1893,thefirst o organizationofphysicianspecialistsin anesthesia,"TheSocietyof Anesthetists" Inthe UnitedStates,thefirst o organizationofphysiciananesthetists was formed in1911.
  • 95. † invented an inhaler for ether † published the first book on general anaesthesia:On the Inhalation of Ether John Snow the father of anaesthesia aninhaler forether publishedthefirst o bookongeneral anaesthesia : Onthe InhalationofEther John Snow the fatherofanaesthesia
  • 96. History of Anesthesia in Turkey-1 † The first publications belong to surgeons † They made great contributions to anesthesia in Turkey † Publication of Miralay Ahmet Bey „ includes the information about the use of ether † Ether anesthesia was first used in Gülhane Askeri Hospital in 1898 by Rieder Paşa Historyof AnesthesiainTurkey-1 Thefirst publications belongtosurgeons Theymadegreatcontributionsto anesthesia inTurkey Publication ofMiralayAhmetBey o the use of ether Etheranesthesia wasfirstusedin o GülhaneAskeriHospitalin1898 by Ri ed e r Pasa
  • 97. History of Anesthesia in Turkey-2 † Dr. Sadi Sun is the first anesthesiologist in Turkey † The first endotracheal entubation was performed by Dr Sun † In 1955, anesthesia was accepted as a medical specialty by Ministry of Health Historyof AnesthesiainTurkey-2 Dr.SadiSunisthe firstanesthesiologist inTurkey Thefirstendotracheal entubationwas performed by DrSun In1955,anesthesia wasacceptedasa medicalspecialtyby MinistryofHealth
  • 98. What is Anesthesiology? †Practice of medicine dedicated to the relief of pain and total care of the surgical patient before, during and after surgery. What isAnesthesiology? Practiceofmedicine o dedicatedtothereliefof painandtotalcareofthe duri ngandaftersurgery.
  • 99. †Anesthesiologists are a physician who complete a six years of medical school and four more year anesthesiology residency training program. Anesthesiologistsarea o physician whocompleteasix yearsofmedicalschooland fourmore yearanesthesiology residencytrainingprogram.
  • 100. † Anesthesiologist is the perioperative physician † Provides medical care to each patient „ Evaluating the patient before surgery (preoperative) „ Consulting with the surgical team „ Providing pain control „ Supporting of life functions during surgery (intraoperative) „ Supervising care after surgery (postoperative) Anesthesiologististhe perioperative o physician Provides medicalcaretoeachpatient o Evaluatingthe patientbefore surgery (preoperative) Consultingwiththe surgicalteam Providing paincontrol Supporting oflifefunctionsduring surgery(intraoperative) Supervisingcareaftersurgery (postoperative)
  • 101. In the operating room † The role of anesthesiologist is to provide continual medical assessment of the patient „ Monitor and control the patient’s vital functions † Heart rate, rhythm, breathing, blood pressure, body temperature, fluid balance † Immediately diagnose and treat any medical problems during surgery or recovery period „ Control pain and level of unconsciousness Intheoperatingroom The roleofanesthesiologististo provide continualmedicalassessmentofthe patient patient'svital functions IHeartrate,rhythm,breathing,blood pressure, bodytemperature,fluid balance Immediately diagnose andtreatany medical o problemsduringsurgery orrecovery period Controlpainand levelofunconsciousness
  • 102. In the postanesthesia care unit † Patients are transferred to recovery room after surgery „ Allowing them to emerge fully from the anesthetics’ effects † They are observed by skilled nursing personnel „ After stabilization sufficiently, transferred to regular room or home Inthe postanesthesiacareunit Patientsare transferredtorecovery roomaftersurgery Allowingthem to emerge fully fromtheanesthetics' effects Theyare observed by skillednursing personnel Afterstabilization sufficiently,transferredto regularroomorhome
  • 103. What is Scope of Anesthesiologist? † Anesthesiologists work in ICU What isScopeof Anesthesiologist? Anesthesiologists work inlCU
  • 104. † Sedation and providing anesthesia outside the operating room „ Magnetic resonance imaging, cardiac catheterization etc. † Pioneers in cardiopulmonary resuscitation † In childbirth, anesthesiologists manage the care of two persons † Anesthesiologists are also involved in pain management, „ to diagnose and treatment of acute and chronic problems. Sedationandprovidinganesthesiaoutside o theoperatingroom Magnetic resonanceimaging,cardiac catheterizationetc. Pioneersincardiopulmonaryresuscitation o Inchildbirth,anesthesiologists managethe o careoftwo persons Anesthesiologistsare alsoinvolvedin pain o management, to diagnoseandtreatmentofacute andchronic problems.
  • 106. Types of Anaesthesia PPT PREPARED BY DR RAJESH T EAPEN ATLAS HOSPITAL RUWI Types of Anaesthesia PPTPREPARED BY DR RAJESH TEAPEN ATLAS HOSPITAL RUWI
  • 107. Sushruta 800B.C. wrote first Surgery textbook Sushruta 800B.C. wrote first Surgery textbook
  • 109. Anesthesia  From Greek anaisthesis means not sensation  Listed in Bailey´s English Dictionary 1721.  When the effect of ether was discovered anesthesia” used as a name for the new phenomenon. Anesthesia From Greek anaisthesis means not sensation Listed in Bailey's English Dictionary 1721. the effect Of ether was discovered anesthesia" used as a name for the new phenomenon.
  • 110. Oxford dictionary definition  insensitivity to pain, especially as artificially induced by the administration of gases or the injection of drugs before surgical operations Oxford dictionary definition insensitivity to pain, especially as artificially induced by the administration of gases or the injection of drugs before surgical operations
  • 111. World Anesthesia Day 16th Oct
  • 112. HISTORY OF ANESTHESIA • General anesthesia was absent until the mid- 1800s. • Ether synthesized in 1540 by Cordus • Ether used as anesthetic in 1842 by Dr. Crawford W.Long • Ether publicized as anesthetic in 1846 by Dr. William Morton. • Ether is no longer used in modern practice, yet considered to be the first ‘ideal’ anesthetic • Chloroform used as anesthetic in 1853 by Dr. John Snow • Endotracheal tube discovered in 1878 • Thiopental first used in 1934 HISTORY OF ANESTHESIA General anesthesia was absent until the mid- 800s. Ether synthesized in 1540 by Cordus Ether used as anesthetic in 1842 by Dr. Crawford W.Long Ether publicized as anesthetic in 1846 by Dr. William Morton. Ether is no longer used in modern practice, yet onsidered to be the first 'ideal' anesthetic Chloroform used as anesthetic in 1853 by Dr. John Snow Endotracheal tube discovered in 1878 Thiopental first used in 1934
  • 113. Pre 1846 - The Foundations of Anaesthesia ……..so the Lord God caused him to fall into a deep sleep. While the man was sleeping, the Lord God took out one of his ribs. He closed up the opening that was in his side……... Genesis 2:21 NIrV Pre 1846 - The Foundations of —Anaesthesia so the Lord God caused him to fa// into a deep sleep, While the man was s/eeping, the Lord God took out one ofhis ribs. He closed up the opening that was in his side Genesis 2:21 /V1rV
  • 114. Primitive Anesthesia  Ancient civilizations- opium poppy, coca leaves, mandrake root, alcohol  Regional anesthesia in ancient times- compression of nerve trunks or the application of cold (cryoanalgesia) Primitive Anesthesia Ancient civilizations- opium poppy, coca leaves, mandrake root, alcohol Regional anesthesia in ancient times- compression of nerve trunks or the application of cold (cryoanalgesia)
  • 115. World Anaesthesia Day  On 16 October 1846, John Collins Warren removed a tumor from the neck of a local printer,Edward Gilbert Abbott. Warren reportedly quipped, "Gentlemen, this is no humbug.  MGH Boston World Anaesthesia Day • On 16 October 1846, John Collins Warren removed a tumor from the neck of a local printer,Edward Gilbert Abbott. Warren reportedly quipped, "Gentlemen, this is no humbug. NIGH Boston
  • 116. Regional Anaesthesia  1884 Sigmund Freud physiology actions cocaine  Carl Koller cocaine ophthalmological surgery Regional Anaesthesia 1884 Sigmund Freud physiology actions cocaine Carl Koller cocaine ophthalmological surgery
  • 117. Birth of modern Anaesthesia  1913,Chevalier Jackson-use of direct laryngoscopy as a means to intubate the trachea  Sodium Pentathal - first used in humans on 8 March 1934 by Ralph M. Waters Birth of modern Anaesthesia Chevalier Jackson-use of direct -1 13, laryngoscopy as a means to intubate the trachea Sodium Pentathal - first used in humans on 8 March 1934 by Ralph M. Waters
  • 118. Slide master Your Text here "Ether Day, 1846" Pictured are Gilbert Abbott (the patient), John Collins Warren, MD (the surgeon), William T. G. Morton (the anesthetist) and Henry J. Bigelow. MD (the junior surgeon).
  • 119. History  1845- Horace Wells- N2O  1846- William Morton- Ether  1847- Simpson- Chloroform  1853-John Snow  1878- ETT  1884- Cocaine  1895-98- Spinal analgesia/anaesthesia History 1845- Horace wells- N20 1846- William Morton- Ether 1847- Simpson- 1853-John Snow 1878- ETT 1884- Cocaine 1895-98- Spinal analgesia/anaesthesia
  • 120. Types Of Anesthesia Types Of Anesthesia and what kind of anesthesia can you afford? cæ.VJ
  • 121. Types . Types Local anesthesia Topo Infiltraton Regional anesthesia Poriphotal nerve blcH Epidural Spinal Intravenous regional Anesthesia Total tnmgation General anesthesia anesthesia inhalant anesthesia Injectable anesthesia Anesthetic adjuncts intravenous anesthesia
  • 122. Triad of General anaesthesia Hypnosis Analgesia Muscle relaxation ofGeneral anaesthesia Hypnosis Analgesia Muscle relaxation
  • 124. INTRODUCTION • General anaesthetics (GAs) are drugs which produce reversible loss of all sensations and consciousness. It usually involves a loss of memory and awareness with insensitivity to painful stimuli, during a surgical procedure General anesthesia need for unconsciousness ‘Amnesia-hypnosis’ need for analgesia ‘Loss of sensory and autonomic reflexes’ need for muscle relaxation INTRODUCTION General anaesthetics (GAS) are drugs which produce reversible loss of all sensations and consciousness. It usually involves a loss of memory and awareness with insensitivity to painful stimuli, during a surgical procedure need for unconsciousness 'Amnesia-hypnosis' General anesthesia need for analgesia 'Loss of sensory and autonomic reflexes' need for muscle relaxation
  • 125. General anesthetics Oyveen Cylinders General anesthetics The anesthetist Vho•s that guy? Nitrous
  • 127. Hypnotic drugs- intravenous  Gold standard- thiopentone  Propofol others  Etomidate  Benzodiazepines  Ketamine Hypnotic drugs- intravenous Gold standard- others Etomidate Benzodiazepines Ketamine
  • 128. Inhalational anaesthetics  Nitrous oxide-weak  Isoflurane  Sevoflurane  Desflurane  Halothane Inhalational anaesthetics Nitrous oxide-weak Isoflurane Desflurane Halothane
  • 129. Analgesia  Good analgesia= good anaesthesia  Hypnotic sparing effect  Opiates  Local anaesthetics  NSAIDS  Paracetamol Analgesia Good analgesia= good anaesthesia Hypnotic sparing effect Opiates Local anaesthetics NSAIDS Paracetamol
  • 130. Analgesia-Opiates  Gold standard – morphine  Derivatives- diamorphine, codeine  Synthetic agents - Pethidine - Fentanyl/Alfentanil-short acting - Remifentanil-ultra short acting Analgesia-Opiates Gold standard — morphine Derivatives- diamorphine, codeine Synthetic agents Pethidine /Alfentanil-short acting Remifentanil-ultra short actina
  • 131. Analgesia-NSAIDS  Gold standard- aspirin  Ibuprofen  Diclofenac  Cox-2 inhibitors Analgesia-NSAIDS Gold standard- aspirin • Ibuprofen • Diclofenac Cox-2 inhibitors
  • 132. Muscle relaxation  Aids intubation  Helps surgeon/surgery  Surgery of long duration  Reduces maintenance dose of anaesthetics agents Muscle relaxation Aids intubation Helps surgeon/surgery Surgery oflong duration Reduces maintenance dose of anaesthetics agents
  • 133. Muscle relaxants  Two types  Depolarising-short acting e.g.; suxmethonium  Non-depolarising- medium/long acting - Tracurium - Vecuronium - Rocuronium - Cisatracurium (NIMBEX) Muscle relaxants Two types Depolarising-short acting e.g.; suxmethonium Non-depolarising- medium/long acting Vecuronium Rocuronium Cisatracurium (NIMBEX)
  • 134. Prerequisites  Oxygen  Suction  Tilting trolley  Resuscitation drugs  Monitoring  Anaesthetist  Skilled assistance  Drugs and machine Prerequisites Oxygen Suction Tilting trolley Resuscitation drugs Monitoring • Anaesthetist Skilled assistance Drugs and machine
  • 135. The 21 st century-digital revolution The21 st céntury• revolution
  • 136. Phases of general anaesthesia  Induction  Maintenance  Recovery Phases of general anaesthesia Induction Maintenance Recovery
  • 137. Induction  Intravenous- majority  Inhalational- children, needle phobics  Monitoring  Preoxygenation  Hypnotic/analgesic and or relaxant  Mask/LMA/ET tube Induction Intravenous- majority Inhalational- children, needle phobics Monitoring 0 Preoxygenation Hypnotic/analgesic and or relaxant Mask/LMA/ET tube
  • 138. Maintenance  Intravenous or inhalational  Oxygen –40%-100%  Nitrous oxide  Muscle relaxant  Analgesia Maintenance Intravenous or inhalational Oxygen —4000-100% Nitrous oxide Muscle relaxant Analgesia
  • 139. Recovery  Turn off agent  Reverse relaxation  Cough reflex  Extubate when awake  Recovery position  Monitor until discharge Recovery Turn offagent Reverse relaxation Cough reflex Extubate when awake Recovery position Monitor until discharge
  • 140. SAMPLE USE ONLY @ 2009 Nucleus Medical Art All Rights Reserved. nucleus MEDICAL
  • 141. Advantages  No absolute contraindications  Quick to establish  Never fails to work Advantages No absolute contraindications Quick to establish Neverfails to work
  • 142. Disadvantages  Poly-pharmacy  Effects on various systems  Allergic reactions  Recovery profile  Post operative Nausea &Vomiting  Awareness Disadvantages Poly-pharmacy Effects on various systems Allergic reactions Recovery profile Post operative Nausea &Vomiting Awareness
  • 144. Regional anaesthesia  Spinal/epidural - surgery below umbilicus - Provides analgesia/muscle relaxation  Plexus blocks eg brachial plexus  Intravenous- Bier’s block Regional anaesthesia Spinal/epidural surgery below umbilicus Provides analgesia/muscle relaxation Plexus blocks eg brachial plexus Intravenous- Bier's block
  • 145. 40 Spinal Block - Position Spinal Block - Position Ll End of cord Spinal block—lateral position. End of cord Spinal block—sitting position. 40
  • 146. Regional anaesthesia Analgesia Muscle relaxation Regional anaesthesia Analgesia Muscle relaxation
  • 147. Local anaesthetics  Lignocaine- quick/short acting  Bupivacaine/levobupicvacaine - slow and long action  Ropivacaine- as above  Amethocaine- topical  Prilocaine- intravenous Local anaesthetics - quick/short acting /levobupicvacaine - slow and long action Ropivacaine- as above Amethocaine- topical j' Prilocaine- intravenous
  • 148. Advantages  Effective alternative to GA  Avoids polypharmacy  Allergic reactions  Extended analgesia  Patient can remain awake  Early drink/feed Advantages Effective alternative to GA Avoids polypharmacy Allergic reactions Extended analgesia Patient can remain awake Early drink/feed
  • 149. Disadvantages  Limited scope  Higher failure rate  Time constraints  Anticoagulants/Bleeding diathesis  Risk of neural injury Disadvantages Limited scope Higherfailure rate Time constraints Anticoagulants/Bleeding diathesis j' Risk ofneural injury
  • 150. Patient is more important than our ego; call for help, whenever patient is in danger Your Text here Patient is more important than our ego; call for help, whenever patient is in 000 "Nurse, get on the internet, go to SURGERY.COM, scroll down and click on the 'Are you totally lost?' icon.
  • 151. Slide master Your Text here THE IDEAL ANESTHETIST Reader Seoee & *neszhesia Eye estim cardiae Free foot fast Counter Loss Ester.atoc FieJd Eye Gas Eye .anaeoev.y 4 4 block anesthetics Srnag Storn•ch Met* Bats droppiro beetles AB Blood Table *4uster Pacifier & chest Shovel Ernergerwy
  • 152. Choice of anesthesia  The patient´s understanding and wishes regarding the type of anesthesia that could be used  The type and duration of the surgical procedure  The patients´s physiologic status and stability  The presence and severity of coexisting disease  The patient´s mental and psychologic status  The postoperative recovery from various kinds of anesthesia  Options for management of postoperative pain  Any particular requiremets of the surgeon  There is major and minor surgery but only major anesthesia hoice of anesthesia The patient's understanding and wishes regarding the type of anesthesia that could be used The type and duration of the surgical procedure The patients's physiologic status and stability The presence and severity of coexisting disease The patient's mental and psychologic status The postoperative recovery from various kinds of anesthesia Options for management of postoperative pain • Any particular requiremets of the surgeon There is major and minorsurgery but only major anesthesia
  • 153. Types of anesthesia care General Anesthesia  Reversible, unconscious state is characterised by amnesia (sleep, hypnosis or basal narcosis), analgesia (freedom from pain) depression of reflexes, muscle relaxation  Put to sleep Types of anesthesia care General Anesthesia Reversible, unconscious state is characterised by amnesia (sleep, hypnosis or basal narcosis), analgesia (freedom from pain) depression of reflexes, muscle relaxation Put to sleep
  • 154. Types of anesthesia care Regional Anesthesia  A local anethetic is injected to block or ansthetize a nerve or nerve fibers  Implies a major nerve block administered by an anesthesiologist (such as spinal, epidural, caudal, or major peripheral block) Types Of anesthesia care Regional Anesthesia A local anethetic is injected to block or ansthetize a nerve or nerve fi Implies a major nerve block administered by an anesthesiologist (such as spinal, epidural, caudal, or major peripheral block)
  • 155. Types of anesthesia care Monitored anesthesia care  Infiltration of the surgical site with a local anesthesia is performed by the surgeon  The anasthesiologist may supplement the local anesthesia with intravenous drugs that provide systemic analgesia and sedation and depress the response of the patient´s autonomic nervous system Types of anesthesia care Monitored anesthesia care Infiltration of the surgical site with a local anesthesia is performed by the surgeon The anasthesiologist may supplement the local anesthesia with intravenous drugs that provide systemic analgesia and sedation and depress the response of the patient's autonomic nervous system
  • 156. Types of anesthesia care local anesthesia  Employed for minor procedures in which the surgical site is infiltrated with a local anesthetic vital signs  May injsuch as lidocaine or bupivacaine  A perioperative nurse usually monitors the patient´s ect intravenous sedatives or analgesic drugs Types of anesthesia care local anesthesia Employed for minor procedures in which the surgical site is infiltrated with a local anesthetic vital signs May injsuch as lidocaine or bupivacaine A perioperative nurse usually monitors the patient's ect intravenous sedatives or analgesic drugs
  • 157.
  • 158. Thank you Macintosh noted: “for the surgeon the spinal ends with the injection of the agent; for the anesthetist it begins with the injection of the agent.” Macintosh noted: "for the surgeon the spinal ends with the injection of the agent; for the anesthetist it begins with the injection of the agent." Thank you
  • 159. Types of Anaesthesia Prof. med. Nabil H. Mohyeddin Anesthesiologist & Intensivist Board certified University Rostock, Germany nhm1955@hotmail.com Types ofAnaesthesia Prof. med, Nabil H, Mohyeddin Anesthesiologist &Intensivist Board certified University Rostock, Germany nhm1955@hotmail.com
  • 160. Objectives  Short History  Definition/types of anaesthesia  General anaesthesia/drugs  Phases of GA  Regional anaesthesia Objectives Short History Definition/types ofanaesthesia General anaesthesia/drugs Phases ofGA Regional anaesthesia
  • 161. Early history  Ancient/Medieval period - Opium - Alcohol - Cannabis Early history Ancient/Medieval period Opium Alcohol Cannabis
  • 162. History  1845- Horace Wells- N2O  1846- William Morton- Ether  1847- Simpson- Chloroform  1853-John Snow  1878- ETT  1884- Cocaine  1895-98- Spinal analgesia/anaesthesia History 1845- Horace Wells- N20 1846- William Morton- Ether 1847- Simpson- 1853-John Snow 1878- ETT 1884- Cocaine 1895-98- Spinal analgesia/anaesthesia
  • 163. History  1921- Epidurals  1934- Thiopentone, cyclopropane  1942- Curare  1946- Lignocaine  1951- Suxamethonium  1952- IPPV  1956-Halothane History 1921- Epidurals 1934- Thiopentone, cyclopropane 1942- Curare 1946- Lignocaine - Suxamethonium 1951 - IPPV 1952 1956-Halothane
  • 164. Definition ‘Loss of sensation’  General  Regional  Local Definition 'Loss ofsensation' General Regional Local
  • 165. Triad of General anaesthesia Hypnosis Analgesia Muscle relaxation Triad ofGeneral anaesthesia Hypnosis Analgesia Muscle relaxation
  • 167. Hypnotic drugs-intravenous  Gold standard- thiopentone  Propofol others  Etomidate  Benzodiazepines  Ketamine Hypnotic drugs-intravenous Gold standard- others Etomidate Benzodiazepines Ketamine
  • 168. Inhalational anaesthetics  Nitrous oxide-weak  Isoflurane  Sevoflurane  Desflurane  Halothane Inhalational anaesthetics Nitrous oxide-weak Isoflurane Desflurane Halothane
  • 169. Analgesia  Good analgesia= good anaesthesia  Hypnotic sparing effect  Opiates  Local anaesthetics  NSAIDS  Paracetamol Analgesia Good analgesia= good anaesthesia Hypnotic sparing effect Opiates Local anaesthetics NSAIDS Paracetamol
  • 170. Analgesia-Opiates  Gold standard – morphine  Derivatives- diamorphine, codeine  Synthetic agents - Pethidine - Fentanyl/Alfentanil-short acting - Remifentanil-ultra short acting Analgesia-Opiates Gold standard — morphine Derivatives- diamorphine, codeine Synthetic agents Pethidine /Alfentanil-short acting Remifentanil-ultra short acting
  • 171. Analgesia-NSAIDS  Gold standard- aspirin  Ibuprofen  Diclofenac  Cox-2 inhibitors Analgesia-NSAIDS Gold standard- aspirin Ibuprofen Diclofenac Cox-2 inhibitors
  • 172. Muscle relaxation  Aids intubation  Helps surgeon/surgery  Surgery of long duration  Reduces maintenance dose of anaesthetics agents Muscle relaxation Aids intubation Helps surgeon/surgery Surgery oflong duration Reduces maintenance dose of anaesthetics agents
  • 173. Muscle relaxants  Two types  Depolarising-short acting eg;suxmethonium  Non-depolarising- medium/long acting - Tracurium - Vecuronium - Rocuronium Muscle relaxants Two types Depolarising-short acting eg;suxmethonium Non-depolarising- medium/long acting Vecuronium Rocuronium
  • 174. Prerequisites  Oxygen  Suction  Tilting trolley  Resuscitation drugs  Monitoring  Anaesthetist  Skilled assistance  Drugs and machine Prerequisites Oxygen • Suction Tilting trolley Resuscitation drugs Monitoring Anaesthetist Skilled assistance Drugs and machine
  • 175. Phases of general anaesthesia  Induction  Maintenance  Recovery Phases of general anaesthesia Induction Maintenance Recovery
  • 176. Induction  Intravenous- majority  Inhalational- children, needle phobics  Monitoring  Preoxygenation  Hypnotic/analgesic and or relaxant  Mask/LMA/ET tube Induction Intravenous- majority Inhalational- children, needle phobics Monitoring Preoxygenation Hypnotic/analgesic and or relaxant Mask/LMA/ET tube
  • 177. Stages of anaesthesia  Alcohol 1.Dizzy, delightful 2.Drunk, disorderly 3.Dead drunk 4.Dangerously deep  General Anaesthesia 1.Amnesia, analgesia 2.Uninhibited response to stimuli 3.Surgical anaesthesia 4.Vital centre depression Stages ofanaesthesia Alcohol 1 Dizzy, delightful 2Drunk, disorderly 3.Dead drunk 4.Dangerously deep General Anaesthesia 1.Amnesia, analgesia 2, Uninhibited response to stimuli 3.Surgical anaesthesia 4. Vital centre depression
  • 178. Maintenance  Intravenous or inhalational  Oxygen –40%-100%  Nitrous oxide  Muscle relaxant  Analgesia Maintenance Intravenous or inhalational Oxygen —4000-100% Nitrous oxide Muscle relaxant Analgesia
  • 179. Recovery  Turn off agent  Reverse relaxation  Cough reflex  Extubate when awake  Recovery position  Monitor until discharge Recovery Turn offagent Reverse relaxation Cough reflex Extubate when awake Recovery position Monitor until discharge
  • 180. Advantages  No absolute contraindications  Quick to establish  Never fails to work Advantages No absolute contraindications Quick to establish Neverfails to work
  • 181. Disadvantages  Polypharmacy  Effects on various systems  Allergic reactions  Recovery profile  Post operative Nausia &Vomiting  Awareness Disadvantages Polypharmacy Effects on various systems Allergic reactions Recovery profile Post operative Nausia &Vomiting Awareness
  • 182. Regional anaesthesia  Spinal/epidural - surgery below umbilicus - Provides analgesia/muscle relaxation  Plexus blocks eg brachial plexus  Intravenous- Bier’s block Regional anaesthesia Spinal/epidural surgery below umbilicus Provides analgesia/muscle relaxation Plexus blocks eg brachial plexus Intravenous- Bier's block
  • 183. iigarnentum llavum cauda equino anterior epidural space supraspinous tigan• ent interspinous ligament posterior pidura• space basivertebral vein
  • 184. Regional anaesthesia Analgesia Muscle relaxation Regional anaesthesia Analgesia Muscle relaxation
  • 185. Local anaesthetics  Lignocaine- quick/short acting  Bupivacaine/levobupicvacaine- slow and long action  Ropivacaine- as above  Amethocaine- topical  Prilocaine- intravenous Local anaesthetics - quick/short acting /levobupicvacaine- slow and long action Ropivacaine- as above Amethocaine- topical Prilocaine- intravenous
  • 186. Advantages  Effective alternative to GA  Avoids polypharmacy  Allergic reactions  Extended analgesia  Patient can remain awake  Early drink/feed Advantages Effective alternative to GA Avoids polypharmacy Allergic reactions Extended analgesia Patient can remain awake Early drink/feed
  • 187. Disadvantages  Limited scope  Higher failure rate  Time constraints  Anticoagulants/Bleeding diathesis  Risk of neural injury Disadvantages Limited scope Higherfailure rate Time constraints Anticoagulants/Bleeding diathesis Risk ofneural injury
  • 188.
  • 189. Autonomic Nervous system S. Parasuraman, M.Pharm., Ph.D., Associate Professor, Faculty of Pharmacy, AIMST University The Autonomic Nervous System Sympathetic NorEpi mydriasis reduced saliva flow increased SV & HR vasoconstriction reduced peristalsis & secretion glycogen* glucose inhibition of bladder contraction Parasympathetic ACh Ganglia (N) miosis Sympathetic ganglia (N) epinephrine release 132 bronchodilation (not innervated) stimulated saliva flow decreased HR Vagal bronchoconstriction nerve stimulates peristalsis & secretion stimulates bile release bladder contraction Autonomic Nervous system S. Parasuraman, M.Pharm., Ph D Associate Professor, Faculty of Pharmacy, AIMST University
  • 190. Learning Outcomes • At the end of this session, the student would be able to: – Briefly describe Sympathetic and parasympathetic outflow and its functions. – List the differences between Sympathetic and Parasympathetic division. – Explain the adrenergic and cholinergic receptors Learning Outcomes ' At the end of this session, the student would be able to: — Briefly describe Sympathetic and parasympathetic outflow and its functions. — List the differences between Sympathetic and Parasympathetic division. — Explain the adrenergic and cholinergic receptors
  • 191. Nervous System Central nervous system Peripheral nervous system Afferent division (Sensory) Efferent division (Motor) Somatic system (voluntary) Autonomic nervous (involuntary) Sympathetic system (thorcolumbar outflow) Come from the thoracic and lumbar regions (T1 to L2/3) of the spinal cord Parasympathetic system (craniosacral outflow) Come from brainstem (Cranial Nerves III, VII, IX, X) or the sacral spinal cord (S2, S3, S4) Enteric nervous system Nervous System Central nervous system Peripheral nervous system Afferent division (Sensory) Efferent division (Motor) Somatic system (voluntary) Sympathetic system (thorcolumbar outflow) Come from the thoracic and lumbar regions (Tl to L2/3) of the spinal cord Autonomic nervous (involuntary) Parasympathetic system (craniosacral outflow) Enteric nervous system Come from brainstem (Cranial Nerves Ill, VII, X) or the sacral spinal cord (S2,
  • 192. Spinal nerves • There are 31 pairs of spinal nerves – 8 cervical – 12 thoracic – 5 lumbar – 5 sacral – 1 coccygeal The human spinal column is made up of 33 bones. • 7 - cervical region • 12 - thoracic region • 5 - lumbar region • 5 - sacral region • 4 - coccygeal region Ci (Atlas) Os sacrum Coccyx Spinal nerves The human spinal column is made up of 33 bones. 7 - cervical region 12 - thoracic region 5 - lumbar region 5 - sacral region 4 - coccygeal region ' There are 31 pairs spinal nerves Cervical nerves Thoracic nerves Lumbar nerves — 8 cervical — 12 thoracic — 5 lumbar — 5 sacral — 1 coccygeal 1 2 3 4 5 6 7 8 1 2 3 4 5 6 7 8 9 10 11 12 1 2 3 Spinal cord End of spinal cord —Cauda equina Sacral and coccygeal nerves 4 5 1 2 3 4 5 Filum terminale
  • 193. Peripheral Nervous System • Most of the nerves of the peripheral nervous system are composed of sensory nerve fibres conveying afferent impulses from sensory end organs to the brain and motor nerve fibres conveying efferent impulses from the brain through the spinal cord to the effector organs. Peripheral nervous system Efferent division (Motor) Afferent division (Sensory) Somatic system (voluntary) Autonomic nervous (involuntary) Peripheral Nervous System ' Most of the nerves of the peripheral nervous system are composed of sensory nerve fibres conveying afferent impulses from sensory end organs to the brain and motor nerve fibres conveying efferent impulses from the brain through the spinal cord to the effector organs. Peripheral nervous system Afferent division Sensor Efferent division (Motor) Somatic system (voluntary) Autonomic nervous (involuntary)
  • 194. Somatic Nervous System • The somatic nervous system (SNS or voluntary nervous system) is the part of the peripheral nervous system. • The somatic nervous system includes both sensory (afferent nerves) and motor (efferent nerves) neurons. • Sensory neurons convey input from receptors for somatic senses (tactile, thermal, pain, and proprioceptive sensations) and from receptors for the special senses (sight, hearing, taste, smell, and equilibrium) Somatic Nervous System ' The somatic nervous system (SNS or voluntary nervous system) is the part of the peripheral nervous system. ' The somatic nervous system includes both sensory afferent nerves) and motor (efferent nerves) neurons. ' Sensory neurons convey input from receptors for somatic (tactile, thermal, pain, senses and proprioceptive sensations) and from receptors for the (sight, hearing, special senses taste, smell, and equilibrium) SKIN AFFERENT NERVE SPINAL CORD MUSCLE EFFERENT NERVE
  • 195. Autonomic Nervous System • The autonomic nervous system is involved in a complex of reflex activities, which depend on sensory input to the brain or spinal cord, and on motor output. • The majority of the organs of the body are supplied by both sympathetic and parasympathetic nerves which have opposite effects that are finely balanced to ensure the optimum functioning of the organ. Autonomic Nervous System ' The autonomic nervous system is involved in a complex of reflex activities, which depend on sensory input to the brain or spinal cord, and on motor output. ' The majority of the organs of the body are supplied by both sympathetic and parasympathetic nerves which have opposite effects that are finely balanced to ensure the optimum functioning of the organ.
  • 196. Autonomic Nervous System • The autonomic nervous system (ANS) is a complex set of neurons that mediate internal homeostasis without conscious intervention or voluntary control. • The ANS maintains blood pressure, regulates the rate of breathing, influences digestion, urination, and modulates sexual arousal. • There are two main branches to the ANS – the sympathetic nervous system and the parasympathetic nervous system. The effects of autonomic control are rapid and essential for homeostasis Autonomic Nervous System ' The autonomic nervous system (ANS) is a complex set of neurons that mediate internal homeostasis without conscious intervention or voluntary control. ' The ANS maintains blood pressure, regulates the rate of breathing, influences digestion, urination, and modulates sexual arousal. ' There are two main branches to the ANS — the sympathetic and the system nervous parasympathetic nervous system The effects of autonomic control are rapid and essential for homeostasis
  • 197. Sympathetic nervous system • Sympathetic nervous system otherwise called as thoracolumbar system. • Sympathetic stimulation prepares the body to deal with exciting and stressful situations, e.g. strengthening its defences in danger. sympathetic stimulation mobilises the body for 'fight or flight'. • Neurones convey impulses from their origin in the hypothalamus, reticular formation and medulla oblongata to effector organs and tissues. The first neurone has its cell body in the brain and its fibre extends into the spinal cord. Sympathetic nervous system ' Sympathetic nervous system otherwise called as thoracolumbar system. prepares the body to deal ' Sympathetic stimulation with exciting and stressful situations strengthening its defences in danger sympathetic stimulation mobilises the body for 'fight or flight Neurones convey impulses from their origin in the hypothalamus, reticular formation and medulla oblongata to effector organs and tissues. The first neurone has its cell body in the brain and its fibre extends into the spinal cord.
  • 198. Sympathetic nervous system • Structure of the Sympathetic Division – Pathway from Spinal Cord to Sympathetic Trunk Ganglia – Organization of Sympathetic Trunk Ganglia – Pathways from Sympathetic Trunk Ganglia to Visceral Effectors Sympathetic nervous system • Structure of the Sympathetic Division — Pathway from Spinal Cord to Sympathetic Trunk Ganglia Organization of Sympathetic Trunk Ganglia — Pathways from Sympathetic Trunk Ganglia to Visceral Effectors
  • 199. Structure of the sympathetic division of the autonomic nervous system Trachea and bronchi: Bronchodilation Liver: Glycogen glucose conversion increased Iris muscle: Pupil dilated Blood vessels in heart : Vasoconstriction Heart: Rate and force of contraction increased Salivary glands: Secretion inhibited Stomach: Peristalsis reduced Sphincters closed Intestines: Peristalsis and tone decreased Vasoconstriction Kidney: Urine secretion decreased Bladder: Smooth muscle wall relaxed Sphincter closed Sex organs: Generally Vasoconstriction SYUPAtHEOC DIVISION (thoracolumbar) pretar*i to rtuscle of blood a' ttueo organs Preganglionic new-ons PostP"91ionÉ nouroru SINEtg1Äi Iris muscle: Pupil dilated Lactrr•l Salivary glands: Secretion inhibited Wjcous rnernbrar,o oc and palate gland Blood vessels in heart : Vasoconstriction Atrial muscle titers Sweat Hair smooth (each trurü tho Sympathetic trunk gan# cte TtO 712 cervical gan•ion Uiddle interior cervical Selan& Crdiac plexus Greater speanehnie / -z Celiae ganglion Aorticore splanchnié Odon Heart SA'AV enuscle Spleen Heart: Rate and force of contraction increased Trachea and bronchi: Bronchodilation Liver: Glycogen glucose conversion increased Stomach: Peristalsis reduced Sphincters closed Intestines: Peristalsis and tone decreased solanchnic meent«ic ganglion Renal ganglions Lumbar splanchnic Interior mesenterie ganglion Preverte&al Rectum Uret•e (hsad gangUa Urnary 'External Hypogastric p&xus Vasoconstriction Kidney: Urine secretion decreased Bladder: Smooth muscle wall relaxed Sphincter closed Uton.n / Sex organs: Generally Vasoconstriction Structure of the sympathetic division of the autonomic nervous system
  • 200. Parasympathetic nervous system • Parasympathetic nervous system otherwise called as craniosacral outflow. • Parasympathetic stimulation has a tendency to slow down body processes except digestion and absorption of food and the functions of the genitourinary systems. Its general effect is that of a 'peace maker' allowing restoration processes to occur quietly and peacefully. • Cell bodies of parasympathetic preganglionic neurons are found in nuclei in the brain stem. Parasympathetic nervous system ' Parasympathetic nervous system otherwise called as craniosacral outflow. ' Parasympathetic stimulation has a tendency to slow down body except digestion and processes absorption of food the functions of the and Its general effect is that of a genitourinary systems peace maker allowing restoration processes to occur quietly and peacefully. ' Cell bodies of parasympathetic preganglionic neurons are found in nuclei in the brain stem.
  • 201. Parasympathetic nervous system • Structure of the Parasympathetic Division – The cranial parasympathetic outflow consists of preganglionic axons that extend from the brain stem in four cranial nerves. The cranial outflow has four pairs of ganglia and the ganglia associated with the vagus (X) nerve. – The sacral parasympathetic outflow consists of preganglionic axons in anterior roots of the second through fourth sacral spinal nerves. Parasympathetic nervous system • Structure of the Parasympathetic Division — The cranial parasympathetic outflow consists of preganglionic axons that extend from the brain stem in four cranial nerves. The cranial outflow has four pairs of ganglia and the ganglia associated with the vagus (X) nerve. parasympathetic outflow consists of — The sacral preganglionic axons in anterior roots of the second through fourth sacral spinal nerves.
  • 202. Structure of the parasympathetic division of the autonomic nervous system Trachea and bronchi: Bronchoconstriction Liver: Blood vessels dilated Secretion of bile increased Iris muscle: Pupil constricted Heart: Rate and force of contraction decreased Salivary glands: Secretion increased Stomach: Secretion of gastric juice and peristalsis increased Intestines: Digestion and absorption increased Kidney: Urine secretion increased Bladder: Muscle of wall contracted Sphincters relaxed Sex organs: Male: erection; Female: variable PARASYMPATHETIC DIVES'ON Koy-, Preganglionic t'ieurms neurons OcüotnDtOt (Ill) ganglia Facsai (VIV, Ciliary to and giards 01 otgat%: Iris muscle: Pupil constricted Eye and Trans•ars.o Ascending Lacnmal q Salivary glands: Secretion increased Mcnous an Parotxi . ganglion Pterygopalatine ganglion Submandibular ganglion Glossopharynpaj (tX) Otic ganglion Vagus (X tto T12 Pelvic nerves Coccygeal Atnai rmscle ibers SAiAVnodes Trac*E0 Bronchi aro bie du Stomact Unnary Extern* Ute Structure of the parasympathetic division o Heart: Rate and force of contraction decreased Trachea and bronchi: Bronchoconstriction Liver: Blood vessels dilated Secretion of bile increased Stomach: Secretion of gastric juice and peristalsis increased Intestines: Digestion and absorption increased Kidney: Urine secretion increased Bladder: Muscle of wall contracted Sphincters relaxed Sex organs: Male: erection; Female: variable t e autonomic nervous system
  • 203. Ref: https://backyardbrains.com/experiments/img/AutonomicNervousSystem_web.jpg AUTONOMIC NERVOUS SYSTEM ( INVOLUNTARY ) PARASYMPATHETIC CONSTRICTS PUPIL STIMULATES SALIVA ANP TEAR PRODUCTION CONSTRICTS BRONCHI SCOWS HEART STIMULATES STOMACH, INTESTINES STIMULATES URINATION PROMOTES ERECTION OF GENITALS SYMPATHETIC PILATES PUPIL INHIBITS SALIVA PRODUCTION PILATES BRONCH ACCELERATES HEART STIMULATES EPINEPHRINE ANP NOREPINEPHRINE RELEASE STIMULATES GLUCOSE RELEASE INHIBITS STOMACH, PANCREAS ANP INTESTINES INHIBITS URINATION PROMOTES EJACULATION ANP VAGINA CONTRACTIONS Ref: https://backyardbrains.com/experiments/img/AutonomicNervousSystem_web.jpg
  • 205. Autonomic Motor Pathways • Each division of the ANS has two motor neurons (preganglionic and postganglionic neuron). • Preganglionic Neurons – In the sympathetic division (thoracolumbar division/ thoracolumbar outflow), the preganglionic neurons have their cell bodies in the lateral horns of the gray matter in the 12 thoracic segments and the first two (and sometimes three) lumbar segments of the spinal cord. – In the parasympathetic division (craniosacral division/ craniosacral outflow), the preganglionic neurons have their cell bodies in in the nuclei of four cranial nerves in the brain stem (III, VII, IX, and X) and in the lateral gray matter of the second through fourth sacral segments of the spinal cord. Autonomic Motor Pathways ' Each division of the ANS has two motor neurons (preganglionic and postganglionic neuron). ' Preganglionic Neurons sympathetic division (thoracolumbar division/ — In the thoracolumbar outflow) the preganglionic neurons have their cell bodies in the lateral horns of the gray matter in the 12 thoracic segments and the first two (and sometimes three) lumbar segments of the spinal cord. parasympathetic division (craniosacral division/ — In the craniosacral outflow) the preganglionic neurons have their cell bodies in in the nuclei of four cranial nerves in the brain stem (Ill, VII, IX, and X) and in the lateral gray matter of the second through fourth sacral segments of the spinal cord.
  • 206. Autonomic Motor Pathways Preganglionic Neurons • Autonomic Ganglia – There are two major groups of autonomic ganglia • sympathetic ganglia • parasympathetic ganglia • Sympathetic Ganglia: – The sympathetic ganglia are the sites of synapses between sympathetic preganglionic and postganglionic neurons. – There are two major types of sympathetic ganglia: • sympathetic trunk ganglia (also called vertebral chain ganglia or paravertebral ganglia) • prevertebral ganglia (collateral)- Five types of prevertebral ganglia are celiac ganglion, superior mesenteric ganglion, inferior mesenteric ganglion, aorticorenal ganglion and renal ganglion. Autonomic Motor Pathways Preqanqlionic Neurons ' Autonomic Ganglia — There are two major groups of autonomic ganglia ' sympathetic ganglia ' parasympathetic ganglia ' Sympathetic Ganglia — The sympathetic ganglia are the sites of synapses between sympathetic preganglionic and postganglionic neurons. — There are two major types of sympathetic ganglia: (also called vertebral chain ' sympathetic trunk ganglia ganglia or paravertebral ganglia) (collateral)- Five types of ' prevertebral ganglia prevertebral ganglia are celiac ganglion, superior mesenteric ganglion, inferior mesenteric ganglion, aorticorenal ganglion and renal ganglion.
  • 207. Autonomic Motor Pathways Preganglionic Neurons • Autonomic Ganglia – There are two major groups of autonomic ganglia • sympathetic ganglia • parasympathetic ganglia • parasympathetic ganglia: – Preganglionic axons of the parasympathetic division synapse with postganglionic neurons in terminal (intramural) ganglia. They are the ciliary ganglion, pterygopalatine ganglion, submandibular ganglion, and otic ganglion Autonomic Motor Pathways Preqanqlionic Neurons Autonomic Ganglia — There are two major groups of autonomic ganglia ' sympathetic ganglia ' parasympathetic ganglia ' parasympathetic ganglia — Preganglionic axons of the parasympathetic division synapse with postganglionic neurons in terminal (intramural) ganglia. They are the ciliary ganglion, pterygopalatine ganglion, submandibular ganglion, and otic ganglion
  • 208. Autonomic Motor Pathways Postganglionic Neurons • Once axons of sympathetic preganglionic neurons pass to sympathetic trunk ganglia, they may connect with postganglionic neurons. • A single sympathetic preganglionic fiber has many axon collaterals (branches) and may synapse with 20 or more postganglionic neurons. Autonomic Motor Pathways Postqanqlionic Neurons ' Once axons of sympathetic preganglionic neurons pass to sympathetic trunk ganglia, they may connect with postganglionic neurons. single sympathetic preganglionic fiber has many axon collaterals (branches) and may synapse with 20 or more postganglionic neurons Dendrites covered with dendritic spines Cytoplasm of Schwann cell Synaptic terminals Axon Cell body collateral Nucleus Axon Nodes of Ranvier Axon Nucleus Myelin sheath Schwann Terminal cell branches
  • 209. Autonomic Motor Pathways Postganglionic Neurons • Axons of preganglionic neurons of the parasympathetic division pass to terminal ganglia near or within a visceral effector. In the ganglion, the presynaptic neuron usually synapses with only four or five postsynaptic neurons, all of which supply a single visceral effector, allowing parasympathetic responses to be localized to a single effector. Autonomic Motor Pathways Postqanqlionic Neurons ' Axons of preganglionic neurons of the parasympathetic division pass to terminal ganglia near or within a visceral effector. In the ganglion, the presynaptic neuron usually synapses with only four or five postsynaptic all of which supply a single visceral neurons effector, allowing parasympathetic responses to be localized to a single effector.
  • 211. ANS Neurotransmitters and Receptors ANS Receptor Receptor Sub-type Parasympathetic nervous system Nicotinic cholinergic receptors Nn, Nm Muscarinic cholinergic receptors M1, M2, M3, M4, M5 Sympathetic nervous system α adrenergic receptor α1, α2 β adrenergic receptor β1, β2, β3 Sympathetic nervous system Parasympathetic nervous system ANS Neurotransmitters and Receptors ANS Parasympathetic nervous system Sympathetic nervous system NICOTINIC RECEPTOR Preganglionic neuron Ganglion Receptor Nicotinic cholinergic Muscarinic cholinergic receptors a adrenergic receptor ß adrenergic receptor Effector cell ADRENERGIC RECEPTOR NE Postganglionic neuron Receptor Sub-type Nn, Nm MI, M2, M3, M4, al, a2 ßl, ß2, ß3 MUSCARINIC NICOTINIC RECEPTOR Effector cell RECEPTOR ACh Sympathetic nervous system Parasympathetic nervous system
  • 212. Comparison of Somatic and Autonomic Motor Neurons Comparison of Somatic and Autonomic Motor Neurons