Anjana Assistant Professor Deptt of Veterinary Pharmacology amp Toxicology Bihar Veterinary College Bihar Animal Sciences University Patna INHALATIONAL ANAESTHETICS MAC MAC is the minimum alveolar concentration ID: 926572
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Slide1
Inhalant Anaesthetics
Dr.Kumari
Anjana
Assistant Professor
Deptt
. of Veterinary Pharmacology & Toxicology
Bihar Veterinary College, Bihar Animal Sciences University, Patna
Slide2INHALATIONAL ANAESTHETICS
MAC:
MAC is the minimum alveolar concentration; the
lowest
concentration of the inhalant
anesthetic
in pulmonary alveoli
in producing immobility due to surgical incision in 50% of the individuals
.
It
is the measure of potency of inhalation anaesthetics
.
The
anaesthetic
potency of an inhaled
anaesthetic
is inversely related to MAC.
Potency = 1/MAC; i.e. an agent having low
anaesthetic
potency will have a high MAC value and vice-versa
.
Slide3INHALATIONAL ANAESTHETICS contd
…
Classification
of Inhalational
Anaesthetics
:
Gaseous agents
:
Nitrous
oxide and Cyclopropane
.
Volatile liquids
:
Methoxyflurane
, Halothane, Ether, Chloroform,
Enflurane
,
Isoflurane
,
Desflurane
,
Sevoflurane
.
Slide4Blood: Gas Partition Coefficient
: The blood/ gas solubility is a
measure of the speed of anaesthetic
induction
, recovery and change of
anaesthetic
levels.
Lower
the blood/ gas partition coefficient, the
more
rapid the
anaesthetic
induction
or rate of change of
anaesthetic
level in response to a stepwise change in
anaesthetic
delivery
.
Slide5Oil:
Gas Partition Coefficient:
A measure of fat solubility, determines the potency of an
anaesthetic
and also influences the kinetics of its distribution in the body, the main effect being that high lipid solubility delays recovery from
anaesthesia
.
Slide6Volatile Anaesthetics
Parameter
Ether
Halothane
Methoxyflurane
Properties
Characteristic
oduour
and sweetish taste. Oxidizes to peroxides (irritate resp. tract) upon exposure to moisture.
Characteristic sweetish
odour
. Decomposes upon exposure to sunlight (0.10%
thymol
is added as preservative).
Characteristic pungent
odour
. Decomposes upon exposure to sunlight. Butylated
hydroxytoulene
is added as preservative.
MAC (%)
3
Least
potent.
Slow
induction
0.75-1.20
.
Induction 3-5 min
0.23
Slow
induction (10 min)
CNS
All stages are seen
Stage II bypassed
Stage II bypassed
CVS
Induction- release of adrenaline: increase in heart rate & BP. Stage III: Fall in BP and COP (depression of VM centre). Does not sensitize heart to
catecholamines
.
Direct myocardial depression (reducing
intracellutar
Ca
++
). Sensitizes heart to
catcholamines
(arrhythmia)
No change in heart rate or mild tachycardia. Adrenaline can induce cardiac arrhythmia.
Slide7Respiration
Initial stimulation followed by progressive depression. Increase bronchial secretion.
Depression with increase in duration of
anaethesia
, may develop acidosis.
Initial stimulation followed by progressive depression with increase in
anaethesia
.
SK. Muscle relaxation
Sig. effect. Dose of
dTC
to be reduced to one-third
Low to satisfactory relaxation.
dTC
can be used if needed.
Adequate relaxation dTC can be used if needed.
Liver
Prolonged anesthesia lowers liver glycogen. Not hepatotoxic
Hepatotoxic like chloroform
No significant effect
Kidney
Long duration: oliguria/anuria due to ADH release
No significant effect
No significant effect
Body Temperature
Hypothermia
Malignant hyperthermia in pig and horse (
persisten
muscle contraction due release of Ca
++
from
sarcoplasmic
reticulum) and hypothermia in others.
Hypothermia
Slide8Foetus
& Uterus
No significant effect
Reduce uterine contractions
.
Neutralizes oxytocin. Readily crosses placenta.
Reduce uterine
contractions
Neutralizes
oxytocin
. Readily crosses placenta.
GIT
Nauses
& vomition common during induction or recovery.
No vomition during induction or recovery.
Nauses
& vomition common during induction or recovery
Merits
Safest in small animals with proper premedication
.
Ready control of
anaethesia
. Good analgesia, muscle relaxation. Cheap.
No
costly equipment is needed.
Potent; used in small or large animals; rapid induction (3-5 min) & recovery (10-15 min): nonirritant, ready control of
anaesthesia
(low blood solubility), nonflammable &
nonexplosive
Most potent
.
Can be used in small or large animals.
Excellent
muscle relaxation and analgesia. Nonflammable.
Slide9Demerits
Highly flammable. Difficult to use in hot climate. irritant to resp. tract. Delayed induction without proper premedication
Resp.
and
cardiac
depression and poor muscle relaxation and analgesia. Malignant hyperthermia in pig and horse.
Expensive
(requires closed circuit apparatus)
Easy control of
anaesthesia
not possible (high blood solubility).
Recovery
prolonged.
Poor
vaporization.
Needs
close circuit apparatus
Contra-
indications
Aminoglycoside
antibiotics (synergistic curariform effect)
Aminoglycoside antibiotics (synergistic
curariform
effect), catecholamine’s and Ca Channel blockers. CHF
Noradrenalin or epinephrine without premedication
Uses
Not used in human or
vety
, surgery.
Mainly
use in lab animals for surgery or euthanasia
Used in small and large (horse) animals, mainly for maintenance (2-8 ml/45 kg/
hr
) of
anaesthesia
with NO
2
, after induction by ultra-short acting barbiturate.
Used in small or large animal surgery for induction (3% MF+N
2
O(70%)+O
2
(27%) and maintenance (2-3%)
Slide10Enflurane
A colorless, pungent, nonflammable volatile liquid, chemically related to methoxyflurane
. The most frequently
used potent
anaesthetic
in human
surgery.
It
is classified as a
convulsive
anaesthetic
(epilepsy like seizures;
disscociative
-cataleptic
anaesthesia
).
Its
MAC for
horse
is 2.12
%.
It
causes
CNS excitation in dogs
causing muscular twitching (face, neck,
limb
and abdomen) if diazepam
preanaethesia
is not given.
In
comparison to halothane this does not sensitize heart to catecholamine’s and has more depressant action on respiration and
better muscle relaxation
.
Slide11Isoflurane
Though an isomer of enflurane does not cause CNS excitation.
It is about one and half times more potent
than
enflurane
MAC 1.3
%.
It provides
satisfactory skeletal muscle relaxation
(synergistic neuromuscular blockade with curariform
agents).
Slide12Chloroform
It is replaced
by other safer anaesthetics, sometimes used for euthanasia.
Its use is associated
with
risk of death
of the animal during induction, prolonged
anaesthesia
and during
post-
anaesthetic
period.
During
induction majority of deaths
occur due to direct toxic effect on heart.
During
stage I the animal tries to avoid inhaling chloroform
vapours
by temporary
breath-holding
, which is followed by reflex
deep breathing
taking a high concentration of chloroform
vapours
into lungs, from there through pulmonary veins into the heart, causing ventricular fibrillation
and/or
cardiac arrest
.
Cardiac toxicity may be
avoided by proper premedication
(sedatives) and slow administration of chloroform.
Prolonged surgical
anaesthesia
may cause
respiratory failure
due depression of medullary respiratory centre.
exposure to
air and light
chloroform
gets oxidized to
phosgene gas
(a marked lung irritant).
Phosgene formation is prevented by
adding ethyl alcohol @ 1 per cent.
Nitrous Oxide (N2
O; Laughing gas)
It is discovered by
joseph Priestly (1772).
It
is a colorless nonirritating and nonflammable gas.
It
causes
excitement, delirium and amnesia in humans
, hence the name laughing gas
.
Has very low
anaesthetic
potency
(MAC 188 (cat) 255 (dog)%)
and hence must be combined with other inhalation anaesthetics (halothane or
methoxyflurone
).
It has good analgesic, but poor muscle relaxant effects.
To
avoid hypoxia, it is used in combination with oxygen (nitrous oxide 70% oxygen 25%) and other inhalation
anaesthetic
(0.2 – 2
%).
Slide14Cyclopropane
Colorless gas with a characteristic
odour.
It
can be used in small animal surgery of short duration after diluting with oxygen (4 times) through a closed circuit system
.
Morphine premedication and
catechloamines
are contraindicated due to marked respiratory depression and cardiac arrhythmic respectively
.
It causes adequate skeletal muscle relaxation. It forms flammable mixture with air
.
Slide15Thank You