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DR N K AGRAWAL
JNMC,SAWANGI
 What are the properties of an ideal IV agent?
 Should act in one arm brain circulation time
 Should not cause pain on induction
 Should not be irritant
 Should have short half life
 Metabolites should be non active
 Not hepatotoxic
 Should not depend on renal for excretion
 No respiratory depression
 Should cause hallucination
 No dissociation
 Should have hemodynamic stability
 Should not change cerebral blood flow
 Least PONV
 No allergic reaction
 Useful for TIVA
 Derivative of phenol
 Have hypnotic properties
 2-6 disopropofol
 Alkyphenol are oil, highly lipid soluble
 Ctenophore is 1% propofol,10% soybean oil,2.25
glycerol, and 1.2% purified egg
 Fospropofol is USA FDA Aqua van
 1 % excreted in urine,2% feces
 Metabolized hepatic,kidney,lungs
 Elimination Half life is 2-8 min
 Distribution half life is 4min to 23 hrs
 Dose is 1-2 mg/kg
 Infusion is 200ug/kg/min
 Act on GABA
 Directly act on neurons of spinal card
 At dose of 2.5 mg/kg induces hypnosis in
90-100 sec
 It causes sedation,hypnosis,amnesia
 Hypnosis lost for 6-10 min
 Hallicination,sexual fantasis,opisthotonus
have been reported
 High doses are needed for less than 2 yr,with
age dose requirement is reduced
 Decreases arterial BP
 Diastolic BP
 Stroke volume
 Peripheral resistance
 Pawp
 Pulmonary vascular resistance
 HR may or may not
 Myocardial blood flow reduced as well
demand
 Decreases ICT
 Tolerance
 Reduces CPP
 Cp50
 Apnea depends on dose, speed of
injection,concommitent premedication
 Uses and Doses of Intravenous Propofol
 Induction of general anaesthesia 1-
2.5 mg/kg IV dose reduced with increasing
age
 Maintenance of general anaesthesia 50-
150 µg/kg/min IV combined with N2O or an
opiate
 Sedation 25-75 µg/kg/min IV Antiemetic
10-20 mg IV, can repeat every 5-10 min or
start infusion of 10 µg/kg/min N2O, nitrous
oxide.
 Pain on injection
 Hypotension
 Myoclonus
 Apnea
 thromboplhebities
 Highly alkaline
 Prepared with water or normal saline
 Stable for one week
 Not compatible with pan.,vec,atra,sufen,alfen
 Excreted through liver
 Metabolites are inactive, water soluble
,excreted in urine
 Bio transformation in four stage
 oxidation
 desulfuration
 dealkylation
 destruction
 Dose is 4-5 mg/kg
 Half life is 7-17 hrs
 its affinity for fat, relatively large volume of
distribution, and low rate of hepatic
clearance, thiopental can accumulate in
tissues, especially if given in large doses over
a prolonged period. The plasma drug level
increases when repeat doses of drug are
given.
 Act in one arm brain circulation time
 Ultra short acting
 Crosses blood brain barrier
 Bound to albumin
 Dose dependant CNS Depression
 Decreases cerebral metabolic rate
 Protect brain from ischemia
 Reduces CMRO2
 On injection garlic or onion test in 40%
 Allergic reaction
 Irritation
 necrosis
 Infuse normal saline
 Heparin
 Nerve block
 Increases HR
 Peripheral vascular resistance decreased
 Negative inotropic effect
 Fall in cardiac out put
 Decreases ventricular filling
 Decreases sympathetic outflow CNS
 Depression
 Apnea
 Wood has listed the contraindications to IV
barbiturate use.[227]
 (1) When there is respiratory obstruction or an
inadequate airway, thiopental may worsen respiratory
depression.
 (2) Severe cardiovascular instability or shock may
preclude its use.
 (3) Status asthmatics is a condition in which airway
control and ventilation may be worsened further by
thiopental.
 (4) Porphyries may be precipitated or acute attacks
may be accentuated by the administration of
thiopental.
 (5) Without proper equipment (IV instrumentation)
and airway equipment (means of artificial ventilation),
thiopental should not be administered.
 It is imidazole derivative
 Molecular wt 342.69
 Water insoluble
 Ph 6.9
 Dose not precipitate
INTRA VENOUS INDUCING AGENTS
 general anaesthesia 0.2-0.6 mg/kg IV
 Maintenance of general anaesthesia
10 µg/kg/min IV with N2O and an opiate
 Sedation and analgesia Limited to periods of
brief sedation because of inhibition of
corticosteroid synthesis N2O, nitrous oxide.
 The primary action of etomidate on the CNS
is hypnosis,
 which is achieved in one arm–brain
circulation after a normal induction dose
(0.3 mg/kg).
 Etomidate has no analgesic activity. Plasma
levels required for the maintenance of
anaesthesia are approximately 300 to
500 ng/mL, for sedation are 150 to
300 ng/mL, and for awakening are 150 to
250 ng/mL
 mechanism by which etomidate produces
hypnosis is fully known
 Reduces CMR and CBF
 No change in MAP
 CPP maintain or increased
 Dose not affect ventilation
 No histamine release
 No effect on co2 response
 No effect on Pao2
 PACO2 slightly increased
 NO CHANGE IN
 HR,MAP,STROKE VOLUME,CARDIAC
INDEX,PAWP,
 CVP,
 It provide sedation hypnosis, anxiolysis
 Analgesia sympatholysis
 DOSE- 0.25 to 1 mg/kg
 Metabolize in liver
 2%
 Metabolite are active
 85% by kidney
 14% via liver
 Rapidly distributed and extensively
metabolized in liver
 Excreted through urine and feces
 Sensitive half life 4-6 min
 Half life 2-4 hours
 SEDATIVE- the patients are awake and
responsive
 ANALGESIA-good analgesic, when given in
epidural space action within 2-20 min
 Absorbed in CSF Little effect on ICP CBF
 Ventilatory response increased
 Response to co2 increased
 RR increased
 Paco2 increased by 20%
 Decrease in HR-Sympathetic vascular
resistance
 Hence decreases cardiac out put cardiac out
put
INTRA VENOUS INDUCING AGENTS

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INTRA VENOUS INDUCING AGENTS

  • 1. DR N K AGRAWAL JNMC,SAWANGI
  • 2.  What are the properties of an ideal IV agent?  Should act in one arm brain circulation time  Should not cause pain on induction  Should not be irritant  Should have short half life  Metabolites should be non active  Not hepatotoxic
  • 3.  Should not depend on renal for excretion  No respiratory depression  Should cause hallucination  No dissociation  Should have hemodynamic stability  Should not change cerebral blood flow  Least PONV  No allergic reaction  Useful for TIVA
  • 4.  Derivative of phenol  Have hypnotic properties  2-6 disopropofol  Alkyphenol are oil, highly lipid soluble  Ctenophore is 1% propofol,10% soybean oil,2.25 glycerol, and 1.2% purified egg  Fospropofol is USA FDA Aqua van
  • 5.  1 % excreted in urine,2% feces  Metabolized hepatic,kidney,lungs  Elimination Half life is 2-8 min  Distribution half life is 4min to 23 hrs  Dose is 1-2 mg/kg  Infusion is 200ug/kg/min
  • 6.  Act on GABA  Directly act on neurons of spinal card  At dose of 2.5 mg/kg induces hypnosis in 90-100 sec  It causes sedation,hypnosis,amnesia  Hypnosis lost for 6-10 min  Hallicination,sexual fantasis,opisthotonus have been reported  High doses are needed for less than 2 yr,with age dose requirement is reduced
  • 7.  Decreases arterial BP  Diastolic BP  Stroke volume  Peripheral resistance  Pawp  Pulmonary vascular resistance  HR may or may not  Myocardial blood flow reduced as well demand
  • 8.  Decreases ICT  Tolerance  Reduces CPP  Cp50
  • 9.  Apnea depends on dose, speed of injection,concommitent premedication
  • 10.  Uses and Doses of Intravenous Propofol  Induction of general anaesthesia 1- 2.5 mg/kg IV dose reduced with increasing age  Maintenance of general anaesthesia 50- 150 µg/kg/min IV combined with N2O or an opiate  Sedation 25-75 µg/kg/min IV Antiemetic 10-20 mg IV, can repeat every 5-10 min or start infusion of 10 µg/kg/min N2O, nitrous oxide.
  • 11.  Pain on injection  Hypotension  Myoclonus  Apnea  thromboplhebities
  • 12.  Highly alkaline  Prepared with water or normal saline  Stable for one week  Not compatible with pan.,vec,atra,sufen,alfen
  • 13.  Excreted through liver  Metabolites are inactive, water soluble ,excreted in urine
  • 14.  Bio transformation in four stage  oxidation  desulfuration  dealkylation  destruction
  • 15.  Dose is 4-5 mg/kg  Half life is 7-17 hrs  its affinity for fat, relatively large volume of distribution, and low rate of hepatic clearance, thiopental can accumulate in tissues, especially if given in large doses over a prolonged period. The plasma drug level increases when repeat doses of drug are given.
  • 16.  Act in one arm brain circulation time  Ultra short acting  Crosses blood brain barrier  Bound to albumin
  • 17.  Dose dependant CNS Depression  Decreases cerebral metabolic rate  Protect brain from ischemia  Reduces CMRO2
  • 18.  On injection garlic or onion test in 40%  Allergic reaction  Irritation  necrosis
  • 19.  Infuse normal saline  Heparin  Nerve block
  • 20.  Increases HR  Peripheral vascular resistance decreased  Negative inotropic effect  Fall in cardiac out put  Decreases ventricular filling  Decreases sympathetic outflow CNS
  • 22.  Wood has listed the contraindications to IV barbiturate use.[227]  (1) When there is respiratory obstruction or an inadequate airway, thiopental may worsen respiratory depression.  (2) Severe cardiovascular instability or shock may preclude its use.  (3) Status asthmatics is a condition in which airway control and ventilation may be worsened further by thiopental.  (4) Porphyries may be precipitated or acute attacks may be accentuated by the administration of thiopental.  (5) Without proper equipment (IV instrumentation) and airway equipment (means of artificial ventilation), thiopental should not be administered.
  • 23.  It is imidazole derivative  Molecular wt 342.69  Water insoluble  Ph 6.9  Dose not precipitate
  • 25.  general anaesthesia 0.2-0.6 mg/kg IV  Maintenance of general anaesthesia 10 µg/kg/min IV with N2O and an opiate  Sedation and analgesia Limited to periods of brief sedation because of inhibition of corticosteroid synthesis N2O, nitrous oxide.
  • 26.  The primary action of etomidate on the CNS is hypnosis,  which is achieved in one arm–brain circulation after a normal induction dose (0.3 mg/kg).  Etomidate has no analgesic activity. Plasma levels required for the maintenance of anaesthesia are approximately 300 to 500 ng/mL, for sedation are 150 to 300 ng/mL, and for awakening are 150 to 250 ng/mL  mechanism by which etomidate produces hypnosis is fully known
  • 27.  Reduces CMR and CBF  No change in MAP  CPP maintain or increased
  • 28.  Dose not affect ventilation  No histamine release  No effect on co2 response  No effect on Pao2  PACO2 slightly increased
  • 29.  NO CHANGE IN  HR,MAP,STROKE VOLUME,CARDIAC INDEX,PAWP,  CVP,
  • 30.  It provide sedation hypnosis, anxiolysis  Analgesia sympatholysis  DOSE- 0.25 to 1 mg/kg
  • 31.  Metabolize in liver  2%  Metabolite are active  85% by kidney  14% via liver
  • 32.  Rapidly distributed and extensively metabolized in liver  Excreted through urine and feces  Sensitive half life 4-6 min  Half life 2-4 hours
  • 33.  SEDATIVE- the patients are awake and responsive  ANALGESIA-good analgesic, when given in epidural space action within 2-20 min  Absorbed in CSF Little effect on ICP CBF
  • 34.  Ventilatory response increased  Response to co2 increased  RR increased  Paco2 increased by 20%
  • 35.  Decrease in HR-Sympathetic vascular resistance  Hence decreases cardiac out put cardiac out put