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Barbiturates
Dr. S. Parthasarathy
MD., DA., DNB, MD (Acu), Dip. Diab.
DCA, Dip. Software statistics-
PhD ( physiology), IDRA
Synthesis
Barbituric acid is not hypnotic
-substitution of 2 and 5 -
Thiobarbituratesoxybarbiturates
Thiobarbiturates
• Thiobarbiturates are
• more lipid soluble,
• has more rapid onset
• and shorter duration of action.
• Oxy barbiturates – excitatory phenomena
• is acidic in nature due to the presence of H+ at
position 1.
• However, the Na+ salt (at position 3) of
barbituric acid is water soluble yielding highly
alkaline solution
History
• 1864 – barbituric acid
• 1903 – diethyl barbituric acid
• 1934 – thiopental
• Volviler , Tabern
• Ralph waters
• Lundy
Some history
• Thiopentone – rapid action and rapid removal –
they thought
• High doses and deaths
• Ideal method of euthanasia
• War casualties in pearl harbor –tragedy
(7th December 1941)
• Brodie and price – redistribution and not
elimination – cause of termination of action
• Don’t saturate the peripheral sites !!
UK or USA
• Thiopentone
• Or
• Thiopental
Classification
• Long acting
• Short acting
• ultra short acting
• Not valid
Chemistry
• Commercially available sodium thiopentone is a pale yellow,
hygroscopic amorphous powder with a smell of hydrogen
sulphide. ? garlic
• The powder contains mixture of 6 parts anhydrous sodium
carbonate as buffer (60 mg/g of thiopental sodium) to
prevent precipitation of the insoluble acid form of
barbiturate by atmospheric carbon dioxide.
• For the above reason, it is prepared in atmosphere of
nitrogen.
Chemistry
• Yellow colour is due to the presence of
sulphur molecule.
• The powder is soluble in distilled water,
normal saline and alcohol
• pH of 2.5% solution is 10.5 which is highly
alkaline
• pKa = 7.60. – deep breath – alkali – less drug
Short acting , ultra short acting – classification –
obsolete
• These highly alkaline solutions are
incompatible for mixture with drugs in acidic
solutions such as opioids, catecholamines,
neuromuscular blocking drugs.
• Block cannula
• No pain on injection
• The bacteriostatic properties of commercial
preparations are due to their highly alkaline pH.
• NO anti- bacterial agents.
• The powder form is stable at room temperature
indefinitely. The reconstituted solution (2.5%) is stable
and sterile for 6 days (? One day ) at room temperature
(22*C) and for 2 weeks at 4 – 8*C.
• Throw out Cloudy solution.
Dosage and route
• The usual IV induction dose of thiopental is
• 3 to 5 mg/kg in adults,
• 5 to 6 mg/kg in children,
• 6 to 8 mg/kg in infants.
• (premedication and age !!)
• Rectal – 6-10 mg / kg
• methohexital 1.5 mg/kg
Calculated
dose
Vs
titrated
dose
• Acutely inebriated
• Less dose
• Chronic alcoholism
• More dose
Loss of eyelash
reflex
Deep sigh
Apnea
Tidal volume
depression than
rate
Mechanism
• GABA A receptor –
• Chloride channels
• Hyperpolarization of
nerve cell -----
• Glutamate antagonism
• Na channel blockade
Pharmacokinetics
• Volume of distribution at steady-state (Vd): 1.7 to
2.5 L/kg; may increase to 4.1 L/kg during pregnancy
at term and to 7.9 L/kg in obese patients.
• Clearance – 3.4 ml /kg/min.
• Protein binding: high protein binding, with albumin
ranging from 72 to 86%.
• Decreased protein binding due to hypoproteinemia
(cirrhosis of liver) or other causes – more action
Redistribution
• Onset
• 15 – 30 seconds
• Duration - 5 – 10
minutes
• Metabolized by the
liver and mostly
excreted as inactive
products
Pharmacodynamics
• Dose dependent depression of cerebral cortex,
ascending reticular activating system and medullary
centre resulting in sedation, hypnosis, anaesthesia,
respiratory depression.
• Decrease in Cerebral metabolic oxygen consumption,
• Reduction of MAP ,CBF and ICP ( CPP is OK )
• Anticonvulsant effect Isoelectric EEG, (not with
methohexitone )
• Antanalgesic effect
Neuroprotection
• It has been suggested that barbiturates also possess
“neuroprotective” properties secondary to their
ability to decrease oxygen demand. Alternative
explanations have been suggested, including a
reverse steal (“Robin Hood effect”) on CBF,
• free-radical scavenging,
• stabilization of liposomal membranes,
Neuroprotection
• experts have concluded that barbiturates have no
place in the therapy following resuscitation of a
cardiac arrest patient.
• In contrast, barbiturates are frequently used for
cerebroprotection during incomplete brain ischemia
• (e.g., carotid endarterectomy, temporary occlusion
of cerebral arteries, profound hypotension, and
cardiopulmonary bypass).
• 15 mg / kg with 7 mg/kg/hour doses
Cardiovascular
• Peripheral vasodilation
• Myocardial depressant
• Blood pressure falls
• More with metho because tachycardic
response is less
• On beta blocker beware !!
• Depression of ventilation
• Decreased sensitivity of respiratory centre to
increase in carbon dioxide.
• Apnoea may be present in 30- 40% cases.
• But laryngeal and bronchial reflexes are not
much depressed in low doses
• Laryngospasm and bronchospasm
Others
• Decrease hepatic blood flow – not much
• Enzyme induction
• Modest decrease in renal blood flow
• Placental transfer is present but acceptable
• Decrease IOP
Clinical uses
• Induction of anesthesia
• Maintenance of anesthesia ( 50 mg / 12
minutes
• Sedation
• Increased ICP - 3 mg/kg
• Anticonvulsant
• Neuroprotection
• Narcoanalysis
Truth serum
• The maddening thing about Truth Serum, and
the damage over the years, is that its
conceptual originator, Dr Robert House,
meant it to exonerate prisoners.
• They spoke automatically and unthinkingly,
• Find out truths
Contraindications
• Acute intermittent porphyria (thiopentone induces
mitochondrial enzyme D- aminolevulinic acid synthetase. As a
result, production of heme is accelerated, and acute
intermittent porphyria may be precipitated in susceptible
patients, (paralysis, collapse )
• 2. Barbiturate allergy
• 3. H/O paradoxic excitation
• 4. Status asthmaticus:
Think before thio
• Shock states
• Stenotic valve states , Rt to left shunts
• Hepatic dysfunction
• Myxedema
• Muscle dystrophies
• On disulfiram
• Thermally injured may need more
Intra arterial injection
• Aberrant ulnar artery superficial to biceps tendon
• The pH of 2.5% drug solution is 10.5 (strong alkali).
When it is injected into artery and mixed with blood
(pH= 7.4= less alkaline) it gets precipitated as solid
crystals of thiopentone and haemoglobin.
• local inflammation and blocks small arterioles,
vasospasm due to local release of noradrenaline.
Intra arterial injection
• Pain
• Blanching
• Edema
• gangrene
• No anesthesia
Five days for
gangrene ??
5 % is very dangerous
that’s why its prepared as
2.5 % or less
Treatment options
• Stop injection
• Leave the needle – dilute with saline
• Inject local and papavarine intra arterial
• 40 – 80 mg
• Inject heparin IV
• Stellate ganglion block
Why not
venous ??
Other side effects
• Euphoria, vertigo, restlessness
• Allergy
• Immunosuppression
• Hemolytic anemia
• Tolerance and physical dependence
• Localized muscle spasm and pronation –
narcotics will lessen
Summary
• Barbiturates – oxy and thio
• Acidic but sodium salt – preparation vials
• History – euthanasia and pearl harbour
• Mechanism
• Dosage and Redistribution
• Effects
• Indications
• Contra indications
• Side effects
Thank you all

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Barbiturates

  • 1. Barbiturates Dr. S. Parthasarathy MD., DA., DNB, MD (Acu), Dip. Diab. DCA, Dip. Software statistics- PhD ( physiology), IDRA
  • 3. Barbituric acid is not hypnotic -substitution of 2 and 5 -
  • 5. Thiobarbiturates • Thiobarbiturates are • more lipid soluble, • has more rapid onset • and shorter duration of action. • Oxy barbiturates – excitatory phenomena
  • 6. • is acidic in nature due to the presence of H+ at position 1. • However, the Na+ salt (at position 3) of barbituric acid is water soluble yielding highly alkaline solution
  • 7. History • 1864 – barbituric acid • 1903 – diethyl barbituric acid • 1934 – thiopental • Volviler , Tabern • Ralph waters • Lundy
  • 8. Some history • Thiopentone – rapid action and rapid removal – they thought • High doses and deaths • Ideal method of euthanasia • War casualties in pearl harbor –tragedy (7th December 1941) • Brodie and price – redistribution and not elimination – cause of termination of action • Don’t saturate the peripheral sites !!
  • 9. UK or USA • Thiopentone • Or • Thiopental
  • 10. Classification • Long acting • Short acting • ultra short acting • Not valid
  • 11. Chemistry • Commercially available sodium thiopentone is a pale yellow, hygroscopic amorphous powder with a smell of hydrogen sulphide. ? garlic • The powder contains mixture of 6 parts anhydrous sodium carbonate as buffer (60 mg/g of thiopental sodium) to prevent precipitation of the insoluble acid form of barbiturate by atmospheric carbon dioxide. • For the above reason, it is prepared in atmosphere of nitrogen.
  • 12. Chemistry • Yellow colour is due to the presence of sulphur molecule. • The powder is soluble in distilled water, normal saline and alcohol • pH of 2.5% solution is 10.5 which is highly alkaline • pKa = 7.60. – deep breath – alkali – less drug Short acting , ultra short acting – classification – obsolete
  • 13. • These highly alkaline solutions are incompatible for mixture with drugs in acidic solutions such as opioids, catecholamines, neuromuscular blocking drugs. • Block cannula • No pain on injection
  • 14. • The bacteriostatic properties of commercial preparations are due to their highly alkaline pH. • NO anti- bacterial agents. • The powder form is stable at room temperature indefinitely. The reconstituted solution (2.5%) is stable and sterile for 6 days (? One day ) at room temperature (22*C) and for 2 weeks at 4 – 8*C. • Throw out Cloudy solution.
  • 15. Dosage and route • The usual IV induction dose of thiopental is • 3 to 5 mg/kg in adults, • 5 to 6 mg/kg in children, • 6 to 8 mg/kg in infants. • (premedication and age !!) • Rectal – 6-10 mg / kg • methohexital 1.5 mg/kg Calculated dose Vs titrated dose
  • 16. • Acutely inebriated • Less dose • Chronic alcoholism • More dose Loss of eyelash reflex Deep sigh Apnea Tidal volume depression than rate
  • 17. Mechanism • GABA A receptor – • Chloride channels • Hyperpolarization of nerve cell ----- • Glutamate antagonism • Na channel blockade
  • 18. Pharmacokinetics • Volume of distribution at steady-state (Vd): 1.7 to 2.5 L/kg; may increase to 4.1 L/kg during pregnancy at term and to 7.9 L/kg in obese patients. • Clearance – 3.4 ml /kg/min. • Protein binding: high protein binding, with albumin ranging from 72 to 86%. • Decreased protein binding due to hypoproteinemia (cirrhosis of liver) or other causes – more action
  • 19. Redistribution • Onset • 15 – 30 seconds • Duration - 5 – 10 minutes • Metabolized by the liver and mostly excreted as inactive products
  • 20. Pharmacodynamics • Dose dependent depression of cerebral cortex, ascending reticular activating system and medullary centre resulting in sedation, hypnosis, anaesthesia, respiratory depression. • Decrease in Cerebral metabolic oxygen consumption, • Reduction of MAP ,CBF and ICP ( CPP is OK ) • Anticonvulsant effect Isoelectric EEG, (not with methohexitone ) • Antanalgesic effect
  • 21. Neuroprotection • It has been suggested that barbiturates also possess “neuroprotective” properties secondary to their ability to decrease oxygen demand. Alternative explanations have been suggested, including a reverse steal (“Robin Hood effect”) on CBF, • free-radical scavenging, • stabilization of liposomal membranes,
  • 22. Neuroprotection • experts have concluded that barbiturates have no place in the therapy following resuscitation of a cardiac arrest patient. • In contrast, barbiturates are frequently used for cerebroprotection during incomplete brain ischemia • (e.g., carotid endarterectomy, temporary occlusion of cerebral arteries, profound hypotension, and cardiopulmonary bypass). • 15 mg / kg with 7 mg/kg/hour doses
  • 23. Cardiovascular • Peripheral vasodilation • Myocardial depressant • Blood pressure falls • More with metho because tachycardic response is less • On beta blocker beware !!
  • 24. • Depression of ventilation • Decreased sensitivity of respiratory centre to increase in carbon dioxide. • Apnoea may be present in 30- 40% cases. • But laryngeal and bronchial reflexes are not much depressed in low doses • Laryngospasm and bronchospasm
  • 25. Others • Decrease hepatic blood flow – not much • Enzyme induction • Modest decrease in renal blood flow • Placental transfer is present but acceptable • Decrease IOP
  • 26. Clinical uses • Induction of anesthesia • Maintenance of anesthesia ( 50 mg / 12 minutes • Sedation • Increased ICP - 3 mg/kg • Anticonvulsant • Neuroprotection • Narcoanalysis
  • 27. Truth serum • The maddening thing about Truth Serum, and the damage over the years, is that its conceptual originator, Dr Robert House, meant it to exonerate prisoners. • They spoke automatically and unthinkingly, • Find out truths
  • 28. Contraindications • Acute intermittent porphyria (thiopentone induces mitochondrial enzyme D- aminolevulinic acid synthetase. As a result, production of heme is accelerated, and acute intermittent porphyria may be precipitated in susceptible patients, (paralysis, collapse ) • 2. Barbiturate allergy • 3. H/O paradoxic excitation • 4. Status asthmaticus:
  • 29. Think before thio • Shock states • Stenotic valve states , Rt to left shunts • Hepatic dysfunction • Myxedema • Muscle dystrophies • On disulfiram • Thermally injured may need more
  • 30. Intra arterial injection • Aberrant ulnar artery superficial to biceps tendon • The pH of 2.5% drug solution is 10.5 (strong alkali). When it is injected into artery and mixed with blood (pH= 7.4= less alkaline) it gets precipitated as solid crystals of thiopentone and haemoglobin. • local inflammation and blocks small arterioles, vasospasm due to local release of noradrenaline.
  • 31. Intra arterial injection • Pain • Blanching • Edema • gangrene • No anesthesia Five days for gangrene ?? 5 % is very dangerous that’s why its prepared as 2.5 % or less
  • 32. Treatment options • Stop injection • Leave the needle – dilute with saline • Inject local and papavarine intra arterial • 40 – 80 mg • Inject heparin IV • Stellate ganglion block Why not venous ??
  • 33. Other side effects • Euphoria, vertigo, restlessness • Allergy • Immunosuppression • Hemolytic anemia • Tolerance and physical dependence • Localized muscle spasm and pronation – narcotics will lessen
  • 34. Summary • Barbiturates – oxy and thio • Acidic but sodium salt – preparation vials • History – euthanasia and pearl harbour • Mechanism • Dosage and Redistribution • Effects • Indications • Contra indications • Side effects