test 5 inhalation anesthetics Flashcards
Inhalation Anesthetics
- Maintenance AFTER administration of an IV agent
- Depth of anesthesia rapidly altered by changing concentration
- Very narrow therapeutic indices
* Difference between surgical anesthesia and severe cardiac and respiratory depression is small - No antagonists exist
Inhalation Anesthetics Mechanism of Action
- NO SPECIFIC RECEPTOR IDENTIFIED for how they work
- Variety of molecular mechanisms may contribute
* Increase sensitivity (affinity for GABA) of GABA receptors to inhibitory neurotransmitter GABA
* CNS activity diminished
* Block excitatory postsynaptic currents of nicotinic receptors
* Increased activity of inhibitory glycine receptors in spinal motor neurons
Inhalation Anesthetics- Common Features
- Nonflammable
- Nonexpolosive
- Volatile (Except nitrous oxide, which is gaseous)
- Decrease cerebral vascular resistance= increased brain perfusion
- Bronchodilation with decreased spontaneous respiration
- Depress normal cardiac contractility
Volatile Anesthetics
- require a precision vaporizer for inhalation
• Often incorporated into CPB circuits!
MAC- Minimal Alveolar Concentration
- Median effective dose (ED50) = concentration of the anesthetic at which 50% of the patients will have no movement upon an incision being made
- Effective dose: elimination of movement during a standard incision
- Expressed as percentage of gas in a mixture
Low MAC
- More potent = need a lower percentage of it to reach that ED50
- More lipid soluble
High MAC
- Less potent
- Less lipid soluble
- Nitrous oxide
Factors that increase MAC
- Hyperthermia
- Drugs that ↑ CNS catecholamines
- Chronic ethanol abuse
Factors that decrease MAC
- Hypothermia
- ↑ age
- Acute intoxication
- Pregnancy
- Sepsis
- Concurrent IV anesthetics
- α2 anesthetics
Inhalation Anesthetic Uptake
• GOAL: constant and optimal brain partial pressure of inhaled anesthetic
• MECHANISM: partial pressure drives anesthetic to move => ALVEOLI → BLOOD → BRAIN
• RESULT: partial pressure between alveoli and brain equilibrate and reach a steady state
Palv = Pbld = Pbr
Rate at which equilibration is reached is dependent upo
- Ventilation
- Solubility
- Cardiac output
- Blood flow distribution
Inhalation Anesthetic Uptake: Ventilation
- Replacement of the normal lung gases with the anesthetic mixture
- Controlled by:
* Inspired concentration
* Ventilation rate
Inhalation Anesthetic Uptake: Solubility
• Blood/Gas partition coefficient
• Physical property of the gas
• Low Solubility → little dissolves into blood → few more molecules necessary to increase partial pressure → arterial tension rises rapidly
- small changes can change the anesthetic depth
• High Solubility → dissolves more completely into blood → more molecules dissolve before partial pressure changes significantly → arterial tension increases less rapidly
• Greater amount of anesthetic and longer time required to increase partial pressure in the blood
• Increased time of induction and recovery
• Slower changes in anesthetic depth with increasing concentration
Inhalation Anesthetic Uptake: Cardiac Output
• Higher pulmonary blood flow removes anesthetic from alveoli and slows the rate of rise of alveolar gas concentration
• Longer time for Palv = Pbld = Pbr
• Slower induction
- Blood flowing through the lungs pulls away the anesthetics so it’s hard to reach a high partial pressure
Inhalation Anesthetic Uptake: Blood Flow Distribution
• Alveolar-venous partial
pressure difference
• Driving force of anesthetic delivery
• Dependent on uptake of anesthesia by tissues
• The greater the A-V difference, the longer the time it will take to achieve equilibrium with the brain
- Palv = Pa = Pbr
Recovery From Inhalation Anesthetics
• Same principals in reverse
- blood travels back to your lungs and into the alveoli -> is ventillated -> then out of your body
• Eliminated via ventilation (only metabolized to small extent) (increase ventillation rate to eliminate it faster)
• Less soluble anesthetics eliminated faster than more soluble anesthetics
• Inspired concentration reduced to 0%
• Alveolar ventilation can speed rate of elimination
Inhalation Anesthetics: Halothane
- Prototype (co-administered)
- Mostly replaced due to adverse effects
- Therapeutic uses:
* Potent anesthetic/weak analgesic
* Potent bronchodilator
* Relaxes skeletal and uterine muscle
Halothane Adverse Effects
- Cardiac
* Vagomimetic- bradycardia (atropine sensitive)
* Arrhythmias
* Hypotension - Malignant hyperthermia
Malignant Hyperthermia (MH)
Life threatening hyper-metabolism involving the skeletal muscle Abnormal receptor interferes with calcium regulation Increased CO2 production Heat production Activation of SNS Hyperkalemia DIC Multiple organ dysfunction Death
Isoflurane (Forane)
- Does not induce cardiac arrhythmias
- Pungent odor
- Stimulates respiratory reflexes so not used for induction
- Higher solubility than others- used when cost is a factor
- Dose-dependent vasodilation
* USEFUL FOR PRESSURE CONTROL ON CPB
Sevoflurane (Ultane)
- Low pungency
- Rapid induction without irritation of airways
- Rapid onset and recovery
- Dose-dependent vasodilation
* USEFUL FOR PRESSURE CONTROL ON CPB
Desflurane (Suprane)
- Low solubility= rapid onset and recovery
- Popular for outpatient procedures
- Decreases vascular resistance
- Stimulates respiratory reflexes- no induction
- Relatively expensive so not used during lengthy procedures
Isoflurane (Forane) dosing
- Bottle must be used with appropriate adaptor to fill forane vaporizer on your pump
* Spillage can cause structural degradation of plastic - Set vaporizer at 0.5% to 2% after initiation of gas flow
- Can be temporarily increased for blood pressure control
- Concentrations reduced before termination of CPB to minimize myocardial depressant effects
- Scavenge oxygenator gas outflow when using anesthetic gas (recommended by Prof Gaspar and most people with a conscience)
AMSECT standard about anesthetic gas scavenge
- An anesthetic gas scavenge line shall be employed whenever inhalation agents are introduced into the circuit during CPB procedures
Short term exposure to Isoflurane (Forane)
- Liver and kidney disease
- Headache
- Irritability
- Fatigue
- Nausea
- Drowsiness
- Compromised performance
* Decreased vigilance
* Slow reaction time
Long term exposure to Isoflurane (Forane)
- Miscarriage
- Genetic damage
- Cancer
- Miscarriage and birth defects in the SPOUSES of exposed workers
Approaches for Scavenging (2)
- Gas Deactivation: activated charcoal
2. Gas removal: active gas scavenger system connected to anesthesia machine vents to outside hospital
Perfusion Relevant Approaches
Gas removal:
- Ventilate to the outside
- Ventilate to vacuum source
Perfusion Concerns
- Generation of back pressure into the oxygenator
- Insufficient oxygenation
- Cracks in polycarbonate components due to spilled agent
Nitrous Oxide
- LAUGHING GAS
* Concentration of 30-50% with oxygen - Potent analgesic
- Weak anesthetic
* Commonly combined with other more potent anesthetics - May cause diffusion hypoxia during recovery
* Poor solubility allows rapid movement
* Fills alveoli upon discontinuation (down concentration gradient)
* O2 and CO2 are diluted, PO2 decreases and leads to hypoxia
* Prevention: Ventilate patient with high FiO2