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266 Cards in this Set
- Front
- Back
Do Volatile inhalation agents depress the Autonomic Nervous System? If so, what part(s)?
|
YES; depresses both the SNS and the PNS
|
|
Which 3 agents inhibit preganglionic sympathetic efferent activity?
|
Halothane, Enflurane and Isoflurane
|
|
Which 3 agents reduce postganglionic sympathetic nerve activity?
|
Halothane, Enflurane adn Isoflurane
|
|
Which 3 agents block postsynaptic nicotinic receptors in the stellate ganglion?
|
Halothane, Enflurane and Isoflurane
|
|
Which 3 aqents induce reductions in norepinephrine release from postganglionic sympathetic nerves?
|
Halothane, Enflurane and Isoflurane
|
|
Which 3 agents may contribute to depression of reflex vasoconstriction in peripheral blood vessels?
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Halothane, Enflurane and Isoflurane
|
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Does Halothane inhibit the Parasympathetic Nervous System (PNS)?
|
YES
|
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TRUE/FALSE: Halothane depresses vagal nerve efferent activity
|
TRUE
|
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Halothane inhibits reflex _____ in response to increases in arterial pressure
|
BRADYCARDIA
|
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Which 2 IAs have equivalent depression of PNS and SNS?
|
Halothane and Isoflurane
|
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Does Halothane depress the baroreceptor reflex control of arterial pressure?
|
YES
|
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Does Halothane depress the sympathetic responses to declines in arterial pressure (such as increased HR in response)?
|
YES
|
|
With Halothane the HR stays stable with increasing MAC concentration; Although the BP is dropping with increasing MAC, HR stays low and stable; what does this mean?
|
the Baroreceptor reflex is NOT intact; Halothane depresses this reflex
|
|
What effect does Halothane have on myocardial contractility?
|
dose related depression of myocardial contractility
|
|
Which 2 IAs have a higher dose-related depression of myocardial contractility than Isoflurane?
|
Halothane and Enflurane
|
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What effect does Halothane and Isoflurane have on preload and afterload?
|
Halothane and Isoflurane produce beneficial decreases in LV preload and afterload in patients eith heart failure and coronary artery disease
|
|
What inotropic effect does Halothane produce?
|
Negative inotropic effects
|
|
What are the negative inotropic effects from Halothane caused by?
|
Alterations in intracellular Ca++
|
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The negative inotropic effects of Halothane and Enflurane cause a depression of what?
|
BP
|
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Routine BP meds such as Beta Blockers and Calcium channel blockers may increase the _____ of BP depression caused by admin. of Halothane or Enflurane
|
magnitude
|
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Although some IAs depress BP, should routine blood pressure medications be continued despite this?
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YES
|
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Does Halothane cause bradycardia or tachycardia?
|
Bradycardia
|
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Is Halothane-induced bradycardia more problematic in adults or peds? Why?
|
Peds; because their BP depends on their HR
|
|
How does Halothane cause bradycardia?
|
Slows the rate of SA node discharge by direct and indirect effects on SA node automaticity; also prolongs AV conduction time and refractoriness
|
|
What drug should you have ready when giving a Pediatric patient Halothane (due to its bradycardic effects)?
|
Atropine
|
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Which IA sensitizes the myocardium to the arrhythmogenic effects of Epinephrine?
|
Halothane
|
|
Which IA reduces the threshold for atrial and ventricular arrhythmias?
|
Halothane
|
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When escalating doses of epinephrine (endogenous or exogenous) is combined with admin. of _____ (IA), PVCs and sustained ventricular tachyarrhythmias are more likely to occur
|
Halothane
|
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TRUE/FALSE: When administering Halothane you should avoid the coadmin. of Epinephrine
|
TRUE
|
|
If patient is to receive Halothane during surgery, why is it important to keep patient calm before/during surgery?
|
to avoid increases in endogenous Epinephrine levels
|
|
What drug can you give patient pre-op to keep them calm in an attempt to decrease/limit endogenous Epi levels?
|
Versed
|
|
When administering Halothane, Epinephrine coadmin needs to be avoided or severely limited; if it's necessary to give Epi, what is the recommended concentration and dosage?
|
1:100,000 (0.1 mg/10 minutes)
1:100,000 (0.3 mg/hour) |
|
0.5% Lidocaine s.q. given with Epi allows you to ____ the dose of Epi you can safely administer with Halothane. Why?
|
Double; because of the cardioprotective effects of Lidocaine
|
|
Halothane causes what changes in PCO2 above 1 MAC? Why does this occur?
|
slight Increase in CO2; occurs because of the Decrease in TV
|
|
What effect does Halothane have on TV?
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Decreases
|
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What effect does Halothane have on RR?
|
Increases
|
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What net effect does Halothane have on overall minute volume?
|
Fairly stable
|
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All IAs depress the response to ______
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HYPOXIA
|
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the depressed response to hypoxia that occurs with IAs can ve overcome by doing what?
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Stimulating the patient
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Which IA depresses the response to hypoxia more severely than other IAs without external stimuli?
|
Halothane
|
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When administering Halothane to a COPD patient is it good to allow them to ventilate spontaneously or to use mechanical ventilation? Why?
|
Mechanical Ventilation; Halothane depresses the hypoxic drive to breathe (which is what COPD patients depend on); mechanical ventilation would be most appropriate
|
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What effect does Halothane have on GFR and renal blood flow?
|
Decreases both
|
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Does Halothane decrease or increase urinary output? Why?
|
Decrease; decreased due to decreased CO and decreased BP; autoregulation of renal blood flow is intact
|
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What intervention is important when giving Halothane to prevent Halothane-induced decrease in GFR, renal blood flow and decreased urinary output?
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Give them fluids; pre-op hydration abolishes or attenuates these effects
|
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What effect does Halothane have on uterine muscle?
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relaxes uterine muscle and inhibits contractions
|
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Does Halothane rapidly cross the placenta?
|
YES
|
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What's a disadvantage for using Halothane alone in a C-section patient? What combo is recommended to use instead?
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Increases blood loss; use 0.5 MAC of Halothane and 0.5 MAC of N2O
|
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While Halothane causes uterine relaxation and can cause excessive bleeding, how can this be useful in a postpartum patient?
|
valuable for uterine relaxation to help remove retained placenta fragments; retained placenta fragments can cause a woman to bleed to death!
|
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Halothane undergoes 2 pathways for metabolism; what are they?
|
Reduction (Low O2)
Oxidative (ample O2) |
|
When Halothane undergoes the Oxidative metabolic pathway, what is it metabolized to?
|
Trifluoroacetic Acid
|
|
All Fluorinated Volatile IAs (EXCEPT Sevoflurane) may produce what metabolite?
|
Trifluoroacetic Acid
|
|
Trifluoroacetic acid is detected in the urine for how long?
|
Many days
|
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In genetically susceptible patients, an antigen is formed that provokes the formation of antibodies to the Trifluoroacetic Acid metabolite of Halothane; this sensitivity reaction is called what?
|
"Halothane Hepatitis"
|
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Which fluorinated IA is the only one that will NOT produce the Trifluoroacetic Acid metabolite?
|
Sevoflurane
|
|
Trifluoroacetic Acid cross sensitivity may occur between which 3 fluorinated IAs?
|
Halothane, Enflurane and Isoflurane
|
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Which fluorinated IA is the least metabolized IA and therefore the least likely to cause hepatic damage?
|
Desflurane
|
|
First reports of liver damage associated with Halothane occurred in _____ (year)?
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1958
|
|
What's the incidence of the "mild form" of "Halothane Hepatitis?" The severe form?
|
Mild form=1:5
severe form=1:10,000 |
|
The mild form of Halothane Hepatitis causes what kind of necrosis? The severe form?
|
Mild form=Focal Necrosis
Severe Form=Massive Hepatic Necrosis |
|
The mild form causes mild elevation of what liver enzymes?
|
ALT, AST
|
|
The severe form of Halothane Hepatitis causes a marked elevation of what liver enzymes?
|
ALT, AST, Bilirubun, Alkaline Phosphatase
|
|
What is the mortality rate of the severe form of Halothane Hepatitis?
|
50%
|
|
Is Halothane a potential triggering agent for Malignant Hyperthermia?
|
YES
|
|
Which agent has replaced Halothane as an induction agent for children in the U.S?
|
Sevoflurane
|
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Pro-arrhythmic potential has been confirmed with the use of Halothane; how would you treat Halothane-induced dysrythmias?
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Treat with Lidocaine
|
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Chemically, Ethrane (Enflurane) is an _____.
|
Ether
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Why is it important NOT to hyperventilate a patient on Ethrane (Enflurane)?
|
Decreasing PaCO2 < 30 torr causes SEIZURE activity
|
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Administering Ethrane above ____ MAC concentrations can cause seizure activity
|
above 2 MAC
|
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If patient on Ethrane (Enflurane) has seizure activity and they are at a MAC concentration above 2, what do you do?
|
Treat by decreasing MAC, returning to normocarbia
|
|
Does increasing MAC of Enflurane (Ethrane) lead to electrical silence (EEG)?
|
NO; can't depress electrical activity of the brain like you can with other agents
|
|
With Ethrane admin. is autoregulation of Cerebral Blood Flow (CBF) completely intact?
|
NO; however increases in BP/MAP cause SMALLER increases in brain perfusion than with Halothane admin
|
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With Ethrane admin, autoregulation of CBF stays relatively normal and stable until approx. what MAC?
|
0.6 MAC
|
|
What effect does Ethrane (Enflurane) have on CSF production and absorption?
|
Increased rate of production and decreased absorption
|
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Because Ethrane increases production and decreases absorption of CSF, what effect does this most likely have on ICP?
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May increase ICP
|
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What 3 factors increase ICP with Ethrane admin?
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increase in CBF, seizure activity, and increased CSF production
|
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What factor decreases ICP with Ethrane admin?
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LOW MAP
|
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Enflurane depresses the Myocardium to a greater extent than which 2 other IAs?
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Halothane and Isoflurane
|
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Enflurane (Ethrane) has what effect on PaCO2?
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Greatly increases PaCO2;
|
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Because Enflurane greatly increases the PaCO2 level in the patient, is it a good drug to chhose for a patient who is going to breathe spontaneously?
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NO
|
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What effect does Enflurane have on TV?
|
Decreases TV
|
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What effect does Enflurane have on RR?
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Increases
|
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What effect does Enflurane have on Minute Ventilation?
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Decreases
|
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Metablism of Enflurane produces what kind of an ion?
|
Inorganic Fluoride ion
|
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Even low fluoride ion concentrations have been associated with a 25% decrease in maximum urine _____ ability
|
Concentrating
|
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Because Enflurane metabolizes into a fluoride ion, what effect does this have on renal function?
|
May temporarily alter renal function
|
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Should you administer Ethrane to patients with pre-existing renal disease?
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NO; may be harmful
|
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Which IA produced the highest serum Fluoride concentrations when metabolized which is why we no longer use it anymore due to its harmful renal effects?
|
Methoxyflurane (Penthrane)
|
|
Does Ethrane produce dose-related skeletal muscle relaxation or rigidity? How?
|
Relaxation; depresses NM function
|
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Does admin of Ethrane potentiate or inhibit muscle relaxants?
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Potentiate
|
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Because Ethrane produces good muscle relaxation, its use may be adequate for what type of surgery?
|
Abdominal
|
|
Usage of Muscle Relaxants allows the dose of Ethrane to be _____.
|
Decreased (synergistic)
|
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Ethrane has a lower incidence of liver damage due to its low degree of ______.
|
Biodegration
|
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Which IA, Halothane or Ethrane, has a higher degree of biodegration?
|
Halothane
|
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Which IA has the highest incidence of biodegration and therefore the highest incidence of liver damage?
|
Halothane
|
|
How is Ethrane metabolized (which pathway)?
|
Oxidative metabolism
|
|
What percentage of Ethrane is metabolized?
|
2.5%
|
|
Although Ethrane is not used in the U.S. anymore, why is it often used in 3rd world countries?
|
It's CHEAP
|
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Structurally, Isoflurane is very similar to which other IA with only one difference? What is that difference?
|
Similar to Desflurane; the Cl- atom in Isoflurane is replaced by a Fluorine atom in Desflurane
|
|
Chemically, what is Forane (Isoflurane) called?
|
a Halogenated methyl, ethyl ether
|
|
Isoflurane (Forane) is an isomer of what other IA?
|
Enflurane (Ethrane)
|
|
Is Isoflurane flammable?
|
NO
|
|
Does Forane (Isoflurane) have a preservative?
|
NO
|
|
Is IV induction with Isoflurane (Forane) more or less rapid than Halothane and Ethrane?
|
More rapid
|
|
What is the major problem with performing a mask induction with Forane?
|
It's irritable to the airway, therefore causing slower inductions (ppl cough, hold their breath,etc; they don't breathe it in as readily)
|
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Recovery with Isoflurane (Forane) is more or less rapid than Enflurane?
|
more rapid
|
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Recovery with Isoflurane (Forane) is more or less rapid than Halothane?
|
Less rapid
|
|
Why is recovery with Halothane more rapid than with Isoflurane (Forane)?
|
due to Halothane's extensive metabolism
|
|
What effect does 1 MAC of Isoflurane (Forane) have on EEG spikes?
|
decreases the amplitude and increases the latency of EEG spikes
|
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What effect does 1.5 MAC of Isoflurane (Forane) have on the EEG?
|
burst suppression and decreased latency
|
|
What effect does 2 MAC of Isoflurane (Forane) have on the EEG?
|
Isoelectric activity (flat line)
|
|
Does Isoflurane (Forane) interfere with evoked potentials?
|
YES (at >1 MAC)
|
|
What is beneficial about Isoflurane (Forane) producing isoelectric activity (on the EEG)?
|
Beneficial because it decreases the cerebral CMRO2 (o2 demand)
|
|
With Isoflurane (Forane) a MAC of 0.6-1.1 produces what kind of change to the CBF?
|
No change
|
|
Isoflurane (Forane) increases CBF by about 19% at what MAC?
|
1.1 MAC
|
|
All agents may increase ICP but effects are attenuated by decreasing what?
|
PCO2
|
|
Which IA requires you to hyperventilate simultaneously with induction (to decrease PCO2 and ICP)?
|
Isoflurane (Forane)
|
|
Which IA requires PREVIOUS hyperventilation (to decrease PCO2 and ICP)?
|
Halothane
|
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Which agent should you NOT hyperventilate at all because decreasing the PCO2 can actually cause seizures?
|
Ethrane (Enflurane)
|
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Because autoregulation of CBF is impaired with Halothane admin, as MAP increases, CBF _____.
|
Increases
|
|
Autoregulation of CBF is intact with Isoflurane (Forane) at 1 MAC; this means as MAP increases, CBF is prevented from _____.
|
Increasing
|
|
Does increased CBF always mean increased Cerebral Blood Volume (CBV)?
|
NO
|
|
What effect does Isoflurane (Forane) have on CSF production and reabsorption?
|
No change in production, increased reabsorption
|
|
Although it has not been proven, it is said that Isoflurane (Forane) is ______ and the agent of choice in neurosurgical cases
|
neuroprotective
|
|
Why is Isoflurane (Forane) considered "neuroprotective?" How is it protective?
|
Isoflurane (Forane) does not cause major disturbances in Cerebral O2 balance during hypotension (due to autoregulation)
|
|
Increasing MAC of IAs typically does what to BP?
|
Decreases
|
|
What effect does Isoflurane (Forane) have on SVR at 1 MAC?
|
decreases it significantly (<80% of normal)
|
|
True/False: Isoflurane peripheralizes circulation to skin, muscle, etc
|
TRUE
|
|
Isoflurane peripheralizes blood flow to skin; what effect does that have on the patient's temp?
|
drops the patient's temp
|
|
With Isoflurane (Forane), as BP drops, HR increases; this means the Baroreceptor reflex is ______.
|
Intact
|
|
Isoflurane (Forane) has a mild _____(receptor) agonist effect; this leaves CO virtually intact and stable
|
Beta agonist
|
|
With Isoflurane, CO and CI are _____.
|
Stable
|
|
Are arrhythmias common with Isoflurane (Forane)?
|
NO
|
|
Why are arrhythmias uncommon with Isoflurane (Forane)?
|
Less sensitivity of the heart to Epinephrine than Halothane and Enflurane
|
|
Because Isoflurane produces less cardiac sensitivity to Epinephrine, how much more of an Epi dose can you give with Isoflurane than Halothane?
|
May triple the dose of Epinephrine with Isoflurane
|
|
Enflurane produces a cardiac sensitivity to Epinephrine that is somewhere between Halothane and Isoflurane; How much more of an Epi dose can you give with Enflurane than Halothane?
|
May double the dose of Epinephrine with Enflurane (Ethrane)
|
|
In a normal, awake patient, a decrease in HR, Preload or Afterload, or a negative inotropic state causes coronary (vasoconstriction or vasodilation)? This is due to metabolic ______.
|
Vasoconstriction; metabolic autoregulation
|
|
Metabolic autoregulation causes coronary vasoconstriction secondary to a decrease in HR, Preload, Afterload, negative inotropic state, etc; what is the overall purpose of this metabolic autoregulatioin?
|
to decrease myocardial oxygen consumption (MVO2) and to decrease myocardial O2 supply
|
|
Which non-IA drug causes "Coronary Steal Syndrome?"
|
Adenosine
|
|
Does Isoflurane (Forane) cause Coronary "Steal" Syndrome?
|
NO
|
|
Which 3 IAs are used for anesthesia cardiac pre-conditioning (preconditions heart and protects against prolonged myocardial ischemia)?
|
Isoflurane, Sevoflurane and Desflurane
|
|
What effect does Isoflurane have on HR?
|
Will increase HR
|
|
With Isoflurane, what is the only hemodynamic parameter that is significantly related to ischemia?
|
Tachycardia
|
|
Because Isoflurane can cause tachycardia which can cause myocardial ischemia, what drug should you give to prevent this ischemia?
|
Beta1-antagonists (Beta Blockers)
|
|
True/False: In patients predisposed to myocardial ischemia, it is important to make sure they continue their heart medications prior to surgery
|
TRUE
|
|
What effect does Isoflurane have on PaCO2?
|
Increases
|
|
What effect does Isoflurane have on TV?
|
Decreases
|
|
What effect does Isoflurane have on RR?
|
increases
|
|
What effect does Isoflurane have on minute ventilation?
|
Decreases
|
|
Isoflurane depresses respiratory system (due to increased PaCO2) more or less than Halothane and N2O?
|
More
|
|
|
|
|
Which IA has the worst bronchodilator properties and should be avoided in asthmatics?
|
Desflurane
|
|
Which 2-drug combination is very bad to admin. to asthmatics because of their poor bronchodilator properties?
|
Thiopental + N2O
|
|
PaCO2-induced respiratory depression is greater or less with Isoflurane alone than with Isoflurane + N2O?
|
Greater with Isoflurane alone
|
|
Using Isoflurane with muscle relaxants allows you to ____ the dose of the muscle relaxants (than if used alone)
|
decrease
|
|
Isoflurane is minimally metabolized; what % is metabolized?
|
<0.2%
|
|
Isoflurane is metabolized by what metabolic pathway?
|
Oxidative pathway
|
|
Isoflurane is metabolized into Trifluoroacetic Acid; what is important about this?
|
Need to be aware of cross-sensitivity (Halothane, Enflurane and Isoflurane)
|
|
Does Isoflurane produce any renal dysfunction? Why or why not?
|
NO; because so little of it is metabolized there are only an insignificant amount of Fluoride ions produced
|
|
Is Isoflurane nephrotoxic?
|
NO
|
|
What effect does Isoflurane have on Renal Blood Flow (RBF), GFR and Urinary output?
|
Decreases all
|
|
Why is RBF, GFR and urinary output decreased with Isoflurane?
|
due to decreased BP and a subsequent decrease in perfusion to the kidneys
|
|
What effect does Isoflurane have on the Liver?
|
Increases hepatic blood flow (O2 supply to the Liver is greater with Isoflurane than Halothane)
|
|
In general, Isoflurane (Forane) is NOT hepatic toxic; what is the one case where it could be?
|
with cross sensitivity reactions(in patients who are genetically susceptible)
|
|
What are the major general advantages of Isoflurane (Forane)?
|
CV stability, Ischemic preconditioning, Lack of sensitization of the heart to circulating catecholamines (Epi), Limited biodegration, decreased hepatorenal toxicity, good muscle relaxation properties, no CNS excitatory effects
|
|
What is the major disadvantage of Isoflurane (Forane)?
|
Not good for mask induction due to irritation to the airways
|
|
There is only one major difference between the chemical structure of Desflurane and Isoflurane. Otherwise they are identical. What is it?
|
Isoflurane has an ethyl group with a Cl- atom on the alpha carbon; Desflurane's same ethyl group has a Fluorine atom on the alpha carbon
|
|
What is the chemical classification of Desflurane (Suprane)?
|
Halogenated methyl ethyl ether
|
|
Desflurane (Suprane) has an increased resistance to metabolism; because of this it has a higher/lower peak concentration of Trifluoroacetic Acid?
|
Lower
|
|
Rank Halothane,Isoflurane and Desflurane in order from greatest to least concentration of Trifluoroacetic Acid produced from metabolism
|
Halothane (500),
Isoflurane (5), Desflurane (<0.5) |
|
Is Desflurane reactive or non-reactive in sunlight?
|
Non-reactive
|
|
Is Desflurane reactive or non-reactive in soda lime?
|
Non-reactive
|
|
Is Deflurane reactive or non-reactive with metals?
|
Non-reactive
|
|
Does Desflurane have a pleasant or a pungent odor? Is this good or bad for mask inductions?
|
Pungent odor; not recommended for mask inductions (like Isoflurane)
|
|
Other than the pungent odor of Desflurane, what's another reason Desflurane is not recommended for mask inductions?
|
Can cause Laryngospasms
|
|
What effect does Desflurane have on CBF and CMRO2?
|
Increases CBF and decreases CMRO2
|
|
Does Desflurane produce any seizure activity?
|
NO
|
|
What kind of EEG changes does Desflurane produce?
|
Dose-related decreases
|
|
What type of test is Desflurane good to be used for during procedures such as Harrington Rod placement where the patient needs to answer questions about their status, etc?
|
The Wake-up Test
|
|
Why is Desflurane a good drug to use for the wake-up test?
|
Its low solubility coefficient allows them to wake up quickly and be put under quickly
|
|
What effect does Desflurane have on HR?
|
Increases
|
|
What effect does Desflurane have on MAP? How does this compare to Isoflurane?
|
Increases MAP; increases MAP more than Isoflurane does
|
|
What effect does Desflurane (Suprane) have on PaCO2?
|
Increases
|
|
What effect does Desflurane have on TV?
|
Decreases
|
|
What effect does Desflurane have on RR?
|
Increases
|
|
What effect does Desflurane have on minute ventilation?
|
fairly stable minute ventilation until 1 MAC and then decreases
|
|
True/False: Desflurane is the most desirable agent to use for an asthmatic
|
False; it's the least desirable agent to use in asthmatics due to it's lack of brochodilator effect
|
|
Is Desflurane an airway irritant?
|
YES
|
|
What occurs (symptoms) due to Desflurane being an airway irritant?
|
Patient coughing, breath-holding and Laryngospasm
|
|
What population should you be cautious with when administering Desflurane due to its airway irritant properties?
|
Smokers
|
|
Is it good to administer Desflurane to a patient with an LMA? Why or why not?
|
NO; Laryngospasm can occur
|
|
Because Desflurane is an airway irritant, it should not be started in a smoker until what occurs first?
|
ET tube is in place
|
|
Rank Desflurane, Sevoflurane, Isoflurane and Halothane in order from greatest to least ability to potentiate muscle relaxation?
|
Des>Sevo>Iso>Halo
|
|
The 2 IAs with the lowest blood/gas solubility coefficients (Desflurane and Sevoflurane) are the best at potentiating muscle relaxation; why is this?
|
decreased blood/gas solubility coefficients allows these agents to move quickly into the NMJ
|
|
Does Desflurane produce any change in serum creatinine or BUN (or any other significant renal effects)?
|
NO
|
|
Does Desflurane produce any change in liver function tests?
|
NO
|
|
What percentage of Desflurane is metabolized?
|
Minimum to none--0.01%
|
|
With Desflurane is there any evidence of organ toxicity?
|
NO
|
|
Is Desflurane a trigger for malignant hyperthermia?
|
YES
|
|
True/False: All inhaled anesthetics produce some CO (Carbon Monoxide).
|
TRUE
|
|
Rank Desflurane, Enflurane and Isoflurane in order from greatest to least production of CO in Baralyme CO2 Absorbent
|
Desflurane>Enflurane>Isoflurane
|
|
Which 2 IAs produce about the same amount of CO in Soda lime CO2 absorbent?
|
Desflurane and Enflurane
|
|
What percentage of Hgb is bound with CO in nonsmokers?
|
1%
|
|
What percentage of Hgb is bound with CO in smokers?
|
10%
|
|
What percentage of Hgb bound with CO causes death?
|
50%
|
|
What factor produces more CO?
|
interaction with strong bases in relatively dry carbon dioxide (CO2) absorbents
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What 3 factors influence the level of CO production?
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Choice of anesthetic agent, inspired anesthetic concentration, and type, temperature and degree of dryness of the CO2 absorbent
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What are some simple ways you can minimize or eliminate CO?
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Use fresh absorbent, Use Soda Lime instead of Baralyme, avoid techniques that dehydrate the CO2 absorbent
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Dehydrating CO2 absorbent increases CO production, so avoiding techniques that dehydrate the CO2 absorbent is critical; what are 2 ways you can avoid dehydrating the CO2 absorbent?
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Use low gas flows or (as a last resort) rehydrate absorbent by adding approx. 1 cup of water (230 ml) per 1.2 kg of absorbent (i.e. standard cannister)
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What are two new absorbents that are now being used (which have a lower incidence of dehydration and CO production)?
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Amsorb and DragerSorb Free
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As an "economical delivery method", how much flow of gas and for how long would you administer it to equilibrate the VRG?
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6L/minute for 10 minutes
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As an "economical delivery method", how much flow of gas and for how long would you administer it to equilibrate the muscle group?
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4L/minute for 20 minutes
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As an "economical delivery method", how much flow of gas and for how long would you administer it to decrease the incidence of absorbent dessication (drying out)?
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2L/minute for 30 minutes
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With Desflurane, is wash-out fast or slow?
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Extremely fast (has low solubility coefficient)
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Because wash-out with Desflurane is extremely fast, what are 2 very important things to remember regarding patient comfort?
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Anticipate early analgesic needs;
Reverse muscle relaxants early |
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Why is Desflurane good to use for obese patients?
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low solubility coefficients--won't hang out in the fat as a reservoir
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How should you administer Desflurane to avoid unacceptable tachycardia?
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Induce and change levels slowly
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What chemical classification does Sevoflurane (Ultane) belong to?
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Halogenated methyl isopropyl ether
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What type of odor does Sevoflurane have?
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"Ethereal;" Non-pungent
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True/False: The odor of Sevoflurane is well tolerated by mask
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TRUE
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Is Sevoflurane stable or unstable in CO2 absorbents?
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Unstable
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What is the major degradation product of Sevoflurane when Sevo comes into contact with Soda lime or Baralyme and CO2 absorbent?
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Compound A
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What chemical classification is "Compound A?" (major degradation product of Sevo)
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Alkene
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Which other IA (other than Sevo) has a similar degradation reaction as Sevo when comes in contact with CO2 absorbents and therefore is not stable in Soda lime CO2 absorbents?
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Halothane
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How is Compound A formed from Sevoflurane?
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By the extraction of the acidic proton in the presence of a strong base (KOH) to form an alkene (Compound A)
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The degree of degradation of Sevoflurane to Compound A increases with (increasing or decreasing) temperature
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Increasing
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The chemical reaction of CO2 with absorbents is endothermic or exothermic?
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Exothermic (heat is produced)
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Dry (or fresh) absorbents produce (more or less) heat?
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More heat
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Increased temperature increases degradation of Sevoflurane and production of Compound A; the temperature increase depends on what factors?
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fresh gas flow in breathing circuit, metabolic status of the patient, ventilation and concentration of Sevoflurane
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Why is it good to use a high flow rate when admin. Sevoflurane?
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High flow rates decrease the production of Compound A by reducing re-breathing
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Are flows of <2L recommended with Sevoflurane admin?
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NO
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What do high concentrations of Compound A cause (in rats)? At what concentrations?
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Cause renal injury and death; occurred when levels reached 25-50 ppm or greater
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Cases of humans with renal changes occurred after Sevoflurane admin (Compound A); Under what conditions did these renal changes occur?
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Prolonged Sevoflurane exposure
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While "renal changes" have been demonstrated in humans after Sevoflurane admin, a large number of studies were done which demonstrated no change in BUN and Creatinine levels after Sevo admin; why could this be?
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may not be sensitive enough markers to demonstrate renal dysfunction
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What's the most important factor in determining how much Compound A a patient will inspire?
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Inspired fresh gas flow is most important factor
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Should we avoid using Sevoflurane in a patient with preexisting renal disease?
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YES
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What effect does Sevoflurane have on CBF and CMRO2?
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Increases CBF (the least among the Volatile IAs) and decreases CMRO2
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Which IA increases CBF the LEAST among the volatile IAs?
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Sevoflurane
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What's interesting about the effect Sevoflurane has on CBF and CMRO2 at 1 MAC?
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decreases CBF by 38% and CMRO2 by 39% (coupled)
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True/False: With Sevoflurane admin, the cranial vessel response to PaCO2 is impaired?
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False; it is intact (you can hyperventilate patient, bringing CO2 and ICP down)
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Sevoflurane produces what general cardiovascular effect?
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dose related depression
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What effect does Sevoflurane have on BP?
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dose related decrease
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What effect does Sevoflurane have on HR?
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up to 1 MAC, decreased;
at 1.5 MAC, increased (baroreceptor reflex is intact) |
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What effect does Sevoflurane have on MAP?
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MAP is decreased until approx. 1.5 MAC and then it levels out (or slightly increases); baroreceptors are intact
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The Epinephrine induced arrhythmogenic effect of Sevoflurane is equivalent to which other IA?
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Isoflurane
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What general effect does Sevoflurane have on the respiratory system?
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Dose related depression
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What effect does Sevoflurane have on PaCO2?
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Increases
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True/False: Sevoflurane is the best bronchodilator and the best IA to use in asthmatics
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TRUE
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Does Sevoflurane potentiate NM blockers?
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YES
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Because Sevoflurane potentiates NM blockers (muscle relaxants), the dosage of Muscle relaxants should be guided by a ____ ____ _____
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Peripheral Nerve Stimulator
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Sevoflurane is the next best drug to ____ for NM Blocker potentiation
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Desflurane
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What percentage of Sevoflurane dose is metabolized?
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3-5%
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Does Sevoflurane form Trifluoroacetic Acid?
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NO
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Since Sevoflurane does not form Trifluoroacetic Acid, what 3 things also do not occur?
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Does not stimulate antibodies to TFA, does not cause immune mediated hepatic toxicity, and no cross-sensitivity with Halothane
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What are the 2 metabolic products of Sevoflurane?
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Hexafluoroisopropanol (HFIP) and Inorganic Fluoride ion
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How is Hexafluoroisopropanol (HFIP) metabolized?
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Conjugated with Glucuronic acid and excreted in the urine
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HFIP (metabolic product of Sevo) represents ____% of Fluorine released from Sevoflurane metabolism; what is the problem with this?
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80%; worry about renal not being able to concentrate urine in Pediatrics (Peds lack UGT enzymes necessary to catalyze the transfer of glucuronic acid)
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Why are we more concerned about Enflurane and renal insufficiency than Sevoflurane and renal insufficiency?
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Because Enflurane has a higher solubility coefficient than Sevoflurane (stays around longer)
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Is Sevoflurane a potential trigger for Malignant Hyperthermia?
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YES
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What is a problem with Sevoflurane upon emergence (particularly in Peds)?
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Emergent Excitement
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Describe "Emergent Excitement"
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Transient confusional state associated with emergence from GA
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Emergent Excitement is not to be confused with what other similar condition that occurs after Ketamine admin?
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Emergence Delerium
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When does Emergent Excitement typically occur?
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Within the 1st 10 minutes of recovery
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The peak incidence of Emergent Excitement occurs in what age of children?
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2-4 year olds
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What 2 IAs are associated with emergent excitement?
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Sevoflurane and Desflurane (esp. Sevoflurane)
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List the etiological factors of emergence excitement
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IA, Post-op pain, type of surgery, age (typically 2-4 year olds), preoperative anxiety, underlying temperament, adjunct medications
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What are the 2 main conditions to be cautious about when admin. Sevoflurane to Pediatrics?
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Increased levels of HFIP, and Emergent Excitement
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