Induction Agents Flashcards
Propofol
Induction dose:
MAC Sedation Dose:
1-2.5 mg/kg IV
MAC — 25-75 mcg/kg/min
The general anesthesia sedation/maintenance dose of Propofol is:
25-200 mcg/kg/min
Indications for Propofol (5)
Induction and MAC
TIVA
Outpatient surgery and endoscopy
Antiemetic
Malignant Hyperthermia
MOA of Propofol:
GABA agonist
Cardiac and respiratory effects of Propofol:
Decreases CO, BP, SVR (slight decrease in HR until pt is asleep then increases to compensate for CV decreases)
dose-dependent respiratory depression
Decreased Vt
Increased RR (at maintenance doses)
Bronchodilator (direct effect on intracellular Ca++)
T or F: Propofol is a neuro protective drug
T
Propofol CNS effects:
- neuroprotective — decrease CBF, CMRO2, and ICP & decreased SVR may cause decreased CPP
- anticonvulsant
Contraindications of Propofol (3)
Allergies to soybean oil or soy products
Allergies to egg and egg products
Allergies to sulfite
Correct onset and duration of Propofol:
Onset: <1 min
**”30 seconds or so…”
Duration: dose and rate dependent
Metabolism of Propofol occurs in:
Hepatic
Kidney and lungs (account for ~ 30%)
Excretion of Propofol is via:
Renal System
unconventional use of propofol and MOA
10 mg IV for PONV and pruritis
MOA related to spinal cord suppression
T or F: propofol is good for WPW ablations because it has no AV or SN node depression
T
clinically when you should avoid propofol use
cardiac unstable or hemorrhaging
is propofol lipid soluble
yes
protein binding of propfol
97-99%
why can propofol injections be painful and what can you do to decrease it
glycerol; lidocaine 1 mg/kg
T or F: propfol has analgesic effects
F
T or F: Propofol is a chiral compound
F– not chiral
how is propofol partially reversed
physostigmine
induction dose of Ketamine:
IV
IM
1-2 mg/kg IV; 4-5 mg/kg IM
***in low dosing can be opioid sparing
infusion dose of Ketamine
1-2 mg/kg/hr
other name for Ketamine
Ketalar
other name for propfol
diprivan
indication for Ketamine (6)
- induction
- sedation
- sedation for mentally challenged or non-compliant such as kids
- CV collapse
- “bad” epidural/spinal
- Good for OB.
- tamponade ***she didnt say this !?
contraindication of Ketamine (4)
- Right heart dysfunction (decreases PVR)
- increased ICP
- Critically ill/shock pts ( catecholamine depletion r/t shock — will cause profound hypotension and unopposed direct myocardial depression)
- psych patients (will make them hallucinate)
MOA of Ketamine (3)
- noncompetitive NMDA antagonist that blocks glutamate
- stimulates the SNS: inhibits the reuptake of norepi
- dissociative anesthesia — dissociation btwn thalamocortical and limbic system
CV system effects of Ketamine
- increase BP, HR, CO, PAP, CVP, CI
- increases myocardial O2 requirements
in what CV patient should you be especially cautious of using Ketamine
pt with severe RIGHT heart dysfunction
Respiratory system effects of Ketamine (4)
- minimal depression
- maintain upper airway reflexes
- increased oral secretions (effects on muscarinic receptors)
- bronchodilator (used in bronchospasm dilator)
Neuro system effects of Ketamine (5)
- cerebral dilator (increased ICP)
- potential to produce myoclonic activity (usually considered an anticonvulsant though)
- prolongs and enhances effects of NMBDs
- emergence delirium
- Hallucinogenic: phencyclidine derivative
other system effects of Ketamine
- increased lacrimation and salivation –> premedicate with anticholinergic
what are a few clinical judgments necessary for Ketamine? (4)
- used in OB (NOT preeclamptic)
- ketamine dart 3-4 mg/kg for mentally challenged
- not good for brain lesions d/t increased ICP
- MAY be used as a last resort for status epilepticus
onset of Ketamine
IV
IM
IV- 30 seconds
IM 2-4 minutes
duration of Ketamine
IV
IM
IV 10-15 min
IM 15-25 min
metabolism of Ketamine
hepatic by demethylation via CYP 450
*active metabolite, Norketamine, is 1/3-1/5 as potent
excretion of Ketamine
Renal
T or F: Ketamine provides analgesia w/o airway compromise
T
more potent stereoisomer of Ketamine
S (+)
T or F: for Ketamine, there is a functional dissociation between thalamocortical and limbic systems
T
protein binding of Ketamine
only anesthetic that has low protein bind (12% or 20% depending on source)
describe the cataleptic state of Ketamine
pt eyes remain open with slow nystagmic gaze
other name for Thiopental
pentathol
induction dose of Thiopental
3-5 mg/kg IV
how should you adjust the induction dose of Thiopental for elderly
reduce by 30%
indications for Thiopental (4)
- induction/sedative
- hypnotic
- anticonvulsant
- treatment of ICP (Neuro cases)
contraindications of Thiopental (3)
- Acute intermittent Porphyria
- variegate Porphyria
- status asthmaticus (**d/t histamine release)
MOA of Thiopental (2)
- activates GABA — short acting barbituate
- decreases RAS (small histamine release)
CV effects of Thiopental
Hypotension
Depresses myocardium and relaxes vascular smooth muscle
respiratorey effects of Thiopental
resp depression
Neuro effects of Thiopental (3)
- potent cerebroconstrictor
- decreased CBF
- decreased ICP
GI effects of Thiopental
N/V
T or F: Thiopental has analgesic effects
F- may actually lower pain threshold; thus increasing sensitivity to pain
onset of thiopental
30-60 seconds
duration of Thiopental
5-30 min
metabolism of Thiopental
hepatic
half life of Thiopental
12 hours
protein binding of Thiopental
80%
** its actually 72-86%**
what does Thiopental precipitate with
- lidocaine
- roc
- succs
THIs LIghter Really Succs
important things to know about Thiopental (5)
- extravation= necrosis
- accidental arterial injection= severe vasoconstriction
- sulfur on 2nd C atom
- “hangover feeling”
- pt can experience garlic/onion taste
other name for etomidate
amidate
induction dose of etomidate
0.2-0.3 mg/kg
infusion dose of etomidate
5-20 mcg/kg/min
indications for etomidate (2)
- induction
- procedural sedation
MOA of etomidate (3)
GABA agonist (increases Cl- influx, hyperpolarizing cell)
Short acting non-barbituate hypnotic
Depresses RAS
CV and respiratory effects of etomidate
CV- minimal effects
resp- depression
neuro effects of etomidate
- potent cerebroconstrictor decreases CMR, CBF, ICP
- myoclonus decrease with opioids
GI effects of etomidate
N/V
other system effects of etomidate
- adrenocorticol supression
in what type of patient is etomidate a good choice for
- cardiac patients with low EF
what procedures/ patients should you use clinical judgment for use of etomidate
- ECT (prolong seizure duration)
- trauma
- elderly patients
onset of etomidate
30-60 seconds
duration of etomidate
3-5 min
Pharm says 5-10 minutes
metabolism of etomidate
hepatic and plasma ester hydrolysis
excretion of etomidate
renal (80%)
Bile (20%)
protein binding of etomidate
76%
more potent isomer of etomidate
R (+)
does etomidate have hypnotic and analgesic effects
hypnotic- yes
analgesic- no
other name for dexmedetomidine
precedex
procedural sedation dexmedetomidine:
For sedation:
For infusion:
Sedation: 0.5-1 mcg/kg over 10 min
Infusion: 0.3-0.7 mcg/kg/hr
awake fiberoptic intubation and infusion dose of dexmedetomidine
intubation: 1 mcg/kg over 10 min
infusion: 0.7 mcg/kg/hour until intubated
indications for dexmedetomidine (4)
- pediatrics
- analgesia (acts on mu, delta, kappa receptors)
- procedural/Postop sedation
- awake fiberoptic intubation
contraindications for dexmedetomidine
- AV block
- 1st degree HB
MOA of dexmedetomidine
- highly selective potent central acting alpha-2 adrenergic agonist (inhibit release of norepinephrine)
CV effects of dexmedetomidine
- bradycardia
- sinus arrest
- hypotension
- rebound HTN
Tx: w/ atropine/ephedrine/volume
respiratory effects of dexmedetomidine
Minimal depression
- less vent depression than other agents
- bonus can decrease minute ventilation
onset and peak of dexmedetomidine
onset: 5-10 min
Peak: 15-30 min
duration of dexmedetomidine
1-2 hours (dose-dependent)
metabolism of dexmedetomidine
hepatic
excretion of dexmedetomidine
renal
protein binding of dexmedetomidine
94%
dexmedetomidine provides what CNS dose dependent effects (3)
- analgesia
- anxiolysis
- sedation
Which is more alpha selective:
dexmedetomidine or clonidine
dexmedetomidine
the hypnotic efects of dexmedetomidine occur in:
locus coeruleus
where do the analgesic effects of dexmedetomidine occur
level of spinal cord
T or F: can develop tolerance and dependence of dexmedetomidine
T
What effects does dexmedetomidine have on the CYP 450 system
inhibitory properties that can increase plasma concentrations of opioids
another name for methohexital
brevital
induction dose (and concentration) of methohexital
1-1.5 mg/kg
Concentration: 500 mg vial reconstituted with 50 cc NS (1% solution —> 10 mg/cc)
indications for methohexital (3)
- ECT
- Endo
- very short procedures
contraindications for methohexital
- acute intermittent porphyria
- variegate porphyria
MOA of methohexital
enhances GABA— rapid ultrashort acting barbiturate
system effects of methohexital (4)
- skeletal muscle hyperactivity
- deep sedation
- pain on injection
- Lowers seizure threshold
methohexital useful in what procedures clinically and why
- ECT–> lower seizure threshold
- Endo–> used when shortage of propofol (very short procedures).
onset and duration of methohexital
onset: < 1 min
duration: 5-7 min
metabolims of methohexital
hepatic
excretion of methohexital
Renal
protein binding of methohexital
75-85%
what med should you be catious of when using methohexital
atropine– it precipitates with it
chemical property of methohexital
oxygen retained on the 2nd C atom
In what 6 groups should we use propofol cautiously and how should each groups dose be adjusted? (6)
- Children — Need more large Vd and quicker clearance= need more
- Chronic ETOH — Need more d/t enzyme abuse
- Obese — Depends base dosing on lean body weight
- CV disease — Need less d/t propofol decreasing SVR
- Trauma/hypotensive/bleeding — Need less d/t the decrease in SVR, BP, CO, SV
- Elderly — Need less decreased sensitive, prolonged effects d/t decreases CO and clearance
Dose of lidocaine
0.5-1.5 mg/kg (dose depend on pt and provider)
Why is lidocaine used on induction (4)
- suppress coughing reflex during laryngoscopy/intubation/EGDs
- reduce airway responsiveness to noxious stimuli
- reduce pain from IV injected agents
- Can attenuate the intracranial hypertensive response to laryngoscopy/intubation.
Lidocaine might increase hypotensive effects of
Sedative-hypnotic agents
Why should you use caution when administering lidocaine to cardiac patients
- indirect evidence that it can attenuate intracranial hypertensive response to laryngoscopy and intubation
- lidocaine (1.5 mg/kg) given 3 min before intubation suppresses cough reflex and attenuates increased airway resistence resulting from laryngoscopy and ETT intubation
How can you prevent emergence delerium from ketamine
- low lights
- quiet room
- versed (2 mg as pretreatment)
T or F: KEtamine causes intense analgesia
T
Ketmine dose for bronchospasms
0.2-1.0 mg/kg IV
Active metabolite of ketamine and how “active “ is it?
Norketamine
1/3-1/5 as potent as ketamine
Level of histamine release from thiopental use
“Some”
How can you decrease myoclonic movements with etomidate
Opioids
How can you treat Precedex induced hypotension
Atropine
Ephedrine
Volume
T or F: Methohexital has anticonvulsant activity
F — does not have anticonvulsant activity (lowers seizure threshold)
For intermittent IV use of methohexital, how should it be reconstituted
Into 1% (10 mg/cc)
T or F: Methohexital has a slow redistribution
F— RAPID
____________ is the shortest-acting barbiturate and (does/does not) have anticonvulsant activity. It (lowers/increases) the seizure threshold.
Methohexital
Does not
Lowers (this is why its good for ECT)
Etomidate is a ____________ derivative
Carboxylated imidazole
Ketamine has (low/high) lipid solubility
High
How do we dose ketamine when using for a “bad spinal/epidural”
- 2 mg Versed
- Ketamine in 10-20 mg doses at a time until pt is unresponsive to glabellar tap, still breathing, not screaming
- If they even bat an eyelash, immediately give 10 mg more
- Repeat until procedure is finished
Lidocaine dose
What do we typically give and when must we adjust it?
1 mg/kg (range is 0.5-1.5 mg/kg)
Typically give 100 mg of 2% solution (5 cc); adjust this for both patients weighing less than 60 kg, as well as hemo unstable
Why don’t we mix propofol and lidocaine in same syringe
After 20 mins, the effect of Propofol are negated and lipid emulsion broken up (risk for embolism)
Propofol:
N/V rescue dose-
N/V background infusion dose -
What MOA is this?
10-15 mg
10-20 mcg/kg/min
Direct effect on CTZ
Cause of PRIS and how is it recognized clinically?
Occurs with propofol doses 4 mg/kg/hr > 48 hours or 67 mcg/kg/min
Bradycardia, EKG changes, Arrhythmias
For which patients would we use TIVA rather than inhalational GA
History of PONV or MH
How do we know pt is unconscious/sedated during TIVA if they are muscle relaxed?
Use BIS (40-60 is ideal for GA)
How does etomidate cause adrenocortical suppression and for how long?
Inhibit 11 B hydroxylase enzyme (Effects last 4-8 hours after induction dose of etomidate)
CNS Ketamine effects
- potent cerebral vasodilator
- increase CBF by 60-80% (hyperventilate to attenuate effects)
- relatively C/I in pt with elevated ICP
Propofol S/E (3)
- injection pain (d/t glycerol)
- allergies/anaphylaxis (d/t phenyl nucleus and di-isopropyl side chain)
- PRIS (bradycardia, ekg changes, arrhythmias)