Top Drawer- S3 Flashcards
Stimulation of GABAa receptors, high lipid solubility.
Uses: TIVA, induction, antiemetic, endoscopy, MAC.
Pain on injection-give w lidocaine
CV: decreased HR and BP, decreased SVR.
Decrease in CBF and ICP.
Propofol
Propofol can support bacteria how long is it good for open.
1. In opened vial infusion?
2. Drawn up in syringe?
12 hours infusion
6 hours syringe
Contraindications to Propofol?
Egg or soy allergies?
Patients with low CO or hypovolemia.
Will decrease HR and BP even more
Propofol dosing?
INDUCTION
MAC/MAINTENANCE
Propofol onset
Propofol Duration
Induction=2mg/kg
MAC=25-200mcg/kg/min
Onset= 30secs rapid
Duration= Dose dependent
Propofol metabolism?
In the liver to 4-hydroxypropofol
excreted in kidneys
Lidocaine is administered to?
1.Suppress coughing reflex during laryngoscopy
2.Reduce the airway responsiveness to noxious stimuli
3.Reduce pain caused by IV injection agents
Lidocaine dosing?
0.5-1mg/kg.
1mg/kg for induction
ERAS= 1-2 mcg/kg/hr
Which drug can attenuate the intracranial hypertensive response to laryngoscopy?
Lidocaine
Synthetic Piperidine
High volume of distribution in lipohillic opiods, low protein binding.
100x more potent than morphine
Metabolized by liver.
0.5-1mcg/kg (50-100mcgs) typically
Fentanyl
Which Opiod receptors does Fentanyl affect?
Mu-1
Mu-2
Kappa
Which opiod receptor affects?
Supraspinal analgesia
Bradycardia
Sedation
Pruritus
N/V
Mu-1
Morphine
Meperidine
Fentanyl
Which opiod receptor affects?
Respiratory depression
Euphoria
pruritis
constipation
dependence
Mu-2
Morphine
Meperidine
Fentanyl
Which opiod receptor affects?
Spinal analgesia
Respiratory depression
Sedation
miosis
Kappa
Fentanyl
Morphine
Nalbuphine
Which opiod receptor affects?
Spinal analgesia
Respiratory depression
Delta
Oxycodone
beta-endorphin
Leu-enkephalin
Noncompetitive NMDA receptor antagonist that blocks glutamate?
Phencyclidine derivative
Inhibits the re-uptake of Norepinephrine
Causes dissociative anesthesia
Given for induction, sedation, trauma, CV collapse.
Causes increase in BP, HR, CO, CVP, CI
Minimal respiratory depression, maintains airway reflexes, increased oral secretions, Bonchodilator
Emergence delirium (give versed)
Ketamine
Which opiod receptors does ketamine affect?
Kappa-agonist
Mu-antagonist
Increase in ICP, CBF, CMRO2,
Norketamine is active metabolite (1/3) potency.
Ketamine
Ketamine Dosing?
Onset?
Duration?
1-2mg/kg IV
4-5mg/kg IM
Onset-30 secs, IM-2 mins
Duration 10-15 mins
Short acting barbiturate
Activates GABA
Used in sedative, hypnotic, anticonvulsant, treatment of ICP in neuro cases.
Histamine release
Decrease CBP/ICP, hypotension.
No longer in the US
Thiopental
Short acting Barbiturate contraindicated in Acute Intermittent Porphyria (AIP).
Dosing 3-5 mg/kg IV
Onset- 30 secs
Duration- 5-30 mins
Hepatic metabolism
Thiopental
Ultrashort acting non-barbiturate hypnotic depressant RAS.
Affects GABA
used for induction or procedural sedation
Minimal CV effects, Minimal respiratory depression
Myoclonic Movements
Adrenocortical suppression (long-term)
Etomidate
Etomidate dosing?
Onset?
metabolism?
0.2-0.3 mg/kg
30-60 secs
Hepatic enzyme and plasma esterase hydrolysis
Highly selective, potent central acting Alpha-2 adrenergic agonist.
Inhibition of norepinephrine release presynaptically.
Used in procedure sedation, analgesia, fiberoptic intubation, post-op sedation.
Bradycardia/Hypotension
Minimal respiratory depression.
Dexmedetomidine
Dexmedetomidine dosing?
Onset?
Duration?
Excretion?
Procedural sedation: 0.5-1mcg/kg over 10 mins
IV infusion 0.3-0.7mcg/kg/hour.
5-10 min onset
duration 1 hour
Hepatic metabolism/urine excretion
Rapid ultrashort acting barbiturate, enhances GABA affect.
Uses: ECT, ENDO, Short
Deep sedation, skeletal muscle hyperactivity
Lowers seizure threshold
Methohexital
Methohexital Dose?
Onset?
Duration?
1-1.5mg/kg.
Onset 30 secs
Duration 5-7 mins
Hepatic metabolism, urine excretion
3 ways to cause muscle relaxation?
- High dose volatile anesthetics
- Regional anesthesia
- NMBA
Depolarizing NMBA?
Succinycholine
Non-depolarizing aminosteroids?
Rocuronium
Vecuronium
Pancuronium
Non-depolarizing Benzylisoquinolines?
Cisatricurium
Atracurium
Mivacurium
Binds to 2 alpha subunits of nicotinic cholinergic receptors, allows Na and Ca influx, K efflux.
Depolarization of muscle
remains depolarized until SCH diffuses away from the receptor.
Succinycholine
What does Succinycholine mimic?
Acetycholine
Used in RSI, very short cases, and laryngospasm?
Succinycholine
Side effects of Succinycholine?
Hyperkalemia + 0.5mg
Malignant hyperthermia
Minimal histamine release
Decreases HR
Fasciculations
Myalgias
Succinycholine metabolism?
Butrycholinesterase/plasma cholinesterase in the plasma hydrolyzed. Succinymonocholine weak active metabolite.
Decreased levels of pseudocholinesterase can prolong the block.
Succinycholine dosing?
Onset?
Duration?
1-1.5 mg/kg
30-60 sec onset
<10 min duration
Malignant hyperthermia triggers?
First sign to look out for?
Succinycholine and volatile anesthetics
Increased etCO2
How do nondepolarizing muscle relaxants work?
Compete with/ block acetycholine at the nicotinic receptor alpha subunits on the motor endplate.
Aminosteroids metabolism?
Hepatic breakdown, kidney excretion, minimal histamine release.
Potential for allergic reactions
Intermediate action, rare histamine release, nondepolarizing NMBA.
Used to defasciculate with Sux.
No effect on BP or HR
Aminosteroid
Rocuronium
Rocuronium dose?
Maintenance dose?
Onset?
Duration?
0.6mg/kg induction
1.2mg/kg RSI
5mg defasciulating dose
0.1mg/kg repeat/maintenance
1-2 min onset
30 min duration
Intermediate nondepolarizing NMBA, no histamine release, cardiac stable.
Precipitate with thiopental.
Vecuronium
Pancuronium dosing
onset?
Duration?
.08-.12 mg/kg
2-3 min onset
60-100 min duration
Vecuronium Dosing?
Onset?
Maintenance?
0.08-0.1mg/kg
2-3 min onset
0.01 mg/kg maintenance
Increased Hoffman elimination is caused by?
Increased pH and temperature
This benzylisoquinoline has histamine release when given quick. Hydrolysis by plasma cholinesterase?
Dose 0.2mg/kg
1 min onset
Mivacurium
Elimination for Benzylisoquinolines?
Hoffman Elimination and ester hydrolysis
Decresased Hoffman elimination is caused by?
Decreased pH and temperature
Long acting aminosteroid NMBA,
No histamine release
Tachycardia due to norepi release
Increase in BP and CO
Pancuronium
Intermediate acting Benzyliso NMBA, small histamine release. Minimal decrease in BP. Primary metabolite is Laudanosine which can produce seizure activity. Tertiary amine.
Atracurium
Atracurium dosing?
Onset
Duration
0.3-0.6mg/kg
2-3 min onset
20-30 min duration
Intermediate/ long acting Benzylisoquionlone NMBA.
No histamine release, No changes in BP/HR.
Cisatricurium
Cisatricurium dosing?
Onset?
Duration
0.1-0.15 mg/kg IV dose
2-3 min onset
40-70 min duration
Most allergic reactions are caused by which 2 drugs?
Sugammadex-32%
Rocuronium-27%
Which factors affect reversal of NMBA?
Intensity of block
Dose and choice of NMB
Drug interactions
Choice of reversal agent
Disease process (Liver faliure)
Blocking or inhibiting the breakdown of ACH at the NMJ results in an _____ in the avaliable pool of ACH at the synaptic cleft and a better change of competing with the nondepolarizing NMBA.
Increase
Side effect of Acetycholinesterase inhibitors?
SLUDGE
muscarinic stimulation
Increased bronchial secretions/bronchospasm
Bradycardia
Treatment for overdose of anticholinergic agent?
Physostigmine, increases Ach amount
tertiary amine that crosses the BBB.
Inhibits hydrolysis of ACh by AChE.
Causes parasympathetic affects, used with glycopyrrolate to decrease muscarinic side effects.
Quaternary ammonium.
Ceiling affect.
used in deep blocks.
Neostigmine
Neostigmine dosing?
70mcg/kg max dose
5mg