Anesthesia Flashcards
What is the ideal thyromental distance in airway evaluation?
Greater than 6 cm
What are the preoperative NPO guidelines
ASA Classifications system
Common sources of error for pulse oximetry
(10 pts)
-Shivering
-Fingernail Polish
-Corboxyhemoglobin
-Methemoglobin
-Methylene Blue
-Hypothermia
-Hypotension
-Hypovolemia
-Hypoxia
-Ambient light
What are the most sensitive EKg monitors to ischemia
Leads II and V5
EKG helps determines
Ischemia, disarrhythmias, and pacemaker function
When is invasive BP indicated
-In major surgeries
-Hemodynamic instability
-Vasocactive meds
-Frequent blood draws.
Too large of a BP cuff?
falsely low BP
Too small of a BP cuff?
Falsely elevated bP
CO2 monitoring allows for measurement of:
-Assessment of ventilation
-Assessment of ciculation
-Identification of intubation
-Identification of anesthetic circuit malfunction (leaks, disconnection)
Bispectral index
Yes EEG data via scalp electrodes to record the depth of anesthesia via IV or inhalation
Levels of consciousness
Responsivness for minimal, moderate, deep, general
Airway, spontaneous ventilation, cardiovascular function
for minimal moderate, deep, general
T/F: LMA’s can be used for airway emergencies when intubation has failed.
True, it is a suprglottic airway and does not protect the airway though.
what does oral RAE stand for?
Ring-Adair-Elwyn
When is a cricothyrotomy used?
It is used during airway emergencies when other nonsurgical attempts at securing the airway have failed.
Volume of distribution
Dose of drug administered/concentration of drug in plasma
-Decreased by high protein binding affinity, ionization, decreased lipid solubility.
What is drug clearance?
The volume of plasma cleared of drug in mL per minute as a result of renal elimination and metabolism (liver and other tissues: kidney, lung, gastrointestinal tract)
How is renal elimination improved
It is improved with increased water solubility and inhibited by protein binding and lipid solubility
Elimination half time:
Time required to decrease drug concentration by 50% _5 half times required for total elimination.
Redistribution
Drugs preferentially distribute to highly perfused tissues (eg brain, heart, kidneys)
Eventually a gradient is reached that allows perfusion to the less perfused tissues (fat, skeletal muscle)
First-pass hepatic effect
Oral drugs are absorbed by the GI tract and pass through the liver via the portal circulation before entering the systemic circulation
Drugs are metabolized in this process
PAP
Pulmonary artery pressure-the partial pressure of volatile agent in the brain is in equilibrium with the blood and alveoli
MAC
Minimum alveolar concentration is the concentration (partial pressure) of volatile anesthetic (at 1 atm and measured during steady state) that prevents movement in 50% of patients during surgical stimulus.
The higher the MAC, the less the potency
MAC of Sevo
2.1
What are the advantages and disadvantages of Sevo?
Advantages-Rapid induction/recovery
Minimal airway irritation
Disadvantages-Potential renal concerns ( compound A)
What are the advantages and disadvantages of Iso?
Advantages-Relatively slower onset of action, Pungent odor
Disadvantages-Coronary steal effect
MAC of Iso
1.15
What are the advantages and disadvantages of Des?
Advantages-Rapid induction/recovery
Disadvantages-Airway irritation
MAC of des
6.0
What are the advantages (4) and disadvantages (6) of Nitrous Oxide?
Advantages-
-Analgesia,
-second gas effect,
-safe in malignant hypothermia susceptible patients,
-rapid induction/recovery
Disadvantages-Expansion of air-filled spaces, higher combustion risk, PONV, megaloblastic anemia, Chronic use may result in peripheral neuropathy, possible teratogen
MAC of Nitrous Oxide
105
True/FalseBlood pressure reduces from halothane, isoflurane, desflurane, sevoflurane
True, only NO seems to cause it to rise
When does HR increase on iso, des, sevo
Only if MAC is greater than 1.5
Cardiac contractility
All volatile agents cause a decrease in contractility
Volatile anesthetics impact on respiratory rate, TV, MV, and CO2 level
Most volatile anesthetics (except isoflurane)
1-Increased respiratory rate
2-Decreased tidal volume
3-Decreased minute ventilation
4-Produce a high carbon dioxide level
Which opioids are included in the Morphine group?
(10 meds)
Morphine
-Codeine
-Hydrocodone
-Oxycodone
-Oxymorphone
-Hydromorphone
-Nalbuphine
-Butorphanol
-Levophanol
-Pentazocine
Which opioids are included in the phenylpiperidine group?
-Meperidine
-Fentanyl
-Sufentanil
-Remfentanil
What is the mechanism of action of opioids?
-Agonist at various endogenous opioid receptors (Mu1, Mu2, delta, kappa, sigma) within the nociceptive pathways.
-Involves decreased presynaptic release of acetylcholine and substance P
What are the effects of opioids on the:
CNS
CV
Respiratory
GI
GU
What concerns do you have with opioids?
-Tolerance and dependence
-Chest Wall rigidity
-Crosses placenta
-Histamine release with morphine and meperidine
How do you reverse opioids?
Naloxone
-Adult dose is 0.04 to 0.4 mg IV; repeat dose or increase dose to 2 mg if no response.
-Pediatric dose: 0.001 to 0.005 mg/kg IV
Pseudoallergy of opioids
Minor symptoms of flushing, hives, diaphoresis, dysphagia, facial/airway swelling,
IV Meds-Bartbituates include
Pentobarbital, methohexital
What is the mechanism of action of barbiturates?
GABA potentiation, direction action on GABA, receptor chloride channels, some action on calcium ion channels
What is the induction/sedation dosage of barbituates
Induction: 1 to 1.5 mg/kg
Sedation: 0.75 to 1 mg/kg followed by 0.5 mg/kg every 2-5 minutes
Ketamine-MOA
(5 receptors)
Various receptors (NMDA agonist, opioid, monoaminergic, muscarinic, calcium ion channels)
What are the pharmacokinetics of Ketamine?
-High lipid solubility: Crosses blood-brain barrier easily
-Hepatic metabolism
What is the dosage of Ketamine
Induction: 1 to 4.5 mg/kg IV
Sedation (IV): 1 to 2 mg/kg IV followed by 0.25 to 0.5 mg/kg IV very 5 to 10 min
Sedation IM: 2 to 5 mg/kg IM
Indications for Ketamine
(3 pts)
-Dissociative anesthetic with analgesic properties
-Induction agent
-Sedation
Effects of Ketamine
CNS
CV
Respiratory
T/F: Ketamine contraindicated in head trauma
True, because it increased CBF and ICP
What can help mitigate the hallucinatory issues of Ketamine?
Benzodiazpines
T/F: Ketamine depresses respiratory rate significantly
False
T/F: Ketamine decreases secretions
False, it increases and so sometimes people pretreat with hypersalivation
Is Ketamine a bronchodilator or bronchoconstrictor
It is a bronchodilator
Benzodiapeines
Midazolam-Versed
Diazepam-Vallium
Lorazepam-Ativan
Alprazolam-Xanax
MOA of benzos
mediated by GABA
Are benzodiazepines anticonvulsants?
Yes, they are
Effects of Benzodiazepines
CNS
CV
Respiratory
Which drug decreases metabolism of Benzodiazpines
Erythromycin
What is the reversal agent for Benzos?
Flumazenil: Competitive Antagonist
Adult dose: 0.2 mg IV; repeated doses may be given at 1 minute intervals to a maximum of 3 mg
Pediatric Dose: 0.01 mg/kg may be repeated at 1 - minute intervals to a maximum dose of 1 mg
What is the danger of flumazenil?
the half life is less then benzodiazepines so the resection is possible of recurring.
Benzodiapines doses…What is the duration for Midazolam (Versed), Diazepam (Vallium), and Lorazepam (Ativan)
What is dexmedetomidine used for?
Sedation in short term in intubated patients?
MOA of dexmedetomidine?
alpha 2 adrenoceptor agonist
What are the effects of alpha, beta receptors.
Effects of dexmedetomidine
CNS
CV
Respiratory
What are the nueromuscular blockers used for?
Skeletal muscle relaxation during intubation, ventilation or during treatment of laryngospams refractory to positive pressure.
What are the depolarizing agents?
Succinylcholine
What are the non depolarizing agents
Rocuronium, Vecuronium, Cisatracurium
What is the reversal agent for neuromuscular blockers?
It is Neostigmine (Anticholinesterase, but this is only for nondepolarzing agents only)
What is neostigmine’s MOA
It inhibits acetyl cholinesterase, leading to a build up of acetylcholine within the neuromuscular junction (NMJ)
Dosage for Neostigmine
0.03 to 0.07 mg/kg over 1 minute